CN103275771B - Anti-static fuel additive and preparation method thereof - Google Patents

Anti-static fuel additive and preparation method thereof Download PDF

Info

Publication number
CN103275771B
CN103275771B CN201310169806.9A CN201310169806A CN103275771B CN 103275771 B CN103275771 B CN 103275771B CN 201310169806 A CN201310169806 A CN 201310169806A CN 103275771 B CN103275771 B CN 103275771B
Authority
CN
China
Prior art keywords
anti static
static additive
fuel anti
additive according
polyamine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN201310169806.9A
Other languages
Chinese (zh)
Other versions
CN103275771A (en
Inventor
刘婕
王树雷
朱志谦
王清亮
曹文杰
顾鹏翔
崔健
薛艳
张冬梅
贺则臣
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Oil Materials Inst Air Force P L A
Original Assignee
Oil Materials Inst Air Force P L A
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Oil Materials Inst Air Force P L A filed Critical Oil Materials Inst Air Force P L A
Priority to CN201310169806.9A priority Critical patent/CN103275771B/en
Publication of CN103275771A publication Critical patent/CN103275771A/en
Application granted granted Critical
Publication of CN103275771B publication Critical patent/CN103275771B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Liquid Carbonaceous Fuels (AREA)

Abstract

The invention relates to a fuel additive and in particular relates to an anti-static fuel additive and a preparation method thereof. The anti-static fuel additive comprises polyamino sulfone shown in a formula (I). Amino and sulfonyl in the anti-static additive are in a same molecule, and the ratio of amino to sulfonyl is fixed, so that the anti-static additive can be also kept in gasoline or diesel in the absence of a stabilizer, the electrical conductivity of an oil product is stable, the production program of the anti-static additive is simplified, and the cost is lowered; and the anti-static additive is not easily adsorbed by metallic media, the electric conductivity of gasoline or diesel is not easily attenuated during transportation and usage processes, and the stability of the electrical conductivity is high.

Description

A kind of fuel anti static additive and preparation method thereof
Technical field
The present invention relates to a kind of fuel dope, specifically, relate to a kind of fuel anti static additive and preparation method thereof.
Background technology
Handling or transportation oil and petroleum products, the fire causing because of static discharge, explosion hazard are at whole world ubiquity, and the financial loss causing is very huge.The every annual in the whole world has Extra Serious Accident 6~10 times, when charge of oil, emptying, occurs.As for road tank car and rail tank car, because of the accident that static discharge causes, happen occasionally.Gasoline, diesel oil poorly conductive, easily gather electric charge, and electrostatic hazard accident occurs.Along with automotive industry is the developing of China, the usage quantity increase year after year of the fuel such as gasoline, diesel oil, and the static firing accident that these fuel in use occur grows with each passing day.Therefore gasoline, diesel oil are used anti static additive very necessary.
The anti static additive that China is used at present mainly contains the anti static additives such as T1502, Stadis450, Stadis425, T1503.T1502 and Stadis450 are the ashless anti static additives of rocket engine fuel, and they have good antistatic effect in rocket engine fuel.Stadis425 and T1503 are the ashless anti static additives of gasoline, diesel oil.They have good antistatic effect in gasoline, diesel oil.
Existing anti static additive is by polysulfones, two kinds of polymers of polyamine and solvent composition.The mechanism of action of existing anti static additive is that polysulfones can lose proton and electronegative, and polyamine easily obtains proton and positively charged, when they meet, forms strong dipole ion pair owing to attracting each other, and is not having under outer electrostatic field, and ion pair is aobvious neutral.Once there be outer electrostatic field to exist, the dipole ion that polysulfones and polyamine form is to aligning, electronegative polysulfones one end turns to outer electrostatic field anodal, polyamine one end of positively charged turns to external electric field negative pole, form dipole ion pair, form contrary " polarized electric field " with external electric field polarity, thereby reduced external electric field intensity, play antistatic property.If outer electrostatic field is very strong, this dipole ion, to being finally separated into and being with plus-minus electric ion under the inductive capacity effect very strong, shows stronger electroconductibility.Polyamine, polysulfones comprise difference but the polar group polymer that attracts each other, mix according to a certain percentage, due to the effect of intermolecular attraction, make the polar group can not be in the state of rolling up, it is many when rolling up to be exposed to outer polar group, thereby strengthens electroconductibility.But polar group to align mobile time distance larger, therefore except being subject to outside the impact of electrostatic field power, be subject to oil product structure and extraneous factor to affect larger as factors such as temperature, times.
US Patent No. 3844732A proposes with alkyl aminomethylene-sulfonic acid as fuel anti static additive.Alkyl aminomethylene -sulfonic acid polarity is strong, and it uses separately the anti static additive that can be used as fuel, but its easily ionizable forms negative oxygen ion, and easy and metal adsorption, thereby the conductive capability of reduction anti static additive make the specific conductivity decay of oil fuel fast, and stability is not good.In vapour, diesel oil actual production, transportation and storage process, because the pipeline of contact, large tank etc. all belong to metal medium, if used as anti static additive alkyl aminomethylene-sulphonic acids is independent, the specific conductivity of vapour, diesel oil will decay to very soon defective in transportation and accumulating, and specific conductivity is lower than 50Ps/m.
For the defect of anti static additive in prior art, special proposition the present invention.
Summary of the invention
Primary goal of the invention of the present invention is to propose a kind of fuel anti static additive.
The second goal of the invention of the present invention is to propose the preparation method of this fuel anti static additive.
In order to realize object of the present invention, the technical scheme of employing is:
The present invention relates to a kind of fuel anti static additive, described fuel anti static additive contains suc as formula the polyamine base sulfone shown in (I);
Wherein, R 1be selected from-(CH 2) 1-16-,-(CH 2-CH=CH) 1-5-; Preferably-(CH 2) 1-12-,-(CH 2-CH=CH) 1-4-;
R 2be selected from the C of straight or branched i-6the C of alkyl, straight or branched 2-4thiazolinyl;
R 3be selected from-(CH 2) 1-6-,-(CH 2-CH=CH) 1-3-;
R 4be selected from the C of straight or branched 1-12alkyl, the C of straight or branched 2-12thiazolinyl;
X is selected from 20~200 integer, preferably 80~120 integer;
N is selected from 30~200 integer, preferably 80~100 integer.
The first optimal technical scheme of the present invention is:
R 1be selected from-(CH 2) 1-12-, preferably-(CH 2) 1-6-, more preferably-(CH 2) 1-3-;
R 2be selected from straight or branched C 1-4alkyl, more preferably straight or branched C 1-3alkyl;
R 3be selected from-(CH 2) 1-3-;
R 4be selected from the C of straight or branched 1-8alkyl, the preferred C of straight or branched 1-6alkyl, the more preferably C of straight or branched 1-3alkyl;
The 3rd optimal technical scheme of the present invention is: R 1be selected from-CH 2-; R 2be selected from ethyl; R 3be selected from-CH 2-CH 2-; R 4be selected from sec.-propyl.
The 4th optimal technical scheme of the present invention is: described fuel anti static additive contains suc as formula polyamine base sulfone 60~96wt%, the organic solvent 4~40wt% shown in (I); Preferably contain suc as formula polyamine base sulfone 60~90wt%, the organic solvent 10~40wt% shown in (I); More contain suc as formula polyamine base sulfone 80~90wt%, the organic solvent 10~20wt% shown in (I); Described organic solvent is selected from one or more the mixture in toluene, dimethylbenzene, trimethylbenzene, ethylbenzene, diethylbenzene, methyl-propyl benzene, preferably the mixture of toluene and dimethylbenzene.
The 4th optimal technical scheme of the present invention is: described fuel anti static additive contains suc as formula polyamine base sulfone 60~96wt%, toluene 2~20wt%, the dimethylbenzene 2~20wt% shown in (I); Preferably contain suc as formula polyamine base sulfone 60~90wt%, toluene 5~20wt%, the dimethylbenzene 5~20wt% shown in (I); More preferably contain suc as formula polyamine base sulfone 80~90wt%, toluene 5~10wt%, the dimethylbenzene 5~10wt% shown in (I).
The invention still further relates to the preparation method of this fuel anti static additive: by stirring 1~5 hour of preparing, preferably 1~3 hour after adding in proportion organic solvent in the polyamine base sulfone shown in (I).
The preparation method of the polyamine base sulfone in the present invention is: the preparation method of described polyamine base sulfone is: polysulfones is first added in reactor, add in proportion organic solvent, stir after 15 minutes~2 hours, add NaOH solid, be preferably the platy shaped particle of NaOH solid; Be warming up to 60 ℃~90 ℃, preferably 65~85 ℃; Under nitrogen protection, add in proportion while stirring polyamine in batches, stir 5~10 hours, preferably 6~8 hours, more preferably 7 hours; Cooling rear reaction completes; With slurry tank sedimentation 36~72 hours, preferably 48~72 hours, more preferably 48 hours; When unreacted NaOH solid settlement is after container bottom, the clear liquid shifting after sedimentation obtains suc as formula the polyamine base sulfone shown in (I).
Reaction molecular formula is:
Wherein, the mol ratio that described polysulfones and polyamine add is 1: 0.8~1.2, preferably 1: 1; The volume ratio of polysulfones and organic solvent is 25: 1~10: 1, preferably 20: 1.Described organic solvent is selected from a kind of in toluene, dimethylbenzene, ethylbenzene, diethylbenzene, preferably toluene.When adding polyamine in proportion while stirring, the mode that adds of polyamine is: polyamine divides 2~10 batches to add, preferably 2~5 batches in batches; The ratio that at every turn adds polyamine is 10%~50% of polyamine total amount, preferably 20%~50%; Stirring velocity is 30~180 revs/min, preferably 60~120 revs/min.Owing to being added with a small amount of solvent in the building-up process at polyamine base sulfone, thus polyamine base sulfone synthetic in prepare the solvent that as far as possible adopts at least one identical type in anti static additive.
The invention still further relates to this application of fuel anti static additive in gasoline or diesel oil, the concentration of described fuel anti static additive in gasoline or diesel oil is 1~2mg/l, preferably 2mg/l.
Below technical scheme of the present invention is made further explanation.
Fuel anti static additive in the present invention and the chemical structure of anti static additive of the prior art and composition and the mechanism of action are all different.Fuel anti static additive of the present invention is by a kind of polymer of polyamine base sulfone and solvent composition.
The chemical structure of poly-amino sulfone is suc as formula shown in I:
The antistatic property mechanism of fuel anti static additive of the present invention is: anti static additive, because the amido of positively charged and electronegative sulfuryl are in same molecular structure, is not having under outer electrostatic field, and molecule is aobvious neutral.When having outer electrostatic field, can form ion pair in molecule, form contrary " polarized electric field " with external electric field polarity, thereby reduced external electric field intensity, play antistatic property.Due to ion pair in molecule to align miles of relative movement less, be subject to oil product structure and extraneous factor to affect less as factors such as temperature, times.
Beneficial effect of the present invention is:
1. anti static additive of the present invention is because the amido of positively charged and electronegative sulfuryl are in same molecular structure, when having outer electrostatic field, can form ion pair in molecule, form contrary " polarized electric field " with external electric field polarity, thereby reduced external electric field intensity, played antistatic property.Due to ion pair in molecule to align miles of relative movement less, in the higher diesel oil of molecular weight, in molecule, in molecule, ion pair spacing is short, the polarized electric field of formation is strong.The ability that derives electric charge increases, so the specific conductivity of anti static additive of the present invention in diesel oil is high.
2. amido and sulfuryl are in same a part, and the ratio of amido and sulfuryl is fixed, and do not need stablizer also can keep anti static additive in vapour, diesel oil, and the stable conductivity of oil product has been simplified the production sequence of static inhibitor, has reduced cost.
Due to ion pair in molecule to align miles of relative movement less, be subject to oil product structure and extraneous factor to affect less as factors such as temperature, times.Therefore the stable conductivity of anti static additive of the present invention in vapour, diesel oil is good, is subject to external interference little.Compare with alkyl aminomethylene-sulphonic acids anti static additive, poly-amino sulfone in the present invention is done vapour, diesel oil anti static additive, it is difficult for being adsorbed by metal medium, and gasoline, diesel oil specific conductivity in transportation and use procedure is difficult for decay, and the stability of specific conductivity is high.
The specific embodiment of the present invention only limits to further explain and explanation the present invention, not to Composition of contents restriction of the present invention.
Embodiment
Embodiment 1:
One, the preparation of polyamine base sulfone
Wherein, x is selected from 80~120 integer, and n is selected from 80~100 integer.
Its preparation method is:
The preparation method of polyamine base sulfone is: polysulfones is first added in reactor, add in proportion toluene, the volume ratio of polysulfones and toluene is 20: 1; Stir after 2 hours, add the platy shaped particle of NaOH solid; Be warming up to 90 ℃; Under nitrogen protection, add in proportion while stirring polyamine, the mol ratio of polysulfones and polyamine is 1: 1 in batches, and polyamine divides 10 batches to add, and the ratio that at every turn adds polyamine is 10% of polyamine total amount; Stir 7 hours, stirring velocity is 120 revs/min; Cooling rear reaction completes; With slurry tank sedimentation 48 hours; When unreacted NaOH platy shaped particle is deposited to after container bottom, the clear liquid shifting after sedimentation obtains suc as formula the polyamine base sulfone shown in (A).
Two, the preparation of fuel anti static additive:
Formula: contain suc as formula polyamine base sulfone 80wt%, toluene 10wt%, the dimethylbenzene 10wt% shown in (A).
Preparation method: under normal temperature condition, by stirring 1 hour after adding in proportion toluene, dimethylbenzene in the polyamine base sulfone shown in (A) of preparing.
Embodiment 2~3:
One, the preparation of polyamine base sulfone
In its molecular formula, each substituting group is as shown in table 1:
Table 1:
Preparation method is: polysulfones is first added in reactor, add in proportion dimethylbenzene, the volume ratio of polysulfones and dimethylbenzene is 10: 1; Stir after 15 minutes, add the platy shaped particle of NaOH solid; Be warming up to 60 ℃, add in proportion while stirring polyamine under nitrogen protection in batches, the mol ratio that polysulfones and polyamine add is 1: 1, and polyamine divides 5 batches to add, and the ratio that at every turn adds polyamine is 20% of polyamine total amount; Stir 5 hours, stirring velocity is 180 revs/min; Cooling rear reaction completes; With slurry tank sedimentation 72 hours; When unreacted NaOH solid sheet particles settling is after container bottom, the clear liquid shifting after sedimentation obtains suc as formula the polyamine base sulfone shown in (I).
Two, the preparation of fuel anti static additive:
Formula: contain suc as formula polyamine base sulfone 60wt%, toluene 20wt%, the dimethylbenzene 20wt% shown in (I).
Preparation method: under normal temperature condition, by stirring 1 hour after adding in proportion toluene, dimethylbenzene in the polyamine base sulfone shown in (1) of preparing.
Embodiment 4~5:
One, the preparation of polyamine base sulfone
In its molecular formula, each substituting group is as shown in table 2:
Table 2:
Preparation method is: polysulfones is first added in reactor, add in proportion ethylbenzene, the volume ratio of polysulfones and ethylbenzene is 25: 1, stirs after 1 hour, adds NaOH solid platy shaped particle; Be warming up to 65 ℃; Under nitrogen protection, add in proportion while stirring polyamine in batches, divide 2 batches and add, the ratio that at every turn adds polyamine is 50% of polyamine total amount; Stir 10 hours, stirring velocity is 60 revs/min; Cooling rear reaction completes; With slurry tank sedimentation 36 hours; When NaOH solid settlement is after container bottom, the clear liquid shifting after sedimentation obtains suc as formula the polyamine base sulfone shown in (I).
Two, the preparation of fuel anti static additive:
Formula: contain suc as formula polyamine base sulfone 80wt%, ethylbenzene 10wt%, the diethylbenzene 10wt% shown in (I).
Preparation method: under normal temperature condition, by stirring 3 hours after adding in proportion ethylbenzene, diethylbenzene in the polyamine base sulfone shown in (1) of preparing.
Embodiment 6~7: the preparation of polyamine base sulfone
In its molecular formula, each substituting group is as shown in table 3:
Table 3:
Preparation method is: polysulfones is first added in reactor, add in proportion dimethylbenzene, the volume ratio of polysulfones and dimethylbenzene is 15: 1; Stir 2 hours, add NaOH solid, be warming up to 80 ℃; Under nitrogen protection, add in proportion while stirring polyamine, the mol ratio that polysulfones and polyamine add is 1: 1 in batches; Polyamine divides 4 batches to add, and the ratio that at every turn adds polyamine is 25% of polyamine total amount, stirs 8 hours, and stirring velocity is 120 revs/min; Cooling rear reaction completes; With slurry tank sedimentation 72 hours; When NaOH solid settlement is after container bottom, the clear liquid shifting after sedimentation obtains suc as formula the polyamine base sulfone shown in (I).Two, the preparation of fuel anti static additive:
Formula: contain suc as formula polyamine base sulfone 70wt%, dimethylbenzene 15wt%, the diethylbenzene 15wt% shown in (I).
Preparation method: under normal temperature condition, by stirring 5 hours after adding in proportion dimethylbenzene, diethylbenzene in the polyamine base sulfone shown in (1) of preparing.
Experimental example 1:
The anti static additive that adds 2mg embodiment 8 preparations in the gasoline of 1L, diesel oil, be mixed with the mensuration solution of 2mg/l concentration, mensuration solution is contained in the metal drum that is coated with tetrafluoroethylene and keeps in Dark Place, and at interval of certain hour, gets and measures the conductivity value of solution under 20 ℃ of conditions.
Get the gasoline, the diesel oil that do not add anti static additive simultaneously and contrast, be also contained in the metal drum that is coated with tetrafluoroethylene, under identical condition, measure conductivity value.
Conductance measurement method: press GB/T6539 and measure specific conductivity, test-results is as shown in table 4.
Table 4:
Get anti static additive prepared by the polyamine base sulfone of other embodiments of the invention and test, obtain similar experimental result.
Comparative example 1: diesel oil contrast experiment:
Comparative example 1: only add polyamine class anti static additive in diesel oil: poly-(2-the hydroxyl)-N-dodecyl propylamine of end dodecyl amido;
Comparative example 2: only add polysulfones anti static additive in diesel oil: poly-(β-hexyl-vinyl sulfone(RemzaolHuo Xingranliaohuoxingjituan));
Comparative example 3: add polyamine class in diesel oil: poly-(2-the hydroxyl)-N-dodecyl propylamine of end dodecyl amido and poly-(β-hexyl-vinyl sulfone(RemzaolHuo Xingranliaohuoxingjituan));
By above-mentioned comparative example under the same conditions, according to the method for experimental example 1, measure specific conductivity, test-results is as shown in table 5:
Table 5:
Comparative example 2: gasoline contrast experiment:
Comparative example 1: only add polyamine class anti static additive in gasoline: poly-(2-the hydroxyl)-N-dodecyl propylamine of end dodecyl amido;
Comparative example 2: only add polysulfones anti static additive poly-(β-hexyl-vinyl sulfone(RemzaolHuo Xingranliaohuoxingjituan)) in gasoline;
Comparative example 3: add the simple combination that polyamine class adds polysulfones anti static additive in gasoline: poly-(2-the hydroxyl)-N-dodecyl propylamine of end dodecyl amido and poly-(β-hexyl-vinyl sulfone(RemzaolHuo Xingranliaohuoxingjituan));
By above-mentioned comparative example under the same conditions, according to the method for experimental example 1, measure specific conductivity, test-results is as shown in table 6:
Table 6:

Claims (1)

1. a fuel anti static additive, is characterized in that, described fuel anti static additive contains polyamine base sulfone as shown in the formula (I);
(I)
R wherein 1be selected from-(CH 2) 1-16-,-(CH 2-CH=CH) 1-5-;
R 2be selected from the C of straight or branched 1-6the C of alkyl, straight or branched 2-4thiazolinyl;
R 3be selected from-(CH 2) 1-6-,-(CH 2-CH=CH) 1-3-;
R 4be selected from the C of straight or branched 1-12alkyl, the C of straight or branched 2-12thiazolinyl;
X is selected from 20~200 integer;
N is selected from 30~200 integer.
2 .fuel anti static additive according to claim 1, is characterized in that, described R 1be selected from-(CH 2) 1-12-,-(CH 2-CH=CH) 1-4-.
3 .fuel anti static additive according to claim 1, is characterized in that, x is selected from 80~120 integer.
4 .fuel anti static additive according to claim 1, is characterized in that, n is selected from 80~100 integer.
5 .fuel anti static additive according to claim 1, is characterized in that R 1be selected from-(CH 2) 1-12-, R 2be selected from straight or branched C 1-4alkyl, R 3be selected from-(CH 2) 1-3-, R 4be selected from the C of straight or branched 1-8alkyl.
6 .fuel anti static additive according to claim 5, is characterized in that R 1be selected from-(CH 2) 1-6-.
7 .fuel anti static additive according to claim 5, is characterized in that R 1be selected from-(CH 2) 1-3-.
8 .fuel anti static additive according to claim 5, is characterized in that R 2be selected from straight or branched C 1-3alkyl.
9 .fuel anti static additive according to claim 5, is characterized in that R 4be selected from the C of straight or branched 1-6alkyl.
10 .fuel anti static additive according to claim 5, is characterized in that R 4be selected from the C of straight or branched 1-3alkyl.
11 .fuel anti static additive according to claim 5, is characterized in that R 1be selected from-CH 2-; R 2be selected from ethyl; R 3be selected from-CH 2-CH 2-; R 4be selected from sec.-propyl.
12 .fuel anti static additive according to claim 1, is characterized in that, described fuel anti static additive contains polyamine base sulfone 60~96wt%, organic solvent 4~40 wt% as shown in the formula (I); Described organic solvent is selected from one or more the mixture in toluene, dimethylbenzene, trimethylbenzene, ethylbenzene, diethylbenzene, methyl-propyl benzene.
13 .fuel anti static additive according to claim 12, is characterized in that, described fuel anti static additive contains polyamine base sulfone 60 ~ 90wt%, organic solvent 10~40 wt% as shown in the formula (I).
14 .fuel anti static additive according to claim 12, is characterized in that, described fuel anti static additive contains polyamine base sulfone 80 ~ 90wt%, organic solvent 10~20 wt% as shown in the formula (I).
15 .fuel anti static additive according to claim 12, is characterized in that, described organic solvent is selected from the mixture of toluene and dimethylbenzene.
16 .fuel anti static additive according to claim 12, is characterized in that, described fuel anti static additive contains polyamine base sulfone 60 ~ 96wt%, toluene 2 ~ 20 wt%, dimethylbenzene 2 ~ 20 wt% as shown in the formula (I).
17 .fuel anti static additive according to claim 16, is characterized in that, described fuel anti static additive contains polyamine base sulfone 60 ~ 90wt%, toluene 5 ~ 20 wt%, dimethylbenzene 5 ~ 20 wt% as shown in the formula (I).
18 .fuel anti static additive according to claim 16, is characterized in that, described fuel anti static additive contains polyamine base sulfone 80 ~ 90wt%, toluene 5 ~ 10 wt%, dimethylbenzene 5 ~ 10 wt% as shown in the formula (I).
19 .fuel anti static additive according to claim 17, is characterized in that, the preparation method of described fuel anti static additive is: after adding in proportion organic solvent in the polyamine base sulfone as shown in the formula (I) preparing, stir 1~5 hour.
20 .fuel anti static additive according to claim 19, is characterized in that, the time of stirring is 1~3 hour.
21 .fuel anti static additive according to claim 1, is characterized in that, the preparation method of described polyamine base sulfone is: polysulfones is first added in reactor, add in proportion organic solvent, stir after 15 minutes~2 hours, add NaOH solid, be warming up to 60 ℃~90 ℃; Under nitrogen protection, add in proportion while stirring polyamine in batches, stir 5~10 hours; Cooling rear reaction completes; With slurry tank sedimentation 36~72 hours; When unreacted NaOH solid settlement is after container bottom, the clear liquid shifting after sedimentation obtains polyamine base sulfone as shown in the formula (I).
22 .fuel anti static additive according to claim 21, is characterized in that, described NaOH solid is the platy shaped particle of NaOH solid.
23 .fuel anti static additive according to claim 21, is characterized in that, is warming up to 65~85 ℃ after adding NaOH solid.
24 .fuel anti static additive according to claim 21, is characterized in that, adds in proportion while stirring polyamine under nitrogen protection in batches, stirs 6~8 hours.
25 .fuel anti static additive according to claim 21, is characterized in that, adds in proportion while stirring polyamine under nitrogen protection in batches, stirs 7 hours.
26 .fuel anti static additive according to claim 21, is characterized in that, with slurry tank sedimentation 36~72 hours.
27 .fuel anti static additive according to claim 21, is characterized in that, with slurry tank sedimentation 48~72 hours.
28 .fuel anti static additive according to claim 21, is characterized in that, with slurry tank sedimentation 48 hours.
29 .fuel anti static additive according to claim 21, is characterized in that, the mol ratio that described polysulfones and polyamine add is 1: 0.8~1.2; The volume ratio of polysulfones and organic solvent is 25: 1~10: 1; Described organic solvent is selected from a kind of in toluene, dimethylbenzene, ethylbenzene, diethylbenzene.
30 .fuel anti static additive according to claim 29, is characterized in that, the mol ratio that described polysulfones and polyamine add is 1: 1.
31 .fuel anti static additive according to claim 29, is characterized in that, the volume ratio of described polysulfones and organic solvent is 20: 1.
32 .fuel anti static additive according to claim 29, is characterized in that, described organic solvent is selected from toluene.
33 .fuel anti static additive according to claim 21, is characterized in that, when adding polyamine in proportion while stirring, the mode that adds of polyamine is: polyamine divides 2~10 batches to add in batches; The ratio that at every turn adds polyamine is 10%~50% of polyamine total amount; Stirring velocity is 30~180 revs/min.
34 .fuel anti static additive according to claim 33, is characterized in that, the mode that adds of polyamine is: polyamine divides 2~5 batches to add.
35 .fuel anti static additive according to claim 33, is characterized in that, the ratio that at every turn adds polyamine is 20%~50% of polyamine total amount.
36 .fuel anti static additive according to claim 33, is characterized in that, stirring velocity is 60~120 revs/min.
37 .application according to the fuel anti static additive described in claim 1~36 in gasoline or diesel oil, the concentration of described fuel anti static additive in gasoline or diesel oil is 1~2mg/l.
38 .application according to described in claim 37, is characterized in that, the concentration of described fuel anti static additive in gasoline or diesel oil is 2mg/l.
CN201310169806.9A 2013-05-10 2013-05-10 Anti-static fuel additive and preparation method thereof Expired - Fee Related CN103275771B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310169806.9A CN103275771B (en) 2013-05-10 2013-05-10 Anti-static fuel additive and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310169806.9A CN103275771B (en) 2013-05-10 2013-05-10 Anti-static fuel additive and preparation method thereof

Publications (2)

Publication Number Publication Date
CN103275771A CN103275771A (en) 2013-09-04
CN103275771B true CN103275771B (en) 2014-12-10

Family

ID=49058399

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310169806.9A Expired - Fee Related CN103275771B (en) 2013-05-10 2013-05-10 Anti-static fuel additive and preparation method thereof

Country Status (1)

Country Link
CN (1) CN103275771B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105296026B (en) * 2015-10-14 2017-09-29 无棣华信石油技术服务有限公司 Fuel oil antistatic agent and preparation method thereof
CN105400555B (en) * 2015-12-11 2017-08-25 广昌达新材料技术服务(深圳)股份有限公司 A kind of environmentally friendly oil antistatic agent and its application method

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007110780A2 (en) * 2006-03-24 2007-10-04 Innospec Limited Enhanced antistatic additives for hydrocarbon fuels & solvents
EP2042584A2 (en) * 2007-09-25 2009-04-01 Afton Chemical Corporation Diesel fuel additive compositions for prolonged antistatic performance
CN101892101A (en) * 2010-08-09 2010-11-24 北京斯伯乐科技发展有限公司 Ashless high-efficiency oil antistatic agent and using method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007110780A2 (en) * 2006-03-24 2007-10-04 Innospec Limited Enhanced antistatic additives for hydrocarbon fuels & solvents
EP2042584A2 (en) * 2007-09-25 2009-04-01 Afton Chemical Corporation Diesel fuel additive compositions for prolonged antistatic performance
CN101892101A (en) * 2010-08-09 2010-11-24 北京斯伯乐科技发展有限公司 Ashless high-efficiency oil antistatic agent and using method thereof

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
司荣等.聚胺型油品抗静电剂的合成与性能研究.《炼油技术与工程》.2009,第39卷(第4期),第58-60页. *
张倩 等.聚砜型油品抗静电剂的合成及性能评价.《现代化工》.2011,第31卷(第2期),第50-52页. *
聚砜型油品抗静电剂的合成及性能评价;张倩 等;《现代化工》;20110228;第31卷(第2期);第50-52页 *
聚胺型油品抗静电剂的合成与性能研究;司荣等;《炼油技术与工程》;20090430;第39卷(第4期);第58-60页 *

Also Published As

Publication number Publication date
CN103275771A (en) 2013-09-04

Similar Documents

Publication Publication Date Title
CN105400555B (en) A kind of environmentally friendly oil antistatic agent and its application method
Huang et al. Effects of amphiphilic copolymer dispersants on rheology and stability of coal water slurry
Atta et al. Use of rosin‐based nonionic surfactants as petroleum crude oil sludge dispersants
CN103275771B (en) Anti-static fuel additive and preparation method thereof
US11052355B2 (en) Gas separation membrane containing heteromorphous shaped silica nanoparticles
CN103265875B (en) The application of hyperbranched polymer in fire retarding conveying band static inhibitor
KR20030003259A (en) Anti-static additive compositions for hydrocarbon fuels
CN106590773B (en) A kind of unleaded aviation gasoline and preparation method thereof
CN109181747A (en) A kind of eutectic solvent and its application method for fuel oil extraction denitrogenation
US20080141582A1 (en) Additive Composition
CN102417839B (en) Fuel antistatic agent and application thereof
EP3317383A1 (en) Hydrogen sulfide scavenging additive compositions, and medium comprising the same
CN108409591A (en) A kind of star-like carboxylic acid group's zwitterionic compound and its preparation method and application
CN111334270A (en) Asphaltene stabilizer and preparation method thereof
DK201670270A1 (en) Use of Magnetic Nanoparticles for Depletion of Aromatic Compounds in Oil
JPH0642414B2 (en) Conductive magnetic fluid composition and method for producing the same
CN110484315B (en) Gasoline detergent and preparation method thereof
Dong et al. Properties of amphoteric polyurethane waterborne dispersions. III. Isoelectric points and precipitation
CN103409180B (en) Vehicle gasoline and preparation method thereof
CN103421557B (en) A kind of multifunctional fuel oil additive
US3729452A (en) Reaction products of an amine and a methyl vinyl ether-maleic anhydride copolymer
Liu et al. Binding of thermo-sensitive and pH-sensitive butylated poly (allylamine) s with lysozyme
US3210169A (en) Hydrocarbon compositions containing salts of certain nitrogen-containing polymers with sulfodicarboxylates
Orrego-Ruiz et al. Characterization of Acid Species in Asphaltenic Fractions by Fourier Transform Ion Cyclotron Resonance Mass Spectrometry and Infrared Spectroscopy
Akhtar et al. Separation of naphthenic acid from an oil‐phase using novel magnetic composite particles

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20141210

Termination date: 20180510