KR920016129A - A method for removing emissions in situ from a gaseous stream by injecting an emission absorbent downstream of the combustion zone. - Google Patents

A method for removing emissions in situ from a gaseous stream by injecting an emission absorbent downstream of the combustion zone. Download PDF

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Publication number
KR920016129A
KR920016129A KR1019910018647A KR910018647A KR920016129A KR 920016129 A KR920016129 A KR 920016129A KR 1019910018647 A KR1019910018647 A KR 1019910018647A KR 910018647 A KR910018647 A KR 910018647A KR 920016129 A KR920016129 A KR 920016129A
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absorbent
effluent
promoter
exhaust gas
mixtures
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KR1019910018647A
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Korean (ko)
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KR940006397B1 (en
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로드리구에즈 도밍고
오. 고메즈 세베르스
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롤프 베커 비.
인테베프, 에스. 에이.
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/14Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/48Sulfur compounds
    • B01D53/50Sulfur oxides
    • B01D53/501Sulfur oxides by treating the gases with a solution or a suspension of an alkali or earth-alkali or ammonium compound

Abstract

내용 없음No content

Description

연소 대역의 하류에 배출물 흡수제를 주입시킴으로써 가스상 스트림으로부터 배출물을 계내에서 제거하는 방법A method for removing emissions in situ from a gaseous stream by injecting an emission absorbent downstream of the combustion zone.

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (30)

연소 대역에서 연료를 T1의 온도로 연소시켜서 배출물을 함유하는 배기가스를 방출시키고 ; 상기 배기기스를 상기 연소대역으로부터 이동시켜, 이 배기가스를 T1보다 낮은 온도 T2까지 냉각시키고 ; 배출물 흡수제를 제공하고 ; 상기 배출물흡수제를 상기 연소대역의 하류, 배기가스의 온도가 T2가 되는 지점에서 배기가스에 주입하여, 이 흡수제가 배기가스로부터 배출물을 흡수하도록 하는 것으로 이루어지는, 연료의 연소에 의해 발생하는 배기가스로부터 배출물을 제거하는 방법.Combusting the fuel at a temperature of T 1 in the combustion zone to release exhaust gas containing emissions; Moving the exhaust gas out of the combustion zone to cool the exhaust gas to a temperature T 2 lower than T 1 ; Providing an exhaust absorber; The exhaust gas generated by combustion of fuel, which is injected into the exhaust gas downstream of the combustion zone and at the point where the temperature of the exhaust gas becomes T 2 so that the absorber absorbs the exhaust gas from the exhaust gas. How to remove emissions from 제 1 항에 있어서, 상기 배출물 흡수제를 주입시키기 전에 물과 혼합하여 수성 배출물 흡수제 혼합물을 제조하는 것을 포함하는 방법.The method of claim 1 comprising mixing the water with water prior to injecting the effluent absorbent to produce an aqueous effluent absorbent mixture. 제 2 항에 있어서, 상기 배출물 흡수제 혼합물을 평균 소적 크기가 100마이크론 미만인 미세한 분무액을 형성할 수 있도록 상기 배기가스에 주입시키는 것을 포함하는 방법.3. The method of claim 2, comprising injecting the effluent absorbent mixture into the exhaust gas to form a fine spray liquid having an average droplet size of less than 100 microns. 제 2 항에 있어서, 상기 배출물 흡수제 혼합물을 평균 소적 크기가 50마이크론 미만인 미세한 분무액을 형성할 수 있도록상기 배기가스에 주입시키는 것을 포함하는 방법.3. The method of claim 2, comprising injecting said effluent absorbent mixture into said exhaust gas to form a fine spray liquid having an average droplet size of less than 50 microns. 제 3 항에 있어서, 칼슘 화합물, 마그네슘 화합물 및 이들의 혼합물로 이루어지는 군으로부터 선택되는 수용성 흡수제 화합물을 혼합시킴으로써 상기 배출물 흡수제 혼합물을 제조하는 것을 포함하는 방법.4. The process of claim 3 comprising preparing said effluent absorbent mixture by mixing a water soluble absorbent compound selected from the group consisting of calcium compounds, magnesium compounds and mixtures thereof. 제 3 항에 있어서, 칼슘 화합물, 마그네슘 화합물 및 이들의 혼합물로 이루어지는 군으로부터 선택되는 수불용성 화합물을 혼합시킴으로써 상기 배출물 흡수제 혼합물을 제조하는 것을 포함하는 방법.4. The process of claim 3 comprising preparing said emission absorbent mixture by mixing a water insoluble compound selected from the group consisting of calcium compounds, magnesium compounds and mixtures thereof. 제 5 항에 있어서, 철, 구리, 망간, 붕소, 알루미늄, 나트륨, 칼륨, 아연 및 니켈의 염, 및 이들의 혼합물로 이루어지는군으로부터 선택되는 수용성 금속염 촉진제를 상기 배출물 흡수제 혼합물과 혼합시키는 것을 더 포함하는 방법.6. The method of claim 5, further comprising mixing a water soluble metal salt promoter selected from the group consisting of salts of iron, copper, manganese, boron, aluminum, sodium, potassium, zinc and nickel, and mixtures thereof with the emission absorbent mixture. How to. 제 6 항에 있어서, 철, 구리, 망간, 붕소, 알루미늄, 나트륨, 칼륨, 아연 및 니켈의 염, 및 이들의 혼합물로 이루어지는군으로부터 선택되는 수용성 금속염 촉진제를 상기 배출물 흡수제 혼합물과 혼합시키는 것을 더 포함하는 방법.7. The method of claim 6, further comprising mixing a water soluble metal salt promoter selected from the group consisting of salts of iron, copper, manganese, boron, aluminum, sodium, potassium, zinc and nickel, and mixtures thereof with the emission absorbent mixture. How to. 제 5 항에 있어서, 상기 촉진제가 철, 구리, 망간 및 붕소의 염, 및 이들의 혼합물로 이루어지는 군으로부터 선택되는 방법.6. The method of claim 5 wherein said promoter is selected from the group consisting of salts of iron, copper, manganese and boron, and mixtures thereof. 제 6 항에 있어서, 상기 촉진제가 철, 구리, 망간 및 붕소의 염, 및 이들의 혼합물로 이루어지는 군으로부터 선택되는 방법.7. The method of claim 6, wherein said promoter is selected from the group consisting of salts of iron, copper, manganese and boron, and mixtures thereof. 제 5 항에 있어서, 상기 촉진제가 철 및 구리의 염, 및 이들의 혼합물로 이루어지는 군으로부터 선택되는 방법.6. The method of claim 5 wherein said promoter is selected from the group consisting of salts of iron and copper, and mixtures thereof. 제 6 항에 있어서, 상기 촉진제가 철 및 구리의 염, 및 이들의 혼합물로 이루어지는 군으로부터 선택되는 방법.7. The method of claim 6, wherein said promoter is selected from the group consisting of salts of iron and copper, and mixtures thereof. 제 7 항에 있어서, 수용성 흡수제 대 배출물의 몰비가 0.4 내지 1.2인 방법.8. The method of claim 7, wherein the molar ratio of water soluble absorbent to effluent is 0.4 to 1.2. 제 7 항에 있어서, 수용성 흡수제 대 배출물의 몰비가 0.6 내지 1.0인 방법.8. The method of claim 7, wherein the molar ratio of water soluble absorbent to effluent is 0.6 to 1.0. 제 8 항에 있어서, 수불용성 흡수제 대 배출물의 몰비가 0.5 내지 2.5인 방법.9. The process of claim 8 wherein the molar ratio of water insoluble absorbent to effluent is from 0.5 to 2.5. 제 8 항에 있어서, 수불용성 흡수제 대 배출물의 몰비가 0.8 내지 2.0인 방법.9. The process of claim 8 wherein the molar ratio of water insoluble absorbent to effluent is between 0.8 and 2.0. 제13항에 있어서, 촉진제 대 흡수제의 몰비가 0.01 내지 0.15인 방법.The method of claim 13, wherein the molar ratio of promoter to absorbent is 0.01 to 0.15. 제14항에 있어서, 촉진제 대 흡수제의 몰비가 0.01 내지 0.05인 방법.The method of claim 14, wherein the molar ratio of promoter to absorbent is 0.01 to 0.05. 제15항에 있어서, 촉진제 대 흡수제의 몰비가 0.01 내지 0.10인 방법.The method of claim 15 wherein the molar ratio of promoter to absorbent is from 0.01 to 0.10. 제16항에 있어서, 촉진제 대 흡수제의 몰비가 0.01 내지 0.10인 방법.The method of claim 16 wherein the molar ratio of promoter to absorbent is from 0.01 to 0.10. 제13항에 있어서, T2가 1093℃(2000℉) 내지 1260℃(2300℉)인 방법.The method of claim 13, wherein T 2 is 1093 ° C. (2000 ° F.) to 1260 ° C. (2300 ° F.). 제15항에 있어서, T2가 982℃(1800℉) 내지 1204℃(2200℉)인 방법.The method of claim 15, wherein T 2 is 982 ° C. (1800 ° F.) to 1204 ° C. (2200 ° F.). 제 7 항에 있어서, T2가 900℃(1650℉) 내지 1538℃(2800℉)인 방법.The method of claim 7 wherein T 2 is between 900 ° C. (1650 ° F.) and 1538 ° C. (2800 ° F.). 제 1 항에 있어서, 상기 연료로서 수성 유제중의 오일을 제조하는 단계를 포함하는 방법.The method of claim 1 including preparing an oil in an aqueous emulsion as said fuel. 제 1 항에 있어서, 상기 연료를 연소시키기 전에 어토마이즈화 시키는 것을 포함하는 방법.2. The method of claim 1 comprising atomizing the fuel prior to combustion. 제 1 항에 있어서, 상기 연료가 액체 연료인 방법.The method of claim 1 wherein the fuel is a liquid fuel. 제 1 항에 있어서, 상기 연료가 고체 연료인 방법.The method of claim 1 wherein the fuel is a solid fuel. 제 6 항에 있어서, 철, 구리, 망간, 붕소, 알루미늄, 나트륨, 칼륨, 아연 및 니켈의 염, 및 이들의 혼합물로 이루어지는군으로 부터 선택되는 수용성 촉진제로 상기 배출물 흡수제를 스파이크 시키는 것을 포함하는 방법.7. A method according to claim 6, comprising the step of spiked the effluent absorber with a water soluble promoter selected from the group consisting of salts of iron, copper, manganese, boron, aluminum, sodium, potassium, zinc and nickel, and mixtures thereof. . 제28항에 있어서, 상기 스파이크시킨 배출물 흡수제 입자를 평균입자 크기 50마이크론 미만의 입자로 제조하는 것을 특징으로 하는 방법.29. The method of claim 28, wherein the spiked effluent absorber particles are prepared from particles having an average particle size of less than 50 microns. 제28항에 있어서, 상기 스파이크시킨 배출물 흡수제 입자를 평균 입자크기 10마이크론 미만의 입자로 제조하는 것을 특징으로 하는 방법.29. The method of claim 28, wherein said spiked effluent absorber particles are prepared from particles having an average particle size of less than 10 microns. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019910018647A 1991-02-19 1991-10-23 In-situ removal drrluent from a gaseous stream by injection of an dffluent sorbent into down stream of the combustion zone KR940006397B1 (en)

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DK170891D0 (en) 1991-10-08
DE4204795C2 (en) 1999-07-08
CA2053965A1 (en) 1992-08-20
KR940006397B1 (en) 1994-07-20
FR2672817A1 (en) 1992-08-21
GB2252967A (en) 1992-08-26
NL9200310A (en) 1992-09-16
BR9104514A (en) 1992-10-27
DK170891A (en) 1992-08-20
DE4204795A1 (en) 1992-08-20
JPH0596128A (en) 1993-04-20
ITTO910955A1 (en) 1992-08-20
GB2252967B (en) 1995-09-13
ITTO910955A0 (en) 1991-12-10
IT1250357B (en) 1995-04-07
GB9121602D0 (en) 1991-11-27

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