CN101003366A - Method for producing hydros by using epoxy compound as auxiliary agent - Google Patents

Method for producing hydros by using epoxy compound as auxiliary agent Download PDF

Info

Publication number
CN101003366A
CN101003366A CN 200610150002 CN200610150002A CN101003366A CN 101003366 A CN101003366 A CN 101003366A CN 200610150002 CN200610150002 CN 200610150002 CN 200610150002 A CN200610150002 A CN 200610150002A CN 101003366 A CN101003366 A CN 101003366A
Authority
CN
China
Prior art keywords
synthetic
pot
auxiliary agent
epoxy compound
sodium
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
CN 200610150002
Other languages
Chinese (zh)
Inventor
张宝健
张心遵
王国清
邹广柱
孙丙谦
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.)
Jinhe Safety Powder Factory Co Ltd Yantai City
Original Assignee
Jinhe Safety Powder Factory Co Ltd Yantai City
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 Jinhe Safety Powder Factory Co Ltd Yantai City filed Critical Jinhe Safety Powder Factory Co Ltd Yantai City
Priority to CN 200610150002 priority Critical patent/CN101003366A/en
Publication of CN101003366A publication Critical patent/CN101003366A/en
Pending legal-status Critical Current

Links

Landscapes

  • Glass Compositions (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Abstract

This invention relates to a method for producing sodium hydrosulfite by using epoxide compound as auxiliary. The method solves the problems of large difficulty in inhibiting side reactions, poor product stability, low yield and high raw material consumption faced by background techniques. In this invention, when the content of Na2S2O3 in the materials in the synthesis pot is greater than or equal to 5 g/L, epoxide compound is added so that the content of Na2S2O3 is less than or equal to 5 g/L. Sodium hydrosulfite produced in this invention has such advantages as inhibited side reactions, high synthesis rate.

Description

A kind of method of producing vat powder with epoxy compound as auxiliary agent
Technical field: the present invention relates to produce the method for vat powder, particularly a kind of method of producing vat powder with epoxy compound as auxiliary agent.
Background technology: at present, produce the method for vat powder, conditions such as the pH value of reaction solution and pressure, temperature are produced vat powder in the synthetic pot of major control.This method exists that side reaction is difficult to suppress, product stability is poor, synthesis yield is low, the shortcomings such as raw materials consumption height.The sodium thiosulfate Na that generates of side reaction particularly 2S 2O 3, increased consumption of raw materials, cause above problem to take place.What therefore effectively suppress side reaction is to produce sodium hydrosulfite method institute problem demanding prompt solution.
Summary of the invention: the objective of the invention is to propose a kind of method of producing vat powder with epoxy compound as auxiliary agent, the solution background technology exists: side reaction is difficult to suppress, product stability is poor, synthesis yield is low, shortcomings such as raw materials consumption height.Solving the technical scheme that above technical problem adopts is: 1, a kind of method of producing sodium hydrosulfite with epoxy compound as auxiliary agent, (1) synthetic bed material preparation: under normal temperature, normal pressure, material (to call the ingredients pot material in the following text No. 1) with refined methanol or synthesis mother liquid, sodium formate and fresh water (FW) preparation adds 1000~1500L in synthetic pot, start synthetic pot and stir, pass into steam to synthetic pot chuck then and slowly heat up; (2) in and tone pitch: when synthetic kettle temperature rises to 75 ℃~80 ℃, the synthetic pot inner pressure 0.05~0.30MPa of control, the acidificated material (to call the ingredients pot material in the following text No. 2) that adds refined methanol or washing methyl alcohol, sodium pyrosulfite or sodium carbonate, sulfur dioxide liquid preparation in the synthetic pot is regulated in the synthetic pot material pH value 4.2~4.6 and o'clock is ended; (3) the big dropping: behind the tone pitch, when synthetic kettle temperature rose to 80~85 ℃, beginning is dropping greatly, namely simultaneously leftover materials in No. 1, No. 2 ingredients pots was evenly added in 50min~90min; (4) little dropping: drip greatly rear a synthetic pot material suitably is incubated 5~15min after, begin little dropping, namely add equably sulfur dioxide liquid with 100~180min thread shape, until from synthetic material during Sodium Hydrosulfite Content 〉=88.5% synthetic droplet add end; (5) insulation: when synthetic reach terminal point after, insulation 30min~90min, 80~84 ℃ of the synthetic pot inner pressure 0.10~0.25MPa of insulating process control, temperature, insulation terminal point PH 〉=4.9; (6) cooling blowing: be incubated complete, opening clamp jacket water valve, synthetic pot inner pressure≤the 0.1MPa of control, 60~70 ℃ of temperature, pH value 〉=4.9 will be synthesized then in the pot material and be put into four unification driers and carry out press filtration, washing, drying, cooling, blending, blowing, packing and make qualified sodium hydrosulfite product; It is characterized in that in the above process Na in the synthetic pot of sample analysis material 2S 2O 3During 〉=5g/L, end when adding epoxide to Na2S203≤5g/L.The epoxy compounds of adding is oxyethane or propylene oxide.
The beneficial effect that the present invention and background technology comparison have is: owing to add epoxy compound as auxiliary agent on the methodological science ground that produces sodium hydrosulfite, play the generation that suppresses side reaction in synthetic sodium hydrosulfite process, reduced accessory substance Na 2S 2O 3Generation, therefore improved product stability, increased synthesis yield, reduced raw materials consumption.
Embodiment:
Embodiment 1, a kind of method of producing sodium hydrosulfite with epoxy compound as auxiliary agent, (1) synthetic bed material preparation: under normal temperature, normal pressure, material (to call the ingredients pot material in the following text No. 1) with refined methanol or synthesis mother liquid, sodium formate and fresh water (FW) preparation adds 1000~1500L in synthetic pot, start synthetic pot and stir, pass into steam to synthetic pot chuck then and slowly heat up; (2) in and tone pitch: when synthetic kettle temperature rises to 75 ℃~80 ℃, the synthetic pot inner pressure 0.05~0.30MPa of control, the acidificated material (to call the ingredients pot material in the following text No. 2) that adds refined methanol or washing methyl alcohol, sodium pyrosulfite or sodium carbonate, sulfur dioxide liquid preparation in the synthetic pot is regulated in the synthetic pot material pH value 4.2~4.6 and o'clock is ended; (3) the big dropping: behind the tone pitch, when synthetic kettle temperature rose to 80~85 ℃, beginning is dropping greatly, namely simultaneously leftover materials in No. 1, No. 2 ingredients pots was evenly added in 50min~90min; (4) little dropping: drip greatly rear a synthetic pot material suitably is incubated 5~15min after, begin little dropping, namely add equably sulfur dioxide liquid with 100~180min thread shape, until from synthetic material during Sodium Hydrosulfite Content 〉=88.5% synthetic droplet add end; (5) insulation: when synthetic reach terminal point after, insulation 30min~90min, 80~84 ℃ of the synthetic pot inner pressure 0.10~0.25MPa of insulating process control, temperature, insulation terminal point PH 〉=4.9; (6) cooling blowing: be incubated complete, open chuck condensed water valve, synthetic pot inner pressure≤the 0.1MPa of control, 60~70 ℃ of temperature, pH value 〉=4.9 will be synthesized then in the pot material and be put into four unification driers and carry out press filtration, washing, drying, cooling, blending, blowing, packing and make qualified sodium hydrosulfite product; It is characterized in that in the above process Na in the synthetic pot of sample analysis material 2S 2O 3During 〉=5g/L, add oxirane to Na 2S 2O 3End during≤5g/L.
Embodiment 2, except that epoxy compounds is propylene oxide, all the other are identical with embodiment 1.

Claims (3)

1, a kind of method of producing sodium hydrosulfite with epoxy compound as auxiliary agent, (1) synthetic bed material preparation: under normal temperature, normal pressure, material (to call the ingredients pot material in the following text No. 1) with refined methanol or synthesis mother liquid, sodium formate and fresh water (FW) preparation adds 1000~1500L in synthetic pot, start synthetic pot and stir, pass into steam to synthetic pot chuck then and slowly heat up; (2) in and tone pitch: when synthetic kettle temperature rises to 75 ℃~80 ℃, the synthetic pot inner pressure 0.05~0.30MPa of control, the good material (to call the ingredients pot material in the following text No. 2) of caproic acidization that adds refined methanol or washing methyl alcohol, sodium pyrosulfite or sodium carbonate, sulfur dioxide liquid preparation in the synthetic pot is regulated in the synthetic pot material pH value 4.2~4.6 and o'clock is ended; (3) the big dropping: behind the tone pitch, when synthetic kettle temperature rose to 80~85 ℃, beginning is dropping greatly, namely simultaneously leftover materials in No. 1, No. 2 ingredients pots was evenly added in 50min~90min; (4) little dropping: drip greatly rear a synthetic pot material suitably is incubated 5~15min after, begin little dropping, namely add equably sulfur dioxide liquid with 100~180min thread shape, until from synthetic material during Sodium Hydrosulfite Content 〉=88.5% synthetic droplet add end; (5) insulation: when synthetic reach terminal point after, insulation 30min~90min, 80~84 ℃ of the synthetic pot inner pressure 0.10~0.25MPa of insulating process control, temperature, insulation terminal point PH 〉=4.9; (6) cooling blowing: be incubated complete, opening clamp jacket water valve, synthetic pot inner pressure≤the 0.1MPa of control, 60~70 ℃ of temperature, pH value 〉=4.9 will be synthesized then in the pot material and be put into four unification driers and carry out press filtration, washing, drying, cooling, blending, blowing, packing and make qualified sodium hydrosulfite product; It is characterized in that in the above process Na in the synthetic pot of sample analysis material 2S 2O 3During 〉=5g/L, add epoxide to Na 2S 2O 3End during≤5g/L.
2, according to the described a kind of method of producing vat powder of claim 1, it is characterized in that the epoxy compounds of adding is an oxyethane with epoxy compound as auxiliary agent.
3, according to the described a kind of method of producing vat powder of claim 1, it is characterized in that the epoxy compounds of adding is a propylene oxide with epoxy compound as auxiliary agent.
CN 200610150002 2006-10-24 2006-10-24 Method for producing hydros by using epoxy compound as auxiliary agent Pending CN101003366A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200610150002 CN101003366A (en) 2006-10-24 2006-10-24 Method for producing hydros by using epoxy compound as auxiliary agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200610150002 CN101003366A (en) 2006-10-24 2006-10-24 Method for producing hydros by using epoxy compound as auxiliary agent

Publications (1)

Publication Number Publication Date
CN101003366A true CN101003366A (en) 2007-07-25

Family

ID=38702802

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 200610150002 Pending CN101003366A (en) 2006-10-24 2006-10-24 Method for producing hydros by using epoxy compound as auxiliary agent

Country Status (1)

Country Link
CN (1) CN101003366A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102530883A (en) * 2011-12-14 2012-07-04 烟台金海化工有限公司 Method for synthetizing sodium hydrosulfite
CN102556980A (en) * 2011-12-14 2012-07-11 烟台金海化工有限公司 Method for synthesizing sodium dithionite
CN102674266A (en) * 2012-05-23 2012-09-19 江苏省东泰精细化工有限责任公司 Drying method of zinc dust process based sodium hydrosulfite
CN103552991A (en) * 2013-10-23 2014-02-05 中盐安徽红四方股份有限公司 Novel continuous large dropwise adding technological method in sodium hydrosulfite production
CN104341328A (en) * 2014-10-16 2015-02-11 烟台市金河保险粉厂有限公司 Method for producing ethanethiol by utilizing distilled crude methanol residue liquid in production process of sodium hydrosulfite
CN106517103A (en) * 2016-12-14 2017-03-22 赤峰瑞阳化工有限公司 Sodium hydrosulfite synthesizing and continuous producing method

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102530883A (en) * 2011-12-14 2012-07-04 烟台金海化工有限公司 Method for synthetizing sodium hydrosulfite
CN102556980A (en) * 2011-12-14 2012-07-11 烟台金海化工有限公司 Method for synthesizing sodium dithionite
CN102530883B (en) * 2011-12-14 2013-10-23 烟台市金河保险粉厂有限公司 Method for synthetizing sodium hydrosulfite
CN102674266A (en) * 2012-05-23 2012-09-19 江苏省东泰精细化工有限责任公司 Drying method of zinc dust process based sodium hydrosulfite
CN103552991A (en) * 2013-10-23 2014-02-05 中盐安徽红四方股份有限公司 Novel continuous large dropwise adding technological method in sodium hydrosulfite production
CN104341328A (en) * 2014-10-16 2015-02-11 烟台市金河保险粉厂有限公司 Method for producing ethanethiol by utilizing distilled crude methanol residue liquid in production process of sodium hydrosulfite
CN106517103A (en) * 2016-12-14 2017-03-22 赤峰瑞阳化工有限公司 Sodium hydrosulfite synthesizing and continuous producing method
CN106517103B (en) * 2016-12-14 2018-07-27 赤峰瑞阳化工有限公司 Sodium hydrosulfite synthesizes continuous production method

Similar Documents

Publication Publication Date Title
CN101003366A (en) Method for producing hydros by using epoxy compound as auxiliary agent
CN104805151A (en) Lignocellulosic feedstock pretreatment method without prepreg
JPS6336760B2 (en)
EP1969175A4 (en) A novel catalytic reactor process for the production of commercial grade pulp, native lignin and unicellular protein
CN103757959B (en) A kind of method using ionic liquid two-step method to obtain fiber-rich cellulosic material from straw
WO2012047832A3 (en) Process for the production of alcohols from biomass
CN109422719A (en) The preparation method of cyclic sulfates
CN107011314A (en) The synthetic method of Atorvastatin calcium chiral intermediate
CN104817443B (en) Benzoin dimethyl ether synthesis process
CN100396598C (en) Process for producing sodium formate using liquid sulfur dioxide and sodium pyrosulfite
CN104744239B (en) The preparation method of hydroxyacetic acid
CN106631777A (en) Method for synthesizing methyl gamma-chlorobutyrate
CN104355990B (en) Method for recycling and mechanically using L- (+) -tartaric acid in D-ethyl ester production
CN102516057A (en) Method for extracting organic acid from yellow water
CN101550118B (en) Synthetic process for vitamin C sodium salts
CN108191731A (en) A kind of novel butyrolactam preparation process based on biomass material aminobutyric acid
CN103613518B (en) The preparation method of a kind of α-benzene ethyl sulfonic acid
CN1284725C (en) Method of producing sodium formate method sodium hydrosulfite using liquid sulfur dioxide and solid sodium carbonate
CN105503777A (en) Preparation method of quaternary ammonium salt GTMAC
CN105002237A (en) Method for synthesizing L-ascorbic acid-2-glucoside through enzyme fermentation process
CN106831513A (en) The preparation method of thioacetic acid potassium
CN106398236B (en) A kind of technique of epoxidized linseed oil and citric acid composite elasticizer
CN203530188U (en) Equipment for refining and bleaching alkyl glycoside
CN105001273B (en) A kind of preparation method of mannose
CN104099378B (en) A kind of method that xylitol is prepared with sugar grass fermentation residue

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C12 Rejection of a patent application after its publication
RJ01 Rejection of invention patent application after publication

Open date: 20070725