CN1235843C - Method for eliminating and reclaiming acid component from oil products - Google Patents
Method for eliminating and reclaiming acid component from oil products Download PDFInfo
- Publication number
- CN1235843C CN1235843C CN 200410008621 CN200410008621A CN1235843C CN 1235843 C CN1235843 C CN 1235843C CN 200410008621 CN200410008621 CN 200410008621 CN 200410008621 A CN200410008621 A CN 200410008621A CN 1235843 C CN1235843 C CN 1235843C
- Authority
- CN
- China
- Prior art keywords
- oil
- acid
- solvent
- phase
- naphthenic acid
- 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
Links
- 238000000034 method Methods 0.000 title claims abstract description 48
- 239000002253 acid Substances 0.000 title claims abstract description 39
- 239000002904 solvent Substances 0.000 claims abstract description 67
- 239000003921 oil Substances 0.000 claims abstract description 48
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 claims abstract description 37
- 239000010779 crude oil Substances 0.000 claims abstract description 35
- 235000011114 ammonium hydroxide Nutrition 0.000 claims abstract description 11
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 6
- 239000000839 emulsion Substances 0.000 claims description 19
- 239000003795 chemical substances by application Substances 0.000 claims description 14
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 8
- 238000005189 flocculation Methods 0.000 claims description 8
- 230000016615 flocculation Effects 0.000 claims description 8
- 229920000570 polyether Polymers 0.000 claims description 8
- 150000001298 alcohols Chemical class 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 6
- 230000005684 electric field Effects 0.000 claims description 6
- 238000004062 sedimentation Methods 0.000 claims description 6
- 150000004703 alkoxides Chemical class 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 150000002430 hydrocarbons Chemical class 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 230000007935 neutral effect Effects 0.000 claims description 4
- -1 polyethylene Polymers 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 3
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 3
- 229910021529 ammonia Inorganic materials 0.000 claims description 3
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052921 ammonium sulfate Inorganic materials 0.000 claims description 3
- 235000011130 ammonium sulphate Nutrition 0.000 claims description 3
- 238000000605 extraction Methods 0.000 claims description 3
- 229920001568 phenolic resin Polymers 0.000 claims description 3
- 239000005011 phenolic resin Substances 0.000 claims description 3
- 229920000768 polyamine Polymers 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- DPDMMXDBJGCCQC-UHFFFAOYSA-N [Na].[Cl] Chemical compound [Na].[Cl] DPDMMXDBJGCCQC-UHFFFAOYSA-N 0.000 claims description 2
- 238000011084 recovery Methods 0.000 abstract description 6
- 238000000926 separation method Methods 0.000 abstract description 3
- 239000002131 composite material Substances 0.000 abstract 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 abstract 1
- 238000004945 emulsification Methods 0.000 abstract 1
- 238000013517 stratification Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 239000003208 petroleum Substances 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 230000008901 benefit Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000006386 neutralization reaction Methods 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000007670 refining Methods 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000002283 diesel fuel Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 125000005608 naphthenic acid group Chemical class 0.000 description 2
- 230000020477 pH reduction Effects 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 208000006558 Dental Calculus Diseases 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- MAZPIOPHRNWBNG-UHFFFAOYSA-N [Cl-].Cl[NH3+].[Na] Chemical compound [Cl-].Cl[NH3+].[Na] MAZPIOPHRNWBNG-UHFFFAOYSA-N 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000008431 aliphatic amides Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000003637 basic solution Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000010612 desalination reaction Methods 0.000 description 1
- 238000011033 desalting Methods 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 229940001516 sodium nitrate Drugs 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Landscapes
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
本发明涉及一种从油品中脱除和回收环烷酸的方法，该方法选用包括C2-5饱和烷醇、氨水和破乳剂的复合溶剂，使待处理油品与复合溶剂混合，于30～70℃之间加热至多60分钟，静置分层后分离出溶剂相，并酸化处理该溶剂相，分离出环烷酸相；还可在复合溶剂中加入适量的絮凝剂以加速分层。本发明所述的方法尤其适用于馏分油和原油的脱酸，既能方便地脱除油品中的酸成分，又能有效回收其中主要包含的、高附加值的环烷酸产品，并且避免了分离和回收过程的乳化现象。The invention relates to a method for removing and reclaiming naphthenic acid from oil products. The method selects a composite solvent comprising C2-5 saturated alkanol, ammonia water and a demulsifier, mixes the oil product to be treated with the composite solvent, and decomposes at 30 Heat to 70°C for up to 60 minutes, separate the solvent phase after standing and stratifying, and acidify the solvent phase to separate the naphthenic acid phase; an appropriate amount of flocculant can also be added to the composite solvent to accelerate the stratification. The method of the present invention is especially suitable for the deacidification of distillate oil and crude oil. It can not only remove the acid components in the oil products conveniently, but also effectively recover the high value-added naphthenic acid products mainly contained therein, and avoid Emulsification phenomenon in the separation and recovery process.
Description
Technical field
The present invention relates to a kind of method that from oil product, removes and reclaim naphthenic acid, relate in particular to the method that from crude oil or heavy distillate, removes and reclaim naphthenic acid.
Background technology
From diesel oil and light ends oil, remove the existing many processing methodes of sour composition at present, for example US4752381 proposed a kind of in and in oil and the petroleum fractions organic acid to obtain neutralization value less than 1.0 method; This method comprises: handle petroleum fractions with monoethanolamine, heat the sufficiently long time more at a certain temperature to form acid amides.These amine can not obtain simple naphthenic acid product as the present invention.
US4634519 discloses with methyl alcohol-ammoniacal liquor double solvents and has removed the method for the sour composition in the distillate.Because solvent for use lacks security, and final step in deacidification, be white emulsion to occur in the useless double solvents process of heating recovery, make the yield of petroleum acid be lower than 50%, this mainly is owing to fail to resolve due to the emulsive problem of petroleum acid ammonium salt decomposition back.
But these methods can not effectively deviate from and reclaim for the sour composition in crude oil and the heavy distillate.Along with the increase of peracidity crude oil on the market, continued to bring out the new technology of processing highly acid crude oil.For crude oil with high acid value, the refinery can't directly refine, because refining equipment is produced serious corrosion, and greatly influence safety in production.One of currently used method be with low acid number crude oil with the crude oil with high acid value blending, be no more than 0.5 with the acid number that guarantees blend.This method also only limits to handle the crude oil of relatively low acid number, and the treatable crude oil with high acid value amount of institute is very limited.Relevant anticorrosion technique also is included in annotates alkali with neutralization sour composition wherein in the refining process.This method may form plain stubborn milk sap, has stayed unnecessary impurity simultaneously in the crude oil of handling, and also can influence the normal operation of refining equipment.
Though in thermal treatment, hydrofining and the calcium and etc. the pre-treatment measure can effectively reduce acid value for crude oil, they change into other product devastatingly with naphthenic acid, can not obtain the naphthenic acid product of high added value.The market value of common naphthenic acid is 2～5 times of identical weight kerosene.Therefore, need a kind of can remove easily sour composition in the oil product, again can efficient recovery naphthenic acid product that wherein mainly comprise, high added value method.
Summary of the invention
The purpose of this invention is to provide a kind of method that from oil product, removes and reclaim naphthenic acid, it can remove the sour composition in the oil product easily, again can efficient recovery naphthenic acid product that wherein mainly comprise, high added value, it may further comprise the steps: select the double solvents that comprises C2-5 saturated alkoxides, ammoniacal liquor and emulsion splitter for use, pending oil product is mixed with double solvents, between 30～70 ℃, be heated to many 60 minutes, isolate solvent phase behind the standing demix, and this solvent phase of acidification, isolate the naphthenic acid phase.
In the method for the invention,, can also comprise the flocculation agent that is selected from the plurality of inorganic salt class in the described double solvents, be preferably and be selected from ammonium sulfate, volatile salt, sodium-chlor and the Repone K one or more for shortening above-mentioned separation time.The weight percentage of described flocculation agent consumption is 0.1%～2%.
In the oil product by the inventive method processing, acid constituents is mainly naphthenic.They are the chemical intermediates with higher-value.
The C2-5 saturated alkoxides that the present invention uses can be ethanol, propyl alcohol, butanols and other low-molecular-weight alcohols, preferred Virahol.
Emulsion splitter described in the present invention can be selected from one or more in alcohols polyethers, polyethylene polyamine block polyether, phenolic resin type, the PEP-101, also can be the small molecules emulsion splitter.
By the inventive method, can adopt concentration is 15% ammoniacal liquor, and Virahol: the volume ratio of ammonia volume is 1: 2～1: 4; The consumption of emulsion splitter is 50～100ppm, and the agent of double solvents and oil in the mixing/oil volume is than between 0.2～1, preferably between 0.5～1.
Acidification solvent phase described in the present invention is that the pH value with solvent phase is adjusted to below 2.
Oil product described in the present invention can be a crude oil with high acid value, can be light ends oil also, comprises diesel oil and kerosene that naphthenic acid content is higher.
The present invention can adopt the oil product phase and the solvent phase that contains the acid of deviating from after the method for natural sedimentation or electric field separates is separated depickling.
In the methods of the invention, described type of heating can adopt steam heating, electric heating or other ordinary method.The general agitator in the pot type operating process is used in described mixing, or uses the extraction tower countercurrent liquid-liquid operation of operate continuously process.Can adopt the method for natural sedimentation or electric field separates separate after the depickling oil product mutually and contain the solvent phase of the acid of deviating from.The neutral oil that is mixed with in the isolated solvent phase can adopt a kind of the extracting in benzene,toluene,xylene, sherwood oil, 90～180 ℃ the liquid hydrocarbon, to improve the thick acid number of naphthenic acid.Add hydrochloric acid or sulfuric acid and regulate the pH value of the solvent phase behind wash-out or make it heating, make system separate out the naphthenic acid layer, can get the naphthenic acid product after the layering.Can recycle and separate the depickling solvent that obtains.
If described oil product is crude oil, then described being separated in the refinery desalting unit carried out, and obtains the former oil phase after the depickling and contains the solvent phase of naphthenic acid salt.
The present invention uses the double solvents of ammoniacal liquor and C2-5 saturated alkoxides, preferred Virahol to remove that its main component is the sour composition of naphthenic acid in crude oil and the distillate thereof, its mechanism is believed: by ammonia with the neutralization reaction of naphthenic acid and utilize the extracting effect of the salt that alcohol in the solvent produces neutralization, naphthenic acid in the oil is transferred in the solvent, oil product and the demixing of solvents that contains naphthenic acid also are separated, reach the purpose that removes naphthenic acid in the oil product.Its advantage is, the solvent safety of use can effectively suppress the generation of emulsion in the extractive process, make the layering of solvent extraction process very fast; The naphthenic acid that obtains is to exist with purer state; Solvent is recycled easily.Also the sulphur of mercaptan can be removed in the lump simultaneously, to reduce the sulphur content of oil product.
The following specifically describes some detail operation stepss of the inventive method.
Described double solvents can followingly be prepared: Virahol: the volume ratio of ammoniacal liquor can be between 1: 2～1: 4.Virahol also can be replaced by ethanol, n-propyl alcohol and propyl carbinol and other low-molecular-weight alcohols.Because the gasification potential of alcohols material is low, boiling point is low, and the energy consumption that reclaims the extract solvent from extract is lower, helps energy-conservation.
Described emulsion splitter can be that (as SPI69, its molecular formula is C to the alcohols polyethers
18H
37-O-(C
3H
6O)
x-(C
2H
4O
y-(C
3H
6O) z-H)), (as AE is two sections block polyethers to the polyethylene polyamine block polyether, AP is three sections block polyethers), in the phenolic resin type (as AR type emulsion splitter, promptly alkylphenol is with EO and PO copolymerization), oxyethane (EO)-propylene oxide (PO) multipolymer (as UD10) one or more.Described emulsion splitter also can be selected one or more in micromolecular ethylenediamine tetraacetic acid (EDTA), lipid acid, aliphatic amide, the negatively charged ion amine etc., to accelerate layered effect; Effect emulsion splitter preferably is SPI69.For some lightweight oils, comprise that crude oil and distillate, flocculation agent may be nonessential.
Described flocculation agent can be selected one or more the mixture in sodium-chlor, ammonium chloride, Repone K, sodium sulfate, ammonium sulfate, vitriolate of tartar, SODIUMNITRATE, ammonium nitrate, the saltpetre for use, and its ratio can be selected arbitrarily.Wherein ammonium salt is best.
Above-mentioned reaction mixture natural subsidence is separated, and system is divided into oil phase and solvent phase two-phase, and the acid number of oil phase can reach below the 0.5mgKOH/g.Utilize the neutral oil in the solvent phase after the depickling of light hydrocarbons wash-out, to improve the thick acid number of naphthenic acid.Add hydrochloric acid or sulfuric acid and regulate below the pH of the solvent phase behind wash-out value to 2, system is separated out the naphthenic acid layer at once, utilizes density difference between naphthenic acid and the solvent phase and immiscible character thereof, and the employing natural sedimentation is told naphthenic acid wherein.Naphthenic acid can wash with water with seawater or general industry earlier mutually, can suitably add emulsion splitter, washes with water with general industry at last, makes the naphthenic acid product.The recyclable utilization of solvent that obtains from delaminating process.
The double solvents amount that the present invention uses and the volume ratio of corresponding crude oil can be between 0.2～1, and be slightly different according to different operating method.
Liquid between agent/oil-liquid contact can be adopted the andnon-continuous operation manner of depickling jar, also can adopt the operate continuously mode of counter-current extraction tower multi-stage solvent extraction.Solvent can prepare the back and add, and adds alcoholic solution and other breakdown of emulsion components again after also can adding basic solution earlier.The adding mode can be the depickling solvent to be joined in the crude oil go, and also crude oil can be joined in the depickling solvent and go.
The method of separating crude oil and solvent can adopt natural sedimentation also can adopt the method for electric field separates.If adopt the latter, can utilize in the refinery existing desalination unit to implement.Can in static mixer, under low-shearing power, mix, to react.
Solvent phase can adopt a kind of washing back in the organic solvents such as benzene,toluene,xylene, sherwood oil, light hydrocarbon to reclaim, and the solvent in the oil phase can distill recovery simply, is recycled.Resistates after the distillation is neutral crude oil, can merge with depickling crude oil.
Depickling temperature of the present invention can be chosen between 30～70 ℃, and preferably between 45～55 ℃, the reaction times is no more than 60 minutes, preferably between 10 minutes～40 minutes.Agent/oil content layer also can carry out under the situation of suitably insulation.
The mode of separating depickling crude oil and solvent can adopt natural sedimentation, and the mixture behind the stirring reaction is left standstill in separating funnel or other separators.Utilize density difference and its immiscible character of crude oil and solvent, the natural subsidence layering.
Solvent after the depickling can directly be regulated pH to alkalescence, as new depickling solvent recycling.Also can after suitable distillation purification processes, reuse.
Can adopt thermal degradation and directly add acid-treated method the processing of naphthenate, obtain the naphthenic acid product.
The present invention compared with prior art, its advantage is: be applicable to the depickling of distillate and crude oil; Depickling and acid treating, recovery are organically combined, avoided the emulsion of separation and removal process; Reduced the technology cost of whole process; The yield and the acid number thereof of the naphthenic acid that is recovered to after removing are higher.Method is simple, economical and effective for this, and favorable economic benefit and social benefit are arranged.And the yield and the acid number thereof of petroleum acid have been improved.
Embodiment
Embodiment 1
In this embodiment, use the Sudan's crude oil, its acid value for crude oil is 10.8mg KOH/g.At volume is to add 250 gram the Sudan crude oil in the still kettle of 2 liters; In Virahol: the volume ratio of 15% ammoniacal liquor is 1: 2 a ratio preparation double solvents, wherein contains commercially available UD10 type emulsion splitter 80ppm; With crude oil and double solvents is to mix at 1: 1 by volume, is heated to 60 ℃; Under 250r/ minute stirring velocity, mixed 30 minutes, left standstill at least 30 minutes; After treating the abundant layering of crude oil and solvent phase, lower floor's solvent phase is told.Measure acid value for crude oil, acid number is reduced to 3.2mg KOH/g from 10.8mg KOH/g.
The solvent of as above gained is regulated pH value to 14 with ammoniacal liquor or NaOH, adds the UD10 emulsion splitter, with its concentration adjustment to the 80ppm.So far the solvent of gained joined again in the crude oil of depickling go.Under 50 ℃, mixed 30 minutes, and mixed system was transferred to left standstill 30 minutes in the separating funnel; Layering; Record its oil phase acid number and reduce to 0.2mg KOH/g.
The solvent that above-mentioned steps is told with petroleum ether after, add hydrochloric acid and also regulate pH to 2, tell the black oil phase on the solvent upper strata at once. upper oil phase is told.Determine that with infrared spectra and mass spectrum it consists of the naphthenic acid of molecular weight ranges between 100～1000.
Embodiment 2
Take by weighing the Sudan's straight run heavy grease of 450～500 ℃ of cuts of 200 grams, its acid number is higher than 18.2mgKOH/g.It is mixed by 1: 0.5 volume ratio with the depickling double solvents among the embodiment 1, and temperature maintenance is at 40 ℃.Mix 30 minutes in beaker after, the impouring separating funnel adds ammonium chloride 2 grams and makes flocculation agent, and suitably insulation; After treating the solution layering, measure the acid number of distillate, acid number is reduced to 0.5mgKOH/g.With the solvent petroleum ether of telling, use salt acid for adjusting pH value to 2 at last.Tell the naphthenic acid of gained, the thick acid number of measuring naphthenic acid is 154mgKOH/g; Pure acid number 168mgKOH/g.
Embodiment 3
Use Peng Lai, Shandong crude oil (total acid value 3.8mgKOH/g) in this embodiment.Mix with following condition preparation double solvents and with this crude oil and to handle:
It is 25% ammoniacal liquor that double solvents in the present embodiment is selected ethanol and concentration for use, and by ethanol: ammoniacal liquor is that 1: 2 volume ratio is mixed, and adds the alcohols polyether-type SPI69 emulsion splitter of 60ppm; Above-mentioned double solvents is 0.3 with the agent/oil volume ratio of oil; Temperature of reaction is 50 ℃, and the reaction times is 30 minutes.Mixture after treatment separated 10 minutes under DC electric field, strength of electric field 1000V/cm.Divide fuel-displaced, agent two-phase, measuring the oil phase acid number is 0.2mgKOH/g.Use the petroleum ether identical with former oil volume, gained raffinate addition sulfuric acid is regulated pH value to 2, and system is layering at once, obtains naphthenic acid, measures its specification and meets SH00922 acidity scale standard.
Claims (9)
1. method that from oil product, removes and reclaim naphthenic acid, it is characterized in that: select the double solvents that comprises C2-5 saturated alkoxides, ammoniacal liquor and emulsion splitter for use, pending oil product is mixed with double solvents, between 30～70 ℃, be heated to many 60 minutes, isolate solvent phase behind the standing demix, and the pH value of solvent phase is adjusted to below 2, isolate the naphthenic acid phase.
2. method according to claim 1 is characterized in that: comprise also in the described double solvents that flocculation agent, this flocculation agent are to be selected from ammonium sulfate, volatile salt, sodium-chlor and the Repone K one or more.
3. method according to claim 2 is characterized in that: described C2-5 saturated alkoxides is a Virahol; Emulsion splitter is selected from one or more in alcohols polyethers, polyethylene polyamine block polyether, the phenolic resin type.
4. method according to claim 3 is characterized in that: employing concentration is 15% ammoniacal liquor, and Virahol: the volume ratio of ammonia volume is 1: 2～1: 4; The consumption of emulsion splitter is 50～100ppm; The weight percentage of described flocculation agent consumption is 0.1%～2%.
5. method according to claim 4 is characterized in that: get agent/oil volume in the mixing than between 0.2～1.
6. according to each described method in the claim 1 to 5, it is characterized in that: described oil product is a crude oil with high acid value.
7. method according to claim 6 is characterized in that: the method for employing natural sedimentation or electric field separates is separated the oil product phase after the depickling and is contained the solvent phase of the acid of deviating from.
8. method according to claim 7 is characterized in that: the neutral oil that is mixed with in the isolated solvent phase adopts a kind of extraction the in benzene,toluene,xylene, sherwood oil, 90～180 ℃ the liquid hydrocarbon.
9. method according to claim 7 is characterized in that: recycle and separate the depickling solvent that obtains.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200410008621 CN1235843C (en) | 2004-03-12 | 2004-03-12 | Method for eliminating and reclaiming acid component from oil products |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200410008621 CN1235843C (en) | 2004-03-12 | 2004-03-12 | Method for eliminating and reclaiming acid component from oil products |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1563283A CN1563283A (en) | 2005-01-12 |
| CN1235843C true CN1235843C (en) | 2006-01-11 |
Family
ID=34477684
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 200410008621 Expired - Fee Related CN1235843C (en) | 2004-03-12 | 2004-03-12 | Method for eliminating and reclaiming acid component from oil products |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1235843C (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100506949C (en) * | 2006-04-18 | 2009-07-01 | 中国海洋石油总公司 | Method of eliminating naphthenic acid from crude oil or fraction oil |
| CN101538477A (en) * | 2008-03-20 | 2009-09-23 | 北京迪威尔石油天然气技术开发有限公司 | Deacidification agent and crude-oil deacidification technique using same |
| CN101353592B (en) * | 2008-09-03 | 2012-07-04 | 西南石油大学 | Method and apparatus for diesel acid stripping |
| CN102311775A (en) * | 2010-07-05 | 2012-01-11 | 中国石油化工股份有限公司 | Method for recovering naphthenic acid from hydrocarbon oil and device thereof |
| CN105419863A (en) * | 2015-12-10 | 2016-03-23 | 广东石油化工学院 | Process method for deacidifying high acid thickened oil |
| CN108535390B (en) * | 2018-03-09 | 2019-11-15 | 中国地质大学（武汉） | A Magnetic Droplet Dispersion Extraction Method for Petroleum Acid Separation |
| CN112795398A (en) * | 2021-01-14 | 2021-05-14 | 武汉润尔华科技有限公司 | Preparation of deacidifying agent for high-acid crude oil and distillate oil thereof |
-
2004
- 2004-03-12 CN CN 200410008621 patent/CN1235843C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN1563283A (en) | 2005-01-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN106753742B (en) | Regeneration method of waste lubricating oil | |
| AU2009327268B2 (en) | Demulsifying of hydrocarbon feeds | |
| CN1276002A (en) | Method of re-refining waste oil by distilation and extraction | |
| CN103080276B (en) | For gained width scope diesel oil, steady broad range diesel oil are carried out stable, desulfurization and dry solvent extraction technology and application thereof | |
| CN103068773B (en) | Novel methods for regeneration of solvents for extractive processes | |
| CN102666799A (en) | Process for de-acidifying hydrocarbons | |
| CN103805227A (en) | Pre-treatment process method of high acid crude oil | |
| CN105316018A (en) | Pretreatment method for deep processing of coal tar | |
| CN101781575B (en) | Method for preparing high-cleanness fuel oil from intermediate-temperature and low-temperature coal tar | |
| CN1235843C (en) | Method for eliminating and reclaiming acid component from oil products | |
| CN105713658A (en) | Low-temperature coal tar pretreatment technology | |
| CN102585870B (en) | Method for quickly separating chain hydrocarbon and phenols from medium and low temperature tar | |
| US2792332A (en) | Desulfurization and dearomatization of hydrocarbon mixtures by solvent extraction | |
| US8329941B2 (en) | Process for the extraction of high molecular weight naphthenic acids from calcium naphthenate salts | |
| Sterpu et al. | Regeneration of used engine lubricating oil by solvent extraction | |
| CN103113912A (en) | Method for separating and extracting crude oil from oil sand | |
| AU2012285743A1 (en) | Method and system for removal of dissolved organic compounds in process water | |
| CN102311775A (en) | Method for recovering naphthenic acid from hydrocarbon oil and device thereof | |
| CN105950212A (en) | Aged sump oil treatment process | |
| CN105419859A (en) | Reverse back extraction refining method for petroleum reduced pressure distillation distillate and application thereof | |
| CN102653686B (en) | Preparation method of aromatic rubber oil | |
| CN1219854C (en) | Method of crude oil and fraction oil deacidification and naphthenic acid refining method | |
| WO2011022832A1 (en) | A process and system for reducing acidity of hydrocarbon feeds | |
| CN101565632B (en) | A method for removing naphthenic acid from diesel oil | |
| CN1142257C (en) | Process for deacidifying from petroleum distillate |
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 | ||
| C19 | Lapse of patent right due to non-payment of the annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |