JPH10330357A - Production of peracid - Google Patents
Production of peracidInfo
- Publication number
- JPH10330357A JPH10330357A JP15571997A JP15571997A JPH10330357A JP H10330357 A JPH10330357 A JP H10330357A JP 15571997 A JP15571997 A JP 15571997A JP 15571997 A JP15571997 A JP 15571997A JP H10330357 A JPH10330357 A JP H10330357A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- peracid
- hydrogen peroxide
- ester
- ester compound
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/24—Peroxy compounds the —O—O— group being bound between a >C=O group and hydrogen, i.e. peroxy acids
- C07C409/26—Peracetic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
- C07C407/003—Separation; Purification; Stabilisation; Use of additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/24—Peroxy compounds the —O—O— group being bound between a >C=O group and hydrogen, i.e. peroxy acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、エステル化合物を
酸化して過酸を製造する方法に関する。本発明の製造方
法により得られる過酸は、エポキシ体、キノン体、ラク
トン体などの製造において酸化剤として用いられる有用
な化合物である。TECHNICAL FIELD The present invention relates to a method for producing a peracid by oxidizing an ester compound. The peracid obtained by the production method of the present invention is a useful compound used as an oxidizing agent in producing an epoxy compound, a quinone compound, a lactone compound and the like.
【0002】従来より、過酸、特に過酢酸を製造する方
法は種々知られている。例えば、過酸の製法としては、
酸触媒存在下にカルボン酸と過酸化水素を反応させる方
法(J.Am.Chem.Soc.,77卷,4037頁(1955年);J.Org.Che
m.,27卷,1336頁(1962年);特開昭53−119813号
公報など)、過酸化水素とカルボン酸無水物または塩化
物を反応させる方法(Bull.Soc.Chim.France,1959年,14
01頁)、過酸化ジアロイルとナトリウムメトキシドを反
応させる方法(Org.Synth.,Coll.1卷,431頁(1946
年))、アルデヒドの自動酸化による方法(J.Am.Chem.S
oc.,79卷,5982頁(1957年);J.Org.Chem.,23卷,1923頁(19
58年);Chem,&Ind.,62卷,1962卷など)などがあげられ
る。Conventionally, various methods for producing peracids, particularly peracetic acid, have been known. For example, as a method for producing peracid,
Method of reacting carboxylic acid and hydrogen peroxide in the presence of acid catalyst (J. Am. Chem. Soc., 77th ed., 4037 (1955); J.Org.Che.
m., 27, 1336 (1962); JP-A-53-119813, etc.), a method of reacting hydrogen peroxide with a carboxylic acid anhydride or chloride (Bull.Soc.Chim.France, 1959). ,14
01), a method of reacting diaroyl peroxide with sodium methoxide (Org.Synth., Coll. 1), 431 (1946).
)), Method by autoxidation of aldehyde (J. Am. Chem. S.
oc., 79, p. 5982 (1957); J. Org. Chem., 23, p. 1923 (19).
58); Chem, & Ind., 62, 1962, etc.).
【0003】これらの方法のなかでも、製造上の容易さ
および経済的観点より、現在では、酸触媒存在下にカル
ボン酸と過酸化水素を反応させる方法が現実的な過酸の
製造方法とされている。しかし、かかる方法は、カルボ
ン酸を溶解する溶媒の選択が難しいという問題があっ
た。そこで、その改良方法として、カルボン酸自体を溶
媒を兼ねる目的で大量に用いる方法が報告されている
(Chem.Pharm.Bull.,34卷(2),445頁(1986年))。しか
し、この改良方法では、カルボン酸を大量に用いている
ため、製造装置の腐食が促進される不利や、生成系より
過酸を分離する際のカルボン酸と過酸との分離が困難で
あるなどの不利がある。Among these methods, the method of reacting a carboxylic acid with hydrogen peroxide in the presence of an acid catalyst is currently regarded as a realistic peracid manufacturing method from the viewpoint of easiness in production and economic efficiency. ing. However, such a method has a problem that it is difficult to select a solvent in which the carboxylic acid is dissolved. Therefore, as an improved method, a method of using a large amount of carboxylic acid itself for the purpose of also serving as a solvent has been reported (Chem.Pharm.Bull., 34 (2), 445 (1986)). However, in this improved method, since a large amount of carboxylic acid is used, there is a disadvantage that the corrosion of the production apparatus is accelerated, and it is difficult to separate the carboxylic acid and the peracid when separating the peracid from the production system. There are disadvantages such as.
【0004】[0004]
【発明が解決しようとする課題】本発明は、製造装置の
腐食等の問題が少なく、しかも生成系内から過酸を容易
に分離することができる過酸の容易な製造方法を提供す
ることを目的とする。SUMMARY OF THE INVENTION It is an object of the present invention to provide a method for producing a peracid which has few problems such as corrosion of the production equipment and which can easily separate the peracid from the production system. Aim.
【0005】[0005]
【課題を解決するための手段】本発明者は、前記従来技
術の課題を解決すべく鋭意研究を重ねた。その結果、酸
触媒存在下で、エステル化合物と過酸化水素を混合した
場合には、エステル化合物の酸触媒による加水分解が、
通常のエステル化合物の加水分解に比べて非常に速い反
応速度で起きると同時に、加水分解生成物であるカルボ
ン酸が過酸化水素により酸化されて、過酸を容易に製造
できることを見出し、本発明を完成するに至った。Means for Solving the Problems The present inventor has made intensive studies to solve the above-mentioned problems of the prior art. As a result, when an ester compound and hydrogen peroxide are mixed in the presence of an acid catalyst, hydrolysis of the ester compound by the acid catalyst is
The present invention has been found to occur at a very high reaction rate as compared with usual hydrolysis of an ester compound, and at the same time, a carboxylic acid as a hydrolysis product is oxidized by hydrogen peroxide to easily produce a peracid. It was completed.
【0006】すなわち、本発明は、エステル化合物と過
酸化水素を、酸触媒存在下で混合し、エステル化合物を
酸化することを特徴とする過酸の製造方法に関する。That is, the present invention relates to a method for producing peracid, comprising mixing an ester compound and hydrogen peroxide in the presence of an acid catalyst to oxidize the ester compound.
【0007】[0007]
【発明の実施の形態】本発明において用いるエステル化
合物は、各種カルボン酸類とアルコール類から得られる
各種のものを特に制限なく使用できる。このようなエス
テル化合物としては、たとえば、一般式(1):R1 −
COO−R2 (式中、R1 は炭素数1〜3のアルキル
基、またはアミノ基、水酸基もしくはハロゲン基を有す
る炭素数1〜3以下のアルキル基を表し、R2 は炭素数
1〜6のアルキル基、もしくはアミノ基、水酸基もしく
はハロゲン基を有する炭素数1〜6の置換アルキル基、
またはフェニル基、もしくはアミノ基、水酸基、ハロゲ
ン基もしくはアルキル基を有する置換フェニル基を表
す。)で表される化合物などがあげられる。これらエス
テル化合物としては、R1 が炭素数1〜3のアルキル
基、R2 が炭素数1〜6のアルキル基の化合物、すなわ
ち、酢酸、プロピオン酸または酪酸と炭素数1〜6アル
コールとのエステル化合物が好ましい。これらのエステ
ル化合物は1種を単独で用いてもよく、また2種類以上
混合して用いてもよい。2種類以上混合して用いる場合
はその混合比率を任意に設定することができる。DESCRIPTION OF THE PREFERRED EMBODIMENTS As the ester compound used in the present invention, various compounds obtained from various carboxylic acids and alcohols can be used without particular limitation. Examples of such an ester compound include, for example, a compound represented by the general formula (1): R 1-
COO-R 2 (In the formula, R 1 represents an alkyl group having 1 to 3 carbon atoms or an alkyl group having 1 to 3 carbon atoms having an amino group, a hydroxyl group or a halogen group, and R 2 represents 1 to 6 carbon atoms. An alkyl group, or a substituted alkyl group having 1 to 6 carbon atoms having an amino group, a hydroxyl group or a halogen group,
Or a phenyl group or a substituted phenyl group having an amino group, a hydroxyl group, a halogen group or an alkyl group. ) And the like. Examples of these ester compounds are compounds in which R 1 is an alkyl group having 1 to 3 carbon atoms and R 2 is an alkyl group having 1 to 6 carbon atoms, that is, an ester of acetic acid, propionic acid or butyric acid and an alcohol having 1 to 6 carbon atoms. Compounds are preferred. One of these ester compounds may be used alone, or two or more thereof may be used in combination. When two or more kinds are mixed and used, the mixing ratio can be set arbitrarily.
【0008】発明において用いる過酸化水素は、通常、
過酸化水素を水または有機溶媒で希釈したもの(以下過
酸化水素溶液)を用いる。希釈に用いることのできる有
機溶媒としては、過酸化水素を溶解でき、過酸化水素に
よって酸化されないアルコール類、ケトン類などが好ま
しい。具体的には、アルコール類としてはメタノール、
エタノール、1−または2−プロパノール、1−、2
−、3−またはtert−ブタノールなどを例示できる。ケ
トン類としてはアセトン、メチルエチルケトン、ジエチ
ルケトン、メチルイソブチルケトン、エチルブチルケト
ンなどを例示できる。その他、これらの化合物が各種官
能基で置換されたものも用いることができる。The hydrogen peroxide used in the invention is usually
A solution obtained by diluting hydrogen peroxide with water or an organic solvent (hereinafter referred to as a hydrogen peroxide solution) is used. As the organic solvent that can be used for dilution, alcohols and ketones that can dissolve hydrogen peroxide and are not oxidized by hydrogen peroxide are preferable. Specifically, methanol as the alcohol,
Ethanol, 1- or 2-propanol, 1-, 2
Examples thereof include-, 3- or tert-butanol. Examples of ketones include acetone, methyl ethyl ketone, diethyl ketone, methyl isobutyl ketone, and ethyl butyl ketone. In addition, those in which these compounds are substituted with various functional groups can also be used.
【0009】過酸化水素溶液の濃度は、特に制限され
ず、市販の各種濃度のものから90重量%を超える高濃
度のものまで各種のものを用いることができる。一般的
には、90重量%を超える高濃度の過酸化水素溶液は、
爆発の危険性が高いことから、安全面を考慮すれば過酸
化水素溶液は、濃度90重量%以下のもの、さらには濃
度75重量%以下のものが望ましい。一方、低濃度の過
酸化水素溶液であっても反応には何ら影響を及ぼさない
が、一定量の過酸を生成するのに用いる過酸化水素溶液
の液量を考慮すると過酸化水素溶液は、濃度5重量%以
上のもの、さらには濃度25重量%以上のものが望まし
い。The concentration of the hydrogen peroxide solution is not particularly limited, and various commercially available ones can be used, and various ones having a high concentration exceeding 90% by weight can be used. Generally, a high-concentration hydrogen peroxide solution exceeding 90% by weight is
Since there is a high risk of explosion, the hydrogen peroxide solution should preferably have a concentration of 90% by weight or less and more preferably have a concentration of 75% by weight or less in consideration of safety. On the other hand, even a low-concentration hydrogen peroxide solution has no effect on the reaction, but considering the amount of the hydrogen peroxide solution used to generate a certain amount of peracid, the hydrogen peroxide solution is It is desirable that the concentration is 5% by weight or more, and further that the concentration is 25% by weight or more.
【0010】前記エステル化合物と過酸化水素の比率に
特に制限はないが、反応の効率と安全性を考慮すると、
エステル化合物のモル数を過酸化水素のモル数で除した
値が1000〜1.2となる範囲が望ましい。さらに前
記値は100以下が望ましく、また2以上が望ましい。The ratio of the ester compound to hydrogen peroxide is not particularly limited, but considering the efficiency and safety of the reaction,
It is desirable that the value obtained by dividing the number of moles of the ester compound by the number of moles of hydrogen peroxide be 1000 to 1.2. Further, the value is preferably 100 or less, and more preferably 2 or more.
【0011】本発明において用いる触媒としては、各種
の酸触媒を特に限定なく使用できる。例えば、酸触媒と
しては硫酸、塩酸、硝酸のような一般的な無機酸触媒、
メタンスルフォン酸、パラトルエンスルフォン酸、ベン
ゼンスルフォン酸、スルフォン酸型強酸型イオン交換樹
脂のようなスルフォン酸化合物、スルフォン酸型以外の
強酸型イオン交換樹脂、シリカアルミナ、酸化ニオブ、
酸化チタン、タングステン酸のような金属酸化物、ナフ
ィオン、トリフルオロ酢酸などを例示できる。これら酸
触媒のなかでも強酸が好ましく、特に硫酸や、スルフォ
ン酸基を有する化合物が好ましい。As the catalyst used in the present invention, various acid catalysts can be used without particular limitation. For example, as the acid catalyst, common inorganic acid catalysts such as sulfuric acid, hydrochloric acid, and nitric acid,
Methanesulfonic acid, paratoluenesulfonic acid, benzenesulfonic acid, sulfonic acid compounds such as sulfonic acid type strong acid type ion exchange resin, strong acid type ion exchange resin other than sulfonic acid type, silica alumina, niobium oxide,
Examples thereof include metal oxides such as titanium oxide and tungstic acid, Nafion, and trifluoroacetic acid. Among these acid catalysts, strong acids are preferred, and sulfuric acid and compounds having a sulfonic acid group are particularly preferred.
【0012】前記酸触媒の使用量は、特に制限されない
が、反応速度および経済面を勘案すると、エステル化合
物の重量に対し、通常、0.001〜50重量%程度が
望ましい。反応速度の低下や反応時間を考慮すれば、酸
触媒の使用量の下限は0.1重量%がより望ましく、経
済面からは上限を20重量%とするのがより望ましい。The amount of the acid catalyst to be used is not particularly limited, but is preferably about 0.001 to 50% by weight, based on the weight of the ester compound, in consideration of the reaction rate and economy. In consideration of a reduction in the reaction rate and the reaction time, the lower limit of the amount of the acid catalyst used is more preferably 0.1% by weight, and the upper limit is more preferably 20% by weight from the viewpoint of economy.
【0013】本発明の過酸の製造は、酸触媒の存在下
で、前記エステル化合物を過酸化水素により酸化するこ
とにより行なう。かかる反応において、前記エステル化
合物は溶媒としても作用するため、前記エステル化合物
が反応温度において液体の場合には、溶媒の使用は特に
必要とされないが、エステル化合物が固体である場合に
はこれを溶解させる水または有機溶媒を加えることがで
きる。添加できる有機溶媒としては、過酸によって酸化
されないものが好ましい。また、被溶解物がエステル化
合物であることから、極性を有するものが好ましい。具
体的には、過酸化水素溶液に用いたアルコール類、ケト
ン類などがあげられる。なお、エステル化合物が液体で
ある場合においても過酸化水素溶液との相溶性をよくす
る目的で適量の有機溶媒を加えることができる。The production of the peracid of the present invention is carried out by oxidizing the ester compound with hydrogen peroxide in the presence of an acid catalyst. In such a reaction, since the ester compound also acts as a solvent, when the ester compound is a liquid at the reaction temperature, use of a solvent is not particularly required, but when the ester compound is a solid, it is dissolved. Precipitated water or organic solvent can be added. Organic solvents that can be added are preferably those that are not oxidized by peracids. Further, since the substance to be dissolved is an ester compound, those having polarity are preferable. Specific examples include alcohols and ketones used in the hydrogen peroxide solution. Even when the ester compound is liquid, an appropriate amount of an organic solvent can be added for the purpose of improving the compatibility with the hydrogen peroxide solution.
【0014】本発明の過酸の製造方法における反応温度
は、反応の効率と安全性を考慮すると、通常、反応系が
固化する低温以上でかつ反応系が沸騰する高温以下で行
われることが望まれる。具体的温度は使用するエステル
化合物、有機溶媒によって異なるが、エステル化合物と
して酢酸イソブチルを用いた場合は、酢酸イソブチルの
融点である−99℃から沸点である117℃の範囲で行
われるのが良い。さらに反応効率の面からすれば−30
℃以上が望ましく、安全性の面からすれば80℃以下が
望ましい。In consideration of the efficiency and safety of the reaction, the reaction temperature in the method for producing peracid of the present invention is usually desirably carried out at a temperature lower than the temperature at which the reaction system solidifies and at a temperature lower than the temperature at which the reaction system boils. Be done. The specific temperature varies depending on the ester compound used and the organic solvent, but when isobutyl acetate is used as the ester compound, it is preferably carried out within the range of −99 ° C. which is the melting point of isobutyl acetate to 117 ° C. which is the boiling point. Furthermore, from the viewpoint of reaction efficiency, it is -30.
C. or higher is desirable, and from the viewpoint of safety, 80.degree. C. or lower is desirable.
【0015】反応は殆どの場合に短時間で終了するが、
完全に反応を終結させるためにはさらに反応時間を延ば
すことができる。通常、反応時間は5分〜24時間程度
である。The reaction is completed in a short time in most cases.
To complete the reaction, the reaction time can be further extended. Usually, the reaction time is about 5 minutes to 24 hours.
【0016】こうして得られた過酸は、生成系から、蒸
留、水または溶剤抽出(エステル化合物と混合しない極
性の有機溶剤)、カラム分離等の手段により分離でき
る。The peracid thus obtained can be separated from the production system by means such as distillation, water or solvent extraction (a polar organic solvent which does not mix with the ester compound), and column separation.
【0017】なお、本発明の製造方法に用いる装置は、
前記の反応温度に耐え、かつ過酸化水素および過酸の急
激な分解を引き起こす物質、例えば金属分、高分子、化
学物質などの付着しないものが安全上望ましい。反応器
の材質も前記の反応温度に耐え、かつ過酸化水素および
過酸の急激な分解を引き起こす材料で作られていなけれ
ば特に制限はない。また、撹拌設備のあるものが望まし
い。The apparatus used in the manufacturing method of the present invention is
From the viewpoint of safety, substances that can withstand the above reaction temperatures and that cause rapid decomposition of hydrogen peroxide and peracid, such as metal components, polymers, and chemical substances, are not attached. The material of the reactor is not particularly limited as long as it is not made of a material that withstands the above-mentioned reaction temperature and causes rapid decomposition of hydrogen peroxide and peracid. Further, a device having a stirring device is desirable.
【0018】[0018]
【発明の効果】本発明では、過酸の原料としてカルボン
酸を用いていないため、製造装置の腐食等の問題を最小
限に止めることができる。また、製造された過酸は、エ
ステル化合物中に存在するため、エステル化合物と過酸
の性質の違いを利用して生成系内から容易に過酸を分離
することができる。According to the present invention, since carboxylic acid is not used as a raw material for peracid, problems such as corrosion of manufacturing equipment can be minimized. Further, since the produced peracid is present in the ester compound, the peracid can be easily separated from the production system by utilizing the difference in properties between the ester compound and the peracid.
【0019】[0019]
【実施例】以下に実施例をあげて本発明をさらに具体的
に説明するが、本発明はこれら実施例に限定されるもの
ではない。なお、%は特記しない限りいずれも重量基準
である。The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples. All percentages are by weight unless otherwise specified.
【0020】実施例1 還流管を備えた100mlのガラス製三つ口フラスコに
酢酸ブチル20g(192ミリモル)、酸触媒としてメ
タンスルフォン酸0.5gを加えた。室温(25℃)に
て電磁撹拌を行いながら60%過酸化水素水1.39g
(24.5ミリモル)を5分かけて滴下した。その後、
室温にて電磁撹拌を行いながら5時間放置した。この反
応液を0.1規定過マンガン酸カリウムで滴定し過酸化
水素量を定量した。続いて、よう素滴定法にて過酢酸量
を定量した。その結果、過酸化水素の残存量は3.36
ミリモル、過酢酸の生成量は、21.14ミリモル(過
酢酸の収率は86モル%)であった。Example 1 20 g (192 mmol) of butyl acetate and 0.5 g of methanesulfonic acid as an acid catalyst were added to a 100 ml glass three-necked flask equipped with a reflux tube. 60% hydrogen peroxide water 1.39g while performing electromagnetic stirring at room temperature (25 ° C)
(24.5 mmol) was added dropwise over 5 minutes. afterwards,
The mixture was left for 5 hours at room temperature with magnetic stirring. This reaction solution was titrated with 0.1 N potassium permanganate to quantify the amount of hydrogen peroxide. Then, the amount of peracetic acid was quantified by the iodine titration method. As a result, the remaining amount of hydrogen peroxide was 3.36.
The amount of production of mmol and peracetic acid was 21.14 mmol (the yield of peracetic acid was 86 mol%).
【0021】実施例2〜10、比較例1〜2 実施例1において、エステル化合物の種類、酸触媒の種
類および反応温度のうち少なくともひとつを表1に示す
ように変えた他は実施例1と同様の操作を行い、また実
施例1と同様にして過酸化水素と過酸を確認した。過酸
の収率を表1に示す。Examples 2 to 10 and Comparative Examples 1 and 2 Example 1 was the same as Example 1 except that at least one of the type of ester compound, the type of acid catalyst and the reaction temperature was changed as shown in Table 1. The same operation was performed, and hydrogen peroxide and peracid were confirmed in the same manner as in Example 1. The yield of peracid is shown in Table 1.
【0022】なお、実施例において得られた過酸は、安
定剤としてジオクチル二水素ピロリン酸エステルを加え
た後減圧蒸留することで原料のエステル化合物から容易
に分離できた。The peracids obtained in the examples could be easily separated from the starting ester compounds by adding dioctyl dihydrogen pyrophosphate ester as a stabilizer and then distilling under reduced pressure.
【0022】[0022]
【表1】 [Table 1]
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI // C07B 61/00 300 C07B 61/00 300 ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 6 Identification code FI // C07B 61/00 300 C07B 61/00 300
Claims (3)
存在下で混合し、エステル化合物を酸化することを特徴
とする過酸の製造方法。1. A method for producing a peracid, which comprises mixing an ester compound and hydrogen peroxide in the presence of an acid catalyst to oxidize the ester compound.
または酪酸と炭素数1〜6のアルコールとのエステル化
合物である請求項1記載の製造方法。2. The method according to claim 1, wherein the ester compound is an ester compound of acetic acid, propionic acid or butyric acid and an alcohol having 1 to 6 carbon atoms.
有する化合物である請求項1または2記載の製造方法。3. The method according to claim 1, wherein the acid catalyst is a compound having a sulfuric acid or a sulfonic acid group.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15571997A JPH10330357A (en) | 1997-05-28 | 1997-05-28 | Production of peracid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15571997A JPH10330357A (en) | 1997-05-28 | 1997-05-28 | Production of peracid |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH10330357A true JPH10330357A (en) | 1998-12-15 |
Family
ID=15612000
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15571997A Pending JPH10330357A (en) | 1997-05-28 | 1997-05-28 | Production of peracid |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH10330357A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014072143A1 (en) | 2012-11-08 | 2014-05-15 | Evonik Industries Ag | Method for producing equilibrium peracetic acid and equilibrium peracetic acid obtainable by the method |
CN107602435A (en) * | 2016-07-12 | 2018-01-19 | 上海利康消毒高科技有限公司 | The method that glyceryl triacetate prepares Peracetic acid |
-
1997
- 1997-05-28 JP JP15571997A patent/JPH10330357A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014072143A1 (en) | 2012-11-08 | 2014-05-15 | Evonik Industries Ag | Method for producing equilibrium peracetic acid and equilibrium peracetic acid obtainable by the method |
JP2015535297A (en) * | 2012-11-08 | 2015-12-10 | エボニック インダストリーズ アクチエンゲゼルシャフトEvonik Industries AG | Method for producing equilibrium peracetic acid and equilibrium peracetic acid obtained by said method |
CN107602435A (en) * | 2016-07-12 | 2018-01-19 | 上海利康消毒高科技有限公司 | The method that glyceryl triacetate prepares Peracetic acid |
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