CN105903333B - 一种镁强化赤泥的烟气深度脱硫方法 - Google Patents
一种镁强化赤泥的烟气深度脱硫方法 Download PDFInfo
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- CN105903333B CN105903333B CN201610463539.XA CN201610463539A CN105903333B CN 105903333 B CN105903333 B CN 105903333B CN 201610463539 A CN201610463539 A CN 201610463539A CN 105903333 B CN105903333 B CN 105903333B
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- red mud
- flue gas
- desulfurization
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- deep
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- 239000011499 joint compounds Substances 0.000 title claims abstract description 203
- 239000003546 flue gases Substances 0.000 title claims abstract description 64
- UGFAIRIUMAVXCW-UHFFFAOYSA-N carbon monoxide Chemical compound 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[O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 title claims abstract description 63
- 239000011777 magnesium Substances 0.000 title claims abstract description 31
- FYYHWMGAXLPEAU-UHFFFAOYSA-N magnesium Chemical compound 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[Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 title claims abstract description 30
- 229910052749 magnesium Inorganic materials 0.000 title claims abstract description 30
- 238000000034 methods Methods 0.000 title claims abstract description 24
- 238000006477 desulfuration reactions Methods 0.000 claims abstract description 171
- 230000003009 desulfurizing Effects 0.000 claims abstract description 134
- 239000007788 liquids Substances 0.000 claims abstract description 102
- 239000002002 slurries Substances 0.000 claims abstract description 72
- 239000003595 mist Substances 0.000 claims abstract description 9
- 239000002994 raw materials Substances 0.000 claims abstract description 9
- 239000007921 sprays Substances 0.000 claims abstract description 9
- 239000010410 layers Substances 0.000 claims abstract description 8
- 239000007789 gases Substances 0.000 claims description 29
- 238000007654 immersion Methods 0.000 claims description 22
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- 239000000395 magnesium oxide Substances 0.000 claims description 12
- 229910000140 magnesium oxide Inorganic materials 0.000 claims description 12
- 238000006297 dehydration reactions Methods 0.000 claims description 9
- JLVVSXFLKOJNIY-UHFFFAOYSA-N magnesium ion Chemical compound data:image/svg+xml;base64,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 data:image/svg+xml;base64,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 [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 claims description 6
- 229910001425 magnesium ion Inorganic materials 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound 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[S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 239000005864 Sulphur Substances 0.000 claims description 5
- 239000000347 magnesium hydroxide Substances 0.000 claims description 5
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 5
- 239000011901 water Substances 0.000 claims description 5
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reactions Methods 0.000 claims description 3
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- 229910001415 sodium ion Inorganic materials 0.000 claims description 3
- 239000007787 solids Substances 0.000 claims description 3
- 238000004062 sedimentation Methods 0.000 claims description 2
- 238000010521 absorption reactions Methods 0.000 abstract description 10
- 239000002918 waste heat Substances 0.000 abstract description 3
- 238000005265 energy consumption Methods 0.000 abstract description 2
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- RAHZWNYVWXNFOC-UHFFFAOYSA-N sulphur dioxide Chemical compound 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- 238000006243 chemical reactions Methods 0.000 description 5
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- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound 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[Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 4
- 239000004127 magnesium sulphate Substances 0.000 description 4
- 239000000779 smoke Substances 0.000 description 4
- 238000005516 engineering processes Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000004064 recycling Methods 0.000 description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound 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[Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L Calcium sulfate Chemical compound 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- PNEYBMLMFCGWSK-UHFFFAOYSA-N al2o3 Chemical compound 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[O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000011957 aluminium oxide Substances 0.000 description 2
- 239000006227 byproducts Substances 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000945 fillers Substances 0.000 description 2
- 239000011521 glasses Substances 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L mgso4 Chemical compound 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- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound 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[Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound 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- 150000003463 sulfur Chemical group 0.000 description 1
- 238000003786 synthesis reactions Methods 0.000 description 1
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/75—Multi-step processes
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/48—Sulfur compounds
- B01D53/50—Sulfur oxides
- B01D53/501—Sulfur oxides by treating the gases with a solution or a suspension of an alkali or earth-alkali or ammonium compound
- B01D53/502—Sulfur oxides by treating the gases with a solution or a suspension of an alkali or earth-alkali or ammonium compound characterised by a specific solution or suspension
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/77—Liquid phase processes
- B01D53/78—Liquid phase processes with gas-liquid contact
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01D—COMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
- C01D5/00—Sulfates or sulfites of sodium, potassium or alkali metals in general
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F11/00—Treatment of sludge; Devices therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2251/00—Reactants
- B01D2251/40—Alkaline earth metal or magnesium compounds
- B01D2251/402—Alkaline earth metal or magnesium compounds of magnesium
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2258/00—Sources of waste gases
- B01D2258/02—Other waste gases
- B01D2258/0283—Flue gases
-
- 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
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/10—Process efficiency
- Y02P20/129—Energy recovery, e.g. by cogeneration, H2recovery or pressure recovery turbines
-
- 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
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
Abstract
Description
一种镁强化赤泥的烟气深度脱硫方法
技术领域
[0001] 本发明属于环境保护领域的工业烟气污染物控制技术领域,涉及一种镁强化赤泥 的烟气深度脱硫方法。
背景技术
[0002] 二氧化硫是对造成光化学烟雾和酸雨污染的主要大气污染物。在我国,电力、化 工、金属冶炼等工业行业使用的燃煤锅炉和窑炉排放烟气量大,且烟气中含有大量的二氧 化硫污染物。因此,工业燃煤和生产产生的烟气必须进行脱硫处理达标后才能排放。
[0003] 目前,针对燃煤烟气脱硫和工业窑炉废气脱硫工艺的报道很多,工程上比较成熟 常用的是石灰石-石膏法、双碱法等。虽然石灰石价格低廉,但进入脱硫系统前需要磨制成 粉状并制成浆液,对于烟气量不大、含硫浓度高的工业烟气来说,建设成本和运行成本均较 高,难以在工业窑炉烟气脱硫领域普遍应用。同时,可以注意到,我国是氧化铝生产大国,氧 化铝生产过程中会排出大量的赤泥,是污染性废渣,一般平均每生产1吨氧化铝,附带产生 1.0〜2.0吨赤泥。赤泥中含有大量铁和碱,pH在10以上。从污染控制和废物利用方面综合考 虑,若能将氧化铝生产环节中的副产物赤泥应用到工业烟气脱硫则具有无比的优越性。利 用赤泥脱硫不仅可以控制S02的排放,而且还可以达到赤泥本身脱碱的作用,为赤泥的进一 步资源化利用提供保证。
[0004] 目前,关于赤泥用于烟气脱硫的研宄也有不少报道,但其在大规模的工业应用则 很少。中国专利ZL200610200499.6和ZL200610098706.1分别报道了采用赤泥吸收烟气中 S02的技术方法,均采用填料吸收塔,在运行中压降较大,动力消耗大,且易出现结垢堵塞的 问题;难以满足深度脱硫的排放要求,且赤泥中碱脱除不彻底;由于赤泥的本身特性所限, 在高pH值下导致赤泥脱硫的硫容有限,导致脱硫过程中需要大量的赤泥浆液循环,不仅是 循环栗的电耗增加,而且还加剧了泵和管道的磨损。因此,针对氧化铝行业赤泥废物资源化 和工业烟气脱硫的需求,开发一种功能加强型赤泥法烟气脱硫技术对于实现工业烟气深度 脱硫和赤泥的资源化利用非常必要。
发明内容
[0005] 本发明的目的就是为了克服上述现有技术存在的缺陷而提供一种能有效实现工 业烟气深度脱硫和赤泥的资源化综合利用,降低有毒有害物质的产生的镁强化赤泥的烟气 深度脱硫方法。
[0006] 本发明的目的可以通过以下技术方案来实现:
[0007] —种镁强化赤泥的烟气深度脱硫方法,该方法具体包括以下步骤:
[0008]第一步:将赤泥原料送入赤泥预浸槽中,并加入从脱硫赤泥浆液脱水池回流的含 镁预脱硫浆液清液进行预浸处理,待预浸结束后,使赤泥预浸槽中的固体赤泥发生自然沉 降,回流的含镁预脱硫浆液清液中的镁离子转化为氢氧化镁并沉积到赤泥上,沉降结束后, 将上层的赤泥预浸清液送入深度脱硫液循环池,而下层的赤泥预浸浆液由赤泥预浸槽底部 送入赤泥架液池;
[0009] 第二步:向赤泥浆液池中加入氧化镁和水,并与赤泥预浸浆液混合均匀,送入脱硫 塔下部的预脱硫区;
[0010] 第三步:含二氧化硫工业烟气从脱硫塔的烟气进口进入预脱硫区,与预脱硫区内 自上而下喷淋的赤泥预浸浆液逆向接触吸收,进行预脱硫;
[0011] 第四步:预脱硫后的赤泥预浸浆液在脱硫塔底部经曝气氧化后,进入脱硫赤泥浆 液脱水池中进行脱水,脱水后得到预脱硫浆液清液及脱碱赤泥,将预脱硫浆液清液回流至 赤泥预浸槽中,同时排出脱碱赤泥;
[0012] 第五步:预脱硫后的烟气经脱硫塔中部的分区塔板进入脱硫塔上部的深度脱硫 区,与深度脱硫区内自上而下喷淋的来自深度脱硫液循环池的赤泥预浸清液逆向接触吸 收,进行深度脱硫;
[0013] 第六步:深度脱硫后的赤泥预浸清液在分区塔板下方的收集槽中收集后,再回流 至深度脱硫液循环池中;
[0014] 第七步:深度脱硫后的烟气经脱硫塔顶部的高效除雾区除雾后,经烟气出口排出 即可。
[0015] 第一步中预浸处理结束后,所述的赤泥预浸清液及赤泥预浸浆液的pH均大于8。
[0016] 所述的预浸处理过程中,利用搅拌器搅拌以增强预浸效果,预浸后关停搅拌器,使 赤泥预浸槽中的赤泥发生自然沉降而分层。
[0017] 第二步中所述的氧化镁的加入量为赤泥预浸浆液质量的0.5-5%。
[0018] 第五步中,当经深度脱硫区后的赤泥预浸清液中钠离子质量浓度高于10%时,向 外界排出一部分赤泥预浸清液,并由赤泥预浸槽向深度脱硫液循环池中补充相同体积新的 赤泥预浸清液。
[0019] 所述的赤泥预浸清液的排出体积为深度脱硫液循环池中赤泥预浸清液总体积的 2-20% 〇
[0020] 所述的脱硫塔为三区式脱硫塔,下部为预脱硫区,中部为深度脱硫区,上部为高效 除雾区。
[0021] 所述的预脱硫区、深度脱硫区分别选自喷淋塔区、填料塔区或板式塔区中的一种。
[0022] 所述的预脱硫区及深度脱硫区中,液气比为1-12L/H13。
[0023]作为优选的技术方案,所述的赤泥预浸槽共设有一对。
[0024]作为优选的技术方案,所述的赤泥预浸槽底部还设有用于将赤泥预浸浆液排送至 赤泥浆液池的出泥管。
[0025]所述的赤泥原料为铝土矿提取氧化铝过程中产生的赤泥废渣。
[0026] 所述的预浸处理能够脱除赤泥中的表面游离碱和弱结合碱,分离后可得到用于预 脱硫的含镁赤泥预浸浆液以及用于深度脱硫的赤泥预浸清液。
[0027]回流至赤泥预浸槽的预脱硫浆液清液中含有硫酸镁及少量钠,与赤泥原料混合预 浸时,预脱硫浆液清液中的硫酸镁转化为氢氧化镁并沉积到赤泥中,从而实现镁的循环利 用。
[0028] 赤泥浆液池中加入的氧化镁能够保证预脱硫区所用的赤泥预浸浆液的脱硫活性 和缓冲作用。
[0029]烟气经预脱硫后,80-90%以上的S〇2能够被脱除。预脱硫后的赤泥预浸浆液在脱 硫赤泥浆液脱水池中进行机械脱水,排出的脱碱赤泥可进行资源化综合利用。
[0030]所述的深度脱硫液循环池中的赤泥预浸清液在经过多次循环后,排出的部分赤泥 预浸清液可进行蒸发结晶回收硫酸钠。
[0031]所述的分区塔板只允许烟气由预脱硫区进入深度脱硫区,防止深度脱硫区内的赤 泥预浸清液向下流动至预脱硫区。
[0032]对赤泥进行预浸处理能够将赤泥中的表面游离碱、弱结合碱以及大部分钠脱除, 同时产生了pH较高的用于深度脱硫的赤泥预浸清液。在赤泥浆液池中补充加入氧化镁,从 而对赤泥预浸浆液进行强化,能够提高赤泥预浸浆液的预脱硫能力,同时预脱硫过程中所 产生的镁离子有利于对结合在赤泥上的碱进行剥离脱除,从而提高对赤泥的脱碱能力。预 脱硫后的镁离子随着预脱硫浆液清液回流至赤泥预浸槽中,并与赤泥原料进行混合,镁离 子转化氢氧化镁,沉积到赤泥上,之后又重新回到赤泥预浸浆液中用于预脱硫,从而实现镁 的循环。
[0033] 整个过程中所涉及的反应方程式主要有:
[0034] (1)赤泥预浸过程所发生的反应:
[0035] 赤泥+H20—Na0H+Ca (0H) 2 (1)
[0036] MgS〇4+赤泥—Mg (0H) 2丄(2)
[0037] (2)预脱硫区的主要反应:
[0038]赤泥+H2〇+S〇2+〇2—MgS〇4+CaS〇4 (3)
[0039] (3)深度脱硫区的主要反应:
[0040] 2Na0H+S02+0.502^Na2S〇4+H20 ⑷
[0041] 本发明方法中,赤泥原料先利用含镁脱硫循环液进行预浸,经沉降后得到稠厚的 赤泥预浸浆液和赤泥预浸清液,并将其分别作为烟气预脱硫浆液和深度脱硫液使用。预焙 阳极煅烧烟气经过余热回收后进入脱硫塔进行喷淋洗涤处理,该脱硫塔按其功能划分为3 个区,分别为预脱硫区、深度脱硫区和高效除雾区。预脱硫区喷淋液为镁强化的稠厚的赤泥 预浸浆液,深度脱硫区喷淋液为赤泥预浸清液。烟气先经过脱硫塔下部的预脱硫区与低pH 值镁强化稠厚赤泥预浸浆液进行逆向接触吸收,使烟气中的80-90%的302在此区被脱除; 之后烟气经过分区塔板,进入深度脱硫区,通过与pH值较高的赤泥预浸清液逆向接触吸收 达到深度脱硫目的。最后,烟气在经过脱硫塔上层高效除雾区除雾后排出脱硫塔,并实现达 标排放。
[0042] 与现有报道的单纯赤泥脱硫技术相比,本发明具有以下特点:
[0043] 1)能够同时实现电解铝预焙阳极煅烧工段中产生的烟气深度脱硫以及氧化铝生 产副产物赤泥的废物资源化综合利用,脱硫效率高、赤泥脱碱彻底且能够降低有毒有害物 质的产生,能耗较低;
[0044] 2)将一个脱硫塔按其功能划分为预脱硫区和深度脱硫区,预脱硫区在低pH情况下 运行有利于赤泥中的结合钠、钙等碱性组分充分脱除或转化,不仅能够提高赤泥作为脱硫 剂的利用率,同时还可充分对赤泥进行脱碱处理;预脱硫区无需达到过高的脱硫效率,从而 降低了液气比并能够保持较低的PH,而残留的二氧化硫将在深度脱硫区利用高pH赤泥预浸 清液进行高效脱除;
[0045] 3)利用镁强化赤泥脱硫,能够有效提高赤泥的脱硫效率及对赤泥的脱碱能力,降 低赤泥预浸浆液的循环量,同时,赤泥预浸浆液中的镁离子还可与赤泥混合后转化为氢氧 化镁,并沉积到赤泥预浸槽中的赤泥上,之后重新返回到预脱硫区,以实现镁的循环利用。
附图说明
[0046]图1为本发明工艺流程示意图;
[0047]图中标记说明:
[0048] 1 一赤泥预浸槽、2—深度脱硫液循环池、3—赤泥浆液池、4 一烟气进口、5—预脱硫 区、6—脱硫赤泥浆液脱水池、7—分区塔板、8—深度脱硫区、9一高效除雾区、10—烟气出 口、11 一收集槽、12—赤泥原料、13—赤泥预浸清液、14一赤泥预浸楽液、15—预脱硫衆液清 液、16—脱硫塔。
具体实施方式
[0049]下面结合附图和具体实施例对本发明进行详细说明。
[0050] 实施例1:
[0051]如图1所示,一种电解铝预焙阳极煅烧烟气脱硫的方法,具体包括以下步骤:
[0052] 第一步:将赤泥原料12送入赤泥预浸槽1中,并加入从脱硫赤泥浆液脱水池6回流 的含镁预脱硫浆液清液15进行预浸处理,待预浸结束后,使赤泥预浸槽1中的固体赤泥发生 自然沉降,回流的含镁预脱硫浆液清液15中的镁离子转化为氢氧化镁并沉积到赤泥上,沉 降结束后,将上层的赤泥预浸清液13送入深度脱硫液循环池2,而下层的赤泥预浸浆液14由 赤泥预浸槽1底部送入赤泥浆液池3;
[0053] 第二步:向赤泥浆液池3中加入氧化镁和水,并与赤泥预浸浆液14混合均匀,送入 脱硫塔16下部的预脱硫区5;
[0054] 第三步:电解铝预焙阳极煅烧烟气经过余热回收后,从脱硫塔16的烟气进口 4进入 预脱硫区5,与预脱硫区5内自上而下喷淋的赤泥预浸浆液14逆向接触吸收,进行预脱硫,脱 硫效率为88 %;
[0055]第四步:预脱硫后的赤泥预浸浆液14在脱硫塔16底部经曝气氧化后,进入脱硫赤 泥浆液脱水池6中进行脱水,脱水后得到预脱硫浆液清液15及脱碱赤泥,将预脱硫浆液清液 15回流至赤泥预浸槽1中,同时排出脱碱赤泥;
[0056]第五步:预脱硫后的烟气经脱硫塔16中部的分区塔板7进入脱硫塔16上部的深度 脱硫区8,与深度脱硫区8内自上而下喷淋的来自深度脱硫液循环池2的赤泥预浸清液13逆 向接触吸收,进行深度脱硫,脱硫效率为75 % ;
[0057]第六步:深度脱硫后的赤泥预浸清液I3在分区塔板7下方的收集槽11中收集后,再 回流至深度脱硫液循环池2中;
[0058]第七步:深度脱硫后的烟气经脱硫塔16顶部的高效除雾区9除雾后,经烟气出口 10 排出即可。
[0059]第一步中预浸处理结束后,赤泥预浸清液I3及赤泥预浸浆液14的pH均大于8。
[0060]第二步中氧化镁的加入量为赤泥预浸浆液14质量的0.5-5%。
[0061]第五步中,当经深度脱硫区8后的赤泥预浸清液13中钠离子质量浓度高于10%时, 向外界排出一部分赤泥预浸清液13,并由赤泥预浸槽1向深度脱硫液循环池2中补充相同体 积新的赤泥预浸清液13。赤泥预浸清液13的排出体积为深度脱硫液循环池2中赤泥预浸清 液13总体积的20%。
[0062]本实施例中,脱硫塔16为三区式脱硫塔,该三区式脱硫塔中的预脱硫区5及深度脱 硫区8均为喷淋塔区。赤泥预浸槽1共设有一对。赤泥预浸槽1底部还设有用于将赤泥预浸浆 液14排送至赤泥浆液池3的出泥管。
[0063]向脱硫塔16中通入含二氧化硫初始浓度为4000mg/m3的模拟烟气,烟气流量控制 在2.5m3/h,烟气温度约为100°C,预脱硫区5液气比为7L/m3,深度脱硫区8液气比为9L/m3。 [0064] 通过对脱硫尾气中二氧化硫浓度的在线监测和记录,结果表明吸收后模拟烟气中 二氧化硫的浓度保持在l〇〇mg/m3左右,据此计算二氧化硫的去除率为97.5 %。
[0065] 实施例2:
[0066] 本实施例中,预脱硫区5的液气比为1 L/m3,深度脱硫区8的液气比为1 L/m3,赤泥预 浸清液13的排出体积为深度脱硫液循环池2中赤泥预浸清液13总体积的2%。
[0067]向脱硫塔16中通入含二氧化硫初始浓度为4000mg/m3的模拟烟气,烟气流量控制 在2.5m3/h,烟气温度约为80°C,预脱硫区5液气比为lL/m3,深度脱硫区8液气比为lL/m3。 [0068]通过对脱硫尾气中二氧化硫浓度的在线监测和记录,结果表明吸收后模拟烟气中 二氧化硫的浓度保持在170mg/m3左右,据此计算二氧化硫的去除率为95.7 %。
[0069] 其余同实施例1。
[0070] 实施例3:
[0071 ]本实施例中,预脱硫区5的液气比为12L/m3,深度脱硫区8的液气比为12L/m3,赤泥 预浸清液13的排出体积为深度脱硫液循环池2中赤泥预浸清液13总体积的20%。
[0072]向脱硫塔16中通入含二氧化硫初始浓度为4000mg/m3的模拟烟气,烟气流量控制 在2.5m3/h,烟气温度约为160°C,预脱硫区5液气比为10L/m3,深度脱硫区8液气比为l〇L/m3。 [0073]通过对脱硫尾气中二氧化硫浓度的在线监测和记录,结果表明吸收后模拟烟气中 二氧化硫的浓度保持在140mg/m3左右,据此计算二氧化硫的去除率为96.5 %。
[0074]其余同实施例1。
[0075] 实施例4:
[0076]利用一个直径l〇cm,高度120cm的有机玻璃制填料喷淋脱硫塔作为主反应器进行 实验。脱硫塔I6分为上下三个区,下部为预脱硫区5,中部为深度脱硫区8,上部为高效除雾 区9。预脱硫区5的吸收液的主要有效组分为预浸后的赤泥加入水和氧化镁制成的赤泥预浸 浆液14,氧化镁含量为赤泥重量的3%;深度脱硫区8的吸收液为赤泥预浸清液13,pH保持在 10-12范围。
[0077]向脱硫塔I6中通入含二氧化硫初始浓度为2200mg/m3的模拟烟气,烟气流量控制 在2.0m3/h,烟气温度约为l〇〇°C,预脱硫区5液气比为3L/m3,深度脱硫区8液气比为5L/m3。 [0078]通过对脱硫尾气中二氧化硫浓度的在线监测和记录,结果表明吸收后模拟烟气中 二氧化硫的浓度保持在106mg/m3左右,据此计算二氧化硫的去除率为95.2%。
[0079] 实施例5:
[0080]利用一个直径10cm,高度120cm的有机玻璃制填料喷淋脱硫塔作为主反应器进行 实验。脱硫塔16分为上下三个区,下部为预脱硫区5,中部为深度脱硫区8,上部为高效除雾 区9。预脱硫区5的吸收液的主要有效组分为预浸后的赤泥加入水和氧化镁制成的赤泥预浸 浆液14,氧化镁含量为赤泥重量的5% ;深度脱硫区8的吸收液为赤泥预浸清液13,pH保持在 12-13范围。
[0081]向脱硫塔16中通入含二氧化硫初始浓度为2200mg/m3的模拟烟气,烟气流量控制 在2 • 0m3/h,烟气温度约为100 °C,预脱硫区5液气比为5L/m3,深度脱硫区8液气比为7L/m3。 [0082]通过对脱硫尾气中二氧化硫浓度的在线监测和记录,结果表明吸收后模拟烟气中 二氧化硫的浓度保持在68mg/m3左右,据此计算二氧化硫的去除率为96.9%。
[0083]上述的对实施例的描述是为便于该技术领域的普通技术人员能理解和使用发明。 熟悉本领域技术的人员显然可以容易地对这些实施例做出各种修改,并把在此说明的一般 原理应用到其他实施例中而不必经过创造性的劳动。因此,本发明不限于上述实施例,本领 域技术人员根据本发明的揭示,不脱离本发明范畴所做出的改进和修改都应该在本发明的 保护范围之内。
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