CN1587293A - Process for preparing high solid single component polyurethane elastor and its use - Google Patents
Process for preparing high solid single component polyurethane elastor and its use Download PDFInfo
- Publication number
- CN1587293A CN1587293A CN 200410053452 CN200410053452A CN1587293A CN 1587293 A CN1587293 A CN 1587293A CN 200410053452 CN200410053452 CN 200410053452 CN 200410053452 A CN200410053452 A CN 200410053452A CN 1587293 A CN1587293 A CN 1587293A
- Authority
- CN
- China
- Prior art keywords
- siloxanes
- solvent
- solid level
- monocomponent polyurethane
- reactive hydrogen
- 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.)
- Granted
Links
Landscapes
- Polyurethanes Or Polyureas (AREA)
Abstract
The polyurethane is prepared through the reaction between polyol and isocyanate and siloxane modification. The preparation process includes first synthesis of polyurethane prepolymer with end isocyanic radical and the subsequent modification with siloxane, or includes first synthesis of polyurethane prepolymer containing end isocyanic radical with siloxane containing isocyanate and the subsequent modification with siloxane containing active hydrogen. The modified polymer may be produced into paint film of 2-3 mm thickness, shore A hardness not lower than 60, elongation at rupture not smaller than 300 %, stretching strength not lower than 3 MPa and stable storage period of 3-6 months. The present invention is applied in making elastic polyurethane coating.
Description
Technical field
The present invention relates to chemical field, is a kind of high-solid level mono-component polyurethane method for producing elastomers and application thereof.
Background technology
At present, generally adopt vulcabond and polyester or polyether glycol to react and makes end isocyano (hereinafter to be referred as NCO) single-component moisture curing polyurethane (hereinafter to be referred as PU) resin, the end NCO base and the airborne moisture reaction formation urea key that contain by polyurethane prepolymer reach the solidified purpose.Usually the urethane resin of high-solid level is mainly used in the less demanding tackiness agent of working viscosity and foaming, cast elastomeric material field, and for varnish and paint field working viscosity and performance demands, the solid content of single-component moisture curing polyurethane that is used for this field at present is generally below 70%.Because the CO2 gas that reaction produces during moisture curing remains in the coating easily, thereby influence the decorate properties and the mechanical property of coating, particularly for thick coating layer, especially obvious to Effect on Performance, reduce hardness, tensile strength and the unit elongation of coating greatly, so that the end application of NCO monocomponent moisture cure PU resin on elastomer material is restricted.In addition, for reach environmental protection to the discharging of VOC (organic volatile branch) limit the quantity of and for the limit index of free tolylene diisocyanate (hereinafter to be referred as m-TDI) in the polyurethane coating, usually adopt direct synthetic method to reduce m-TDI and have certain limitation, and too big with the film evaporation method investment, the application of solvent-borne type end NCO base single-component moisture curing polyurethane is restricted.
Summary of the invention
The purpose of this invention is to provide a kind of excellent performance, high-solid level mono-component polyurethane method for producing elastomers and application thereof.
A kind of high-solid level monocomponent polyurethane method for producing elastomers that the present invention proposes, elder generation is with isocyanic ester or contain the siloxanes of isocyano and the polyurethane prepolymer of polyol reaction preparation end isocyano, again through containing the silicone-modified of reactive hydrogen, used polyvalent alcohol is a polyether glycol, or polyester polyol, or epoxy polyol; Used isocyanic ester is an aromatic diisocyanate, or aliphatic diisocyanate; Used siloxanes is the siloxanes that contains reactive hydrogen, and used catalyzer is tin class or amines catalyst, and used solvent is not for containing the solvent of reactive hydrogen: above-mentioned by weight percentage each raw material consumption is as follows:
Polyvalent alcohol 30-80%
Isocyanate-monomer 10-30%
The siloxanes 0.1-10% that contains reactive hydrogen
Catalyzer 0-0.2%
Solvent 0-10%,
Polyvalent alcohol 30-80%
The siloxanes 0-10% that contains isocyano
The siloxanes 0.1-10% that contains reactive hydrogen
Catalyzer 0-0.2%
Solvent 0-10%,
Concrete preparation process is as follows: having the agitator that is equipped with of vacuum dewatering plant; thermometer; in the reactor of prolong; add the isocyanates monomer; solvent; catalyzer; polyvalent alcohol and the evenly slow permanent dropping in back of solvent with vacuum-drying; under nitrogen protection, slowly be warming up to 70-90 ℃ of reaction 3-4 hour; the siloxanes that maybe will contain isocyano; solvent; catalyzer; add earlier in the reactor with polyol reaction 0.5-1.5 hour after; add the isocyanates monomer again and continue reaction 3-4 hour; till the end isocyano-content remains unchanged substantially; cooling; dropping contains the siloxanes of reactive hydrogen; in 60-80 ℃ of reaction 1-2 hour, cooling; discharging also packs.
Among the present invention, polyvalent alcohol adopts vacuum hydro-extraction, vacuum tightness 0.06-0.09MPa, temperature 80-110 ℃; Perhaps dewater with refluxing toluene.
Among the present invention, used polyvalent alcohol molecular weight is 50-10000, hydroxyl value is at 25～300mgKOH/g, polyvalent alcohol can be 1,4 butyleneglycols, neopentyl glycol, TriMethylolPropane(TMP), tetramethylolmethane, polyether Glycols, polyether-tribasic alcohol, polyester diol, polyester trivalent alcohol, epoxy dibasic alcohol, amido polyethers, PTMG etc. adopt one or more mixing wherein to use.
Among the present invention, used isocyanic ester is tolylene diisocyanate, diphenylmethanediisocyanate, naphthalene-1,5 vulcabond, many phenyl polymethine polyisocyanates, one or more in aliphatics hexamethylene diisocyanate, the isophorone diisocyanate mix use.
Among the present invention, the used siloxanes that contains isocyano is isocyanic ester methoxy silane, isocyanic ester Ethoxysilane, isocyanate-containing alkyl methoxy silane, isocyanate-containing alkyl Ethoxysilane, adopts wherein one or two or more kinds mixing to use.
Among the present invention, the used siloxanes coupling agent that contains reactive hydrogen is sulfydryl, epoxy group(ing), urea groups, primary amino, secondary amino group siloxanes, and adopting wherein, one or more mix use.
Among the present invention, used catalyzer is dibutyl tin laurate, stannous acetate, triethylenediamine, adopts wherein one or two or more kinds mixing to use.
Among the present invention, used solvent is toluene, dimethylbenzene, N-BUTYL ACETATE, vinyl acetic monomer, 4-methyl 2 pentanone, methylethylketone, solvent 100, solvent 150, uses wherein one or two or more kinds mixing to use.
Among the present invention, high-solid level monocomponent polyurethane elastomerics prepolymer solids constituent 〉=90% that makes at 25 ℃, solidifies thick-layer elastic coating shore A hardness 〉=60 of making after 7 days, elongation at break 〉=300%, tensile strength 〉=3Mpa during humidity 50%RH.
Among the present invention, the high-solid level monocomponent polyurethane elastomerics that makes is as the application of coating.
Mono-component polyurethane elastomerics solids constituent 〉=90% that the present invention obtains, free NCO≤0.4%, and reach the viscosity requirement of construction.(1) at 25 ℃, during humidity 50%RH, solidify the thick-layer elastic coating of making after 7 days, coating is bright and clean still, shore A hardness 〉=60, elongation at break 〉=300%, tensile strength 〉=3Mpa.Can be applicable to the thick elastic coating that is coated with of PU, PU pavement material such as floor varnish, sports field are decorated varnish etc.(2) the polyurethane elastomer prepolymer that makes of the present invention has the wetting and dispersing property with pigment, filler excellence, can be mixed with elastic polyurethane coating with pigment, filler.High solid, the nontoxic thick elastic coating that is coated with; Coat-thickness can reach 2-3mm.Therefore, but adopt the elastomerics widespread use of preparation method's gained of the present invention.
Embodiment
1, the elastomeric preparation of mono-component polyurethane
Example 1:
Having the agitator that is equipped with of vacuum dewatering plant; thermometer; in the 500ml round-bottomed flask of prolong; the adding hydroxyl value is 80KOH/g; molecular weight is 3000 polyether-tribasic alcohol 80 grams; hydroxyl value is 100KOH/g; molecular weight is 2000 polyester diol 160 grams; be warming up to 100 ℃; stir vacuum hydro-extraction down 1 hour; be cooled to 50 ℃; add tolylene diisocyanate 50 grams; dimethylbenzene 15 grams; catalyzer 0.06 gram; be warming up under the 80-90 ℃ of logical nitrogen protection and reacted 3-4 hour; with Di-n-Butyl Amine titration measuring NCO content; when NCO content remains unchanged substantially, be cooled to 40 ℃, drip aminopropyl trimethoxysilane coupling agent 8 grams; 60 ℃ of reactions were measured the discharging of NCO content after 2 hours.
Example 2:
Having the agitator that is equipped with of vacuum dewatering plant; thermometer; in the 500ml round-bottomed flask of prolong; the adding hydroxyl value is 60KOH/g; molecular weight is 1000 epoxy dibasic alcohol 60 grams; hydroxyl value is 200KOH/g; molecular weight is 2000 polyester diol 120 grams; be warming up to 100 ℃; stir vacuum hydro-extraction down 1 hour; be cooled to 50 ℃; add isocyanic ester propyl group Ethoxysilane 4.35 grams; toluene and N-BUTYL ACETATE solvent 10 grams are warming up to 70-90 ℃; nitrogen protection was reacted 1 hour down; add diphenylmethanediisocyanate 30 grams and continue reaction 3-4 hour; with Di-n-Butyl Amine titration measuring NCO content; when NCO content remains unchanged substantially, be cooled to 50 ℃, drip mercaptopropyl trimethoxysilane 1.99 grams; NCO content, discharging are measured in 100 ℃ of reactions after 2 hours.
Example 3
Having the agitator that is equipped with of vacuum dewatering plant; thermometer; in the 500ml round-bottomed flask of prolong; add neopentyl glycol 40 grams; hydroxyl value is 100KOH/g; molecular weight is 1000 PTMG 120 grams; be warming up to 100 ℃; stir vacuum hydro-extraction down 1 hour; be cooled to 50 ℃; add 1; 6-second vulcabond 30 grams; N-BUTYL ACETATE and methylpentanone 5 grams; catalyzer 0.08 gram; be warming up under the 80-90 ℃ of logical nitrogen protection and reacted 3-4 hour; with Di-n-Butyl Amine titration measuring NCO content; when NCO content remains unchanged substantially, be cooled to 40 ℃, drip cyclohexyl-aminopropyl methyl dimethoxysilane 0.2 gram; NCO content, discharging are measured in 80 ℃ of reactions after 2 hours.
Performance:
Example 1-3 makes colourless to little yellow transparent viscous liquid, and solid content 〉=90% is at 25 ℃, during humidity 50%RH, did solid work in 24 hours, solidify the thick-layer elastic coating of making after 7 days, coating is bright and clean still, hardness 〉=60shore A, elongation at break 〉=300%, tensile strength 〉=3Mpa.
2, the application of the silicone-modified polyurethane elastomer of monocomponent moisture cure
Get any elastomerics prepolymer among the example 1-3, press following recipe ratio and pigment, filler blending dispersion under agitation:
Silicone-modified prepolymer 12-15
N-BUTYL ACETATE 2-3
Lime carbonate (10um) 20-25
Titanium dioxide (whitening agent) 0.5-1
T-12 0.02-0.03％
The coating normal temperature of making 2-3mm solidifies down, does solid work 7 days mensuration coating shore A hardness 〉=70, elongation at break 〉=100%, tensile strength 〉=1.6Mpa after 24 hours.
Claims (10)
1, a kind of high-solid level monocomponent polyurethane method for producing elastomers, it is characterized in that earlier holding the polyurethane prepolymer of isocyano with isocyanic ester or the siloxanes that contains isocyano and polyol reaction preparation, again through containing the silicone-modified of reactive hydrogen, used polyvalent alcohol is a polyether glycol, or polyester polyol, or epoxy polyol; Used isocyanic ester is an aromatic diisocyanate, or aliphatic diisocyanate; Used siloxanes is the siloxanes that contains reactive hydrogen, and used catalyzer is tin class or amines catalyst, and used solvent is not for containing the solvent of reactive hydrogen; Above-mentioned by weight percentage each raw material consumption is as follows:
Polyvalent alcohol 30-80%
Isocyanate-monomer 10-30%
The siloxanes 0.1-10% that contains reactive hydrogen
Catalyzer 0-0.2%
Solvent 0-10%,
Polyvalent alcohol 30-80%
The siloxanes 0-10% that contains isocyano
The siloxanes 0.1-10% that contains reactive hydrogen
Catalyzer 0-0.2%
Solvent 0-10%,
Concrete preparation process is as follows: having the agitator that is equipped with of vacuum dewatering plant; thermometer; in the reactor of prolong; add the isocyanates monomer; solvent; catalyzer; polyvalent alcohol and the evenly slow permanent dropping in back of solvent with vacuum-drying; under nitrogen protection, slowly be warming up to 70-90 ℃ of reaction 3-4 hour; the siloxanes that maybe will contain isocyano; solvent; catalyzer; add earlier in the reactor with polyol reaction 0.5-1.5 hour after; add the isocyanates monomer again and continue reaction 3-4 hour; till the end isocyano-content remains unchanged substantially; cooling; dropping contains the siloxanes of reactive hydrogen; in 60-80 ℃ of reaction 1-2 hour, cooling; discharging also packs.
2, high-solid level monocomponent polyurethane method for producing elastomers according to claim 1 is characterized in that polyvalent alcohol adopts vacuum hydro-extraction, vacuum tightness 0.06-0.09MPa, temperature 80-110 ℃; Perhaps dewater with refluxing toluene.
3, according to right 1 described high-solid level monocomponent polyurethane method for producing elastomers, it is characterized in that used polyvalent alcohol molecular weight is 50-10000, hydroxyl value is at 25～300mgKOH/g.
4, high-solid level monocomponent polyurethane method for producing elastomers according to claim 1, it is characterized in that used isocyanic ester is tolylene diisocyanate, diphenylmethanediisocyanate, naphthalene-1,5 vulcabond, many phenyl polymethine polyisocyanates, in aliphatics hexamethylene diisocyanate, the isophorone diisocyanate one or more mix use.
5, high-solid level monocomponent polyurethane method for producing elastomers according to claim 1, it is characterized in that the used siloxanes that contains isocyano is isocyanic ester methoxy silane, isocyanic ester Ethoxysilane, isocyanate-containing alkyl methoxy silane, isocyanate-containing alkyl Ethoxysilane, adopt wherein one or two or more kinds mixing to use.
6, high-solid level monocomponent polyurethane method for producing elastomers according to claim 1, it is characterized in that the used siloxanes coupling agent that contains reactive hydrogen is sulfydryl, epoxy group(ing), urea groups, primary amino, secondary amino group siloxanes, adopting wherein, one or more mix use.
7, according to the described high-solid level monocomponent polyurethane of claim 1 method for producing elastomers, it is characterized in that used catalyzer is dibutyl tin laurate, stannous acetate, triethylenediamine, adopt wherein one or two or more kinds mixing to use.
8, high-solid level monocomponent polyurethane method for producing elastomers according to claim 1, it is characterized in that: used solvent is toluene, dimethylbenzene, N-BUTYL ACETATE, vinyl acetic monomer, 4-methyl 2 pentanone, methylethylketone, solvent 100, solvent 150, uses wherein one or two or more kinds mixing to use.
9, high-solid level monocomponent polyurethane elastomerics prepolymer solids constituent 〉=90% that makes according to the described method of claim 1-8, at 25 ℃, solidify thick-layer elastic coating shore A hardness 〉=60 of making after 7 days, elongation at break 〉=300%, tensile strength 〉=3Mpa during humidity 50%RH.
10, the high-solid level monocomponent polyurethane elastomerics that makes according to the described method of claim 1-8 is as the application of coating.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2004100534522A CN100528920C (en) | 2004-08-05 | 2004-08-05 | Process for preparing high solid single component polyurethane elastor and its use |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2004100534522A CN100528920C (en) | 2004-08-05 | 2004-08-05 | Process for preparing high solid single component polyurethane elastor and its use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1587293A true CN1587293A (en) | 2005-03-02 |
| CN100528920C CN100528920C (en) | 2009-08-19 |
Family
ID=34602863
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2004100534522A Expired - Fee Related CN100528920C (en) | 2004-08-05 | 2004-08-05 | Process for preparing high solid single component polyurethane elastor and its use |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100528920C (en) |
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100513500C (en) * | 2007-04-09 | 2009-07-15 | 周树东 | Self-curing polyurethane insulating varnish and its production |
| CN102140243A (en) * | 2010-11-26 | 2011-08-03 | 山东东大一诺威聚氨酯有限公司 | Plastic sizing agent for silane-modified single component wet cured polyurethane playing court and preparation method thereof |
| CN102391454A (en) * | 2011-09-09 | 2012-03-28 | 北京高盟新材料股份有限公司 | Preparation method of polyurethane adhesive for extrusion lamination |
| CN101319130B (en) * | 2008-07-22 | 2012-04-11 | 四川省隆鑫科技包装有限公司 | Adhesion agent for battle cap |
| CN102408825A (en) * | 2011-09-14 | 2012-04-11 | 吴江市汇丰材料科技有限公司 | Single-component thermosetting polyurethane elastomer composition and preparation method thereof |
| CN102031056B (en) * | 2009-09-29 | 2013-04-10 | 比亚迪股份有限公司 | Coating as well as preparation method and use method thereof |
| CN103741490A (en) * | 2013-12-30 | 2014-04-23 | 辽宁恒星精细化工有限公司 | Tear-resistant finishing agent for pure cotton woven fabric and preparation method thereof |
| CN104231219A (en) * | 2014-09-18 | 2014-12-24 | 东莞市吉鑫高分子科技有限公司 | TPU (thermoplastic polyurethane) elastomer for keyboard film and preparation method of elastomer |
| CN105315878A (en) * | 2015-12-05 | 2016-02-10 | 四川蜀羊防水材料有限公司 | Solvent-free one-component polyurethane waterproof coating |
| CN106118428A (en) * | 2016-07-28 | 2016-11-16 | 上海乘鹰新材料有限公司 | A kind of waterproof scratch resistant aqueous polyurethane coating and preparation method thereof |
| CN106978059A (en) * | 2017-03-09 | 2017-07-25 | 上海台安实业集团有限公司 | Silane end-cappers modified double components polyurethane water-proof paint and preparation method thereof |
| CN108485586A (en) * | 2018-02-09 | 2018-09-04 | 广东普赛达密封粘胶有限公司 | A kind of dendritic silane modified polyurethane composition of high shear strength and preparation method thereof |
| CN109666115A (en) * | 2017-10-16 | 2019-04-23 | 万华化学集团股份有限公司 | A kind of amino-silane terminated modified polyurethane resin and preparation method thereof |
| CN111454425A (en) * | 2012-09-04 | 2020-07-28 | 科思创德国股份有限公司 | Isocyanatosilanes with thiocarbamate Structure |
| CN114292574A (en) * | 2021-08-13 | 2022-04-08 | 荆门科顺新材料有限公司 | Single-component polyurethane waterproof coating and preparation method thereof |
| CN115678018A (en) * | 2022-11-04 | 2023-02-03 | 海洋化工研究院有限公司 | Polyurethane-organic silicon resin prepolymer and preparation method and application thereof |
| CN116284639A (en) * | 2023-02-09 | 2023-06-23 | 上海博盛聚氨酯制品有限公司 | Polyurethane elastomer for petroleum pipeline cleaner and preparation method thereof |
| CN117777395A (en) * | 2023-12-26 | 2024-03-29 | 马鞍山采石矶涂料有限公司 | Isocyanate-terminated elastomer resin, preparation method thereof, coating component and application |
-
2004
- 2004-08-05 CN CNB2004100534522A patent/CN100528920C/en not_active Expired - Fee Related
Cited By (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100513500C (en) * | 2007-04-09 | 2009-07-15 | 周树东 | Self-curing polyurethane insulating varnish and its production |
| CN101319130B (en) * | 2008-07-22 | 2012-04-11 | 四川省隆鑫科技包装有限公司 | Adhesion agent for battle cap |
| CN102031056B (en) * | 2009-09-29 | 2013-04-10 | 比亚迪股份有限公司 | Coating as well as preparation method and use method thereof |
| CN102140243A (en) * | 2010-11-26 | 2011-08-03 | 山东东大一诺威聚氨酯有限公司 | Plastic sizing agent for silane-modified single component wet cured polyurethane playing court and preparation method thereof |
| CN102140243B (en) * | 2010-11-26 | 2012-07-25 | 山东东大一诺威聚氨酯有限公司 | Plastic sizing agent for silane-modified single component wet cured polyurethane playing court and preparation method thereof |
| CN102391454A (en) * | 2011-09-09 | 2012-03-28 | 北京高盟新材料股份有限公司 | Preparation method of polyurethane adhesive for extrusion lamination |
| CN102391454B (en) * | 2011-09-09 | 2013-12-18 | 北京高盟新材料股份有限公司 | Preparation method of polyurethane adhesive for extrusion lamination |
| CN102408825A (en) * | 2011-09-14 | 2012-04-11 | 吴江市汇丰材料科技有限公司 | Single-component thermosetting polyurethane elastomer composition and preparation method thereof |
| CN111454425A (en) * | 2012-09-04 | 2020-07-28 | 科思创德国股份有限公司 | Isocyanatosilanes with thiocarbamate Structure |
| CN111454425B (en) * | 2012-09-04 | 2023-04-07 | 科思创德国股份有限公司 | Isocyanatosilanes with thiocarbamate Structure |
| CN103741490B (en) * | 2013-12-30 | 2016-01-13 | 辽宁恒星精细化工有限公司 | Textile shuttle-woven fabric anti tear finishing agent and preparation method |
| CN103741490A (en) * | 2013-12-30 | 2014-04-23 | 辽宁恒星精细化工有限公司 | Tear-resistant finishing agent for pure cotton woven fabric and preparation method thereof |
| CN104231219A (en) * | 2014-09-18 | 2014-12-24 | 东莞市吉鑫高分子科技有限公司 | TPU (thermoplastic polyurethane) elastomer for keyboard film and preparation method of elastomer |
| CN104231219B (en) * | 2014-09-18 | 2017-08-29 | 东莞市吉鑫高分子科技有限公司 | It is a kind of for TPUE of keyboard membrane and preparation method thereof |
| CN105315878A (en) * | 2015-12-05 | 2016-02-10 | 四川蜀羊防水材料有限公司 | Solvent-free one-component polyurethane waterproof coating |
| CN106118428A (en) * | 2016-07-28 | 2016-11-16 | 上海乘鹰新材料有限公司 | A kind of waterproof scratch resistant aqueous polyurethane coating and preparation method thereof |
| CN106978059B (en) * | 2017-03-09 | 2020-01-10 | 上海台安实业集团有限公司 | Silane end-capping agent modified two-component polyurethane waterproof coating and preparation method thereof |
| CN106978059A (en) * | 2017-03-09 | 2017-07-25 | 上海台安实业集团有限公司 | Silane end-cappers modified double components polyurethane water-proof paint and preparation method thereof |
| CN109666115A (en) * | 2017-10-16 | 2019-04-23 | 万华化学集团股份有限公司 | A kind of amino-silane terminated modified polyurethane resin and preparation method thereof |
| CN108485586A (en) * | 2018-02-09 | 2018-09-04 | 广东普赛达密封粘胶有限公司 | A kind of dendritic silane modified polyurethane composition of high shear strength and preparation method thereof |
| CN108485586B (en) * | 2018-02-09 | 2021-01-05 | 广东普赛达密封粘胶有限公司 | High-shear-strength dendritic silane modified polyurethane composition and preparation method thereof |
| CN114292574A (en) * | 2021-08-13 | 2022-04-08 | 荆门科顺新材料有限公司 | Single-component polyurethane waterproof coating and preparation method thereof |
| CN115678018A (en) * | 2022-11-04 | 2023-02-03 | 海洋化工研究院有限公司 | Polyurethane-organic silicon resin prepolymer and preparation method and application thereof |
| CN115678018B (en) * | 2022-11-04 | 2023-10-20 | 海洋化工研究院有限公司 | Polyurethane-organic silicon resin prepolymer and preparation method and application thereof |
| CN116284639A (en) * | 2023-02-09 | 2023-06-23 | 上海博盛聚氨酯制品有限公司 | Polyurethane elastomer for petroleum pipeline cleaner and preparation method thereof |
| CN116284639B (en) * | 2023-02-09 | 2024-05-17 | 上海博盛聚氨酯制品有限公司 | Polyurethane elastomer for petroleum pipeline cleaner and preparation method thereof |
| CN117777395A (en) * | 2023-12-26 | 2024-03-29 | 马鞍山采石矶涂料有限公司 | Isocyanate-terminated elastomer resin, preparation method thereof, coating component and application |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100528920C (en) | 2009-08-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100528920C (en) | Process for preparing high solid single component polyurethane elastor and its use | |
| US8394909B2 (en) | Silane-terminated polyurethanes with high strength and high elongation | |
| CA1038540A (en) | Moisture curable polyurethane systems | |
| CA2414411C (en) | Silylated polyurethanes for adhesives and sealants with improved mechanical properties | |
| EP2010588B1 (en) | Organosilicon polyurea polymers, elastomers manufactured therefrom and their use | |
| KR20080063814A (en) | Moisture-hardened polyurethane compositions containing compounds comprising aldimine | |
| KR100461621B1 (en) | Polyurethane resin | |
| TW200306990A (en) | Polyurethane prepolymers with reduced functionality having terminal alkoxysilane and OH groups, a method of preparing them and their use | |
| CN1986641B (en) | Encapsulating polyurethane material recipe and encapsulating material containing said recipe | |
| CN109851738B (en) | Preparation method of fluorine-silicon modified carbamido compound | |
| CN113980563B (en) | Method for preparing one-component semi-polyurea waterproof coating composition and one-component semi-polyurea waterproof coating composition | |
| CN108949090A (en) | A kind of solvent-free dual-component polyurethane sealant and preparation method thereof | |
| KR20170040097A (en) | Urethane adhesive composition | |
| CN103834034B (en) | Polyureas copolymer with main chain containing siloxane composition unit and preparation method thereof | |
| CN102203207B (en) | Dry-to-the-touch moisture-curable compositions and products made therefrom | |
| CN117106366B (en) | Single-component polyurea coating and preparation method and application thereof | |
| US20060057394A1 (en) | System and method for coating a substrate | |
| CN101528801A (en) | Polysulfide curable composition | |
| JP2006506490A5 (en) | ||
| US11499001B2 (en) | Single-component polysiloxane non-skid / non-slip coatings | |
| WO2006032034A2 (en) | Polyurethane-polyurea polymer | |
| CN1108678A (en) | Water-proof polyurethane coating film and preparation method thereof | |
| CN104119499A (en) | Method for preparing epoxy-modified aromatic polysulfideurethane | |
| CN115260228B (en) | Silicon-containing compound and preparation method thereof, and single-component polyurethane waterproof coating and preparation method thereof | |
| JP2916967B2 (en) | Method for producing crosslinked polyurethane elastomer |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20090819 Termination date: 20160805 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |