JP2005278523A - Microorganism carrying material - Google Patents

Microorganism carrying material Download PDF

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JP2005278523A
JP2005278523A JP2004097863A JP2004097863A JP2005278523A JP 2005278523 A JP2005278523 A JP 2005278523A JP 2004097863 A JP2004097863 A JP 2004097863A JP 2004097863 A JP2004097863 A JP 2004097863A JP 2005278523 A JP2005278523 A JP 2005278523A
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microorganism
cellulose sponge
cleaner
weight
dry
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Tomiji Matsuki
富二 松木
Ichiro Murakami
一郎 村上
Yukiyoshi Mori
幸由 森
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Toyo Shokusan Inc
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Toyo Shokusan Inc
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W10/00Technologies for wastewater treatment
    • Y02W10/10Biological treatment of water, waste water, or sewage

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  • Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
  • Soil Conditioners And Soil-Stabilizing Materials (AREA)
  • Fertilizers (AREA)
  • Farming Of Fish And Shellfish (AREA)
  • Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
  • Biological Treatment Of Waste Water (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a microorganism carrying material avoiding the environmental conservation problem of the residue of carrier in an extended slow-acting fertilizer, keeping sufficient water-absorption and water retention, developing good fermentation culture property in the production of extended slow-acting fertilizer, and giving an extended slow-acting fertilizer exhibiting excellent performance as a fermentation material such as the decomposition and composting of organic materials. <P>SOLUTION: The purpose can be achieved by a microorganism carrying material prepared by impregnating an organic carrier obtained by mixing a cellulose sponge having an apparent density of 0.025-0.05 [g(dry)/cm<SP>3</SP>(wet)] with a cellulose sponge having an apparent density of 0.025-0.05 [g(dry)/cm<SP>3</SP>(wet)], preferably a cellulose sponge, in an amount of ≥5 wt.% in dried state with an aqueous solution of microorganisms, and carrying out the fermentation culture of the microorganism. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は微生物が担持された資材、さらに詳しくは、微生物培養液をセルロース製スポンジが混合された有機物担体に含浸し、発酵培養させて成る微生物担持資材に関する。   The present invention relates to a material on which microorganisms are supported, and more specifically to a microorganism-supporting material obtained by impregnating a microorganism culture solution into an organic carrier mixed with cellulose sponge and subjecting it to fermentation culture.

微生物は、一般的に水溶液状の培地に添加されて市販されている。この微生物含有の培養液は、排水の環境浄化効果および無農薬肥料源等のボカシ肥を製造する際の原液として有効であり注目されている。ボカシ肥製造で用いる場合には、担体物質として籾殻、米糠、椰子殻、蕎麦殻等の穀物の殻、大鋸屑、木屑等の有機物に、培養液を噴霧状、シャワー状等で混合して含浸し、発酵培養することが知られている(例えば特許文献1および2)。   Microorganisms are generally added to an aqueous medium and marketed. This microorganism-containing culture solution is effective as an undiluted solution for producing a blur fertilizer such as an environmental purification effect of drainage and an agrochemical-free fertilizer source. When used in the manufacture of Bokashi fertilizer, the culture medium is mixed and impregnated as a carrier material in organic matter such as grain husks, rice husks, coconut husks, buckwheat husks, etc. It is known to perform fermentation culture (for example, Patent Documents 1 and 2).

これに対する改善策としては、鋳物砂、セラミックス、コンクリート片、汚泥砂、レンガ、ガラス繊維、ロックウール、瓦、パーライト、廃粘土、焼却炉灰等の多孔質の無機物担体を有機物に併用させることが知られている(例えば特許文献3および4)。
特開平9−328682号公報 特開2002−306158号公報 特開2002−121092号公報 特開2003−199434号公報
As an improvement measure against this, it is possible to use a porous inorganic carrier such as foundry sand, ceramics, concrete pieces, sludge sand, brick, glass fiber, rock wool, tile, perlite, waste clay, incinerator ash, etc. in combination with organic matter. Known (for example, Patent Documents 3 and 4).
Japanese Patent Laid-Open No. 9-328682 JP 2002-306158 A JP 2002-121092 A JP 2003-199434 A

従来の微生物担持資材、特にボカシ肥の場合、担体物質として用いる上記有機物のみでは(1)吸水性および保水性が不十分、(2)微生物の定着に必要な空隙部の存在が不十分で微生物繁殖のための好気性と嫌気性のバランスが不良となり、発酵培養させるのに長期間必要となり、(3)期待するボカシ肥としての効果が小さい、等の問題があり十分満足できるものではなかった。   In the case of conventional microorganism-carrying materials, especially Bokashi fertilizer, the above organic substance used as a carrier substance alone is (1) insufficient water absorption and water retention, and (2) the presence of voids necessary for colonization of microorganisms is insufficient. The balance between aerobic and anaerobic for breeding was poor, and it was necessary for fermentation culture for a long time, and (3) it was not satisfactory because there were problems such as small effect as expected bog fertilizer .

上述の従来技術のように、無機物担体を併用した場合、これら無機物は自然界において通常極めて分解し難く、無機物担体そのものがボカシ肥に残存し、更に、長期的には土壌中等に残存蓄積してしまうという課題があった。   When the inorganic carrier is used together as in the above-described conventional technology, these inorganic substances are usually extremely difficult to decompose in nature, and the inorganic carrier itself remains in the blurry fertilizer and further accumulates in the soil in the long term. There was a problem.

そこで本発明は、上記課題を解決するべく成されたものであり、その目的とするところは、十分な吸水性および保水性を保持し、製造時の発酵培養性が良好であり、得られたものが有機物の分解・堆肥化等の発酵資材として優れた性能を発揮できる微生物担持資材を提供することを課題とする。   Therefore, the present invention has been made to solve the above-mentioned problems, and the object of the present invention is to retain sufficient water absorption and water retention, have good fermentation culture properties during production, and have been obtained. It is an object of the present invention to provide a microorganism-carrying material that can exhibit excellent performance as a fermentation material for decomposition and composting of organic matter.

本発明は上記目的を達成するために、微生物担持資材を調製するときの発酵培養性を向上でき、かつ、自然環境下で生分解可能な素材との組合せを鋭意探索し、次の構成を有する要素技術が極めて有効であることを見出した。
すなわち、本発明に係わる微生物担持資材としては、
1.有機物担体に発酵培養された微生物が定着した微生物担持資材であって、有機物担体がセルロース製スポンジを5重量%以上含有する微生物担持資材、
2.セルローススポンジが、含水率60重量%での見掛密度が0.025〜0.05[g(dry)/cm3(wet)]のものである前記の微生物担持資材、
3.セルローススポンジが平均孔径0.3〜3.5mm、最大含水率20〜35[g(水)/g(dry)]であることを特徴とする前記いずれかの微生物担持資材、
4.肥料、土壌改良剤、発酵開始・促進剤、消臭剤、廃水浄化剤、生け簀浄化剤、河川・湖沼浄化剤および空気浄化剤のいずれかである前記いずれかの微生物担持資材、
であり、微生物担持資材の製造方法としては、
6.セルロース製スポンジを乾燥重量で5重量%以上混合した有機物担体に微生物培養液を含浸し、発酵培養させることを特徴とする微生物担持資材の製造方法、
7.微生物培養液が、[A];納豆菌、[B];酵母、[C];乳酸菌の微生物群および該微生物群の栄養源を含む培養液であることを特徴とする前記微生物担持資材の製造方法、
8.セルローススポンジが、含水率60重量%での見掛密度が0.025〜0.05[g(dry)/cm3(wet)]のものである前記いずれかのの微生物担持資材の製造方法、
9.セルローススポンジが平均孔径0.3〜3.5mm、最大含水率20〜35[g(水)/g(dry)]である前記いずれかの微生物担持資材の製造方法、
10.微生物培養液中の該微生物群の菌体数比率が、[A]:[B]:[C]=1:101〜105:102〜106 の範囲であることを特徴とする前記いずれかの微生物担持資材の製造方法、
11.微生物担持資材が肥料、土壌改良剤、発酵開始・促進剤、消臭剤、廃水浄化剤、生け簀浄化剤、河川・湖沼浄化剤および空気浄化剤のいずれかである前記いずれかの微生物担持資材の製造方法
である。
In order to achieve the above-mentioned object, the present invention can improve fermentation culture properties when preparing a microorganism-supporting material, and eagerly search for a combination with a material that can be biodegraded in a natural environment, and has the following configuration. We found that elemental technology is extremely effective.
That is, as the microorganism-supporting material according to the present invention,
1. A microorganism-supporting material in which microorganisms fermented and cultured on an organic material carrier are fixed, wherein the organic material carrier contains 5% by weight or more of cellulose sponge,
2. The above microorganism-supporting material, wherein the cellulose sponge has an apparent density at a water content of 60% by weight of 0.025 to 0.05 [g (dry) / cm 3 (wet)],
3. Cellulose sponge has an average pore diameter of 0.3 to 3.5 mm and a maximum water content of 20 to 35 [g (water) / g (dry)],
4). Fertilizer, soil conditioner, fermentation starter / accelerator, deodorant, wastewater cleaner, ginger cleaner, river / lake cleaner and air cleaner,
As a method for producing a microorganism-supporting material,
6). A method for producing a microorganism-supporting material, comprising impregnating a microorganism carrier with an organic substance carrier in which a cellulose sponge is mixed in an amount of 5% by weight or more by dry weight, followed by fermentation culture;
7). Production of the microorganism-supporting material, wherein the microorganism culture solution is a culture solution containing [A]; natto, [B]; yeast, [C]; Method,
8). The method for producing any one of the above microorganism-supporting materials, wherein the cellulose sponge has an apparent density at a water content of 60% by weight of 0.025 to 0.05 [g (dry) / cm 3 (wet)].
9. The method for producing any one of the above microorganism-supporting materials, wherein the cellulose sponge has an average pore size of 0.3 to 3.5 mm and a maximum water content of 20 to 35 [g (water) / g (dry)],
10. The cell number ratio of the microorganism group in the microorganism culture solution is in the range of [A]: [B]: [C] = 1: 10 1 to 10 5 : 10 2 to 10 6 , A method for producing any microorganism-supporting material,
11. The microorganism-supporting material is any one of the above-mentioned microorganism-supporting materials, wherein the microorganism-supporting material is any one of fertilizers, soil improvers, fermentation starters / accelerators, deodorants, wastewater cleaners, ginger cleaners, river / lake cleaners, and air cleaners. It is a manufacturing method.

本発明によれば、微生物の定着に必要な空隙部のあるセルロース製スポンジを混合し含ませることで旺盛に繁殖した微生物が定着し、肥料、土壌改良剤、発酵開始・促進剤、消臭剤、廃水浄化剤、生け簀浄化剤、河川・湖沼浄化剤および空気浄化剤などの公的な有機物担体を有利に得ることができる。   According to the present invention, microorganisms propagated vigorously by mixing and including a cellulosic sponge having voids necessary for colonization of microorganisms is established, fertilizer, soil improver, fermentation start / accelerator, deodorant In addition, it is possible to advantageously obtain a public organic substance carrier such as a waste water purification agent, a sacrifice purification agent, a river / lake purification agent and an air purification agent.

本発明において、有機物担体の一部または全部として使用されるセルロース製スポンジは、セルロースを重量で半分以上含有するもので、さらに好ましくは90重量%以上のものである。また構造としては、スポンジ状、すなわち多孔質体であればよく、多孔質の構造が連通孔体,非連通孔体,連通孔と非連通孔の混合体の何れであってもよい。この多孔質体が水分を吸収して膨張し空隙部が生じる機能は、微生物の定着にとって好ましい機能である。該セルロース製スポンジの特性としては、含水率60重量%下の見掛密度が0.025〜0.05[g(dry)/cm3(wet)]であり、また、平均孔径が0.3〜3.5mm、最大含水率が20〜35[g(水)/g(dry)]であることが好ましい。これら各特性が上記範囲の場合、2次培養時のセルロース製スポンジへの微生物定着が良好となり、本発明の微生物担持資材としての性能がさらに優れることになる。 In the present invention, the cellulosic sponge used as part or all of the organic carrier contains cellulose by half or more, more preferably 90% by weight or more. The structure may be sponge-like, that is, a porous body, and the porous structure may be any one of a communicating hole body, a non- communicating hole body, and a mixture of communicating holes and non- communicating holes. The function that the porous body absorbs moisture and expands to form voids is a preferable function for fixing microorganisms. As the characteristics of the cellulose sponge, the apparent density at a moisture content of 60% by weight is 0.025 to 0.05 [g (dry) / cm 3 (wet)], and the average pore diameter is 0.3. It is preferable that the maximum water content is 20 to 35 [g (water) / g (dry)]. When these properties are within the above ranges, the microorganisms are well fixed on the cellulose sponge during the secondary culture, and the performance as the microorganism-supporting material of the present invention is further improved.

また、上記セルロース製スポンジの形状については特に限定されず、長方四角状,サイコロ状、球状、その他不定形状のもの、これら形状の混合されたもの等が使用でき、更に、これら形状物の大きさは、取扱い面および他の有機物担体との混合面等で、結果として微生物担持資材として支障が出なければ良く、目安として最大長さとして1〜100mm程度のものが好ましく、特に5〜50mm程度が好ましい。   In addition, the shape of the cellulose sponge is not particularly limited, and rectangular, dice, spherical, other irregular shapes, a mixture of these shapes, and the like can be used. As long as the handling surface and the mixing surface with other organic carriers do not interfere with the microorganism-supporting material as a result, the maximum length is preferably about 1 to 100 mm, particularly about 5 to 50 mm. Is preferred.

また、上記セルロース製スポンジと混合でき、かつ任意成分である他の有機物担体は、特に限定されないが、自然環境で生分解性であり、微生物の定着性があるもので、また安価で容易に入手できるものが好ましく、例えば、籾殻、蕎麦殻、米糠、椰子殻等の穀物殻、木屑、大鋸屑、サトウキビ茎廃物、米藁、麦藁、綿天然繊維類、枯れ草、落ち葉、紙屑等の天然素材廃物、食品製造廃物等が挙げられ、これら有機物の単独系あるい2種以上の混合系で用いらることもできる。   Other organic carriers that can be mixed with the above cellulose sponge and are optional components are not particularly limited, but are biodegradable in the natural environment and have microbial fixability, and are inexpensive and easily available. Preferred are, for example, grain husks such as rice husk, buckwheat husk, rice bran, coconut husk, wood waste, large sawdust, sugarcane stem waste, rice straw, wheat straw, cotton natural fibers, dead grass, fallen leaves, paper waste, etc. Examples include food manufacturing wastes, and these organic substances can be used alone or in a mixture of two or more.

さらに、上記セルロース製スポンジの有機物担体における含有量は、用いる他の有機物と組み合わせての吸水性、保水性、微生物定着性、2次培養性等を維持できるよう配慮すればよい。従って、上記特性のセルロース製スポンジの配合量は、全有機物担体に対して乾燥重量で5重量%以上が好ましく、更に、10重量%以上、さらに80重量%以上が特に好ましい。   Furthermore, the content of the cellulose sponge in the organic carrier may be considered so as to maintain water absorption, water retention, microbial fixation, secondary culture, etc. in combination with other organic substances to be used. Therefore, the blending amount of the cellulose sponge having the above characteristics is preferably 5% by weight or more by dry weight, more preferably 10% by weight or more, and further preferably 80% by weight or more based on the total organic carrier.

微生物担持資材に定着される発酵培養された微生物群の好ましい例としては、食物製造用微生物であり、例えば、納豆、アルコール類、食酢、醤油、ヨーグルト等の食物を製造するもので、具体的に納豆菌、酵母、麹菌、乳酸菌、酢酸菌などが挙げられる。   Preferred examples of the fermentation-cultured microorganism group fixed on the microorganism-supporting material are microorganisms for food production, for example, for producing foods such as natto, alcohols, vinegar, soy sauce, yogurt, specifically Examples include natto, yeast, koji, lactic acid, and acetic acid.

本発明において上述の効果を充分に高めるために、[A];納豆菌、[B];酵母、[C];乳酸菌の3種の微生物群の併用であることが好ましい。   In order to sufficiently enhance the above-described effects in the present invention, it is preferable to use a combination of three types of microorganisms: [A]; natto, [B]; yeast, [C];

本発明の[A];納豆菌は、Bacillus subtilis、Bacillus cereus、Bacillus megaterium、Bacillus circulans、Bacillus licheniformisなどのBacillus属が好ましく、納豆生産に使用されるBacillus subtilisで強力糸引納豆菌とされる菌株がさらに好ましい。   [A] of the present invention is preferably a Bacillus genus such as Bacillus subtilis, Bacillus cereus, Bacillus megaterium, Bacillus circulans, Bacillus licheniformis, etc. Further preferred.

本発明の[B];酵母は、有胞子酵母科に分類される酵母であり、Saccharomyces cerevisiae、Saccharomyces uvarum、Saccharomyces diastaticus、Kluyveromyces fragilis、Hanseniaspora valbyensis、Shizosaccharomyces pombe、Pichia membranaefaciens、Lipomyces starkeyi、Brettanomyces sp.、Candida utilis、Trichosporon sp.などが好ましく、パン酵母として市販されているSaccharomyces cerevisiaeがさらに好ましい。   [B] of the present invention is a yeast classified into the spore yeast family, Saccharomyces cerevisiae, Saccharomyces uvarum, Saccharomyces diastaticus, Kluyveromyces fragilis, Hanseniaspora valbyensis, Shizosaccharomyces pombe, Pichia membpo Candida utilis, Trichosporon sp. And the like are preferable, and Saccharomyces cerevisiae commercially available as baker's yeast is more preferable.

本発明の[C];乳酸菌は、Lactobacillus delbrukii、 Lactobacillus bulgaricus、Lactobacillus casei、Streptococcus thermophilus、Streptococcus lactis、Leuconostoc mesenteroides、Lactobacillus pentoacetiusなどの乳酸発酵性を有する菌株が好ましく、ヨーグルト用種菌として入手しやすいLactobacillus delbrukii、 Lactobacillus bulgaricus、Streptococcus thermophilusがさらに好ましい。   Lactobacillus delbrukii, Lactobacillus bulgaricus, Lactobacillus casei, Streptococcus thermophilus, Streptococcus lactis, Leuconostoc mesenteroides, Lactobacillus pentoacetius, and the like, Lactobacillus pentoacetius, which is easily obtained as an inoculum for Lactobacillus pentoacetius Lactobacillus bulgaricus and Streptococcus thermophilus are more preferable.

微生物担持資材を分解・堆肥化等のための発酵材として使用するときや、土壌改良材、消臭材等におけるボカシ肥として使用する場合の性能の観点から、微生物培養液中の上記微生物群の比率は、[A]:[B]:[C]=1:101〜105:102〜106が好ましく、1:102〜104:103〜105が特に好ましい。 From the viewpoint of performance when using microorganism-supporting material as a fermenting material for decomposition and composting, or as a fertilizer for soil improvement materials, deodorizing materials, etc., the above microorganism group in the microorganism culture solution The ratio is preferably [A]: [B]: [C] = 1: 10 1 to 10 5 : 10 2 to 10 6 , particularly preferably 1:10 2 to 10 4 : 10 3 to 10 5 .

本発明のセルロース製スポンジを含む有機物担体に含侵させる微生物培養液は、栄養源を添加して上記微生物群を培養させたものであり、この培養は特に限定されず通常法でよく、例えば、液全体を加温し混合できる容器内に、先ず所定量の栄養源の糖蜜やシロップなどの糖類を常温水に溶かし、そこへ、[A];納豆菌、[B];酵母、[C];乳酸菌の所定量を各々添加混合して全体の水溶液を緩やかに撹拌しながら約37℃保温の条件下で3日間位温めて、培養液1ml当たりの微生物群の総数を100万以上に培養するという方法などがある。   The microorganism culture solution impregnated in the organic carrier containing the cellulose sponge of the present invention is obtained by culturing the above-mentioned microorganism group by adding a nutrient source, and this culture is not particularly limited and may be a normal method, for example, First, a predetermined amount of saccharides such as molasses and syrup are dissolved in room temperature water in a container that can be heated and mixed with the whole liquid, [A]; natto, [B]; yeast, [C] Each of which is added and mixed with a predetermined amount of lactic acid bacteria, and the whole aqueous solution is warmed for about 3 days under a condition of keeping at about 37 ° C. while gently stirring, and the total number of microbial groups per 1 ml of the culture is cultured to 1 million or more There is a method.

なお、本発明の微生物担持資材製造に用いる該微生物培養液としては、環境浄化微生物を培養した培養液状態であれば使用できる。例えば、後述の実施例に記載された組み合わせの他、愛媛県工業技術センター開発の環境浄化微生物”えひめAI−1”が適用できる。   The microorganism culture solution used for the production of the microorganism-supporting material of the present invention can be used as long as it is in a culture solution state in which environmentally purified microorganisms are cultured. For example, in addition to the combinations described in Examples described later, the environmental purification microorganism “Ehime AI-1” developed by Ehime Industrial Technology Center can be applied.

次に、上記微生物培養液を有機物担体に含浸した後に行う2次培養の方法としては、特に限定されず通常の方法で行う。例えば、外気に触れずほぼ密閉可能な容器内へ所定量のセルロース製スポンジと他有機物を入れて全体を混合し、そこへ予め調製しておいた所定量の微生物培養液および栄養源の糖蜜を混ぜた溶液を全有機物担体に均一に含浸した後、容器を密閉にする。この容器全体を約40℃の保温条件下にて適度にガス抜きしながら1週間位かけて発酵させる方法などで行われる。因みに、この2次培養を適切に行うためには、全原料を仕込んだ容器全体の保温条件を30〜45℃、好ましくは35〜40℃の範囲に保つことが好ましい。また、各原料の仕込み重量比としては、微生物培養液を1〜6重量部および糖蜜などの栄養源を1〜3重量部、上記特性のセルロース製スポンジを乾燥重量で5重量%以上混合した有機物担体を1〜6重量部の範囲内として調製することが好ましい。    Next, the secondary culturing method carried out after impregnating the above-mentioned microorganism culture solution into an organic substance carrier is not particularly limited and is carried out by a usual method. For example, put a predetermined amount of cellulose sponge and other organic matter in a container that can be sealed almost without touching the outside air, mix the whole, and add a predetermined amount of microbial culture solution and nutrient molasses prepared beforehand. After the mixed solution is uniformly impregnated into the whole organic carrier, the container is sealed. The entire container is fermented over about a week while properly degassing under a temperature maintaining condition of about 40 ° C. Incidentally, in order to appropriately perform this secondary culture, it is preferable to keep the temperature maintaining conditions of the whole container charged with all the raw materials in the range of 30 to 45 ° C, preferably 35 to 40 ° C. Moreover, as for the charge ratio of each raw material, 1 to 6 parts by weight of a microorganism culture solution, 1 to 3 parts by weight of a nutrient source such as molasses, and an organic substance in which a cellulose sponge having the above characteristics is mixed by 5% by weight or more by dry weight It is preferable to prepare the carrier in the range of 1 to 6 parts by weight.

このような構成の微生物担持資材は、その微生物の活性の高さから肥料、土壌改良剤、発酵開始・促進剤、消臭剤、廃水浄化剤、生け簀浄化剤、河川・湖沼浄化剤、空気浄化剤に使用することができる。なお、本発明の微生物担持資材は、その用途が許容するのであれば、有機物担体の他に、微生物を担持していない有機物や無機物を含有することも可能である。   Due to the high activity of the microorganisms, the microorganism-supporting material with such a structure is fertilizer, soil improver, fermentation starter / accelerator, deodorant, wastewater cleaner, ginger cleaner, river / lake cleaner, air cleaner. Can be used in the preparation. Note that the microorganism-carrying material of the present invention may contain an organic substance or an inorganic substance that does not carry microorganisms in addition to the organic substance carrier, as long as the use permits.

以下、実施例により本発明をさらに詳細に説明する。本例中、微生物培養液中の微生物群比率、また、セルロース製スポンジの含水率、見掛密度、平均孔径、最大含水率、更に、微生物担持資材の消臭試験は次の方法にて求めたものである。   Hereinafter, the present invention will be described in more detail with reference to examples. In this example, the microorganism group ratio in the microorganism culture solution, the moisture content of the cellulose sponge, the apparent density, the average pore diameter, the maximum moisture content, and the deodorization test of the microorganism-supporting material were determined by the following method. Is.

(1)微生物群菌体数比率
マイクロピペットにより採取した微生物培養液10μlをスリット入スライド(10mm枠の中に0.1mm間隔のスリット)上に垂らした後、カバーガラスを被せて400倍の倍率で顕微鏡観察を行い、1スリット(1mm2)当たりに存在する乳酸菌、酵母、納豆菌の数をそれぞれ数える。
(1) Microbe group cell number ratio 10 μl of microorganism culture solution collected with a micropipette is hung on a slide with slits (slits with a spacing of 0.1 mm in a 10 mm frame) and then covered with a cover glass to give a magnification of 400 × And the number of lactic acid bacteria, yeast, and natto bacteria present per slit (1 mm 2 ) is counted.

(2)含水率
湿潤セルロース製スポンジの乾燥前サンプルの重量を測定(Ag)し、次に、同サンプルを乾燥機中105℃で6時間乾燥した後の重量を測定(Bg)して次式
含水率(wt%)=(A−B)×100/A
から算出する。
(2) Moisture content The weight of the wet cellulose sponge before drying is measured (Ag), then the weight of the sample after drying for 6 hours at 105 ° C. in a dryer (Bg) is Moisture content (wt%) = (A−B) × 100 / A
Calculate from

(3)見掛密度
湿潤状態のセルロース製スポンジを乾燥機105℃で6時間乾燥した後、デシケータ内で室温(約23℃)に冷却し、乾燥セルロース製スポンジを得る。この乾燥品を面辺長5cmの立方体に切断して作製したサンプルの重量を測定(Cg)する。次に、この立方体サンプルに水を含浸させ、含水率60重量%に調製した後、各面の寸法を測定して含水サンプルの体積を算出(Dcm3)し、次式
見掛密度[g(dry)/cm3(wet)] =C/D
から求める。
(3) Apparent density After the wet cellulose sponge is dried at 105 ° C. for 6 hours, it is cooled to room temperature (about 23 ° C.) in a desiccator to obtain a dry cellulose sponge. A weight of a sample prepared by cutting the dried product into a cube having a side length of 5 cm is measured (Cg). Next, after impregnating this cubic sample with water to prepare a moisture content of 60% by weight, the dimensions of each surface were measured to calculate the volume of the moisture sample (Dcm3).
Apparent density [g (dry) / cm3 (wet)] = C / D
Ask from.

(4)平均孔径
予め、含水率60重量%に調製したセルロース製スポンジサンプルを鋭利な刃物で切断し、その切断面の細孔を無作為に50個所抽出して細孔の円相当径(直径)を測定し、その平均値を平均細孔とする。
(4) Average pore diameter A cellulose sponge sample prepared to a moisture content of 60% by weight in advance was cut with a sharp blade, and 50 pores on the cut surface were randomly extracted to obtain the equivalent circle diameter (diameter of the pores). ) And the average value is taken as the average pore.

(5)最大含水率
湿潤状態のセルロース製スポンジを辺長5cmの立方体に切断し、そのサンプルを常温水に入れ脱泡して5分間浸漬後、取り出して金網上で1分間放置し、直ちに重量を測定(Eg)する。次に、このサンプルを脱水機850rpmで5分間脱水した後、乾燥機105℃で6時間乾燥し、デシケータ内で室温まで冷却した重量を測定(Fg)して次式
最大含水率[g(水)/g(dry)] =(E−F)/E
から求める。
(5) Maximum moisture content A cellulose sponge in a wet state is cut into cubes with a side length of 5 cm, the sample is defoamed in room temperature water, immersed for 5 minutes, taken out, left on a wire mesh for 1 minute, and immediately weighted. Is measured (Eg). Next, this sample was dehydrated at 850 rpm for 5 minutes, then dried at 105 ° C. for 6 hours, measured in a desiccator at room temperature (Fg), and the maximum water content [g (water ) / G (dry)] = (E−F) / E
Ask from.

(6)消臭試験
内径約9cm、高さ約17cmの蓋付き1000ml容器内に、28〜30%アンモニア水試薬(和光純薬工業(株)製)を使って濃度1000mg/Lに調製したアンモニア水溶液を400ml入れた
。そこへ各実施例、比較例で製造した微生物担持資材を80gを添加浸漬し緩やかに混合し、容器の蓋をした状態で室温下5分間放置した後、蓋を開けて液面から5cm上の気相部をガス検知管方式(北川式のガス採取器AP−20およびアンモニアガス検知管2.5〜1000mg/L、光明理化学工業(株)製)にてアンモニアガス濃度を測定した。
(6) Deodorization test Ammonia prepared at a concentration of 1000 mg / L using a 28-30% ammonia water reagent (manufactured by Wako Pure Chemical Industries, Ltd.) in a 1000 ml container with a lid having an inner diameter of about 9 cm and a height of about 17 cm. 400 ml of an aqueous solution was added. 80 g of the microorganism-supporting material produced in each example and comparative example was added and immersed there, and the mixture was gently mixed. After leaving the container covered for 5 minutes at room temperature, the cover was opened and 5 cm above the liquid level. The gas phase portion was measured for ammonia gas concentration by a gas detector tube method (Kitakawa gas collector AP-20 and ammonia gas detector tube 2.5 to 1000 mg / L, manufactured by Komyo Chemical Co., Ltd.).

以下、実施例1〜3および比較例1では、有機物担体の種類を変更し、微生物培養液として環境浄化微生物”えひめAI−1”を用いた微生物担持資材であるボカシ肥の製造例、更に、これら製造例から得られた微生物担持資材であるボカシ肥の性能試験例を示す。なお、実施例中の仕込み割合は、全て重量比で示したものである。   Hereinafter, in Examples 1 to 3 and Comparative Example 1, the type of the organic substance carrier is changed, and a manufacturing example of Bokasi fertilizer that is a microorganism-supporting material using the environmentally purified microorganism “Ehime AI-1” as a microorganism culture solution, The performance test example of Bokashi fertilizer which is a microorganism-supporting material obtained from these production examples is shown. In addition, all the preparation ratios in the examples are shown by weight ratio.

[実施例1]
含水率60重量%下の見掛密度:0.03[g(dry)/cm3(wet)]、平均孔径:1.8mm、最大含水率:31[g(水)/g(dry)]の特性である乾燥セルロース製スポンジの最長径30mmの不定形切断品を100重量%を全有機物担体として使用し、表1の仕込み割合で密閉容器に仕込んだ後、ガス抜きをしながら容器全体を約40℃の保温で発酵培養させ、約3日間で芳醇なアルコール臭のする「微生物担持資材:イ」を得た。
[Example 1]
Apparent density under water content of 60% by weight: 0.03 [g (dry) / cm3 (wet)], average pore diameter: 1.8 mm, maximum water content: 31 [g (water) / g (dry)] Using 100% by weight of an amorphous cut product of dry cellulose sponge with the longest diameter of 30 mm as the characteristic organic carrier as the total organic substance carrier, and charging it into a sealed container at the charging rate shown in Table 1, the entire container is degassed. Fermentation culture was performed at a temperature of 40 ° C., and “microorganism-supporting material: i” having a rich alcohol odor in about 3 days was obtained.

[実施例2]
有機物担体として、実施例1使用の乾燥セルロース製スポンジを50重量%および他の有機物に米糠を50重量%用いた以外は実施例1と同様に行い、約3日間で芳醇なアルコール臭のする「微生物担持資材:ロ」を得た。
[Example 2]
As an organic carrier, the same procedure as in Example 1 was carried out except that 50% by weight of the dry cellulose sponge used in Example 1 and 50% by weight of rice bran were used for other organic substances. Microorganism carrying material: B ”was obtained.

[実施例3]
有機物担体として、実施例1使用の乾燥セルロース製スポンジを15重量%と他の有機物に実施例1使用の米糠を50重量%および籾殻を35重量%用いた以外は実施例1と同様に行い、約4日間で芳醇なアルコール臭のする「微生物担持資材:ハ」を得た。
[Example 3]
As an organic substance carrier, it was carried out in the same manner as in Example 1 except that 15% by weight of the dry cellulose sponge used in Example 1 and 50% by weight of rice bran used in Example 1 and 35% by weight of rice husk were used as other organic substances. In about 4 days, “microorganism-supporting material: C” having a rich alcohol odor was obtained.

[比較例1]
有機物担体として、実施例2,3使用の米糠を50重量%および実施例3使用の籾殻を50重量%用いた以外は実施例1と同様に行い、約6日間で芳醇なアルコール臭のする「微生物担持資材:ニ」を得た。
[Comparative Example 1]
As an organic carrier, the same procedure as in Example 1 was carried out except that 50% by weight of rice bran used in Examples 2 and 3 and 50% by weight of rice husk used in Example 3 were used. Microbe-supporting material: D ”was obtained.

[実施例4,5,6]、[比較例2,3]
実施例1〜3および比較例1で得た「微生物担持資材イ〜二」を用い、ブランク(微生物担持資材無添加)と比較して消臭試験を行った結果を表2に示す。
この消臭性に関する試験結果からも本発明のセルロース製スポンジを混合した微生物担持資材の有効性が高いことが確認された。
[Examples 4, 5, 6], [Comparative Examples 2, 3]
Table 2 shows the results of the deodorization test using the “microorganism-supporting materials 1 to 2” obtained in Examples 1 to 3 and Comparative Example 1 in comparison with the blank (no added microorganism-supporting material).
Also from the test results regarding the deodorizing property, it was confirmed that the microorganism-carrying material mixed with the cellulose sponge of the present invention is highly effective.

[実施例7]
実施例1〜3および比較例1で得た「微生物担持資材イ〜二」のサンプル各々を自然の土中に埋めて分解する様子を観察したところ、土中埋設してから約5ヶ月間で全サンプルとも有機物担体のスタート時の形状が壊れて保持されていなく、小片状および粉末状になっていることを確認できた。この現象結果から、土壌中のバクテリア等により良好に生分解されたものと判断できる。
[Example 7]
When observing how each of the samples of “microorganism-supporting materials 1 to 2” obtained in Examples 1 to 3 and Comparative Example 1 was buried in natural soil and decomposed, it was about 5 months after being embedded in the soil. In all the samples, it was confirmed that the shape of the organic carrier at the start was broken and not held, and was in the form of small pieces and powder. From this phenomenon result, it can be determined that the biodegradation was satisfactorily caused by bacteria in the soil.

Figure 2005278523
Figure 2005278523

Figure 2005278523
Figure 2005278523

本発明の微生物担持資材は、生分解性が高いことから環境保全上で担体残存の問題が小さく、かつ、吸水性および保水性が良好であり、ボカシ肥などの肥料、土壌改良剤、発酵開始・促進剤、消臭剤、廃水浄化剤、生け簀浄化剤、河川・湖沼浄化剤および空気浄化剤として使用できる。   The microorganism-carrying material of the present invention has high biodegradability, so that there are few problems with remaining carriers in environmental conservation, and water absorption and water retention are good. Fertilizers such as bokeh fertilizer, soil improver, and fermentation start -It can be used as an accelerator, deodorant, wastewater cleaner, ginger cleaner, river / lake cleaner, and air cleaner.

Claims (4)

有機物担体に発酵培養された微生物が定着した微生物担持資材であって、有機物担体がセルロース製スポンジを5重量%以上含有する微生物担持資材。 A microorganism-carrying material in which microorganisms fermented and cultured on an organic carrier are fixed, wherein the organic carrier contains 5% by weight or more of a cellulose sponge. 肥料、土壌改良剤、発酵開始・促進剤、消臭剤、廃水浄化剤、生け簀浄化剤、河川・湖沼浄化剤および空気浄化剤のいずれかである請求項1記載の微生物担持資材。 The microorganism-carrying material according to claim 1, which is any one of a fertilizer, a soil conditioner, a fermentation starter / accelerator, a deodorant, a wastewater cleaner, a ginger cleaner, a river / lake cleaner, and an air cleaner. セルロース製スポンジを5重量%以上混合した有機物担体に、微生物培養液を含浸し、発酵培養させることを特徴とする微生物担持資材の製造方法。 A method for producing a microorganism-supporting material, comprising impregnating a microorganism culture solution into an organic carrier mixed with 5% by weight or more of a cellulose sponge and subjecting it to fermentation culture. 微生物担持資材が肥料、土壌改良剤、発酵開始・促進剤、消臭剤、廃水浄化剤、生け簀浄化剤、河川・湖沼浄化剤および空気浄化剤のいずれかである請求項3記載の製造方法。 The production method according to claim 3, wherein the microorganism-supporting material is any one of fertilizer, soil improver, fermentation starter / accelerator, deodorant, wastewater cleaner, ginger cleaner, river / lake cleaner, and air cleaner.
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JP2014185277A (en) * 2013-03-25 2014-10-02 Michiyo Takenaka Liquid composition
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010041502A1 (en) * 2008-10-09 2010-04-15 独立行政法人農業・食品産業技術総合研究機構 Solid support comprising microorganisms capable of conducting parallel multiple mineralization immobilized thereon, catalyst column and method for producing solid medium for cultivating plants
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JP2010221213A (en) * 2009-02-27 2010-10-07 Keisuke Takenouchi Water treatment technique using filamentous fungus or actinomycete
WO2014101764A1 (en) * 2012-12-25 2014-07-03 Zhu Yongqiang Biological membrane fluidized bed wastewater treatment method
JP2014185277A (en) * 2013-03-25 2014-10-02 Michiyo Takenaka Liquid composition
JP2017047136A (en) * 2015-09-04 2017-03-09 株式会社スギノマシン Environment cleaning agent, environment cleaning method, and production method for environment cleaning agent
JP2018122275A (en) * 2017-02-03 2018-08-09 田中 聡 Method for producing deodorant
CN108461170A (en) * 2018-04-24 2018-08-28 海南大学 A kind of novel Deep Geological Disposal of High-level Radioactive Wastes padded coaming and its construction method
CN111533416A (en) * 2020-05-18 2020-08-14 宇恒(南京)环保装备科技有限公司 Method for solid-liquid synergistic aerobic biological fermentation of high-nutrition waste organic matters

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