JPH0160537B2 - - Google Patents
Info
- Publication number
- JPH0160537B2 JPH0160537B2 JP60047800A JP4780085A JPH0160537B2 JP H0160537 B2 JPH0160537 B2 JP H0160537B2 JP 60047800 A JP60047800 A JP 60047800A JP 4780085 A JP4780085 A JP 4780085A JP H0160537 B2 JPH0160537 B2 JP H0160537B2
- Authority
- JP
- Japan
- Prior art keywords
- flue gas
- sintering machine
- absorption liquid
- acid
- desulfurization method
- 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
Links
- 238000010521 absorption reaction Methods 0.000 claims description 20
- 239000007788 liquid Substances 0.000 claims description 19
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 16
- 239000003546 flue gas Substances 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 15
- 238000005245 sintering Methods 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 11
- 239000002455 scale inhibitor Substances 0.000 claims description 10
- 150000005846 sugar alcohols Polymers 0.000 claims description 9
- 238000006477 desulfuration reaction Methods 0.000 claims description 8
- 230000023556 desulfurization Effects 0.000 claims description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
- 229940043430 calcium compound Drugs 0.000 claims description 6
- 150000001674 calcium compounds Chemical class 0.000 claims description 6
- 229920000642 polymer Chemical class 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical class OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 3
- 235000011187 glycerol Nutrition 0.000 claims description 3
- 239000004386 Erythritol Substances 0.000 claims description 2
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 claims description 2
- 235000019414 erythritol Nutrition 0.000 claims description 2
- 229940009714 erythritol Drugs 0.000 claims description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 1
- 239000003595 mist Substances 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000010440 gypsum Substances 0.000 description 4
- 229910052602 gypsum Inorganic materials 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- JSZVAKSQKFZKNG-UHFFFAOYSA-K P(=O)(O)(O)C(C(C(=O)[O-])(C(=O)[O-])C(=O)[O-])CC.[Na+].[Na+].[Na+] Chemical compound P(=O)(O)(O)C(C(C(=O)[O-])(C(=O)[O-])C(=O)[O-])CC.[Na+].[Na+].[Na+] JSZVAKSQKFZKNG-UHFFFAOYSA-K 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 230000003009 desulfurizing effect Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- BAERPNBPLZWCES-UHFFFAOYSA-N (2-hydroxy-1-phosphonoethyl)phosphonic acid Chemical compound OCC(P(O)(O)=O)P(O)(O)=O BAERPNBPLZWCES-UHFFFAOYSA-N 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OELQSSWXRGADDE-UHFFFAOYSA-N 2-methylprop-2-eneperoxoic acid Chemical compound CC(=C)C(=O)OO OELQSSWXRGADDE-UHFFFAOYSA-N 0.000 description 1
- SZHQPBJEOCHCKM-UHFFFAOYSA-N 2-phosphonobutane-1,2,4-tricarboxylic acid Chemical compound OC(=O)CCC(P(O)(O)=O)(C(O)=O)CC(O)=O SZHQPBJEOCHCKM-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- GBAOBIBJACZTNA-UHFFFAOYSA-L calcium sulfite Chemical compound [Ca+2].[O-]S([O-])=O GBAOBIBJACZTNA-UHFFFAOYSA-L 0.000 description 1
- 235000010261 calcium sulphite Nutrition 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- BXLLINKJZLDGOX-UHFFFAOYSA-N dimethoxyphosphorylmethanamine Chemical compound COP(=O)(CN)OC BXLLINKJZLDGOX-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000011508 lime plaster Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical class OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001444 polymaleic acid Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- -1 styrene sulfone Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/25—Process efficiency
Landscapes
- Waste-Gas Treatment And Other Accessory Devices For Furnaces (AREA)
- Treating Waste Gases (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
〔産業上の利用分野〕
この発明は高炉装入原料等として用いられる焼
結鉱を製造する際、発生する排煙を効率よく脱硫
処理する方法に関するものである。
〔従来の技術〕
砂鉄や、鉄鋼石の予備処理によつて生じる粉鉱
は貴重な鉄鋼原料であり、これらを利用したもの
に焼結鉱がある。焼結鉱は粒度、強度、被還元性
が制御できるため、特に高炉装入原料として多用
されている。
一般に焼結鉱は粉鉱や砂鉄等を焼結原料とし、
これにコークスや石灰、水等を必要に応じて加え
てドラムミキサー等で混練、造粒化し、粗大化し
た後、これを焼結機に装入し、1300℃前後の高温
にさらして焼結反応を行なわせ、その後、破砕、
冷却して製造されている。
このとき、焼結原料等の焼結層を通過した前記
高温ガスには、焼結原料から除去したイオウが
SO2の形で含有されている。そこで、このような
焼結機排煙は、例えば、石灰石膏法などによつて
脱硫される。具体的には、排煙を先ず冷却塔に導
入して、水等と接触させて、ある程度の冷却、除
塵を行なつた後、吸収塔へ供給する。吸収塔で、
石灰等のカルシウム化合物含有液を噴霧して排煙
と接触させ、排煙中のイオウを亜硫酸カルシウム
や硫酸カルシウムの形で吸収液中に捕促する。
こうして、除塵、脱硫、冷却された排煙は排風
機によつて系外へ放出する。
〔発明が解決しようとする問題点〕
しかしながら、このようなカルシウム化合物含
有液を用いた焼結機排煙脱硫方法においては、噴
霧した吸収液の一部が排煙と接触後、ミストとな
つて飛散し、噴霧面より上部の壁面やミストセパ
レータに付着する。そうすると、これらの付着物
は比較的高温の排煙と常時接触することになり、
付着物中の水分は蒸発し、付着物は乾固してしま
う。この乾固付着物はケイ酸カルシウムや石膏、
酸化鉄等を含んでおり、極めて硬質のスケールと
なる。
一方、噴霧された吸収液は吸収塔下部で集液さ
れ、酸化塔で酸化されて石膏が作られるが、この
水系でも多量のスケールが発生する。
従来、このようなスケールの生成を防止するた
めには、吸収液に重合リン酸や高分子化合物等の
スケール防止剤を添加する方法などがあつた。し
かし、これらのスケール防止剤が有効に作用する
のは吸収液と接触している所のみであつて、前述
のようなミストの付着により生成する付着物によ
るスケールの生成には効果がなかつた。
〔問題点を解決するための手段〕
この発明は、前述の従来技術の問題点を解決す
るために完成されたものである。
この発明は焼結機から排出される排煙をカルシ
ウム化合物を含む吸収液と接触させる焼結機排煙
脱硫方法において、前記吸収液に多価アルコール
系化合物とスケール防止剤とを添加することを特
徴とする焼結機排煙脱硫方法である。
この発明に用いられるカルシウム化合物として
は消石灰、炭酸カルシウム、廃アルカリなどが例
示される。通常、これらのカルシウム化合物は水
溶液化またはスラリー化して吸収液とする。
この発明に用いられる多価アルコール系化合物
は、1分子中に複数のアルコール性水酸基を有す
る化合物であつて、具体的には、エチレングリコ
ール、グリセリン、エリトリツト、プロピレング
リコール、および前記ポリオール類のエチレンオ
キサイド付加物が例示される。このうち、エチレ
ンオキサイドまたはプロピレンオキサイドの分子
量は10111以下とすることが好ましい。
この発明では、上記の多価アルコール系化合物
と共にスケール防止剤を用いるものであるが、こ
こで用いられるスケール防止剤としては特に限定
されず、公知の水系用スケール防止剤を用いるこ
とができる。具体的にはトリポリリン酸、ヘキサ
メタリン酸などの重合リン酸またはその塩、アミ
ノトリメチルホスホン酸、ヒドロキシエチリデン
ジホスホン酸、エチレンジアミンテトラメチルホ
スホン酸、ホスホノブタントリカルボン酸などの
ホスホン酸、ホスホノカルボン酸またはそれらの
塩、およびカルボン酸系高分子化合物などが挙げ
られる。カルボン酸系高分子化合物としてはポリ
アクリル酸、ポリメタクリル酸、ポリマレイン
酸、ポリイタコン酸などのホモポリマーもしくは
その塩、またはアクリル酸、メタクリル酸、マレ
イン酸、無水マレイン酸と他の重合性単量体―ア
クリルアミドやイソブテン、ブテン、ヒドロキシ
メタクリレート、スチレン、スチレンスルホンの
コポリマーもしくはその塩が例示される。これら
の高分子化合物の分子量は500〜100000程度、好
ましくは1000〜10000程度の範囲とする。
これら多価アルコール系化合物またはスケール
防止剤の吸収液への添加量は焼結原料の種類の応
じて変動するが、標準的にはいずれも1〜100
mg/程度とする。
〔作 用〕
多価アルコール系化合物は各アルコール性水酸
基が水と水素結合等によつて強く結びついてい
る。従つて、多価アルコール系化合物を含む吸収
液の一部がミスト化して、噴霧面より上の壁面や
ミストセパレータに付着しても、水の蒸発が遅
く、ぬれ膜を形成する。この結果、ミスト中の懸
濁固形物の乾固を防止し、軟質のものにとどめる
作用を果たす。
一方、吸収液中のスケール防止剤はスケール形
成性折出物の表面に吸着されて結晶の成長や折出
物の凝集を阻害し、スケール化を防止する。
以下、実施例によりこの発明をさらに説明す
る。
〔実施例〕
実施例 1
アクリル製吸収塔(60mmφ×1000mmH)内に6
%の炭酸カルシウム水溶液(石膏50gを含む)を
入れ、吸収液内及び水面より上部にテストピース
を懸垂させた。この吸収塔に下部からSO2濃度
450mg/、温度60℃の空気を模凝焼結機排煙と
して15/分の流速で供給した。1日7時間の運
転を10日間行なつた。次に吸収液にさらに、薬剤
として、多価アルコール系化合物としてグリセリ
ンのプロピレンオキサイド付加物(分子量700)
を60mg/、及びホスホノブタントリカルボン酸
ソーダを5mg/それぞれ加えた以外は前記と全
く同一条件で運転を行なつた。これらの運転をそ
れぞれ2回くり返した、両運転終了後、テストピ
ースに付着した石膏の量からスケール付着速度を
求めた。水面上のテストピースの結果を第1表
に、吸収液中のテストピースの結果を第2表にそ
れぞれ示す。
[Industrial Field of Application] The present invention relates to a method for efficiently desulfurizing flue gas generated when producing sintered ore used as a raw material for blast furnace charging. [Prior Art] Iron sand and powder ore produced by preliminary treatment of iron ore are valuable raw materials for steel, and sintered ore is a product that utilizes these materials. Sintered ore is often used as a raw material for blast furnace charging because its particle size, strength, and reducibility can be controlled. Generally, sintered ore uses powdered ore, iron sand, etc. as the raw material for sintering.
Coke, lime, water, etc. are added to this as necessary, and the mixture is kneaded and granulated using a drum mixer to make it coarse, and then it is charged into a sintering machine and exposed to high temperatures of around 1300℃ to sinter it. Let the reaction take place, then crush,
Manufactured by cooling. At this time, the high temperature gas that has passed through the sintered layer of the sintered raw material contains sulfur removed from the sintered raw material.
Contains in the form of SO 2 . Therefore, such sintering machine exhaust gas is desulfurized by, for example, a lime plaster method. Specifically, flue gas is first introduced into a cooling tower, brought into contact with water, etc. to perform some degree of cooling and dust removal, and then supplied to an absorption tower. In the absorption tower
A liquid containing calcium compounds such as lime is sprayed and brought into contact with flue gas, and sulfur in the flue gas is captured in the absorption liquid in the form of calcium sulfite or calcium sulfate. In this way, the dust-removed, desulfurized, and cooled flue gas is discharged outside the system by the exhaust fan. [Problems to be solved by the invention] However, in the sintering machine flue gas desulfurization method using such a calcium compound-containing liquid, a part of the sprayed absorption liquid becomes a mist after coming into contact with the flue gas. It scatters and adheres to the wall surface and mist separator above the spray surface. As a result, these deposits are constantly in contact with relatively high temperature flue gas,
The moisture in the deposit evaporates and the deposit dries up. This dry deposit is composed of calcium silicate, gypsum,
Contains iron oxide, etc., and forms an extremely hard scale. On the other hand, the sprayed absorption liquid is collected at the bottom of the absorption tower and oxidized in the oxidation tower to produce gypsum, but even in this aqueous system, a large amount of scale is generated. Conventionally, in order to prevent the formation of such scale, there has been a method of adding a scale inhibitor such as polymerized phosphoric acid or a polymer compound to the absorption liquid. However, these scale inhibitors act effectively only in areas that are in contact with the absorbing liquid, and are not effective against the formation of scale due to deposits caused by adhesion of mist as described above. [Means for Solving the Problems] The present invention has been completed in order to solve the problems of the prior art described above. This invention provides a sintering machine flue gas desulfurization method in which flue gas discharged from a sintering machine is brought into contact with an absorbing liquid containing a calcium compound, in which a polyhydric alcohol compound and a scale inhibitor are added to the absorbing liquid. This is a unique method for desulfurizing sintering machine flue gas. Examples of the calcium compound used in this invention include slaked lime, calcium carbonate, and waste alkali. Usually, these calcium compounds are made into an aqueous solution or slurry to form an absorption liquid. The polyhydric alcohol compound used in this invention is a compound having multiple alcoholic hydroxyl groups in one molecule, and specifically includes ethylene glycol, glycerin, erythritol, propylene glycol, and ethylene oxide of the above polyols. An example is an adduct. Among these, the molecular weight of ethylene oxide or propylene oxide is preferably 10111 or less. In this invention, a scale inhibitor is used together with the above polyhydric alcohol compound, but the scale inhibitor used here is not particularly limited, and any known aqueous scale inhibitor can be used. Specifically, polymerized phosphoric acids or their salts such as tripolyphosphoric acid and hexametaphosphoric acid, phosphonic acids such as aminotrimethylphosphonic acid, hydroxyethylidene diphosphonic acid, ethylenediaminetetramethylphosphonic acid, phosphonobutanetricarboxylic acid, phosphonocarboxylic acids, or the like. and carboxylic acid-based polymer compounds. Carboxylic acid-based polymer compounds include homopolymers or salts thereof such as polyacrylic acid, polymethacrylic acid, polymaleic acid, and polyitaconic acid, or acrylic acid, methacrylic acid, maleic acid, maleic anhydride, and other polymerizable monomers. - Copolymers of acrylamide, isobutene, butene, hydroxymethacrylate, styrene, styrene sulfone, or salts thereof are exemplified. The molecular weight of these polymer compounds is approximately 500 to 100,000, preferably approximately 1,000 to 10,000. The amount of these polyhydric alcohol-based compounds or scale inhibitors added to the absorption liquid varies depending on the type of sintering raw material, but the standard amount is 1 to 100%.
mg/degree. [Function] In polyhydric alcohol compounds, each alcoholic hydroxyl group is strongly bound to water through hydrogen bonds, etc. Therefore, even if a part of the absorption liquid containing the polyhydric alcohol compound becomes a mist and adheres to the wall surface or the mist separator above the spray surface, the water evaporates slowly and forms a wet film. As a result, the suspended solids in the mist are prevented from drying and remain soft. On the other hand, the scale inhibitor in the absorption liquid is adsorbed on the surface of the scale-forming precipitates, inhibits crystal growth and aggregation of the precipitates, and prevents scaling. The present invention will be further explained below with reference to Examples. [Example] Example 1 6 in an acrylic absorption tower (60 mmφ x 1000 mmH)
% calcium carbonate aqueous solution (containing 50 g of gypsum), and a test piece was suspended in the absorption liquid and above the water surface. SO 2 concentration from the bottom to this absorption tower
Air at a temperature of 60° C. and a flow rate of 450 mg/min was supplied as flue gas from the simulated sintering machine at a flow rate of 15/min. I drove 7 hours a day for 10 days. Next, a propylene oxide adduct of glycerin (molecular weight 700) is added to the absorption liquid as a drug and as a polyhydric alcohol compound.
The operation was carried out under exactly the same conditions as above, except that 60 mg of sodium phosphonobutanetricarboxylate and 5 mg of sodium phosphonobutanetricarboxylate were added. Each of these operations was repeated twice, and after both operations were completed, the scale adhesion rate was determined from the amount of gypsum adhering to the test piece. The results for the test piece on the water surface are shown in Table 1, and the results for the test piece in the absorption liquid are shown in Table 2.
【表】【table】
この発明方法によれば、従来有効な対処方法が
かつた焼結機排煙脱硫装置における吸収塔内のミ
スト付着による乾固物の生成が大巾に軽減される
とともに、付着物自体軟質であり、高圧水を噴射
する等、簡便な手段により容易に剥離することが
できる。また、吸収液の循環系でもスケール生成
に基くトラブルは極めて軽減される等、脱硫装置
の維持管理が著しく容易になる。
According to the method of this invention, the generation of dry solids due to mist adhesion in the absorption tower in the sintering machine flue gas desulfurization equipment, for which there was an effective countermeasure in the past, can be greatly reduced, and the adhesion itself is soft. It can be easily peeled off by simple means such as spraying high-pressure water. In addition, troubles caused by scale formation in the absorption liquid circulation system are greatly reduced, and maintenance and management of the desulfurization equipment is greatly facilitated.
Claims (1)
物を含む吸収液と接触させる焼結機排煙脱硫方法
において、前記吸収液に多価アルコール系化合物
とスケール防止剤とを添加することを特徴とする
焼結機排煙脱硫方法。 2 多価アルコール系化合物がエチレングリコー
ル、グリセリン、エリトリツトおよびそれらのエ
チレンオキサイドまたはプロピレンオキサイド付
加物から成る群から選ばれる1種以上である特許
請求の範囲第1項記載の脱硫方法。 3 スケール防止剤が重合リン酸、ホスホン酸及
び高分子化合物から成る群から選ばれる1種以上
である特許請求の範囲第1項又は第2項に記載の
脱硫方法。[Claims] 1. A sintering machine flue gas desulfurization method in which flue gas discharged from a sintering machine is brought into contact with an absorption liquid containing a calcium compound, in which a polyhydric alcohol compound and a scale inhibitor are added to the absorption liquid. A sintering machine flue gas desulfurization method characterized by adding. 2. The desulfurization method according to claim 1, wherein the polyhydric alcohol compound is one or more selected from the group consisting of ethylene glycol, glycerin, erythritol, and their ethylene oxide or propylene oxide adducts. 3. The desulfurization method according to claim 1 or 2, wherein the scale inhibitor is one or more types selected from the group consisting of polymerized phosphoric acid, phosphonic acid, and polymer compounds.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60047800A JPS61207527A (en) | 1985-03-11 | 1985-03-11 | Desulfurizing method for flue gas from sintering machine |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60047800A JPS61207527A (en) | 1985-03-11 | 1985-03-11 | Desulfurizing method for flue gas from sintering machine |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61207527A JPS61207527A (en) | 1986-09-13 |
JPH0160537B2 true JPH0160537B2 (en) | 1989-12-22 |
Family
ID=12785443
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60047800A Granted JPS61207527A (en) | 1985-03-11 | 1985-03-11 | Desulfurizing method for flue gas from sintering machine |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61207527A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4590001B2 (en) | 2008-02-27 | 2010-12-01 | 新日本製鐵株式会社 | Method for producing sintered ore and sintering machine |
BRPI0903986B1 (en) * | 2009-04-20 | 2019-09-17 | Vale S/A | PROCEDURE FOR INHIBITING PARTICULATE DUTIES DURING THE TERMINATION OF IRON ORE PELLETS THREADED |
-
1985
- 1985-03-11 JP JP60047800A patent/JPS61207527A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS61207527A (en) | 1986-09-13 |
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