JPS6012559B2 - How to remove deposits from boilers, heat exchangers, etc. - Google Patents
How to remove deposits from boilers, heat exchangers, etc.Info
- Publication number
- JPS6012559B2 JPS6012559B2 JP1002076A JP1002076A JPS6012559B2 JP S6012559 B2 JPS6012559 B2 JP S6012559B2 JP 1002076 A JP1002076 A JP 1002076A JP 1002076 A JP1002076 A JP 1002076A JP S6012559 B2 JPS6012559 B2 JP S6012559B2
- Authority
- JP
- Japan
- Prior art keywords
- deposits
- cleaning
- boilers
- heat exchangers
- water
- 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
- 238000004140 cleaning Methods 0.000 claims description 59
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 20
- 239000007921 spray Substances 0.000 claims description 15
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 claims description 10
- 235000019270 ammonium chloride Nutrition 0.000 claims description 10
- 239000000843 powder Substances 0.000 claims description 6
- 238000012546 transfer Methods 0.000 claims description 4
- 238000013467 fragmentation Methods 0.000 claims 1
- 238000006062 fragmentation reaction Methods 0.000 claims 1
- 239000007788 liquid Substances 0.000 description 19
- 239000000243 solution Substances 0.000 description 18
- 239000000126 substance Substances 0.000 description 17
- 238000007796 conventional method Methods 0.000 description 11
- 238000005406 washing Methods 0.000 description 10
- 239000002699 waste material Substances 0.000 description 10
- -1 205・NaV60 Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- 239000013505 freshwater Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 230000009471 action Effects 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000007922 dissolution test Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000009423 ventilation Methods 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Landscapes
- Incineration Of Waste (AREA)
Description
【発明の詳細な説明】
本発明は、ボイラ・熱交換器等の付着物の除去方法に関
するもので、特殊な洗浄液を使用することによって従釆
この種の除去方法の有する欠点を解決した付着物の除去
方法の改良に関する。Detailed Description of the Invention The present invention relates to a method for removing deposits from boilers, heat exchangers, etc., which solves the drawbacks of this type of removal method by using a special cleaning liquid. This invention relates to improvements in removal methods.
火力プラント、その他蒸気発生プラントのボィラ・熱交
換器等の外面には燃焼ガスの付着灰による汚れが生じる
。特に大型の舶用ボィラ過熱器管外面は、燃料油の粗悪
化に伴い付着灰による汚れが激しく、過熱器ガス通路の
閉塞、管村支持金具の高温腐食等の問題が生じているの
で、従来は一般に過熱器管外面の付着物は第1表に示す
水洗法で除去している。第1表
注)水洗法にょり20万トンクラスのタンカーのボィラ
過熱器管外面付着物を除去した場合で、表中の数値は1
缶分である。BACKGROUND OF THE INVENTION The outer surfaces of boilers, heat exchangers, etc. of thermal power plants and other steam generation plants are contaminated by ash adhering to combustion gas. In particular, the outer surface of superheater tubes in large marine boilers is heavily contaminated with adhering ash as the fuel oil deteriorates, causing problems such as blockage of superheater gas passages and high-temperature corrosion of tube support fittings. Generally, deposits on the outer surface of superheater tubes are removed by the water washing method shown in Table 1. Table 1 Note) The values in the table are based on the case where deposits on the outside surface of the boiler superheater tube of a 200,000 ton class tanker are removed using the water washing method.
That's a can.
第1図は、この水洗系統をポイラの概要と共に示したも
ので、1はバーナ、2は火炉水冷壁、3は過熱器、4は
蒸発管、6は蒸気ドラム、6は水ドラム、7は筋炭器で
ある。Fig. 1 shows this water washing system together with an outline of the boiler. 1 is a burner, 2 is a furnace water wall, 3 is a superheater, 4 is an evaporator tube, 6 is a steam drum, 6 is a water drum, and 7 is a It is a muscle charcoal machine.
第1図において、洗浄系統は、100〜120k9/地
の高圧ジェット洗浄系統と、3〜5k9/地の清水スプ
レー洗浄系統の2系統が使えるようになっている。In FIG. 1, two cleaning systems are available: a high-pressure jet cleaning system with a capacity of 100 to 120 k9/ground and a fresh water spray cleaning system with a capacity of 3 to 5 k9/ground.
ジェット洗浄系統では、上甲板に設置されたタンク8中
の洗浄用清水が弁9を通ってポンプ10から高圧でホー
ス11に送水され、高圧ホースの先端に取付けられたジ
ェット洗浄ノズル12から過熱器3に噴射され、高圧ジ
ェット洗浄で付着物を除去する。一方低圧の清水スプレ
ー洗浄系統では、清水がポンプ10から低圧のままホー
ス13に送水され、ホース先端に取付けられたスプレー
ノズル14から過熱器3に頃霧され、付着物を湿潤、軟
化する。また、これらの2系統の洗浄廃液は火炉のドレ
ン抜きからホース15を経て船外タンク16に溜められ
る。これら2系統による洗浄法は、第1表に示すように
第1工程としてジェット洗浄系統を用いて第1回のジェ
ット洗浄を行ない、煤状ならびに欧質付着物を除去し、
第ロ工程ではスプレー洗浄系統で清水スプレー洗浄を行
ない、残存付着物を湿潤、軟化させ、第m工程では湿潤
、軟化した付着物を第2回のジェット洗浄で除去する。
また第1〜m工程で除去されなかった付着物は鎌W工程
でェアハンマ−、たがね等の手工具を用いて除去される
。このように操作する従来法では次のような欠点があっ
た。In the jet cleaning system, clean water for cleaning in a tank 8 installed on the upper deck passes through a valve 9 and is sent from a pump 10 to a hose 11 at high pressure, and from a jet cleaning nozzle 12 attached to the tip of the high-pressure hose to a superheater. 3, and removes deposits with high-pressure jet cleaning. On the other hand, in the low-pressure fresh water spray cleaning system, fresh water is sent from the pump 10 to the hose 13 at a low pressure, and is sprayed from the spray nozzle 14 attached to the end of the hose to the superheater 3 to moisten and soften deposits. Further, the cleaning waste liquid from these two systems is stored in an outboard tank 16 via a hose 15 from the drain of the furnace. In the cleaning method using these two systems, as shown in Table 1, the first step is to perform the first jet cleaning using the jet cleaning system to remove soot and dirt deposits.
In the b-th step, fresh water spray cleaning is performed in a spray cleaning system to moisten and soften the remaining deposits, and in the m-th step, the moistened and softened deposits are removed by a second jet cleaning.
Further, the deposits not removed in the first to mth steps are removed in the sickle W step using a hand tool such as a pneumatic hammer or a chisel. The conventional method operated in this manner has the following drawbacks.
‘1’蒸気温度が約400qo以下の過熱器管外面付着
物は、軟質ポーラスでNa2S04が主成分であるもの
が多いため、従来の水洗法のみでも長時間洗浄も行なえ
ば除去できる。Since most of the deposits on the outer surface of the superheater tube with a '1' steam temperature of about 400 qo or less are soft porous and mainly composed of Na2S04, they can be removed by the conventional water washing method or by long-term washing.
しかし、約400℃以上の高温部付着成分はV、Fe、
Ni系化合物が多く繊密な堆積層となるため、従来法で
は長時間洗浄を行なっても付着物は殆んど除去できない
。そのため第W工程で残存付着物をェアハンマー、たが
ね等の手工具で除去しており多くの工数を必要としてい
る。■ 従来法は、特に第0工程の清水スプレー洗浄に
長時間を要しているので廃液量が多くなり、これらの廃
液は付着物中のS、V等の化合物の溶解によりpH2〜
5程度の弱酸性で汚濁物質が含まれており、中和後、沈
降分離等の処理を必要とするが廃液処理量が多いためコ
スト高となる。However, the components adhering to the high temperature area above about 400℃ are V, Fe,
Since the deposited layer is dense and contains a large amount of Ni-based compounds, it is almost impossible to remove the deposits using the conventional method even if cleaning is performed for a long time. Therefore, in the W step, the remaining deposits are removed using a hand tool such as an air hammer or a chisel, which requires a large number of man-hours. ■ In the conventional method, the amount of waste liquid is large because it takes a long time, especially for clean water spray cleaning in the 0th step.
It has a weak acidity of about 5.5 and contains pollutants, and requires treatment such as sedimentation and separation after neutralization, but the cost is high because the amount of waste liquid to be treated is large.
‘31 火炉内でェアハンマ−、たがね等の手工具によ
る作業を行なうことは、粉塵の発生、換気不良等の問題
があり、作業員の健康面と管外面に傷が付くので保守の
点から好ましくない。'31 Working with hand tools such as air hammers and chisels inside the furnace causes problems such as the generation of dust and poor ventilation, which is a health issue for the workers and damages the outer surface of the pipes, so maintenance is important. undesirable.
本発明者等は、上記従来法の欠点を解消するため数多く
の実験研究を重ねた結果、上記従来法の第0工程である
清水スプレー洗浄の代りに、特定組成の薬液を含む洗浄
液によるスプレーを行なうことによって、湿潤、軟化、
除去の困難な付着物を短時間で溶解、粉末化しうろこと
、そのために上記従来法の第W工程のようなェアハンマ
ー、たがね等の使用を不必要にならしめ、且つ発生廃液
の量を低減しうろことを確認した。As a result of numerous experimental studies to eliminate the drawbacks of the conventional method, the present inventors have discovered that instead of the clean water spray cleaning, which is the 0th step of the conventional method, spraying with a cleaning solution containing a chemical solution of a specific composition has been carried out. By doing this, wetting, softening,
The scale dissolves and powders the deposits that are difficult to remove in a short time, making the use of air hammers, chisels, etc. in Step W of the conventional method unnecessary, and reducing the amount of waste liquid generated. It was confirmed that the scales were reduced.
本発明は上記の知見に塞いて完成されたもので、ボィラ
・熱交換器等の伝熱面に対し、まず高圧水によるジェッ
ト洗浄を行なって煤状付着物や欧質付着物を除去し、つ
いで上記伝熱面に残存する付着物に対し、過酸化水素、
硝酸アンモニウムおよび塩化アンモニウムを含む洗浄液
をスプレーして付着物を溶解あるいは粉末、細片化させ
たのち、さらに高圧水によるジェット洗浄を行ない粉末
、細片化した残存付着物を除去することを特徴とするボ
ィラ・熱交換器等の付着物の除去方法を要旨とするもの
である。The present invention was completed based on the above knowledge, and the heat transfer surfaces of boilers, heat exchangers, etc. are first jet-cleaned using high-pressure water to remove soot-like deposits and foreign deposits. Next, the deposits remaining on the heat transfer surface are treated with hydrogen peroxide,
It is characterized by spraying a cleaning solution containing ammonium nitrate and ammonium chloride to dissolve the deposits or turning them into powder and pieces, and then jet washing with high-pressure water to remove the remaining deposits that have turned into powder and pieces. The gist of this article is a method for removing deposits from boilers, heat exchangers, etc.
本発明は火力プラントおよび化学プラント等のボィラ・
熱交換器等の付着物の洗浄法に適用しうる。The present invention is applicable to boilers such as thermal power plants and chemical plants.
It can be applied to a method for cleaning deposits on heat exchangers, etc.
以下、更に本発明の洗浄液の組成並にその洗浄液の使用
温度について詳述する。Hereinafter, the composition of the cleaning liquid of the present invention and the temperature at which the cleaning liquid is used will be further explained in detail.
‘1’洗浄液の配合と濃度範囲
付着物除去用化学洗浄液としては、過酸化水素、硝酸ア
ンモニウム、塩化アンモニウムの3種を併用できるよう
に調合する。'1' Combination and Concentration Range of Cleaning Solution As a chemical cleaning solution for removing deposits, hydrogen peroxide, ammonium nitrate, and ammonium chloride are mixed so that they can be used together.
また濃度は過酸化水素0.5〜10%、硝酸アンモニウ
ム1〜10%、塩化アンモニウム1〜10%を含むよう
にする。これ以下の濃度では洗浄に長時間を必要とし作
業面から実用的でない。一方、各々10%以上含有して
も付着物の溶解、粉末化に顕著な効果が得られないので
経済性から好ましくない。【2} 使用温度20〜4ぴ
0温度が高くなると付着物の溶解、粉末化の反応は遠く
なる反面、鉄鋼面の腐食が大きくなり、加温用の熱源を
必要とする上、発生蒸気により作業性が悪くなる等の問
題が生じるので、20℃以上〜4ぴ○以下が好ましい。The concentration is such that hydrogen peroxide is 0.5 to 10%, ammonium nitrate is 1 to 10%, and ammonium chloride is 1 to 10%. A concentration lower than this requires a long time for cleaning and is not practical from a work standpoint. On the other hand, even if each of them is contained in an amount of 10% or more, no significant effect on dissolving or pulverizing deposits can be obtained, which is not preferable from an economic point of view. [2] If the operating temperature is 20 to 40 mm, the melting of deposits and powdering reaction will be delayed, but on the other hand, the corrosion of the steel surface will increase, a heat source for heating will be required, and the generated steam will Since problems such as poor workability occur, the temperature is preferably 20°C or higher and 4 pi or lower.
次に、本発明において使用する洗浄液の作用について説
明する。Next, the action of the cleaning liquid used in the present invention will be explained.
付着物の成分はNa、S、V、Fe、Ni等でその化合
状態は水落性付着物ではその主成分がNa2S04、水
に溶け難い付着物では主成分が、Na,。The components of deposits are Na, S, V, Fe, Ni, etc., and their combination state is Na2S04 as the main component in water-repellent deposits, and Na as the main component in deposits that are difficult to dissolve in water.
V240敗、Nも○・V204・V205、Nも.鑓V
205・NaV60,5等のNa−V−○系化合物で、
Fe、Ni系化合物の割合も水溶性付着物の場合より多
い。本発明において用いる過酸化水素、硝酸アンモニウ
ム、塩化アンモニウムからなる洗浄液の上記付着物に対
する溶解および粉末化作用は次のように考えられる。過
酸化水素は付着物を最大の酸化状態まで強力に酸化する
一方、付着物の表面で酸素を盛んに発生しながら分解す
る。V240 lost, N also ○, V204, V205, N too. Sword V
Na-V-○ type compounds such as 205・NaV60,5,
The proportions of Fe and Ni-based compounds are also higher than in the case of water-soluble deposits. The dissolving and pulverizing effects of the cleaning liquid comprising hydrogen peroxide, ammonium nitrate, and ammonium chloride used in the present invention on the above-mentioned deposits can be considered as follows. Hydrogen peroxide strongly oxidizes deposits to the maximum oxidation state, while decomposing them while actively generating oxygen on the surface of the deposits.
この過程で付着物は酸化による体積変化と付着物表面で
発生する酸素ガス圧によって付着物が分解、粉末化し、
また殆んどの付着物は程度の差はあっても水溶性成分が
幾分かは含まれているので、これらの結果として液が逐
次浸透し、付着物は洗浄、除去されてゆく。また、硝酸
アンモニウム、塩化アンモニウムは酸性塩で水溶液をp
H4〜5の弱酸性にするが、これらの塩のみの水溶液で
は付着物に対する溶解作用は殆んどない。しかし、強い
酸化剤である過酸化水素の共存下では、これらの酸性塩
が対応する酸として、付着物中のNa−V−○系化合物
やFe、Ni等の酸化物に作用し、付着物の溶解が進む
と共に、前述の過酸化水素単独の付着物に対する分解、
粉末化作用とあいまつて付着物は溶解、粉末化し除去さ
れるものと考えられる。この結果、本発明によれば以下
のような効果を奏することができる。In this process, the deposits are decomposed and powdered due to the volume change due to oxidation and the oxygen gas pressure generated on the surface of the deposits.
Furthermore, since most of the deposits contain some water-soluble components, although the degree may vary, as a result of these, the liquid gradually penetrates and the deposits are washed and removed. In addition, ammonium nitrate and ammonium chloride can be used to purge aqueous solutions with acid salts.
Although it is made weakly acidic such as H4-5, an aqueous solution containing only these salts has almost no dissolving effect on deposits. However, in the coexistence of hydrogen peroxide, which is a strong oxidizing agent, these acid salts act as corresponding acids on Na-V-○ compounds and oxides such as Fe and Ni in the deposits, causing the deposits to deteriorate. As the dissolution of hydrogen peroxide progresses, the aforementioned hydrogen peroxide alone decomposes the deposits,
It is thought that together with the powdering action, the deposits are dissolved, powdered, and removed. As a result, according to the present invention, the following effects can be achieved.
‘1’過酸化水素、硝酸アンモニウム、塩化アンモニウ
ムを含む水溶液を用いて付着物を少ない液量で短時間に
溶解、粉末化させることが可能である。'1' Using an aqueous solution containing hydrogen peroxide, ammonium nitrate, and ammonium chloride, deposits can be dissolved and powdered in a small amount of liquid in a short time.
{21 従って、本発明の洗浄液で洗浄後の残存付着物
は粉末、細片化されているから、高圧水洗浄で容易に除
去可能であり、作業時間が大幅に短縮されると共に工数
も低減できる。{21 Therefore, since the remaining deposits after cleaning with the cleaning solution of the present invention are powdered and fragmented, they can be easily removed by high-pressure water cleaning, and the work time and man-hours can be reduced significantly. .
{3’洗浄廃液量が少ないので、中和、沈降、分離等の
廃液処理コストが安くてすむ。{3' Since the amount of washing waste liquid is small, the cost of waste liquid treatment such as neutralization, sedimentation, and separation is low.
■ 換気の悪い粉塵の発生する炉内で、ハンマー、たが
ね等による手工臭作業をしないで済むので、作業者の安
全衛生面から好ましく、また被洗浄面に錫も生じない。■ It is preferable from the safety and health standpoint of the workers because it is not necessary to carry out manual work using hammers, chisels, etc. in a dusty furnace with poor ventilation, and no tin is produced on the surfaces to be cleaned.
第2図に、本発明方法で使用する化学洗浄液を用いた化
学洗浄系統を示す。第2図において、1〜7はボィラ構
成機器を、8〜12は高圧水によるジェット洗浄系統を
、15〜16は洗浄廃液ラインを示しており、これら前
記した第1図の場合と同じであるが、第2図では従来法
の清水スプレー洗浄系統に代え、本発明の化学洗浄液ス
プレー洗浄系統が設置されている。FIG. 2 shows a chemical cleaning system using a chemical cleaning solution used in the method of the present invention. In Figure 2, 1 to 7 are boiler components, 8 to 12 are high-pressure water jet cleaning systems, and 15 to 16 are cleaning waste liquid lines, which are the same as in Figure 1 above. However, in FIG. 2, the chemical cleaning solution spray cleaning system of the present invention is installed in place of the conventional clean water spray cleaning system.
即ち、本発明の化学洗浄液はタンク17から弁18を経
て低圧ポンプ19からホース201こ送られ、過熱器3
のガス側と内側に導かれ、その上部のへツダ21に取付
けられたスプレーノズル22から過熱器3に噴霧され、
付着物を短時間に溶解、粉末、細片化する。また破線で
示した部分は本発明の化学洗浄液の有効利用を計るため
、該洗浄液を循環させる場合に使用するもので、23は
濃厚洗浄液の注入ライン、24は洗浄液の回収ラインで
ある。、次に、本発明の実験例および実施例をあげる。That is, the chemical cleaning solution of the present invention is sent from the tank 17 through the valve 18 to the low pressure pump 19 through the hose 201, and then to the superheater 3.
is guided to the gas side and inside of the superheater 3 from a spray nozzle 22 attached to the header 21 at the top thereof,
Dissolves deposits into powder and pieces in a short time. The parts indicated by broken lines are used to circulate the chemical cleaning solution of the present invention in order to make effective use of it, and 23 is the injection line for the concentrated cleaning solution, and 24 is the recovery line for the cleaning solution. Next, experimental examples and examples of the present invention will be given.
実験例 1第2表は本発明方法で使用する化学洗浄液の
熔解試験結果の例を水の溶解試験結果と併せて示したも
のである。Experimental Example 1 Table 2 shows examples of the results of the dissolution test of the chemical cleaning liquid used in the method of the present invention, together with the results of the dissolution test of water.
試験方法は舶用ボィラ過熱器管外面付着物の魂り2.0
〜2.2夕を糟秤して、12メッシュの網目を有するポ
リエチレンネットに入れ、液量100泌を入れたビーカ
ー中に浸済する。室温で5時間静直後、ポリエチレンネ
ットに残った付着物を110℃で乾燥させ、試験前後の
重量差から溶解量を求めた。第2表からわかる通り本発
明方法で使用する化学洗浄液で付着物A〜Cは90〜1
00%溶解された。The test method is to determine the amount of deposits on the outer surface of marine boiler superheater tubes 2.0
~2.2 Weigh out the solution, place it in a polyethylene net with a 12-mesh mesh, and immerse it in a beaker containing 100ml of liquid. Immediately after leaving it at room temperature for 5 hours, the deposits remaining on the polyethylene net were dried at 110°C, and the amount dissolved was determined from the difference in weight before and after the test. As can be seen from Table 2, the chemical cleaning solution used in the method of the present invention has deposits A to C of 90 to 1
00% dissolved.
また水での溶解量が10%以下の雛溶性付着物D、Eで
も50〜85%が溶解し、ポリエチレンネットに残った
付着物はかなりもろくなっているので、高圧水で洗浄す
れば容易に細片化、除去できる。第2表
注)付着物A−Eは20万トン級のタンカー5隻のボィ
ラ過熱器管外面から剥離したものである。In addition, 50 to 85% of the brood-soluble deposits D and E, which dissolve in water at a rate of 10% or less, are dissolved, and the deposits remaining on the polyethylene net are quite brittle, so they can be easily washed with high-pressure water. Can be fragmented and removed. Table 2 Note: Deposits A to E were separated from the outer surface of the boiler superheater tubes of five 200,000 ton class tankers.
実験例 2
第3表は本発明方法で使用する化学洗浄液の濃度を変え
て溶解率の変化を調べた実験例である。Experimental Example 2 Table 3 shows an experimental example in which changes in dissolution rate were investigated by varying the concentration of the chemical cleaning solution used in the method of the present invention.
過酸化水素0.5%、硝酸アンモニウム1%、塩化アン
モニウム1%の場合、溶解率は付着物Bで75%、付着
物Eで30%であるが、ポリエチレンネットに残った付
着物はいずれも酸化や割れでもろ・〈なっているから、
本発明方法の化学洗浄後に高圧水で洗浄すればほぼ除去
できる。しかし、これ以下の濃度では溶解率が悪く、化
学洗浄時間を長く必要とするので実用的でない。また過
酸化水素10%、硝酸アンモニウム10%、塩化アンモ
ニウム10%以上含有しても顕著な効果は認められない
から、これ以上の濃度は経済面から好ましくない。In the case of 0.5% hydrogen peroxide, 1% ammonium nitrate, and 1% ammonium chloride, the dissolution rate is 75% for deposit B and 30% for deposit E, but all deposits remaining on the polyethylene net are oxidized. Even if it cracks or cracks,
It can be almost removed by washing with high-pressure water after the chemical washing according to the method of the present invention. However, concentrations lower than this are not practical because the dissolution rate is poor and chemical cleaning requires a long time. Moreover, no significant effect is observed even if the content exceeds 10% hydrogen peroxide, 10% ammonium nitrate, and 10% ammonium chloride, so higher concentrations are not preferred from an economic standpoint.
第 3表 注)付着物B,Eは実験例1と同じものである。Table 3 Note) Deposits B and E are the same as in Experimental Example 1.
実施例第4表は従来法の清水スプレー洗浄に代え本発明
における化学洗浄液でスプレー洗浄した場合の付着物除
去工程を示している。第4表
注)本発明の方法によって20万トンクラスのタンカー
のボィラ過熱器管外面付着物を除去した場合で、表中の
数値は1缶分である。Table 4 of Examples shows the deposit removal process when spray cleaning was performed using a chemical cleaning solution according to the present invention instead of the conventional clear water spray cleaning. Table 4 Note) The values in the table are for the case where deposits on the outer surface of the boiler superheater tube of a 200,000 ton class tanker are removed by the method of the present invention, and the values in the table are for one can.
化学洗浄液の組成は、過酸化水素3%、硝酸アンモニウ
ム5%、塩化アンモニウム5%を含む常温の水溶液であ
る。第1表に示した従釆法では第D工程の清水スプレー
洗浄に10〜7頚時間を要し、廃液量は20〜200め
であったが、本発明方法の化学洗浄液でスプレー洗浄を
行なえば、洗浄時間は5時間、廃液量は1過式でも10
めで済み、循環式にすれば更に減少できる。The composition of the chemical cleaning solution is an aqueous solution at room temperature containing 3% hydrogen peroxide, 5% ammonium nitrate, and 5% ammonium chloride. In the conventional method shown in Table 1, it took 10 to 7 hours for clean water spray cleaning in step D, and the amount of waste liquid was 20 to 200 g. , the cleaning time is 5 hours, and the amount of waste liquid is 10 hours even with a 1-pass method.
This can be reduced further by using a circulating system.
また、本発明の化学洗浄液のスプレー洗浄で付着物は袷
んど溶解、粉末化されるので、従来法で行なっていた第
1表の第W工程の残存付着物除去作業は不q瓢こなった
。結局、本発明の洗浄方法によって、廃液量は従来法の
1′2〜1/40となり、所要日数は従来法の3〜7日
から1日に低減された。In addition, since the deposits are thoroughly dissolved and powdered by spray cleaning with the chemical cleaning solution of the present invention, the removal of remaining deposits in step W in Table 1, which was performed in the conventional method, is no longer necessary. Ta. In the end, with the cleaning method of the present invention, the amount of waste liquid was reduced to 1/40 of the conventional method, and the required number of days was reduced from 3 to 7 days of the conventional method to 1 day.
第1図は従来法による水洗系統をボィラの概要と共に示
した説明図、第2図は本発明による化学洗浄系統を同じ
くボィラの概要と共に示した説明図である。
第1図
オ2図FIG. 1 is an explanatory diagram showing a water washing system according to a conventional method together with an outline of a boiler, and FIG. 2 is an explanatory diagram showing a chemical cleaning system according to the present invention together with an outline of a boiler. Figure 1 Figure 2
Claims (1)
よるジエツト洗浄を行なつて煤状付着物や軟質付着物を
除去し、ついで上記伝熱面に残存する付着物に対し、過
酸化水素、硝酸アンモニウムおよび塩化アンモニウムを
含む洗浄液をスプレーして付着物を溶解あるいは粉末、
細片化さたのち、さらに高圧水によるジエツト洗浄を行
ない粉末、細片化した残存付着物を除去することを特徴
とするボイラ・熱交換器等の付着物の除去方法。1 Heat transfer surfaces of boilers, heat exchangers, etc. are first jet-cleaned with high-pressure water to remove soot-like deposits and soft deposits, and then any deposits remaining on the heat transfer surfaces are cleaned with excess water. Spray a cleaning solution containing hydrogen oxide, ammonium nitrate, and ammonium chloride to dissolve deposits or remove powder.
A method for removing deposits from boilers, heat exchangers, etc., characterized in that after fragmentation, jet cleaning is performed using high-pressure water to remove powder and fragmented residual deposits.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1002076A JPS6012559B2 (en) | 1976-02-03 | 1976-02-03 | How to remove deposits from boilers, heat exchangers, etc. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1002076A JPS6012559B2 (en) | 1976-02-03 | 1976-02-03 | How to remove deposits from boilers, heat exchangers, etc. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5293803A JPS5293803A (en) | 1977-08-06 |
| JPS6012559B2 true JPS6012559B2 (en) | 1985-04-02 |
Family
ID=11738706
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1002076A Expired JPS6012559B2 (en) | 1976-02-03 | 1976-02-03 | How to remove deposits from boilers, heat exchangers, etc. |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6012559B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008241078A (en) * | 2007-03-26 | 2008-10-09 | Kurita Water Ind Ltd | Clinker suppression method |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6361897A (en) * | 1986-09-01 | 1988-03-18 | Mitsubishi Heavy Ind Ltd | Cleaning method for exhaust gas economizer |
| CN105000613A (en) * | 2015-07-24 | 2015-10-28 | 中山沃尔威多水处理设备有限公司 | Billowing evaporation system and technology applied to high-salt and high-scale-rate waste water |
-
1976
- 1976-02-03 JP JP1002076A patent/JPS6012559B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008241078A (en) * | 2007-03-26 | 2008-10-09 | Kurita Water Ind Ltd | Clinker suppression method |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5293803A (en) | 1977-08-06 |
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