Patent Application
20120308824
The present disclosure relates to a silica particle, a method for producing thereof, and a resin composition containing it.
Recently, highly-pure silica came to be used for producing electronic materials and semiconductors with the rapid developments in electronic industry (see patent document 1, for example). Especially, a method using a sealing resin composition containing a resin and spherical silica which is being as filler is known. In such the use, silica particles having the sharp particle size distribution without coarse particles are needed with the size downing and the refinement of electronic parts.
For example, a method for producing spherical silica particles which comprises hydrolysis reaction of alkoxysilane in the presence of a basic catalyst, such as ammonia, and polycondensation of the obtained hydrolysate to produce spherical silica particles (see patent document 2, for example). A method for producing spherical silica having the sharp particle size distribution through the use of this sol-gel method has been investigated (Patent documents 3, 4, 5, and 6).
When the sealing resin composition becomes solidified, a problem that a resin film is swollen to generate cracks occurs because silanol groups existing at the surface of silica particle absorb moisture. As the moisture absorption increases, the sealing condition will be broken and the main body of semiconductor device will be exposed to the air. It tends to reduce the thickness of the sealing material to reduce the size and weight of the semiconductor device. However, in this case, the moisture may penetrate inside the sealing material trough the wall surface thereof. Even if the above-mentioned silica particle is used, such a problem cannot be solved.
To solve the problem, patent document 7 discloses a method to inhibit the crack occurrence at the resin part by using amorphous silica having high moisture absorbency. However, this method cannot obtain sufficient effect because the moisture is still remained in the sealing material part.
Patent document 8 discloses silica particles having fine pores of the certain size. However, the silica disclosed in patent document 8 is not high-density, because it has fine pores. Additionally, the amount of the silanol groups contained in the silica are controlled to surface treat by a silane coupling agent, and the silica are treated by a silane coupling agent. However, when the added amount of the silane coupling agent is low, the silanol groups which do not reacted with the silane coupling agent remains so that the remained silanol groups may reduce the humidity resistance. When the added amount of the silane coupling agent is large, the free silane coupling agents which are not used in the reaction may inhibit the adhesion to the resin and generate the change in color of the resin.
According to the above mentioned state of the art, the object of the present disclosure is to obtain silica particles having the sharp particle size distribution and low water-absorbing rate and being used suitably as a filler of a sealing resin composition, a method for producing it, and a resin composition containing the silica particle and a resin.
The present disclosure relates to a silica particle having a water-absorbing rate of less than 1.0% measured 500 hours after being kept at a temperature of 50° C. and at a humidity of 90%, and at a temperature of 85° C. and at a humidity of 85%, D90/D10 of 3 or less, a true specific gravity of 2.1 g/cm3 or more, and an average particle diameter of 10 μm or less.
The silica particle is preferably surface treated by using a silane coupling agent and/or a silane compound.
The present disclosure relates to a method for producing the silica particle comprising a step (1) of obtaining silica particles by a hydrolysis reaction of tetraethoxysilane and/or a derivative thereof, and a step (2) of calcinating the obtained silica particles in said step (1) at 900 to 1050° C.
The calcinating is preferably proceeded at the calcinating temperature of 950 to 1050° C.
The method for producing the silica particle preferably comprises surface treating with use of a silane coupling agent and/or a silane compound.
The surface treating is preferably proceeded by means of a spray drying.
The present disclosure relates to a resin composition containing the silica particle and a resin.
The silica particle of the present disclosure has the sharp particle size distribution (that is, the amount of coarse particles having extremely-large particle diameter is little) and remarkable lower water-absorbing rate than ordinary silica particles at a wide range of temperatures over time. The silica particles can obtain excellent filling property, humidity resistance, and dimension stability which are needed for use of a sealing filler of a semiconductor and so on.
The present disclosure is described in more detail below. The silica particle of the present disclosure has a water-absorbing rate of less than 1.0% measured 500 hours after being kept at a temperature of 50° C. and at a humidity of 90%, and at a temperature of 85° C. and at a humidity of 85%. The above-mentioned silica particle has not been known and had been produced by the inventors for the first time. The water-absorbing rate of ordinary silica particles are about 2 to 5% under the above-mentioned conditions. So, it may be said that the water-absorbing rate of the silica particle of the present disclosure is exceptionally-low. The water-absorbing rate is preferably less than 0.5%, and the lower limit is not particularly limited but preferably 0.01% or more. In the present disclosure, the water-absorbing rate can be measured by the following method. First, silica powder 10 g is weighed in a 300 cc-beaker, and weighed before absorbing the moisture. The beaker containing the silica powder is put in a thermo-hygrostat and after another 500 hours, the silica powder absorbing the moisture is weighed. The calculation method of the water-absorbing rate is showed by the formula (1).
Water-absorbing rate(%)=(weight after absorbing the moisture−weight before absorbing the moisture)/(weight before absorbing the moisture)×100 (1)
For example, the temperature and the humidity when the water-absorbing rate is measured may be controlled by using a thermo-hygrostat (LH-113 manufactured by ESPEC CORP.).
The silica particle of the present disclosure has D90/D10 of 3 or less. When the particle size distribution of the powder is measured, D10 and D90 correspond to the point where the cumulative weight from the small-particle-diameter side reaches 10% and 90% in the cumulative particle size distribution. The silica particle of the present disclosure has the sharp particle size distribution because the D90/D10 thereof is 3 or less. It is preferred that the particles have the sharp particle size distribution, because the control of the filling ratio becomes easier. The D90/D10 is preferably 2.9 or less. D10 and D90 are values obtained by measuring the particle size distribution. In the present disclosure, the particle size distribution is measured by using a laser diffraction particle size analyzer (Microtrac MT 3300 EX manufactured by NIKKISO CO., LTD.).
The silica particle of the present disclosure has the true specific gravity of 2.1 g/cm3 or more. The true specific gravity becomes smaller with the increasing of cracks and fine pores at the surface and inside of the particle. The silica particle of the present disclosure has the true specific gravity larger than ordinary silica particles, so the number of fine pores therein is small and the amount of Si—OH groups contained at the surface is small. The Si—OH group is highly hydrophilic functional group; the hydrophilic property becomes less with the reduction of the amount of the Si—OH groups so that the water-absorbing rate becomes less. The silica having the true specific gravity of 2.1 g/cm3 or more has a low number of fine pores and a high-density netlike constitution is formed therein, so the amount of Si—OH groups is little. Therefore, hydrophilic property becomes less to reduce the water-absorbing rate of the silica particle.
The true specific gravity is preferably 2.10 g/cm3 or more, more preferably 2.15 g/cm3 or more. The upper limit of the true specific gravity is not particularly limited but is preferably 2.20 g/cm3. When the true specific gravity is less than 2.1 g/cm3, the water-absorbing rate may not be reduced sufficiently. The true specific gravity can be measured by using Beckmann air comparison pycnometer.
The silica particle of the present disclosure has an average particle diameter of 10 μm or less. It is not preferred to use particle having the average particle diameter of more than 10 μm as a sealing material, because the thickness of a sealing material cannot be reduced so that the size downing and the weight saving of a semiconductor device become difficult. The average particle diameter is preferably 8 μm or less, more preferably 5 μm or less. The lower limit of the average particle diameter is not particularly limited but preferably 0.01 μm, and more preferably 0.03 μm. In the present disclosure, the average particle diameter of the silica particle can be measured by using a laser diffraction particle size analyzer.
A particle shape of the silica particle of the present disclosure is not particularly limited but includes needle shape, bar-like shape, plate-like shape, spherical shape and the like. Preferably, the particle shape is nearly spherical shape. In addition, the particle shape can be observed by Scanning Electron Microscope (JSM-7000f manufactured by JEOL Ltd.).
The silica particle is preferably surface treated by using a silane coupling agent and/or a silane compound. By this surface treating, the compatibility with a resin can be increased, and the resin physicality and the molding processability when the particle is composed in a resin can be improved.
The silane coupling agent and/or silane compound are not particularly limited but a compound expressed by the general formula (I) is preferably used;
Xm-Si—(OR)4-m (I)
(in the formula, X expresses an organic group having a reactive organic functional group, R expresses an alkyl group having 1 to 5 carbon atoms, and m expresses integer of 0 to 3) The reactive organic functional group in the organic group includes, for example, vinyl group, epoxy group, amino group, mercapto group, chlorine atom, acryloyloxy group, methacryloyloxy group and so on. Therefore, the organic group X having such a reactive organic functional group includes, for example, vinyl group, 2-(3,4-epoxy cyclohexyl)ethyl group, γ-glycidoxy propyl group, γ-aminopropyl group, N-2-(aminoethyl)-3-aminopropyl group, N-phenyl-3-aminopropyl group, γ-mercaptopropyl group, 3-chloropropyl group, 3-methacryloxy propyl group and so on. The alkyl group R may include, for example, methyl group, ethyl group, propyl group, butyl group, pentyl group, methoxyethoxyl group, and so on.
Therefore, in the present disclosure, a preferred specific example includes, for example, tetraethoxysilane, vinyltriethoxysilane, vinyl tris(2-methoxyethoxy)silane, γ-methacryloxy propyl trimethoxysilane, γ-aminopropyl trimethoxysilane, 2-(3,4-epoxycyclohexyl)ethyl trimethoxysilane, γ-glicycloxy propyl trimethoxysilane, γ-mercapto propyl trimethoxysilane, 3-chloropropyl trimethoxysilane and so on.
A method for producing the silica particle is not particularly limited but includes, for example, a method comprising a step (1) of obtaining silica particles by a hydrolysis reaction of tetraethoxysilane and/or a derivative thereof, and a step (2) of calcinating the obtained silica particle in said step (1) at 900 to 1050° C. The method for producing is one aspect of the present disclosure.
The method for producing a silica particle of the present disclosure comprises calcinating the silica particle obtained by a hydrolysis reaction with use of tetraethoxysilane and/or a derivative thereof at the calcinating temperature of 900 to 1050° C. Though the reason is unknown, silica particles which have a sharper particle size distribution than the case when the other silane compound (for example, tetramethoxysilane and so on) is used as a material can be obtained when the tetraethoxysilane and/or a derivative thereof is used as a material.
The tetraethoxysilane derivative is not particularly limited but includes, for example, a low condensate obtained by partial hydrolysis of tetraethoxysilane. Other silane compound may be used unless the compound has little effect on the particle size distribution.
The hydrolysis may be done under the condition of a hydrolysis reaction used in the ordinary sol-gel method. That is, it can be obtained by hydrolysis and condensation of the tetraethoxysilane and/or derivative thereof as a material in an organic solvent containing water.
The organic solvent is not particularly limited but includes, for example, alcohols such as methanol, ethanol, isopropanol, n-butanol, t-butanol, pentanol, ethylene glycol, propyrene glycol, and 1,4-butanediol, ketones such as acetone and methyl ethyl ketone, esters such as ethyl acetate, paraffins such as isooctane, and cyclohexane, ethers such as dioxane, and diethyl ether, and aromatic compounds such as benzene, and toluene. The organic solvent may be used singly or two or more of them may be used in admixture. In the present disclosure, it is preferred to use alcohols, more preferred to use methanol, ethanol, and isopropanol.
An amount of the organic solvent to be used is not particularly limited but preferably 0.1 to 50 mol per 1 mol of the used material. If less than 0.1 mol, the compatibility with the materials may be reduced. If more than 50 mol, it is not preferred because the production efficiency may be extremely decreased. The amount of water is not particularly limited but preferably 0.5 to 15 mol per 1 mol of the used materials. The amount of water to be used has an effect on the particle diameter of the formed silica fine particles. With the increase in the amount of water relatively, the particle diameter of the silica fine particle may be lessened. With the decrease in the amount of water relatively, the particle diameter of the silica fine particles may be enlarged. Therefore, the particle diameter of the silica fine particles may be adjusted by controlling the ratio of water and the organic solvent.
In addition, a catalyst such as ammonia, urea, ethanolamine, and tetramethylammonium hydroxide may be added in the organic solvent. When the catalyst is used, the amount is not particularly limited but preferably 0.05 to 10 mol per 1 mol of the used materials.
The step (1) is more preferably done in a solution of homogeneous solvent to obtain the high-density silica particle of the present disclosure. That is, a reaction in a mixed solution of a solvent which can be mixed in all proportions with water and can dissolve a silane compound being the material and water, is preferred. The reaction in the mixed solution of the solvent and water is preferred because it is easy to obtain the high-density silica. The solvent which can dissolve the silane compound being the material may include alcohols such as ethanol, methanol, isopropanol, n-butanol, t-butanol, pentanol, ethyleneglycol, propyrene glycol, and 1,4-butanediol.
The hydrolysis and condensation of the materials in an organic solvent containing water may be done by adding the materials in the organic solvent containing water and stirring at 0 to 100° C., preferably 0 to 70° C. In this way, a slurry containing spherical silica may be obtained by stirring the materials in the organic solvent containing water, hydrolysis and condensation.
Usually, silica particle is calcinated at low temperature of about 200 to 700° C. This is due to the feature that the silanol groups existing at the silica surface are connected to form aggregates by calcinating at high temperature. The present disclosure can reduce the silanol group amount and fine pores to obtain silica particles having the low water-absorbing rate, by setting the calcinating temperature which is usually about 200 to 700° C. at the high temperature. The present disclosure found that the effect of the invention can be achieved efficiency by using the tetraethoxysilane and/or the derivative thereof as a material.
The calcinating temperature is 900 to 1050° C. If less than 900° C., the water-absorbing rate cannot be reduced sufficiently. If more than 1050° C., it becomes hard to obtain silica particles having the sharp particle size distribution because the fusion between the particles occurs to form an aggregate. The calcinating temperature is more preferably 950 to 1050° C. The calcinating is preferably done for 10 min. to 10 hours. If the calcinating time is less than 10 min., it is not preferred because the calcinating may be insufficient.
The silica particle obtained according to the above-mentioned method has a sharp particle size distribution but the particles may be pulverized or classified using a sieve if sharper particle size distribution is required or in order to remove a few coarse particles contained therein. A method for pulverization is not particularly limited but includes, for example, a method using an atomizer and so on. The classification using a sieve includes wet classification and dry classification.
The method for producing a silica particle of the present disclosure preferably comprises surface treating with use of a silane coupling agent and/or a silane compound. By doing the surface treatment, the water-absorbing rate can be reduced because the silanol group amount existing at the surface of the silica particle can be reduced. The silane coupling agent and/or the silane compound are not particularly limited but include the above-mentioned compounds.
A method for the surface treatment is not particularly limited but ordinary known methods may be used. Among them, a spray drying is preferred. The silica particle of the present disclosure has low reactivity with a silane coupling agent because the silanol group amount existing at the surface thereof is reduced. However, the silane coupling agent can be applied suitably by surface treating through use of a spray drying and baking (drying step). In a method of the spray drying, a spray drier is used and a charge amount is controlled so that the exit temperature is set at 90 to 100° C.
The silica particle may be used as an additive of a resin. A resin composition containing the silica particle and a resin is one aspect of the present disclosure. In this case, a resin to be used is not particularly limited but may be a thermoplastic resin or a thermosetting resin. There may be mentioned, for example, epoxy resins, phenol resins, polyphenylene sulfide resin (PPS), polyester resins, polyamides, polyimides, polystyrenes, polyethylenes, polypropylenes, polyvinyl chloride, polyvinylidene chloride, fluorine resins, polymethylmethacrylate, ethylene/ethyl acetate copolymer resin (EEA), polycarbonate, polyurethanes, polyacetals, polyphenylene ethers, polyether imides, acrylonitrile butadiene styrene copolymer resin (ABS), liquid crystal resins (LCP), silicone resins, acrylic resins and so on. Two or more of the resins may be used. Especially, a resin composition containing the silica particle and the epoxy resin may be used suitably as a sealing composition.
The resin composition may be a composition containing the silica particle and a photo-curable resin. The photo-curable resin may include a compound containing two or more acrylate groups or methacrylate groups. As this compound, specifically, there may be mentioned EO-modified bisphenol A di(meth)acrylate, trimethylolpropane tri(meth)acrylate, pentaerythritol tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, dipentaerythritol hexa(meth)acrylate, dipentaerythritol tetra(meth)acrylate, tricyclodecanedimethanol(meth)acrylate, hexanediol di(meth)acrylate, dipentaerythritol hydroxypenta(meth)acrylate, pentaerythritol ethoxytetra(meth)acrylate, tris(acryloxy ethyl)isocyanurate, trimethylolpropane benzoate(meth)acrylate, neopentyl glycol di(meth)acrylate, polypropyleneglycol di(meth)acrylate, polyethylene glycol di(meth)acrylate, imido(meth)acrylate, amino(meth)acrylate, polyester(meth)acrylate, ester(meth)acrylate, urethane(meth)acrylate, epoxy(meth)acrylate, isocyanuric acid-modified tri(meth)acrylate, and so on. In the disclosure, (meth)acrylate means methacrylate and acrylate.
An amount of the silica particle to be added in the resin composition is not particularly limited but may be controlled according to need. Specifically, the amount is preferably 10 to 950 weight parts, more preferably 100 to 900 weight parts relative to 100 weight parts of the resin, when the resin composition is used as a sealing resin composition.
In the resin composition, two kinds of the silica particles having the different particle diameters may be used. More specifically, coarse particles having large particle diameter and fine silica particles having the particle diameter of ⅓ to 1/40 of the silica particles having large particle diameter may be used in combination. The mixing ratio between the coarse particles and fine particles is preferably the coarse particles 90 to 40%: the fine particles 10 to 60% in volume. More preferably, it is within the range of the coarse particles 80 to 60%: the fine particles 20 to 40%. It is preferred to set the mixing ratio between the coarse particles and the fine particles within the above-mentioned range because the filling constitution becomes nearly closest filling to increase the filling ratio of particles.
The resin composition of the present disclosure is superior in the humidity resistance, processability, dimensional stability, and so on, because the silica particles to be used as the filling material have the above-mentioned performances. The use of the resin composition is not particularly limited but includes, for example, a sealing resin composition for a semiconductor and an electronic component, an adhesive agent, a toner external additive and so on. When used in such the use, other additives than the silica particle and the resin may be added according to use.
The silica particle of the present disclosure may be used for a liquid sealing material, a liquid crystal sealing agent, a seal agent, a polyimide film, a sputtering target, a CMP slurry (abrading agent), a dental material, a food additive, and cosmetics.
Hereinafter, the present disclosure will be described in more detail by way of examples, but the present disclosure is not limited to these examples. In examples, “%” means “weight %”, unless otherwise specified.
In the following, the particle size distribution of the obtained silica particles were measured by using a laser diffraction particle size analyzer (Microtrac MT 3300 EX manufactured by NIKKISO CO., LTD.). The particles were observed by using Scanning Electron Microscope (JSM-7000f manufactured by JEOL, Ltd.). The average particle diameter was measured by using a laser diffraction particle size analyzer (Microtrac MT 3300 EX manufactured by NIKKISO CO., LTD.). The true specific gravity was measured by using Beckmann air comparison pycnometer 930 type.
A 2 L-reaction vessel equipped with an agitator was set in a constant-temperature bath, ethanol 205 g, water 246 g, and 25 wt % ammonia water 232 g were put into the vessel. The mixture was mixed by using the agitator with heating to 50° C. Next, with stirring the mixture, tetraethoxysilane 267 g was added continuously for 200 min. After adding, the solution was filtered to obtain silica particles. Then, the particles were dried at 130° C. one night, and calcinated at 1000° C. The calcinating condition was that the temperature was raised to 1000° C. for 10 hours, kept for 5 hours, and then lowered. The obtained silica particle was spherical, the average particle diameter was 0.05 μm, and the D90/D10 value was 1.7.
A 2 L-reaction vessel equipped with an agitator was set in a constant-temperature bath, ethanol 102 g, water 184 g, and 25 wt % ammonia water 204 g were put into the vessel. The mixture was mixed by using the agitator with heating to 33° C. Next, with stirring the mixture, tetraethoxysilane 421 g was added continuously for 45 min. After adding, the solution was filtered to obtain silica particles. Then, the particles were dried at 130° C. one night, and calcinated at 1000° C. The calcinating condition was that the temperature was raised to 1000° C. for 10 hours, kept for 5 hours, and then lowered. The obtained silica particle was spherical, the average particle diameter was 0.1 μm, and the D90/D10 value was 1.9.
A 2 L-reaction vessel equipped with an agitator was set in a constant-temperature bath, ethanol 85.5 g, water 184 g, and 25 wt % ammonia water 204 g were put into the vessel. The mixture was mixed by using the agitator with heating to 25° C. Next, with stirring the mixture, tetraethoxysilane 421 g was added continuously for 45 min. After adding, the solution was filtered to obtain silica particles. Then, the particles were dried at 130° C. one night, and calcinated at 1000° C. The calcinating condition was that the temperature was raised to 1000° C. for 10 hours, kept for 5 hours, and then lowered. The obtained silica particle was spherical, the average particle diameter was 0.4 μm, and the D90/D10 value was 1.8.
A 2 L-reaction vessel equipped with an agitator was set in a constant-temperature bath, ethanol 171 g, water 184 g, and 25 wt % ammonia water 204 g were put into the vessel. The mixture was mixed by using the agitator with heating to 25° C. Next, with stirring the mixture, tetraethoxysilane 421 g was added continuously for 45 min. After adding, the solution was filtered to obtain silica particles. Then, the particles were dried at 130° C. one night, and calcinated at 1000° C. The calcinating condition was that the temperature was raised to 1000° C. for 10 hours, kept for 5 hours, and then lowered. The obtained silica particle was spherical, the average particle diameter was 0.7 μm, and the D90/D10 value was 1.7.
A 2 L-reaction vessel equipped with an agitator was set in a constant-temperature bath, ethanol 342 g, water 184 g, and 25 wt % ammonia water 204 g were put into the vessel. The mixture was mixed by using the agitator with heating to 25° C. Next, with stirring the mixture, tetraethoxysilane 421 g was added continuously for 45 min. After adding, the solution was filtered to obtain silica particles. Then, the particles were dried at 130° C. one night, and calcinated at 1000° C. The calcinating condition was that the temperature was raised to 1000° C. for 10 hours, kept for 5 hours, and then lowered. The obtained silica particle was spherical, the average particle diameter was 1.5 μm, and the D90/D10 value was 1.7.
The silica particles were obtained by following the same procedure as that of Examples 1 to 5 except that the calcinating temperature was changed to 900° C. The obtained silica particles were spherical and the average particle diameters thereof were 0.05, 0.1, 0.4, 0.7 and 1.5 μm, respectively. The D90/D10 values thereof were 1.7, 1.9, 1.8, 1.7, and 1.7, respectively.
The silica particles were obtained by following the same procedure as that of Examples 0.1 to 5 except that the calcinating temperature was changed to 950° C. The obtained silica particles were spherical and the average particle diameters thereof were 0.05, 0.1, 0.4, 0.7 and 1.5 μm, respectively. The D90/D10 values thereof were 1.7, 1.9, 1.8, 1.7, and 1.7, respectively.
The silica particles were obtained by following the same procedure as that of Examples 1 to 5 except that the calcinating temperature was changed to 1050° C. The obtained silica particles were spherical and the average particle diameters thereof were 0.05, 0.1, 0.4, 0.7 and 1.5 μm, respectively. The D90/D10 values thereof were 1.7, 1.9, 1.8, 1.7, and 1.7, respectively.
The silica particles were obtained by following the same procedure as that of Examples 1 to 5 except that the calcinating temperature was changed to 700° C. The obtained silica particles were spherical and the average particle diameters thereof were 0.05, 0.1, 0.4, 0.7 and 1.5 μm, respectively. The D90/D10 values thereof were 1.7, 1.9, 1.8, 1.7, and 1.7, respectively.
The silica particles were obtained by following the same procedure as that of Examples 1 to 5 except that the calcinating temperature was changed to 750° C. The obtained silica particles were spherical and the average particle diameters thereof were 0.05, 0.1, 0.4, 0.7 and 1.5 μm, respectively. The D90/D10 values thereof were 1.7, 1.9, 1.8, 1.7, and 1.7, respectively.
The silica particles were obtained by following the same procedure as that of Examples 1 to 5 except that the calcinating temperature was changed to 800° C. The obtained silica particles were spherical and the average particle diameters thereof were 0.05, 0.1, 0.4, 0.7 and 1.5 μm, respectively. The D90/D10 values thereof were 1.7, 1.9, 1.8, 1.7, and 1.7, respectively.
The silica particles were obtained by following the same procedure as that of Examples 1 to 5 except that the calcinating temperature was changed to 850° C. The obtained silica particles were spherical and the average particle diameters thereof were 0.05, 0.1, 0.4, 0.7 and 1.5 μm, respectively. The D90/D10 values thereof were 1.7, 1.9, 1.8, 1.7, and 1.7, respectively.
The water-absorbing rate was measured after the obtained silica particles 10 g was put in a 300 mL-beaker and kept in a thermo-hygrostat (LH-113 manufactured by ESPEC corp.) at 50° C. temperature and 90% humidity for 500 hours.
The water-absorbing rate was measured by following the same procedure as that of the water-absorbing rate 1 except that the condition was changed to 85° C. temperature and 85% humidity.
The specific gravity of the silica particles obtained by calcinating at the several calcinating temperature was measured by using Beckmann air comparison pycnometer 930 type. The true specific gravity of the obtained silica particles were shown in Table 1. The water-absorbing rate of the each particle at 50° C. temperature and 90% humidity was shown in table 2. The water-absorbing rate of the each particle at 85° C. temperature and 85% humidity was shown in table 3. The relationship between the true specific gravity and the water-absorbing rate of the particle having the average particle diameter of 0.4 μm was shown in
From the results, it was shown that there is a correlation between the true specific gravity and the water-absorbing rate. Concerning the silica particle having the average particle diameter of 0.4 μm, the silica particle having the true specific gravity of 2.1 g/cm3 or more had the water-absorbing rate less than 1.0%, so the silica particle which is superior in the humidity resistance could be achieved.
Silica powder of Example 2 was re-pulped at 400 g/L, and wet pulverized by using a sand mill. After then, a coupling agent KBM-403 (manufactured by Shin-Etsu Chemical Co., Ltd.) which is hydrolyzed at room temperature in advance was added to the slurry, and stirred at 60° C. for two hours. This slurry was spray-dried by using L-12 type spray drier (manufactured by Ohkawara Kakohki Co., LTD.). This time, the charge amount was controlled so that the exit temperature was 90 to foot. The obtained silica powder was dried at 130° C. in a drying machine to bind KBM-403 to the silica particle.
Silica powder of Example 4 was re-pulped at 400 g/L, and wet pulverized by using a sand mill. After then, a coupling agent KBM-403 (manufactured by Shin-Etsu Chemical Co., Ltd.) which is hydrolyzed at room temperature in advance was added to the slurry, and stirred at 60° C. for two hours. This slurry was spray-dried by using L-12 type spray drier (manufactured by Ohkawara Kakohki Co., LTD.). This time, the charge amount was controlled so that the exit temperature was 90 to 100° C. The obtained silica powder was dried at 130° C. in a drying machine to bind KBM-403 to the silica particle.
The silica particle was surface treated by following the same procedure as that of Example 21 except that the silane coupling agent was changed to hexamethyldisilazane being alkoxysilane (HMDS) (manufactured by Shin-Etsu Chemical Co., Ltd.).
The silica particle was surface treated by following the same procedure as that of Example 22 except that the silane coupling agent was changed to hexamethyldisilazane being alkoxysilane (HMDS) (manufactured by Shin-Etsu Chemical Co., Ltd.).
Silica particle of example 2 having the particle diameter of 0.1 μm and silica particle of example 4 having the particle diameter of 0.7 μm were mixed in the ratio of 3:7 (weight ratio), and a resin composition was prepared by mixing this mixture 232 weight parts relative to EEA resin 100 weight parts. The resin composition obtained by this way was molded to a test piece of 2 square mm.
Silica particle of example 21 having the particle diameter of 0.1 μm and silica particle of example 22 having the particle diameter of 0.7 μm were mixed in the ratio of 3:7 (weight ratio), and a resin composition was prepared by mixing this mixture 232 weight parts relative to EEA resin 100 weight parts. The resin composition obtained by this way was molded to a test piece of 2 square mm.
Silica particle of example 23 having the particle diameter of 0.1 μm and silica particle of example 24 having the particle diameter of 0.7 μm were mixed in the ratio of 3:7 (weight ratio), and a resin composition was prepared by mixing this mixture 232 weight parts relative to EEA resin 100 weight parts. The resin composition obtained by this way was molded to a test piece of 2 square mm.
The dynamic viscoelasticity of the test pieces of Examples 25 to 27 were measured (measuring condition was 190° C., a capillary to be used has the capillary diameter of 2.0 mm) by using a capillary rheometer (type 1D, manufactured by Toyo Seiki Seisaku-Sho, Ltd.). The method for measuring it was according to JIS K 7199.
The result was shown in
The present disclosure can obtain silica particle having the sharp particle size distribution and lower water-absorbing rate than ordinary particles. Such the silica particle can be used suitably for the fields such as a sealing resin composition of electronic components, an adhesive agent, and a toner external additive.
The silica particle of the present disclosure can be used for a liquid sealing material, a liquid crystal sealing agent, a seal agent, a polyimide film, a sputtering target, a CMP slurry (abrading agent), a dental material, a food additive, and cosmetics.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2010-014016 | Jan 2010 | JP | national |
| 2010-178811 | Aug 2010 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2011/050491 | 1/14/2011 | WO | 00 | 7/23/2012 |
