ZA200307430B - Adhesive filled with surface-treated chalk and soot. - Google Patents
Adhesive filled with surface-treated chalk and soot. Download PDFInfo
- Publication number
- ZA200307430B ZA200307430B ZA200307430A ZA200307430A ZA200307430B ZA 200307430 B ZA200307430 B ZA 200307430B ZA 200307430 A ZA200307430 A ZA 200307430A ZA 200307430 A ZA200307430 A ZA 200307430A ZA 200307430 B ZA200307430 B ZA 200307430B
- Authority
- ZA
- South Africa
- Prior art keywords
- stands
- radical
- groups
- silane
- isocyanate
- Prior art date
Links
- 239000000853 adhesive Substances 0.000 title claims abstract description 58
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 58
- 239000004071 soot Substances 0.000 title claims description 27
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 61
- 229920000642 polymer Polymers 0.000 claims abstract description 37
- 239000000203 mixture Substances 0.000 claims abstract description 28
- 239000004814 polyurethane Substances 0.000 claims abstract description 28
- 238000004132 cross linking Methods 0.000 claims abstract description 26
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 25
- 229920005862 polyol Polymers 0.000 claims abstract description 25
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000000945 filler Substances 0.000 claims abstract description 20
- 150000003077 polyols Chemical class 0.000 claims abstract description 18
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 16
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000012948 isocyanate Substances 0.000 claims abstract description 14
- 229910000077 silane Inorganic materials 0.000 claims abstract description 14
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 13
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 11
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 9
- 239000002245 particle Substances 0.000 claims abstract description 9
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 6
- 239000000194 fatty acid Substances 0.000 claims abstract description 6
- 229930195729 fatty acid Natural products 0.000 claims abstract description 6
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 6
- 125000004185 ester group Chemical group 0.000 claims abstract description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims abstract 3
- 235000010216 calcium carbonate Nutrition 0.000 claims description 28
- 229960003563 calcium carbonate Drugs 0.000 claims description 23
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 229920001730 Moisture cure polyurethane Polymers 0.000 claims description 15
- 230000008030 elimination Effects 0.000 claims description 15
- 238000003379 elimination reaction Methods 0.000 claims description 15
- -1 dryers Substances 0.000 claims description 13
- 239000010419 fine particle Substances 0.000 claims description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 150000004756 silanes Chemical class 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 239000003054 catalyst Substances 0.000 claims description 7
- 125000005442 diisocyanate group Chemical group 0.000 claims description 7
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000000470 constituent Substances 0.000 claims description 4
- 239000004014 plasticizer Substances 0.000 claims description 4
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 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 description 3
- 239000000049 pigment Substances 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 3
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 claims description 2
- AGJCSCSSMFRMFQ-UHFFFAOYSA-N 1,4-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=C(C(C)(C)N=C=O)C=C1 AGJCSCSSMFRMFQ-UHFFFAOYSA-N 0.000 claims description 2
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 claims description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- 229920002121 Hydroxyl-terminated polybutadiene Polymers 0.000 claims description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 2
- 239000012963 UV stabilizer Substances 0.000 claims description 2
- 239000002318 adhesion promoter Substances 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- 239000000835 fiber Substances 0.000 claims description 2
- 239000012760 heat stabilizer Substances 0.000 claims description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 2
- 239000011256 inorganic filler Substances 0.000 claims description 2
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 150000002895 organic esters Chemical class 0.000 claims description 2
- 239000012766 organic filler Substances 0.000 claims description 2
- 229920001083 polybutene Polymers 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 239000002562 thickening agent Substances 0.000 claims description 2
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 claims description 2
- LFSYUSUFCBOHGU-UHFFFAOYSA-N 1-isocyanato-2-[(4-isocyanatophenyl)methyl]benzene Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=CC=C1N=C=O LFSYUSUFCBOHGU-UHFFFAOYSA-N 0.000 claims 1
- 150000002009 diols Chemical class 0.000 claims 1
- 229920002635 polyurethane Polymers 0.000 abstract description 24
- 238000002360 preparation method Methods 0.000 abstract description 9
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 abstract description 3
- 239000006229 carbon black Substances 0.000 abstract 4
- 239000011575 calcium Substances 0.000 abstract 2
- 239000004033 plastic Substances 0.000 abstract 2
- 229920003023 plastic Polymers 0.000 abstract 2
- 150000003254 radicals Chemical class 0.000 description 21
- 239000000306 component Substances 0.000 description 10
- 238000004026 adhesive bonding Methods 0.000 description 7
- 238000001125 extrusion Methods 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000013466 adhesive and sealant Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 239000012763 reinforcing filler Substances 0.000 description 5
- 238000009472 formulation Methods 0.000 description 4
- GVGLGOZIDCSQPN-PVHGPHFFSA-N Heroin Chemical compound O([C@H]1[C@H](C=C[C@H]23)OC(C)=O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4OC(C)=O GVGLGOZIDCSQPN-PVHGPHFFSA-N 0.000 description 3
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000000565 sealant Substances 0.000 description 3
- 239000012790 adhesive layer Substances 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 2
- 229910021485 fumed silica Inorganic materials 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000003707 silyl modified polymer Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- 239000004970 Chain extender Substances 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 235000010210 aluminium Nutrition 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- UOYUSRMQWUMMNJ-UHFFFAOYSA-N aminosilylbenzene Chemical compound N[SiH2]C1=CC=CC=C1 UOYUSRMQWUMMNJ-UHFFFAOYSA-N 0.000 description 1
- 229940009098 aspartate Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229940000425 combination drug Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- VSNLCLFPPHBFLV-LBPRGKRZSA-N diethyl (2s)-2-(3-trimethoxysilylpropylamino)butanedioate Chemical compound CCOC(=O)C[C@@H](C(=O)OCC)NCCC[Si](OC)(OC)OC VSNLCLFPPHBFLV-LBPRGKRZSA-N 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- ARYZCSRUUPFYMY-UHFFFAOYSA-N methoxysilane Chemical compound CO[SiH3] ARYZCSRUUPFYMY-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000004588 polyurethane sealant Substances 0.000 description 1
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 1
- 230000036647 reaction Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000012945 sealing adhesive Substances 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
-
- 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
-
- 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
- C08G2190/00—Compositions for sealing or packing joints
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01111158A EP1256595A1 (de) | 2001-05-10 | 2001-05-10 | Klebstoff, gefüllt mit oberflächenbehandelter Kreide und Russ |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200307430B true ZA200307430B (en) | 2003-12-05 |
Family
ID=8177359
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200307430A ZA200307430B (en) | 2001-05-10 | 2003-09-25 | Adhesive filled with surface-treated chalk and soot. |
Country Status (10)
Country | Link |
---|---|
US (3) | US20040127622A1 (ja) |
EP (2) | EP1256595A1 (ja) |
JP (2) | JP4546030B2 (ja) |
AT (1) | ATE462742T1 (ja) |
BR (1) | BR0209486B1 (ja) |
CA (1) | CA2446677A1 (ja) |
DE (1) | DE50214315D1 (ja) |
MX (1) | MXPA03010167A (ja) |
WO (1) | WO2002090411A1 (ja) |
ZA (1) | ZA200307430B (ja) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10351802A1 (de) * | 2003-11-06 | 2005-06-09 | Consortium für elektrochemische Industrie GmbH | alpha-Alkoxysilane sowie ihre Anwendung in alkoxysilanterminierten Prepolymeren |
US7718730B2 (en) * | 2003-12-19 | 2010-05-18 | Bayer Materialscience Llc | Two-component silylated polyurethane adhesive, sealant, and coating compositions |
EP1717254A1 (de) * | 2005-04-29 | 2006-11-02 | Sika Technology AG | Feuchtigkeitshärtende Zusammensetzung mit erhöhter Dehnbarkeit |
DE102005054008A1 (de) * | 2005-11-10 | 2007-05-16 | Henkel Kgaa | Silanvernetzender Kleb-, Dicht-oder Beschichtungsstoff und seine Verwendung |
DE102006006975A1 (de) * | 2006-02-14 | 2007-08-30 | Bostik Gmbh | Einkomponentiger, lösemittelfreier Kontaktklebstoff |
US8530573B2 (en) * | 2006-05-10 | 2013-09-10 | Designer Molecules, Inc. | Modified calcium carbonate-filled adhesive compositions and methods for use thereof |
EP1860167A1 (de) * | 2006-05-24 | 2007-11-28 | Sika Technology AG | Klebverbundkörper mit erhöhter Haftung |
DE102007011511A1 (de) | 2007-03-09 | 2008-09-11 | Henkel Ag & Co. Kgaa | Ein-Komponenten-Montageklebstoff mit hoher Anfangshaftung |
BRPI0817385A2 (pt) * | 2007-11-07 | 2015-03-31 | Dow Global Technologies Inc | Composição e método para ligar vidro ou um plástico revestido com camada resistente à abrasão a um substrato |
US8008419B2 (en) | 2008-08-13 | 2011-08-30 | Designer Molecules, Inc. | Siloxane monomers and methods for use thereof |
ATE509972T1 (de) | 2008-10-31 | 2011-06-15 | Sika Technology Ag | Organomethoxysilan enthaltende polyurethanzusammensetzung mit anisotropen materialeigenschaften |
DE102009057600A1 (de) * | 2009-12-09 | 2011-06-16 | Bayer Materialscience Ag | Polyurethan-Prepolymere |
JP5972910B2 (ja) | 2011-02-17 | 2016-08-17 | ダウ グローバル テクノロジーズ エルエルシー | カルシウムカーボネートを含有するアルコキシシラン含有ポリウレタン接着剤組成物 |
DE102011087603A1 (de) | 2011-12-01 | 2013-06-06 | Wacker Chemie Ag | Vernetzbare Massen auf Basis von organyloxysilanterminierten Polyurethanen |
DE102011087604A1 (de) | 2011-12-01 | 2013-06-06 | Wacker Chemie Ag | Vernetzbare Massen auf Basis von organyloxysilanterminierten Polyurethanen |
DE102012201734A1 (de) | 2012-02-06 | 2013-08-08 | Wacker Chemie Ag | Massen auf Basis von organyloxysilanterminierten Polymeren |
DE102016202196A1 (de) * | 2016-02-12 | 2017-08-17 | Wacker Chemie Ag | Vernetzbare Massen auf Basis von organyloxysilanterminierten Polymeren |
EP3416809A1 (de) * | 2016-02-19 | 2018-12-26 | Basf Se | Kaolin zur mechanischen verstärkung von polymerem lasersinter-pulver |
US10563662B2 (en) | 2016-11-04 | 2020-02-18 | General Electric Company | Metal surface preparation |
CN109485238A (zh) * | 2018-10-16 | 2019-03-19 | 惠州大唐伟业电子有限公司 | 一种手机盖板的加工工艺 |
NL2022496B1 (en) | 2019-02-01 | 2020-08-19 | Strongbond B V | High strength and elongation, label free, silyl modified polymer adhesive composition |
EP3882289A1 (de) | 2020-03-17 | 2021-09-22 | Sika Technology Ag | Zusammensetzungen auf basis von silan-terminierten polymeren und acetylen-russ |
CN113896951B (zh) * | 2021-11-15 | 2023-02-14 | 南京曙光精细化工有限公司 | 一种以炭黑为载体的含硫硅烷偶联剂的制备方法 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1207594A (en) | 1967-03-16 | 1970-10-07 | Union Carbide Corp | One component room temperature vulcanizable silicon terminated polymers |
US4222925A (en) * | 1978-08-02 | 1980-09-16 | Inmont Corporation | Vulcanizable silicon terminated polyurethane polymer compositions having improved cure speed |
US5703146A (en) | 1991-09-12 | 1997-12-30 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Curable composition containing an oxypropylene polymer and calcium carbonate which has been surface treated with a fatty acid |
DE4237468A1 (de) | 1992-11-06 | 1994-05-11 | Bayer Ag | Alkoxysilan- und Aminogruppen aufweisende Verbindungen |
JP2594024B2 (ja) | 1994-04-08 | 1997-03-26 | オーエスアイ・スペシヤルテイーズ・インコーポレーテツド | アリールアミノシラン末端キヤツプドウレタンのシーラント |
US6136446A (en) * | 1995-05-19 | 2000-10-24 | Prc-Desoto International, Inc. | Desiccant matrix for an insulating glass unit |
KR100445015B1 (ko) * | 1995-08-01 | 2004-11-06 | 요코하마 고무 가부시키가이샤 | 접착성조성물및이의제조방법 |
DE19619538A1 (de) * | 1996-05-15 | 1997-11-20 | Bayer Ag | Alkoxysilan- und Hydantoingruppen aufweisende Polyurethanprepolymere, ein Verfahren zu ihrer Herstellung sowie ihre Verwendung zur Herstellung von Dichtstoffen |
ES2297844T3 (es) | 1996-07-18 | 2008-05-01 | Bostik B.V. | Composicion de adhesivo. |
US6001946A (en) | 1996-09-23 | 1999-12-14 | Witco Corporation | Curable silane-encapped compositions having improved performances |
US5990257A (en) * | 1998-01-22 | 1999-11-23 | Witco Corporation | Process for producing prepolymers which cure to improved sealants, and products formed thereby |
EP1080126B1 (en) | 1998-04-27 | 2003-10-22 | Essex Specialty Products, Inc. | Method of bonding a window to a substrate using a silane functional adhesive composition |
US6121354A (en) * | 1998-11-19 | 2000-09-19 | Bostik, Inc. | High performance single-component sealant |
US6124387A (en) * | 1998-12-22 | 2000-09-26 | Adco Products, Inc. | Fast-cure silylated polymer adhesive |
DE19923300A1 (de) * | 1999-05-21 | 2000-11-23 | Bayer Ag | Phosphatstabilisierte, kondensationsvernetzende Polyurethanmassen, ein Verfahren zu ihrer Herstellung sowie ihre Verwendung |
JP2000351894A (ja) * | 1999-06-11 | 2000-12-19 | Yokohama Rubber Co Ltd:The | 一液湿気硬化型ウレタン組成物 |
US6197912B1 (en) * | 1999-08-20 | 2001-03-06 | Ck Witco Corporation | Silane endcapped moisture curable compositions |
US6498210B1 (en) * | 2000-07-13 | 2002-12-24 | Adco Products, Inc. | Silylated polyurethanes for adhesives and sealants with improved mechanical properties |
-
2001
- 2001-05-10 EP EP01111158A patent/EP1256595A1/de not_active Withdrawn
-
2002
- 2002-04-18 BR BRPI0209486-0A patent/BR0209486B1/pt not_active IP Right Cessation
- 2002-04-18 JP JP2002587485A patent/JP4546030B2/ja not_active Expired - Fee Related
- 2002-04-18 CA CA002446677A patent/CA2446677A1/en not_active Abandoned
- 2002-04-18 WO PCT/IB2002/001247 patent/WO2002090411A1/de active Application Filing
- 2002-04-18 AT AT02720361T patent/ATE462742T1/de not_active IP Right Cessation
- 2002-04-18 US US10/476,525 patent/US20040127622A1/en not_active Abandoned
- 2002-04-18 MX MXPA03010167A patent/MXPA03010167A/es not_active Application Discontinuation
- 2002-04-18 DE DE50214315T patent/DE50214315D1/de not_active Expired - Lifetime
- 2002-04-18 EP EP02720361A patent/EP1397406B1/de not_active Revoked
-
2003
- 2003-09-25 ZA ZA200307430A patent/ZA200307430B/en unknown
-
2006
- 2006-04-07 US US11/399,364 patent/US20060183846A1/en not_active Abandoned
-
2007
- 2007-11-30 US US11/948,836 patent/US7589134B2/en not_active Expired - Fee Related
-
2009
- 2009-11-02 JP JP2009252374A patent/JP2010024461A/ja not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
WO2002090411A1 (de) | 2002-11-14 |
JP4546030B2 (ja) | 2010-09-15 |
US20060183846A1 (en) | 2006-08-17 |
BR0209486B1 (pt) | 2011-09-06 |
EP1256595A1 (de) | 2002-11-13 |
US7589134B2 (en) | 2009-09-15 |
EP1397406A1 (de) | 2004-03-17 |
JP2010024461A (ja) | 2010-02-04 |
US20080255286A1 (en) | 2008-10-16 |
US20040127622A1 (en) | 2004-07-01 |
JP2005501928A (ja) | 2005-01-20 |
EP1397406B1 (de) | 2010-03-31 |
DE50214315D1 (de) | 2010-05-12 |
MXPA03010167A (es) | 2005-08-16 |
BR0209486A (pt) | 2004-07-06 |
ATE462742T1 (de) | 2010-04-15 |
CA2446677A1 (en) | 2002-11-14 |
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