JP2011012051A - Fumigation agent composition, fumigation equipment and fumigation method - Google Patents

Fumigation agent composition, fumigation equipment and fumigation method Download PDF

Info

Publication number
JP2011012051A
JP2011012051A JP2010115502A JP2010115502A JP2011012051A JP 2011012051 A JP2011012051 A JP 2011012051A JP 2010115502 A JP2010115502 A JP 2010115502A JP 2010115502 A JP2010115502 A JP 2010115502A JP 2011012051 A JP2011012051 A JP 2011012051A
Authority
JP
Japan
Prior art keywords
smoke
fumigation
agent
component
effect
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
Application number
JP2010115502A
Other languages
Japanese (ja)
Other versions
JP5647815B2 (en
Inventor
Satomi Murata
里美 村田
Hiroshi Yamagishi
弘 山岸
Keiya Takahara
啓也 高原
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.)
Lion Corp
Original Assignee
Lion Corp
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 Lion Corp filed Critical Lion Corp
Priority to JP2010115502A priority Critical patent/JP5647815B2/en
Publication of JP2011012051A publication Critical patent/JP2011012051A/en
Application granted granted Critical
Publication of JP5647815B2 publication Critical patent/JP5647815B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/16Heavy metals; Compounds thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01MCATCHING, TRAPPING OR SCARING OF ANIMALS; APPARATUS FOR THE DESTRUCTION OF NOXIOUS ANIMALS OR NOXIOUS PLANTS
    • A01M13/00Fumigators; Apparatus for distributing gases
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/20Combustible or heat-generating compositions
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N65/00Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L9/00Disinfection, sterilisation or deodorisation of air
    • A61L9/015Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
    • A61L9/02Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air by heating or combustion

Abstract

PROBLEM TO BE SOLVED: To provide a fumigation agent composition, fumigation equipment and a fumigation method, little in remaining odor after fumigation and excellent in microorganism suppressing effect and deodorant effect.SOLUTION: The fumigation agent composition comprises an agent containing silver and an organic foaming agent. The former agent preferably has a 0.01-1,000 μm volume-average particle diameter, the organic foaming agent is preferably azodicarbonamide, and more preferably contains as an foaming auxiliary one or more selected from the group consisting of zinc oxide, zinc carbonate, zinc stearate, magnesium stearate, magnesium oxide, calcium carbonate and calcium phosphate. The fumigation equipment 10 comprises a fumigation agent part 32 filled with the fumigation agent composition, a heating part 20, and a heat transfer part transferring heat generated in the heating part to the fumigation agent part. The fumigation method comprises indirectly heating the fumigation composition.

Description

本発明は、燻煙剤組成物、燻煙装置及び燻煙方法に関する。   The present invention relates to a smoke composition, a smoke device, and a smoke method.

近年、一般家庭では、住宅の気密性向上に伴い、細菌、カビ等の微生物が生活空間に繁殖しやすくなっている。微生物の繁殖は、美観を損ねるだけでなく、感染症リスクとなる等の衛生上の大きな問題となる。特に、湿気の多い浴室は、細菌、カビ等の微生物が繁殖しやすい環境である。浴室の天井や壁の上部等の高い部分は、カビ取り剤の吸引を防止する観点から手入れがしにくく、このため微生物が繁殖しやすい場所である。加えて、換気口等、奥深くまで手が届かないような複雑な構造物の内部等は、さらに手入れが困難である。このような場所に微生物が繁殖すると、不快な臭いの発生源となる。浴室の臭いに対しては、その発生源を取り除くことが主な対処法であるが、発生源が不明であることも多く、対処が困難であった。  In recent years, in general households, microorganisms such as bacteria and molds are easily propagated in living spaces as the airtightness of houses is improved. The propagation of microorganisms not only detracts from aesthetics but also becomes a major hygiene problem such as risk of infectious diseases. In particular, a humid bathroom is an environment in which microorganisms such as bacteria and molds can easily propagate. High parts such as the ceiling of the bathroom and the upper part of the wall are difficult to maintain from the viewpoint of preventing the fungicide from being sucked in, and are therefore places where microorganisms tend to propagate. In addition, the inside of a complex structure that cannot be reached deeply such as a ventilation opening is further difficult to maintain. When microorganisms propagate in such places, they become a source of unpleasant odors. For the smell of the bathroom, removing the source is the main countermeasure, but the source is often unknown and it is difficult to cope with it.

こうした問題に対し、有害生物駆除用薬剤と、有機発泡剤(有機揮散剤)とを含有する燻煙剤組成物を加熱し、屋内を燻煙する方法が知られている(例えば、特許文献1〜3)。このような燻煙による手入れは、浴室における微生物繁殖や臭気発生を容易に予防できる。  For such problems, a method is known in which a smoke composition containing a pest control agent and an organic foaming agent (organic volatilizer) is heated to smoke indoors (for example, Patent Document 1). ~ 3). Such care with smoke can easily prevent microbial growth and odor generation in the bathroom.

特開2008−127299号公報JP 2008-127299 A 特開2005−89453号公報JP 2005-89453 A 特開昭56−77202号公報JP-A-56-77202

しかしながら、浴室に使用する燻煙剤組成物は、手軽に浴室を手入れできるものであるが、燻煙後に特有の臭気が残りやすい。加えて、燻煙剤組成物には、さらなる抗菌、殺菌、防カビ、抗カビ等の微生物抑制効果、消臭効果の向上が望まれている。
そこで、本発明は、燻煙後の臭気の残留が少なく、かつ、微生物抑制効果及び消臭効果に優れる燻煙剤組成物、燻煙装置及び燻煙方法を目的とする。
However, the smoke agent composition used in the bathroom can easily clean the bathroom, but a characteristic odor tends to remain after the smoke. In addition, the smoke composition is desired to have further antibacterial, antibacterial, antifungal, antifungal and other antimicrobial effects and an improved deodorizing effect.
Therefore, the present invention has an object of a smoke composition, a smoke device, and a smoke method that have little odor residue after smoke and are excellent in microbial control effect and deodorization effect.

本発明の燻煙剤組成物は、銀を含有する薬剤と、有機発泡剤とを含有することを特徴とする。
前記薬剤は、体積平均粒子径0.01〜1000μmであることが好ましく、前記有機発泡剤は、アゾジカルボンアミドであることが好ましく、さらに、発泡助剤として酸化亜鉛、炭酸亜鉛、ステアリン酸亜鉛、ステアリン酸マグネシウム、酸化マグネシウム、炭酸カルシウム及びリン酸カルシウムからなる群から選択される1種以上を含有することがより好ましい。
The smoke agent composition of the present invention is characterized by containing an agent containing silver and an organic foaming agent.
The agent preferably has a volume average particle diameter of 0.01 to 1000 μm, the organic foaming agent is preferably azodicarbonamide, and zinc oxide, zinc carbonate, zinc stearate as a foaming aid, More preferably, it contains at least one selected from the group consisting of magnesium stearate, magnesium oxide, calcium carbonate, and calcium phosphate.

本発明の燻煙装置は、前記燻煙剤組成物を充填した燻煙剤部と、加熱部と、該加熱部で生じた熱を前記燻煙剤部に伝える伝熱部とを有することを特徴とする。   The smoke device of the present invention has a smoke agent part filled with the smoke agent composition, a heating part, and a heat transfer part that transmits heat generated in the heating part to the smoke agent part. Features.

本発明の燻煙方法は、前記燻煙剤組成物を間接的に加熱することを特徴とする。   The smoke method of the present invention is characterized by indirectly heating the smoke composition.

本発明によれば、燻煙後の臭気の残留を少なくし、かつ、微生物抑制効果及び消臭効果の向上が図れる。   According to the present invention, it is possible to reduce residual odor after smoking, and to improve the microorganism suppressing effect and the deodorizing effect.

本発明の燻煙装置の一例を示す断面図である。It is sectional drawing which shows an example of the soot device of this invention. 微生物抑制効果の評価に用いた実験系を示す模式図である。It is a schematic diagram which shows the experimental system used for evaluation of the microorganisms inhibitory effect.

(燻煙剤組成物)
本発明の燻煙剤組成物(以下、単に燻煙剤という)は、銀を含有する薬剤(以下、(A)成分という)と、有機発泡剤(以下、(B)成分という)とを含有するものである。
(Smoke agent composition)
The smoke agent composition of the present invention (hereinafter simply referred to as smoke agent) contains a drug containing silver (hereinafter referred to as component (A)) and an organic foaming agent (hereinafter referred to as component (B)). To do.

<(A)成分:銀を含有する薬剤>
本発明の(A)成分は、銀を含有する薬剤である。このような(A)成分を用いることで、(A)成分を気化させずに、燻煙対象である室内(対象空間)に拡散することができる。加えて、銀は、殺菌、抗菌、防カビ又は抗カビ等の微生物抑制効果、消臭効果に優れるためである。
(A)成分は、燻煙剤の目的に応じ、従来用いられている銀を含有する無機化合物等を使用することができる。薬剤としては、例えば、殺菌剤、抗菌剤、防カビ剤、抗カビ剤、消臭剤、殺虫剤等として作用する薬剤が挙げられ、中でも、殺菌剤、抗菌剤、防カビ剤、抗カビ剤、消臭剤を好適に用いることができる。
<(A) component: a drug containing silver>
The component (A) of the present invention is a drug containing silver. By using such a component (A), the component (A) can be diffused into a room (target space) that is a smoke target without being vaporized. In addition, silver is excellent in sterilizing, antibacterial, antifungal, antifungal and other microorganism control effects and deodorizing effects.
As the component (A), a conventionally used inorganic compound containing silver can be used according to the purpose of the smoke agent. Examples of the agent include agents that act as antibacterial agents, antibacterial agents, antifungal agents, antifungal agents, deodorants, insecticides, etc., among others, antibacterial agents, antibacterial agents, antifungal agents, antifungal agents A deodorant can be preferably used.

(A)成分の気化温度は、後述する(B)成分の気化温度よりも高いことが好ましい。このような(A)成分を用いることで、燻煙処理の際に(A)成分の気化に由来する臭気を防止できる。ここで気化とは、(A)成分が溶液である場合の水等の溶媒の蒸発や、(A)成分が酸化物である場合の酸素が離脱する等の分解反応は含まない。なお、気化温度(沸点)は、熱分析を用いて測定できる。   It is preferable that the vaporization temperature of (A) component is higher than the vaporization temperature of (B) component mentioned later. By using such (A) component, the odor derived from vaporization of (A) component can be prevented in the case of smoke treatment. Here, the vaporization does not include a decomposition reaction such as evaporation of a solvent such as water when the component (A) is a solution, or separation of oxygen when the component (A) is an oxide. The vaporization temperature (boiling point) can be measured using thermal analysis.

(A)成分としては、例えば、有効成分として、抗菌・殺菌・防カビ・抗カビ・消臭作用を持つ銀単体、銀の酸化物、塩化物塩、硝酸塩、硫酸塩、スルホン酸塩、炭酸塩等の無機銀塩、蟻酸塩、酢酸塩等の有機銀塩等の銀化合物が挙げられる。   As the component (A), for example, as an active ingredient, silver alone having antibacterial / sterilizing / mold / antifungal / deodorizing action, silver oxide, chloride salt, nitrate, sulfate, sulfonate, carbonate Examples thereof include inorganic silver salts such as salts, and silver compounds such as organic silver salts such as formate and acetate.

また、(A)成分は、これらの有効成分をゼオライト、シリカゲル、低分子ガラス、リン酸カルシウム、ケイ酸塩、酸化チタン等の物質(以下、担体ということがある)に担持させたもの等が挙げられ、例えば、銀単体、酸化銀、硝酸銀等の無機銀塩、有機銀塩等の銀化合物を担持したゼオライト系抗菌剤、シリカゲル系抗菌剤、酸化チタン系抗菌剤、ケイ酸塩系抗菌剤等が挙げられる。このような(A)成分を用いることで、燻煙処理した後の臭気の残留を防止できる。
中でも、(A)成分としては、臭気の残留をより低減する観点から、銀単体、酸化銀、硝酸銀等の無機銀塩又はこれらを担体に担持させた無機系薬剤が好ましい。
また、(A)成分は1種単独で又は2種以上を適宜組み合わせて用いることができる。
Examples of the component (A) include those obtained by supporting these active ingredients on a substance (hereinafter sometimes referred to as a carrier) such as zeolite, silica gel, low molecular glass, calcium phosphate, silicate, and titanium oxide. Examples include zeolite antibacterial agents, silica gel antibacterial agents, titanium oxide antibacterial agents, silicate antibacterial agents that carry silver compounds such as simple silver, silver oxide and silver nitrate, and silver compounds such as organic silver salts. Can be mentioned. By using such a component (A), it is possible to prevent the odor from remaining after the smoke treatment.
Among these, as the component (A), from the viewpoint of further reducing residual odor, inorganic silver salts such as single silver, silver oxide and silver nitrate, or inorganic chemicals in which these are supported on a carrier are preferable.
Moreover, (A) component can be used individually by 1 type or in combination of 2 or more types as appropriate.

(A)成分の形態は特に限定されないが、燻煙の処理対象とする空間の広さ等を勘案して決定できる。(A)成分は、粒子が微細であるほど煙化率を向上できると共に、広域に拡散できる。一方、(A)成分の粒子は、小さすぎると拡散した後に落下しにくくなり、処理対象とする空間の下方への薬剤効果の発現までに時間を要する。例えば、(A)成分の体積平均粒子径は、0.01〜1000μmが好ましく、0.5〜100μmがより好ましく、1〜5μmがさらに好ましい。本発明の燻煙剤組成物においては、このような比較的大きな粒子径の(A)成分であっても、煙化して拡散することができる。ここで、「煙化」とは、(A)成分を対象空間に拡散できる状態にすることを意味する。
なお、体積平均粒子径は、レーザー回析/散乱式粒度分布測定装置(LA910、株式会社堀場製作所製)により求められる値をいい、次のようにして測定できる。(A)成分を固形分1質量%となるように蒸留水に分散して試料とする。この試料をレーザー回析/散乱式粒度分布測定装置に投入し、装置内で超音波による分散後レーザーを照射して粒度分布を測定する。体積頻度の累積が50%(体積)となる径を平均粒子径とする。
The form of the component (A) is not particularly limited, but can be determined in consideration of the size of the space to be treated with smoke. The component (A) can improve the smoke conversion rate as the particles are finer and can diffuse in a wide area. On the other hand, if the particle of component (A) is too small, it will be difficult to fall after diffusing, and it will take time to develop a drug effect below the space to be treated. For example, the volume average particle diameter of the component (A) is preferably 0.01 to 1000 μm, more preferably 0.5 to 100 μm, and further preferably 1 to 5 μm. In the smoke agent composition of the present invention, even such a component (A) having a relatively large particle size can be smoked and diffused. Here, “smoke” means that component (A) can be diffused into the target space.
The volume average particle diameter is a value determined by a laser diffraction / scattering particle size distribution measuring device (LA910, manufactured by Horiba, Ltd.), and can be measured as follows. The component (A) is dispersed in distilled water so as to have a solid content of 1% by mass to obtain a sample. This sample is put into a laser diffraction / scattering type particle size distribution measuring apparatus, and the particle size distribution is measured by irradiating a laser after dispersion by ultrasonic waves in the apparatus. The diameter at which the cumulative volume frequency is 50% (volume) is defined as the average particle diameter.

燻煙剤における(A)成分の配合量は、(A)成分の種類や有効成分濃度、燻煙剤に求める機能に応じて決定することができる。例えば、銀又はその化合物を有効成分とする(A)成分は、燻煙剤中の銀濃度を0.0001〜1質量%とすることが好ましく、0.01〜0.1質量%とすることがより好ましい。上記下限値未満であると、所望する薬剤効果が発揮されにくく、上記上限値を超えて配合しても薬剤の効果が飽和し、さらなる効果の向上が望めないためである。  The blending amount of the component (A) in the smoke agent can be determined according to the type of the component (A), the effective component concentration, and the function required for the smoke agent. For example, the component (A) containing silver or a compound thereof as an active ingredient preferably has a silver concentration in the smoke agent of 0.0001 to 1% by mass, preferably 0.01 to 0.1% by mass. Is more preferable. This is because if it is less than the lower limit, the desired drug effect is hardly exhibited, and even if it exceeds the upper limit, the effect of the drug is saturated and further improvement of the effect cannot be expected.

<(B)成分:有機発泡剤>
有機発泡剤である(B)成分は、特に限定されず、従来公知のものを利用できる。
(B)成分としては、加熱により熱分解して多量の熱を発生すると共に、炭酸ガスや窒素ガス等(以下、総じて発泡ガスという)を発生するものが用いられ、例えば、アゾジカルボンアミド、p,p’−オキシビス(ベンゼンスルホニルヒドラジド)、N,N’−ジニトロソペンタメチレンテトラミン、アゾビスイソブチロニトリル等が挙げられる。中でも、分解温度、発泡ガスの発生量等の観点から、アゾジカルボンアミドが好ましい。
これらの(B)成分は、1種単独で又は2種以上を適宜組み合わせて用いることができる。これら(B)成分は加熱により(A)成分と発泡溶融し(B)成分の熱分解ガスの作用により、(A)成分を有効に煙化させることができる。
<(B) component: Organic foaming agent>
(B) component which is an organic foaming agent is not specifically limited, A conventionally well-known thing can be utilized.
As the component (B), those which are pyrolyzed by heating to generate a large amount of heat and generate carbon dioxide gas, nitrogen gas or the like (hereinafter generally referred to as foaming gas) are used. For example, azodicarbonamide, p , P′-oxybis (benzenesulfonylhydrazide), N, N′-dinitrosopentamethylenetetramine, azobisisobutyronitrile and the like. Of these, azodicarbonamide is preferable from the viewpoints of decomposition temperature, amount of foaming gas, and the like.
These (B) components can be used individually by 1 type or in combination of 2 or more types. These components (B) are foamed and melted with the component (A) by heating, and the component (A) can be effectively smoked by the action of the pyrolysis gas of the component (B).

燻煙剤中の(B)成分の配合量は、(B)成分の種類や(A)成分の粒子径等を勘案して決定することができ、例えば、50〜80質量%が好ましく、60〜70質量%がより好ましい。上記下限値未満であると(A)成分を効率よく拡散できず、上記上限値を超えると(B)成分の多くの分解物(残渣)が飛散して対象空間を汚す傾向にある。   The blending amount of the component (B) in the smoke agent can be determined in consideration of the type of the component (B), the particle size of the component (A), etc., and is preferably 50 to 80% by mass, for example, 60 -70 mass% is more preferable. If it is less than the lower limit, component (A) cannot be efficiently diffused, and if it exceeds the upper limit, many decomposition products (residues) of component (B) tend to scatter and contaminate the target space.

<(C)成分:発泡助剤>
本発明の燻煙剤には、発泡助剤である(C)成分を配合できる。(C)成分を配合することで、(B)成分の異常分解を抑制し、発泡ガス以外の物質の発生を抑制することができる。加えて、(C)成分は、(B)成分の発泡温度を低下、即ちより低温で(B)成分を発泡することで、(A)成分の煙化・拡散力を高め、対象空間の隅々まで(A)成分を拡散できる。(C)成分は、酸化亜鉛、炭酸亜鉛、ステアリン酸亜鉛、ステアリン酸マグネシウム、酸化マグネシウム、炭酸カルシウム及びリン酸カルシウムからなる群から選択される1種以上であり、中でも酸化亜鉛、炭酸カルシウムが好ましく、酸化亜鉛がさらに好ましい。酸化亜鉛は、(B)成分の分解を促進し、(A)成分を速やかに煙化すると共に、広範囲に拡散できる。また、炭酸カルシウムは、(B)成分の異常分解を抑制する効果に優れ、燻煙剤を設置した床等の汚染を抑制できる。
燻煙剤中の(C)成分の配合量は、例えば、0.1〜20質量%が好ましく、0.1〜15質量%がより好ましく、0.5〜5質量%が最も好ましい。
0.1質量%未満では発泡助剤(揮散助剤)としての効果が小さく、20質量%を超えると不安定な発泡となる場合がある。また、(B)成分と(C)成分との質量比は、(B)/(C)=1〜700であることが好ましく、10〜150であることがより好ましい。上記範囲とすることで、(B)成分の発泡性が向上し、(A)成分の煙化・拡散が良好となり、微生物抑制効果をより向上させることができる。
<(C) component: foaming aid>
(C) component which is a foaming adjuvant can be mix | blended with the smoke agent of this invention. By mix | blending (C) component, abnormal decomposition | disassembly of (B) component can be suppressed and generation | occurrence | production of substances other than foaming gas can be suppressed. In addition, the component (C) lowers the foaming temperature of the component (B), that is, foams the component (B) at a lower temperature, thereby increasing the smoke / diffusion power of the component (A) and increasing the corner of the target space. The component (A) can be diffused as much as possible. The component (C) is at least one selected from the group consisting of zinc oxide, zinc carbonate, zinc stearate, magnesium stearate, magnesium oxide, calcium carbonate, and calcium phosphate. Among them, zinc oxide and calcium carbonate are preferable, and oxidation Zinc is more preferred. Zinc oxide accelerates the decomposition of the component (B), quickly smokes the component (A), and can diffuse widely. Moreover, calcium carbonate is excellent in the effect which suppresses abnormal decomposition | disassembly of (B) component, and can suppress contamination of the floor etc. which installed the smoke agent.
0.1-20 mass% is preferable, for example, the compounding quantity of (C) component in a smoke agent is more preferable, 0.1-15 mass% is more preferable, and 0.5-5 mass% is the most preferable.
If it is less than 0.1% by mass, the effect as a foaming aid (volatilization aid) is small, and if it exceeds 20% by mass, unstable foaming may occur. Moreover, it is preferable that it is (B) / (C) = 1-700, and, as for mass ratio of (B) component and (C) component, it is more preferable that it is 10-150. By setting it as the said range, the foamability of (B) component improves, the smoke formation and spreading | diffusion of (A) component become favorable, and the microorganisms inhibitory effect can be improved more.

<任意成分>
燻煙剤には、本発明の効果を阻害しない範囲で(A)成分、(B)成分、(C)成分以外の任意成分を配合できる。任意成分としては、例えば、安定剤、結合剤、賦形剤、香料、色素等の添加剤が挙げられる。これらのうち、特に、安定剤、結合剤及び賦形剤のいずれか1種又は2種以上を含有することが好ましい。
<Optional component>
An optional component other than the component (A), the component (B), and the component (C) can be blended with the smoke agent so long as the effects of the present invention are not impaired. As an arbitrary component, additives, such as a stabilizer, a binder, an excipient | filler, a fragrance | flavor, a pigment | dye, are mentioned, for example. Among these, it is particularly preferable to contain one or more of stabilizers, binders and excipients.

安定化剤としては、ソルビタン脂肪酸エステル、ジブチルヒドロキシトルエン、ブチルヒドキシアニソール、没食子酸プロピル、エポキシ化合物(エポキシ化大豆油、エポキシ化アマニ油等)等が挙げられる。
結合剤としては、メチルセルロース、エチルセルロース、カルボキシメチルセルロース、ヒドロキシプロピルメチルセルロース、ヒドロキシプロピルセルロース、デンプン、デキストリン、ヒドロキシプロピルスターチ、ゼラチン、ポリビニルアルコール、ポリビニルアセテート、ポリビニルピロリドン、ポリアクリル酸ナトリウム等が挙げられる。
賦形剤としては、クレー(含水ケイ酸アルミニウム)、タルク、珪藻土、カオリン、ベントナイト、ホワイトカーボン等が挙げられる。
Examples of the stabilizer include sorbitan fatty acid ester, dibutylhydroxytoluene, butylhydroxyanisole, propyl gallate, epoxy compounds (epoxidized soybean oil, epoxidized linseed oil, etc.) and the like.
Examples of the binder include methyl cellulose, ethyl cellulose, carboxymethyl cellulose, hydroxypropyl methyl cellulose, hydroxypropyl cellulose, starch, dextrin, hydroxypropyl starch, gelatin, polyvinyl alcohol, polyvinyl acetate, polyvinyl pyrrolidone, sodium polyacrylate, and the like.
Examples of the excipient include clay (hydrous aluminum silicate), talc, diatomaceous earth, kaolin, bentonite, and white carbon.

<製造方法>
本発明の燻煙剤は、粉状、粒状、錠剤等の固形製剤として調製される。固形製剤は、目的とする剤形に応じて、公知の製造方法を用いて調製することができる。例えば、粒状の製剤とする場合は、押出し造粒法、圧縮造粒法、撹拌造粒法、転動造粒法、流動層造粒法等、公知の造粒物の製造方法により製造できる。
押出し造粒法による製造方法の具体例としては、燻煙剤の各成分を、ニーダー等により混合し、さらに適量の水を加えて混合し、得られた混合物を一定面積の開孔を有するダイスを用い、前押し出しあるいは横押し出し造粒機を用い造粒する。該造粒物は、さらにカッター等を用いて一定の大きさに切断し乾燥してもよい。
<Manufacturing method>
The smoke agent of the present invention is prepared as a solid preparation such as powder, granules and tablets. The solid preparation can be prepared using a known production method according to the intended dosage form. For example, in the case of a granular preparation, it can be produced by a known granulated production method such as extrusion granulation method, compression granulation method, stirring granulation method, tumbling granulation method, fluidized bed granulation method and the like.
As a specific example of the production method by the extrusion granulation method, each component of the smoke agent is mixed by a kneader and the like, and an appropriate amount of water is added and mixed, and the resulting mixture is a die having an opening of a certain area. And granulate using a pre-extrusion or horizontal extrusion granulator. The granulated product may be further cut into a certain size using a cutter or the like and dried.

<燻煙方法>
本発明の燻煙方法は、本発明の燻煙剤を間接的に加熱するものである。間接的にとは、燻煙剤を燃焼させることなく、(B)成分を熱分解して得られる温度(熱エネルギー)を容器や伝熱面等を介して供給する方法である。例えば、任意の金属製容器、セラミック製容器等の容器に燻煙剤を収容して、前記容器を加熱することによって燻煙できる。燻煙剤を間接的に加熱することで、燻煙剤の燃えカス等による屋内汚染を低減できる。また、後述する燻煙装置に組み込んで、対象空間を燻煙してもよい。対象空間としては、特に限定されず、浴室、居間、押入れ等が挙げられる。
加熱方法は、特に限定されず、従来、間接加熱方式として知られているものを用いることができる。例えば、水と接触して発熱する物質を水と接触させ、その反応熱を利用する方法、鉄粉と酸化剤(塩素酸アンモニウム等)との混合、金属と該金属よりイオン化傾向の小さい金属酸化物又は酸化剤とを混合し酸化反応を利用する方法等が挙げられる。水と接触して発熱する物質としては、酸化カルシウム、塩化マグネシウム、塩化アルミニウム、塩化カルシウム、塩化鉄等が挙げられる。中でも、実用性の観点から、水と接触して発熱する物質を水と接触させ、その反応熱を利用する方法が好ましく、酸化カルシウムと水との反応熱を利用する方法がより好ましい。
<How to smoke>
The smoke method of the present invention indirectly heats the smoke agent of the present invention. Indirectly is a method of supplying the temperature (thermal energy) obtained by pyrolyzing the component (B) via a container, a heat transfer surface or the like without burning the smoke smoke agent. For example, smoke can be smoked by storing a smoke agent in a container such as an arbitrary metal container or ceramic container and heating the container. By indirectly heating the soot agent, indoor pollution due to the burning residue of the soot agent can be reduced. Further, the target space may be smoked by being incorporated in a smoke device described later. The target space is not particularly limited, and examples include a bathroom, a living room, and a closet.
The heating method is not particularly limited, and a conventionally known indirect heating method can be used. For example, a method in which a substance that generates heat in contact with water is brought into contact with water and the reaction heat is used, mixing of iron powder and an oxidizing agent (ammonium chlorate, etc.), metal oxidation with less ionization tendency than the metal And a method of using an oxidation reaction by mixing a product or an oxidizing agent. Examples of substances that generate heat upon contact with water include calcium oxide, magnesium chloride, aluminum chloride, calcium chloride, and iron chloride. Among these, from the viewpoint of practicality, a method of bringing a substance that generates heat upon contact with water into contact with water and utilizing the reaction heat thereof is preferred, and a method of utilizing the reaction heat between calcium oxide and water is more preferred.

本発明の燻煙剤の使用量は、対象空間の容積に応じて適宜設定すればよく、通常、1m当たり、0.1〜2.4gが好ましく、0.4g〜2.0gがより好ましい。
燻煙処理時間(燻煙開始後、対象空間を密閉する時間)は、特に限定されず、1時間以上が好ましく、1.5時間以上がより好ましい。
The amount of the fumigant of the present invention may be appropriately set according to the volume of the object space, usually, 1 m 3 per, 0.1~2.4G and more preferably 0.4g~2.0g .
The soot treatment time (time for sealing the target space after the start of soot) is not particularly limited, but is preferably 1 hour or longer, and more preferably 1.5 hours or longer.

(燻煙装置)
本発明の燻煙装置は、上述した燻煙剤が充填された燻煙剤部と、前記燻煙剤部を加熱する加熱部と、該加熱部で生じた熱を前記燻煙剤部に伝える伝熱部とを有する。
(Smoke device)
The smoke device of the present invention transmits the smoke agent part filled with the smoke agent described above, a heating part for heating the smoke agent part, and heat generated in the heating part to the smoke agent part. And a heat transfer section.

燻煙装置について、一例を挙げて説明する。図1は、本発明の燻煙装置10の断面図である。燻煙装置10は、筐体12と、筐体12の内部に設けられた加熱部20と、筐体12の内部に設けられた燻煙剤部32とで概略構成されている。筐体12は略円筒状の本体14と、底部16と、蓋部18とで構成されている。筐体12内には、燻煙剤容器30が設けられ、燻煙剤容器30には燻煙剤が充填され燻煙剤部32が形成されている。   The smoke device will be described with an example. FIG. 1 is a cross-sectional view of a smoke device 10 of the present invention. The smoke device 10 is roughly configured by a housing 12, a heating unit 20 provided in the housing 12, and a smoke agent unit 32 provided in the housing 12. The housing 12 includes a substantially cylindrical main body 14, a bottom portion 16, and a lid portion 18. A smoke agent container 30 is provided in the housing 12, and the smoke agent container 30 is filled with a smoke agent and a smoke agent part 32 is formed.

蓋部18は、孔を有するものであり、メッシュ、パンチングメタル、格子状の枠体等が挙げられる。蓋部18の材質は、例えば、金属、セラミック等が挙げられる。
本体14の材質は蓋部18と同じである。
The lid portion 18 has a hole, and examples thereof include a mesh, punching metal, and a lattice frame. Examples of the material of the lid portion 18 include metals and ceramics.
The material of the main body 14 is the same as that of the lid 18.

燻煙剤容器30は、燻煙剤部32を充填する容器として機能すると共に、加熱部20で生じた熱エネルギーを燻煙剤部32に伝える伝熱部として機能するものである。燻煙剤容器30は、例えば金属製の容器等が挙げられる。   The smoke agent container 30 functions as a container that fills the smoke agent part 32 and also functions as a heat transfer part that transmits the thermal energy generated in the heating part 20 to the smoke agent part 32. Examples of the smoke agent container 30 include a metal container.

加熱部20は、特に限定されず、燻煙剤部32の煙化に必要な熱量を考慮して決定することができ、例えば、水と接触して発熱する物質(例えば、酸化カルシウム等)を充填しておいてもよいし、鉄粉と酸化剤とを仕切り材で仕切って充填しておいてもよいし、金属と該金属よりイオン化傾向の小さい金属酸化物又は酸化剤とを仕切り材で仕切って充填しておいてもよい。中でも、水と接触して発熱する物質を充填しておくことが好ましく、酸化カルシウムを充填しておくことが好ましい。   The heating unit 20 is not particularly limited, and can be determined in consideration of the amount of heat necessary for the smoke of the smoke agent unit 32. For example, a substance that generates heat upon contact with water (for example, calcium oxide) is used. It may be filled, iron powder and an oxidant may be partitioned and filled with a partition material, or a metal and a metal oxide or oxidizer having a lower ionization tendency than the metal may be filled with a partition material. You may partition and fill. Among them, it is preferable to fill with a substance that generates heat upon contact with water, and it is preferable to fill with calcium oxide.

底部16は、加熱部20の機構に応じて決定することができ、例えば、加熱部20が水と接触して発熱する物質(酸化カルシウム等)により構成されている場合、底部16には不織布や金属製のメッシュ等を用いることができる。底部16を不織布やメッシュとすることで、底部16から水を加熱部20内に浸入させ加熱することができる。  The bottom part 16 can be determined according to the mechanism of the heating part 20, for example, when the heating part 20 is made of a substance (calcium oxide or the like) that generates heat when in contact with water, the bottom part 16 has a nonwoven fabric or A metal mesh or the like can be used. By making the bottom part 16 into a nonwoven fabric or a mesh, water can penetrate into the heating part 20 from the bottom part 16 and can be heated.

燻煙装置10を用いた燻煙方法について説明する。まず、燻煙装置10を対象空間内に設置する。次いで、加熱部20の機構に応じて加熱部20を発熱させる。例えば、酸化カルシウムを充填した加熱部20が設けられている場合、底部16を水に浸漬する。加熱部20が発熱すると、燻煙剤容器30を介して燻煙剤部32が加熱される。加熱された燻煙剤部32の燻煙剤は、その(B)成分の分解によりガスを生じ、生じたガスと共に(A)成分が煙化し、蓋部18の孔を通過して拡散する。こうして、対象空間内に(A)成分が拡散することで、微生物抑制効果や消臭効果を得ることができる。   A smoke method using the smoke device 10 will be described. First, the smoke device 10 is installed in the target space. Next, the heating unit 20 generates heat according to the mechanism of the heating unit 20. For example, when the heating part 20 filled with calcium oxide is provided, the bottom part 16 is immersed in water. When the heating unit 20 generates heat, the smoke agent part 32 is heated via the smoke agent container 30. The smoke smoke agent of the heated smoke agent portion 32 generates gas by decomposition of the component (B), and the component (A) is smoked together with the generated gas and diffuses through the hole of the lid portion 18. Thus, the component (A) is diffused in the target space, so that a microorganism suppressing effect and a deodorizing effect can be obtained.

以上、説明したとおり、(A)成分は、抗菌、殺菌、防カビ、抗カビ、消臭等の微生物抑制効果に優れるため、対象空間の臭気発生源となる微生物を減少させ、また、微生物の増殖を防止できる。(A)成分は、カビ等の微生物と接触すると短時間で微生物抑制効果を発揮する。一方、3−ヨード−2−プロピニルブチルカーバメイト(IPBC)や2−イソプロピル−5−メチルフェノール(IPMP)等の有機系薬剤は、殺菌等の処理対象となる部分(例えば、天井等)に長時間滞留することで殺菌作用を示す。このように、本発明の燻煙剤は、浴室のように、湿気が多く、薬剤が長時間滞留しにくいような場所においても、従来の燻煙剤に比べ、高い微生物抑制効果及び消臭効果を発揮できる。
加えて、(B)成分の一般的な気化温度(200〜300℃)では気化しない(A)成分を有効成分とすることで、(A)成分を気化させずに対象空間に拡散できる。(A)成分は、元来、臭気が低い。また、(A)成分自体は熱分解しにくいため、刺激性の高い副生物や、異臭を発する副生物を生じない。このため、従来の燻煙剤の有効成分として用いられていた有機物のように、燻煙処理時の有効成分の気化による臭気の発生を抑制できる。
さらに(B)成分に(C)成分を組み合わせることにより、(B)成分をより低い温度で安定的に気化すること可能となり(A)成分を対象空間の隅々まで効率的に燻煙しやすくなる。
(A)成分を無機銀塩や無機銀塩を担体に担持した無機系薬剤とすることで、有効成分が分解されず、細菌やカビと接触した後も長期にわたってその効力を維持することができる。
As described above, since the component (A) has an excellent antimicrobial effect such as antibacterial, sterilizing, antifungal, antifungal, and deodorizing, it reduces the microorganisms that are the source of odor generation in the target space. Proliferation can be prevented. When the component (A) comes into contact with microorganisms such as mold, it exerts a microorganism suppressing effect in a short time. On the other hand, organic chemicals such as 3-iodo-2-propynyl butyl carbamate (IPBC) and 2-isopropyl-5-methylphenol (IPMP) are applied to a part to be treated such as sterilization (for example, ceiling) for a long time. It shows bactericidal action by staying. Thus, the smoke agent of the present invention has a high microbial control effect and deodorant effect compared to conventional smoke agents, even in places where the humidity is high and the drug is difficult to stay for a long time, such as in a bathroom. Can be demonstrated.
In addition, by using the component (A) that does not vaporize at a general vaporization temperature (200 to 300 ° C.) of the component (B) as an active component, the component (A) can be diffused into the target space without vaporizing. Component (A) has a low odor originally. In addition, since the component (A) itself is difficult to be thermally decomposed, it does not produce a highly irritating by-product or a by-product that generates a bad odor. For this reason, generation | occurrence | production of the odor by the vaporization of the active ingredient at the time of soot processing can be suppressed like the organic substance used as an active ingredient of the conventional smoke agent.
Furthermore, by combining the component (B) with the component (B), the component (B) can be stably vaporized at a lower temperature, and the component (A) is easily smoked to every corner of the target space. Become.
(A) By making an inorganic chemical | medical agent which carry | supported the component (A) inorganic silver salt and inorganic silver salt on the support | carrier, an active ingredient is not decomposed | disassembled but can maintain the efficacy over a long term even after contacting with bacteria and mold. .

本発明の燻煙装置は、燻煙剤を間接的に加熱するものであり、すり板式燻煙剤のように燻煙剤自体を燃焼させる炎の発生がない。また、エアゾールのように可燃性ガス等を用いない。従って、ガスを用いた風呂釜が設置されている環境下においても、取り扱いが容易である。  The soot device of the present invention indirectly heats the soot agent, and does not generate a flame that burns the soot agent itself like a sliding plate soot agent. Moreover, flammable gas etc. are not used like aerosol. Therefore, it is easy to handle even in an environment where a bath using gas is installed.

以下に、実施例を示して本発明をより詳細に説明するが、本発明はこれに限定されるものではない。
(使用原料)
<(A)成分:銀を含有する薬剤>
A−1:銀担持シリカ・アルミナ系無機抗菌剤(商品名:ATOMY BALL−(UA)、体積平均粒子径15nm、銀含量0.07質量%、日揮触媒化成株式会社製)
A−2:銀担持ケイ酸塩系無機抗菌剤(商品名:AIS−NAZ320、体積平均粒子径2μm、銀含量1.2質量%、日揮触媒化成株式会社製)
A−3:銀担持ゼオライト系無機抗菌剤(商品名:セラメディックCW、体積平均粒子径2μm、真比重2g/cm(20℃)、嵩比重0.4g/cm(20℃)、銀含量0.6質量%、株式会社シナネンゼオミック製)
A−4:酸化銀(特級、体積平均粒子径0.1μm、和光純薬工業株式会社製)
A−5:銀担持ゼオライト系無機抗菌剤(商品名:ゼオミックAJ10N、体積平均粒子径2.5μm、真比重2g/cm(20℃)、嵩比重0.4g/cm(20℃)、銀含量2.5質量%、株式会社シナネンゼオミック製)
Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited thereto.
(Raw material)
<(A) component: a drug containing silver>
A-1: Silver-supported silica / alumina inorganic antibacterial agent (trade name: ATOMY BALL- (UA), volume average particle diameter 15 nm, silver content 0.07% by mass, manufactured by JGC Catalysts & Chemicals Co., Ltd.)
A-2: Silver-supported silicate-based inorganic antibacterial agent (trade name: AIS-NAZ320, volume average particle diameter 2 μm, silver content 1.2% by mass, manufactured by JGC Catalysts & Chemicals Co., Ltd.)
A-3: Silver-supported zeolite inorganic antibacterial agent (trade name: Ceramedic CW, volume average particle diameter 2 μm, true specific gravity 2 g / cm 3 (20 ° C.), bulk specific gravity 0.4 g / cm 3 (20 ° C.), silver 0.6% by mass, made by Sinanen Zeomic Co., Ltd.)
A-4: Silver oxide (special grade, volume average particle size 0.1 μm, manufactured by Wako Pure Chemical Industries, Ltd.)
A-5: Silver-supported zeolite inorganic antibacterial agent (trade name: Zeomic AJ10N, volume average particle diameter 2.5 μm, true specific gravity 2 g / cm 3 (20 ° C.), bulk specific gravity 0.4 g / cm 3 (20 ° C.), (Silver content 2.5% by mass, manufactured by Sinanen Zeomic Co., Ltd.)

<(A’)成分:(A)成分の比較品>
A’−1:3−ヨード−2−プロピニルブチルカーバメイト(IPBC)(商品名:Glycacil 2000、ロンザジャパン株式会社製)
A’−2:2−イソプロピル−5−メチルフェノール(IPMP)(試薬鹿特級、関東化学株式会社製)
<(A ′) component: Comparative product of component (A)>
A′-1: 3-iodo-2-propynylbutyl carbamate (IPBC) (trade name: Glycacil 2000, manufactured by Lonza Japan Ltd.)
A′-2: 2-isopropyl-5-methylphenol (IPMP) (reagent deer special grade, manufactured by Kanto Chemical Co., Inc.)

<(B)成分:有機発泡剤>
B−1:アゾジカルボンアミド(ADCA)(商品名:ダイブローAC.2040(C)、大日精化工業株式会社製)
<(B) component: Organic foaming agent>
B-1: Azodicarbonamide (ADCA) (trade name: Daiburo AC.2040 (C), manufactured by Dainichi Seika Kogyo Co., Ltd.)

<(C)成分:発泡助剤>
C−1:酸化亜鉛(日本薬局方 酸化亜鉛、平均粒径0.6μm、真比重5.6g/cm(20℃)、堺化学工業株式会社製)
C−2:炭酸カルシウム(試薬鹿1級、関東化学株式会社製)
C−3:リン酸三カルシウム(食品添加物、関東化学株式会社製)
<(C) component: foaming aid>
C-1: Zinc oxide (Japanese Pharmacopoeia Zinc oxide, average particle size 0.6 μm, true specific gravity 5.6 g / cm 3 (20 ° C.), manufactured by Sakai Chemical Industry Co., Ltd.)
C-2: Calcium carbonate (reagent deer first grade, manufactured by Kanto Chemical Co., Inc.)
C-3: Tricalcium phosphate (food additive, manufactured by Kanto Chemical Co., Inc.)

<その他成分>
結合剤:ヒドロキシプロピルメチルセルロース(HPMC)(商品名:メトローズ60SH−50、信越化学工業株式会社製)
賦形剤:クレー(商品名:NK−300、昭和KDE株式会社製)
<Other ingredients>
Binder: Hydroxypropyl methylcellulose (HPMC) (trade name: Metroles 60SH-50, manufactured by Shin-Etsu Chemical Co., Ltd.)
Excipient: Clay (trade name: NK-300, Showa KDE Co., Ltd.)

(評価方法)
<微生物抑制効果の評価>
≪対カビ評価≫
[暴露試験]
図2に示す実験系100を用い、暴露試験を行った。図2に示すように、1818mmタイプ(メーターモジュール用)の浴室と同体積で、密閉可能な評価室102を対象空間として用意した。評価室102の床104の略中央部に、加熱装置110を設置した。加熱装置110は、ホットプレート上にアルミニウム箔を敷いて作製した。評価室102の天井106には、カビ付き平板培地120、130を設置し、評価室102の床104には、カビ付き平板培地140を設置した。カビ付き平板培地120は、加熱装置110の略真上に位置するものとし、カビ付き平板培地130は、天井106の隅部に位置するものとした。
(Evaluation methods)
<Evaluation of microbial control effect>
≪Anti-mold evaluation≫
[Exposure test]
An exposure test was conducted using the experimental system 100 shown in FIG. As shown in FIG. 2, an evaluation chamber 102 having the same volume as a 1818 mm type (for meter module) bathroom and capable of being sealed was prepared as a target space. A heating device 110 is installed at a substantially central portion of the floor 104 of the evaluation chamber 102. The heating device 110 was produced by laying an aluminum foil on a hot plate. On the ceiling 106 of the evaluation chamber 102, mold-containing flat media 120 and 130 were installed, and on the floor 104 of the evaluation chamber 102, a mold-containing flat media 140 was installed. The mold-containing plate medium 120 is located almost immediately above the heating device 110, and the mold-containing plate medium 130 is located at the corner of the ceiling 106.

各例の燻煙剤を加熱装置110のアルミニウム箔上に載せ、350℃に設定したホットプレートで加熱した。ホットプレートでの加熱は、燻煙剤からの発煙開始10分後に停止した。燻煙試験1では発煙開始90分後、燻煙試験2では30分後に、評価室102内の空気を排気し暴露試験を終了した。  The smoke agent of each example was placed on the aluminum foil of the heating device 110 and heated with a hot plate set at 350 ° C. Heating on the hot plate was stopped 10 minutes after the start of smoking from the smoke smoke agent. In the soot test 1, after 90 minutes from the start of smoke generation, and in the soot test 2, after 30 minutes, the air in the evaluation chamber 102 was exhausted and the exposure test was completed.

[カビ付き平板培地の作製]
ポテトデキストロース寒天(Difco社製)の斜面培地にて25℃、1週間培養したCladosporium cladosporioides HMC1064(浴室分離菌、以下、評価用カビという)を用意した。別途、ポテトデキストロース寒天(Difco社製)をシャーレに充填し、初期平板培地を用意した。初期平板培地の中央に、鉤形にしたニクロム線を用いて、評価用カビを1点接種し、25℃で3日間培養した。こうして、培養により平板培地にカビのコロニーが形成されたカビ付き平板培地120(効果1用)、130(効果2用)、140(効果3用)を作製した。カビ付き平板培地120、130、140それぞれの暴露試験前のカビコロニーの直径を初期直径とした。
[Preparation of mold plate with mold]
Cladospodium cladosporoides HMC1064 (bathroom isolate, hereinafter referred to as mold for evaluation) was prepared by culturing at 25 ° C. for 1 week on a potato dextrose agar (Difco) slant medium. Separately, potato dextrose agar (Difco) was filled into a petri dish to prepare an initial plate medium. One point of mold for evaluation was inoculated into the center of the initial plate medium using a nichrome wire in the shape of a cage and cultured at 25 ° C. for 3 days. In this way, mold plate culture mediums 120 (for effect 1), 130 (for effect 2), and 140 (for effect 3) in which mold colonies were formed on the plate medium by culture were prepared. The diameter of the mold colony before the exposure test for each of the mold plates 120, 130, and 140 was set as the initial diameter.

[暴露試験の効果測定]
暴露試験後のカビ付き平板培地120、130、140を回収し、回収したカビ付き平板培地120(効果1:燻煙剤真上)、130(効果2:天井の隅部)、140(効果3:床)を25℃で5日間培養し、下記評価基準に従い、対カビ効果を評価した。
[Measurement of effect of exposure test]
Mold plate media 120, 130, 140 after the exposure test were collected, and the collected mold plate media 120 (effect 1: just above the smoke agent), 130 (effect 2: corner of the ceiling), 140 (effect 3) : Floor) was cultured at 25 ° C. for 5 days, and the antifungal effect was evaluated according to the following evaluation criteria.

[評価基準]
5日間培養した後、カビコロニーの直径(培養後直径)を測定し、下記(1)式により直径差を求めた。
求めた直径差を下記基準に従って分類し、対カビ評価とした。
A:直径差が0〜10mm
B:直径差が10mm超、15mm以下
C:直径差が15mm超
[Evaluation criteria]
After culturing for 5 days, the diameter of the mold colony (the diameter after culturing) was measured, and the difference in diameter was determined by the following formula (1).
The obtained difference in diameter was classified according to the following criteria, and was evaluated against mold.
A: Diameter difference is 0-10mm
B: Diameter difference exceeds 10 mm, 15 mm or less C: Diameter difference exceeds 15 mm

直径差(mm)=培養後直径(mm)−初期直径(mm) ・・・(1)  Diameter difference (mm) = diameter after culture (mm) −initial diameter (mm) (1)

≪対酵母評価≫
[暴露試験]
カビ付き平板培地120(効果1:燻煙剤真上)、130(効果2:天井の隅部)、140(効果3:床)を下記の酵母付き平板培地に換えた以外は、対カビ評価と同様にして暴露試験を行った。
≪Evaluation against yeast≫
[Exposure test]
Evaluation for molds except that the mold-containing plate medium 120 (effect 1: just above the smoke agent), 130 (effect 2: corner of the ceiling), and 140 (effect 3: floor) were replaced with the following plate medium with yeast. The exposure test was conducted in the same manner as above.

[酵母付き平板培地の作製]
ポテトデキストロース寒天の平板培地にて25℃、2日間培養したRhodotorula rubra HIC3420(浴室分離菌、以下、評価用酵母という)を、滅菌した0.05質量%Tween80水溶液にて初発菌数が1×10〜3×10CFU/mLとなるように調整し菌液とした。別途、ポテトデキストロース寒天(Difco社製)をシャーレに充填し、初期平板培地を用意した。初期平板培地に前記菌液0.1mLを塗抹接種し、酵母付き平板培地を作製した。
[Preparation of plate medium with yeast]
Rhodotorula rubra HIC3420 (bathroom isolate, hereinafter referred to as “evaluation yeast”) cultured at 25 ° C. for 2 days in a plate medium of potato dextrose agar has a starting bacterial count of 1 × 10 5 in a sterilized 0.05 mass% Tween 80 aqueous solution. A bacterial solution was prepared by adjusting to 3 to 3 × 10 3 CFU / mL. Separately, potato dextrose agar (Difco) was filled into a petri dish to prepare an initial plate medium. The initial plate medium was smeared with 0.1 mL of the bacterial solution to prepare a plate medium with yeast.

[暴露試験の効果測定]
暴露試験後の酵母付き平板培地を回収し、回収した酵母付き平板培地を25℃で5日間培養した。別途、暴露試験に供さない酵母付き平板培地を同様に培養した。培養後、発現したコロニーを計数し、下記評価基準に従い、対酵母効果を評価した。
[Measurement of effect of exposure test]
The plate medium with yeast after the exposure test was collected, and the collected plate medium with yeast was cultured at 25 ° C. for 5 days. Separately, a plate medium with yeast not subjected to the exposure test was cultured in the same manner. After culturing, the expressed colonies were counted, and the effect on yeast was evaluated according to the following evaluation criteria.

[評価基準]
培養後菌数を常用対数に変換し、下記(2)式によりΔlogを求めた。求めたΔlogを下記基準に従って分類し、対酵母評価とした。
A:Δlogが2以上
B:Δlogが1以上2未満
C:Δlogが1未満
[Evaluation criteria]
After culturing, the number of bacteria was converted to a common logarithm, and Δlog was determined by the following equation (2). The obtained Δlog was classified according to the following criteria and used as a yeast evaluation.
A: Δlog is 2 or more B: Δlog is 1 or more and less than 2 C: Δlog is less than 1

Δlog=log(暴露試験に供さない酵母付き平板培地の培養後菌数)−log(暴露試験に供した酵母付き平板培地の培養後菌数) ・・・(2)  Δlog = log (the number of bacteria after culturing of the plate medium with yeast not subjected to the exposure test) −log (the number of bacteria after the culturing of the plate medium with yeast subjected to the exposure test) (2)

<消臭評価、基剤臭残留評価>
≪暴露試験≫
一般的な家庭で使用されている浴室(1818mmタイプ(メーターモジュール用)の浴室)内の床面の略中央部にホットプレートを設置し、該ホットプレートにアルミニウム箔を敷いた加熱装置を用意した。該加熱装置のアルミニウム箔上に各例の燻煙剤を載せ、350℃に設定したホットプレートで加熱した。ホットプレートでの加熱は、燻煙剤からの発煙開始10分後に停止した。発煙開始90分後に、浴室内の空気を排気し暴露試験を終了した。暴露試験終了後、3名のパネラーが6段階強度表示法により浴室内の臭気を確認した。
<Deodorization evaluation, base odor residue evaluation>
≪Exposure test≫
A hot plate was installed in the approximate center of the floor in a bathroom (1818 mm type (for meter module) bathroom) used in a general household, and a heating device was prepared by laying aluminum foil on the hot plate. . The smoke agent of each example was placed on the aluminum foil of the heating device and heated with a hot plate set at 350 ° C. Heating on the hot plate was stopped 10 minutes after the start of smoking from the smoke smoke agent. 90 minutes after the start of smoke generation, the air in the bathroom was exhausted and the exposure test was completed. After the exposure test, three panelists confirmed the odor in the bathroom using a six-level intensity display method.

≪消臭評価≫
消臭評価は、3名のパネラーが暴露後の浴室臭気(暴露後臭気)について、暴露試験前の浴室内の臭気(初期臭気)を対象とし、6段階強度表示法により採点し、3名の採点結果の平均点を下記評価基準に従って分類し、消臭評価とした。
≪Deodorization evaluation≫
The deodorant evaluation was conducted by three panelists, and the bathroom odor after exposure (post-exposure odor) was targeted for the odor in the bathroom (initial odor) before the exposure test. The average score of the scoring results was classified according to the following evaluation criteria and used as deodorant evaluation.

≪基剤臭残留評価≫
基剤臭残留評価は、3名のパネラーが暴露後臭気について、基剤臭(燻煙剤由来の臭気)を対象とし6段階強度表示法により採点した。3名の採点結果の平均点を下記評価基準に従って分類し、消臭評価とした。
≪Base odor residue evaluation≫
The base odor residual evaluation was scored by a six-level strength display method for the base odor (smell-derived odor) for the odor after exposure by three panelists. The average score of the scoring results of three people was classified according to the following evaluation criteria, and deodorant evaluation was performed.

≪6段階強度表示法≫
0点:臭気は感じられない
1点:臭気をやっとかすかに感じる(検知閾値)
2点:対象とする臭気をらくに感じる(臭気の性質を想像しうる認知閾値)
3点:対象とする臭気を明らかに感じる
4点:対象とする臭気を強く感じる
5点:対象とする臭気を著しく強く感じる
≪6-level intensity display method≫
0 point: The odor is not felt 1 point: The odor is finally felt slightly (detection threshold)
2 points: Easily feel the target odor (recognition threshold that can imagine the nature of the odor)
3 points: The target odor is clearly felt. 4 points: The target odor is strongly felt. 5 points: The target odor is felt strongly.

≪評価基準≫
A:1点未満
B:1点以上、2点未満
C:2点以上、3点未満
D:3点以上
≪Evaluation criteria≫
A: Less than 1 point B: 1 point or more, less than 2 points C: 2 points or more, less than 3 points D: 3 points or more

(実施例1〜29、比較例1〜4)
表1〜5に示す組成に従い、各成分をニーダー(S5−2G型、株式会社モリヤマ製)で攪拌混合した後、水を加えて混合し混合物を得た。得られた混合物を直径2mmの開孔を有するダイスの前押し出し造粒機(EXK−1、株式会社不二パウダル製)を用い造粒し造粒物を得た。得られた造粒物を長さ2〜5mmに切断し、70℃に設定した乾燥機(RT−120HL、アルプ株式会社製)により乾燥させ、顆粒状の燻煙剤を得た。得られた燻煙剤について、表1〜5に記載の使用量を用いて、微生物効力の評価、消臭評価、基剤臭残留評価を行い、その結果を表1〜5に示す。
表中の(A−1)〜(A−3)、(A−5)の組成(質量%)はAg量として記載した。また、表中、微生物効力の対カビ効果の欄には直径差の値、対酵母評価の欄にはΔlogの値、消臭評価及び基剤臭評価には平均点をそれぞれカッコ内に記載した。
(Examples 1 to 29, Comparative Examples 1 to 4)
According to the composition shown in Tables 1 to 5, each component was stirred and mixed with a kneader (S5-2G type, manufactured by Moriyama Co., Ltd.), then water was added and mixed to obtain a mixture. The obtained mixture was granulated using a die pre-extruding granulator (EXK-1, manufactured by Fuji Powder Co., Ltd.) having an opening having a diameter of 2 mm to obtain a granulated product. The obtained granulated product was cut into a length of 2 to 5 mm and dried by a dryer (RT-120HL, manufactured by Alp Co., Ltd.) set at 70 ° C. to obtain a granular smoke agent. About the obtained smoke agent, microbial efficacy evaluation, deodorant evaluation, and base odor residual evaluation were performed using the usage-amount of Tables 1-5, and the result is shown to Tables 1-5.
The composition (mass%) of (A-1) to (A-3) and (A-5) in the table is described as the Ag amount. Also, in the table, the value of the difference in diameter in the column of microbial efficacy against mold, the value of Δlog in the column of evaluation against yeast, and the average score are described in parentheses for deodorant evaluation and base odor evaluation, respectively. .

Figure 2011012051
Figure 2011012051

Figure 2011012051
Figure 2011012051

Figure 2011012051
Figure 2011012051

Figure 2011012051
Figure 2011012051

Figure 2011012051
Figure 2011012051

表1〜5の実施例1〜29の結果のとおり、本発明の燻煙剤は、カビ及び酵母に対して優れた微生物抑制効果を示した。加えて、本発明の燻煙剤は、浴室の消臭効果が高く、かつ基剤臭の残留が少なかった。
(A)成分、(B)成分に(C)成分を併用した実施例19〜29(表4〜5)は、(C)成分を配合しない実施例1〜18に比べ、カビに対する微生物抑制効果が向上した。中でも、(C)成分として酸化亜鉛を用いた実施例22は、(C)成分の種類を変えた実施例23、24に比べて微生物抑制効果の向上が見られた。加えて、(B)成分/(C)成分=10〜140(質量比)とした実施例19〜24、26、27、29には、微生物抑制効果のさらなる向上が見られた(燻煙試験1、カビ評価2)。
As shown in the results of Examples 1 to 29 in Tables 1 to 5, the smoke agent of the present invention showed an excellent microbial inhibitory effect against mold and yeast. In addition, the smoke agent of the present invention has a high deodorizing effect in the bathroom and a small amount of residual base odor.
In Examples 19 to 29 (Tables 4 to 5) in which the (C) component is used in combination with the (A) component and the (B) component, the microbial inhibitory effect against mold is compared to Examples 1 to 18 in which the (C) component is not blended. Improved. Among them, Example 22 using zinc oxide as the component (C) showed an improvement in the microorganism suppressing effect as compared with Examples 23 and 24 in which the type of the component (C) was changed. In addition, in Examples 19 to 24, 26, 27, and 29 in which (B) component / (C) component = 10 to 140 (mass ratio), a further improvement in the microbial control effect was observed (smoke test) 1. Mold evaluation 2).

一方、(A)成分に換えて有機系薬剤であるIPBCを用いた比較例1〜3は、カビに対する微生物抑制効果はあるものの、浴室の消臭効果が低く、かつ基剤臭が残留していた。また、(A)成分に換えて有機系薬剤であるIPMPを用いた比較例4は、カビ及び酵母に対する微生物抑制効果が低かった。加えて、比較例4は、浴室の消臭効果が低く、基剤臭が残留していた。  On the other hand, Comparative Examples 1 to 3 using IPBC, which is an organic chemical instead of component (A), have a microbial control effect against mold, but have a low deodorizing effect in the bathroom and a base odor remains. It was. Moreover, the comparative example 4 which used IPMP which is an organic chemical | medical agent instead of (A) component had a low microorganisms inhibitory effect with respect to mold and yeast. In addition, Comparative Example 4 had a low bathroom deodorizing effect and a base odor remained.

実施例6及び8と、これらの実施例の(A)成分と同量の(A’)成分を配合した比較例3との比較において、本発明の燻煙剤は薬剤の配合量が同じであれば、より高い微生物抑制効果と消臭効果を奏していた。  In comparison between Examples 6 and 8 and Comparative Example 3 in which the same amount of component (A ′) as that of component (A) of these examples was compared, the smoke compound of the present invention had the same compounding amount. If there was, the higher microorganism suppression effect and deodorizing effect were exhibited.

以上の結果から、(A)成分を用いることで、微生物抑制効果、消臭効果の向上が図れると共に、基剤臭の残留を抑制できることが判った。  From the above results, it was found that by using the component (A), the effect of suppressing microorganisms and the effect of deodorizing can be improved, and the residual base odor can be suppressed.

燻煙装置 10
加熱部 20
燻煙剤容器 30
燻煙剤部 32
Smoke device 10
Heating unit 20
Smoke container 30
Smoke agent part 32

Claims (6)

銀を含有する薬剤と、有機発泡剤とを含有することを特徴とする燻煙剤組成物。   A smoke composition comprising a drug containing silver and an organic foaming agent. 前記薬剤は、体積平均粒子径0.01〜1000μmであることを特徴とする、請求項1に記載の燻煙剤組成物。   The smoke agent composition according to claim 1, wherein the drug has a volume average particle diameter of 0.01 to 1000 μm. 前記有機発泡剤は、アゾジカルボンアミドであることを特徴とする、請求項1又は2に記載の燻煙剤組成物。   The soot agent composition according to claim 1 or 2, wherein the organic foaming agent is azodicarbonamide. さらに、発泡助剤として酸化亜鉛、炭酸亜鉛、ステアリン酸亜鉛、ステアリン酸マグネシウム、酸化マグネシウム、炭酸カルシウム及びリン酸カルシウムからなる群から選択される1種以上を含有することを特徴とする、請求項1〜3のいずれか1項に記載の燻煙剤組成物。   Furthermore, it contains at least one selected from the group consisting of zinc oxide, zinc carbonate, zinc stearate, magnesium stearate, magnesium oxide, calcium carbonate and calcium phosphate as a foaming aid. 4. The smoke agent composition according to any one of 3 above. 請求項1〜4のいずれか1項に記載の燻煙剤組成物を充填した燻煙剤部と、加熱部と、該加熱部で生じた熱を前記燻煙剤部に伝える伝熱部とを有することを特徴とする、燻煙装置。   A smoke agent part filled with the smoke agent composition according to any one of claims 1 to 4, a heating part, and a heat transfer part that transmits heat generated in the heating part to the smoke agent part. A smoke device characterized by comprising: 請求項1〜4のいずれか1項に記載の燻煙剤組成物を間接的に加熱することを特徴とする、燻煙方法。   A smoke method, wherein the smoke agent composition according to any one of claims 1 to 4 is indirectly heated.
JP2010115502A 2009-06-02 2010-05-19 Smoke agent composition for indirect heating method, indirect heating method smoke device and smoke method Active JP5647815B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2010115502A JP5647815B2 (en) 2009-06-02 2010-05-19 Smoke agent composition for indirect heating method, indirect heating method smoke device and smoke method

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2009133119 2009-06-02
JP2009133119 2009-06-02
JP2010115502A JP5647815B2 (en) 2009-06-02 2010-05-19 Smoke agent composition for indirect heating method, indirect heating method smoke device and smoke method

Publications (2)

Publication Number Publication Date
JP2011012051A true JP2011012051A (en) 2011-01-20
JP5647815B2 JP5647815B2 (en) 2015-01-07

Family

ID=43506582

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010115502A Active JP5647815B2 (en) 2009-06-02 2010-05-19 Smoke agent composition for indirect heating method, indirect heating method smoke device and smoke method

Country Status (2)

Country Link
JP (1) JP5647815B2 (en)
KR (1) KR101681774B1 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013032427A (en) * 2011-08-01 2013-02-14 Eiwa Kasei Kogyo Kk Gas generating agent for producing foam
WO2013179805A1 (en) * 2012-05-30 2013-12-05 ライオン株式会社 Smoking agent and smoking device
JP2013249264A (en) * 2012-05-30 2013-12-12 Lion Corp Smoking agent and smoking device
JP2014047150A (en) * 2012-08-30 2014-03-17 Lion Corp Smoking agent and smoking device
JP2014224103A (en) * 2013-04-17 2014-12-04 ライオン株式会社 Granular smoking agent composition
WO2015159816A1 (en) * 2014-04-16 2015-10-22 ライオン株式会社 Self-jetting spatial processing agent
JP2016008201A (en) * 2014-06-25 2016-01-18 ライオン株式会社 Smoking agent
JP2016202868A (en) * 2015-04-17 2016-12-08 大日本除蟲菊株式会社 Smoking antifungal method
JP2017008042A (en) * 2015-06-18 2017-01-12 アース製薬株式会社 Bactericidal agent

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07309706A (en) * 1991-12-04 1995-11-28 Taihei Kagaku Sangyo Kk Antibacterial/antifungal spray liquid
JP3048323U (en) * 1997-10-23 1998-05-06 株式会社共栄商興 Antibacterial candle
JP3051248U (en) * 1997-10-23 1998-08-21 株式会社共栄商興 Antibacterial incense stick
JPH11246306A (en) * 1998-02-25 1999-09-14 Chugai Pharmaceut Co Ltd Fumigant composition
JP2003286104A (en) * 2002-03-26 2003-10-07 Nippon Soda Co Ltd Mildewproofing method for bathroom
JP2004059442A (en) * 2002-07-25 2004-02-26 Chugai Pharmaceut Co Ltd Fungicide for washing tub, fungicidal apparatus for washing tub comprising the same and fungicidal method for washing tub

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5677202A (en) 1980-08-06 1981-06-25 Earth Chem Corp Ltd Fumigating drug composition
JP3035829B2 (en) * 1989-04-06 2000-04-24 株式会社小森コーポレーション A method for adjusting a gap in a sheet feeding safety device of a sheet-fed printing press
JP3051248B2 (en) * 1992-02-07 2000-06-12 株式会社宮本工業所 Cremation furnace
JP3941893B2 (en) * 1997-04-24 2007-07-04 アース製薬株式会社 Fumigant composition and fumigation method
JP4410057B2 (en) 2003-08-08 2010-02-03 ライオン株式会社 Antifungal fumigating agent, apparatus, and processing method
JP4920377B2 (en) 2006-11-17 2012-04-18 ライオン株式会社 Smoke composition

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07309706A (en) * 1991-12-04 1995-11-28 Taihei Kagaku Sangyo Kk Antibacterial/antifungal spray liquid
JP3048323U (en) * 1997-10-23 1998-05-06 株式会社共栄商興 Antibacterial candle
JP3051248U (en) * 1997-10-23 1998-08-21 株式会社共栄商興 Antibacterial incense stick
JPH11246306A (en) * 1998-02-25 1999-09-14 Chugai Pharmaceut Co Ltd Fumigant composition
JP2003286104A (en) * 2002-03-26 2003-10-07 Nippon Soda Co Ltd Mildewproofing method for bathroom
JP2004059442A (en) * 2002-07-25 2004-02-26 Chugai Pharmaceut Co Ltd Fungicide for washing tub, fungicidal apparatus for washing tub comprising the same and fungicidal method for washing tub

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013032427A (en) * 2011-08-01 2013-02-14 Eiwa Kasei Kogyo Kk Gas generating agent for producing foam
CN104349670B (en) * 2012-05-30 2016-05-25 狮王株式会社 Fumigant and fumigating device
WO2013179805A1 (en) * 2012-05-30 2013-12-05 ライオン株式会社 Smoking agent and smoking device
JP2013249264A (en) * 2012-05-30 2013-12-12 Lion Corp Smoking agent and smoking device
JP2013249262A (en) * 2012-05-30 2013-12-12 Lion Corp Smoking agent and smoking device
CN104349670A (en) * 2012-05-30 2015-02-11 狮王株式会社 Smoking agent and smoking device
TWI574620B (en) * 2012-05-30 2017-03-21 獅子股份有限公司 Smoking agent and smoking device
JP2014047150A (en) * 2012-08-30 2014-03-17 Lion Corp Smoking agent and smoking device
JP2014224103A (en) * 2013-04-17 2014-12-04 ライオン株式会社 Granular smoking agent composition
JP2015044874A (en) * 2013-04-17 2015-03-12 ライオン株式会社 Method for manufacturing granular smoking agent composition
WO2015159816A1 (en) * 2014-04-16 2015-10-22 ライオン株式会社 Self-jetting spatial processing agent
JP2016008201A (en) * 2014-06-25 2016-01-18 ライオン株式会社 Smoking agent
JP2016202868A (en) * 2015-04-17 2016-12-08 大日本除蟲菊株式会社 Smoking antifungal method
JP2017008042A (en) * 2015-06-18 2017-01-12 アース製薬株式会社 Bactericidal agent
JP2021001233A (en) * 2015-06-18 2021-01-07 アース製薬株式会社 Bactericidal agent
JP7051967B2 (en) 2015-06-18 2022-04-11 アース製薬株式会社 Disinfectant

Also Published As

Publication number Publication date
JP5647815B2 (en) 2015-01-07
KR20100130151A (en) 2010-12-10
KR101681774B1 (en) 2016-12-01

Similar Documents

Publication Publication Date Title
JP5647815B2 (en) Smoke agent composition for indirect heating method, indirect heating method smoke device and smoke method
JP5903335B2 (en) Smoke agent for indirect heating method and smoke device for indirect heating method
JP5903334B2 (en) Smoke agent and smoke device
JP4920377B2 (en) Smoke composition
JP2010280577A (en) Fumigant composition and fumigation apparatus
JP2014210714A (en) Smoking agent composition
JP6014423B2 (en) Smoke agent and smoke device
JP6621324B2 (en) Smoke agent and smoke device
JP6850668B2 (en) Smoke agent composition
JP6688703B2 (en) Smoke agent composition
JP2017225356A (en) Indirect heating type smoking device
JP5887395B2 (en) Mold anti-smoke composition for bathroom and anti-smoke device for bathroom
JP6225354B2 (en) Smoke agent
JP2015091876A (en) Antifungal smoking apparatus for bath room
JP6635589B2 (en) Antifungal composition
JP6850669B2 (en) Smoke agent composition
JP6489696B2 (en) Indirect heating smoke composition
JP5891289B2 (en) Mold-proof smoke smoking agent composition for bathroom
JP6322176B2 (en) Disinfection method
JP6614961B2 (en) Smoke agent and smoke device
JP2014210712A (en) Smoking agent composition and smoking device
JP7149814B2 (en) disinfectant composition
JP2021183570A (en) Microorganism control method
JP2023064833A (en) Antibacterial or antivirus treatment method
JP2019048772A (en) Smoking agent composition

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20130121

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20140220

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20140225

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20140428

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: 20141014

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20141110

R150 Certificate of patent or registration of utility model

Ref document number: 5647815

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350