Porous resin film

TECHNICAL FIELD

[0001] The present invention relates to a porous resin film having excellent aqueous liquid absorbency and ink absorbency. The invention also relates to a recording medium which exhibits good ink jet recording properties and which allows the formation of a fine image.

BACKGROUND OF THE INVENTION

[0002] A film-based synthetic paper having excellent water resistance comprises a resin as a main component and has heretofore been mainly used for offset printing, seal printing using oil-based or UV curing ink, sublimation, or melt type heat transfer, etc. As the film-based synthetic paper has found more applications, however, there has been a growing demand for printing methods using an aqueous ink and aqueous paste for environmental protection purposes. To this end, synthetic paper having good absorption of aqueous ink, aqueous paste, or water, which acts as a solvent therefor, would be desirable.

[0003] The recent progress of multimedia techniques means that ink jet process printers have become popular for use in both business or consumer applications. The ink jet process printer can be easily provided in the form of a multi-color display, and it can easily provide a large image. Thus, it desirably reduces the printing cost. In particular, ink jet printers using aqueous ink, which has fewer environmental or safety problems as compared with oil-based ink, have become popular recently.

[0004] The ink jet printer has been widely used to obtain a hard copy with characters as well as images. Therefore, the printed image must be finer. The image fineness depends on the dryability of the ink printed on the recording medium. For example, when repeated printing is made on a plurality of recording medium sheets, other sheets of recording medium are often imposed on the printed recording medium. In this case, if the printed recording medium sheet has absorbed the ink insufficiently, the ink can transfer to the preceding recording medium sheet, causing image stain.

[0005] In order to enhance the fineness of image, a method has been widely employed which comprises coating an ink-receptive material that contains a hydrophilic resin or inorganic finely divided powder onto a recording medium such as plastic film or paper (Japanese Patent Laid-Open No. 1991-82589, Japanese Patent Laid-Open No. 1997-216456). A recording medium for ink jet recording having an ink-receptive layer mainly composed of a hydrophilic resin formed by heat lamination or extrusion lamination has also been proposed (Japanese Patent Laid-Open No. 1996-12871, Japanese Patent Laid-Open No. 1997-1920). However, the recording media formed by these methods have the disadvantage in that when the ejected amount of ink is great, the media cannot absorb the ink sufficiently, which requires that the thickness of the coat layer be increased, and which requires a plurality of coating steps.

[0006] An aim of the invention is to solve the problems of the conventional techniques. In other words, an aim of the invention is to provide a porous resin film having good water absorption from aqueous inks or aqueous pastes and a recording medium which can absorb ink without density unevenness even if solid printing is carried out in which the ejected amount of ink is great in ink jet recording. Another aim of the invention is to provide a porous resin film constituting such a recording medium having excellent properties.

DISCLOSURE OF THE INVENTION

[0007] The inventors made extensive studies for the purpose of solving the aforementioned problems. As a result, it was found that a porous resin film comprising a thermoplastic resin and an inorganic and/or organic finely divided powder treated with a specific surface treating agent and having a liquid absorption capacity of not smaller than 0.5 ml/m2 as measured by “Japan TAPPI No. 51-87” exhibits good aqueous liquid absorbency and, when it has a surface contact angle of not greater than 110°, can absorb ink without density unevenness even if the elected amount of ink is great and thus can be preferably used as a recording medium for ink jet recording or the like. Thus, the invention has been worked out.

[0008] In other words, the invention lies in a porous resin film comprising a thermoplastic resin and an inorganic and/or organic finely divided powder treated with a specific surface treating agent and having a liquid absorption capacity of not smaller than 0.5 ml/m2 as measured by “Japan TAPPI No. 51-87”. In a preferred embodiment, the average contact angle of the film with respect to water is not greater than 110°. More preferably, the porous resin film has pores in the surface and the interior thereof and exhibits a porosity of not smaller than 10%.

[0009] In a preferred embodiment, the film preferably has pores in the surface layer in an amount of 1×106/m2, and the average diameter of the pores in the surface layer is preferably from 0.01 to 50 μm. Further, it is preferred that at least a part of the inorganic or organic finely divided powder be present in the pores in the surface layer and/or the interior of the film.

[0010] The thermoplastic resin is preferably a polyolefin-based resin, and the inorganic or organic finely divided powder preferably has an average particle diameter of from 0.01 μm to 20 μm. The specific surface area of the inorganic or organic finely divided powder preferably falls within a range of not smaller than 0.5 m2/g.

[0011] Referring to a preferred embodiment of the mixing proportion of the constituents, the content of the thermoplastic resin is from 30 to 90% by weight, the content of the surface-treated inorganic or organic finely divided powder is from 10 to 70% by weight, and the proportion of the surface treating agent is from 0.01 to 40 parts by weight based on 100 parts by weight of the inorganic and/or organic finely divided powder.

[0012] The surface treating agent preferably exhibits an HLB value, which indicates the balance between inorganic properties and organic properties, of from 5 to 100. Specific examples of such a surface treating agent include sulfonate having an alkyl group having from 4 to 40 carbon atoms, and quaternary ammonium compound having an alkyl group having from 4 to 40 carbon atoms.

[0013] In another preferred embodiment, the porous resin film is stretched. The invention includes a laminated film comprising a porous resin film layer provided on at least one surface of a substrate, a recording medium comprising same, and an ink jet recording medium comprising a colorant-fixing layer provided thereon.

[0014] In another preferred embodiment, the porous resin film is stretched. The invention includes a laminated film comprising a porous resin film layer provided on at least one surface of a substrate, a recording medium comprising same, and an ink jet recording medium comprising an ink-receptive layer provided thereon.

[0015] The ink-receptive layer preferably comprises an inorganic filler of not greater than 350 nm and a binder resin incorporated therein in an amount of from 70 to 95% by weight and from 5 to 30% by weight, respectively. The inorganic filler is preferably an amorphous silica and/or alumina and/or alumina hydrate, and in particular, the amorphous silica is obtained by agglomerating primary particles having an average diameter of from 1 nm to 10 nm. The amorphous silica is preferably a cationically treated silica.

[0016] The alumina is preferably δ-alumina, and the alumina hydrate is preferably pseudo-boehmite.

[0017] The ink-receptive layer preferably comprises a crosslinking agent and an ink fixing agent incorporated therein each in an amount of from 1 to 20% by weight.

[0018] A top coat layer is preferably provided on the ink-receptive layer, and the surface gloss of the top coat layer is preferably not smaller than 50% (as measured at 60° according to JIS-8741). The top coat layer preferably comprises an inorganic filler having an average particle diameter of not greater than 350 nm and a binder resin and an ink fixing agent incorporated therein in an amount of from 70 to 95% by weight and from 5 to 30% by weight and from 1 to 20% by weight, respectively.

BEST MODE FOR CARRYING OUT THE INVENTION

[0019] The porous resin film and recording medium of the invention will be further described hereinafter.

[0020] The liquid absorption capacity of the porous resin film of the invention is not smaller than 0.5 ml/m2 preferably from 3 to 2,600 ml/m2, more preferably from 5 to 100 ml/m2, still more preferably from 7 to 100 ml/m2.

[0021] When the liquid absorption capacity of the porous resin film falls below 0.5 ml/m2, the porous resin film exhibits an insufficient absorption of aqueous ink and aqueous paste. Since it is also necessary that the thickness of the porous resin film be taken into account to increase the absorption, the upper limit of the liquid absorption capacity is properly predetermined depending on the purpose.

[0022] The liquid absorption capacity of the porous resin film of the invention is measured according to “Japan TAPPI No. 51-87” (JAPAN TAPPI, paper pulp testing method No. 51-87; Bristow Method). In the present invention, the value measured in 2 seconds of absorption time is defined as liquid absorption capacity. The solvent used in the measurement is obtained by adding a coloring dye to 100% by weight of a mixture of 70% by weight of water and 30% by weight of ethylene glycol. As the coloring dye malachite green or the like is used in an amount of about 2 parts by weight based on 100 parts by weight of the mixed solvent, but the kind and amount of the coloring dye to be used is not specifically limited so far as they do not change drastically the surface tension of the solvent used in the measurement.

[0023] The measuring instrument may be, e.g., a liquid absorbency testing machine produced by Kumagai Riki Kogyo K.K.

[0024] The greater the liquid absorption capacity in a short period of absorption time is, the less likely that an aqueous paste, if used, can come out from the edge of paper. In the present invention, the liquid absorption capacity in 40 milliseconds is preferably not smaller than 0.8 ml/M2, more preferably from 1 to 500 ml/m2.

[0025] The greater the liquid absorption speed measured with the measurement of the aforementioned liquid absorption capacity is, the better the results of absorption by and drying of color-imposed area tend to be. In the present invention, the absorption speed between 20 milliseconds to 400 milliseconds is normally not smaller than 0.02 ml/{m2·(ms)1/2}, preferably from 0.1 to 100 ml/{m2·(ms)1/2}.

[0026] The surface contact angle of the porous resin film of the present invention with respect to water is not greater than 110°, preferably from 0 to 100°, more preferably from 0 to 90°.

[0027] When the surface contact angle of the porous resin film exceeds 100°, the penetration of a liquid such as paste comprising an aqueous ink or aqueous medium is not sufficient. From the standpoint of the requirements that the spread of an aqueous ink droplet in the direction parallel to the surface of film and the penetration of the aqueous ink droplet into the film in the thickness direction be balanced, there can be a proper range of contact angle, and the contact angle is properly predetermined according to the type of ink.

[0028] The surface contact angle of the film of the invention with respect to water is measured by dropping purified water onto the surface of the film, and then measuring the contact angle of the film after 1 minute. Ten measurements are made on one specimen. Once measured, the specimen is replaced by an unmeasured specimen which is not yet wet with purified water for measurement of contact angle. These measurements are then averaged to determine the contact angle with water. An example of commercially available contact angle meter which can be used to measure the contact angle of the present invention is a Type CA-D contact angle meter produced by KYOWA INTERFACE SCIENCE CORPORATION LIMITED.

[0029] The smaller the “difference between maximum value and minimum value” in the ten measurements of contact angle is, the more uniform the absorption of the ink or the liquid comprising an aqueous medium tends to be and the better is the print quality given by the printing medium. By way of example, the difference between maximum value and minimum value is not greater than 40°, preferably not greater than 30′, more preferably not greater than 20°.

[0030] The porous resin film of the present invention has fine pores in the surface thereof and absorbs an aqueous ink or aqueous liquid in contact with the surface through the pores.

[0031] The number and shape of the pores in the surface of the porous resin film and the presence of at least a part of the inorganic and/or organic finely divided powder in the surface pores can be determined by observation under an electron microscope.

[0032] The shape of pores in the surface of the porous resin film can be observed by cutting an arbitrary part out of the porous resin film specimen, sticking the specimen to an observation specimen carrier, vacuum-evaporating gold, gold-palladium or the like onto the surface of the specimen to be observed, and then observing the specimen under a Type S-2400 scanning electron microscope produced by HITACHI LTD. or the like at any magnification power allowing easy observation to determine the number, size and shape of pores. The number of pores per unit area on the surface of the porous resin film is not smaller than 1×106/m2, preferably not smaller than 1×107/m2, more preferably not smaller than 1×108/m2 from the standpoint of enhancement of absorption of aqueous liquid. From the standpoint of enhancement of surface strength to a higher level, it is preferably not greater than 1×1015/m2, more preferably not greater than 1×1012/m2.

[0033] The shape of pores in the vicinity of the surface of the porous resin film can vary from circular to ellipsoidal. The average [(L+M)/2] of measurements of the maximum diameter (L) of each of the pores and the maximum diameter (M) in the direction perpendicular thereto is defined to be the average diameter of the pore. The measurement is repeatedly made on at least 20 surface pores, and the average of the measurements is defined to be the average diameter of pores in the surface of the porous resin film. From the standpoint of enhancement of liquid absorbency to a higher level, the average diameter is preferably not smaller than 0.01 μm, more preferably not smaller than 0.1 μm, even more preferably not smaller than 1 μm. In order to enhance the surface strength of the porous resin film to a higher level, the average diameter is not greater than 50 μm, preferably not greater than 30 μm, more preferably not greater than 20 μm.

[0034] Preferably, at least a partr preferably not less than about 30% of the pores in the surface layer and in its vicinity has an inorganic and/or organic finely divided powder present in the interior thereof and its surrounding. As the number of such pores increases, the absorbency tends to increase.

[0035] The porous resin film of the invention has a porous structure with numerous fine pores in the interior thereof, and from the standpoint of enhancement of absorption and dryability of aqueous ink, the porosity thereof is not smaller than 10%, preferably from 20 to 75%, more preferably from 30 to 65%. When the porosity is not greater than 75%, the strength of the film material is on a good level.

[0036] Preferably, at least a part of the internal pores has an inorganic and/or organic finely divided powder present in the interior thereof and its surrounding. As the number of such pores increases, the absorbency tends to increase.

[0037] The presence of pores in the interior of the porous resin film and the presence of an inorganic and/or organic finely divided powder in the internal pores can be confirmed by observing the section of the film under an electron microscope. The porosity in the present description indicates the porosity represented by the following equation (1) or the percent area proportion (%) of pores in the region on the section observed under an electron microscope.

Porosity
(%)=100 (ρ0−ρ)/ρ0 (1)

[0038] (ρ0: Density of nonporous portion of porous resin film, ρ: Density of porous resin film)

[0039] In some detail, the porous resin film is embedded in an epoxy resin which is then solidified, cut by a microtome so that sections are formed in the direction parallel to the thickness direction and in the direction perpendicular to the surface of the film, respectively, metallized on the sections, and then observed on the sections at an arbitrary power of magnification allowing easy observation, e.g., from 500 to 2,000. By way of example, the region thus observed is photographed. The photograph of pores is then traced to a tracing film. The drawing obtained by smearing away the area of pores can then be image-processed by an image analyzer (LUZEX IID, produced by NIRECO CORPORATION) to determine the percent area of pores from which the porosity can be calculated. In the case of a laminated film having a porous resin film of the present invention provided on the surface thereof, the thickness and basis weight of the porous resin film of the present invention are calculated from the thickness and basis weight (g/m2) of the laminated film and the portion obtained by excluding the porous resin film of the present invention from the laminated film to determine the density (ρ). The density (ρ0) of the nonporous portion is determined from the formulation of the constituents. Then, the porosity can be determined by the equation (1).

[0040] The shape or dimension of the internal pores can be observed at a power of magnification allowing easy observation under a scanning electron microscope, e.g., 500 to 2,000. The dimension of the internal pores is determined by averaging the measurements of dimension of at least 10 internal pores in the surface direction and thickness direction.

[0041] The average dimension of the pores in the porous resin film in the surface direction is from 0.1 μm to 1,000 μm, preferably from 1 μm to 500 μm. From the standpoint of enhancement of the mechanical strength of the porous resin film to a higher level, the maximum dimension of the pores in the surface direction is preferably not greater than 1,000 μm. From the standpoint of enhancement of absorbency of aqueous liquid to a higher level, the maximum dimension of the pores in the surface direction is preferably not smaller than 0.1 μm.

[0042] The average dimension of the pores in the porous resin film in the thickness direction is normally from 0.01 μm to 50 μm, preferably from 0.1 μm to 10 μm. From the standpoint of enhancement of absorbency of aqueous liquid, the dimension of the pores in the thickness direction is preferably greater, but the upper limit of the pore dimension in the thickness direction can be predetermined depending on the purpose to provide the film with a proper mechanical strength.

[0043] <Formulation and Preparation Method of Porous Resin Film>

[0044] The porous resin film of the present invention comprises in combination a thermoplastic resin, an inorganic and/or organic finely divided powder, and a surface treating agent as constituent components.

[0045] Examples of the thermoplastic resin to be used in the porous resin film of the present invention include ethylene-based resin such as high density polyethylene, middle density polyethylene and low density polyethylene, propylene-based resin, polyolefin-based resin such as polymethyl-1-pentene and ethylene-cyclic olefin copolymer, polyamide-based resin such as nylon-6, nylon-6,6, nylon-6,10 and nylon-6,12, thermoplastic polyester-based resin such as polyethylene terephthalate, copolymer thereof, polyethylene naphthalate and aliphatic polyester, and thermoplastic resin such as polycarbonate, atactic polystyrene, syndiotactic polystyrene and polyphenylene sulfide. Two or more of these thermoplastic resins may be used in admixture.

[0046] Preferred among these thermoplastic resins is an ethylene-based resin or a polyolefin-based resin such as propylene-based resin, more preferably propylene-based resin from the standpoint of chemical resistance, low specific gravity, cost, etc. Examples of the propylene-based resin include isotactic polymer or syndiotactic polymer obtained by homopolymerization of propylene. Alternatively, a copolymer comprising as main component a polypropylene having various stereoregularities obtained by the copolymerization of α-olefin such as ethylene, 1-butene, 1-hexene, 1-heptene and 4-methyl-1-pentene with propylene may be used. The copolymer may be in the form of binary or ternary or higher system or may be either a random copolymer or a block copolymer. The propylene-based resin preferably comprises a resin having a melting point lower than that of propylene hompolymer incorporated therein in an amount of from 2 to 25% by weight. Examples of such a resin having a low melting point include high density or low density polyethylene.

[0047] The organic or inorganic finely divided powder to be used in the porous resin film of the present invention is not specifically limited, but specific examples of the organic or inorganic finely divided powder will be given below.

[0048] Examples of the inorganic finely divided powder include heavy calcium carbonate, light calcium carbonate, agglomerated light calcium carbonate, silica having various pore volumes, zeolite, clay, talc, titanium oxide, barium sulfate, zinc oxide, magnesium oxide, diatomaceous earth, silicon oxide, composite inorganic finely divided powder having a hydroxyl group-containing inorganic finely divided powder such as silica as nucleus surrounded by an aluminum oxide or hydroxide, etc. Among these inorganic finely divided powders, heavy calcium carbonate, clay and diatomaceous earth are preferably used because they are inexpensive and have good pore-forming properties if the film is stretched.

[0049] The organic finely divided powder is selected from non-compatible organic finely divided powders having a higher melting point or glass transition point than that of the thermoplastic resin to be used in the porous resin film of the present invention for the purpose of forming pores. Specific examples of the organic finely divided powder include polyethylene terephthalate, polybutylene terephthalate, polyamide, polycarbonate, polyethylene naphthalate, polystyrene, polymer or copolymer of acrylic acid ester or methacrylic acid ester, melamine resin, polyethylene sulfite, polyimide, polyethyl ether ketone, polyphenylene sulfide, homopolymer of cyclic olefin, copolymer of cyclic olefin with ethylene, etc. An organic finely divided powder having a melting point of from 120° C. to 300° C. or a glass transition temperature of from 120° C. to 280° C. is preferably used.

[0050] Preferred among inorganic finely divided powder and organic finely divided powder is inorganic finely divided powder because it generates little amount of heat when combusted.

[0051] The average particle diameter of the inorganic finely divided powder or organic finely divided powder is preferably from 0.01 μm to 20 μm, more preferably from 0.1 μm to 10 μm, even more preferably from 0.5 μm to 10 μm. The average particle diameter of the inorganic finely divided powder or organic finely divided powder is preferably not smaller than 0.01 μm from the standpoint of ease of mixing with the thermoplastic resin. In the case where the porous resin film is stretched to form pores in the interior thereof, enhancing the absorbency thereof, the average particle diameter of the inorganic finely divided powder or organic finely divided powder is preferably not greater than 20 μm from the standpoint of difficulty in the occurrence of troubles such as sheet breakage and deterioration of strength of surface layer during stretching.

[0052] The particle diameter of the inorganic finely divided powder or organic finely divided powder can be determined by the particle diameter corresponding to 50% of cumulation of particle diameter (50% cumulative particle diameter) measured by a particle diameter meter, e.g., laser diffraction type particle diameter meter “Microtrack” (produced by NIKKISO CO., LTD.). Further, the particle diameter of finely divided powder dispersed in the thermoplastic resin by melt kneading and dispersion can be determined as an average value by measuring at least 10 particles on the section of the porous resin film under an electron microscope.

[0053] The specific surface area of the inorganic finely divided powder or organic finely divided powder is measured by BET method and is, by way of example, preferably from 0.1 to 1,000 m2/g, more preferably from 0.2 to 500 m2/g, even more preferably from 0.5 to 100 m2/g.

[0054] When an inorganic finely divided powder or organic finely divided powder having a large specific surface area is used, the absorption of an aqueous solvent or ink tends to improve. In the case where the mixing and dispersion with the hydrophilic thermoplastic resin or non-hydrophilic thermoplastic resin tends to cause trouble such as insufficient dispersion due to classification and foaming due to entrained air, the upper limit of specific surface area suitable for use is properly predetermined. Moreover, inorganic or organic finely divided powders having various oil absorptions can be used, and, by way of example, the oil absorption (JIS K5101-1991, etc.) of the inorganic or organic finely divided powder is from 1 to 300 ml/100 g, preferably from 10 to 200 ml/100 g.

[0055] As the organic finely divided powder or inorganic finely divided powder to be used in the porous resin film of the invention there may be singly selected and used one among those described above or selected or used in combination two or more among those described above. In the case where two or more of inorganic or organic finely divided powders are used in combination, an organic finely divided powder and an inorganic finely divided powder may be used in combination.

[0056] The surface treating agent of the invention exhibits, by way of example, an HLB value of from 5 to 100, preferably from 5.5 to 50. A surface treating agent having an HLB value falling within the aforementioned range greatly improves the absorbency of aqueous solvent or aqueous ink by the porous resin film of the invention.

[0057] The HLB value of the invention can be determined by the method described in Oda, “Teijin Times”, 22, No. 9 (1952), Oda, Teramura, “Kaimen Kasseizai no Gosei to Sono Ouyou (Synthesis and Application of Surface Active Agents)”, page 501, Maki Shoten, (1957), Fujimoto, “Shin Kaimen Kasseizai Nyumon (New Introduction to Surface Active Agents)”, pp. 197-198, SANYO CHEMICAL INDUSTRIES, LTD., (1981), etc. and indicates the ratio of inorganic properties to organic properties determined by the following equation.

[0058] HLB=10×sum of inorganic values/sum of organic values

[0059] The organic properties and inorganic properties can be determined by summing the organic and inorganic values of units constituting the molecule of the surface treating agent, respectively. The organic and inorganic values of units constituting the surface treating agent molecule are disclosed in Fujita, “Kagaku Jikkengaku, Yuki Kagakuhen, Ippan Sousahou(Chemical Experiment, Organic Chemistry, General Operation Method)”, page 511, Kawade Shobou (1952), Fujita, “Kagaku no Ryouiki (Chemical Region)”, 11, page 719, (1957), Fujimoto, “Shin Kaimen Kasseizai Nyumon (New Introduction to Surface Active Agents)”, pp. 197-198, SANYO CHEMICAL INDUSTRIES, LTD., (1981), etc.

[0060] The quaternary nitrogen atom in quaternary ammonium is considered identical with amine salt. Sodium sulfonate and potassium sulfonate are regarded as light metal salt. These light metal salts have an inorganic value of 500. The amine salt and ammonium salt are considered to have an inorganic value of 400.

[0061] Among known metal soaps are those having an inorganic value falling within the aforementioned range. However, these metal soaps can cause a white powder to be attached to the machine at a step of rendering the film porous. Therefore, these metal soaps are excluded from the scope of the invention.

[0062] Specific examples of the surface treating agent will be given below. These surface treating agents may be properly selected such that the effect of the invention can be exerted.

[0063] In other words, there may be used the following compounds:

[0064] (K) Sulfonate having a hydrocarbon group having from 4 to 40 carbon atoms;

[0065] (L) Phosphoric acid ester salt having a hydrocarbon group having from 4 to 40 carbon atoms, phosphoric acid mono- or diester salt of higher alcohol having from 4 to 40 carbon atoms, phosphoric acid ester salt of ethylene oxide adduct of higher alcohol having from 4 to 40 carbon atoms;

[0066] (M) Higher aliphatic alcohol, alkyl phenol, higher aliphatic amine or ethylene oxide adduct of higher aliphatic acid amide with from 4 to 40 carbon atoms having a molecular weight of not greater than about 3,000;

[0067] (N) Alkylbetaine or alkylsulfobetaine having a hydrocarbon group having from 4 to 40 carbon atoms;

[0068] (P) N-alkyl-α-, β- and γ-amino acid salt having an alkyl group having from 4 to 30 carbon atoms on nitrogen atom; and

[0069] (Q) Ammonium compound having at least one hydrocarbon group having from 4 to 40 carbon atoms

[0070] The term “salt” as used hereinabove and hereinafter indicates lithium salt, sodium salt, potassium salt, calcium salt, magnesium salt, primary to quaternary ammonium salt or primary to quaternary phosphonium salt. Preferred salts among these include lithium salt, sodium salt, potassium salt, and quaternary ammonium salt, more preferably sodium salt or potassium salt.

[0071] (K) Examples of the sulfonate having a hydrocarbon group having from 4 to 40 carbon atoms include sulfonate and sulfoalkane carboxylate having. a hydrocarbon group having a straight-chain, branched or cyclic structure having from 4 to 40, preferably from 8 to 20 carbon atoms. Specific examples' of these compounds include alkylbenzenesulfonate and naphthalenesulfonic acid salt having from 4 to 40, preferably from 8 to 20 carbon atoms, alkylnaphthalenesulfonic acid salt having a straight-chain, branched or cyclic structure having from 4 to 30, preferably from 8 to 20 carbon atoms, monosulfonate or disulfonate of diphenylether or biphenyl having an alkyl group having a straight-chain or branched structure having from 1 to 30, preferably from 8 to 20 carbon atoms, alkanesulfonic acid salt having a straight-chain, branched or cyclic structure having from 1 to 30, preferably from 8 to 20 carbon atoms, alkylsulfuric acid ester salt having from 1 to 30, preferably from 8 to 20 carbon atoms, sulfoalkanecarboxylic acid ester salt, sulfonic acid salt of alkylene oxide adduct of alkyl alcohol having from 8 to 30, preferably from 10 to 20 carbon atoms, etc

[0072] Specific examples of these compounds include alkanesulfonic acid or aromatic sulfonic acid, i.e., octanesulfonic acid salt, dodecanesulfonic acid salt, hexadecanesulfonic acid salt, octadecanesulfonic acid salt, 1- or 2-dodecylbenzenesulfonic acid salt, 1- or 2-hexadecylbenzenesulfonic acid salt, 1- or 2-octadecylbenzenesulfonic acid salt, various isomers of naphthalenesulfonic acid salt, various isomers of dodecylnaphthalenesulfonic acid salt, β-naphthalenesulfonic acid-formalin condensate salt, various isomers of octylbiphenylsulfonic acid salt, dodecylbiphenylsulfonic acid salt, various isomers of dodecylphenoxybenzenesulfonic acid salt, dodecyldiphenylether disulfonic acid salt, dodecyl lignin sulfonic acid salt, alkylsulfuric acid ester salt, i.e., dodecylsulfuric acid salt, hexadecylsulfuric acid salt, sulfoalkanecarboxylic acid salt, i.e., sulfosuccinic acid dialkylester the alkyl moiety of which has a straight-chain, branched or cyclic structure having from 1 to 30, preferably from 4 to 20 carbon atoms, e.g., sulfosuccinic acid di(2-ethylhexyl) salt, N-methyl-N-(2-sulfoethyl)alkylamide salt (alkyl group has from 1 to 30, preferably from 12 to 18 carbon atoms) (e.g., amide compound derived from N-methyltaurin and oleic acid), 2-sulfoethylester salt of carboxylic acid having from 1 to 30, preferably from 10 to 18 carbon atoms, laurylsulfuric acid triethanolamine, laurylsulfuric acid ammonium, polyoxyethylene laurylsulfuric acid salt, polyoxyethylene cetylsulfuric acid salt, sulfonate of alkylene oxide adduct of alkyl alcohol having from 8 to 30, preferably from 10 to 20 carbon atoms (e.g., sulfuric acid ester salt of ethylene oxide adduct of lauryl alcohol, sulfuric acid ester salt of ethylene oxide adduct of cetyl alcohol, sulfuric acid ester salt of ethylene oxide adduct of stearyl alcohol), etc.

[0073] (L) Phosphoric acid mono- or diester salt or phosphoric acid triester having a hydrocarbon group having a straight-chain, branched or cyclic structure having from 4 to 40, preferably from 8 to 20 carbon atoms. Specific examples of such compounds include phosphoric acid dodecyl disodium salt or dipotassium salt, phosphoric acid hexadecyl disodium salt or dipotassium salt, phosphoric acid didodecyl disodium salt or dipotassium salt, phosphoric acid dihexadecyl sodium salt or potassium salt, phosphoric acid triester of ethylene oxide adduct of dodecyl alcohol, etc.

[0074] (M) Higher aliphatic alcohol, alkyl phenol, higher aliphatic amine or ethylene oxide adduct of higher aliphatic acid amide with from 4 to 40 carbon atoms having a molecular weight of not greater than about 3,000, preferably not greater than 1,000. Specific examples of such compounds include ethylene oxide adduct of lauryl alcohol, ethylene oxide adduct of cetyl alcohol, ethylene oxide adduct of stearyl alcohol, ethylene oxide adduct of octyl phenol, ethylene oxide adduct of dodecyl phenol, ethylene oxide adduct of stearic acid, ethylene oxide adduct of oleic acid, ethylene oxide adduct of lauric acid, ethylene oxide adduct of laurylamine, ethylene oxide adduct of stearylamine, ethylene oxide adduct of laurylic acid amide, ethylene oxide adduct of stearic acid amide, ethylene oxide adduct of oleic acid amide, etc.

[0075] (N) Alkylbetaine or alkylsulfobetaine having a hydrocarbon group having from 4 to 40, preferably from 10 to 20 carbon atoms. Specific examples of such compounds include lauryl dimethylbetaine, stearyl dimethylbetaine, dodecyl dimethyl(3-sulfopropyl)ammonium inner salt, cetyl dimethyl(3-sulfopropyl)ammonium inner salt, stearyl dimethyl(3-sulfopropyl)ammonium inner salt, 2-octyl-N-carboxyethyl-N-hydroxyethylimidazolinium betaine, 2-lauryl-N-carboxymethyl-N-hydroxyethylimidazolinium betaine, etc.

[0076] (P) N-alkyl-α-, β- and ƒÁ-amino acid salt having an alkyl group having from 4 to 30, preferably from 10 to 20 carbon atoms on nitrogen atom. Specific examples of such a compound include laurylaminopropionic acid, cetylaminopropionic acid, stearylaminopropionic acid, and salt thereof, i.e., laurylaminopropionic acid salt, cetylaminopropionic acid salt, stearylaminopropionic acid salt, etc.

[0077] (Q) Ammonium compound having at least one hydrocarbon group having from 4 to 40, preferably from 10 to 20 carbon atoms. Examples of the ammonium compound include those represented by the following general formula (I).

R1XN+R2R3R4Y− (I)

[0078] X: group such as —CH2—, —CONHCH2CH2—, —CONHCH2CH2CH2—, —NHCOCH2—, —NHCOCH2CH2—, —COOCH2CH2—, —COOCH2CH2CH2—, —OCOCH2— and —OCOCH2CH2—;

[0079] R1: alkyl group having from 10 to 20 carbon atoms;

[0080] R2: alkyl group having from 1 to 20 carbon atoms;

[0081] R3: methyl, ethyl or polyalkyeneoxy group;

[0082] R4: methyl, ethyl or polyalkyleneoxy group; and

[0083] Y−: anion selected from the group consisting of chloride ion, bromide ion, hydroxide ion, methanesulfonic acid ion, ethanesulfonic acid ion, methylsulfuric acid ion, ethylsulfuric acid ion, nitric acid ion, sulfuric acid ion and acetic acid ion

[0084] Specific examples of R1 include undecyl group, lauryl group, tridecyl group, cetyl group, pentadecyl group, stearyl group, and oleyl group. Specific examples Of R2 include methyl group, ethyl group, propyl group, lauryl group, cetyl group, and stearyl group. Specific examples of R3 and R4 other than methyl group and ethyl group include 2-hydroxyethyl group, 2-(2-hydroxyethyl)ethyl group, trioxyethyleneoxy group, tetraoxyethyleneoxy group, pentaoxyethyleneoxy group, hexaoxyethyleneoxy group, etc.

[0085] Further examples of the compound (Q) include chloride, bromide, hydroxide, methosulfate, ethosulfate, nitrate, sulfate and acetate of ammonium derived from laurylamine and coconut amine, lauryl dimethyl benzyl ammonium, imidazolinium-based quaternary ammonium, polydimethyl diallyl ammonium, polymethyl diallyl ammonium, polydiallyl ammonium, dimethyl diallyl ammonium-acrylamide copolymer, methyl diallyl ammonium-acrylamide copolymer, diallyl ammonium-acrylamide copolymer, etc. Preferred ammonium compounds are those that contain a hydrocarbon group having from 10 to 20 carbon atoms represented by the foregoing general formula (I).

[0086] Preferred among these compounds is sulfonic acid salt containing a hydrocarbon group having from 4 to 40 carbon atoms (K) or ammonium compound containing at least one hydrocarbon group preferably having from 10 to 20 carbon atoms (Q). Preferred examples of these compounds include sodium or potassium salt of dodecanesulfonic acid, sodium or potassium salt of di(2-ethylhexyl)sulfosuccinate, sodium or potassium salt of dodecylbenzenesulfonic acid, lauryl trimethyl ammonium chloride, lauryl dimethyl ethyl ammonium ethosulfate, lauryl trimethyl ammonium methosulfate 3-(lauroylamino)propyldimethyl(2-hydroxyethyl)ammonium nitrate, and dilauryldi(polyoxyethyleneoxy)ammonium chloride which has oxyethylene groups added in a total amount of from 2 to 4.

[0087] The surface treating agents may be used in combination with a auxiliary surface treating agent so far as their effects cannot be impaired. The amount of the auxiliary surface treating agent is not greater than 30% by weight, preferably not greater than 20% by weight based on the sum of the amount of the surface treating agent and the auxiliary surface treating agent.

[0088] Specific examples of the auxiliary surface treating agent (R) include amide compound of higher aliphatic acid and higher alcohol having from 4 to 40 carbon atoms. Specific examples of these compounds include stearic acid amide, ethylenebisstearic acid amide, N-methylstearic acid amide, N-ethylstearic acid amide, oleic acid amide, behenic acid amide, lauroyl monoethanolamide, stearoyl monoethanolamide, lauryl diethanolamine, stearyl diethanolamine, lauryl alcohol, stearyl alcohol, etc.

[0089] (Process for Surface Treatment of Inorganic and/or Organic Finely Divided Powder)

[0090] As the process for the preparation of the inorganic and/or organic finely divided powder surface-treated with a surface treating agent in the invention there may be used various known processes without any special restriction. The kind of the mixing machine to be used and the mixing temperature and time may be properly predetermined according to the properties and physical properties of the components used. The L/D (axial length/axial diameter) ratio of the mixing machine used, the shape, shearing speed and specific energy of the agitating blade, the retention time, the processing time, the processing temperature, etc. may be predetermined according to the properties of the—components used.

[0091] Specific examples of the process for the preparation of the inorganic and/or organic finely divided powder surface-treated with a surface treating agent include:

[0092] (I) Process which comprises adding the aforementioned surface treating agent in the form of powder, liquid, paste or solution or dispersion in water or an organic solvent or in the form of solution or dispersion having a proper concentration obtained by removing part of solvent or no solvent from the surface treating agent, if it has been prepared using a solvent, to the finely divided powder, and then stirring the mixture at a low or high speed to attach the surface treating agent to the periphery of the finely divided powder;

[0093] (II) Process which comprises adding a surface treating agent to a finely divided powder suspended in water or an organic solvent, or adding a finely divided powder to a solution of the aforementioned cationic polymer-based surface treating agent in a solvent, mixing the two components, removing the solvent from the mixture, and then drying the mixture to attach the surface treating agent to the periphery of the finely divided powder;

[0094] (III) Process which comprises adding a surface treating agent to a finely divided powder before or during grinding, if the finely divided powder is prepared by a dry or wet grinding method, so that the surface treating agent is attached to the periphery of the finely divided powder during grinding;

[0095] (IV) Process which comprises adding a necessary amount of a surface treating agent to a part of the finely divided powder to be used in a concentration higher than the required concentration to prepare a master batch made of finely divided powder and surface treating agent, mixing the master batch with the balance of the finely divided powder to attach the master batch to the periphery of the finely divided powder, and then mixing the finely divided powder with a thermoplastic resin;

[0096] (V) Process which comprises adding a surface treating agent in the form of powder, liquid, paste or solution or dispersion in a solvent to a finely divided powder before, during or after polymerization, if the finely divided powder is an organic finely divided powder prepared by polymerization, to attach the surface treating agent to the periphery of the organic finely divided powder; and

[0097] (VI) Process which, if the finely divided powder is an organic finely divided powder obtained by dispersing a finely divided powder in a thermoplastic resin continuous phase during melt kneading, comprises adding a surface treating agent to a thermoplastic resin and an undispersed organic finely divided powder or a mixture of thermoplastic resin and undispersed filler during melt kneading so that the surface treating agent is attached to the periphery of the organic finely divided powder while the organic finely divided powder is being finely dispersed during melt kneading.

[0098] In the case where the surface treating agent in the form of solution or dispersion in a solvent or paste is mixed with an inorganic and/or organic finely divided powder, the mixing temperature may be properly predetermined according to the properties of the finely divided powder or surface treating agent. By way of example, the mixing temperature is from room temperature to 120° C., and if drying is needed, from 40° C. to 120° C., preferably from 80° C. to 120° C. Alternatively, vacuum drying or drying with dried air or hot air may be employed as necessary.

[0099] (Proportion of Constituent Components)

[0100] Referring to preferred proportion of components constituting the porous resin film of the present invention, the content of the thermoplastic resin is from 30 to 90% by weight, the content of the surface-treated inorganic and/or organic finely divided powder is from 10 to 70% by weight, and the proportion of the surface treating agent is from 0.01 to 40 parts by weight based on 100 parts by weight of the inorganic and/or organic finely divided powder.

[0101] The content of the thermoplastic resin is more preferably from 30 to 60% by weight, even more preferably from 35 to 55% by weight. From the standpoint of further enhancement of the strength of the porous resin film (i), it is not smaller than 30 parts by weight, and in order to further enhance the absorption of aqueous solvent or ink, it is not greater than 90% by weight.

[0102] The amount of the surface-treated inorganic and/or organic finely divided powder is by way of example from 10 to 70% by weight. The amount of the inorganic finely divided powder is preferably from 40 to 70% by weight, more preferably from 45 to 65% by weight. In order to increase pores, it is preferred that the amount of the finely divided powder be greater. However, for the purpose of enhancing the surface strength of the porous resin film to a higher level, the amount of the finely divided powder is preferably not greater than 70% by weight. Most organic finely divided powders have a small specific gravity. The amount of the organic finely divided powder is preferably from 10 to 50% by weight, more preferably from 15 to 40% by weight.

[0103] The amount of the surface treating agent used varies with the purpose of the porous resin film. In practice, however, the amount of the surface treating agent to be used is from 0.01 to 40 parts by weight, preferably from 0.1 to 20 parts by weight, more preferably from 1 to 10 parts by weight based on 100 parts by weight of the inorganic or organic finely divided powder. From the standpoint of enhancement of absorption of aqueous solvent or aqueous ink, the amount of the surface treating agent used is preferably not smaller than 0.01 parts by weight. When the amount of the surface treating agent used exceeds 40 parts by weight, the effect of the surface treating agent reaches the upper limit. Accordingly, in order to make smooth operation in the mixing and/or melt kneading with the thermoplastic resin and the inorganic or organic finely divided powder without troubles such as agglomeration and maldispersion, the amount of the surface treating agent is preferably not greater than 20 parts by weight.

[0104] (Arbitrary components)

[0105] When these finely divided powders are kneaded with the thermoplastic resin, a dispersant, an oxidation inhibitor, a compatibilizer, a fire retardant, an ultraviolet stabilizer, a coloring pigment, etc. may be added as necessary. In the case where the porous resin film of the present invention is used as a durable material, an oxidation inhibitor, ultraviolet stabilizer, etc. are preferably added.

[0106] The porous resin film of the present invention may comprise a hydrophilic resin incorporated therein as an arbitrary additional component in addition to the aforementioned components so far as the effect of the present invention is not impaired.

[0107] The hydrophilic resin is not specifically limited so far as it is dissolved in or swells with water and becomes plastic at a temperature of not lower than ordinary temperature.

[0108] For example, polyvinyl-based resins such as polyvinyl alcohol, copolymer or crosslinked material thereof, polyvinyl pyrrolidone and copolymer thereof as synthetic resins, polyacrylic resins and salt thereof (e.g., sodium salt, potassium salt, lithium salt, primary to quaternary ammonium salt) such as polymer or copolymer of acrylic acid, methacrylic acid or maleic acid containing a hydroxyalkyl group such as 2-hydroxyethyl and 2-hydroxypropyl group or crosslinking product thereof, polyacrylamide or copolymer thereof, hydrolyzate of polymer or crosslinking product of acrylonitrile and polymer or copolymer of acrylic acid or methacrylic acid or crosslinking product thereof, resins or salt thereof (e.g., sodium salt, potassium salt, lithium salt, primary to quaternary ammonium salt) such as polymaleic acid or maleic acid copolymer or crosslinking product thereof, hydrolyzate of copolymer of vinyl acetate and methyl methacrylate, water-soluble nylon, urethane-based resin, i.e., water-soluble polyurethane, high water absorption polyurethane, thermoplastic polyurethane, polyalkylene oxide-based resins such as polyethylene oxide or copolymer thereof and polypropylene oxide or copolymer thereof, polyether amide, polyether ester amide, polyester polyol, polyvinylamine, polyallylamine or copolymer thereof, etc. may be used. Alternatively, the hydrophilic resin can be selected from those described in references such as “Kobunshi Kako”, No. 9, 1984, pp. 32-38. Among these hydrophilic resins, the polyalkylene oxide-based resins, which becomes plastic at a temperature of not lower than ordinary temperature and can be relatively easily formed into film, are preferably used.

[0109] various methods may be used for mixing the components constituting the porous resin film of the present invention. Thus, the method for mixing the components constituting the porous resin film of the present invention is not specifically limited. The mixing temperature and time are properly predetermined according to the properties of the components used.

[0110] Examples of the mixing method include a method which comprises mixing the components while being dissolved or dispersed in a solvent, and a melt-kneading method. The melt-kneading method gives a good production efficiency.

[0111] A method which comprises mixing a thermoplastic resin in the form of powder or pellet, an inorganic finely divided powder and/or organic finely divided powder and a surface treating agent in a Henschel mixer, ribbon blender, super mixer or the like, melt-kneading the mixture in a single-screw or twin-screw kneader, extruding the mixture into a strand form, and then cutting the strand to form pellets, or a method which comprises extruding the mixture into water, and then cutting the material with a rotary blade mounted on the forward end of the die may be employed. As the single-screw or twin-screw kneader to be used there may be selected one having various L/D (axial length/axial diameter) ratios, shear rate, specific energies, retention times, temperatures, etc. according to the properties of the components used.

[0112] The porous resin film and recording medium of the present invention can be prepared by using various methods known to those skilled in the art in combination. Any porous resin film or recording medium prepared by these known methods can be included in the scope of the present invention so far as it comprises a porous resin film satisfying the requirements of the present invention.

[0113] To prepare a porous resin film of the present invention having a liquid absorption capacity of not smaller than 0.5 ml/m2, any of the various film preparation techniques or a combination thereof may be used. For example, a film stretching method utilizing the formation of pores by stretching, a rolling method or calendering method involving the formation of pores during rolling, a foaming method using a foaming agent, a method using pore-containing particles, a solvent extraction method, a method involving dissolution and extraction of mixed components, etc. may be used. Preferred among these methods is the film stretching method.

[0114] In the case where the film stretching method is employed, it is not necessarily required that only the porous resin film of the present invention be stretched. For example, in the case where it is tried to finally prepare a (laminated) recording medium having the porous resin film of the present invention formed on a substrate layer, an unstretched porous resin film and a substrate layer may be laminated, and then together stretched. When these layers are previously laminated before combined stretching, it gives simplicity and reduced cost as compared with the case where these layers are separately stretched before being laminated. In addition, this method makes it easier to control the pores formed in the porous resin film of the present invention and the substrate layer. In particular, when the laminate is used as a recording medium, it is preferably controlled such that the porous resin film has more pores than the substrate layer to effectively act as a layer capable of improving ink absorbency.

[0115] The thermoplastic resin film forming the substrate layer may have a single layer structure, a two-layer structure consisting of a core layer and a surface layer, a three-layer structure comprising a surface layer provided on the both surfaces of a core layer or a multi-layer structure comprising other resin film layers interposed between the core layer and the surface layer and may be stretched at least monoaxially. In the case where the multi-layer structure film is stretched, the three-layer structure film may be stretched monoaxially all at the three layers, stretched monoaxially both at the surface layer and the core layer and biaxially at the back layer, stretched monoaxially at the surface layer, biaxially at the core layer and monoaxially at the back layer, stretched biaxially at the surface layer and monoaxially both at the core layer and the back layer, stretched monoaxially at the surface layer and biaxially both at the core layer and the back layer, stretched biaxially both at the surface layer and the core layer and monoaxially at the back layer or stretched biaxially all at the three layers. In the case of a structure having more layers, the number of stretching axes is arbitrarily combined.

[0116] As the thermoplastic resin, inorganic finely divided powder and organic finely divided powder to be used in the substrate layer there may be used materials similar to those used in the aforementioned porous resin film.

[0117] In the case where the thermoplastic resin layer is a single-layer polyolefin-based resin film comprising an inorganic and/or organic finely divided powder incorporated therein, the thermoplastic resin film layer normally comprises a polyolefin-based resin and an inorganic and/or organic finely divided powder in an amount of from 40 to 99.5% by weight and from 0.5 to 60% by weight, preferably from 50 to 97% by weight and from 3 to 50% by weight, respectively.

[0118] In the case where the thermoplastic resin film has a multi-layer structure and the core layer and surface layer comprise an inorganic and/or organic finely divided powder incorporated therein, the core layer normally comprises a polyolefin-based resin and an inorganic and/or organic finely divided powder incorporated therein in an amount of from 40 to 99.5% by weight and from 0.5 to 60% by weight, preferably from 50 to 97% by weight and from 3 to 50% by weight, respectively, and the surface layer normally comprises a polyolefin-based resin and an inorganic and/or organic finely divided powder incorporated therein in an amount of from 25 to 100% by weight and from 0 to 75% by weight, preferably from 30 to 97% by weight and from 3 to 70% by weight, respectively.

[0119] When the amount of the inorganic and/or organic finely divided powder incorporated in the core layer having a single-layer or multi-layer structure exceeds 60% by weight, the resin film which has been longitudinally stretched can easily break during crosswise stretching. When the amount of the inorganic and/or organic finely divided powder to be incorporated in the surface layer exceeds 75% by weight, the surface layer which has been crosswise stretched has a lowered surface strength and the surface layer can easily break due to mechanical in use to disadvantage.

[0120] For the stretching, various known methods can be employed. The stretching can be effected at a temperature of not lower than the glass transition point of the thermoplastic resin used in the case of amorphous resin or at a temperature suitable for thermoplastic resin from not lower than the glass transition point of the amorphous portion to not higher than the melting point of the crystalline portion in the case of crystalline resin. In some detail, the stretching can be accomplished by longitudinal stretching utilizing the difference in circumferential speed between rolls, rolling, crosswise stretching using a tenter oven, inflation stretching using a mandrel on tube-like film, simultaneous biaxial stretching using a tenter oven and a linear motor in combination or the like.

[0121] The draw ratio is not specifically limited and is properly predetermined taking into account the purpose of the porous resin film of the present invention and the properties of the thermoplastic resin. For example, in the case where a propylene homopolymer or copolymer is used as the thermoplastic resin, the draw ratio is from about 1.2 to 12, preferably from 2 to 10 for monoaxial stretching or from 1.5 to 60, preferably from 10 to 50 as calculated in terms of area for biaxial stretching. In the case where other thermoplastic resins are used, the draw ratio is from 1.2 to 10, preferably 2 to 7 for monoaxial stretching or from 1.5 to 20, preferably from 4 to 12 as calculated in terms of area for biaxial stretching.

[0122] Further, the film may be subjected to heat treatment at a high temperature as necessary. The stretching temperature is from 2 to 60° C. lower than the melting point of the thermoplastic resin used, and the stretching speed is preferably from 10 to 350 m/min.

[0123] The thickness of the porous resin film of the present invention is not specifically limited. For example, it is not smaller than 5 μm, preferably not smaller than 25 μm, more preferably not smaller than 30 μm from the standpoint of further enhancement of absorption of aqueous solvent or aqueous ink. The upper limit of the thickness of the porous resin film is properly predetermined by the required absorption of aqueous liquid. By way of example, it may be adjusted to not greater than 1,000 μm, preferably not greater than 500 μm, more preferably not greater than 300 μm.

[0124] The porous resin film of the present invention can be used as it is or may be laminated on another thermoplastic resin, laminated paper, pulp paper, nonwoven cloth, cloth, etc, before use. Examples of the another thermoplastic resin film on which the porous resin film of the present invention is laminated include transparent or opaque films such as polyester film, polyamide film and polyolefin film. In particular, a proper functional layer as described in the examples below can be formed on the porous resin film of the present invention to form a recording medium. For example, the porous resin film of the present invention can be formed as a surface layer on a substrate layer made of a thermoplastic resin film to prepare a recording medium. The recording medium comprising the porous resin film of the present invention as a surface layer is useful particularly as a recording medium for ink jet recording. The kind of the substrate layer is not specifically limited, but a film comprising a polypropylene-based resin and an inorganic finely divided powder incorporated therein may be exemplified.

[0125] The recording medium thus formed by laminating the porous resin film of the present invention with other films may have a total thickness of, e.g., from 50 μm to 1 mm.

[0126] The aforementioned porous resin film or a laminate comprising same may be subjected to surface oxidation treatment as necessary. There are some cases where surface oxidation treatment makes it possible to enhance the hydrophilicity or absorbency of the surface of the film or enhance the coatability of the film with an ink-fixing agent or ink-receptive layer or the adhesivity of the film with the substrate. As the surface oxidation treatment there may be used one selected from corona discharge treatment, flame treatment, plasma treatment, glow discharge treatment and ozone treatment, preferably corona treatment or flame treatment, more preferably corona treatment.

[0127] The amount of treatment is from 600 to 12,000 J/m2 (from 10 to 200 W·min/m2), preferably from 1,200 to 9,000 j/m2 (from 20 to 180 W·min/m2) in the case of corona treatment. In order to sufficiently exert the effect of corona discharge treatment, it is not smaller than 600 J/m2 (10 W·min/m2). When the amount of treatment exceeds 12,000 J/m2 (200 W·min/m2), the effect of treatment reaches the upper limit. Thus, the amount of treatment suffices if it is not greater than 12,000 J/m2 (200 W·min/m2). The amount of treatment is from 8,000 to 200,000 J/m2, preferably from 20,000 to 100,000 J/m2 in the case of flame treatment. In order to exert a definite effect of flame treatment, the amount of treatment is not smaller than 8,000 J/m2. When the amount of treatment exceeds 200,000 J/m2, the effect of treatment reaches the upper limit. Thus, the amount of treatment suffices if it is not greater than 200,000 J/m2.

[0128] In the case where the porous resin film of the present invention is used as a recording medium, the porous resin film of the present invention may have an ink-receptive layer for fixing a dye or pigment colorant formed on the surface thereof. The combination of such a colorant-fixing layer or ink-receptive layer with the porous resin film of the present invention having a good absorption of aqueous solvent makes it possible to reduce the occurrence of running, enhance the absorbency and reduce the thickness of the ink-receptive layer.

[0129] The ink-receptive layer acts to round the ink dot, thereby providing a sharper image as well as preventing the flow of colorant due to water or moisture. Accordingly, in the case where the porous resin film of the present invention is used as an ink jet recording medium, the ink-receptive layer is particularly useful.

[0130] (Ink-Receptive Layer)

[0131] In the present invention, an ink-receptive layer is provided to obtain water resistance in addition to ink absorbency. Preferably, an ink-receptive layer having a surface gloss (as measured at 60° according to JIS Z-8741) of not smaller than 40% is provided to obtain a high gloss.

[0132] The ink-receptive layer may have either a single-layer structure or a multi-layer structure consisting of two or more layers. In the case of multi-layer structure, the various layers may have the same or different formulations. In order to form a multi-layer structure, two or more layers may be coated at once or successively.

[0133] <Inorganic Filler>

[0134] The ink-receptive layer comprises an inorganic filler having an average particle diameter of not greater than 350 nm and a binder resin incorporated therein in an amount of from 70 to 95% by weight and from 5 to 30% by weight, respectively, for the purpose of enhancing ink absorbency and realizing a high gloss.

[0135] When an inorganic filler having an average particle diameter of not smaller than 350 nm is used, the resulting ink-receptive layer exhibits a drastically lowered surface gloss, which is undesirable.

[0136] Examples of the inorganic filler to be used in the present invention include colloidal silica, colloidal calcium carbonate, aluminum oxide, amorphous silica, pearl necklace-like colloidal silica, fibrous aluminum oxide, tabular aluminum oxide, alumina, alumina hydrate, etc.

[0137] Amorphous silica is preferred among the aforementioned inorganic fillers from the standpoint of ink jet printing ink absorbency or because of low cost. Also preferred among the aforementioned inorganic fillers is alumina or alumina hydrate because it has a positive charge on the surface of particle to fix the ink jet printing ink fairly.

[0138] In particular, to obtain a high gloss ink-receptive layer, amorphous silica obtained by agglomerating primary particles having an average diameter of from 1 to 10 nm is preferred.

[0139] An amorphous silica comprises agglomerated primary particles having an average diameter of from 1 to 50 nm. An amorphous silica having a primary particle diameter of from 1 to 10 nm is preferably used to enhance ink absorbency.

[0140] When an amorphous silica having a primary particle diameter of not smaller than 10 nm is used in the ink-receptive layer, the resulting ink-receptive layer exhibits a drastic deterioration of gloss and ink absorbency, which is undesirable. The reason why an amorphous silica falling within the scope of the present invention exhibits a high performance is unknown. However, this is presumably because the amorphous silica having a primary particle diameter of from 1 to 10 nm has a high gloss as well as has an increased gap between primary particles and hence an enhanced ink absorbency.

[0141] Processes for preparing amorphous silica can be roughly divided into two groups, i.e., dry process and wet process. In the present invention, silica prepared by any process can be used so far as it is an amorphous silica having a primary particle diameter of from 1 to 10 nm and an average particle diameter of not greater than 350 nm.

[0142] Alternatively, in the present invention, an amorphous silica having an average particle diameter of not greater than 350 nm obtained by crushing a commercially available amorphous silica having an average particle diameter of from 2 to 10 μm can be used. The method for crushing amorphous silica is not specifically limited. However, mechanical grinding using a grinder is preferably employed from the standpoint of uniformity. in quality and because it allows grinding at a reduced cost. Specific examples of the grinder include ultrasonic grinding, jet mill, sand grinder, roller mill, high speed rotary mill, etc.

[0143] Further, the amorphous silica to be used in the present invention is preferably subjected to cationic treatment on the surface thereof to enhance the fixability of an ink jet printing ink, which is anionic.

[0144] Cationic treatment is treatment for covering the surface of silica with a cationic chemical during grinding or preparation of silica. Examples of such a cationic chemical include inorganic metal salt, cationic coupling agent, cationic polymer, etc.

[0145] Specific examples of the inorganic metal salt include hydrates of inorganic metal oxide such as aluminum oxide hydrate, zirconium oxide hydrate and tin oxide hydrate, water-soluble inorganic metal salt such as aluminum hydroxide, aluminum sulfate, aluminum chloride, aluminum acetate, aluminum nitrate, zirconium sulfate, zirconium chloride and tin chloride, etc.

[0146] Specific examples of the cationic coupling agent include cationic silane coupling agent such as amino group-containing silane coupling agent and quaternary ammonium group-containing silane coupling agent, cationic zirconium coupling agent such as amino group-containing zirconium coupling agent and quaternary ammonium group-containing zirconium coupling agent, cationic titanium coupling agent such as amino group-containing titanium coupling agent and quaternary ammonium group-containing titanium coupling agent, and cationic glycidyl coupling agent such as amino group-containing glycidyl coupling agent and quaternary ammonium group-containing glycidyl coupling agent.

[0147] Specific examples of the cationic polymer include polyalkylene polyamine such as polyethyleneimine and polypropylene polyamine, derivative thereof, amino group-containing acrylic polymer, quaternary ammonium group-containing acrylic polymer, amino group-containing polyvinyl alcohol, quaternary ammonium group-containing polyvinyl alcohol, etc.

[0148] The average particle diameter and primary particle diameter of the inorganic filler used in the ink-receptive layer of the present invention can be measured by the same apparatus used in the measurement of the inorganic finely divided powder or organic finely divided powder in the aforementioned porous substrate.

[0149] Specific examples of alumina include α-alumina, β-alumina, γ-alumina, δ-alumina, η-alumina, θ-alumina, etc. From the standpoint of ink absorbency and gloss, δ-alumina is preferred.

[0150] Specific examples of the alumina hydrate include alumina hydrate having a pseudo-boehmite structure (pseudo-boehmite), alumina hydrate having an amorphous structure (amorphous alumina hydrate), etc. Pseudo-boehmite is preferred from the standpoint of ink absorbency and gloss.

[0151] <Binder resin>

[0152] In the ink-receptive layer of the present invention, a binder resin is used as an adhesive.

[0153] In the present invention, the ink-receptive layer comprises a binder resin incorporated therein as an adhesive in addition to the inorganic filler. Referring to the mixing proportion of inorganic filler and binder resin, the proportion of the organic filler and the binder resin are preferably from 70 to 95% by weight and from 5 to 30% by weight, respectively.

[0154] When the proportion of the inorganic filler exceeds 95% by weight, the resulting ink-receptive layer exhibits a drastically reduced adhesivity to the porous resin film. On the contrary, when the proportion of the inorganic filler falls below 70% by weight, the resulting ink-receptive layer exhibits a drastically reduced ink absorbency.

[0155] Specific examples of the binder resin employable herein include water-soluble resins such as polyvinyl alcohol, derivative thereof, polyvinyl pyrrolidone, polyacrylamide, hydroxyethyl cellulose, casein and starch, and water-insoluble resins such as urethane-based resin, ester-based resin, epoxy-based resin, ethylene-based resin, ethylene-vinyl acetate copolymer resin, vinyl acetate-based resin, vinyl chloride-based resin, vinyl chloride-vinyl acetate-based copolymer resin, vinylidene chloride-based resin, vinyl chloride-vinylidene copolymer resin, acrylic acid-based resin, methacrylic acid-based resin, polybutyral-based resin, silicon resin, nitrocellulose resin, styrene-acryl copolymer resin, styrene-butadiene-based copolymer resin and acrylonitrile-butadiene-based copolymer resin. The aforementioned water-soluble resin may be used in the form of aqueous solution, and the aforementioned water-insoluble resin may be used in the form of solution, emulsion or latex.

[0156] Preferred among the aforementioned binder resins is polyvinyl alcohol from the standpoint of compatibility with the inorganic filler or ink absorbency. In particular, from the standpoint of strength of coat film, a polyvinyl alcohol having a polymerization degree of not smaller than 3,000 and a saponification degree of from 80% to 95% is preferred. In the present invention, a crosslinking agent is preferably used in an amount of from 1 to 20% by weight based on the amount of the ink-receptive layer to enhance the water resistance of the binder resin. Specific examples of the crosslinking agent include urea-formaldehyde resin, melamine-formaldehyde resin, polyamide polyurea-formaldehyde resin, glyoxal, epoxy-based crosslinking agent, polyisocyanate resin, boric acid, borax, various borates, etc.

[0157] In addition, in the present invention, the ink-receptive layer preferably comprises an ink-fixing agent incorporated therein in an amount of from 1 to 20% by weight based on the amount of the ink-receptive layer to improve the ink fixability. Examples of the ink-fixing agent include inorganic metal salt, cationic coupling agent, cationic polymer, etc.

[0158] Specific examples of the inorganic metal salt, cationic coupling agent and cationic polymer include those described with reference to the cationic chemical used in the cationic treatment of the aforementioned amorphous silica.

[0159] The ink-receptive layer of the present invention may also comprise various auxiliaries such as dispersant, thickening agent, antifoaming agent, preservative, ultraviolet absorber, oxidation inhibitor and surface active agent, which are normally used in coated paper as necessary.

[0160] The coated amount of the ink-receptive layer of the present invention is properly predetermined according to the liquid absorption capacity of the porous resin film used as a support. This coated amount is preferably from 5 to 30 g/m2. When the coated amount of the ink-receptive layer falls below 5 g/m2, the resulting ink-receptive layer lacks gloss, oozing properties and water resistance. On the other hand, when the coated amount of the ink-receptive layer exceeds 30 g/m2, the resulting ink-receptive layer exhibits a satisfactory ink absorbency but exhibits deteriorated surface strength.

[0161] (Top Coat Layer)

[0162] In the present invention, for the purpose of improving gloss and surface fretting abrasion resistance, it is preferred that a top coat layer having a gloss (as measured at 60° according to JIS Z-8741) of not smaller than 50% be provided on the ink-receptive layer.

[0163] The top coat layer of the present invention preferably comprises an inorganic filler and a binder resin incorporated therein in an amount of from 70 to 95% by weight and from 5 to 30% by weight, respectively. As the inorganic filler and binder resin there may be used the same filler and binder as the inorganic filler and binder resin used in the ink-receptive layer.

[0164] The top coat layer preferably comprises a cationic ink-fixing agent incorporated therein in an amount of from 1 to 20% by weight for the purpose of enhancing ink fixability. As the ink-fixing agent there may be used the same fixing agent as the ink-fixing agent used in the aforementioned ink-receptive layer.

[0165] The coated amount of the top coat layer of the present invention is properly predetermined according to the porous resin film or ink-receptive layer but is from 0.1 to 5.0 g/m2 preferably from 0.5 to 3.0 g/m2. When the coated amount of the top coat layer falls below 0.1 g/m2, the effect of the top coat layer is not sufficiently exerted. On the other hand, when the coated amount of the top coat layer exceeds 5.0 g/m2, the effect of the top coat layer is saturated.

[0166] The top coat layer of the present invention may comprise various auxiliaries such as dispersant, thickening agent, antifoaming agent, preservative, ultraviolet absorber, oxidation inhibitor and surface active agent which are normally used in coated paper as necessary.

[0167] (Coating Method)

[0168] The method for coating the aforementioned ink-receptive layer and top coat layer on the porous resin film can be properly selected from known methods. Examples of the coating method include blade coating method, rod bar coating method, roll coating method, air knife coating method, spray coating method, gravure coating method, curtain coating method, die coating method, comma coating method, etc.

[0169] (Other Printing Methods)

[0170] The porous resin film of the present invention may be subjected to printing other than ink jet printing depending on the purpose. The kind and process of printing are not specifically limited. For example, printing can be accomplished by a known printing method such as gravure printing, aqueous flexographic printing, silk screen printing, melt heat transfer printing and sublimation heat transfer printing using an ink having a pigment dispersed in a known vehicle. Alternatively, printing can be accomplished by metallization, gloss printing, mat printing or the like. The pattern to be printed may be properly selected from natural pattern such as animal, scenery, lattice and polka dots and abstract pattern.

[0171] The porous resin film of the present invention is also suited for applications requiring the absorption of aqueous liquid other than printing purposes. For example, the porous resin film of the present invention can be used as an adhesive label comprising an aqueous adhesive, label paper to be stuck on vessels such as bottles and cans, water-absorbing film, wall paper, surface decorative paper for veneer board and plasterboard, film for preventing the production of water drop, drip preventive wrapping paper for food, coaster, paper for working, colored paper used for making figures by folding, water-retaining sheet, soil drying preventive sheet, concrete drying aid material, drying agent, dehumidifier or the like.

EXAMPLES

[0172] The present invention will be further described hereinafter in the following examples, comparative examples and test examples. Proper changes can be made in the materials, added amount, proportion, operation, etc. described in the following examples so far as they don't depart from the spirit of the present invention. Accordingly, the scope of the present invention is not limited to the specific examples described hereinafter.

[0173] Porous resin films of the present invention, recording media comprising same and recording media comprising comparative resin films were prepared according to the following procedures.

Experiment Example 1

[0174] 100 parts by weight of a heavy calcium carbonate (average particle diameter: 3 μm; specific surface area: 1.8 m2/g; oil absorption: 31 ml/100 g as measured according to JIS-K5101-1991; abbreviation: tankaru 1) as a finely divided powder were heated to a temperature of from 80° C. to 100° C. with stirring in a super mixer. To the finely divided powder were then added 4 parts by weight of a surface treating agent (mixture of 50% of sodium dodecanesulfonate and 50% of sodium hexadecanesulfonate; HLB value: 17.9; reagent grade produced by TOKYO KASEI KOGYO CO., LTD.; abbreviation: ST1). The mixture was then heated with stirring to obtain a surface-treated calcium carbonate. The temperature in the super mixer was from about 100° C. to 110° C. The abbreviation of the surface-treated calcium carbonate is SC1.

[0175] The particle diameter of the calcium carbonate powder used in the examples of the specification is 50% cumulative particle diameter measured by a laser diffraction type particle measuring instrument “Microtrack” (trade name, produced by NIKKISO CO., LTD.).

Experiment Example 2

[0176] A surface-treated calcium carbonate (abbreviation: SC2) was obtained in the same manner as in Experiment Example 1 except that as the surface treating agent there was used oleic acid (HLB value: 4.7; abbreviation: ST2).

Experiment Example 3

[0177] A surface-treated calcium carbonate (abbreviation: SC3) was obtained in the same manner as in Experiment Example 1 except that as the surface treating agent there was used lauryl trimethyl ammonium methosulfate (HLB value: 13.3; abbreviation; ST3).

Experiment Example 4

[0178] A surface-treated calcium carbonate (abbreviation: SC4) was obtained in the same manner as in Experiment Example 1 except that as the surface treating agent there was used 3-lauroylaminopropyldimethyl(2-hydroxyethyl)nitrate (HLB value: 18.4; abbreviation: ST4).

Experiment Example 5

[0179] A surface-treated calcium carbonate (abbreviation: SC5) was obtained in the same manner as in Experiment Example 1 except that as the surface treating agent there was used a mixture of dilauryldi(diethyleneoxy)ammonium chloride and dilauryl(2-hydroxyethyl) (trioxyethyleneoxy)chloride (HLB value: 11.7; abbreviation: ST5).

Example 1

[0180] <Preparation and Longitudinal Stretching of Substrate Layers

[0181] A mixture of 75% by weight of a polypropylene having a melt flow rate (MFR; temperature: 230° C.; load: 2.16 kg) of 1 g/10 min. and 5% by weight of a high density polyethylene having a melt flow rate (MFR; temperature: 190° C.; load: 2.16 kg) of 8 g/10 min. was kneaded with a composition [a] having 20% by weight of calcium carbonate having an average particle diameter of 3 μm incorporated therein by means of an extruder the temperature of which had been set at 250° C., and then extruded into strands which were then cut to form pellets. The pellets of the composition [a] were then extruded through a T-die connected to the extruder the temperature of which had been set at 250° C. into a sheet which was then cooled by a cooling machine to obtain an unstretched sheet. Subsequently, the unstretched sheet was heated to a temperature of 145° C., and then longitudinally stretched at a draw ratio of 4.5 to obtain a stretched sheet.

[0182] In the melt kneading of the resin component or the mixture thereof with the finely divided powder in the present example, BHT (4-methyl-2,6-di-t-butylphenol) and Irganox 1010 (trade name of phenol-based oxidation inhibitor produced by Ciba Geigy Inc.) as an oxidation inhibitor were added to the resin component and the finely divided powder in an amount of 0.2 parts by weight and 0.1 parts by weight, respectively, based on 100 parts by weight of the total weight of the resin component and the finely divided powder.

[0183] <Formation of Surface Porous Resin Film>

[0184] Separately, 40% by weight of a polypropylene (abbreviation: PP1) having MFR of 20 g/10 minutes and 60% by weight of the surface-treated calcium carbonate (abbreviation: SC1) were thoroughly mixed in the form of powder, and then extruded through a biaxial kneader which had been set at a temperature of 240° C. into strands which were then cut to prepare pellets (composition [b]).

[0185] The pellets of the composition [b] were then extruded through a T-die connected to the extruder which had been set at a temperature of 230° C. (temperature a) into a sheet. The sheet thus obtained was then laminated on both surfaces of the sheet which had been stretched at a draw ratio of 4.5 in the aforementioned manner, cooled to a temperature of 50° C. (temperature b) and then stretched at a draw ratio of 8.5 in the crosswise direction by means of a tenter at an elevated temperature of 154° C. (temperature c). Thereafter, the laminate was annealed at a temperature of 155° C. (temperature d), cooled to a temperature of 55° C. (temperature e), and then slit at the edge thereof to obtain a laminate comprising a porous resin film having a total thickness of 137 μm having a three-layer structure (surface absorption layer [b]/substrate layer [a]/back absorption layer [b]: thickness 45 μm/56 μm/36 μm).

[0186] The laminates of the examples and comparative examples were then evaluated on the surface absorption layer.

[0187] These laminates were evaluated in the following manner.

[0188] <Evaluation>

[0189] (1) Liquid Absorption Capacity

[0190] The liquid absorption capacity of the aforementioned porous resin film at 2 seconds was measured by means of a liquid absorbency testing machine produced by Kumagai Riki Kogyo K.K. according to “Japan TAPPI No. 51-87” (JAPAN TAPPI, paper pulp testing method No. 51-87; Bristow Method). The measurement solvent was obtained by mixing 70% by weight of water and 30% by weight of ethylene glycol, and then dissolving malachite green in the mixed solvent in an amount of 2 parts by weight based on 100 parts by weight of the mixed solvent.

[0191] (2) Average Contact Angle of Porous Resin Film with Respect to Water and Difference between Maximum Value and Minimum Value Thereof

[0192] The contact angle of the surface of the aforementioned porous resin film was determined by dropping purified water onto the surface of the film, and then measuring the surface of the film for contact angle by means of a contact angle meter (Type CA-D, produced by KYOWA INTERFACE SCIENCE CORPORATION LIMITED) after 1 minute. This measurement was effected 10 times (the specimen was replaced by an unmeasured film which had not been wet with purified water every measurement), and the average value of the ten measurements of contact angle and the difference between the maximum value and the minimum value of contact angle were then determined.

[0193] (3) Confirmation of Presence of Surface Pores and Measurement of Number and Dimension of Surface Pores

[0194] The aforementioned porous resin film was cut to sample a portion out of the film to confirm that pores were present in the surface and section of the film. An arbitrary portion was cut out of the porous resin film sample, The sample was then vacuum-metallized with gold or gold-palladium on the surface to be observed. The sample was then observed at a magnification power of 500 under a Type S-2400 scanning electron microscope produced by Hitachi Ltd. to confirm the presence of pores in the surface of the film and the presence of an inorganic finely divided powder in the interior or end of the majority of all pores, i.e., at least 50% of all pores. Further, the electron microscope image was outputted onto paper or taken in photograph on which the number of pores in the surface of the film was then counted. As a result, the number of pores was about 4.3×109/m2. Subsequently, the measurements of the aforementioned 118 pores were averaged. As a result, the major axis was 13.3 μm, the minor axis was 8.2 μm, and the average diameter was 8.3 μm. In the case where two pores are connected to both sides of a finely divided particle or upper and lower sides of a finely divided particle, respectively, the two pores were collectively regarded as a pore assuming that pores are formed with the finely divided particle as a center.

[0195] (4) Confirmation of Presence of Internal Pores and Measurement of Internal Porosity

[0196] The porous resin film was embedded in an epoxy resin which was then solidified, cut by a microtome so that sections were formed in the direction parallel to the thickness direction and in the direction perpendicular to the surface of the film, respectively, metallized with gold-palladium on the sections, and then observed on the sections at a magnification power of 1,000 to confirm the presence of internal pores and the presence of a finely divided powder in at least some of the internal pores.

[0197] The total thickness and basis weight (g/M2) of the porous resin film were measured. Subsequently, the surface absorption layer was peeled off the laminate at a predetermined area. The thickness and basis weight of the remaining film were then measured. From these differences were then determined the thickness and basis weight (g/m2) of the porous resin film layer, respectively The density (ρ) of the absorption layer was then calculated by dividing the basis weight by the thickness. Subsequently, the composition [b] was formed into a press sheet having a thickness of 1 mm at a temperature of 230° C. The density (σo) of the press sheet was then measured. The porosity of the porous resin film was then calculated by the following equation (2).

% Porosity=100(ρo−ρ)/ρo (2)

[0198] (ρo density of press sheet having a thickness of 1 mm;

[0199] ρ: density of absorption layer in porous resin film)

[0200] (5) Ink Absorbency

[0201] A color chart for evaluation (50% printed monochromatic color and 100% printed monochromatic color on 2 cm×2 cm area, 200% printed polychromatic color on 2 cm×2 cm area) was prepared, and printing was then made on the various recording media on its porous resin film as surface layer with pigment inks (yellow, magenta, cyan, black) using an ink jet printer (Type JP2115, produced by GRAPHTEC CORPORATION). Thereafter, a filter paper was pressed onto the printed area at a predetermined interval of time to observe to see if the ink returned to the filter paper. The time at which the ink no longer returns to the filter paper was recorded. The ink absorbency was then evaluated according to the following criterion.

[0202] 6: Time in which the ink no longer returns to the filter paper is shortly after printing;

[0203] 5: Time in which the ink no longer returns to the filter paper is not more than 1 minute;

[0204] 4: Time in which the ink no longer returns to the filter paper is from more than 1 minute to not more than 2 minutes;

[0205] 3: Time in which the ink no longer returns to the filter paper is from more than 2 minutes to not more than 3 minutes;

[0206] 2: Time in which the ink no longer returns to the filter paper is from more than 3 minutes to not more than 4 minutes;

[0207] 1: Time in which the ink no longer returns to the filter paper is from more than 4 minutes to not more than 5 minutes; and

[0208] 0: The ink still returns to the filter paper and doesn't dry even after more than 5 minutes

[0209] (Evaluation of Density Unevenness)

[0210] The porous resin film which had absorbed the ink was visually observed for density unevenness, and then evaluated according to the following criterion.

[0211] 4: No density unevenness;

[0212] 3: Little density unevenness;

[0213] 2: Some density unevenness; and

[0214] 1: Remarkable density unevenness

[0215] (Evaluation of Running)

[0216] The porous resin film which had absorbed the ink was visually observed for running, and then evaluated according to the following criterion.

[0217] 4: No running, sharp image;

[0218] 3: Little running, little difficulty in recognition of image;

[0219] 2: Some running, some difficulty in recognition of image; and

[0220] 1: Remarkable running, disabled to use

[0221] (Evaluation of Surface Unevenness After Printing)

[0222] The porous resin film on which printing had been made was allowed to stand in a room for 1 hour, visually observed for the occurrence of surface unevenness (roughness), and then evaluated according to the following criterion.

[0223] 3: No unevenness, flat surface, little or no change from before printing;

[0224] 2: Little unevenness; and

[0225] 1: Remarkable unevenness

[0226] These results of evaluation are together set forth in Table 1.

[0227] (Evaluation of Water Resistance)

[0228] The printed sample which had been prepared under the same conditions as in the aforementioned evaluation of ink absorbency was dipped in a sufficient amount of tap water (temperature: 25° C.) for 4 hours, air-dried on the surface thereof, visually observed for the degree of ink retention, and then evaluated according to the following criterion.

[0229] 3: Percent ink retention is from 80% to 100%;

[0230] 2: Percent ink retention is from 50% to 80%; and

[0231] 1: Percent ink retention is from 0% to 50%

[0232] The results of the aforementioned various tests and evaluations are set forth in Table 1.

[0233] (Comparative Example 1)

[0234] A laminated film having a porous resin film provided on the surface thereof was prepared and evaluated in the same manner as in Example except that the surface-treated calcium carbonate SC1 was replaced by the heavy calcium carbonate (average particle diameter: 3 μm; specific surface area: 1.8 m2/g; oil absorption: 31 ml/100 g as measured according to JIS-K5101-1991; abbreviation: tankaru 1) used in Experiment Example 1 which had been not subjected to surface treatment. The results of evaluation are set forth in Table 1.

Comparative Example 2

[0235] A laminated film having a porous resin film provided on the surface thereof was prepared and evaluated in the same manner as in Example 1 except that the surface-treated calcium carbonate was replaced by the calcium carbonate which had been surface-treated with stearic acid as a surface treating agent (Experiment Example 2; abbreviation: SC2). The results of evaluation are set forth in Table 1.

Example 2

[0236] A laminated film having a porous resin film provided on the surface thereof was prepared and evaluated in the same manner as in Example 1 except that the mixing proportion and forming conditions were as set forth in Table 1. The results of evaluation are set forth in Table 1.

Example 3

[0237] A laminated film having a porous resin film provided on the surface thereof was prepared and evaluated in the same manner as in Example 1 except that the thickness of the surface porous resin film layer was as set forth in Table 1. The results of evaluation are set forth in Table 1.

Example 4

[0238] A laminated film having a porous resin film provided on the surface thereof was prepared and evaluated in the same manner as in Example 1 except that the surface-treated calcium carbonate was replaced by the surface-treated calcium carbonate (abbreviation: SC3) as set forth in Experiment Example 3. The results of evaluation are set forth in Table 1.

Example 5

[0239] A laminated film having a porous resin film provided on the surface thereof was prepared and evaluated in the same manner as in Example 1 except that the surface-treated calcium carbonate was replaced by the surface-treated calcium carbonate (abbreviation: SC4) as set forth in Experiment Example 4. The results of evaluation are set forth in Table 1.

Example 6

[0240] A laminated film having a porous resin film provided on the surface thereof was prepared and evaluated in the same manner as in Example 1 except that the surface-treated calcium carbonate was replaced by the surface-treated calcium carbonate (abbreviation: SC5) as set forth in Experiment Example 5. The results of evaluation are set forth in Table 1.

1TABLE 1Com-Com-Com-parativeparativeparativeUnitExample 1Example 1Example 2Example 2Example 3Example 4Example 5Example 6Constituent componentsKind of thermoplastic resin—PP1PP1PP1PP1PP1PP1PP1PP1Mixing proportion ofwt-%4040404540404040thermoplastic resin<Finely divided powder andsuface treating agent>Kind of surface-treated—SC1UntreatedSC2SC1SC1SC3SC4SC5finely divided powder(abbrev.)Mixing proportion ofwt-%60Untreated:605560606060surface-treated finely60divided powderKind of surface treating—ST1—ST2ST1ST1ST3ST4ST5agentAmount of surface treatingparts6—666666agent based finelyby wtdivided powderForming conditionsTemperature a° C.230230230230230230230230Temperature b° C.5050505050505050Temperature c° C.154154154153154154154154Temperature d° C.155155155154155155155155Temperature e° C.5555555555555555Results of evaluationof filmTotal thickness of filmμm137135134135175140143141Thickness of porous resinμm4645425573485046filmThickness of substrateμm5655565059565755layerLiquid absorption capacityml/m215.2006.118.712.516.714(2 sec.)Surface gloss%3323252230333232Average surface contact angle°841141158883879195with waterDifference between maximum°32344101210value and minimum valueof contact angle withwaterInternal porosity%6555575560646262Number of surface pores/m24.3E+93.8E+91.9E+98.4E+92.5E+91.8E+91E+92.1E+9Average diameter ofμm889121091212surface poresSurface pores having finelyVisuallyNotNotNotNotNotNotNotNotdivided powder in interiorobservedsmallersmallersmallersmallersmallersmallersmallersmallerthereof or at end thereofthan halfthan halfthan halfthan halfthan halfthan halfthan halfthan halfInternal pores havingVisuallyObservedObservedObservedObservedObservedObservedObservedObservedfinely divided powderobservedin interior thereofor at end thereofInk absorbencyVisually60066666(monochromatic 50%)observedInk absorbencyVisually60066666(monochromatic 100%)observedInk absorbencyVisually60056666(polychromatic 200%)observedDensity unevennessVisually41134444observedRunningVisually31133333observedSurface unevenness afterVisually33333333printingobserved

Example 7

[0241] The pellets as used in the formation of the surface porous resin film of Example 4 were melted and pressed at 50 kg/cm2 in a press-molding machine the temperature of which had been set at 230° C., and then cooled to a temperature of 30° C. to obtain a sheet having a length of 120 mm, a width of 120 mm and a thickness of about 1 mm. The density of the sheet was 1.5 g/cm3.

[0242] The sheet was heated to 159° C. (temperature al) in a small-sized biaxial stretching machine (produced by Iwamoto Seisakujo K.K.), stretched at a draw ratio of 5.2 in one direction, and then cooled to a temperature of 90° C. (temperature b1) by cold air to obtain a porous resin film having a thickness of 325 μm, a basis weight of 207 g/m2 and a density (p) of 0.64 g/cm3. The porous resin film thus obtained has an internal porosity of 58%. Subsequently, the porous resin film was evaluated in the same manner as in Example 1. The results of evaluation are set forth in Table 2.

Comparative Example 3

[0243] The pellets as used in the formation of the surface porous resin film of Comparative Example 1 were melted and pressed at 50 kg/cm2 in a press-molding machine the temperature of which had been set at 230° C., and then cooled to a temperature of 30° C. to obtain a sheet having a length of 120 mm, a width of 120 mm and a thickness of about 1 mm. The density of the sheet was 1.5 g/cm3.

[0244] The sheet was heated to 160° C. (temperature a1) in a small-sized biaxial stretching machine (produced by Iwamoto Seisakujo K.K.), stretched at a draw ratio of 5.2 in one direction, and then cooled to a temperature of 90° C. (temperature b1) by cold air to obtain a porous resin film having a thickness of 306 μm, a basis weight of 208 g/m2 and a density (p) of 0. 68 g/cm3. The porous resin film thus obtained has an internal porosity of 55%. Subsequently, the porous resin film was evaluated in the same manner as in Example 1. The results of evaluation are set forth in Table 2.

2TABLE 2ComparativeUnitExample 7Example 3ConstituentKind of—PP1PP1componentsthermoplastic resinMixing proportionwt-%4040of thermoplasticresin<Finely dividedpowder and surfacetreating agent>Kind of surface-—SC3tankaru 1treated finelydivided powder(abbrev.)Mixing proportionwt-%6060of surface-treatedfinely dividedpowderKind of surface—ST2—treating agentAmount of surfaceparts by6—treating agent basedwt.finely dividedpowderFormingTemperature a1° C.160160conditionsTemperature b1° C.9090Draw ratioTimes5.25.2Results ofThickness of porousμm325306evaluationresin filmof filmLiquid absorptionml/m2230capacity (2 sec.)Surface gloss%2724Average surface°0115contact angle withwaterDifference between°02maximum value andminimum value ofcontact angle withwaterInternal porosity%5855Number of surface/m21E + 101.6E + 10poresAverage diameter ofμm5.25.5surface poresSurface poresVisuallyNot smallerNot smallerhaving finelyob-thanthan halfdivided powderservedhalfin interiorthereof or atend thereofInternal poresVisuallyObservedObservedhaving finelyob-divided powder inservedinterior thereof or atend thereofInk absorbencyVisually60(monochromaticob-50%)servedInk absorbencyVisually60(monochromaticob-100%)servedInk absorbencyVisually60(polychromaticob-200%)servedDensity unevennessVisually31ob-servedRunningVisually31ob-servedSurface unevennessVisually33after printingob-served

Examples 8, 9

[0245] The laminates having a porous resin film provided on the surface thereof described in Examples 1 and 3 were each subjected to corona treatment on the surface thereof at a density of 3,600 J/m2 (60 W·min/m2). These laminates were each then evaluated in the same manner as in Example 1. The results of evaluation are set forth in Table 3.

Example 10

[0246] The porous resin film prepared in Example 3 was subjected to corona treatment at a density of 3,600 J/m2 (60 W·min/m2). Onto the porous resin film (on one surface thereof) was then coated a coating solution for ink-receptive layer having the following formulation in an amount of 5 g/m2 as calculated in terms of solid content. The coated material was dried, and then subjected to smoothing by super calendering to obtain an ink jet recording paper.

[0247] Formulation of coating solution:

3Synthetic silica powder (Mizukasil100 parts by P-78D, produced by MIZUSAWA INDUSTRIALweightCHEMICALS, LTD.)Polyvinyl alcohol (PVA-117, produced by30 parts byKURARAY CO., LTD.)weightPolyamide polyamide epichlorohydrin10 parts byadduct (WS-570, produced by JAPAN PMCweightCORPORATION)Sodium polyacrylate (reagent, produced by5 parts by Wako Pure Chemical Industries, Ltd.)weightWater1,600 parts by weight

[0248] The ink jet recording paper thus obtained was then evaluated in the same manner as in Example 1. The results of evaluation are set forth in Table 3.

Comparative Example 4

[0249] A commercially available pulp paper-based ink jet recording paper (Epson Superfine Paper MJA4SP1) was evaluated in the same manner as in Example 1. The results are set forth in Table 3.

4TABLE 3ComparativeUnitExample 8Example 9Example 10Example 4Substrate/Kind of substrate or—Example 1Example 3Example 3Pulp-basedsupportsupportpaperKind of surface—CoronaCoronaCoronaoxidation treatmenttreatmenttreatmenttreatmentIntensity of surfaceJ/m23,6003,6003,600oxidation treatmentLiquid absorptionml/m2151515capacity after surfaceoxidation treatmentContact angle with°244124water after surfaceoxidation treatmentDifference between°121412maximum value andminimum value ofcontact angle withwater after surfaceoxidation treatmentCoatingSolid content of ink-g/m2——5receptive layerResults ofInk dryabilityVisually6666evaluation(monochromatic 50%)observedInk dryabilityVisually6666(monochromatic 100%)observedInk dryabilityVisually6666(polychromatic 200%)observedDensity unevennessVisually4444observedRunningVisually3344observedSurface unevennessVisually3331after printingobserved

Examples 11 to 15, Comparative Examples 5 to 10

[0250] The materials set forth in Table 4 were used in predetermined amounts, and then processed in the following manner to prepare an ink jet recording sheet.

[0251] An amorphous silica, a binder resin, a crosslinking agent, an ink-fixing agent, and water were mixed to prepare a coating solution for forming an ink-receptive layer. The coating solution was applied to the surface of the porous resin film by means of a mayor bar in a dried amount of 15 g/m2, and then dried and solidified in a 110° C. oven for 5 minutes to form a receptive layer, thereby obtaining an ink jet recording paper. The ink jet recording paper was then evaluated for adaptability to ink jet printer in the same manner as for the porous resin film.

[0252] The formulation and the results of evaluation of surface gloss and adaptability to ink jet recording are set forth in Table 5.

Examples 16 to 18

[0253] The materials set forth in Table 4 were used in predetermined amounts, and then processed in the following manner to prepare an ink jet recording sheet.

[0254] An inorganic filler, a binder resin, an ink-fixing agent, and water were mixed to prepare a coating solution for top coat layer.

[0255] An ink-receptive layer was then formed on the porous resin film in the same manner as in Example 11. The coating solution for top coat layer was applied to the porous resin film by means of a mayor bar in a dried amount of 1.0 g/m2, and then dried and solidified in a 110° C. oven for 1 minute to form a top coat layer, thereby obtaining an ink jet recording paper.

[0256] The formulation and the results of evaluation of surface gloss and adaptability to ink jet printer are set forth in Table 5.

5TABLE 4Name ofmaterialContentsAmorphousAqueous dispersion of particulate silicasilica 1having a primary particle diameter of 7 nmand an average particle diameter of 300 nmobtained by grinding silica prepared by gelmethod (solid content: 20%) “Cyclojet 703A”(trade name, produced by Grace Japan Co.,Ltd.)AmorphousAqueous dispersion of particulatesilica 2silica having a primary particle diameter of6 nm and an average particle diameter of 300nm obtained by dispersing silica having anaverage particle diameter of 2.5 μm“Mizukasil P-73” (trade name, produced byMIZUSAWA INDUSTRIAL CHEMICALS, LTD.)prepared by gel method (solid content:10%) by a sand grinderAmorphousAqueous dispersion of particulatesilica 3cationically-treated silica having a primaryparticle diameter of 7 nm and an averageparticle diameter of 300 nm obtained bygrinding silica prepared by gel method(solid content: 18%) “Cyclojet 703C” (tradename, produced by Grace Japan Co., Ltd.)AmorphousAqueous dispersion of silica having asilica 4primary particle diameter of 7 nm and anaverage particle diameter of 100 nm obtainedby dispersing silica “Aerosil 300CF” (tradename, Nippon Aerosil Co., Ltd.) prepared bygas phase method by a sand grinder (solidcontent: 8%)AmorphousAqueous dispersion of silica having asilica 5primary particle diameter of 6 nm and anaverage particle diameter of 800 nm obtainedby dispersing silica “Mizukasil P-73” (tradename, MIZUSAWA INDUSTRIAL CHEMICALS, LTD.)having an average particle diameter of 2.5μm prepared by gel method by a sand grinder(solid content: 10%)AmorphousAqueous dispersion of silica having asilica 6primary particle diameter of 25 nm and anaverage particle diameter of 300 nm obtainedby dispersing silica “Mizukasil P-526”(trade name, MIZUSAWA INDUSTRIAL CHEMICALS,LTD.) having an average particle diameter of3.0 μm prepared by precipitation method by asand grinder (solid content: 10%)Colloidal“Snowtechs YL” (trade name, produced bysilica 1Nissan Chemical Industries, Ltd.), which isan aqueous dispersion of spherical colloidalsilica having an average particle diameterof 75 nm (solid content: 40%)Binder resinAqueous solution of “Kuraray Poval PVA-235”(trade name, KURARAY CORP.) (solid content:10%), which is a polvinyl alcohol having apolymerization degree of 3,500 and asaponification degree of 88%CrosslinkingAqueous dispersion of a melamine-formalineagent 1resin (solid content; 80%) “Uramine P-6300”(trade name, produced by Mitsui ChemicalInc.)Crosslinking4% Aqueous dispersion of sodium tetraborateagent 2decahydrate (alias: borax, reagent grade,produced by Wako Pure Chemical Industries,Ltd.)Ink-fixingAqueous dispersion of cationic acryl polymeragent 1(solid content: 30%) “Sumirez Resin 1001”(trade name, produced by SUMITOMO CHEMICALCO., LTD.)Ink-fixing10% Aqueous dispersion of aluminum chlorideagent 2hexahydrate (reagent, produced by Wako PureChemical Industries, Ltd.)

[0257]

6

TABLE 5

Example
Example
Example
Example
Example
Example
Example

11
12
13
14
15
16
17

Support
Example 3
Example 3
Example 3
Example 3
Example 3
Example 3
Example 3

Ink-receptive layer

Amorphous silica 1
76
76

76
76

Amorphous silica 2

76

Amorphous silica 3

76

(cation)

Amorphous silica 4

76

Amorphous silica 5

Amorphous silica 6

Binder resin
20
20
20
20
20
20
20

Crosslinking agent 1
2
2
2
2

2
2

Crosslinking agent 1

2

Ink-fixing agent 1
2

2
2

2
2

Ink-fixing agent 2

2

2

Coated amount (g/m2)
15
15
15
15
15
15
15

Top coat layer

Amorphous silica 1

90

Colloidal silica 1

90

Binder resin

10
10

Ink-fixing agent 2

Results of evaluation

of film

Surface gloss (%)
45
46
45
42
44
55
59

Ink dryability
Visually
6
6
6
6
6
6
6

(polychromatic
observed

200%)

Density
Visually
4
4
4
4
4
4
4

unevenness
observed

Running
Visually
4
4
4
4
4
4
4

observed

Water
Visually
3
3
3
3
3
3
3

resistance
observed

Surface
Visually
3
3
3
3
3
3
3

unevenness
observed

after printing

Com-

Com-
Com-
Com-
Com-
Com-
parative

Example
parative
parative
parative
parative
parative
Example

18
Example 5
Example 6
Example 7
Example 8
Example 9
10

Support
Example 3
Example 3
Example 3
Com-
Example 3
Example 3
Example 3

parative

Example 2

Ink-receptive layer

Amorphous silica 1
76
80
76

60
97

Amorphous silica 2

Amorphous silica 3

(cation)

Amorphous silica 4

Amorphous silica 5

76

Amorphous silica 6

76

Binder resin
20
20
20
20
20
40
3

Crosslinking agent 1
2

2
2
2

Crosslinking agent 2

Ink-fixing agent 1
2

2
2
2

Ink-fixing agent 2

Coated amount (g/m2)
15
15
15
15
15
15
15

Top coat layer

Amorphous silica 1

Colloidal silica 1
80

Binder resin
10

Ink-fixing agent 2
10

Results of evaluation

of film

Surface gloss (%)
60
47
37
15
18
44
3

Ink dryability
Visually
6
6
6
0
6
6
6

(polychromatic
observed

200%)

Density
Visually
4
4
1
4
4
4
4

unevenness
observed

Running
Visually
4
4
1
4
4
4
4

observed

Water
Visually
3
1
1
1
1
1
1

resistance
observed

Surface
Visually
3
3
3
3
3
3
3

unevenness

after printing

Examples 19 to 22, Comparative Examples 11 to 14

[0258] The materials set forth in Table 6 were used in predetermined amounts, and then processed in the following manner to prepare an ink jet recording sheet.

[0259] In some detail, alumina or alumina hydrate, and a binder resin were mixed to prepare a coating solution for forming an ink-receptive layer. The coating solution was applied to the surface of the porous resin film by means of a mayor bar in a dried amount of 15 g/m2, and then dried and solidified in a 110° C. oven for 5 minutes to form a receptive layer, thereby obtaining an ink jet recording paper. The ink jet recording paper was then evaluated for adaptability to ink jet printer in the same manner as for the porous resin film.

[0260] The formulation and the results of evaluation of surface gloss and adaptability to ink jet recording are set forth in Table 7.

Examples 23, 24

[0261] The materials set forth in Table 6 were used in predetermined amounts, and then processed in the following manner to prepare an ink jet recording sheet.

[0262] An ink-receptive layer was formed on the porous resin film in the same manner as in Example 19. An inorganic filler and a binder resin were mixed to prepare a coating solution for top coat layer. The coating solution for top coat layer was then applied to ink-receptive layer by means of a mayor bar in a dried amount of 1.0 g/m2, and then dried and solidified in a 110° C. oven for 1 minute to form a top coat layer, thereby obtaining an ink jet recording paper.

[0263] The formulation and the results of evaluation of surface gloss and adaptability to ink jet printer are set forth in Table 7.

7TABLE 6Name ofmaterialContentsAlumina 1Dispersion of “Aluminum Oxide C” (tradename, produced by Nippon Aerosil Co.,Ltd.), which is δ-alumina having anaverage particle diameter of 20 nm, ina 80/20 (by weight) mixture of waterand isopropyl alcohol obtained bydispersion using a homogenizer and aultrasonic dispersing machineAlumina 2Dispersion of “AKP3000” (trade name,produced by SUMITOMO CHEMICALCORPORATION), which is α-alumina havingan average particle diameter of 550 nm,in a 80/20 (by weight) mixture of waterand isopropyl alcohol obtained bydispersion using a homogenizer and aultrasonic dispersing machineAluminaAqueous dispersion of fibrous pseudohydrate 1boehmite having an average particlediameter of 100 nm (solid content: 7%)(Cataloid AS-3) (trade name, produced byCATALYSTS & CHEMICALS IND. CO., LTD.)AluminaAqueous dispersion of fibrous pseudohydrate 2boehmite having an average particlediameter of 25 nm (solid content: 10%)(Cataloid AS-2) (trade name, produced byCATALYSTS & CHEMICALS IND. CO., LTD.)BinderAqueous solution of “Kuraray Poval PVA-resin 1235” (trade name, KURARAY CORP.) (solidcontent: 10%), which is a polvinylalcohol having a polymerization degreeof 3,500 and a saponification degree of88%BinderAqueous solution of “Kuraray Poval PVA-resin 2124” (trade name, KURARAY CORP.) (solidcontent: 15%), which is a polvinylalcohol having a polymerization degreeof 2,400 and a saponification degree of95%Colloidal“Snowtechs PL-M” (trade name, produced bysilica 1Nissan Chemical Industries, Ltd.),which is an aqueous dispersion ofspherical colloidal silica having anaverage particle diameter of 70 nm(solid content: 40%)Colloidal“Snowtechs YL” (trade name, producedsilica 2by Nissan Chemical Industries, Ltd.),which is an aqueous dispersion of pearlnecklace-like colloidal silica havingan average particle diameter of 150 nm(solid content: 20%)

[0264]

8

TABLE 7

Example
Example
Example
Example
Example
Example

19
20
21
22
23
24

Support
Example 3
Example 3
Example 3
Example 3
Example 3
Example 3

Ink-receptive layer

Alumina 1
80

80
80

Alumina 2

Alumina hydrate 1

90

Alumina hydrate 2

90
90

Binder resin 1
20
10
10

20
20

Binder resin 2

10

Coated amount (g/m2)
15
15
15
15
15
15

Top coat layer

Colloidal silica 1

90

Colloidal silica 2

90

Binder resin 1

10
10

Results of evaluation

of film

Surface gloss (%)
49
52
55
53
63
62

Ink dryability
Visually
6
6
6
6
6
6

(polychromatic
observed

200%)

Density
Visually
4
4
4
4
4
4

unevenness
observed

Running
Visually
4
4
4
4
4
4

observed

Water
Visually
3
3
3
3
3
3

resistance
observed

Surface
Visually
3
3
3
3
3
3

unevenness
observed

after printing

Comparative
Comparative
Comparative
Comparative

Example 11
Example 12
Example 13
Example 14

Support
Comparative
Example 3
Example 4
Example 4

Example 2

Ink-receptive layer

Alumina 1
80

60
97

Alumina 2

80

Alumina hydrate 1

Alumina hydrate 2

Binder resin 1
20
20
40
3

Binder resin 2

Coated amount (g/m2)
15
15
15
15

Top coat layer

Colloidal silica 1

Colloidal silica 2

Binder resin 1

Results of evaluation of film

Surface gloss (%)
38
15
51
46

Ink dryability
Visually
0
6
6
6

(polychromatic
observed

200%)

Density unevenness
Visually
1
4
4
4

observed

Running
Visually
1
4
4
4

observed

Water resistance
Visually
1
1
1
1

observed

Surface unevenness
Visually
3
3
3
3

after printing
observed

[0265] As can be seen in Tables 1 to 7, the porous resin film of the present invention (Examples 1 to 9) exhibits little density unevenness and a very good ink absorbency even if the ejected amount of ink is great. Further, in the case where an ink-receptive layer comprising the inorganic filler and binder of the present invention is provided on the porous resin film (Examples 10 to 15, 19 to 22), the porous resin film exhibits a good ink absorbency and a good running resistance, demonstrating that the effect of the present can be definitely exerted. Further, the provision of a top coat layer on the ink-receptive layer (Examples 16 to 18, 23, 24) causes enhancement of surface gloss.

[0266] On the contrary, all the films having a liquid absorption capacity deviating from the scope of the present invention (Comparative Examples 1 to 3) exhibit a deteriorated ink absorbency. Further, the comparison of the examples with Comparative Example 4 shows that the porous resin film of the present invention exhibits no surface unevenness after printing, demonstrating that the effect of the present can be definitely exerted. Further, the ink jet recording paper comprising a porous resin film deviating from the scope of the present invention (Comparative Examples 6, 11) and the ink jet recording paper comprising an ink-receptive layer deviating from the scope of the present invention (Comparative Examples 5, 7 to 10, 12 to 14) cannot meet the aforementioned requirements and thus exhibit deteriorated performance.

[0267] industrial Applicability

[0268] The porous resin film of the present invention exhibits an extremely good absorption of aqueous solvent and ink. Further, the recording medium of the present invention comprising the aforementioned porous resin film can form a fine image free of density unevenness thereon even if the ejected amount of ink is great. Accordingly, the porous resin film and recording medium of the present invention can be preferably provided for a wide printing purpose such as recording with an aqueous ink, particularly ink jet recording medium, or purpose using an aqueous solvent.

Number	Date	Country
11-347828	Dec 1999	JP
2000-156094	May 2000	JP
2000-156095	May 2000	JP

	Number	Date	Country
Parent	PCT/JP00/08633	Dec 2000	US
Child	10163372	Jun 2002	US

Porous resin film

Information

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Abstract

Description

Claims

Priority Claims (3)

Continuations (1)