[go: up one dir, main page]

CN101121557A - Preparation method for disinfection algicide for swimming pool - Google Patents

Preparation method for disinfection algicide for swimming pool Download PDF

Info

Publication number
CN101121557A
CN101121557A CNA2007100257523A CN200710025752A CN101121557A CN 101121557 A CN101121557 A CN 101121557A CN A2007100257523 A CNA2007100257523 A CN A2007100257523A CN 200710025752 A CN200710025752 A CN 200710025752A CN 101121557 A CN101121557 A CN 101121557A
Authority
CN
China
Prior art keywords
preparation
saturated
carbon atom
treatment agent
reaction solution
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
Application number
CNA2007100257523A
Other languages
Chinese (zh)
Other versions
CN100584769C (en
Inventor
李胜兵
陈军
冯志德
刘效兵
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.)
Solvay Zhangjiagang Specialty Chemicals Co Ltd
Original Assignee
Feixiang Chemicals Zhangjiagang Co Ltd
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 Feixiang Chemicals Zhangjiagang Co Ltd filed Critical Feixiang Chemicals Zhangjiagang Co Ltd
Priority to CN200710025752A priority Critical patent/CN100584769C/en
Publication of CN101121557A publication Critical patent/CN101121557A/en
Application granted granted Critical
Publication of CN100584769C publication Critical patent/CN100584769C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The present invention discloses a manufacturing method of the high-efficient, innoxious and safe sterilizing and alga-destroying thing used in the natatorium. The method mainly comprises the following steps: under the protection of the inert gases, the frank-chain fat diamines is reacted with the dihydroxy ethyl aether in the water solution, and then are treated by the treating thing. The reaction liquid is adjusted to litmusless. The sterilizing and alga-destroying thing with the structure can be obtained. Thereinto, R1, R2, R3, R4 are respectively selected from H and a saturated or unsaturated alkyl including at least one carbon atom; m is among 1 to 14; n is among 1 to 5000; X represents a halogen ion combined with a positive ion. The product can be widely used for sterilizing and alga-destroying for the natatorium.

Description

A kind of preparation method of disinfection algicide for swimming pool
Technical field
The present invention relates to a kind of preparation method of disinfection algicide for swimming pool.
Background technology
Generally use chlorine, dioxide peroxide, clorox as disinfection algicide for swimming pool at present, chlorine must be closed Shi Caike at swimming pool and carry out sterilization algae removal because human body is had pungency and danger; Though clorox danger reduces greatly, pungency still exists; Dioxide peroxide is non-stimulated to human body, but preparation is difficult, product stock is unstable.
Summary of the invention
Technical problem to be solved by this invention is: the preparation method that a kind of disinfection algicide for swimming pool efficient, nontoxic, safe in utilization will be provided.
For solving the problems of the technologies described above; the technical solution used in the present invention is: the preparation method of described disinfection algicide for swimming pool; it is characterized in that: comprise the steps: under certain temperature T1; and under protection of inert gas; straight-chain fat diamine is added in the mixed solution of dihalo-ethyl ether and water; be warming up to the T2 reaction then and obtain a kind of polyquaternium; the pH value of monitoring reaction liquid; after the pH of reaction solution value is less than A; reaction solution is cooled to T3; adding post-treatment agent then handles; after post-treatment agent is handled, again reaction solution is transferred to neutrality, promptly get required Biocidal algae-killing agent.This Biocidal algae-killing agent has following general formula:
Figure A20071002575200041
Wherein R1 be selected from H, by a kind of saturated or undersaturated alkyl that has at least one carbon atom, R2 is selected from H, by a kind of saturated or undersaturated alkyl that has at least one carbon atom, R3 is selected from H, by a kind of saturated or undersaturated alkyl that has at least one carbon atom, R4 is selected from H, by a kind of saturated or undersaturated alkyl that has at least one carbon atom; M is 1~14; N is 1~5000; X-represents a kind of halide-ions that combines with positively charged ion.
The mol ratio of above-mentioned straight-chain fat diamine and dihalo-ethyl ether is 1.5: 1~1: 1.5.
Above-mentioned temperature T 1 is 30-90 ℃, preferred 50-70 ℃; T2 is 60-150 ℃, preferred 90-120 ℃.T3 is 0-70 ℃, preferred 30-60 ℃.
Above-mentioned pH value A is 4.0-7.0.
Above-mentioned rare gas element can be nitrogen, carbonic acid gas.
Above-mentioned X-can be selected from fluorine, chlorine, bromine, iodine.
Above-mentioned post-treatment agent is selected from sodium bisulfite, S-WAT, hydrogen peroxide, Sodium Pyrosulfite, sodium hydroxide, Sulfothiorine, sodium borohydride.And the add-on of post-treatment agent is 0.01%~2% of a reaction solution total mass.
The invention has the beneficial effects as follows: preparation method's environmental protection of the present invention, there are not any three wastes, no high temperature, high pressure; Resulting product has excellent biodegradability, and eco-toxicity is low, has excellent Environmental compatibility and skin-friendliness, to human body nonirritant, nontoxic.
Embodiment
The invention will be further described below by specific embodiment, but the present invention should not only limit to these embodiment.
Embodiment 1
In reactor, add 600g deionized water, 3.5mol Dichloroethyl ether, with nitrogen replacement to oxygen level less than 100ppm, open stirring, be warming up to 60 ℃, begin to drip tetraethylethylenediamine (3.51mol altogether), slowly be warming up to 80-95 ℃ after diamines drips off, constant temperature 20 hours, control in the sampling, less than 6.0, be cooled to below 50 ℃ as pH.Add 30% aqueous solution that contains the 3.0g sodium bisulfite, stirred 2 hours, regulate pH to 7.0, get product with sodium hydroxide.
Embodiment 2
In reactor, add 600g deionized water, 3.44mol dibromo ethyl ether, with nitrogen replacement to oxygen level less than 100ppm, open stirring, be warming up to 50 ℃, begin to drip 4-methyl-diaminopropane (3.50mol altogether), slowly be warming up to 100-105 ℃ after diamines drips off, constant temperature 10-15 hour, control in the sampling, less than 6.0, be cooled to below 50 ℃ as pH.Add 30% aqueous solution and 1.5g (30%) sodium borohydride solution that contain the 1.0g S-WAT, stir more than half an hour, regulate pH to 7.0, get product with sodium hydroxide.
Embodiment 3
In reactor, add 600g deionized water, 3.60mol dibromo ethyl ether, with nitrogen replacement to oxygen level less than 60ppm, open stirring, be warming up to 75 ℃, begin to drip 4-methyl-diaminopropane (3.40mol altogether), slowly be warming up to 110-120 ℃ after diamines drips off, constant temperature 8 hours, control in the sampling, less than 6.0, be cooled to below 50 ℃ as pH.Add 30% solution that contains 2.0g Sulfothiorine, stir more than 1 hour, regulate pH to 7.0, get product with sodium hydroxide.
Embodiment 4
In reactor, add 600g deionized water, 3.44mol dibromo ethyl ether, 3.51mol Tetramethyl Ethylene Diamine, with nitrogen replacement to oxygen level less than 60ppm, begin to stir, be warming up to 65 ℃, constant temperature slowly is warming up to 100-105 ℃ after 4 hours, constant temperature 12 hours is controlled in the sampling,, be cooled to below 50 ℃ less than 6.0 as pH.Add 30% aqueous solution that contains the 2.0g sodium bisulfite, stir more than 2 hours, dropping sodium is neutralized to pH7.0, adds 1.5g (30%) sodium borohydride solution then, stirs to get product half an hour.

Claims (9)

1. the preparation method of a disinfection algicide for swimming pool; it is characterized in that: comprise the steps: under the certain temperature T1 and under protection of inert gas; straight-chain fat diamine is added in the mixed solution of dihalo-ethyl ether and water; be warming up to the T2 reaction then and obtain a kind of polyquaternium; the pH value of monitoring reaction liquid; after the pH of reaction solution value is less than A; reaction solution is cooled to T3; adding post-treatment agent then handles; after post-treatment agent is handled, again reaction solution is transferred to neutrality, promptly get required Biocidal algae-killing agent.This Biocidal algae-killing agent has following general formula:
Figure A2007100257520002C1
Wherein R1 be selected from H, by a kind of saturated or undersaturated alkyl that has at least one carbon atom, R2 is selected from H, by a kind of saturated or undersaturated alkyl that has at least one carbon atom, R3 is selected from H, by a kind of saturated or undersaturated alkyl that has at least one carbon atom, R4 is selected from H, by a kind of saturated or undersaturated alkyl that has at least one carbon atom; M is 1~14; N is 1~5000; X-represents a kind of halide-ions that combines with positively charged ion.
2. preparation method as claimed in claim 1 is characterized in that: the mol ratio of described straight-chain fat diamine and dihalo-ethyl ether is 1.5: 1~1: 1.5.
3. preparation method as claimed in claim 1 or 2 is characterized in that: described temperature T 1 is 30-90 ℃; T2 is 60-150 ℃; T3 is 0-70 ℃.
4. preparation method as claimed in claim 3 is characterized in that: described temperature T 1 is 50-70 ℃; T2 is 90-120 ℃; T3 is 30-60 ℃.
5. preparation method as claimed in claim 1 or 2 is characterized in that: described pH value A is 4.0-7.0.
6. preparation method as claimed in claim 1 or 2 is characterized in that: described rare gas element is nitrogen, carbonic acid gas.
7. preparation method as claimed in claim 1 or 2 is characterized in that: described X-is selected from fluorine, chlorine, bromine, iodine.
8. preparation method as claimed in claim 1 or 2 is characterized in that: described post-treatment agent is selected from sodium bisulfite, S-WAT, hydrogen peroxide, Sodium Pyrosulfite, sodium hydroxide, Sulfothiorine, sodium borohydride.
9. preparation method as claimed in claim 1 or 2 is characterized in that: the add-on of described post-treatment agent is 0.01%~2% of a reaction solution total mass.
CN200710025752A 2007-08-02 2007-08-02 A kind of preparation method of swimming pool bactericidal algicide Expired - Fee Related CN100584769C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN200710025752A CN100584769C (en) 2007-08-02 2007-08-02 A kind of preparation method of swimming pool bactericidal algicide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN200710025752A CN100584769C (en) 2007-08-02 2007-08-02 A kind of preparation method of swimming pool bactericidal algicide

Publications (2)

Publication Number Publication Date
CN101121557A true CN101121557A (en) 2008-02-13
CN100584769C CN100584769C (en) 2010-01-27

Family

ID=39084082

Family Applications (1)

Application Number Title Priority Date Filing Date
CN200710025752A Expired - Fee Related CN100584769C (en) 2007-08-02 2007-08-02 A kind of preparation method of swimming pool bactericidal algicide

Country Status (1)

Country Link
CN (1) CN100584769C (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102453257A (en) * 2010-10-15 2012-05-16 中国石油化工股份有限公司 A kind of polyquaternium salt and its preparation method and application
CN102757558A (en) * 2011-04-28 2012-10-31 中国石油化工股份有限公司 A polyquaternary salt, preparation method and application thereof
CN103012782A (en) * 2011-09-22 2013-04-03 中国石油化工股份有限公司 Polyquaternary ammonium salt, and preparation method and application thereof
CN103621502A (en) * 2013-11-28 2014-03-12 常州大学 Preparation method and applications of organic polymer heterotrophic bacteria fungicide
CN103975948A (en) * 2014-06-10 2014-08-13 山东瑞爱特环保科技有限公司 Biocide-algaecide for circulating water and preparation method thereof
CN110326616A (en) * 2019-04-16 2019-10-15 骏雁新材料科技(上海)有限公司 A kind of cationic polymerization Biocidal algae-killing agent and its manufacturing method

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102453257A (en) * 2010-10-15 2012-05-16 中国石油化工股份有限公司 A kind of polyquaternium salt and its preparation method and application
CN102757558A (en) * 2011-04-28 2012-10-31 中国石油化工股份有限公司 A polyquaternary salt, preparation method and application thereof
CN102757558B (en) * 2011-04-28 2014-07-02 中国石油化工股份有限公司 A polyquaternary salt, preparation method and application thereof
CN103012782A (en) * 2011-09-22 2013-04-03 中国石油化工股份有限公司 Polyquaternary ammonium salt, and preparation method and application thereof
CN103621502A (en) * 2013-11-28 2014-03-12 常州大学 Preparation method and applications of organic polymer heterotrophic bacteria fungicide
CN103975948A (en) * 2014-06-10 2014-08-13 山东瑞爱特环保科技有限公司 Biocide-algaecide for circulating water and preparation method thereof
CN103975948B (en) * 2014-06-10 2015-11-11 山东瑞爱特环保科技有限公司 Cycle water Biocidal algae-killing agent and preparation method thereof
CN110326616A (en) * 2019-04-16 2019-10-15 骏雁新材料科技(上海)有限公司 A kind of cationic polymerization Biocidal algae-killing agent and its manufacturing method

Also Published As

Publication number Publication date
CN100584769C (en) 2010-01-27

Similar Documents

Publication Publication Date Title
AU784846B2 (en) Process for generating stabilized bromine compounds
CN101121557A (en) Preparation method for disinfection algicide for swimming pool
JP2002512885A (en) Stable oxidizing bromine formulations, methods for their preparation and methods used for controlling microbial fouling
JP5649976B2 (en) Apparatus and method for sterilizing water
JP3832399B2 (en) Bactericidal algicide composition and water-based bactericidal algae method
WO1999062339A1 (en) Concentrated aqueous bromine solutions and their preparation
JP2010527337A (en) Disinfectant based on aqueous hypochlorous acid (HOCl) containing solution, process for making it and use thereof
JP6807219B2 (en) Reverse osmosis membrane treatment system and reverse osmosis membrane treatment method
KR102040042B1 (en) Treatment method of ammonia-nitrogen containing wastewater and ammonia nitrogen decomposing agent
KR102132462B1 (en) Water treatment system and water treatment method using reverse osmosis membrane
KR102675437B1 (en) Water treatment method and water treatment device using reverse osmosis membrane
JP3729432B2 (en) Hypochlorite production equipment
CN106395749A (en) Method for preparing high-purity chlorine dioxide through solid-state heterogeneous catalysis
CN101492193B (en) Method for treating wastewater containing methanal and methanoic acid
JP2017025046A (en) One-component water treatment composition with improved storage stability
TWI725215B (en) Treatment method and treatment system for water containing low-molecular weight organic matter
KR100376913B1 (en) Preparation method of chlorine dioxide, an apparatus used therefor and uses thereof
CN111675294A (en) Degradable bactericide for sewage
CN101480197A (en) Stable disinfectant and preparation method thereof
TWI772292B (en) Water treatment agent composition and water treatment method
JP5281465B2 (en) Bactericidal algicide composition, water-based bactericidal algicide method, and method for producing bactericidal algicide composition
JP2004224626A (en) Method of manufacturing chlorine dioxide water and sterilization apparatus
CN109673663B (en) Amphoteric asymmetric efficient bactericide for polymer-containing sewage
JP4470121B2 (en) Disinfecting and algae killing method of circulating cooling water system
JP2021080140A (en) Chlorine dioxide aqueous solution composition retaining concentration for long terms at ordinary temperature and method for producing the same

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
C56 Change in the name or address of the patentee

Owner name: ROHDIA FEIXIANG FINE CHEMICAL CO., LTD.

Free format text: FORMER NAME: FEIXIANG CHEMICALS ZHANGJIAGANG CO., LTD.

CP01 Change in the name or title of a patent holder

Address after: 215613 Fenghuang Town, Zhangjiagang, Jiangsu

Patentee after: Rhodia fly Fine Chemical Co.

Address before: 215613 Fenghuang Town, Zhangjiagang, Jiangsu

Patentee before: Feixiang Chemicals Zhangjiagang Co., Ltd.

ASS Succession or assignment of patent right

Owner name: SOLVAY (ZHANGJIAGANG) PRECISION CHEMICAL CO., LTD.

Free format text: FORMER OWNER: ROHDIA FEIXIANG FINE CHEMICAL CO., LTD.

Effective date: 20130710

C41 Transfer of patent application or patent right or utility model
TR01 Transfer of patent right

Effective date of registration: 20130710

Address after: 215613 Fenghuang Town, Zhangjiagang, Jiangsu

Patentee after: Solvay (Zhangjiagang) Fine Chemical Co. Ltd.

Address before: 215613 Fenghuang Town, Zhangjiagang, Jiangsu

Patentee before: Rhodia fly Fine Chemical Co.

CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20100127

Termination date: 20200802

CF01 Termination of patent right due to non-payment of annual fee