DE3339981C2 - - Google Patents
Info
- Publication number
- DE3339981C2 DE3339981C2 DE3339981A DE3339981A DE3339981C2 DE 3339981 C2 DE3339981 C2 DE 3339981C2 DE 3339981 A DE3339981 A DE 3339981A DE 3339981 A DE3339981 A DE 3339981A DE 3339981 C2 DE3339981 C2 DE 3339981C2
- Authority
- DE
- Germany
- Prior art keywords
- polyamide
- silane
- melt
- groups
- formula
- 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.)
- Expired
Links
- 229920002647 polyamide Polymers 0.000 claims description 78
- 239000004952 Polyamide Substances 0.000 claims description 77
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 52
- 229910000077 silane Inorganic materials 0.000 claims description 52
- 238000000034 method Methods 0.000 claims description 35
- 238000006243 chemical reaction Methods 0.000 claims description 16
- 125000003277 amino group Chemical group 0.000 claims description 15
- 239000000155 melt Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 230000008569 process Effects 0.000 claims description 12
- 238000006460 hydrolysis reaction Methods 0.000 claims description 11
- 238000002844 melting Methods 0.000 claims description 11
- 239000008187 granular material Substances 0.000 claims description 10
- 230000007062 hydrolysis Effects 0.000 claims description 10
- 230000008018 melting Effects 0.000 claims description 9
- 125000001931 aliphatic group Chemical group 0.000 claims description 7
- 125000000524 functional group Chemical group 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 3
- 229920006020 amorphous polyamide Polymers 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 125000004018 acid anhydride group Chemical group 0.000 claims description 2
- 125000003368 amide group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000012298 atmosphere Substances 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 claims description 2
- 239000012948 isocyanate Substances 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 230000007717 exclusion Effects 0.000 claims 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 1
- 108010055615 Zein Proteins 0.000 claims 1
- 229920002494 Zein Polymers 0.000 claims 1
- 239000012876 carrier material Substances 0.000 claims 1
- 150000002513 isocyanates Chemical class 0.000 claims 1
- 238000004898 kneading Methods 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 238000004132 cross linking Methods 0.000 description 12
- 229920001169 thermoplastic Polymers 0.000 description 11
- 239000004416 thermosoftening plastic Substances 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 10
- 229920000098 polyolefin Polymers 0.000 description 8
- 239000000843 powder Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- -1 Poly ethylene Polymers 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 229920002292 Nylon 6 Polymers 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 229920000570 polyether Polymers 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 230000006855 networking Effects 0.000 description 4
- 150000004756 silanes Chemical class 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 229910002808 Si–O–Si Inorganic materials 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 235000019241 carbon black Nutrition 0.000 description 2
- 238000010382 chemical cross-linking Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000004035 construction material Substances 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- SYECJBOWSGTPLU-UHFFFAOYSA-N hexane-1,1-diamine Chemical compound CCCCCC(N)N SYECJBOWSGTPLU-UHFFFAOYSA-N 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- BUZRAOJSFRKWPD-UHFFFAOYSA-N isocyanatosilane Chemical compound [SiH3]N=C=O BUZRAOJSFRKWPD-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000013112 stability test Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 230000035882 stress Effects 0.000 description 2
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical compound [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 2
- 230000000007 visual effect Effects 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
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 description 1
- 239000004953 Aliphatic polyamide Substances 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000237858 Gastropoda Species 0.000 description 1
- 239000004609 Impact Modifier Substances 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910008051 Si-OH Inorganic materials 0.000 description 1
- 229910006358 Si—OH Inorganic materials 0.000 description 1
- 229910009257 Y—Si Inorganic materials 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 229920003231 aliphatic polyamide Polymers 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 238000010640 amide synthesis reaction Methods 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229920006018 co-polyamide Polymers 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920006017 homo-polyamide Polymers 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 238000002789 length control Methods 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229940100630 metacresol Drugs 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- ZETYUTMSJWMKNQ-UHFFFAOYSA-N n,n',n'-trimethylhexane-1,6-diamine Chemical compound CNCCCCCCN(C)C ZETYUTMSJWMKNQ-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- 125000005646 oximino group Chemical group 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229920006114 semi-crystalline semi-aromatic polyamide Polymers 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000009718 spray deposition Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000011191 terminal modification Methods 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/48—Polymers modified by chemical after-treatment
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Polyamides (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH6444/82A CH660744A5 (de) | 1982-11-05 | 1982-11-05 | Verfahren zur herstellung hochviskoser bzw. thermisch formstabiler, mindestens teilvernetzter polyamide. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE3339981A1 DE3339981A1 (de) | 1984-05-17 |
| DE3339981C2 true DE3339981C2 (en, 2012) | 1989-01-19 |
Family
ID=4309732
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19833339981 Granted DE3339981A1 (de) | 1982-11-05 | 1983-11-04 | Verfahren zur herstellung hochviskoser bzw. thermisch formstabiler, mindestens teilvernetzter polyamide |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4647630A (en, 2012) |
| JP (1) | JPS59117536A (en, 2012) |
| AT (1) | AT384815B (en, 2012) |
| CH (1) | CH660744A5 (en, 2012) |
| DE (1) | DE3339981A1 (en, 2012) |
| FR (1) | FR2535729B1 (en, 2012) |
| GB (1) | GB2131037B (en, 2012) |
| IT (1) | IT1169341B (en, 2012) |
| NL (1) | NL189860C (en, 2012) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1992007020A1 (de) * | 1990-10-17 | 1992-04-30 | Henkel Kommanditgesellschaft Auf Aktien | Feuchtigkeitshärtbare polyamide |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4783511A (en) * | 1984-10-29 | 1988-11-08 | Ems-Inventa Ag | Process for preparing moulded bodies from modified thermoplastic polyamides |
| US5061746A (en) * | 1984-11-07 | 1991-10-29 | General Electric Company | Silane derivatives which improve properties of PPE-polyamide compositions |
| DE3545032C1 (de) * | 1985-12-19 | 1990-01-25 | Inventa Ag | Verfahren zur Herstellung von Formkoerpern aus thermoplastischen Polyamiden |
| DE3714763A1 (de) * | 1987-05-04 | 1988-11-24 | Henkel Kgaa | Feuchtigkeitsvernetzende schmelzkleber |
| US5032635A (en) * | 1988-03-18 | 1991-07-16 | General Electric Company | Silane derivatives which improve properties of pre-polyamide compositions |
| US4871788A (en) * | 1988-06-03 | 1989-10-03 | Dow Corning Corporation | Inomeric coupling agents based on amic acid-functional silanes |
| DE58900397D1 (de) * | 1988-06-07 | 1991-11-28 | Inventa Ag | Verfahren zur herstellung von vernetzten polyamidformkoerpern. |
| DE3917926A1 (de) * | 1988-06-07 | 1989-12-14 | Inventa Ag | Verfahren zur herstellung von vernetzten polyamidformkoerpern |
| DE3840220A1 (de) | 1988-11-29 | 1990-05-31 | Henkel Kgaa | Verfahren zur herstellung und applikation von unter feuchtigkeitseinwirkung nachvernetzenden schmelzkleber- und/oder dichtmassen |
| AT390069B (de) * | 1988-12-01 | 1990-03-12 | Egger Karl | Verfahren zur herstellung von fuer wasserfuehrende leitungen, insbesondere brauchbzw. heisswasserleitungen, bestimmten rohren oder formstuecken |
| US5112919A (en) * | 1989-10-30 | 1992-05-12 | Union Carbide Chemicals & Plastics Technology Corporation | Solid feeding of silane crosslinking agents into extruder |
| US5519109A (en) * | 1990-10-17 | 1996-05-21 | Henkel Kommanditgesellschaft Auf Aktien | Moisture-curing polyamides |
| JP2722915B2 (ja) * | 1992-01-17 | 1998-03-09 | 信越化学工業株式会社 | 硬化性樹脂及びその製造方法並びに電子部品用保護膜 |
| US5919441A (en) * | 1996-04-01 | 1999-07-06 | Colgate-Palmolive Company | Cosmetic composition containing thickening agent of siloxane polymer with hydrogen-bonding groups |
| US5874069A (en) * | 1997-01-24 | 1999-02-23 | Colgate-Palmolive Company | Cosmetic composition containing silicon-modified amides as thickening agents and method of forming same |
| US6037421A (en) * | 1997-09-30 | 2000-03-14 | Solutia Inc. | Functionalized polymers |
| US6946174B1 (en) * | 2000-10-12 | 2005-09-20 | Boston Scientific Scimed, Inc. | Moisture curable balloon materials |
| US8114515B2 (en) * | 2007-02-05 | 2012-02-14 | Sabic Innovative Plastics Ip B.V. | Crosslinked polyester compositions, method of manufacture, and uses thereof |
| US9771498B2 (en) * | 2009-11-20 | 2017-09-26 | Henkel IP & Holding GmbH | Moisture curable polyamides and methods for using the same |
| CN104804424B (zh) * | 2015-05-12 | 2017-02-01 | 华东理工大学 | 用于尼龙/玻璃纤维增强复合材料的界面增容剂及其制备方法 |
| FR3061182B1 (fr) | 2016-12-22 | 2019-05-31 | Setup Performance | Poudre de particules spheriques de polyamide reticulable, procede de preparation et utilisation avec la technique de frittage par laser selectif |
| EP3559095B1 (de) | 2016-12-22 | 2021-08-04 | Covestro Deutschland AG | Kunststofffolien für id-dokumente mit verbesserter lasergravierbarkeit und verbesserter chemikalienbeständigkeit |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3341501A (en) * | 1963-05-31 | 1967-09-12 | Monsanto Co | Polyamides containing silane end groups |
| GB1127625A (en) * | 1964-09-28 | 1968-09-18 | Johnson & Johnson | Method of cross-linking polymers |
| US3637550A (en) * | 1970-01-23 | 1972-01-25 | Du Pont | Silanated polyamide adhesive and its preparation |
| JPS4847929A (en, 2012) * | 1971-10-15 | 1973-07-07 | ||
| JPS4910158A (en, 2012) * | 1972-05-29 | 1974-01-29 | ||
| US3948835A (en) * | 1973-06-07 | 1976-04-06 | Ciba-Geigy Corporation | Silicon-modified prepolymers |
| JPS5223198A (en) * | 1975-08-15 | 1977-02-21 | Hitachi Ltd | Preparation of aromatic polyether amide resin |
| NZ190052A (en) * | 1978-03-31 | 1980-11-14 | Union Carbide Corp | Water-curable silane-modified alkylene alkylacrylate copolymers |
| US4319007A (en) * | 1980-03-10 | 1982-03-09 | Allied Corporation | High melt strength polycaprolactam compositions |
| JPS5740528A (en) * | 1980-08-25 | 1982-03-06 | Teijin Ltd | Aromatic polyamide formed article |
| EP0046954A3 (en) * | 1980-08-25 | 1982-03-24 | Teijin Limited | Shaped article of aromatic polyamide |
| US4429082A (en) * | 1982-05-10 | 1984-01-31 | Ppg Industries, Inc. | Film-forming resins containing alkoxy silane groups |
-
1982
- 1982-11-05 CH CH6444/82A patent/CH660744A5/de not_active IP Right Cessation
-
1983
- 1983-11-03 GB GB08329336A patent/GB2131037B/en not_active Expired
- 1983-11-03 FR FR8317490A patent/FR2535729B1/fr not_active Expired
- 1983-11-04 NL NLAANVRAGE8303811,A patent/NL189860C/xx not_active IP Right Cessation
- 1983-11-04 DE DE19833339981 patent/DE3339981A1/de active Granted
- 1983-11-04 IT IT49274/83A patent/IT1169341B/it active
- 1983-11-04 AT AT0389983A patent/AT384815B/de not_active IP Right Cessation
- 1983-11-04 JP JP58206044A patent/JPS59117536A/ja active Granted
- 1983-11-07 US US06/549,574 patent/US4647630A/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1992007020A1 (de) * | 1990-10-17 | 1992-04-30 | Henkel Kommanditgesellschaft Auf Aktien | Feuchtigkeitshärtbare polyamide |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59117536A (ja) | 1984-07-06 |
| AT384815B (de) | 1988-01-11 |
| CH660744A5 (de) | 1987-06-15 |
| GB8329336D0 (en) | 1983-12-07 |
| GB2131037B (en) | 1986-01-29 |
| FR2535729A1 (fr) | 1984-05-11 |
| NL8303811A (nl) | 1984-06-01 |
| NL189860C (nl) | 1993-08-16 |
| IT1169341B (it) | 1987-05-27 |
| JPH0240249B2 (en, 2012) | 1990-09-11 |
| DE3339981A1 (de) | 1984-05-17 |
| US4647630A (en) | 1987-03-03 |
| ATA389983A (de) | 1987-06-15 |
| IT8349274A0 (it) | 1983-11-04 |
| FR2535729B1 (fr) | 1986-05-23 |
| GB2131037A (en) | 1984-06-13 |
| NL189860B (nl) | 1993-03-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OP8 | Request for examination as to paragraph 44 patent law | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |