CN1552827A - Low-sulfur diesel oil multi-effect additive composition - Google Patents
Low-sulfur diesel oil multi-effect additive composition Download PDFInfo
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Abstract
A multi-effect additive composition for low-sulfur diesel includes: components A and B at weight ratio of (A):(B) = 1:0.1-10, wherein, component A consisting of reacted product or mixture of Mannich base, which is prepared from polyolefin phenol, C1-C6 aldehyde and polyenoic polyamines, and phenol acid; and component B consisting of reacted product or mixture of natural oil fat and amine and/or alcohol. The additive achieves additive amount 50-2000ppm as diesel wear resisting agent, stabilizing agent and dispersing agent.
Description
Technical field
The invention belongs to diesel oil multi-efficient additive, definite saying so both can be used as diesel antiwear additive, also can be used as the multipurpose additive of diesel oil stabilizing agent, diesel oil ashless dispersant.
Technical background
Along with the pay attention to day by day of countries in the world to environmental issue, pollute in order to reduce diesel exhaust gas, produce high-quality clean diesel, become the developing direction of modern petroleum refining industry.This diesel oil has generally that sulphur content is low, and it is low to contain aromatic hydrocarbons, cetane value height, characteristics such as cut is light.Studies show that sulphur is the harmful element that increases CH, CO, particularly pellet (PM) in the diesel engine emissions, so it is particularly important to improving topsoil to reduce in the diesel oil sulphur content.The diesel oil specification of the present U.S., Canada, every Western Europe country, all regulation diesel oil contains the S amount less than 0.05%, and aromaticity content is also lower.Because they have generally adopted harsh hydrogenation technique, the content that polarity in the diesel oil contains oxygen, nitrogenous compound is all very low, the content of many rings, double ring arene is also less, thereby reduced the natural lubricity of diesel oil, some oil injection pumps that rely on diesel oil itself to be lubricated have been caused, wearing and tearing occur as rotor pump (rotary pumps), proportioning pump (distributor pumps), reduced their work-ing life.
As everyone knows, non-hydrocarbon compounds such as the alkene in the diesel oil, diolefin and sulfide, nitride generate a series of intermediate oxidation product under the effect of oxygen, and these intermediate products produce insoluble precipitation through condensation.These insoluble particles that generate in the diesel oil storage process can have influence on the use properties of fuel, cause filtering system to stop up, and cause the prime the fuel system unit failure; influence oil atomizing; cause incomplete combustion, even in engine, form too much carbon deposit, make spray nozzle clogging.
The problems referred to above can be alleviated by add additive in diesel oil.It is generally acknowledged that diesel antiwear additive can remedy because of diesel oil causes the loss that plays lubricated composition in the oil through hydrotreatment, improves diesel fuel lubricity; Diesel oil stabilizing agent can stop, weakens or disturb above-mentioned various reaction, and is rotten to suppress diesel oil, improves its stability; Diesel cleaning and dispersing agent can wash down established carbon deposit on the nozzle, and forms protective membrane at nozzle surface, prevents that new carbon deposit from producing, and also can disperse established sediment in the diesel oil simultaneously, improves purifier and spray nozzle clogging, and improves exhaust emissions.
Diesel antiwear additive mostly is the derivative of fatty acid ester, acid amides or salt.EP773279 discloses and has used the carboxylicesters of dimeracid and hydramine prepared in reaction as diesel antiwear additive.EP798364 discloses with the salt of lipid acid and aliphatic amide prepared in reaction or acid amides as diesel antiwear additive.EP1209217 discloses C
6～C
50The reaction product of saturated fatty acid and dicarboxylic acid and short chain oils dissolubility primary, the second month in a season, tertiary amine is as diesel antiwear additive.WO9915607 discloses the reaction product of dimer (fatty acid) yl and epoxide as diesel antiwear additive.But these additives to the stability of diesel oil and detergent-dispersant performance to no effect, and may also can make the oxidation stability and the dispersed variation of diesel oil in many cases.
CS275894, EP605857 disclose with fatty acid ester such as rapeseed oil, sunflower oil, castor-oil plant wet goods directly as diesel antiwear additive.Though these products have advantages such as raw material is easy to get, price is more cheap, result of use is relatively poor relatively, because its viscosity is big, separates out easily at low temperatures simultaneously, and this practical application to it is also made troubles.
GB 2,245, and the replacement triazine that 588 reports generate with primary amine, secondary amine and formaldehyde reaction, replacement methane compound are as diesel oil stabilizing agent.This class additive has certain stabilization to color, but accelerating under the oxidizing condition (SH/T0175-94,95 ℃, logical oxygen 16 hours), the diesel oil oxidation sediment is suppressed indifferent, and its oil soluble is also not so good simultaneously.And above-mentioned diesel oil stabilizing agent does not have peace and quiet dissemination.
Mannich base (Mannich base) class lubricating oil and oil fuel ashless dispersant are the big classes in the dispersion agent that uses at present, US 3,649,229 reports are with high molecular (600～3000) alkylphenol, aldehyde, the mannich base product that contains the amine of the H-N＜group detergent-dispersant additive that acts as a fuel.
Mannich base is carried out chemical modification can make effects such as its dispersion, antioxygen all strengthen to some extent.As US 5,399,273 reports with the derivative of the mannich base product of high molecular (900～4000) alkylphenol, aldehyde, polyamines and two-ketone/sulfo-ketone compound as lubricating oil and fuel dispersants etc.
Summary of the invention
The purpose of this invention is to provide a kind of multipurpose additive with functions such as wear-resistant, stable, dispersions, it can not only improve the oilness of low-sulfur diesel-oil and can also stop condensation between alkene, diolefin oxidation and the non-hydrocarbon compound in the diesel oil, gathering between the small oxidation products that prevents to have produced, make it to be dispersed among the diesel oil, thereby improve the stability of diesel oil, delay engine filter and spray nozzle clogging.
Diesel oil multi-efficient additive provided by the invention comprises following component:
(A) reaction product of mannich base and phenol acids or product mixtures, wherein mannich base is by polyolefin-based phenol, C
1～C
6Aldehyde and polyamines polyene reaction generate;
(B) reaction product or the product mixtures of natural fats and oils and amine and/or alcohol;
Wherein component (A) is 1: 0.1～10 with the weight ratio of component (B), preferred 1: 0.2～6, more preferably 1: 0.3～3.
About component (A)
Said component (A) prepares by following method:
With mannich base and phenol acids according to 1: 0.5～5, preferred 1: 1～4 mixed in molar ratio (mole number of mannich base in wherein the mole number of polyamines polyene), in 50～200 ℃, preferred 80～160 ℃ were reacted preferred 1～10 hour 0.5～20 hour in the presence of solvent.Available nitrogen protection in the reaction system perhaps allows and carries out under the condition that is reflected at solvent refluxing.This reaction can not add catalyzer, also can add a small amount of (0.01～1%) acidic cpd such as sulfuric acid, tosic acid or acidic white earth as catalyzer, so that fast reaction speed.Said reaction solvent is hydrocarbon polymer such as benzene,toluene,xylene, aromatic hydrocarbons thinning oil, industrial naptha or mineral oil (boiling point is more than 120 ℃), or their mixture.Solvent load generally is 30～150% of a monomer material gross weight.For the ease of postorder operation and storage, last product can be made into about 50% diluent with the aromatic hydrocarbons thinning oil.
Said phenol acids is selected from Whitfield's ointment (salicylic acid), m-Salicylic acid, P-hydroxybenzoic acid, 3-hydroxyl 2-naphthoic acid, 3,4,5-trihydroxybenzoic acid (gallic acid), 4, two (4-hydroxyphenyl) valeric acids (diphenolic acid) of 4-etc. or their mixture.
Said mannich base is made by polyolefin-based phenol, aldehyde and polyamines polyene reaction, and three's mol ratio is generally 1: 0.1～10: 0.1～1 0, be preferably 1: 1～4: 0.5～and 2.The mannich reaction temperature is generally 50～200 ℃, is preferably within 70～150 ℃ of scopes.Reaction medium can be hydrocarbon polymer such as benzene,toluene,xylene, aromatic hydrocarbons thinning oil (boiling range is 159～185 ℃), industrial naptha or mineral oil (boiling point is more than 120 ℃), or their mixture.Solvent load generally is 30～150% of a monomer material gross weight.Available nitrogen protection in the reaction system perhaps allows system carry out under the condition of solvent refluxing.The preparation method is at US 3,413, and 347, US3,649,229, description is all arranged in US 3,798,165, US 4,116,644, US 4,553,979 patent documentations such as grade.
Polyolefin-based phenol wherein is the macromolecular compound with following structure, and wherein R is not for having
Isotactic polypropylene, polybutene, polyisobutene or ethylene-propylene copolymer, the number-average molecular weight of R are 300～3000, preferred 500～2000.The preparation of polyolefin-based phenol can be adopted existing alkylation of phenol technology.For example, under a small amount of acid catalyst action, 0.1～10 moles of phenol (being preferably 1～2.5 mole) and 1 mole of polyolefine are carried out alkylated reaction under 50～150 ℃.An acidic catalyst can be sulfuric acid, phosphoric acid or Lewis acid, as BF
3-diethyl ether solution, BF
3-ethanolic soln, BF
3-phenol solution etc., preferred Lewis acids.Reaction finishes back distilled water flush away catalyzer, and underpressure distillation or wet distillation are removed unreacted phenol again.
Aldehyde wherein is meant C
1～C
6Aldehyde, as formaldehyde, acetaldehyde, propionic aldehyde, hexamethylene aldehyde etc., formaldehyde preferably, 36% formaldehyde solution or Paraformaldehyde 96 all can.
The structural formula of polyamines polyene wherein is H
2N[(CH
2)
nNH]
mH, n are 2～4, and preferred 2～3 integer, m are 1～5, preferred 3～4 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.
About component (B)
Said component (B) is the reaction product or the product mixtures of natural fats and oils and amine and/or alcohol.Amine wherein or alcohol can be one or more in Fatty Alcohol(C12-C14 and C12-C18), hydramine, aliphatic amide, Cycloalkyl amine and the heterocyclic amine.
Said natural fats and oils can be vegetables oil or animal oil, can be fresh, also can be the waste oil that reclaims.Wherein vegetables oil is selected from peanut oil, Semen Maydis oil, Oleum Gossypii semen, rape seed oil, soybean oil, plam oil, Thistle oil, linseed oil, Oleum Cocois, Oak Tree oil, Prunus amygdalus oil, walnut oil, Viscotrol C, sesame oil, sweet oil, sunflower seeds wet goods, preferred peanut oil, Oleum Gossypii semen, rape seed oil, soybean oil, Viscotrol C, sesame wet goods.Animal oil is selected from lard, chicken fat, duck oil, goose oil, sheep oil, house oil, haco oil, shark wet goods, preferred lard, chicken fat, sheep oil, butter etc.
Said alcohol refers to C
1～C
18Fatty Alcohol(C12-C14 and C12-C18) can be a monohydroxy-alcohol, also can be polyvalent alcohol.Monohydroxy-alcohol can be ethanol, propyl alcohol, butanols, amylalcohol, hexanol, octanol etc., and just structure and isomery all can.Polyvalent alcohol can be ethylene glycol, polyoxyethylene glycol, 1, and 2-propylene glycol, 1, ammediol, glycerol, the butyleneglycol of various structures, pentanediol, hexylene glycol, heptanediol, ethohexadiol, nonanediol, decanediol, tetramethylolmethane, sorbyl alcohol, anhydrous sorbitol etc.Preferred C
2～C
8Fatty Alcohol(C12-C14 and C12-C18), more preferably polyvalent alcohol.
Said amine is that carbon number is C
1～C
18, preferred C
2～C
10Aliphatic amide, Cycloalkyl amine or heterocyclic amine.Wherein aliphatic amide can be primary amine or secondary amine, can be monoamine, also can be polyamine.Monoamine such as ethamine, propylamine, butylamine, amylamine, hexylamine etc., just structure and isomery all can.Polyamine can be quadrol, propylene diamine, diethylenetriamine, triethylene tetramine, tetraethylene pentamine, five ethene hexamines etc.Cycloalkyl amine can be cyclopentamine, hexahydroaniline etc.; Heterocyclic amine can be morpholine, piperazine etc.
Said hydramine is thanomin, diethanolamine, trolamine, methyldiethanolamine etc.
When natural fats and oils and amine and/or alcohol reacted, the mol ratio of grease and various alcohol or amine was 1: 0.1～5, preferred 1: 0.5～3, be preferably 1: 1.0～and 2.5.Because natural fats and oils all is the mixed glyceride based on 18 carbon, for calculating the convenience of feed ratio, its molecular weight can be considered as roughly identical with glycerol stearate (molecular weight 890).Reaction can be used acid catalysis such as sulfuric acid, tosic acid etc., also can use base catalysis such as sodium hydroxide, potassium hydroxide, organic bases such as dimethylcyclohexylamine etc.; Can also be without catalyzer.Reaction times is 1～20 hour, preferred 2～10 hours.Temperature of reaction is 50～200 ℃, preferred 80～160 ℃.
The addition of multipurpose additive provided by the invention in diesel oil generally is 50～2000ppm, preferred 100～1000ppm.
According to using needs, additive provided by the invention can also with other additive, use simultaneously as FLOW IMPROVERS, cetane number improver, metal passivator, sanitas etc.
Diesel oil multi-efficient additive provided by the invention not only has preferably resistance to abrasion, also has resistance of oxidation and a detergent-dispersant performance energy, colloid isopolarity compound and fine particles had very strong absorption and capturing ability, can stop its further oxidation, gathering, thereby reduce the generation of oxidation sediment in the diesel oil.
In addition, additive of the present invention also has other function, as improves the copper corrosion of diesel oil, reduces the discharging of diesel motor exhaust.
Embodiment
Example 1
This example is the preparation of polyolefin-based phenol:
In a 1000ml three-necked bottle, add 363.3 gram polyisobutene (polyisobutene number average relative molecular mass Mn=1100, source are Jinzhou petro-chemical corporation) and 62.1 gram phenol, be heated with stirring to 50 ℃, with 14.1 gram BF
3-diethyl ether solution divides and is added drop-wise in the reaction system about two hours for three times.Be warming up to 60 ℃, clock reaction 4.5 hours.Stopped reaction, it is inferior to give a baby a bath on the third day after its birth with the distilled water of heat, and unreacted phenol is removed in underpressure distillation again.Adopt the column chromatography analysis method to calculate transformation efficiency, unreacted polyisobutene is 32% in the sherwood oil, and then alkylating transformation efficiency is 68%.
Example 2
This example is the preparation of polyolefin-based phenol:
In a 1000ml three-necked bottle, add 200 gram polyisobutene (polyisobutene number average relative molecular mass Mn=1000, source are German BASF AG) and 37.6 gram phenol, be heated with stirring to 60 ℃, with 8.6 gram BF
3-diethyl ether solution divides and is added drop-wise in the reaction system about two hours for three times.Be warming up to 70 ℃, clock reaction 4 hours.Stopped reaction, it is inferior to give a baby a bath on the third day after its birth with the distilled water of heat, and unreacted phenol is removed in underpressure distillation again.Adopt the column chromatography analysis method to calculate transformation efficiency, unreacted polyisobutene is 30% in the sherwood oil, and then alkylating transformation efficiency is 70%.
Example 3
This example is the synthetic of mannich base:
In three-necked bottle, add polyolefin-based phenol, 9.4 gram triethylene tetramines and the 120 gram toluene of 100 grams by example 1 preparation, heated and stirred to 70 ℃ was added drop-wise to (mol ratio of polyolefin-based phenol, formaldehyde, triethylene tetramine is 1: 3: 1.2) in the reaction system with the formaldehyde solution of 13.4 grams 36% in 2 hours.Be warmed up to 100 ℃ after dripping off, and 100 ℃ of clock reactions 2 hours.Remove toluene solvant and water with underpressure distillation then, add 50 gram aromatic hydrocarbons thinning oils again, be made into about 50% diluent.
Example 4
This example is the synthetic of mannich base:
In three-necked bottle, add polyolefin-based phenol, 1.8 gram Paraformaldehyde 96s, 11.3 gram tetraethylene pentamine and the 50 gram aromatic hydrocarbons thinning oils (mol ratio of polyolefin-based phenol, formaldehyde, tetraethylene pentamine be 1: 1: 1) of 100 grams by example 2 preparations, heated and stirred to 90 ℃, reaction is 6 hours under nitrogen purging, divide water outlet, add 10 gram aromatic hydrocarbons thinning oils again, be made into about 50% diluent.
Example 5～8th, the preparation of component (A).
Example 5
In three-necked bottle, add mannich base and the 3.5 gram P-hydroxybenzoic acid (P-hydroxybenzoic acid and triethylene tetramine mol ratio be about 1.3: 1) of 50 grams by example 3 preparations, and 4 gram aromatic hydrocarbons thinning oil, logical nitrogen, reacted 5 hours down at 100 ℃, be cooled to room temperature then, make product A 1 of the present invention.
Example 6
In three-necked bottle, add mannich base and 4.9 gram salicylic acids (Whitfield's ointment) and the 5 gram aromatic hydrocarbons thinning oils (salicylic acid and triethylene tetramine mol ratio be about 1.8: 1) of 50 grams by example 3 preparations, in the presence of nitrogen, reacted 3 hours in 130 ℃, be cooled to room temperature then, make product A 2 of the present invention.
Example 7
In three-necked bottle, add mannich base and 4.3 gram P-hydroxybenzoic acid and the 5 gram aromatic hydrocarbons thinning oils (P-hydroxybenzoic acid and tetraethylene pentamine mol ratio be about 1.8: 1) of 50 grams by example 4 preparations, in the presence of nitrogen, reacted 6 hours in 80 ℃, be cooled to room temperature then, make product A 3 of the present invention.
Example 8
With 4.8 grams 3,4, the 5-trihydroxybenzoic acid replaces 4.3 gram P-hydroxybenzoic acid of example 7, in 120 ℃ of reactions 5 hours, is cooled to room temperature in the presence of nitrogen, makes product A 4 of the present invention.
Example 9～13rd, the preparation of component (B).
Example 9
With 100g Viscotrol C, 1 7g 1,2-propylene glycol (Viscotrol C and 1, the mol ratio of 2-propylene glycol is about 1: 2) and the 1.2g tosic acid place a reactor that electric mixer, thermometer, reflux condensing tube and nitrogen ingress pipe be housed, fed nitrogen 5～10 minutes, and in reaction process, keep faint nitrogen gas stream, heated and stirred is warming up to 150 ℃, reacts 5 hours, adds 0.5gCa (OH) then
2, the cooling suction filtration promptly gets product B 1.
Example 10
100g peanut oil, 25g trolamine (mol ratio of peanut oil and trolamine is about 1: 1.5) and 2.8g sodium methylate/catalyst for methanol are placed a reactor that electric mixer, thermometer, reflux condensing tube and nitrogen ingress pipe be housed, fed nitrogen 5～10 minutes, and in reaction process, keep faint nitrogen gas stream, heated and stirred is warming up to 160 ℃, reacted 6 hours, be cooled to 90 ℃ and add neutralization of 3.2g acidic white earth and filtration, promptly get product B 2.
Example 11
100g Oleum Gossypii semen, 17g triethylene tetramine (mol ratio of Oleum Gossypii semen and triethylene tetramine is about 1: 2) and 1.5g dimethylcyclohexylamine are placed a reactor that electric mixer, thermometer, reflux condensing tube and nitrogen ingress pipe be housed, fed nitrogen 5～10 minutes, and in reaction process, keep faint nitrogen gas stream, heated and stirred is warming up to 150 ℃, reacted 7 hours, cooling promptly gets product B 3.
Example 12
100g Viscotrol C, 24g morpholine (mol ratio of Viscotrol C and morpholine is about 1: 2.5) and 1.0g dimethylcyclohexylamine are placed a reactor that electric mixer, thermometer, reflux condensing tube and nitrogen ingress pipe be housed, fed nitrogen 5～10 minutes, and in reaction process, keep faint nitrogen gas stream, heated and stirred is warming up to 140 ℃, reacted 8 hours, cooling promptly gets product B 4.
Example 13
100g butter, 14.8g n-Butyl Amine 99 (mol ratio of butter and n-Butyl Amine 99 is about 1: 1.8) and 2.0g dimethylcyclohexylamine are placed a reactor that electric mixer, thermometer, reflux condensing tube and nitrogen ingress pipe be housed, slowly fed nitrogen 5～10 minutes, and in reaction process, keep nitrogen atmosphere, the heated and stirred temperature rising reflux, when temperature rises to 140 ℃ of quantity of reflux seldom the time, stopped reaction, cooling promptly gets product B 5.
Example 14～20 is the preparation of diesel oil multi-efficient additive composition of the present invention.
To be selected from the component A of example 5～8, the B component of example 9～13, mix, obtain different compositions according to the weight ratio shown in the table 1.
The preparation of table 1 multi-effect composite additive
Example component A B component A, B weight ratio
Example 14 A1 (example 5) B1 (example 9) 1: 0.5
Example 15 A1 (example 5) B2 (example 10) 1: 2
Example 16 A2 (example 6) B5 (example 13) 1: 0.25
Example 17 A2 (example 6) B1 (example 9) 1: 3
Example 18 A3 (example 7) B3 (example 11) 1: 1
Example 19 A3 (example 7) B4 (example 12) 1: 0.5
Example 20 A4 (example 8) B2 (example 10) 1: 0.8
Example 21
This example is the result of use of multi-effect composite additive in diesel oil that example 14～20 makes.Select huge port 0 for use
#The mixed oil (a) and the Yanshan Mountain 0
#Processed oil (b).Its physicochemical property sees Table 2, adds HFRR method (ISO12156-1) the grinding defect diameter WSD of agent front and back diesel oil
1.4, the oxidation stability total insoluble substance of accelerating oxidation style (SH/T0175-94) evaluation oil product sees Table 3, when grinding defect diameter during less than 460um (60 ℃), then the oilness of diesel oil is qualified; Total insoluble substance is less than or equal to 2.5mg/100ml, and then the oxidation stability of diesel oil is qualified.
The physicochemical property of table 2 diesel oil
Diesel oil
(a)???????????????(b)
Density (20 ℃)/gcm
-30.8576 0.8401
Viscosity (20 ℃)/mm
2S
-13.998 3.902
S content/mgkg
-1238 158
N content/mgkg
-1120 187
Paraffinic hydrocarbons/m% 38.5 43.9
Total naphthenic hydrocarbon/m% 18.4 20.6
Total mononuclear aromatics/m% 29.6 25.2
Total double ring arene/m% 11.9 9.3
Thrcylic aromatic hydrocarbon/m% 1.6 1.0
CFPP/℃??????????????????????????4?????????????????-2
SP/℃????????????????????????????1?????????????????-7
Initial boiling point/℃ 188 190
20% heat up in a steamer a little/℃ 230 225
50% heat up in a steamer a little/℃ 252 258
90% heat up in a steamer a little/℃ 343 326
Do/℃ 353 351
By table 3 as can be seen, diesel oil multi-efficient additive composition provided by the invention can improve low-sulfur diesel-oil energy oilness, can improve the stability of diesel oil again.
Table 3 multi-effect composite additive is to the effect of improving of diesel fuel lubricity and oxidation stability
Addition
Oilness Oxidation stability
Diesel-dope/mgkg
-1Total insoluble substance
WSD
1.4/um
/mg·100ml
-1
a???????????/?????????????/??????????????5.30????????????2.3
A example 5 400 480 1.5
A example 9 400 278 2.7
A example 14 500 219 1.0
A example 15 500 235 1.5
A example 16 600 289 0.7
A example 17 500 223 1.0
A example 18 600 219 1.6
A example 19 500 232 1.8
A example 20 350 241 1.5
b???????????/?????????????/??????????????474?????????????2.5
B example 5 300 382 1.4
B example 9 300 240 3.5
B example 14 500 195 1.2
B example 15 600 208 1.1
B example 16 500 234 1.4
B example 17 600 217 0.9
B example 18 500 213 1.3
B example 19 600 208 1.2
B example 20 400 245 2.0
Example 22
This example employing tinsel sedimentation is carried out simulation evaluation to the dispersing property of additive.
Present method is at the character of diesel oil, the tinsel sedimentation that the rotary oxygen bomb method that is used for measuring lubricating oil oxidation stability and SAE 872112 (Society of automotive engineers report) is used to evaluate the gasoline detergent dispersiveness has been carried out comprehensive improvement, and experimental installation and test method are referring to Chinese patent CN1382777.Test-results sees Table 4, wherein deposits improvement rate=(blank value-experimental value)/blank value * 100%.
Table 4 tinsel sedimentation evaluation diesel oil deposition conditions on tinsel
Add dosage deposition deposition improvement rate
Sample
/mg.kg
-1????????/mg?????????????/％
Blank diesel oil b 0 14.8 0
B+ example 14 produces 300 10.9 26.3
B+ example 15 produces 300 11.4 22.9
B+ example 16 produces 300 11.1 25.0
B+ example 17 produces 300 10.5 29.1
B+ example 18 produces 300 9.4 36.5
B+ example 19 produces 300 11.7 20.9
B+ example 20 produces 300 9.9 33.1
Example 23
This example is estimated the dispersiveness of multi-effect composite additive with the spot test method.
Spotting method is with after carbon black ointment (or engine sludge) and the dispersant, disperse through high-speed stirring and sonic oscillation, in 50 ℃ of baking ovens, left standstill 18 hours then, drop in after the taking-up on the filter paper, the oil droplet amount is controlled at 0.02～0.025g, the latter is placed in 50 ℃ of baking ovens and leaves standstill 2 hours, take out then and measure diffusion circle diameter (d) and greasy filth loop diameter (D), its ratio r=d/D * 100 are as the index of weighing dispersive ability, and the r value is big more, and dispersiveness is good more.The results are shown in Table 5.
Table 5 spotting method is estimated the dispersiveness of multipurpose additive
| Sample r | Sample r |
| Blank sample 24 examples 14 66.5 examples 15 65.8 examples 16 66.5 | Example 17 65.6 examples 18 67.5 examples 19 65.8 examples 20 64.3 |
From table 4 and table 5 as can be seen, the diesel oil multi-efficient additive composition of the present invention's preparation has detergent-dispersant performance preferably.
Claims (15)
1. low sulphur diesel oil multi-efficient additive composition comprises following component:
(A) reaction product of mannich base and phenol acids or product mixtures, wherein mannich base is by polyolefin-based phenol, C
1～C
6Aldehyde and polyamines polyene reaction generate;
(B) reaction product or the product mixtures of natural fats and oils and amine and/or alcohol;
Wherein component (A) is 1: 0.1～10 with the weight ratio of component (B).
2. according to the described composition of claim 1, it is characterized in that component (A) is 1: 0.2～6 with the weight ratio of component (B).
3. according to the described composition of claim 1, it is characterized in that wherein component (A) is 1: 0.3～3 with the weight ratio of component (B).
4. according to the described composition of claim 1, it is characterized in that, said component (A) prepares by following method: with mannich base and phenol acids according to 1: 0.5～5 mixed in molar ratio, in the presence of solvent in 50～200 ℃ of reactions 0.5～20 hour.
5. according to the described composition of claim 4, it is characterized in that said component (A) prepares by following method: with mannich base and phenol acids according to 1: 1～4 mixed in molar ratio, in the presence of solvent in 80～160 ℃ of reactions 1～10 hour.
6. according to the described composition of claim 1, it is characterized in that said phenol acids is selected from Whitfield's ointment, m-Salicylic acid, P-hydroxybenzoic acid, 3-hydroxyl 2-naphthoic acid, 3,4,5-trihydroxybenzoic acid, 4, two (4-hydroxyphenyl) valeric acids of 4-or their mixture.
7. according to the described composition of claim 1, it is characterized in that said mannich base is by polyolefin-based phenol, C
1～C
6Aldehyde and polyamines polyene make 50～200 ℃ of reactions, and three's mol ratio is 1: 0.1～10: 0.1～10.
8. according to the described composition of claim 7, it is characterized in that polyolefin-based phenol wherein is the macromolecular compound with following structure:
Wherein R is Atactic Polypropelene, polybutene, polyisobutene or ethylene-propylene copolymer, and the number-average molecular weight of R is 300～3000, preferred 500～2000.
9. according to the described composition of claim 7, it is characterized in that polyamines polyene wherein is selected from diethylenetriamine, triethylene tetramine, tetraethylene pentamine, five ethene hexamines, two propylene triamines, three propylene tetramines, tetrapropylene five amine, five propylene hexamines.
10. according to the described composition of claim 1, it is characterized in that said component (B) is natural fats and oils and amine and/or alcohol according to 1: 0.1～5 the mol ratio reaction product at 50～200 ℃, amine wherein or alcohol are C
1～C
18Fatty Alcohol(C12-C14 and C12-C18), hydramine, C
1～C
18In aliphatic amide, Cycloalkyl amine or the heterocyclic amine one or more.
11. according to claim 1 or 10 described compositions, it is characterized in that, said natural fats and oils is vegetables oil or animal oil, and wherein vegetables oil is selected from peanut oil, Semen Maydis oil, Oleum Gossypii semen, rape seed oil, soybean oil, plam oil, Thistle oil, linseed oil, Oleum Cocois, Oak Tree oil, Prunus amygdalus oil, walnut oil, Viscotrol C, sesame oil, sweet oil, sunflower seed oil; Animal oil is selected from lard, chicken fat, duck oil, goose oil, sheep oil, house oil, haco oil, shark oil shai.
12., it is characterized in that animal oil is selected from lard, chicken fat, sheep oil, butter according to the described composition of claim 11; Vegetables oil is selected from peanut oil, Oleum Gossypii semen, rape seed oil, soybean oil, Viscotrol C, sesame oil.
13., it is characterized in that said Fatty Alcohol(C12-C14 and C12-C18) is selected from ethylene glycol, polyoxyethylene glycol according to the described composition of claim 10,1,2-propylene glycol, 1, ammediol, glycerol, butyleneglycol, pentanediol, hexylene glycol, heptanediol, ethohexadiol.
14. according to the described composition of claim 10, it is characterized in that, said aliphatic amide is selected from ethamine, propylamine, butylamine, amylamine, hexylamine, quadrol, propylene diamine, diethylenetriamine, triethylene tetramine, tetraethylene pentamine, five ethene hexamines, said Cycloalkyl amine is cyclopentamine, hexahydroaniline, and said heterocyclic amine is morpholine, piperazine.
15., it is characterized in that said hydramine is thanomin, diethanolamine, trolamine or methyldiethanolamine according to the described composition of claim 1.
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| CN 03137919 CN1234820C (en) | 2003-05-30 | 2003-05-30 | Low-sulfur diesel oil multi-effect additive composition |
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| CN 03137919 CN1234820C (en) | 2003-05-30 | 2003-05-30 | Low-sulfur diesel oil multi-effect additive composition |
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1900794A3 (en) * | 2006-09-14 | 2009-02-11 | Afton Chemical Corporation | Biodegradable fuel performance additives |
| CN102453561A (en) * | 2010-10-27 | 2012-05-16 | 中国石油化工股份有限公司 | Diesel oil additive and application thereof to low-sulfur diesel oil |
| CN102453558A (en) * | 2010-10-27 | 2012-05-16 | 中国石油化工股份有限公司 | Low-sulfur diesel oil lubricating additive composition and application thereof |
| CN103060029A (en) * | 2011-10-21 | 2013-04-24 | 中国石油化工股份有限公司 | Diesel additive composition containing alkyl ethylene glycol acetic acid polyol ester and application thereof |
| CN103060030A (en) * | 2011-10-21 | 2013-04-24 | 中国石油化工股份有限公司 | Diesel additive composition containing alkyl ethylene glycol acetamide and application thereof |
| CN103060028A (en) * | 2011-10-21 | 2013-04-24 | 中国石油化工股份有限公司 | Diesel additive composition containing alkyl ethylene glycol acetic acid and application thereof |
| CN101993744B (en) * | 2009-08-19 | 2016-01-13 | 中国石油化工股份有限公司 | The method of biodiesel composition and raising oxidation stability of biodiesel |
| CN109852446A (en) * | 2019-02-28 | 2019-06-07 | 盘锦辽河油田大力集团有限公司 | A kind of preparation process of organic ashless class anti-knock agent |
-
2003
- 2003-05-30 CN CN 03137919 patent/CN1234820C/en not_active Expired - Lifetime
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1900794A3 (en) * | 2006-09-14 | 2009-02-11 | Afton Chemical Corporation | Biodegradable fuel performance additives |
| CN101993744B (en) * | 2009-08-19 | 2016-01-13 | 中国石油化工股份有限公司 | The method of biodiesel composition and raising oxidation stability of biodiesel |
| CN102453561A (en) * | 2010-10-27 | 2012-05-16 | 中国石油化工股份有限公司 | Diesel oil additive and application thereof to low-sulfur diesel oil |
| CN102453558A (en) * | 2010-10-27 | 2012-05-16 | 中国石油化工股份有限公司 | Low-sulfur diesel oil lubricating additive composition and application thereof |
| CN102453558B (en) * | 2010-10-27 | 2014-03-12 | 中国石油化工股份有限公司 | Low-sulfur diesel oil lubricating additive composition and application thereof |
| CN102453561B (en) * | 2010-10-27 | 2014-05-28 | 中国石油化工股份有限公司 | Diesel oil additive and application thereof to low-sulfur diesel oil |
| CN103060029A (en) * | 2011-10-21 | 2013-04-24 | 中国石油化工股份有限公司 | Diesel additive composition containing alkyl ethylene glycol acetic acid polyol ester and application thereof |
| CN103060030A (en) * | 2011-10-21 | 2013-04-24 | 中国石油化工股份有限公司 | Diesel additive composition containing alkyl ethylene glycol acetamide and application thereof |
| CN103060028A (en) * | 2011-10-21 | 2013-04-24 | 中国石油化工股份有限公司 | Diesel additive composition containing alkyl ethylene glycol acetic acid and application thereof |
| CN103060028B (en) * | 2011-10-21 | 2015-03-18 | 中国石油化工股份有限公司 | Diesel additive composition containing alkyl ethylene glycol acetic acid and application thereof |
| CN109852446A (en) * | 2019-02-28 | 2019-06-07 | 盘锦辽河油田大力集团有限公司 | A kind of preparation process of organic ashless class anti-knock agent |
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| Publication number | Publication date |
|---|---|
| CN1234820C (en) | 2006-01-04 |
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