FI76115B - Derivat av med hydrokarbyl substituerat, karboxylacylerande medel innehaolllande sammansaettningar, och braenslen som innehaoller saodana. - Google Patents
Derivat av med hydrokarbyl substituerat, karboxylacylerande medel innehaolllande sammansaettningar, och braenslen som innehaoller saodana. Download PDFInfo
- Publication number
- FI76115B FI76115B FI832802A FI832802A FI76115B FI 76115 B FI76115 B FI 76115B FI 832802 A FI832802 A FI 832802A FI 832802 A FI832802 A FI 832802A FI 76115 B FI76115 B FI 76115B
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- carbon atoms
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- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 239000011273 tar residue Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- NBRKLOOSMBRFMH-UHFFFAOYSA-N tert-butyl chloride Chemical compound CC(C)(C)Cl NBRKLOOSMBRFMH-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 125000004853 tetrahydropyridinyl group Chemical group N1(CCCC=C1)* 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical class C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000000101 thioether group Chemical group 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-N trans-cinnamic acid Chemical compound OC(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- HQYCOEXWFMFWLR-UHFFFAOYSA-K vanadium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[V+3] HQYCOEXWFMFWLR-UHFFFAOYSA-K 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
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Claims (10)
1. Komposition, kännetecknad därav, att den i kombination innefattar: (A) en första komponent utvald ur gruppen bestaende av: (i) en oljelöslig etylenskelettpolymer med en numerär medelmolekylvikt inom intervallet cirka 500 till cirka 50 000; (ii) en kolvätesubstituerad fenol med formeln (R*)a-Ar-(0H)b (I) väri R* är en kolvätegrupp utvald ur gruppen bestaende av kolvä-tegrupper av fran cirka 8 till cirka 30 kolatomer och polymerer av minst 30 kolatomer, Ar är en aromatisk enhet med 0 till 4 eventuella substituenter utvalda ur gruppen bestaende av lägre alkyl, lägre alkoxyl, nitro, halo eller kombinationer av tvä el-ler flera av nämnda eventue11a substituenter och a och b varde-ra är oberoende ett helt tai av 1 upp till 5 ganger antalet aromatiska kärnor närvarande i Ar, med det förbehallet att summan av a och b ej överstiger de icke upptagna valenserna i Ar; (iii) blandningar av (i) och (ii); och (B) som en andra komponent reaktionsprodukten av (B)(1) ett kolvätesubstituerat karboxylacyleringsmedel med (BHII) en eller flera aminer, en eller flera alkoholer eller en blandning av en eller flera aminer och/eller en eller flera alkoholer, varvid kolvätesubstituenten av (B)(1) är utvald ur gruppen be-stäende av (i') ett eller flera monoolefiner av fran cirka 8 till cirka 30 kolatomer; (ii1) blandningar av ett eller flera monoolefiner av fran cirka 8 till cirka 30 kolatomer med en eller flera olefin-polymerer av minst 30 kolatomer utvald ur gruppen bestaende av polymerer av mono-l-olefiner med fran 2 till 8 kolatomer eller de klorerade eller bromerade analogerna av sadana polymerer; och (iii1) en eller flera olefinpolymerer av minst 30 kolatomer utvald ur gruppen best&ende av ” 76115 (a) polymerer av monoolefiner med fran cirka 8 till cirka 30 kolatomer; (b) interpolymerer av mono-l-olefiner med fran 2 till 8 kolatomer med monoolefiner med fran cirka 8 till cirka 30 kolatomer; (c) en eller flera blandningar av homopolymerer och/ eller interpolymerer av mono-l-olefiner med fran 2 till 8 kolatomer med homopolymerer och/eller interpolymerer av monoolefiner med fran virka 8 till cirka 30 kolatomer; och (d) klorerade eller bromerade analoger av (a), (b) eller (c) .
2. Komposition enligt patentkravet 1, känneteck-n a d därav, att nämnda acyleringsmedel (B)(1) är härlett fran ett eller flera alfa-beta-olefiniskt omättade karboxyliska rea-gens innehallande 2 till cirka 20 kolatomer utom de karboxyl-baserade grupperna.
3. Komposition enligt patentkravet 2, känneteck- n a d därav, att nämnda karboxyliska reagens är utvalt ur grup-pen bestaende av akrylsyra, metakrylsyra, fumarsyra, maleinsy-ra, lägre alkylestrar av sädana syror, maleinsyraanhydrid och blandningar av tva eller flera av dessa.
4. Komposition enligt patentkravet 1, känneteck-n a d därav, att komponenten (B)(II) innefattar minst en amin karakteriserad av närvaron i sin struktur av minst en grupp H-N .
5. Komposition enligt patentkravet 1, känneteck-n a d därav, att komponenten (B)(II) är utvald ur gruppen bestaende av (a) primära, sekundära och tertiMra alkanolaminer som kan representeräs med formlerna: 78 761 1 5 H ^ N - R' - OH H ^ - R' - OH R^ R ^ - R' - OH R^ (b) hydroxylsubstituerade oxialkylenanaloger av nämnda alkanol-aminer representerade med formlerna: H\ >——H H' H\ -*'0*2=15-H R' R\ N-eR,Q)2-i5-H R' väri varje R oberoende är en kolvätegrupp med en tili cirka 8 kolatomer eller hydroxylsubstituerad kolvätegrupp med 2 tili cirka 8 kolatomer och R* är en tvävärd kolvätegrupp med 2 tili cirka 18 kolatomer, och (c) blandningar av tv! eller flera därav.
6. Komposition enligt patentkravet 1, känne t e c k - n a d därav, att komponenten (A)(i) är en homopolymer eller in-terpolymer av en etyleniskt omättad alkylester med £ormeln: T --f r2 r3 väri Ri äv väte eller Ci-Cg-kolväte; R2 är en --OOCR4- eller -C00R4~grupp; R3 är väte eller -COOR4; och R4 är väte eller en Ci~ tili C3o-alkylgrupp.
7. Komposition enligt patentkravet 1, känne teck-
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US06/404,845 US4564460A (en) | 1982-08-09 | 1982-08-09 | Hydrocarbyl-substituted carboxylic acylating agent derivative containing combinations, and fuels containing same |
US40484582 | 1982-08-09 |
Publications (4)
Publication Number | Publication Date |
---|---|
FI832802A0 FI832802A0 (fi) | 1983-08-03 |
FI832802A FI832802A (fi) | 1984-02-10 |
FI76115B true FI76115B (fi) | 1988-05-31 |
FI76115C FI76115C (sv) | 1988-09-09 |
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ID=23601284
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI832802A FI76115C (sv) | 1982-08-09 | 1983-08-03 | Derivat av med hydrokarbyl substituerat, karboxylacylerande medel inne hållande sammansättningar, och bränslen som innehåller sådana |
Country Status (11)
Country | Link |
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US (1) | US4564460A (sv) |
BE (1) | BE897486A (sv) |
CA (1) | CA1212835A (sv) |
DE (1) | DE3328739C2 (sv) |
DK (1) | DK164791C (sv) |
FI (1) | FI76115C (sv) |
FR (1) | FR2531448B1 (sv) |
IN (1) | IN161461B (sv) |
NL (1) | NL190787C (sv) |
NO (1) | NO174512B (sv) |
SE (1) | SE459814B (sv) |
Families Citing this family (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4569679A (en) * | 1984-03-12 | 1986-02-11 | Exxon Research & Engineering Co. | Additive concentrates for distillate fuels |
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US4724091A (en) * | 1983-03-31 | 1988-02-09 | The Lubrizol Corporation | Alkyl phenol and amino phenol compositions and two-cycle engine oils and fuels containing same |
-
1982
- 1982-08-09 US US06/404,845 patent/US4564460A/en not_active Expired - Lifetime
-
1983
- 1983-07-29 NL NL8302704A patent/NL190787C/xx not_active IP Right Cessation
- 1983-08-03 FI FI832802A patent/FI76115C/sv not_active IP Right Cessation
- 1983-08-05 NO NO832825A patent/NO174512B/no unknown
- 1983-08-08 SE SE8304318A patent/SE459814B/sv not_active IP Right Cessation
- 1983-08-08 BE BE0/211320A patent/BE897486A/fr not_active IP Right Cessation
- 1983-08-08 IN IN988/CAL/83A patent/IN161461B/en unknown
- 1983-08-08 DK DK361283A patent/DK164791C/da active
- 1983-08-08 CA CA000434074A patent/CA1212835A/en not_active Expired
- 1983-08-09 FR FR8313082A patent/FR2531448B1/fr not_active Expired
- 1983-08-09 DE DE3328739A patent/DE3328739C2/de not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
FR2531448B1 (fr) | 1987-02-27 |
IN161461B (sv) | 1987-12-12 |
DE3328739A1 (de) | 1984-02-09 |
CA1212835A (en) | 1986-10-21 |
FI76115C (sv) | 1988-09-09 |
SE8304318L (sv) | 1984-02-10 |
NO174512C (sv) | 1994-05-18 |
DK164791B (da) | 1992-08-17 |
SE459814B (sv) | 1989-08-07 |
US4564460A (en) | 1986-01-14 |
DE3328739C2 (de) | 1996-03-28 |
NO174512B (no) | 1994-02-07 |
FI832802A (fi) | 1984-02-10 |
SE8304318D0 (sv) | 1983-08-08 |
DK361283A (da) | 1984-02-10 |
BE897486A (fr) | 1984-02-08 |
NL8302704A (nl) | 1984-03-01 |
NO832825L (no) | 1984-02-10 |
DK164791C (da) | 1993-01-04 |
NL190787B (nl) | 1994-03-16 |
FI832802A0 (fi) | 1983-08-03 |
FR2531448A1 (fr) | 1984-02-10 |
NL190787C (nl) | 1994-08-16 |
DK361283D0 (da) | 1983-08-08 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM | Patent lapsed | ||
MM | Patent lapsed |
Owner name: THE LUBRIZOL CORPORATION |