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JPH0519481B2 - - Google Patents
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JPH0519481B2 - - Google Patents

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Publication number
JPH0519481B2
JPH0519481B2 JP62278347A JP27834787A JPH0519481B2 JP H0519481 B2 JPH0519481 B2 JP H0519481B2 JP 62278347 A JP62278347 A JP 62278347A JP 27834787 A JP27834787 A JP 27834787A JP H0519481 B2 JPH0519481 B2 JP H0519481B2
Authority
JP
Japan
Prior art keywords
raw material
reaction tube
reaction zone
gas
reaction
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
Application number
JP62278347A
Other languages
Japanese (ja)
Other versions
JPH01122901A (en
Inventor
Yutaka Tsukuda
Masaya Hashimoto
Kazuhiro Ando
Mamoru Hotsukedo
Toshio Ito
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.)
Mitsui Zosen KK
Original Assignee
Mitsui Zosen KK
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 Mitsui Zosen KK filed Critical Mitsui Zosen KK
Priority to JP27834787A priority Critical patent/JPH01122901A/en
Publication of JPH01122901A publication Critical patent/JPH01122901A/en
Publication of JPH0519481B2 publication Critical patent/JPH0519481B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27BSAWS FOR WOOD OR SIMILAR MATERIAL; COMPONENTS OR ACCESSORIES THEREFOR
    • B27B17/00Chain saws; Equipment therefor
    • B27B17/12Lubricating devices specially designed for chain saws
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/06Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds in tube reactors; the solid particles being arranged in tubes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27BSAWS FOR WOOD OR SIMILAR MATERIAL; COMPONENTS OR ACCESSORIES THEREFOR
    • B27B17/00Chain saws; Equipment therefor
    • B27B17/02Chain saws equipped with guide bar
    • B27B17/025Composite guide bars, e.g. laminated, multisectioned; Guide bars of diverse material

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Forests & Forestry (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
  • Hydrogen, Water And Hydrids (AREA)

Description

【発明の詳細な説明】 〔発明の技術分野〕 本発明は炭化水素と水蒸気の混合物から触媒作
用により水素富化ガス(改質ガス)を製造する改
質管の反応管に関する。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to a reaction tube of a reforming tube for producing hydrogen-enriched gas (reformed gas) from a mixture of hydrocarbons and steam by catalytic action.

〔従来技術〕[Prior art]

改質器内に配置された、改質触媒が充填された
反応管内において、原料炭化水素と水蒸気の混合
物を加熱下に改質触媒と接触させる改質反応によ
つて水素富化ガスが製造される。
Hydrogen-enriched gas is produced through a reforming reaction in which a mixture of raw material hydrocarbons and steam is brought into contact with a reforming catalyst under heating in a reaction tube filled with a reforming catalyst placed in a reformer. Ru.

そして改質反応は強い吸熱反応であり、かつ改
質に必要な温度が700〜950℃と高温のために、バ
ーナでの燃焼で発生する高温燃焼ガスにより反応
管を加熱し、この管内を通る原料の改質反応に必
要な熱量が与えられる。
Since the reforming reaction is a strong endothermic reaction, and the temperature required for reforming is as high as 700 to 950°C, the reaction tube is heated by high-temperature combustion gas generated by combustion in a burner, and the gas passes through the tube. The amount of heat required for the reforming reaction of the raw material is provided.

第5図〜第8図に従来の水素富化ガス製造用改
質器の反応管を示す。
5 to 8 show reaction tubes of a conventional reformer for producing hydrogen-enriched gas.

第5図においては反応管1に改質触媒2が充填
されており、原料炭化水素と水蒸気との混合物が
矢印Aに沿つて供給され、矢印Bに沿つて反応管
1中を流れ、矢印Cに沿つて排出される。
In FIG. 5, a reaction tube 1 is filled with a reforming catalyst 2, and a mixture of raw material hydrocarbon and steam is supplied along arrow A, flows through the reaction tube 1 along arrow B, and flows through arrow C. is discharged along the

一方、高温燃焼ガスが矢印Dに沿つて供給さ
れ、原料混合物と向流熱交換される。
On the other hand, high-temperature combustion gas is supplied along arrow D and undergoes countercurrent heat exchange with the raw material mixture.

しかしながら、高温の改質ガスが流れる反応管
の出口部3が火炎に近い高温燃焼ガスから伝熱さ
れるので、特に出口部3近傍の反応管表面温度が
極めて高温となり、従つて反応管材料として非常
に高価な耐熱材料(高ニツケル鋼等)が必要とな
るので経済的でなく、また反応管表面温度が高い
ので反応管の寿命が短くなる欠点があつた。
However, since the exit section 3 of the reaction tube through which the high-temperature reformed gas flows, heat is transferred from the high-temperature combustion gas near the flame, so the surface temperature of the reaction tube, especially near the exit section 3, becomes extremely high. This method is not economical because it requires expensive heat-resistant materials (such as high-nickel steel), and it also has the disadvantage of shortening the life of the reaction tube because the surface temperature of the reaction tube is high.

第6図は、原料混合物の流れA,B,Cと燃焼
ガス流Dが並流の場合を示し、火炎に近い高温燃
焼ガスと接触する反応管入口部4における原料混
合物温度は400〜600℃と低く、反応管表面温度は
低くなる。
Fig. 6 shows a case where the raw material mixture flows A, B, and C and the combustion gas flow D flow in parallel, and the temperature of the raw material mixture at the reaction tube inlet 4 where it comes into contact with the high-temperature combustion gas near the flame is 400 to 600°C. and the surface temperature of the reaction tube becomes low.

しかし反応管出口部3では、高温の改質ガスに
熱を与えねばならないので、より高い燃焼ガス温
度が必要となり、このため燃焼により生じた熱を
有効に利用できず、熱効率が悪く、燃焼ガス形成
のために多量の燃料を必要とし、多くの運転経費
が必要となる。
However, at the reaction tube outlet 3, heat must be given to the high-temperature reformed gas, so a higher combustion gas temperature is required, and therefore the heat generated by combustion cannot be used effectively, resulting in poor thermal efficiency and It requires a large amount of fuel to form and has high operating costs.

第7図の反応管1は内部伝熱管5を有し、原料
混合物は矢印A,B,B′に沿つて反応管1中を
流れ、矢印Cに沿つて排出される。
The reaction tube 1 of FIG. 7 has an internal heat exchanger tube 5, and the raw material mixture flows through the reaction tube 1 along arrows A, B, B' and is discharged along arrow C.

そして、内部伝熱管5によつて改質ガスの有す
る熱量は、原料混合物と熱交換することによつて
回収される。
The heat of the reformed gas is recovered by the internal heat transfer tube 5 by exchanging heat with the raw material mixture.

しかしながら、第5図の場合と同様に原料混合
物の流れBと燃焼ガスの流れDは向流となり、反
応管表面温度が高くなる欠点がある。
However, as in the case of FIG. 5, the flow B of the raw material mixture and the flow D of the combustion gas flow countercurrently, which has the drawback of increasing the reaction tube surface temperature.

第8図は内部伝熱管5によつて原料混合物が予
熱される場合を示し、前記第6図のの場合と同様
に原料混合物と燃焼ガスは並流となり、熱効率が
悪い。
FIG. 8 shows a case where the raw material mixture is preheated by the internal heat transfer tube 5, and as in the case of FIG. 6, the raw material mixture and combustion gas flow in parallel, resulting in poor thermal efficiency.

〔発明の目的〕[Purpose of the invention]

本発明は上記従来の欠点を解消し、熱効率を高
め、燃料使用量を削減し、反応管表面温度の低い
水素富化ガス製造用改質器の反応管を提供するこ
とを目的とするものである。
The present invention aims to eliminate the above-mentioned conventional drawbacks, increase thermal efficiency, reduce fuel consumption, and provide a reaction tube for a hydrogen-enriched gas production reformer with a low reaction tube surface temperature. be.

〔発明の構成〕[Structure of the invention]

上記目的を達成する本発明は、水素富化ガス製
造用改質器の反応管において、該反応管を隔壁に
よつて上部反応帯と下部反応帯に区分し、前記隔
壁を貫通して該下部反応帯中を下方に延びる原料
ガス導管と、前記隔壁を貫通して該上部反応帯中
を上方に延びる改質ガス導管をそれぞれ設け、該
改質ガス導管を前記反応管外に導き、前記上部反
応帯に原料ガス供給管を設けると共に、前記上部
反応帯、下部反応帯および原料ガス導管に改質触
媒を充填したことを特徴とするものである。
To achieve the above object, the present invention provides a reaction tube for a reformer for producing hydrogen-enriched gas, in which the reaction tube is divided into an upper reaction zone and a lower reaction zone by a partition, and the A raw material gas conduit extending downward in the reaction zone and a reformed gas conduit penetrating the partition wall and extending upward in the upper reaction zone are provided, and the reformed gas conduit is guided outside the reaction tube and The present invention is characterized in that a raw material gas supply pipe is provided in the reaction zone, and a reforming catalyst is filled in the upper reaction zone, lower reaction zone, and raw material gas conduit.

第1図は本発明の反応管の第1実施例を示し、
反応管1は隔壁6によつて上部反応帯7と下部反
応帯8に区分されている。そして隔壁6を貫通し
て下部反応帯8中を下方に延びる原料ガス導管9
と、隔壁6を貫通して上部反応帯7中を上方に延
びる改質ガス導管10が設けられ、改質ガス導管
10は改質ガス排出管12を経て反応管1外に導
かれる。
FIG. 1 shows a first embodiment of the reaction tube of the present invention,
The reaction tube 1 is divided into an upper reaction zone 7 and a lower reaction zone 8 by a partition wall 6. A raw material gas conduit 9 passes through the partition wall 6 and extends downward in the lower reaction zone 8.
A reformed gas conduit 10 is provided that penetrates the partition wall 6 and extends upward in the upper reaction zone 7, and the reformed gas conduit 10 is led out of the reaction tube 1 via a reformed gas exhaust pipe 12.

更に、上部反応帯7、下部反応帯8および原料
ガス導管9には夫々、改質触媒が充填されてい
る。
Furthermore, the upper reaction zone 7, the lower reaction zone 8, and the raw material gas conduit 9 are each filled with a reforming catalyst.

かかる反応管1においては、原料炭化水素と水
蒸気との原料混合物が原料供給管11から矢印A
に沿つて供給され、上部反応帯7において改質触
媒と接触しながら矢印B,Bに沿つて流下し、改
質反応を開始する。
In this reaction tube 1, a raw material mixture of raw material hydrocarbon and steam is supplied from a raw material supply pipe 11 to an arrow A.
It flows down along the arrows B and B while contacting the reforming catalyst in the upper reaction zone 7, and starts the reforming reaction.

なお、本発明において使用される改質触媒は特
に限定されるものではなく、従来使用されている
水素製造用改質触媒が使用される。
Note that the reforming catalyst used in the present invention is not particularly limited, and conventionally used reforming catalysts for producing hydrogen can be used.

また原料炭化水素としても、従来用いられてい
る天然ガス、プロパン、ブタンおよびナフサなど
が用いられる。
Furthermore, conventionally used natural gas, propane, butane, naphtha, and the like are used as raw material hydrocarbons.

上部反応帯7における改質反応に必要な熱量
は、比較的低温な燃焼ガスの流れD1,D1と向流
熱交換することにより供給される。
The amount of heat required for the reforming reaction in the upper reaction zone 7 is supplied by countercurrent heat exchange with relatively low temperature combustion gas flows D 1 and D 1 .

上部反応帯7を流下した原料混合物は、隔壁6
によつて流下がさまたげられ、原料ガス導管9中
を矢印B1に沿つて流下し、反応管1の底部から
反転して反応管1の管壁側を矢印B2,B2に沿つ
て上昇する。
The raw material mixture flowing down the upper reaction zone 7 passes through the partition wall 6
The flow is blocked by the raw material gas conduit 9 and flows down along the arrow B 1 , reverses from the bottom of the reaction tube 1 and rises along the wall side of the reaction tube 1 along the arrows B 2 and B 2 do.

そして、原料ガス導管9中における改質反応に
必要な熱量は、高温の燃焼ガスの流れD2,D2
並流するB2,B2の流れと熱交換することにより
供給される。
The amount of heat required for the reforming reaction in the raw gas conduit 9 is supplied by heat exchange with the flows of B 2 and B 2 flowing in parallel with the flows of high-temperature combustion gases D 2 and D 2 .

改質反応は流れB2,B2の隔壁6近傍において
ほぼ終了し、この高温の改質ガスの流れB2,B2
は、隔壁6において集められ、改質ガス導管10
中を矢印B3に沿つて上昇する間に、原料混合物
の流れB,Bと熱交換により熱を与え、温度低下
しながら反応管外に排出される。
The reforming reaction is almost completed in the vicinity of the partition wall 6 of the streams B 2 , B 2 , and the high temperature reformed gas flows B 2 , B 2
is collected at the partition wall 6, and the reformed gas conduit 10
While rising along the arrow B3 inside, it exchanges heat with the raw material mixture flows B and B, giving it heat, and is discharged to the outside of the reaction tube while its temperature decreases.

なお、上部反応帯7における改質触媒層温度は
通常、400〜700℃、原料ガス導管9中における触
媒層温度は500〜800℃、原料ガス導管9をとり巻
く触媒層の温度は600〜950℃、である。
Note that the temperature of the reforming catalyst layer in the upper reaction zone 7 is usually 400 to 700°C, the temperature of the catalyst layer in the raw gas conduit 9 is 500 to 800°C, and the temperature of the catalyst layer surrounding the raw gas conduit 9 is 600 to 950°C. ℃, is.

第2図Aおよび第2図Bは本発明の第2実施例
を示し、改質ガス導管が101,102と2本設け
られている点のみが第1実施例と異なつている。
2A and 2B show a second embodiment of the present invention, which differs from the first embodiment only in that two reformed gas conduits 10 1 and 10 2 are provided.

第3図は本発明の第3実施例を示し、改質ガス
導管が101,102,103および104と四本設
けられている。
FIG. 3 shows a third embodiment of the present invention, in which four reformed gas conduits 10 1 , 10 2 , 10 3 and 10 4 are provided.

かかる本発明の反応管1は、第4図に示すよう
に、バーナ13を有する加熱炉14に設置されて
改質器15が構成される。
The reaction tube 1 of the present invention is installed in a heating furnace 14 having a burner 13 to constitute a reformer 15, as shown in FIG.

なお、燃焼ガスは燃焼ガス排出口16から排出
される。
Note that the combustion gas is discharged from the combustion gas outlet 16.

〔発明の効果〕〔Effect of the invention〕

以上述べたように本発明によれば、一本の反応
管内に向流と並流を合せ持つている。すなわち原
料ガスの流れBと向流する燃焼ガスの流れD1
およびB2と並流するD2である。
As described above, according to the present invention, a single reaction tube has both countercurrent and parallel current. That is, the combustion gas flow D 1 countercurrent to the raw material gas flow B,
and D 2 cocurrent with B 2 .

従つて、火炎に近い高温の燃焼ガスの流れD2
によつて伝熱される部分は、比較的低温の、すな
わち改質反応が終了する以前のガス流B2である
ため反応管表面温度を低くすることができ、従来
のように反応管材料に高価な耐熱材料を必要とす
ることがなくなる。
Therefore, the flow of hot combustion gases D 2 near the flame
Since the part where the heat is transferred is relatively low temperature gas flow B 2 before the reforming reaction is completed, the reaction tube surface temperature can be lowered, and the reaction tube material is expensive as in the past. This eliminates the need for heat-resistant materials.

低温の燃焼ガスD1は、低温の原料ガスBに伝
熱すれば良いので、熱を有効に利用することがで
き、高い熱効率を得ることができる。
Since the low-temperature combustion gas D 1 only needs to transfer heat to the low-temperature raw material gas B, heat can be used effectively and high thermal efficiency can be obtained.

更に、上部反応帯中に改質ガス導管を設けたの
で、改質反応を終えた改質ガスの持つ高い保有熱
量を原料ガスと熱交換することによつて原料ガス
へ与えることができるので、燃焼ガスから原料ガ
スに与える熱を少なくすることができ、従つて燃
焼ガス形成に要する燃料量を減少させることがで
きる。
Furthermore, since the reformed gas conduit is provided in the upper reaction zone, the high amount of heat held by the reformed gas after the reforming reaction can be given to the raw material gas by exchanging heat with the raw material gas. The heat imparted from the combustion gas to the raw material gas can be reduced, and therefore the amount of fuel required to form the combustion gas can be reduced.

また、反応管から排出される改質ガスの温度が
原料ガスとの熱交換によつて低下するので、改質
ガス排出管12から他の設備(図示せず)に至る
連絡管をあまり高価な耐熱材料を使わずにすみ経
済的である。
In addition, since the temperature of the reformed gas discharged from the reaction tube is lowered by heat exchange with the raw material gas, it is not necessary to connect the connecting pipe from the reformed gas discharge pipe 12 to other equipment (not shown) in an expensive manner. It is economical as it does not require the use of heat-resistant materials.

つまり本発明の反応管は、第5図に示した従来
の反応管が有する燃焼ガス温度の有効利用と、第
6図の反応管が有する反応管材料のグレード・ダ
ウンおよび第7図の反応管が持つ高い熱回収効率
という各々の特徴を兼えた反応管と云うことがで
きる。
In other words, the reaction tube of the present invention makes effective use of the combustion gas temperature of the conventional reaction tube shown in FIG. 5, downgrades the reaction tube material of the reaction tube shown in FIG. It can be said that the reaction tube combines the characteristics of each type, such as high heat recovery efficiency.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の反応管の第1実施例を示す縦
断面概要図、第2図Aは第2実施例を示す縦断面
概要図、第2図BはそのX−X矢印横断面概要
部、第3図は第3実施例を示す横断面概要図、第
4図は本発明の反応管を設けた改質器の縦断面概
要図、第5図、第6図、第7図および第8図は従
来の反応管の縦断面概要図である。 1…反応管、6…隔壁、7…上部反応帯、8…
下部反応帯、9…原料ガス導管、10…改質ガス
導管。
Fig. 1 is a longitudinal cross-sectional schematic diagram showing the first embodiment of the reaction tube of the present invention, Fig. 2 A is a longitudinal cross-sectional schematic diagram showing the second embodiment, and Fig. 2 B is a cross-sectional schematic diagram of the X-X arrow. Fig. 3 is a schematic cross-sectional view showing the third embodiment, Fig. 4 is a schematic vertical cross-sectional view of a reformer equipped with the reaction tube of the present invention, Fig. 5, Fig. 6, Fig. 7, and FIG. 8 is a schematic vertical cross-sectional view of a conventional reaction tube. DESCRIPTION OF SYMBOLS 1... Reaction tube, 6... Partition wall, 7... Upper reaction zone, 8...
Lower reaction zone, 9... raw material gas conduit, 10... reformed gas conduit.

Claims (1)

【特許請求の範囲】[Claims] 1 水素富化ガス製造用改質器の反応器におい
て、該反応管を隔壁によつて上部反応帯と下部反
応帯に区分し、前記隔壁を貫通して該下部反応帯
中を下方に延びる原料ガス導管と、前記隔壁を貫
通して該上部反応帯中を上方に延びる改質ガス導
管をそれぞれ設け、該改質ガス導管を前記反応管
外に導き、前記上部反応帯に原料ガス供給管を設
けると共に、前記上部反応帯、下部反応帯および
原料ガス導管に改質触媒を充填したことを特徴と
する水素富化ガス製造用改質器の反応管。
1. In a reactor of a reformer for producing hydrogen-enriched gas, the reaction tube is divided into an upper reaction zone and a lower reaction zone by a partition wall, and a raw material that penetrates the partition wall and extends downward into the lower reaction zone. A gas conduit and a reformed gas conduit penetrating the partition wall and extending upward in the upper reaction zone are provided, the reformed gas conduit is guided outside the reaction tube, and a raw material gas supply pipe is connected to the upper reaction zone. A reaction tube for a reformer for producing hydrogen-enriched gas, characterized in that the upper reaction zone, the lower reaction zone, and the raw material gas conduit are filled with a reforming catalyst.
JP27834787A 1987-11-05 1987-11-05 Reaction tube of reformer for producing hydrogen-enriched gas Granted JPH01122901A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27834787A JPH01122901A (en) 1987-11-05 1987-11-05 Reaction tube of reformer for producing hydrogen-enriched gas

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27834787A JPH01122901A (en) 1987-11-05 1987-11-05 Reaction tube of reformer for producing hydrogen-enriched gas

Publications (2)

Publication Number Publication Date
JPH01122901A JPH01122901A (en) 1989-05-16
JPH0519481B2 true JPH0519481B2 (en) 1993-03-16

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP27834787A Granted JPH01122901A (en) 1987-11-05 1987-11-05 Reaction tube of reformer for producing hydrogen-enriched gas

Country Status (1)

Country Link
JP (1) JPH01122901A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5025561A (en) * 1989-05-08 1991-06-25 Sugihara Trading Co., Ltd. Guide bar for a chain saw
WO2006006479A1 (en) * 2004-07-12 2006-01-19 Sumitomo Seika Chemicals Co., Ltd. Hydrogen production system and reforming apparatus

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK165946C (en) * 1985-03-21 1993-07-05 Haldor Topsoe As REFORMING PROCESS DURING HEAT EXCHANGE AND REACTOR THEREOF
JPS625091A (en) * 1985-06-28 1987-01-12 Jgc Corp Double tube type heat transfer tube

Also Published As

Publication number Publication date
JPH01122901A (en) 1989-05-16

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