JP2012502151A5 - - Google Patents
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- JP2012502151A5 JP2012502151A5 JP2011526432A JP2011526432A JP2012502151A5 JP 2012502151 A5 JP2012502151 A5 JP 2012502151A5 JP 2011526432 A JP2011526432 A JP 2011526432A JP 2011526432 A JP2011526432 A JP 2011526432A JP 2012502151 A5 JP2012502151 A5 JP 2012502151A5
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- acid
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- -1 carboxy compound Chemical class 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 230000005494 condensation Effects 0.000 claims description 3
- 238000009833 condensation Methods 0.000 claims description 3
- 230000007062 hydrolysis Effects 0.000 claims description 3
- 238000006460 hydrolysis reaction Methods 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 claims 2
- 230000001070 adhesive effect Effects 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 229920002635 polyurethane Polymers 0.000 claims 2
- 239000004814 polyurethane Substances 0.000 claims 2
- 239000000565 sealant Substances 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 description 8
- 125000000524 functional group Chemical group 0.000 description 8
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 125000006165 cyclic alkyl group Chemical group 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- 150000001336 alkenes Chemical group 0.000 description 3
- 125000003710 aryl alkyl group Chemical group 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 description 2
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 2
- 125000004103 aminoalkyl group Chemical group 0.000 description 2
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 150000002118 epoxides Chemical class 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
- 239000010438 granite Substances 0.000 description 2
- 125000001188 haloalkyl group Chemical group 0.000 description 2
- 125000006038 hexenyl group Chemical group 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 125000005358 mercaptoalkyl group Chemical group 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 238000007142 ring opening reaction Methods 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- BITHHVVYSMSWAG-KTKRTIGZSA-N (11Z)-icos-11-enoic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCC(O)=O BITHHVVYSMSWAG-KTKRTIGZSA-N 0.000 description 1
- GWHCXVQVJPWHRF-KTKRTIGZSA-N (15Z)-tetracosenoic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCCCC(O)=O GWHCXVQVJPWHRF-KTKRTIGZSA-N 0.000 description 1
- FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 description 1
- 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
- FPAQLJHSZVFKES-UHFFFAOYSA-N 5-Eicosenoic acid Natural products CCCCCCCCCCCCCCC=CCCCC(O)=O FPAQLJHSZVFKES-UHFFFAOYSA-N 0.000 description 1
- AFSDNFLWKVMVRB-UHFFFAOYSA-N Ellagic acid Chemical compound OC1=C(O)C(OC2=O)=C3C4=C2C=C(O)C(O)=C4OC(=O)C3=C1 AFSDNFLWKVMVRB-UHFFFAOYSA-N 0.000 description 1
- ATJXMQHAMYVHRX-CPCISQLKSA-N Ellagic acid Natural products OC1=C(O)[C@H]2OC(=O)c3cc(O)c(O)c4OC(=O)C(=C1)[C@H]2c34 ATJXMQHAMYVHRX-CPCISQLKSA-N 0.000 description 1
- 229920002079 Ellagic acid Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000208202 Linaceae Species 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- XJXROGWVRIJYMO-SJDLZYGOSA-N Nervonic acid Natural products O=C(O)[C@@H](/C=C/CCCCCCCC)CCCCCCCCCCCC XJXROGWVRIJYMO-SJDLZYGOSA-N 0.000 description 1
- 235000021319 Palmitoleic acid Nutrition 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000021322 Vaccenic acid Nutrition 0.000 description 1
- UWHZIFQPPBDJPM-FPLPWBNLSA-M Vaccenic acid Natural products CCCCCC\C=C/CCCCCCCCCC([O-])=O UWHZIFQPPBDJPM-FPLPWBNLSA-M 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 235000021342 arachidonic acid Nutrition 0.000 description 1
- 229940114079 arachidonic acid Drugs 0.000 description 1
- 239000002928 artificial marble Substances 0.000 description 1
- 239000002969 artificial stone Substances 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- KHAVLLBUVKBTBG-UHFFFAOYSA-N caproleic acid Natural products OC(=O)CCCCCCCC=C KHAVLLBUVKBTBG-UHFFFAOYSA-N 0.000 description 1
- 239000011111 cardboard Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- KJDZDTDNIULJBE-QXMHVHEDSA-N cetoleic acid Chemical compound CCCCCCCCCC\C=C/CCCCCCCCCC(O)=O KJDZDTDNIULJBE-QXMHVHEDSA-N 0.000 description 1
- SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 1
- GWHCXVQVJPWHRF-UHFFFAOYSA-N cis-tetracosenoic acid Natural products CCCCCCCCC=CCCCCCCCCCCCCCC(O)=O GWHCXVQVJPWHRF-UHFFFAOYSA-N 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000005725 cyclohexenylene group Chemical group 0.000 description 1
- 125000004990 dihydroxyalkyl group Chemical group 0.000 description 1
- 229940090949 docosahexaenoic acid Drugs 0.000 description 1
- 235000020669 docosahexaenoic acid Nutrition 0.000 description 1
- 229960002852 ellagic acid Drugs 0.000 description 1
- 235000004132 ellagic acid Nutrition 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 239000011381 foam concrete Substances 0.000 description 1
- VZCCETWTMQHEPK-UHFFFAOYSA-N gamma-Linolensaeure Natural products CCCCCC=CCC=CCC=CCCCCC(O)=O VZCCETWTMQHEPK-UHFFFAOYSA-N 0.000 description 1
- VZCCETWTMQHEPK-QNEBEIHSSA-N gamma-linolenic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/CCCCC(O)=O VZCCETWTMQHEPK-QNEBEIHSSA-N 0.000 description 1
- 235000020664 gamma-linolenic acid Nutrition 0.000 description 1
- 229960002733 gamolenic acid Drugs 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- FAARLWTXUUQFSN-UHFFFAOYSA-N methylellagic acid Natural products O1C(=O)C2=CC(O)=C(O)C3=C2C2=C1C(OC)=C(O)C=C2C(=O)O3 FAARLWTXUUQFSN-UHFFFAOYSA-N 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- WBHHMMIMDMUBKC-QJWNTBNXSA-N ricinoleic acid Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O WBHHMMIMDMUBKC-QJWNTBNXSA-N 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000001443 terpenyl group Chemical group 0.000 description 1
- UWHZIFQPPBDJPM-BQYQJAHWSA-N trans-vaccenic acid Chemical compound CCCCCC\C=C\CCCCCCCCCC(O)=O UWHZIFQPPBDJPM-BQYQJAHWSA-N 0.000 description 1
- 229960002703 undecylenic acid Drugs 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008041920.6 | 2008-09-09 | ||
| DE102008041920A DE102008041920A1 (de) | 2008-09-09 | 2008-09-09 | Neue Katalysatoren für die Vernetzung von funktionellen Silanen oder funktionellen Siloxanen, insbesondere mit Substraten |
| PCT/EP2009/058723 WO2010028877A1 (de) | 2008-09-09 | 2009-07-09 | Neue katalysatoren für die vernetzung von funktionellen silanen oder funktionellen siloxanen, insbesondere mit substraten |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2012502151A JP2012502151A (ja) | 2012-01-26 |
| JP2012502151A5 true JP2012502151A5 (US06244707-20010612-C00007.png) | 2012-06-14 |
Family
ID=41055304
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011526432A Withdrawn JP2012502151A (ja) | 2008-09-09 | 2009-07-09 | 官能性シラン又は官能性シロキサンを基質と架橋するための新規触媒 |
Country Status (6)
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007040802A1 (de) * | 2007-08-28 | 2009-03-05 | Evonik Degussa Gmbh | VOC-arme aminoalkyl-funktionelle Siliciumverbindungen enthaltende Zusammensetzung für Streichfarben zur Behandlung von Papier oder Folie |
| DE102008041918A1 (de) | 2008-09-09 | 2010-03-11 | Evonik Degussa Gmbh | Silanolkondensationskatalysatoren zur Vernetzung von gefüllten und ungefüllten Polymer-Compounds |
| WO2010130457A1 (en) * | 2009-05-14 | 2010-11-18 | Borealis Ag | Cross-linkable polyolefin composition comprising two types of silane groups |
| DE102009027090A1 (de) | 2009-06-23 | 2010-12-30 | Evonik Degussa Gmbh | Magnetische Partikel und Polyethylen enthaltendes Kompositmaterial |
| DE102010002358A1 (de) | 2010-02-25 | 2011-08-25 | Evonik Degussa GmbH, 45128 | Carboxyfunktionalisierte Silicium enthaltende Vorläuferverbindung verschiedener organischer Carbonsäuren |
| DE102011001962A1 (de) | 2011-04-11 | 2012-10-11 | Thyssenkrupp Uhde Gmbh | Verfahren und Anlage zur biologischen Reinigung von Kokereiabwasser |
| JP5867325B2 (ja) * | 2011-07-12 | 2016-02-24 | 株式会社デンソー | 撥水性基材の製造方法 |
| DE102011086865A1 (de) | 2011-11-22 | 2013-05-23 | Evonik Degussa Gmbh | Chloridarme Zusammensetzungen olefinisch funktionalisierter Siloxanoligomere basierend auf Alkoxysilanen |
| DE102011086862A1 (de) | 2011-11-22 | 2013-05-23 | Evonik Degussa Gmbh | Zusammensetzung olefinisch funktionalisierter Siloxanoligomere basierend auf Alkoxysilanen |
| DE102011086863A1 (de) | 2011-11-22 | 2013-05-23 | Evonik Degussa Gmbh | Besonders VOC-arme Gemische olefinisch funktionalisierter Siloxanoligomere basierend auf Alkoxysilanen |
| JP2013170264A (ja) * | 2012-02-23 | 2013-09-02 | Shinshu Univ | シリコーン系接着剤組成物およびその硬化体 |
| US8753443B1 (en) | 2013-01-02 | 2014-06-17 | Jones-Blair Company | Universal tint paste having high solids |
| US9914809B2 (en) * | 2013-08-30 | 2018-03-13 | Momentive Performance Materials Inc. | Moisture curable composition with amino acids |
| EP3080194B1 (en) * | 2013-12-13 | 2018-07-04 | Momentive Performance Materials Inc. | Process for the production of silane-crosslinked polyolefin in the presence of non-tin catalyst and resulting crosslinked polyolefin |
| JP6784676B2 (ja) * | 2014-12-19 | 2020-11-11 | ダウ シリコーンズ コーポレーション | 縮合架橋粒子の調製方法 |
| JP2017008320A (ja) * | 2016-06-30 | 2017-01-12 | 信越化学工業株式会社 | ゲル状組成物および吸水防止剤 |
| WO2018181650A1 (ja) * | 2017-03-29 | 2018-10-04 | 信越化学工業株式会社 | （メタ）アクリル変性シロキサン化合物 |
| WO2018180983A1 (ja) * | 2017-03-31 | 2018-10-04 | 住友化学株式会社 | 組成物 |
| US10480189B2 (en) * | 2017-11-06 | 2019-11-19 | Johns Manville | Aerogel containing construction board |
| EP3802684B1 (en) | 2018-05-25 | 2022-08-17 | Union Carbide Corporation | Moisture-curable polyolefin formulation |
| US11396637B2 (en) * | 2018-06-18 | 2022-07-26 | Chemetall U.S., Inc. | Amine-functionalized organosilane/organophosphate combination systems as EP agents / corrosion inhibitors in compositions for treating metal surfaces |
| EP3725753B1 (de) | 2019-04-15 | 2021-09-29 | PAGEL Spezial-Beton GmbH & Co. KG | Hydrophobierungsmittel für mineralische materialien |
| CN111454687B (zh) * | 2020-04-15 | 2022-06-07 | 隆基乐叶光伏科技有限公司 | 双组份硅酮胶及其生产方法及应用 |
| EP3904463A1 (de) * | 2020-04-30 | 2021-11-03 | Flooring Technologies Ltd. | Zusammensetzung zur mattierung und reduzierung von anti-fingerprint-effekten von oberflächen auf trägermaterialien |
| WO2022006394A1 (en) * | 2020-07-02 | 2022-01-06 | Momentive Performance Materials Inc. | Hybrid siloxane oligomers |
| PL242889B1 (pl) | 2020-09-12 | 2023-05-08 | Wysokinski Karol | Metoda modyfikowania metali za pomocą lasera |
| WO2022212137A1 (en) | 2021-03-31 | 2022-10-06 | Dow Global Technologies Llc | Moisture-curable semiconductive formulation |
| TW202239854A (zh) | 2021-03-31 | 2022-10-16 | 美商陶氏全球科技有限責任公司 | 可濕固化半導電調配物 |
| CN114082521B (zh) * | 2021-11-24 | 2022-08-09 | 贺州久源矿业有限公司 | 一种从花岗岩风化壳型钾长石综合回收云母的工艺 |
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| DE4443824A1 (de) | 1994-12-09 | 1996-06-13 | Huels Chemische Werke Ag | Organopolysiloxan-haltige Zusammensetzungen auf Wasserbasis, Verfahren zu deren Herstellung sowie deren Verwendung |
| DE19624032A1 (de) | 1996-06-17 | 1997-12-18 | Huels Chemische Werke Ag | Oligomerengemisch kondensierter Alkylalkoxysilane |
| DE19639782A1 (de) | 1996-09-27 | 1998-04-02 | Huels Chemische Werke Ag | Glycidether-, Acryl- und/oder Methacryl-funktionelle Organopolysiloxan-haltige Zusammensetzungen auf Wasser-Basis, Verfahren zu deren Herstellung sowie deren Verwendung |
| DE19649955A1 (de) | 1996-12-03 | 1998-06-04 | Huels Chemische Werke Ag | Fluoralkyl-funktionelle Organopolysiloxan-haltige Zusammensetzungen auf Wasser/Alkohol-Basis, Verfahren zu deren Herstellung sowie deren Verwendung |
| DE19649954A1 (de) | 1996-12-03 | 1998-06-04 | Huels Chemische Werke Ag | Fluoralkyl-funktionelle Organosiloxan-haltige Zusammensetzungen auf Alkoholbasis, Verfahren zu deren Herstellung sowie deren Verwendung |
| DE19649953A1 (de) | 1996-12-03 | 1998-06-04 | Huels Chemische Werke Ag | Fluoralkyl-funktionelle Organopolysiloxan-haltige Zusammensetzungen auf Wasserbasis, Verfahren zu deren Herstellung sowie deren Verwendung |
| DE19721699A1 (de) | 1997-05-23 | 1998-11-26 | Huels Silicone Gmbh | Aminosiliconöl-Microemulsionen |
| TW436500B (en) | 1997-06-17 | 2001-05-28 | Huels Chemische Werke Ag | N-[ω-(methyl),ω-(silyl)]alkyl-N-organocarboxamides, oligomeric and polycondensed Si-containing compounds thereof, processes for their preparation, and their use |
| DE19802069A1 (de) | 1998-01-21 | 1999-07-22 | Huels Silicone Gmbh | Aminofunktionelle Polyorganosiloxane, deren Herstellung und Verwendung |
| DE19818924A1 (de) | 1998-04-28 | 1999-11-04 | Degussa | Oberflächenmodifizierte Füllstoffe, Verfahren zu deren Herstellung sowie deren Verwendung |
| DE19818923A1 (de) | 1998-04-28 | 1999-11-04 | Degussa | Stabile Zusammensetzungen wasserlöslicher, Amino- und Alkenyl-funktioneller Organosiloxane, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE19823390A1 (de) | 1998-05-26 | 1999-12-16 | Degussa | Oligomerisiertes Organopolysiloxan-Cokondensat, dessen Herstellung und dessen Verwendung |
| DE19830128A1 (de) | 1998-07-06 | 2000-02-10 | Degussa | Oberflächenmodifizierte Flammschutzmittel, Verfahren zu deren Herstellung sowie deren Verwendung |
| DE19848351A1 (de) * | 1998-10-21 | 2000-04-27 | Degussa | Vernetzbare Polymere, Verfahren zu deren Herstellung und Formkörper aus vernetzten Polymeren |
| DE19904132C2 (de) | 1999-02-03 | 2002-11-28 | Degussa | Zusammensetzung fluororganofunktioneller Silane und Siloxane, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE19908636A1 (de) | 1999-02-27 | 2000-08-31 | Degussa | Wasserbasierende Zusammensetzung aminofunktioneller Siliciumverbindungen |
| DE19955047C2 (de) | 1999-11-15 | 2003-07-03 | Degussa | Triamino- und fluoralkylfunktionelle Organosiloxane |
| TW468241B (en) * | 2000-11-14 | 2001-12-11 | United Microelectronics Corp | Method to improve adhesion of dielectric material of semiconductor |
| JP3656545B2 (ja) | 2000-11-17 | 2005-06-08 | 日立電線株式会社 | シラン架橋ポリオレフィン成型物 |
| DE10159952A1 (de) * | 2001-12-06 | 2003-06-18 | Degussa | Verwendung flüssiger oder auf Trägermaterial aufgebrachter ungestättigter Organosilan/-mischungen zur Herstellung von feuchtigkeitsvernetzten und gefüllten Kabelcompounds |
| DE10240756A1 (de) * | 2002-08-30 | 2004-03-11 | Degussa Ag | Alkoxysiloxanhaltiges Trockenmittel für vernetzbare Polymermassen |
| JP2007045980A (ja) | 2005-08-11 | 2007-02-22 | Tosoh Corp | ポリウレタン樹脂製造用触媒組成物及びポリウレタン樹脂の製造方法 |
-
2008
- 2008-09-09 DE DE102008041920A patent/DE102008041920A1/de not_active Withdrawn
-
2009
- 2009-07-09 EP EP09780357A patent/EP2331622A1/de not_active Withdrawn
- 2009-07-09 JP JP2011526432A patent/JP2012502151A/ja not_active Withdrawn
- 2009-07-09 US US13/062,225 patent/US20110282024A1/en not_active Abandoned
- 2009-07-09 WO PCT/EP2009/058723 patent/WO2010028877A1/de active Application Filing
- 2009-07-09 CN CN2009801352081A patent/CN102149759A/zh active Pending
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