NZ210165A - Gasification of pulverulent carbonaceous starting material - Google Patents
Gasification of pulverulent carbonaceous starting materialInfo
- Publication number
- NZ210165A NZ210165A NZ210165A NZ21016584A NZ210165A NZ 210165 A NZ210165 A NZ 210165A NZ 210165 A NZ210165 A NZ 210165A NZ 21016584 A NZ21016584 A NZ 21016584A NZ 210165 A NZ210165 A NZ 210165A
- Authority
- NZ
- New Zealand
- Prior art keywords
- gas
- gasification chamber
- shaft
- gasification
- starting material
- Prior art date
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
- C10J3/06—Continuous processes
- C10J3/08—Continuous processes with ash-removal in liquid state
-
- 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
-
- 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
- C10J2200/00—Details of gasification apparatus
- C10J2200/15—Details of feeding means
- C10J2200/152—Nozzles or lances for introducing gas, liquids or suspensions
-
- 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
- C10J2300/12—Heating the gasifier
- C10J2300/123—Heating the gasifier by electromagnetic waves, e.g. microwaves
- C10J2300/1238—Heating the gasifier by electromagnetic waves, e.g. microwaves by plasma
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Carbon And Carbon Compounds (AREA)
- Processing Of Solid Wastes (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Hydrogen, Water And Hydrids (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Description
<div class="application article clearfix" id="description">
<p class="printTableText" lang="en">2101 <br><br>
r~ 1 <br><br>
j ;1L Lr- I <br><br>
j -9 NOV 1984 <br><br>
[~~ RECEIVED <br><br>
PATENTS ACT 1953 PATENTS FORM NO. 5 COMPLETE SPECIFICATION CARBON GASIFICATION <br><br>
WE, SKF STEEL ENGINEERING AB, a Swedish Company, (Sweden) P.n. sn* ?n?f s-813 00 HOFORS, Sweden, hereby declare the invention for which we pray that a patent may be granted to us and the method by which it is to be performed, to be particularly described in and by the following statement: <br><br>
- 1 - <br><br>
The present invention relates to a process for generating a hot (above about 1000°C, preferably above about 1400°C) gas consisting primarily of CO and from a carbonaceous starting material which, in pulverulent form, together with oxidizing agent and optionally also a slag-former, is introduced with the aid of a transport gas, into a gasification chamber, said starting material in said chamber being partially combusted and at least partially gasified. <br><br>
Reduction or combustion gas. based on a content of carbon monoxide and hydrogen is currently generated using several types of processes, which operate in accordance with a variety of entirely different principles, and all of which have certain drawbacks. The energy required is usually generated by combustion of a carbonaceous starting material injected into an empty chamber with oxidizing agent. To cover the energy requirement in the process a certain amount of the CO and formed must be combusted to CO2 and 1^0, and this results in the gas having higher contents of carbon dioxide and water than desired. <br><br>
Consequently, the gas generated in known carbon gasification processes must be relieved of a part of its carbon dioxide content and this means that the gas must <br><br>
first be cooled before being'heated again. In other processes such a low temperature is used that tar and phenols are formed. The gas must therefore be washed and then reheated if it is to be used in subsequent process 5 steps. <br><br>
Against the background of the above, the prime object of the present invention is to effect a process for generating a hot (above about 1000°C, preferably above about 1400°C) reduction or combustion gas consisting primarily of carbon 10 monoxide and hydrogen, said process permitting control of the temperature and composition of the emerging gas, as well as the process offering optimal utilization of energy. <br><br>
This and other objects are achieved with the proces according to the present invention, in which the starting 15 material is partially combusted and at least partially gasified in a gasification chamber, after which the resultant mixture is introduced into a shaft containing a bed of solid carbonaceous lump material; the thermal energy content of the mixture emerging from the 20 gasification chamber is used in the bed of solid carbonaceous lump material to reduce the content of carbon dioxide and water in the gas, and the gas generating process is controlled so that the gas leaving has a temperature and a composition suitable for the following 25 process step. <br><br>
- 3 - f*29JUl»87 <br><br>
210165 <br><br>
( % <br><br>
5 <br><br>
10 <br><br>
Preferably the solid carbonaceous lump material is coke. <br><br>
The oxidizing agent may consist of 0^ i C02' H2^' a"*"r °r various arbitrary mixtures thereof. <br><br>
According to one embodiment of the invention, the energy required is generated in the gasification chamber by supplying an excess of air and/or oxygen gas with a maximum ' of about 20% H2O which reacts exothermically or autothermically with a part of the carbonaceous starting material. <br><br>
According to a second embodiment of the invention, external thermal energy is supplied to the gasification chamber. This external thermal energy may be supplied by means of a carrier gas heated in one or more plasma generators, the gas being selected from a group consisting of 02, 1^0, air and recycled gas containing CO + H2 + CO2 + I^O, or mixtures of two or more components from the <br><br>
According to an embodiment of the invention, the transport gas consists of the oxidizing agent. <br><br>
According to a further embodiment of the invention, water vapour: for introducing material and/or for use as carrier gas is partially or wholly generated with <br><br>
4 <br><br>
210165 <br><br>
coolant heated in a pressurized cooling system in water-cooled parts of the installation and/or by making use of the physical heat in the gas generated. <br><br>
According to a further embodiment of the invention the 5 physical thermal content of the ^reaction gas emerging from the gasification chamber is used to convert gas injected into the coke bed, and containing carbon dioxide and/or water, to carbon monoxide and hydrogen. <br><br>
According to a further embodiment of the invention the 10 entire gas generating proces is controlled by analyzing the oxygen potential in the gas mixture before and/or after the coke-filled shaft. <br><br>
According to a further embodiment of the invention the slag is fed separately out of the gasification chamber and 15 the coke-filled shaft. Alternatively all the slag may be removed from the shaft. <br><br>
According to a further embodiment of the invention sulphur acceptors are injected in pulverulent form into the gasification chamber and/or in lump form into the coke 20 shaft. <br><br>
According to yet another embodiment of the invention the terial injected into the gasification chamber is given a <br><br>
- 5 - <br><br>
210165 <br><br>
rotary motion produce a slag layer protecting the inner walls of the gasification chamber. <br><br>
In another embodiment, recycled product gas is used as the transport gas for injecting the pulverulent starting 5 material. <br><br>
Additional features, advantages and embodiments of the invention will be revealed in the following detailed description. <br><br>
The process is of course not limited to only one gasi-10 fication chamber per shaft. On the contrary, several gasification chambers are preferably arranged in connection with one coke-filled shaft. <br><br>
There are considerable advantages in preforming the majority of the gasification reactions in a gasification •^5 chamber and then completing the reactions in a coke bed. <br><br>
0n& advantage is that gasification can be performed at a high temperature which shall always be above the melting point of the slag, and generally above about 14 00°C, after which the thermal energy content of the gas can be 2o utilized in the subsequent shaft to perform the carburizing reactions which are discontinued at about <br><br>
<r>v <br><br>
,rtn ! <br><br>
,iooo°c. <br><br>
-8DEC1987 <br><br>
a As intimated above, the excess heat in the gas can be used in several ways. For instance, a relatively high content <br><br>
25 oflf-carbon dioxide is permitted in the gas generated in the <br><br>
- 6 - <br><br>
210165 <br><br>
gasification chamber, and this is then converted to carbon monoxide in the coke bed, utilizing the physical thermal content of the gas. <br><br>
The advantage of working with increased COj content in the 5 gasification stage is that the resultant higher oxygen potential gives higher reaction speed between the fuel and the oxidizing agent and at the same time, the process is caused to operate further from the limit where soot deposits occur. <br><br>
10 Another, or supplementary method of exploiting the surplus heat is to inject carbon dioxide and/or water into the coke bed. This can be achieved, for instance, by utilizing a partially spent recycled gas with a high content of carbon dioxide and water. <br><br>
15 The coke bed fulfils a number of important functions, as indicated above, and as will be described in more detail below. <br><br>
The coke bed collects any coke particles and slag drops accompanying the gas mixture from the gasification <br><br>
20 chamber. These particles and drops will then be returned to the process as the coke in the coke bed is spent. The fuel is thus used extremely efficiently. <br><br>
2 10165 <br><br>
The coke bed also functions as a heat store, equalizing any variations in the heat supplied in the gasification chamber. It also acts as carbon store, equalizing any variations in the quantity of carbonaceous material 5 supplied in relation to the quantity of oxidizing agent supplied. This in turn gives reduced risk of explosion, in practice entirely eliminating this risk, even should pure oxygen be added without an equivalent quantity of carbonaceous material being supplied to the gasification 10 chamber. The risk of explosion is otherwise an extremely serious problem. <br><br>
The fuel or the carbonaceoous starting material is supplied in finely distributed form. If it consists of pulverulent, solid material this may be injected with the 15 aid of water vapour, for instance, according to the preferred embodiment of the invention. <br><br>
The carbonaceous starting material may. be selected from a group consisting of oil, coal, coke, charcoal, gas, peat, saw-dust and various mixtures thereof. This offers 20 considerable economic advantages over the known gasification processes, all of which are limited with respect to the choice of starting material. To a great extent the coke consumption is kept low since the oxidizing agent is forced to react with the carbonaceous 25 material in the gasification chamber before it reaches the hot, and thus reactive, coke. <br><br>
- 8 - <br><br>
2101 <br><br>
If only combustion is utilized to generate the heat required for the reactions, a limitation is caused by the thermal balance of the reactions, which results in a relatively high carbon dioxide content. This has 5 previously meant that carbon dioxide must be subsequently removed from the gas in a separate process stage. <br><br>
However, in the process according to the invention, this involves no problem. When oxygen is used as oxidizing agent with the addition of 1^0, autothermic conditions 10 will occur if ca.20% water is added, i.e. the reactions continue but no excess energy is generated. If thermal energy is supplied externally, excess energy is obtained which, according to the above, can be used in the following coke bed. Electric energy can thus be used, 15 preferably by the use of plasma generators in which a carrier gas is heated to a considerable temperature upon passage through an electric arc generated between electrodes in the plasma generated. In the preferred embodiment, the carrier gas used is oxygen and water 20 vapour. However, water vapour, a mixture of H2O and oxygen, pure oxygen or even air may be used as carrier gas. <br><br>
The supply of external energy enables the use of a spent reducing gas containing high contents of carbon dioxide 25 and water as oxidizing agent. <br><br>
- 9 - <br><br>
210165 <br><br>
According to a preferred embodiment, the process can be controlled by analyzing the content of CC>2 or potential in the gas generated, immediately after the gasification'chamber, prior to entering the coke bed 5 and/or in the gas outlet after the coke bed. The analysis immediately after the gasification chamber is preferably utilized to control the ratio between carbonaceous material fed in and oxidizing agent, and possibly also the temperature of the gas leaving, whereas the analysis of 10 the gas after the coke bed is used to control the quantity of CO2 and/or H20 fed into the coke bed. A final gas can thus be produced having the composition and temperature desired for the process following, which may be a sponge-iron proces, for instance, while at the same time 15 almost optimal energy consumption is achieved. <br><br>
In view of the high temperatures used in the process, at least parts of the shaftf and the entire gasification chamber with its burners, should preferably be water-cooled. Arranging the cooling system to operate under pressure, preferably 20 in the vicinity of 5-6 bar over-pressure, enables the heated coolant to be used to generate steam which can then be used as carrier and/or transport gas. Heat losses from the cooling system can thus be utilized. <br><br>
The gasification chamber shall preferably have . 25 substantially circular inner walls. According to th~ <br><br>
10 <br><br>
-» <? fs | 6 5 <br><br>
i. z >«. y invention the flows of gas and material introduced into the gasification chamber can then be given a rotatory motion. Slag particles will then be separated off and form a protective layer on the inner walls of the 5 gasification chamber. The thickness of this slag deposit is determined by the thermal balance between thermal energy removed to the cooling casing and thermal energy supplied to the slag surface by convection and radiation. Excess slag runs out 10 through a slag overflow which may be arranged separately for the gasification chamber, or may be combined with the slag overflow for the shaft. <br><br>
Slag-formers and/or sulphur acceptors in finely divided form, may be injected into the gasification chamber 15 together with the carbonaceous material or separately from it and/or they may be introduced together with the solid carbonaceous material in lump form in the shaft, thus forming a part of the coke bed. <br><br>
To achieve rapid and efficient mixing between the hot gas 20 generated in the plasma generator and the pulverulent, <br><br>
carbon-carrying fuel supplied, the hot gas is introduced through the orifice of the plasma generator into the gasification chamber. This is achieved by the carrier gas being given a rotary motion during its passage through the 25 plasma generator, the pulverulent fuel having been given a rotary motion prior to entering the gasification <br><br>
- 11 _ <br><br>
210165 <br><br>
chamber, and/or by the plasma generator and/or supply means for carbonaceous fuel being arranged to open tangentially into the gasification chamber. This will cause the hot gas to expand upon entering the gasification 5 chamber and this turbulence will provide an extremely short mixing space. <br><br>
The invention will now be described more fully with reference to the accompanying drawing showing one embodiment of an installation for performing the process 10 according to the invention. <br><br>
The figure shows a gasification plant having a gasification chamber 1, and a shaft 2 filled with coke 3. <br><br>
The gasification chamber 1 has an outer, water-cooled casing 4 and a refractory lining 5 and is preferably 15 essentially cylindrical. Several gasification chambers are preferably arranged in connection with one shaft. <br><br>
The shaft 2 has a lower slag outiet 6 and an upper gas outlet 7. Coke in lump form is supplied to the shaft through a gas-tight supply means 8 at the top of the 20 shaft. The gasification chamber 1 leads into the lower part of the shaft, from whence the gas passes up through the coke bed and out through the gas outlet. In the embodiment shown the slag outlet 6 is common for both gasification chamber and shaft. <br><br>
- 12 - <br><br>
210165 <br><br>
Associated with the gasification chamber is at least one burner consisting, in the embodiment shown, of a plasma generator 9. The plasma generator is connected to the gasification chamber via a valve means 10. Oxidizing 5 agent is introduced into the plasma generator through a supply pipe 11. The oxidizing agent may comprise a carrier gas which is led through the plasma generator or a separate carrier gas may be used. The hot, turbulent gas generated in the plasma generator, is introduced into the 10 gasification chamber through the opening 12 of the plasma generator. The carbonaceous fuel, preferably in pulverulent form, is introduced with the aid of a transport gas through a supply pipe 13 into an annular gap 14 arranged concentrically around the plasma generator, 15 and/or lance 15 which may also be used with advantage for the supply of any additive, such as slag-former. <br><br>
Lances 16, 17 are also arranged in the shaft for the supply, if necessary, of additional oxidizing agent, such as 1^0 or CO2, to exploit the physical surplus heat in the 20 gas. This also allows for control of the temperature and composition of the gas. <br><br>
At the end of the gasification chamber close to the coke bed, a first sensing device 18 is arranged and a second sensing device 19 is arranged in the gas outlet 7 from the 25 shaft for measuring temperature and/or analyzing the gas. <br><br>
- 13 - <br><br>
210165 <br><br>
These two sensing devices enable control of the process by regulation of the external energy supplied and/or by variation in the flows of material supplied. <br><br>
The figure shows only one embodiment of a plant for 5 performing the process according to the invention and many other solutions are feasible. For example, the plasma generators or burners may be arranged tangentially on the periphery of the gasification chamber so as to produce a circulating flow in the gasification chamber. 10 Furthermore, to facilitate slag separation, the gasification chamber may be vertical, or the gasification chamber and shaft may have separate slag outlets. <br><br>
The matter contained in each, of the following claims is to be read as part of the general description of the present 15 invention. <br><br>
- 14 - <br><br></p>
</div>
Claims (1)
- <div class="application article clearfix printTableText" id="claims"> <p lang="en"> 210165<br><br> What we claim is:<br><br> 1. A method for generating a gas consisting primarily of CO and ^ from a carbonaceous starting material, which method comprises<br><br> 1) heating a carrier gas stream containing oxygen and a gasification medium, particularly water vapour, in a plasma generator;<br><br> 2) conducting the hot (above 1000°C) carrier gas emerging from the plasma generator to a gasification chamber and giving it a rotary movement before it enters the gasification chamber;<br><br> 3) injecting, with the aid of a transport gas, a carbonaceous starting material in pulverulent form concentrically around the hot carrier gas flowing into the gasification chamber;<br><br> 4) giving the starting material a rotary movement in the gasification chamber where it is partially combusted and at least partially gasified to form reaction gas containing CO, H2> H2° and CC^, the rotary movement causing a layer of slag to^ be formed on the inner wall of the gasification chamber;<br><br> 5) introducing the reaction gas which emerges from the gasification chamber into a shaft containing a bed of solid carbonaceous lump material, wherein the thermal energy content of the reaction gas is used in the bed of lump material to reduce the content of carbon dioxide and water in the reaction gas and thereby to form a gas consisting primarily of carbon monoxide and hydrogen; and"removing this<br><br> - 15 -<br><br> //\r O -1L ■<br><br> fN<br><br> •8 DEC 1987<br><br> 210165<br><br> product gas from the shaft.<br><br> 2. A method according to claim 1 wherein the entire gasification chamber and at least part of the shaft is water-cooled.<br><br> 3. A method according to claim 1 or 2 wherein recycled product gas is used as the transport gas for injecting the pulverulent starting material.<br><br> 4. A method according to any one of the preceding claims wherein sulphur acceptors are injected in pulverulent form into the gasification chamber and/or in lump form into the shaft.<br><br> preceding claims wherein the gas generating process is controlled by analysing the carbon dioxide content or oxygen potential in the gas mixture before and/or after the shaft.<br><br> preceding claims wherein the slag is fed separately out of the gasification chamber and the shaft furnace.<br><br> preceding claims wherein the slag from the gasification chamber is fed to the shaft, from whence all the slag is then removed.<br><br> 8. A method according to any one of the preceding claims carried out in apparatus comprising a shaft containing a bed of solid carbonaceous lump material, a<br><br> 5. A method according to any one of the<br><br> 6. A method according to any one of the<br><br> 7. A method according to any one of the supply means for the carbonaceous lump material, a g~~<br><br> 16<br><br> 210165<br><br> m<br><br> 5 outlet, a slag outlet, at least one plasma generator to which a first supply pipe for a carrier gas is connected, and a second supply pipe for pulverulent carbonaceous starting material and transport gas, the plasma generator and the<br><br> 10. second supply pipe being connected to a gasification chamber joined to the shaft furnace, and an annular gap which is arranged concentrically around the opening of the plasma generator being joined to the second supply pipe for the pulverulent carbonaceous starting material.<br><br> 9. A method according to claim 8 wherein the plasma generator and the second supply pipe are arranged tangentially to the periphery of the gasification chamber.<br><br> 10. A method according to claim 8 or 9 wherein several gasification chambers are joined to the periphery of the shaft.<br><br> /<br><br> 11. A method according to any one of claims 8 to<br><br> 10>substantially as hereinbefore described with reference to th£ drawings.<br><br> 12. a mixture of gases comprising carbon monoxide and hydrogen whenever produced by a method according to any one of claims 1 to 11.<br><br> DATED this .day of Docombor; A^D.—1987<br><br> SKF STEEL ENGINEERING AB,<br><br> By its Patent Attorneys,<br><br> HENRY HUGHES LIMITED By:<br><br> - 17 -<br><br> </p> </div>
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE8403190A SE453750B (en) | 1984-06-14 | 1984-06-14 | KIT FOR GASING OF FINE DISTRIBUTED COAL CONTENTS |
Publications (1)
Publication Number | Publication Date |
---|---|
NZ210165A true NZ210165A (en) | 1988-02-12 |
Family
ID=20356228
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NZ210165A NZ210165A (en) | 1984-06-14 | 1984-11-09 | Gasification of pulverulent carbonaceous starting material |
Country Status (19)
Country | Link |
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JP (1) | JPS614788A (en) |
KR (1) | KR860000354A (en) |
CN (1) | CN85101040A (en) |
AT (1) | AT389524B (en) |
AU (1) | AU577071B2 (en) |
BE (1) | BE901156A (en) |
BR (1) | BR8406068A (en) |
CA (1) | CA1265340A (en) |
DE (1) | DE3441359A1 (en) |
ES (1) | ES538141A0 (en) |
FR (1) | FR2565993B1 (en) |
GB (1) | GB2160219B (en) |
IN (1) | IN162480B (en) |
IT (1) | IT1177078B (en) |
NO (1) | NO844797L (en) |
NZ (1) | NZ210165A (en) |
SE (1) | SE453750B (en) |
YU (1) | YU45682B (en) |
ZA (1) | ZA848215B (en) |
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IT1218575B (en) * | 1987-05-28 | 1990-04-19 | Valerio Tognazzo | RECOVERY PROCEDURE FROM FOSSIL, VEGETABLE PRODUCTS, AGGREGATES OF WASTE AND NON-POLLUTANTS, OF PURE GASEOUS FUELS, INERT USEFUL AND POLLUTANT SUBSTANCES, BY SEPARATION IN FUNCTION OF THE ENERGY CONTENT, WITHOUT PROVIDING AN ENVIRONMENT OF ELEVATION AND A LESS HEAT OF SUPERIOR TO HEAT FROM ABOVE WATER TO PURIFY IT |
JP2512061B2 (en) * | 1987-11-26 | 1996-07-03 | 日本碍子株式会社 | Homogeneous silicon nitride sintered body and method for producing the same |
DE4030554A1 (en) * | 1990-09-27 | 1992-04-09 | Bergmann Michael Dr | Procedure and device for thermal treatment of waste materials - comprises reactor combustion zone charged with waste, coke and lime, and gas produced passes through hot coke be also located in reactor |
WO2000013785A1 (en) * | 1998-09-02 | 2000-03-16 | Jacobus Swanepoel | Treatment of solid carbonaceous material |
KR100391121B1 (en) * | 2000-12-11 | 2003-07-16 | 김현영 | Method of gasifying high molecular weight organic material and apparatus therefor |
EP1474500A1 (en) * | 2002-02-06 | 2004-11-10 | Félicien Absil | Gazeification de dechets par plasma |
US20070225382A1 (en) * | 2005-10-14 | 2007-09-27 | Van Den Berg Robert E | Method for producing synthesis gas or a hydrocarbon product |
FR2892127B1 (en) * | 2005-10-14 | 2012-10-19 | Commissariat Energie Atomique | DEVICE FOR GASIFYING BIOMASS AND ORGANIC WASTE AT HIGH TEMPERATURE AND WITH EXTERNAL ENERGY DELIVERY FOR THE GENERATION OF A HIGH-QUALITY SYNTHESIS GAS |
JP5277741B2 (en) * | 2008-06-11 | 2013-08-28 | 株式会社Ihi | Gasification method and gasification apparatus |
JP2011006295A (en) * | 2009-06-26 | 2011-01-13 | Teijin Chem Ltd | Method for producing carbon monoxide and method for producing phosgene using the same |
US8852693B2 (en) | 2011-05-19 | 2014-10-07 | Liquipel Ip Llc | Coated electronic devices and associated methods |
JP6041451B2 (en) * | 2013-05-16 | 2016-12-07 | Global Energy Trade株式会社 | Gasification method and gasification apparatus for solid organic raw material |
AU2015201766B1 (en) * | 2015-04-08 | 2016-06-09 | Mitsubishi Power, Ltd. | Gasifying system including a gasifier |
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DE859191C (en) * | 1949-01-20 | 1952-12-11 | Basf Ag | Process for generating fuel, in particular synthesis gases, in gas generators |
GB720598A (en) * | 1952-01-16 | 1954-12-22 | Power Jets Res & Dev Ltd | Gas producer plant |
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US4153426A (en) * | 1977-07-18 | 1979-05-08 | Arthur G. Mckee & Company | Synthetic gas production |
CH644149A5 (en) * | 1978-12-29 | 1984-07-13 | Voest Alpine Ag | METHOD AND DEVICE FOR GASIFYING COAL. |
GB2093070B (en) * | 1981-02-11 | 1984-10-31 | Skf Steel Eng Ab | Manufacturing sponge iron |
SE434163B (en) * | 1981-03-10 | 1984-07-09 | Skf Steel Eng Ab | SET AND DEVICE FOR PREPARING A MAIN COOLOXIDE AND VETGAN CONTAINING GAS FROM COAL AND / OR CARBON-CONTAINING INGREDIENTS |
DE3132506A1 (en) * | 1981-08-18 | 1983-03-03 | Hoechst Ag, 6000 Frankfurt | METHOD AND DEVICE FOR PRODUCING SYNTHESIS GAS |
SE8201263L (en) * | 1982-03-01 | 1983-09-02 | Skf Steel Eng Ab | INSTALLATION AND INSTALLATION FOR GASATION OF CARBONIC MATERIAL |
DE3239774A1 (en) * | 1982-10-27 | 1984-05-03 | Hoechst Ag, 6230 Frankfurt | METHOD AND DEVICE FOR PRODUCING SYNTHESIS GAS |
IT1177076B (en) * | 1983-12-02 | 1987-08-26 | Skf Steel Eng Ab | PROCESS AND PLANT TO REDUCE OXIDE MATERIAL SIMULTANEOUSLY GENERATING A GAS SUITABLE FOR THE RECOVERY OF THERMAL ENERGY |
IT1177077B (en) * | 1983-12-02 | 1987-08-26 | Skf Steel Eng Ab | PROCEDURE AND PLANT TO REDUCE OXIDE MATERIAL SIMULTANEOUSLY GENERATING A GAS SUITABLE AS COMBUSTIBLE GAS |
IT1177075B (en) * | 1983-12-02 | 1987-08-26 | Skf Steel Eng Ab | PROCEDURE AND PLANT TO REDUCE OXIDE MATERIAL |
-
1984
- 1984-06-14 SE SE8403190A patent/SE453750B/en not_active IP Right Cessation
- 1984-10-22 ZA ZA848215A patent/ZA848215B/en unknown
- 1984-10-23 CA CA000466103A patent/CA1265340A/en not_active Expired - Fee Related
- 1984-10-30 IT IT23371/84A patent/IT1177078B/en active
- 1984-10-30 IN IN811/MAS/84A patent/IN162480B/en unknown
- 1984-11-05 GB GB8427969A patent/GB2160219B/en not_active Expired
- 1984-11-09 NZ NZ210165A patent/NZ210165A/en unknown
- 1984-11-09 AU AU35254/84A patent/AU577071B2/en not_active Ceased
- 1984-11-13 DE DE19843441359 patent/DE3441359A1/en active Granted
- 1984-11-27 FR FR848418041A patent/FR2565993B1/en not_active Expired - Fee Related
- 1984-11-28 YU YU202084A patent/YU45682B/en unknown
- 1984-11-29 BR BR8406068A patent/BR8406068A/en not_active IP Right Cessation
- 1984-11-29 BE BE0/214074A patent/BE901156A/en not_active IP Right Cessation
- 1984-11-30 AT AT0381784A patent/AT389524B/en not_active IP Right Cessation
- 1984-11-30 NO NO844797A patent/NO844797L/en unknown
- 1984-11-30 ES ES538141A patent/ES538141A0/en active Granted
- 1984-12-01 JP JP59252851A patent/JPS614788A/en active Pending
- 1984-12-01 KR KR1019840007575A patent/KR860000354A/en not_active Application Discontinuation
-
1985
- 1985-04-01 CN CN198585101040A patent/CN85101040A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
ES8602099A1 (en) | 1985-12-01 |
GB2160219A (en) | 1985-12-18 |
SE8403190D0 (en) | 1984-06-14 |
ZA848215B (en) | 1986-06-25 |
BR8406068A (en) | 1986-06-17 |
CA1265340A (en) | 1990-02-06 |
DE3441359A1 (en) | 1985-12-19 |
FR2565993A1 (en) | 1985-12-20 |
AU3525484A (en) | 1985-12-19 |
IT1177078B (en) | 1987-08-26 |
SE453750B (en) | 1988-02-29 |
SE8403190L (en) | 1985-12-15 |
YU202084A (en) | 1987-12-31 |
FR2565993B1 (en) | 1990-06-22 |
IT8423371A0 (en) | 1984-10-30 |
ES538141A0 (en) | 1985-12-01 |
IN162480B (en) | 1988-05-28 |
DE3441359C2 (en) | 1989-01-12 |
AU577071B2 (en) | 1988-09-15 |
NO844797L (en) | 1985-12-16 |
IT8423371A1 (en) | 1986-04-30 |
GB8427969D0 (en) | 1984-12-12 |
KR860000354A (en) | 1986-01-28 |
BE901156A (en) | 1985-03-15 |
JPS614788A (en) | 1986-01-10 |
YU45682B (en) | 1992-07-20 |
GB2160219B (en) | 1989-06-07 |
AT389524B (en) | 1989-12-27 |
CN85101040A (en) | 1987-01-10 |
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