CA2123524A1 - Process for the production of polymer-bound rubber chemicals - Google Patents
Process for the production of polymer-bound rubber chemicalsInfo
- Publication number
- CA2123524A1 CA2123524A1 CA002123524A CA2123524A CA2123524A1 CA 2123524 A1 CA2123524 A1 CA 2123524A1 CA 002123524 A CA002123524 A CA 002123524A CA 2123524 A CA2123524 A CA 2123524A CA 2123524 A1 CA2123524 A1 CA 2123524A1
- Authority
- CA
- Canada
- Prior art keywords
- polymer
- rubber chemicals
- rubber
- production
- optionally
- 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.)
- Abandoned
Links
- 229920001971 elastomer Polymers 0.000 title claims abstract description 35
- 239000000126 substance Substances 0.000 title claims abstract description 30
- 229920000642 polymer Polymers 0.000 title claims abstract description 16
- 238000000034 method Methods 0.000 title claims abstract description 8
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 6
- 239000007788 liquid Substances 0.000 claims abstract description 9
- 239000000654 additive Substances 0.000 claims abstract description 4
- 239000008240 homogeneous mixture Substances 0.000 claims abstract description 4
- 239000007787 solid Substances 0.000 claims abstract description 3
- 239000011230 binding agent Substances 0.000 abstract description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- AFZSMODLJJCVPP-UHFFFAOYSA-N dibenzothiazol-2-yl disulfide Chemical compound C1=CC=C2SC(SSC=3SC4=CC=CC=C4N=3)=NC2=C1 AFZSMODLJJCVPP-UHFFFAOYSA-N 0.000 description 3
- -1 inter alia retarders Chemical class 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 238000004073 vulcanization Methods 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 2
- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical compound C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 2
- 229960002447 thiram Drugs 0.000 description 2
- 150000003626 triacylglycerols Chemical class 0.000 description 2
- OBMHSNXMHVKVSA-UHFFFAOYSA-L zinc;n-benzylcarbamodithioate Chemical compound [Zn+2].[S-]C(=S)NCC1=CC=CC=C1.[S-]C(=S)NCC1=CC=CC=C1 OBMHSNXMHVKVSA-UHFFFAOYSA-L 0.000 description 2
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000945 filler 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
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- FIMHASWLGDDANN-UHFFFAOYSA-M methyl sulfate;tributyl(methyl)azanium Chemical compound COS([O-])(=O)=O.CCCC[N+](C)(CCCC)CCCC FIMHASWLGDDANN-UHFFFAOYSA-M 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003566 thiocarboxylic acids Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229960001296 zinc oxide Drugs 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
- C08J3/226—Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- 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
- C08K9/00—Use of pretreated ingredients
- C08K9/08—Ingredients agglomerated by treatment with a binding agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2321/00—Characterised by the use of unspecified rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2491/00—Characterised by the use of oils, fats or waxes; Derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4316429A DE4316429A1 (de) | 1993-05-17 | 1993-05-17 | Verfahren zur Herstellung polymergebundener Kautschukchemikalienbinder |
| DEP4316429.3 | 1993-05-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2123524A1 true CA2123524A1 (en) | 1994-11-18 |
Family
ID=6488266
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002123524A Abandoned CA2123524A1 (en) | 1993-05-17 | 1994-05-13 | Process for the production of polymer-bound rubber chemicals |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5624988A (enExample) |
| EP (1) | EP0625543A1 (enExample) |
| JP (1) | JPH06329837A (enExample) |
| CN (1) | CN1096794A (enExample) |
| CA (1) | CA2123524A1 (enExample) |
| DE (1) | DE4316429A1 (enExample) |
| TW (1) | TW290572B (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19727848B4 (de) * | 1997-06-26 | 2005-09-29 | Schill & Seilacher (Gmbh & Co) | Kautschukadditivgranulat, ein Verfahren zu seiner Herstellung sowie seine Verwendung |
| DE10010072A1 (de) * | 2000-03-02 | 2001-09-06 | Rheinchemie Rheinau Gmbh | Biozid-Batche auf Basis vernetzter Öle, Verfahren zu ihrer Gerstellung und ihre Verwendung in thermoplastischen Formmassen |
| DE102007050728A1 (de) * | 2007-10-22 | 2009-04-23 | Sachtleben Chemie Gmbh | Additiv für Polymere und Verfahren zu dessen Herstellung |
| DE102008040138A1 (de) * | 2008-07-03 | 2010-01-07 | Rhein Chemie Rheinau Gmbh | Verfahren und Vorrichtung zur Herstellung einer vernetzbaren Kautschukmischung |
| EP2284217B1 (de) * | 2009-08-07 | 2011-12-07 | Rhein Chemie Rheinau GmbH | Vulkanisationsbeschleunigende Mischung |
| CN105793343B (zh) * | 2013-11-12 | 2018-05-22 | 罗宾逊兄弟有限公司 | 促进剂组合物和方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1865728A (en) * | 1931-05-28 | 1932-07-05 | Rubber Service Lab Co | Process for vulcanization of rubber |
| US2450771A (en) * | 1944-03-06 | 1948-10-05 | Shell Dev | Plastic sulfur vulcanizing agent, method for its utilization and vulcanizable compositions containing the same |
| US2454862A (en) * | 1944-04-13 | 1948-11-30 | Allied Chem & Dye Corp | Product and process of reacting alkenyl succinic esters with sulfur |
| US2609373A (en) * | 1949-03-26 | 1952-09-02 | Monsanto Chemicals | Mercapto thiazole-sulfur halide reaction products |
| US3635859A (en) * | 1968-12-31 | 1972-01-18 | Sir Soc Italiana Resine Spa | Improvements relating to alkyd resins |
| US3920623A (en) * | 1972-02-18 | 1975-11-18 | Du Pont | Treatment of chloroprene-sulfur copolymers with benzothiazole sulfenamides |
| US4190460A (en) * | 1978-04-03 | 1980-02-26 | Suntech, Inc. | Sulfur plasticization with olefins |
| DE2901774A1 (de) * | 1979-01-18 | 1980-07-24 | Elastogran Gmbh | Rieselfaehiges, mikrobenbestaendiges farbstoff- und/oder hilfsmittelkonzentrat auf basis eines polyurethan-elastomeren und verfahren zu seiner herstellung |
| DE3307421A1 (de) * | 1983-03-03 | 1984-09-06 | Rhein-Chemie Rheinau Gmbh, 6800 Mannheim | Herstellung und verwendung vernetzter, epoxidierter fetter oele |
| DE3920411A1 (de) * | 1989-06-22 | 1991-01-03 | Rhein Chemie Rheinau Gmbh | Granulierte kautschukchemikalien |
| DE4231073A1 (de) * | 1992-09-17 | 1994-03-24 | Rhein Chemie Rheinau Gmbh | Phosphorylierung von Epoxiden |
-
1993
- 1993-05-17 DE DE4316429A patent/DE4316429A1/de not_active Withdrawn
-
1994
- 1994-04-25 TW TW083103654A patent/TW290572B/zh active
- 1994-05-04 EP EP94106970A patent/EP0625543A1/de not_active Ceased
- 1994-05-11 JP JP6120817A patent/JPH06329837A/ja active Pending
- 1994-05-13 CA CA002123524A patent/CA2123524A1/en not_active Abandoned
- 1994-05-17 CN CN94105698A patent/CN1096794A/zh active Pending
-
1995
- 1995-03-23 US US08/409,904 patent/US5624988A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP0625543A1 (de) | 1994-11-23 |
| CN1096794A (zh) | 1994-12-28 |
| JPH06329837A (ja) | 1994-11-29 |
| DE4316429A1 (de) | 1994-11-24 |
| US5624988A (en) | 1997-04-29 |
| TW290572B (enExample) | 1996-11-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Dead |