CN101322900A - Compositional type reclaiming agent - Google Patents

Compositional type reclaiming agent Download PDF

Info

Publication number
CN101322900A
CN101322900A CNA2008100227861A CN200810022786A CN101322900A CN 101322900 A CN101322900 A CN 101322900A CN A2008100227861 A CNA2008100227861 A CN A2008100227861A CN 200810022786 A CN200810022786 A CN 200810022786A CN 101322900 A CN101322900 A CN 101322900A
Authority
CN
China
Prior art keywords
compositional type
type reclaiming
reclaiming agent
agent
antioxidant
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.)
Pending
Application number
CNA2008100227861A
Other languages
Chinese (zh)
Inventor
顾泽元
龚六兴
陈政
顾晓峰
张炜
王玉莲
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CNA2008100227861A priority Critical patent/CN101322900A/en
Publication of CN101322900A publication Critical patent/CN101322900A/en
Pending legal-status Critical Current

Links

Landscapes

  • Gas Separation By Absorption (AREA)

Abstract

The invention relates to a high-effective remover of hydrogen sulfide at normal temperature and a preparation method thereof, in particular to a compound high-effective sulfur remover and the preparation method thereof. The sulfur remover contains N-methyl diethanol amine with the content of 93.5 weight percent to 96 weight percent, and the other components are an anti-foaming agent, a corrosion inhibitor, an antioxidant and an intensifier. The preparation method of the sulfur remover is that 93.5 portions to 96 portions (all portions are weight portions) of N-methyl diethanol amine, 0.05 portion to 0.2 portion of anti-foaming agent, 0.02 portion to 0.05 portion of corrosion inhibitor, 0.05 portion to 0.2 portion of antioxidant and 3 portions to 6 portions of intensifier are stirred in a stirring kettle into uniform solution, that is, the compound sulfur remover. The compound sulfur remover of the invention solves the problem that the present MDEA compound sulfur remover can affect the sulfur removing effect by reacting with CO2.

Description

A kind of Compositional type reclaiming agent
Technical field
The present invention relates to normal temperature high efficient remover of a kind of hydrogen sulfide and preparation method thereof, especially a kind of Compositional type efficient desulfurizing agent and preparation method thereof.
Background technology
Both at home and abroad the research of Treatment of Hydrogen Sulfide Waste Gas is more and more paid attention to, the method for carrying out desulfurization according to its faintly acid and strong reducing property can be divided into dry method and wet method.Dry method is to utilize the reproducibility and the combustibility of hydrogen sulfide, comes desulfurization or directly burning with solid oxidizer or adsorbent, comprising Claus method, iron oxide process, activated carbon method and Ka Taisuerfufa etc.Wet method is divided into liquid absorption method and absorbs oxidizing process two classes by its used different Compositional type reclaiming agents.Chemical absorption method that utilizes alkaline solution and the Physical Absorption method of utilizing organic solvent and physical chemistry absorption process are arranged in the liquid absorption method.Absorbing oxidizing process mainly utilizes various oxidants, catalyst to carry out desulfurization.With regard to present dry method and wet method two big sulfur removal technologies, dry desulfurization is to remove sulfide with solid absorbent, desulfuration efficiency is higher, but equipment investment is bigger, need super regeneration or replacing, its sulfur capacity is relatively low, and Compositional type reclaiming agent can not be regenerated mostly, need to handle, mainly be suitable for the meticulous desulfurization of gas.Wet desulphurization is to remove sulfide with liquid-absorbant, and the device processes amount is big, and investment and operating cost are little, but continued operation can adapt to the desulfurization requirement of higher load, the application surface broad, and wherein the advantage with liquid phase oxidation is comparatively outstanding especially.Industrialized absorption oxidizing process at present just, arsyl technology does not re-use substantially; Vanadium base technology also will be subjected to the restriction of environmental regulation because use contains the vanadium washing lotion; PDS (the alert sulfonate that bores of double-core phthalein) desulfur technology is owing to catalyst system therefor PDS cost height, and desulphurization cost is corresponding wants high; Iron-based technology desulfuration efficiency height, sulfur capacity is big, but these class methods remain the problem that needs solution many at aspects such as stability of solution, side reaction control and regeneration.At present, it is N methyldiethanol amine that a kind of Compositional type reclaiming agent MDEA that is widely used is arranged in the wet desulphurization, MDEA and H 2S forms more stable soda acid complex compound in water, but also can with a large amount of CO that exist in the gas 2Form the soda acid complex compound, absorb H thereby influence MDEA 2The problem of the amount of S.
Summary of the invention
The technical problem to be solved in the present invention is: present MDEA Compositional type reclaiming agent exists and CO 2Reaction influences the problem of the effect of desulfurization, the invention provides a kind of Compositional type reclaiming agent.
The technical solution adopted for the present invention to solve the technical problems is: the invention provides a kind of Compositional type reclaiming agent, wherein contain N methyldiethanol amine, N methyldiethanol amine content in Compositional type reclaiming agent is 93.5~96wt%, and all the other are defoamer, corrosion inhibiter, antioxidant and reinforcing agent.
The purity of employed N methyldiethanol amine is more than or equal to 95wt% among the present invention.
Defoamer used in the present invention is a dimethicone, its use amount accounts for 0.05~0.2wt% of whole Compositional type reclaiming agent, dimethicone is a kind of defoamer commonly used, can well eliminate the foam that Compositional type reclaiming agent produces when absorbing sulfurous gas, reaches the purpose of fast Absorption.
Corrosion inhibiter used in the present invention is thiocarbamide, dimethyl sulfourea, 1,4-succinimide mercaptans or sulfo-diethylene glycol (DEG), and its use amount accounts for 0.02~0.05wt% of whole Compositional type reclaiming agent, and corrosion inhibiter can form film in equipment surface, less absorption H 2Behind the S, the H+ that ionization goes out in solution is to the erosion of equipment surface.
Employed antioxidant is 2 among the present invention, and 6-DI-tert-butylphenol compounds, hydroquinones, MEHQ or diethyl hydroxylamine, the content in described Compositional type reclaiming agent are 0.05~0.2wt%.
Employed reinforcing agent is boric acid, phosphoric acid, phosphorous acid, polyethers phosphoric acid, butyric acid, valeric acid or oleic acid among the present invention, and the content in described Compositional type reclaiming agent is 3~6wt%.
Preparation method of the present invention stirs the reinforcing agent of the N methyldiethanol amine of 93.5~96 parts (following umber is mass fraction), 0.05~0.2 part of defoamer, 0.02~0.05 part of corrosion inhibiter, 0.05~0.2 part of antioxidant and 3~6 minutes and makes uniform solution, i.e. Compositional type reclaiming agent in stirred tank.
The present invention is applicable to the holder H of natural gas, refinery gas 2S handles, in particular for CO in the unstripped gas 2(vol%)/H 2The natural gas that S (vol%) volume ratio is high, the desulfurization of refinery gas are handled.
The invention has the beneficial effects as follows that the present invention has than MDEA or based on the higher selection of common Compositional type reclaiming agent of MDEA and absorbs H when handling the raw material of high carbon-sulfur ratio 2The ability of S can make the H in the regenerated acidic gas 2The S volume content increases by 5~10%, and desulphurization system solvent internal circulating load can descend 10% simultaneously, is the new product of a kind of energy-conservation, consumption reduction, environmental protection.
The specific embodiment
The invention will be further described below by embodiment, and its purpose is to be better understanding content of the present invention.
Example one
With the N methyldiethanol amine of 95 parts of purity 98wt%, 0.2 part of dimethicone, 0.05 part of dimethyl sulfourea, 0.2 part 2,6-DI-tert-butylphenol compounds and 6 fens phosphoric acid stir in stirred tank makes uniform solution, i.e. Compositional type reclaiming agent.
Example two
With the N methyldiethanol amine of 93.5 parts of purity 99wt%, 0.1 part of dimethicone, 0.03 part 1,4-succinimide mercaptans, 0.05 part of MEHQ and 4 fens butyric acid stir in stirred tank makes uniform solution, i.e. Compositional type reclaiming agent.
Example three
The N methyldiethanol amine of 96 parts of purity 95wt%, 0.1 part of dimethicone, 0.03 portion of sulfo-diethylene glycol (DEG), 0.05 part of hydroquinones and 4 segregation ether phosphoric acids are stirred in stirred tank make uniform solution, i.e. Compositional type reclaiming agent.
Specific embodiment described herein only is illustrating spirit of the present invention, real name person of ordinary skill in the field can do various modifications or replenishes or adopt similar mode to substitute described specific embodiment, but can not depart from spirit of the present invention.

Claims (8)

1. a Compositional type reclaiming agent wherein contains N methyldiethanol amine, it is characterized in that: described N methyldiethanol amine content in described Compositional type reclaiming agent is 93.5~96wt%, and all the other are defoamer, corrosion inhibiter, antioxidant and reinforcing agent.
2. Compositional type reclaiming agent according to claim 1 is characterized in that: the purity of described N methyldiethanol amine is more than or equal to 95wt%.
3. Compositional type reclaiming agent according to claim 1, it is characterized in that: the content of described defoamer in described Compositional type reclaiming agent is 0.05~0.2wt%, the content of described corrosion inhibiter in described Compositional type reclaiming agent is 0.02~0.05wt%, the content of described antioxidant in described Compositional type reclaiming agent is 0.05~0.2wt%, and the content of described reinforcing agent in described Compositional type reclaiming agent is 3~6wt%.
4. Compositional type reclaiming agent according to claim 1 and 2 is characterized in that: described defoamer is a dimethicone.
5. Compositional type reclaiming agent according to claim 1 and 2 is characterized in that: described corrosion inhibiter is thiocarbamide, dimethyl sulfourea, 1,4-succinimide mercaptans or sulfo-diethylene glycol (DEG).
6. Compositional type reclaiming agent according to claim 1 and 2 is characterized in that: described antioxidant is 2,6-DI-tert-butylphenol compounds, hydroquinones, MEHQ or diethyl hydroxylamine.
7. Compositional type reclaiming agent according to claim 1 and 2 is characterized in that: described reinforcing agent is boric acid, phosphoric acid, phosphorous acid, polyethers phosphoric acid, butyric acid, valeric acid or oleic acid.
8. Compositional type reclaiming agent preparation method according to claim 1, it is characterized in that: the reinforcing agent of the N methyldiethanol amine of 93.5~96 parts (following umber is mass fraction), 0.05~0.2 part of defoamer, 0.02~0.05 part of corrosion inhibiter, 0.05~0.2 part of antioxidant and 3~6 minutes is stirred in stirred tank make uniform solution, i.e. Compositional type reclaiming agent.
CNA2008100227861A 2008-07-29 2008-07-29 Compositional type reclaiming agent Pending CN101322900A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNA2008100227861A CN101322900A (en) 2008-07-29 2008-07-29 Compositional type reclaiming agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNA2008100227861A CN101322900A (en) 2008-07-29 2008-07-29 Compositional type reclaiming agent

Publications (1)

Publication Number Publication Date
CN101322900A true CN101322900A (en) 2008-12-17

Family

ID=40186699

Family Applications (1)

Application Number Title Priority Date Filing Date
CNA2008100227861A Pending CN101322900A (en) 2008-07-29 2008-07-29 Compositional type reclaiming agent

Country Status (1)

Country Link
CN (1) CN101322900A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101773783A (en) * 2010-03-17 2010-07-14 南京碳环生物质科技有限公司 Wet catalytic oxidative desulfurization method for biogas
CN101822932A (en) * 2010-06-12 2010-09-08 中国石油集团工程设计有限责任公司 Composite decarbonization solvent for eliminating carbon dioxide in natural gases
CN103537170A (en) * 2013-10-10 2014-01-29 盘锦鑫安源化学工业有限公司 Highly selective desulfurization solvent and preparation method thereof
CN103664651A (en) * 2013-11-22 2014-03-26 江苏汉光实业股份有限公司 Desulfurizer production system
CN107081052A (en) * 2017-06-13 2017-08-22 中国石油集团工程设计有限责任公司 Acid gas absorbent and application containing double (3 aminopropyl) polyethylene glycol
CN108816196A (en) * 2018-07-24 2018-11-16 淄博凯美可工贸有限公司 Highly selective Compositional type reclaiming agent and preparation method thereof
CN111054198A (en) * 2018-10-16 2020-04-24 上海赛思特新能源科技有限公司 Compound desulfurizer and preparation method thereof
CN111117689A (en) * 2019-12-27 2020-05-08 江苏科创石化有限公司 Efficient desulfurization composite solvent and preparation method thereof
CN116550100A (en) * 2023-05-30 2023-08-08 江苏太湖新材料控股有限公司 Desulfurizing agent and preparation method thereof

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101773783A (en) * 2010-03-17 2010-07-14 南京碳环生物质科技有限公司 Wet catalytic oxidative desulfurization method for biogas
CN101822932A (en) * 2010-06-12 2010-09-08 中国石油集团工程设计有限责任公司 Composite decarbonization solvent for eliminating carbon dioxide in natural gases
CN101822932B (en) * 2010-06-12 2013-01-02 中国石油集团工程设计有限责任公司 Composite decarbonization solvent for eliminating carbon dioxide in natural gases
CN103537170A (en) * 2013-10-10 2014-01-29 盘锦鑫安源化学工业有限公司 Highly selective desulfurization solvent and preparation method thereof
CN103537170B (en) * 2013-10-10 2015-09-30 盘锦鑫安源化学工业有限公司 Desulfurization solvent of a kind of high selectivity and preparation method thereof
CN103664651A (en) * 2013-11-22 2014-03-26 江苏汉光实业股份有限公司 Desulfurizer production system
CN107081052A (en) * 2017-06-13 2017-08-22 中国石油集团工程设计有限责任公司 Acid gas absorbent and application containing double (3 aminopropyl) polyethylene glycol
CN107081052B (en) * 2017-06-13 2019-10-25 中国石油工程建设有限公司 Acid gas absorbent and application containing bis- (3- aminopropyl) polyethylene glycol
CN108816196A (en) * 2018-07-24 2018-11-16 淄博凯美可工贸有限公司 Highly selective Compositional type reclaiming agent and preparation method thereof
CN108816196B (en) * 2018-07-24 2021-05-14 淄博凯美可工贸有限公司 High-selectivity compound desulfurizer and preparation method thereof
CN111054198A (en) * 2018-10-16 2020-04-24 上海赛思特新能源科技有限公司 Compound desulfurizer and preparation method thereof
CN111117689A (en) * 2019-12-27 2020-05-08 江苏科创石化有限公司 Efficient desulfurization composite solvent and preparation method thereof
CN111117689B (en) * 2019-12-27 2021-08-31 江苏科创石化有限公司 Efficient desulfurization composite solvent and preparation method thereof
CN116550100A (en) * 2023-05-30 2023-08-08 江苏太湖新材料控股有限公司 Desulfurizing agent and preparation method thereof

Similar Documents

Publication Publication Date Title
CN101264411A (en) Desulfurization solvent
CN101322900A (en) Compositional type reclaiming agent
CN102151476B (en) Method for removing hydrogen sulfide in gas phase through oxidization under high gravity field
CN101264413A (en) Total sulfides removing solvent and preparation thereof
CN101274750B (en) Tail gas-recycled sulfur recovery method
CN103265988B (en) Method for purifying natural gas
CN108816196B (en) High-selectivity compound desulfurizer and preparation method thereof
WO2010126694A1 (en) Self-concentrating absorbent for acid gas separation
RU2696467C2 (en) Method of renewed wet desulphurisation using a suspension layer
RU2678698C1 (en) Method of wet desulfurization using suspension layer
CN103357261A (en) Compound desulfurizer and preparation method thereof
CN103949147A (en) Desulfurization method for purifying flue gas
CN105126380A (en) Coking exhaust gas treatment method
CN113289458B (en) Application of amine compound in removing organic sulfide
CN103146416B (en) Method for separating disulfide from alkali liquor
CN1169335A (en) Method for taking off hydrogen sulfide from mixed gas
CN108355463A (en) A kind of sulfur method and device of tail gas of sulphur
CN103205296A (en) Wet method and dry method series-connected biogas desulfurization purifying process
Zhang et al. Removal of sulfide from fuels by ionic liquids: prospects for the future
CN105169879B (en) Coked tail gas processing method
CN102179147B (en) Polymer organic amine desulfurizer
CN102218260B (en) Absorbent used for removing sulfides in malodorous gases
CN105126530A (en) Coking exhaust gas purification method
CN109351126A (en) Sulphur-containing exhaust gas processing method
CN102133500B (en) Method for removing sulfur dioxide in smoke

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Open date: 20081217