JP2583902B2 - Control device for wet flue gas desulfurization unit - Google Patents
Control device for wet flue gas desulfurization unitInfo
- Publication number
- JP2583902B2 JP2583902B2 JP62203404A JP20340487A JP2583902B2 JP 2583902 B2 JP2583902 B2 JP 2583902B2 JP 62203404 A JP62203404 A JP 62203404A JP 20340487 A JP20340487 A JP 20340487A JP 2583902 B2 JP2583902 B2 JP 2583902B2
- Authority
- JP
- Japan
- Prior art keywords
- absorbent slurry
- flow rate
- signal
- acid gas
- exhaust gas
- 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
Links
- 238000006477 desulfuration reaction Methods 0.000 title claims description 22
- 230000023556 desulfurization Effects 0.000 title claims description 22
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 title claims description 9
- 239000003546 flue gas Substances 0.000 title claims description 9
- 239000002250 absorbent Substances 0.000 claims description 93
- 230000002745 absorbent Effects 0.000 claims description 93
- 239000002002 slurry Substances 0.000 claims description 93
- 239000007789 gas Substances 0.000 claims description 89
- 229910005965 SO 2 Inorganic materials 0.000 claims description 50
- 239000002253 acid Substances 0.000 claims description 40
- 238000001514 detection method Methods 0.000 claims description 22
- 230000003472 neutralizing effect Effects 0.000 claims description 14
- 239000003245 coal Substances 0.000 claims description 9
- 230000002378 acidificating effect Effects 0.000 claims description 8
- 238000006386 neutralization reaction Methods 0.000 claims description 3
- 238000011144 upstream manufacturing Methods 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 17
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 15
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 15
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 15
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 14
- 229910052815 sulfur oxide Inorganic materials 0.000 description 9
- 238000010521 absorption reaction Methods 0.000 description 8
- 239000002585 base Substances 0.000 description 8
- 238000010248 power generation Methods 0.000 description 6
- 239000006096 absorbing agent Substances 0.000 description 5
- 238000010586 diagram Methods 0.000 description 5
- 239000000428 dust Substances 0.000 description 5
- 239000000446 fuel Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- TVZRAEYQIKYCPH-UHFFFAOYSA-N 3-(trimethylsilyl)propane-1-sulfonic acid Chemical compound C[Si](C)(C)CCCS(O)(=O)=O TVZRAEYQIKYCPH-UHFFFAOYSA-N 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 239000010881 fly ash Substances 0.000 description 3
- 239000003595 mist Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 238000003915 air pollution Methods 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
- GBAOBIBJACZTNA-UHFFFAOYSA-L calcium sulfite Chemical compound [Ca+2].[O-]S([O-])=O GBAOBIBJACZTNA-UHFFFAOYSA-L 0.000 description 2
- 235000010261 calcium sulphite Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052602 gypsum Inorganic materials 0.000 description 2
- 239000010440 gypsum Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 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
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000003009 desulfurizing effect Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
Landscapes
- Treating Waste Gases (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は湿式排煙流装置に係り、特に亜硫酸ガスの他
に酸性ガスやフライアツシユを含む排ガスを安定して処
理するのに好適な湿式排煙脱硫装置の制御装置に関す
る。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a wet flue gas flow apparatus, and more particularly to a wet flue gas suitable for stably treating an exhaust gas containing an acid gas and a fly ash in addition to a sulfurous acid gas. The present invention relates to a control device for a smoke desulfurization device.
近年、発電需要が増大するにつれて、化石燃料を主燃
料とするボイラも大型化し、発電用ボイラが大気汚染を
与える影響度も増加しつつある。In recent years, as the demand for power generation has increased, the size of boilers using fossil fuel as a main fuel has also increased, and the degree of influence of power generation boilers on air pollution has been increasing.
この大気汚染を拡大する公害物質のうち、多大な比率
をしめるSOxの排出規制は年々きびしくなる傾向にあ
る。この状勢下で第二次石油シヨツク以来、石油を主燃
料としてきた我が国の発電業界は、より安価で、かつ十
分な供給源をもつ石炭燃料へと燃料転換しつつある。SOx emission regulations, which account for a large proportion of the pollutants that increase this air pollution, tend to become more stringent year after year. Under this circumstance, the power generation industry in Japan, which has been using oil as its main fuel since the Second Petroleum Shock, is switching to coal fuel, which is cheaper and has a sufficient supply.
ところが、ボイラが大型化する一方、発電コストを低
下する目的で、発電需要に応じて頻繁な負荷変動を行な
うために、一日単位でボイラの起動停止運動を行なう毎
日起動停止(Daily Start Stop以下単にDSSという)運
転や、週末起動停止(Weekly Start Stop以下単にWSSと
いう)運転が繰り返されている。However, in order to increase the size of the boiler and reduce the power generation cost, the boiler starts and stops on a daily basis to carry out frequent load fluctuations according to the power generation demand (Daily Start Stop or less). DSS) operation and weekend start / stop operation (WSS).
それは最近の電力需要の特徴として、原子力発電の伸
びと共に、電力負荷の最大,最小差も増大し、火力発電
用ボイラをベースロード用から負荷調整用へと移行する
傾向にあり、この火力発電用ボイラを負荷に応じて圧力
を変化させて変圧運転を行なう、いわゆる全負荷では超
臨界圧域、部分負荷では亜臨界圧域で運転する変圧運転
ボイラとすることによつて、部分負荷での発電効率を数
%向上させることができるからである。As a characteristic of recent power demand, the difference between the maximum and minimum power loads has increased with the increase in nuclear power generation, and there has been a tendency to shift thermal power boilers from base load to load adjustment. The boiler performs a variable-pressure operation by changing the pressure according to the load, so-called a variable-pressure operation boiler that operates in a supercritical pressure region for a full load and a subcritical pressure region for a partial load, thereby generating electricity at a partial load. This is because the efficiency can be improved by several percent.
ところが、この様に一日単位で頻繁にDSS運転や週単
位でWSS運転を行なうために、この負荷変動によつて排
ガス量が変動し、石炭の炭種によつても可溶性酸性ガス
量やフライアツシユ量が異るために、例えば1/4,1/2,3/
4負荷などの部分負荷時には目標SOx値以下にすることが
できない。However, since the DSS operation is performed frequently on a daily basis and the WSS operation is performed on a weekly basis, the amount of exhaust gas fluctuates due to the load fluctuation, and the amount of soluble acid gas or fly ash is also dependent on the type of coal. For example, 1/4, 1/2, 3 /
At the time of partial load such as 4 loads, it cannot be reduced below the target SOx value.
例えば火力発電所等に設置される湿式排煙脱硫装置
は、炭酸カルシウム(CaCO3)、水酸化カルシウム〔Ca
(OH2)〕または酸化カルシウム(CaO)などを吸収剤と
したスラリからなる吸収剤スラリを用い、ボイラ等の排
ガス中の硫黄酸化物(SOx)を吸収し、得られた亜硫酸
カルシウムを酸化して、硫酸カルシウム、すなわち石膏
として回収する方法が最も一般的である。For example, a wet-type flue gas desulfurization device installed in a thermal power plant or the like includes calcium carbonate (CaCO 3 ), calcium hydroxide [Ca
(OH 2 )] or an absorbent slurry consisting of calcium oxide (CaO) as an absorbent, absorbs sulfur oxides (SOx) in the exhaust gas from boilers and the like, and oxidizes the resulting calcium sulfite. Most commonly, calcium sulfate is recovered as gypsum.
一方、エネルギーの多様化に伴い、発電所や工場のボ
イラ燃料として石炭が多く用いられている。この石炭の
燃料排ガスは通常重油焚排ガスと比較して数十倍もの高
濃度のフツ化水素(HF),塩化水素(HCI)などの酸性
ガスとフライアツシユを含んでおり、これらの成分は脱
硫性能に対して種々の悪影響を及ぼす。HCI及びHFは、
吸収剤スラリと反応して塩化カルシウム(CaCl2)とな
り、SOxに見合つて供給される吸収剤(CaCO3)を消費す
るとともに、吸収剤(CaCO3)スラリの溶解速度を低下
させる。また、フライアツシユは吸収剤スラリ中に混入
すると、Al3+,Fe3+等の重金属が溶出し、特にAl3+はHF
と化合し、吸収剤スラリであるCaCO3の粒子表面に難溶
性化合物を形成し吸収剤スラリ溶解速度を極めて低下さ
せる。On the other hand, with the diversification of energy, coal is widely used as boiler fuel for power plants and factories. The fuel exhaust gas from this coal contains acid gas such as hydrogen fluoride (HF) and hydrogen chloride (HCI) and fly ash, which are several tens of times higher than those of heavy oil fired exhaust gas. Have various adverse effects. HCI and HF are
It reacts with the absorbent slurry to form calcium chloride (CaCl 2 ), consumes the absorbent (CaCO 3 ) supplied in proportion to the SOx, and reduces the dissolution rate of the absorbent (CaCO 3 ) slurry. Further, when Furaiatsushiyu is mixed into the absorbent slurry, Al 3+, heavy metals and dissolution of such Fe 3+, in particular Al 3+ HF
And form a poorly soluble compound on the surface of the particles of CaCO 3 which is the absorbent slurry, and extremely reduce the dissolution rate of the absorbent slurry.
この石炭焚排ガスを用いる従来の湿式排煙脱硫装置の
概略系統図を第3図に示す。FIG. 3 shows a schematic system diagram of a conventional wet flue gas desulfurization apparatus using this coal-fired exhaust gas.
第3図において、図示してしないボイラ等からの排ガ
スは煙道1により除じん塔2に導入され、除じん塔2に
おいては、除じん塔循環タンク3、除じん塔循環ポンプ
4により供給される吸収剤スラリと気液接触により、排
ガス中に含有されるダストが除去されるとともに、SOx
の一部が吸収されて除去される。なお、吸収塔5に送ら
れるガス中のミストを除去するために、ミストエリミネ
ータ6が設置される場合もある。In FIG. 3, exhaust gas from a boiler or the like (not shown) is introduced into a dust tower 2 by a flue 1, and is supplied to the dust tower 2 by a dust tower circulation tank 3 and a dust tower circulation pump 4. The dust contained in the exhaust gas is removed by the gas-liquid contact with the absorbent slurry and the SOx
Is absorbed and removed. Note that a mist eliminator 6 may be installed in order to remove mist in the gas sent to the absorption tower 5.
吸収塔5においては、吸収塔循環タンク7、吸収液循
環ポンプ8、吸収剤スラリ循環配管9から供給された吸
収剤スラリと排ガスとの気液接触により排ガス中のSOx
が吸収、除去された後、デミスタ10で同伴ミストが除去
され、煙道11より処理ガスとして排出される。In the absorption tower 5, the SOx in the exhaust gas is brought into contact with the exhaust gas by gas-liquid contact between the absorbent slurry supplied from the absorption tower circulation tank 7, the absorption liquid circulation pump 8 and the absorbent slurry circulation pipe 9.
After being absorbed and removed, the accompanying mist is removed by the demister 10 and discharged from the flue 11 as a processing gas.
吸収塔5の吸収塔循環タンク7には排ガス中のSOxを
吸収するに必要な吸収剤スラリ12が吸収剤スラリタンク
13,ポンプ14,吸収剤スラリ調節弁15を経て吸収剤スラリ
供給配管16から供給される。Absorber slurry 12 necessary for absorbing SOx in the exhaust gas is stored in the absorber circulation tank 7 of the absorber 5.
13, supplied from an absorbent slurry supply pipe 16 via a pump 14, an absorbent slurry control valve 15.
この吸収塔循環タンク7内のSOxを吸収し生成した亜
硫酸カルシウムを含有する吸収剤スラリの一部は吸収塔
ブリードポンプ17により抜き出され、図示していない酸
化塔において石膏となつて回収される。A part of the absorbent slurry containing calcium sulfite generated by absorbing SOx in the absorption tower circulation tank 7 is extracted by the absorption tower bleed pump 17 and collected as gypsum in an oxidation tower (not shown). .
なお、図中18は排ガス流量検出器、19は入口SO2農度
検出器、20は出口SO2濃度検出器、21は吸収剤スラリ流
量検出器である。In the figure, 18 is an exhaust gas flow rate detector, 19 is an inlet SO 2 agricultural degree detector, 20 is an outlet SO 2 concentration detector, and 21 is an absorbent slurry flow rate detector.
従来用いられている代表的な吸収剤スラリ流量制御系
統図を第4図に示すが、この制御系統について説明す
る。出口SO2濃度検出器20から出口SO2濃度検出信号22を
入口SO2濃度検出器19から入口SO2濃度検出信号23を検出
し、引算器24,割算器25を用いて脱硫率信号26を演算す
る。また、排ガス流量検出器18において検出した排ガス
流量検出信号27に掛算器28において水分補正のための定
数(ドライガスに換算)を掛け、排ガス中の水分を除い
たドライベース排ガス流量検出信号29を演算する。この
ドライベース排ガス流量検出信号29と入口SO2濃度検出
信号23を掛算器30において掛け、総SO2量信号31を得
る。この総SO2量信号31と脱硫率信号26を掛算器32で演
算し、除去SO2量信号33を演算する。関数発生器34で
は、SO2との反応に必要な吸収剤スラリ過剰率を求める
が、一般には過剰率を一定とするいわゆる過剰率一定制
御である、これに対し、吸収剤スラリのPHでこの過剰率
を補正する方法もとられているが、基本的には除去SO2
量に対して吸収剤スラリが投入される制御である。FIG. 4 shows a typical diagram of a conventional absorbent slurry flow rate control system, which will be described. Detecting the outlet SO 2 concentration detector 20 from the outlet SO 2 concentration detection signal 22 to the inlet SO 2 concentration detector 19 from the inlet SO 2 concentration detection signal 23, the desulfurization ratio signal using the subtractor 24, the divider 25 Calculate 26. Further, a multiplier 28 multiplies the exhaust gas flow rate detection signal 27 detected by the exhaust gas flow rate detector 18 by a constant for moisture correction (converted to dry gas) to obtain a dry base exhaust gas flow rate detection signal 29 from which moisture in the exhaust gas has been removed. Calculate. The multiplier 30 multiplies the dry base exhaust gas flow rate detection signal 29 by the inlet SO 2 concentration detection signal 23 to obtain a total SO 2 amount signal 31. The total SO 2 amount signal 31 and the desulfurization rate signal 26 are calculated by a multiplier 32 to calculate a removed SO 2 amount signal 33. A function generator 34, while obtaining the absorbent slurry excess required for reaction with SO 2, generally is a so-called excess constant control to constant excess, whereas in this PH of absorbent slurry Although a method of correcting the excess ratio has been proposed, basically, the removal SO 2
This is a control in which the absorbent slurry is added to the amount.
掛算器35では除去SO2量信号33と吸収剤過剰率信号36
より吸収剤スラリ流量設定信号37を求め吸収剤スラリ流
量調節計(演算器)38に入力される。In the multiplier 35, the removed SO 2 amount signal 33 and the absorbent excess ratio signal 36
An absorbent slurry flow rate setting signal 37 is further obtained and input to an absorbent slurry flow rate controller (calculator) 38.
一方、吸収剤スラリ流量検出器21からの吸収剤スラリ
流量検出器信号39は演算器38に入力され、演算器28では
吸収剤スラリ流量設定信号37と吸収剤スラリ流量検出信
号39の偏差信号40が演算され、この偏差信号40によつて
吸収剤スラリ供給配管16の吸収剤スラリ調節弁15が開閉
される。On the other hand, the absorbent slurry flow detector signal 39 from the absorbent slurry flow detector 21 is input to a calculator 38, and the calculator 28 outputs a deviation signal 40 between the absorbent slurry flow setting signal 37 and the absorbent slurry flow detection signal 39. The deviation signal 40 causes the absorbent slurry control valve 15 of the absorbent slurry supply pipe 16 to open and close.
従来技術の制御装置においては、吸収剤スラリの供給
量を除去SO2量に一定の過剰率設定信号を掛け合せて、
吸収剤スラリ流量設定信号が設定されていたので、酸性
ガス量に見合う吸収剤スラリ量が不足し、脱硫率が低下
する欠点があつた。The control device of the prior art, by multiplying a constant excess ratio setting signal to remove SO 2 amount supplied amount of absorbent slurry,
Since the absorbent slurry flow rate setting signal was set, the amount of the absorbent slurry corresponding to the amount of the acid gas was insufficient, and the desulfurization rate was reduced.
本発明は従来技術の欠点を解決するもので、その目的
とするところは除去SO2量、酸性ガス量に応じて吸収剤
スラリ量が制御でき、しかも酸性ガスの吸収剤スラリ消
費による脱硫性能の低下を防止するものである。The present invention solves the drawbacks of the prior art, and the object is to control the amount of the absorbent slurry according to the amount of SO 2 removed and the amount of the acidic gas, and to improve the desulfurization performance by consuming the absorbent slurry of the acidic gas. This is to prevent the drop.
本発明は前述の目的を達成するために、演算器の上硫
に、炭種によつて酸性ガス濃度を設定する酸性ガス濃度
設定器と、酸性ガス濃度設定器からの酸素濃度信号と排
ガス流量検出器からのドライベース排ガス流量検出信号
から酸性ガス中和用吸収剤スラリ流量設定信号を演算す
る掛算器と、吸収剤スラリ流量設定信号と酸性ガス中和
用吸収剤スラリ流量設定信号を加算する加算器を設け、
吸収剤スラリ流量設定信号を酸性ガス中和用吸収剤スラ
リ流量設定信号によつて補正するようにしたものであ
る。In order to achieve the above object, the present invention provides an acid gas concentration setting device for setting an acid gas concentration according to the type of coal, an oxygen concentration signal from the acid gas concentration setting device, and an exhaust gas flow rate. A multiplier for calculating an acid gas neutralizing absorbent slurry flow setting signal from the dry base exhaust gas flow detecting signal from the detector, and adding the absorbent slurry flow setting signal and the acidic gas neutralizing absorbent slurry flow setting signal. Adder is provided,
An absorbent slurry flow rate setting signal is corrected by an acid gas neutralizing absorbent slurry flow rate setting signal.
以下、本発明の実施例を説明する前に湿式排煙脱硫装
置内での脱硫反応、酸性ガス除去反応について述べる。Hereinafter, a desulfurization reaction and an acid gas removal reaction in a wet flue gas desulfurization apparatus will be described before describing the embodiments of the present invention.
(1) 脱硫反応(空気を吹込まない場合) SO2+Ag→H2SO3 ……(1) 1/2CaCO3+H2SO3→1/2Ca(HSO3)2+1/2CO2+Ag ……(2)1/2Ca(HSO3)2+1/2CaCO3→CaCO3・1/2H2O+1/2CO2 ……(3) (OVERALL)SO2+CaCO3+Ag→CaSO3・1/2H2O+CO2 ……(4) この様に脱硫反応における吸収剤(O3)(CaCO3)ス
ラリとSO2との反応は1:1である系内で除去されたSO2量
と当量の吸収剤スラリが必要であるが、実際には、SO2
を吸収剤スラリ内に固定するには、SO2と当量以上の吸
収剤スラリが必要である。(1) Desulfurization reaction (when air is not blown) SO 2 + Ag → H 2 SO 3 … (1) 1 / 2CaCO 3 + H 2 SO 3 → 1 / 2Ca (HSO 3 ) 2 + 1 / 2CO 2 + Ag (2) 1 / 2Ca (HSO 3 ) 2 + 1 / 2CaCO 3 → CaCO 3・ 1 / 2H 2 O + 1 / 2CO 2 … (3) (OVERALL) SO 2 + CaCO 3 + Ag → CaSO 3・ 1 / 2H 2 O + CO 2 (4) Thus, the reaction between the absorbent (O 3 ) (CaCO 3 ) slurry and SO 2 in the desulfurization reaction is 1: 1. The amount of the absorbent slurry equivalent to the amount of SO 2 removed in the system is 1: 1. Required, but in fact, SO 2
To secure the absorbent in the slurry, it is necessary or more equivalents of the absorbent slurry and SO 2.
(2) 酸性ガス除去反応 (a) HCl除去反応 HCl+Ag→H++Cl- ……(5)H++Cl-+1/2CaCO3→1/2CaCl2+1/2CO2+Ag ……(6) (OVERALL)HCl+1/2CaCO3+Ag→1/2CaCl2+1/2CO2 ……(7) (b) HF除去反応 HF+Ag→H++F- ……(8)H++F-+1/2CaCO3→1/2CaF2+1/2CO2+Ag ……(9) (OVERALL)HF+1/2CaCO3+Ag→1/2CaF2+1/2CO2 ……(10) 酸性ガスの除去反応は、HClは(5)式、HFは(8)
式で示される様に水により液中に溶解するSO2の除去反
応と異なり殆んど放散せず液中に固定できるので、水だ
けで除去できる。しかしながら、これに伴ない液中のH+
濃度は高くなる(即ち、PHが低くなる)ので、脱硫吸収
液で酸性ガスも除去する場合には、SO2吸収の為にPHを
少くとも3.5以上とする必要があり、この場合には、HCl
では(6)式、HFでは(9)式の反応が不可欠で、その
為に吸収剤スラリは必要不可欠である。尚、このHCl,HF
と吸収剤スラリとの反応は、1:1/2で、酸性ガスに対し1
/2当量の吸収剤スラリが必要である。この酸性ガスと吸
収剤スラリとの反応は、SO2と吸収剤スラリの反応に比
べて比較的速く起こるので、SO2の様に過剰率を考慮す
る必要はなく、高々、2〜3%で良い。(2) acid gas removal reaction (a) HCl removal reaction HCl + Ag → H + + Cl - ...... (5) H + + Cl - + 1 / 2CaCO 3 → 1 / 2CaCl 2 + 1 / 2CO 2 + Ag ...... (6) (OVERALL) HCl + 1 / 2CaCO 3 + Ag → 1 / 2CaCl 2 + 1 / 2CO 2 ...... (7) (b) HF removing reaction HF + Ag → H + + F - ...... (8) H + + F - + 1 / 2CaCO 3 → 1 / 2CaF 2 +1 / 2CO 2 + Ag (9) (OVERALL) HF + 1 / 2CaCO 3 + Ag → 1 / 2CaF 2 + 1 / 2CO 2 (10) For the removal reaction of acid gas, HCl is formula (5) and HF is (8)
As shown in the formula, unlike the reaction for removing SO 2 dissolved in water by water, it can be fixed in the liquid without being diffused, and can be removed only with water. However, H +
Since the concentration becomes high (that is, the PH becomes low), when removing the acidic gas with the desulfurization absorption solution, the PH needs to be at least 3.5 or more to absorb SO 2. In this case, HCl
In formula (6), the reaction of formula (9) is indispensable in HF, and an absorbent slurry is indispensable. In addition, this HCl, HF
And the reaction with the absorbent slurry is 1: 1/2,
/ 2 equivalents of absorbent slurry is required. Reaction of the acid gas and the absorbent slurry, so place relatively faster than the reaction of the absorbent slurry and SO 2, is no need to consider the excess as the SO 2, at most, with 2-3% good.
この様に、石炭焚排ガスの様なHCl、HFなどの酸性ガ
スを多く含んだ排ガスを脱硫吸収剤スラリで洗浄する場
合には、HCl,HFによる吸収剤スラリの消費を考慮した吸
収剤スラリの供給量制御を行うことにより、SO2,HCl,HF
に対して常に必要最低限に吸収剤がスラリが供給できる
ので、吸収剤スラリ供給不足による脱硫性能の低下が起
こることはない。As described above, when exhaust gas containing a large amount of acid gas such as HCl and HF such as coal-fired exhaust gas is washed with the desulfurizing absorbent slurry, the use of the absorbent slurry in consideration of the consumption of the absorbent slurry by HCl and HF is considered. By controlling the supply amount, SO 2 , HCl, HF
Therefore, since the slurry can always be supplied to the minimum necessary amount of the absorbent, there is no possibility that the desulfurization performance is deteriorated due to the insufficient supply of the absorbent slurry.
以下本発明の実施例を第1図,第2図を用いて説明す
る。Hereinafter, an embodiment of the present invention will be described with reference to FIGS.
第1図および第2図において、符号15から40までは従
来のものと同一のものを示す。In FIGS. 1 and 2, reference numerals 15 to 40 denote the same components as conventional ones.
41は炭種によつて酸性ガス濃度を設定する酸性ガス濃
度設定器、42は酸性ガス濃度信号、43はドライベース排
ガス流量信号29と酸性ガス濃度信号42から酸性ガス中和
用吸収剤スラリ流量設定信号44を演算する掛算器、45は
SO2側吸収剤スラリ流量設定信号37と酸性ガス中和用吸
収剤流量スラリ設定信号44を加算する加算器、46は吸収
剤スラリ流量設定信号である。41 is an acid gas concentration setting device for setting the acid gas concentration according to the type of coal, 42 is an acid gas concentration signal, 43 is a dry base exhaust gas flow signal 29 and an acid gas neutralizing absorbent slurry flow rate from the acid gas concentration signal 42. A multiplier for calculating the setting signal 44, 45 is
An adder adds the SO 2 side absorbent slurry flow rate setting signal 37 and the acidic gas neutralizing absorbent flow rate slurry setting signal 44, and 46 is an absorbent slurry flow rate setting signal.
第1図において、出口SO2濃度検出器20から出口SO2濃
度検出信号22、入口SO2濃度検出器19から入口SO2濃度検
出信号23を検出し、引算器24、割算器25を用いて脱硫率
信号26を演算する。また、排ガス流量検出器18において
検出した排ガス流量検出信号27に掛算器28(32)におい
て水分補正のための定数を掛け、排ガス中の水分を除い
たドイラベース排ガス流量信号29を演算する。このドラ
イベース排ガス流量信号29と入口SO2濃度検出信号23を
掛算器30において掛け総SO2重信号31を演算する。得ら
れた総SO2量信号31と脱硫率信号26を掛算器32で演算
し、除去SO2量信号33を得る。関数発生器34では、SO2と
の反応に必要な吸収剤スラリ過剰率を求めるが、基本的
には過剰率を一定する。掛算器35では除去SO2量信号33
と吸収剤過剰率信号36よりSO2の吸収に必要なSO2側吸収
剤スラリ流量設定信号37を求める。In FIG. 1, an exit SO 2 concentration detector 20 detects an exit SO 2 concentration detection signal 22 from an exit SO 2 concentration detector 20, and an entrance SO 2 concentration detector 19 detects an entrance SO 2 concentration detection signal 23. The desulfurization rate signal 26 is calculated using the above. Further, a multiplier 28 (32) multiplies the exhaust gas flow rate detection signal 27 detected by the exhaust gas flow rate detector 18 by a constant for moisture correction to calculate a Doyer base exhaust gas flow rate signal 29 excluding moisture in the exhaust gas. The dry base exhaust gas flow rate signal 29 and the inlet SO 2 concentration detection signal 23 and calculates the total SO 2 double signal 31 multiplied by the multiplier 30. The obtained total SO 2 amount signal 31 and desulfurization rate signal 26 are operated by a multiplier 32 to obtain a removed SO 2 amount signal 33. The function generator 34 calculates the excess amount of the absorbent slurry required for the reaction with SO 2, and basically keeps the excess ratio constant. Multiplier 35 removes SO 2 amount signal 33
And determine the SO 2 side absorbent slurry flow rate setting signal 37 required than absorbent excess signal 36 to the absorption of SO 2.
一方、排ガス中に含まれる酸性ガス(HCl,HF)も吸収
剤スラリと容易に反応し吸収剤スラリを消費する為、こ
れに対しても吸収剤スラリを供給する必要がある。酸性
ガス濃度設定器41により入口排ガス中の酸性ガス濃度信
号42を与え、掛算器43において、これに水分を差し引い
たドライベース排ガス流量信号29を掛け、更に吸収剤ス
ラリと酸性ガスの反応は1:2で起こるための補正(基本
的には0.5を掛ける)を行い最終的に酸性ガス量を中和
するに必要な酸性ガス中和用吸収剤スラリ流量設定信号
44を演算する。On the other hand, the acid gas (HCl, HF) contained in the exhaust gas easily reacts with the absorbent slurry and consumes the absorbent slurry. Therefore, it is necessary to supply the absorbent slurry to this. An acid gas concentration setter 41 gives an acid gas concentration signal 42 in the inlet exhaust gas, a multiplier 43 multiplies this by a dry base exhaust gas flow rate signal 29 from which moisture has been subtracted, and the reaction between the absorbent slurry and the acid gas is 1 : Absorber slurry flow rate setting signal for neutralization of acid gas necessary to correct for (2 basically multiply by 0.5) and finally neutralize the amount of acid gas
Calculate 44.
そして、SO2側吸収剤スラリ流量設定信号37と酸性ガ
ス中和用吸収剤スラリ流量設定信号44は加算器45で加算
され、吸収剤スラリ流量設定信号46となり、吸収剤スラ
リ流量検出信号39と吸収剤スラリ流量設定信号46は演算
器38で演算され、偏差信号40によつて吸収剤スラリ供給
配管16の吸収剤スラリ調節弁15が開,閉される。Then, the SO 2 side absorbent slurry flow rate setting signal 37 and the acid gas neutralizing absorbent slurry flow rate setting signal 44 are added by an adder 45 to become an absorbent slurry flow rate setting signal 46, and an absorbent slurry flow rate detection signal 39 and The absorbent slurry flow rate setting signal 46 is calculated by the calculator 38, and the deviation signal 40 causes the absorbent slurry control valve 15 of the absorbent slurry supply pipe 16 to open and close.
このように第1図における制御装置においては吸収剤
スラリ流量設定信号46がSO2側吸収剤スラリ流量設定信
号37と酸性ガス中和用吸収剤スラリ流量設定信号44によ
つて補正されるので、SO2,HCl,HFに対して必要最小限の
吸収剤スラリが供給でき、脱硫性態の低下も防止でき
る。Since absorbent slurry flow rate setting signal 46 is by connexion corrected SO 2 side absorbent slurry flow rate setting signal 37 and the acid gas neutralizing absorbent slurry flow rate setting signal 44 in this control device in the first view, The required minimum amount of absorbent slurry can be supplied to SO 2 , HCl, and HF, and a decrease in desulfurization state can be prevented.
また、DSS運転時、WSS運転時あるいは炭種が変更され
ても追従して吸収剤スラリが供給できる。In addition, the absorbent slurry can be supplied during DSS operation, WSS operation, or even when the coal type is changed.
第2図に示す制御装置は酸性ガスの中和用として可溶
性アルカリを添加する場合に有効な制御装置である。The control device shown in FIG. 2 is an effective control device when a soluble alkali is added for neutralizing acid gas.
第1図の制御装置と異なる点は、第1図の制御装置に
中和剤流量検出器47、引算器48を設け、中和剤流量検出
器47からの中和剤流量検出信号49を引算器48に入力し、
酸性ガス側中和用吸収剤スラリ流量設定信号44を中和剤
流量検出信号49だけ小さくして酸性ガス中和用吸収剤ス
ラリ流量設定信号44aを得るもので、他の説明は第1図
のものと同一である。1 is different from the control device of FIG. 1 in that a neutralizer flow rate detector 47 and a subtracter 48 are provided in the controller of FIG. 1 and a neutralizer flow rate detection signal 49 from the neutralizer flow rate detector 47 is provided. Input to the subtractor 48,
The acid gas-side neutralizing absorbent slurry flow rate setting signal 44 is reduced by the neutralizing agent flow rate detection signal 49 to obtain an acidic gas neutralizing absorbent slurry flow rate setting signal 44a. It is the same as the one.
なお、ガス中のHClやHFなどの酸性ガス濃度を連続し
て測定できる方法は、例えば「工業計測法ハンドブッ
ク」539〜542ページ1982年3月10日朝倉書店発行、特公
昭53−9877号公報、特開昭57−104853号公報、特開昭60
−114761号公報などによって広く知られている。Incidentally, a method for continuously measuring the concentration of acid gas such as HCl or HF in a gas is described in, for example, "Industrial Measurement Method Handbook", pages 539 to 542, published by Asakura Shoten on March 10, 1982, and JP-B-53-9877. JP-A-57-104853 and JP-A-60
It is widely known, for example, from JP-A-1114761.
本発明によれば酸性ガス及びSO2を含む排ガスに対し
て常に所定の過剰な吸収剤スラリが供給でき、吸収剤ス
ラリの不足による脱硫性能の低下が防止できる。According to the present invention can always supply a predetermined excess absorbent slurry against exhaust gas containing acidic gases and SO 2, lowering of desulfurization performance due to lack of the absorbent slurry can be prevented.
また、酸性ガス中和に必要な吸収剤スラリ供給量も制
御できるので、炭種が変化しても脱硫性能は追従でき
る。Further, since the supply amount of the absorbent slurry required for neutralizing the acid gas can be controlled, the desulfurization performance can be followed even if the type of coal changes.
第1図および第2図は本発明の実施例に係る湿式排煙脱
硫装置の制御系統図、第3図は湿式排煙脱硫装置の概略
構成図、第4図は従来の制御系統図である。 15……吸収剤スラリ調節弁、18……排ガス流量検出器、
19……入口SO2濃度検出器、20……出口SO2濃度検出器、
21……吸収剤スラリ流量検出器、22……出口SO2濃度検
出信号、23……入口SO2濃度検出信号、27……排ガス流
量検出信号、29……ドライベース排ガス流量信号、37…
…吸収剤スラリ設定信号、38……演算器、39……吸収剤
スラリ流量検出信号、40……偏差信号、41……酸性ガス
濃度設定器、42……酸性ガス濃度設定信号、43……掛算
器、44……酸性ガス中和用吸収剤スラリ流量設定信号、
45……加算器、46……吸収剤スラリ流量設定信号。1 and 2 are control system diagrams of a wet flue gas desulfurization device according to an embodiment of the present invention, FIG. 3 is a schematic configuration diagram of the wet flue gas desulfurization device, and FIG. 4 is a conventional control system diagram. . 15 ... absorbent slurry control valve, 18 ... exhaust gas flow detector,
19 ...... inlet SO 2 concentration detector, 20 ...... outlet SO 2 concentration detector,
21 ...... absorbent slurry flow detector, 22 ...... outlet SO 2 concentration detection signal, 23 ...... inlet SO 2 concentration detection signal, 27 ...... exhaust gas flow rate detection signal, 29 ...... dry basis exhaust gas flow rate signal, 37 ...
... absorbent slurry setting signal, 38 ... calculator, 39 ... absorbent slurry flow rate detection signal, 40 ... deviation signal, 41 ... acid gas concentration setting device, 42 ... acid gas concentration setting signal, 43 ... Multiplier, 44 ... Absorbent slurry flow rate setting signal for acid gas neutralization,
45: Adder, 46: Absorber slurry flow rate setting signal.
フロントページの続き (72)発明者 勝部 利夫 広島県呉市宝町6番9号 バブコツク日 立株式会社呉工場内 (56)参考文献 特開 昭63−224719(JP,A) 特開 昭56−105729(JP,A) 特開 昭59−32924(JP,A) 特開 昭64−47425(JP,A)Continuation of the front page (72) Inventor Toshio Katsube 6-9 Takara-cho, Kure City, Hiroshima Prefecture Inside the Kure Plant of Babkotsuk Hitachi Ltd. (56) References JP-A-63-224719 (JP, A) JP-A-56-105729 (JP, A) JP-A-59-32924 (JP, A) JP-A-64-47425 (JP, A)
Claims (1)
出口SO2濃度検出器からの検出信号によつて吸収剤スラ
リ流量設定信号を算出すると共に、吸収剤スラリ流量検
出器から吸収剤スラリ流量検出信号を検出し、この吸収
剤スラリ設定信号と吸収剤スラリ流量検出信号を演算器
に入力して偏差信号を求め、この偏差信号によつて吸収
剤スラリ調節弁開,閉するものにおいて、前記演算器の
上流に、炭種によつて酸性ガス濃度を設定する酸性ガス
濃度設定器と、酸性ガス濃度設定器からの酸性ガス濃度
信号と排ガス流量検出器からのドライベース排ガス流量
検出信号から酸性ガス中和用吸収剤スラリ流量設定信号
を演算する掛算器と、吸収剤スラリ流量設定信号と酸性
ガス中和用吸収剤スラリ流量設定信号を加算する加算器
を設け、吸収剤スラリ流量設定信号を酸性ガス中和用吸
収剤スラリ流量設定信号によつて補正するようにしたこ
とを特徴とする湿式排煙脱硫装置の制御装置。An absorbent slurry flow rate setting signal is calculated based on detection signals from an exhaust gas flow rate detector, an inlet SO 2 concentration detector, and an outlet SO 2 concentration detector. When the slurry flow rate detection signal is detected, the absorbent slurry setting signal and the absorbent slurry flow rate detection signal are input to a calculator to obtain a deviation signal, and the deviation signal is used to open and close the absorbent slurry control valve. Upstream of the computing unit, an acid gas concentration setting device for setting the acid gas concentration according to the type of coal, an acid gas concentration signal from the acid gas concentration setting device, and a dry base exhaust gas flow detection signal from the exhaust gas flow detector. A multiplier for calculating an acid gas neutralizing absorbent slurry flow rate setting signal from the controller and an adder for adding the absorbent slurry flow rate setting signal and the acidic gas neutralizing absorbent slurry flow rate setting signal. Controller of the wet flue gas desulfurization apparatus characterized by the flow rate setting signal so as to by connexion corrected to absorbent slurry flow rate setting signal for acid gas neutralization.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62203404A JP2583902B2 (en) | 1987-08-18 | 1987-08-18 | Control device for wet flue gas desulfurization unit |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62203404A JP2583902B2 (en) | 1987-08-18 | 1987-08-18 | Control device for wet flue gas desulfurization unit |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6447426A JPS6447426A (en) | 1989-02-21 |
| JP2583902B2 true JP2583902B2 (en) | 1997-02-19 |
Family
ID=16473495
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62203404A Expired - Lifetime JP2583902B2 (en) | 1987-08-18 | 1987-08-18 | Control device for wet flue gas desulfurization unit |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2583902B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2740970B2 (en) * | 1989-10-05 | 1998-04-15 | 株式会社日立製作所 | Operating method of coal boiler |
| JP4821102B2 (en) * | 2004-09-10 | 2011-11-24 | Jfeエンジニアリング株式会社 | Desalination control device and desalination control method |
| JP6053606B2 (en) * | 2013-05-10 | 2016-12-27 | 三菱電機株式会社 | Measurement method for insulation deterioration of electrical equipment |
-
1987
- 1987-08-18 JP JP62203404A patent/JP2583902B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6447426A (en) | 1989-02-21 |
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