CN1724616A - New method of producing oil productwith ultra low sulfur content using potassium ferrate oxidation method - Google Patents
New method of producing oil productwith ultra low sulfur content using potassium ferrate oxidation method Download PDFInfo
- Publication number
- CN1724616A CN1724616A CN 200510069861 CN200510069861A CN1724616A CN 1724616 A CN1724616 A CN 1724616A CN 200510069861 CN200510069861 CN 200510069861 CN 200510069861 A CN200510069861 A CN 200510069861A CN 1724616 A CN1724616 A CN 1724616A
- Authority
- CN
- China
- Prior art keywords
- potassium ferrate
- low sulfur
- sulfur content
- acid
- productwith
- 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.)
- Granted
Links
Images
Landscapes
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
The invention supplies a method to manufacture super low sulfur oil product by potassium ferrate green oxidation process that adds certain acid water solution into oil product and adds potassium ferrate while whisking, then forms polar compound by oxidation process to realize produce super low sulfur oil product. The invention has advantages of mild reaction situation, and simple de-sulfurization technology, low cost, etc. It could be widely used in the field that needs super low sulfur oil product.
Description
The present invention relates to a kind of novel method that removes sulfide in the oil product, specifically provide a kind ofly when removing in the oil product sulfide, make the novel method of oxidant production super low sulfur oil product with potassium ferrate with oxidation style.
Traditional hydrodesulfurization has the history of decades, and the hydrogenation catalyst that generally uses at present is the sulfide system of Co-Mo, Ni-Mo, W-Ni etc., the SO that produces when catalyst vulcanization and regeneration
XSerious to topsoil, owing to require the temperature of reaction height, reaction pressure is big simultaneously, and the hydrogen consumption is big, to the requirement height of reactor, causes this method desulphurization cost higher.When particularly production sulphur content was the oil product of following " zero sulphur " standard of 10ppm, industrial cost can increase sharply.And non-hydrogenation method desulfurization such as extraction, alkali cleaning or process for adsorption desulfuration, existence form to sulfide in the oil product requires harsh, better to mercaptan sulfides removal effect in the oil product, but the removal effect for the thiophene-based organic sulfide is not good, is difficult to make sulphur content to drop to satisfied " zero sulphur " standard.
The objective of the invention is in order to overcome the deficiencies in the prior art, the novel method of potassium ferrate green oxidation method production super low sulfur oil product is provided.The sweetening process of this method is pollution-free, reaction conditions relaxes, technological process is simple, desulfurization degree is high, can remove various forms of sulfide in the oil product effectively.
The objective of the invention is to be achieved through the following technical solutions.The novel method of the producing oil productwith ultra low sulfur content using potassium ferrate oxidation method that the present invention proposes is one or two Sauerstoffatom to be linked on the sulphur atom of thiophenes by method for oxidation, to increase its polarity, adopts methods such as extraction, alkali cleaning or absorption to remove sulphur then.Concrete steps are: at first under normal temperature, normal pressure, in oil product, add an amount of aqueous acid, under agitation add potassium ferrate, after reaction for some time, the product that obtains is filtered, remove sulfide in the product with methods such as extraction, alkali cleaning or absorption again, thereby obtain the super low sulfur oil product.
The oxidation desulfurizing method that the present invention proposes has adopted green oxidation agent potassium ferrate, and its technological process is green, to environment without any pollution; Because the aqueous acid that adds, generated the stronger intermediate of oxidisability with the potassium ferrate effect, further improved the oxidation activity of potassium ferrate, effectively one or two Sauerstoffatom is linked and generated sulfoxide and sulfone class on the sulphur atom of thiophenes in the oil product, increased the polarity of sulfide, it is removed easilier by extraction, alkali cleaning or adsorption method, thereby the desulfurization degree height, can production super low sulfur oil product.Characteristics such as this method also has reaction conditions and relaxes, and sulfur removal technology is simple, and production cost is lower needing can be widely used in the field of super low sulfur oil product.
Below in conjunction with embodiment the present invention is further introduced.
Fig. 1 is the influence curve of oxidization time to residual sulfur content
Embodiment 1, be example with the desulfurization of pentane cut, raw material sources are in Fine, Chemical Plant, Daqing Oil Field, and wherein pentane content 73.0%, total sulfur content 49.3ppm.Experimental procedure is as follows:
Step 1, add in the pentane cut: (1) concentration is the aqueous acetic acid of 20~70% (w), and the volume ratio of aqueous acetic acid and pentane cut is 0.2~1.0: 20; (2) adding concentration respectively is 0.01~0.2g/mL phospho-molybdic acid, phospho-wolframic acid, oxalic acid aqueous solution, and the volume ratio of aqueous acid and pentane cut is 0.2~2.0: 20.
Step 2, measure 20mL pentane cut, add above-mentioned (1) or (2) solution of 0.5mL, stir and add the 0.1786g potassium ferrate down, control reaction temperature is 10~70 ℃, reacts 0.5~4 hour.
Step 3, filtering reacting liquid extract filtrate respectively and to remove sulphur with 50% ethylene glycol.
Result's contrast when adding experimental result that different acid obtain and not adding any acid sees Table 1.As can be seen from Table 1, under the identical prerequisite of other condition, when not adding acid in the product residual sulfur content be 16.8ppm, all can significantly improve sweetening effectiveness and add various acid, residual sulfur content is less than 4.02ppm in the product; The sweetening effectiveness of these several acid that experiment is added is differentiated, and when wherein adding other acid except that acetic acid, the sulphur content in the product is all less than 2ppm.
The result of result when adding different acid in table 1 oil product when not adding any acid relatively
Sequence number | Oxygenant/additive | Temperature of reaction/℃ | Reaction times/h | Oxygenant and residual sulfur content/ppm |
1 | K 2FeO 4 | 30 | 1 | 16.8 |
2 | K
2FeO
4/ | 30 | 1 | 1.44 |
3 | K
2FeO
4/ phospho- | 30 | 1 | 1.66 |
4 | K
2FeO
4/ phospho- | 30 | 1 | 1.90 |
5 | K
2FeO
4/ | 30 | 1 | 4.02 |
Embodiment 2, the phospho-molybdic acid of measuring 20ml pentane raw material, 0.5mL 10% are respectively put into Florence flask and are shaken all, add the 0.1786g potassium ferrate under the magnetic agitation, control reaction temperature is 30 ℃, change oxidation time, the reaction solution that obtains filters, sulfide in the filtrate adopts alkali cleaning (pH=11.5) method to remove, and the experimental result of the different oxidization times that obtain is seen shown in Figure 1.Along with the increase in reaction times, the residual sulfur content in the product reduces as seen from Figure 1, begins to reduce comparatively fast, slows down subsequently; During reaction 60min, residual sulfur content has been dropped to below the 1ppm by 49.3ppm in the pentane, and desulfurization degree is greater than 97.97%.
Embodiment 3, the phospho-molybdic acid of measuring 20ml pentane raw material, 0.5mL 10% are respectively put into Florence flask and are shaken all, add the 0.1786g potassium ferrate under the magnetic agitation, control reaction temperature is 30 ℃, oxidation 60min, filtering reacting liquid, filtrate adopt respectively under normal temperature, normal pressure: (1) extraction removes sulphur (making solvent as the ethylene glycol with 50%); (2) alkali cleaning (as the aqueous solution of pH=11.5) removes sulphur; (3) adsorbing and removing sulphur (as solid molecular sieves).The sweetening effectiveness of sweetening effectiveness when reaction solution that these three kinds of method separation removal oxidizing reactions obtain when handling inoxidized pentane raw material with corresponding separation method compares, and the results are shown in Table shown in 2.As can be seen from Table 2: after the pentane oil product through oxidation extracts, alkali cleaning or fractionation by adsorption remove sulphur, in the pentane residual sulfur content all less than 2ppm, sweetening effectiveness obviously than the oil product that not oxidised is handled directly extract, effective when alkali cleaning or absorption.Show Sauerstoffatom to be linked and generate sulfoxide and sulfone class on the sulphur atom of organic sulfide in the raw material by oxidation, increased the moment of dipole of sulfide, therefore, during with oil product after oxidation extraction, alkali cleaning or absorption, can will be directly during with extraction, alkali cleaning or absorption the difficult nonpolar sulfide that removes separate effectively, thereby the purpose that realizes producing the super low sulfur oil product that satisfies " zero sulphur " standard.
The comparison of the experimental result the when experimental result of table 2 oxidation sweetening and not oxidised
The removal methods of sulphur in the product | Separation removal sulphur method | Pentane residual sulfur content/ppm | |
Not oxidised is directly separated | After oxidation, | ||
Extraction | |||
50% ethylene glycol extraction | 24.5 | 1.66 | |
Alkali cleaning | The aqueous solution of PH=11.5 cleans | 26.5 | <1.0 |
Absorption | Solid molecular sieves absorption | 18.8 | <1.0 |
Claims (5)
1, a kind of novel method of producing oil productwith ultra low sulfur content using potassium ferrate oxidation method is characterized in that the oxygenant of use is a potassium ferrate when the oxidation sweetening of oil product.
2, the novel method of the described a kind of producing oil productwith ultra low sulfur content using potassium ferrate oxidation method of claim 1 is characterized in that at first adding an amount of aqueous acid in oil product when adding potassium ferrate.
3, the novel method of the described a kind of producing oil productwith ultra low sulfur content using potassium ferrate oxidation method of claim 1 is characterized in that the aqueous acid that is added is the aqueous solution of heteropolyacids such as phospho-molybdic acid.
4, the novel method of the described a kind of producing oil productwith ultra low sulfur content using potassium ferrate oxidation method of claim 1 is characterized in that the aqueous acid that is added is the aqueous solution of phospho-molybdic acid.
5, the novel method of the described a kind of producing oil productwith ultra low sulfur content using potassium ferrate oxidation method of claim 1 is characterized in that the aqueous acid that is added is phospho-wolframic acid, oxalic acid or aqueous acetic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100698616A CN100560694C (en) | 2005-04-30 | 2005-04-30 | A kind of method of producing oil productwith ultra low sulfur content using potassium ferrate oxidation method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100698616A CN100560694C (en) | 2005-04-30 | 2005-04-30 | A kind of method of producing oil productwith ultra low sulfur content using potassium ferrate oxidation method |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1724616A true CN1724616A (en) | 2006-01-25 |
CN100560694C CN100560694C (en) | 2009-11-18 |
Family
ID=35924250
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2005100698616A Expired - Fee Related CN100560694C (en) | 2005-04-30 | 2005-04-30 | A kind of method of producing oil productwith ultra low sulfur content using potassium ferrate oxidation method |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN100560694C (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101851529A (en) * | 2010-06-24 | 2010-10-06 | 东北石油大学 | Deep desulphurization method for oil by catalytic oxidation of potassium ferrate serving as oxidant with solid super acid |
-
2005
- 2005-04-30 CN CNB2005100698616A patent/CN100560694C/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101851529A (en) * | 2010-06-24 | 2010-10-06 | 东北石油大学 | Deep desulphurization method for oil by catalytic oxidation of potassium ferrate serving as oxidant with solid super acid |
Also Published As
Publication number | Publication date |
---|---|
CN100560694C (en) | 2009-11-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101653690B (en) | Sulfur and mercury removing agent | |
RU2006134728A (en) | METHOD FOR HIGH-EFFECTIVE SULFUR EXTRACTION FROM ACID GAS FLOW | |
CN102515447B (en) | Method for treating wastewater produced in process for directly liquefying coal | |
CN101962566B (en) | Mercaptan removed alkali liquid oxidation regeneration method and device thereof | |
CN110218576B (en) | Efficient selective catalytic oxidation desulfurization method for diesel oil | |
CN103331161B (en) | Catalyst for diesel desulfurization, preparation method and application | |
CN103146416B (en) | Method of separating disulfide from lye | |
CN105170133B (en) | A kind of preparation method of catalytic oxidation desulfurization catalyst | |
CN1952050B (en) | Oxidation sweetening method of hydrogenated diesel oil | |
CN101173192B (en) | Desulfurization method for diesel oil | |
CN103525453B (en) | Petroleum oil product oxidation coupling abstraction desulfurization and ionic liquid and preparation method thereof | |
CN104307469B (en) | It is a kind of for desulfuration adsorbent of refined diesel oil deep desulfuration and preparation method thereof | |
CN100489063C (en) | Method for preparing desulfurized diesel oil | |
CN101091869A (en) | Method for cleansing exhaust gas of sulfureted hydrogen in low concentration | |
CN100560694C (en) | A kind of method of producing oil productwith ultra low sulfur content using potassium ferrate oxidation method | |
CN105771892A (en) | Oil product desulfurizing agent and desulfurizing method thereof | |
CN104694151A (en) | An oxidation regeneration method for a thiolate-containing alkali solution | |
JPS60190241A (en) | Regeneration of waste hydrogenation catalyst | |
CN105126768A (en) | Light-weight oil desulfurizing agent based on supra-molecular inclusion effect and application method thereof | |
CN117358027A (en) | Desulfurizing agent for removing hydrogen sulfide and carbonyl sulfide, and preparation method and application thereof | |
CN101302441A (en) | Method for removing sulfide in catalytically cracked gasoline by oxidation-extraction | |
CN113117650B (en) | Defect metal-organic framework desulfurization adsorbent and preparation method and application thereof | |
CN102757811B (en) | Diesel oil oxidative desulphurization method | |
CN101525549B (en) | Hydrocracking tail oil ultra-deep adsorbent desulfurizing and denitrifying method | |
CN101851529A (en) | Deep desulphurization method for oil by catalytic oxidation of potassium ferrate serving as oxidant with solid super acid |
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 | ||
C17 | Cessation of patent right | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20091118 Termination date: 20100430 |