CA1045804A - Aides de traitement pour composes de caoutchouc naturel et synthetique - Google Patents

Aides de traitement pour composes de caoutchouc naturel et synthetique

Info

Publication number: CA1045804A
Authority: CA; Canada
Prior art keywords: processing aid; thioether; acid; rubber; aid according
Prior art date: 1973-11-01
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

Application number

CA212,200A

Other languages

English (en)

Other versions

CA212200S (en

Inventor

Erwin Aron

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Technical Processing Inc

Original Assignee

Technical Processing Inc

Priority date (The priority date 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 date listed.)

1973-11-01

Filing date

1974-10-24

Publication date

1979-01-09

1974-01-03 Priority claimed from US430566A external-priority patent/US3882062A/en

1974-10-24 Application filed by Technical Processing Inc filed Critical Technical Processing Inc

1979-01-09 Application granted granted Critical

1979-01-09 Publication of CA1045804A publication Critical patent/CA1045804A/fr

Status Expired legal-status Critical Current

Links

150000001875 compounds Chemical class 0.000 title claims abstract description 43
239000006057 Non-nutritive feed additive Substances 0.000 title claims abstract description 26
229920003052 natural elastomer Polymers 0.000 title abstract description 7
229920001194 natural rubber Polymers 0.000 title abstract description 7
229920003051 synthetic elastomer Polymers 0.000 title abstract description 4
239000005061 synthetic rubber Substances 0.000 title abstract description 4
239000000203 mixture Substances 0.000 claims abstract description 35
150000003568 thioethers Chemical class 0.000 claims abstract description 30
-1 aromatic sulfonic acids Chemical class 0.000 claims abstract description 16
150000003839 salts Chemical class 0.000 claims abstract description 5
150000004668 long chain fatty acids Chemical class 0.000 claims abstract description 4
229920001971 elastomer Polymers 0.000 claims description 35
239000005060 rubber Substances 0.000 claims description 35
125000003118 aryl group Chemical group 0.000 claims description 17
238000010057 rubber processing Methods 0.000 claims description 17
150000004665 fatty acids Chemical class 0.000 claims description 16
239000000344 soap Substances 0.000 claims description 16
LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 claims description 15
235000014113 dietary fatty acids Nutrition 0.000 claims description 14
239000000194 fatty acid Substances 0.000 claims description 14
229930195729 fatty acid Natural products 0.000 claims description 14
125000004432 carbon atom Chemical group C* 0.000 claims description 13
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims description 12
239000002480 mineral oil Substances 0.000 claims description 12
XXSIKMDLPWYFIJ-UHFFFAOYSA-N 2-[2-[2-[2-(2-nonylphenoxy)ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCOCCOCCOCCO XXSIKMDLPWYFIJ-UHFFFAOYSA-N 0.000 claims description 11
235000010446 mineral oil Nutrition 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 10
239000000463 material Substances 0.000 claims description 10
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 9
229910052751 metal Inorganic materials 0.000 claims description 9
239000002184 metal Substances 0.000 claims description 9
239000000654 additive Substances 0.000 claims description 8
238000013329 compounding Methods 0.000 claims description 8
235000019271 petrolatum Nutrition 0.000 claims description 8
PZTAGFCBNDBBFZ-UHFFFAOYSA-N tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCCC1CO PZTAGFCBNDBBFZ-UHFFFAOYSA-N 0.000 claims description 8
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 7
239000004264 Petrolatum Substances 0.000 claims description 7
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 7
239000007788 liquid Substances 0.000 claims description 7
229940066842 petrolatum Drugs 0.000 claims description 7
239000011591 potassium Substances 0.000 claims description 7
229910052700 potassium Inorganic materials 0.000 claims description 7
239000011734 sodium Substances 0.000 claims description 7
229910052708 sodium Inorganic materials 0.000 claims description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
125000003710 aryl alkyl group Chemical group 0.000 claims description 6
229960000541 cetyl alcohol Drugs 0.000 claims description 6
DWNAQMUDCDVSLT-UHFFFAOYSA-N diphenyl phthalate Chemical compound C=1C=CC=C(C(=O)OC=2C=CC=CC=2)C=1C(=O)OC1=CC=CC=C1 DWNAQMUDCDVSLT-UHFFFAOYSA-N 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
238000000034 method Methods 0.000 claims description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
229940114930 potassium stearate Drugs 0.000 claims description 5
ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 claims description 5
LPEBYPDZMWMCLZ-CVBJKYQLSA-L zinc;(z)-octadec-9-enoate Chemical compound [Zn+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LPEBYPDZMWMCLZ-CVBJKYQLSA-L 0.000 claims description 5
ODJQKYXPKWQWNK-UHFFFAOYSA-N 3,3'-Thiobispropanoic acid Chemical group OC(=O)CCSCCC(O)=O ODJQKYXPKWQWNK-UHFFFAOYSA-N 0.000 claims description 4
239000003490 Thiodipropionic acid Substances 0.000 claims description 4
125000002877 alkyl aryl group Chemical group 0.000 claims description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
238000010077 mastication Methods 0.000 claims description 4
230000018984 mastication Effects 0.000 claims description 4
229910052717 sulfur Inorganic materials 0.000 claims description 4
239000011593 sulfur Substances 0.000 claims description 4
235000019303 thiodipropionic acid Nutrition 0.000 claims description 4
SASYRHXVHLPMQD-UHFFFAOYSA-N 2-(1,2-dicarboxyethylsulfanyl)butanedioic acid Chemical group OC(=O)CC(C(O)=O)SC(C(O)=O)CC(O)=O SASYRHXVHLPMQD-UHFFFAOYSA-N 0.000 claims description 3
NDVLTZFQVDXFAN-UHFFFAOYSA-N 3-(2-cyanoethylsulfanyl)propanenitrile Chemical group N#CCCSCCC#N NDVLTZFQVDXFAN-UHFFFAOYSA-N 0.000 claims description 3
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
VXYFARNRGZWHTJ-UHFFFAOYSA-N [3-(4-hydroxyphenyl)-1-methoxy-1-oxopropan-2-yl]azanium;chloride Chemical group Cl.COC(=O)C(N)CC1=CC=C(O)C=C1 VXYFARNRGZWHTJ-UHFFFAOYSA-N 0.000 claims description 3
230000001476 alcoholic effect Effects 0.000 claims description 3
239000003513 alkali Substances 0.000 claims description 3
150000001447 alkali salts Chemical class 0.000 claims description 3
229910052788 barium Inorganic materials 0.000 claims description 3
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 3
238000009835 boiling Methods 0.000 claims description 3
239000011575 calcium Substances 0.000 claims description 3
229910052791 calcium Inorganic materials 0.000 claims description 3
239000003925 fat Substances 0.000 claims description 3
239000011777 magnesium Substances 0.000 claims description 3
229910052749 magnesium Inorganic materials 0.000 claims description 3
MYWWWNVEZBAKHR-UHFFFAOYSA-N methyl 3-(3-methoxy-3-oxopropyl)sulfanylpropanoate Chemical group COC(=O)CCSCCC(=O)OC MYWWWNVEZBAKHR-UHFFFAOYSA-N 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
150000003460 sulfonic acids Chemical class 0.000 claims description 3
UVZICZIVKIMRNE-UHFFFAOYSA-N thiodiacetic acid Chemical group OC(=O)CSCC(O)=O UVZICZIVKIMRNE-UHFFFAOYSA-N 0.000 claims description 3
229910052725 zinc Inorganic materials 0.000 claims description 3
239000011701 zinc Substances 0.000 claims description 3
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 2
UFONUKZQWFSQLP-UHFFFAOYSA-N [N].NC#N Chemical compound [N].NC#N UFONUKZQWFSQLP-UHFFFAOYSA-N 0.000 claims description 2
125000003368 amide group Chemical group 0.000 claims description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
LUFPJJNWMYZRQE-UHFFFAOYSA-N benzylsulfanylmethylbenzene Chemical group C=1C=CC=CC=1CSCC1=CC=CC=C1 LUFPJJNWMYZRQE-UHFFFAOYSA-N 0.000 claims description 2
VXTYCJJHHMLIBM-UHFFFAOYSA-N carboxysulfanylformic acid Chemical group OC(=O)SC(O)=O VXTYCJJHHMLIBM-UHFFFAOYSA-N 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims description 2
239000000945 filler Substances 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
239000001301 oxygen Substances 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims description 2
239000012188 paraffin wax Substances 0.000 claims description 2
239000000049 pigment Substances 0.000 claims description 2
125000000547 substituted alkyl group Chemical group 0.000 claims description 2
230000000996 additive effect Effects 0.000 claims 2
150000007524 organic acids Chemical class 0.000 claims 2
UTXPMECBRCEYCI-UHFFFAOYSA-N 2-[2-[2-[2-(4-nonylphenoxy)ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCO)C=C1 UTXPMECBRCEYCI-UHFFFAOYSA-N 0.000 claims 1
239000002585 base Substances 0.000 claims 1
238000012545 processing Methods 0.000 abstract description 3
239000002253 acid Substances 0.000 description 8
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 7
YPIFGDQKSSMYHQ-UHFFFAOYSA-N 7,7-dimethyloctanoic acid Chemical compound CC(C)(C)CCCCCC(O)=O YPIFGDQKSSMYHQ-UHFFFAOYSA-N 0.000 description 7
235000021355 Stearic acid Nutrition 0.000 description 7
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 7
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 7
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 7
239000008117 stearic acid Substances 0.000 description 7
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 5
150000001412 amines Chemical class 0.000 description 5
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 5
239000003921 oil Substances 0.000 description 5
244000043261 Hevea brasiliensis Species 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
150000007513 acids Chemical class 0.000 description 4
238000009472 formulation Methods 0.000 description 4
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 3
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
229940126062 Compound A Drugs 0.000 description 3
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
AUZONCFQVSMFAP-UHFFFAOYSA-N disulfiram Chemical compound CCN(CC)C(=S)SSC(=S)N(CC)CC AUZONCFQVSMFAP-UHFFFAOYSA-N 0.000 description 3
CFNDRVCFJKQSHT-UHFFFAOYSA-N dodecyl benzenesulfonate;potassium Chemical compound [K].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 CFNDRVCFJKQSHT-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
150000002430 hydrocarbons Chemical class 0.000 description 3
239000004615 ingredient Substances 0.000 description 3
239000011630 iodine Substances 0.000 description 3
229910052740 iodine Inorganic materials 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
235000013311 vegetables Nutrition 0.000 description 3
239000011787 zinc oxide Substances 0.000 description 3
NXQMCAOPTPLPRL-UHFFFAOYSA-N 2-(2-benzoyloxyethoxy)ethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOCCOC(=O)C1=CC=CC=C1 NXQMCAOPTPLPRL-UHFFFAOYSA-N 0.000 description 2
LXODQLXKQIJVNK-UHFFFAOYSA-N 2-(2-benzoyloxypropoxy)propyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C)COC(C)COC(=O)C1=CC=CC=C1 LXODQLXKQIJVNK-UHFFFAOYSA-N 0.000 description 2
BHVFARXULURYAW-UHFFFAOYSA-N 2-[2-[2-[2-(4-nonylphenyl)peroxyethoxy]ethoxy]ethoxy]ethanol Chemical compound C(CCCCCCCC)C1=CC=C(OOCCOCCOCCOCCO)C=C1 BHVFARXULURYAW-UHFFFAOYSA-N 0.000 description 2
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
125000002768 hydroxyalkyl group Chemical group 0.000 description 2
238000011065 in-situ storage Methods 0.000 description 2
239000012669 liquid formulation Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
239000004200 microcrystalline wax Substances 0.000 description 2
235000019808 microcrystalline wax Nutrition 0.000 description 2
239000012184 mineral wax Substances 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
238000010058 rubber compounding Methods 0.000 description 2
239000007787 solid Substances 0.000 description 2
150000008054 sulfonate salts Chemical class 0.000 description 2
239000003760 tallow Substances 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
BTUUFEOXIVJCMZ-UHFFFAOYSA-N 1-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]-2-phenoxyundecan-2-ol Chemical compound OCCOCCOCCOCC(O)(CCCCCCCCC)OC1=CC=CC=C1 BTUUFEOXIVJCMZ-UHFFFAOYSA-N 0.000 description 1
LLMLGZUZTFMXSA-UHFFFAOYSA-N 2,3,4,5,6-pentachlorobenzenethiol Chemical compound SC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LLMLGZUZTFMXSA-UHFFFAOYSA-N 0.000 description 1
IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 1
AHSGHEXYEABOKT-UHFFFAOYSA-N 2-[2-(2-benzoyloxyethoxy)ethoxy]ethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOCCOCCOC(=O)C1=CC=CC=C1 AHSGHEXYEABOKT-UHFFFAOYSA-N 0.000 description 1
OJCFEGKCRWEVSN-UHFFFAOYSA-N 2-[2-[2-[2-[2-(2-dodecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCO OJCFEGKCRWEVSN-UHFFFAOYSA-N 0.000 description 1
DOJWGMZWXSGSII-UHFFFAOYSA-N 2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]-1,1-bis(2-octylphenoxy)ethanol;phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O.CCCCCCCCC1=CC=CC=C1OC(O)(COCCOCCOCCOCCOCCO)OC1=CC=CC=C1CCCCCCCC DOJWGMZWXSGSII-UHFFFAOYSA-N 0.000 description 1
FCWOBTLJAOFFCI-UHFFFAOYSA-N 2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]-3-phenoxy-1-phenylpentadecan-3-ol;phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O.C=1C=CC=CC=1CC(OCCOCCOCCOCCOCCO)C(O)(CCCCCCCCCCCC)OC1=CC=CC=C1 FCWOBTLJAOFFCI-UHFFFAOYSA-N 0.000 description 1
TWIMUEGVLWNOMO-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-(2-nonylphenoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCOCCOCCOCCOCCOCCO TWIMUEGVLWNOMO-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
229920001368 Crepe rubber Polymers 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
241001441571 Hiodontidae Species 0.000 description 1
229930194542 Keto Natural products 0.000 description 1
241000276489 Merlangius merlangus Species 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
235000021314 Palmitic acid Nutrition 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
230000002730 additional effect Effects 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
HCHHNNBICUNCTE-UHFFFAOYSA-N bis(2-phenoxyethyl) benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCCOC=2C=CC=CC=2)C=1C(=O)OCCOC1=CC=CC=C1 HCHHNNBICUNCTE-UHFFFAOYSA-N 0.000 description 1
KAPPEHYHCPRBGI-UHFFFAOYSA-N bis(2-phenoxyundecyl) benzene-1,2-dicarboxylate Chemical compound C=1C=CC=CC=1OC(CCCCCCCCC)COC(=O)C1=CC=CC=C1C(=O)OCC(CCCCCCCCC)OC1=CC=CC=C1 KAPPEHYHCPRBGI-UHFFFAOYSA-N 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
JNGZXGGOCLZBFB-IVCQMTBJSA-N compound E Chemical compound N([C@@H](C)C(=O)N[C@@H]1C(N(C)C2=CC=CC=C2C(C=2C=CC=CC=2)=N1)=O)C(=O)CC1=CC(F)=CC(F)=C1 JNGZXGGOCLZBFB-IVCQMTBJSA-N 0.000 description 1
238000001816 cooling Methods 0.000 description 1
UCVPKAZCQPRWAY-UHFFFAOYSA-N dibenzyl benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC=2C=CC=CC=2)C=1C(=O)OCC1=CC=CC=C1 UCVPKAZCQPRWAY-UHFFFAOYSA-N 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
229940113120 dipropylene glycol Drugs 0.000 description 1
238000000893 electron nuclear double resonance spectroscopy Methods 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000008240 homogeneous mixture Substances 0.000 description 1
150000002431 hydrogen Chemical group 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
125000000468 ketone group Chemical group 0.000 description 1
238000005259 measurement Methods 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
235000014593 oils and fats Nutrition 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
235000021313 oleic acid Nutrition 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
230000000704 physical effect Effects 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920001343 polytetrafluoroethylene Polymers 0.000 description 1
229960004063 propylene glycol Drugs 0.000 description 1
235000013772 propylene glycol Nutrition 0.000 description 1
LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
239000013638 trimer Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000001993 wax Substances 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1
235000014692 zinc oxide Nutrition 0.000 description 1
ONSIBMFFLJKTPT-UHFFFAOYSA-L zinc;2,3,4,5,6-pentachlorobenzenethiolate Chemical compound [Zn+2].[S-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl.[S-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl ONSIBMFFLJKTPT-UHFFFAOYSA-L 0.000 description 1
DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
- C08K5/42—Sulfonic acids; 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)
Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Processes Of Treating Macromolecular Substances (AREA)

CA212,200A 1973-11-01 1974-10-24 Aides de traitement pour composes de caoutchouc naturel et synthetique Expired CA1045804A (fr)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US41197573A	1973-11-01	1973-11-01
US42168973A	1973-12-04	1973-12-04
US430566A US3882062A (en)	1973-12-04	1974-01-03	Novel processing aids for natural and synthetic rubber compounds

Publications (1)

Publication Number	Publication Date
CA1045804A true CA1045804A (fr)	1979-01-09

Family

ID=27410924

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA212,200A Expired CA1045804A (fr)	1973-11-01	1974-10-24	Aides de traitement pour composes de caoutchouc naturel et synthetique

Country Status (4)

Country	Link
JP (1)	JPS521930B2 (fr)
CA (1)	CA1045804A (fr)
FR (1)	FR2249921B1 (fr)
GB (1)	GB1477371A (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SK285498B6 (sk) *	2002-05-20	2007-03-01	Matador Holding, A. S.	Vulkanizačné činidlo a spôsob jeho výroby
BRPI0622084A2 (pt) *	2006-10-30	2014-06-17	Pirelli	Pneu para rodas de veículo, artigo elastomérico,e, composição elastomérica reticulável

1974
- 1974-10-24 CA CA212,200A patent/CA1045804A/fr not_active Expired
- 1974-10-31 FR FR7436478A patent/FR2249921B1/fr not_active Expired
- 1974-10-31 GB GB4713874A patent/GB1477371A/en not_active Expired
- 1974-11-01 JP JP12559074A patent/JPS521930B2/ja not_active Expired

Also Published As

Publication number	Publication date
GB1477371A (en)	1977-06-22
JPS521930B2 (fr)	1977-01-19
FR2249921A1 (fr)	1975-05-30
FR2249921B1 (fr)	1976-10-22
JPS5075235A (fr)	1975-06-20
DE2451567B2 (de)	1976-02-26
DE2451567A1 (de)	1975-05-07

Publication	Publication Date	Title
USRE29821E (en)	1978-10-31	Novel processing aids for natural and synthetic rubber compounds
JPS5811896B2 (ja)	1983-03-05	ハロゲン化ビニル用安定剤組成物
US4010129A (en)	1977-03-01	Novel processing aids for natural and synthetic rubber compounds
JPH05125231A (ja)	1993-05-21	ゴムおよびプラスチツクの加工性を改良する方法
US3882062A (en)	1975-05-06	Novel processing aids for natural and synthetic rubber compounds
US2343835A (en)	1944-03-07	Method of compounding rubber
US3855165A (en)	1974-12-17	Novel processing aids for rubber compounds
US2052607A (en)	1936-09-01	Rubber compounding material and method of using
CA1064245A (fr)	1979-10-16	Adjuvants dans la fabrication de produits en caoutchouc naturel et artificiel
US2189417A (en)	1940-02-06	Antioxidant
US2871191A (en)	1959-01-27	Greases stabilized with organic carbonates
US2268501A (en)	1941-12-30	Vulcanization of rubber
JPH05295178A (ja)	1993-11-09	充填剤配合ポリオレフィンの色の安定化
US2352950A (en)	1944-07-04	Antioxidant
JPH0135019B2 (fr)	1989-07-21
US2662864A (en)	1953-12-15	Rubber compositions with oxidized microcrystalline wax
DE602005000555T2 (de)	2007-11-08	Thermische Stabilisatorzusammensetzungen für halogenhaltige Vinylpolymere
US3434991A (en)	1969-03-25	Rubber dispersing agents comprising fatty acid salts,alcohol and hydrocarbon
US2380129A (en)	1945-07-10	Antioxidants
US1669491A (en)	1928-05-15	Treatment of fatty still residues
US1924170A (en)	1933-08-29	Method for preparing latex compositions
JPH1180421A (ja)	1999-03-26	水素化ニトリルゴム用可塑剤及び水素化ニトリルゴム組成物並びに水素化ニトリルゴムの可塑化方法
US2373375A (en)	1945-04-10	Plasticized rubber and method of making
US2361543A (en)	1944-10-31	Treatment of rubber
JP2000191836A (ja)	2000-07-11	難燃性ゴム組成物及び難燃性ゴム成形体