CN1364860A - Clean disperser for lubricating oil - Google Patents
Clean disperser for lubricating oil Download PDFInfo
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- CN1364860A CN1364860A CN 01102235 CN01102235A CN1364860A CN 1364860 A CN1364860 A CN 1364860A CN 01102235 CN01102235 CN 01102235 CN 01102235 A CN01102235 A CN 01102235A CN 1364860 A CN1364860 A CN 1364860A
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- aldehyde
- described detergent
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Abstract
The clean disperser for lubricating oil is prepared through the following steps: adding aldehyde into the mixture of methoxyphenol and polyene polyamine, heating to 120-200 deg.c for dewatering reaction of 1-8 hr and collecting condensated polyamine with the molar ratio of penol, amine and aldehyde being 1 to 0.l5-2.5 to 2-5; mixing the condensation compound of hydroxyl capped epoxy compound and polyalkenyl succinic acid (anhydride)in the molar ratio of 0.1-0.4:1 and dewatering reaction at 100-180 deg.c for 2-8 hr; and mixing the product of the foregoing steps in the molar ratio of 1:01-0.5, reaction at 90-180 deg.c for 2-8 hr and collecting the product. The clean disperser for lubricating oil of the present invention has better cleaning performance than available ones.
Description
The present invention relates to be used for the detergent-dispersant additive of I. C. engine oil.
Along with the raising day by day of environmental protection and energy-conservation requirement, each engine manufacturer constantly dwindles size of engine, increases compression ratio, improves the service temperature of engine.Particularly the apical ring groove temperature of high-power diesel engine will be brought up to 310 ℃ by 270 ℃, and this antioxidant property and cleansing performance to I. C. engine oil and oil fuel is had higher requirement.In addition, because the use of particulate matter trap, palpus reduces the ash of oil product, and the detergency under the low ash of oil product is also had higher requirement.Dispersion agent special consumption in lubricating oil in oil product is very big, and the antioxygen and the cleansing performance that therefore improve dispersion agent become this area main research work.The antioxygen that improves dispersion agent can be by introducing different antioxygen functional groups in the structure of dispersion agent, used antioxygen functional group is based on phenols.Improve the cleansing performance of dispersion agent and then can introduce different ester functional groups.
For example, US 5182038 has reported a kind of succimide dispersion agent that generates with nonyl phenol coupling amide group.US 4636322, US 4699724, US 4713189 disclosed dispersion agents are to be prepared from by the coupling succimide by phenol, bisphenol-A, Resorcinol, single nonyl phenol and 2-Naphthol.CN 1169464A discloses a kind of link coupled succimide dispersion agent, is by a kind of phenol in Resorcinol, pyrocatechol and the p-cresol or its mixture the coupling of succimide dispersion agent to be formed.EP 253,668 discloses a kind of succinate dispersion agent based on polyethers, is to be made by polyvinyl ether and Succinic anhydried reaction.
The purpose of this invention is to provide a kind of polyfunctional group detergent-dispersant additive with good detergency.
Detergent-dispersant additive of the present invention is to be made by the reaction of the condenses of polyamines polyene, methoxyphenol, aldehyde, alkenyl succinic acid and epoxy compounds, and its preparation method may further comprise the steps:
1) add aldehyde in the mixture of methoxyphenol and polyamines polyene, be warming up to 120～200 ℃ of dehydration reactions 1～8 hour, collect amine condensation, wherein the mol ratio of phenol, amine, aldehyde is 1: 0.5～2.5: 2～5;
2) with the condenses of the epoxy compounds of hydroxyl end socket and polyolefin-based Succinic Acid (acid anhydride) according to 0.1～0.4: 1 mixed in molar ratio, 100～180 ℃ of dehydration reactions 2～8 hours;
3) in step 2) product in add amine condensation according to 1: 0.1～0.5 mol ratio, 90～180 ℃ of reactions 2～8 hours, collect product.
Specifically, detergent-dispersant additive provided by the invention can prepare in accordance with the following methods:
1) with methoxyphenol and polyamines polyene according to 1: 0.5～2.5, preferred 1: 1～2 mixed in molar ratio drips 2～5 times of phenol mole numbers under nitrogen protection; preferred 2.5～3.5 times aldehyde; for the ease of mixing, can suitably be warming up to 50～100 ℃, and fully stir 0.5～4 hour; elevated temperature to 120～200 ℃ then; preferred 130～180 ℃, reacted preferred 2～5 hours 1～8 hour; stripping water and unreacted aldehyde promptly obtain amine condensation.
2) with the condenses of the epoxy compounds of hydroxyl end socket and polyolefin-based Succinic Acid (acid anhydride) according to 0.1～0.6: 1, preferred 0.2～0.4: 1 mixed in molar ratio, can suitably be heated to 50～100 ℃ and also fully stir 0.5～4 hour so that mix, at 100～180 ℃, preferred 125～145 ℃ of dehydration reactions 2～10 hours, preferred 2～6 hours, obtain intermediate product.
3) in above-mentioned intermediate product according to 1: 0.1～0.5, preferred 1: 0.2～0.3 mol ratio adds amine condensation (mole number of amine condensation calculates with amine wherein), at 90～180 ℃, preferred 100～150 ℃ of reactions 2～8 hours, preferred 4～6 hours, promptly obtain detergent-dispersant additive of the present invention after filtration.
Said polyamines polyene is meant to have H
2N[(CH
2)
nNH]
mThe amine of H general formula, wherein n is 2～4 integer, m is 1～5 integer.As quadrol, diethylenetriamine, triethylene tetramine, tetraethylene pentamine, five ethene hexamines, propylene diamine, two propylene triamines, three propylene tetramines, tetrapropylene five amine, five propylene hexamines etc., preferred triethylene tetramine, tetraethylene pentamine and five ethene hexamines.
Said phenol is a kind of or its mixture in p methoxy phenol, hydroxyanisole and the meta-methoxy phenol.
The condenses of the epoxy compounds of said hydroxyl end socket, the condenses of optimization ethylene oxide, propylene oxide and butylene oxide ring, or the condenses of two or more epoxy compoundss wherein, number-average molecular weight Mn can be 100～3000, preferred 200～2200.
The polyolefin-based C that comes from the said polyolefin-based Succinic Acid (acid anhydride)
3～C
4The multipolymer of monoolefine or homopolymer can be polyisobutene, Atactic Polypropelene, ethylene-propylene copolymer.Its number-average molecular weight Mn=850～5000 are preferably 950～2500.
Said aldehyde can be formaldehyde, acetaldehyde, propionic aldehyde, butyraldehyde, salicylic aldehyde or phenyl aldehyde, or the polymer of above-mentioned aldehyde or the aqueous solution, preferred formaldehyde, Paraformaldehyde 96 and salicylic aldehyde.The adding mode of aldehyde preferably drips.
Clean disperser for lubricating oil provided by the invention is compared existing detergent-dispersant additive and is had better cleansing performance.
The invention will be further described below by example.
Example 1
This example is the preparation of amine condensation.
In the there-necked flask of 250ml, add 75g (0.4mol) tetraethylene pentamine (TEPA); 21.4g (0.17mol) p methoxy phenol; under nitrogen protection, rise to 70 ℃; drip 44g formaldehyde (0.53mol) aqueous solution (containing 36% formaldehyde); 0.5 hour add; stir and made the material thorough mixing in 2 hours, rise to 130 ℃ of reactions 3 hours, get amine condensation AN
1102g.
Example 2
This example is the preparation of amine condensation.
Add 75g (0.4mol) tetraethylene pentamine (TEPA) in the 250ml there-necked flask, 32.8g (0.26mol) p methoxy phenol rises to 80 ℃ under nitrogen protection, drips salicylic aldehyde 65g (0.53mol), adds in 0.5 hour.Stir and made the material thorough mixing in 2 hours, rise to 180 ℃ of reactions 3 hours, get amine condensation AN
2163g.
Example 3
In the 250ml there-necked flask, add 100g polyisobutenyl succinic anhydride (the soap valency is 50mgKOH/g, contains 40%150SN neutral oil, and the polyisobutene number-average molecular weight is 1300, and specialty oil products factory in Suzhou produces), behind the nitrogen replacement, rise to 70 ℃, stir.Add 2.6g (0.011mol) five glycol (propylene oxide condenses, molecular weight 238), stirred 1 hour, rise to 120 ℃, dehydration reaction is cooled to 80 ℃ after 3 hours, obtain intermediate product XN
1, add 2.9g example 1 gained amine condensation AN
1, added in 1 hour, stir, rise to 130 ℃, dehydration reaction gets product E N after 3 hours
1
Example 4
(the soap valency is 50mgKOH/g to add the 100g polyisobutenyl succinic anhydride in the 250ml there-necked flask, contain 40%150SN, the polyisobutene number-average molecular weight is 1300, Suzhou specialty oil products factory produces) and 17.5g150SN neutral oil (Dalian Petrochemical Industry Company's production), behind the nitrogen replacement, rise to 80 ℃, stir.Add 9g polyethers L31 (chemical plant, Lvshun produces for the condenses of oxyethane and propylene oxide, molecular weight Mn=1000) again, added in 2 hours, rise to 135 ℃, dehydration reaction was cooled to 85 ℃ in 5 hours, added 3.5g example 2 gained amine condensation AN
2, obtain intermediate product XN
2, adding in 1 hour, restir rises to 110 ℃ after 1 hour, and dehydration reaction 3 hours gets product E N after the filtration
2
Example 5
After in the 250ml there-necked flask, adding 91g polyisobutenyl succinic anhydride (the soap valency is 50.mgKOH/g, contains 40%150SN, and the polyisobutene number-average molecular weight is 1300, and specialty oil products factory in Suzhou produces) nitrogen replacement, rise to 70 ℃, stir.Add 9g polyethers L31 (chemical plant, Lvshun produces, molecular weight Mn=1000) again, added in 2 hours, rise to 135 ℃, dehydration reaction was cooled to 85 ℃ in 5 hours, obtained intermediate product XN
2, add 1.6g amine condensation AN
1, added in 1 hour, stirred 1 hour, rise to 100 ℃ after stirring, dehydration reaction 3 hours gets product E N after the filtration
3
Comparative Examples 1
Contrast with traditional esteramides class dispersion agent LZ6401 (production of Lubrizol company).
Comparative Examples 2
Contrast with traditional succimide dispersion agent OLOA1200 (production of Chevron company).
Example 6
This example is that detergent-dispersant performance can be evaluated.The gained dispersion agent is joined in the non-dispersant 10W30 SF/CC oil by 2.5% weight ratio, carry out coke test by the SH/T0300-92 method, it the results are shown in Table 1.
Table 1
| Numbering | The sample title | Burnt heavy, mg |
| Example 3 | ????EN 1 | ????15.8 |
| Example 4 | ????EN 2 | ????13.8 |
| Example 5 | ????EN 3 | ????11.5 |
| Comparative Examples 1 | ????LZ6401 | ????16.4 |
| Comparative Examples 2 | ????OLOA1200 | ????24.7 |
The result shows in the table, and the heavy dispersion agent less than prior art of Jiao of detergent-dispersant additive provided by the invention has the good high-temperature cleansing performance.
Claims (14)
1. clean disperser for lubricating oil, its preparation method may further comprise the steps:
1) add aldehyde in the mixture of methoxyphenol and polyamines polyene, be warming up to 120～200 ℃ of dehydration reactions 1～8 hour, collect amine condensation, wherein the mol ratio of phenol, amine, aldehyde is 1: 0.5～2.5: 2～5;
2) with the condenses of the epoxy compounds of hydroxyl end socket and polyolefin-based Succinic Acid (acid anhydride) according to 0.1～0.4: 1 mixed in molar ratio, 100～180 ℃ of dehydration reactions 2～8 hours;
3) in step 2) product in add amine condensation according to 1: 0.1～0.5 mol ratio, 90～180 ℃ of reactions 2～8 hours, collect product.
2. according to the described detergent-dispersant additive of claim 1, it is characterized in that 1) in the step, the mol ratio of phenol, amine, aldehyde is 1: 1～2: 2.5～3.5,130～180 ℃ of temperature of reaction, 2～5 hours reaction times.
3. according to the described detergent-dispersant additive of claim 1, it is characterized in that 2) in the step, the mol ratio of the condenses of the epoxy compounds of hydroxyl end socket and polyolefin-based Succinic Acid (acid anhydride) is 0.2～0.4: 1,125～145 ℃ of temperature of reaction, 2～6 hours reaction times.
4. according to the described detergent-dispersant additive of claim 1, it is characterized in that 3) in the step, in step 2) product in add amine condensation, 100～150 ℃ of temperature of reaction, 4～6 hours reaction times according to 1: 0.2～0.3 mol ratio.
5. according to the described detergent-dispersant additive of claim 1, it is characterized in that said polyamines polyene is selected from has H
2N[(CH
2)
nNH]
mThe compound of H general formula, wherein n is 2～4 integer, m is 1～5 integer.
6. according to claim 1 or 5 described detergent-dispersant additives, it is characterized in that said polyamines polyene is selected from quadrol, diethylenetriamine, triethylene tetramine, tetraethylene pentamine, five ethene hexamines, propylene diamine, two propylene triamines, three propylene tetramines, tetrapropylene five amine, five propylene hexamines.
7. according to the described detergent-dispersant additive of claim 6, it is characterized in that said polyamines polyene is selected from triethylene tetramine, tetraethylene pentamine and five ethene hexamines.
8. according to the described detergent-dispersant additive of claim 1, it is characterized in that said phenol is a kind of or its mixture in p methoxy phenol, hydroxyanisole and the meta-methoxy phenol.
9. according to the described detergent-dispersant additive of claim 1, it is characterized in that the condenses of the epoxy compounds of said hydroxyl end socket is selected from the condenses of oxyethane, propylene oxide and butylene oxide ring, or the condenses of two or more epoxy compoundss wherein.
10. according to the described detergent-dispersant additive of claim 1, it is characterized in that the number-average molecular weight of the condenses of the epoxy compounds of said hydroxyl end socket is 100～3000.
11., it is characterized in that the polyolefin-based C that comes from the said polyolefin-based Succinic Acid (acid anhydride) according to the described detergent-dispersant additive of claim 1
3～C
4The multipolymer of monoolefine or homopolymer, its number-average molecular weight are 850～5000.
12., it is characterized in that said aldehyde is selected from formaldehyde, acetaldehyde, propionic aldehyde, butyraldehyde, salicylic aldehyde and phenyl aldehyde according to the described detergent-dispersant additive of claim 1, or the polymer of above-mentioned aldehyde or the aqueous solution.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB011022353A CN1141370C (en) | 2001-01-18 | 2001-01-18 | Clean disperser for lubricating oil |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB011022353A CN1141370C (en) | 2001-01-18 | 2001-01-18 | Clean disperser for lubricating oil |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1364860A true CN1364860A (en) | 2002-08-21 |
| CN1141370C CN1141370C (en) | 2004-03-10 |
Family
ID=4652578
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB011022353A Expired - Lifetime CN1141370C (en) | 2001-01-18 | 2001-01-18 | Clean disperser for lubricating oil |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1141370C (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1775934B (en) * | 2004-11-16 | 2011-06-15 | 英菲诺姆国际有限公司 | Lubricating oil additive concentrates |
| CN101709242B (en) * | 2009-11-11 | 2012-07-04 | 济南开发区星火科学技术研究院 | Lubricant dispersant |
-
2001
- 2001-01-18 CN CNB011022353A patent/CN1141370C/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1775934B (en) * | 2004-11-16 | 2011-06-15 | 英菲诺姆国际有限公司 | Lubricating oil additive concentrates |
| CN101709242B (en) * | 2009-11-11 | 2012-07-04 | 济南开发区星火科学技术研究院 | Lubricant dispersant |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1141370C (en) | 2004-03-10 |
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Granted publication date: 20040310 |