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JPH09316022A - Prevention of polymerization of (meth)acrylic acid and its ester - Google Patents

Prevention of polymerization of (meth)acrylic acid and its ester

Info

Publication number
JPH09316022A
JPH09316022A JP12830296A JP12830296A JPH09316022A JP H09316022 A JPH09316022 A JP H09316022A JP 12830296 A JP12830296 A JP 12830296A JP 12830296 A JP12830296 A JP 12830296A JP H09316022 A JPH09316022 A JP H09316022A
Authority
JP
Japan
Prior art keywords
polymerization
acrylic acid
meth
ester
hydroquinone
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
JP12830296A
Other languages
Japanese (ja)
Inventor
Katsuji Imi
勝治 伊美
Kozo Kato
幸三 加藤
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP12830296A priority Critical patent/JPH09316022A/en
Publication of JPH09316022A publication Critical patent/JPH09316022A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a method for preventing the polymerization of the subject compound, capable of exhibiting extremely excellent polymerization preventing effects by addition of a small amount of a polymerization inhibitor even in a high-temperature state in distillation, by using a specific polymerization inhibitor and hydroquinone. SOLUTION: (A) At least one of benzoquinone, 1,2-naphtoquinone and its derivative and (B) hydroquinone are used. The amounts of the components A and B are 1-5,000ppm based on the objective compound, respectively and the ratio of the components A to B is preferably (1:100) to (100:1). For example, potassium 1,2-naphtoquinone-4sulfonate is preferably used as the component B.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明が属する技術分野】本発明は、(メタ)アクリル
酸およびそのエステルの重合防止方法に関する。さらに
詳しくは、本発明は(メタ)アクリル酸およびそのエス
テルを含む系において、重合防止剤としてハイドロキノ
ンに加えて、ベンゾキノン、1,2−ナフトキノン及び
その誘導体の少なくとも1種を併用する重合防止方法に
関する。
TECHNICAL FIELD The present invention relates to a method for preventing polymerization of (meth) acrylic acid and its ester. More specifically, the present invention relates to a method for preventing polymerization in a system containing (meth) acrylic acid and its ester, in which at least one of benzoquinone, 1,2-naphthoquinone and its derivative is used in combination with hydroquinone as a polymerization inhibitor. .

【0002】[0002]

【従来の技術】(メタ)アクリル酸およびそのエステル
は、熱、光、過酸化物等によって容易に、しかも極めて
激しい重合を起こす性質を有しているため、これらを蒸
留塔により精製する際に、多量の重合物の発生による蒸
留塔の能力の低下や、蒸留塔リボイラー伝熱面への重合
物の付着による伝熱性能の低下をもたらすばかりでな
く、蒸留塔内での重合物による閉塞も起こすことが知ら
れている。これらの現象は、(メタ)アクリル酸および
そのエステルを製造するプロセスにおいては、極めて大
きな支障となっており、重合をいかに制御するかが、工
業的製造には重要である。
2. Description of the Related Art (Meth) acrylic acid and its esters have the property of easily and extremely violently polymerizing due to heat, light, peroxides, etc., and therefore, when they are purified by a distillation column. Not only does the capacity of the distillation column decrease due to the generation of a large amount of polymer, and the heat transfer performance decreases due to the adhesion of the polymer to the heat transfer surface of the distillation column reboiler, but also clogging by the polymer in the distillation column occurs. Known to cause. These phenomena are extremely serious obstacles in the process of producing (meth) acrylic acid and its ester, and how to control the polymerization is important for industrial production.

【0003】従来、(メタ)アクリル酸およびそのエス
テルの重合防止法の1つとして、重合防止剤を添加する
ことが、古くから提案され実施されている。代表的な重
合防止剤としては、ハイドロキノン、ハイドロキノンモ
ノメチルエーテル等のフェノール類、フェノチアジン、
ジフェニルアミン等のアミン類、ジブチルジチオカルバ
ミン酸銅等の銅塩、酢酸マンガン等のマンガン塩、ニト
ロ化合物、ニトロソ化合物が知られている。そして、こ
れらの重合防止剤を単独の形で用いたり、或いは分子状
酸素含有ガスとこれらの重合防止剤との併用による方法
などがいろいろ提案されている。
Conventionally, addition of a polymerization inhibitor has been proposed and practiced for a long time as one of methods for preventing polymerization of (meth) acrylic acid and its ester. Representative polymerization inhibitors include hydroquinone, phenols such as hydroquinone monomethyl ether, phenothiazine,
Known are amines such as diphenylamine, copper salts such as copper dibutyldithiocarbamate, manganese salts such as manganese acetate, nitro compounds and nitroso compounds. Various proposals have been made on the method in which these polymerization inhibitors are used alone or in combination with the molecular oxygen-containing gas and these polymerization inhibitors.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、このよ
うに提案されている重合防止剤は(メタ)アクリル酸製
造プロセスの蒸留工程などの高温状態では、その重合防
止効果が小さいため、多量に添加しなければならず、工
業的実施において満足すべきものではない。
However, the polymerization inhibitor proposed in this way has a small effect of inhibiting polymerization at high temperatures such as in the distillation step of the (meth) acrylic acid production process, so that a large amount should be added. Must be satisfied in industrial practice.

【0005】[0005]

【課題を解決するための手段】本発明者らは、(メタ)
アクリル酸およびそのエステルの重合防止法について鋭
意検討を行った結果、個々にはアクリル酸の重合防止剤
として公知であるハイドロキノンと特定の重合防止剤を
併用する場合には、単独では得られなかった顕著な重合
防止効果を相乗効果として発現し得ることを見出し、本
発明を完成するに至った。すなわち本発明は、重合防止
剤としてベンゾキノン、1,2−ナフトキノンおよびそ
の誘導体の少なくとも1種とハイドロキノンを用いるこ
とを特徴とする(メタ)アクリル酸およびそのエステル
の重合防止方法を提供するにある。
Means for Solving the Problems The present inventors have proposed (meth)
As a result of diligent studies on a method for preventing polymerization of acrylic acid and its ester, when hydroquinone, which is known as a polymerization inhibitor of acrylic acid, and a specific polymerization inhibitor are used in combination, they cannot be obtained alone. It has been found that a remarkable polymerization inhibiting effect can be exhibited as a synergistic effect, and the present invention has been completed. That is, the present invention provides a method for preventing polymerization of (meth) acrylic acid and its ester, which comprises using at least one of benzoquinone, 1,2-naphthoquinone and its derivative and hydroquinone as a polymerization inhibitor.

【0006】[0006]

【発明の実施の形態】以下、本発明方法について詳細に
説明する。本発明方法は(メタ)アクリル酸およびその
エステルに適用し得る。アクリル酸エステルとしては、
アクリル酸メチル、アクリル酸エチル、アクリル酸ブチ
ル、アクリル酸2−エチルヘキシル、アクリル酸2−ヒ
ドロキシエチル、アクリル酸2−ヒドロキシプロピル
等、またメタクリル酸エステルとしては、メタクリル酸
メチル、メタクリル酸エチル、メタクリル酸ブチル、メ
タクリル酸2−ヒドロキシエチル、メタクリル酸2−ヒ
ドロキシプロピル等が挙げられる。
BEST MODE FOR CARRYING OUT THE INVENTION The method of the present invention will be described in detail below. The method of the invention can be applied to (meth) acrylic acid and its esters. As acrylic acid ester,
Methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, etc. As the methacrylic acid ester, methyl methacrylate, ethyl methacrylate, methacrylic acid Butyl, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate and the like can be mentioned.

【0007】本発明方法に於いて、(メタ)アクリル酸
およびそのエステルの重合防止方法は、重合防止剤とし
てハイドロキノンにベンゾキノン、1,2−ナフトキノ
ンおよびその誘導体(以下1,2−ナフトキノン類と記
す場合がある)の少なくとも1種を併せ用いることを必
須とする。 重合防止剤としてのハイドロキノンは、
(メタ)アクリル酸およびそのエステルに対して約1〜
約5000ppm、好ましくは、約10〜約500pp
m添加される。ベンゾキノン、または1,2−ナフトキ
ノン類は、(メタ)アクリル酸およびそのエステルに対
して約1〜約5000ppm、好ましくは、約10〜約
500ppm添加される。この際、両者は共存させて使
用するが、その比率(重量比)は約1:約100〜約1
00:約1、好ましくは約1:約10〜約10:約1の
範囲から選ばれる。前記重合防止剤の添加量がこの範囲
未満の場合には重合防止効果が十分ではなく、また、こ
の範囲を越える場合には十分な重合防止効果は得られる
ものの経済的ではない。
In the method of the present invention, the method for preventing the polymerization of (meth) acrylic acid and its ester is as follows: Hydroquinone, benzoquinone, 1,2-naphthoquinone and its derivative (hereinafter referred to as 1,2-naphthoquinones) as a polymerization inhibitor. In some cases), it is essential to use at least one of them together. Hydroquinone as a polymerization inhibitor,
About 1 to (meth) acrylic acid and its ester
About 5000 ppm, preferably about 10 to about 500 pp
m is added. Benzoquinone or 1,2-naphthoquinones are added in an amount of about 1 to about 5000 ppm, preferably about 10 to about 500 ppm, based on (meth) acrylic acid and its ester. At this time, both are used together, but the ratio (weight ratio) is about 1: about 100 to about 1.
00: about 1, preferably about 1: about 10 to about 10: about 1. If the amount of the polymerization inhibitor added is less than this range, the polymerization inhibitory effect is not sufficient, and if it exceeds this range, a sufficient polymerization inhibitory effect is obtained, but it is not economical.

【0008】1,2−ナフトキノンの誘導体としては
1,2−ナフトキノン−4−スルホン酸カリウム、1,
2−ナフトキノン−4−スルホン酸ナトリウム、ブロモ
−1,2−ナフトキノン、クロロ−1,2−ナフトキノ
ン等が挙げられる。
Derivatives of 1,2-naphthoquinone include potassium 1,2-naphthoquinone-4-sulfonate, 1,
Examples thereof include sodium 2-naphthoquinone-4-sulfonate, bromo-1,2-naphthoquinone, and chloro-1,2-naphthoquinone.

【0009】本発明に於いて、重合防止剤の添加方法は
特に限定されるものではないが、例えば、アクリル酸を
製造する場合に関して説明すれば、それぞれの重合防止
剤を固体、または粉体のまま直接アクリル酸に添加する
方法や、適当な有機溶剤にそれぞれまたはその両方を溶
解して添加しても良い。これらは例えばアクリル酸の製
造直後に添加することもできるが、蒸留を行う直前に添
加することが好ましく、工業的には蒸留装置へ供給され
るアクリル酸の供給原液中や蒸留によって蒸留缶液側へ
還流される液中に溶解させて供給することもできる。一
般に、アクリル酸またはアクリル酸を含む系の蒸留は約
50〜約150℃、約100〜約500mmHgの条件
で行われるが、本発明方法によれば、このような高温状
態での処理においても十分に重合を防止することがで
き、長期の連続運転が可能になる。
In the present invention, the method of adding the polymerization inhibitor is not particularly limited. For example, in the case of producing acrylic acid, each polymerization inhibitor may be solid or powder. It may be added directly to acrylic acid as it is, or may be added by dissolving each or both in an appropriate organic solvent. These can be added, for example, immediately after the production of acrylic acid, but it is preferable to add them immediately before carrying out the distillation. Industrially, the acrylic acid is fed to the distillation apparatus in the stock solution or by distillation. It can also be supplied by dissolving it in a liquid refluxed. Generally, the distillation of acrylic acid or a system containing acrylic acid is carried out under the conditions of about 50 to about 150 ° C. and about 100 to about 500 mmHg, but according to the method of the present invention, the treatment at such a high temperature is sufficient. Moreover, polymerization can be prevented, and long-term continuous operation becomes possible.

【0010】本発明方法に於いては重合防止剤としてハ
イドロキノンにベンゾキノン、1,2−ナフトキノンお
よびその誘導体の少なくとも1種を併用することによ
り、優れた重合防止効果が得られるが、公知の他の重合
防止剤を更に添加・併用することも可能である。かかる
公知の重合防止剤としてはハイドロキノンモノメチルエ
ーテル等のフェノール類、フェノチアジン、ジフェニル
アミン等のアミン類、ジブチルジチオカルバミン酸銅等
の銅塩、酢酸マンガン等のマンガン塩、ニトロ化合物、
ニトロソ化合物等が挙げられる。 これらの使用は上記
した本発明方法に於いて適用する重合防止剤と同様の方
法で使用することができる。
In the method of the present invention, by using at least one of benzoquinone, 1,2-naphthoquinone and its derivative in combination with hydroquinone as a polymerization inhibitor, an excellent polymerization inhibiting effect can be obtained. It is also possible to further add / combine the polymerization inhibitor. Such known polymerization inhibitors include phenols such as hydroquinone monomethyl ether, phenothiazine, amines such as diphenylamine, copper salts such as copper dibutyldithiocarbamate, manganese salts such as manganese acetate, nitro compounds,
A nitroso compound etc. are mentioned. These can be used in the same manner as the polymerization inhibitor applied in the above-mentioned method of the present invention.

【0011】また、本発明方法に於いては、必要に応じ
て分子状酸素を用いることも可能である。分子状酸素は
エアーバブリング等によりアクリル酸に混入させればよ
く、工業的には、アクリル酸の精留塔や、アクリル酸と
溶剤の分離塔、アクロレインやメタクロレイン等の軽沸
分のストリッパー等の蒸留操作を行う箇所で実施するこ
とができる。
Further, in the method of the present invention, molecular oxygen can be used if necessary. Molecular oxygen may be mixed with acrylic acid by air bubbling or the like, and industrially, a rectification column for acrylic acid, a separation column for acrylic acid and a solvent, a stripper for light boiling components such as acrolein and methacrolein, etc. It can be carried out at the place where the distillation operation is performed.

【0012】[0012]

【発明の効果】以上詳述した本発明方法によれば、少量
の重合防止剤で効果的に(メタ)アクリル酸およびその
エステルの重合防止を可能ならしめるもので、特に蒸留
時の高温状態においても、個々に重合防止剤を用いる場
合に比較し、極めて優れた(メタ)アクリル酸およびそ
のエステルの重合防止効果を発揮するもので、その産業
上の利用価値は頗る大である。
According to the method of the present invention described in detail above, it is possible to effectively prevent the polymerization of (meth) acrylic acid and its ester with a small amount of a polymerization inhibitor, especially in a high temperature state during distillation. Also, compared with the case where a polymerization inhibitor is used individually, it exhibits an extremely excellent polymerization inhibiting effect of (meth) acrylic acid and its ester, and its industrial utility value is extremely large.

【0013】[0013]

【実施例】以下実施例によって本発明を具体的に説明す
るが、本発明はこれらの実施例に限定されるものではな
い。
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.

【0014】実施例1 アクリル酸50%水溶液にハイドロキノンを100pp
mを添加し、さらに表1に示す重合防止剤を添加した溶
液5gを、内容積20mlの蓋付き試験管に入れ、窒素
ボックス中で100ppmの酸素を含む窒素により5分
間バブリングした後、試験管をその雰囲気下で密栓し
た。次いでこの試験管を100℃のオイルバスに30分
浸けた後、取り出し冷却した。この冷却後の溶液を水で
希釈し、4級アンモニウム塩と反応させ、その濁りの度
合いから溶液中のポリアクリル酸量を定量した。
Example 1 100 pp of hydroquinone was added to a 50% acrylic acid aqueous solution.
m was added, and 5 g of a solution to which the polymerization inhibitor shown in Table 1 was added was placed in a test tube with a lid having an internal volume of 20 ml, and after bubbling with nitrogen containing 100 ppm of oxygen in a nitrogen box for 5 minutes, the test tube Was sealed under the atmosphere. Then, the test tube was immersed in an oil bath at 100 ° C. for 30 minutes, taken out, and cooled. The cooled solution was diluted with water and reacted with a quaternary ammonium salt, and the amount of polyacrylic acid in the solution was determined from the degree of turbidity.

【0015】[0015]

【表1】 (表中のPAはポリアクリル酸を示す)[Table 1] (PA in the table indicates polyacrylic acid)

【0016】表1から明らかな如く重合防止剤としてハ
イドロキノンとベンゾキノン、又はハイドロキノンと
1,2−ナフトキノンおよびその誘導体を併用した本発
明方法はハイドロキノン単独或いはハイドロキノンと本
発明方法以外の重合防止剤との併用に比較し、重合防止
効果に優れていることがわかる。
As is apparent from Table 1, the method of the present invention in which hydroquinone and benzoquinone, or hydroquinone and 1,2-naphthoquinone and its derivatives are used in combination as a polymerization inhibitor is a combination of hydroquinone alone or hydroquinone and a polymerization inhibitor other than the method of the present invention. It can be seen that the effect of preventing polymerization is superior to that of the combined use.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 重合防止剤としてベンゾキノン、1,2
−ナフトキノンおよびその誘導体の少なくとも1種とハ
イドロキノンを用いることを特徴とする(メタ)アクリ
ル酸およびそのエステルの重合防止方法。
1. Benzoquinone, 1,2 as a polymerization inhibitor
A method for preventing polymerization of (meth) acrylic acid and its ester, which comprises using at least one of naphthoquinone and its derivative and hydroquinone.
【請求項2】 ベンゾキノン、1,2−ナフトキノンお
よびその誘導体の使用量が(メタ)アクリル酸およびそ
のエステルに対して1〜5000ppmであることを特
徴とする請求項1記載の(メタ)アクリル酸およびその
エステルの重合防止方法。
2. The (meth) acrylic acid according to claim 1, wherein the amount of benzoquinone, 1,2-naphthoquinone and its derivative used is 1 to 5000 ppm based on (meth) acrylic acid and its ester. And a method for preventing the polymerization of the ester thereof.
【請求項3】 ハイドロキノンの使用量が(メタ)アク
リル酸およびそのエステルに対して1〜5000ppm
であることを特徴とする請求項1記載の(メタ)アクリ
ル酸およびそのエステルの重合防止方法。
3. The amount of hydroquinone used is 1 to 5000 ppm based on (meth) acrylic acid and its ester.
The method for preventing polymerization of (meth) acrylic acid and its ester according to claim 1, wherein
【請求項4】 ベンゾキノン、1,2−ナフトキノンお
よびその誘導体の少なくとも1種とハイドロキノンの使
用割合が1:100〜100:1であることを特徴とす
る請求項1記載の(メタ)アクリル酸のおよびそのエス
テルの重合防止方法。
4. The (meth) acrylic acid according to claim 1, wherein the use ratio of at least one of benzoquinone, 1,2-naphthoquinone and its derivative and hydroquinone is 1: 100 to 100: 1. And a method for preventing the polymerization of the ester thereof.
JP12830296A 1996-05-23 1996-05-23 Prevention of polymerization of (meth)acrylic acid and its ester Pending JPH09316022A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12830296A JPH09316022A (en) 1996-05-23 1996-05-23 Prevention of polymerization of (meth)acrylic acid and its ester

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12830296A JPH09316022A (en) 1996-05-23 1996-05-23 Prevention of polymerization of (meth)acrylic acid and its ester

Publications (1)

Publication Number Publication Date
JPH09316022A true JPH09316022A (en) 1997-12-09

Family

ID=14981432

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12830296A Pending JPH09316022A (en) 1996-05-23 1996-05-23 Prevention of polymerization of (meth)acrylic acid and its ester

Country Status (1)

Country Link
JP (1) JPH09316022A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005336082A (en) * 2004-05-26 2005-12-08 Mitsubishi Chemicals Corp Polymerization inhibitor, composition containing the same, and method for producing easily polymerizable compound by using the polymerization inhibitor
JP2011520948A (en) * 2008-05-22 2011-07-21 ルーサイト インターナショナル ユーケー リミテッド Production of ethylenically unsaturated acids or their esters
KR20200026793A (en) 2017-07-04 2020-03-11 가와사끼가세이고오교 가부시끼가이샤 Radical polymerization control agent and radical polymerization control method

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005336082A (en) * 2004-05-26 2005-12-08 Mitsubishi Chemicals Corp Polymerization inhibitor, composition containing the same, and method for producing easily polymerizable compound by using the polymerization inhibitor
JP4556491B2 (en) * 2004-05-26 2010-10-06 三菱化学株式会社 Polymerization inhibitor, composition containing the same, and method for producing easily polymerizable compound using the polymerization inhibitor
JP2011520948A (en) * 2008-05-22 2011-07-21 ルーサイト インターナショナル ユーケー リミテッド Production of ethylenically unsaturated acids or their esters
US8592624B2 (en) 2008-05-22 2013-11-26 Lucite International Uk Limited Production of ethylenically unsaturated acids or esters thereof
JP2015007142A (en) * 2008-05-22 2015-01-15 ルーサイト インターナショナル ユーケー リミテッド Production of ethylenically unsaturated acids or esters thereof
KR20200026793A (en) 2017-07-04 2020-03-11 가와사끼가세이고오교 가부시끼가이샤 Radical polymerization control agent and radical polymerization control method
US11613509B2 (en) 2017-07-04 2023-03-28 Kawasaki Kasei Chemicals Ltd. Radical polymerization control agent and radical polymerization control method

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