Patent Grant
8092654
The present invention relates to a polyurethane process belt for papermaking used in a papermaking machine as shoe press belt, transfer belt, calender belt and the like, having high hardness and high extensibility and flexural properties. In a papermaking machine, a shoe press belt is for example compressed together with a papermaking press felt (also called press fabric), on which a wet paper web has been placed, by a press roll and a shoe for squeezing moisture comprised in the wet paper web. The present invention also relates to a method for making the process belt.
In the papermaking process, a papermaking machine is conventionally equipped with a wire part, a press part and a dryer part for squeezing water from a wet paper web. The wire part, press part and dryer part are arranged in this order in the transfer direction of the wet paper web. The wet paper web is squeezed while being transferred by passing from one papermaking equipment to the next provided in the wire part, the press part and the dryer part, and is finally dried in the dryer part.
In these parts, papermaking equipment is used which corresponds to the functions of dewatering the wet paper web (wire part), squeezing water from the wet paper web (press part) and drying the wet paper web (dryer part). Moreover, the press part is generally equipped with one or more press devices arranged in series next to each other in the direction in which the wet paper web is transferred.
In each press device, an endless felt (closed type) or an open-ended felt that has been formed into an endless felt by connecting it in the papermaking machine is provided. Each press device also comprises a pair of rolls, which face each other (namely, a roll press), or a roll and a shoe press; the wet paper web is placed on the felt, and, while it is moving together with the felt in the wet paper web transfer direction, moisture is squeezed from the wet paper web by pressing the wet paper web together with the felt and the shoe press belt in the roll press or in the shoe press; the moisture pressed from the wet paper web is continuously absorbed by the felt or passes through the felt to be discharged to the outside of the felt.
Hereinafter, one example of the above-mentioned press device part will be described with reference to
As shown in
For these reasons, polyurethane having good crack resistance is widely used as resin material for forming the outer circumferential polyurethane layer 21 of the shoe press belt 2.
JP, A, 2002-146694 (Patent Document 1), for example, proposes a shoe press belt made from an integrated structure of a reinforcing fibrous base material and polyurethane, the polyurethane comprising an outer circumferential layer and an inner circumferential layer, the reinforcing fibrous base material being embedded in the polyurethane, wherein
a polyurethane of the outer circumferential layer is a polyurethane with a “JIS A hardness” of 89 to 94 made by curing mixed composition of
a polyurethane of the inner circumferential layer is a polyurethane made by curing a mixed composition of
JP, A, 2002-146694 (Patent Document 1) further proposes a papermaking process belt made from an integrated structure of a reinforcing base material and thermosetting polyurethane, the reinforcing base material being embedded in the polyurethane, the outer circumferential surface and the inner circumferential surface being made from the polyurethane, wherein a polyurethane, which forms the outer circumferential surface, is made from polyurethane of a composition comprising a urethane prepolymer having a terminal isocyanate group and a curing agent containing dimethylthiotoluene diamine.
JP, A, 2008-285784 (Patent Document 2), moreover, proposes a shoe press belt, shown in
an urethane prepolymer (A) produced by reacting an isocyanate compound selected from p-phenylene-diisocyanate and 4,4′-methylenebis(phenylisocyanate) with a polytetramethylene glycol (PTMG) and having a terminal isocyanate group, and
a curing agent mixture (B) comprising 1,4-butanediol and an aromatic polyamine having an active hydrogen group (H).
Compared to the shoe press belt according to Patent Document 1, the shoe press belt according to Patent Document 2 uses a straight chain polyol compound as polyol component and an isocyanate compound selected from p-phenylene-diisocyanate and 4,4′-methylenebis(phenylisocyanate) of which the hardness, flexural resistance and curing speed as polyisocyanate of the polyurethane material are difficult to adjust; therefore, it has the excellent properties such as resistance against flexural fatigue, resistance to crack propagation, resistance to groove closure, hardness, elongation properties and toughness of the wear characteristics.
JP, T, 2007-530800 (Patent Document 3), moreover, proposes a papermaking process belt having a polyurethane layer comprising a coating which has polyurethane, as its base, using TDI and MDI as isocyanate compounds and including an amount from about 0.01 to about 10% by weight, preferably 1 to 5% by weight, of nanoparticles ranging in lengths from about 100 nm to about 500 nm but not exceeding an average size distribution of 100 nm. Patent Document 3 mentions that this papermaking process belt improves at least one of the following characteristics: resistance to flex fatigue, resistance to crack propagation, resistance to groove closure, hardness, elongation characteristics and wear characteristics.
The specification of Japanese Patent No. 3264461 (Patent Document 4) is related to a transfer belt (conveyor belt) and discloses a transfer belt used in a papermaking or paperboard-making machine and the like for carrying a web from a first transfer point, where the transfer belt is subjected to compression, in a closed draw to a second transfer point. The transfer belt comprises a reinforcing base fabric and an aliphatic polyurethane polymer coating on the paper side (outer layer) of the reinforcing base fabric, wherein
the reinforcing base fabric has a back side and the above-mentioned paper side,
the polymer film is formed by coating and drying an aliphatic polyurethane aqueous dispersion liquid comprising 23.6% by weight of kaolin clay and 67.5% by weight of aliphatic polyurethane (solid volume) on the reinforcing base fabric surface, and has a hardness ranging from Shore A 50 to Shore A 90,
the polymer film comprises a web-contacting surface with a pressure-responsive recoverable degree of roughness,
the roughness before the polymer film is compressed is in the range from Rz=2 microns to 80 microns,
when the transfer belt is in the press nip, this roughness is in the range from Rz=0 micron to 20 microns, and
after exiting the press nip, it is capable of returning to the roughness it had before the compression.
Patent Document 3 lists clay, carbon black, silica, silicon carbide, or metallic oxides such as alumina as examples of nanoparticles. As examples of metallic oxides are listed aluminum oxide, titanium oxide, iron oxide, zinc oxide, indium oxide, tin oxide, antimony oxide, cerium oxide, yttrium oxide, zirconium oxide, copper oxide, nickel oxide and/or tantalum oxide and combinations thereof. For example, in one embodiment, up to 1% by weight of uncoated alumina, alumina coated with epoxysilane or octylsilane was added. It is further mentioned that clays may include montmorillonite such as Cloisite (registered trade name) 30B, saponite, hectorite, mica, vermiculite, bentonite, nontronite, volkonskoite, manadiite and henyaite and combinations thereof.
The papermaking process belt according to Patent Document 3 has a higher surface hardness than the transfer belt disclosed in Patent Document 4; moreover the figures for resistance to flex fatigue and resistance to crack propagation disclosed in its specification are about 4 to 5 times better than those for the papermaking process belt according to Patent Document 1; however, resistance to flex fatigue and resistance to crack propagation of the papermaking process belt according to Patent Document 3 are inferior to the corresponding figures for the shoe press belt according to Patent Document 2.
The shoe press belt according to Patent Document 2 uses an isocyanate compound selected from p-phenylene-diisocyanate and 4,4′-methylenebis(phenylisocyanate); therefore, there is the disadvantage that it is difficult to control the temperature when the polyisocyanate compound and the curing agent are heated.
The process belt of Patent Document 4 uses an aliphatic polyurethane aqueous dispersion liquid comprising 23.6% by weight of kaolin clay and 67.5% by weight of aliphatic polyurethane (solid volume) as coating agent; therefore, there is an increase in the “JIS A hardness” of the belt due to the kaolin clay and an improvement of the extensibility of the belt due to the aliphatic polyurethane; however, the improvement of the durability is still insufficient.
[Patent Document 1] JP, A, 2002-146694
[Patent Document 2] JP, A, 2008-285784
[Patent Document 3] JP, T, 2007-530800
[Patent Document 4] JP, B, 3264461
The means for increasing the effect of suppressing the fatigue crack growth rate of a papermaking shoe press belt by blending nanoparticles according to Patent Document 3 has the advantage that it can be used without specifying the type of polyisocyanate compound of the polyurethane raw material. Nevertheless, there is the disadvantage that the dispersion of the nanoparticles in the urethane prepolymer and, when the curing agent is mixed, the further uniform dispersion of the nanoparticles in the curable urethane composition causes the nanoparticles to absorb the moisture in the air and react with the polyisocyanate compound and induces secondary aggregation of the nanoparticles; thus it is difficult to use more than 10% by weight of nanoparticles. Mixtures with 0.1 to 10% by weight of nanoparticles may also be employed for shoe press belts; however, for process belts which require hydrophilic properties a higher blending ratio of the nanoparticles is preferred.
During the evaluation of the effect of suppressing the fatigue crack growth rate in papermaking process belts produced from polyurethane using an inorganic filler of an average particle size of 1 to 20 μm which is homogeneously dispersed in a curable urethane composition, the present inventors discovered that an inorganic filler comprising 50% by weight or more of a silicon oxide component from calcined kaolin clay, fused silica, zeolite of an average particle size of 1 to 20 μm, or from particles thereof that have been surface treated by an organic silane coupling agent can further improve the suppression of the fatigue crack growth rate by a factor of 2 to 10.
The invention of claim 1 proposes a papermaking process belt comprising an integrated structure of a reinforcing fibrous base material and a polyurethane layer, the reinforcing fibrous base material being embedded in the polyurethane; wherein one part of the polyurethane or all of the polyurethane is formed by heat curing of a curable urethane composition comprising a urethane prepolymer having a terminal isocyanate group and which is obtained by reacting an aromatic isocyanate compound and polyol, a curing agent having an active hydrogen group, and 0.3 to 30% by weight of an inorganic filler of which the main component is a silicon oxide component selected from calcined kaolin clay, fused silica and zeolite of an average particle size of 1 to 20 μm.
The invention of claim 2 proposes a papermaking process belt according to claim 1, wherein, in the inorganic filler, the particle surfaces of the calcined kaolin clay or the fused silica are treated with 0.2 to 3% by weight (as a percentage of the weight of the inorganic filler that is surface-treated by the organic silane coupling agent) of an organic silane coupling agent.
The invention of claim 3 proposes a papermaking process belt according to claim 1, wherein the “JIS A hardness” of the polyurethane outer layer side of the papermaking process belt that is in contact with the wet paper web is 91 to 100.
The invention of claim 4 proposes a method for making a papermaking process belt comprising an integrated structure of a reinforcing fibrous base material and a polyurethane layer, the reinforcing fibrous base material being embedded in the polyurethane; wherein are comprised
a process for obtaining a curable urethane composition by mixing a urethane prepolymer, a curing agent having an active hydrogen group and an inorganic filler, and
a process for forming a polyurethane layer by heat-curing a curable urethane composition, wherein one part or all the polyurethane is made from the curable urethane composition and a reinforcing fibrous base material is embedded therein, and wherein
the inorganic filler comprises, as main component, a silicon oxide component selected from calcined kaolin clay, fused silica and zeolite of an average particle size of 1 to 20 μm, and wherein the inorganic filler is 0.3 to 30% by weight of the curable urethane composition, and
the urethane prepolymer having a terminal isocyanate group is made by reacting an aromatic isocyanate compound and a polyol.
The papermaking process belt of the present invention uses an inorganic filler of which the main component are silicon oxide particles from calcined kaolin clay, fused silica and zeolite which, with an average particle size of 1 to 20 μm, have a large particle size; therefore, the inorganic filler can be easily blended with the curable urethane composition, and the bonding of the inorganic filler with the aromatic-type polyurethane to be formed is also strong. Moreover, with a blending ratio of 0.3 to 30% by weight, the inorganic filler can also be blended at an increased ratio, and it is possible to provide a polyurethane process belt with high hardness and a fatigue crack growth rate suppressing effect 5 to 20 times higher than that of the commercially available polyurethane shoe press belts, transfer belts, calender belts and other papermaking process belts.
Hereinafter, the present invention will be described in still greater detail with reference to the drawings.
In any one of the above-mentioned shoe press belt structures, one part of the polyurethane or all of the polyurethane in a polyurethane process belt is formed by curing a curable urethane composition comprising a urethane prepolymer having a terminal isocyanate group, a curing agent having an active hydrogen group, and an inorganic filler of which the main component is a silicon oxide component selected from calcined kaolin clay, fused silica, zeolite of an average particle size of 1 to 20 μm, preferably 1 to 10 μm, and surface treated inorganic fillers of the calcined kaolin clay, fused silica of which the particle surface has been treated with an organic silane coupling agent having an active hydrogen group (II). The above-mentioned curable urethane composition comprises the inorganic filler in an amount of 0.3 to 30% by weight, preferably 1.0 to 20% by weight in the case of a shoe press belt, 12 to 28% by weight in the case of transfer belt in which hydrophilic properties are desirable, and 3 to 20% by weight in the case of a calender belt.
The above-mentioned urethane prepolymer (A) has an isocyanate group (—NCO) at its terminal and is obtained by reacting an aromatic polyisocyanate compound (a) and a polyol (b). The terminal isocyanate group of the urethane prepolymer (A) may be masked with a blocking agent of phenol, oxime, alcohol, organic aliphatic amine, organic carboxylic acid and the like.
Examples of the aromatic polyisocyanate compound (a) include one or more polyisocyanates selected from 2,4-tolylene-diisocyanate, 2,6-tolylene-diisocyanate, 1,5-napthalene-diisocyanate, p-phenylene-diisocyanate, 4,4′-methylenebis(phenylisocyanate) and metaxylene diisocyanate. Particularly preferred are TDI, MDI because they require little heat curing energy when the polyurethane is produced.
Examples of the polyol (b) include one or more polyols selected from polyether polyols such as polytetramethylene glycol, polyethylene glycol, polypropylene glycol and the like, and polyester polyols such as polycaprolactone ester, polycarbonate, polyethylene adipate, polybutylene adipate, polyhexane adipate and the like. Particularly preferred are polyether polyols with a molecular weight of 230 to 3000 such as polytetramethylene glycol, polyethylene glycol, polypropylene glycol and the like.
The isocyanate group (—NCO) of the aromatic polyisocyanate compound (a) is reacted such that the equivalent ratio in relation to the hydroxyl group (—OH) of the polyol (b) is L or more and isocyanate groups remain at the terminal of the urethane prepolymer produced.
Examples of the curing agent (B) having an active hydrogen group (—H) include one or more curing agents selected from aliphatic polyols such as 1,4-butandiol, glycerin, pentaerythritol and the like, aromatic polyamines with a molecular weight of 108 to 380, preferably 198 to 342, selected from a mixture of 3,5-diethyltoluene-2,4-diamine and 3,5-diethyltoluene-2,6-diamine (trade name Ethacure 100), 4,4′-bis(2-chloroaniline), a mixture of 3,5-dimethylthio-2,4-toluenediamine and 3,5-dimethylthio-2,6-toluenediamine (trade name Ethacure 300), 4,4′-bis(sec-butylamino)-diphenylmethane, N,N′-dialkyldiaminodiphenylmethane, 4,4′-methylenedianiline (MDA), 4,4′-methylene-bis(2,3-dichloroaniline) (TCDAM), 4,4′-methylene-bis(2-chloroaniline) (MOCA), 4,4′-methylene-bis(2-ethyl-6-methylaniline) (trade name CUREHARD MED), trimethylene-bis(4-aminobenzoate) (trade name CUA-4), and m-phenylenediamine (MPDA).
The isocyanate group (—NCO) of the urethane prepolymer (A) and the active hydrogen group (—H) of the curing agent (B) are used at such a proportion that the equivalent ratio (—H/—NCO) with the isocyanate group (—NCO) of the urethane prepolymer (A) is 0.88≦N/NCO≦1.12, and preferably 0.95≦N/NCO≦1.0. The polyurethane layer of the outer layer is formed by heat curing the curable urethane mixed composition of the urethane prepolymer and the curing agent and 0.3 to 30% by weight of the inorganic filler at 70 to 140° C. for 2 to 20 hours. A low H/NCO ratio is desirable for increasing the wear resistance of a polyurethane belt, whereas a high H/NCO ratio is desirable for increasing the crack prevention properties of a polyurethane belt.
Examples of the inorganic filler (C) include inorganic fillers of which the main component is a silicon oxide component selected from calcined kaolin clay, fused silica, zeolite of an average particle size of 1 to 20 μm, preferably 1 to 10 μm, and surface treated inorganic fillers of the calcined kaolin clay, fused silica of which the particle surface has been treated with an organic silane coupling agent. These inorganic fillers (C) are used with a moisture content of less than 1.0% by weight, and preferably 0.0001% by weight or less.
Examples of organic silane coupling agents preferably include organic silane coupling agents having an active hydrogen group (—H) such as amine group (—NH2)-modified organosilane coupling agent, mercapto group (—SH)-modified organosilane coupling agent, carboxyl group (—COOH)-modified organosilane coupling agent and the like, and modified organosilane coupling agents having an alkoxy group (OR) and an active hydrogen group (—H). These coupling agents may be used on their own, or two or more may be used together. Moreover, organic silane coupling agents having an active hydrogen group (—H) also include alkoxy group-modified organic silane coupling agents and amide group-modified organic silane coupling agents which exhibit an active hydrogen group (—H) by dissolving due to heating and reacting with the moisture in the air.
Specific examples of modified-organosilane coupling agents include 3-octanoylthiopropyltriethoxysilane, γ-ureidepropyltriethoxysilane, β-(3,4-epoxycyclohexyl)ethyltrimethoxysilane and the like.
Specific examples of the amino group-modified organosilane coupling agents include N-β(aminoethyl)γ-aminopropyltrimethoxysilane, N-β(aminoethyl)γ-aminopropylmethyldimethoxysilane, γ-aminopropyltriethoxysilane, N-phenyl-γ-aminopropyltrimethoxysilane, N-2-(aminoethyl)3-aminopropylmethyldimethoxysilane, N-2-(aminoethyl)3-aminopropyltrimethoxysilane, N2-(aminoethyl)-3-aminopropyltriethoxysilane, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3-triethoxysilyl-N-(1,3-dimethyl-butylidene) propylamine, N-phenyl-3-aminopropyltrimethoxysilane, γ-chloropropyltrimethoxysilane and the like.
Specific examples of the epoxy group-modified organosilane coupling agents include γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropyltriethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, γ-glycidoxypropyltrimethyldiethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane and the like.
Specific examples of mercapto group (—SH)-modified organosilane coupling agents include γ-mercaptopropyltrimethoxysilane, 3-octanoylthiopropyltriethoxysilane, 3-mercaptopropylmethyldimethoxysilane, 3-mercaptopropyltrimethoxysilane, bis(triethoxysilylpropyl)tetrasulfide and the like.
Specific examples of carboxyl group (—COOH)-modified organosilane coupling agents include 3-methacryloxypropylmethyldiethoxysilane, 3-methacryloxypropyltriethoxysilane, 3-acryloxypropyltrimethoxysilane and the like.
Among these, 3-aminopropyltriethoxysilane, 3-(2-aminoethyl)aminopropyltrimethoxysilane are preferred because of their excellent affinity with fused silica, calcined kaolin clay and polyurethane. In other words, the organic silane coupling agent has good affinity with the inorganic filler having SiO2 as main component, and the active hydrogen group (—H) of the organic silane coupling agent reacts with the isocyanate group when the curable urethane composition is cured; therefore, the bond between the polyurethane produced and the inorganic filler is stronger.
The amount used of the organic silane coupling agent having an active hydrogen group is 0.2 to 3% by weight, preferably 0.5 to 1.5% by weight, of the inorganic filler.
As a calcined kaolin clay (C), for example, 3-aminopropyltriethoxysilane-modified calcined kaolin clay is available under the trade name of Translink 445 (average particle size: 1.4 μm, specific surface area: 10.4 m2/g) from the German BASF company, calcined kaolin clay is available under the trade names of Satintone W (average particle size: 1.4 μm, specific surface area: 10.4 m2/g) from BASF, under the trade names of Polestar 200R from Imerys Mineral Ltd. and under the trade names of Calconed China Clay from JETRO. Moreover, fused silica (C) is available under the trade names of Fuselex X (average particle size: 2.5 μm, specific surface area 12.8 m2/g) and Fuselex RD-8 (average particle size: 15.1 μm, specific surface area: 2.2 m2/g), both from Tatsumori Co., Ltd. The 3-(2-aminoethyl)aminopropyltrimethoxysilane used for producing the 3-(2-aminoethyl)aminopropyltrimethoxysilane-modified calcined kaolin (C) and fused silica (C) is commercially available under the trade names of KBM-603from Shinetsu Chemical Industry, Z-6020 and Z-6094 from Dow Corning Toray Co., Ltd. and A-1120 and A-1122 from Momentive. Moreover, the 3-aminopropyltriethoxysilane used for producing the 3-aminopropyltriethoxysilane-modified calcined kaolin (C) and fused silica (C) is commercially available under the trade names of KBE-903 from Shinetsu Chemical Industry, Z-6011 from Dow Corning Toray Co., Ltd. and A-1100 from Momentive. The zeolite used has a water content of less than 1% by weight. Natural zeolite (silicate-water-containing substance) is a water-containing substance, even commercially available zeolite and synthetic zeolite contain water; therefore, zeolite with a water content exceeding 1.0% by weight is dried by heating so as to volatilize the water content.
The amount of inorganic filler (C) comprising 50% by weight or more of the SiO2 contained in the polyurethane is in the range from 0.3 to 30% by weight. With less than 0.3% by weight, an increase in hardness and the fatigue crack growth rate suppressing effect cannot be expected. With more than 30% by weight, a further increase in hardness and the fatigue crack growth rate suppressing effect cannot be expected, it is difficult to uniformly mix the urethane prepolymer (A), the curing agent (B) and the inorganic filler (C), and the layering of the curable urethane composition for the outer layer becomes cumbersome.
The polyurethane raw material and the curing agent used for forming the inner layer and the intermediate layer are also selected from the polyisocyanate compound (a), polyol (b) and curing agent (B). The material composition of polyurethane of the outer layer, the polyurethane of the intermediate layer and the polyurethane of the inner layer may be identical or different. Moreover, the polyurethane of the intermediate layer and the polyurethane of the inner layer may or may not comprise 0.3 to 30% by weight of the inorganic filler.
The process belt shown in
As reinforcing fibrous base material 6, not only the woven fabrics mentioned in Patent Documents 1 to 4 but also the reinforcing base materials mentioned in other documents can be used. For example, a grid-like web can be made from CMD (Cross Machine Direction) yarns comprising multifilament twisted yarns of 5,000 dtex made from polyethylene terephthalate (PET) fibers and MD (Machine Direction) yarns comprising multifilament yarns of 550 dtex; wherein the MD yarns are sandwiched by the CMD yarns and the crossings of the MD yarns and the CMD yarns are joined by a polyurethane adhesive. As fiber material, aramid fibers, Nylon 6,6, Nylon 6,10, Nylon 6 and other polyamide fibers can also be used instead of polyethylene terephthalate. Moreover, fibers of different materials can also be used for the MD yarns and the CMD yarns. It is also possible to use different fiber sizes such as 800 dtex and 7,000 dtex and the like for the CMD yarns and the MD yarns.
Even though the outer circumferential polyurethane layer is made from polyurethane of a “JIS A hardness” of 91 to 100, preferably 95 to 98, it has excellent wear resistance, crack resistance and flexural fatigue resistance.
In the manufacture of papermaking process belts, for example, a mixture of a urethane prepolymer and a curing agent for forming an inner circumferential polyurethane layer is coated onto the surface of a mandrel, which has been coated by a parting agent, while the mandrel is being rotated so as to form an inner circumferential polyurethane layer with a thickness of 0.8 to 3.5 mm on the mandrel surface. The layer of the coated mixture is then heated to a temperature between 70 and 140° C. and precured for 0.5 to 1 hour. Then, a woven reinforcing fibrous base material is placed on top of this inner circumferential polyurethane layer, and a mixture of a urethane prepolymer and a curing agent for forming the intermediate layer is coated to a thickness of 0.5 to 2 mm. The mixture for forming the intermediate layer impregnates the base fabric and bonds with the inner circumferential polyurethane layer. The layer of the coated mixture is precured at 50 to 120° C. for 0.5 to 1 hour to form the intermediate polyurethane layer reinforced by the fibrous base material. Then, while the mandrel is being rotated, a curable urethane composition comprising the urethane prepolymer (A), the curing agent (B) and the inorganic filler (C) for forming an outer circumferential polyurethane layer is coated onto the surface of the woven reinforcing fibrous base material, impregnating the same, to form the outer circumferential polyurethane layer with a thickness of 1.5 to 4 mm. The layer of the coated mixture is then cured by being heated to a temperature between 70 and 140° C. for 2 to 20 hours. Thereafter, grooves 24 shown in
In another method for manufacturing a papermaking process belt, for example, a mixture of a urethane prepolymer and a curing agent for forming an inner circumferential polyurethane layer is coated onto a mandrel, the surface of which has been coated by a parting agent, so as to form a polyurethane layer with a thickness of 0.8 to 3 mm, which is then precured for 0.5 to 2 hours at a temperature between 70 and 140° C. Then, a reinforcing fibrous base material is placed on the outer surface of the cured polyurethane layer, and thereafter, a mixture of a urethane prepolymer and a curing agent for forming the intermediate layer is coated to a thickness of 0.5 to 2 mm. The mixture for forming the intermediate layer impregnates the base fabric and bonds with the inner circumferential layer. The layer of the coated mixture is precured at 50 to 120° C. for 0.5 to 1 hour to form the intermediate polyurethane layer reinforced by the fibrous base material. Next, a curable urethane composition comprising the urethane prepolymer (A), the curing agent (B) and the inorganic filler (C) for forming an outer circumferential surface is coated to form the outer circumferential polyurethane layer with a thickness of 2 to 4 mm, which is then post-cured at a temperature between 70 and 140° C. for 4 to 16 hours. Then grooves are cut with a cutting tool into the surface of the layered outer circumferential polyurethane layer in which the reinforcing fibrous base material is embedded, after which the outer circumferential polyurethane surface is polished by sandpaper or a polyurethane polishing cloth.
In another method for manufacturing a papermaking process belt comprising an intermediate layer, for example, a mixture of a urethane prepolymer and a curing agent for forming an inner circumferential layer is coated onto a mandrel, the surface of which has been coated by a parting agent, so as to form an inner circumferential layer with a thickness of 0.6 to 3 mm, which is then precured for 0.5 to 2 hours at a temperature between 50 and 140° C. Then, a previously manufactured intermediate polyurethane layer with a thickness of 1 to 2 mm in which a reinforcing fibrous base material is embedded is wound around the outer surface of the inner circumferential layer. Then, the intermediate layer is pressed by a nip roll which is heated to between 50 and 140° C. Next, a composition of the urethane prepolymer (A), the curing age at (B) and the inorganic filler (C) for producing the outer circumferential surface is further coated to form an outer circumferential polyurethane layer with a thickness of 2 to 4 mm, which is post-cured at 90 to 140° C. for 2 to 20 hours. Then, the outer circumferential surface of the layered polyurethane in which the reinforcing fibrous base material has been embedded is polished by sandpaper or a polyurethane polishing cloth; thereafter, grooves are cut in the surface of the outer circumferential surface by a cutting tool.
In another method for manufacturing a papermaking process belt, two rolls are used instead of the mandrel. An endless woven reinforcing fibrous base material is stretched between the two rolls. First, the surface of the fibrous reinforcing base material is coated with a blend of a urethane prepolymer and a curing agent, which impregnates the fibrous base material and is then precured at 50 to 120° C. for 0.5 to 3 hours. Thereafter, a mixture of a urethane prepolymer and a curing agent for forming the inner circumferential polyurethane layer of the process belt is coated so as to form the inner circumferential polyurethane layer with a thickness of 0.5 to 3 mm, which is then cured at 70 to 140° C. for 2 to 12 hours. The surface of the inner circumferential polyurethane layer is polished by sandpaper or a polishing cloth. Thus, the integral structure in which the inner circumferential polyurethane layer and the fibrous reinforcing base material are bonded is produced. Next, this partially finished process belt is reversed and stretched on the two rolls. Then, the surface of the stretched partially finished process belt is coated with a blend of a urethane prepolymer and a curing agent which impregnates the fibrous base material. The surface is further coated with a curable urethane composition comprising the urethane prepolymer (A), the curing agent (B) and the inorganic filler (C) to a thickness of 1.5 to 4 mm, which is cured at 70 to 140° C. for 2 to 20 hours. After completing the curing, the surface layer is polished to a prescribed thickness and grooves are formed by cutting the outer circumferential layer with a cutting tool.
Hereinafter, the production of polyurethane specimens for evaluating the physical properties of the polyurethane used for producing papermaking process belts will be described.
A curable urethane composition (with an H/NCO equivalent ratio of 0.95) was prepared by mixing a urethane prepolymer (NCO: 6.04%, preheating temperature: 30° C.), obtained by reacting tolylenediisocyanate (TDI) and polytetramethylene glycol (PTMG), and a curing agent mixture (Ethacure 300) of 3,5-dimethylthio-2,4-toluenediamine and 3,5-dimethylthio-2,6-toluenediamine. This curable urethane composition was poured into a preheated mold and heated to 100° C. After precuring at 100° C. for 30 minutes, post-curing was performed at 100° C. for 16 hours to obtain a cured polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) of a “JIS A hardness” of 95.8. The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 1 except that calcined kaolin clay (average particle size: 1.4 μm, specific surface area: 10.4 m2/g) modified by 0.5% by weight of 3-aminopropyltriethoxysilane, which had been dried at 100° C. for 2 hours, was mixed beforehand with the prepolymer to obtain the ratios shown in Table 1 for 100 parts by weight of the urethane prepolymer and the curing agent after mixing (Reference Example 2: 1 part by weight, Reference Example 3: 5 parts by weight, Reference Example 4: 12 parts by weight, Reference Example 5: 20 parts by weight, Reference Example 6: 30 parts by weight, Reference Example 7: 40 parts by weight). The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 5 except that a mixture of 3,5-diethyltoluene-2,4-diamine and 3,5-diethyltoluene-2,6-diamine (Ethacure 100) was used instead of the mixture of 3,5-dimethylthio-2,4-toluenediamine and 3,5-dimethylthio-2,6-toluenediamine (Ethacure 300) as curing agent for mixing with the prepolymer to obtain an equivalent ratio H/NCO of 1.00. The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 8 except that a mixture of 50 molar % of 3,5-diethyltoluene-2,4-diamine and 3,5-diethyltoluene-2,6-diamine (Ethacure 100) and 50 molar % of 3,5-dimethylthio-2,4-toluenediamine and 3,5-dimethylthio-2,6-toluenediamine (Ethacure 300) was used as curing agent instead of the mixture of 3,5-diethyltoluene-2,4-diamine and 3,5-diethyltoluene-2,6-diamine (Ethacure 100). The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 5 except that fused silica available under the trade name of Fuselex RD-8 (average particle size 15.1 μm, specific surface area 2.2 m2/g) was used instead of the calcined kaolin clay modified by 0.5% by weight of 3-aminopropyltriethoxysilane. The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 5 except that zeolite available under the trade name of SP 600 from Nitto Funka Kogyo K. K. (average particle size: 1.9 μm) which had been heated to 100° C. for reducing the moisture content to 1% or less was used instead of the calcined kaolin clay modified by 0.5% by weight of 3-aminopropyltriethoxysilane. The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 5 except that mica available under the trade name of SJ-005 from Yamaguchi Mica Co., Ltd. (average particle size: 5.1 μm) was used instead of the calcined kaolin clay modified by 0.5% by weight of 3-aminopropyltriethoxysilane. The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 1 except that a urethane prepolymer with an NCO of 4.41% obtained by reacting tolylenediisocyanate (TDI) and polytetramethylene glycol (PTMG) was used instead of the methane prepolymer with an NCO of 6.04% obtained by reacting tolylenediisocyanate (TDI) and polytetramethylene glycol (PTMG). The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 13 except that calcined kaolin clay available under the trade name of Satintone W (average particle size: 1.4 μm, specific surface area: 10.4 m2/g), which had been dried at 100° C. for 2 hours, was mixed beforehand with the prepolymer to obtain a ratio of 10 weight parts for 100 weight parts of the mixture of the urethane prepolymer and the curing agent. The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 14 except that calcined kaolin clay modified by 0.5% by weight of 3-aminopropyltriethoxysilane (average particle size: 1.4 μm, specific surface area: 10.4 m2/g) was used instead of the calcined kaolin clay. The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 14 except that fused silica available under the trade name of Fuselex X (average particle size: 2.5 μm, specific surface area: 12.8 m2/g) was used instead of the calcined kaolin clay. The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 14 except that fused silica modified by 1.0% by weight of 3-aminopropyltriethoxysilane (average particle size: 2.5 μm, specific surface area: 12.8 m2/g) was used instead of the calcined kaolin clay. The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 14 except that fused silica modified by 0.5% by weight of 3-(2-aminoethyl)aminopropyltrimethoxysilane (average particle size: 2.5 μm, specific surface area: 12.8 m2/g) was used instead of the calcined kaolin clay. The specimens were made from this sheet.
A curable urethane composition (with an H/NCO equivalent ratio of 0.90) was prepared by mixing a urethane prepolymer (NCO: 9.04%, preheating temperature: 30° C.), obtained by reacting methylenebis(1,4-phenylene)diisocyanate (MDI) and polytetramethylene glycol (PTMG), and a curing agent mixed from 90 molar % of 1,4-butandiol and a 10 molar % of a mixture (Ethacure 300) of 3,5-dimethylthio-2,4-toluenediamine and 3,5-dimethylthio-2,6-toluenediamine. This curable urethane composition was poured into a mold which had been preheated at 115° C. After precuring at 115° C. for 3 hours, post-curing was performed at 115° C. for 14 hours to obtain a polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius). The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 19 except that calcined kaolin clay (average particle size: 1.4 μm, specific surface area: 10.4 m2/g) modified by 0.5% by weight of 3-aminopropyltriethoxysilane, which had been dried at 100° C. for 2 hours, was mixed beforehand with the prepolymer to obtain a ratio of 20 weight parts for 100 weight parts of the mixture of the urethane prepolymer and the curing agent. The specimens were made from this sheet.
A curable urethane composition (with an H/NCO equivalent ratio of 0.90) was prepared by mixing a urethane prepolymer (NCO: 5.80%), obtained by mixing 70 parts by weight of a urethane prepolymer (NCO: 4.41%), obtained by reacting tolylenediisocyanate (TDI) and polytetramethylene glycol (PTMG), and 30 parts by weight of a urethane prepolymer (NCO: 9.04%), obtained by reacting methylenebis(1,4-phenylene)diisocyanate (MDI) and polytetramethylene glycol (PTMG), and a curing agent mixture (Ethacure 300) of 3,5-dimethylthio-2,4-toluenediamine and 3,5-dimethylthio-2,6-toluenediamine. This curable urethane composition was poured into a mold which had been preheated at 115° C. After precuring at 115° C. for 3 hours, post-curing was performed at 115° C. for 14 hours to obtain a polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius). The specimens were made from this sheet.
A polyurethane sheet (with a thickness of 3.4 mm, and having at its center a semicircular groove of 1.5 mm radius) was obtained as in Reference Example 21 except that calcined kaolin clay (average particle size: 1.4 μm, specific surface area: 10.4 m2/g) modified by 0.5% by weight of 3-aminopropyltriethoxysilane, which had been dried at 100° C. for 2 hours, was mixed beforehand with the prepolymer to obtain a ratio of 20 weight parts for 100 weight parts of the mixture of the urethane prepolymer and the curing agent. The specimens were made from this sheet.
The “JIS A hardness” and the flexural tests for the specimens produced in Reference Examples 1 to 22 were evaluated. The results obtained are shown in Table 1.
The test apparatus shown in
The size of a specimen 61 was: width=25 mm, length=185 mm (including 20 mm on each side for grips), thickness=3.4 mm; the distance between grips 62 was 150 mm; the specimen had a semicircular dimple 61a with a radius of 1.5 mm at their center. The back and forth movement of the grips took place with a speed of 360 strokes/minute over a distance of 65 mm between the greatest grip distance of 100 mm and the smallest grip distance of 35 mm. A notch with a 2 mm length in the width direction was provided at the center of the specimens. The grips 62, 62 on the left and right sides are provided so as to form an angle of 45°, respectively, in the back and forth directions. The specimens were repeatedly flexed under these conditions, and after prescribed stroke counts, the length of cracks was measured. The term stroke count used here represents a value which is the sum of the test time multiplied by the speed of the back and forth movement. The test was finished when the cracks, which had an initial notch length of about 2 mm, exceeded 15 mm. Approximate curves of the stroke count and the crack length were plotted, and the stroke counts at the crack length of 15 mm were read from the approximate curves. The length of the cracks that had grown (the measured value of the crack length of 15 mm−value of the initial notch length) was divided by the corresponding stroke count (De Mattia flexing test results) to obtain the fatigue crack growth rate (crack growth speed μm/stroke count).
Hereinafter, examples of manufacturing shoe press belts using the curable urethane composition used in Reference Examples 1 to 22 will be described.
Step 1: A parting agent (KS-61, manufactured by Sin-Etsu Chemical Co., Ltd.) was coated on the polished surface of a mandrel having a diameter of 1,500 mm which can be rotated by a suitable driving means. Next, a polyurethane layer was formed by coating a polyurethane resin mixture (H/NCO equivalent ratio: 0.95), obtained by mixing the urethane prepolymer (TDI/PTMG prepolymer) and a curing agent mixture (Ethacure 300) of 3,5-dimethylthio-2,4-toluenediamine and 3,5-dimethylthio-2,6-toluenediamine used in Reference example 1, to a thickness of 1.4 mm onto the rotating mandrel by using a doctor bar. The polyurethane resin mixture was left on the rotating mandrel at room temperature (30° C.) for 40 minutes. Then, a shoe-side inner circumferential polyurethane layer was produced by heat-precuring the polyurethane resin mixture with a heating device attached to the mandrel at 100° C. for 30 minutes.
Step 2: A grid-like web (MD yarn density 1 yarn/cm, CMD yarn density: 4 yarns/cm) was prepared from CMD yarns comprising multifilament twisted yarns of 5,000 dtex made from polyethylene terephthalate fibers and MD yarns comprising multifilament yarns of 550 dtex; wherein the MD yarns are sandwiched by the CMD yarns and the crossings of the MD yarns and the CMD yarns are joined by a urethane resin adhesive. A plurality of grid-like webs was placed as one layer, without gaps therebetween, on the outer circumference of the shoe-side layer so that the CMD yarns extend along the axis direction of the mandrel. Then, a wound-yarn layer was formed by helically winding multifilament yarns of 6,700 dtex polyethylene terephthalate fibers around the outer circumference of the grid-like web at a pitch of 30 yarns/5 cm. Thereafter, an integral structure was formed by coating the polyurethane resin mixture as intermediate layer to a thickness of 1.6 mm sufficiently to close the gap between the grid-like web and the wound-yarn layer; thereby, a reinforcing fibrous base material polyurethane intermediate layer was formed.
Step 3: The curable urethane composition, used in Reference Example 2 was coated to a thickness of about 2.5 mm onto the wound-yarn layer by using a doctor blade and left to stand at room temperature for 40 minutes. Then, a wet paper web-side layer (outer circumferential polyurethane layer) was produced by post-curing by heating at 110° C. for 4 hours. Next, the surface of the wet paper web-side layer was polished until the overall thickness was 5.2 mm, and a plurality of concave grooves (width: 0.8 mm, depth: 0.8 mm, and pitch: 2.54 mm) was formed in the MD direction of the belt by using a rotating blade. In this manner a shoe press belt was produced.
The shoe press belts in Inventive Examples 2 to 17 were produced in the same manner as in Inventive Example 1 except that, instead of the curable urethane composition of Reference Example 2, the curable urethane compositions used in Reference Examples 3 to 11, Reference Examples 14 to 18, Reference Example 20 and Reference Example 22 were used for the outer polyurethane layer.
The shoe press belts in Comparative Examples 1 to 5 were produced in the same manner as in Inventive Example 1 except that, instead of the curable urethane composition of Reference Example 2, the curable urethane compositions used in Reference Examples 1, 12, 13, 19 and 21 were used for the outer polyurethane layer.
Wear tests were performed with the shoe press belts produced in Inventive Examples 1 to 17 and Comparative Examples 1 to 5. In the wear tests, the test apparatus shown in
The reduction of the thickness (depth of wear) of the belt specimens is shown in Table 1.
From Table 1 it can be seen that the specimens with polyurethane comprising calcined kaolin clay, fused silica or zeolite as urethane for papermaking process belts according to the present invention had, without reducing wear resistance, a better fatigue crack growth rate suppressing effect and flexural resistance than the specimens with the polyurethane of the Comparative Examples.
A polyurethane papermaking process belt according to the present invention has better wear resistance, crack resistance and fatigue crack resistance than existing belts and 2 to 20 times the operational life of existing commercially available process belts using TDI and MDI as isocyanate compounds.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2009-269408 | Nov 2009 | JP | national |
| Number | Name | Date | Kind |
|---|---|---|---|
| 4923520 | Anzai et al. | May 1990 | A |
| 5298124 | Eklund et al. | Mar 1994 | A |
| 6905734 | Withers et al. | Jun 2005 | B2 |
| 20040029474 | Watanabe et al. | Feb 2004 | A1 |
| 20050208288 | Li et al. | Sep 2005 | A1 |
| 20060191658 | Watanabe et al. | Aug 2006 | A1 |
| 20090014143 | Kobayashi et al. | Jan 2009 | A1 |
| 20100032121 | Nakagawa et al. | Feb 2010 | A1 |
| 20100147480 | Yazaki et al. | Jun 2010 | A1 |
| 20100186920 | Yazaki et al. | Jul 2010 | A1 |
| 20100314067 | Yazaki et al. | Dec 2010 | A1 |
| 20110017419 | Yazaki et al. | Jan 2011 | A1 |
| Number | Date | Country |
|---|---|---|
| 0 576 115 | Dec 1993 | EP |
| 1 338 696 | Aug 2003 | EP |
| 2284772 | Jun 1995 | GB |
| 2001-263427 | Sep 2001 | JP |
| 3264461 | Dec 2001 | JP |
| 2002-146694 | May 2002 | JP |
| 2007-9389 | Jan 2007 | JP |
| 2007-530800 | Nov 2007 | JP |
| 2008-111220 | May 2008 | JP |
| 2008-156779 | Jul 2008 | JP |
| 2008-285784 | Nov 2008 | JP |
| 2009-173839 | Aug 2009 | JP |
| 4616403 | Oct 2010 | JP |
| WO 2005090429 | Sep 2005 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 20110127000 A1 | Jun 2011 | US |
