US4297298A
Expired / Lapsed
US
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Method of preparing stable dilute solutions of aliphatic carboxylic peracids, and the resulting solutions
Assignee: LAir Liquide SA pour lEtude et lExploitation des Procedes Georges Claude
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Filing: 1980-07-22
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Granted: 1981-10-27
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Expires: 2000-07-22
Abstract
Abstract The invention relates to the preparation of dilute solutions of aliphatic rboxylic peracids. In a first step, a concentrated solution of aliphatic peracid is prepared from the corresponding acid or anhydride and concentrated hydrogen peroxide in the presence of a strong acid catalyst, preferably the minimum quantity necessary for obtaining equilibrium in the system within 48 hours; and in a second step, the concentrated solution of aliphatic peracid is diluted with a solution containing at least one of the reagents, so as to bring the concentration of aliphatic peracid to the rated concentration of the mixture. The method is applicable inter alia to the preparation of stable dilute solutions of peracetic acid.
Inventors
- 👤 Francois Crommelynck
- 👤 Michel Granger
- 👤 Michel Rio
- 👤 Jacques Tourdot
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-24 22:25
CPC Classifications
C; C07; C07C; C07C409/00; C07C409/24; C07C409/26; C07C407/00
Claims Analysis
Total Claims: 15
Claim 1
Independent Claim
189 words
A method of preparing a dilute solution, containing a rated concentration between 1 and 20% by weight, of an aliphatic carboxylic peracid with a stable concentration titer in time, notwithstanding the possible presence of trace amounts of decomposition catalysts, comprising the steps of: preparing a concentrated solution of aliphatic peracid from the corresponding carboxylic acid or anhydride and hydrogen peroxide in a concentration of between 60 and 90% in the presence of the substantially minimal amount of a strong acid catalyst necessary to obtain equilibrium of the system in a maximum period of 48 hours; and diluting the concentrated solution of aliphatic peracid, prepared in said preparing step, with a solution containing at least one of the reagents used in said preparing step in an amount and concentration sufficient to bring the concentration of aliphatic peracid at least to the rated concentration of the mixture and such that (a) the maximum concentration of peracid during storage at ambient temperature is at most 10% above the rated concentration of peracid and (b) the concentration after storage for 12 months is at least equal to the rated concentration of aliphatic peracid.
Claim 2
Independent Claim
189 words
A method of preparing a dilute solution, containing a rated concentration between 1 and 20% by weight, of an aliphatic carboxylic peracid with a stable concentration titer in time, notwithstanding the possible presence of trace amounts of decomposition catalysts, comprising the steps of: preparing a concentrated solution of aliphatic peracid from the corresponding carboxylic acid or anhydride and hydrogen peroxide in a concentration of between 60 and 90% in the presence of the substantially minimal amount of a strong acid catalyst necessary to obtain equilibrium of the system in a maximum period of 48 hours; and diluting the concentrated solution of aliphatic peracid, prepared in said preparing step, with a solution containing at least one of the reagents used in said preparing step in an amount and concentration sufficient to bring the concentration of aliphatic peracid at least to the rated concentration of the mixture and such that (a) the maximum concentration of peracid during storage at ambient temperature is at most 10% above the rated concentration of peracid and (b) the concentration after storage for 12 months is at least equal to the rated concentration of aliphatic peracid.
Claim 3
Dependent Claim
22 words
A method, according to claim 1, wherein a stabilizer is introduced into the concentrated solution of aliphatic peracid in said preparing step.
Claim 4
Dependent Claim
21 words
A method according to claim 1, wherein the strong acid catalyst used in the preforming step is a strong mineral acid.
Claim 5
Dependent Claim
37 words
A method according to claim 3, wherein the strong acid catalyst is selected from sulphuric and orthophosphoric acids and organo-mineral acids and is used in a proportion of 0.1 to 5% by weight of the reaction mixture.
Claim 6
Dependent Claim
25 words
A method according to claim 4, wherein the said acid is used in a proportion of 0.2 to 0.5% by weight of the reaction mixture.
Claim 7
Dependent Claim
35 words
A method according to claim 1, wherein in the preparing step, the carboxylic acid is selected from monocarboxylic acids containing 2 or 3 carbon atoms in the molecule and di-carboxylic acids containing 3-5 carbon atoms.
Claim 8
Dependent Claim
24 words
A method according to claim 1, wherein, in said preparing step, said hydrogen peroxide is at a concentration of 70 to 85% by weight.
Claim 9
Dependent Claim
32 words
A method according to claim 1, wherein, in the diluting step, the concentrated solution of aliphatic peracid is diluted with hydrogen peroxide at a concentration of from 40 to 70% by weight.
Claim 10
Dependent Claim
25 words
A method according to claim 8, wherein, in the diluting step, the hydrogen peroxide is used at a concentration of 40 to 50% by weight.
Claim 11
Dependent Claim
25 words
A method in accordance with claim 1 wherein said acid is present in an amount of 0.1-5% by weight in relation to said reaction mixture.
Claim 12
Dependent Claim
56 words
A method in accordance with claim 1 wherein, in said preparing step, said strong acid is a strong inorganic acid in an amount of 0.2-0.5% by weight in relation to the reaction mixture, and, in said diluting step, the concentrated solution of aliphatic peracid is diluted with hydrogen peroxide at a concentration of 40-50% by weight.
Claim 13
Dependent Claim
15 words
A method in accordance with claim 1, wherein said strong inorganic acid is mineral acid.
Claim 14
Dependent Claim
77 words
A method in accordance with claim 1, wherein said aliphatic carboxylic peracid is peracetic acid; wherein, in said preparing step, said corresponding carboxylic acid or anhydride is acetic acid or anhydride and said strong acid catalyst is present in an amount of 0.1-0.5% by weight in relation to the reaction mixture; and wherein, in said diluting step, the concentrated peracetic acid solution prepared in said preparing step is diluted with hydrogen peroxide at a concentration of 40-70%.
Claim 15
Dependent Claim
99 words
A method in accordance with claim 1, wherein the aliphatic carboxylic peracid is peracetic acid and the rated concentration of the final product is 2-5% by weight; wherein, in said preparing step said corresponding carboxylic acid or anhydride is acetic acid, said hydrogen peroxide is present in a concentration of 70-90% and said strong acid catalyst is sulfuric acid present in an amount of 0.2-0.5% by weight in relation to said reaction mixture; and wherein, in said diluting step, the concentrated peracetic acid solution prepared in said preparing step is diluted with hydrogen preoxide at a concentration of 40-70%.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1984-10-26 | 1985-04-27 | 1985-10-27 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1988-10-26 | 1989-04-27 | 1989-10-27 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1992-10-26 | 1993-04-27 | 1993-10-27 | $7700.00 | Window Closed / Lapsed |