SU298206A1 - METHOD OF OBTAINING MULTIFUNCTIONAL FITTINGS - Google Patents
METHOD OF OBTAINING MULTIFUNCTIONAL FITTINGSInfo
- Publication number
- SU298206A1 SU298206A1 SU1241927A SU1241927A SU298206A1 SU 298206 A1 SU298206 A1 SU 298206A1 SU 1241927 A SU1241927 A SU 1241927A SU 1241927 A SU1241927 A SU 1241927A SU 298206 A1 SU298206 A1 SU 298206A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- fittings
- xylene
- obtaining multifunctional
- additive
- stirring
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 7
- 239000000654 additive Substances 0.000 description 7
- 239000008096 xylene Substances 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 239000003921 oil Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- PCSMJKASWLYICJ-UHFFFAOYSA-N Succinic aldehyde Chemical compound O=CCCC=O PCSMJKASWLYICJ-UHFFFAOYSA-N 0.000 description 1
- SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical compound NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/086—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type polycarboxylic, e.g. maleic acid
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/022—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
Изобретение относитс к способам получейи присадок к маслам, в частности сукцииимидных присадок.The invention relates to methods for producing additives for oils, in particular succinamide additives.
Известен способ получени присадки к маслам путем взаимодействи полимера, например полиолефина (мол. вес 300-3000), с малеиновым ангидридом в присутствии перекиси бензоила с последующим взаимодействием полученного сукцинангидрида с полиамином . Однако присадка, полученна этим способом, недостаточно эффективна.A known method for producing an additive to oils by reacting a polymer, such as a polyolefin (mol. Weight 300-3000), with maleic anhydride in the presence of benzoyl peroxide followed by reacting the resulting succinic anhydride with a polyamine. However, the additive obtained in this way is not sufficiently effective.
C-b- CH7-CH4-f H N- -CHsCHoNH-bHI XУ 1д-пC-b-CH7-CH4-f H N- -CHsCHoNH-bHI XY 1d-p
СН-СН,CH-CH,
с,with,
С целью повышени эффективности присадки , предлагаетс использовать в качестве исходного полимера полимер с мол. весом 6000-200000.In order to increase the effectiveness of the additive, it is proposed to use a polymer with mol. weighing 6000-200000.
Реакцию в зависимости от в зкОСти среды « примен емого инициатора провод т в растворителе или без растворител при температурах от 50 до 250°С (преимущественно в преде ..1е температур 100-200°С).The reaction, depending on the viscosity of the medium "used initiator, is carried out in a solvent or without a solvent at temperatures from 50 to 250 ° C (mainly in the range of 100-200 ° C).
Реакци получени сукцинимидов протекает по схеме:The reaction of obtaining succinimides proceeds according to the scheme:
RRRR
-ffCHo-C-b-tCH.-CH L --ffCHo-C-b-tCH.-CH L -
СН-СН7CH-CH7
T 4CH7-CH-2NH- HT 4CH7-CH-2NH- H
Пример 1. В трехтубусную колбу о.бъемом 0,5 л, снабженную мешалкой, обратным холодильником и термометром, загрулсают 100 г атактического полипропилена (мол. вес ), 10 г ыалеипового ангидрида, 200 мл ксилола и 3 г перекиси бензоила. Смесь при перемешивании нагревают до кипени (140°С). Затем при перемешивапип кии т т в течеиие 5 час. После этого ксилол отгон ют при атмосферном давлеиии до температуры в парах 150°С. Затем постепенно создают вакуум (до 15 мм рт. ст.) и отгоп ют не вступивший в реакцию малеииовый ангидрид. После этого выдерживают ири 150°С и 15 мм рт. ст. в течение 0,5 час, ИК-сиектр полученного продукта доказывает, что IB нем содержатс сукцинангидридные ripynnH. Содержание их, рассчитанное на основании элементарного анализа и числа омылени , составл ет 8,8 вес. %. П р и м е р 2. В трехтубусную колбу объемом 2 л, еиабженпую мешалкой, обратным холодильником и капельной вороикой загружают 750 г расплавленпого атактического полиироиилена (мол. вес 10000), 500 мл ксилола и 40 г малеинового ангидрида. В капельную воронку заливают раствор 7,5 г перекиси бепзоила в 100 мл ксилола. Смесь при перемешивании н.агревают до кипеии и подают по капл м раствор перекиси бепзоила в течение 2 час. Затем при атмосферпом давлении отгоп ют ксилол до температуры в парах 150°С, и иостеиеипо снижают давление до 100 мм рт. ст., отгон от остатки ксилола и не вступивший в реакцию малеииовый ангидрид. Затем давление сиижают до 10-15 мм рт. ст. и поднимают темиературу до 200°С. При этих услови х отгоику ведут в течение 1 час. Содержаппе суикцинангидридных груип в полученном полимере 4,1 вес. %. П р и м е р 3. Реакцию провод т в трехтубуспой колбе объемом 2 л, снабженной обратным холодильником с ловушкой Дина-Старка, мешалкой и капельной воронкой. Довод т смесь до кииени и подают при перемешивании полиэтилепполиамип с такой скоростью, чтобы не происходило слишком сильное вспеиивание . Затем кии т т еще 1 час. В течение этого времени выдел етс около 3 мл воды ( теоретическое количество 3,5 мл). После этого отгон ют ксилол при атмосферном давлении до температуры в иарах 150°С. Далее постепенно снижают давленпе до 200 мм рт. ст. и довод т темиературу до 200°С. При этих услови х выдерживают 0,5 час. Затем остаточное давление довод т до 15 мм рт. ст. и выдерживают еще 0,5 час, иосле чего охлаждают в вакууме до 150°С и добавл ют ири перемешивании еще 510 г веретенного масла «АУ. Содержание азота в присадке 1,8%. Полученна присадка представл ет собой 50%-ный раствор иолииропиленсукцинимида в масле. Данные, представленные в таблице, показывают эффективиость получеииой ирисадки.Example 1. A three-liter flask with a volume of 0.5 l equipped with a stirrer, a reflux condenser and a thermometer was charged with 100 g of atactic polypropylene (mol. Weight), 10 g of type anhydride, 200 ml of xylene and 3 g of benzoyl peroxide. The mixture is heated to boiling with stirring (140 ° C). Then, with stirring, the cues are t for 5 hours. After that, xylene is distilled off at atmospheric pressure to a vapor temperature of 150 ° C. Then, a vacuum is gradually created (up to 15 mmHg) and the unreacted maleium anhydride is prepared. After that, stand iri 150 ° C and 15 mm Hg. Art. for 0.5 hours, the infrared spectrum of the product obtained proves that IB contains succinic hydride ripynnH. Their content, calculated on the basis of the elementary analysis and the saponification number, is 8.8 wt. % EXAMPLE 2 A three liter flask with a volume of 2 liters, equipped with a stirrer, a reflux condenser and a droplet tube, was charged with 750 g of melted atactic polyyroylene (mol. Weight 10,000), 500 ml of xylene and 40 g of maleic anhydride. A solution of 7.5 g of bepzoyl peroxide in 100 ml of xylene is poured into the dropping funnel. The mixture, while stirring, heated to boiling and a solution of bepsoyl peroxide was added dropwise for 2 hours. Then, at atmospheric pressure, xylene is heated to a vapor temperature of 150 ° C, and the pressure is reduced to 100 mm Hg. Art., distilled from xylene residues and unreacted maleic anhydride. Then the pressure shine up to 10-15 mm Hg. Art. and raise the temperature to 200 ° C. Under these conditions, the offal is maintained for 1 hour. Content suiccinium hydride in the resulting polymer is 4.1 wt. % PRI me R 3. The reaction was carried out in a 2 l three-flask flask equipped with a reflux condenser with a Dean-Stark trap, a stirrer and an addition funnel. Bring the mixture to a kiyena and serve, with stirring, polyelelectrolipes at such a rate that there is no excessive melting. Then cues t another 1 hour. During this time, about 3 ml of water is released (theoretical amount is 3.5 ml). After that, xylene is distilled at atmospheric pressure to a temperature in the vapors of 150 ° C. Then gradually reduce pressure to 200 mm Hg. Art. and adjusted to 200 ° C. Under these conditions, it is kept for 0.5 hour. Then the residual pressure is adjusted to 15 mm Hg. Art. and incubated for another 0.5 hour, and then cooled in vacuum to 150 ° C, and another 510 g of spun “AU” oil was added under stirring. The nitrogen content in the additive is 1.8%. The resulting additive is a 50% solution of iothiropylenesuccinimide in oil. The data presented in the table show the effectiveness of the obtained iris.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU1241927A SU298206A1 (en) | 1968-05-20 | 1968-05-20 | METHOD OF OBTAINING MULTIFUNCTIONAL FITTINGS |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU1241927A SU298206A1 (en) | 1968-05-20 | 1968-05-20 | METHOD OF OBTAINING MULTIFUNCTIONAL FITTINGS |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU298206A1 true SU298206A1 (en) | 1973-09-17 |
Family
ID=20442507
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1241927A SU298206A1 (en) | 1968-05-20 | 1968-05-20 | METHOD OF OBTAINING MULTIFUNCTIONAL FITTINGS |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU298206A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0490454A1 (en) * | 1990-12-12 | 1992-06-17 | Shell Internationale Researchmaatschappij B.V. | Alkenyl succinimides as luboil additives |
-
1968
- 1968-05-20 SU SU1241927A patent/SU298206A1/en active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0490454A1 (en) * | 1990-12-12 | 1992-06-17 | Shell Internationale Researchmaatschappij B.V. | Alkenyl succinimides as luboil additives |
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