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JPS585104B2 - Dust collection electrode for electrostatic precipitator - Google Patents
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JPS585104B2 - Dust collection electrode for electrostatic precipitator - Google Patents

Dust collection electrode for electrostatic precipitator

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Publication number
JPS585104B2
JPS585104B2 JP51071813A JP7181376A JPS585104B2 JP S585104 B2 JPS585104 B2 JP S585104B2 JP 51071813 A JP51071813 A JP 51071813A JP 7181376 A JP7181376 A JP 7181376A JP S585104 B2 JPS585104 B2 JP S585104B2
Authority
JP
Japan
Prior art keywords
dust collection
dust
electrode
electrostatic precipitator
collection electrode
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
Application number
JP51071813A
Other languages
Japanese (ja)
Other versions
JPS52155480A (en
Inventor
一行 辻野
兼政 野間口
功 内ケ崎
毅 丹野
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.)
Resonac Corp
Original Assignee
Hitachi Chemical Co 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 Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP51071813A priority Critical patent/JPS585104B2/en
Publication of JPS52155480A publication Critical patent/JPS52155480A/en
Publication of JPS585104B2 publication Critical patent/JPS585104B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 従来、電気集じん装置はガス中に浮遊する粉鉄、ミスト
などの集じんに広く利用され、放電極(−)には鉛、銅
、ニッケル、ニクロム、チタン、白金などを用い、集じ
ん極(+)には、鉄、鉛、金網などを用いる方法がとら
れている。
[Detailed Description of the Invention] Conventionally, electrostatic precipitators have been widely used to collect dust such as iron powder and mist floating in gas, and the discharge electrode (-) contains lead, copper, nickel, nichrome, titanium, and platinum. For the dust collection electrode (+), iron, lead, wire mesh, etc. are used.

電極に金属を使用するためC12,Cr、SO2゜HC
l、H2SO4、アンモニアなどの腐食性ガス体を含む
集じん(例えば都市ゴミ焼却、排煙脱硫など)において
は当然、装置の腐食の問題が発生し、特に高温での使用
においてはさらに腐食が著しく促進され、使用に耐えな
い場合も多々発生し、装置の材料の検討が強く望まれて
いる。
Since metal is used for the electrode, C12, Cr, SO2°HC
Naturally, when collecting dust containing corrosive gases such as L, H2SO4, and ammonia (e.g., municipal waste incineration, flue gas desulfurization, etc.), equipment corrosion problems occur, and especially when used at high temperatures, corrosion becomes even more severe. However, there are many cases in which the device cannot withstand use due to the acceleration, and there is a strong need to consider the material of the device.

これら高温下における腐食、強度の問題点を解決する手
段としては、従来、合成樹脂を利用したものが実公昭3
8−9088号、特公昭49−8142号、特公昭50
−2463号、特公昭50−2464号などに示される
が、これらはいずれも、耐食性および強度の点から常用
使用温度は80℃以下が限界であり、それ以上の温度で
は強度低下、強度劣化、変形、腐食劣化が著しくなり使
用に耐えない。
Conventionally, as a means to solve these problems of corrosion and strength under high temperatures, synthetic resins have been used.
No. 8-9088, Special Publication No. 1984-8142, Special Publication No. 1973
-2463, Japanese Patent Publication No. 50-2464, etc., but in terms of corrosion resistance and strength, the limit for normal use is 80°C or less, and at higher temperatures, strength decreases, strength deteriorates, etc. Deformation and corrosion deterioration are significant, making it unusable.

特開昭49−10464号公報には、熱硬化性樹脂をガ
ラス繊維、石綿繊維等で強化された素材を用いる例が示
され、また特公昭49−8141号公報には無機繊維層
と高分子化合物から成る板を用いる例が示されているが
、これらは上記の合成樹脂を用いた素材と比べると、強
度、耐熱性の面からは優れるが、その性能は熱硬化性樹
脂の性能に左右される。
JP-A-49-10464 discloses an example of using a thermosetting resin reinforced with glass fiber, asbestos fiber, etc., and JP-A-49-8141 discloses an example in which a thermosetting resin is reinforced with glass fiber, asbestos fiber, etc. An example of using a board made of a compound is shown, but these are superior in terms of strength and heat resistance compared to the materials using synthetic resins mentioned above, but their performance depends on the performance of the thermosetting resin. be done.

例えば、特公昭49−8141号公報に示される不飽和
ポリエステル樹脂、エポキシ樹脂、フラン樹脂、ウレタ
ン樹脂は耐薬品性に優れるが80℃以上では強度劣化が
著しい。
For example, unsaturated polyester resins, epoxy resins, furan resins, and urethane resins disclosed in Japanese Patent Publication No. 49-8141 have excellent chemical resistance, but their strength deteriorates significantly at temperatures above 80°C.

ふっ素樹脂は耐熱性には優れるが、耐薬品性に弱く、フ
ェノール樹脂も使用温度の限界は100℃位である。
Although fluororesin has excellent heat resistance, it has poor chemical resistance, and phenolic resin also has a usage temperature limit of about 100°C.

100℃を越える高温域では、特公昭47−28609
号などにより無機材料である耐熱ガラス、耐熱レンガ、
耐熱モルタルなどを利用することにより常用使用温度2
00℃を可能にしているが、これらの装置は施工に熟練
を要し、かつ構造が複雑となるため施工不良が生じやす
く、これにより耐用年数が短くなり、トータルコストが
高価につく。
In high temperature ranges exceeding 100℃,
Heat-resistant glass, heat-resistant brick, which are inorganic materials, depending on the number etc.
By using heat-resistant mortar etc., the normal operating temperature 2
However, these devices require skill to install and have a complicated structure, making them prone to construction defects, which shortens their service life and increases the total cost.

また材料強度が低いため施工、取扱いに難点があり、使
用時の破損も生じやすいなどの欠点がある。
Furthermore, due to the low material strength, it is difficult to construct and handle, and it is easily damaged during use.

また、無機材料のため、導電性材料とすることは不可能
である。
Furthermore, since it is an inorganic material, it is impossible to use it as a conductive material.

したがって乾式集じん装置とはなりえず、湿式集じん装
置のみの使用しかできず用途的に限界がある。
Therefore, it cannot be used as a dry-type dust collector, and can only be used as a wet-type dust collector, which limits its use.

本発明は従来の集じん装置のこれら欠点の改良に関する
ものであり、常用温度200℃でも耐食性、強度ともに
十分使用に耐え、かつ、導電性を有する乾式集じん装置
にも有効な耐熱性、耐食性、導電性を有する電気集じん
装置用集じん極に関する。
The present invention relates to improving these drawbacks of conventional dust collectors, and provides heat resistance and corrosion resistance that are sufficiently durable even at a normal temperature of 200°C, and are also effective in dry type dust collectors that have conductivity. , relates to a dust collecting electrode for an electrostatic precipitator having conductivity.

本発明は、多官能エポキシ化合物および多官能インシア
ネート化合物を反応して得られる熱硬化性樹脂、補強材
ならびに導電性材料を含有してなる電気集じん装置用集
じん極に関する。
The present invention relates to a dust collecting electrode for an electrostatic precipitator, which contains a thermosetting resin obtained by reacting a polyfunctional epoxy compound and a polyfunctional incyanate compound, a reinforcing material, and a conductive material.

図面には通常使用される平板式電気集じん装置の集じん
極安部および全体図を示すが、本発明における集じん極
の形状は筒状、板状、板を組み合わせたます目状等とさ
れ、その形状には制限がない。
The drawing shows the lowest part of dust collection and an overall view of a commonly used flat plate electrostatic precipitator, but the shape of the dust collection electrode in the present invention may be cylindrical, plate-like, square-shaped by combining plates, etc. , there are no restrictions on its shape.

第1〜第3図は通常使用される平板式、電気集じん装置
であり、本発明による組成物は集じん極1に用いられる
1 to 3 show a commonly used flat plate type electrostatic precipitator, and the composition according to the present invention is used for the dust collection electrode 1.

ここで集じん極の形式は他に管形、円筒形、格子形など
があり、これらへも利用することができる。
Here, there are other types of dust collection electrodes, such as tube, cylinder, and lattice shapes, and these can also be used.

放電極2は下部に重錘3を付し、上部は導線4で結線さ
れている。
A weight 3 is attached to the lower part of the discharge electrode 2, and the upper part is connected with a conductive wire 4.

2にはチタン、白金、バナジウムなどの金属を使用する
Metals such as titanium, platinum, and vanadium are used for 2.

5はダスト除去用水受皿を示すが、これは湿式、半湿式
と呼び、機械的槌打による払い落し方式を乾式と呼び、
いずれでも可能である。
5 shows a water tray for removing dust, which is called a wet type or a semi-wet type, and a method of removing dust by mechanical hammering is called a dry type.
Either is possible.

6は粉じん粒子に電荷を与える直流電源(ハ)であり、
荷電粒子の集じん作用が7のアースにより同−電界内で
行なわれる1段式と呼ばれるものであり、別に荷電部と
集じん部との電解が分かれている2段式のものもある。
6 is a DC power supply (c) that charges the dust particles,
There is a so-called one-stage type in which the dust collecting action of charged particles is carried out in the same electric field by means of a ground (7), and there is also a two-stage type in which electrolysis is carried out separately in the charged part and the dust collection part.

本発明において用いられる熱硬化性樹脂は、多官能エポ
キシ化合物および多官能イソシアネート化合物を反応し
て得られる熱硬化性樹脂である。
The thermosetting resin used in the present invention is a thermosetting resin obtained by reacting a polyfunctional epoxy compound and a polyfunctional isocyanate compound.

多官能エポキシ化合物としては、例えばビスフェノール
Aのジグリシジルエーテル、ブタジェンジェポキシサイ
ド、3,4−エポキシシクロヘキシルメチル−(3,4
−エポキシ)シクロヘキサンカルボキシレート、等の2
官能のエポキシ化合物、パラアミノフェノールのトリグ
リシジルエーテル、ポリアリルグリシジルエーテル、ト
リメチロールプロパンのトリグリシジルエーテル等の3
官能以上のエポキシ化合物が用いられる。
Examples of polyfunctional epoxy compounds include diglycidyl ether of bisphenol A, butadiene jepoxide, and 3,4-epoxycyclohexylmethyl-(3,4
-epoxy) cyclohexane carboxylate, etc. 2
Functional epoxy compounds, triglycidyl ether of para-aminophenol, polyallyl glycidyl ether, triglycidyl ether of trimethylolpropane, etc.
Epoxy compounds with higher functionality are used.

多官能イソシアネート化合物としては、メタンジイソン
アネート、ブタン−1,1−ジイソシアネート、ジフェ
ニルスルホン−4,4′−ジイソシアネートの2官能の
イソシアネート、ポリメチレンポリフェニルイソシアネ
ート、3,3’、4.4’−ジフェニルメタンテトライ
ソシアネートなどの3官能以上のインシアネートが用い
られる。
Examples of polyfunctional isocyanate compounds include bifunctional isocyanates such as methanedisonanate, butane-1,1-diisocyanate, diphenylsulfone-4,4'-diisocyanate, polymethylene polyphenylisocyanate, 3,3', 4.4' - A trifunctional or higher functional incyanate such as diphenylmethane tetraisocyanate is used.

多官能エポキシ化合物と多官能イソシアネート化合物と
の反応は、トリメチルアミン、トリエチルアミド、等の
3級アミン類、ジメチルアミノエタノール、ジメチルア
ミノペンタノール等のオキシアルキルアミン、ジメチル
アニリン、トリスジメチルアミノメチルフェノール等の
各種のアミン類、セチルトリメチルアンモニウムブロマ
イド、ベンジルジメチルテトラデシルアンモニウムアセ
チレート等の第4級アンモニウム塩、2−メチルイミダ
ゾール、2−エチルイミダゾール類などの触媒の存在下
で行なわれる。
The reaction between a polyfunctional epoxy compound and a polyfunctional isocyanate compound can be performed using tertiary amines such as trimethylamine and triethylamide, oxyalkylamines such as dimethylaminoethanol and dimethylaminopentanol, dimethylaniline, trisdimethylaminomethylphenol, etc. The reaction is carried out in the presence of various amines, quaternary ammonium salts such as cetyltrimethylammonium bromide and benzyldimethyltetradecylammonium acetylate, and catalysts such as 2-methylimidazole and 2-ethylimidazole.

多官能エポキシ化合物と多官能イソシアネート化合物と
の配合割合は、前者1当量に対し後者1.5当量以上5
当量以下とすることが好ましい。
The blending ratio of the polyfunctional epoxy compound and the polyfunctional isocyanate compound is 1 equivalent of the former to 1.5 equivalent or more of the latter.
It is preferable to use an equivalent amount or less.

補強材としては無機、有機繊維を使用し、要求される強
度、耐熱、耐食性、成形法などからその種類、所要重量
を決定する。
Inorganic or organic fibers are used as the reinforcing material, and the type and required weight are determined based on the required strength, heat resistance, corrosion resistance, molding method, etc.

例えば、比較的低温で使用する耐アルカリ性の場合は有
機繊維を利用することも効果があり、通常は無機繊維を
多く使用する。
For example, in the case of alkali resistance used at relatively low temperatures, it is also effective to use organic fibers, and usually a large amount of inorganic fibers is used.

また、さらに強度向上には金網などの金属の繊維を挿入
することも効果がある。
Furthermore, it is also effective to insert metal fibers such as wire mesh to further improve the strength.

導電性材料としては、カーボン粉、カーボン繊維等が用
いられる。
Carbon powder, carbon fiber, etc. are used as the conductive material.

カーボン粉、カーボン繊維は単独で使用または併用され
、要求される導電性能および強要によりその種類、粒子
、組み合わせなどを変えることができる。
Carbon powder and carbon fibers can be used alone or in combination, and their types, particles, combinations, etc. can be changed depending on the required conductive performance and requirements.

カーボン粉、カーボン繊維は集じん他成分に対して5〜
40重量%の範囲とされる。
Carbon powder and carbon fiber have a rating of 5 to 50% compared to dust collection and other components.
The range is 40% by weight.

上記組成物の成形法は、通常使用するハンドレイアツブ
成形、スプレーアップ成形、コールドプレス成形、引抜
き成形、押出成形、バック成形、FW成形、プレス成形
などが適用できる。
The above-mentioned composition can be formed by commonly used hand lay-on molding, spray-up molding, cold press molding, pultrusion molding, extrusion molding, back molding, FW molding, press molding, etc.

先にのべた熱硬化性樹脂と補強材の混合比率は成形法、
強度、耐食、耐熱性などにより変化するが通常補強材含
有量は上記の熱硬化性樹脂、補強材および導電性材料に
対し10〜60重量%である。
The mixing ratio of the thermosetting resin and reinforcing material mentioned above depends on the molding method,
Although it varies depending on strength, corrosion resistance, heat resistance, etc., the reinforcing material content is usually 10 to 60% by weight based on the above-mentioned thermosetting resin, reinforcing material, and conductive material.

また成形温度と時間は通常60〜200℃、30〜30
0分の範囲が使用される。
In addition, the molding temperature and time are usually 60-200℃, 30-30℃
A range of 0 minutes is used.

本発明における熱硬化性樹脂、補強材、および導電性材
料を含有する組成物の機械加工(切断、切削、穴あけ、
ネジ加工など)は従来のFRPと同様に容易にできる。
Machining (cutting, cutting, drilling,
(screw processing, etc.) can be easily done in the same way as with conventional FRP.

また、この組成物の接合法は機械的接合(ボルト、リベ
ットなど)、接着接合(接着剤によるスカーフ、バット
、ラップジョイトなど)などの従来のFRPと同様に容
易にできる。
Further, this composition can be easily bonded using mechanical bonding (bolts, rivets, etc.), adhesive bonding (scarfs, batts, lap joints, etc. using adhesives) in the same manner as conventional FRP.

実施例 ビスフェノールAのジグリシジルエーテル(米国ダウケ
ミカル社製、DER332、エポキシ当量174、粘度
5000センチポイズ/25℃)100gと4,4′−
ジフェニルメタンイソシアネート(以下MDIと略す)
174gおよびN−メチルモルホリン0.27gを常温
でよく混合した。
Example 100 g of diglycidyl ether of bisphenol A (manufactured by Dow Chemical Company, USA, DER332, epoxy equivalent weight 174, viscosity 5000 centipoise/25°C) and 4,4'-
Diphenylmethane isocyanate (hereinafter abbreviated as MDI)
174 g and 0.27 g of N-methylmorpholine were thoroughly mixed at room temperature.

また導電性付与のため樹脂に対しグラファイト(申越黒
鉛■AP−6)を20重量%混合し、さらにカーボン繊
維(大洋化器■EP−100)を組成物の表裏に各1枚
ずつ設置した。
In addition, 20% by weight of graphite (Shen-Etsu Graphite AP-6) was mixed with the resin to impart conductivity, and one carbon fiber (Taiyokaki EP-100) was placed on each side of the composition. .

補強材としては無機繊維のガラスクロス(FFG■FE
CR−2521−22B、平織、200g/m重量)1
5枚を使用した。
As a reinforcing material, inorganic fiber glass cloth (FFG■FE
CR-2521-22B, plain weave, 200g/m weight)1
Five sheets were used.

成形はカーボン繊維、およびガラスクロスにガラスクロ
スと同重量の樹脂を含浸させ、これを真空脱気したのち
80℃、100℃各1時間の加圧プレス(プレス圧50
kg/cm2G)にて平板(1m×2m)を作成した。
For molding, carbon fiber and glass cloth were impregnated with the same weight of resin as the glass cloth, and after vacuum degassing, pressurization was carried out at 80℃ and 100℃ for 1 hour each (press pressure 50℃).
A flat plate (1 m x 2 m) was prepared using 100 kg/cm2G).

この平板を平板式集じん極として機械加工し使用した。This flat plate was machined and used as a flat plate type dust collection electrode.

本発明になる集じん極と、従来のビニルエステル系樹脂
(ノボラック系エポキシ樹脂のメタクリレートのスチレ
ン溶液)を用い他の材料構成は同一の組成で、成形S度
、時間は60℃、3時間の手積成形による。
The dust collecting electrode of the present invention and the conventional vinyl ester resin (a styrene solution of methacrylate of novolak epoxy resin) were used, the other material composition was the same, the molding time was 60℃, 3 hours. Made by hand molding.

集じん極を150℃の硫酸ミスト用電気集じん装置にお
いて、2ケ月稼動後の集じん極板の切出し試片の150
℃における試験結果を表1に示す。
The dust collection electrode was placed in an electrostatic precipitator for sulfuric acid mist at 150°C, and 150% of the cut-out specimen of the dust collection electrode plate was used after two months of operation.
The test results at ℃ are shown in Table 1.

即ち本発明になる集じん極は、機械特性、電気特性、他
の特性などいずれもほとんど変化しないが、従来の素材
による集じん極は機械特性で40係の保持率、強度劣化
は著しくまた表面アラサ、外観などは大幅に変化し、そ
れにより電気的特性はほとんど非導電性に近い状況にな
り、装置全体の強度は構造物として限界に近い状況を呈
し長期の使用は不可であることが確認された。
In other words, the dust collecting electrode according to the present invention has almost no change in mechanical properties, electrical properties, or other properties, but the dust collecting electrode made of conventional materials has a retention rate of 40 coefficients in terms of mechanical properties, significant strength deterioration, and surface deterioration. The roughness, appearance, etc. changed significantly, and as a result, the electrical characteristics became almost non-conductive, and the strength of the entire device was close to its limit as a structure, and it was confirmed that long-term use was impossible. It was done.

上記の表において、表面あらさば、東京精密製表面あら
さ計SURFCOMにより測定し、表面あらさの表示法
はJIS B 0601の最大高さくHmax)とした
In the above table, the surface roughness was measured using a surface roughness meter SURFCOM manufactured by Tokyo Seimitsu Co., Ltd., and the surface roughness was expressed using the maximum height (Hmax) of JIS B 0601.

重量減少率は、集じん極板の初期の重量Wおよび2力月
後の重量W′を測定した。
The weight reduction rate was determined by measuring the initial weight W of the dust collecting electrode plate and the weight W' after 2 months.

次式により求めた。It was calculated using the following formula.

その他の特性はJIS K 6911−1970によ
って測定した。
Other properties were measured according to JIS K 6911-1970.

150℃硫酸ミスト用電気集じん装置に用いた本発明に
なる集じん極は1年間の実績を有するが変化は見られず
、集じん効率も初期と同等の性能にを有し、耐食、耐熱
、導電性などは十分である。
The dust collection electrode of the present invention used in an electrostatic precipitator for sulfuric acid mist at 150°C has been used for one year, but no change has been observed, the dust collection efficiency is the same as the initial performance, and it is corrosion resistant and heat resistant. , conductivity, etc. are sufficient.

本発明になる電気集じん装置用集じん極は高強度、耐熱
性の特性の他に、電気集じん装置用集じん極として要求
される耐アーク性、高温耐食性、高温寸法安定性、じん
あい除去性等の諸性能が、従来の集じん極に比較して大
幅に改善される。
The dust collecting electrode for an electrostatic precipitator according to the present invention has the characteristics of high strength and heat resistance, as well as arc resistance, high temperature corrosion resistance, high temperature dimensional stability, and dust resistance required for a dust collecting electrode for an electrostatic precipitator. Various performances such as removability are significantly improved compared to conventional dust collection electrodes.

上記の性能について、本発明になる集じん極と従来の集
じん極とを比較して表2に示す。
Regarding the above performance, Table 2 shows a comparison between the dust collecting electrode according to the present invention and the conventional dust collecting electrode.

表2において、本発明になる集じん極板は、上記の実施
例に記載した集じん極板であり、従来の集じん極板は、
樹脂としてノボラック系エポキシ樹脂のメタクリレート
のスチレン溶液を用い、他の材料構成、成形温度、時間
は本発明になる集じん極と同一として手積成形によって
得たものである。
In Table 2, the dust collection electrode plate according to the present invention is the dust collection electrode plate described in the above embodiment, and the conventional dust collection electrode plate is
The electrode was obtained by hand molding using a styrene solution of methacrylate of novolak epoxy resin as the resin, and the other material composition, molding temperature, and time were the same as those of the dust collecting electrode of the present invention.

1)耐アーク性について 電気集じん装置では、放電極と集じん極に一定の電圧を
かけるため集じん極にアークが発生し、従来の集じん極
では、極板表面の劣化が進み、平滑性が失われ、集じん
性能の低下をきたす。
1) About arc resistance In electrostatic precipitators, arcs occur on the dust collecting electrode because a constant voltage is applied between the discharge electrode and the dust collecting electrode. This results in a loss of properties and a decline in dust collection performance.

本発明になる集じん極では、耐アーク性が大幅に改善さ
れる。
In the dust collecting electrode according to the present invention, arc resistance is significantly improved.

表に集じん極板の表面あらさの比較を示す。The table shows a comparison of the surface roughness of the dust collection electrode plates.

2)高温耐食性について 電気集じん装置は、通常腐食性ガス体を処理するため、
強度劣化と高温時における耐食劣化が重要な問題となる
2) Regarding high temperature corrosion resistance Electrostatic precipitators usually process corrosive gases, so
Deterioration of strength and corrosion resistance at high temperatures are important issues.

従来の集じん極では、その性能に限界があったが、本発
明においては大幅に改善される。
Conventional dust collecting electrodes had limited performance, but the present invention significantly improves its performance.

表にSO2,HFを処理した場合の集じん極板の重量変
化率を示す。
The table shows the weight change rate of the dust collection electrode plate when treated with SO2 and HF.

3)高温寸法安定性について 電気集じん装置の生命とも言える放電極と集じん極との
間隔は常に一定の精度を確保せねばならず、精度不良の
場合には集じん性能は著しく低下をきたす。
3) Regarding high-temperature dimensional stability, the interval between the discharge electrode and the dust collecting electrode, which is the lifeblood of an electrostatic precipitator, must always maintain a certain degree of accuracy, and if the accuracy is poor, the dust collection performance will deteriorate significantly. .

従来の集じん極では、高温時の使用により集じん極が変
形を起こすが、本発明の乗じん極ではこの変形が大幅に
防止され、性能低下は少なくなる。
In conventional dust collection electrodes, the dust collection electrode is deformed when used at high temperatures, but in the dust collection electrode of the present invention, this deformation is largely prevented, and the deterioration in performance is reduced.

表に集じん極板のそり、ねじれを示す。The table shows warpage and twisting of the dust collection electrode plate.

そりは、集じん極板の長さ方向のそりを単位mmで表わ
し、ねじれは幅方向のねじれの角度で示す。
Warpage is expressed by the warpage in the length direction of the dust collecting electrode plate in units of mm, and twist is expressed by the angle of twist in the width direction.

4)じんあい除去性について 集じん極に付着したじんあいは、集じん性能の低下をき
たすため、通常は一定期間毎に集じん極を振動作動させ
、付着したじんあいを下方に脱落させる手法を採用し、
集じん性能のレベルを保持している。
4) Regarding dust removal ability: Dust that adheres to the dust collection electrode will cause a decline in dust collection performance, so the method is usually to vibrate the dust collection electrode at regular intervals to cause the dust that has adhered to fall off downward. adopted,
The level of dust collection performance is maintained.

しかしながら、振動させる作業は少ない方がメンテナン
ス上有利でありか集じん性能上も有利となる。
However, less vibration work is advantageous in terms of maintenance and dust collection performance.

従来の集じん極は、短期間にじんあいが付着するため、
ひんばんに振動させる必要があったが、本発明の集じん
極は従来のものに比べて振動は少なくてすむ。
Conventional dust collection electrodes collect dust in a short period of time, so
Although it was necessary to vibrate frequently, the dust collection electrode of the present invention requires less vibration than conventional ones.

表に1力月の振動作動回数を示す。The table shows the number of vibration operations per power month.

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

第1図は平板式電気集じん装置の全体組立略図、第2図
は集じん装置の要部を示すもので、第3図は第2図のA
A矢視図である。 符号の説明、1・・・・・・集じん極、2・・・・・・
放電極、3・・・・・・重錘、4・・・・・・導線、5
・・・・・・ダスト除去用水受皿、6・・・・・・直流
電源(−)、7・・・・・・アース(+)。
Figure 1 is a schematic diagram of the overall assembly of a flat plate type electrostatic precipitator, Figure 2 shows the main parts of the dust collector, and Figure 3 is a diagram of A in Figure 2.
It is a view from arrow A. Explanation of symbols, 1... Dust collection pole, 2...
Discharge electrode, 3... Weight, 4... Conductor, 5
...Water tray for removing dust, 6...DC power supply (-), 7... Earth (+).

Claims (1)

【特許請求の範囲】[Claims] 1 多官能エポキシ化合物および多官能イソシアネート
化合物を反応して得られる熱硬化性樹脂、補強材ならび
に導電性材料を含有してなる電気集じん装置用集じん極
1. A dust collecting electrode for an electrostatic precipitator comprising a thermosetting resin obtained by reacting a polyfunctional epoxy compound and a polyfunctional isocyanate compound, a reinforcing material, and a conductive material.
JP51071813A 1976-06-18 1976-06-18 Dust collection electrode for electrostatic precipitator Expired JPS585104B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51071813A JPS585104B2 (en) 1976-06-18 1976-06-18 Dust collection electrode for electrostatic precipitator

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51071813A JPS585104B2 (en) 1976-06-18 1976-06-18 Dust collection electrode for electrostatic precipitator

Publications (2)

Publication Number Publication Date
JPS52155480A JPS52155480A (en) 1977-12-23
JPS585104B2 true JPS585104B2 (en) 1983-01-29

Family

ID=13471368

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51071813A Expired JPS585104B2 (en) 1976-06-18 1976-06-18 Dust collection electrode for electrostatic precipitator

Country Status (1)

Country Link
JP (1) JPS585104B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63305950A (en) * 1987-06-08 1988-12-13 Kyowa Kako Kk Corrosion resistant electrostatic precipitator

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5635949B2 (en) * 1972-06-01 1981-08-20
JPS5054660A (en) * 1973-09-17 1975-05-14

Also Published As

Publication number Publication date
JPS52155480A (en) 1977-12-23

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