BR112014007102B1 - Plastificante, composição polimérica e condutor revestido - Google Patents
Plastificante, composição polimérica e condutor revestido Download PDFInfo
- Publication number
- BR112014007102B1 BR112014007102B1 BR112014007102-0A BR112014007102A BR112014007102B1 BR 112014007102 B1 BR112014007102 B1 BR 112014007102B1 BR 112014007102 A BR112014007102 A BR 112014007102A BR 112014007102 B1 BR112014007102 B1 BR 112014007102B1
- Authority
- BR
- Brazil
- Prior art keywords
- plasticizer
- weight
- polymeric composition
- fact
- transesterified
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 61
- 239000004020 conductor Substances 0.000 title claims abstract description 26
- 239000004014 plasticizer Substances 0.000 claims abstract description 66
- 235000019387 fatty acid methyl ester Nutrition 0.000 claims abstract description 13
- 235000012424 soybean oil Nutrition 0.000 claims abstract description 13
- 239000003549 soybean oil Substances 0.000 claims abstract description 13
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000003878 thermal aging Methods 0.000 claims abstract description 7
- 238000004383 yellowing Methods 0.000 claims description 19
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 17
- 229920005989 resin Polymers 0.000 claims description 13
- 239000011347 resin Substances 0.000 claims description 13
- 239000004800 polyvinyl chloride Substances 0.000 claims description 10
- 241001550224 Apha Species 0.000 claims description 9
- 239000011248 coating agent Substances 0.000 claims description 9
- 238000000576 coating method Methods 0.000 claims description 9
- 239000003921 oil Substances 0.000 claims description 7
- 235000019198 oils Nutrition 0.000 claims description 7
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 6
- 235000010469 Glycine max Nutrition 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 150000004702 methyl esters Chemical class 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 244000068988 Glycine max Species 0.000 claims 1
- 150000007824 aliphatic compounds Chemical group 0.000 claims 1
- 229920000642 polymer Polymers 0.000 abstract description 8
- 230000000052 comparative effect Effects 0.000 description 16
- 238000000034 method Methods 0.000 description 8
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 8
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000014759 maintenance of location Effects 0.000 description 5
- 102100039510 Cancer/testis antigen 2 Human genes 0.000 description 4
- 101000889345 Homo sapiens Cancer/testis antigen 2 Proteins 0.000 description 4
- -1 Phthalic acid diesters Chemical class 0.000 description 4
- 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 4
- 238000005259 measurement Methods 0.000 description 4
- 239000002952 polymeric resin Substances 0.000 description 4
- 229920003002 synthetic resin Polymers 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 102100025570 Cancer/testis antigen 1 Human genes 0.000 description 3
- 101000856237 Homo sapiens Cancer/testis antigen 1 Proteins 0.000 description 3
- 101000938702 Homo sapiens N-acetyltransferase ESCO1 Proteins 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 150000002924 oxiranes Chemical group 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000005809 transesterification reaction Methods 0.000 description 3
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- 239000004641 Diallyl-phthalate Substances 0.000 description 2
- 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 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004262 Ethyl gallate Substances 0.000 description 2
- 239000004399 Polyvinyl alcohol-polyethylene glycol-graft co-polymer Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 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 description 2
- 238000006735 epoxidation reaction Methods 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 125000005498 phthalate group Chemical class 0.000 description 2
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 2
- 229920001169 thermoplastic Polymers 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
- MQWCQFCZUNBTCM-UHFFFAOYSA-N 2-tert-butyl-6-(3-tert-butyl-2-hydroxy-5-methylphenyl)sulfanyl-4-methylphenol Chemical compound CC(C)(C)C1=CC(C)=CC(SC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O MQWCQFCZUNBTCM-UHFFFAOYSA-N 0.000 description 1
- DEXFNLNNUZKHNO-UHFFFAOYSA-N 6-[3-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-3-oxopropyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)C(CCC1=CC2=C(NC(O2)=O)C=C1)=O DEXFNLNNUZKHNO-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 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
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 101000686984 Xenopus laevis 26S proteasome regulatory subunit 6A-A Proteins 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 239000013307 optical fiber Substances 0.000 description 1
- CABDEMAGSHRORS-UHFFFAOYSA-N oxirane;hydrate Chemical compound O.C1CO1 CABDEMAGSHRORS-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000013047 polymeric layer Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/307—Other macromolecular compounds
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
- C08K5/103—Esters; Ether-esters of monocarboxylic acids with polyalcohols
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1515—Three-membered rings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/04—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C09D127/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
- H01B3/443—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from vinylhalogenides or other halogenoethylenic compounds
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2967—Synthetic resin or polymer
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Insulated Conductors (AREA)
- Organic Insulating Materials (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161541323P | 2011-09-30 | 2011-09-30 | |
| US61/541,323 | 2011-09-30 | ||
| PCT/US2012/055307 WO2013048771A1 (en) | 2011-09-30 | 2012-09-14 | Plasticizer for color retention during heat aging |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BR112014007102A2 BR112014007102A2 (pt) | 2017-04-11 |
| BR112014007102B1 true BR112014007102B1 (pt) | 2020-03-03 |
Family
ID=46982939
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR112014007102-0A BR112014007102B1 (pt) | 2011-09-30 | 2012-09-14 | Plastificante, composição polimérica e condutor revestido |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US10262767B2 (enExample) |
| EP (1) | EP2751185A1 (enExample) |
| JP (2) | JP2014534985A (enExample) |
| KR (1) | KR101963925B1 (enExample) |
| CN (1) | CN103930477B (enExample) |
| BR (1) | BR112014007102B1 (enExample) |
| CA (1) | CA2850430C (enExample) |
| MX (1) | MX378342B (enExample) |
| TW (1) | TW201326279A (enExample) |
| WO (1) | WO2013048771A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10262767B2 (en) | 2011-09-30 | 2019-04-16 | Dow Global Technologies Llc | Plasticizer for color retention during heat aging |
| CA2850326C (en) * | 2011-09-30 | 2019-11-12 | Dow Global Technologies Llc | Process for mixing polyvinyl chloride with a bio-based plasticizer |
| ES2619029T3 (es) | 2011-10-14 | 2017-06-22 | Galata Chemicals Llc | Plastificantes derivados de materia prima renovable |
| CN104004303B (zh) * | 2014-06-16 | 2016-01-13 | 福建致尚生物质材料发展有限公司 | 一种复合型生物酯增塑剂 |
| JP6428101B2 (ja) * | 2014-09-26 | 2018-11-28 | 住友電気工業株式会社 | 光ファイバ心線及び光ファイバテープ心線 |
| EP3212702B1 (en) * | 2014-10-27 | 2021-08-25 | Dow Global Technologies LLC | Plasticizer compositions and methods for making plasticizer compositions |
| WO2025128797A1 (en) | 2023-12-13 | 2025-06-19 | Blue Evolution, Inc | Ecofriendly, biodegradable biological polysaccharide composition for packaging materials |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2852563A (en) | 1955-10-17 | 1958-09-16 | Eastman Kodak Co | Condensation of isoaldehydes with lower aliphatic aldehydes |
| US3070608A (en) | 1958-07-07 | 1962-12-25 | Swift & Co | Selective alcoholysis of epoxy fatty acid esters |
| US3377304A (en) * | 1959-04-22 | 1968-04-09 | Swift & Co | High oxirane fatty esters |
| US3607805A (en) * | 1969-01-15 | 1971-09-21 | Scm Corp | Process for stabilizing vinyl halide resins |
| DE2646595C3 (de) | 1976-10-15 | 1979-07-26 | Hoechst Ag, 6000 Frankfurt | Sinterfähige feinteilige Polyvinylchlorid-Fonnmassen |
| DE3932049A1 (de) | 1989-09-26 | 1991-04-04 | Huels Chemische Werke Ag | Dihydropyridine als costabilisatoren fuer formmassen auf basis von polymerisaten des vinylchlorids |
| EP0432096A1 (de) | 1989-12-06 | 1991-06-12 | Ciba-Geigy Ag | Stabilisierte chlorhaltige Zusammensetzung |
| DE59108223D1 (de) | 1990-11-30 | 1996-10-31 | Ciba Geigy Ag | Stabilisierte chlorhaltige Polymere |
| US5283273A (en) | 1990-11-30 | 1994-02-01 | Ciba-Geigy Corporation | Stabilized chlorine-containing polymers |
| US5324846A (en) * | 1992-01-30 | 1994-06-28 | Elf Atochem North America, Inc. | Partial esters of epoxy containing compounds |
| DE4425266C1 (de) | 1994-07-16 | 1995-10-19 | Metallgesellschaft Ag | Schichtgitterverbindungen und deren Verwendung |
| ATE312874T1 (de) | 1996-03-22 | 2005-12-15 | Wolfgang Wehner | Stabilisatorkombination für chlorhaltige polymere |
| US5880310A (en) | 1997-05-21 | 1999-03-09 | Mitsubishi Gas Chemical Company, Inc. | Process for producing plasticizer esters |
| US6797753B2 (en) | 2000-06-20 | 2004-09-28 | Battelle Memorial Institute | Plasticizers derived from vegetable oils |
| DE10104815A1 (de) * | 2001-02-01 | 2002-08-08 | Cognis Deutschland Gmbh | Verfahren zur Herstellung von epoxidierten Glyceridacetaten |
| EP1433794B1 (en) | 2002-12-11 | 2008-02-20 | Kuraray Co., Ltd. | Dispersion stabilizer for suspension polymerization of vinyl compound and method of producing the same |
| KR100573479B1 (ko) | 2003-12-23 | 2006-04-24 | 주식회사 엘지화학 | 균일질 무정형 마블바닥재 및 이의 제조방법 |
| DE102005031945A1 (de) | 2005-07-08 | 2007-01-11 | Construction Research & Technology Gmbh | Verwendung von entfärbtem Biodiesel als Weichmacher |
| CN1966497A (zh) * | 2006-09-11 | 2007-05-23 | 罗春妹 | 环氧脂肪酸甲酯 |
| BRPI0705276A2 (pt) | 2007-12-10 | 2009-08-11 | Nexoleum Bioderivados Ltda | plastificantes primários de pvc derivados de óleos vegetais, processo de obtenção de plastificantes primários de pvc derivados de oléos vegetais e composição de pvc plastificado |
| US8481767B2 (en) * | 2008-01-24 | 2013-07-09 | Polyone Corporation | Catalysts for esterification of epoxidized soyates and methods of using same |
| CN101939307B (zh) * | 2008-02-12 | 2015-04-22 | 普立万公司 | 环氧化大豆油脂肪酸二酯及其使用方法 |
| CA2715287C (en) * | 2008-02-15 | 2016-01-05 | Union Carbide Chemicals & Plastics Technology Llc | A replacement plasticizer system for phthalate-plasticized formulations |
| MX341364B (es) * | 2008-06-17 | 2016-08-18 | Resinas Y Mat S A De C V | Bioplastificantes o plastificantes oleoquimicos primarios, que a su vez actuan como estabilizadores termicos y de radiacion ultravioleta en resinas moldeables de pvc y proceso para obtencion de los mismos. |
| CA2775993C (en) * | 2009-09-30 | 2017-07-18 | Dow Global Technologies Llc | Acetylated glycerin esters and their blends with epoxidized fatty acid esters |
| WO2011041396A1 (en) | 2009-09-30 | 2011-04-07 | Dow Global Technologies Llc | Heat stabilized polymeric composition with epoxidized fatty acid ester plasticizer |
| BR112012017956B1 (pt) * | 2010-01-22 | 2020-04-07 | Archer Daniels Midland Co | composição de poli (haleto de vinila) |
| CA2798296C (en) * | 2010-05-10 | 2016-12-13 | Dow Global Technologies Llc | Flexible pvc compositions made with plasticizers derived from renewable sources |
| US10262767B2 (en) | 2011-09-30 | 2019-04-16 | Dow Global Technologies Llc | Plasticizer for color retention during heat aging |
-
2012
- 2012-09-14 US US14/347,069 patent/US10262767B2/en active Active
- 2012-09-14 KR KR1020147007917A patent/KR101963925B1/ko active Active
- 2012-09-14 MX MX2014003842A patent/MX378342B/es unknown
- 2012-09-14 JP JP2014533586A patent/JP2014534985A/ja not_active Withdrawn
- 2012-09-14 CN CN201280042944.4A patent/CN103930477B/zh active Active
- 2012-09-14 WO PCT/US2012/055307 patent/WO2013048771A1/en not_active Ceased
- 2012-09-14 EP EP12769545.0A patent/EP2751185A1/en not_active Ceased
- 2012-09-14 CA CA2850430A patent/CA2850430C/en active Active
- 2012-09-14 BR BR112014007102-0A patent/BR112014007102B1/pt active IP Right Grant
- 2012-09-26 TW TW101135319A patent/TW201326279A/zh unknown
-
2017
- 2017-10-20 JP JP2017203233A patent/JP2018059105A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CA2850430A1 (en) | 2013-04-04 |
| KR20140071378A (ko) | 2014-06-11 |
| MX2014003842A (es) | 2014-04-30 |
| JP2014534985A (ja) | 2014-12-25 |
| BR112014007102A2 (pt) | 2017-04-11 |
| US10262767B2 (en) | 2019-04-16 |
| WO2013048771A1 (en) | 2013-04-04 |
| MX378342B (es) | 2025-03-10 |
| EP2751185A1 (en) | 2014-07-09 |
| JP2018059105A (ja) | 2018-04-12 |
| TW201326279A (zh) | 2013-07-01 |
| CN103930477B (zh) | 2015-08-19 |
| CA2850430C (en) | 2019-11-12 |
| CN103930477A (zh) | 2014-07-16 |
| KR101963925B1 (ko) | 2019-03-29 |
| US20140234622A1 (en) | 2014-08-21 |
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Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 14/09/2012, OBSERVADAS AS CONDICOES LEGAIS. |