CS227302B2 - Způsob inhibice oxidačního odbourání organického materiálu - Google Patents

Způsob inhibice oxidačního odbourání organického materiálu Download PDF

Info

Publication number: CS227302B2
Authority: CS; Czechoslovakia
Prior art keywords: hydroxyphenyl; tert; radical; butyl; mol
Prior art date: 1978-08-04

Application number

CS536979A

Other languages

Czech (cs)

English (en)

Inventor

Edward L Wheeler

Elmar H Jancis

Richard A Gencarelli

Franklin H Barrows

Original Assignee

Uniroyal 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.)

1978-08-04

Filing date

1979-08-03

Publication date

1984-04-16

1979-08-03 Application filed by Uniroyal Inc filed Critical Uniroyal Inc

1984-04-16 Publication of CS227302B2 publication Critical patent/CS227302B2/cs

Links

238000000034 method Methods 0.000 title claims description 24
239000011368 organic material Substances 0.000 title claims description 15
238000010525 oxidative degradation reaction Methods 0.000 title claims description 10
230000002401 inhibitory effect Effects 0.000 title claims description 6
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-1 alkyl radical Chemical class 0.000 claims description 64
125000004432 carbon atom Chemical group C* 0.000 claims description 20
150000003254 radicals Chemical class 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 8
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
UIYCHXAGWOYNNA-UHFFFAOYSA-N vinyl sulfide Chemical group C=CSC=C UIYCHXAGWOYNNA-UHFFFAOYSA-N 0.000 claims description 2
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239000000203 mixture Substances 0.000 description 75
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 70
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POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
238000001035 drying Methods 0.000 description 4
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239000007858 starting material Substances 0.000 description 4
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239000000853 adhesive Substances 0.000 description 1
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PWAXUOGZOSVGBO-UHFFFAOYSA-N adipoyl chloride Chemical compound ClC(=O)CCCCC(Cl)=O PWAXUOGZOSVGBO-UHFFFAOYSA-N 0.000 description 1
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125000003368 amide group Chemical group 0.000 description 1
150000001414 amino alcohols Chemical class 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
150000005840 aryl radicals Chemical class 0.000 description 1
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150000001559 benzoic acids Chemical class 0.000 description 1
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229910052794 bromium Inorganic materials 0.000 description 1
239000000378 calcium silicate Substances 0.000 description 1
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OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
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230000015556 catabolic process Effects 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000003610 charcoal Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
239000003026 cod liver oil Substances 0.000 description 1
235000012716 cod liver oil Nutrition 0.000 description 1
235000005687 corn oil Nutrition 0.000 description 1
239000002285 corn oil Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
MMXKVMNBHPAILY-UHFFFAOYSA-N dodecanoic acid ethyl ester Natural products CCCCCCCCCCCC(=O)OCC MMXKVMNBHPAILY-UHFFFAOYSA-N 0.000 description 1
NQGIJDNPUZEBRU-UHFFFAOYSA-N dodecanoyl chloride Chemical compound CCCCCCCCCCCC(Cl)=O NQGIJDNPUZEBRU-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003480 eluent Substances 0.000 description 1
CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 1
ZCWSUZJGZZFSHM-UHFFFAOYSA-N ethyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 ZCWSUZJGZZFSHM-UHFFFAOYSA-N 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000003925 fat Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
239000000446 fuel Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
239000000944 linseed oil Substances 0.000 description 1
235000021388 linseed oil Nutrition 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000010687 lubricating oil Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
YMVXPZAKIVJWBR-UHFFFAOYSA-N n'-(3-hydroxypropyl)oxamide Chemical compound NC(=O)C(=O)NCCCO YMVXPZAKIVJWBR-UHFFFAOYSA-N 0.000 description 1
GTBODJTVLNPEEM-UHFFFAOYSA-N n-(3-hydroxypropyl)octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCCO GTBODJTVLNPEEM-UHFFFAOYSA-N 0.000 description 1
229930014626 natural product Natural products 0.000 description 1
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
MVLVMROFTAUDAG-UHFFFAOYSA-N octadecanoic acid ethyl ester Natural products CCCCCCCCCCCCCCCCCC(=O)OCC MVLVMROFTAUDAG-UHFFFAOYSA-N 0.000 description 1
WVJVHUWVQNLPCR-UHFFFAOYSA-N octadecanoyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(=O)CCCCCCCCCCCCCCCCC WVJVHUWVQNLPCR-UHFFFAOYSA-N 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
239000003209 petroleum derivative Substances 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
229960005235 piperonyl butoxide Drugs 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002857 polybutadiene Polymers 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
229920000306 polymethylpentene Polymers 0.000 description 1
239000011116 polymethylpentene Substances 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920006324 polyoxymethylene Polymers 0.000 description 1
229920006380 polyphenylene oxide Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000005033 polyvinylidene chloride Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
238000003825 pressing Methods 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
238000002390 rotary evaporation Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000003760 tallow Substances 0.000 description 1
238000003878 thermal aging Methods 0.000 description 1
239000000326 ultraviolet stabilizing agent Substances 0.000 description 1
239000001993 wax Substances 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Compositions Of Macromolecular Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Lubricants (AREA)
Anti-Oxidant Or Stabilizer Compositions (AREA)

CS536979A 1978-08-04 1979-08-03 Způsob inhibice oxidačního odbourání organického materiálu CS227302B2 (cs)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US93108778A	1978-08-04	1978-08-04

Publications (1)

Publication Number	Publication Date
CS227302B2 true CS227302B2 (cs)	1984-04-16

Family

ID=25460209

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS536979A CS227302B2 (cs)	1978-08-04	1979-08-03	Způsob inhibice oxidačního odbourání organického materiálu

Country Status (4)

Country	Link
JP (2)	JPS5543080A (ja)
BR (1)	BR7904999A (ja)
CS (1)	CS227302B2 (ja)
ZA (2)	ZA794012B (ja)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5837051A (ja) *	1981-08-27	1983-03-04	Toyobo Co Ltd	安定化されたポリウレタン弾性繊維
US4435253A (en) *	1983-01-28	1984-03-06	Omi International Corporation	Gold sulphite electroplating solutions and methods
JP2604166B2 (ja) *	1987-07-31	1997-04-30	日清製油株式会社	潤滑油
BE1014162A3 (fr) *	1997-05-26	2003-06-03	Ciba Sc Holding Ag	Produits stabilisants, compositions et concentres les contenant, et leur procede d'utilisation.
JP4974136B2 (ja) *	2006-03-31	2012-07-11	株式会社興人	バイオディーゼル燃料の加水分解抑制剤及び該抑制剤を含有したバイオディーゼル燃料

1979
- 1979-08-03 CS CS536979A patent/CS227302B2/cs unknown
- 1979-08-03 ZA ZA00794012A patent/ZA794012B/xx unknown
- 1979-08-03 BR BR7904999A patent/BR7904999A/pt not_active IP Right Cessation
- 1979-08-03 ZA ZA00794013A patent/ZA794013B/xx unknown
- 1979-08-03 JP JP9939179A patent/JPS5543080A/ja active Granted
- 1979-08-03 JP JP9939079A patent/JPS5531073A/ja active Granted

Also Published As

Publication number	Publication date
JPS5531073A (en)	1980-03-05
JPS6254298B2 (ja)	1987-11-13
JPS5543080A (en)	1980-03-26
ZA794013B (en)	1981-06-24
JPS6129348B2 (ja)	1986-07-05
ZA794012B (en)	1980-08-27
BR7904999A (pt)	1980-02-12

Publication	Publication Date	Title
JP3668898B2 (ja)	2005-07-06	安定剤としての液体酸化防止剤
EP0022749B1 (de)	1983-05-18	Alkanolamid-beta-ketocarbonsäureester und ihre Verwendung zur Stabilisierung von chlorhaltigen Thermoplasten
DE69317008T2 (de)	1998-08-27	Substituierte 1-Hydroxy-2,6-Diaryl-4-Piperidonketal-Stabilisatoren
US6194493B1 (en)	2001-02-27	4-hydroxyquinoline-3-carboxylic acid derivatives as light stabilizers
FR2763338A1 (fr)	1998-11-20	Nouveaux composes a base de derives de polyalkyl-1-oxa- diazaspirodecane
CS227302B2 (cs)	1984-04-16	Způsob inhibice oxidačního odbourání organického materiálu
AU701742B2 (en)	1999-02-04	Bisphenol ester derivatives
US4305868A (en)	1981-12-15	Phenolic esteramide antioxidants
US5190999A (en)	1993-03-02	α-carbonylphenylacetonitrile derivatives as stabilizers for organic materials
US5250592A (en)	1993-10-05	Isoindolinone compounds as stabilizers for organic materials
US4304714A (en)	1981-12-08	Polyfunctional phenolic oxamide antioxidants
JPH0212235B2 (ja)	1990-03-19
JPH09501673A (ja)	1997-02-18	２，２’，２”−ニトリロ［トリエチル−トリス−（３，３’，５，５’−テトラ−第三−ブチル−１，１’−ビフェニル−２，２’−ジイル）ホスフィット］のガンマ結晶変態
JPS6318597B2 (ja)	1988-04-19
US5169885A (en)	1992-12-08	Bis[2-tert-butyl-4-(2-octadecyloxycarbonylethyl)-6-methylphenyl]phosphite useful as a stabilizing agent
EP0009866B1 (en)	1982-08-04	Phenolic esteramide antioxidants and their use
JP2764282B2 (ja)	1998-06-11	長鎖Ｎ−アルキル−α−アルキルニトロン及び安定剤としてのそれらの使用方法
US4601839A (en)	1986-07-22	Stabilized polymers, novel stabilizers, and synthesis thereof
JPH054953A (ja)	1993-01-14	オルト−ヒドロキシフエニルアセタミド
US4107137A (en)	1978-08-15	Phenolic antioxidants for synthetic polymers
JPH08113545A (ja)	1996-05-07	有機材料のための安定剤
EP0008507B1 (en)	1985-02-13	Derivatives of 2-oxazolines as antioxidants and compositions thereof
US3681358A (en)	1972-08-01	Hindered phenolic esters of cyclic amino carboxylic acids
US4309336A (en)	1982-01-05	Polymeric compositions containing antioxidants
FR2540111A1 (fr)	1984-08-03	Esters polyalkyl-piperidyliques d'acides tetracarboxyliques aliphatiques, et polymeres organiques qui ont ete stabilises a l'aide de ces composes