CN101077861A - Technique for preparing peroxyacetic acid - Google Patents
Technique for preparing peroxyacetic acid Download PDFInfo
- Publication number
- CN101077861A CN101077861A CN 200610040553 CN200610040553A CN101077861A CN 101077861 A CN101077861 A CN 101077861A CN 200610040553 CN200610040553 CN 200610040553 CN 200610040553 A CN200610040553 A CN 200610040553A CN 101077861 A CN101077861 A CN 101077861A
- Authority
- CN
- China
- Prior art keywords
- reaction
- peroxyacetic acid
- technique
- superoxide
- preparing peroxyacetic
- 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
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The present invention relates to new process of preparing peroxy acetic acid serving as bleaching agent, pesticide and bactericide. Acetic anhydride as the material is oxidized with peroxide solution of 10-50 % concentration through reaction at the temperature controlled in 20-60 deg.c for 4 hr to produce peroxy acetic acid.
Description
Technical field
The present invention relates to a kind of SYNTHETIC OPTICAL WHITNER, new preparation process of in weaving, being used as in hospital as the new preparation process, particularly Peracetic Acid of the sterilant of sterilant.
Background technology
At present, industrial synthetic Peracetic Acid method remains two kinds of hydrogen peroxide and acetaldehyde oxidations, though these two kinds of methods have had new development and improvement at present, need to adopt the strong acid class to do catalyzer and condition of high voltage, not only increase cost and increased the three wastes and danger.Though this technology also is peroxide oxidation method but to have adopted aceticanhydride be raw material as long as single step reaction has at normal temperatures and pressures been avoided deficiency in the former technology, has improved Working environment and has reduced production costs.
Summary of the invention
It is not enough in order to solve in the former technology that purpose of the present invention is exactly, and a kind of safe and convenient and technology that cost is low is provided, and is that the direct and superoxide of raw material reacts the generation Peracetic Acid at normal temperatures and pressures with aceticanhydride.
The technology of the present invention solution:
A kind of technique for preparing peroxyacetic acid, its feature are to be raw material with the aceticanhydride, with superoxide oxidizing reaction generation in the 4 hours at a certain temperature Peracetic Acid of proper concn.The superoxide of proper concn refers to react the superoxide that initial peroxide level is 10-50%, and certain temperature refers to that temperature of reaction is controlled at 20-60 ℃.
Embodiment
A kind of technique for preparing peroxyacetic acid, its feature are to be raw material with the aceticanhydride, are added drop-wise in the aceticanhydride with the 10-50% superoxide, and the control rate of addition makes temperature of reaction remain on 20-60 ℃, and oxidizing reaction generated Peracetic Acid in 4 hours under this temperature.
Example one
Under fully stirring, the hydrogen peroxide of 100g30% is added drop-wise in the 450g aceticanhydride the outer cooling of control feed rate and bottle, make temperature of reaction dimension built in 40 ℃, reinforced finishing was 40 ℃ of following stirring reactions 4 hours, spend the night in the room temperature placement, the Peracetic Acid concentration that makes is 1mol/L.
Embodiment two
Under fully stirring, the chlorine peroxide of 303g30% is added drop-wise in the 450g aceticanhydride the outer cooling of control feed rate and bottle, make temperature of reaction dimension built in 40 ℃, reinforced finishing was 40 ℃ of following stirring reactions 4 hours, spend the night in the room temperature placement, the Peracetic Acid concentration that makes is 1mol/L.
Implement three
Under fully stirring, the hydrogen peroxide of 75g40% is added drop-wise in the 450g aceticanhydride the outer cooling of control feed rate and bottle, make temperature of reaction dimension built in 30 ℃, reinforced finishing was 30 ℃ of following stirring reactions 4 hours, spend the night in the room temperature placement, the Peracetic Acid concentration that makes is 1mol/L.
Claims (4)
1, a kind of technique for preparing peroxyacetic acid, its feature are to be raw material with the aceticanhydride, with superoxide oxidizing reaction generation in the 4 hours at a certain temperature Peracetic Acid of proper concn.The superoxide of proper concn refers to react the superoxide that initial peroxide level is 10-50%, and certain temperature refers to that temperature of reaction is controlled at 20-60 ℃.
2, by the described technique for preparing peroxyacetic acid of claim 1, it is characterised in that superoxide is hydrogen peroxide, chlorine peroxide etc., and its initial concentration is 10-50%.
3, by the described technique for preparing peroxyacetic acid of claim 1, the described temperature of reaction of its feature is 20-60 ℃.
4, by the described technique for preparing peroxyacetic acid of claim 1, the described reaction times of its feature is 4 hours for dripping the back insulation reaction time.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 200610040553 CN101077861A (en) | 2006-05-24 | 2006-05-24 | Technique for preparing peroxyacetic acid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 200610040553 CN101077861A (en) | 2006-05-24 | 2006-05-24 | Technique for preparing peroxyacetic acid |
Publications (1)
Publication Number | Publication Date |
---|---|
CN101077861A true CN101077861A (en) | 2007-11-28 |
Family
ID=38905551
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 200610040553 Pending CN101077861A (en) | 2006-05-24 | 2006-05-24 | Technique for preparing peroxyacetic acid |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN101077861A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102757375A (en) * | 2011-04-29 | 2012-10-31 | 中国石油化工股份有限公司 | Preparation method of peroxyacetic acid |
CN103651585A (en) * | 2013-12-06 | 2014-03-26 | 何小刚 | Insect-resisting agent |
CN108658823A (en) * | 2017-03-30 | 2018-10-16 | 中国石油化工股份有限公司 | The method for preparing Peracetic acid |
CN113728076A (en) * | 2019-04-24 | 2021-11-30 | 杰富意钢铁株式会社 | Method for producing low-sulfur coal |
-
2006
- 2006-05-24 CN CN 200610040553 patent/CN101077861A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102757375A (en) * | 2011-04-29 | 2012-10-31 | 中国石油化工股份有限公司 | Preparation method of peroxyacetic acid |
CN102757375B (en) * | 2011-04-29 | 2014-03-12 | 中国石油化工股份有限公司 | Preparation method of peroxyacetic acid |
CN103651585A (en) * | 2013-12-06 | 2014-03-26 | 何小刚 | Insect-resisting agent |
CN108658823A (en) * | 2017-03-30 | 2018-10-16 | 中国石油化工股份有限公司 | The method for preparing Peracetic acid |
CN108658823B (en) * | 2017-03-30 | 2020-06-16 | 中国石油化工股份有限公司 | Process for the preparation of peroxyacetic acid |
CN113728076A (en) * | 2019-04-24 | 2021-11-30 | 杰富意钢铁株式会社 | Method for producing low-sulfur coal |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FI20050913A (en) | Process for the preparation of peroxyacids | |
WO2009023492A3 (en) | Dilute stabilized peracetic acid production and treatment process | |
CN101077861A (en) | Technique for preparing peroxyacetic acid | |
MX2012003966A (en) | Perhydrolase for enzymatic peracid production. | |
BR0209833A (en) | Process for the production of a benzenedicarboxylic acid | |
CN102140073A (en) | Cocoyl dimethyl ammonium iodine oxide complex | |
CN1803771A (en) | Method for preparing peroxy acetic acid | |
CA2407605A1 (en) | Precious metal recovery from organics-precious metal compositions with supercritical water reactant | |
MX2009012234A (en) | Start-up of high selectivity catalysts in olefin oxide plants. | |
ITMI962753A1 (en) | PROCEDURE FOR THE PRODUCTION OF AROMATIC ACIDS | |
CN101391750B (en) | Method for preparing high-purity chlorine dioxide by using starchiness raw material and method for preparing catalyst used therein | |
CN103772141B (en) | Hydroperoxide reduction reaction technique | |
CN101092428B (en) | New technique for preparing glyphosate by oxidizing N-Phosphonomethyl iminodiacetic acid in air | |
CN101391751B (en) | Method for preparing high-purity chlorine dioxide by using agronomic crop stalk and method for preparing catalyst used therein | |
CN101497045B (en) | Catalyst for producing epoxypropane by liquid phase one-step oxidation of propylene and preparation method | |
CN111533097A (en) | Yellow phosphorus oxidation dearsenification method | |
WO2003082735A8 (en) | Process for the production of hydrogen peroxide | |
CN102838484A (en) | Polyoxyethylene laurate (400) ester-iodine complex | |
CN116003370A (en) | Preparation device and method for continuously synthesizing ester from peroxyacid and cyclohexanone | |
CN100575328C (en) | The preparation technology of dichloroacetyl chloride | |
CN104513198A (en) | 2-chloronicotinic acid synthetic method | |
CN103193204B (en) | Method for improving oxidation yield of hydrogenated liquid of hydrogen peroxide prepared by utilizing anthraquinone process | |
CN102229621B (en) | Method for preparing glyphosate by catalyzing and oxidizing glyphosine in the presence of ultraviolet light source | |
CN113845421B (en) | Method for preparing ethyl propiolate by one-pot method | |
CN1807388A (en) | Method for producing sodium gluconate using dual oxidative catalysis method |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |