JP3160860B2 - Eradication and antibacterial agents - Google Patents

Eradication and antibacterial agents

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Publication number
JP3160860B2
JP3160860B2 JP29101398A JP29101398A JP3160860B2 JP 3160860 B2 JP3160860 B2 JP 3160860B2 JP 29101398 A JP29101398 A JP 29101398A JP 29101398 A JP29101398 A JP 29101398A JP 3160860 B2 JP3160860 B2 JP 3160860B2
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Prior art keywords
rice vinegar
experimental example
component
bacteria
concentration
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JP2000119117A (en
Inventor
勇 能沢
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有限会社まるイ ノザワ物産
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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は除菌・抗菌剤に関す
る。
[0001] The present invention relates to a disinfectant / antibacterial agent.

【0002】[0002]

【従来の技術】広葉樹(ナラ)、針葉樹(松、桧)の間
伐材を炭化させて発生する排煙を冷却して得られる液体
物質としての木酢は、防虫、消臭、作物の活性化、土壌
改良など農業を中心に多くの用途に活用されている。こ
れらの乾留物質は、天然物質から生成されたものであ
り、これが流出しても分解力が高いため、環境汚染に与
える影響が殆どないものと考えられる。これらの乾留液
体は、80乃至90%が水分であり、これに酢酸、アル
コール、エステル、アルデヒド、フェノールなど200
数種の含有成分が定性的に知られている。したがって、
土壌消臭効果は、ホルムアルデヒドとその誘導体類を中
心として、他に酢酸、蟻酸、アルコール類によるものと
考えられる。一方、籾殻の乾留物質である籾酢液は、木
酢に比べて、タールなどの粘稠性物質が少ないため、原
液と水の親和性が高く、水道水で希釈しても容器を汚す
可能性が小さい。従って、容易に希釈できる利点が有る
ため、経済的な面も含めて木酢以上に利用価値が有るも
のと推定される。すなわち、籾殻は米作農業の副産物と
して多量に発生するため、籾殻の新しい有効利用が期待
できる。また、細菌では、各種の抗菌商品が開発されて
いるが、大部分が化学物質を利用しているため、副作用
が危惧される。
2. Description of the Related Art Wood vinegar as a liquid substance obtained by cooling flue gas generated by carbonizing thinned wood (oak) and conifer (pine, cypress) thinned wood is used as an insect repellent, deodorant, activating crops, It is used for many purposes mainly in agriculture such as soil improvement. These carbonized substances are generated from natural substances and have a high decomposability even if they flow out, so they are considered to have little effect on environmental pollution. In these dry distillation liquids, 80 to 90% is moisture, and acetic acid, alcohol, ester, aldehyde, phenol, etc.
Several components are qualitatively known. Therefore,
The soil deodorizing effect is considered to be mainly due to formaldehyde and its derivatives, and also to acetic acid, formic acid, and alcohols. On the other hand, rice husk liquor, which is a dry distillation material of rice husks, has less affinity for tar and other viscous substances than wood vinegar. Is small. Therefore, it has an advantage that it can be easily diluted, and it is presumed that it has more utility value than wood vinegar including economical aspects. In other words, rice husk is generated in large quantities as a by-product of rice agriculture, and new effective use of rice husk can be expected. In addition, various antibacterial products have been developed for bacteria, but most of them use chemical substances, so there are concerns about side effects.

【0003】[0003]

【発明が解決しようとする課題】解決しようとする課題
は、除菌及び抗菌能力が高く、しかも、副作用がなくて
且つ燻醸臭をともなわない有用な除菌・抗菌剤を提供す
ることにある。
An object of the present invention is to provide a useful disinfectant / antibacterial agent which has high antibacterial and antibacterial abilities, has no side effects, and has no smoked odor. .

【0004】[0004]

【課題を解決するための手段】本発明は前記した課題を
達成するため、原籾酢成分と希釈成分からなり、この
希釈成分としての生理食塩水で希釈される前記原籾酢成
分が全体の1〜5%になる比率関係に調整してある燻醸
臭が無いことを特徴とする。
Means for Solving the Problems In order to achieve the above-mentioned object, the present invention comprises a raw rice vinegar component and a diluting component, and the raw rice vinegar component diluted with a physiological saline as the diluting component is used as a whole. Characterized in that there is no smoked odor adjusted to a ratio relationship of 1 to 5% of

【0005】[0005]

【発明の実施の形態】以下、本発明の実施の1形態につ
いて詳細に説明する。除菌・抗菌剤は、原籾酢成分と希
釈成分で構成しており、この希釈成分としての生理食塩
水で希釈される前記原籾酢成分が全体の1〜5%になる
比率関係になるように調整してある。 <具体例1> 除菌・抗菌剤は、原籾酢成分と希釈成分の比率関係が、
原籾酢成分が全体の1%になるように希釈成分としての
生理食塩水で希釈して構成してある。 <具体例2> 除菌・抗菌剤は、原籾酢成分と希釈成分の比率関係が、
原籾酢成分が全体の3%になるように希釈成分としての
生理食塩水で希釈して構成してある。 <具体例3> 除菌・抗菌剤は、原籾酢成分と希釈成分の比率関係が、
原籾酢成分が全体の5%になるように希釈成分としての
生理食塩水で希釈して構成してある。 <比較例1> 試験剤は、生理食塩水のみで構成してある。 <比較例2> 試験剤は、原籾酢成分と希釈成分の比率関係が、原籾酢
成分が全体の7%になるように希釈成分としての生理食
塩水で希釈して構成した。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS One embodiment of the present invention will be described below in detail. The disinfecting and antibacterial agent is composed of raw rice vinegar and a diluting component.
The ratio is adjusted so that the ratio of the raw rice vinegar component diluted with water is 1 to 5% of the whole. <Specific example 1> The ratio of the ratio between the raw rice vinegar component and the diluting component is
Raw rice vinegar is diluted with physiological saline as a diluting component so as to make up 1% of the whole. <Specific Example 2> The ratio of the ratio between the unhulled vinegar component and the diluting component in the disinfecting / antibacterial agent was
Raw rice vinegar is diluted with a physiological saline solution as a diluting component so that the component becomes 3% of the whole. <Specific Example 3> The ratio of the ratio between the unhulled rice vinegar component and the diluting component is as follows.
Raw rice vinegar is diluted with physiological saline as a diluting component so that the vinegar component is 5% of the whole. <Comparative Example 1> The test agent was composed of only physiological saline. <Comparative Example 2> The test agent was configured by diluting with physiological saline as a diluting component so that the ratio relationship between the raw rice vinegar component and the diluting component was 7% of the whole.

【0006】実験に供する大腸菌および黄色ぶどう球菌
含有溶液の調整は、スラント上の大腸菌(Eshelichia c
oli AHU1714)或いは黄色ぶどう球菌(Staphy loco
cusaureus cowan)を白金耳でかき取り、減菌済みの0.8
5%生理食塩水9mlで混合希釈した。さらに、この混合
希釈液を生理食塩水で100倍に希釈した。実験は、先
ず、各試験管に生理食塩水を8ml加え、これに大腸菌群
又は黄色ぶどう球菌含有溶液を1mlづつ加えた後、前記
した具体例1、具体例2、具体例3の各除菌・抗菌剤、
そして、比較例2の試験剤を夫々1ml加えて、各全容量
を10mlにした。後の表1では、具体例1を加えたもの
を実験例1とし、具体例2を加えたものを実験例2と
し、具体例3を加えたものを実験例3とし、比較例2を
加えたものを実験例Bとした。尚、比較例1による実験
例Aについては、大腸菌群又は黄色ぶどう球菌含有溶液
各1mlと生理食塩水9ml加えて、各全容量を10mlにし
た。次に、タッチミキサーで30秒間攪拌し、20℃で2
時間保温した。その後、試験管内の溶液を1ml取り出
し、生菌数の測定に供した。大腸菌の測定は、デスオキ
シコレート培地をシャーレに約15ml加えて固めた後、
更に、5ml加えて重層後、37℃で24時間培養後のコ
ロニー数を計測した。又、黄色ぶどう球菌の測定は、標
準寒天培地をシャーレに約15ml加え、37℃で48時
間培養後、シャーレ中のコロニー数を計測(表1参照)
した。
[0006] Preparation of the E. coli and Staphylococcus aureus-containing solution to be used for the experiment was carried out by using Eshelichia c.
oli AHU1714) or Staphylococcus
cusaureus cowan) with a platinum loop and sterilized 0.8
The mixture was diluted with 9 ml of 5% saline. Further, this mixed diluted solution was diluted 100 times with physiological saline. In the experiment, first, 8 ml of physiological saline was added to each test tube, and 1 ml of a solution containing coliform bacteria or Staphylococcus aureus was added thereto at a time, and then each of the eradication of the above-mentioned specific examples 1, 2 and 3 was removed.・ Antibacterial agent,
Then, 1 ml of each of the test agents of Comparative Example 2 was added to bring the total volume to 10 ml. In Table 1 below, the result obtained by adding the specific example 1 is referred to as Experimental example 1, the result obtained by adding the specific example 2 is referred to as Experimental example 2, the result obtained by adding the specific example 3 is referred to as Experimental example 3, and the comparative example 2 is added. This was designated as Experimental Example B. In the case of Experimental Example A according to Comparative Example 1, 1 ml each of a solution containing coliform bacteria or Staphylococcus aureus and 9 ml of physiological saline were added to make the total volume of each solution 10 ml. Next, stir with a touch mixer for 30 seconds,
Incubated for hours. Thereafter, 1 ml of the solution in the test tube was taken out and provided for measurement of the viable cell count. For the measurement of Escherichia coli, about 15 ml of desoxycholate medium was added to a petri dish and hardened.
Further, 5 ml was added, and after overlaying, the number of colonies after culturing at 37 ° C for 24 hours was counted. For measurement of Staphylococcus aureus, about 15 ml of a standard agar medium was added to a Petri dish, and after culturing at 37 ° C. for 48 hours, the number of colonies in the Petri dish was counted (see Table 1).
did.

【0007】[0007]

【表1】 [Table 1]

【0008】表1によれば、実験例1〜3は、大腸菌
群、黄色ぶどう球菌ともに実験例Aに比べて著しく減少
した。この除菌能力は実験例Bに示されるように原籾酢
濃度が高いほど効果が大きく、実験例3では、大腸菌群
で約95%、黄色ぶどう球菌で100%除菌したことに
なる。一方、除菌能力が高い実験例Bでは、燻醸臭が有
る。このことから、原籾酢濃度が1〜5%である実験例
1〜3が、大腸菌群、黄色ぶどう球菌を効率良く除菌で
き且つ燻醸臭が無いことが確認された。
According to Table 1, in Examples 1 to 3, both the coliforms and Staphylococcus aureus were significantly reduced as compared to Example A. As shown in Experimental Example B, the higher the concentration of raw rice vinegar, the greater the effect of this sterilization ability. In Experimental Example 3, about 95% of the coliform bacteria were removed and 100% of the Staphylococcus aureus were removed. On the other hand, in Experimental Example B having a high sterilization ability, there is a smoked smell. From this, it was confirmed that in Experimental Examples 1 to 3 in which the raw rice vinegar concentration was 1 to 5%, the coliform group and Staphylococcus aureus could be efficiently eliminated and there was no smoked smell.

【0009】[0009]

【表2】 [Table 2]

【0010】表2には、前記した表1の実験における大
腸菌群数が約2倍多い溶液を供試して、同様に実験し、
30分および7日間保温した場合の除菌能力を示してい
る。30分間保温では、表1の2時間保温に比べて実験
例4及び5は除菌率が低かったが、実験例6は96%の
高い除菌率を示した。さらに、7日間保温した場合に
は、実験例4〜6ともに菌数が検出されなかった。した
がって、大腸菌群数が多い場合においても、30分保温
では原籾酢が5%濃度である実験例6のもののように9
5%除菌でき、そして、7日間保温では原籾酢が1%濃
度の実験例4のものでも100%除菌できることが確認
され、且つ、燻醸臭が無いことが確認された。
[0010] In Table 2, a solution containing about twice the number of coliform bacteria in the experiment of Table 1 was used, and the same experiment was performed.
It shows the germicidal ability when the temperature was kept for 30 minutes and for 7 days. In the 30-minute incubation, the eradication rates of Experimental Examples 4 and 5 were lower than those of the 2-hour incubation in Table 1, but Experimental Example 6 showed a high 96% eradication rate. Furthermore, when the temperature was kept for 7 days, the number of bacteria was not detected in all of Experimental Examples 4 to 6. Therefore, even when the number of coliforms is large, 9 hours, as in the case of Experimental Example 6, where the raw rice vinegar has a 5% concentration in the 30-minute incubation.
It was confirmed that 5% of the bacteria could be removed, and that it was possible to remove 100% of the unhulled vinegar even in the case of Experimental Example 4 having a concentration of 1%, and that there was no smoked smell when kept warm for 7 days.

【0011】表3は、下水処理水の流入量が多くて、大
腸菌群及び栄養塩濃度が高い水質の河川(新川河川:札
幌市手稲区第1新川橋地点)から採取した試料の測定結
果である。除菌・抗菌剤の調整及び大腸菌群の測定は、
前記した表1における方法にしたがった。すなわち、各
試験管に全容積10mlとなるように試料8mlをそれぞれ
加え、これに調整済みの大腸菌群含有溶液及び具体例1
〜3の各除菌・抗菌剤、比較例2を1mlづつ加え、タッ
チミキサーで30秒間攪拌した後、20℃で30分間保
温して大腸菌群の測定をし、また、20℃で2時間保温
して一般生菌数の測定を行なった。後の表3では、具体
例1を加えたものを実験例7とし、具体例2を加えたも
のを実験例8とし、具体例3を加えたものを実験例9と
し、比較例2を加えたものを実験例Eとした。
[0011] Table 3 shows the measurement results of samples collected from a river (Shinkawa River: No. 1 Shinkawa Bridge, Teine-ku, Sapporo-shi) with a high inflow of treated sewage water and a high quality of coliform bacteria and nutrient salts. is there. Preparation of eradication and antibacterial agents and measurement of coliform bacteria
According to the method in Table 1 described above. That is, 8 ml of the sample was added to each test tube so that the total volume became 10 ml, and the adjusted E. coli group-containing solution and the specific example 1 were added thereto.
Add 1 ml of each of the bactericidal and antibacterial agents of Comparative Example 2 to Comparative Example 2 and stir with a touch mixer for 30 seconds. Then, keep the temperature at 20 ° C for 30 minutes to measure coliform bacteria, and keep the temperature at 20 ° C for 2 hours. Then, the number of general viable bacteria was measured. In Table 3 below, the result obtained by adding the specific example 1 is referred to as Experimental example 7, the result obtained by adding the specific example 2 is referred to as Experimental example 8, the result obtained by adding the specific example 3 is referred to as Experimental example 9, and the comparative example 2 is added. This was designated as Experimental Example E.

【0012】[0012]

【表3】 [Table 3]

【0013】[0013]

【表4】 [Table 4]

【0014】表3は、試料水の腸内細菌に対する30分
間保温後の除菌能力を示しており、除菌能は籾酢濃度が
高いほど上昇し、籾酢濃度が1%である実験例7のもの
では20%、籾酢濃度が3%である実験例8のものでは
80%、籾酢濃度が5%である実験例9のものでは85
%の除菌率を示した。これにより、汚染の進んでいる河
川では籾酢濃度が3%以上であると除菌能が高くなるこ
とが確認された。表4は、試料水の一般生菌に対する2
時間保温後の除菌能力を示しており、除菌率は籾酢濃度
が1%である実験例7のもので60%、籾酢濃度が3%
である実験例8のもので85%、籾酢濃度が5%である
実験例9のもので94%であり、大腸菌群と同様に籾酢
濃度が高くなるのにつれて除菌効果が高まることが確認
された。また、一般生菌は大腸菌群に比べて除菌され易
く、これは保温時間の影響によるものと考えられる。以
上のことから、籾酢濃度が5%である実験例9のもので
は約2時間保温により大腸菌群及び/又は黄色ぶどう球
菌の90%以上の除菌が可能で且つ燻醸臭が無いことが
確認された。
Table 3 shows the disinfecting ability of the sample water after incubating for 30 minutes against intestinal bacteria. The disinfecting ability increases as the concentration of rice vinegar increases and the concentration of rice vinegar is 1%. In the case of Example 7, 20%, in the case of Experimental Example 8 in which the concentration of rice vinegar is 3%, 80%, and in the case of Experimental Example 9, in which the concentration of rice vinegar is 5%, 85%.
% Eradication rate. Thus, it was confirmed that in a river with a high degree of contamination, the sterilization ability was increased when the concentration of rice vinegar was 3% or more. Table 4 shows 2 samples for general living bacteria of sample water.
It shows the bactericidal ability after heat retention for 60 hours, and the bactericidal rate is 60% in the case of Experimental Example 7 in which the concentration of rice vinegar is 1%, and the concentration of rice vinegar is 3%.
It is 85% in the case of Experimental Example 8 and 94% in the case of Experimental Example 9 in which the concentration of rice vinegar is 5%. Like the coliform group, the eradication effect increases as the concentration of rice vinegar increases. confirmed. In addition, general viable bacteria are more easily eradicated than the coliform group, which is considered to be due to the effect of the heat retention time. From the above, in the case of Experimental Example 9 in which the concentration of rice vinegar is 5%, it is possible to eliminate 90% or more of the coliform bacteria and / or Staphylococcus aureus by keeping the temperature for about 2 hours, and there is no smoked smell. confirmed.

【0015】表5は、海水が混じった河口(小樽運河:
小樽市手宮側の仲川河口部地点)から採取した試料の測
定結果である。除菌・抗菌剤の調整及び大腸菌群の測定
は、前記した表1における方法にしたがった。全容積1
0mlとなるように各試験管に試料9mlを入れ、これに具
体例3の除菌・抗菌剤、籾酢濃度が10%の試験剤を1
ml加えて、タッチミキサーで30秒間攪拌した後、20
℃で2時間保温した。その後に、試験管内から試料1ml
を取り出し、これを減菌済みシャーレに入れ、一般生菌
と大腸菌群数を測定した。一般生菌数の測定は標準寒天
培地をシャーレに約15ml加え、48時間培養後、シャ
ーレ中のコロニー数を計測した。生菌数の測定は前記し
た表1のものと同様である。後の表5では、具体例3を
加えたものを実験例10とし、籾酢濃度10%の試験剤
を加えたものを実験例Fとした。
Table 5 shows the estuary (Otaru Canal:
This is a measurement result of a sample collected from the Nakagawa estuary point on the Temiya side of Otaru City. Preparation of the bacteria-eliminating / antibacterial agent and measurement of the coliform bacteria were performed according to the methods in Table 1 described above. Total volume 1
9 ml of a sample is put into each test tube so as to be 0 ml, and the sterilizing / antibacterial agent of Example 3 and the test agent having a rice vinegar concentration of 10% are added to each tube.
Add 30 ml with a touch mixer and stir for 20 seconds.
Incubated at 2 ° C. for 2 hours. Then, sample 1 ml from the test tube
Was taken out and placed in a sterilized petri dish, and the numbers of general viable bacteria and coliforms were measured. For the measurement of the number of general viable bacteria, about 15 ml of a standard agar medium was added to a Petri dish, and after culturing for 48 hours, the number of colonies in the Petri dish was counted. The measurement of the viable cell count is the same as that in Table 1 described above. In Table 5 below, the one to which the specific example 3 was added was set as an experimental example 10, and the one to which a test agent having a rice vinegar concentration of 10% was added was set as an experimental example F.

【0016】[0016]

【表5】 [Table 5]

【0017】表5は、籾酢濃度5%の除菌・抗菌剤によ
る2時間保温後の大腸菌群及び一般生菌の除菌能力を示
しており、除菌率は大腸菌群で85%、一般生菌で80
%であり、除菌率は試料の生菌数が少ない割には表1及
び表3における実験例と比べて10%程度低かった。こ
れは、試料に海水が約8割程度含まれ、このことが、生
菌の耐除菌性を高めたのかもしれない。このように、籾
酢濃度が5%である除菌・抗菌剤を用いて2時間保温す
ることにより、大腸菌群、一般生菌ともに約90%以上
の除菌が可能であり、さらに、7日間保温では100%
除菌可能であると推定され、且つ、燻醸臭が無いことが
確認された。
Table 5 shows the bactericidal abilities of the coliforms and general viable bacteria after incubation for 2 hours with a sterilizing / antibacterial agent having a rice vinegar concentration of 5%. 80 with live bacteria
%, And the eradication rate was about 10% lower than the experimental examples in Tables 1 and 3 in spite of the small number of viable bacteria in the sample. This means that the sample contains about 80% of seawater, which may have improved the bactericidal resistance of viable bacteria. In this way, by maintaining the temperature for 2 hours using a disinfectant / antibacterial agent having a rice vinegar concentration of 5%, it is possible to remove about 90% or more of both the coliforms and general viable bacteria, and further for 7 days 100% for keeping warm
It was estimated that the bacteria could be removed, and it was confirmed that there was no smoking odor.

【0018】[0018]

【発明の効果】A.請求項1により、除菌及び抗菌能力
が高く、しかも、副作用がなくて且つ燻醸臭をともなわ
ないから、河川、調整池、汚水処理場等に有用であると
共に、食品、食器の洗浄に有用であり、消毒、除菌、抗
菌を必要とされる用途に広範囲に活用できる。
A. Effects of the Invention According to claim 1, since it has high antibacterial and antibacterial abilities, and has no side effects and no odor of smoking, it is useful for rivers, regulating ponds, sewage treatment plants, etc., and also for cleaning foods and dishes. It can be widely used for applications requiring disinfection, disinfection, and antibacterial.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 原籾酢成分と希釈成分からなり、この
希釈成分としての生理食塩水で希釈される前記原籾酢成
分が全体の1〜5%になる比率関係に調整してある燻醸
臭が無いことを特徴とする除菌・抗菌剤。
1. A smoke comprising a raw rice vinegar component and a diluting component , wherein the ratio of the raw rice vinegar component diluted with physiological saline as a diluting component is adjusted to 1 to 5% of the whole. Disinfectant and antibacterial agent characterized by no odor.
JP29101398A 1998-10-13 1998-10-13 Eradication and antibacterial agents Expired - Fee Related JP3160860B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29101398A JP3160860B2 (en) 1998-10-13 1998-10-13 Eradication and antibacterial agents

Publications (2)

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JP2000119117A JP2000119117A (en) 2000-04-25
JP3160860B2 true JP3160860B2 (en) 2001-04-25

Family

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Application Number Title Priority Date Filing Date
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Country Link
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Also Published As

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