JP2008542416A - シラン修飾尿素誘導体、その製造方法及びレオロジー補助剤としての利用 - Google Patents
シラン修飾尿素誘導体、その製造方法及びレオロジー補助剤としての利用 Download PDFInfo
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- JP2008542416A JP2008542416A JP2008515126A JP2008515126A JP2008542416A JP 2008542416 A JP2008542416 A JP 2008542416A JP 2008515126 A JP2008515126 A JP 2008515126A JP 2008515126 A JP2008515126 A JP 2008515126A JP 2008542416 A JP2008542416 A JP 2008542416A
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- silane
- modified urea
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- 150000003672 ureas Chemical class 0.000 title claims abstract description 35
- 238000000518 rheometry Methods 0.000 title claims abstract description 8
- 238000004519 manufacturing process Methods 0.000 title description 2
- 239000013008 thixotropic agent Substances 0.000 claims abstract description 16
- 229910000077 silane Inorganic materials 0.000 claims abstract description 14
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000005442 diisocyanate group Chemical group 0.000 claims abstract description 9
- 238000006243 chemical reaction Methods 0.000 claims abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 25
- 239000011230 binding agent Substances 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 17
- 229920000642 polymer Polymers 0.000 claims description 16
- -1 silane compound Chemical class 0.000 claims description 15
- 239000012876 carrier material Substances 0.000 claims description 14
- 239000000654 additive Substances 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 239000012024 dehydrating agents Substances 0.000 claims description 8
- 239000000203 mixture Chemical class 0.000 claims description 8
- 229920005862 polyol Polymers 0.000 claims description 7
- 150000003077 polyols Chemical class 0.000 claims description 7
- 230000000996 additive effect Effects 0.000 claims description 6
- 239000000945 filler Substances 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 5
- 239000004014 plasticizer Substances 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- 229920001296 polysiloxane Polymers 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000000732 arylene group Chemical group 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 239000004814 polyurethane Substances 0.000 claims description 3
- 229920002635 polyurethane Polymers 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- 239000002318 adhesion promoter Substances 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 150000001343 alkyl silanes Chemical class 0.000 claims description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
- 150000001555 benzenes Chemical class 0.000 claims description 2
- 239000002274 desiccant Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000005395 methacrylic acid group Chemical group 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000005077 polysulfide Substances 0.000 claims description 2
- 229920001021 polysulfide Polymers 0.000 claims description 2
- 150000008117 polysulfides Polymers 0.000 claims description 2
- 150000004760 silicates Chemical class 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical class [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 claims description 2
- 239000010457 zeolite Substances 0.000 claims description 2
- 125000005498 phthalate group Chemical class 0.000 claims 1
- 239000000326 ultraviolet stabilizing agent Substances 0.000 claims 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract description 5
- TXDNPSYEJHXKMK-UHFFFAOYSA-N sulfanylsilane Chemical compound S[SiH3] TXDNPSYEJHXKMK-UHFFFAOYSA-N 0.000 abstract description 4
- 239000011248 coating agent Substances 0.000 abstract description 3
- 238000004132 cross linking Methods 0.000 abstract description 3
- 239000003973 paint Substances 0.000 abstract description 3
- 239000013466 adhesive and sealant Substances 0.000 abstract description 2
- 239000004922 lacquer Substances 0.000 abstract 1
- 230000008092 positive effect Effects 0.000 abstract 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 abstract 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 238000002156 mixing Methods 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 239000000565 sealant Substances 0.000 description 4
- 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 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 150000004756 silanes Chemical class 0.000 description 3
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 2
- UWSMKYBKUPAEJQ-UHFFFAOYSA-N 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O UWSMKYBKUPAEJQ-UHFFFAOYSA-N 0.000 description 2
- 102100036301 C-C chemokine receptor type 7 Human genes 0.000 description 2
- 101000716065 Homo sapiens C-C chemokine receptor type 7 Proteins 0.000 description 2
- 238000004566 IR spectroscopy Methods 0.000 description 2
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- YCZJVRCZIPDYHH-UHFFFAOYSA-N ditridecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCC YCZJVRCZIPDYHH-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 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 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 235000011837 pasties Nutrition 0.000 description 2
- 239000008029 phthalate plasticizer Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000012974 tin catalyst Substances 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ATOUXIOKEJWULN-UHFFFAOYSA-N 1,6-diisocyanato-2,2,4-trimethylhexane Chemical compound O=C=NCCC(C)CC(C)(C)CN=C=O ATOUXIOKEJWULN-UHFFFAOYSA-N 0.000 description 1
- HXLAEGYMDGUSBD-UHFFFAOYSA-N 3-[diethoxy(methyl)silyl]propan-1-amine Chemical compound CCO[Si](C)(OCC)CCCN HXLAEGYMDGUSBD-UHFFFAOYSA-N 0.000 description 1
- WJIOHMVWGVGWJW-UHFFFAOYSA-N 3-methyl-n-[4-[(3-methylpyrazole-1-carbonyl)amino]butyl]pyrazole-1-carboxamide Chemical compound N1=C(C)C=CN1C(=O)NCCCCNC(=O)N1N=C(C)C=C1 WJIOHMVWGVGWJW-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- NBFCDPUURVHFFF-UHFFFAOYSA-N 5-[dimethoxy(propyl)silyl]oxypentan-1-amine Chemical compound CCC[Si](OC)(OC)OCCCCCN NBFCDPUURVHFFF-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- IGGHSANJNRYSQB-UHFFFAOYSA-N OS([SiH3])(=O)=O Chemical class OS([SiH3])(=O)=O IGGHSANJNRYSQB-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004650 Polymer ST Substances 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 150000001278 adipic acid derivatives Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000003225 biodiesel Substances 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 150000002118 epoxides Chemical group 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- BUZRAOJSFRKWPD-UHFFFAOYSA-N isocyanatosilane Chemical class [SiH3]N=C=O BUZRAOJSFRKWPD-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- FRDNYWXDODPUJV-UHFFFAOYSA-N n-ethyl-2-methyl-3-trimethoxysilylpropan-1-amine Chemical compound CCNCC(C)C[Si](OC)(OC)OC FRDNYWXDODPUJV-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000000191 radiation effect Effects 0.000 description 1
- 150000003329 sebacic acid derivatives Chemical class 0.000 description 1
- 125000005372 silanol group Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000004354 sulfur functional group Chemical group 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/544—Silicon-containing compounds containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/288—Compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/289—Compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
- C08G18/758—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing two or more cycloaliphatic rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/541—Silicon-containing compounds containing oxygen
- C08K5/5415—Silicon-containing compounds containing oxygen containing at least one Si—O bond
- C08K5/5419—Silicon-containing compounds containing oxygen containing at least one Si—O bond containing at least one Si—C bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/548—Silicon-containing compounds containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polyurethanes Or Polyureas (AREA)
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
【解決手段】本発明のシラン修飾尿素誘導体は、特にレオロジー補助剤、好ましくはシラン架橋系用のチキソトロピック剤、特に1液型と2液型接着剤やシーラント、塗料、ラッカーやコーティング剤に適しており、実質的に粘度を増やさず、退色せず、反応性であり、機械的性質にプラスの影響を及ぼす。
【選択図】なし
Description
最初に60gのフタル酸エステル系可塑剤(Jayflex DIUP)と、13.12gのジイソシアネート(Vestanat H12MDI、MG 262.35)とをあわせて容器に入れる。次に、22.14gのアミノシラン(Dynasylan AMEO、重量平均分子量221)を、十分に混合しながら、30分間以上かけて少しずつ添加する。温度は50℃を超えないようにする。無色、乳状、無臭、高粘性のペーストが得られる。ASTM D 1638に準拠した滴定法と赤外分光法の結果から、残存イソシアネート含量はゼロである。最後に、0.5重量%の脱水剤(Dynasylan VTMO)を加える。
最初に60gのシリル化ポリウレタンプレポリマー(ハンセ−ケミ製Polymer ST−67)と、6.55gのジイソシアネート(Vestanat H12MDI)と13.05gのフタル酸エステル系可塑剤(Jayflex DIUP)とをあわせて混合容器に入れる。次に、8.94gのアミノシラン(Dynasylan AMMO、分子量179)を、十分に混合及び攪拌しながら15分間以上かけて少しずつ添加する。ASTM D 1638に準拠した滴定法と赤外分光法の結果から、残存イソシアネート含量はゼロである。その後すぐに、このようにして得られた結合剤を、シーラントを生成するために充填剤及び追加的な添加剤を用いて調合する。
モルテニ ラボマックス(Molteni Labmax)実験室用ミキサーで調合を実施した。調合済シーラントの流動挙動は、材料試験装置 タイプ ズウィック(Zwick) Z2.5/TN 1Sを用いる手法によって、23℃での3mmノズル使用時の吐出力として測定した。機械的特性は打抜き標準試料を用いて測定した。
本発明のチキソトロピック剤 200g
シリル化結合剤 ST−67、ハンセ (Hanse) 200g
チョーク BLR2充填剤、オムヤ(Omya) 350g
フタル酸エステル系可塑剤 DIUP、エクソン(Exxon) 50g
チヌビン(Tinuvin)327、紫外線吸収剤、チバ(Ciba) 2g
スズ触媒 DBTL、ローム+ハース(Rohm+Haas) 4g
ダインシラン(Dynsylan)VTMO脱水剤、デグサ(Degussa) 6g
吐出力(調製時) 720N
吐出力(60℃で一週間後) 770N
皮膜形成時間 80分
伸張強度 2.9MPa
品質保持期間(60℃で4週間) 満足
シリル化結合剤ST−67、ハンセ(Hanse)中の本発明のチキソトロピック剤 400g
チョーク BLR2充填剤、オムヤ(Omya) 350g
フタル酸エステル系可塑剤 DIUP、エクソン(Exxon) 50g
チヌビン(Tinuvin)327、紫外線吸収剤、チバ(Ciba) 2g
スズ触媒 DBTL、ローム+ハース(Rohm+Haas) 4g
ダインシラン(Dynsylan)VTMO脱水剤、デグサ(Degussa) 6g
吐出力(調製時) 510N
吐出力(60℃で一週間後) 550N
皮膜形成時間 90分
伸張強度 2.3MPa
品質保持期間(60℃で4週間) 満足
Claims (19)
- 一般式(I)のシラン修飾尿素誘導体
- nは0〜2であり、xは0〜1である、請求項1に記載のシラン修飾尿素誘導体。
- R3は、炭素数1〜4のアルキル基又はフェニル基である、請求項1又は2に記載のシラン修飾尿素誘導体。
- 前記ジイソシアネートと前記シラン化合物との反応がキャリア物質と任意に脱水剤存在下で行われる、請求項1〜8のいずれか1項に記載の方法。
- 非反応性キャリア物質が、例えばシリコーン類又はポリオール類等の長鎖ポリマー類、エステル類、アルキル化ベンゼン類、フタル酸エステル類、脂肪族炭化水素、芳香族炭化水素又はこれらの混合物から成る群から選択される、請求項9に記載の方法。
- ポリエーテル類、ポリウレタン類、ポリスルフィド類、シリコーン類、アクリル酸エステル類、メタクリル酸エステル類、又はこれらの物質の混合物を基本とするシリル化ポリマー類が、反応性キャリア物質として使用される、請求項9に記載の方法。
- ビニルシラン類、CaO、ゼオライト類、ケイ酸エステル類、アルキルシラン類及びこれらの混合物が脱水剤として使用される、請求項9〜11のいずれか1項に記載の方法。
- 前記脱水剤の濃度が、キャリア物質及び尿素誘導体の総重量に基づいて0.01〜40重量%に、好ましくは0.1〜10重量%に、特に好ましくは0.2〜5重量%で存在する、請求項9〜12のいずれか1項に記載の方法。
- 前記キャリア物質中の前記シラン修飾尿素誘導体の濃度が5〜90重量%、特に10〜60重量%、特に好ましくは15重量%〜50重量%である、請求項9〜13のいずれか1項に記載の方法。
- 前記シラン修飾尿素誘導体が、結合剤の存在下で調製される、請求項4〜14のいずれか1項に記載の方法。
- 請求項1〜3のいずれか1項に記載のシラン修飾尿素誘導体のレオロジー補助剤、特に1液型又は2液型硬化性高分子系用のチキソトロピック剤としての使用。
- 前記シラン修飾尿素誘導体が結合剤中に、0.1〜80重量%、好ましくは2〜50重量%で、特に好ましくは5〜30重量%の濃度で存在する、請求項16に記載の使用。
- 前記シラン修飾尿素誘導体が結合剤中に存在する、請求項16又は17に記載の使用。
- 前記シラン修飾尿素誘導体が結合剤中に、充填剤、可塑剤、接着促進剤、乾燥剤、溶剤、触媒及び紫外線安定剤からなる添加剤と共に、ペースト状の添加剤として結合剤に添加される、請求項16〜18のいずれか1項に記載の使用。
Applications Claiming Priority (2)
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DE102005026085A DE102005026085A1 (de) | 2005-06-07 | 2005-06-07 | Silan-modifizierte Harnstoff-Derivate, Verfahren zu ihrer Herstellung und deren Verwendung als Rheologiehilfsmittel |
PCT/EP2006/005385 WO2006131314A1 (de) | 2005-06-07 | 2006-06-06 | Silan-modifizierte harnstoff-derivate, verfahren zu ihrer herstellung und deren verwendung als rheologiehilfsmittel |
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JP2008542416A true JP2008542416A (ja) | 2008-11-27 |
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JP2008515126A Pending JP2008542416A (ja) | 2005-06-07 | 2006-06-06 | シラン修飾尿素誘導体、その製造方法及びレオロジー補助剤としての利用 |
Country Status (12)
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US (1) | US8138277B2 (ja) |
EP (1) | EP1888665B1 (ja) |
JP (1) | JP2008542416A (ja) |
KR (1) | KR20080026594A (ja) |
CN (1) | CN101193930A (ja) |
AT (1) | ATE478905T1 (ja) |
AU (1) | AU2006256946B2 (ja) |
BR (1) | BRPI0611246A2 (ja) |
CA (1) | CA2610784A1 (ja) |
DE (2) | DE102005026085A1 (ja) |
ES (1) | ES2351227T3 (ja) |
WO (1) | WO2006131314A1 (ja) |
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JP7547379B2 (ja) | 2019-05-06 | 2024-09-09 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツング | シラン系コーティング組成物 |
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DE102008030304A1 (de) | 2008-06-25 | 2009-12-31 | Basf Coatings Ag | Verwendung teilsilanisierter Verbindungen auf Polyisocyanatbasis als Vernetzungsmittel in Beschichtungszusammensetzungen und Beschichtungszusammensetzung enthaltend die Verbindungen |
DE102008038488A1 (de) * | 2008-08-20 | 2010-02-25 | Henkel Ag & Co. Kgaa | Feuchtigkeitshärtende wasserfeste Beschichtung |
DE102008047362A1 (de) | 2008-09-15 | 2010-04-15 | Henkel Ag & Co. Kgaa | Zusammensetzung zur Hautaufhellung |
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US8900668B2 (en) * | 2011-04-11 | 2014-12-02 | Eastern Michigan University | Corrosion-resistant coatings and methods using polyureasil precursors |
EP2617778B1 (en) * | 2012-01-19 | 2021-03-17 | Jotun A/S | Fouling release coatings |
WO2014158535A1 (en) * | 2013-03-14 | 2014-10-02 | The Government Of The United States Of America, As Represented By The Secretary Of The Navy | Single-component moisture-curable coatings based on n-substituted urea polymers with extended chains and terminal alkoxysilanes |
DE102014106841A1 (de) | 2014-05-15 | 2015-12-03 | Barbara Röckinghausen | Beschichtungsmittel für Schuhe |
US9587143B2 (en) | 2014-10-22 | 2017-03-07 | The United States Of America, As Represented By The Secretary Of The Navy | Two-component siloxane-based coatings containing polymers with urea linkages and terminal alkoxysilanes |
JP6826362B2 (ja) * | 2015-06-30 | 2021-02-03 | リンテック株式会社 | 粘着シート |
EP3613786A1 (de) | 2018-08-21 | 2020-02-26 | Covestro Deutschland AG | Trocknungsmittel für feuchtigkeitshärtende zusammensetzungen |
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- 2006-06-06 CA CA002610784A patent/CA2610784A1/en not_active Abandoned
- 2006-06-06 JP JP2008515126A patent/JP2008542416A/ja active Pending
- 2006-06-06 DE DE502006007735T patent/DE502006007735D1/de active Active
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- 2006-06-06 BR BRPI0611246-3A patent/BRPI0611246A2/pt not_active IP Right Cessation
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013527867A (ja) * | 2010-04-21 | 2013-07-04 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツング | 改善された流れ傾向を有する被覆剤 |
JP7547379B2 (ja) | 2019-05-06 | 2024-09-09 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツング | シラン系コーティング組成物 |
Also Published As
Publication number | Publication date |
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KR20080026594A (ko) | 2008-03-25 |
US8138277B2 (en) | 2012-03-20 |
AU2006256946A1 (en) | 2006-12-14 |
EP1888665B1 (de) | 2010-08-25 |
CN101193930A (zh) | 2008-06-04 |
DE102005026085A1 (de) | 2006-12-14 |
ES2351227T3 (es) | 2011-02-01 |
CA2610784A1 (en) | 2006-12-14 |
US20080125529A1 (en) | 2008-05-29 |
AU2006256946B2 (en) | 2012-04-26 |
EP1888665A1 (de) | 2008-02-20 |
BRPI0611246A2 (pt) | 2010-08-24 |
DE502006007735D1 (de) | 2010-10-07 |
WO2006131314A1 (de) | 2006-12-14 |
ATE478905T1 (de) | 2010-09-15 |
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