• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
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    • 专利摘要:

    公开号:WO1980001490A1
    申请号:PCT/EP1980/000002
    申请日:1980-01-14
    公开日:1980-07-24
    发明作者:A Johansson
    申请人:Battelle Memorial Institute；A Johansson；
    IPC主号:D21C11-00
    专利说明:
    [0001] BLACK-LIQUOR PROCESSING
    [0002] TECHNICAL FIELD
    [0003] The present invention concerns an improved process for treating the black liquor involved in chemical pulping process i.e. as issuing from the digestion of wood and other cellulosic materials with alkali hydroxide solution in the soda pulping process or with alkali sulfide solution in the Kraft pulping process.
    [0004] In the alkaline processes for manufacturing cellulosic pulp, lignocellulosic material such as straw or wood in comminuted form is digested in a sodium hydroxide solution, either in the presence or in the absence of sodium sulfide (depending on the process) whereby the lignin and hemi-cellulosic fractions get dissolved by forming what is σalled "black-liquor". The pulp is separated fram the black-liquor, for instance by filtration or centrifugation and used for making carton or other high tenacity cellulosic products. Then the black-liquor, which still contains dissolved about 50% organic matter based on the original wooden products having undergone digestion, must be processed for recovering the mineral sulfur and sodium compounds and for separating the organics which can be used as fuel to provide power to the plant. BACKGPOUND OF THE AKT There exists several processes for recovering black-liquor components, some of which are described in the following publication: Proceedings from the Gunnar Sundblad Seminar at Billingehus, Skövde, STFI Meddelande Serie D No. 7. Whatever differences between such processes, they all involve eliminating the water from the black-liquor by putting it into the gaseous State (concentrating by evaporation, drying, spraying or direct burning) which, energywise, is quite une-conomical. For instance, in the process most used today (the TCMLINSON process) the black liquor is first concentrated by evaporation, then it is sprayed in a burner furnace where it undergoes partial combustion with evolution of flue gases and Separation of the mineral compounds in the form of sodium carbonate (and sulfate in the Kraft process). Thereafter, the latter must be reduced again to sulfide with part of the flue gases. It is common knowledge that besides its poor energy conversion efficiency, the above-described reactor is hazardous to operate (many have exploded) and the maintenance costs are very high. The other processes, among which the ST. REGIS (USP 3.762.989), the WEYERHAUSER and the SCA-BILLERUD (see the abovementioned reference) are possibly less hazardous to operate but their energy look-out is hardly better and their econαnies have not been fully demonstrated yet.
    [0005] Obviously, a process whereby the organic product salts in the aqueous phase of the black-liquor could be separated fron the aqueous phase without having to convert the water of such phase to vapor and in which such organic material would be in a form easy enough to handle and to convey to other locations (most present processes produce carbon residues and tars which stick to and rapidly foul the equipments) would be much appreciated. Thus, recently Houssni El-Saied J. Appl. Chem. Biotechnol. 1977, 27, 443-462, reported the Separation of ligno-hemicellulosic materials fron waste black-liquor by acidification with H2SO4 and settling, followed by the conversion of the isolated solid material to oil by heating under pressure with water and carbon monoxide. Indeed, under such conditions, hydrogen is produced according to the reaction,
    [0006] CO + H2O → H2 + CO2
    [0007] and achieves liquefaction of solid lignocellulosic materials by depolymerization, hydrogenation and hydrogenolysis of the ether bonds present in such materials. However, this method proved to be unsatisfactory on an industrial point of view for the following reasons: this Separation technique is tedious and consumes H2SO4; the filtered liquor having been acidified, the mineral reagents can no more be conveniently recovered and recycled; the liquefaction Operation leaves some part of the material in solid form which must be separated from the oil by hydrocarbon extraction. DISCLOSURE CF THE INVENTION
    [0008] It has been discovered now with great surprise that black-liquor can be subjected directly to treatment with CO, H2 or both, under heat and pressure, which treatment leads to the formation of an oil phase insoluble in the water phase and which can be separated by decantation. In this process, most of the organics are converted to oil, a small part of it is gasefied and the araount remaining in the water phase is negligible with regard to further recovery operations.
    [0009] Therefore, the process of the invention comprises contacting the black-liquor directly issuing fron the digester tank (or from the evaporation units) with carbon monoxide, hydrogen or mixtures of both under heat and pressure until substantially all the organic matter dissolved therein is converted to liquid and gaseous products, the liquefied portion thereof forming a liquid phase insoluble in the water phase and easily separable therefrom. In this process, any preliminary treatment of the black-liquor is unnecessary and can be performed only if desired, e.g. partial evaporation. This invention was most unexpected and its practically quantitative yields are perhaps due to the presence of' the minerals in the black-liquor which possibly act as catalysts. This possibility is actually backed up by some findings of El Saied (see above reference) that some added minerals such as NaOH, Na2CO3 or Ca(OH)2 acted as catalysts in his liquefaction experiments of the solid black-liquor extracts.
    [0010] BEST METHODS OF CARRYING OUT THE INVENTION
    [0011] The preferred conditions to perform the process of the present invention are 100 to 300 bars, 200-350°C. Below 200°C, the reaction becomes somewhat sluggish and above 350°C the pressure build-up is hard on the equipment. Temperature ranges of 270-330°C are actually preferred at least for one step conversion. The concentration in solids of the black-liquor used is not critical and can be comprised for instance between 100 and 500 g/l of organics and 50-200 g/l of mineral ccmpounds. In practice all types of black-liquors involved in the chemical pulping industry can be treated that way. Also, the types of reactors in which the above oil conversion treatment can be carried out are not at all critical and most usual types of reactors for treating liquids under heat and pressure can be used. For instance, the reaction operates as well in a 1 liter laboratory autoclave as in a large scale industrial high pressure reactor. The conversion Operation can be conducted in one stage or, otherwise in two or more stages. If the conversion is carried out in, say, two stages, the heating under CO and/or H pressure is interrupted at some point at which all or part of the CO formed during the reaction is allowed to escape. This can be done without interrupting the heating or, better, by allowing the autoclave to cool to some extent, even down to room temperature, releasing the pressure and refilling the autoclave with a fresh portion of reducing gases. This method has two main advantages: a) it improves the Overall yield of about 10% as compared with the one stage conversion under similar conditions; b) it permits using more gentle overall conditions. Thus, for instance, in one preferred operational sequence, the working conditions of the first conversion stage are set up at relatively high initial pressure (about 50-80 bar of reducing gases at room temperature) and relatively low temperature (about 200-220°C); then, in the second stage, the initial pressure is set at lower initial values (about 30-40 bar) and the heating is carried out at higher temperatures (in the range of 300-350°C). Therefore, by this method the overall pressure build-up on the equipment at final operating temperature is maintained under more reasonable limits without lowering the ultimate oil yields.
    [0012] The invention will now be more fully illustrated with reference to the accompanying drawing which represents schematically a Kraft pulping plant in which the invention is incorporated.
    [0013] The plant comprises a digester tank 1 into which the wooden chips to be pulped and the chemicals are introduced through the inlets represented by the arrows 2 and 3. After digestion, the pulp is separated and removed at bottom of tank as shown by arrow 4 and the blackliquor is sent to an evaporator 5 where it gets concentrated (the evaporator is a purely optional Step in the present invention). Then, the black-liquor enters a pressure reactor 6 comprising a heating System represented schematically by a coil 7. Carbon monoxide, or hydrogen or both, compressed by compressor 8, is introduued into reactor 6 whereby the black-liquor is subjected to heat and pressure until all its organic components are converted to oil and gas. Then, the gas, oil and water phases are all sent to a settling tank 9 whereby the gas is collected as shown by the arrow 10 and the oil and water phases are separated by decantation (or centrifugation). It is to be understood that the various phases in this process are driven from and to the above described processing units by means known in the art (pumps, valves, etc.) and not shown here for the sake of simplicity and to avoid overcrowding. The oil is collected and cooled in a heat-exchanger 11 wherein the heat can be recovered and used elsewhere whereas the water phase which does not contain any significant quantity of organics is flown to a tank 12 wherein the Separation of the mineral compounds in the form of Na2SO4 and Na2CO3 is effected. Such Separation can be achieved by classical means, e.g. evaporation and crystallization or by ultra-filtration under pressure (such pressure can be provided easily because of the existence of the high operating pressures required for reactor 6). The water from this Separation can either be discarded or reused as shown in the drawing and to be discussed hereinunder. Then, the solid salts are subjected to reduction in the kiln 13 by means of either coal provided from an outside source (see arrow 14) or oil (see arrows 15 and 14). The carbon monoxide produced during reduction is compressed by pump 8 and fed to the reactor 6. The reduced salts which consist now of Na2s and Na2CO3 are then reacted in a reactor 16 with a lime slurry (see arrcw 17), whereby the sodium carbonate is converted to hydroxide with simultaneous precipitation of chalk which is separated in tank 18 from the concentrated solution of Na2S + NaOH. This concentrated sulfide and caustic solution is further diluted with water, e.g. the water separated from the minerals in tank 12 and transported by line 19 and the resulting liquor (white-liquor) is recycled in the process through line 20 and the inlet represented by arrow 3. It should be noted that only a small part of the oil generated in reactor 6 may be required to effect the reduction of the salts in kiln 13. Therefore, most of this oil can be used as fuel or stored as a refining stock.
    [0014] In a modification of the present installation, another (or more) reactor 6' could be inserted in the circuit between present react or 6 and tank 9, means being provided between the two reactors 6 and 6' to have the mixture cooled (cooling coil), the pressure be released (valve opening in order to allow CO2 formed to escape) and then be introduced into reactor 6', whereby it would be subjected again to heat and reducing gases pressure by means of the same pump 8 or another separate pump 8' supplying the same or a different gas mixture. Additional items 6', 8' and the above means are not shown on the drawing since they can be visualized and selected easily by any average man skilled in the art. This embodiment modification is for ensuring a two (or more) stage conversion, as discussed above with reference to a lab autoclave experiment, with consecutive yield improvement and the setting of milder overall conversion conditions. REDUCTION TO PRACTICE
    [0015] The following Examples illustrate the invention in further detail.
    [0016] Example 1
    [0017] In a one liter autoclave were introduced 240 g of black-liquor from a Kraft pulp mill containing 64% solids and 210 g of Ho. The autoclave was connected to a CD supply and set to an initial pressure of 70 atm. The mixture was heated to 290°C (corresponding to a maximum pressure of 185 atm), for 2 hours.
    [0018] After cooling to room temperature the autoclave was opened and it was found that the organic material in the black-liquor had separated into an oily viscous layer floating on the light brown aqueous phase containing the inorganic constituents of the black-liquor. The amount of oil recovered was 40 g corresponding to more than 70% oil conversion of the total organics in the black-liquor. The water phase of brownish color did not contain any significant amount of organic matter, the remaining 30% having been converted to gas. Example 2
    [0019] 240 g black-liquor, 210 g H2O and 10 g NaOH were introduced in the same reactor mentioned in Example 1. The initial CO pressure was 70 atm; heating was done for 1 hr to 305°C corresponding to a maximum pressure of 220 atm; 42 g of oil pourable at room temperature separated as layer floating on light green aqueous phase. Composition of oil: C 63.3%, H 6.05%, 017.65%, N 0.1%, H2O 13%. Example 3
    [0020] 300 g black-liquor, 150 g H2O and 5 g NaOH were introduced into a 1 liter reactor and subjected to an initial CO pressure of 70 atm. Then the reactor was heated for 1 hr at a temperature of 300°C corresponding to a pressure of 145 atm. There were recovered 56 g of an anthracenerlike product corresponding to more than 75% conversion efficiency. Composition: C 73.1%, H 8.1%, N traces, 0 15.3%, S 3.1%. H2O 9%. Corresponding to approximate fuel value 8330 of kcal/kg.
    [0021] Example 4
    [0022] 200 g black-liquor, 50 g H2O and 80 g of oil from previous experiments were introduced into the reactor which was subjected to an initial CO pressure of 70 atm and to heat. The final temperature was 300°C and the pressure reached 200 atm during 1 hour. There were recovered 112 g of oil pourable at room temperature.
    [0023] Analysis of the undried product gave: C 66.9%, H 7.5%, N 0.1%,
    [0024] 0 13.8%, S 2.7%, H2O 9%. Corresponding to approximate fuel value of 7660 kcal/kg.
    [0025] Example 5
    [0026] 240 g black-liquor were put into an autoclave like in Example
    [0027] 1 and heated to 210°C for one hour under a 50:50 (V/V) mixture of 00 and H2; the initial pressure was 70 atm. Then, the autoclave was cooled, the pressure was fully relieved for allowing all gases, including CO2, to escape, then a fresh portion of CO/H2 was reintroduced (initial pressure 30 atm) and the reaction was pursued for 1 hr at 310°C.
    [0028] After cooling and work-up as in the previous Examples, 46 g of oil were recovered.
    [0029] Further comments on the prior art
    [0030] After this application was filed for securing a priority date, a Standard Seareh was condueted and provided the following references:
    [0031] 1. FR 1.319.466 (DELIBRAT0R)
    [0032] 2. USP 3,864,096 (URBAN)
    [0033] 3. USP 3,733,255 (APPELL)
    [0034] 4. DE 382.367 (FISCHER)
    [0035] 5. I. Appl. Chem. Biotechnol. 27, 443-452 (1977) (EL-SAIED) 6. Abstract, No. 9473, Abstr. Bull. Inst. Paper Chem. 47 (9) 29-34 (1977) (HILL)
    [0036] Reference 1 concerns a process for the treatment of Solutions or effluents arising from cellulose processing. It consists in spraying the liquor to be treated in a stream of not gas such as water vapor, CO2, CO, -H2, N2 or mixtures thereof. The heat necessary for heating the gas is obtained from the burning of a fuel such as coal, liquid fuel or the gases evolved during said processing. There is no question in this reference of heating the liquor with CO and H2 under pressure in order to quantitatively convert the organic matter therein into oil or gas. Therefore, Reference 1 does not anticipate the invention.
    [0037] Reference 2 concerns a process for converting cellulose products into a hydrocarbon liquid oil by heating with hydrogen or a mixture of H2 and CO plus ammonia and water. By looking at the Examples, it is found that the conversion yields do not exceed about 50% in the best case. Therefore, since in the invention the conversion is nearly quantitative (this being possibly due to the nature of the products under treatment or to the catalytic effect of the minerals dissolves in the black-liquor), Reference 2 does not anticipate the invention or makes it obvious.
    [0038] Reference 3 concerns the treatment of sewage sludge with CO plus water and heat in order to form heavy oils. The reference indicates that alkali and earth-alkali hydroxides and carbonates act as catalysts in the reaction. However, the yields are very low (around 25%) which seems to indicate, with reference to the present invention, that black-liquor behaves quite differently in such circumstances fron ordinary sludge. Since the Substrate to be treated and the yields are different frαn the invention, the novelty of the latter is not impaired by Reference 3. However, the reason why black-liquor behaves differently from sludge is not clear. It is however pointed out that, in the reference, large amounts of heavy products and biturnen are obtained and that conversion ratios are generally below 40% whereas, in the invention, the amount of products other than oil, gases or water dissolved products, is generally negligible. It seems therefore that the organic content of black-liquor favors its convertibility to oil as compared to municipal sludge. Reference 4 is an old German Patent (1920) which concerns a process for reducing organic matter such as coal, peat or heavy oil into ether soluble oils by heating with water and carbon monoxide in an autoclave, optionally using basic agents. The yields are low (about 30%) . This reference teaches nothing more than the previous references.
    [0039] Reference 5 is the article by El-Saied which was already discussed in the introduction of the present application. It is not believed that this reference can damage the novelty of the present invention. On the contrary, it puts into evidence the simplicity of the method of the invention, this simplicity being, in itself, surprising.
    [0040] Reference 6 concerns the converting of organic wastes into oil by heating with CO and H2O. The reference speaks of "wood wastes" and more particularly of lignin, but not of black-liquor. Further, the reference provides no detail on yield, the catalysts and the conditions used.
    权利要求:
    Claims
    1. A process for treating black-liquor and separating the organic components thereof from the water phase without having to convert said water to water vapor, which comprises contacting said blackliquor with a reducing gas such as carbon monoxide and/or hydrogen under heat and pressure until substantially all the organic matter dissolved therein is converted to liquid and gas products, the liquefied portion thereof forming a liquid oil phase insoluble in the water phase and easily separable therefrom.
    2. The process of Claim 1, wherein the oil and the water phases are separated by decantation, centrifugation or other conventional means.
    3. In a chemical pulping process for ligno-cellulosic materials including the following steps: a) digesting the lignocellulosic material with aqueous NaOH or NaOH + Na2S, thus forming pulp and the black-liquor, b) separating the pulp fron the black-liquor, c) treating the black-liquor for separating the organic compounds dissolved therein from the water phase, d) separating the used mineral chemicals from said water phase, e) regenerating the Na s from said used chemicals by reduction and the NaOH by treatment with lime and f) recycling said NaOH or said NaOH + Na2s, the improvement to Step c) consisting in subjecting the black-liquor to heat and high pressure of reducing gas such as carbon monoxide and/or hydrogen until said organic compounds are converted to gas and oil, said oil being insoluble in the water phase and separable therefrom by decantation or centrifugation.
    4. The process of Claim 3, wherein the reduction of the used chemicals of Step e) is effected by using the oil obtained in Step c).
    5. The process of Claim 3, wherein the carbon monoxide prcduced by the reduction of the used chemicals in Step e) is used to achieve the improvement of Step c).
    6. The process of Claim 1, wherein said Operation of converting black-liquor into oil is separated into two - or more - stages, the temperatures and pressures being different from stage to stage and part or all of the carbon dioxide formed during the one stage being removed after that stage and before undertaking the next stage.
    7. The process of Claim 6, wherein the temperature is relatively moderate and the initial pressure relatively high in the first stage, the temperature is relatively high and the initial pressure relatively lσw in the second stage and wherein, between said stages, the mixture is cooled to some extent and the pressure is temporari- ly released in order to drive off the CO2 formed in the first stage.
    8. The process of Claim 3, in which said subjecting the black- liquor to heat and pressures with a reducing gas is carried out in two or more stages, the temperatures and pressures being different fron stage to stage and the carbon dioxide resulting from the reaction being at least partly eliminated between two consecutive stages.
    9. The process of Claim 8, in which the two or more stages of black-liquor conversion to oil are carried out in two or more independent reactors, the elimination of CO2 being carried out between two consecutive stages by cooling to some extent the reaction mixture flow and partly or totally releasing the pressure before going to the next reactor.
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    同族专利:
    公开号 | 公开日
    FI70057C|1986-09-12|
    CA1130959A1||
    FI800099A|1980-07-17|
    DE3068925D1|1984-09-20|
    CA1130959A|1982-09-07|
    EP0022841B1|1984-08-15|
    FI70057B|1986-01-31|
    EP0022841A1|1981-01-28|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1980-07-24| AK| Designated states|Designated state(s): BR NO US |
    1980-07-24| AL| Designated countries for regional patents|Designated state(s): CH DE FR SE |
    1980-09-12| WWE| Wipo information: entry into national phase|Ref document number: 1980900300 Country of ref document: EP |
    1981-01-28| WWP| Wipo information: published in national office|Ref document number: 1980900300 Country of ref document: EP |
    1984-08-15| WWG| Wipo information: grant in national office|Ref document number: 1980900300 Country of ref document: EP |
    优先权:
    申请号 | 申请日 | 专利标题
    CH38879||1979-01-16||
    CH388/79||1979-01-16||DE8080900300T| DE3068925D1|1979-01-16|1980-01-14|Black-liquor processing|
    NO802737A| NO156458C|1979-01-16|1980-09-15|Fremgangsmaate for behandling av kraftsvartlut og anvendelse av fremgangsmaaten for opparbeidelse av denne svartlut fra kjemisk masseomdannelse.|
    BR8005902A| BR8005902A|1979-01-16|1980-09-15|Processos de tratamento de licor preto e de formacao de polpa para materiais lignocelulosicos|
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