CA2069281C - Multi-level sulfide content pulping - Google Patents
Multi-level sulfide content pulping Download PDFInfo
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- CA2069281C CA2069281C CA 2069281 CA2069281A CA2069281C CA 2069281 C CA2069281 C CA 2069281C CA 2069281 CA2069281 CA 2069281 CA 2069281 A CA2069281 A CA 2069281A CA 2069281 C CA2069281 C CA 2069281C
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- liquor
- white liquor
- cooking
- supply
- white
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- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 title abstract description 20
- 238000004537 pulping Methods 0.000 title description 10
- 238000010411 cooking Methods 0.000 claims abstract description 74
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 59
- 239000002655 kraft paper Substances 0.000 claims abstract description 43
- 229920005610 lignin Polymers 0.000 claims abstract description 12
- 229910052717 sulfur Inorganic materials 0.000 claims description 49
- 239000011593 sulfur Substances 0.000 claims description 49
- 238000000034 method Methods 0.000 claims description 37
- 239000007789 gas Substances 0.000 claims description 23
- 239000002657 fibrous material Substances 0.000 claims description 13
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 9
- 229910000037 hydrogen sulfide Inorganic materials 0.000 claims description 9
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 8
- 238000010438 heat treatment Methods 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 4
- 239000002002 slurry Substances 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 3
- 150000002898 organic sulfur compounds Chemical class 0.000 claims 1
- 229920001021 polysulfide Polymers 0.000 abstract description 23
- 239000005077 polysulfide Substances 0.000 abstract description 23
- 150000008117 polysulfides Polymers 0.000 abstract description 23
- 239000000126 substance Substances 0.000 abstract description 22
- 150000001720 carbohydrates Chemical class 0.000 abstract description 9
- 230000015556 catabolic process Effects 0.000 abstract description 9
- 238000006731 degradation reaction Methods 0.000 abstract description 9
- 230000002708 enhancing effect Effects 0.000 abstract description 9
- 239000002023 wood Substances 0.000 abstract description 9
- 229920001131 Pulp (paper) Polymers 0.000 abstract description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 abstract description 4
- 238000006243 chemical reaction Methods 0.000 abstract description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
- 238000005470 impregnation Methods 0.000 description 20
- 230000008569 process Effects 0.000 description 19
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 9
- 229910052979 sodium sulfide Inorganic materials 0.000 description 9
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 9
- 235000014633 carbohydrates Nutrition 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 5
- 150000004056 anthraquinones Chemical class 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 3
- 238000006477 desulfuration reaction Methods 0.000 description 3
- 230000023556 desulfurization Effects 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 230000008685 targeting Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910001182 Mo alloy Inorganic materials 0.000 description 2
- 241001062472 Stokellia anisodon Species 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 229920002488 Hemicellulose Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- WHDPTDWLEKQKKX-UHFFFAOYSA-N cobalt molybdenum Chemical compound [Co].[Co].[Mo] WHDPTDWLEKQKKX-UHFFFAOYSA-N 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- VDQVEACBQKUUSU-UHFFFAOYSA-M disodium;sulfanide Chemical compound [Na+].[Na+].[SH-] VDQVEACBQKUUSU-UHFFFAOYSA-M 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- DDTIGTPWGISMKL-UHFFFAOYSA-N molybdenum nickel Chemical compound [Ni].[Mo] DDTIGTPWGISMKL-UHFFFAOYSA-N 0.000 description 1
- HEDOODBJFVUQMS-UHFFFAOYSA-N n-[2-(5-methoxy-1h-indol-3-yl)ethyl]-n-methylpropan-2-amine Chemical compound COC1=CC=C2NC=C(CCN(C)C(C)C)C2=C1 HEDOODBJFVUQMS-UHFFFAOYSA-N 0.000 description 1
- 125000001741 organic sulfur group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- -1 sulfide ions Chemical class 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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- Paper (AREA)
Abstract
Paper pulp (e.g. kraft pulp or sulfite pulp) is produced utilizing at least two different supplies of cooking liquor (e. g. white liquor), having different percentages of lignin reaction enhancing or carbohydrate degradation slowing chemicals (e.g. one having low sulfide content, and the other high sulfide content). The high sulfide content supply is typically used to impregnate the pulp, while the second supply is used in other cooking stages (whether co-current or countercurrent). At least 60%
of the sulfide of the cooking chemicals may be prodded in the first supply. Some of the sulfide in the first supply is desirably provided in the form of polysulfide or elemental sulfur. When about 2%
polysulfide on wood is utilized yield is significantly increased. Utilizing multiple chemical (e. g. sulfide) content supplies results in an optimum viscosity/kappa ratio and/or pulp strength properties for the pulp produced.
of the sulfide of the cooking chemicals may be prodded in the first supply. Some of the sulfide in the first supply is desirably provided in the form of polysulfide or elemental sulfur. When about 2%
polysulfide on wood is utilized yield is significantly increased. Utilizing multiple chemical (e. g. sulfide) content supplies results in an optimum viscosity/kappa ratio and/or pulp strength properties for the pulp produced.
Description
2~~~~~~.
t~ULTI-LEVEL SULFIDE CONTENT
BAGKGFiOUND AND SUi~iIHARX OF THfE INi~EN:CIOrI
Far many years it has been known that a higher sulfide concentration in white liquor for kraft pulping in the pulp and paper industry (i.e. higher white liquor sulfur content) could produce kraft pulp with higher viscosity and better physical properties. It has also been known that the beneficial effect of higher white liquor sulfur content is more profound in the early stages of the kraft cook than in the later stages. However in the past there have been a number of technical and practical concerns and conditions which have precluded practical utilization of these concepts.
Similarly maximum utilization has not been commercially made of the known ability of polysulfide to stabilize carbohydrates and wood against degradation during chemical pulping by oxidatively converting the reducing end groups in celluloses and hemi-cellulose to carboxylic groups.
(See U.S. patent 2,944,925.) According to the most specific aspects of the present invention, the concepts described above are utilized in a practical manner to provide kraft pulp that has an optimum viscosity/kappa ratio, and/or good strength properties, and with good yield. The invention is applicable to a wide variety of different kraft cooking processes, both batch and continuous. for example the invention can be utilized ire continuous digesters having an impregnation zone, or in cooking systems utilizing a separate impregnation vessel from the continuous digester, or in batch digesters. The invention can also be utilized in association with co-current movements of white liquor with the pulp, or countercurrent movements, such as are provided in the commercial digesting process marketed by Kamyr, Inc. of Glens Falls, New York under the trademark "MCC".
'White liquor is that treatment liquid in a kraft process which contains 'the active cooking chemicals, sodium hydroxide (NaOH) and sodium sulfide (Na2S); or white liquor in an extreme situation may contain substantially only NaOH as active ingredient. According to standard practice, the white liquor cooking sulfur content is maintained in the range of 25-35% (this overall sulfur content ratio is the amount of sodium sulfide to the sum of sodium sulfide and sodium hydroxide applied to the whole cooking process), and according to standard practice in the art, a sulfur content level below 15% results in a deterioration in the cooking rate and pulp quality. During the production of kraft pulp, residual or °'black liquor"
containing the reaction products of lignin solublization is withdrawn from the digester, concentrated, arid burned in a recovery furnace to yield an inorganic smelt of sodium carbonate and sodium sulfide. The smelt is dissolved to form green liquor which is reacted with quick lime (Ca0) to convert the sodium carbonate into sodium hydroxide and thereby regenerate the original white liquor.
According to the present invention, it has been found that by making two (or more) supplies or 2flo~2~1 streams of white liquor, with different sulfur contents, and applying them to different portions in the kraft cycle, significantly improved results can be achieved. In fact it has been found that it is highly desirable to add the majority of the sulfide in the total white liquor (total cooking chemical) -- at least about 60-90%, in fact even almost all the sulfide -- at the initial stages (e. g.
impxegnation) of the kraft cycle, while adding white liquor with primarily only sodium hydroxide at the later stages (e. g. co-current or countercurrent cooks). practicing the invention, it is possible to optimize the viscosity/kappa ratio of the produced pulp for any given level of sulfur content, and/or to optimize pulp strength properties. The increase can be dramatic, easily on the order of 25% for conventional cooks with multiple white liquor additions (co-current), about the same increase for modified continuous cooking (MCCTM), and 15% or more for extended modified continuous cooking (EMCCT~).
Comparable increases occur for batch treatment too.
When about 2% polysulfide on wood, expressed as elemental sulfur, is provided in the white liquor, a yield equal to kappa 1g-20 for a conventional kraft cook is produced with a kappa of about 12.5, and pulp with a viscosity comparable to conventional cook kraft pulp at a kappa of about 26 is produced.
Elemental sulfur (in dry or slurry form) may be used instead of polysulfide; elemental sulfur is about 60-75% as effective as polysulfide.
While the exact source of the sulfur for producing the high sulfur content stream or supply of white liquor according to the invention is not critical, one exceptionally good source that allows a practical, industrial scale process to be practiced is that shown in U.S. patent 4,929,307 wherein sulfate black liquor is heated to above the cooking temperature so as to split the macro-molecular lignin fraction, to produce sulfur containing off gases. Those off gases may be reacted to produce primarily methane and hydrogen sulfide, and then brought into contact with sulfur depleted white liquor from the normal chemical manufacturing facility o~ the pulp mill, to produce an extremely high sulfur content white liquor, the hydrogen sulfide being selectively absorbed into the white liquor. That high sulfur content white liquor may then be acted upon to produce at least some significant portions of polysulfide, and then utilized in early stages of the kraft cook.
According to one specific aspect of the present invention, a method of producing kraft pulp from cellulosic comminuted fibrous material utilizing white liquor, is provided. It comprises the following steps: (a) Making at least two streams of white liquor, including a second stream having relatively low sulfur content, and a first stream having relatively high sulfur content, substantially higher than the sulfur content of the second stream. (b) Impregnating the cellulosic comminuted fibrous material with the first stream o~ white liquor. (c) Cooking the cellulosic comminuted fibrous material under kraft coo)cing conditions, in a cooking zone with cooking chemicals to produce kraft pulp. (d) Supplying the second stream of white liquor to the cooking zone as cooking chemicals. And, (e) washing the kraft pulp produced.
According to another specific aspect of the present invention there is provided a method of producing kraft pulp comprising the following steps: (a) Treating a slurry of cellulosic fibrous material in a plurality of consecutive stages with white liquor, including at least first and second stages, using a first supply of white liquor to the first stage and a second supply to the second stage. (b) Subjecting the material treated with white liquor to cooking conditions in at least one stage of the stages to effect kraft cooking thereof, and producing black liquor. (c) Recovering sulfur from the black liquor. And, (d) adding the recovered sulfur to the first supply of white liquor to significantly increase the sulfur content thereof so that it is greater. than the sulfur content of the second supply.
According to still another specific aspect of the present invention there is provided a method of producing kraft pulp comprising the steps of: (a) Treating cellulosic comminuted fibrous material in a first stage with a first supply of white liquor.
(b) Treating the material in a second stage with a second supply of white liquor. And, (c) controlling the relative sulfur contents of the first and second supplies of white liquor so as to optimize the viscosity/kappa ratio and/or physical strength properties of the kraft pulp produced.
While the invention will primarily be described in this application with respect to kraft cooking, there is a broader aspect of the present invention.
t~ULTI-LEVEL SULFIDE CONTENT
BAGKGFiOUND AND SUi~iIHARX OF THfE INi~EN:CIOrI
Far many years it has been known that a higher sulfide concentration in white liquor for kraft pulping in the pulp and paper industry (i.e. higher white liquor sulfur content) could produce kraft pulp with higher viscosity and better physical properties. It has also been known that the beneficial effect of higher white liquor sulfur content is more profound in the early stages of the kraft cook than in the later stages. However in the past there have been a number of technical and practical concerns and conditions which have precluded practical utilization of these concepts.
Similarly maximum utilization has not been commercially made of the known ability of polysulfide to stabilize carbohydrates and wood against degradation during chemical pulping by oxidatively converting the reducing end groups in celluloses and hemi-cellulose to carboxylic groups.
(See U.S. patent 2,944,925.) According to the most specific aspects of the present invention, the concepts described above are utilized in a practical manner to provide kraft pulp that has an optimum viscosity/kappa ratio, and/or good strength properties, and with good yield. The invention is applicable to a wide variety of different kraft cooking processes, both batch and continuous. for example the invention can be utilized ire continuous digesters having an impregnation zone, or in cooking systems utilizing a separate impregnation vessel from the continuous digester, or in batch digesters. The invention can also be utilized in association with co-current movements of white liquor with the pulp, or countercurrent movements, such as are provided in the commercial digesting process marketed by Kamyr, Inc. of Glens Falls, New York under the trademark "MCC".
'White liquor is that treatment liquid in a kraft process which contains 'the active cooking chemicals, sodium hydroxide (NaOH) and sodium sulfide (Na2S); or white liquor in an extreme situation may contain substantially only NaOH as active ingredient. According to standard practice, the white liquor cooking sulfur content is maintained in the range of 25-35% (this overall sulfur content ratio is the amount of sodium sulfide to the sum of sodium sulfide and sodium hydroxide applied to the whole cooking process), and according to standard practice in the art, a sulfur content level below 15% results in a deterioration in the cooking rate and pulp quality. During the production of kraft pulp, residual or °'black liquor"
containing the reaction products of lignin solublization is withdrawn from the digester, concentrated, arid burned in a recovery furnace to yield an inorganic smelt of sodium carbonate and sodium sulfide. The smelt is dissolved to form green liquor which is reacted with quick lime (Ca0) to convert the sodium carbonate into sodium hydroxide and thereby regenerate the original white liquor.
According to the present invention, it has been found that by making two (or more) supplies or 2flo~2~1 streams of white liquor, with different sulfur contents, and applying them to different portions in the kraft cycle, significantly improved results can be achieved. In fact it has been found that it is highly desirable to add the majority of the sulfide in the total white liquor (total cooking chemical) -- at least about 60-90%, in fact even almost all the sulfide -- at the initial stages (e. g.
impxegnation) of the kraft cycle, while adding white liquor with primarily only sodium hydroxide at the later stages (e. g. co-current or countercurrent cooks). practicing the invention, it is possible to optimize the viscosity/kappa ratio of the produced pulp for any given level of sulfur content, and/or to optimize pulp strength properties. The increase can be dramatic, easily on the order of 25% for conventional cooks with multiple white liquor additions (co-current), about the same increase for modified continuous cooking (MCCTM), and 15% or more for extended modified continuous cooking (EMCCT~).
Comparable increases occur for batch treatment too.
When about 2% polysulfide on wood, expressed as elemental sulfur, is provided in the white liquor, a yield equal to kappa 1g-20 for a conventional kraft cook is produced with a kappa of about 12.5, and pulp with a viscosity comparable to conventional cook kraft pulp at a kappa of about 26 is produced.
Elemental sulfur (in dry or slurry form) may be used instead of polysulfide; elemental sulfur is about 60-75% as effective as polysulfide.
While the exact source of the sulfur for producing the high sulfur content stream or supply of white liquor according to the invention is not critical, one exceptionally good source that allows a practical, industrial scale process to be practiced is that shown in U.S. patent 4,929,307 wherein sulfate black liquor is heated to above the cooking temperature so as to split the macro-molecular lignin fraction, to produce sulfur containing off gases. Those off gases may be reacted to produce primarily methane and hydrogen sulfide, and then brought into contact with sulfur depleted white liquor from the normal chemical manufacturing facility o~ the pulp mill, to produce an extremely high sulfur content white liquor, the hydrogen sulfide being selectively absorbed into the white liquor. That high sulfur content white liquor may then be acted upon to produce at least some significant portions of polysulfide, and then utilized in early stages of the kraft cook.
According to one specific aspect of the present invention, a method of producing kraft pulp from cellulosic comminuted fibrous material utilizing white liquor, is provided. It comprises the following steps: (a) Making at least two streams of white liquor, including a second stream having relatively low sulfur content, and a first stream having relatively high sulfur content, substantially higher than the sulfur content of the second stream. (b) Impregnating the cellulosic comminuted fibrous material with the first stream o~ white liquor. (c) Cooking the cellulosic comminuted fibrous material under kraft coo)cing conditions, in a cooking zone with cooking chemicals to produce kraft pulp. (d) Supplying the second stream of white liquor to the cooking zone as cooking chemicals. And, (e) washing the kraft pulp produced.
According to another specific aspect of the present invention there is provided a method of producing kraft pulp comprising the following steps: (a) Treating a slurry of cellulosic fibrous material in a plurality of consecutive stages with white liquor, including at least first and second stages, using a first supply of white liquor to the first stage and a second supply to the second stage. (b) Subjecting the material treated with white liquor to cooking conditions in at least one stage of the stages to effect kraft cooking thereof, and producing black liquor. (c) Recovering sulfur from the black liquor. And, (d) adding the recovered sulfur to the first supply of white liquor to significantly increase the sulfur content thereof so that it is greater. than the sulfur content of the second supply.
According to still another specific aspect of the present invention there is provided a method of producing kraft pulp comprising the steps of: (a) Treating cellulosic comminuted fibrous material in a first stage with a first supply of white liquor.
(b) Treating the material in a second stage with a second supply of white liquor. And, (c) controlling the relative sulfur contents of the first and second supplies of white liquor so as to optimize the viscosity/kappa ratio and/or physical strength properties of the kraft pulp produced.
While the invention will primarily be described in this application with respect to kraft cooking, there is a broader aspect of the present invention.
According to the broadest aspect of the present invention, any lignin reaction enhancing or carbohydrate degradation slowing chemicals are targeted to one or more specific parts of the cook, such as the impregnation, co-current, or countercurrent stages. Thus the invention is applicable not just to kraft white liquor, but to sulfite process cooking liquors (containing a cationic base), anthraquinone, derivatives of or equivalents to anthraquinone, or the like. The anthraquinone may replace all or some of the sodium sulfide in a cooking liquor containing NaOH, or may be used in other liquor compositions.
According to the broadest aspect of the present invention, a method of treating comminuted cellulosic fibrous material with cooking Liquor to obtain cellulasic pulp, is provided. The method comprises the following steps: (a) Providing at least first and second cooking liquors, including a first cooking liquor having a first concentration of lignin enhancing or carbohydrate degradation slowing chemical, and a second cooking liquor having a second concentration of that lignin enhancing or carbohydrate degradation slowing chemical, the second concentration being from zero to much less than the first concentration. (b) Cooking the comminuted cellulosic fibrous material in several cook stages. (c) Targeting the first cooking liquor to one or more, but less than all, of the cook stages, to provide cooking liquor for that one or more stages; and (d) utilizing the second cooking liquor in at least one cook stage in which the first cooking liquor is not utilized.
The cooking liquor utilized above may be a kraft cooking liquor, sulfite cooking liquor, or the like. It may contain a cationic base, sodium sulfide, anthraquinone or its derivatives or equivalents, or the like, and the first liquor may be targeted to an impregnation stage, co-current cook stage, or countercurrent cook stage.
It is the primary object of the present invention to provide a substantially improved cook cycle for the production of paper pulp. This and other objects of the invention will become clear from an inspection of the detailed description of the invention, and from the appended claims.
DRIEF DESCRIPTION OF TPIE DRAWING
FIGURE 1 is a schematic view of exemplary apparatus for practicing an exemplary method according to the present invention.
DETAILED DESCRIPTION OF TAE DRAWING
FIGURE 1 illustrates exemplary apparatus for use in a kraft pulping process. However, as indicated above, the invention is applicable to other processes for the production of paper pulp from comminuted cellulosic fibrous material in which any lignin reaction enhancing or carbohydrate degradation slowing chemicals are targeted to one or more specific parts of the cook, such as the impregnation, co-current, or countercurrent stages.
In a typical kraft pulping process, as illustrated in FIGURE 1, a digester 12 -- which preferably is a continuous digester such as that sold by Kamyr, Inc. of Glens Falls, New York, but may be a batch digester -- has a stream of off gases 13, and blac)c liquor (residual white liquor containing the reaction products of lignin solubilization) is withdrawn at an intermediate position as indicated at 14, while the kraft pulp produced is discharged at 15. When the black liquor in line 1~ is discharged, it may be passed directly to black liquor evaporators, and preferably it is subjected, somewhere in the evaporator chain, 'to a heat treatment process at step 17 to produce off gases in line 18. The heat treatment of block 17 is preferably that described in U.S. patent 4,929,307.
After heat treatment at 17 the black liquor passes to evaporators 19 (evaporators 19' may concentrate the black liquor before heat treatment 17 too), which also produce off gases in line 20, then to a conventional recovery boiler 22, with conventional white liquor manufacture at block 23, to produce white liquor in line 24 having depleted sulfur content.
The off gases in line 18 -- which may include only those from the heat treatment 17, or also those from the digester line 13, only and from the black liquor evaporators in line 20, or a combination of any two of them -- are preferably first subjected to a drying or absorption stage (as indicated schematically at 27 in FIGURE 1) in order to remove a majority of the water vapor. The removal of the water vapor increases the concentration of organic sulfur gases. Step 27 is accomplished by drying the gas stream by any conventional means and/or by absorbing or adsorbing the organic portion of the gas onto a solid, or additionally by absorbing the off gas into one of any non-polar liquids (e. g.
kerosene or mineral oil). Treatment may be provided of a liquid mixture, but preferably according to the invention further treatment is of the concentrated gas.
The next steps in the treatment of the off gases as illustrated in FIGURE 1 are to add hydrogen, and then pass the gas in the presence of the added hydrogen past a hydrogen desulfurization catalyst. This may be accomplished, for example, in the hydrogen desulfurization (HDS) unit 28, with the hydrogen gas from line 29 added to the unit 28 along with the gas in line 18. The hydrogen gas in line 2.9 can come from any source (e.g. be purchased , from water electroylsis, etc.), It is preferred that the hydrogen desulfurization catalyst consist essentially of a transition metal-molybdenum alloy, particularly a nickel molybdenum or cobalt molybdenum alloy.
Typically, in gaseous processing, the product gas stream in line 30 is further acted upon. The gas stream in line 3Q contains primarily methane, and hydrogen sulfide, with hydrogen also present.
Preferably the hydrogen sulfide is then separated out from the gas in stream 30. While the hydrogen sulfide may be separated as a gas and then used in its gaseous form in conventional pulping techniques, it may be fed to a scrubber 32 in which it is brought into contact with a caustic solution, preferably kraft white liquor, which contains sodium hydroxide and most likely at least some sodium ~~~~2~1 to sulfide. While in the preferred embodiment illustrated in the drawings white liquor is utilized, under some circumstances green liquor may be advantageously utilized, with white liquor subsequently made from the green liquor.
White liquor from line 24 is passed into inlet 33 of scrubber 32, the hydrogen sulfide being absorbed in the white liquor and thereby significantly enhancing its sulfur content. The significantly enhanced sulfur content white liquor then passes through the outlet 34 of the scrubber into line 35, to be used in the pulping process.
Desirably, the white liquor in line 35 passes through a polysulfide treatment stage, as illustrated at 36, and then to the impregnation vessel 37 (if a separate impregnation vessel is used)'or the like, to be utilized in the pulping cycle. Elemental sulfur may be added at 36 instead of polysulfide.
The gas stream that remains, in line 38, contains primarily methane, but also some hydrogen.
Ultimately, the gas in line 38 may become the source of. the hydrogen for line 29.
According to the invention, the high sulfur content white liquor in lina 35 is provided at an early stage of the cook, e. g. at the beginning of 'the impregnation vessel 37, or impregnation stage if impregnation takes place in the digester 12 itself, or at multiple places in the impregnation zone and/or vessel 37. A countercurrent impregnation flow may be provided, in which case the higher sulfur content liquor is added near the end of the impregnation stage. Part of the sulfide depleted white liquor in line 24 is passed unto line 41, and it is then introduced into the cook, preferably at multiple locations, as indicated at 42 and 43 in FIGURE 1.
according to the invention, where the low sulfur content white liquor in line 41 is introduced into the kraft cook may vary widely. For example, it may be added to the middle of the impregnation vessel 37, at one, two, or more co-current stages in the digester 12, or at one, two, or more countercurrent stages in the digester 12 (e.g. for modified continuous cooking, ox extended modified continuous cooking). Of course, the liquor in line 41 may also be utilized in a batch process.
While -the drawing illustrates only two streams or supplies of white liquor, 35, 41, having different sulfur content, as many different sulfur content streams as desired may be produced. For example 'two series connected units 32 may be utilized, the first producing the highest sulfur content level white liquor, while the second produces an intermediate (between lines 35 and 41) sulfur content level white liquor. The intermediate sufidity white liquor is added earlier in the cook than the white liquor in line 41.
The relative amount of sulfur content of the white liquor added at various stages within the kraft cycle may also be varied widely according to the invention. For example, if the kraft. pulping process is to be a mufti-level conventional cook, that is white liquor is added at two or more points in the cook and flows co-currently with the pulp, then about 60% of the total cooking chemical is added to the impregnation vessel (e. g. in line 35), while about 2'5% is added to the first co-current stage (e. g. at 42) and about 15% to the second co-current stage (e. g. at 43). In this procedure, preferably the amount of sulfide provided in line 35 is about 60--90%, and if practical may be almost 100%
of the total sulfide in all of the white liquor streams, that is the white liquor in stream 41 is substantially fully sulfide depleted. The stream in line 35 in this embodiment may be made by manufactured by passing 35-65% of the total volume of white liquor through the unit 32, the remaining 65--35% of the white liquor being added through line 41. According to another embodiment, about 35% of the total volume of white liquor is passed through unit 32, and this high sulfur content white liquor is then added to the top circulation in the conventional impregnation vessel 37. The sulfide-depleted white liquor in line 41 is added to middle circtalation in the vessel 37 in the amount of about 25-35% of the total cooking chemical from white liquor, while about 20-25% of the total cooking chemical, in the sulfide depleted white liquor in line 41, is added to the continuous digester 12 first cooking circulation.
The low sodium sulfide content liquor in line 41 may also be added at 44 to an oxygen delignification or bleaching stage 45 as a source of sodium hydroxide.
When utilizing the multiple level sulphitiy white liquors according to the invention in modified continuous cooking and extended modified continuous cooking sequences, the viscosity to kappa ratio may ~~~2~~.
be increased by about 0.?,-0.3 units if almost all sulfide is added to the impregnation stage (e.g. in line 35 to vessel 37). Preferably at least about 60% (e.g. 60-90%) of the total sulfur content is added in the impregnation stage (line 35), the total volume of white liquor added in line 35 being about 40-65% of the total volume of white liquor used in the pulping process.
In stage 36, polysulfide is added to the white liquor. For example, this can be done by the MOXY
(TM) process in which some of the sodium sulfide in the white liquor is partially oxidized to produce polysulfide, or by other known polysulfide processes. Alternatively, in stage 35 polysulfide from an external source may merely be introduced into the white liquor, e.g. polysulfide groduced by reacting elemental sulfur with sulfide ions in an aqueous solution under proper conditions; or elemental sulfur may be added to the white liquor instead of polysulfide.
The amount of polysulfide produced, or added, in stage 36 is about 0.5%-8% on wood, expressed as elemental sulfur. Typically, about 2% polysulfide is desirable. If 2% polysulfide is used in conjunction with extended modified continuous cooking, a kraft pulp with a kappa of about 12.5, a viscosity of about 33.7 cp, and a yield of about 44.6% can be made. This yield is equal to that of a conventional cook or extended modified continuous cook pulp at a kappa of about 18-20 without polysulfide, and the viscosity is equivalent to that of a conventional cook pulp at kappa 26, or an extended modified continuous cook pulp at kappa 17.
_2~~~28~
If an amount of elemental sulfur equivalent to about 0.5-8% polysulfide is used, the results are about 60-75% as good as when polysulfide is used.
Utilizing the apparatus schematically illustrated in the drawings, various methods may be practiced according to the invention. According to one method:
(a) Two (or more) streams of white liquor, 35, 41, are made up, the first stream (35) having relatively high sulfur content, and the second (41) relatively low sulfur content (even approaching zero).
(b) Cellulosic comminuted fibrous material (e. g. wood chips) are impregnated with the first stream 35 (e. g. in vessel 37).
(c) The material is cooked under kraft cooking conditions, in a cooking zone (in vessel 12) with cooking chemicals (the sodium hydroxide and sodium sulfide in the white liquor) to produce kraft pulp.
(d) The second stream, 41, of white liquor is supplied to the cooking zone (e.g. digester 12) as cooking chemicals; and (e) the kraft pulp is washed (e. g. in a wash zone in digester 12, and/or in a separate wash vessel).
According to another aspect of the invention, a slurry of wood chips is treated in a plurality of consecutive stages (e. g. impregnation stage, first and second co-current or countercurrent cooking stages) with white liquor using first and second supplies, differing in the sulfur content thereof.
The chips are treated with white liquor under cooking conditions (e. g. in digester 12) in at least one stage, to effect kraft cooking thereof. Slack.
liquor is withdrawn (at 14) and sulfur is recovered from the black licyuor, as by heating treating it (at 17) according to the process of US Patent 4,929,307, evaporating it (in 19), etc. (see 22 and 23 in FIGURE 1). The recovered sulfur is added to the first supply of white liquor, as in unit 32, to significantly increase the sulfur content thereof, so that the sulfur content'of the liquor in line 35 is substantially greater than that in line 24 (which is sulfur depleted, and may be near zero). The relative sulfur contents of the white liquors in lines 35 and 24 are controlled so as to optimize the viscosity/kappa ratio and/or physical strength properties.
The invention allows advantageous production of kraft pulp to be practiced on an industrial scale --that is, larger production than reasonably possible in a laboratory, with complete chemical recovery.
The invention may be illustrated by various examples.
Tables IA-IE provide the results of laboratory batch cooks using split white liquor streams with variable sulfur content, according to the invention, and conventional cooks for comparison purposes. In these tables, "CK" means conventional kraft cooking, "MCK" means kraft cooking with multiple introductions of white liquor, with more than one co-current cooking stage, "MCC" refers to Kamyr, Int.'s trademarked modified continuous cooking process in which multiple introductions of white liquor are provided, and a countercurrent cook stage, and "EMCC" refers to Kamyr, Inc.'s trademarked extended modified continuous coolc9.ng process in which a second countercurrent cook is provided.
Table II illustrates the advantages achieved when polysulfide is used. The liquid to wood ratio for all cooks in Table II is 4/1. "Sulfidity"
refers to sodium sulfide content.
The wood utilized in all of TABLES IA-E and II
is southern pins from the Mississippi area.
However, the results are applicable to a wide variety of wood species.
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P~8F8T~bMI tiB 8 Tim~, mia 110 110 110 110 110 C
T~a~pezatury I S6-66dui VHb J c6 H6.
a 30 30 30 30 30 30 Tita~, miry 110 110 110 :L10 110 110 ' Tamperetturov 150 150 150 9.50 150 li ~
g~e~auzo, p8lg e 3.nitial ~7~~ ~ Na~N $1'd 25 Initial lib, ~ Na2D 5 73.5 62.5 62.5 62.5 52 5x.6 8ulfidity, ~ on bR . 2 2 3 2n0 gb ~ 5 min, ~ teac~H 0 ld.~ 15.9 6 22 15.7 ttea~l~u~nl fib, g/~ t~a2~ . . 1.9 2.6 -8 1 1.6 . H,csi~. p~lysulfi~~, gll~.
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Tit~~ bt max, min 6 5 5 g ~
t Ha~F~ _ - d.?5 5.85 ~A, ~ Ha2~ 0 0 O 0 0 0 sulfidity, ~ 8.5 1d.0 8.0 10.Z 9.6 R~si0ual ~by g!L NAZD
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As can be seen from the above examples, the method according to the invention optimizes the viscosity/kappa ratio and/or strength properties of kraft pulp produced, and achieves other advantageous results. The utilization of polysulfide or elemental sulfur as part of the sulfide content of the white liquor also significantly increases yield.
While the Tables describe the results of kraf_t cooks, and white liquor, the invention is applicable to other cooking processes and cooking liquors for the production of paper pulp. With sulfite cooking liquor, and when using other lignin reaction enhancing or carbohydrate degradation slowing chemicals, such as anthraquinone or its derivatives or equivalents, or the like, significant increases in viscosity/kappa ratio or pulp strength properties can be obtained by targeting one cooking liquor to a specific stage (or stages) of the cook, while another cooking liquor is used in other portions.
In general, a method is provided in which comrninuted cellulosic fibrous material is treated with cooking liquor to obtain cellulosic pulp in the following steps: (a) Providing at least .first and second cooking liquors, including a first cooking liquor having a first concentration of lignin enhancing or carbohydrate degradation slowing chemical (e. g. in line 3~) , and a second cooking liquor (e. g. in line 41) having a second concentration of that lignin enhancing or carbohydrate degradation slowing chemical, the second concentration being from zero to much less than the first concentration. (b) Cooking the comminuted cellulosic fibrous material in several 2~~~~8.~
cook stages {e. g. in vessels 12, 37). {c) Targeting the first cooking liquor to one or more, but less than all, of the cook stages, to provide cooking liquor for that one or more stages (e.g. to the co-current impregnation stage in vessel 37). And (d) utilizing the second cooking liquor in at least one cook stage in which the first cooking liquor is not utilized {e. g. introducing it at 42., 43 into co-current or countercurrent cook stages).
While the invention has been herein shown and described in what is presently conceived to be the most practical embodiment thereof, it will be appreciated by those in the art that many modifications may be made thereof within the scope of the invention, which scope is to be accorded the broadest interpretation of the appended claims so as to encompass all equivalent methods and procedures.
a
According to the broadest aspect of the present invention, a method of treating comminuted cellulosic fibrous material with cooking Liquor to obtain cellulasic pulp, is provided. The method comprises the following steps: (a) Providing at least first and second cooking liquors, including a first cooking liquor having a first concentration of lignin enhancing or carbohydrate degradation slowing chemical, and a second cooking liquor having a second concentration of that lignin enhancing or carbohydrate degradation slowing chemical, the second concentration being from zero to much less than the first concentration. (b) Cooking the comminuted cellulosic fibrous material in several cook stages. (c) Targeting the first cooking liquor to one or more, but less than all, of the cook stages, to provide cooking liquor for that one or more stages; and (d) utilizing the second cooking liquor in at least one cook stage in which the first cooking liquor is not utilized.
The cooking liquor utilized above may be a kraft cooking liquor, sulfite cooking liquor, or the like. It may contain a cationic base, sodium sulfide, anthraquinone or its derivatives or equivalents, or the like, and the first liquor may be targeted to an impregnation stage, co-current cook stage, or countercurrent cook stage.
It is the primary object of the present invention to provide a substantially improved cook cycle for the production of paper pulp. This and other objects of the invention will become clear from an inspection of the detailed description of the invention, and from the appended claims.
DRIEF DESCRIPTION OF TPIE DRAWING
FIGURE 1 is a schematic view of exemplary apparatus for practicing an exemplary method according to the present invention.
DETAILED DESCRIPTION OF TAE DRAWING
FIGURE 1 illustrates exemplary apparatus for use in a kraft pulping process. However, as indicated above, the invention is applicable to other processes for the production of paper pulp from comminuted cellulosic fibrous material in which any lignin reaction enhancing or carbohydrate degradation slowing chemicals are targeted to one or more specific parts of the cook, such as the impregnation, co-current, or countercurrent stages.
In a typical kraft pulping process, as illustrated in FIGURE 1, a digester 12 -- which preferably is a continuous digester such as that sold by Kamyr, Inc. of Glens Falls, New York, but may be a batch digester -- has a stream of off gases 13, and blac)c liquor (residual white liquor containing the reaction products of lignin solubilization) is withdrawn at an intermediate position as indicated at 14, while the kraft pulp produced is discharged at 15. When the black liquor in line 1~ is discharged, it may be passed directly to black liquor evaporators, and preferably it is subjected, somewhere in the evaporator chain, 'to a heat treatment process at step 17 to produce off gases in line 18. The heat treatment of block 17 is preferably that described in U.S. patent 4,929,307.
After heat treatment at 17 the black liquor passes to evaporators 19 (evaporators 19' may concentrate the black liquor before heat treatment 17 too), which also produce off gases in line 20, then to a conventional recovery boiler 22, with conventional white liquor manufacture at block 23, to produce white liquor in line 24 having depleted sulfur content.
The off gases in line 18 -- which may include only those from the heat treatment 17, or also those from the digester line 13, only and from the black liquor evaporators in line 20, or a combination of any two of them -- are preferably first subjected to a drying or absorption stage (as indicated schematically at 27 in FIGURE 1) in order to remove a majority of the water vapor. The removal of the water vapor increases the concentration of organic sulfur gases. Step 27 is accomplished by drying the gas stream by any conventional means and/or by absorbing or adsorbing the organic portion of the gas onto a solid, or additionally by absorbing the off gas into one of any non-polar liquids (e. g.
kerosene or mineral oil). Treatment may be provided of a liquid mixture, but preferably according to the invention further treatment is of the concentrated gas.
The next steps in the treatment of the off gases as illustrated in FIGURE 1 are to add hydrogen, and then pass the gas in the presence of the added hydrogen past a hydrogen desulfurization catalyst. This may be accomplished, for example, in the hydrogen desulfurization (HDS) unit 28, with the hydrogen gas from line 29 added to the unit 28 along with the gas in line 18. The hydrogen gas in line 2.9 can come from any source (e.g. be purchased , from water electroylsis, etc.), It is preferred that the hydrogen desulfurization catalyst consist essentially of a transition metal-molybdenum alloy, particularly a nickel molybdenum or cobalt molybdenum alloy.
Typically, in gaseous processing, the product gas stream in line 30 is further acted upon. The gas stream in line 3Q contains primarily methane, and hydrogen sulfide, with hydrogen also present.
Preferably the hydrogen sulfide is then separated out from the gas in stream 30. While the hydrogen sulfide may be separated as a gas and then used in its gaseous form in conventional pulping techniques, it may be fed to a scrubber 32 in which it is brought into contact with a caustic solution, preferably kraft white liquor, which contains sodium hydroxide and most likely at least some sodium ~~~~2~1 to sulfide. While in the preferred embodiment illustrated in the drawings white liquor is utilized, under some circumstances green liquor may be advantageously utilized, with white liquor subsequently made from the green liquor.
White liquor from line 24 is passed into inlet 33 of scrubber 32, the hydrogen sulfide being absorbed in the white liquor and thereby significantly enhancing its sulfur content. The significantly enhanced sulfur content white liquor then passes through the outlet 34 of the scrubber into line 35, to be used in the pulping process.
Desirably, the white liquor in line 35 passes through a polysulfide treatment stage, as illustrated at 36, and then to the impregnation vessel 37 (if a separate impregnation vessel is used)'or the like, to be utilized in the pulping cycle. Elemental sulfur may be added at 36 instead of polysulfide.
The gas stream that remains, in line 38, contains primarily methane, but also some hydrogen.
Ultimately, the gas in line 38 may become the source of. the hydrogen for line 29.
According to the invention, the high sulfur content white liquor in lina 35 is provided at an early stage of the cook, e. g. at the beginning of 'the impregnation vessel 37, or impregnation stage if impregnation takes place in the digester 12 itself, or at multiple places in the impregnation zone and/or vessel 37. A countercurrent impregnation flow may be provided, in which case the higher sulfur content liquor is added near the end of the impregnation stage. Part of the sulfide depleted white liquor in line 24 is passed unto line 41, and it is then introduced into the cook, preferably at multiple locations, as indicated at 42 and 43 in FIGURE 1.
according to the invention, where the low sulfur content white liquor in line 41 is introduced into the kraft cook may vary widely. For example, it may be added to the middle of the impregnation vessel 37, at one, two, or more co-current stages in the digester 12, or at one, two, or more countercurrent stages in the digester 12 (e.g. for modified continuous cooking, ox extended modified continuous cooking). Of course, the liquor in line 41 may also be utilized in a batch process.
While -the drawing illustrates only two streams or supplies of white liquor, 35, 41, having different sulfur content, as many different sulfur content streams as desired may be produced. For example 'two series connected units 32 may be utilized, the first producing the highest sulfur content level white liquor, while the second produces an intermediate (between lines 35 and 41) sulfur content level white liquor. The intermediate sufidity white liquor is added earlier in the cook than the white liquor in line 41.
The relative amount of sulfur content of the white liquor added at various stages within the kraft cycle may also be varied widely according to the invention. For example, if the kraft. pulping process is to be a mufti-level conventional cook, that is white liquor is added at two or more points in the cook and flows co-currently with the pulp, then about 60% of the total cooking chemical is added to the impregnation vessel (e. g. in line 35), while about 2'5% is added to the first co-current stage (e. g. at 42) and about 15% to the second co-current stage (e. g. at 43). In this procedure, preferably the amount of sulfide provided in line 35 is about 60--90%, and if practical may be almost 100%
of the total sulfide in all of the white liquor streams, that is the white liquor in stream 41 is substantially fully sulfide depleted. The stream in line 35 in this embodiment may be made by manufactured by passing 35-65% of the total volume of white liquor through the unit 32, the remaining 65--35% of the white liquor being added through line 41. According to another embodiment, about 35% of the total volume of white liquor is passed through unit 32, and this high sulfur content white liquor is then added to the top circulation in the conventional impregnation vessel 37. The sulfide-depleted white liquor in line 41 is added to middle circtalation in the vessel 37 in the amount of about 25-35% of the total cooking chemical from white liquor, while about 20-25% of the total cooking chemical, in the sulfide depleted white liquor in line 41, is added to the continuous digester 12 first cooking circulation.
The low sodium sulfide content liquor in line 41 may also be added at 44 to an oxygen delignification or bleaching stage 45 as a source of sodium hydroxide.
When utilizing the multiple level sulphitiy white liquors according to the invention in modified continuous cooking and extended modified continuous cooking sequences, the viscosity to kappa ratio may ~~~2~~.
be increased by about 0.?,-0.3 units if almost all sulfide is added to the impregnation stage (e.g. in line 35 to vessel 37). Preferably at least about 60% (e.g. 60-90%) of the total sulfur content is added in the impregnation stage (line 35), the total volume of white liquor added in line 35 being about 40-65% of the total volume of white liquor used in the pulping process.
In stage 36, polysulfide is added to the white liquor. For example, this can be done by the MOXY
(TM) process in which some of the sodium sulfide in the white liquor is partially oxidized to produce polysulfide, or by other known polysulfide processes. Alternatively, in stage 35 polysulfide from an external source may merely be introduced into the white liquor, e.g. polysulfide groduced by reacting elemental sulfur with sulfide ions in an aqueous solution under proper conditions; or elemental sulfur may be added to the white liquor instead of polysulfide.
The amount of polysulfide produced, or added, in stage 36 is about 0.5%-8% on wood, expressed as elemental sulfur. Typically, about 2% polysulfide is desirable. If 2% polysulfide is used in conjunction with extended modified continuous cooking, a kraft pulp with a kappa of about 12.5, a viscosity of about 33.7 cp, and a yield of about 44.6% can be made. This yield is equal to that of a conventional cook or extended modified continuous cook pulp at a kappa of about 18-20 without polysulfide, and the viscosity is equivalent to that of a conventional cook pulp at kappa 26, or an extended modified continuous cook pulp at kappa 17.
_2~~~28~
If an amount of elemental sulfur equivalent to about 0.5-8% polysulfide is used, the results are about 60-75% as good as when polysulfide is used.
Utilizing the apparatus schematically illustrated in the drawings, various methods may be practiced according to the invention. According to one method:
(a) Two (or more) streams of white liquor, 35, 41, are made up, the first stream (35) having relatively high sulfur content, and the second (41) relatively low sulfur content (even approaching zero).
(b) Cellulosic comminuted fibrous material (e. g. wood chips) are impregnated with the first stream 35 (e. g. in vessel 37).
(c) The material is cooked under kraft cooking conditions, in a cooking zone (in vessel 12) with cooking chemicals (the sodium hydroxide and sodium sulfide in the white liquor) to produce kraft pulp.
(d) The second stream, 41, of white liquor is supplied to the cooking zone (e.g. digester 12) as cooking chemicals; and (e) the kraft pulp is washed (e. g. in a wash zone in digester 12, and/or in a separate wash vessel).
According to another aspect of the invention, a slurry of wood chips is treated in a plurality of consecutive stages (e. g. impregnation stage, first and second co-current or countercurrent cooking stages) with white liquor using first and second supplies, differing in the sulfur content thereof.
The chips are treated with white liquor under cooking conditions (e. g. in digester 12) in at least one stage, to effect kraft cooking thereof. Slack.
liquor is withdrawn (at 14) and sulfur is recovered from the black licyuor, as by heating treating it (at 17) according to the process of US Patent 4,929,307, evaporating it (in 19), etc. (see 22 and 23 in FIGURE 1). The recovered sulfur is added to the first supply of white liquor, as in unit 32, to significantly increase the sulfur content thereof, so that the sulfur content'of the liquor in line 35 is substantially greater than that in line 24 (which is sulfur depleted, and may be near zero). The relative sulfur contents of the white liquors in lines 35 and 24 are controlled so as to optimize the viscosity/kappa ratio and/or physical strength properties.
The invention allows advantageous production of kraft pulp to be practiced on an industrial scale --that is, larger production than reasonably possible in a laboratory, with complete chemical recovery.
The invention may be illustrated by various examples.
Tables IA-IE provide the results of laboratory batch cooks using split white liquor streams with variable sulfur content, according to the invention, and conventional cooks for comparison purposes. In these tables, "CK" means conventional kraft cooking, "MCK" means kraft cooking with multiple introductions of white liquor, with more than one co-current cooking stage, "MCC" refers to Kamyr, Int.'s trademarked modified continuous cooking process in which multiple introductions of white liquor are provided, and a countercurrent cook stage, and "EMCC" refers to Kamyr, Inc.'s trademarked extended modified continuous coolc9.ng process in which a second countercurrent cook is provided.
Table II illustrates the advantages achieved when polysulfide is used. The liquid to wood ratio for all cooks in Table II is 4/1. "Sulfidity"
refers to sodium sulfide content.
The wood utilized in all of TABLES IA-E and II
is southern pins from the Mississippi area.
However, the results are applicable to a wide variety of wood species.
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TABLE II
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P~8F8T~bMI tiB 8 Tim~, mia 110 110 110 110 110 C
T~a~pezatury I S6-66dui VHb J c6 H6.
a 30 30 30 30 30 30 Tita~, miry 110 110 110 :L10 110 110 ' Tamperetturov 150 150 150 9.50 150 li ~
g~e~auzo, p8lg e 3.nitial ~7~~ ~ Na~N $1'd 25 Initial lib, ~ Na2D 5 73.5 62.5 62.5 62.5 52 5x.6 8ulfidity, ~ on bR . 2 2 3 2n0 gb ~ 5 min, ~ teac~H 0 ld.~ 15.9 6 22 15.7 ttea~l~u~nl fib, g/~ t~a2~ . . 1.9 2.6 -8 1 1.6 . H,csi~. p~lysulfi~~, gll~.
C~CtIRFL~~tT BTDsO~:
61 d0 60 ?3 ?5 b0 T~tal tl~~v mid 16d 1a5 16d 1?0 1?0 165 ~ d5 d5 d5 d5 d5 d5 ~iax ta~lpe~atura~
Tit~~ bt max, min 6 5 5 g ~
t Ha~F~ _ - d.?5 5.85 ~A, ~ Ha2~ 0 0 O 0 0 0 sulfidity, ~ 8.5 1d.0 8.0 10.Z 9.6 R~si0ual ~by g!L NAZD
GL~ClI~~~P'iT 8'I'b~~ I o T a Time, minv _ 1?O 1?~
~ro~p~ra~ur~/ C" ~ 2.85 3.1.5 sb~ % ~ta2G ~ ' 0 0 8ultit~ity ~
CntDNT~RCURRBI~T BTACU~ r t 2d0 2d0 Zd0 2d0 Ti~tg, miTi 16d 150 16d = m 165 ' C 35. 15. 15. ~ 0 15 ~
Tompa~aDura, 3 ~ d v~oQ
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Hullidity, ~ _ _ 9 13 ix 12 . O
11 . .
o 0 ~~0 9/L 88 t'iaOFi . 16 0.16_ a 0.16 ~laplacamantv Llmin. . . d a ~ 38~~
d 36 Displacac! volume. L . . .
~laDlae~mant ~taai~ubl t 60 minut~a, ~b g/L NaZD 6.9 10.d _ 0 1Z0 aaix~utea, ~b g/L ?.6 9.9. .. ~.
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, a.? ~.s 9.s ~!L ~aoa x fact~z 2'733 2239 2695 1935 29d?
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As can be seen from the above examples, the method according to the invention optimizes the viscosity/kappa ratio and/or strength properties of kraft pulp produced, and achieves other advantageous results. The utilization of polysulfide or elemental sulfur as part of the sulfide content of the white liquor also significantly increases yield.
While the Tables describe the results of kraf_t cooks, and white liquor, the invention is applicable to other cooking processes and cooking liquors for the production of paper pulp. With sulfite cooking liquor, and when using other lignin reaction enhancing or carbohydrate degradation slowing chemicals, such as anthraquinone or its derivatives or equivalents, or the like, significant increases in viscosity/kappa ratio or pulp strength properties can be obtained by targeting one cooking liquor to a specific stage (or stages) of the cook, while another cooking liquor is used in other portions.
In general, a method is provided in which comrninuted cellulosic fibrous material is treated with cooking liquor to obtain cellulosic pulp in the following steps: (a) Providing at least .first and second cooking liquors, including a first cooking liquor having a first concentration of lignin enhancing or carbohydrate degradation slowing chemical (e. g. in line 3~) , and a second cooking liquor (e. g. in line 41) having a second concentration of that lignin enhancing or carbohydrate degradation slowing chemical, the second concentration being from zero to much less than the first concentration. (b) Cooking the comminuted cellulosic fibrous material in several 2~~~~8.~
cook stages {e. g. in vessels 12, 37). {c) Targeting the first cooking liquor to one or more, but less than all, of the cook stages, to provide cooking liquor for that one or more stages (e.g. to the co-current impregnation stage in vessel 37). And (d) utilizing the second cooking liquor in at least one cook stage in which the first cooking liquor is not utilized {e. g. introducing it at 42., 43 into co-current or countercurrent cook stages).
While the invention has been herein shown and described in what is presently conceived to be the most practical embodiment thereof, it will be appreciated by those in the art that many modifications may be made thereof within the scope of the invention, which scope is to be accorded the broadest interpretation of the appended claims so as to encompass all equivalent methods and procedures.
a
Claims (4)
1. A method of producing kraft pulp by cooking comminuted cellulosic fibrous material with white liquor to produce kraft pulp and black liquor, comprising the steps of:
(a) treating a slurry of cellulosic fibrous material in a plurality of consecutive stages with white liquor, including at least first and second stages, using a first supply of white liquor on the first stage and a second supply of white liquor on another stage;
(b) subjecting the material treated with white liquor to cooking conditions in at least one of the stages to effect kraft cooking thereof, and producing black liquor;
(c) removing and treating sulfur from the black liquor and making at least two streams of white liquors from the remaining black liquor, and wherein the second stream of white liquor is used as the second supply of white liquor;
(d) adding the treated sulfur to the first stream of white liquor to produce the first supply of white liquor with a sulfur content greater than the sulfur content of the second supply of white liquor; and wherein steps (a), (c) and (d) are practiced by: (i) heating the black liquor at a temperature and for a time period such that off gases containing organic sulfur compounds are produced; (ii) treating the off gases from step (i) to produce primarily hydrogen sulfide and methane; and (iii) using the hydrogen sulfide to produce the first supply of white liquor.
(a) treating a slurry of cellulosic fibrous material in a plurality of consecutive stages with white liquor, including at least first and second stages, using a first supply of white liquor on the first stage and a second supply of white liquor on another stage;
(b) subjecting the material treated with white liquor to cooking conditions in at least one of the stages to effect kraft cooking thereof, and producing black liquor;
(c) removing and treating sulfur from the black liquor and making at least two streams of white liquors from the remaining black liquor, and wherein the second stream of white liquor is used as the second supply of white liquor;
(d) adding the treated sulfur to the first stream of white liquor to produce the first supply of white liquor with a sulfur content greater than the sulfur content of the second supply of white liquor; and wherein steps (a), (c) and (d) are practiced by: (i) heating the black liquor at a temperature and for a time period such that off gases containing organic sulfur compounds are produced; (ii) treating the off gases from step (i) to produce primarily hydrogen sulfide and methane; and (iii) using the hydrogen sulfide to produce the first supply of white liquor.
2. A method as recited in claim 1 wherein step (a) is practiced to add the first supply of white liquor to the first stage, and the second supply of white liquor to the second stage.
3. A method as recited in claim 1 wherein sub-step (iii) is practiced by absorbing the hydrogen sulfide into a stream of white liquor.
4. A method as recited in claim 1 wherein sub-step (i) is practiced by raising the temperature of the black liquor above the cooking temperature so as to split the macro-molecular lignin fraction contained in the liquor and maintain the black liquor at the raised temperature for about 1 to 60 minutes, to produce sulfur-containing off gases.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9111256.5 | 1991-05-24 | ||
GB919111256A GB9111256D0 (en) | 1991-05-24 | 1991-05-24 | Pulping process |
US78815191A | 1991-11-05 | 1991-11-05 | |
US07/788,151 | 1991-11-05 |
Publications (2)
Publication Number | Publication Date |
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CA2069281A1 CA2069281A1 (en) | 1992-11-25 |
CA2069281C true CA2069281C (en) | 2002-11-05 |
Family
ID=26298949
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Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA 2069281 Expired - Fee Related CA2069281C (en) | 1991-05-24 | 1992-05-22 | Multi-level sulfide content pulping |
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CA (1) | CA2069281C (en) |
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1992
- 1992-05-22 CA CA 2069281 patent/CA2069281C/en not_active Expired - Fee Related
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