CN102120877A - Ultralow-hardness polyurethane elastomer and preparation method thereof - Google Patents

Ultralow-hardness polyurethane elastomer and preparation method thereof Download PDF

Info

Publication number
CN102120877A
CN102120877A CN2011100089384A CN201110008938A CN102120877A CN 102120877 A CN102120877 A CN 102120877A CN 2011100089384 A CN2011100089384 A CN 2011100089384A CN 201110008938 A CN201110008938 A CN 201110008938A CN 102120877 A CN102120877 A CN 102120877A
Authority
CN
China
Prior art keywords
component
molecular weight
mass ratio
hardness
polyurethane elastomer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN2011100089384A
Other languages
Chinese (zh)
Inventor
石飞
钟宁庆
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
China Leather and Footwear Research Institute Co Ltd
Original Assignee
China Leather and Footwear Research Institute Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by China Leather and Footwear Research Institute Co Ltd filed Critical China Leather and Footwear Research Institute Co Ltd
Priority to CN2011100089384A priority Critical patent/CN102120877A/en
Publication of CN102120877A publication Critical patent/CN102120877A/en
Pending legal-status Critical Current

Links

Landscapes

  • Polyurethanes Or Polyureas (AREA)

Abstract

The invention relates to an ultralow-hardness polyurethane elastomer which comprises three components: a component A is diphenylmethane diisocyanate or a prepolymer thereof, wherein the prepolymer is formed by polymerizing the diphenylmethane diisocyanate and a modifier thereof with polypropylene oxide ether polyol with the functionality of 2-3 and the number-average molecular weight of 1000-8000; a component B consists of polymer polyol, a catalyst and an antiaging agent; and a component C is polymer linear monoalcohol with the number-average molecular weight of 1000-4000. When the component A is the prepolymer, the mass ratio of the component A to the component B is 1:(0.8-1.3). When the component A is the diphenylmethane diisocyanate, the mass ratio of the component A to the component B is 1:(19-27). The mass ratio of the component B to the component C is 1:(0-0.3). The invention also provides a preparation method of the ultralow-hardness polyurethane elastomer material, which is simple to formulate and easy for manufacturing; and the obtained product is environment-friendly and safe, has favorable buffering performance and compression resisting performance, the Shore hardness ranging between 0 and 15, and smooth surface or extremely low viscosity, and is used for manufacturing shoe products for buffering, resisting wearing, and the like.

Description

Super-low-hardness polyurethane elastomer and preparation method thereof
Technical field
The present invention relates to polyurethane elastomer and preparation method thereof, particularly super-low-hardness polyurethane elastomer and preparation method thereof.
Background technology
Cast urethane elastomer is the chemical system of cast liquid reaction mixture article of manufacture in die cavity, has physical strength height, wear-resisting, oil resistant, anti-skidding, incompressible, excellent characteristics such as durometer level is wide, shock-absorbing capacity is good, is suitable for making the footwear parts.The shoe-pad that is used for damping adopts the soft resilient material more, and common low hardness polyurethane elastic body all is to obtain by adding softening agent, and this product is by placing for a long time, softening agent can be moved to the surface of shoe-pad, pollute footgear, the hardness of shoe-pad also can raise, and its application is restricted.
Provided some examples about low hardness polyurethane elastic body in the prior art:
200910256449.3 a low hardness polyurethane elastic body composite, the preparation functionality of prepolymer is 2 or 3 in this patent, and molecular weight is at the poly(propylene oxide) ethoxylated polyhydric alcohol of 1000-3000; Having used another component functionality in the reaction is 2 or 3, and molecular weight is at poly-epoxy propyl ether polyvalent alcohol and catalyzer, the antiager etc. of 300 to 6000 scopes; Product hardness is equivalent to Shao Shi C 10 to 40 between Shao Shi A 0 to 20.
03805398.5 Thermocurable polyurethane elastomeric compositions, polyurethane elastomer and manufacture method thereof, the preparation of performed polymer macromolecule polyvalent alcohol in this patent, its molecular weight ranges is at the polyvalent alcohol of 4000-20000, and optimum molecular weight is at 8000-15000; Used solidifying agent polyoxygenated tetramethylene polyvalent alcohol and chain propagation agent small molecular weight dibasic alcohol in the reaction, as 1,4-butyleneglycol etc.; Product hardness focuses mostly between Shao Shi A 30-40 between Shao Shi A 10-70.
200580018314.3 low-hardness thermosetting polyurethane elastomer and production method thereof, the preparation of performed polymer macromolecule polyvalent alcohol in this patent, its molecular weight ranges is at the polyvalent alcohol of 5000-20000, and optimum molecular weight is at 8000-12000; In the reaction to have adopted carbonatoms be 2 to 10 to solidifying agent, is in particular 2 to 4, has the polyoxyalkylene polyol and the catalyzer of 2 to 3 hydroxyls; Product hardness is between Shao Shi A 10-40.
Summary of the invention
The objective of the invention is to overcome the defective of conventional art, super-low-hardness polyurethane elastomer and preparation method thereof is provided, the resulting product Environmental Safety, has comfortable sense of touch, good shock-absorbing capacity and anti-compression properties, durometer level between Shao Shi A 0-15, smooth surface or extremely low viscosity is arranged.
For achieving the above object, super-low-hardness polyurethane elastomer provided by the invention, made by the raw material cast of following mass fraction: the mass ratio of A component and B component is 1: 19-1: 27, the mass ratio of B component and C component is 1: 0 to 1: 0.3, wherein:
The A component is a diphenylmethanediisocyanate;
The B component is 6000-10000 by number-average molecular weight, and functionality is 3 poly(propylene oxide) ethoxylated polyhydric alcohol, catalyzer and antiaging agent composition; Wherein catalyzer is one or both in dibutyl tin laurate, the stannous octoate, accounts for the 0.01-0.5% of B component total amount, and antiaging agent is 1010, among BHT, UV-531, the UV-328 one or more, accounts for the 0.01-0.5% of B component total amount;
The C component is that number-average molecular weight is the single alcohol of polymeric linear of 1000-4000.
Super-low-hardness polyurethane elastomer of the present invention, raw material cast by following mass fraction is made: A component and B component blended mass ratio are 1: 22.1, B component and C component blended mass ratio are 1: 0.1, wherein the B component is the mixture of 3 functionality molecular weight, 7600 poly(propylene oxide) ethoxylated polyhydric alcohol Z-221,3 functionality molecular weight, 10000 poly(propylene oxide) ethoxylated polyhydric alcohol Z-3100 and dibutyl tin laurate and UV-531, and mass ratio is 1000: 1000: 3: 5; Linear single pure D-2000 of C component molecular weight 2000.
Super-low-hardness method for preparing polyurethane elastic body provided by the invention, A component, B component, C component are deposited separately, and when producing, respectively at 110 ℃, dehydration is 4 hours under the-0.08MPa condition, is cooled to 53 ℃ with B component and C component.The A component is warming up to 55 ℃, join in the component C, mix, reacted ten minutes, the B component is joined in A, the C mixture again, mixing is poured in 50 ℃ of mold cavities the demoulding in 20 minutes rapidly, 80 ℃ of slakings are 4 hours then, normal temperature was placed after 24 hours again, and smooth surface is inviscid, and the hardness of the polyurethane elastomer that obtains is Shao Shi A 5.
For achieving the above object, another kind of super-low-hardness polyurethane elastomer provided by the invention, made by the raw material cast of following mass fraction: the mass ratio of A component and B component is 1: 0.8-1: 3, the mass ratio of B component and C component is 1: 0 to 1: 0.3, wherein:
The A component is a biphenyl methane diisocyanate prepolymer, and this prepolymer is that 2-3, number-average molecular weight are that the poly(propylene oxide) ethoxylated polyhydric alcohol of 1000-8000 is polymerized by diphenylmethanediisocyanate and modifier thereof and functionality;
The B component is 6000-10000 by number-average molecular weight, and functionality is 3 poly(propylene oxide) ethoxylated polyhydric alcohol, catalyzer and antiaging agent composition; Wherein catalyzer is one or both in dibutyl tin laurate, the stannous octoate, accounts for the 0.01-0.5% of B component total amount, and antiaging agent is 1010, among BHT, UV-531, the UV-328 one or more, accounts for the 0.01-0.5% of B component total amount;
The C component is that number-average molecular weight is the single alcohol of polymeric linear of 1000-4000.
The another kind of super-low-hardness polyurethane elastomer of the present invention, make by the raw material cast of following mass fraction:
The mass ratio of A component and B component is 1: 0.94, and the mass ratio of B component and C component is 1: 0.1, and wherein B is that component is the mixture of 3 functionality molecular weight, 7600 poly(propylene oxide) ethoxylated polyhydric alcohol Z-221 and dibutyl tin laurate, and mass ratio is 1000: 2; The C component is linear single pure D-2000 of molecular weight 2000.
Another kind of super-low-hardness method for preparing polyurethane elastic body provided by the invention, A component, B component, C component are deposited separately, and when producing, respectively at 110 ℃, dehydration is 4 hours under the-0.08MPa condition, is cooled to 53 ℃ with B component and C component.The A component is warming up to 55 ℃, join in the component C, mix, reacted ten minutes, the B component is joined in A, the C mixture again, mixing is poured in 50 ℃ of mold cavities the demoulding in 20 minutes rapidly, 80 ℃ of slakings are 4 hours then, normal temperature was placed after 24 hours again, and smooth surface is inviscid, and the hardness of the polyurethane elastomer that obtains is Shao Shi A 5.
For achieving the above object, the third super-low-hardness polyurethane elastomer provided by the invention, made by the raw material cast of following mass fraction: the mass ratio of A component and B component is 1: 0.8-1: 3, wherein:
The A component is a biphenyl methane diisocyanate prepolymer, and this prepolymer is that 2-3, number-average molecular weight are that the poly(propylene oxide) ethoxylated polyhydric alcohol of 1000-8000 is polymerized by diphenylmethanediisocyanate and modifier thereof and functionality;
The B component is 6000-10000 by number-average molecular weight, and functionality is 3 poly(propylene oxide) ethoxylated polyhydric alcohol, catalyzer and antiaging agent composition; Wherein catalyzer is one or both in dibutyl tin laurate, the stannous octoate, accounts for the 0.01-0.5% of B component total amount, and antiaging agent is 1010, among BHT, UV-531, the UV-328 one or more, accounts for the 0.01-0.5% of B component total amount.
The third super-low-hardness polyurethane elastomer of the present invention, raw material cast by following mass fraction is made: the mass ratio of A component and B component is 1: 1.9, wherein the B component is the mixture of 3 functionality molecular weight, 7600 poly(propylene oxide) ethoxylated polyhydric alcohol Z-221 and dibutyl tin laurate and 1010, and its mass ratio is 1000: 2: 1.
The third super-low-hardness method for preparing polyurethane elastic body provided by the invention, A component, B component are deposited separately, when producing, with the B component at 110 ℃, dehydration was cooled to room temperature after 4 hours under the-0.08MPa condition, got 31 gram A components and joined to mix rapidly in the 60 gram B components and be poured in the normal temperature mould self-vulcanizing demoulding in 2 minutes, the rear surface was little sticking in static 24 hours, and the hardness of the polyurethane elastomer that obtains is Shao Shi A 0.
Super-low-hardness polyurethane elastomer of the present invention since single alcohol in reaction system with isocyanate reaction, play the effect of chain termination, formed the less polyurethane oligomer of a part of molecular weight, with the polyurethane elastomer that forms the later infiltration that is interweaved, played the plastifying effect, this oligopolymer is bigger with respect to the plasticizer molecule amount of little branch, has similar molecular structure to polyurethane elastomer again, therefore, can reduce the hardness of polyurethane elastomer, again can be not elongated and precipitate into elastomeric surface along with the time.In addition, do not use micromolecular chainextender and linking agent.Super-low-hardness method for preparing polyurethane elastic body prescription provided by the invention is simple, makes easily the resulting product Environmental Safety, has comfort feel, good shock-absorbing capacity and anti-compression properties, durometer level between Shao Shi A 0-15, smooth surface or extremely low viscosity is arranged.
Embodiment
Super-low-hardness polyurethane elastomer of the present invention, the cast starting material are made of three kinds of components:
A component: constitute by in diphenylmethanediisocyanate and the prepolymer thereof any one.Prepolymer is 2-3 by diphenylmethanediisocyanate and modifier thereof and functionality, and number-average molecular weight is that the poly(propylene oxide) ethoxylated polyhydric alcohol of 1000-8000 is polymerized according to known method.
B component: form by polymer polyatomic alcohol, catalyzer and antiaging agent.Wherein polymer polyatomic alcohol is that number-average molecular weight is 6000 to 10000, and functionality is 3 poly(propylene oxide) ethoxylated polyhydric alcohol.Catalyzer is one or both in dibutyl tin laurate, the stannous octoate, accounts for the 0.01-0.5% of B component total amount.Antiaging agent one or more by 1010, among BHT, UV-531, the UV-328 are formed, and account for the 0.01-0.5% of B component total amount.
The C component: be made up of the single alcohol of polymeric linear, wherein the number-average molecular weight of single alcohol is 1000 to 4000.
The mass ratio of three kinds of components is:
When the A component is diphenylmethanediisocyanate and the B component mixed according to 1: 19 to 1: 27.
When the A component is prepolymer and the B component mix according to mass ratio 1: 0.8 to 1: 3;
The mass ratio of B component and C component is 1: 0 to 1: 0.3.
Its preparation method is: A component, B component, C component are deposited separately, and A component and C component are 45 ℃-60 ℃ in temperature when producing, pre-mixing 10-30 minute, add the B component again, mix rapidly and be poured in the mould, the demoulding in 1-20 minute, 80 ℃ of slakings 4 hours.The hardness of the polyurethane elastomer that obtains is Shao Shi A 0-16.
Further specify the technical scheme of super-low-hardness polyurethane elastomer its preparation method of the present invention below in conjunction with embodiment:
Embodiment 1:
The A component is a biphenyl methane diisocyanate prepolymer; B is that component is the mixture of 3 functionality molecular weight, 7600 poly(propylene oxide) ethoxylated polyhydric alcohol Z-221 and dibutyl tin laurate, and mass ratio is 1000: 2; The C component is linear single pure D-2000 of molecular weight 2000.
The mass ratio of A component and B component is 1: 0.94, gets 43 grams and 40.3 grams respectively, and the mass ratio of B component and C component is 1: 0.1, and the C component is got 4 grams.
Respectively at 110 ℃, dehydration is 4 hours under the-0.08MPa condition, is cooled to 60 ℃ with B component and C component.43 gram A components are warming up to 60 ℃, join in the 4 gram component C, mix, reacted ten minutes, again 40.3 gram B components are joined in A, the C mixture, mixing is poured in the mold cavity demoulding in 10 minutes rapidly, 80 ℃ of slakings are 4 hours then, normal temperature was placed after 24 hours again, and smooth surface is inviscid, hardness Shao Shi A 7.
Embodiment 2:
The A component is diphenylmethanediisocyanate MDI-100; The B component is the mixture of 3 functionality molecular weight, 7600 poly(propylene oxide) ethoxylated polyhydric alcohol Z-221,3 functionality molecular weight, 10000 poly(propylene oxide) ethoxylated polyhydric alcohol Z-3100 and dibutyl tin laurate and UV-531, and mass ratio is 1000: 1000: 3: 5; Linear single pure D-2000 of C component molecular weight 2000.
A component and B component blended mass ratio are 1: 22.1, get 1.81 grams and 40 grams respectively, and B component and C component blended mass ratio are 1: 0.1, and the C component is got 4 grams.
Respectively at 110 ℃, dehydration is 4 hours under the-0.08MPa condition, is cooled to 53 ℃ with B component and C component.1.81 gram A components are warming up to 55 ℃, join in the 4 gram component C, mix, reacted ten minutes, again 40 gram B components are joined in A, the C mixture, mixing is poured in 50 ℃ of mold cavities the demoulding in 20 minutes rapidly, 80 ℃ of slakings are 4 hours then, normal temperature was placed after 24 hours again, and smooth surface is inviscid, hardness Shao Shi A 5.
Embodiment 3:
The A component is a biphenyl methane diisocyanate prepolymer; The B component is the mixture of 3 functionality molecular weight, 7600 poly(propylene oxide) ethoxylated polyhydric alcohol Z-221 and dibutyl tin laurate and 1010, and its mass ratio is 1000: 2: 1.
The mass ratio of A component and B component is 1: 1.9, gets 31 grams and 60 grams respectively.
At 110 ℃, dehydration was cooled to room temperature after 4 hours under the-0.08MPa condition with the B component, got 31 gram A components and joined to mix rapidly in the 60 gram B components and be poured in the normal temperature mould, the self-vulcanizing demoulding in 2 minutes, the rear surface was little sticking in static 24 hours, and hardness Shao Shi A 0 is equivalent to Shao Shi C 6.
Super-low-hardness polyurethane elastomer of the present invention is made with single alcohol reaction by diphenylmethanediisocyanate and poly-epoxy propyl ether polyvalent alcohol, single alcohol in reaction system with isocyanate reaction, play the effect of chain termination, formed the less polyurethane oligomer of a part of molecular weight, with the polyurethane elastomer that forms the later infiltration that is interweaved, played the plastifying effect, this oligopolymer is bigger with respect to the plasticizer molecule amount of little branch, has similar molecular structure to polyurethane elastomer again, therefore, can reduce the hardness of polyurethane elastomer, again can be not elongated and precipitate into elastomeric surface along with the time.Another characteristics are not use micromolecular chainextender and linking agent in three components of reaction.Super-low-hardness method for preparing polyurethane elastic body prescription is simple, make easily, the resulting product Environmental Safety, has comfort feel, good shock-absorbing capacity and anti-compression properties, durometer level is between Shao Shi A 0-15, and smooth surface or extremely low viscosity is arranged is applicable to the goods such as buffering, spats, abrasionproof at positions such as making shoe-pad and flank, half sole, heel, bung, shoestring in shoe industry.
Above-described embodiment is described preferred implementation of the present invention; be not that scope of the present invention is limited; design under the prerequisite of spirit not breaking away from the present invention; various distortion and improvement that the common engineering technical personnel in this area make technical scheme of the present invention all should fall in the definite protection domain of claims of the present invention.

Claims (9)

1. super-low-hardness polyurethane elastomer is characterized in that: the raw material cast by following mass fraction is made: the mass ratio of A component and B component is 1: 19-1: 27, and the mass ratio of B component and C component is 1: 0 to 1: 0.3, wherein:
The A component is a diphenylmethanediisocyanate;
The B component is 6000-10000 by number-average molecular weight, and functionality is 3 poly(propylene oxide) ethoxylated polyhydric alcohol, catalyzer and antiaging agent composition; Wherein catalyzer is one or both in dibutyl tin laurate, the stannous octoate, accounts for the 0.01-0.5% of B component total amount, and antiaging agent is 1010, among BHT, UV-531, the UV-328 one or more, accounts for the 0.01-0.5% of B component total amount;
The C component is that number-average molecular weight is the single alcohol of polymeric linear of 1000-4000.
2. according to the described super-low-hardness polyurethane elastomer of claim 1, it is characterized in that: the raw material cast by following mass fraction is made: A component and B component blended mass ratio are 1: 22.1, B component and C component blended mass ratio are 1: 0.1, wherein the B component is the mixture of 3 functionality molecular weight, 7600 poly(propylene oxide) ethoxylated polyhydric alcohol Z-221,3 functionality molecular weight, 10000 poly(propylene oxide) ethoxylated polyhydric alcohol Z-3100 and dibutyl tin laurate and UV-531, and mass ratio is 1000: 1000: 3: 5; Linear single pure D-2000 of C component molecular weight 2000.
3. according to claim 1 or 2 described super-low-hardness method for preparing polyurethane elastic body, it is characterized in that: A component, B component, C component are deposited separately, when producing, with B component and C component respectively at 110 ℃, dehydration is 4 hours under the-0.08MPa condition, is cooled to 53 ℃.The A component is warming up to 55 ℃, join in the component C, mix, reacted ten minutes, the B component is joined in A, the C mixture again, mixing is poured in 50 ℃ of mold cavities the demoulding in 20 minutes rapidly, 80 ℃ of slakings are 4 hours then, normal temperature was placed after 24 hours again, and smooth surface is inviscid, and the hardness of the polyurethane elastomer that obtains is Shao Shi A 5.
4. super-low-hardness polyurethane elastomer is characterized in that: the raw material cast by following mass fraction is made: the mass ratio of A component and B component is 1: 0.8-1: 3, and the mass ratio of B component and C component is 1: 0 to 1: 0.3, wherein:
The A component is a biphenyl methane diisocyanate prepolymer, and this prepolymer is that 2-3, number-average molecular weight are that the poly(propylene oxide) ethoxylated polyhydric alcohol of 1000-8000 is polymerized by diphenylmethanediisocyanate and modifier thereof and functionality;
The B component is 6000-10000 by number-average molecular weight, and functionality is 3 poly(propylene oxide) ethoxylated polyhydric alcohol, catalyzer and antiaging agent composition; Wherein catalyzer is one or both in dibutyl tin laurate, the stannous octoate, accounts for the 0.01-0.5% of B component total amount, and antiaging agent is 1010, among BHT, UV-531, the UV-328 one or more, accounts for the 0.01-0.5% of B component total amount;
The C component is that number-average molecular weight is the single alcohol of polymeric linear of 1000-4000.
5. according to the described super-low-hardness polyurethane elastomer of claim 4, it is characterized in that: the raw material cast by following mass fraction is made:
The mass ratio of A component and B component is 1: 0.94, and the mass ratio of B component and C component is 1: 0.1, and wherein B is that component is the mixture of 3 functionality molecular weight, 7600 poly(propylene oxide) ethoxylated polyhydric alcohol Z-221 and dibutyl tin laurate, and mass ratio is 1000: 2; The C component is linear single pure D-2000 of molecular weight 2000.
6. according to claim 4 or 5 described super-low-hardness method for preparing polyurethane elastic body, it is characterized in that: A component, B component, C component are deposited separately, when producing, with B component and C component respectively at 110 ℃, dehydration is 4 hours under the-0.08MPa condition, is cooled to 53 ℃.The A component is warming up to 55 ℃, join in the component C, mix, reacted ten minutes, the B component is joined in A, the C mixture again, mixing is poured in 50 ℃ of mold cavities the demoulding in 20 minutes rapidly, 80 ℃ of slakings are 4 hours then, normal temperature was placed after 24 hours again, and smooth surface is inviscid, and the hardness of the polyurethane elastomer that obtains is Shao Shi A 5.
7. super-low-hardness polyurethane elastomer is characterized in that: the raw material cast by following mass fraction is made: the mass ratio of A component and B component is 1: 0.8-1: 3, wherein:
The A component is a biphenyl methane diisocyanate prepolymer, and this prepolymer is that 2-3, number-average molecular weight are that the poly(propylene oxide) ethoxylated polyhydric alcohol of 1000-8000 is polymerized by diphenylmethanediisocyanate and modifier thereof and functionality;
The B component is 6000-10000 by number-average molecular weight, and functionality is 3 poly(propylene oxide) ethoxylated polyhydric alcohol, catalyzer and antiaging agent composition; Wherein catalyzer is one or both in dibutyl tin laurate, the stannous octoate, accounts for the 0.01-0.5% of B component total amount, and antiaging agent is 1010, among BHT, UV-531, the UV-328 one or more, accounts for the 0.01-0.5% of B component total amount.
8. according to the described super-low-hardness polyurethane elastomer of claim 7, it is characterized in that: the raw material cast by following mass fraction is made: the mass ratio of A component and B component is 1: 1.9, wherein the B component is the mixture of 3 functionality molecular weight, 7600 poly(propylene oxide) ethoxylated polyhydric alcohol Z-221 and dibutyl tin laurate and 1010, and its mass ratio is 1000: 2: 1.
9. according to claim 7 or 8 described super-low-hardness method for preparing polyurethane elastic body, it is characterized in that: A component, B component are deposited separately, when producing, with the B component at 110 ℃, dehydration was cooled to room temperature after 4 hours under the-0.08MPa condition, got 31 gram A components and joined to mix rapidly in the 60 gram B components and be poured in the normal temperature mould self-vulcanizing demoulding in 2 minutes, the rear surface was little sticking in static 24 hours, and the hardness of the polyurethane elastomer that obtains is Shao Shi A 0.
CN2011100089384A 2011-01-17 2011-01-17 Ultralow-hardness polyurethane elastomer and preparation method thereof Pending CN102120877A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2011100089384A CN102120877A (en) 2011-01-17 2011-01-17 Ultralow-hardness polyurethane elastomer and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2011100089384A CN102120877A (en) 2011-01-17 2011-01-17 Ultralow-hardness polyurethane elastomer and preparation method thereof

Publications (1)

Publication Number Publication Date
CN102120877A true CN102120877A (en) 2011-07-13

Family

ID=44249553

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2011100089384A Pending CN102120877A (en) 2011-01-17 2011-01-17 Ultralow-hardness polyurethane elastomer and preparation method thereof

Country Status (1)

Country Link
CN (1) CN102120877A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103694440A (en) * 2013-12-14 2014-04-02 常熟市永利化工有限公司 Low-hardness polyurethane elastomer material
CN104004157A (en) * 2014-06-03 2014-08-27 奥斯汀新材料(张家港)有限公司 Preparation method of soft thermoplastic polyurethane elastomers
CN108720170A (en) * 2018-04-28 2018-11-02 东莞市顺风运动器材有限公司 A kind of cool insole
CN110003429A (en) * 2019-04-02 2019-07-12 百恩实业(深圳)有限公司 A kind of soft, high-strength pouring type polyurethane elastomer and preparation method thereof
CN112876638A (en) * 2021-01-08 2021-06-01 东莞市中森新材料有限公司 Formula and production process of non-adhesive polyurethane elastomer

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103694440A (en) * 2013-12-14 2014-04-02 常熟市永利化工有限公司 Low-hardness polyurethane elastomer material
CN103694440B (en) * 2013-12-14 2016-08-03 常熟市永利化工有限公司 Low hardness polyurethane elastic body material
CN104004157A (en) * 2014-06-03 2014-08-27 奥斯汀新材料(张家港)有限公司 Preparation method of soft thermoplastic polyurethane elastomers
CN104004157B (en) * 2014-06-03 2016-04-13 奥斯汀新材料(张家港)有限公司 A kind of preparation method of soft thermoplastic polyurethane elastomers
CN108720170A (en) * 2018-04-28 2018-11-02 东莞市顺风运动器材有限公司 A kind of cool insole
CN110003429A (en) * 2019-04-02 2019-07-12 百恩实业(深圳)有限公司 A kind of soft, high-strength pouring type polyurethane elastomer and preparation method thereof
CN112876638A (en) * 2021-01-08 2021-06-01 东莞市中森新材料有限公司 Formula and production process of non-adhesive polyurethane elastomer

Similar Documents

Publication Publication Date Title
CN103665319B (en) The preparation method of resistance to polyurethane elastomeric compositions of subduing
CN101948616B (en) Microporous polyurethane elastomer shock absorption element for high-speed railway and preparation method thereof
US10544253B2 (en) Method for improving fracture toughness of polyisocyanurate comprising reaction products
CN102120877A (en) Ultralow-hardness polyurethane elastomer and preparation method thereof
AU2008328999B2 (en) Novel tennis ball
EP2997063A2 (en) Thermoplastic polyurethane from low free monomer prepolymer
SG193457A1 (en) Auto-crusting microporous elastomer composition foruse in polyurethane foam-filled tire
TW201708294A (en) Hard polyurethane resin composition, hard polyurethane resin, molded article, and fiber-reinforced plastic
KR20130114608A (en) Polymer compositions
AU2012327770B2 (en) Preparation method of rigid polyurethane
WO2009117630A3 (en) Polyether natural oil polyols and polymers thereof
CN102250307B (en) Biobased micro-porous polyurethane material and preparation method thereof
CN103965433B (en) The soft low-density polyurethane foam materials of sole
CN105504209B (en) Polyurethane elastomer that mechanical property improves and preparation method thereof
ES2645887T3 (en) Composition of segmented copolymer with improved properties
CN102040721A (en) Environment-friendly polyurethane elastomer
KR102280968B1 (en) Eco-friendly Integral skin polyurethane foam composition with excellent durability and elongation and Integral skin polyurethane foam manufactured using the same
EP3077439B1 (en) Storage stable polyol composition for polyurethane elastomers
JP2023504859A (en) ultralight ski boots
TWI846317B (en) Thermoplastic polyurethane foam material, midsole of sports shoes and manufacturing method of foam material
KR101276578B1 (en) Breaker diaphragm composition made of temperature polyurethane and breaker diaphragm using thereof
KR20110027970A (en) Synthesis and composition of one-type polyurethane for abrasion and grip excellent
JPH02296816A (en) Reaction injection molding
KR20210021615A (en) Preparing method for high functionality polyether carbonate polyol and preparing method for rigid polyurethane foam using the same
CN110606973A (en) Preparation method of polybutylene succinate-polyurethane composite micro-foaming material

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20110713