JPS586233A - Removing filter for gaseous sulfide - Google Patents

Removing filter for gaseous sulfide

Info

Publication number
JPS586233A
JPS586233A JP56103270A JP10327081A JPS586233A JP S586233 A JPS586233 A JP S586233A JP 56103270 A JP56103270 A JP 56103270A JP 10327081 A JP10327081 A JP 10327081A JP S586233 A JPS586233 A JP S586233A
Authority
JP
Japan
Prior art keywords
filter
fibers
soln
ferrite
fine powder
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
JP56103270A
Other languages
Japanese (ja)
Inventor
Sotoharu Goto
外治 後藤
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.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy Industries Ltd
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 Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP56103270A priority Critical patent/JPS586233A/en
Publication of JPS586233A publication Critical patent/JPS586233A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a filter for sulfides which permits an increase in the volume of the gases to be treated in one hour per apparent volume of adsorbents, is easy to regenerated and can be molded into a cartridge type by depositing active ferrite powder directly on fibers. CONSTITUTION:A ferrous sulfate soln. and a ferric chloride soln. are mixed at a 1:2 ratio, and this soln. is neutralized with an NaOH soln., whereby active ferrite of fine powder having no water of crystallization is obtd. The fine powder 2 of active ferrite is deposited by arbitrary methods on fibers 1 such as paper, synthetic fibers, glass, asbestos, or the like, whereby a filter element is produced. In use, the element is worked to a wave- or star-shaped filter and this filter is incorporated into a desulfurizer. The surfaces of the fine powder of the active ferrite which is an adsorbent is utilized entirely and the increase in an SV value are made possible. This filter is easy to regenerate by repetition of washing and drying followed by air oxidation.

Description

【発明の詳細な説明】 本発明は、硫化ガス、主として硫化水素及びメル★グタ
ン磐O悪臭ガスの除去フィルターに関する。更に詳細に
社、本発明社、従来から使用されているC紬晶置酸化鉄
ベレッ)Kかえて、活性7エライ)0黴細粉末を使用し
、これを有機質又は鍼機質繊維に担持させてなる硫化ガ
ス除去フィルターEmmする。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a filter for removing sulfide gases, mainly hydrogen sulfide and Mel*GtanO malodor gases. In more detail, the present invention company uses an active 7 element (0) microscopic powder instead of the conventionally used C-crystalline iron oxide beret (K), and supports this on organic or acupuncture fibers. Sulfide gas removal filter Emm.

硫化ガスO発生社、各種の化学工場、特に製紙工場(タ
57トパルプ法)をはじめとし、ゴム、プラスチツタ関
連及び石油精製工場等にみもれ、更に都市のし尿処履場
(消化#&)や下水処麿場*Kかいて4与られ、悪臭ガ
ス。主要成分となって−る。これら硫化ガスの除去手段
として社、従来からアルiIす洗滌法(次O反応式1に
よるもの)及び酸化鉄吸着法(次の反応式2によるもの
)が用−られて−る。
Sulfide gas generation companies, various chemical factories, especially paper mills (T57 pulp method), rubber and plastic ivy related plants, oil refineries, etc., as well as urban human waste disposal facilities (digestion #&). And sewage treatment facility Maroba *K + 4 was given, foul-smelling gas. It is the main ingredient. Conventionally, as means for removing these sulfide gases, the Al iI washing method (according to the following O reaction formula 1) and the iron oxide adsorption method (according to the following reaction formula 2) have been used.

)IaOH+ Ha I  −4Wall 十Ha O
”拳”  D)?eOz + 1IaH−h F@1!
 + 1ilO@11@・・・(2)上記O従来方法に
&!夫夫々寄書得失To)、前者のアルカリ洗滌法(1
1式法)紘、硫化ガスO1k収効率は棗好であるが、l
ll1処履O問題が残)、後者の酸化鉄吸着法(乾式法
)は、酸化鉄O再生は簡単であるが、硫化ガス011着
効率が悪iなどO問題がある。
)IaOH+ Ha I -4Wall 10Ha O
“Fist” D)? eOz + 1IaH−h F@1!
+ 1ilO@11@...(2) The above O conventional method &! The former's alkaline cleaning method (1)
1 equation method) Hiro, the sulfide gas O1k yield rate is better than Natsume, but l
In the latter iron oxide adsorption method (dry method), regeneration of iron oxide O is easy, but there are problems such as poor adhesion efficiency of sulfide gas.

本発WJ4鉱、螢者O酸化鉄歇着法(11,弐渋)の改
良に関する。すなわち、従来O乾式法に用−られて−る
吸着、剤は、a結晶層酸化鉄の@末を、粘結剤を使用し
て錠剤(Tablet)中粒状ベレツ) (p*xxe
t) K 11. I! シた%O″eToるが、硫化
ガスを含む処理ガスがζ011着剤を兜填しえ容器を通
過する際、この吸着剤と硫化ガスとが実質的KII触す
る表面積が小iIh #従って、規定の吸着性能を得る
ためには、ay値(中間速IF)を小さくシ、多量O吸
着剤を必要とする欠点が存在する。
This article relates to the improvement of the WJ4 ore developed in the present invention and the firewood O iron oxide intercalation method (11, Nishibu). That is, the adsorption agent conventionally used in the O dry method is to form a powder of iron oxide in the crystal layer into a tablet (tablet) using a binder (p*xxe).
t) K 11. I! However, when the processing gas containing the sulfide gas passes through the container filled with the ζ011 adhesive, the surface area where the adsorbent and the sulfide gas come into substantial contact is small. Therefore, In order to obtain a specified adsorption performance, the ay value (intermediate speed IF) must be small and a large amount of O adsorbent is required.

なお、Bマ値とは空間速度(8paa@Veloait
y)と1づけられるもので、次O式O如く、1時間轟)
O熟思lス量・(0℃換算)を、吸着剤(触媒等を含む
)見掛は容積で除したもので H−1単位で表示される
In addition, the Bma value is the spatial velocity (8 paa @ Veloait
y) and 1, as in the following O type O, 1 hour roar)
The amount of oxygen (converted to 0°C) divided by the apparent volume of the adsorbent (including catalyst, etc.) is expressed in units of H-1.

通常用いられている従来の吸着剤の8マ値は1・O以下
であ艶、錫層ガス量が毎時1・〇−〇場舎脱硫用吸着剤
は1冑8以上を必要とする。
Conventional adsorbents commonly used have a glossy value of less than 1.O, while adsorbents for desulfurization in which the amount of tin layer gas is 1.0-0 per hour require a value of 8 or more.

本発明は、上記欠点を歇嵐しえものでTo)、そO改良
点は次の2点にある。
The present invention overcomes the above-mentioned drawbacks and has the following two improvements.

口) 吸着剤を、従来Og結晶渥酸化鉄から活性フェラ
イトにか見え点。
) The adsorbent can be changed from conventional Og crystalline iron oxide to activated ferrite.

(2)成型手段を、従来O@結剤併用Oベレット源から
粘結剤を使用せず活性フェライト粉末を直接有機質又は
−横貫繊維に担持させた点。
(2) The active ferrite powder is directly supported on the organic material or transverse fibers without using a binder from the conventional O pellet source in combination with a binder as the molding means.

すなわち、本発明は雛−鉄塩と第二鉄塩とO温合溶液を
アルカリで中和して得られる活性フェライト粉末を、有
機質又は無機質繊維に!1持させてなることを特徴とす
る硫化ガス除去フィルターでTol)、これによって、
従来の一マ値を約10倍向上する効果を奏する%Oであ
る。
That is, the present invention uses activated ferrite powder obtained by neutralizing a mixed solution of iron salt, ferric salt, and O warm with an alkali to produce organic or inorganic fiber! This is a sulfide gas removal filter that is characterized by having a
%O has the effect of improving the conventional one-ma value by about 10 times.

本発明を従来法と比較して、より詳細に説明すると、脱
硫用吸着剤01[科である酸化鉄は、従来法では、酸性
の鉄イオン溶液をアルカ菅で中和して水酸化鉄の沈殿を
作)、とれかも直結晶型の酸化鉄を製造してか)、とO
酸化鉄は軸径が大きい40である。これに対して、本発
明で使用する吸着剤Fi活性アエツイトであ)、とれは
、単一〇酸性の鉄イオン溶液をアに*すで中和する上述
の方法を用いず、予め第一鉄イオン溶液と第二鉄イオン
溶液とを1対意の比で温合しておき、これを中和して調
造するものである。こO方法によると、結晶水をもえ壜
−微粉末(粒径(Ll々り四ン以下)の活性フェライト
が得られる。上記O結晶層酸化鉄及び活性フエ94)の
製法は、いずれも従来よシ知られている方法でる〕、そ
れらの反応は次に示すとおりである。
To explain the present invention in more detail by comparing it with a conventional method, the desulfurization adsorbent 01 [family iron oxide] is produced by neutralizing an acidic iron ion solution in an alkali tube and producing iron hydroxide. Precipitate), or produce recrystalline iron oxide), and O
Iron oxide has a large shaft diameter of 40. On the other hand, with the adsorbent Fi activated It is prepared by heating an ionic solution and a ferric ion solution at a ratio of 1 to 1, and then neutralizing the mixture. According to this O method, activated ferrite with a fine powder (particle size (Ll-4) or less) can be obtained by burning crystal water. [by a well-known method], and their reactions are as follows.

a結晶型酸化鉄の場合 21aO1g 十411aO)! −+ 2νe(OH
%+ 611aojν・(OH)s−47N Ol ・
n% 。
For a-crystalline iron oxide, 21aO1g 1411aO)! −+ 2νe(OH
%+ 611aojν・(OH)s-47N Ol・
n%.

活性フェライトの場合 シeilQ4−4−2シe04 + 8MaOH−41
1J@O−Fil QI+ lfa@ go@+!1i
aoj + 4島0本発゛明では、上記したように、結
晶水を有しない微粉末の活性フェライト(磁性酸化鉄)
を吸着剤として使用するものでtblとれはtそ0粒径
が極めて小さいので、比表面積(単位重量当夛の表面積
)が極めて大きくな〕、吸着剤としての性能向上に役立
つ基礎的要因をなす亀のである。
In the case of active ferrite, sheil Q4-4-2 sheil e04 + 8MaOH-41
1J@O-Fil QI+ lfa@go@+! 1i
aoj + 4 islands 0 In the present invention, as mentioned above, fine powdered active ferrite (magnetic iron oxide) without crystal water is used.
Since the particle size of TBL is extremely small, the specific surface area (surface area per unit weight) is extremely large], which is a fundamental factor that helps improve the performance as an adsorbent. It's a turtle.

次に成型手段であるが、従来は例えId4/4(直径4
■、長−s4 m ) 0ベレツト状に成層しえものを
用いてか)、その結果、酸化鉄と処llスとの接触面積
が小さい欠点がある・これに対して、本発明では、微粉
末era性フェライトそれ自体が、1個づつ自由に熟思
ガスと接触で自るようKする大め、繊維に謹持堪せる成
型手段を採用するものである0本発明で用iる繊維とし
ては、紙、綿、羊毛、絹などの天然繊維の他ナイーン、
ビニロン、テ)翳ンなど0会成繊維及びガラス、アスベ
スト、竜うミツタスなどの無機繊維でhシ、これら担持
眉鐵維は熟思ガスの性状、’f#に処層ガス温度に応じ
て適宜選択するものである。まえ、本発明KTh−て、
繊維KJI持させる手段としては任意であるが、例えば
、紙に担持させる場合には、抄紙法による製紙工程にお
いて、フエライ)It!粉末を懸濁(8usp@n5i
on) 0状態で混合し成形する方法を用−ることがで
きる、まえ、本発明にシいて、フェライト微粉末Oat
持量は任意であるか、通’1lFilO〜40重量s”
t’in、好tL(は11〜40重量−てめる、壜大、
本発@にお−て、活性フェライト粉末を担持しえ絨−を
そIDままフィルターとしてw!用で自るが、好ましく
鉱、PIl、すなわち舐、織布、不絨布力どのフィルタ
ーエレメ/)K加工し、さらに、波形又は星状フィルタ
ーに加工するOが好適である。
Next is the molding means. Conventionally, for example, Id4/4 (diameter 4
■, Length - s4 m) As a result, the contact area between the iron oxide and the treatment layer is small.In contrast, in the present invention, The fibers used in the present invention are large enough to allow the powdered ferrite to self-destruct one by one when it comes in contact with a contemplative gas, and a molding method is adopted that allows the fibers to endure. , natural fibers such as paper, cotton, wool, silk, etc.
0-component fibers such as vinylon, TE), and inorganic fibers such as glass, asbestos, and mitsutus are used. It is a choice. First, the present invention KTh-te,
The means for supporting the fiber KJI is arbitrary, but for example, when supporting it on paper, it can be used in the papermaking process using the papermaking method. Suspend the powder (8usp@n5i
In accordance with the present invention, a method of mixing and molding in a zero state can be used.
The carrying amount is arbitrary, or the total weight is 1 l to 40 wt.
t'in, good tL (is 11-40 weight-temel, bottle size,
In this development @, the carpet carrying activated ferrite powder can be used as a filter as it is! However, it is preferable to use filter elements such as mineral, PIl, filtrate, woven fabric, non-woven fabric, etc., and further process it into a corrugated or star-shaped filter.

添付v:J#iについて本発明をよクーSに説明すると
、第1図は本発明のフィルターの一部拡大図であり、繊
維10間に活性フェライト粉末2が粉末1個づつ夫々7
リーで存在してiる状態を示す。本発明は、第1図に示
すように1各粉末が夫々自由に繊維間に存在しているた
め、各粉末0表面が充分に処理ガスと接触することとな
)、吸着性能が最大限に発揮されるもθである。
Attachment v: J#i To explain the present invention to Yokoo S, Fig. 1 is a partially enlarged view of the filter of the present invention, in which activated ferrite powder 2 is placed between fibers 10, one powder each 7
Indicates the state of existence in Lee. In the present invention, as shown in Fig. 1, each powder exists freely between the fibers, so the surface of each powder comes into sufficient contact with the processing gas), and the adsorption performance is maximized. The effect is also θ.

第1図は、本発明のフィルターの形部を例示し丸もので
るり、(ム)は5層のフィルター(f)層シらな墨もの
であn、(lは1つのフィルター(f)を*IIK加工
したもOである。
Figure 1 shows examples of the shapes of the filters of the present invention; (mu) is a five-layer filter (f) is a thin black black one; (l is one filter (f)). It is also O after *IIK processing.

閣中矢印鉱処理ガスの流れ方向を示す、フイ羨タ一層七
通過する処理ガスの抵抗値を少なくすることを意図する
場合は、(ム)より%CB)のフィルター形11にする
のが好ましi。これは(1) 011111は、(A)
(IそtLK比較して、フィルターのaim積が大11
%A大め、熟思lス0椙対流速が両者同一であっても、
フイにター曹0絶対流速は(1)の方が極めて小さ0〕
、ζO結果、フィルター〇通過抵抗を小さくする仁とと
なるからである。
If the intention is to reduce the resistance value of the processing gas passing through the filter, it is preferable to use a filter type 11 of (%CB) rather than (MU). Mashii. This is (1) 011111 is (A)
(Compared to I and LK, the aim product of the filter is large 11
%A is larger, I think about it. Even if the convection velocity is the same for both,
Finally, the absolute flow velocity of (1) is extremely small.
This is because, as a result, the resistance to passing through the filter becomes small.

第3図紘、本発明0フイルターを綴込んだ脱硫装置01
例でTo夛、本発明Oフィルターを長さ方向KfIIL
形KN)―けて星状フィhp−(m)とし、これを2本
の円筒容all(ム)、(ムI)内にセットし、外筒(
1)と叢(0)中に配設しえ40である。図中矢印社熟
思ガスの流れを示す。
Figure 3 Hiro, desulfurization equipment 01 with the present invention 0 filter installed
For example, the present invention O filter in the longitudinal direction KfIIL
Form KN) - a star-shaped fi hp- (m), set it in two cylindrical volumes all (mu), (mu I), and outer cylinder (
1) and 40 disposed in the plexus (0). The arrow in the figure shows the flow of the gas.

本発Ij!h、上記したように、従来0#結晶■酸化鉄
にかえて微粉末の活性フェライトをw!用し、これを直
接繊維Km持させえ構成からなるフィルターであるから
、I!東0%OK比し、吸着剤でh為活性フィルター黴
粉末のすべて011画を活用できるので、−マ値が高め
ることがてき(#11倍に向上させるeとがで自、)、
★丸、吸着剤O使用量が小量とすることがで龜る顕著を
効果を奏する4のである。さらに、本発明0フィルター
は、水洗、屹燥を()返し、空気酸化で簡単に再生する
ことがで自るも0であItえ、本発明oフィルターは、
これを組込んに脱硫装置をコンパクトにすることがで自
ると共にこ0フイルターをカートリッジ弐に成形するこ
とがで龜る4のであるから、堆扱i及びメンテナンスが
容易であるなどO利点が生ずる%Oである。
Original Ij! h, As mentioned above, instead of the conventional 0# crystal ■ iron oxide, use fine powder active ferrite lol! Since this is a filter consisting of a structure in which the fibers Km are directly retained, I! Compared to 0% OK, since all of the active filter mold powder can be utilized with the adsorbent, the -ma value can be increased (e and the value are increased by #11 times),
* Circle 4 shows that using a small amount of adsorbent O has a significant effect. Furthermore, the O filter of the present invention can be easily regenerated by air oxidation after washing with water and drying.
By incorporating this, the desulfurization equipment can be made more compact, and the filter can also be molded into the cartridge, which makes it easier to handle and maintain the cartridge. %O.

実施例 硫酸嬉−鉄(y・#偽り40)!111液と塩化第二鉄
(ν・04・aha)zswi液とを混合し、むOI&
舎液をM*OH$111で中和して活性7エ2イトを製
造した。得られえ7エライト粉末14・麺をパルプ抄紙
液体に諷合し、繊維転体重量221α推持させ、巾1飼
、長さtz=、厚さ104mのフィルクーエレメントを
製造しえ。
Example sulfate-iron (y/#false 40)! 111 liquid and ferric chloride (ν・04・aha)zswi liquid,
The solution was neutralized with M*OH$111 to produce active 7E2ite. The obtained 7-elite powder 14 and noodles were combined with a pulp papermaking liquid to maintain a fiber inversion weight of 221α, and a film element having a width of 1, a length of tz, and a thickness of 104 m was produced.

このエレメントを、ll5l!!!lK示すように、長
1方肉に液形に折り−げて星状フィルター(ml)K成
層し、辷れを直II (L S m lびLlwaで長
さ1鯛Oパンチメタルで作うえ2本O円曽容−(ム)、
(7)04’にセットし、外筒(1)と蓋(0)0’t
”に取付け、脱硫フィルター装置を製造し* e e 
o 装置に1硫化水素1 @ 5 @ ’Iipmsメ
チルメ#★ブタン221S)ν鳳を會む空気を毎時4・
〇−通過させ良とζろ、硫化水素、メテルメ羨カプタン
共!!−以上O除去率を得え。
This element, ll5l! ! ! As shown, fold the meat into a liquid shape on one length, layer it with a star-shaped filter (ml), and make a length of sea bream with punched metal. 2 O Ensoyo-(mu),
(7) Set to 04', outer cylinder (1) and lid (0) 0't
” to manufacture a desulfurization filter device* e e
o The equipment is supplied with 1 hydrogen sulfide 1 @ 5 @ 'Iipms methylmethane #★butane 221S) ν 4 hours per hour.
〇- Let it pass and ζro, hydrogen sulfide, meterume envy captan! ! Obtain an O removal rate of - or more.

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

第11!i it 、本発明Oフィルター〇一部拡大図
でToシ、Kz図は、本発明0フイルターの形態を例示
した図てあり、第易■線、本発明のフィルターを組込ん
だ脱硫装置01例を示す。 復代理人  内 1)  明 豐代薯人  藪 原 亮 −
11th! i it, O filter of the present invention; Toshi and Kz diagrams are partially enlarged views illustrating the form of the O filter of the present invention; shows. Sub-agents 1) Akihiro Yabuhara Ryo -

Claims (1)

【特許請求の範囲】[Claims] 嬉−鉄環と諺二鉄塩との混合溶液をアルカリで中和して
得られる活性7エライト粉末を、有機質又紘無機質繊艙
に担持させてなることを特徴とする硫化ガス除去フィル
ター。
A sulfide gas removal filter characterized in that an active 7-elite powder obtained by neutralizing a mixed solution of iron salts and ferrous salts with an alkali is supported on an organic or inorganic fiber.
JP56103270A 1981-07-03 1981-07-03 Removing filter for gaseous sulfide Pending JPS586233A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56103270A JPS586233A (en) 1981-07-03 1981-07-03 Removing filter for gaseous sulfide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56103270A JPS586233A (en) 1981-07-03 1981-07-03 Removing filter for gaseous sulfide

Publications (1)

Publication Number Publication Date
JPS586233A true JPS586233A (en) 1983-01-13

Family

ID=14349710

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56103270A Pending JPS586233A (en) 1981-07-03 1981-07-03 Removing filter for gaseous sulfide

Country Status (1)

Country Link
JP (1) JPS586233A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6342735A (en) * 1986-08-11 1988-02-23 Mitsubishi Heavy Ind Ltd Honeycomb-shaped desulfurizing agent
CN106190428A (en) * 2016-08-30 2016-12-07 温州乐享科技信息有限公司 A kind of method that coal is burnt
CN106190429A (en) * 2016-08-30 2016-12-07 温州乐享科技信息有限公司 A kind of method for burning coal
CN106221853A (en) * 2016-08-30 2016-12-14 温州乐享科技信息有限公司 The method of coal burning
CN106281574A (en) * 2016-08-30 2017-01-04 温州乐享科技信息有限公司 A kind of method for burning coal
CN106281573A (en) * 2016-08-30 2017-01-04 温州乐享科技信息有限公司 method for burning coal
CN106318513A (en) * 2016-08-30 2017-01-11 温州乐享科技信息有限公司 Coal combustion method
CN106318514A (en) * 2016-08-30 2017-01-11 温州乐享科技信息有限公司 Coal combustion method

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6342735A (en) * 1986-08-11 1988-02-23 Mitsubishi Heavy Ind Ltd Honeycomb-shaped desulfurizing agent
CN106190428A (en) * 2016-08-30 2016-12-07 温州乐享科技信息有限公司 A kind of method that coal is burnt
CN106190429A (en) * 2016-08-30 2016-12-07 温州乐享科技信息有限公司 A kind of method for burning coal
CN106221853A (en) * 2016-08-30 2016-12-14 温州乐享科技信息有限公司 The method of coal burning
CN106281574A (en) * 2016-08-30 2017-01-04 温州乐享科技信息有限公司 A kind of method for burning coal
CN106281573A (en) * 2016-08-30 2017-01-04 温州乐享科技信息有限公司 method for burning coal
CN106318513A (en) * 2016-08-30 2017-01-11 温州乐享科技信息有限公司 Coal combustion method
CN106318514A (en) * 2016-08-30 2017-01-11 温州乐享科技信息有限公司 Coal combustion method

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