JP3168387B2 - Deodorizing material and method for producing the same - Google Patents

Deodorizing material and method for producing the same

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Publication number
JP3168387B2
JP3168387B2 JP33094194A JP33094194A JP3168387B2 JP 3168387 B2 JP3168387 B2 JP 3168387B2 JP 33094194 A JP33094194 A JP 33094194A JP 33094194 A JP33094194 A JP 33094194A JP 3168387 B2 JP3168387 B2 JP 3168387B2
Authority
JP
Japan
Prior art keywords
weight
activated carbon
deodorizing material
toluene
producing
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.)
Expired - Lifetime
Application number
JP33094194A
Other languages
Japanese (ja)
Other versions
JPH08155239A (en
Inventor
多美夫 野田
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.)
Nippon Steel Corp
Original Assignee
Nippon Steel 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 Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP33094194A priority Critical patent/JP3168387B2/en
Publication of JPH08155239A publication Critical patent/JPH08155239A/en
Application granted granted Critical
Publication of JP3168387B2 publication Critical patent/JP3168387B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Separation Of Gases By Adsorption (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Description

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

【0001】[0001]

【産業上の利用分野】本発明はトルエン、キシレン等の
溶剤の臭気を除去する脱臭材およびその製造方法に関す
る。本発明の脱臭材は、例えば塗装工場、印刷工場用の
脱臭材として用いることができる。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a deodorizing material for removing odors from solvents such as toluene and xylene and a method for producing the same. The deodorizing material of the present invention can be used, for example, as a deodorizing material for a painting factory and a printing factory.

【0002】[0002]

【従来の技術】トルエン、キシレン等の溶剤の臭気に対
しては、活性炭を用いる吸着法や、直接燃焼法、触媒燃
焼法が行われている。しかし、活性炭を用いる吸着法は
吸着熱による発火、火災が起きやすいという安全上の問
題があり、直接燃焼法では燃料コストが高く悪臭成分を
完全燃焼させるには燃焼温度を高く保つ必要があり窒素
酸化物が発生する等問題があり、触媒燃焼法では触媒が
塗料に含まれる珪酸等の顔料によって被毒し短期間に脱
臭性能が劣化し、高価な触媒交換する為の費用が必要と
なる問題があった。
2. Description of the Related Art An adsorption method using activated carbon, a direct combustion method, and a catalytic combustion method are used for the odor of a solvent such as toluene and xylene. However, the adsorption method using activated carbon has a safety problem that ignition and fire easily occur due to the heat of adsorption.The direct combustion method requires high fuel costs and requires a high combustion temperature to completely combust odorous components. There is a problem such as the generation of oxides. In the catalytic combustion method, the catalyst is poisoned by pigments such as silicic acid contained in the paint, and the deodorizing performance deteriorates in a short period of time. was there.

【0003】[0003]

【発明が解決しようとする課題】活性炭は可燃性物質で
あり火災の危険性があるものの、トルエン、キシレン等
の溶剤吸着性能には優れている。
Activated carbon is a flammable substance and has a risk of fire, but has an excellent ability to adsorb solvents such as toluene and xylene.

【0004】従って、粒状活性炭を通気性の良い不燃物
質でコーティングする等の対策が考えられる。また、粉
末活性炭を不燃性の物質と混練して成形する方法も考え
られる。
Therefore, measures such as coating granular activated carbon with a non-combustible substance having good air permeability can be considered. A method of kneading powdered activated carbon with a nonflammable substance and molding the same is also conceivable.

【0005】しかし、不燃性の物質で成形性が良く、形
状を保持できる強度を持ち、かつ活性炭の吸着性能を損
なわない製造方法は一般的に極めて難しい。
However, it is generally extremely difficult to use a non-combustible substance which has good moldability, has sufficient strength to maintain its shape, and does not impair the adsorption performance of activated carbon.

【0006】成形性について言えば、例えば押し出し成
形をする場合は流動性が求められるが流動性の良いカオ
リン等の粘度鉱物等を混合材として選択すれば成形はで
きるようになるが乾燥しても充分な強度が得られない。
With respect to the moldability, for example, in the case of extrusion molding, fluidity is required, but if a viscous mineral such as kaolin having good fluidity is selected as a mixed material, molding can be performed, but even if it is dried, Sufficient strength cannot be obtained.

【0007】そのような場合は成型後に焼結処理をしな
いと搬送や使用に耐える強度は保てないし通気性が悪い
ので活性炭の吸着性能が著しく損なわれる。焼結処理の
ときに活性炭が酸化して消耗してしまうことも問題であ
る。焼結費用もかかる。
In such a case, if the sintering treatment is not performed after molding, the strength that can withstand transportation and use cannot be maintained or the air permeability is poor, so that the adsorption performance of activated carbon is significantly impaired. Another problem is that activated carbon is oxidized and consumed during the sintering process. It also requires sintering costs.

【0008】形状保持強度については、例えば成形後の
強度を保つ為の接着剤は活性炭との親和性が高く活性炭
の吸着性能の本質的特徴である微細孔を被覆してしまい
吸着性能を損なう。
Regarding the shape retention strength, for example, an adhesive for maintaining the strength after molding has a high affinity for activated carbon and covers the fine pores which are an essential feature of the activated carbon adsorption performance, thereby impairing the adsorption performance.

【0009】[0009]

【課題を解決するための手段】不燃性で通気性がある粘
度鉱物として鎖状珪酸マグネシウムを選定し、成型時の
流動性を改善する素材としてハロイサイトを選び、粉末
活性炭と混合成形した場合に成形性、強度、脱臭性能及
び火災の危険性が無い適正な配合と混練液の調合法につ
いて研究を行い、本発明を開発するに到った。
[Means for Solving the Problems] Chain magnesium silicate is selected as a nonflammable and air-permeable viscous mineral, halloysite is selected as a material for improving fluidity during molding, and molding is performed when mixed with powdered activated carbon. The present invention was developed by conducting research on a proper compounding method without mixing property, strength, deodorizing performance and danger of fire and a method of preparing a kneading liquid.

【0010】即ち、多孔質で通気性に富む鎖状珪酸マグ
ネシウムを主体の配合として不燃性を確保し、流動性の
良いハロイサイトを少量配合して成形性を高めると同時
に燐酸とヒドラジンの混合水溶液で混練することにより
粘土鉱物が硬化し強度が出せることを見出し、粉末活性
炭の性能を引き出すことに成功した。
[0010] That is, a non-flammable composition is ensured by blending a porous, highly breathable chain-like magnesium silicate as a main component, and a small amount of flowable halloysite is blended to enhance moldability, and at the same time, a mixed aqueous solution of phosphoric acid and hydrazine is used. It was found that the clay mineral was hardened by kneading and strength could be obtained, and the performance of powdered activated carbon was successfully brought out.

【0011】なお、トルエン、キシレン等の吸着容量の
評価では活性炭の配合量以上の吸着容量を示しており鎖
状珪酸マグネシウムも燐酸とヒドラジンの効果でトルエ
ン、キシレン等の吸着性能が付加されていることを示唆
している。
In the evaluation of the adsorption capacities of toluene, xylene, etc., the adsorbing capacities are equal to or more than the amount of activated carbon. The chain magnesium silicate also has the adsorbing capacity of toluene, xylene, etc. due to the effect of phosphoric acid and hydrazine. Suggest that.

【0012】[0012]

【実施例】次に本発明の実施例について述べる。Next, an embodiment of the present invention will be described.

【0013】セピオライト粉末(昭和61年丸善株式会
社発行の「セラミックス辞典」によれば、繊維状形態を
もつ粘土鉱物の一種で複鎖構造類似の構造をもち、化学
組成はMg4Si615(OH)2(OH2)・4H2O。
ドロマイト中に脈状で産し、蛇紋岩の変質によっても生
ずる。)、ハロイサイト粉末(前出の「セラミックス辞
典」によれば、カオリン鉱物の一種で、1:1層の間に
1分子層のH2Oがはさまって交互に積み重なってお
り、組成はAl2Si25(O H)4・2H2Oで表され
る。)、活性炭粉末を表1に示した重量配合比で混合
し、ヒドラジンと硫酸アルミニウム、燐酸を表2の配合
で調製した水溶液を固形分に対して100重量%前後
(後述の押し出し成形の適正水分は95%から110%
であり、90%未満や115%以上では成形不可能であ
った。)添加して混練し、押し出し成形機で成形した。
Sepiolite powder (Maruzen Co., Ltd. in 1986)
According to the "Ceramics Dictionary" published by the company, fibrous forms
A type of clay mineral that has a structure similar to a double-chain structure.
Composition is MgFourSi6OFifteen(OH)Two(OHTwo) ・ 4HTwoO.
Produced in a vein form in dolomite and also produced by alteration of serpentine
Cheating. ), Halloysite powder ("Ceramics"
According to the ceremony, a kind of kaolin mineral, between 1: 1 layers
One molecular layer of HTwoO is sandwiched between layers
And the composition is AlTwoSiTwoOFive(O H)Four・ 2HTwoRepresented by O
You. ), Activated carbon powder mixed at the weight ratio shown in Table 1.
And hydrazine, aluminum sulfate and phosphoric acid as shown in Table 2.
Around 100% by weight of the aqueous solution prepared in
(Appropriate moisture for extrusion molding to be described later is 95% to 110%
If it is less than 90% or 115% or more, molding is impossible.
Was. ), Kneaded, and molded by an extrusion molding machine.

【0014】押し出し成形機のダイスは直径2mmφの
円形の穴を配しており成形品は円柱状の形状を持つ。成
形品は麺状に長くできるが、本実施例では50mmに切
り揃えた。また、押し出し成形品は乾燥機で100℃に
加熱して乾燥し、最終成品とした。
The die of the extrusion molding machine has a circular hole having a diameter of 2 mmφ, and the molded product has a columnar shape. Although the molded article can be lengthened like a noodle, it is cut to 50 mm in this example. The extruded product was heated to 100 ° C. with a dryer and dried to obtain a final product.

【0015】各種配合の中で押し出し成形が不可能なも
のがあり、流動性の評価ではそれらを×と判定した。成
形可能なものは○と判定した。成形性不良の組み合わせ
については脱臭性能、強度、不燃性等の評価は省略し
た。
Extrusion molding was impossible among various compounds, and they were judged as x in the evaluation of fluidity. Those that can be molded were judged as ○. The evaluation of deodorizing performance, strength, nonflammability, etc. was omitted for combinations of poor moldability.

【0016】成形できたものはそれらの成品と市販の粒
状活性炭を使い、トルエンとキシレンの脱臭性能を比較
した。評価装置は図1に示した構造で内容積1m3のア
クリル製の箱の中に、循環ファンを設置し、脱臭材各4
0gを80mm角の底が網でできた箱に入れてファンの
入口にセットし、トルエン、キシレンの除去性能を検知
管で測定した。
The molded products were compared with the deodorizing performance of toluene and xylene using those products and commercially available granular activated carbon. The evaluation device was constructed as shown in Fig. 1 and a circulating fan was installed in an acrylic box with an internal volume of 1 m 3 , and each deodorizing material was
0 g was put in an 80 mm square bottom box made of a net and set at the entrance of the fan, and the removal performance of toluene and xylene was measured with a detector tube.

【0017】初期濃度はそれぞれ500ppm、循環風
量は400 l/分で30分後の濃度がどこまで低下し
ているかを調べて吸着能力を比較した。市販粒状活性炭
はトルエン、キシレンともに30ppmまで低下してお
り、脱臭材を入れないブランクテストでは全く低下せず
30分後も初期濃度が保たれていた。
The initial concentration was 500 ppm and the circulating air flow was 400 l / min, and the adsorption capacity was compared by examining how much the concentration was reduced after 30 minutes. The commercial granular activated carbon was reduced to 30 ppm for both toluene and xylene, and did not decrease at all in the blank test without the deodorizing material, and the initial concentration was maintained after 30 minutes.

【0018】脱臭性能については活性炭との競争力を考
慮して30分後の濃度が60ppm以下であれば○、6
1ppm以上で120ppm以下であれば△、121p
pm以上では×と評価した。
Regarding the deodorizing performance, considering the competitiveness with activated carbon, if the concentration after 30 minutes is 60 ppm or less, 、, 6
If it is 1 ppm or more and 120 ppm or less, Δ, 121p
At pm or more, it was evaluated as x.

【0019】また、成形品の強度については試料100
gを100mmφ*1000mmLのパイプに入れ、パ
イプの上下の蓋の位置関係が交互に切り変わるように1
0回、回転させることによって粉化の程度を調べること
により評価した。
As for the strength of the molded article,
g into a pipe of 100 mmφ * 1000 mmL, so that the positional relationship between the upper and lower lids of the pipe is alternately switched.
Evaluation was made by examining the degree of powdering by rotating 0 times.

【0020】粉の発生は1mm目の篩で篩い分け、その
重量を測定した。粉の発生が1%未満を○、1%以上で
3%未満を△、3%以上を×と判定した。
The generation of the powder was sieved with a 1 mm sieve, and the weight was measured. Less than 1% of powder generation was evaluated as ○, 1% or more and less than 3%, Δ as 3% or more.

【0021】また成品の着火性については試料10gを
ガスバーナーで1分間加熱し、着火が認められたら×、
着火しない場合は○と判定した。
Regarding the ignitability of the product, 10 g of the sample was heated with a gas burner for 1 minute.
When it did not ignite, it was judged as ○.

【0022】[0022]

【表1】 [Table 1]

【0023】[0023]

【表2】 [Table 2]

【0024】評価結果を表3に纏めて示した。成形性、
脱臭性能、強度、不燃性を全て満足できるものとして、
鎖状珪酸マグネシウム55〜80重量%、ハロイサイト
10〜15重量%、粉末活性炭10〜30重量%を含む
混合粉末に燐酸0.5〜1.0mol/lとヒドラジン
0.5〜1.0mol/lを含む水溶液を95〜110
重量%添加して混練、成形したものを得ることができ
た。
The evaluation results are summarized in Table 3. Moldability,
Deodorizing performance, strength, and nonflammability are all satisfied.
A mixed powder containing 55 to 80% by weight of chain magnesium silicate, 10 to 15% by weight of halloysite, and 10 to 30% by weight of powdered activated carbon is mixed with 0.5 to 1.0 mol / l of phosphoric acid and 0.5 to 1.0 mol / l of hydrazine. Aqueous solution containing 95 to 110
It was possible to obtain a kneaded, molded product with the addition of about 10% by weight.

【0025】[0025]

【表3】 [Table 3]

【0026】[0026]

【発明の効果】本発明により、トルエン、キシレンの除
去効率が高く、不燃性で、実用的なレベルで成形性、強
度が確保できる脱臭材が製造できる。
According to the present invention, it is possible to produce a deodorizing material which has high removal efficiency of toluene and xylene, is nonflammable, and can secure moldability and strength at a practical level.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の脱臭材の評価装置を示す図。FIG. 1 is a view showing an apparatus for evaluating a deodorant according to the present invention.

【符号の説明】 1 密閉容器 2 循環ファン 3 脱臭材 4 ガス導入口 5 ガスサンプル採取口 6 ガス循環方向[Description of Signs] 1 Closed container 2 Circulation fan 3 Deodorizing material 4 Gas inlet 5 Gas sampling port 6 Gas circulation direction

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 鎖状珪酸マグネシウム55〜70重量
%、ハロイサイト10〜15重量%、粉末活性炭10〜
30重量%を含む混合粉末に、燐酸0.5〜1.0mo
l/lとヒドラジン0.5〜1.0mol/lを含む水
溶液を固形分に対して95〜110重量%添加して混
練、成形することを特徴とする脱臭材の製造方法。
1. A chain magnesium silicate of 55 to 70% by weight, halloysite of 10 to 15% by weight, powdered activated carbon of 10 to 10% by weight.
0.5 to 1.0 mol of phosphoric acid is added to the mixed powder containing 30% by weight.
A method for producing a deodorizing material, characterized in that an aqueous solution containing 1 / l and 0.5 to 1.0 mol / l of hydrazine is added to a solid content in an amount of 95 to 110% by weight, kneaded and molded.
【請求項2】 請求項1にて製造された、トルエン、キ
シレン等の溶剤の臭気を除去する脱臭材。
2. A deodorizing material for removing odor of a solvent such as toluene or xylene produced in claim 1.
JP33094194A 1994-12-09 1994-12-09 Deodorizing material and method for producing the same Expired - Lifetime JP3168387B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP33094194A JP3168387B2 (en) 1994-12-09 1994-12-09 Deodorizing material and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP33094194A JP3168387B2 (en) 1994-12-09 1994-12-09 Deodorizing material and method for producing the same

Publications (2)

Publication Number Publication Date
JPH08155239A JPH08155239A (en) 1996-06-18
JP3168387B2 true JP3168387B2 (en) 2001-05-21

Family

ID=18238139

Family Applications (1)

Application Number Title Priority Date Filing Date
JP33094194A Expired - Lifetime JP3168387B2 (en) 1994-12-09 1994-12-09 Deodorizing material and method for producing the same

Country Status (1)

Country Link
JP (1) JP3168387B2 (en)

Also Published As

Publication number Publication date
JPH08155239A (en) 1996-06-18

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