GB1335933A - Curing of chloroprene polymers - Google Patents
Curing of chloroprene polymersInfo
- Publication number
- GB1335933A GB1335933A GB1562071*[A GB1562071A GB1335933A GB 1335933 A GB1335933 A GB 1335933A GB 1562071 A GB1562071 A GB 1562071A GB 1335933 A GB1335933 A GB 1335933A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amine
- curing
- propanol
- organic radical
- attached
- 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
- 229920000642 polymer Polymers 0.000 title abstract 5
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 title abstract 4
- 150000001412 amines Chemical class 0.000 abstract 5
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 abstract 2
- 229920001084 poly(chloroprene) Polymers 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 abstract 2
- JGVZJRHAZOBPMW-UHFFFAOYSA-N 1,3-bis(dimethylamino)propan-2-ol Chemical compound CN(C)CC(O)CN(C)C JGVZJRHAZOBPMW-UHFFFAOYSA-N 0.000 abstract 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 abstract 1
- QIJIUJYANDSEKG-UHFFFAOYSA-N 2,4,4-trimethylpentan-2-amine Chemical compound CC(C)(C)CC(C)(C)N QIJIUJYANDSEKG-UHFFFAOYSA-N 0.000 abstract 1
- XRIBIDPMFSLGFS-UHFFFAOYSA-N 2-(dimethylamino)-2-methylpropan-1-ol Chemical compound CN(C)C(C)(C)CO XRIBIDPMFSLGFS-UHFFFAOYSA-N 0.000 abstract 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 abstract 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 238000004132 cross linking Methods 0.000 abstract 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 abstract 1
- -1 hexadecyl radicals Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- WINHZLLDWRZWRT-SFQUDFHCSA-N n-[2-(diethylamino)ethyl]-5-[(e)-(5-fluoro-2-oxo-1h-indol-3-ylidene)methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide Chemical compound CCN(CC)CCNC(=O)C1=C(C)NC(\C=C\2C3=CC(F)=CC=C3NC/2=O)=C1C WINHZLLDWRZWRT-SFQUDFHCSA-N 0.000 abstract 1
- 235000006408 oxalic acid Nutrition 0.000 abstract 1
- WLCAJVVSNAVBSM-UHFFFAOYSA-N oxalic acid;piperidine Chemical compound C1CCNCC1.OC(=O)C(O)=O WLCAJVVSNAVBSM-UHFFFAOYSA-N 0.000 abstract 1
- 239000008281 solid sol Substances 0.000 abstract 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 abstract 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 abstract 1
- 239000011787 zinc oxide Substances 0.000 abstract 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4070670A | 1970-05-26 | 1970-05-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1335933A true GB1335933A (en) | 1973-10-31 |
Family
ID=21912475
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1562071*[A Expired GB1335933A (en) | 1970-05-26 | 1971-05-18 | Curing of chloroprene polymers |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3686156A (enExample) |
| JP (1) | JPS5030669B1 (enExample) |
| DE (1) | DE2125546A1 (enExample) |
| FR (1) | FR2093767A5 (enExample) |
| GB (1) | GB1335933A (enExample) |
| ZA (1) | ZA712048B (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3849372A (en) * | 1972-10-20 | 1974-11-19 | Du Pont | Viscosity-stable chloroprene sol polymer |
| US3926912A (en) * | 1973-02-10 | 1975-12-16 | Bayer Ag | Polymerizing chloroprene in the presence of xanthogen disulphides with functional groups |
| US4054731A (en) * | 1973-05-17 | 1977-10-18 | Denki Kagaku Kogyo Kabushiki Kaisha | Process for curing liquid chloroprene polymer containing xanthate active terminal groups using polyfunctional amines |
| CA1014295A (en) * | 1973-11-08 | 1977-07-19 | John R. Dunn | Amine modified remoldable rubbers |
| US3925340A (en) * | 1974-05-08 | 1975-12-09 | Du Pont | Preparation of sol chloroprene polymers |
| GB0407908D0 (en) * | 2004-04-07 | 2004-05-12 | Univ York | Ionic liquids |
| DE102008040135A1 (de) * | 2008-07-03 | 2010-01-07 | Leibniz-Institut Für Polymerforschung Dresden E.V. | Modifizierte Polychloropren-Materialien und Verfahren zu ihrer Herstellung |
| EP2417167B1 (en) * | 2009-04-10 | 2013-09-04 | Saudi Basic Industries Corporation (Sabic) | Process for the production of an ethylene polymer using a chromium containing catalyst |
| US20130018134A1 (en) | 2011-07-11 | 2013-01-17 | E I Du Pont De Nemours And Company | Polychloroprene compositions with improved adhesion properties |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2455697A (en) * | 1944-10-13 | 1948-12-07 | Goodrich Co B F | Vulcanization of neoprene |
| NL262295A (enExample) * | 1960-03-23 | 1964-05-25 | ||
| US3300433A (en) * | 1964-02-20 | 1967-01-24 | Du Pont | Xanthogen disulfide and amine preparation of polychloroprene |
| FR1497462A (fr) * | 1964-07-15 | 1967-10-06 | Interchem Corp | Procédé perfectionné de calfeutrage |
-
1970
- 1970-05-26 US US40706A patent/US3686156A/en not_active Expired - Lifetime
-
1971
- 1971-03-30 ZA ZA712048A patent/ZA712048B/xx unknown
- 1971-05-11 JP JP46030893A patent/JPS5030669B1/ja active Pending
- 1971-05-18 GB GB1562071*[A patent/GB1335933A/en not_active Expired
- 1971-05-22 DE DE19712125546 patent/DE2125546A1/de active Pending
- 1971-05-26 FR FR7119106A patent/FR2093767A5/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE2125546A1 (de) | 1971-12-02 |
| US3686156A (en) | 1972-08-22 |
| ZA712048B (en) | 1971-12-29 |
| JPS5030669B1 (enExample) | 1975-10-02 |
| FR2093767A5 (enExample) | 1972-01-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PE20 | Patent expired after termination of 20 years |