JP2007217573A - Cleanser composition for food production line - Google Patents

Cleanser composition for food production line Download PDF

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JP2007217573A
JP2007217573A JP2006040180A JP2006040180A JP2007217573A JP 2007217573 A JP2007217573 A JP 2007217573A JP 2006040180 A JP2006040180 A JP 2006040180A JP 2006040180 A JP2006040180 A JP 2006040180A JP 2007217573 A JP2007217573 A JP 2007217573A
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dichloroisocyanurate
food production
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sodium metasilicate
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JP4947266B2 (en
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Masayuki Yamazaki
雅之 山崎
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Nissan Chemical Corp
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Nissan Chemical Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a cleanser composition for food production lines, which exhibits excellent cleansing forces also for stains, especially protein stains, adhered to the surfaces of pipes, has excellent storage stability, has low corrosiveness to various metals, when used as aqueous solutions, and does not produce irritative odors even in a high concentration aqueous solution. <P>SOLUTION: This cleanser composition for the food production lines contains a dichloroisocyanurate and sodium metasilicate pentahydrate only whose particle surfaces are subjected to a low hydration treatment, as essential components. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

食品製造ライン用の洗浄剤組成物に関する。   The present invention relates to a detergent composition for a food production line.

食生活の変化と食品加工技術の進歩により、食の世界は多様化し、食品工場は多品種の製造を余儀なくされてきている。近年、消費者の健康意識が変化しており、加工品の衛生面及び安全面に対して敏感になってきているため、食品製造にあたっては、衛生管理がきわめて重要なこととなっており、食品製造において、その配管などのラインの洗浄度合を検出する方法(例えば、特許文献1参照)などが提示されている。   Due to changes in dietary habits and advances in food processing technology, the world of food has diversified, and food factories have been forced to produce a wide variety of foods. In recent years, consumers' health consciousness has changed and it has become more sensitive to the hygiene and safety aspects of processed products, so hygiene management has become extremely important in food production. In manufacturing, a method for detecting the degree of cleaning of a line such as a pipe (see, for example, Patent Document 1) is presented.

配管などのラインの微生物汚染を防ぐために、汚れの塊を洗い流す高圧スプレーによる予備洗浄工程や、洗浄剤(界面活性剤やアルカリ、酸など)を使用して機械的に汚れを洗い落とす洗浄工程、残留薬剤を洗い流す濯ぎ工程、更に、次亜塩素酸ナトリウム液やジクロロイソシアヌル酸塩などの塩素系化合物を使用して除菌する工程が必要である。最終工程で使用される塩素系化合物の作用機構は、いずれも次亜塩素酸の酸化作用によるもので、その強力な酸化力により細胞膜を破壊し、核タンパクのSH基や酵素タンパクを酸化変性して効果を発揮する。しかし、塩素系化合物は酸化力が強い為に、金属等に対して腐食性を有し、アルミニウム、鋳鉄、ステンレスといった金属への腐食が懸念される。また、配管表面にこびり付いた汚れ、特にタンパク汚れに対する洗浄効果は十分とはいえない。一種類の洗浄剤により除菌、洗浄を同時に行うことができれば、作業が著しく簡素化されることになる。
特開2004−329978(特許請求の範囲)
To prevent microbial contamination of lines such as piping, pre-cleaning process using high-pressure spray to wash away lump of dirt, cleaning process to wash off dirt mechanically using detergent (surfactant, alkali, acid, etc.), residual A rinsing step for washing away the drug and a step for sterilization using a chlorine-based compound such as sodium hypochlorite solution or dichloroisocyanurate are required. The mechanism of action of the chlorinated compounds used in the final process is based on the oxidation of hypochlorous acid. The strong oxidizing power destroys the cell membrane and oxidizes and denatures the SH group of the nuclear protein and the enzyme protein. To be effective. However, since chlorinated compounds have strong oxidizing power, they are corrosive to metals and the like, and there is concern about corrosion of metals such as aluminum, cast iron, and stainless steel. Moreover, it cannot be said that the cleaning effect with respect to dirt stuck to the piping surface, particularly protein dirt, is sufficient. If sterilization and cleaning can be performed simultaneously with one type of cleaning agent, the operation will be greatly simplified.
JP-A-2004-329978 (Claims)

本発明に使用されているジクロロイソシアヌル酸塩を水に溶かした液の性能面における長所は、各種細菌類に対する除菌力が確実なことである。その反面、欠点としては反応性が著しいため、保存安定性が低いとともに、金属に対する腐食性が激しく、金属類が多く存在する条件での除菌には利用しにくい点が挙げられる。また、水溶液濃度を高くした場合に、強い刺激臭を発生するといった使用場面における環境面での欠点も挙げられる。よって、保存安定性が高いとともに、腐食抑制能力を確保すること、及び水溶液濃度を高くしても刺激臭を発生しないことが、実用化のための必須条件である。   The advantage of the performance of the solution obtained by dissolving the dichloroisocyanurate used in the present invention in water is that the sterilizing power against various bacteria is reliable. On the other hand, since the reactivity is remarkably low, the storage stability is low, the corrosiveness to metals is intense, and it is difficult to use for sterilization under conditions where a lot of metals exist. In addition, when the concentration of the aqueous solution is increased, there is also an environmental disadvantage in use scenes such that a strong irritating odor is generated. Therefore, it is an indispensable condition for practical use that the storage stability is high, that the corrosion-inhibiting ability is ensured, and that no irritating odor is generated even when the concentration of the aqueous solution is increased.

本発明は、上記従来技術の課題及び現状等に鑑み、これを解消しようとするものであり、食品製造において、その配管などのラインの汚れ、特にタンパク汚れに対して優れた洗浄力を発揮するとともに、保存安定性に優れ、水溶液にして使用した場合に各種金属に対する腐食性が低く、しかも高濃度水溶液にしても刺激臭を発生しない食品製造ライン用洗浄剤組成物を提供することを目的とする。   The present invention is to solve this problem in view of the problems and current situation of the prior art described above, and in food production, exhibits excellent cleaning power against dirt on lines such as piping, particularly protein dirt. In addition, an object of the present invention is to provide a cleaning composition for food production lines that is excellent in storage stability, has low corrosiveness to various metals when used as an aqueous solution, and does not generate an irritating odor even in a high concentration aqueous solution. To do.

本発明は、ジクロロイソシアヌル酸塩と粒子表面のみを低水和化処理したメタケイ酸ナトリウム五水和物とを必須成分として含有する、食品製造ライン用洗浄剤組成物である。   The present invention is a detergent composition for a food production line containing dichloroisocyanurate and sodium metasilicate pentahydrate obtained by subjecting only the particle surface to a low hydration treatment as essential components.

好ましい形態は、以下の通りである。   Preferred forms are as follows.

ジクロロイソシアヌル酸塩がジクロロイソシアヌル酸ナトリウムであること。 ジクロロイソシアヌル酸塩100質量部に対して、メタケイ酸ナトリウム五水和物の配合量が、150質量部以上であること。   The dichloroisocyanurate is sodium dichloroisocyanurate. The compounding quantity of sodium metasilicate pentahydrate is 150 mass parts or more with respect to 100 mass parts of dichloroisocyanurate.

ジクロロイソシアヌル酸塩100質量部に対して、メタケイ酸ナトリウム五水和物の配合量が、150質量部以上、かつ2000質量部以下であること。   The blending amount of sodium metasilicate pentahydrate is 150 parts by mass or more and 2000 parts by mass or less with respect to 100 parts by mass of dichloroisocyanurate.

組成物の1質量%水溶液のpHが11以上であること。   The pH of a 1% by mass aqueous solution of the composition is 11 or more.

組成物中のジクロロイソシアヌル酸塩の配合量が、0.5〜40質量%であること。   The blending amount of dichloroisocyanurate in the composition is 0.5 to 40% by mass.

組成物中のジクロロイソシアヌル酸塩の配合量が、3〜40質量%であること。   The blending amount of dichloroisocyanurate in the composition is 3 to 40% by mass.

本発明の組成物は、食品製造ラインにこびりついた汚れ、特にタンパク汚れに対して優れた洗浄力を発揮するとともに、水に溶かして使用した場合の金属腐食性及び刺激臭の発生が極めて少なく、保存安定性に優れている。   The composition of the present invention exhibits excellent detergency against dirt stuck to food production lines, particularly protein dirt, and extremely little metal corrosiveness and generation of irritating odors when dissolved in water, Excellent storage stability.

ジクロロイソシアヌル酸塩を水に溶かした液の除菌力については、十分な効果があることは知られている。しかし金属腐食性及び高濃度水溶液からの刺激臭の発生については、これまで十分な対策がなかったことから、利用できる範囲が限定されていた。本発明により、従来の常識は変更されることになり、ジクロロイソシアヌル酸塩の殺菌力を高濃度水溶液のかたちでも、幅広く有効に利用できることになった。   It is known that the sterilizing power of a solution obtained by dissolving dichloroisocyanurate in water has a sufficient effect. However, with respect to the generation of irritating odors from metal corrosive and high-concentration aqueous solutions, there has been no sufficient countermeasures so far, so the range that can be used has been limited. According to the present invention, the conventional common sense is changed, and the bactericidal power of dichloroisocyanurate can be widely and effectively used even in the form of a high-concentration aqueous solution.

本発明について、以下に説明する。   The present invention will be described below.

ジクロロイソシアヌル酸塩を水に溶かして使用した場合の金属防錆及び、高濃度水溶液からの刺激臭発生防止を目的として、組成物中に必須成分として、ジクロロイソシアヌル酸塩と粒子表面のみを低水和化処理したメタケイ酸ナトリウム五水和物(メタケイ酸ナトリウム5H2O:Na2O・SiO2・5H2O)とを必須成分として含有させる。 For the purpose of preventing metal rust when dichloroisocyanurate is dissolved in water and preventing the generation of irritating odors from high-concentration aqueous solutions, only dichloroisocyanurate and the particle surface are low water as essential components in the composition. sodium metasilicate was divided treated pentahydrate (sodium metasilicate 5H 2 O: Na 2 O · SiO 2 · 5H 2 O) and a is contained as an essential component.

ここで、従来のメタケイ酸ナトリウム五水和物と粒子表面のみを低水和化処理したメタケイ酸ナトリウム五水和物とは、下記の付着水分量の測定方法により識別することができる。   Here, the conventional sodium metasilicate pentahydrate and the sodium metasilicate pentahydrate obtained by subjecting only the particle surface to a low hydration treatment can be distinguished by the following method for measuring the amount of adhered water.

付着水分量の測定方法は、日本薬局方一般試験法強熱減量試験法を参考にして、アルミナ坩堝を用いて800℃、2時間強熱乾燥した後、次式(式1)によって付着水分量(水和物水分量)を算出する。   The method for measuring the amount of adhering water is as follows. Refer to the Japanese Pharmacopoeia General Test Method and the ignition loss test method. Calculate (hydrate water content).

付着水分量(%)=[1−A×(W3−W1)/(W2−W1)]×100 (式1)
上記式1の記号については、下記の通りに定める。
Adhering moisture amount (%) = [1-A × (W3-W1) / (W2-W1)] × 100 (Formula 1)
The symbol of the above formula 1 is determined as follows.

A:1.7377(係数) [=212(分子質量Na2O・SiO2・5H2O)/122(分子質量Na2O・SiO2)]
W1:坩堝質量(g)
W2:強熱乾燥前のW1と試料精秤量との合計質量(g)
W3:強熱乾燥後のW1と試料精秤量との合計質量(g)
前記式1による、本発明に使用される粒子表面のみを低水和化処理したメタケイ酸ナトリウム五水和物の付着水分量測定値は、−0.01〜−1.00質量%となる。
A: 1.7377 (coefficient) [= 212 (molecular mass Na 2 O.SiO 2 .5H 2 O) / 122 (molecular mass Na 2 O.SiO 2 )]
W1: crucible mass (g)
W2: Total mass (g) of W1 and the sample weighed before ignition drying
W3: Total mass (g) of W1 after ignitable drying and the exact sample weight
The measured value of the attached water content of sodium metasilicate pentahydrate in which only the particle surface used in the present invention is subjected to a low hydration treatment according to the formula 1 is -0.01 to -1.00% by mass.

この−0.01〜−1.00質量%は、低水和化処理によりメタケイ酸ナトリウム五水和物の粒子表面から水和物としての水が粒子表面から離脱した水分量比率に対応する。   This -0.01--1.00 mass% respond | corresponds to the moisture content ratio from which the water as a hydrate separated from the particle | grain surface of the sodium metasilicate pentahydrate from the particle | grain surface by the low hydration process.

メタケイ酸ナトリウム五水和物の粒子表面のみを低水和化処理する方法としては、流動層式乾燥、気流式乾燥などの通気流熱風乾燥方式による乾燥方法が採用される。   As a method for subjecting only the particle surface of sodium metasilicate pentahydrate to a low hydration treatment, a drying method using an aeration flow hot air drying method such as fluidized bed drying or airflow drying is employed.

本発明の好ましい形態について、説明する。   A preferred embodiment of the present invention will be described.

本発明で使用するジクロロイソシアヌル酸塩としては、例えばジクロロイソシアヌル酸のナトリウム塩、カリウム塩等が挙げられるが、好ましいものはジクロロイソシアヌル酸ナトリウムである。   Examples of the dichloroisocyanuric acid salt used in the present invention include sodium salt and potassium salt of dichloroisocyanuric acid, with sodium dichloroisocyanurate being preferred.

金属腐食抑制効果を確実にするとともに、高濃度水溶液からの刺激臭発生を防止するために、ジクロロイソシアヌル酸塩100質量部に対して、粒子表面のみを低水和化処理したメタケイ酸ナトリウム五水和物の配合量を、150質量部以上にして、組成物の1質量%水溶液のpHを11以上にする。また、メタケイ酸ナトリウム五水和物の配合量の上限としては、ジクロロイソシアヌル酸塩100質量部に対して、2000質量部である。   Sodium metasilicate pentahydrate in which only the particle surface is subjected to low hydration treatment with respect to 100 parts by mass of dichloroisocyanurate in order to ensure the metal corrosion inhibitory effect and prevent the generation of irritating odors from highly concentrated aqueous solutions. The blending amount of the Japanese product is 150 parts by mass or more, and the pH of the 1% by mass aqueous solution of the composition is 11 or more. Moreover, as an upper limit of the compounding quantity of sodium metasilicate pentahydrate, it is 2000 mass parts with respect to 100 mass parts of dichloro isocyanurate.

組成物の1質量%水溶液のpHを11以上にすることにより、金属腐食抑制効果を確実にするとともに、高濃度水溶液からの刺激臭発生を防止する。   By making the pH of the 1% by mass aqueous solution of the composition 11 or more, the metal corrosion inhibiting effect is ensured and the generation of irritating odors from the high concentration aqueous solution is prevented.

組成物の保存安定性を高めるために、組成物中のジクロロイソシアヌル酸塩の配合量を0.5〜40質量%又は3〜40質量%にする。   In order to improve the storage stability of the composition, the blending amount of dichloroisocyanurate in the composition is 0.5 to 40% by mass or 3 to 40% by mass.

ジクロロイソシアヌル酸塩100質量部に対して、粒子表面のみを低水和化処理したメタケイ酸ナトリウム五水和物の配合量を、150質量部以上にすることにより、鉄、ステンレス、銅、真鍮、アルミニウム等の金属表面に、ケイ酸陰イオンの特異吸着が起こり、生成された吸着膜が金属表面の保護膜となることによって、金属腐食因子のアタックを防止しているものと考える。これは金属と溶液界面の電気二重層の電位に関するものである。更に、粒子表面のみを低水和化処理したメタケイ酸ナトリウム五水和物中のアルカリ分が水溶液中でジクロロイソシアヌル酸塩の有効成分である次亜塩素酸をイオン化することにより、刺激臭の発生を抑制しているものと考える。また、ジクロロイソシアヌル酸塩とメタケイ酸ナトリウム五水和物を配合した組成物は、保存安定性が決して良くない為、比較的高い温度条件で保存された場合、急激にケーキング(固結)してしまう傾向が認められるが、粒子表面のみを低水和化処理したメタケイ酸ナトリウム五水和物を使用し、ジクロロイソシアヌル酸塩配合量を3〜40質量%にすることにより、これを抑えることができる。粒子表面のみを低水和化処理したメタケイ酸ナトリウム五水和物は、市販品として容易に入手できる。   By adding 150 parts by mass or more of sodium metasilicate pentahydrate with a low hydration treatment only on the particle surface to 100 parts by mass of dichloroisocyanurate, iron, stainless steel, copper, brass, It is considered that specific adsorption of silicate anions occurs on a metal surface such as aluminum, and the produced adsorbed film serves as a protective film on the metal surface, thereby preventing attack of metal corrosion factors. This concerns the electric double layer potential at the metal / solution interface. In addition, the alkali content in sodium metasilicate pentahydrate, which is a hypohydrated treatment only on the particle surface, ionizes hypochlorous acid, which is an active ingredient of dichloroisocyanurate, in an aqueous solution. We think that we are suppressing. In addition, a composition containing dichloroisocyanurate and sodium metasilicate pentahydrate has a poor storage stability, so when stored at a relatively high temperature, it rapidly caking (consolidates). However, it is possible to suppress this by using sodium metasilicate pentahydrate with a low hydration treatment only on the particle surface, and by adjusting the amount of dichloroisocyanurate to 3 to 40% by mass. it can. Sodium metasilicate pentahydrate obtained by subjecting only the particle surface to a low hydration treatment can be easily obtained as a commercial product.

以下、実施例及び比較例を挙げて更に詳しく本発明を説明するが、本発明の技術的範囲はこれによって制限されるものではない。   EXAMPLES Hereinafter, although an Example and a comparative example are given and this invention is demonstrated in detail, the technical scope of this invention is not restrict | limited by this.

ここでは、メタケイ酸ナトリウム五水和物(未処理品)として、商品名「メタ珪酸ソーダ5水塩」(三宝化学工業株式会社製)を使用した。一方、粒子表面のみを低水和化処理したメタケイ酸ナトリウム五水和物(乾燥処理品)として、商品名「メタエース5(高流動性5水和物)」(三宝化学工業株式会社製)を使用した。前記の付着水分量の測定方法では、使用した「メタ珪酸ソーダ5水塩」(三宝化学工業株式会社製)の付着水分量は、1.09質量%を示した。また、使用した「メタエース5(高流動性5水和物)」(三宝化学工業株式会社製)の付着水分量は、−0.51質量%を示した。   Here, the trade name “Sodium Silicate Pentahydrate” (manufactured by Sanpo Chemical Industry Co., Ltd.) was used as sodium metasilicate pentahydrate (untreated product). On the other hand, the product name “Metaace 5 (high fluidity pentahydrate)” (manufactured by Sanpo Chemical Industry Co., Ltd.) is used as sodium metasilicate pentahydrate (dried product) that has been subjected to low hydration treatment only on the particle surface. used. In the method for measuring the amount of adhering moisture, the amount of adhering moisture of the used “sodium metasilicate pentahydrate” (manufactured by Sanpo Chemical Industry Co., Ltd.) was 1.09% by mass. Moreover, the amount of adhering water of “Metaace 5 (high fluidity pentahydrate)” (manufactured by Sanpo Chemical Industry Co., Ltd.) used was −0.51% by mass.

実施例1〜7及び比較例1〜2では、表1に示す配合の組成物を作成し、以下の評価を行った。   In Examples 1-7 and Comparative Examples 1-2, the composition of the mixing | blending shown in Table 1 was created, and the following evaluation was performed.

[金属腐食試験]
有効塩素濃度が1000ppmになるように、表1に示す実施例1〜7及び比較例1〜2の組成物をそれぞれ蒸留水に溶解し、この溶解液をポリ容器に入れ、各種金属のテストピースを浸漬した状態で密閉し、40℃、24時間保存する。保存後の腐食度を測定し、腐食度の格付けを決定した。結果を表1に示す。
[Metal corrosion test]
Each of the compositions of Examples 1 to 7 and Comparative Examples 1 and 2 shown in Table 1 was dissolved in distilled water so that the effective chlorine concentration was 1000 ppm. Is immersed and stored at 40 ° C. for 24 hours. The degree of corrosion after storage was measured and the rating of the degree of corrosion was determined. The results are shown in Table 1.

腐食度:腐食によるテストピースの減少質量(mdd:mg/dm2・d)
腐食度は次の基準(格付け)で分類した。
Corrosion degree: Reduced mass of test piece due to corrosion (mdd: mg / dm 2 · d)
Corrosion degree was classified according to the following criteria (rating).

A(優良):0〜10、B(可)10〜50、C(否)>100。   A (excellent): 0 to 10, B (possible) 10 to 50, C (no)> 100.

[1%水溶液のpH測定]
表1に示す実施例1〜7及び比較例1〜2の組成物をそれぞれ蒸留水に溶解し、1%水溶液を作成後、pHを測定した。結果を表1に示す。
[PH measurement of 1% aqueous solution]
The compositions of Examples 1 to 7 and Comparative Examples 1 and 2 shown in Table 1 were each dissolved in distilled water to prepare a 1% aqueous solution, and then the pH was measured. The results are shown in Table 1.

[刺激臭確認試験]
有効塩素濃度が1000ppmになるように、表1に示す実施例1〜7及び比較例1〜2の組成物をそれぞれ蒸留水に溶解し、この溶解液をポリ容器に入れ、密閉した状態で温度40℃にて、それぞれ2時間、4時間、6時間保存後の刺激臭発生量を塩素ガス検知管にて測定した。結果を表1に示す。
[Irritating odor confirmation test]
The compositions of Examples 1 to 7 and Comparative Examples 1 and 2 shown in Table 1 were each dissolved in distilled water so that the effective chlorine concentration was 1000 ppm, and this solution was put in a plastic container and sealed in a temperature state. The amount of irritating odor generated after storage at 40 ° C. for 2 hours, 4 hours and 6 hours was measured with a chlorine gas detector tube. The results are shown in Table 1.

Figure 2007217573
Figure 2007217573

実施例8〜9及び比較例3〜4では、表2に示す配合の組成物を作成し、以下の評価を行った。   In Examples 8 to 9 and Comparative Examples 3 to 4, compositions having the composition shown in Table 2 were prepared and evaluated as follows.

[安定性試験]
表2に示す実施例8〜9の組成物及び比較例3〜4の組成物を、それぞれアルミ袋(15cm×10cm)に100g充填し、ヒートシールした後、55℃条件で密閉保存し、それぞれ24時間、48時間保存後にケーキングの有無を確認した。結果を表2に示す。
[Stability test]
The compositions of Examples 8 to 9 and the compositions of Comparative Examples 3 to 4 shown in Table 2 were each filled with 100 g of aluminum bags (15 cm × 10 cm), heat sealed, and hermetically stored at 55 ° C., respectively. The presence or absence of caking was confirmed after storage for 24 hours and 48 hours. The results are shown in Table 2.

Figure 2007217573
Figure 2007217573

表3に示す実施例10及び比較例5〜6の組成物を、有効塩素濃度が150ppmになるように蒸留水に溶解した試験液を作成し、これらの試験液を用いて、以下の評価を行った。   Test solutions in which the compositions of Example 10 and Comparative Examples 5 to 6 shown in Table 3 were dissolved in distilled water so that the effective chlorine concentration was 150 ppm were prepared, and the following evaluation was performed using these test solutions. went.

[洗浄力評価]
食品製造ラインの汚れとして代表的なタンパク汚れに対する洗浄力評価を行うために、卵を約0.8gスライドガラス(76mm×26mm)に塗り、乾燥させたものを被洗浄体のサンプルとした。各試験液にスライドガラスを浸漬し、20℃にて1時間及び24時間静置した後、蒸留水の入ったビーカー中でスライドガラスを軽く濯ぎ、室温で乾燥する。洗浄力効果を下記の判定基準で評価するとともに、試験前後のスライドガラスの重量を測定し、下記の計算式により、汚れ除去率を算出した。結果を表3に示す。
[Detergency evaluation]
In order to evaluate the detergency against protein stains typical of food production line stains, about 0.8 g of a glass slide (76 mm × 26 mm) coated and dried was used as a sample of the object to be cleaned. The slide glass is immersed in each test solution and allowed to stand at 20 ° C. for 1 hour and 24 hours. Then, the slide glass is lightly rinsed in a beaker containing distilled water and dried at room temperature. The cleaning power effect was evaluated according to the following criteria, the weight of the slide glass before and after the test was measured, and the stain removal rate was calculated by the following formula. The results are shown in Table 3.

判定基準:
○…大半の汚れが除去されていた △…半分程度の汚れが除去されていた ×…大半の汚れが除去されずに残っていた
汚れ除去率(%)=(W1−W2)/(W1−W3) × 100 (式2)
上記式2の記号については、下記の通りに定める。
Judgment criteria:
○: Most of the dirt was removed Δ: About half of the dirt was removed ×: Most of the dirt remaining without being removed (%) = (W1-W2) / (W1- W3) × 100 (Formula 2)
The symbol of the above formula 2 is determined as follows.

W1:汚れ成分を塗った試験前のスライドガラスの重量(g)
W2:試験後のスライドガラスの重量(g)
W3:汚れ成分を塗る前のスライドガラスの重量(g)
[金属腐食試験]
実施例10及び比較例5〜6の試験液をポリ容器に入れ、金属(SS−400)のテストピースを浸漬した状態で密閉し、40℃、24時間保存する。保存後の腐食度を測定し、腐食度の格付けを決定した。結果を表3に示す。
W1: Weight (g) of the slide glass before the test on which the soil component was applied
W2: Weight of slide glass after test (g)
W3: Weight of slide glass before applying dirt component (g)
[Metal corrosion test]
The test solutions of Example 10 and Comparative Examples 5 to 6 are placed in a plastic container, sealed with a metal (SS-400) test piece immersed therein, and stored at 40 ° C. for 24 hours. The degree of corrosion after storage was measured and the rating of the degree of corrosion was determined. The results are shown in Table 3.

腐食度:腐食によるテストピースの減少質量(mdd:mg/dm2・d)
腐食度は次の基準(格付け)で分類した。
Corrosion degree: Reduced mass of test piece due to corrosion (mdd: mg / dm 2 · d)
Corrosion degree was classified according to the following criteria (rating).

A(優良):0〜10、B(可)10〜50、C(否)>100。   A (excellent): 0 to 10, B (possible) 10 to 50, C (no)> 100.

Figure 2007217573
Figure 2007217573

表1〜表3に示すように、本発明の組成物は、食品製造において、その配管などのラインの汚れ、特にタンパク汚れに対して優れた洗浄力を発揮するとともに、水に溶かして使用した場合の金属腐食性及び刺激臭の発生が極めて少なく、保存安定性に優れている。   As shown in Tables 1 to 3, the composition of the present invention exhibited excellent detergency against dirt on lines such as piping, particularly protein dirt, in food production, and was used by dissolving in water. In this case, the metal corrosiveness and the generation of irritating odor are extremely small, and the storage stability is excellent.

従前より、ジクロロイソシアヌル酸塩を水に溶かした液の除菌力については、十分な効果があることは知られていた。しかしながら、金属腐食性及び高濃度水溶液からの刺激臭の発生については、これまで十分な対策法がなかったことから、利用できる範囲が限定されていた。本発明により、食品製造ラインにこびりついた汚れ、特にタンパク汚れに対して優れた洗浄力を発揮するとともに、保存安定性に優れ、水溶液にして使用した場合に各種金属に対する腐食性が低く、しかも高濃度水溶液にしても刺激臭を発生しない食品製造ライン用洗浄剤組成物の提供が可能となった。これにより、特定用途のみに利用範囲が限定されていたジクロロイソシアヌル酸塩の水溶液が有する殺菌力を、金属類が多く存在する条件下や、高濃度水溶液形態などにおいても、幅広く有効に利用できることとなり、該水溶液の用途の拡大が期待できることとなった。
Conventionally, it has been known that the sterilizing power of a solution obtained by dissolving dichloroisocyanurate in water has a sufficient effect. However, with respect to the generation of irritating odors from metal corrosive and high-concentration aqueous solutions, there has been no sufficient countermeasures so far, so the range of use has been limited. According to the present invention, it exhibits excellent detergency against dirt stuck to food production lines, especially protein stains, has excellent storage stability, and has low corrosiveness to various metals when used in aqueous solution. It has become possible to provide a detergent composition for food production lines that does not generate an irritating odor even with a concentrated aqueous solution. As a result, the sterilizing power of aqueous solutions of dichloroisocyanurate, whose range of use was limited to specific applications, can be used widely and effectively even under conditions where there are many metals and in the form of highly concentrated aqueous solutions. Therefore, it was expected that the application of the aqueous solution could be expanded.

Claims (6)

ジクロロイソシアヌル酸塩と粒子表面のみを低水和化処理したメタケイ酸ナトリウム五水和物とを必須成分として含有する、食品製造ライン用洗浄剤組成物。 A detergent composition for a food production line, containing dichloroisocyanurate and sodium metasilicate pentahydrate obtained by subjecting only the particle surface to a low hydration treatment as essential components. ジクロロイソシアヌル酸塩がジクロロイソシアヌル酸ナトリウムである、請求項1に記載の食品製造ライン用洗浄剤組成物。 The detergent composition for food production lines according to claim 1, wherein the dichloroisocyanurate is sodium dichloroisocyanurate. ジクロロイソシアヌル酸塩100質量部に対して、メタケイ酸ナトリウム五水和物の配合量が、150質量部以上である、請求項1に記載の食品製造ライン用洗浄剤組成物。 The detergent composition for a food production line according to claim 1, wherein the compounding amount of sodium metasilicate pentahydrate is 150 parts by mass or more with respect to 100 parts by mass of dichloroisocyanurate. ジクロロイソシアヌル酸塩100質量部に対して、メタケイ酸ナトリウム五水和物の配合量が、150質量部以上、かつ2000質量部以下である、請求項1に記載の食品製造ライン用洗浄剤組成物。 The detergent composition for food production lines according to claim 1, wherein the amount of sodium metasilicate pentahydrate is 150 parts by mass or more and 2000 parts by mass or less with respect to 100 parts by mass of dichloroisocyanurate. . 組成物の1質量%水溶液のpHが11以上である、請求項1に記載の食品製造ライン用洗浄剤組成物。 The detergent composition for food production lines according to claim 1, wherein the pH of the 1 mass% aqueous solution of the composition is 11 or more. 組成物中のジクロロイソシアヌル酸塩の配合量が、0.5〜40質量%である、請求項1に記載の食品製造ライン用洗浄剤組成物。 The cleaning composition for food production lines according to claim 1, wherein the blending amount of dichloroisocyanurate in the composition is 0.5 to 40% by mass.
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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5516014A (en) * 1978-07-19 1980-02-04 Asahi Denka Kogyo Kk Detergent removing hard surface filmy dirt
JPS56139406A (en) * 1980-04-02 1981-10-30 Uehara Kagaku:Kk Preparation of sterilizing detergent
JPS5964523A (en) * 1982-07-09 1984-04-12 ロ−ヌ−プ−ラン・シミ・ド・バ−ズ Novel sodium metasilicate granule, manufacture and use for dish washing detergent composition
JPS62104899A (en) * 1985-10-31 1987-05-15 日産化学工業株式会社 Sterilizing detergent
JPS6335697A (en) * 1986-07-24 1988-02-16 ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチェン Low fomable and/or foam control surfactant mixture and its use
JP2003027095A (en) * 2001-07-16 2003-01-29 Asahi Denka Kogyo Kk Powdered cartridge detergent composition for automatic dishwasher
JP2005023120A (en) * 2003-06-30 2005-01-27 Niitaka:Kk Cleanser composition for cleansing surface of plastic container

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5516014A (en) * 1978-07-19 1980-02-04 Asahi Denka Kogyo Kk Detergent removing hard surface filmy dirt
JPS56139406A (en) * 1980-04-02 1981-10-30 Uehara Kagaku:Kk Preparation of sterilizing detergent
JPS5964523A (en) * 1982-07-09 1984-04-12 ロ−ヌ−プ−ラン・シミ・ド・バ−ズ Novel sodium metasilicate granule, manufacture and use for dish washing detergent composition
JPS62104899A (en) * 1985-10-31 1987-05-15 日産化学工業株式会社 Sterilizing detergent
JPS6335697A (en) * 1986-07-24 1988-02-16 ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチェン Low fomable and/or foam control surfactant mixture and its use
JP2003027095A (en) * 2001-07-16 2003-01-29 Asahi Denka Kogyo Kk Powdered cartridge detergent composition for automatic dishwasher
JP2005023120A (en) * 2003-06-30 2005-01-27 Niitaka:Kk Cleanser composition for cleansing surface of plastic container

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