JPS6247472B2 - - Google Patents

Info

Publication number
JPS6247472B2
JPS6247472B2 JP805081A JP805081A JPS6247472B2 JP S6247472 B2 JPS6247472 B2 JP S6247472B2 JP 805081 A JP805081 A JP 805081A JP 805081 A JP805081 A JP 805081A JP S6247472 B2 JPS6247472 B2 JP S6247472B2
Authority
JP
Japan
Prior art keywords
ash
temperature
grain structure
gasification
reaction temperature
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
Application number
JP805081A
Other languages
Japanese (ja)
Other versions
JPS5712094A (en
Inventor
Shorutsu Gyuntaa
Deyururitsuhi Manfuriito
Sopuka Kaaru
Hofuman Berunaa
Rihitaa Geruharuto
Endaa Haintsu
Biinhoruto Deiitoritsuhi
Gurafu Heruman
Kunauto Berutoruto
Domen Furanku
Menaruto K Eeberuharuto
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Gaskombinat Schwarze Pumpe VEB
Original Assignee
Gaskombinat Schwarze Pumpe VEB
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Gaskombinat Schwarze Pumpe VEB filed Critical Gaskombinat Schwarze Pumpe VEB
Publication of JPS5712094A publication Critical patent/JPS5712094A/en
Publication of JPS6247472B2 publication Critical patent/JPS6247472B2/ja
Granted legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/02—Fixed-bed gasification of lump fuel
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/02—Fixed-bed gasification of lump fuel
    • C10J3/20—Apparatus; Plants
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/02—Fixed-bed gasification of lump fuel
    • C10J3/20—Apparatus; Plants
    • C10J3/34—Grates; Mechanical ash-removing devices
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/02—Fixed-bed gasification of lump fuel
    • C10J3/20—Apparatus; Plants
    • C10J3/34—Grates; Mechanical ash-removing devices
    • C10J3/40—Movable grates
    • C10J3/42—Rotary grates
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/72—Other features
    • C10J3/74—Construction of shells or jackets
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00—Details of gasification processes
    • C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0913—Carbonaceous raw material
    • C10J2300/093—Coal
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00—Details of gasification processes
    • C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0913—Carbonaceous raw material
    • C10J2300/0943—Coke
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00—Details of gasification processes
    • C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0953—Gasifying agents
    • C10J2300/0956—Air or oxygen enriched air
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00—Details of gasification processes
    • C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0953—Gasifying agents
    • C10J2300/0959—Oxygen
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00—Details of gasification processes
    • C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0953—Gasifying agents
    • C10J2300/0973—Water
    • C10J2300/0976—Water as steam
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00—Details of gasification processes
    • C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0983—Additives
    • C10J2300/0996—Calcium-containing inorganic materials, e.g. lime

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Solid-Fuel Combustion (AREA)
  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)

Description

【発明の詳細な説明】 本発明は、各種炭化度を有する褐炭または石炭
ガス化用固定層圧力ガス発生炉の単位堅炉荷重を
高めプロセス遂行を最適化する方法に関する。そ
のさい、通常の単位堅炉荷重は越えられる。ガス
化剤大抵、酸素・蒸気混合物または空気・蒸気混
合物内で非酸化分は最少にされる。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for increasing the unit hard furnace load and optimizing the process performance of a fixed bed pressure gas generator for lignite or coal gasification with various degrees of carbonization. In that case, the normal unit hard-hearth load is exceeded. The non-oxidizing content of the gasifying agent is usually minimized in the oxygen/steam mixture or the air/steam mixture.

本方法は、好ましくは、石炭に含まれた鉱物質
が灰融点以下でのガス化にさいして石炭に天然に
与えられた性質によつて微粒・粉末構造を獲得
し、プロセス中ガス化材の崩壊傾向および微粒生
成傾向が強い所で使用される。
Preferably, in this method, the mineral substances contained in the coal acquire a fine grain/powder structure due to the naturally endowed properties of the coal during gasification below the ash melting point, and the gasification material is Used where there is a strong tendency to disintegrate and form fine particles.

固定層ガス化において能力限界を決定する要因
が主としてダスト排出量であることは一般に知ら
れている。燃料の特有性に応じてさまざまな能力
限界においても発生しプロセスを妨げるこの現象
を最少にするため、すでにさまざまな設計上およ
び方法技術上の提案がなされている。これらの提
案は幾つかのグループに分けることができる。例
えば、熱的過程および化学過程を通じて生じる煙
道ダストが可能な限り少なくなるよう燃料をプロ
セス開始前および遂行中に処理することが目的と
して追求される。この解決法は例えば東ドイツ特
許明細書第26392号、第38791号、第119814号およ
び東ドイツ特許明細書CIOJ/205413に見られ
る。
It is generally known that the factor that determines the capacity limit in fixed bed gasification is primarily the amount of dust discharged. Various design and process proposals have already been made in order to minimize this process-interfering phenomenon, which occurs even at various capacity limits depending on the specificity of the fuel. These proposals can be divided into several groups. For example, the aim is to treat the fuel before and during the process so that it generates as little flue dust as possible through thermal and chemical processes. This solution can be found, for example, in East German Patent Specifications No. 26392, No. 38791, No. 119814 and East German Patent Specification CIOJ/205413.

反応器上部、例えばガス出口近くで最適な流れ
分布を惹き起こそうとの設計上の解決法は例えば
東ドイツ特許明細書第132980号、第110297号、第
133817号および第133819号で提案されている。過
去においては固定層圧力ガス化の最適化にあたつ
てガス化剤の供給と合わせ回転火格子の設計構造
およびその運転法にやはり大きな注意が向けられ
た。この種の提案は例えば東ドイツ特許明細書第
133571号、第134243号および東ドイツ特許明細書
C10J/209772でなされている。
Design solutions aimed at inducing an optimal flow distribution in the upper part of the reactor, e.g. near the gas outlet, are described, for example, in East German Patent Specifications No. 132980, No. 110297,
Proposed in Nos. 133817 and 133819. In the past, when optimizing fixed bed pressure gasification, great attention was also given to the design and operation of the rotating grate, as well as the supply of gasifying agent. Proposals of this kind can be found, for example, in the East German Patent Specification No.
No. 133571, No. 134243 and East German patent specification
It was made in C10J/209772.

上記両グループの解決法提案の根底には、充填
進入前および進出後流れを制御してできるだけ均
一な分布、したがつてプロセス案内の最適化を達
成するという共通の関心がある。
Underlying the solution proposals of both groups is a common interest in controlling the pre-filling and post-filling flow to achieve as uniform a distribution as possible and thus an optimization of the process guidance.

これらの提案の欠点は、固定層の性能の決定的
プロセス量としての流れ分布が例えば石炭分配
器、ガス溜めまたは火格子等の前置および後置さ
れた諸機構によつて影響をうけるという間違つた
理論命題と結びついている。この命題は正しくな
い。流れ分布はむしろ、特に、プロセス中に生じ
る粒構造の影響をうける。
A disadvantage of these proposals is that the flow distribution, as a critical process variable for fixed bed performance, is influenced by upstream and downstream mechanisms, such as coal distributors, gas reservoirs or grate. It is connected to different theoretical propositions. This proposition is incorrect. Rather, the flow distribution is influenced inter alia by the grain structure produced during the process.

反応器内の微粒子ばら材層は、例えば、ガス溜
めの内部構造の抵抗または回転火格子の抵抗より
数十乗高い流れ抵抗を有しうる。更に微粒子は、
充填部内で流体によつて動かされ反応器の任意の
個所に沈積しばら材構造の不均一性を増大すると
いう不利な特性を有する。それによつて反応器の
特定範囲が完全に詰まり、反応器の貫通が通路の
形で行われるにすぎなくなり、事実上向流式反応
器の原理および諸利点が相殺されることさえあ
る。
The particulate bulk material layer in the reactor can have a flow resistance that is, for example, several orders of magnitude higher than the resistance of the internal structure of the gas reservoir or the resistance of the rotating grate. Furthermore, fine particles are
It has the disadvantageous property of being moved by the fluid within the packing and deposited anywhere in the reactor, increasing the non-uniformity of the bulk structure. As a result, certain areas of the reactor are completely clogged, and the passage through the reactor only takes place in the form of passages, which in effect even cancels out the principle and advantages of a countercurrent reactor.

それゆえ、過去において行われた上述の処置は
すべて、その効果が充填開始時および終了時の意
味のない範囲に限られていたのであるから、部分
的成果をおさめたにすぎない。
Therefore, all the above-mentioned measures carried out in the past were only partially successful, since their effectiveness was limited to a meaningless area at the beginning and end of filling.

石炭の圧力ガス化にあたつてのプロセス改善に
係る別グループの提案は灰排出量の制御を扱つて
いる。そのさい特に流れの均一性および通路形成
の回避が目ざされる。例えば東ドイツ特許明細書
第133247号の目的もこの点にある。
Another group's proposals for process improvements in the pressure gasification of coal address the control of ash emissions. In particular, uniformity of the flow and the avoidance of channel formations are aimed at. This is also the purpose of East German patent specification no. 133247, for example.

類似の目的を有する別の提案は反応器での灰収
支に基づく灰排出量の制御を予定している。
Another proposal with a similar objective envisages controlling ash emissions based on ash balance in the reactor.

これらの解決法提案でも、固定層の均一な貫流
にとつて固定層内の粒構造が灰排出量制御の決定
的判定基準である点が見失われる。
These proposed solutions also miss the point that for uniform flow through the fixed bed, the grain structure within the fixed bed is a decisive criterion for controlling the ash output.

灰排出量の制御はやはり燃焼帯を一定に保つこ
とができない。なぜなら固定層の粒構造に注意が
向けられないなら燃焼帯は偏平な面を現示しない
からである。それに反し燃焼帯は顕著な通路その
中をかなりの量の固体流が流体の流れ方向に移動
しうる形で固定層のかなりの縦範囲にわたつて延
びている。
Control of ash emissions still cannot keep the combustion zone constant. This is because if attention is not paid to the grain structure of the fixed bed, the combustion zone will not exhibit a flat surface. The combustion zone, on the other hand, extends over a considerable longitudinal extent of the fixed bed in such a way that a considerable amount of solids flow can be moved in the direction of the flow of the fluid through the pronounced channels.

灰排出量の制御に灰収支を関連づけても所期の
改善は得られない。なぜなら粗ガス流による固体
排出量が多いと偏平な灰床層および火床層は成立
せず、その他流体によつて併出される固体流の定
性的および定量的検出に関し実用可能な測定法は
知られていないからである。
Even if ash balance is linked to the control of ash emissions, the desired improvement will not be achieved. This is because flat ash and fire beds do not form when the amount of solids discharged by the crude gas flow is high, and there are no practical measurement methods known for the qualitative and quantitative detection of the solids flow co-expelled by other fluids. This is because it has not been done.

本発明の目的は各種炭化度を有する褐炭または
石炭ガス化用固定層圧力ガス発生炉の単位堅炉荷
重を高めその経済性を向上させる方法であり、該
方法によつて粒構造を改質する好適な方法を手段
にして、プロセスを最適に案内し経済性を向上さ
せるにあたつて充填物の負荷容量を高め単位性能
を高める決定的前提条件として最適な流れ事情を
生じる諸条件がつくり出され、そのことによつて
灰排出量と合わせてプロセスの自動化が可能とな
る。
The object of the present invention is to provide a method for increasing the unit hard-furnace load of a fixed-bed pressure gas generating furnace for gasifying lignite or coal having various degrees of carbonization and improving its economic efficiency, by which the grain structure is modified. By means of suitable methods, the conditions leading to optimal flow conditions are created as a decisive prerequisite for increasing the loading capacity of the packing and increasing the unit performance in order to optimally guide the process and improve its economic efficiency. This allows automation of the process along with ash emissions.

本発明の課題は、石炭分配器、ガス溜め、火格
子等の発生炉内部構造が流れ分布およびそれと結
びついた停滞に及ぼす影響に関してこれまで主張
されてきた見解をプロセス案内が一段と向上され
る形で克服することである。
The object of the present invention is to improve the process guidance by further improving the previously held views regarding the influence of the internal structure of the generator, such as the coal distributor, gas reservoir, and grate, on the flow distribution and associated stagnation. It is about overcoming.

この課題は本発明により、固定層内での粒構造
の形成がプロセスの決定的案内量としてそれぞれ
の方法諸条件に依存して安定固定層および充填物
均一貫流を実現するよう制御されることによつ
て、解決される。
This problem is solved according to the invention by the fact that the formation of the grain structure in the fixed bed is controlled as a decisive guiding variable of the process, depending on the respective process conditions, in order to achieve a stable fixed bed and a uniform flow of the packing. Therefore, it is resolved.

粒構造の流れ工学的品質は一般に平均粒径の計
量値dsmといわゆる間隙容量とによつて定義さ
れ、ここで必要となるその粒構造の判定は本発明
により反応器充填物の各高さ要素の渦点速度とい
う判定基準に基づいて行われる。
The flow engineering quality of the grain structure is generally defined by the measured value dsm of the average grain size and the so-called void volume, the determination of which is required here according to the invention for each height element of the reactor packing. This is done based on the criterion of vortex point velocity.

反応器固定層内の粒構造への影響はさまざまな
方法で行いうる。
Influencing the grain structure within the reactor fixed bed can be done in various ways.

まず第1に、ガス化にさいして発生する灰の粒
構造および圧力気化器中央に存在する灰・コーク
ス灰・石炭混合物の粒構造を酸化帯内の反応温度
変化によつて制御するよう提案される。例えば酸
化帯内の反応温度変化によつて灰、特にその微粒
子分の粒構造だけでなく還元帯、すなわち半ガス
化コークスの範囲の微粒子分も変化しうること
が、大規模に操業している圧力気化器で突き止め
られた。
First, it was proposed to control the grain structure of the ash generated during gasification and the grain structure of the ash/coke ash/coal mixture present in the center of the pressure vaporizer by changing the reaction temperature in the oxidation zone. Ru. For example, in large-scale operations, it is possible to change not only the grain structure of the ash, especially its particulate content, but also the particulate content in the reduction zone, i.e. in the range of semi-gasified coke, by changing the reaction temperature in the oxidation zone. It was tracked down with a pressure vaporizer.

石炭の鉱物質の少なくとも重量部30%が焼結点
または融点を上まわるほどに酸化還元帯の反応温
度が高められることは有利である。それによつて
達成可能な均一に貫流される固定層によつて大型
スラグ凝集が生成する危険は少なくなる。なぜな
ら、灰およびコークス・灰粒子から成る微粒分は
渦点速度を越えることがないのでより広い範囲で
流体によつてより高い層に転送され、したがつて
選別過程によつて容易に融解する共融混合物を形
成するからである。更に、隣接領域への微粒子の
運搬が防がれることによつて化学・物理的プロセ
ス条件は常に保障され、ガス化剤の性質が同じで
あるなら反応温度の違いは生じえない。これによ
つてスラグ発生の危険は最小限におさえられる。
固定層での渦点速度が特に酸化還元帯のどの個所
でも越えられることがないなら、反応最終温度は
鉱物質の大部分を貫流可能な粗粒子ばら材の形に
移行させるほどに高められうる。更に、還元帯内
の反応温度が十分高い場合半ガス化コークス内で
始まつた焼結過程によつて粒子崩壊およびダスト
生成はすでに著しく制限される。
Advantageously, the reaction temperature in the redox zone is increased to such an extent that at least 30% by weight of the mineral matter of the coal is above the sintering or melting point. Owing to the uniformly flowing fixed bed that can thereby be achieved, the risk of large slag agglomerates forming is reduced. This is because the fine fraction, consisting of ash and coke/ash particles, does not exceed the vortex velocity and is thus transferred to higher layers by the fluid over a wider area and is therefore more easily melted by the sorting process. This is because a molten mixture is formed. Furthermore, the chemical and physical process conditions are always ensured by preventing the transport of fine particles to adjacent areas, and no difference in reaction temperature can occur if the nature of the gasifying agent is the same. This minimizes the risk of slag formation.
If the vortex velocity in the fixed bed is not exceeded at any point in the redox zone, the final reaction temperature can be increased enough to transfer most of the mineral material into the form of coarse-grained bulk material that can be flowed through. . Moreover, if the reaction temperature in the reduction zone is high enough, the particle breakdown and dust formation are already significantly limited by the sintering process initiated in the semi-gasified coke.

酸化還元帯の反応温度および粒構造の変化を実
際に可能とするのはガス化剤内の酸素分の変化ま
たはその組成およびガス化剤の温度の選択であ
る。
It is the change in the oxygen content in the gasifying agent or the selection of its composition and the temperature of the gasifying agent that actually allows a change in the reaction temperature and grain structure of the redox zone.

酸化帯での、さまざまな要因に依存した特定最
大温度の正確な維持は、プロセス制御コンピユー
タによつて絶えず監視制御して行われる。この維
持は、1方で高い反応温度の諸利点を完全に利用
しまた他方でスラグ発生または大型スラグ片の発
生を防ぐためにも必要である。
The precise maintenance of a specified maximum temperature in the oxidation zone, which depends on various factors, is constantly monitored and controlled by a process control computer. This maintenance is necessary, on the one hand, to fully utilize the advantages of high reaction temperatures and, on the other hand, to prevent slag formation or the formation of large slag pieces.

最適な反応温度調整のため補助量として本発明
により1方で好ましくは灰帯の高さの発生炉内ジ
ヤケツトで測定した温度値が利用され、該温度値
は不安定な時間的推移および急激な変化によつて
充填物内で渦状態が達成されたことを示す。この
ことから粒構造の貫流性が悪いこと、すなわち反
応温度が低すぎることを知りうる。他方、最適な
反応温度を調整するための補助量として発生炉か
ら排出されるべき灰量の目標値が利用され、この
目標値は反応器内で時間単位当りにガス化された
石炭量から生じる。この目標値を越えた場合発生
炉本体内の粒構造は微粒すぎ、灰粒子またはコー
クス・灰粒子のかなりの量は火格子でなく粗ガス
出口を介して排出される。更に本発明の提案によ
り、灰または固体排出量を基準に酸化帯の反応温
度を最適化することと合わせてプロセスは回転火
格子の操作を介して制御され、酸化帯から生じた
灰の温度と逆流ガス化剤とから生じる特定の平衡
温度が常に維持される。
For optimal reaction temperature adjustment, according to the invention, on the one hand, a temperature value is used which is preferably measured in the jacket of the generator at the height of the ash zone, which temperature value is subject to unstable temporal changes and abrupt changes. The change indicates that a vortex state has been achieved within the filling. This indicates that the flowability of the grain structure is poor, that is, the reaction temperature is too low. On the other hand, the target value for the amount of ash to be discharged from the generator is used as an auxiliary variable for adjusting the optimum reaction temperature, which target value results from the amount of coal gasified per time unit in the reactor. . If this target value is exceeded, the grain structure in the generator body is too fine and a significant amount of ash particles or coke-ash particles are discharged through the coarse gas outlet rather than through the grate. Furthermore, according to the present invention, the process is controlled through the operation of a rotating grate in conjunction with optimizing the reaction temperature of the oxidation zone on the basis of the ash or solids emissions, and the temperature of the ash produced from the oxidation zone and the A certain equilibrium temperature resulting from the backflow gasifying agent is always maintained.

好ましくはこの温度の検出は直接反応器内で、
および酸化帯のすぐ下の反応器外周面の複数個所
で行われる。灰または固体排出量の案内量とし
て、好ましくは、少なくとも2個所、好ましくは
4〜6の測定個所の平均値から算出した平均温度
が利用される。
Preferably the detection of this temperature is carried out directly within the reactor,
and at multiple locations on the outer circumferential surface of the reactor immediately below the oxidation zone. The average temperature calculated from the average value of at least two, preferably 4 to 6, measuring points is preferably used as a guideline for the amount of ash or solids discharged.

固体または灰排出機構の制御は本発明では温度
測定値、全系の時間特性および平衡温度制限値を
考慮したアルゴリズムに従つて行われる。更に酸
化帯反応温度および時間単位当たりに反応器から
排出される灰量が前記補助量と合わせてこのアル
ゴリズムに含まれ、安定した火床および反応器か
ら排出すべき固体量の最適な最終温度が保障され
る。反応器から排出すべき灰の温度と灰床を貫流
するガス化剤の入口温度との温度差の目標値とし
て好ましくは最大50Kの値が確定される。これに
よつて最適かつ効果的なプロセス案内が達成され
るとともに、大抵耐熱損傷性が不十分である固体
排出部材の構造部品が保護される。
The control of the solids or ash evacuation mechanism is carried out according to the invention according to an algorithm that takes into account the temperature measurements, the time characteristics of the entire system and the equilibrium temperature limit. Furthermore, the oxidation zone reaction temperature and the amount of ash to be discharged from the reactor per unit of time are included in this algorithm together with the said auxiliary amounts to determine the stable firebed and the optimal final temperature of the amount of solids to be discharged from the reactor. Guaranteed. A value of at most 50 K is preferably determined as the target value for the temperature difference between the temperature of the ash to be discharged from the reactor and the inlet temperature of the gasifying agent flowing through the ash bed. This achieves optimal and effective process guidance and protects the structural parts of the solids discharge element, which usually have insufficient resistance to heat damage.

更に本発明の提案により、ガス化材のブリケツ
テイングの場合該ガス化材に好適な鉱物質が混和
され、そのことによつて粒構造およびプロセスを
損う微粒子分は反応器酸化帯より上の範囲でも微
粒子生成による粒子崩壊に対抗するように影響を
うける。この種の混和物として最適なのは、熱荷
重をうけると石炭質の粒状組織を固化する鉱物成
分またはガス化過程の結果としてそれ自身が強固
でコンパクトな組織を形成する鉱物成分である。
このような性質は例えば粘土鉱物が有しており、
CaOの形で石炭に含まれた石灰も加熱されるとカ
ーボネート(CaCO3)を生成する。これも特定の
温度水準に至るまでは組織固化を惹き起こし、し
たがつて微粒子生成に対抗する。
Furthermore, according to the present invention, in the case of briquetting the gasification material, suitable mineral substances are incorporated into the gasification material, so that the grain structure and the particulate content which impairs the process are eliminated above the reactor oxidation zone. The range is also affected to counteract particle disintegration due to particulate generation. The most suitable admixtures of this type are mineral components that solidify a coaly grain structure when subjected to thermal loading, or that form themselves a strong, compact structure as a result of the gasification process.
For example, clay minerals have such properties,
Lime contained in coal in the form of CaO also produces carbonate (CaCO 3 ) when heated. This also causes tissue solidification up to a certain temperature level, thus counteracting particulate formation.

他の鉱物諸成分またはその組合わせ成分も混和
物の形で、または特定の石炭選択または石炭混合
によつて自ら上記のプロセス安定化効果を惹き起
こす。
Other mineral components or combinations thereof can also bring about the process stabilizing effects mentioned above, either in the form of admixtures or by themselves through specific coal selection or coal blends.

高い反応温度の調整およびブリケツテイング材
への鉱物質の混和は発生炉堅炉内での顕著な固化
という形の後続現象と結びついている。軟化鉱物
質は場合によつては、堅炉壁が普通の耐火物、例
えばシヤモツトれんがで保護してあるならこの壁
と結合する。本発明の提案により、酸化帯内の高
い反応温度の達成は好ましくは高い熱伝導率を有
するセラミツク材料から成るまたは金属をベース
にした耐スラグ性内張りと合わせて実現される。
The setting of high reaction temperatures and the incorporation of mineral substances into the briquetting material are associated with subsequent phenomena in the form of significant solidification in the production furnace. The softened mineral material may optionally be bonded to the hardness wall if it is protected by a conventional refractory material, for example a brick. According to the proposal of the invention, the achievement of high reaction temperatures in the oxidation zone is preferably achieved in conjunction with a slag-resistant lining made of ceramic material with high thermal conductivity or based on metal.

本発明を以下1実施例に基づいて詳述する。 The present invention will be described in detail below based on one embodiment.

発生炉からの灰排出は一般に回転火格子を介し
て行われ、いわゆる掃除器(Ra¨umer)が排出
部材として使用される。灰排出量は掃除器の断面
積、その後、移動速度および移動時間によつて算
出される。回転火格子の回転速度および運転時間
は実際上灰排出時間の目標量として使用される。
Ash removal from the generator is generally carried out via a rotating grate, so-called vacuum cleaners being used as removal elements. The amount of ash discharged is calculated by the cross-sectional area of the vacuum cleaner, then by the speed of movement and the time of movement. The rotational speed and operating time of the rotating grate are used in practice as target quantities for the ash evacuation time.

回転火格子の回転速度調整および運転時間確定
またはそれらの変化は、本発明により、灰帯温度
測定個所でガス化剤の温度と灰の温度との許容温
度差の表現としての許容温度、好ましくは最大
50K以下が達成されるまで灰排出が確定時間内で
段階的に高まるよう行われる。
According to the invention, the adjustment of the rotational speed of the rotary grate and the determination of the operating time or their variation are carried out in accordance with the invention at the permissible temperature, preferably as an expression of the permissible temperature difference between the temperature of the gasifying agent and the temperature of the ash, at the ash zone temperature measurement point. maximum
Ash discharge is increased step by step within a defined time period until below 50K is achieved.

この温度が灰帯内の複数の温度測定個所の平均
値の形で達成されたなら、灰排出の出発値は調整
され、これによつて、安定した発生炉運転におい
て発生炉内での灰床高さの2点制御が自動的に与
えられたことになる。この系の制御は、灰床高さ
の端位置が大きな時間間隔でのみ、好ましくは2
時間おきに達成されるよう行われる。この周期内
に灰帯において灰排出量に相当しない温度上昇が
生じるなら、これは固定層の渦状態達成を暗示す
るのであるから、酸化帯の反応温度は好ましくは
ガス化剤内の酸化成分の割合を増やすことによつ
て高めなければならない。同様に、灰帯内の温度
勾配の傾向に依存することなく時間単位当たり火
格子を介して反応器から排出される灰量が目標値
を下まわるなら、反応温度を高めねばならない。
これは周知の如く灰調整門内の相当する充填レベ
ル表示器を介してコントロールしうる。反応温度
の上昇はやはり石炭種に適合された歩調で行う。
灰排出の目標値または灰帯内で安定した温度勾配
が達成されたなら昇温は終えられる。
If this temperature has been achieved in the form of an average value of several temperature measurement points in the ash zone, the starting value for the ash discharge can be adjusted, so that the ash bed in the generator can be adjusted in stable generator operation. This means that two-point height control is automatically provided. The control of this system is such that the end position of the ash bed height is controlled only at large time intervals, preferably two
It is done in such a way that it is achieved every hour. If a temperature rise not corresponding to the ash discharge occurs in the ash zone within this period, this implies the attainment of a vortex state in the fixed bed, so the reaction temperature in the oxidation zone is preferably adjusted to It must be increased by increasing the proportion. Similarly, if the amount of ash discharged from the reactor via the grate per time unit, independent of the trend of the temperature gradient in the ash zone, falls below the target value, the reaction temperature must be increased.
This can be controlled in a known manner via a corresponding fill level indicator in the ash control gate. The reaction temperature is again increased at a rate adapted to the type of coal.
The heating is terminated when the target value of ash discharge or a stable temperature gradient within the ash zone is achieved.

高い反応温度の調整およびブリケツテイング材
への鉱物質混和によつて発生炉の堅炉が損傷しう
るが、しかしこれは本発明により好ましくはセラ
ミツク材料から成るまたは金属をベースにした耐
スラグ性内張りによつて防ぐことができる。
Due to the setting of high reaction temperatures and the incorporation of mineral substances into the briquetting material, the hard furnace of the generator furnace can be damaged, but this is preferably avoided by the invention with a slag-resistant lining made of ceramic material or based on metal. This can be prevented by

Claims (1)

【特許請求の範囲】 1 プロセス制御用案内量として固定層内の粒構
造を利用し、また最適なプロセス案内の決定的前
提条件である固定層の安定性および貫流均一性の
判定基準として反応器の各高さ要素での渦点速度
を利用し、流体の許容流れ速度をつねに渦点速度
以下に調整することを特徴とする、各種炭化度を
有する褐炭または石炭ガス化用固定層圧力ガス発
生炉の単位堅炉荷重を高める方法。 2 平均粒径dsmと隙間率とによつて定義される
粒構造を変えるため酸化および還元帯において、
好ましくはガス化剤の酸化分またはその出発温度
が容易に融解する共融混合物選択によつて変えら
れ、発生炉の耐スラグ性セラミツクまたは金属内
張りを用いて石炭の鉱物諸成分の焼結点および融
点が超えられるような反応温度を酸化帯で使用す
ることを特徴とする特許請求の範囲第1項記載の
方法。 3 反応最終温度を介して酸化および還元帯の粒
構造を最適に制御するため補助量としてまず第1
に反応器周囲で測定した灰床温度そして次に灰門
を介して排出すべき鉱物質に関するプロセスの固
体収支から生じる目標値を、灰床温度が上昇する
なら火格子を介しての鉱物質排出速度が減速され
またその逆に灰床温度が高くて火格子によつて排
出される灰量が少なすぎるなら反応最終温度がガ
ス化混合物の変化を介して上昇されるよう、利用
することを特徴とする特許請求の範囲第1項記載
の方法。 4 プロセス制御はアルゴリズムに従いプロセス
制御コンピユーターを使つて行われ、少なくとも
2個所またはそれ以上の測定個所の平均値を灰床
温度用出発量として利用し、石灰調節門と灰調節
門との調節過程の比を排出すべき灰の目標値と見
做し、灰調節回数に対する石灰調節回数の比が前
記目標値を越えたなら反応温度を高めることを特
徴とする特許請求の範囲第1項若しくは第2項記
載の方法。 5 有効的かつ最適なプロセス案内のため灰床温
度の平均値を灰排出量の調節によつて、ガス化剤
の温度より上の50絶対温度の最大値に制限するこ
とを特徴とする特許請求の範囲第1項若しくは第
2項記載の方法。 6 フリケツテイングの場合ガス化剤の粒構造に
影響を与えるため好ましくは粘土、石灰等の鉱物
質が混和され、該鉱物質は反応器内でのガス化過
程の間大きな平均粒径を生成し、またはガス化用
石炭の選択によつてかかる成分の富化に影響を及
ぼすことを特徴とする特許請求の範囲第1、第
3、第4若しくは第5項記載の方法。
[Scope of Claims] 1. The use of the grain structure in the fixed bed as a guide variable for process control and as a criterion for the stability of the fixed bed and the uniformity of flow through, which are decisive prerequisites for optimal process guidance. Fixed bed pressure gas generation for lignite or coal gasification with various degrees of carbonization, characterized by adjusting the allowable flow velocity of the fluid to always be below the vortex velocity by using the vortex velocity at each height element of A method to increase the unit hardness load of a furnace. 2. In the oxidation and reduction zones, in order to change the grain structure defined by the average grain size dsm and the void ratio,
Preferably, the oxidation content of the gasifying agent or its starting temperature is varied by selecting an easily melting eutectic mixture, and the slag-resistant ceramic or metal lining of the generator is used to reduce the sintering point and the mineral content of the coal. 2. Process according to claim 1, characterized in that a reaction temperature is used in the oxidation zone such that the melting point is exceeded. 3. In order to optimally control the grain structure of the oxidation and reduction zones through the final reaction temperature, the first
the ash bed temperature measured around the reactor and then the target value resulting from the solids balance of the process with respect to the minerals to be discharged via the ash gate, and if the ash bed temperature increases, the mineral discharge via the grate. It is characterized in that the speed is reduced and, conversely, if the ash bed temperature is high and the amount of ash discharged by the grate is too small, the final reaction temperature is increased through a change in the gasification mixture. The method according to claim 1. 4 Process control is performed using a process control computer according to an algorithm, using the average value of at least two or more measurement points as the starting amount for the ash bed temperature, and controlling the adjustment process of the lime control gate and the ash control gate. The ratio is regarded as a target value of the ash to be discharged, and if the ratio of the number of times of lime adjustment to the number of times of ash adjustment exceeds the target value, the reaction temperature is increased. The method described in section. 5. A patent claim characterized in that the average value of the ash bed temperature is limited to a maximum value of 50 absolute temperatures above the temperature of the gasifying agent by adjusting the ash discharge rate for effective and optimal process guidance. The method according to item 1 or 2 of the scope. 6 In the case of friketing, mineral substances such as clay or lime are preferably mixed in to influence the grain structure of the gasifying agent, which minerals produce a large average particle size during the gasification process in the reactor. 6. A method according to claim 1, 3, 4 or 5, characterized in that the enrichment of such components is influenced by the selection of coal for gasification.
JP805081A 1980-06-03 1981-01-23 Enhancing of unit shaft furnace load of fixed layer pressure gas generating furnace Granted JPS5712094A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DD22153080A DD159010A3 (en) 1980-06-03 1980-06-03 METHOD FOR INCREASING THE SPECIFIC BAY LOADS OF FIXED BEDGED GAS GENERATORS

Publications (2)

Publication Number Publication Date
JPS5712094A JPS5712094A (en) 1982-01-21
JPS6247472B2 true JPS6247472B2 (en) 1987-10-08

Family

ID=5524484

Family Applications (1)

Application Number Title Priority Date Filing Date
JP805081A Granted JPS5712094A (en) 1980-06-03 1981-01-23 Enhancing of unit shaft furnace load of fixed layer pressure gas generating furnace

Country Status (5)

Country Link
JP (1) JPS5712094A (en)
CS (1) CS266781A1 (en)
DD (1) DD159010A3 (en)
DE (1) DE3046249A1 (en)
YU (1) YU58481A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4453949A (en) * 1983-03-08 1984-06-12 The United States Of America As Represented By The United States Department Of Energy Ash bed level control system for a fixed-bed coal gasifier
US4615713A (en) * 1983-05-10 1986-10-07 Sasol Operations (Proprietary) Limited Ash temperature measurement means for a fixed bed gasifier
JPS6078334A (en) * 1983-10-05 1985-05-04 Hitachi Ltd Fluorophotometer
JPH0519801Y2 (en) * 1986-11-07 1993-05-25

Also Published As

Publication number Publication date
DD159010A3 (en) 1983-02-16
JPS5712094A (en) 1982-01-21
DE3046249A1 (en) 1981-12-10
CS266781A1 (en) 1984-05-14
YU58481A (en) 1983-04-30

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