JPH0143596B2 - - Google Patents
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- Publication number
- JPH0143596B2 JPH0143596B2 JP10262682A JP10262682A JPH0143596B2 JP H0143596 B2 JPH0143596 B2 JP H0143596B2 JP 10262682 A JP10262682 A JP 10262682A JP 10262682 A JP10262682 A JP 10262682A JP H0143596 B2 JPH0143596 B2 JP H0143596B2
- Authority
- JP
- Japan
- Prior art keywords
- ash
- coal
- slurry
- water
- 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
Links
Description
〔産業上の利用分野〕
本発明は、石炭火力発電所において石炭灰を水
スラリー輸送する場合に発生する灰処理水のPH調
節方法に関するものである。
〔従来の技術〕
一般に、石炭火力発電所では石炭の燃焼に伴つ
てその燃焼量の10〜20%が石炭灰となつて発生
し、そのうち約85%はフライアツシユとなつて電
気集じん機で捕集され、残りはボイラ下部よりク
リンカアツシユとして排出される。この石炭灰は
極力セメント混和剤などへの有効利用が図られて
いるが、その割合は高々20〜30%であり、残りは
埋立処分されている。最近の石炭火力発電所は、
海外からの輸入炭を使用する揚地大型石炭火力で
あり、臨海に立地することが多く、灰処理も発電
所近傍に確保された灰捨場(灰捨池)へ最も経済
的な水スラリー輸送する型式がとられることが多
い。
石炭灰の埋立処分に当たつては、廃棄物の処理
および清掃に関する法律に従つた処分を実施する
ことになつており、石炭灰は管理型物質としての
適用を受ける。石炭灰は水と接触混合した場合、
溶出液のPHが高くなることが問題であり、スラリ
ー輸送の際にも、灰捨場余水が排水基準のPH5〜
9を上回わる値となることがしばしば生じてい
た。
従来技術として、特開昭57―30594号公報に示
されるように、塵芥焼却炉におけるオーバーフロ
ー槽15からの灰汚水と塵芥焼却炉の排ガスとを
気液触装置17で気液接触させて、排ガス中の
CO2で処理する方法が知られている。しかしこの
方法は、灰水洗槽13で灰を水洗し、灰沈澱槽1
4で沈澱させた後のオーバーフロー水を処理する
ものであり、かつ排ガスとして脱硫工程前のガス
を使用するか、または脱硫工程後のガスを使用す
るかについては何ら記載されていない。
また特開昭57―32787号公報には、石炭焚き火
力発電プラントから排出される粉塵、酸性排出
物、アルカリ性排出物を公害を起こさぬ状態に処
理し、かつ消費水量を極力少なくすることを目的
とする処理方法が記載されている。すなわちこの
公報には、「排ガスを冷却塔7aに導き、スロー
ト部に液を噴霧して、SO3,SO2,粉塵、HC1,
HFを捕捉し、液は冷却塔7aの底部に溜る。こ
の貯溜液は循環ポンプ21により噴霧ノズルから
冷却塔7aのスロート部に供給される。循環ポン
プ21を流れる液はPH1〜2の強い酸性であるの
で、管路23で抽出しかつ管路24による捕給水
でその酸を薄める。また吸収塔7cの底部より抜
き出した石膏は反応槽25、ポンプ26、酸化塔
27を経由してシツクナ槽28に送られる。その
上澄み液はPH9〜10のアルカリ液であり、これを
排水処理槽29に供給する。」旨が記載されてい
る(3頁左上欄9行〜右上欄3行参照)。
このようにこの公報記載の方法においては、ア
ルカリ液は石膏の濃縮時の上澄み液であり、また
フライアツシユを気流搬送することを前提として
いる(2頁右下欄下から2行〜3頁左上欄4行参
照)。
〔発明が解決しようとする問題点〕
しかし上記の特開昭57―32787号公報記載の方
法は、何ら石炭灰のスラリー輸送による灰捨場投
棄によつて起こり得る灰捨場水のPH上昇に対する
解決策とはなつておらず、範囲をパワーステーシ
ヨン内に限定しているものの、石炭灰のスラリー
輸送による灰捨場での問題については何ら言及さ
れていない。
本発明は上記の諸点に鑑み、本発明者らが後述
のように実験により知見し確認した事実、すなわ
ち石炭灰スラリー(スラリー濃度約10〜30重量
%、PH8〜11)に、CO2を約13〜14%含むガスを
導入すると、約1時間後にスラリー中のPHが6〜
7程度になるという事実に着目してなされたもの
で、石炭焚ボイル排ガス中の酸性ガスであるCO2
を用いて、石炭灰を水スラリー輸送する場合に発
生する灰処理水のPHの調節を行う方法を提供せん
とするものである。
〔問題点を解決するための手段および作用〕
本発明の灰処理水のPH調節方法は、石炭焚ボイ
ラにおいて石炭灰を灰捨池までスラリー輸送して
灰処理するに際し、石炭灰・水スラリーを脱硫後
の排ガスの全部または一部と反応塔内で気液接触
させ、排ガス中のCO2を前記スラリーに吸収させ
てPHを調節した後、このスラリーを灰捨池に貯留
し、オーバーフロー水を放流および/または灰輸
送用の水として循環使用することを特徴としてい
る。
本発明の方法においては、石炭灰・水スラリー
を脱硫後のSO2を含有しない排ガスと接触させる
ことを特徴としている。脱硫前のCO2およびSO2
を含有する排ガスでスラリーを処理すれば、次式
のようにPHの関係で一旦生成したCaCO3が分解
する可能性があり好ましくないからである。
CaCO3+H2SO3→CaSO3+H2O+CO2↑
〔実施例〕
以下、本発明の実施例を図面に基づいて説明す
る。第1図は本発明の方法を実施する装置の一例
を示すもので、石炭を専焼または混焼で燃焼させ
る石炭焚ボイラ1の排ガスダクトに電気集じん機
などの集じん装置2、脱硫装置3、煙突4などが
直列に接続されている。集じん装置としては電気
集じん機の代りに他の装置、たとえばグラベル式
ろ過集じん装置、マルチサイクロン、バグフイル
タなどを用いることも可能である。なお集じん装
置2の上流側または下流側に空気予熱器が設けら
れるが、図示を省略している。
石炭焚ボイラ1の排ガスは集じん装置2に導入
され除じんされた後、脱硫処理される。一方、石
炭灰は灰捨池5まで水スラリー輸送される。この
場合の灰スラリー濃度は、通常、好適には10〜15
重量%である。
灰スラリーを、そのままCO2吸収反応塔6に導
入して脱硫後の排ガスと気液接触させ、PHを調節
した後、灰捨池5に貯留し、オーバーフロー水
(上澄)を放流および/または灰輸送用の水とし
て循環使用する。なおCO2吸収反応塔6を簡便に
する場合は、排ガス中にミストが含まれるので、
排ガスを脱硫装置3の前に戻してミストの除去を
図る。
つぎに実験例について説明する。
例 1
第1表に示す組成の石炭灰(試料A,B,C)
を用い、海水および蒸留水により溶出液を調製
し、溶出液のPHの経時変化を測定した。スラリー
中の石炭灰の混入量は10重量%であつた。CO2含
有ガスとしては、CO2 13%と空気87%とからな
るガスを用い、2/minの割合で溶出液と接触
させた。結果は第2図に示す如くであつた。な
お、第2図において、丸印は試料Aを、三角印は
試料Bを、四角印は試料Cを示し、白印は海水の
場合を、黒印は蒸留水の場合を示している。
[Industrial Application Field] The present invention relates to a method for adjusting the pH of ash treatment water generated when coal ash is transported as a water slurry in a coal-fired power plant. [Conventional technology] In general, when coal is burned at a coal-fired power plant, 10 to 20% of the amount of coal is generated as coal ash, of which about 85% becomes fly ash and is collected by an electrostatic precipitator. The remainder is discharged from the bottom of the boiler as clinker ash. Efforts are being made to use this coal ash as effectively as possible in cement admixtures, etc., but the proportion is only 20-30% at most, and the rest is disposed of in landfills. Recent coal-fired power plants are
This is a large-scale coal-fired power plant that uses coal imported from overseas, and is often located on the coast.Ash treatment is carried out by transporting water slurry to an ash disposal site (ash disposal pond) secured near the power plant, which is the most economical method. A format is often taken. When disposing of coal ash in a landfill, it is supposed to be disposed of in accordance with the Waste Disposal and Public Cleansing Act, and coal ash is treated as a controlled substance. When coal ash comes into contact with water and mixes,
The problem is that the pH of the eluate becomes high, and even during slurry transportation, the ash dumping site surplus water has a pH of 5 to 5, which is the drainage standard.
Values exceeding 9 often occurred. As a conventional technique, as shown in Japanese Patent Application Laid-Open No. 57-30594, sewage ash from an overflow tank 15 in a garbage incinerator and exhaust gas from the garbage incinerator are brought into gas-liquid contact with a gas-liquid contact device 17, and the exhaust gas is In
A method of processing with CO 2 is known. However, in this method, the ash is washed with water in the ash washing tank 13, and then the ash is washed in the ash settling tank 1.
This method treats the overflow water after precipitation in step 4, and there is no description as to whether the gas before the desulfurization process or the gas after the desulfurization process is used as the exhaust gas. Furthermore, Japanese Patent Application Laid-open No. 57-32787 states that the purpose is to treat dust, acidic waste, and alkaline waste discharged from coal-fired power plants to a state that does not cause pollution, and to reduce water consumption as much as possible. A processing method is described. In other words, this publication states, ``Exhaust gas is led to the cooling tower 7a, and a liquid is sprayed at the throat to remove SO 3 , SO 2 , dust, HC1,
The HF is captured and the liquid accumulates at the bottom of the cooling tower 7a. This stored liquid is supplied by the circulation pump 21 from the spray nozzle to the throat portion of the cooling tower 7a. Since the liquid flowing through the circulation pump 21 is strongly acidic with a pH of 1 to 2, it is extracted in a pipe 23 and the acid is diluted with water captured in a pipe 24. Further, the gypsum extracted from the bottom of the absorption tower 7c is sent to a stylus tank 28 via a reaction tank 25, a pump 26, and an oxidation tower 27. The supernatant liquid is an alkaline liquid with a pH of 9 to 10, and is supplied to the wastewater treatment tank 29. (See page 3, upper left column, line 9 to upper right column, line 3). As described above, in the method described in this publication, the alkaline solution is the supernatant liquid during the concentration of gypsum, and it is assumed that the flyash is conveyed by air flow (from the second line from the bottom of the lower right column on page 2 to the upper left column on page 3). (See line 4). [Problems to be solved by the invention] However, the method described in JP-A No. 57-32787 does not provide a solution to the PH increase in ash dump water that can occur due to coal ash slurry transportation and dumping at ash dump sites. Although the scope is limited to power stations, there is no mention of problems at ash dumps due to transport of coal ash slurry. In view of the above-mentioned points, the present invention is based on the fact that the present inventors found and confirmed through experiments as described later . When a gas containing 13 to 14% is introduced, the pH in the slurry increases to 6 to 6 after about 1 hour.
This was done by focusing on the fact that CO2 , an acid gas in coal-fired boiler exhaust gas,
The present invention aims to provide a method for adjusting the pH of ash treatment water generated when coal ash is transported as a water slurry. [Means and effects for solving the problem] The method for adjusting the pH of ash treatment water of the present invention is such that when transporting the slurry of coal ash to the ash disposal pond in a coal-fired boiler for ash treatment, All or part of the flue gas after desulfurization is brought into gas-liquid contact in the reaction tower, and the CO 2 in the flue gas is absorbed into the slurry to adjust the pH. This slurry is then stored in an ash disposal pond and the overflow water is drained. It is characterized by being used for circulation as water for discharge and/or ash transportation. The method of the present invention is characterized in that the coal ash/water slurry is brought into contact with the desulfurized exhaust gas that does not contain SO 2 . CO2 and SO2 before desulfurization
This is because if the slurry is treated with exhaust gas containing CaCO 3 , CaCO 3 once generated may be decomposed due to the pH as shown in the following equation, which is not preferable. CaCO 3 +H 2 SO 3 →CaSO 3 +H 2 O+CO 2 ↑ [Examples] Examples of the present invention will be described below based on the drawings. FIG. 1 shows an example of an apparatus for carrying out the method of the present invention, in which a dust collector 2 such as an electrostatic precipitator, a desulfurizer 3, a desulfurizer 3, a dust collector 2 such as an electrostatic precipitator, etc. Chimneys 4 and the like are connected in series. Instead of the electrostatic precipitator, it is also possible to use other devices such as a gravel filter dust collector, multi-cyclone, bag filter, etc. as the dust collector. Note that an air preheater is provided upstream or downstream of the dust collector 2, but is not shown. The exhaust gas from the coal-fired boiler 1 is introduced into a dust collector 2, where the dust is removed and then desulfurized. On the other hand, the coal ash is transported to the ash disposal pond 5 in a water slurry. The ash slurry concentration in this case is usually preferably 10-15
Weight%. The ash slurry is directly introduced into the CO 2 absorption reaction tower 6, brought into gas-liquid contact with the desulfurized exhaust gas, and after adjusting the pH, is stored in the ash disposal pond 5, and overflow water (supernatant) is discharged and/or The water will be recycled and used for transporting ash. In addition, when simplifying the CO 2 absorption reaction tower 6, since mist is included in the exhaust gas,
The exhaust gas is returned to the front of the desulfurization device 3 to remove mist. Next, an experimental example will be explained. Example 1 Coal ash with the composition shown in Table 1 (Samples A, B, C)
An eluate was prepared using seawater and distilled water, and the change in pH of the eluate over time was measured. The amount of coal ash mixed in the slurry was 10% by weight. A gas containing 13% CO 2 and 87% air was used as the CO 2 -containing gas, and was brought into contact with the eluate at a rate of 2/min. The results were as shown in FIG. In FIG. 2, circles indicate sample A, triangles indicate sample B, square marks indicate sample C, white marks indicate seawater, and black marks indicate distilled water.
以上説明したように、本発明の方法は、石炭
灰・水スラリーと脱硫後の排ガスとを直接接触さ
せてCO2の吸収を図るものであるので、吸収効率
が高く、灰処理水のPHを大幅に下げることがで
き、従来、灰処理水のPH調節用に必要としていた
薬品使用量を零にすることができるという効果を
有している。
As explained above, the method of the present invention aims to absorb CO2 by bringing the coal ash/water slurry into direct contact with the flue gas after desulfurization, so the absorption efficiency is high and the PH of the ash treated water is reduced. This has the effect of reducing the amount of chemicals used to adjust the pH of ash treatment water to zero.
第1図は本発明の方法を実施する装置の一例を
示すフローシート、第2図は石炭灰スラリーに
CO2を含むガスを接触させた場合のPHの経時変化
を示すグラフである。
1…石炭焚ボイラ、2…集じん装置、3…脱硫
装置、4…煙突、5…灰捨池、6…CO2吸収反応
塔。
Figure 1 is a flow sheet showing an example of an apparatus for carrying out the method of the present invention, and Figure 2 is a flow sheet showing an example of an apparatus for carrying out the method of the present invention.
It is a graph showing a change in pH over time when a gas containing CO 2 is brought into contact. 1... Coal-fired boiler, 2... Dust collector, 3... Desulfurization device, 4... Chimney, 5... Ash disposal pond, 6... CO 2 absorption reaction tower.
Claims (1)
ラリー輸送して灰処理するに際し、石炭灰・水ス
ラリーを脱硫後の排ガスの全部または一部と反応
塔内で気液接触させ、排ガス中のCO2を前記スラ
リーに吸収させてPHを調節した後、このスラリー
を灰捨池に貯留し、オーバーフロー水を放流およ
び/または灰輸送用の水として循環使用すること
を特徴とする灰処理水のPH調節方法。1. When transporting coal ash as a slurry to an ash disposal pond in a coal-fired boiler for ash treatment, the coal ash/water slurry is brought into gas-liquid contact with all or part of the flue gas after desulfurization in a reaction tower, and CO in the flue gas is removed. 2 is absorbed into the slurry to adjust the PH, the slurry is stored in an ash disposal pond, and the overflow water is recycled and used as water for discharge and/or ash transportation. Adjustment method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10262682A JPS58219991A (en) | 1982-06-15 | 1982-06-15 | Ph control of water after treating ash |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10262682A JPS58219991A (en) | 1982-06-15 | 1982-06-15 | Ph control of water after treating ash |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58219991A JPS58219991A (en) | 1983-12-21 |
| JPH0143596B2 true JPH0143596B2 (en) | 1989-09-21 |
Family
ID=14332445
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10262682A Granted JPS58219991A (en) | 1982-06-15 | 1982-06-15 | Ph control of water after treating ash |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58219991A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61227890A (en) * | 1985-04-02 | 1986-10-09 | Teijin Ltd | Adjusting method for ph of waste water |
| KR100406932B1 (en) * | 1999-03-19 | 2003-11-21 | 주식회사 포스코 | APPARATUS FOR AUTOMATIC CONTROLLING pH OF THICKENER DEDUSTING WATER |
-
1982
- 1982-06-15 JP JP10262682A patent/JPS58219991A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58219991A (en) | 1983-12-21 |
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