[go: up one dir, main page]

CN102336886A - Polyurethane for transmission friction wheels and preparation method thereof - Google Patents

Polyurethane for transmission friction wheels and preparation method thereof Download PDF

Info

Publication number
CN102336886A
CN102336886A CN2011101870501A CN201110187050A CN102336886A CN 102336886 A CN102336886 A CN 102336886A CN 2011101870501 A CN2011101870501 A CN 2011101870501A CN 201110187050 A CN201110187050 A CN 201110187050A CN 102336886 A CN102336886 A CN 102336886A
Authority
CN
China
Prior art keywords
parts
friction wheel
gearing friction
urethane
polyester polyol
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
CN2011101870501A
Other languages
Chinese (zh)
Inventor
方正千
白开军
杨九成
谢计怀
郭大宏
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.)
SHENGZHOU KEDING POLYURETHANE PRODUCTS FACTORY
Jiangsu Miracle Logistics System Engineering Co Ltd
Original Assignee
SHENGZHOU KEDING POLYURETHANE PRODUCTS FACTORY
Jiangsu Miracle Logistics System Engineering 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 SHENGZHOU KEDING POLYURETHANE PRODUCTS FACTORY, Jiangsu Miracle Logistics System Engineering Co Ltd filed Critical SHENGZHOU KEDING POLYURETHANE PRODUCTS FACTORY
Priority to CN2011101870501A priority Critical patent/CN102336886A/en
Publication of CN102336886A publication Critical patent/CN102336886A/en
Pending legal-status Critical Current

Links

Landscapes

  • Polyurethanes Or Polyureas (AREA)

Abstract

The invention relates to polyurethane applied for manufacturing transmission friction wheels and a preparation method thereof. The polyurethane comprises, by weight, 90 to 100 parts of polycaprolactone polyol, 15 to 25 parts of polyester polyol, 20 to 30 parts of toluene diisocyanate, 5 to 10 parts of a curing agent and 15 to 20 parts of a chain extender. According to the invention, polycaprolactone polyol and polyester polyol are used as raw materials to prepare a polyurethane elastic colloidal material; an elastic colloidal layer made of the elastic colloidal material has the advantages of good wear resistance, good elasticity, small deformation, good dynamic performance, good temperature tolerance, etc., and manufacture cost for the elastic colloidal layer is low.

Description

The gearing friction wheel is with urethane and preparation method thereof
Technical field
The present invention relates to a kind of urethane and preparation method thereof, specifically is a kind of urethane that is applied to make the gearing friction wheel and preparation method thereof.
Background technology
The frictionwheel transmission is a kind of widely used mechanical drive mode, and the frictional force that it passes through frictionwheel and wipes part is mutually utilized the turning handle another one object drive rotation of frictionwheel or the drive object moves.It has that compact construction, transmission noise are low, control flexibly, maintenance cost is low, can produce in overload fashion and skid and avoid damaging advantage such as device.During work, frictionwheel the most important thing is will avoid producing skidding, with the anti-tamper frictionwheel, influences normal transmission.In order to overcome skidding, must suitably increase the frictional force of contact position, increase the approach of frictional force, the one, increase positive pressure, the 2nd, increase frictional coefficient.But the method that adopt to increase positive pressure can increase the load that acts on axle and the bearing, causes increasing the size of driving member, makes mechanism's heaviness.Therefore, positive pressure can only suitably increase.Therefore, increasing the surperficial frictional coefficient of frictionwheel is a more feasible scheme.
In the prior art; The scheme that increases the frictionwheel skin friction coefficient normally coats the elastic gel layer in the core wheel outer rim; Utilize the elastic gel layer as friction surface,, make it produce enough big frictional force and drive the rotation of other objects or mobile through the elasticity variable characteristic of elastic gel layer.The material of elastic gel layer commonly used is generally selected polyurethane elastomer for use at present; The special elastomer material that urethane is a kind of good springiness, distortion is little, intensity is high, wear resistance is good; Its wear resistance and tensile strength are 2~5 times of tree elastomer; The raw material variety of polyurethane elastomer is many, and the hardness regulation range is wide, and various raw materials have relative merits separately; Wherein more typical urethane raw has: polyester polyol, THF homopolymer ethoxylated polyhydric alcohol, polycaprolactone polyol etc., and its relative merits separately are following:
(1) polyurethane elastomer made of polyester polyol have intensity height, good springiness, advantages such as wear resistance is good, tear resistance is good, oil resistant, but its water tolerance and anti-mould sex change are poor.
Advantages such as (2) polyurethane elastomer made of THF homopolymer ethoxylated polyhydric alcohol has that intensity height, good springiness, distortion are little, excellent in abrasion resistance, water tolerance and anti-mould sex change are good; But its oil resistant is than polyester difference; Tear resistance is poor, be prone to directed cracking, and cost of material is somewhat expensive.
(3) polyurethane elastomer of polycaprolactone polyol making is because molecular structure has polyester and polyethers two-sidedness; Polyester polyols pure and mild PTMG polyvalent alcohol advantage such as intensity height, good springiness, distortion are little, water-fast so its performance has concurrently, oil resistant, ageing-resistant performance are good; And dynamic deformation little, restorative good, high thermal resistance is good; Excellent combination property etc., but its cost of material is more expensive than the pure and mild PTMG polyvalent alcohol of polyester polyols, and also raw material production enterprise is few.
Summary of the invention
The objective of the invention is to overcome the deficiency that exists in the prior art; A kind of urethane that is applicable to the elastic gel layer of making the gearing friction wheel and preparation method thereof is provided; This urethane has advantages such as wear resisting property is good, good springiness, distortion is little, dynamic property good, heat resistance is good, and manufacturing cost is cheap relatively.
According to technical scheme provided by the invention: the gearing friction wheel use urethane, it is characterized in that: calculating by weight comprises following component: polycaprolactone polyol, 90~100 parts; Polyester polyol, 15~25 parts; Tolylene diisocyanate, 20~30 parts; Solidifying agent, 5~10 parts; Chainextender, 15~20 parts.
As the further improvement of said frictionwheel with urethane, the parts by weight of said each component are specially: polycaprolactone polyol, 100 parts; Polyester polyol, 20 parts; Tolylene diisocyanate, 25 parts, diphenylmethanediisocyanate, 7 parts; Chainextender, 18 parts.
As the further improvement of said frictionwheel with urethane, the molecular weight of said polycaprolactone polyol is 1500~2000.
As the further improvement of said frictionwheel with urethane, the molecular weight of said polyester polyol is 1500~2000.
As the further improvement of said frictionwheel with urethane, said polyester polyol adopts and gathers hexanodioic acid butyleneglycol glycol ester.Because the unit molecule chain length of gathering hexanodioic acid butyleneglycol glycol ester, flexibility is good.
As the further improvement of said frictionwheel with urethane, described tolylene diisocyanate is pure Toluene-2,4-diisocyanate, the 4-vulcabond.
As the further improvement of said frictionwheel with urethane, said employing diphenylmethanediisocyanate.Owing to contain a large amount of isocyanato (NCO) in the diphenylmethanediisocyanate; Isocyanato (NCO) easily with polycaprolactone polyol and polyester polyol resin in the hydroxyl long flexible chain of generation that reacts; Make prepared urethane flexibility good, intensity is high.
As the further improvement of said frictionwheel with urethane, described chainextender is the mixture of diformazan sulfenyl tolylene diamine and TriMethylolPropane(TMP), and the parts by weight of diformazan sulfenyl tolylene diamine and TriMethylolPropane(TMP) are 3: 1.The urethane intensity of being done like this is high, and good springiness is out of shape restorative fast.
The gearing friction wheel is characterized in that: may further comprise the steps with the preparation method of urethane:
(1), proportioning takes by weighing following component by weight: polycaprolactone polyol, 90~100 parts; Polyester polyol, 15~25 parts; Tolylene diisocyanate, 20~30 parts; Diphenylmethanediisocyanate, 5~10 parts; Chainextender, 15~20 parts;
(2), tolylene diisocyanate and diphenylmethanediisocyanate are added in the container with temperature regulation function together, mix, and the temperature in the container is raised to 65~75 ℃;
(3), join polycaprolactone polyol and polyester polyol together in the above-mentioned container then and fully mix; Under 70~85 ℃ temperature, reacted 1.5~2.5 hours, and vacuumized then, reaction is 0.5~1.5 hour under vacuum state; Temperature 85~95 degree obtain performed polymer;
(4), measure the percentage composition of the isocyanato (NCO) in the above-mentioned performed polymer, when the percentage composition of isocyanato (NCO) was lower than 4.5%, stopped reaction obtained satisfactory performed polymer, performed polymer is used for next step or pours out hermetically stored; If the percentage composition of isocyanato (NCO) still is higher than 4.5%, continue reaction under vacuum state, until meeting the requirements;
(5), performed polymer that step (4) is obtained is heated to 80 ℃~90 ℃, adds chainextender then, fully stir 1~2 minute after, can directly pour in the good gearing friction wheel shaping mould of preheating, as the material of gearing friction wheel elastic gel layer.
As said polyurethane preparation further improvements in methods, being evacuated to vacuum tightness in the said step (3) is 0.095~0.098MPa.
The present invention compared with prior art; Advantage is: the present invention adopts polycaprolactone polyol and polyester polyol to process the elastic polyurethane colloidal materials as raw material; The elastic gel layer that utilizes this elastic gel material to process has advantages such as wear resisting property is good, good springiness, distortion is little, dynamic property good, heat resistance is good, and manufacturing cost is cheap relatively.
Embodiment
Below in conjunction with specific embodiment the present invention is described further.
Embodiment 1
(1), proportioning takes by weighing following component by weight: polycaprolactone polyol (molecular weight is 1800), 100 parts; Gather hexanodioic acid butyleneglycol glycol ester (molecular weight is 1600), 20 parts; Tolylene diisocyanate (TDI-100), 25 parts; Diphenylmethanediisocyanate, 7 parts; The mixture of diformazan sulfenyl tolylene diamine and TriMethylolPropane(TMP), 18 parts;
(2), tolylene diisocyanate and diphenylmethanediisocyanate are added in the container with temperature regulation function together, mix, and the temperature in the container is raised to 70 ℃;
(3), join polycaprolactone polyol and polyester polyol together in the above-mentioned container then and fully mix; Reaction is 2 hours under 90 ℃ temperature; Be evacuated to 0.095MPa then; Reaction is 1 hour under vacuum state, and the temperature of reaction under the vacuum state is controlled at below 100 degree, obtains performed polymer;
(4), the percentage composition that records the isocyanato (NCO) in the above-mentioned performed polymer is 4.2%, stopped reaction obtains satisfactory performed polymer;
(5), performed polymer that step (4) is obtained is heated to 85 ℃, the mixture that adds diformazan sulfenyl tolylene diamine and TriMethylolPropane(TMP) then is as chainextender, fully stir 1~2 minute after; Directly pour in the good gearing friction wheel shaping mould of preheating; 120 ℃ of following vulcanization reactions 1 hour, product was taken out in die sinking then, put into 100 ℃~120 ℃ constant temperature oven heat tracing 8~10 hours again; The room temperature cooling was tested its physicals (seeing table 1) after 48 hours.
Embodiment 2
(1), proportioning takes by weighing following component by weight: polycaprolactone polyol (molecular weight is 1600), 90 parts; Gather hexanodioic acid butyleneglycol glycol ester (molecular weight is 2000); Tolylene diisocyanate, 20 parts; Diphenylmethanediisocyanate, 10 parts; The mixture of diformazan sulfenyl tolylene diamine and TriMethylolPropane(TMP), 16 parts;
(2), tolylene diisocyanate and diphenylmethanediisocyanate are added in the container with temperature regulation function together, mix, and the temperature in the container is raised to 65 ℃;
(3), then polycaprolactone polyol and polyester polyol; Join together in the above-mentioned container and fully mix; Reaction is 2.5 hours under 85 ℃ temperature, is evacuated to 0.098MPa then, and reaction is 1.5 hours under vacuum state; Temperature of reaction under the vacuum state is controlled at below 100 degree, obtains performed polymer;
(4), the percentage composition that records the isocyanato (NCO) in the above-mentioned performed polymer is 4%, stopped reaction obtains satisfactory performed polymer;
(5), performed polymer that step (4) is obtained is heated to 80 ℃, the mixture that adds diformazan sulfenyl tolylene diamine and TriMethylolPropane(TMP) then is as chainextender, fully stir 1~2 minute after; Directly pour in the good gearing friction wheel shaping mould of preheating; 120 ℃ of following vulcanization reactions 1 hour, product was taken out in die sinking then, put into 100 ℃~120 ℃ constant temperature oven heat tracing 8~10 hours again; The room temperature cooling was tested its physicals (seeing table 1) after 48 hours.
Embodiment 3
(1), proportioning takes by weighing following component by weight: polycaprolactone polyol (molecular weight is 1500), 95 parts; Gather hexanodioic acid butyleneglycol glycol ester (molecular weight is 1500), 20 parts; Tolylene diisocyanate (TDI-100), 20 parts; Diphenylmethanediisocyanate, 5 parts; The mixture of diformazan sulfenyl tolylene diamine and TriMethylolPropane(TMP), 15 parts;
(2), tolylene diisocyanate and diphenylmethanediisocyanate are added in the container with temperature regulation function together, mix, and the temperature in the container is raised to 75 ℃;
(3), then polycaprolactone polyol and polyester polyol; Join together in the above-mentioned container and fully mix; Reaction is 1.5 hours under 95 ℃ temperature, is evacuated to 0.096MPa then, and reaction is 0.5 hour under vacuum state; Temperature of reaction under the vacuum state is controlled at below 100 degree, obtains performed polymer;
(4), the percentage composition that records the isocyanato (NCO) in the above-mentioned performed polymer is 4.5% o'clock, stopped reaction obtains satisfactory performed polymer;
(5), performed polymer that step (4) is obtained is heated to 90 ℃, adds diformazan sulfenyl tolylene diamine mixture then as chainextender, fully stir 1~2 minute after; Directly pour in the good gearing friction wheel shaping mould of preheating; 120 ℃ of following vulcanization reactions 1 hour, product was taken out in die sinking then, put into 100 ℃~120 ℃ constant temperature oven heat tracing 8~10 hours again; The room temperature cooling was tested its physicals (seeing table 1) after 48 hours.
Table 1: the product physicals of embodiment 1-3
Figure BDA0000073734250000041

Claims (10)

1. the gearing friction wheel is used urethane, it is characterized in that: calculating by weight comprises following component: polycaprolactone polyol, 90~100 parts; Polyester polyol, 15~25 parts; Tolylene diisocyanate, 20~30 parts; Solidifying agent, 5~10 parts; Chainextender, 15~20 parts.
2. gearing friction wheel as claimed in claim 1 is used urethane, and the parts by weight of said each component are specially: polycaprolactone polyol, 100 parts; Polyester polyol, 20 parts; Tolylene diisocyanate, 25 parts; Diphenylmethanediisocyanate, 7 parts; Chainextender, 18 parts.
3. according to claim 1 or claim 2 gearing friction wheel is used urethane, and it is characterized in that: the molecular weight of said polycaprolactone polyol is 1500~2000.
4. according to claim 1 or claim 2 gearing friction wheel is used urethane, and it is characterized in that: the molecular weight of said polyester polyol is 1500~2000.
5. according to claim 1 or claim 2 gearing friction wheel use urethane, and it is characterized in that: said polyester polyol employing gathers hexanodioic acid butyleneglycol glycol ester.
6. according to claim 1 or claim 2 gearing friction wheel is used urethane, and it is characterized in that: described tolylene diisocyanate is pure Toluene-2,4-diisocyanate, the 4-vulcabond.
7. gearing friction wheel according to claim 1 and 2 is used urethane, and it is characterized in that: described chainextender is the mixture of diformazan sulfenyl tolylene diamine and TriMethylolPropane(TMP), and the parts by weight of diformazan sulfenyl tolylene diamine and TriMethylolPropane(TMP) are 3: 1.
8. gearing friction wheel according to claim 1 and 2 is used urethane, it is characterized in that: said isocyanic ester adopts diphenylmethanediisocyanate to make chain extension agent.
9. the gearing friction wheel is characterized in that: may further comprise the steps with the preparation method of urethane:
(1), proportioning takes by weighing following component by weight: polycaprolactone polyol, 90~100 parts; Polyester polyol, 15~25 parts; Tolylene diisocyanate, 20~30 parts; Solidifying agent, 5~10 parts; Chainextender, 15~20 parts;
(2), tolylene diisocyanate and solidifying agent are added in the container with temperature regulation function together, mix, and the temperature in the container is raised to 65~75 ℃;
(3), then join polycaprolactone polyol and polyester polyol together in the above-mentioned container and fully mix, under 85~95 ℃ temperature, reacted 1.5~2.5 hours, vacuumize then, reaction is 0.5~1.5 hour under vacuum state, obtains performed polymer;
(4), measure the percentage composition of the isocyanato (NCO) in the above-mentioned performed polymer, when the percentage composition of isocyanato (NCO) was lower than 4.5%, stopped reaction obtained satisfactory performed polymer, performed polymer is used for next step or pours out hermetically stored; If the percentage composition of isocyanato (NCO) still is higher than 4.5%, continue reaction under vacuum state, until meeting the requirements;
(5), performed polymer that step (4) is obtained is heated to 80 ℃~90 ℃, adds chainextender then, fully stir 1~2 minute after, can directly pour in the good gearing friction wheel shaping mould of preheating, as the material of gearing friction wheel elastic gel layer.
10. gearing friction wheel as claimed in claim 9 is with the preparation method of urethane, and it is characterized in that: being evacuated to vacuum tightness in the said step (3) is 0.095~0.098MPa.
CN2011101870501A 2011-07-05 2011-07-05 Polyurethane for transmission friction wheels and preparation method thereof Pending CN102336886A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2011101870501A CN102336886A (en) 2011-07-05 2011-07-05 Polyurethane for transmission friction wheels and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2011101870501A CN102336886A (en) 2011-07-05 2011-07-05 Polyurethane for transmission friction wheels and preparation method thereof

Publications (1)

Publication Number Publication Date
CN102336886A true CN102336886A (en) 2012-02-01

Family

ID=45512865

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2011101870501A Pending CN102336886A (en) 2011-07-05 2011-07-05 Polyurethane for transmission friction wheels and preparation method thereof

Country Status (1)

Country Link
CN (1) CN102336886A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102585684A (en) * 2012-02-24 2012-07-18 天津德威涂料化工有限公司 Polyurethane gel coat combination capable of spraying blades of fan conventionally and preparation method of polyurethane gel coat combination
CN103630355A (en) * 2013-12-18 2014-03-12 沈阳飞研航空设备有限公司 Machine wheel rotating equipment
CN116515077A (en) * 2023-05-23 2023-08-01 武汉理工大学 A thermosetting polyurethane material for water-lubricated bearings and its preparation method
CN119978289A (en) * 2025-02-26 2025-05-13 青岛科技大学 A low temperature resistant HV type low temperature hydraulic oil resistant polyurethane elastomer and preparation method thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101522741A (en) * 2006-09-13 2009-09-02 科聚亚公司 Isocyanate terminated polycaprolactone polyurethane prepolymers
CN101768249A (en) * 2009-12-30 2010-07-07 洛阳双瑞特种装备有限公司 Filling resin for poured and cured type height-adjustable supports and preparing method thereof
CN101851325A (en) * 2010-04-12 2010-10-06 浙江深蓝轻纺科技有限公司 Polyester high-hydrolysis resistance and high-peeling strength polyurethane resin for wet-method synthetic leather and preparation method thereof
CN101974305A (en) * 2010-09-21 2011-02-16 华南理工大学 Method for preparing waterborne polyurethane adhesive used for compound soft packaging
CN102060973A (en) * 2010-12-21 2011-05-18 浙江华峰合成树脂有限公司 Cold-resistant high-wear-resistant polyurethane resin for synthetic leather
CN102093696A (en) * 2010-12-14 2011-06-15 上海应用技术学院 Ketone-group-containing aqueous polyurethane resin capable of being cured at room temperature and preparation method thereof

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101522741A (en) * 2006-09-13 2009-09-02 科聚亚公司 Isocyanate terminated polycaprolactone polyurethane prepolymers
CN101768249A (en) * 2009-12-30 2010-07-07 洛阳双瑞特种装备有限公司 Filling resin for poured and cured type height-adjustable supports and preparing method thereof
CN101851325A (en) * 2010-04-12 2010-10-06 浙江深蓝轻纺科技有限公司 Polyester high-hydrolysis resistance and high-peeling strength polyurethane resin for wet-method synthetic leather and preparation method thereof
CN101974305A (en) * 2010-09-21 2011-02-16 华南理工大学 Method for preparing waterborne polyurethane adhesive used for compound soft packaging
CN102093696A (en) * 2010-12-14 2011-06-15 上海应用技术学院 Ketone-group-containing aqueous polyurethane resin capable of being cured at room temperature and preparation method thereof
CN102060973A (en) * 2010-12-21 2011-05-18 浙江华峰合成树脂有限公司 Cold-resistant high-wear-resistant polyurethane resin for synthetic leather

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102585684A (en) * 2012-02-24 2012-07-18 天津德威涂料化工有限公司 Polyurethane gel coat combination capable of spraying blades of fan conventionally and preparation method of polyurethane gel coat combination
CN103630355A (en) * 2013-12-18 2014-03-12 沈阳飞研航空设备有限公司 Machine wheel rotating equipment
CN116515077A (en) * 2023-05-23 2023-08-01 武汉理工大学 A thermosetting polyurethane material for water-lubricated bearings and its preparation method
CN119978289A (en) * 2025-02-26 2025-05-13 青岛科技大学 A low temperature resistant HV type low temperature hydraulic oil resistant polyurethane elastomer and preparation method thereof

Similar Documents

Publication Publication Date Title
EP3083271B1 (en) Polyurethane filled tires
CN101550327B (en) High hardness high-toughness polyurethane casting compound and application thereof
CN104987488B (en) Polyurethane elastomer that a kind of soft high intensity low pressure becomes and preparation method thereof
CN105408379B (en) Polyurethane elastomeric seals for hydraulic pumps
CN103804622B (en) A kind of high-performance thermoplastic polyurethane and preparation method thereof
CN102260368A (en) Polyurethane elastomer damper material and its preparation method
KR20080003268A (en) Foamed and solid polyurethane elastomers based on a high melting polyisocyanate and processes for their production and their use
CN102336886A (en) Polyurethane for transmission friction wheels and preparation method thereof
CN106866924A (en) Shock insulation polyurethane elastomer material composition and preparation method thereof
CN110684174A (en) Low-hardness 1, 5-naphthalene diisocyanate-based polyurethane elastomer and preparation method thereof
CN104558498A (en) Method for preparing polyurethane elastomer
AU2012327770B2 (en) Preparation method of rigid polyurethane
CN110511390B (en) Graphene end-crosslinked elastomer material and preparation method thereof
KR101682505B1 (en) Polyurethane elastomer for nonair-type tire and manufacturing method thereof
US10717854B2 (en) Solution polymerized styrene-butadiene rubber-polyurethane elastomer material for high performance tire and preparation method thereof
CN101397400B (en) Nano modified urethane elastomer tyre material for tracked vehicle road wheel and moulding technique thereof
CN105037676A (en) A kind of PPDI-based polyurethane elastomer with low compression set and preparation method thereof
CN111961186A (en) Thermoplastic polyurethane elastomer and preparation method thereof
CN102250307B (en) Biobased micro-porous polyurethane material and preparation method thereof
CN102719084A (en) Polyurethane elastomer for molds and manufacturing method of polyurethane elastomer
JP2003519699A5 (en)
KR101642415B1 (en) Heterogeneous polyurethane prepolymer for nonpneumatic-type tire and method for manufacturing the same
CN106674480B (en) Preparation method of NDI (Newcastle disease) -modified MDI (diphenylmethane diisocyanate) -based polyurethane microporous elastomer
CN104109225A (en) In-situ preparation of TPU light conversion luminous film
CN101128499A (en) Process for producing cylindrical moldings based on cellular polyurethane elastomers

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
AD01 Patent right deemed abandoned

Effective date of abandoning: 20120201

C20 Patent right or utility model deemed to be abandoned or is abandoned