PL429845A1 - Kompozycja biobójczo - stabilizująca do biopaliw - Google Patents
Kompozycja biobójczo - stabilizująca do biopaliwInfo
- Publication number
- PL429845A1 PL429845A1 PL429845A PL42984519A PL429845A1 PL 429845 A1 PL429845 A1 PL 429845A1 PL 429845 A PL429845 A PL 429845A PL 42984519 A PL42984519 A PL 42984519A PL 429845 A1 PL429845 A1 PL 429845A1
- Authority
- PL
- Poland
- Prior art keywords
- tert
- bis
- butylphenol
- butyl
- methylene
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 5
- 230000003115 biocidal effect Effects 0.000 title abstract 2
- 239000002551 biofuel Substances 0.000 title abstract 2
- 230000000087 stabilizing effect Effects 0.000 title 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 6
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 abstract 2
- BVUXDWXKPROUDO-UHFFFAOYSA-N 2,6-di-tert-butyl-4-ethylphenol Chemical compound CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BVUXDWXKPROUDO-UHFFFAOYSA-N 0.000 abstract 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 abstract 2
- 239000003139 biocide Substances 0.000 abstract 2
- 239000006184 cosolvent Substances 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 2
- KMBPCQSCMCEPMU-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-methylpropane-1,3-diamine Chemical compound NCCCN(C)CCCN KMBPCQSCMCEPMU-UHFFFAOYSA-N 0.000 abstract 2
- 230000003647 oxidation Effects 0.000 abstract 2
- 238000007254 oxidation reaction Methods 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- 239000004094 surface-active agent Substances 0.000 abstract 2
- LQPOOAJESJYDLS-UHFFFAOYSA-N 1,3-oxazinane Chemical compound C1CNCOC1 LQPOOAJESJYDLS-UHFFFAOYSA-N 0.000 abstract 1
- PFEFOYRSMXVNEL-UHFFFAOYSA-N 2,4,6-tritert-butylphenol Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 PFEFOYRSMXVNEL-UHFFFAOYSA-N 0.000 abstract 1
- ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 abstract 1
- OPLCSTZDXXUYDU-UHFFFAOYSA-N 2,4-dimethyl-6-tert-butylphenol Chemical compound CC1=CC(C)=C(O)C(C(C)(C)C)=C1 OPLCSTZDXXUYDU-UHFFFAOYSA-N 0.000 abstract 1
- LXWZXEJDKYWBOW-UHFFFAOYSA-N 2,4-ditert-butyl-6-[(3,5-ditert-butyl-2-hydroxyphenyl)methyl]phenol Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)C)C(C)(C)C)O)=C1O LXWZXEJDKYWBOW-UHFFFAOYSA-N 0.000 abstract 1
- JZODKRWQWUWGCD-UHFFFAOYSA-N 2,5-di-tert-butylbenzene-1,4-diol Chemical compound CC(C)(C)C1=CC(O)=C(C(C)(C)C)C=C1O JZODKRWQWUWGCD-UHFFFAOYSA-N 0.000 abstract 1
- JFGVTUJBHHZRAB-UHFFFAOYSA-N 2,6-Di-tert-butyl-1,4-benzenediol Chemical compound CC(C)(C)C1=CC(O)=CC(C(C)(C)C)=C1O JFGVTUJBHHZRAB-UHFFFAOYSA-N 0.000 abstract 1
- SLUKQUGVTITNSY-UHFFFAOYSA-N 2,6-di-tert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SLUKQUGVTITNSY-UHFFFAOYSA-N 0.000 abstract 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 abstract 1
- JBYWTKPHBLYYFJ-UHFFFAOYSA-N 2,6-ditert-butyl-4-(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 JBYWTKPHBLYYFJ-UHFFFAOYSA-N 0.000 abstract 1
- NKRVGWFEFKCZAP-UHFFFAOYSA-N 2-ethylhexyl nitrate Chemical compound CCCCC(CC)CO[N+]([O-])=O NKRVGWFEFKCZAP-UHFFFAOYSA-N 0.000 abstract 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 abstract 1
- 229940044119 2-tert-butylhydroquinone Drugs 0.000 abstract 1
- GJBKLYJVZOTRSP-UHFFFAOYSA-N 3-(1,3-oxazinan-3-ylmethyl)-1,3-oxazinane Chemical compound C1CCOCN1CN1CCCOC1 GJBKLYJVZOTRSP-UHFFFAOYSA-N 0.000 abstract 1
- GUQMDNQYMMRJPY-UHFFFAOYSA-N 4,4-dimethyl-1,3-oxazolidine Chemical compound CC1(C)COCN1 GUQMDNQYMMRJPY-UHFFFAOYSA-N 0.000 abstract 1
- MIFZZKZNMWTHJK-UHFFFAOYSA-N 4-(morpholin-4-ylmethyl)morpholine Chemical compound C1COCCN1CN1CCOCC1 MIFZZKZNMWTHJK-UHFFFAOYSA-N 0.000 abstract 1
- KJWMCPYEODZESQ-UHFFFAOYSA-N 4-Dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C=C1 KJWMCPYEODZESQ-UHFFFAOYSA-N 0.000 abstract 1
- WTWGHNZAQVTLSQ-UHFFFAOYSA-N 4-butyl-2,6-ditert-butylphenol Chemical compound CCCCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 WTWGHNZAQVTLSQ-UHFFFAOYSA-N 0.000 abstract 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 abstract 1
- BNKGKERDFRIJPU-UHFFFAOYSA-N 5-methyl-3-[(5-methyl-1,3-oxazolidin-3-yl)methyl]-1,3-oxazolidine Chemical compound C1OC(C)CN1CN1CC(C)OC1 BNKGKERDFRIJPU-UHFFFAOYSA-N 0.000 abstract 1
- ZRCMGIXRGFOXNT-UHFFFAOYSA-N 7a-ethyl-1,3,5,7-tetrahydro-[1,3]oxazolo[3,4-c][1,3]oxazole Chemical compound C1OCN2COCC21CC ZRCMGIXRGFOXNT-UHFFFAOYSA-N 0.000 abstract 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- -1 alkylated bis-phenols hydroquinones Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 235000019387 fatty acid methyl ester Nutrition 0.000 abstract 1
- 125000000160 oxazolidinyl group Chemical group 0.000 abstract 1
- 239000003208 petroleum Substances 0.000 abstract 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Przedmiotem wynalazku jest kompozycja biobójczo - stabilizująca do biopaliw, zwłaszcza do estrów metylowych kwasów tłuszczowych, zawierająca surfaktant, związek wybrany spośród biocydów, w tym zawierających grupy oksazolidynowe, rozpuszczalnik węglowodorowy, współrozpuszczalnik i inhibitor utleniania wybrany z grupy obejmującej alkilowane monofenole, alkilowane bis-fenole alkilowane hydrochinony, która charakteryzuje się tym, że zawiera, w przeliczeniu na całkowitą masę kompozycji: - od 5,0(m/m) do 10,0%(m/m) surfaktanta, będącego adduktem 4-nonylofenolu z N,N-bis(3-aminopropylo)metyloaminą i formaldehydem w stosunku molowym 2:1:2 lub adduktem 4-dodecylofenolu z N,N-bis(3-aminopropylo)metyloaminą i formaldehydem w stosunku molowym 2:1:2 lub mieszaniną tych adduktów w proporcji masowej 4:1 do 1:4; - od 5,0(m/m) do 10,0%(m/m) biocydu wybranego z grupy obejmującej 4,4-dimetylo-1,3-oksazolidynę, 3,3'-metyleno-bis(5-metylo-1,3-oksazolidynę), 7-etylo-bicyklooksazolidynę, tetrahydro-1,3-oksazynę, 3,3'-metyleno-bis(tetrahydro-2H-1,3-oksazynę), N,N'-metyleno-bis-morfolinę; - od 20,0%(m/m) do 30,0%(m/m) rozpuszczalnika węglowodorowego, którym jest aromatyczna frakcja naftowa o zakresie wrzenia od 150°C do 300°C, o ilości atomów węgla w cząsteczkach co najmniej 9, z grupami alkilowymi prostołańcuchowymi i/lub rozgałęzionymi; - od 3,0%(m/m) do 20,0%(m/m) współrozpuszczalnika, którym jest mieszanina butanolu alkoksylowanego tlenkiem etylenu z azotanem 2-etyloheksylu zmieszanych w stosunku masowym w zakresie od 1:10 do 100:1; - od 5,0%(m/m) do 30,0%(m/m) inhibitora utleniania wybranego z grupy obejmującej 2-tert-butylofenol, 4-tertbutylofenol, 2,6-ditert-butylofenol, 2,4-ditert-butylofenol, 2-tert-butylo-4,6-dimetylofenol, 2,6-ditert-butylo-4-etylofenol, 2,6-ditert-butylo-4-metylofenol, 2,6-ditert-butylo-4-butylofenol, 2,6-ditert-butylo-4-izobutylofenol, 2,4,6-tritert-butylofenol, 2,6-ditert-butylo-4-metoksyfenol, 2,2'-metyleno-bis(6-tert-butylo-4-metylofenol), 2,2'-metyleno-bis(4,6-ditert-butylofenol), 2-tert-butylohydrochinon, 2,5-ditert-butylohydrochinon, 2,6-ditert-butylohydrochinon.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL429845A PL237018B1 (pl) | 2019-05-06 | 2019-05-06 | Kompozycja biobójczo - stabilizująca do biopaliw |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL429845A PL237018B1 (pl) | 2019-05-06 | 2019-05-06 | Kompozycja biobójczo - stabilizująca do biopaliw |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL429845A1 true PL429845A1 (pl) | 2020-11-16 |
| PL237018B1 PL237018B1 (pl) | 2021-03-08 |
Family
ID=73196998
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL429845A PL237018B1 (pl) | 2019-05-06 | 2019-05-06 | Kompozycja biobójczo - stabilizująca do biopaliw |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL237018B1 (pl) |
-
2019
- 2019-05-06 PL PL429845A patent/PL237018B1/pl unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PL237018B1 (pl) | 2021-03-08 |
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