EP0327576B1 - Procede de production de cellulose a partir de matieres premieres contenant de la lignine - Google Patents
Procede de production de cellulose a partir de matieres premieres contenant de la lignine Download PDFInfo
- Publication number
- EP0327576B1 EP0327576B1 EP87907315A EP87907315A EP0327576B1 EP 0327576 B1 EP0327576 B1 EP 0327576B1 EP 87907315 A EP87907315 A EP 87907315A EP 87907315 A EP87907315 A EP 87907315A EP 0327576 B1 EP0327576 B1 EP 0327576B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- lignin
- process according
- reaction
- redox potential
- enzyme
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims abstract description 33
- 229920005610 lignin Polymers 0.000 title claims abstract description 29
- 239000002994 raw material Substances 0.000 title claims abstract description 6
- 239000001913 cellulose Substances 0.000 title description 7
- 229920002678 cellulose Polymers 0.000 title description 7
- 108090000790 Enzymes Proteins 0.000 claims abstract description 35
- 102000004190 Enzymes Human genes 0.000 claims abstract description 35
- 238000006243 chemical reaction Methods 0.000 claims abstract description 21
- 150000002989 phenols Chemical class 0.000 claims abstract description 12
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 10
- 239000007800 oxidant agent Substances 0.000 claims abstract description 9
- 150000003839 salts Chemical class 0.000 claims abstract description 8
- 238000004061 bleaching Methods 0.000 claims abstract description 7
- 239000000463 material Substances 0.000 claims abstract description 7
- 239000007864 aqueous solution Substances 0.000 claims abstract description 3
- 239000002253 acid Substances 0.000 claims abstract 2
- OEGPRYNGFWGMMV-UHFFFAOYSA-N (3,4-dimethoxyphenyl)methanol Chemical compound COC1=CC=C(CO)C=C1OC OEGPRYNGFWGMMV-UHFFFAOYSA-N 0.000 claims description 10
- 238000001042 affinity chromatography Methods 0.000 claims description 7
- 239000003446 ligand Substances 0.000 claims description 6
- 230000002479 lignolytic effect Effects 0.000 claims description 6
- 238000000926 separation method Methods 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims description 3
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 claims description 3
- 235000005985 organic acids Nutrition 0.000 claims description 3
- 102000004169 proteins and genes Human genes 0.000 claims description 3
- 108090000623 proteins and genes Proteins 0.000 claims description 3
- 235000018553 tannin Nutrition 0.000 claims description 3
- 229920001864 tannin Polymers 0.000 claims description 3
- 239000001648 tannin Substances 0.000 claims description 3
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 claims description 2
- 239000007844 bleaching agent Substances 0.000 claims description 2
- 239000007857 degradation product Substances 0.000 claims description 2
- 238000000746 purification Methods 0.000 claims description 2
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 239000004155 Chlorine dioxide Substances 0.000 claims 1
- 239000005708 Sodium hypochlorite Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 235000019398 chlorine dioxide Nutrition 0.000 claims 1
- 230000000593 degrading effect Effects 0.000 claims 1
- 239000004289 sodium hydrogen sulphite Substances 0.000 claims 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims 1
- 244000005700 microbiome Species 0.000 abstract description 11
- 230000001590 oxidative effect Effects 0.000 abstract description 2
- 238000013019 agitation Methods 0.000 abstract 1
- 238000000354 decomposition reaction Methods 0.000 abstract 1
- 230000001131 transforming effect Effects 0.000 abstract 1
- 235000013311 vegetables Nutrition 0.000 abstract 1
- 241000222393 Phanerochaete chrysosporium Species 0.000 description 15
- 239000000126 substance Substances 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 8
- 230000015556 catabolic process Effects 0.000 description 7
- 238000006731 degradation reaction Methods 0.000 description 6
- 239000002023 wood Substances 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 5
- 239000011572 manganese Substances 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 239000002351 wastewater Substances 0.000 description 4
- 241000233866 Fungi Species 0.000 description 3
- 102000003992 Peroxidases Human genes 0.000 description 3
- 230000001533 ligninolytic effect Effects 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- 238000006065 biodegradation reaction Methods 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 229940093915 gynecological organic acid Drugs 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- MMIPFLVOWGHZQD-UHFFFAOYSA-N manganese(3+) Chemical compound [Mn+3] MMIPFLVOWGHZQD-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 108040007629 peroxidase activity proteins Proteins 0.000 description 2
- 150000005839 radical cations Chemical class 0.000 description 2
- 239000010902 straw Substances 0.000 description 2
- 229910021577 Iron(II) chloride Inorganic materials 0.000 description 1
- 108010029541 Laccase Proteins 0.000 description 1
- 108010059896 Manganese peroxidase Proteins 0.000 description 1
- WAEMQWOKJMHJLA-UHFFFAOYSA-N Manganese(2+) Chemical compound [Mn+2] WAEMQWOKJMHJLA-UHFFFAOYSA-N 0.000 description 1
- 108700020962 Peroxidase Proteins 0.000 description 1
- 241000218657 Picea Species 0.000 description 1
- 108010059820 Polygalacturonase Proteins 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 102000003425 Tyrosinase Human genes 0.000 description 1
- 108060008724 Tyrosinase Proteins 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000031018 biological processes and functions Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 238000001784 detoxification Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 108010093305 exopolygalacturonase Proteins 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 108010002430 hemicellulase Proteins 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 108010062085 ligninase Proteins 0.000 description 1
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 description 1
- 229910000357 manganese(II) sulfate Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C3/00—Pulping cellulose-containing materials
- D21C3/22—Other features of pulping processes
- D21C3/228—Automation of the pulping processes
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C5/00—Other processes for obtaining cellulose, e.g. cooking cotton linters ; Processes characterised by the choice of cellulose-containing starting materials
- D21C5/005—Treatment of cellulose-containing material with microorganisms or enzymes
Definitions
- the invention relates to a method for removing and / or converting lignin from lignocellulose-containing material.
- the lingocellulose-containing material such as wood or annual plants, must be freed from the lignin, since this considerably improves the mechanical and physicochemical properties of the paper produced from the cellulose.
- Conventional processes work with high pressures and temperatures using environmentally harmful chemicals.
- P.J. Harvey et al examined the role of radical cations in the breakdown of lignin. They have observed that veratryl alcohol can act as a mediator in the in-vivo process for lignin degradation using Phanerochaete chrysosporium (Abstract Bulletin of the Institute of Paper Chemistry, Volume 57, No. 7, January 1987, Appieton, Wisconsin, USA) P.J. Harvey et al: "Lignin-degrading enzymes and the role of radical cations in lignin biodegradation", see page 958, summary 8575, & STFI / SPCI Int. Conf. Biotechnol. Pulp & Paper Ind.
- Phanerochaete chrysosporium produces a peroxidase, which causes the oxidation of manganese (II) to manganese (III).
- the manganese (III) in turn causes the oxidation of the lignin molecules.
- Mn peroxidase production plays a crucial role in the degradation of lignin.
- “Paszczgnski, A. et al .:” Composition of Ligninase-l and Peroxidase-M2 from the White-Red Fungus Phanerochaete chrysosporium. Arch. Biochem. Biophys. Vol. 244. No. 2 "that the addition of reducing agents inhibits the Mn-dependent peroxidase of Phanerochaete chrysosporium. Dithionite, on the other hand, acts as an activator.
- veratryl alcohol only serves to promote the formation of lignin-degrading enzymes.
- the present invention has now set itself the task of a method for removing and / or converting lignin or its degradation products from lignocellulose-containing material with the aid of lignolytic enzymes obtained, in which the disadvantages of the use of microorganisms, enzymes and chemicals shown above are avoided, to provide.
- This object is achieved in that a) by adding oxidizing agents, reducing agents, salts and phenolic compounds to an aqueous solution of the lignin-containing raw materials, a redox potential in the range from 200 to 500 mV is set, b) subsequently adding a lignin-degrading reaction by adding the lignolytic enzymes simultaneous bleaching started, c) the reaction at a value between 200 and 500 mV, constant temperature between 20 and 60 ° C, constant pH between 2 and 5 and maintained with constant stirring for 2 to 6 hours d) the redox potential is continuously determined by means of a redox electrode and by means of a regulator and actuator during the entire reaction by adding oxidizing agents. Reducing agents, salts, phenolic compounds and organic acids are kept between 200 and 500 mV and e) after the end of the reaction, the enzyme is passed over a separation column, purified there and returned to the reaction process.
- the redox potential is preferably 250 to 350 mV. Hydrogen peroxide, oxygen and ozone are preferably used as the oxidizing agent. Ascorbic acid, dithionite and sodium bisulfite are suitable as reducing agents. MnSO4 and / or FeCl2 is preferably suitable as the salt. Veratryl alcohol can be used as the phenolic compound. The organic acid comes e.g. Lactic acid into consideration.
- Lignolytic enzymes are preferably used as enzymes in the method according to the invention. These preferably include phenol oxidases, laccases and peroxidases.
- the effectiveness of the method according to the invention can be increased by adding pectinases and / or hemicellulases.
- the pH in the process according to the invention is between 2 and 5. A pH of 3 is particularly preferred.
- the temperature is 20 to 60 ° C.
- the reaction is preferably carried out at 40 ° C.
- a redox potential of 250-350 mV can be set.
- the lignin content of wheat straw (approx. 18% lignin content) can be reduced to almost 0%.
- Spruce wood (about 28-30% lignin content) can be broken down to similar end values.
- these results can be achieved in 2 to 6 hours, in many cases even within 2 hours. This does not include the physical and / or chemical pretreatment that is particularly necessary when using wood or annual plants.
- the redox potential is set by the ratio of the various substances added in the reaction vessel. By measuring and controlling the addition of the oxidizing and reducing agents, the salts, the phenolic compounds and organic acids, a certain redox potential can be maintained throughout the course of the reaction.
- the aim of the operation of the redox system set in this way is to intercept the radicals arising in the oxidation reaction and thus to prevent the repolymerization of the lignin.
- the process also has a significant bleaching effect during the degradation and / or conversion reaction, which allows it to be done with significantly less pollution Bleach to work.
- the process according to the invention is therefore also suitable as a bleaching or post-bleaching process for various processes.
- the process can therefore also be used for the biological bleaching and biological wastewater treatment of pulp industry wastewater and other wastewater.
- the method can be used wherever decolorization and detoxification of waste water is to be achieved.
- Another advantage of the process according to the invention is the possibility of continuous process control.
- the process can be carried out particularly economically if the used enzymes are reprocessed and returned to the reaction process. This goal can be achieved with the help of affinity chromatography.
- the enzyme is passed over a separation column, purified there and returned to the reaction process.
- the enzyme purification is carried out in the separation column by means of affinity chromatography.
- affinity chromatography For this purpose, new specific types of ligands have been developed, which are used together with the corresponding enzyme technology know-how.
- phenolic compounds can be used here.
- Protein-specific ligands are also suitable. Tannin is an example.
- Microorganisms or enzymes are added to the reactor via the inflow 7.
- the microorganisms or enzymes can optionally also be immobilized in the reactor.
- Conventional fillers and carriers can be used for the immobilization.
- Oxidizing agents, reducing agents, salts or phenolic compounds can be metered in via the inflow 4.
- the dosage can be controlled depending on the respective redox potential.
- a redox electrode must be attached to the reactor (not shown in the picture), by means of which the redox potential is continuously determined. By connecting to an appropriate control system, the redox potential can then be kept constant during the entire course of the reaction.
- the raw materials are also added via the feed line 7.
- chemically and / or physically pretreated straw and wood come into consideration.
- Lignin and waste water containing lignin can also be treated in the plant according to the invention.
- the lignin is broken down in the reactor with the aid of lignolytic enzymes or microorganisms.
- Particularly suitable enzymes are those which have been obtained from the fungus Phanerochaete chrysosporium. Cellulase- and hemicellulase-free mutants are particularly suitable as microorganisms.
- mutants of Phanerochaete chrysosporium can be used.
- the converted raw material flows out of the reactor via the drain 8 together with the used chemicals, microorganisms or enzymes.
- the mixture of substances is passed, for example, through a filter 3, where dissolved and undissolved substances are separated from one another.
- the enzyme-containing solution is passed through a chromatography column 2. This column works on the principle of affinity chromatography. Here the enzymes are reprocessed and then fed back to the reaction process via line 5.
- the substances separated from the enzymes are discharged via line 6.
- Special enzyme-specific ligands, in particular phenolic compounds are used for affinity chromatography. Protein-specific ligands, in particular tannin, can also be used.
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Paper (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Compounds Of Unknown Constitution (AREA)
- Enzymes And Modification Thereof (AREA)
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
- Processing Of Solid Wastes (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Audible-Bandwidth Dynamoelectric Transducers Other Than Pickups (AREA)
Claims (11)
- Procédé d'élimination et/ou de transformation de la lignine ou de ses produits de décomposition à base de matière lignocellulosique, à l'aide des enzymes ligninolytiques produites,
caractérisé par le fait que :(a) par l'addition d'agents oxydants, d'agents réducteurs, de sels et de composés phénoliques à une solution aqueuse des matières premières à teneur en lignine, on règle un potentiel redox pour qu'il ce situe dans la plage de 200 à 500 mV ;(b) ensuite, par l'addition de l'enzyme ligninolytique, on fait démarrer une réaction de décomposition de la lignine avec un blanchiment simultané ;(c) on maintient la réaction, pour la valeur comprise entre 200 et 500 mV, à une température constante comprise entre 20 et 60°C, à une valeur de pH constante comprise entre 2 et 5, et sous agitation continue pendant un laps de temps de 2 à 6 heures ;(d) on calcule le potentiel redox en continu au moyen d'une électrode redox et on maintient ledit potentiel redox à une valeur comprise entre 200 et 500 mV, au moyen d'un régulateur et d'un composant de réglage, pendant la totalité de la réaction, par addition d'agents oxydants, d'agents réducteurs, de sels, de composés phénoliques et d'acides organiques ; ete) après l'achèvement de la réaction, on amène l'enzyme sur une colonne de rectification, on l'y purifie, et on la recycle dans le procédé de réaction. - Procédé selon la revendication 1, caractérisé par le fait que l'on règle le potentiel redox pour qu'il se situe dans la plage de 250 à 350 mV.
- Procédé selon l'une des revendications 1 ou 2, caractérisé par le fait que l'on utilise, comme agent d'oxydation, H₂O₂, O₂ ou l'ozone.
- Procédé selon l'une des revendications 1 à 3, caractérisé par le fait que l'on utilise, comme agent réducteur, l'acide ascorbique, le dithionite ou le bisulfite de sodium.
- Procédé selon l'une des revendications 1 à 4, caractérisé par le fait que l'on utilise, comme composé phénolique, l'alcool vératrylique.
- Procédé selon l'une des revendications 1 à 5, caractérisé par le fait que l'on règle à une valeur de pH de 3.
- Procédé selon l'une des revendications 1 à 6, caractérisé par le fait que l'on règle à une température de 40°C.
- Procédé selon l'une des revendications 1 à 7, caractérisé par le fait que, dans la colonne de rectification, on conduit la purification de l'enzyme par chromatographie d'affinité.
- Procédé selon la revendication 8, caractérisé par le fait que l'on conduit la chromatographie d'affinité avec des ligands spécifiques de l'enzyme, en particulier des composés phénoliques.
- Procédé selon la revendication 9, caractérisé par le fait que l'on conduit la chromatographie d'affinité avec des ligands spécifiques de protéines, en particulier le tanin.
- Procédé selon l'une des revendications 1 à 10, caractérisé par le fait que l'on réalise un blanchiment supplémentaire avec des agents de blanchiment d'usage courant, comme l'hypochlorite de sodium, le chlore, l'ozone, O₂, le dioxyde de chlore.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT87907315T ATE86318T1 (de) | 1986-10-24 | 1987-10-24 | Verfahren zur herstellung von zellstoff aus ligninhaltigen rohstoffen. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3636208 | 1986-10-24 | ||
DE19863636208 DE3636208A1 (de) | 1986-10-24 | 1986-10-24 | Verfahren zur delignifizierung und bleichung von lignicellulosehaltigem bzw. ligninhaltigem material bzw. lignin durch enzymatische behandlung |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0327576A1 EP0327576A1 (fr) | 1989-08-16 |
EP0327576B1 true EP0327576B1 (fr) | 1993-03-03 |
Family
ID=6312392
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP87907315A Expired - Lifetime EP0327576B1 (fr) | 1986-10-24 | 1987-10-24 | Procede de production de cellulose a partir de matieres premieres contenant de la lignine |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP0327576B1 (fr) |
JP (1) | JPH0718108B2 (fr) |
AT (1) | ATE86318T1 (fr) |
AU (1) | AU605215B2 (fr) |
BR (1) | BR8707844A (fr) |
DE (2) | DE3636208A1 (fr) |
DK (1) | DK170810B1 (fr) |
FI (1) | FI95289C (fr) |
HU (2) | HU202938B (fr) |
NO (1) | NO175104C (fr) |
WO (1) | WO1988003190A1 (fr) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA894239B (en) * | 1988-06-08 | 1990-03-28 | Int Paper Co | Enzymatic delignification of lignocellulosic material |
FI88316C (fi) * | 1989-07-10 | 1993-04-26 | Enso Gutzeit Oy | Foerfarande foer blekning av cellulosamassa |
DE69015294T2 (de) * | 1989-09-12 | 1995-05-18 | Sandoz Ag | Bleichen von Holzstoff mit Enzymen. |
NZ235983A (en) * | 1989-11-08 | 1993-01-27 | Novo Nordisk As | Process for hydrolysis of resins in lignocellulosic pulp using enzymes simultaneously with peroxy bleaching; ctmp fluff-pulp and absorbent articles produced therefrom |
FI895501A (fi) * | 1989-11-17 | 1991-05-18 | Enso Gutzeit Oy | Foerfarande foer tillverkning av massa. |
FI92414B (fi) * | 1989-11-27 | 1994-07-29 | Enso Gutzeit Oy | Menetelmä massan valmistamiseksi |
FI85389C (fi) * | 1989-12-12 | 1992-04-10 | Enso Gutzeit Oy | Foerfarande foer tillverkning av massa. |
FI900544A (fi) * | 1990-02-02 | 1991-08-03 | Enso Gutzeit Oy Tutkimuskeskus | Foerfarande foer tillverkning av massa. |
DE4008893A1 (de) * | 1990-03-20 | 1991-09-26 | Call Hans Peter | Verfahren zum enzymatischen bleichen von zellstoffen |
DE4008894A1 (de) * | 1990-03-20 | 1991-09-26 | Call Hans Peter | Verfahren zur altpapieraufbereitung mit enzymatischer druckfarbenentfernung |
DK249990D0 (da) * | 1990-10-17 | 1990-10-17 | Novo Nordisk As | Fremgangsmaade til enzymatisk pulpbehandling |
EP0486125A1 (fr) * | 1990-11-13 | 1992-05-20 | JAPAN PULP & PAPER RESEARCH INSTITUTE, INC. | Composition lignocellulolytique, procédé pour sa fabrication et son application |
FI905954A (fi) * | 1990-12-03 | 1992-06-04 | Enso Gutzeit Oy | Foerfarande foer blekning av cellulosamassa. |
JPH04240287A (ja) * | 1991-01-21 | 1992-08-27 | Kobe Steel Ltd | パルプの漂白方法 |
FI93230C (fi) * | 1991-03-22 | 1995-03-10 | Genencor Int Europ | Menetelmä mekaanisen massan pihkavaikeuksien vähentämiseksi |
AT400153B (de) * | 1991-05-02 | 1995-10-25 | Voest Alpine Ind Anlagen | Verfahren zum bleichen von xylan- und lignocellulosehältigen materialien |
DE4137761A1 (de) * | 1991-05-17 | 1992-11-19 | Call Hans Peter | Verfahren zur delignifizierung von lignocellulosehaltigem material, bleiche und behandlung von abwaessern mittels laccasen mit erweiteter wirksamkeit |
FI914780A0 (fi) * | 1991-10-10 | 1991-10-10 | Valtion Teknillinen | Foerfarande foer entsymatisk behandling av lignocellulosahaltiga material, i synnerhet cellulosamassor. |
CA2115881C (fr) * | 1993-02-25 | 2000-05-23 | Michael G. Paice | Methode de blanchiment sans chlore de la pate kraft |
JP3262646B2 (ja) * | 1993-07-09 | 2002-03-04 | 日本製紙株式会社 | パルプの漂白方法 |
SE505980C2 (sv) * | 1993-12-23 | 1997-10-27 | Bim Kemi Ab | Sätt att förhindra peroxidnedbrytande enzymer vid blekning med väteperoxid |
JP3970930B2 (ja) * | 1996-02-08 | 2007-09-05 | ノボザイムス アクティーゼルスカブ | リグノセルロース系材料の製造方法、および該方法により得られる生成物 |
DE19820947B4 (de) * | 1997-05-12 | 2005-12-01 | Call, Krimhild | Enzymatisches Bleichsystem mit neuen enzymwirkungsverstärkenden Verbindungen zum Verändern, Abbau oder Bleichen von Lignin, ligninhaltigen Materialien oder Verändern oder Abbau von Kohle sowie Verfahren unter Verwendung des Bleichsystems |
US6824646B2 (en) | 1999-03-23 | 2004-11-30 | Oji Paper Co., Ltd. | Process for oxygen bleaching and enzyme treating lignocellulosic pulp with liquid treatment and recovery |
US6942754B2 (en) | 1999-03-23 | 2005-09-13 | Oji Paper Co., Ltd. | Process for producing xylooligosaccharide from lignocellulose pulp |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1262117B (de) * | 1964-05-05 | 1968-02-29 | Aschaffenburger Zellstoffwerke | Verfahren zur Kontrolle der Bleiche mit Chlordioxyd |
FR1524581A (fr) * | 1966-05-25 | 1968-05-10 | Solvay | Procédé de réglage de la blancheur d'une pâte cellulosique traitée par le peroxyde d'hydrogène ou un produit similaire |
CA1232850A (fr) * | 1985-01-17 | 1988-02-16 | Albert D. Friesen | Purification de la superoxyde-dismutase |
-
1986
- 1986-10-24 DE DE19863636208 patent/DE3636208A1/de not_active Withdrawn
-
1987
- 1987-10-24 AT AT87907315T patent/ATE86318T1/de not_active IP Right Cessation
- 1987-10-24 EP EP87907315A patent/EP0327576B1/fr not_active Expired - Lifetime
- 1987-10-24 HU HU875790A patent/HU202938B/hu not_active IP Right Cessation
- 1987-10-24 AU AU82303/87A patent/AU605215B2/en not_active Ceased
- 1987-10-24 HU HU875790A patent/HUT50894A/hu unknown
- 1987-10-24 BR BR8707844A patent/BR8707844A/pt not_active IP Right Cessation
- 1987-10-24 JP JP62506759A patent/JPH0718108B2/ja not_active Expired - Lifetime
- 1987-10-24 DE DE8787907315T patent/DE3784515D1/de not_active Expired - Fee Related
- 1987-10-24 WO PCT/EP1987/000635 patent/WO1988003190A1/fr active IP Right Grant
-
1988
- 1988-06-23 DK DK344888A patent/DK170810B1/da not_active IP Right Cessation
- 1988-06-24 NO NO882808A patent/NO175104C/no unknown
-
1989
- 1989-04-21 FI FI891909A patent/FI95289C/fi not_active IP Right Cessation
Non-Patent Citations (4)
Title |
---|
Abatract Bulletin of the Institute of Paper Chemistry, vol.57, No.7, January 1987, (Appleton, Wisconsin, US), M. Asther et al.: "Production of ligninolytic enzymes of Phanerochaete chrysosporium INA-12 in submerged agitated cultures", pages 956-957, abstract 8558 * |
Abstract Bulletin of the Institute of Paper Chemistry, vol. 57, No. 7, January 1987, (Appleton, Wisconsin, US), P.J. Harvey et al.: "Lignin-degrading enzymes and the role of radical cations in lignin biodegradation", page 958, abstract 8575 * |
Abstract Bulletin of the Institute of Paper Chemistry, vol. 57, No. 7, January 1987, (Appleton, Wisconsin, US), V.-B. Huynh et al.: "Oxidation of lignin model compounds by a manganese-dependent enzyme from phanerochaete chrysosporium as compared to chemically generated Mn(III)", page 959, abstract 8578 * |
Tappi, vol. 61, No. 6, June 1978, B.I. Fleming et al.: "Soda pulping with anthraquinone. A mechanism", pages 43-46 * |
Also Published As
Publication number | Publication date |
---|---|
ATE86318T1 (de) | 1993-03-15 |
NO882808L (no) | 1988-06-24 |
FI891909A0 (fi) | 1989-04-21 |
DK344888D0 (da) | 1988-06-23 |
WO1988003190A1 (fr) | 1988-05-05 |
AU8230387A (en) | 1988-05-25 |
FI95289B (fi) | 1995-09-29 |
DE3784515D1 (de) | 1993-04-08 |
BR8707844A (pt) | 1989-10-03 |
DE3636208A1 (de) | 1988-05-05 |
DK344888A (da) | 1988-06-23 |
DK170810B1 (da) | 1996-01-22 |
JPH02500990A (ja) | 1990-04-05 |
JPH0718108B2 (ja) | 1995-03-01 |
AU605215B2 (en) | 1991-01-10 |
HUT50894A (en) | 1990-03-28 |
NO882808D0 (no) | 1988-06-24 |
NO175104C (no) | 1994-08-31 |
NO175104B (no) | 1994-05-24 |
FI891909A (fi) | 1989-04-21 |
HU202938B (en) | 1991-04-29 |
FI95289C (fi) | 1996-01-10 |
EP0327576A1 (fr) | 1989-08-16 |
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