JP2015514848A5 - - Google Patents
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- JP2015514848A5 JP2015514848A5 JP2015507106A JP2015507106A JP2015514848A5 JP 2015514848 A5 JP2015514848 A5 JP 2015514848A5 JP 2015507106 A JP2015507106 A JP 2015507106A JP 2015507106 A JP2015507106 A JP 2015507106A JP 2015514848 A5 JP2015514848 A5 JP 2015514848A5
- Authority
- JP
- Japan
- Prior art keywords
- isocyanate
- terminated prepolymer
- mol
- group
- oxide
- 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.)
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- 239000000203 mixture Substances 0.000 claims description 46
- 229920005862 polyol Polymers 0.000 claims description 39
- 150000003077 polyols Chemical class 0.000 claims description 39
- 125000001931 aliphatic group Chemical group 0.000 claims description 32
- 229920000515 polycarbonate Polymers 0.000 claims description 27
- 239000004417 polycarbonate Substances 0.000 claims description 27
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 22
- 239000001569 carbon dioxide Substances 0.000 claims description 11
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 11
- 150000002118 epoxides Chemical class 0.000 claims description 9
- -1 glycidyl ester Chemical class 0.000 claims description 9
- 239000012948 isocyanate Substances 0.000 claims description 8
- 150000002513 isocyanates Chemical class 0.000 claims description 8
- 239000005056 polyisocyanate Substances 0.000 claims description 7
- 229920001228 polyisocyanate Polymers 0.000 claims description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 6
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 5
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 claims description 4
- FDWQGNULGGFFDP-UHFFFAOYSA-N 5-ethenyl-7-oxabicyclo[4.1.0]heptane Chemical compound C=CC1CCCC2OC12 FDWQGNULGGFFDP-UHFFFAOYSA-N 0.000 claims description 4
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 4
- ZWAJLVLEBYIOTI-UHFFFAOYSA-N cyclohexene oxide Chemical compound C1CCCC2OC21 ZWAJLVLEBYIOTI-UHFFFAOYSA-N 0.000 claims description 4
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohexene oxide Natural products O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 claims description 4
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 4
- 229920001897 terpolymer Polymers 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 238000007334 copolymerization reaction Methods 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- 239000012986 chain transfer agent Substances 0.000 claims description 2
- 229920005906 polyester polyol Polymers 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 125000003107 substituted aryl group Chemical group 0.000 claims description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims 2
- UNVGBIALRHLALK-UHFFFAOYSA-N 1,5-Hexanediol Chemical compound CC(O)CCCCO UNVGBIALRHLALK-UHFFFAOYSA-N 0.000 claims 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims 2
- 239000005058 Isophorone diisocyanate Substances 0.000 claims 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims 2
- 150000001298 alcohols Chemical class 0.000 claims 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims 2
- 239000004711 α-olefin Substances 0.000 claims 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 claims 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims 1
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 claims 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 claims 1
- FQXGHZNSUOHCLO-UHFFFAOYSA-N 2,2,4,4-tetramethyl-1,3-cyclobutanediol Chemical compound CC1(C)C(O)C(C)(C)C1O FQXGHZNSUOHCLO-UHFFFAOYSA-N 0.000 claims 1
- RWLALWYNXFYRGW-UHFFFAOYSA-N 2-Ethyl-1,3-hexanediol Chemical compound CCCC(O)C(CC)CO RWLALWYNXFYRGW-UHFFFAOYSA-N 0.000 claims 1
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 claims 1
- JVGDVPVEKJSWIO-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)cyclohexyl]ethanol Chemical compound OCCC1CCC(CCO)CC1 JVGDVPVEKJSWIO-UHFFFAOYSA-N 0.000 claims 1
- DSKYSDCYIODJPC-UHFFFAOYSA-N 2-butyl-2-ethylpropane-1,3-diol Chemical compound CCCCC(CC)(CO)CO DSKYSDCYIODJPC-UHFFFAOYSA-N 0.000 claims 1
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims 1
- KLDXJTOLSGUMSJ-JGWLITMVSA-N Isosorbide Chemical compound O[C@@H]1CO[C@@H]2[C@@H](O)CO[C@@H]21 KLDXJTOLSGUMSJ-JGWLITMVSA-N 0.000 claims 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 claims 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 claims 1
- XDODWINGEHBYRT-UHFFFAOYSA-N [2-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCCCC1CO XDODWINGEHBYRT-UHFFFAOYSA-N 0.000 claims 1
- LUSFFPXRDZKBMF-UHFFFAOYSA-N [3-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCCC(CO)C1 LUSFFPXRDZKBMF-UHFFFAOYSA-N 0.000 claims 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 claims 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 claims 1
- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 claims 1
- PMMYEEVYMWASQN-IMJSIDKUSA-N cis-4-Hydroxy-L-proline Chemical compound O[C@@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-IMJSIDKUSA-N 0.000 claims 1
- RLMGYIOTPQVQJR-UHFFFAOYSA-N cyclohexane-1,3-diol Chemical compound OC1CCCC(O)C1 RLMGYIOTPQVQJR-UHFFFAOYSA-N 0.000 claims 1
- KQWGXHWJMSMDJJ-UHFFFAOYSA-N cyclohexyl isocyanate Chemical compound O=C=NC1CCCCC1 KQWGXHWJMSMDJJ-UHFFFAOYSA-N 0.000 claims 1
- NUUPJBRGQCEZSI-UHFFFAOYSA-N cyclopentane-1,3-diol Chemical compound OC1CCC(O)C1 NUUPJBRGQCEZSI-UHFFFAOYSA-N 0.000 claims 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 claims 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 claims 1
- 125000005442 diisocyanate group Chemical group 0.000 claims 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims 1
- 229960002479 isosorbide Drugs 0.000 claims 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 claims 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 229920001451 polypropylene glycol Polymers 0.000 claims 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 claims 1
- 235000013772 propylene glycol Nutrition 0.000 claims 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims 1
- 239000000853 adhesive Substances 0.000 description 46
- 230000001070 adhesive effect Effects 0.000 description 46
- 229920002635 polyurethane Polymers 0.000 description 28
- 239000004814 polyurethane Substances 0.000 description 28
- 238000009472 formulation Methods 0.000 description 8
- 239000000758 substrate Substances 0.000 description 5
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000003384 small molecules Chemical class 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 239000004970 Chain extender Substances 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261625065P | 2012-04-16 | 2012-04-16 | |
| US61/625,065 | 2012-04-16 | ||
| US201261683277P | 2012-08-15 | 2012-08-15 | |
| US61/683,277 | 2012-08-15 | ||
| PCT/US2013/036751 WO2013158621A1 (en) | 2012-04-16 | 2013-04-16 | Adhesive compositions and methods |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017220107A Division JP6599418B2 (ja) | 2012-04-16 | 2017-11-15 | 接着剤組成物および方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2015514848A JP2015514848A (ja) | 2015-05-21 |
| JP2015514848A5 true JP2015514848A5 (enExample) | 2016-06-16 |
Family
ID=49325658
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015507106A Withdrawn JP2015514848A (ja) | 2012-04-16 | 2013-04-16 | 接着剤組成物および方法 |
| JP2017220107A Active JP6599418B2 (ja) | 2012-04-16 | 2017-11-15 | 接着剤組成物および方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017220107A Active JP6599418B2 (ja) | 2012-04-16 | 2017-11-15 | 接着剤組成物および方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (3) | US20130274401A1 (enExample) |
| EP (1) | EP2838954B1 (enExample) |
| JP (2) | JP2015514848A (enExample) |
| KR (1) | KR102110746B1 (enExample) |
| CN (3) | CN110791246B (enExample) |
| WO (1) | WO2013158621A1 (enExample) |
Families Citing this family (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102089887B1 (ko) | 2008-09-08 | 2020-03-16 | 사우디 아람코 테크놀로지스 컴퍼니 | 폴리카보네이트 폴리올 조성물 |
| KR101401925B1 (ko) * | 2010-12-28 | 2014-06-02 | 에스케이이노베이션 주식회사 | 열안정성이 개선된 폴리프로필렌 카보네이트의 제조방법 |
| ES2749324T3 (es) | 2011-07-25 | 2020-03-19 | Saudi Aramco Tech Co | Composiciones poliméricas y métodos |
| KR102110746B1 (ko) | 2012-04-16 | 2020-05-14 | 사우디 아람코 테크놀로지스 컴퍼니 | 접착제 조성물 및 방법 |
| KR102096761B1 (ko) | 2012-08-24 | 2020-04-03 | 사우디 아람코 테크놀로지스 컴퍼니 | 금속 착물 |
| EP3584267A1 (en) | 2012-11-07 | 2019-12-25 | Saudi Aramco Technologies Company | High strength polyurethane foam compositions and methods |
| JP6045908B2 (ja) * | 2012-12-21 | 2016-12-14 | ヘンケルジャパン株式会社 | 湿気硬化型ホットメルト接着剤 |
| KR20160006775A (ko) | 2013-05-13 | 2016-01-19 | 노보머, 인코포레이티드 | Ｃｏ₂ 포함 폼 및 관련 방법 |
| US10414269B2 (en) * | 2014-02-19 | 2019-09-17 | Floats and Fuel Cells, Inc. | Hydrocarbon storage vessels |
| EP3126424B1 (en) | 2014-04-03 | 2020-09-30 | Saudi Aramco Technologies Company | Aliphatic polycarbonate polyol compositions |
| DE102014209019A1 (de) * | 2014-05-13 | 2015-11-19 | Henkel Ag & Co. Kgaa | Bindemittel-System mit schnellerer Aushärtung |
| CN106459352B (zh) * | 2014-06-16 | 2020-01-14 | 3M创新有限公司 | 具有耐洗性珠粘结层的回射制品 |
| WO2016120406A1 (en) | 2015-01-28 | 2016-08-04 | Repsol, S.A. | A polyurethane adhesive formulation based on polyether carbonate polyol |
| JP6080876B2 (ja) * | 2015-02-04 | 2017-02-15 | 日新製鋼株式会社 | 塗装金属素形材と化学繊維を含む布とが接合された複合体およびその製造方法 |
| WO2016166165A1 (en) | 2015-04-13 | 2016-10-20 | Repsol, S.A. | New formulations for polyurethane applications |
| DE102015207792A1 (de) * | 2015-04-28 | 2016-11-03 | Henkel Ag & Co. Kgaa | Polyurethan-basiertes Bindemittel-System |
| DE102015107174B4 (de) | 2015-05-07 | 2022-07-07 | Lisa Dräxlmaier GmbH | Cyclodextrinhaltige Heißschmelzklebemassen und Verfahren zur Herstellung |
| ES2936086T3 (es) | 2015-08-03 | 2023-03-14 | Repsol Sa | Composición adhesiva que comprende poliéter carbonato polioles |
| JP2018528997A (ja) * | 2015-08-04 | 2018-10-04 | レプソル・ソシエダッド・アノニマＲｅｐｓｏｌ．Ｓ．Ａ． | 感圧接着剤のための新規調製物 |
| CN105601861B (zh) * | 2016-02-23 | 2018-08-28 | 同光（江苏）信息科技有限公司 | 一种有机硅改性水性聚氨酯树脂的合成方法 |
| BR112018069664B1 (pt) * | 2016-03-28 | 2022-10-04 | Rohm And Haas Company | Composição adesiva sem solvente com dois componentes, método para formar um laminado e laminado |
| US10119223B2 (en) * | 2016-07-15 | 2018-11-06 | Covestro Llc | Carpet and synthetic turf backings prepared from a polyether carbonate polyol |
| JP6501991B2 (ja) * | 2016-12-26 | 2019-04-17 | 公立大学法人横浜市立大学 | 蛍光性樹脂組成物、成形体及び医療用機器並びに蛍光性樹脂組成物の製造方法 |
| CN107033829A (zh) * | 2017-04-28 | 2017-08-11 | 东华大学 | 一种聚碳酸亚丙酯基湿固化聚氨酯热熔胶及其制备方法 |
| US20180312623A1 (en) * | 2017-04-28 | 2018-11-01 | Liang Wang | Polyurethane Elastomer with High Ultimate Elongation |
| EP3424967A1 (de) * | 2017-07-07 | 2019-01-09 | Covestro Deutschland AG | Verfahren zur herstellung von funktionalisierten polyoxyalkylenpolyolen |
| BR112020002884A2 (pt) * | 2017-08-11 | 2020-08-04 | Vision Ease, Lp | adesivos ópticos e laminados ópticos e lentes formadas com os mesmos |
| KR101998781B1 (ko) * | 2017-11-20 | 2019-10-01 | 한국신발피혁연구원 | 내수성이 우수한 수분산 폴리우레탄 접착제의 제조방법 및 이 방법에 의해 제조된 수분산 폴리우레탄 접착제 |
| CN108384500B (zh) * | 2018-02-10 | 2020-06-26 | 中国科学院长春应用化学研究所 | 二氧化碳基反应型聚氨酯热熔胶及其制备方法 |
| US11230625B2 (en) | 2018-04-18 | 2022-01-25 | Saudi Aramco Technologies Company | End-group isomerization of poly(alkylene carbonate) polymers |
| WO2020028606A1 (en) | 2018-08-02 | 2020-02-06 | Saudi Aramco Technologies Company | Sustainable polymer compositions and methods |
| CN109266290B (zh) * | 2018-08-31 | 2020-11-24 | 浙江华峰热塑性聚氨酯有限公司 | 反应型热塑性聚氨酯及其制备方法 |
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2013
- 2013-04-16 KR KR1020147032074A patent/KR102110746B1/ko active Active
- 2013-04-16 CN CN201910967728.4A patent/CN110791246B/zh active Active
- 2013-04-16 CN CN202210364405.8A patent/CN114774053A/zh active Pending
- 2013-04-16 EP EP13778334.6A patent/EP2838954B1/en active Active
- 2013-04-16 WO PCT/US2013/036751 patent/WO2013158621A1/en not_active Ceased
- 2013-04-16 US US13/864,095 patent/US20130274401A1/en not_active Abandoned
- 2013-04-16 CN CN201380029221.5A patent/CN104428370A/zh active Pending
- 2013-04-16 US US14/394,762 patent/US9834710B2/en active Active
- 2013-04-16 JP JP2015507106A patent/JP2015514848A/ja not_active Withdrawn
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2015
- 2015-05-22 US US14/720,242 patent/US20150344751A1/en not_active Abandoned
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2017
- 2017-11-15 JP JP2017220107A patent/JP6599418B2/ja active Active
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