JPH0611293B2 - Functional composition - Google Patents

Functional composition

Info

Publication number
JPH0611293B2
JPH0611293B2 JP61300714A JP30071486A JPH0611293B2 JP H0611293 B2 JPH0611293 B2 JP H0611293B2 JP 61300714 A JP61300714 A JP 61300714A JP 30071486 A JP30071486 A JP 30071486A JP H0611293 B2 JPH0611293 B2 JP H0611293B2
Authority
JP
Japan
Prior art keywords
acid
compound
acid compound
component
stability
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.)
Expired - Lifetime
Application number
JP61300714A
Other languages
Japanese (ja)
Other versions
JPS63153066A (en
Inventor
恒久 植田
良明 三木
伊男 夏梅
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.)
Zeon Corp
Original Assignee
Nippon Zeon 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 Nippon Zeon Co Ltd filed Critical Nippon Zeon Co Ltd
Priority to JP61300714A priority Critical patent/JPH0611293B2/en
Publication of JPS63153066A publication Critical patent/JPS63153066A/en
Publication of JPH0611293B2 publication Critical patent/JPH0611293B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は機能性組成物に関し、更に詳しくは(A)酸性リ
ン酸化合物及び/又は酸性ホスホン酸化合物、(B)2価
鉄化合物、(C)オキシカルボン酸化合物及び/又はオキ
ソカルボン酸化合物及び必要に応じて(D)水を含有して
成ることを特徴とする、消臭性、殺菌性、防カビ性等に
優れた機能性組成物に関する。
The present invention relates to a functional composition, more specifically, (A) an acidic phosphoric acid compound and / or an acidic phosphonic acid compound, (B) a divalent iron compound, ( C) Oxycarboxylic acid compound and / or oxocarboxylic acid compound and optionally (D) water, which is a functional composition excellent in deodorant property, bactericidal property, antifungal property, etc. Regarding things.

(従来の技術) 従来、無機酸、硫酸塩、リン酸塩、ホスホン酸塩、有機
酸等はアンモニア、アミン等に有効な脱臭剤として知ら
れている。なかでもリン酸塩やホスホン酸塩は貯蔵安定
性や熱安定性に優れ、またアンモニア等のアルカリ性物
質の脱臭時に沈澱が生成しないなどの利点があったが、
硫化水素等の脱臭性能に劣ることが問題となっていた。
(Prior Art) Conventionally, inorganic acids, sulfates, phosphates, phosphonates, organic acids and the like are known as effective deodorants for ammonia, amines and the like. Among them, phosphates and phosphonates have advantages such as excellent storage stability and heat stability, and that no precipitate is formed when deodorizing alkaline substances such as ammonia.
Poor deodorizing performance of hydrogen sulfide has been a problem.

一方、硫酸第一鉄や塩化第一鉄などの2価の鉄化合物
は、脱臭剤、鉄黒、媒染剤、し尿処理剤、医薬、製革、
ベンガラ等の種々の用途の原料として利用されている。
しかし、これらの2価鉄化合物は空気中の酸素や溶存し
ている酸素により酸化されやすく安定性に劣ることが問
題となっており、また、脱臭性能の面でも満足のいくも
のではなかった。
On the other hand, divalent iron compounds such as ferrous sulfate and ferrous chloride are used for deodorizing agents, iron black, mordants, human waste treating agents, pharmaceuticals, leather,
It is used as a raw material for various purposes such as red iron oxide.
However, these divalent iron compounds have been problematic in that they are easily oxidized by oxygen in the air or dissolved oxygen and are inferior in stability, and they are not satisfactory in terms of deodorizing performance.

この問題に対処するため、最近、2価の鉄化合物にオキ
シカルボン酸やオキソカルボン酸を添加する方法(特開
昭61−106161号公報、特開昭61−14671
8号公報等)が開発されているが、これらの方法では2
価鉄化合物の安定性は一時的には向上するものの長期に
わたる安定性や紙等に含浸させた時に褐色に着色してし
まうといった問題があり、まだ充分なものではなかっ
た。
In order to deal with this problem, recently, a method of adding an oxycarboxylic acid or an oxocarboxylic acid to a divalent iron compound (Japanese Patent Laid-Open Nos. 61-106161 and 61-14671).
No. 8, etc.) have been developed.
Although the stability of the valent iron compound is temporarily improved, it is still not sufficient because of problems such as long-term stability and brown coloring when impregnated into paper or the like.

(発明が解決しようとする問題点) そこで本発明者らは、従来技術に見られるこれらの問題
を解決すべく鋭意研究の結果、(A)酸性リン酸化合物及
び/又は酸性ホスホン酸化合物、(B)2価鉄化合物、(C)
オキシカルボン酸化合物及び/又はオキソカルボン酸化
合物及び必要に応じて(D)水を含有して成る組成物が、
安定性に優れ、かつ硫化水素等の脱臭性能にも優れるこ
とを見い出し、本発明を完成するに到った。
(Problems to be Solved by the Invention) The present inventors have, as a result of earnest research to solve these problems found in the prior art, (A) an acidic phosphoric acid compound and / or an acidic phosphonic acid compound, (A) B) divalent iron compound, (C)
A composition comprising an oxycarboxylic acid compound and / or an oxocarboxylic acid compound, and optionally (D) water,
The inventors have found that they are excellent in stability and deodorizing performance of hydrogen sulfide and the like, and have completed the present invention.

(問題点を解決するための手段) かくして本発明によれば(A)酸性リン酸化合物及び/又
は酸性ホスホン酸化合物、(B)2価鉄化合物、(C)オキシ
カルボン酸化合物及び/又はオキソカルボン酸化合物及
び必要に応じて(D)水を含有して成る機能性組成物が提
供される。
(Means for Solving Problems) Thus, according to the present invention, (A) acidic phosphoric acid compound and / or acidic phosphonic acid compound, (B) divalent iron compound, (C) oxycarboxylic acid compound and / or oxo Provided is a functional composition containing a carboxylic acid compound and optionally (D) water.

本発明で用いられる(A)成分は酸性リン酸化合物及び/
又は酸性ホスホン酸化合物であり、例えば、リン酸、ピ
ロリン酸、メタリン酸、ヒドロキシエチリデン−1,1
−ジホスホン酸、アミノトリメチレンホスホン酸、エチ
レンジアミンテトラメチレンホスホン酸及びこれらの酸
性塩などが挙げられる。かかる塩の種類としては例え
ば、ナトリウム、カリウム、カルシウム、アルミニウ
ム、亜鉛及びアンモニウム塩等が挙げられる。上記化合
物の中では、酸性ピロリン酸塩が賞用される。
The component (A) used in the present invention is an acidic phosphoric acid compound and /
Or an acidic phosphonic acid compound, for example, phosphoric acid, pyrophosphoric acid, metaphosphoric acid, hydroxyethylidene-1,1
-Diphosphonic acid, aminotrimethylenephosphonic acid, ethylenediaminetetramethylenephosphonic acid, and acid salts thereof. Examples of such salts include sodium, potassium, calcium, aluminum, zinc and ammonium salts. Among the above compounds, acid pyrophosphate is preferred.

(B)成分の2価の鉄化合物の具体例としては、硫酸第一
鉄、硫酸第一鉄アンモニウム、塩化第一鉄、硝酸第一鉄
などが挙げられるが、コストや入手の容易性から硫酸第
一鉄が最も好んで使用される。
Specific examples of the divalent iron compound as the component (B) include ferrous sulfate, ferrous ammonium sulfate, ferrous chloride, and ferrous nitrate, but sulfuric acid is used because of its cost and availability. Ferrous iron is most often used.

(C)成分のオキシカルボン酸化合物及びオキソカルボン
酸化合物は夫々単独で用いてもよいし、併用してもよ
い。オキシカルボン酸化合物は分子中に水酸基とカルボ
キシル基をそれぞれ一つ以上含有するオキシカルボン酸
または水溶性塩であり、その具体例として、例えば乳
酸、ヒドロキシ酢酸、ヒドロキシ酪酸、リンゴ酸、酒石
酸、グリセリン酸、クエン酸、α−メチルリンゴ酸、β
−ヒドロキシグルタル酸、デソキサル酸、酒石酸モノエ
チル、クエン酸モノエチル、グルコン酸、ガラクタル
酸、グルクロン酸、ケトグルコン酸、サリチル酸、p−
ヒドロキシ安息香酸、没食子酸、ヒドロキシフタル酸な
どのごとき脂肪族または芳香族化合物、これらナトリウ
ム塩、カリウム塩、アンモニウム塩などのごとき水溶性
塩が例示される。なかでも脂肪族化合物が賞用される。
The oxycarboxylic acid compound and oxocarboxylic acid compound as the component (C) may be used alone or in combination. The oxycarboxylic acid compound is an oxycarboxylic acid or a water-soluble salt containing at least one hydroxyl group and one or more carboxyl group in the molecule, and specific examples thereof include lactic acid, hydroxyacetic acid, hydroxybutyric acid, malic acid, tartaric acid, and glyceric acid. , Citric acid, α-methylmalic acid, β
-Hydroxyglutaric acid, desoxalic acid, monoethyl tartrate, monoethyl citrate, gluconic acid, galactaric acid, glucuronic acid, ketogluconic acid, salicylic acid, p-
Examples thereof include aliphatic or aromatic compounds such as hydroxybenzoic acid, gallic acid and hydroxyphthalic acid, and water-soluble salts such as sodium salts, potassium salts and ammonium salts thereof. Among them, aliphatic compounds are prized.

また、オキソカルボン酸は、分子中にアルデヒド基また
はケト基とカルボキシル基をそれぞれ一つ以上含有する
オキソカルボン酸化合物またはその水溶性塩であり、そ
の具体例として、例えばグリオキシル酸、マロンアルデ
ヒド酸、スクシンアルデヒド酸、ピルビン酸、2−ケト
酪酸、4−アセチル酪酸、2−ケトグルタル酸、4−ケ
ト−n吉草酸、アセト酢酸、オキソマロン酸、アセトン
ジカルボン酸などのごとき化合物、これらのナトリウム
塩、カリウム塩、アンモニウム塩などの如き水溶性塩が
例示される。
Further, the oxocarboxylic acid is an oxocarboxylic acid compound or a water-soluble salt thereof having one or more aldehyde groups or keto groups and carboxyl groups in the molecule, and specific examples thereof include glyoxylic acid and malonaldehyde acid. Compounds such as succinaldehyde acid, pyruvic acid, 2-ketobutyric acid, 4-acetylbutyric acid, 2-ketoglutaric acid, 4-keto-n valeric acid, acetoacetic acid, oxomalonic acid, and acetonedicarboxylic acid, their sodium salts, Water-soluble salts such as potassium salts and ammonium salts are exemplified.

本発明における各化合物の配合比は目的物の要求性能に
応じ適宜選択しうるが、通常は(A)成分100重量部に
対し、(B)成分は2重量部以上、好ましくは5〜100
0重量部、さらに好ましくは10〜500重量部であ
る。一方、(C)成分は1〜1000重量部、好ましくは
5〜500重量部である。
The compounding ratio of each compound in the present invention can be appropriately selected depending on the required performance of the target object, but usually 100 parts by weight of the component (A), 2 parts by weight or more of the component (B), preferably 5 to 100 parts.
The amount is 0 parts by weight, more preferably 10 to 500 parts by weight. On the other hand, the component (C) is 1 to 1000 parts by weight, preferably 5 to 500 parts by weight.

この場合、(A)成分の量が過度に少ないと安定性に劣る
場合があり、逆に過度に多いと硫化水素等の脱臭性能に
劣る場合がある。また、(C)成分の量が過度に少ないと
安定性に劣る場合があり、逆に過度に多いと経済性に劣
る場合がある。
In this case, if the amount of the component (A) is too small, the stability may be poor, and if it is excessively large, the deodorizing performance of hydrogen sulfide or the like may be poor. Further, if the amount of the component (C) is excessively small, the stability may be poor, and conversely, if it is excessively large, the economical efficiency may be poor.

又、本発明の効果を損なわない限りであれば既存の消臭
剤、脱臭剤、殺菌剤、防カビ剤等と併用したり、顔料、
着色剤、安定剤、酸化防止剤等の各種添加剤を必要に応
じて添加することができる。
Further, as long as the effects of the present invention are not impaired, existing deodorants, deodorants, germicides, fungicides and the like may be used in combination, pigments,
Various additives such as colorants, stabilizers and antioxidants can be added as necessary.

本発明における組成物の調製方法は特に制限されるもの
ではなく、例えば各成分を均一に溶解し水溶液にする方
法、該水溶液を凍結乾燥、粉霧乾燥等により乾燥化する
方法、結晶粉末を均一に混合する方法等が挙げられる。
The method for preparing the composition in the present invention is not particularly limited, and for example, a method of uniformly dissolving each component into an aqueous solution, a method of drying the aqueous solution by freeze-drying, atomization drying, etc., a uniform crystal powder And the like.

又、組成物の性状も特に制限されるものではなく、例え
ば水溶液、粉末、錠剤にして単独で用いる他、必要に応
じて水溶液を紙、布、発泡シート、パルプ、繊維等の含
浸塗布可能な物質及び無機担体に含浸、塗布、担持させ
て用いることもできる。本発明で用いられる無機担体は
該組成物が担持可能なものであれば特に制限されるもの
ではなく、具体例としては、活性炭、アルミナ、シリカ
ゲル、ゼオライト、クレー、ベンナイト、ケイソウ土、
酸性白土等が挙げられる。無機担体の形状は、粉末、粒
状、針状繊維状等があるが特に制限されるものではな
い。含浸、塗布、担持させる場合、対象となる部材に対
する組成物の使用量は特に制限はなく、用途及び使用方
法等に応じて異なるが、通常固形分として10〜20重
量%の範囲である。使用量が過度に少ないと機能が不充
分である場合があり、逆に過度に多い場合には経済性に
劣る場合がある。
Further, the property of the composition is not particularly limited, and for example, an aqueous solution, a powder or a tablet may be used alone, and the aqueous solution may be impregnated and applied to paper, cloth, foamed sheet, pulp, fiber or the like as necessary. It is also possible to use it by impregnating, coating and supporting a substance and an inorganic carrier. The inorganic carrier used in the present invention is not particularly limited as long as the composition can be supported, and specific examples include activated carbon, alumina, silica gel, zeolite, clay, bentonite, diatomaceous earth,
Acid clay etc. are mentioned. The shape of the inorganic carrier may be powder, granules, needle-like fibers or the like, but is not particularly limited. In the case of impregnation, coating and supporting, the amount of the composition used with respect to the target member is not particularly limited and varies depending on the application and method of use, but is usually in the range of 10 to 20% by weight as solid content. If the amount used is too small, the function may be insufficient, and if it is excessively large, the economy may be poor.

かくして得られた本発明の組成物は消臭剤、殺菌剤、防
カビ剤等に有用である。
The composition of the present invention thus obtained is useful as a deodorant, a bactericide, a fungicide and the like.

(発明の効果) かくして本発明によれば、従来技術に比較して安定性を
改善し、かつ硫化水素等の脱臭性能に優れた組成物を得
ることができる。
(Effects of the Invention) Thus, according to the present invention, it is possible to obtain a composition having improved stability as compared with the prior art and excellent deodorizing performance of hydrogen sulfide and the like.

(実施例) 以下に実施例を挙げて本発明をさらに具体的に説明す
る。なお、実施例及び比較例中の部及び%はとくに断り
のないかぎり重量基準である。
(Example) Hereinafter, the present invention will be described more specifically with reference to Examples. Parts and% in Examples and Comparative Examples are based on weight unless otherwise specified.

実施例1 第1表に示した(A),(B)及び(C)成分の合計量が10%に
なるように(D)成分を加え、溶解し、試料水溶液を調製
し、その水溶液20gを50mlビーカーに入れガラス板
をのせて調製時及び20日間放置後の水溶液の外観変化
を観察した。
Example 1 The component (D) was added and dissolved so that the total amount of the components (A), (B) and (C) shown in Table 1 was 10%, and a sample aqueous solution was prepared. Was placed in a 50 ml beaker, a glass plate was put on the beaker, and appearance changes of the aqueous solution were observed at the time of preparation and after standing for 20 days.

また、各種水溶液100mgを100ml三角フラスコに入
れて密詮した後、2.8%アンモニア水溶液50μlを
加え、30分後の溶液の外観を観察し、ガスクロマトグ
ラフィーにて気相部分のアンモニア量を定量し、アンモ
ニア脱臭性能の評価とした。
Also, after pouring 100 mg of various aqueous solutions into a 100 ml Erlenmeyer flask and pouring, 50 μl of 2.8% ammonia aqueous solution was added, and the appearance of the solution was observed after 30 minutes, and the amount of ammonia in the gas phase portion was measured by gas chromatography. It was quantified and evaluated as the ammonia deodorizing performance.

一方、各種水溶液1gを100ml三角フラスコに入れて
密詮した後、硫化水素0.02mgを含むガス1mlを注入し、
ガスクロマトグラフィーにて気相部分の硫化水素量を定
量し、硫化水素脱臭性能の評価とした。結果を第1表に
示す。
On the other hand, after putting 1 g of each aqueous solution into a 100 ml Erlenmeyer flask and purging, 1 ml of gas containing 0.02 mg of hydrogen sulfide was injected,
The amount of hydrogen sulfide in the gas phase was quantified by gas chromatography to evaluate the hydrogen sulfide deodorizing performance. The results are shown in Table 1.

第1表より、本発明例は初期の外観を長期にわたり維持
しており系の安定性に優れ、さらにアンモニアや硫化水
素の脱臭性能に優れていることがわかる。これに対し、
(A)成分単独(実験番号1−12)の場合には硫化水素
脱臭性に劣り、また(B)及び(C)の2成分(実験番号1−
14)の場合には長期間放置すると着色を生じ安定性能
に劣ることがわかる。
It can be seen from Table 1 that the examples of the present invention maintain the initial appearance for a long period of time, are excellent in system stability, and are also excellent in deodorizing performance of ammonia and hydrogen sulfide. In contrast,
When the component (A) alone (Experiment No. 1-12) was inferior in deodorizing hydrogen sulfide, the two components (B) and (C) (Experiment No. 1-
In the case of 14), it can be seen that when left for a long period of time, coloring occurs and the stability performance is poor.

実施例2 第2表に示す(A),(B)及び(C)成分の所定量を用い、(B)
成分の量が10%になるように(D)成分を加えて溶解し
試料水溶液を調製した。得られた各試料水溶液にガーゼ
を浸し、十分紋り余分の試料を除去した後、風乾し、2
時間後のガーゼの着色の有無を調べた。結果を第2表に
示す。
Example 2 Using the predetermined amounts of the components (A), (B) and (C) shown in Table 2, (B)
A sample aqueous solution was prepared by adding and dissolving the component (D) so that the amount of the component was 10%. Gauze was dipped in each of the obtained sample aqueous solutions to remove the excess sample and then air-dried.
The presence or absence of coloration of the gauze after the elapse of time was examined. The results are shown in Table 2.

この結果からも本発明例は安定性に優れることがわか
る。
From these results, it can be seen that the inventive examples are excellent in stability.

実施例3 第3表に示す各成分の所定量を水を加えて溶解し、減算
乾燥して乾燥粉末を得た後、110℃、熱風オーブン中
に2時間放置し外観変化を観察した。結果を第3表に示
す。
Example 3 A predetermined amount of each component shown in Table 3 was added with water to dissolve it, and subtractive drying was performed to obtain a dry powder, which was then left in a hot air oven at 110 ° C. for 2 hours to observe a change in appearance. The results are shown in Table 3.

第2表より、本発明例は熱安定性に優れていることがわ
かる。
It can be seen from Table 2 that the inventive examples are excellent in thermal stability.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】(A)酸性リン酸化合物及び/又は酸性ホス
ホン酸化合物、(B)2価鉄化合物、(C)オキシカルボン酸
化合物及び/又はオキソカルボン酸化合物及び必要に応
じて(D)水を含有して成ることを特徴とする機能性組成
物。
1. An (A) acidic phosphoric acid compound and / or an acidic phosphonic acid compound, (B) a divalent iron compound, (C) an oxycarboxylic acid compound and / or an oxocarboxylic acid compound, and (D) if necessary. A functional composition comprising water.
JP61300714A 1986-12-17 1986-12-17 Functional composition Expired - Lifetime JPH0611293B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61300714A JPH0611293B2 (en) 1986-12-17 1986-12-17 Functional composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61300714A JPH0611293B2 (en) 1986-12-17 1986-12-17 Functional composition

Publications (2)

Publication Number Publication Date
JPS63153066A JPS63153066A (en) 1988-06-25
JPH0611293B2 true JPH0611293B2 (en) 1994-02-16

Family

ID=17888211

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61300714A Expired - Lifetime JPH0611293B2 (en) 1986-12-17 1986-12-17 Functional composition

Country Status (1)

Country Link
JP (1) JPH0611293B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5268128B2 (en) * 2007-03-19 2013-08-21 南姜エフニカ株式会社 Deodorant composition, deodorant aqueous solution, deodorant aqueous slurry, deodorant powder composition and deodorant masterbatch

Also Published As

Publication number Publication date
JPS63153066A (en) 1988-06-25

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