JP2018044077A - Cleaning bactericidal agent composition - Google Patents
Cleaning bactericidal agent composition Download PDFInfo
- Publication number
- JP2018044077A JP2018044077A JP2016180328A JP2016180328A JP2018044077A JP 2018044077 A JP2018044077 A JP 2018044077A JP 2016180328 A JP2016180328 A JP 2016180328A JP 2016180328 A JP2016180328 A JP 2016180328A JP 2018044077 A JP2018044077 A JP 2018044077A
- Authority
- JP
- Japan
- Prior art keywords
- cleaning
- weight
- nonionic surfactant
- test
- composition
- 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.)
- Granted
Links
Abstract
Description
本発明は、食品を取り扱う環境下での、食器および容器用自動洗浄機による洗浄除菌、および、製造装置、包装機、壁面、床面等の硬質表面の洗浄除菌に用いる洗浄除菌剤組成物に関する。 The present invention relates to a cleaning and disinfecting agent used for cleaning and disinfecting a table and container automatic cleaning machine in an environment where food is handled, and for cleaning and disinfecting hard surfaces such as manufacturing apparatuses, packaging machines, wall surfaces, and floor surfaces. Relates to the composition.
ホテルやレストラン、食品製造工場、食品加工工場、病院、飲食店、給食センター、事業所給食等、大量の食器やトレー、コンテナを洗浄する現場においては、自動洗浄機の普及が進んでいる。一般的に使用されている自動洗浄機は、加温した洗浄液をスプレーノズルやシャワーノズルから食器や容器等に向けて噴射し、汚れを除去するものが知られている。また、食品製造工場や加工工場での、製造装置や包装機などの洗浄では、配管やタンク等の取り外し洗浄が困難である場合、CIP(Cleaning in place)洗浄が行われている。CIP洗浄とは、装置等を分解することなく、そのままの状態で洗浄液を流通させてその内部を満たして循環させたり、さらには洗浄液をスプレーしたりして、汚れを洗浄・除去する洗浄方法であり、定置洗浄または定置循環洗浄とも呼ばれる。食品を取り扱う環境下でも自動洗浄機による洗浄、およびCIP洗浄においてはいずれも、洗浄液が発泡することでスプレー装置に空気が入り噴射圧が低下したり、洗浄槽や装置から泡が溢れ出したりしないよう、低発泡性の洗浄液を使用することが必要条件とされている。さらに該洗浄液は、低発泡性を維持しつつ十分な洗浄力を得るために、水酸化ナトリウムや水酸化カリウムなどの水酸化アルカリ金属塩を添加し、強アルカリ性に調節されているものがほとんどである。しかしながら、水酸化ナトリウムや水酸化カリウムを5%以上含む洗浄液は、「医薬用外劇物」となり、保管する上では専門的な知識や注意を要する他、洗浄液が飛散し皮膚や眼に接触する等、作業上の危険性があり、また、廃液の際に中和処理を必要とする等の取り扱い上の課題もある。さらに、強アルカリ性の洗浄剤は、ガラスやアルミを侵食したり、界面活性剤の不安定化を招く。従って、近年では、自動洗浄機による洗浄およびCIP洗浄においては、低発泡性に加え、弱アルカリ性の洗浄剤が求められている。 Automatic washing machines are becoming increasingly popular in places where large amounts of tableware, trays, and containers are washed, such as hotels, restaurants, food manufacturing factories, food processing factories, hospitals, restaurants, lunch centers, and establishments. As for the automatic washing machine generally used, what wash | cleans the washing | cleaning liquid from a spray nozzle or a shower nozzle toward a tableware, a container, etc., and removes dirt is known. In addition, when cleaning a manufacturing apparatus, a packaging machine, or the like in a food manufacturing factory or a processing factory is difficult, it is difficult to remove and clean pipes or tanks, and CIP (Cleaning in Place) cleaning is performed. CIP cleaning is a cleaning method that cleans and removes dirt by circulating the cleaning liquid as it is without disassembling the device and filling it, or spraying the cleaning liquid. Yes, also called stationary cleaning or stationary circulation cleaning. Even in food handling environments, in both automatic cleaning and CIP cleaning, the cleaning solution foams, so that air enters the spray device and the spray pressure does not drop, and bubbles do not overflow from the cleaning tank or device. Thus, it is considered necessary to use a low foaming cleaning liquid. Furthermore, in order to obtain a sufficient detergency while maintaining low foamability, most of the cleaning liquid is adjusted to strong alkalinity by adding an alkali metal hydroxide such as sodium hydroxide or potassium hydroxide. is there. However, a cleaning solution containing 5% or more of sodium hydroxide or potassium hydroxide is a “non-medicinal deleterious substance”, and requires specialized knowledge and caution when stored, and the cleaning solution scatters and comes into contact with the skin and eyes. There is also a problem in handling such as there is a danger in work and a neutralization treatment is required in the case of waste liquid. Furthermore, a strong alkaline cleaning agent erodes glass and aluminum, or causes destabilization of the surfactant. Therefore, in recent years, a weak alkaline cleaning agent is required in addition to low foaming properties in cleaning by an automatic cleaning machine and CIP cleaning.
一方、自動洗浄機およびCIP洗浄向けの洗浄液を弱アルカリ性にした場合、洗浄力が劣ることで洗浄機や装置にカビや雑菌が発生する等の問題がある。また、これらの洗浄には常温水や温水を使用する場合も多く、この場合は芽胞菌による汚染も懸念される。よって、自動洗浄機およびCIP洗浄向けの洗浄剤においては、殺菌効果があるものが望まれる。例えば、特許文献1では、カチオン系殺菌剤0.05〜20重量%、アルカリ剤1〜95重量%、非イオン界面活性剤から選ばれる1種類上の界面活性剤0.5〜30重量%を含有することを特徴とする非発泡性の硬質表面用固形殺菌洗浄剤組成物が提案されている。しかしながら、アルカリ剤の含有量が多いために、上記のような取扱い上の問題があるうえに、アルカリ性が強いことで、殺菌剤の効果に影響を及ぼしたり、殺菌剤や界面活性剤の組み合わせによっては、洗浄液が白濁してしまう可能性もある。 On the other hand, when the washing liquid for automatic washing machine and CIP washing is made weakly alkaline, there is a problem that mold and germs are generated in the washing machine and apparatus due to poor cleaning power. Moreover, room temperature water or warm water is often used for these washings, and in this case, contamination by spore bacteria is a concern. Therefore, what has a bactericidal effect is desired in the washing | cleaning agent for automatic washing machines and CIP washing | cleaning. For example, in Patent Document 1, 0.05 to 20% by weight of a cationic fungicide, 1 to 95% by weight of an alkali agent, and 0.5 to 30% by weight of a surfactant on one type selected from nonionic surfactants. A non-foaming solid sterilizing detergent composition for hard surfaces characterized by containing is proposed. However, since the content of the alkaline agent is large, there are problems in handling as described above, and the strong alkalinity affects the effect of the bactericidal agent. May cause the cleaning liquid to become cloudy.
また、特許文献2には、アルカリ金属水酸化物を1.2〜9.8質量%、次亜塩素酸アルカリ金属塩を有効塩素量として1〜10質量%、腐食防止剤として、有機ホスホン酸、ポリカルボン酸型ポリマー、スルホン酸型ポリマー及びこれらの塩より選ばれた少なくとも一種以上を1〜7.5質量%、及び水を含有する洗浄剤組成物を、使用時に、洗浄液の25℃でのpHが9.1〜10.9になるように水又は湯で希釈して自動食器洗浄機の洗浄液として用いることを特徴とする食器類の洗浄方法が提案されている。しかしながら、次亜塩素酸アルカリ金属塩は分解しやすく保管安定性に問題があり、また、金属と反応しやすいため洗浄に水道水を使用できなかったり、金属製の装置に悪影響を及ぼす懸念がある。 Patent Document 2 discloses that 1.2 to 9.8% by mass of an alkali metal hydroxide, 1 to 10% by mass of an alkali metal hypochlorite as an effective chlorine content, and an organic phosphonic acid as a corrosion inhibitor. At least one selected from polycarboxylic acid type polymers, sulfonic acid type polymers and salts thereof, 1 to 7.5% by mass, and a cleaning composition containing water at the time of use at 25 ° C. of the cleaning liquid A dishwashing method has been proposed, which is diluted with water or hot water so as to have a pH of 9.1 to 10.9 and used as a washing liquid of an automatic dishwashing machine. However, alkali metal hypochlorite is easy to decompose and has a problem in storage stability, and since it easily reacts with metals, there is a concern that tap water cannot be used for washing or that metal equipment is adversely affected. .
本発明の目的は、自動洗浄機の使用やCIP洗浄に際し、優れた洗浄力と殺菌力を発揮し、保管中に分離や白濁を生じることない保管安定性に優れた、低発泡性の洗浄除菌剤組成物を提供することにある。 The object of the present invention is to provide an excellent washing power and sterilizing power when using an automatic washing machine or CIP washing, and it has excellent storage stability without separation or clouding during storage, and has a low foaming washing and removal. The object is to provide a fungus composition.
本発明者らは、上記課題を解決するために鋭意検討した結果、ポリヘキサメチレンビグアナイド塩酸塩と特定の非イオン界面活性剤を有効成分とし、組成物における非イオン界面活性剤の含有量が、ポリヘキサメチレンビグアナイド塩酸塩1重量部に対し1.2〜2.5重量部であり、組成物の原液pHが8〜11である洗浄除菌剤組成物が、低発泡性でありながら、優れた洗浄力と殺菌力を発揮し、かつ保管中に分離や白濁を生じることなく保管安定性に優れることを見出し、本発明を完成するに至った。 As a result of intensive studies to solve the above problems, the present inventors have polyhexamethylene biguanide hydrochloride and a specific nonionic surfactant as active ingredients, and the content of the nonionic surfactant in the composition is The cleaning disinfectant composition having 1.2 to 2.5 parts by weight with respect to 1 part by weight of polyhexamethylene biguanide hydrochloride and having a stock solution pH of 8 to 11 is excellent in spite of its low foaming property. The present inventors have found that the present invention has been completed by exhibiting excellent washing stability and sterilizing power and excellent storage stability without causing separation or cloudiness during storage.
すなわち本発明は、ポリヘキサメチレンビグアナイド塩酸塩と式(1)で表される非イオン界面活性剤を有効成分とする洗浄除菌剤組成物であって、組成物における非イオン界面活性剤の含有量が、ポリヘキサメチレンビグアナイド塩酸塩1重量部に対し1.2〜2.5重量部であり、組成物の原液pHが8〜11である洗浄除菌剤組成物を提供する:
ポリヘキサメチレンビグアナイドは、ビグアナイド基とヘキサメチレン基が交互に多数連結したカチオン系界面活性剤であり、ポリヘキサメチレンビグアナイド塩酸塩(以下「PHMB」とも称する)とは、その塩酸塩であり、優れた抗菌効果を有する。本発明の洗浄除菌剤組成物に用いるポリヘキサメチレンビグアナイド塩酸塩は、公知の方法によって製造できる他、市販の製剤を使用してもよい。その市販品としては、例えば、Vantocil IB(登録商標)(発売元:株式会社ウエノフードテクノ)、BG−1(三洋化成工業株式会社製)などが挙げられる。本発明の洗浄除菌剤組成物におけるポリヘキサメチレンビグアナイド塩酸塩の割合は、0.1〜10重量%であることが好ましく、0.5〜8重量%であることがより好ましく、1〜5重量%であることがさらに好ましい。 Polyhexamethylene biguanide is a cationic surfactant in which a large number of biguanide groups and hexamethylene groups are alternately connected, and polyhexamethylene biguanide hydrochloride (hereinafter also referred to as “PHMB”) is its hydrochloride and is excellent. Has antibacterial effect. The polyhexamethylene biguanide hydrochloride used in the cleaning disinfectant composition of the present invention can be produced by a known method, or a commercially available formulation may be used. Examples of the commercially available products include Vantocil IB (registered trademark) (release source: Ueno Food Techno Co., Ltd.), BG-1 (manufactured by Sanyo Chemical Industries, Ltd.), and the like. The proportion of polyhexamethylene biguanide hydrochloride in the cleaning disinfectant composition of the present invention is preferably 0.1 to 10% by weight, more preferably 0.5 to 8% by weight, and 1 to 5%. More preferably, it is% by weight.
本発明の洗浄除菌剤組成物に用いる非イオン界面活性剤は、上記式(1)で表され、Rが炭素数8〜16の直鎖または分岐状の炭化水素基であり、エチレンオキサイドの平均付加モル数lが2〜10であり、プロピレンオキサイドの平均付加モル数mが2〜10であり、かつlとmの和l+mが5〜12である非イオン界面活性剤である。ここで、平均付加モル数とは、式(1)で表される非イオン界面活性剤1モルに付加されたエチレンオキシド、またはプロピレンオキシドのモル数の平均値を意味する。本発明の洗浄除菌剤組成物における、該界面活性剤の含有量は、ポリヘキサメチレンビグアナイド塩酸塩1重量部に対し、1.2〜2.5重量部であることが好ましく、1.5〜2.0重量部含であることがより好ましい。 The nonionic surfactant used in the cleaning disinfectant composition of the present invention is represented by the above formula (1), R is a linear or branched hydrocarbon group having 8 to 16 carbon atoms, ethylene oxide It is a nonionic surfactant having an average addition mole number 1 of 2 to 10, an average addition mole number m of propylene oxide of 2 to 10, and a sum 1 + m of l and m of 5 to 12. Here, the average added mole number means an average value of the number of moles of ethylene oxide or propylene oxide added to 1 mole of the nonionic surfactant represented by the formula (1). In the cleaning disinfectant composition of the present invention, the content of the surfactant is preferably 1.2 to 2.5 parts by weight with respect to 1 part by weight of polyhexamethylene biguanide hydrochloride, It is more preferable that the content is -2.0 parts by weight.
さらに、本発明の洗浄除菌剤組成物は、洗浄力や殺菌力、低発泡性のさらなる向上を目的に、式(1)においてRが炭素数8〜16の直鎖または分岐状の、好ましくは分岐状の炭化水素基であり、エチレンオキサイドの平均付加モル数lが2〜10であり、プロピレンオキサイドの平均付加モル数mが2〜10であり、かつlとmの和l+mが13〜20である非イオン界面活性剤を含むことができる。本発明の洗浄除菌剤組成物における、該非イオン界面活性剤の含有量は、式(1)においてRが炭素数8〜16の直鎖または分岐状の、好ましくは分岐状の炭化水素基であり、エチレンオキサイドの平均付加モル数lが2〜10であり、プロピレンオキサイドの平均付加モル数mが2〜10であり、かつlとmの和l+mが5〜12である非イオン界面活性剤1重量部に対し、0.1〜0.9重量部であることが好ましく、0.2〜0.8重量部であることがより好ましい。 Furthermore, the cleaning disinfectant composition of the present invention is preferably a linear or branched R having 8 to 16 carbon atoms in the formula (1) for the purpose of further improving detergency, bactericidal activity and low foamability. Is a branched hydrocarbon group, the average addition mole number 1 of ethylene oxide is 2 to 10, the average addition mole number m of propylene oxide is 2 to 10, and the sum of l and m l + m is 13 to A nonionic surfactant that is 20 can be included. In the cleaning disinfectant composition of the present invention, the content of the nonionic surfactant is a linear or branched, preferably branched hydrocarbon group having 8 to 16 carbon atoms in the formula (1). A nonionic surfactant having an average addition mole number l of ethylene oxide of 2 to 10, an average addition mole number m of propylene oxide of 2 to 10 and a sum of l and m, i + m of 5 to 12 The amount is preferably 0.1 to 0.9 part by weight, more preferably 0.2 to 0.8 part by weight with respect to 1 part by weight.
なお、式(1)において、(EO)l(PO)mの重合様式は、ブロック重合、ランダム重合、交互重合のいずれの様式であってもよく、これらの重合様式が混合されていてもよい。このような非イオン界面活性剤の具体例としては、ポリオキシエチレンポリオキシプロピレンラウリルエーテル、ポリオキシエチレンポリオキシプロピレンミリスチルエーテル、ポリオキシエチレンポリオキシプロピレンセチルエーテル、ポリオキシエチレンポリオキシプロピレンデシルエーテル、ポリオキシエチレンポリオキシプロピレンオクチルエーテル、ポリオキシエチレンポリオキシプロピレンイソドデシルエーテル、ポリオキシエチレンポリオキシプロピレンイソテトラデシルエーテル、ポリオキシエチレンポリオキシプロピレンイソセチルエーテル、ポリオキシエチレンポリオキシプロピレンイソデシルエーテル、ポリオキシエチレンポリオキシプロピレンイソオクチルエーテル、ポリオキシエチレンポリオキシプロピレン−2−エチルヘキシルエーテルが挙げられるが、中でもポリオキシエチレンポリオキシプロピレンイソデシルエーテルを用いるのが好ましい。ポリオキシエチレンポリオキシプロピレンイソデシルエーテルを用いる場合、一つの態様として、本発明の洗浄除菌剤組成物は、エチレンオキサイドの平均付加モル数lが8であり、プロピレンオキサイドの平均付加モル数mが2であるポリオキシエチレンポリオキシプロピレンイソデシルエーテルと、エチレンオキサイドの平均付加モル数lが8であり、プロピレンオキサイドの平均付加モル数mが9であるポリオキシエチレンポリオキシプロピレンイソデシルエーテルを含む。 In the formula (1), the polymerization mode of (EO) 1 (PO) m may be any of block polymerization, random polymerization, and alternating polymerization, and these polymerization modes may be mixed. . Specific examples of such nonionic surfactants include polyoxyethylene polyoxypropylene lauryl ether, polyoxyethylene polyoxypropylene myristyl ether, polyoxyethylene polyoxypropylene cetyl ether, polyoxyethylene polyoxypropylene decyl ether, Polyoxyethylene polyoxypropylene octyl ether, polyoxyethylene polyoxypropylene isododecyl ether, polyoxyethylene polyoxypropylene isotetradecyl ether, polyoxyethylene polyoxypropylene isocetyl ether, polyoxyethylene polyoxypropylene isodecyl ether, Polyoxyethylene polyoxypropylene isooctyl ether, polyoxyethylene polyoxypropylene-2 Although ethylhexyl ether, preferably used among them polyoxyethylene polyoxypropylene isodecyl ether. When polyoxyethylene polyoxypropylene isodecyl ether is used, as one embodiment, the cleaning disinfectant composition of the present invention has an average added mole number 1 of ethylene oxide of 8 and an average added mole number of propylene oxide m. A polyoxyethylene polyoxypropylene isodecyl ether having an average addition mole number of ethylene oxide of 8 and an average addition mole number of propylene oxide of 9 is 9 Including.
本発明の洗浄除菌剤組成物は、液体製剤として提供され、限定するものではないが水溶液の形態で提供される。本発明の殺菌洗浄剤組成物の調製方法は、特に限定されず、例えば、本発明に係る有効成分と他の成分とを水に溶解させることによって調製することができる。上記水溶液の形態の液体製剤の調製に用いられる水は、脱イオン水、蒸留水、ろ過水などの精製水;地下水、伏流水などの天然水;または水道水であってよく、塩素や金属イオンの含有量が少ないことから精製水が好ましい。 The cleaning disinfectant composition of the present invention is provided as a liquid preparation, and is provided in the form of an aqueous solution, although not limited thereto. The method for preparing the sterilizing detergent composition of the present invention is not particularly limited, and for example, it can be prepared by dissolving the active ingredient according to the present invention and other ingredients in water. The water used for the preparation of the liquid preparation in the form of the above aqueous solution may be purified water such as deionized water, distilled water or filtered water; natural water such as ground water or underground water; or tap water, and chlorine or metal ions. Purified water is preferred because of its low content.
本発明の洗浄除菌剤組成物は、原液のpHが8〜11に調整されたものであり、8.5〜10.5であることが好ましく、9.0〜10.0であることがより好ましく、9.3〜9.7であることがさらに好ましい。本発明の洗浄除菌剤組成物の原液のpHが11よりも高い場合には、組成物の保管安定性が悪くなり、また、泡立ち易くなる傾向がある。さらに、アルカリ性が強いために、作業に危険を伴ったり、取扱いが煩雑になる。本発明の洗浄除菌剤組成物の原液のpHが8よりも低い場合には、組成物を希釈して使用する際にpHが低くなり洗浄力が劣る傾向がある。なお、pHの調整には、水酸化ナトリウム、水酸化カリウムなどの水酸化アルカリ金属塩をアルカリ剤として用いることができる。pH調整を行う段階は、特に限定されず、例えば、調製された水溶液の形態の組成物にアルカリ剤を添加して、pH調整してもよい。 In the cleaning disinfectant composition of the present invention, the pH of the stock solution is adjusted to 8 to 11, preferably 8.5 to 10.5, and preferably 9.0 to 10.0. More preferably, it is more preferably 9.3 to 9.7. When the pH of the stock solution of the cleaning disinfectant composition of the present invention is higher than 11, the storage stability of the composition tends to deteriorate and foaming tends to occur. Further, since the alkalinity is strong, the work is dangerous and handling is complicated. When the pH of the stock solution of the cleaning disinfectant composition of the present invention is lower than 8, when the composition is diluted for use, the pH tends to be low and the cleaning power tends to be poor. For adjusting the pH, an alkali metal hydroxide such as sodium hydroxide or potassium hydroxide can be used as an alkali agent. The step of adjusting the pH is not particularly limited. For example, the pH may be adjusted by adding an alkali agent to the prepared composition in the form of an aqueous solution.
本発明の洗浄除菌剤組成物は、水溶液の形態で提供される場合、水で希釈した希釈液を使用することができる。希釈の濃度は、用途により適宜調整されるが、一つの態様として、0.1〜2.0重量%、好ましくは0.5〜1.0重量%を目安に希釈される。本発明の洗浄除菌剤組成物の希釈後のpHは、中性域または弱アルカリ性域であることが、廃液処理が煩雑にならず好ましい。 When the cleaning disinfectant composition of the present invention is provided in the form of an aqueous solution, a diluted solution diluted with water can be used. The concentration of dilution is appropriately adjusted depending on the application. In one embodiment, the dilution is 0.1 to 2.0% by weight, preferably 0.5 to 1.0% by weight. It is preferable that the pH after dilution of the cleaning disinfectant composition of the present invention is in a neutral range or a weak alkaline range because the waste liquid treatment is not complicated.
また、本発明の洗浄除菌剤組成物は、本発明の効果を阻害しない範囲内で、所望により、香料、染料、消臭剤、金属腐食抑制剤などの任意成分を、適宜の割合で含むことができる。 Moreover, the cleaning disinfectant composition of the present invention contains optional components such as a fragrance, a dye, a deodorant, and a metal corrosion inhibitor in an appropriate ratio as desired within a range not inhibiting the effects of the present invention. be able to.
本発明の洗浄除菌剤組成物は、ガラス、セラミック、金属、プラスチックなどの材質からなる硬質表面の洗浄に適しており、食器用に留まらず、各種製造工場や加工工場における器具や容器、コンテナ等を洗浄するための自動洗浄機に使用可能である。また、各種製造装置、加工装置、包装機などのCIP洗浄の他、各種製造工場、加工工場、調理場等の作業台、タイル、床、壁等の洗浄にも好適に用いることができる。
[試験例]
The cleaning disinfectant composition of the present invention is suitable for cleaning hard surfaces made of materials such as glass, ceramic, metal, plastic, etc., and is not limited to tableware, but is used in instruments, containers, and containers in various manufacturing factories and processing factories. It can be used for an automatic washing machine for washing etc. Further, in addition to CIP cleaning of various manufacturing apparatuses, processing apparatuses, packaging machines, etc., it can be suitably used for cleaning various manufacturing factories, processing factories, work tables such as kitchens, tiles, floors, walls, and the like.
[Test example]
試験例1〜14
まず、表1に示す非イオン界面活性剤の泡立ちと、ポリヘキサメチレンビグアナイド塩酸塩と混合した時の相溶性を、下記に示す方法で評価した。
Test Examples 1-14
First, the foaming of the nonionic surfactant shown in Table 1 and the compatibility when mixed with polyhexamethylene biguanide hydrochloride were evaluated by the methods shown below.
泡立ち試験
表1に示す各種非イオン界面活性剤を水道水で0.01重量%に希釈し、Φ28mm×250mmの試験管に泡が立たないよう注ぎ込み、栓をした。液が入った試験管を上下に30回激しく振とうし、振とう直後と5分後の泡の高さを測定した。5分後の泡の高さが振とう直後の泡の高さの4分の1以上である場合を×(不可)、4分の1未満である場合を○(可)として評価した。結果を表2に示す。
Foaming test Various nonionic surfactants shown in Table 1 were diluted with tap water to 0.01% by weight, poured into a test tube of Φ28 mm × 250 mm so as not to cause foaming, and capped. The test tube containing the liquid was vigorously shaken up and down 30 times, and the height of the foam was measured immediately after shaking and after 5 minutes. The case where the height of the foam after 5 minutes was ¼ or more of the height of the foam immediately after shaking was evaluated as x (impossible), and the case where it was less than ¼ (good). The results are shown in Table 2.
相溶性試験
ポリヘキサメチレンビグアナイド塩酸塩(Vantocil IB、発売元:株式会社ウエノフードテクノ)3重量%と各種非イオン界面活性剤10重量%含む試験液を作成し、白濁、分離あるいは沈殿が発生する場合を×(不可)、発生しない場合を○(可)とした。結果を表2に示す。
Compatibility test Polyhexamethylene biguanide hydrochloride (Vantocil IB, Publisher: Uenofood Techno Co., Ltd.) 3% by weight and 10% by weight of various nonionic surfactants are made, and cloudiness, separation or precipitation occurs. Cases were marked with x (impossible), and cases not occurring were marked with ◯ (possible). The results are shown in Table 2.
試験例15〜19
試験例1〜14において、泡立ち評価とポリヘキサメチレンビグアナイド塩酸塩との相溶性が良好であった界面活性剤について、表3に示す製剤を作成し、泡立ちおよび洗浄力の評価を行った。
Test Examples 15-19
In Test Examples 1 to 14, preparations shown in Table 3 were prepared for surfactants having good foaming evaluation and compatibility with polyhexamethylene biguanide hydrochloride, and foaming and detergency were evaluated.
泡立ち試験
表3に記載の製剤を作成し、水道水で1.0重量%に希釈したものを試験液とした。試験液をΦ28mm×250mmの試験管に泡が立たないよう注ぎ込んで栓をし、試験管を上下に30回激しく振とうし、振とう直後、1分後、3分後の泡の高さを測定した。評価は、以下に示す起泡性または消泡性いずれかの基準に該当する場合を×(不可)、いずれにも該当しない場合を○(可)とした。
<評価基準>
起泡性・・・振とう直後に泡の高さが84mm以上ある
消泡性・・・振とう3分後に振とう直後からの泡の残存率が12%以上且つ泡の高さが
6mmを超える
Foaming test Formulations described in Table 3 were prepared and diluted to 1.0% by weight with tap water to obtain a test solution. Pour the test solution into a Φ28mm x 250mm test tube so that no bubbles are formed, cap it, and shake the test tube up and down 30 times. Immediately after shaking, the height of the foam after 1 minute and 3 minutes It was measured. In the evaluation, a case corresponding to one of the following foaming properties or antifoaming properties was evaluated as x (impossible), and a case not corresponding to any of the criteria was evaluated as ◯ (possible).
<Evaluation criteria>
Foaming property: The height of the foam is 84 mm or more immediately after shaking. Defoaming property: The residual rate of the foam immediately after shaking after 3 minutes of shaking is 12% or more and the height of the foam is
Over 6mm
洗浄力試験
リーナッツ試験法(JIS K3362)に記載のリーナッツ試験機を用いて試験を行った。スライドグラスに常温の牛乳を付着させ、80℃のオーブンで40分間乾燥させ、放冷した後、付着量を量り、これを4枚1組としてモデル汚れガラス片とした。表3に記載の製剤を水道水で0.5重量%に希釈し、60±1℃に加温した試験液700ml中に、支持板にセットしたモデル汚れガラス片を入れ、洗浄力試験機を用い、回転速度250±10rpmで3分間洗浄した。洗浄後、80±1℃の水道水700ml中に入れて、洗浄力試験機を用いて1分間すすいだ。すすぎが完了したモデル汚れガラス片を室温で一昼夜乾燥後、重量を量り、以下の式(A)で洗浄力を算出した。なお、本試験においては、弱アルカリ性低発泡性洗浄剤のクリアロンL(花王株式会社製)を基準品とし、基準品の洗浄力を1とした場合の試験液の洗浄力が0.96以下の場合を×(不可)、0.96を超える場合を○(可)と評価した。
Detergency test A test was conducted using a peanut tester described in the peanut test method (JIS K3362). Room temperature milk was attached to a slide glass, dried in an oven at 80 ° C. for 40 minutes, allowed to cool, and then the amount of attachment was measured. Dilute the formulation shown in Table 3 to 0.5% by weight with tap water and put it in 700 ml of test solution heated to 60 ± 1 ° C. Used and washed at a rotational speed of 250 ± 10 rpm for 3 minutes. After washing, it was put into 700 ml of 80 ± 1 ° C. tap water and rinsed for 1 minute using a detergency tester. After rinsing, the model soiled glass piece was dried at room temperature for a whole day and night, then weighed, and the detergency was calculated by the following formula (A). In this test, the weak alkaline low foaming detergent Clearon L (manufactured by Kao Corporation) is used as a reference product, and the cleaning power of the test solution is 0.96 or less when the reference product has a cleaning power of 1. The case was evaluated as x (impossible), and the case exceeding 0.96 was evaluated as ◯ (possible).
界面活性剤12を使用した製剤3は泡立ちが抑えられ、かつ十分な洗浄力を発揮した。一方、他の界面活性剤を使用した製剤は、泡立ちの抑制が不十分であるか、あるいは洗浄力が不十分であった。結果を表4に示す。 Formulation 3 using Surfactant 12 suppressed foaming and exhibited sufficient detergency. On the other hand, preparations using other surfactants have insufficient suppression of foaming or insufficient detergency. The results are shown in Table 4.
以下、実施例により本発明を詳細に説明するが、本発明は、これらの実施例に何ら限定されるものではない。 EXAMPLES Hereinafter, although an Example demonstrates this invention in detail, this invention is not limited to these Examples at all.
実施例1〜2および比較例1〜5
試験例で評価が良好であった界面活性剤12を用いて製剤を作成し、下記の方法で、相溶性試験、泡立ち試験、および洗浄力試験を実施した。なお、製剤の消泡性について更なる改良を目的に、消泡性評価が良好であった界面活性剤14を併用する場合についても検討した。作成した製剤の処方は表5の通りである。
Examples 1-2 and Comparative Examples 1-5
A preparation was prepared using the surfactant 12 that was evaluated well in the test examples, and a compatibility test, a foaming test, and a detergency test were performed by the following methods. For the purpose of further improving the antifoaming property of the preparation, the case of using the surfactant 14 having a good antifoaming property evaluation was also examined. The formulation of the prepared preparation is as shown in Table 5.
相溶性試験
表5に記載の製剤を作成し、水道水で使用想定濃度である0.5重量%および1.0重量%に希釈したものを試験液とした。原液および試験液において、白濁、分離あるいは沈殿が見られた場合を×(不可)、見られない場合を○(可)として評価した。
Compatibility test The preparations shown in Table 5 were prepared, and diluted with tap water to 0.5% by weight and 1.0% by weight, which were assumed to be used, were used as test solutions. In the undiluted solution and the test solution, the case where white turbidity, separation or precipitation was observed was evaluated as x (impossible), and the case where it was not observed was evaluated as o (possible).
泡立ち試験
表5に記載の製剤を作成し、水道水で使用想定濃度である0.5重量%および1.0重量%に希釈したものを試験液とし、Φ28mm×250mmの試験管に泡が立たないよう注ぎ込み、栓をした。試験液が入った試験管を上下に30回激しく振とうし、振とう直後、1分後、3分後の泡の高さを測定した。評価は、以下の基準に該当する場合を×(不可)、該当しない場合を○(可)とした。
<評価基準(0.5重量%試験液)>
起泡性・・・振とう直後に泡の高さが70mm以上ある
消泡性・・・振とう3分後に振とう直後からの泡の残存率が10%以上且つ泡の高さが
5mmを超える
<評価基準(1.0重量%試験液)>
起泡性・・・振とう直後に泡の高さが84mm以上ある
消泡性・・・振とう3分後に振とう直後からの泡の残存率が12%以上且つ泡の高さが
6mmを超える
Foaming test Preparations described in Table 5 were prepared, diluted with tap water to 0.5% by weight and 1.0% by weight, which were assumed to be used, as test solutions, and bubbles were formed in a test tube of Φ28 mm × 250 mm. Poured and plugged. The test tube containing the test solution was vigorously shaken up and down 30 times, and immediately after shaking, the height of the foam was measured after 1 minute and 3 minutes. In the evaluation, a case where the following criteria were met was evaluated as x (impossible), and a case where the criteria were not met was evaluated as ◯ (possible).
<Evaluation criteria (0.5 wt% test solution)>
Foaming property: The height of the foam is 70 mm or more immediately after shaking. Defoaming property: The residual ratio of the foam immediately after shaking after 3 minutes of shaking is 10% or more and the height of the foam is
Over 5mm
<Evaluation criteria (1.0 wt% test solution)>
Foaming property: The height of the foam is 84 mm or more immediately after shaking. Defoaming property: The residual rate of the foam immediately after shaking after 3 minutes of shaking is 12% or more and the height of the foam is
Over 6mm
洗浄力試験
表5の通り製剤を作成した他は、上記試験例で実施した方法と同様の方法で洗浄力を求め、評価した。
Detergency test The detergency was determined and evaluated in the same manner as in the above test example, except that the preparation was prepared as shown in Table 5.
試験例でも示した通り、実施例1(製剤3)は、ポリヘキサメチレンビグアナイド塩酸塩との相溶性に問題なく、泡立ちも抑えられ、かつ十分な洗浄力を発揮した。また、実施例2(製剤6)においては、相溶性と洗浄力の品質を維持しつつ、消泡性がさらに抑えられた。結果を表6に示す。 As shown in the test examples, Example 1 (Formulation 3) exhibited no problem with compatibility with polyhexamethylene biguanide hydrochloride, suppressed foaming, and exhibited sufficient detergency. Moreover, in Example 2 (formulation 6), the antifoaming property was further suppressed while maintaining the compatibility and the quality of detergency. The results are shown in Table 6.
実施例3〜6および比較例6〜7
実施例2の製剤処方をもとに、表7の通りpHを7〜12に調整した製剤を作成し、泡立ち試験、洗浄力試験、および殺菌力試験を実施した。
Examples 3-6 and Comparative Examples 6-7
Based on the formulation of Example 2, a formulation having a pH adjusted to 7 to 12 as shown in Table 7 was prepared, and a foaming test, a detergency test, and a bactericidal test were performed.
泡立ち試験
表7の通り製剤を作成し、水道水で0.5重量%に希釈した他は、上記実施例に記載の方法と同様の方法で泡立ち試験を実施した。
Foaming test A foaming test was carried out in the same manner as described in the above examples except that the preparation was prepared as shown in Table 7 and diluted to 0.5% by weight with tap water.
洗浄力試験
表7の通り製剤を作成したほかは、上記試験例に記載の方法と同様の方法で洗浄力試験を実施した。
Detergency test A detergency test was performed in the same manner as described in the above test example except that the preparation was prepared as shown in Table 7.
殺菌力試験
殺菌力試験は、石炭酸係数法に準じた方法で行った。まず表7に示す製剤を作成し、脱イオン水で0.5重量%に希釈し、10mlずつ試験管に分注した。これにウマ血清(GIBCO社製)500μlと生理食塩水で下記供試菌を約106cfu/mlに調製した菌液100μlを接種し、供試液とした。菌接種後1分後の供試液10μlを白金耳でブレインハートインフュージョン培地(日水製薬株式会社製)に植え、48時間後の菌の生育を確認し、菌の生育が確認されなかった場合を○(可)、菌の生育が確認された場合を×(不可)として評価した。
供試菌
E.coli NIHJ−JC2
B.cereus IAM1029 芽胞液
Bactericidal power test The bactericidal power test was performed by the method according to the carboxylic acid coefficient method. First, preparations shown in Table 7 were prepared, diluted to 0.5% by weight with deionized water, and dispensed in 10 ml aliquots. This was inoculated with 500 μl of horse serum (GIBCO) and 100 μl of a bacterial solution prepared with about 10 6 cfu / ml of the following test bacteria with physiological saline, and used as a test solution. When 10 μl of the test solution 1 minute after the inoculation is planted in a brain heart infusion medium (manufactured by Nissui Pharmaceutical Co., Ltd.) with a platinum ear The case where the growth of bacteria was confirmed was evaluated as x (impossible).
Test bacteria E. coli NIHJ-JC2
B. cereus IAM1029 Spore fluid
原液pH8〜11の製剤(製剤3および製剤11〜16)は、泡立ちが抑制され、かつ十分な洗浄力と殺菌力を有することが示された。一方、原液pH7.0の製剤(製剤15)は洗浄力が不十分であり、原液pH12の製剤(製剤16)は起泡性の抑制が不十分な傾向であった。結果を表8に示す。 It was shown that the preparations (preparation 3 and preparations 11 to 16) having the stock solution pH 8 to 11 were suppressed in foaming and had sufficient cleaning power and bactericidal power. On the other hand, the undiluted solution pH 7.0 formulation (formulation 15) had insufficient detergency, and the undiluted solution pH 12 formulation (formulation 16) tended to have insufficient foaming suppression. The results are shown in Table 8.
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2016180328A JP6933354B2 (en) | 2016-09-15 | 2016-09-15 | Cleaning disinfectant composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2016180328A JP6933354B2 (en) | 2016-09-15 | 2016-09-15 | Cleaning disinfectant composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2018044077A true JP2018044077A (en) | 2018-03-22 |
JP6933354B2 JP6933354B2 (en) | 2021-09-08 |
Family
ID=61692894
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2016180328A Active JP6933354B2 (en) | 2016-09-15 | 2016-09-15 | Cleaning disinfectant composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP6933354B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2019199554A (en) * | 2018-05-17 | 2019-11-21 | 株式会社ウエノフードテクノ | Cleaning bactericidal agent composition |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001521574A (en) * | 1997-04-24 | 2001-11-06 | ヘンケル−エコラープ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング・ウント・コンパニー・オッフェネ・ハンデルスゲゼルシャフト | Liquid enzyme preparation and its use |
JP2003531247A (en) * | 2000-04-14 | 2003-10-21 | ザ、プロクター、エンド、ギャンブル、カンパニー | Method for cleaning and / or disinfecting hard surfaces with a composition comprising a biguanide antibacterial agent |
JP2006160822A (en) * | 2004-12-03 | 2006-06-22 | Kao Corp | Liquid detergent for clothes |
JP2008184500A (en) * | 2007-01-29 | 2008-08-14 | Kao Corp | Liquid cleanser composition for automatic dish washer |
JP2011208062A (en) * | 2010-03-30 | 2011-10-20 | Kobayashi Pharmaceutical Co Ltd | Lavatory cleaning composition |
JP2011208063A (en) * | 2010-03-30 | 2011-10-20 | Kobayashi Pharmaceutical Co Ltd | Lavatory cleaning composition |
JP2014227442A (en) * | 2013-05-20 | 2014-12-08 | ライオン株式会社 | Detergent for dishwasher |
JP2016011385A (en) * | 2014-06-30 | 2016-01-21 | ライオンハイジーン株式会社 | Detergent composition for pre-dipping |
-
2016
- 2016-09-15 JP JP2016180328A patent/JP6933354B2/en active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001521574A (en) * | 1997-04-24 | 2001-11-06 | ヘンケル−エコラープ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング・ウント・コンパニー・オッフェネ・ハンデルスゲゼルシャフト | Liquid enzyme preparation and its use |
JP2003531247A (en) * | 2000-04-14 | 2003-10-21 | ザ、プロクター、エンド、ギャンブル、カンパニー | Method for cleaning and / or disinfecting hard surfaces with a composition comprising a biguanide antibacterial agent |
JP2006160822A (en) * | 2004-12-03 | 2006-06-22 | Kao Corp | Liquid detergent for clothes |
JP2008184500A (en) * | 2007-01-29 | 2008-08-14 | Kao Corp | Liquid cleanser composition for automatic dish washer |
JP2011208062A (en) * | 2010-03-30 | 2011-10-20 | Kobayashi Pharmaceutical Co Ltd | Lavatory cleaning composition |
JP2011208063A (en) * | 2010-03-30 | 2011-10-20 | Kobayashi Pharmaceutical Co Ltd | Lavatory cleaning composition |
JP2014227442A (en) * | 2013-05-20 | 2014-12-08 | ライオン株式会社 | Detergent for dishwasher |
JP2016011385A (en) * | 2014-06-30 | 2016-01-21 | ライオンハイジーン株式会社 | Detergent composition for pre-dipping |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2019199554A (en) * | 2018-05-17 | 2019-11-21 | 株式会社ウエノフードテクノ | Cleaning bactericidal agent composition |
JP7046363B2 (en) | 2018-05-17 | 2022-04-04 | 株式会社ウエノフードテクノ | Cleaning disinfectant composition |
Also Published As
Publication number | Publication date |
---|---|
JP6933354B2 (en) | 2021-09-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US10091988B2 (en) | Wetting agents for aseptic filling | |
JP7223791B2 (en) | Interactions between antimicrobial quaternary compounds and anionic surfactants | |
JP3566454B2 (en) | Product disinfection and bleaching methods and compositions used therefor | |
EP0756620B1 (en) | Peroxyacetic acid rinse method | |
EP1373455B1 (en) | Methods and compositions for cleaning, rinsing, and antimicrobial treatment of medical equipment | |
JP5198769B2 (en) | Antimicrobial composition comprising a carboxylic acid and an alkoxylated amine | |
JP4098357B2 (en) | Rinsing method with sanitary treatment | |
JP5937410B2 (en) | Cleaning composition for hard surface | |
JPH10330792A (en) | Bactericidal detergent composition and its use | |
CN117050817A (en) | Antimicrobial multipurpose cleaners and methods of making and using the same | |
JP4260249B2 (en) | Aqueous liquid cleaning agent | |
JP5784965B2 (en) | Disinfectant cleaning composition and disinfectant cleaning method | |
JP6933354B2 (en) | Cleaning disinfectant composition | |
JP2011246677A (en) | Cleaning-sterilizing agent composition | |
JP3607606B2 (en) | Sterilization method | |
JP7046363B2 (en) | Cleaning disinfectant composition | |
JP5784963B2 (en) | Disinfectant cleaning composition and disinfectant cleaning method | |
JP2019202976A (en) | Cleaning bactericidal agent composition | |
JP4468010B2 (en) | Disinfectant cleaning composition | |
JP4351768B2 (en) | Sterilizer lubricant for conveyor | |
WO2012148004A1 (en) | Bactericide composition and bactericidal cleaning composition | |
JP5188950B2 (en) | Hard surface cleaning and sterilization method | |
WO2012148005A1 (en) | Bactericide composition and bactericidal cleaning composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20190801 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20200605 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20200707 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20200904 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20210309 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20210416 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20210803 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20210812 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6933354 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |