JP2001219061A - Porous absorbing material and its manufacturing method - Google Patents

Porous absorbing material and its manufacturing method

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Publication number
JP2001219061A
JP2001219061A JP2000074961A JP2000074961A JP2001219061A JP 2001219061 A JP2001219061 A JP 2001219061A JP 2000074961 A JP2000074961 A JP 2000074961A JP 2000074961 A JP2000074961 A JP 2000074961A JP 2001219061 A JP2001219061 A JP 2001219061A
Authority
JP
Japan
Prior art keywords
powder
particles
zeolite
porous
mineral particles
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.)
Pending
Application number
JP2000074961A
Other languages
Japanese (ja)
Inventor
Yoshiya Kikuchi
與志也 菊地
Yasuo Tamura
靖夫 田村
Katsuaki Tanaka
勝昭 田中
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP2000074961A priority Critical patent/JP2001219061A/en
Publication of JP2001219061A publication Critical patent/JP2001219061A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain porous particles enhanced in moisture absorbing/releasing property by granulating fine powder, which has 1 mm or smaller particle size and is produced when a porous mineral is pulverized and is originally to be dumped, and reusing it and to provide a method for manufacturing the porous particles. SOLUTION: An excess of porous mineral fine particles is mixed in an aqueous solution containing a water-soluble macromolecule as a principal component, which is then kneaded. The kneaded material is granulated into large aggregated (granulated) particles, which are then dried to form granular coarse particles so that the objective porous particles more enhanced in performance to absorb moisture content or gas are obtained.

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】本発明は微細な孔隙を有する
粒径が1mm以下の鉱物粒子を主成分とする粉末を団粒
化して粗粒の多孔性粒子に成形することにより、水分な
らびにアンモニアガス、ホルムアルデヒドガスなどのガ
スを吸放出する機能を有して環境調整材料として好適な
多孔性吸収材およびその製造方法に関するものである。
BACKGROUND OF THE INVENTION The present invention relates to a method for producing water and ammonia gas by agglomerating a powder mainly composed of mineral particles having a fine pore size of 1 mm or less and having fine pores into coarse porous particles. The present invention relates to a porous absorbent having a function of absorbing and releasing a gas such as formaldehyde gas and suitable as an environmental control material, and a method for producing the same.

【0002】[0002]

【従来の技術】わが国においてはゼオライトや珪藻土の
ような微細な孔隙を有する鉱物資源の埋蔵量が多く、微
細な孔隙を有して軽く、各種の物質を吸着する性質を有
することから、コンクリートの軽量骨材をはじめとし
て、肥料や農薬の増量剤、土壌改良剤などを含めた種々
の用途に利用されている。その中でもゼオライトはわが
国の埋蔵量が特に多く、吸放湿性などの性質が顕著にあ
ることから、その性質に着目して、近年、ゼオライトを
粉砕して粗粒の粒度のものを住宅の床下に敷いて、地面
から上昇する湿気を吸収させる床下乾燥材としての利用
が進められている。
2. Description of the Related Art In Japan, a large amount of mineral resources having fine pores such as zeolite and diatomaceous earth are buried, light with fine pores, and a property of adsorbing various substances. It is used for various purposes including light weight aggregates, fertilizers, agricultural chemical extenders, soil conditioners, and the like. Among them, zeolite has a large amount of reserves in Japan and has remarkable properties such as moisture absorption and desorption properties, so focusing on these properties, in recent years, zeolite has been crushed and coarse-grained It is being used as an underfloor drying material that can be laid and absorb moisture rising from the ground.

【0003】しかし、ゼオライトを始めとする多孔性の
鉱石を粉砕する際には、粒径が1mm以下の微粉が多量
に発生して、結局その大部分は利用されないままに投棄
しているのが現状である。
However, when pulverizing porous ore such as zeolite, a large amount of fine powder having a particle size of 1 mm or less is generated, and most of the fine powder is eventually discarded without being used. It is the current situation.

【0004】しかし、ゼオライトは多孔質であるものの
孔隙率はあまり大きくなく、比重も比較的高いので、住
宅の床下乾燥材として施工するときに重量があり、取扱
が容易でない問題がある。また吸湿性も予想するほど強
くはない。それに加えて湿度の変化に伴うゼオライトの
吸放湿量の変化は緩慢である、という問題も認められて
いた。
However, although zeolite is porous, its porosity is not so large and its specific gravity is relatively high. Therefore, there is a problem that the zeolite is heavy when applied as a drying material under the floor of a house and is not easy to handle. Also, the hygroscopicity is not as strong as expected. In addition, the problem that the change in the amount of moisture absorbed and released by the zeolite due to the change in humidity was slow was also recognized.

【0005】さらに、このような吸湿剤として使用する
場合、粒度が1mm以下になると、堆積されたゼオライ
ト層が緻密になり、その層内への空気やガスの流通が著
しく低下するために、吸放湿性能がさらに低下するとい
う問題もある。これはゼオライトに限らず、珪藻土やセ
ピオライトなどの孔隙を有する鉱物粉には共通する問題
でもある。
Further, when used as such a hygroscopic agent, if the particle size is 1 mm or less, the deposited zeolite layer becomes dense, and the flow of air and gas into the layer is significantly reduced. There is also a problem that the moisture release performance is further reduced. This is a problem common not only to zeolite but also to mineral powder having pores such as diatomaceous earth and sepiolite.

【0006】[0006]

【発明が解決しようとする課題】本発明の課題は、多孔
性の鉱物を粉砕する際に発生する、本来は投棄されるべ
き粒度が1mm以下の微粉を顆粒状にして再利用するこ
とであり、それによって吸放湿性を改善向上させた多孔
性粒子およびその製造方法を提供することにある。
SUMMARY OF THE INVENTION An object of the present invention is to recycle a fine powder having a particle size of 1 mm or less, which should be discarded, which is generated when pulverizing a porous mineral, into granules. Another object of the present invention is to provide a porous particle having improved and improved moisture absorption and release properties and a method for producing the same.

【0007】[0007]

【課題を解決するための手段】上記課題を解決するため
に、粉砕する際に発生する多孔性の鉱物微粒子を団粒化
(顆粒化)する目的で、水溶性高分子を主成分とする水
溶液に過剰の多孔性鉱物微粒子を配合して混練し、大き
な団粒化粒子に造粒したのち乾燥して顆粒状の粗大粒子
を形成することにより水分やガスの吸収性能を一段と改
善向上させることができる。
In order to solve the above-mentioned problems, an aqueous solution containing a water-soluble polymer as a main component for the purpose of aggregating (granulating) porous mineral fine particles generated during pulverization. It is possible to further improve moisture and gas absorption performance by compounding and kneading excess porous mineral fine particles, kneading them, granulating them into large aggregated particles, and drying them to form granular coarse particles. it can.

【0008】その際に使用する水溶性高分子はポリエチ
レングリコール、ポリビニルアルコールおよびその誘導
体、ポリビニルピロリドン、ポリアクリル酸またはポリ
メタアクリル酸などのナトリウム塩あるいはアンモニウ
ム塩またはそれらの尿素付加物、ポリアクリルアミド、
カルボキシメチルセルロースやメチルセルロースなどの
セルロース誘導体、キトサンおよびその誘導体、アルギ
ン酸およびその塩類、寒天、アラビアガムなどの植物性
ガム類、デンプンおよびその誘導体、ニカワやミルクカ
ゼインなどのタンパク質などのごとき水溶性高分子化合
物があり、それらのうち選ばれた1種または2種以上の
混合物を使用することができる。
[0008] The water-soluble polymer used in this case is polyethylene glycol, polyvinyl alcohol and its derivatives, polyvinylpyrrolidone, sodium or ammonium salts such as polyacrylic acid or polymethacrylic acid or urea adduct thereof, polyacrylamide,
Cellulose derivatives such as carboxymethylcellulose and methylcellulose, chitosan and its derivatives, alginic acid and its salts, agar, vegetable gums such as arabic gum, starch and its derivatives, and water-soluble polymer compounds such as proteins such as glue and milk casein And a selected one or a mixture of two or more of them can be used.

【0009】これらの水溶性高分子を水溶液にするとき
は、種類や重合度によって異なるが、一般には1〜50
%の濃度に調整したものを使用する。さらにその水溶液
にポリ酢酸ビニル樹脂やポリアクリル酸エステル樹脂な
どの熱可塑性樹脂エマルジョン、あるいはスチレン・ブ
タジエンゴム、アクリロニトリル・ブタジエンゴムなど
の合成ゴムラテックス、あるいは天然ゴムラテックスな
どを任意の割合で混合してもよい。
When these water-soluble polymers are made into an aqueous solution, they vary depending on the type and the degree of polymerization.
Use the one adjusted to the concentration of%. Furthermore, a thermoplastic resin emulsion such as a polyvinyl acetate resin or a polyacrylate resin, or a synthetic rubber latex such as styrene-butadiene rubber, acrylonitrile-butadiene rubber, or a natural rubber latex is mixed with the aqueous solution in an arbitrary ratio. Is also good.

【0010】また本発明で使用される多孔性の鉱物粒子
としては珪藻土、ゼオライト、パーライトやセピオライ
トなどのごとき安価な鉱物が用いられるが、入手の容易
さや資源の豊富さからゼオライトを用いるのが好適であ
る。
As the porous mineral particles used in the present invention, inexpensive minerals such as diatomaceous earth, zeolite, perlite and sepiolite are used, but zeolite is preferably used in view of the availability and the abundance of resources. It is.

【0011】さらにはこれらの鉱物に活性炭やノコクズ
や木質廃材チップの炭化物、または藁やトウモロコシ茎
などの農産廃棄物の炭化物、スギ、ヒノキやカラマツな
どの樹皮粉末などを混合使用することにより、吸放湿性
能、ホルムアルデヒドやアンモニアガスなどの吸着性能
などを一段と向上改善することができる。その際に、こ
れらの添加物の添加量は鉱物粉末に対して1〜50%、
好ましくは5〜30%とするのがよい。
[0011] Furthermore, by mixing and using activated carbon, sawdust and charcoal of wood waste chips, or charcoal of agricultural waste such as straw and corn stalk, bark powder of cedar, hinoki and larch, etc. Moisture release performance, adsorption performance for formaldehyde, ammonia gas, and the like can be further improved and improved. At that time, the amount of these additives is 1 to 50% based on the mineral powder,
Preferably, it is 5 to 30%.

【0012】また尿素やアミン化合物、あるいはアミノ
化合物などのごときアミノ化合物のようにホルムアルデ
ヒドなどと容易に反応する化合物を粉末のまま、あるい
は水溶性高分子の水溶液に溶解することにより、本発明
の効果はさらに向上することができる。
The effect of the present invention can be obtained by dissolving a compound which easily reacts with formaldehyde, such as an amino compound such as urea, an amine compound or an amino compound, as a powder or in an aqueous solution of a water-soluble polymer. Can be further improved.

【0013】本発明の多孔性吸収材を製造する方法は、
例えば、水溶性高分子としてポリビニルアルコールを使
用したとき、その水溶液1重量部に対して目開き1mm
のふるいを通過した粒度の多孔性鉱物の粒子を攪拌しな
がら0.5〜100重量部、好ましくは1〜20重量部
の割合で加えて二次凝集させる。そのときには通常の攪
拌機、混練り機などの装置が使用される。混練して顆粒
化したものは50〜200℃の温度に保たれた乾燥器中
で乾燥するが、その際にエポキシ化合物やイソシアネー
ト化合物などのごとき水溶性高分子と反応して架橋する
耐水化剤を水溶性高分子の水溶液に対して1〜20%添
加してもよい。
[0013] The method for producing the porous absorbent material of the present invention comprises:
For example, when polyvinyl alcohol is used as the water-soluble polymer, the aperture is 1 mm for 1 part by weight of the aqueous solution.
The particles of the porous mineral having a particle size that has passed through the sieve are added with stirring at a ratio of 0.5 to 100 parts by weight, preferably 1 to 20 parts by weight, and secondary aggregated. At that time, a device such as a usual stirrer or kneader is used. The kneaded and granulated product is dried in a drier kept at a temperature of 50 to 200 ° C. At that time, a water-proofing agent that reacts with a water-soluble polymer such as an epoxy compound or an isocyanate compound to crosslink. May be added to the aqueous solution of the water-soluble polymer in an amount of 1 to 20%.

【0014】水溶性高分子の水溶液の濃度は一般に水溶
性高分子の重合度が高いほど低濃度の水溶液に調整し、
また水溶液の粘度が低いほど添加する多孔性鉱物の粒子
の割合を増やすことができる。
The concentration of the aqueous solution of the water-soluble polymer is generally adjusted to a lower concentration as the degree of polymerization of the water-soluble polymer becomes higher.
In addition, as the viscosity of the aqueous solution is lower, the ratio of the porous mineral particles to be added can be increased.

【0015】次に本発明による多孔性吸収材について、
以下に試験例を示して説明する。
Next, regarding the porous absorbent according to the present invention,
The following describes test examples.

【0016】[試験例1]ポリビニルアルコール(信越
化学製PA−05GA)の10%水溶液50gに粒径が
1mm以下のゼオライト粉末200gを激しく攪拌しな
がら加えることにより団粒化したのち、110℃に保持
した乾燥器中に3時間放置して乾燥した。このように調
整した試料と3〜6mmの粒度に粉砕したゼオライトと
を、それぞれ直径90mmシャーレに採り、再度絶乾な
るまで乾燥したのち、重量を測定してその時の重量を基
準100とした。30℃で90%RHの恒温恒湿室に3
時間放置して重量変化率を測定した。さらに10時間同
条件に放置したのち、30℃で30%RHの恒温恒湿室
に移し、3時間後の重量変化率を測定した。その結果は
表1のようになった。この結果から明らかなように団粒
化したゼオライトは粒状ゼオライトに比べて優れた吸放
湿性を示した。
Test Example 1 200 g of zeolite powder having a particle size of 1 mm or less was added to 50 g of a 10% aqueous solution of polyvinyl alcohol (PA-05GA manufactured by Shin-Etsu Chemical Co., Ltd.) with vigorous stirring to form an aggregate, and the mixture was heated to 110 ° C. It was left to dry in the held dryer for 3 hours. The sample thus adjusted and zeolite pulverized to a particle size of 3 to 6 mm were each taken in a Petri dish having a diameter of 90 mm, dried again until absolutely dry, and then weighed. The weight at that time was defined as 100. 3 in a constant temperature and humidity room at 30 ° C and 90% RH
After allowing to stand for a time, the weight change rate was measured. After leaving it under the same conditions for further 10 hours, it was transferred to a thermo-hygrostat at 30 ° C. and 30% RH, and the weight change rate after 3 hours was measured. The results are shown in Table 1. As is clear from these results, the aggregated zeolite exhibited superior moisture absorption / release properties as compared with the granular zeolite.

【0017】[0017]

【表1】 [Table 1]

【0018】[試験例2〜4]ポリビニルアルコール
(クラレ製PVA−117)の10%水溶液50gに粒
径が1mm以下のゼオライト粉末500gとスギ樹皮粉
末、活性炭、および粉末尿素をそれぞれ50gずつ混ぜ
て激しく攪拌しながら加えて団粒化したのち、110℃
に保持した乾燥器中に3時間放置して乾燥した。このよ
うに調整した試料と試験例1にて団粒化したゼオライト
とを、それぞれ直径90mmのシャーレに採り、再度絶
乾になるまで乾燥したのち、重量を測定した。その時の
重量を基準100とした。ついで内容積約10lのデシ
ケータの底に300mlの蒸溜水を入れた直径12c
m、高さ6cmの結晶皿を設置して、その中に37%ホ
ルマリン0.2mlを蒸溜水5mlで希釈した溶液を
0.5mlずつ加えた10mlの秤量瓶を置き、それに
シャーレに入れたそれぞれの試料を置いてた。このホル
マリンのみを入れた48時間密封放置したデシケータ内
のホルムアルデヒドガスの測定値は11.9mg/lで
あった。さらに各試料を設置したデシケータを密封した
のち、温度20℃、関係湿度65%に保った恒温恒湿室
に48時間静置した。さらに所定に時間が経過したのち
デシケータ中に設置した結晶皿内の蒸溜水に吸収された
ホルムアルデヒドの濃度を、JIS−5908に規定さ
れたアセチルアセトン法により測定した。その結果を表
2に記した。この結果から明らかなように団粒化したゼ
オライトよりもそれにスギ樹皮チップや活性炭、尿素粉
末を加えて団粒化したものの方がホルムアルデヒドガス
をよく吸収することが明らかである。
Test Examples 2 to 4 500 g of zeolite powder having a particle size of 1 mm or less, 50 g of cedar bark powder, activated carbon, and powdered urea were mixed with 50 g of a 10% aqueous solution of polyvinyl alcohol (Kuraray PVA-117). After adding with vigorous stirring and aggregating, 110 ° C
For 3 hours in a drier kept for 1 hour. The sample thus adjusted and the zeolite agglomerated in Test Example 1 were each taken in a Petri dish having a diameter of 90 mm, dried again until absolutely dry, and then weighed. The weight at that time was defined as 100. Next, a desiccator having an internal volume of about 10 l and a diameter of 12 c containing 300 ml of distilled water at the bottom.
A crystal dish having a height of 6 cm and a height of 6 cm was placed, and a 10-ml weighing bottle in which 0.5 ml of a solution prepared by diluting 0.2 ml of 37% formalin with 5 ml of distilled water was placed therein, and each was placed in a petri dish. Sample was placed. The measured value of formaldehyde gas in the desiccator containing only formalin and sealed for 48 hours was 11.9 mg / l. Furthermore, after the desiccator on which each sample was placed was sealed, the sample was allowed to stand in a constant temperature and humidity room maintained at a temperature of 20 ° C. and a relative humidity of 65% for 48 hours. After a predetermined time, the concentration of formaldehyde absorbed in the distilled water in the crystallizing dish placed in the desiccator was measured by the acetylacetone method specified in JIS-5908. The results are shown in Table 2. As is clear from the results, it is clear that cedar bark chips, activated carbon, and urea powder added to the aggregated zeolite and the aggregated form of zeolite absorb formaldehyde gas better.

【0019】[0019]

【表2】 [Table 2]

【0020】以上の各試験例の結果から、粒度が1mm
以下の多孔性鉱物粉末に水溶性高分子を主体とする水溶
液を攪拌しながら加えて団粒化させ、乾燥して団粒化鉱
物粉末にすることによって吸放湿性能を大幅に改善する
ことを見出すと共に、団粒化の際に樹皮粉末あるいはチ
ップ、活性炭や炭化物粉末、アミノ化合物粉末などを添
加することにより、吸放湿性やホルムアルデヒドガスな
どの吸収性能を一層向上改善することができる。
From the results of the above test examples, the particle size was 1 mm
By adding an aqueous solution mainly composed of a water-soluble polymer to the following porous mineral powder with stirring and aggregating, and drying to form an aggregated mineral powder, it is possible to significantly improve the moisture absorption / release performance. In addition, by adding bark powder or chips, activated carbon, carbide powder, amino compound powder and the like during agglomeration, it is possible to further improve and improve the moisture absorption / release properties and the absorption performance of formaldehyde gas and the like.

【0021】[0021]

【本発明の効果】本発明の効果は多孔性鉱物粉末粒子の
孔隙を一層増加させることによるもので、水分やガスの
吸着面積を増やすことに起因している。またこの鉱物粒
子に樹皮粉末やチップ、アミノ化合物などを添加するこ
とにより吸着したホルムアルデヒドガスなどと反応して
固定化させる効果を有する。
The effect of the present invention is due to the fact that the pores of the porous mineral powder particles are further increased, and is caused by increasing the adsorption area of water and gas. The addition of bark powder, chips, amino compounds and the like to the mineral particles has the effect of reacting with formaldehyde gas and the like adsorbed to immobilize the mineral particles.

【0022】このような効果を有する団粒化鉱物粒子は
住宅の床下に敷いて、地面から放散される水分を防止す
る床下防湿材と利用することができる。
The aggregated mineral particles having such an effect can be laid under the floor of a house and used as a moisture proof material under the floor for preventing moisture radiated from the ground.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C01B 39/04 C01B 39/04 4J002 C08J 3/12 CEP C08J 3/12 CEPZ CER CERZ C08K 7/24 C08K 7/24 C08L 101/14 C08L 101/14 Fターム(参考) 4D052 HA03 HA21 HA22 HA23 HA24 HA39 HB02 4F070 AA26 AB13 AC04 AC22 AC46 AC49 AC96 AD03 DA56 DA60 DC02 DC04 DC05 DC11 4G004 GA00 NA01 4G066 AA04B AA05B AA61B AA64B AA67B AA70B AB06D AB07D AB29D AC02D AC06D AC07B AC07D AC10D AC16D AC25B AC26B AC27B AC39B AD10B AE20D BA09 BA20 BA23 CA29 CA43 CA52 DA03 EA20 FA03 FA21 FA26 FA37 4G073 BB71 BB75 BC10 BD11 CZ00 FA10 FB30 FD26 GA11 UA06 UB60 4J002 AB03W AB04W AB05W AD01W AD02W AH00X BE02W BG01W BG13W BJ00W CH01W DA016 DJ006 EN006 EN116 ET016 FB27X FB276 FD140 GD02──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) C01B 39/04 C01B 39/04 4J002 C08J 3/12 CEP C08J 3/12 CEPZ CER CERZ C08K 7/24 C08K 7 / 24 C08L 101/14 C08L 101/14 F term (reference) 4D052 HA03 HA21 HA22 HA23 HA24 HA39 HB02 4F070 AA26 AB13 AC04 AC22 AC46 AC49 AC96 AD03 DA56 DA60 DC02 DC04 DC05 DC11 4G004 GA00 NA01 4G066 AA04B AA07BA AABB ABB AB29D AC02D AC06D AC07B AC07D AC10D AC16D AC25B AC26B AC27B AC39B AD10B AE20D BA09 BA20 BA23 CA29 CA43 CA52 DA03 EA20 FA03 FA21 FA26 FA37 4G073 BB71 BB75 BC10 BD11 CZ00 FA10 FB30 FD26 GA11 UA06 UB60 4J002 AB03W AB04W AB05W AD01W AD02W AH00X BE02W BG01W BG13W BJ00W CH01W DA016 DJ006 EN006 EN116 ET016 FB27X FB276 FD140 GD0 Two

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】水溶性高分子を主成分とする水溶液を用い
て粒径1mm以下の微細な孔隙を有する鉱物粒子を主成
分とする粉末を団粒状(顆粒状)に成形した多孔性吸収
材。
1. A porous absorbent formed by using an aqueous solution containing a water-soluble polymer as a main component, and forming a powder mainly containing mineral particles having fine pores having a particle diameter of 1 mm or less into a granular form. .
【請求項2】微細な孔隙を有する鉱物粒子がゼオライト
である請求項1に記載の多孔性吸収材。
2. The porous absorbent according to claim 1, wherein the mineral particles having fine pores are zeolite.
【請求項3】微細な孔隙を有する鉱物粒子を主成分とす
る粉末がゼオライトと活性炭、木質または農産廃棄物の
炭化物粉末、樹皮粉末、あるいは尿素、アミン化合物、
アミノ酸などのアミノ基を有する化合物を混合してなる
請求項1に記載する多孔性吸収材。
3. A powder mainly composed of mineral particles having fine pores is selected from the group consisting of zeolite and activated carbon, charcoal powder of woody or agricultural waste, bark powder, urea, amine compound,
The porous absorbent according to claim 1, wherein a compound having an amino group such as an amino acid is mixed.
【請求項4】水溶性高分子を主成分とする水溶液に粒径
1mm以下の微細な孔隙を有する鉱物粒子を主成分とす
る粉末を加えて攪拌あるいは混練して団粒化させた後、
乾燥することを特徴とする多孔性吸収材の製造方法。
4. An aqueous solution containing a water-soluble polymer as a main component is mixed with a powder mainly containing mineral particles having fine pores having a particle size of 1 mm or less and stirred or kneaded to form an aggregate.
A method for producing a porous absorbent material, comprising drying.
【請求項5】微細な孔隙を有する鉱物粒子がゼオライト
である請求項4に記載する多孔性吸収材の製造方法。
5. The method for producing a porous absorbent according to claim 4, wherein the mineral particles having fine pores are zeolite.
【請求項6】粒径1mm以下の微細な孔隙を有する鉱物
粒子を主成分とする粉末がゼオライトと活性炭、木質ま
たは農産廃棄物の炭化物粉末、樹皮粉末、あるいは尿
素、アミン化合物、アミノ酸などのアミノ基を有する化
合物を混合してなる請求項4に記載する多孔性吸収材の
製造方法。
6. A powder mainly composed of mineral particles having fine pores having a particle diameter of 1 mm or less is selected from the group consisting of zeolite and activated carbon, charcoal powder of woody or agricultural waste, bark powder, and amino such as urea, amine compound and amino acid. The method for producing a porous absorbent according to claim 4, wherein a compound having a group is mixed.
JP2000074961A 2000-02-10 2000-02-10 Porous absorbing material and its manufacturing method Pending JP2001219061A (en)

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Country Status (1)

Country Link
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008183536A (en) * 2007-01-31 2008-08-14 Shiga Pref Gov Porous body manufacturing method and composite material
EP2263533A1 (en) 2009-06-18 2010-12-22 Deutsche Telekom AG Enhancing security and emergency functionalities in mobile phones based on detection of physical shocks
JP2018531090A (en) * 2015-10-07 2018-10-25 ロディア・アツェトウ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングRhodia Acetow GmbH Use of composite materials in building materials, building materials and air purification methods
CN116082043A (en) * 2023-02-28 2023-05-09 福建华清电子材料科技有限公司 Continuous preparation method for aluminum nitride powder by sintering

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008183536A (en) * 2007-01-31 2008-08-14 Shiga Pref Gov Porous body manufacturing method and composite material
EP2263533A1 (en) 2009-06-18 2010-12-22 Deutsche Telekom AG Enhancing security and emergency functionalities in mobile phones based on detection of physical shocks
JP2018531090A (en) * 2015-10-07 2018-10-25 ロディア・アツェトウ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングRhodia Acetow GmbH Use of composite materials in building materials, building materials and air purification methods
CN116082043A (en) * 2023-02-28 2023-05-09 福建华清电子材料科技有限公司 Continuous preparation method for aluminum nitride powder by sintering
CN116082043B (en) * 2023-02-28 2023-09-22 福建华清电子材料科技有限公司 Continuous preparation method for aluminum nitride powder by sintering

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