WO2015007953A1 - A method of producing oxidized or microfibrillated cellulose - Google Patents
A method of producing oxidized or microfibrillated cellulose Download PDFInfo
- Publication number
- WO2015007953A1 WO2015007953A1 PCT/FI2014/050572 FI2014050572W WO2015007953A1 WO 2015007953 A1 WO2015007953 A1 WO 2015007953A1 FI 2014050572 W FI2014050572 W FI 2014050572W WO 2015007953 A1 WO2015007953 A1 WO 2015007953A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- suspension
- consistency
- mfc
- pulp
- oxidation
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 41
- 229920002678 cellulose Polymers 0.000 title claims abstract description 24
- 239000001913 cellulose Substances 0.000 title claims abstract description 24
- 239000000725 suspension Substances 0.000 claims abstract description 66
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 51
- 230000003647 oxidation Effects 0.000 claims abstract description 49
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methyl-cyclopentane Natural products CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 claims abstract description 24
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000003054 catalyst Substances 0.000 claims abstract description 19
- 239000007800 oxidant agent Substances 0.000 claims abstract description 19
- 230000001590 oxidative effect Effects 0.000 claims abstract description 19
- 230000001965 increasing effect Effects 0.000 claims abstract description 17
- 238000002156 mixing Methods 0.000 claims abstract description 13
- 239000003513 alkali Substances 0.000 claims abstract description 12
- BCJCJALHNXSXKE-UHFFFAOYSA-N azado Chemical compound C1C(C2)CC3CC1N([O])C2C3 BCJCJALHNXSXKE-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000010008 shearing Methods 0.000 claims abstract description 10
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims abstract description 6
- 238000000265 homogenisation Methods 0.000 claims abstract description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- 206010061592 cardiac fibrillation Diseases 0.000 claims description 23
- 230000002600 fibrillogenic effect Effects 0.000 claims description 23
- 239000002655 kraft paper Substances 0.000 claims description 9
- 229920005610 lignin Polymers 0.000 claims description 8
- 229920002201 Oxidized cellulose Polymers 0.000 claims description 5
- 229940107304 oxidized cellulose Drugs 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 3
- 238000005119 centrifugation Methods 0.000 claims description 2
- 238000003825 pressing Methods 0.000 claims description 2
- 238000004537 pulping Methods 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 8
- 239000002131 composite material Substances 0.000 abstract description 3
- 230000001105 regulatory effect Effects 0.000 abstract description 2
- 239000000243 solution Substances 0.000 description 35
- 235000010980 cellulose Nutrition 0.000 description 20
- 239000000047 product Substances 0.000 description 20
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 238000011282 treatment Methods 0.000 description 12
- 239000005708 Sodium hypochlorite Substances 0.000 description 11
- 239000003153 chemical reaction reagent Substances 0.000 description 11
- 239000000835 fiber Substances 0.000 description 11
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 238000007670 refining Methods 0.000 description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 238000000879 optical micrograph Methods 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000012467 final product Substances 0.000 description 5
- 239000003446 ligand Substances 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 238000005243 fluidization Methods 0.000 description 4
- -1 poly(acrylamide) Polymers 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000007853 buffer solution Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 210000001724 microfibril Anatomy 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108010001336 Horseradish Peroxidase Proteins 0.000 description 2
- 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 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 108010029541 Laccase Proteins 0.000 description 2
- 229920001131 Pulp (paper) Polymers 0.000 description 2
- QYTDEUPAUMOIOP-UHFFFAOYSA-N TEMPO Chemical group CC1(C)CCCC(C)(C)N1[O] QYTDEUPAUMOIOP-UHFFFAOYSA-N 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 239000003426 co-catalyst Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 description 2
- 229910001882 dioxygen Inorganic materials 0.000 description 2
- 238000005265 energy consumption Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 2
- LBSANEJBGMCTBH-UHFFFAOYSA-N manganate Chemical class [O-][Mn]([O-])(=O)=O LBSANEJBGMCTBH-UHFFFAOYSA-N 0.000 description 2
- 230000001404 mediated effect Effects 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical class [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- PBYZMCDFOULPGH-UHFFFAOYSA-N tungstate Chemical class [O-][W]([O-])(=O)=O PBYZMCDFOULPGH-UHFFFAOYSA-N 0.000 description 2
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical class [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 241000609240 Ambelania acida Species 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 239000004155 Chlorine dioxide Substances 0.000 description 1
- 229920000875 Dissolving pulp Polymers 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 229920001046 Nanocellulose Polymers 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000010905 bagasse Substances 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000003842 bromide salts Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 235000019398 chlorine dioxide Nutrition 0.000 description 1
- 229940099041 chlorine dioxide Drugs 0.000 description 1
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical class OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000002608 ionic liquid Substances 0.000 description 1
- 229960004592 isopropanol Drugs 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 239000012978 lignocellulosic material Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006194 liquid suspension Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 150000004967 organic peroxy acids Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000005385 peroxodisulfate group Chemical group 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000013341 scale-up Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical class [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/16—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only modified by a particular after-treatment
- D21H11/20—Chemically or biochemically modified fibres
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
- C08B15/02—Oxycellulose; Hydrocellulose; Cellulosehydrate, e.g. microcrystalline cellulose
-
- 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
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
-
- 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
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/001—Modification of pulp properties
- D21C9/002—Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives
- D21C9/004—Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives inorganic compounds
-
- 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
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/001—Modification of pulp properties
- D21C9/002—Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives
- D21C9/005—Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives organic compounds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/16—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only modified by a particular after-treatment
- D21H11/18—Highly hydrated, swollen or fibrillatable fibres
Definitions
- the present invention concerns a method of producing oxidized cellulose.
- the invention even comprises a method of producing microfibrillated cellulose (MFC) as well as a method of increasing the viscosity of a suspension of a MFC product.
- MFC microfibrillated cellulose
- NFC nanofibrillated cellulose
- Microfibrillated cellulose is hereby defined as fibrous material comprised of cellulosic fibrils and fibril aggregates. Fibrils are very thin, usually of a diameter of about 5 to 100 nm, in average about 20 nm, and have a fibre length of about 20 nm to 200 ⁇ although usually of 100 nm to 100 ⁇ . Nanofibrillated cellulose (NFC) is a specific class of MFC with fibre dimensions at the low end of said fibril size range. In the MFC individual microfibrils are partly or totally detached from each other.
- MFC Fibres that have been fibrillated and which have microfibrils on the surface and microfibrils that are separated and located in a water phase of slurry are included in the definition MFC.
- MFC has a very large open active surface area, generally in the range of about 1 to 300 m 2 /g, and is useful for a wide range of end uses, notably in the field of papermaking but al- so in composites like plastic or rubber, food, pharmaceuticals, home care products, dispersions like paints, etc.
- Prior art methods of manufacturing MFC include mechanical disintegration by refining, milling, beating, homogenizing, and fibrillation by e.g. an extruder. These mechanical methods may be enhanced by chemical or chemoenzymatic treatments as a preliminary step.
- US patent 4,341 ,807 describes production of MFC by passing a fibrous suspension repeatedly through a small diameter orifice subjecting the liquid suspension to a pressure drop.
- the starting suspension contains 0.5 to 10 wt-% of cellulose.
- the product is a homogenous gel-formed suspension of MFC.
- WO 2007/091942 A1 describes a process, in which chemical pulp is first refined, then treated with one or more wood degrading enzymes, and finally homogenized to produce MFC as the final product.
- the consistency of the pulp is taught to be preferably from 0.4 to 10 %.
- the advantage is said to be avoidance of clogging in the high-pressure fluidizer or homogenizer.
- a fibrous slurry of 1 wt-% consistency at pH 10 was oxidized by adding 1 .3 to 5.0 mmol NaCIO, 0.1 mmol TEMPO, and 1 mmol sodium bromide per 1 g of cellulose, and stirring the mixture at room temperature while adding NaOH. The oxidized cellulose was then agitated to swell the fibres and finally to turn the dispersion highly viscous and transparent. Very similar descriptions are found from Fuku-/2017i et al. and Okita et al. also.
- LC low consistency
- WO 2012/097446 A1 instead describes a process of making NFC by multipass high consistency (HC) refining of chemical or mechanical fibres.
- HC is defined as referring to a discharge consistency of more than 20 wt-%
- WO 2012/072874 A1 teaches a multistep process of producing NFC, in which cellulose is refined with a first refiner, the product is divided into an accept fraction and reject fraction, water is removed from the accept fraction, and finally the accept fraction is refined with a second refiner to obtain a gel-like product with fibre diameter of 2 to 200 nm.
- the consistency of the material is under 10 wt-% but increased by removal of water to about 15 wt-% or even 20 wt-% to enhance washing of the same.
- the pulp would be diluted back to a consistency under 10 wt-%.
- WO 201 1/1 14004 there is described a different approach of fibrillating ligno- cellulosic material based on treatment with ionic liquid, i.e. molten salt, which preserves fibres basically intact. Salts comprising an imidazolium type cation are mentioned as an example of such liquids. The process is said to weaken the binding between fibrils or tracheids and separate fibrils or tracheids from fi- bre walls.
- ionic liquid i.e. molten salt
- WO2012/050589 describes treating cellulose raw material in a high consistency with at least one chemical at least partly in an extruder, and optionally performing another refining step in the refining part of the extruder in a consistency of at least 5%.
- a problem with conventional low-consistency refining with hammer or ball mills is that large amounts of energy is consumed for continued fibrillation after the initial phase of the process. Partial hydrolysis of semicrystalline lignocellulose by use of chemicals (e.g. TEMPO) or enzymes is helpful, especially when gellike MFC products are aimed at, but the main drawback then is high material and energy costs. The use of excess chemicals may also require further chemical recovery solutions to be utilized.
- chemicals e.g. TEMPO
- enzymes is helpful, especially when gellike MFC products are aimed at, but the main drawback then is high material and energy costs.
- the use of excess chemicals may also require further chemical recovery solutions to be utilized.
- a microfluidizer or homogenizator may be used instead of refining with hammer or ball mills.
- the fibrillation process requires pre-treatment of the pulp suspension and a relatively low concentration in order to operate smooth- ly and energy efficiently.
- a common drawback of low consistency fibrillations is that the resulting suspension is dilute, difficult to handle and requires further process steps especially if transporting to another location for being used.
- high consistency fibrillation has relatively high energy consumption, initial runnability of the refiner is poor, and the known high consistency methods therefore are not economically viable.
- the problem solved by the invention is to improve oxidative treatment of cellu- losic pulp, in particular in the production of MFC, so as to reduce the material costs and turn this route of manufacture economically viable.
- the goal is also to reduce overall energy consumption, and to obtain oxidized pulp at an increased consistency, which is suitable for being further dried or then transported wet or dry to another location, where it is turned to MFC for use as the final product.
- a further goal is to obtain a final MFC product in the form of a suspension with an increased viscosity.
- the solution according to the invention is production of oxidized cellulose through the steps of (i) providing an aqueous pulp suspension with a consistency of at least 15 wt-%, (ii) adding at least one oxidant to the suspension, and (iii) oxidizing the suspension under mechanical mixing or shearing.
- a gel-like suspension comprising MFC is obtained by the further step of (iv) subjecting the oxidized suspension from step (iii) to fibrillation, preferably homogenization. Oxidation in relatively high consistency, as defined above, under light and gentle mechanical mixing with low shearing forces improves the fibre structure and homogeneity and reduces formation of fines.
- the amount of chemicals used is typically lower compared to oxidation in lower consistencies.
- the mild treatment together with the high consistency avoids cutting of the fibres and is thereby conducive to obtaining MFC with a high aspect ratio. Fibrillation of the oxidized pulp effectively breaks down fibres into individual fibrils and yields a suspension of MFC, which surprisingly was found to have a much increased viscosity as compared to pulp oxidized at a conventional low consistency.
- an increased consistency enhances shearing of fibres and opens their inner structure so as to produce a uniform oxidation throughout the material.
- Such disruption brings fibrillation and yields suspensions of increasing transparency, which require very little further fibrillation to obtain MFC as final product.
- the amount of mediating oxidation catalyst is reduced to a fraction of the dose needed for oxidation at a con- ventional low consistency.
- oxidation may be carried out at the pulp mill where the cellulosic pulp originates, and the resulting oxidized suspension, still at a high consistency, is then transported to another location, e.g. the site of final use of the MFC product, for being washed and fibrillated at a lower consistency to ob- tain the final product.
- the oxidized suspension may even be dried for the transport, as it is readily redisperged in water for regenerating the aqueous suspension.
- the high surface charge density of the fibrils obtained according to this method enhances the re-wettability and dispergation.
- an oxidized suspension at a high consistency may constitute the final product.
- the final fibrillation step yielding MFC is not necessary for the invention in its broadest terms.
- Such suspension of high consistency is useful as a constituent of coating or barrier dispersions for instance.
- the fibrillation step for producing MFC may be me- chanical grinding, fluidization, mechanical fibrillation, extrusion etc., such alternative fibrillation techniques being as such known to a skilled person.
- the consistency of the pulp suspension subjected to oxidation is in the range of 20 to 30 wt- %. Even higher consistencies up to 40 wt-%, 50 wt-% or 60 wt-% or more may be useful. Due to drying the consistency may increase in the course of oxidation, which may take several hours.
- Figure 1 Light microscopy image (2,5x magnification) of example 1 (5 w-% consistency oxidation) after oxidation (before fibrillative treatment). Bar length 1 mm.
- Figure 5 Light microscopy image of example 3 (20 wt-% consistency oxidation) after oxidation and Ultra Turrax treatment. Bar length 100 ⁇ .
- Figure 6. Light microscopy image of example 4 (20 wt-% consistency oxidation) after oxidation and Ultra Turrax treatment. Bar length 100 ⁇ .
- microfibrillated cellulose is produced by first providing an aqueous cellulosic pulp suspension with a consistency of at least 15 wt-%, preferably 20 to 30 wt-% without limiting to the upper limit.
- the starting cellulosic material has a low lignin content of less than 5 wt-% of lignin of the dry content of the pulp suspension.
- At least one oxidant and preferably a cocatalyst are added to the suspension and mixed by continued mechanical agitation. Oxidation is then started and carried out by addition of a mediating catalyst while mechanical mixing or shearing is continued.
- the steps so far may be performed at a pulp mill, which produces the starting material, e.g. an undried kraft pulp, which is centrifuged or pressed to the desired high consistency.
- the oxidized suspension still at a high consistency, may then be transported to the site of use of the final MFC product, where the pulp is optionally washed and finally homogenized or fibrillated at a lower consistency to obtain the gel-like product. From increased consistency follows an increase of the mechanical energy that is needed for agitating the suspension.
- the oxidation step as carried out in the invention turns part of the hydroxyl groups of the cellulosic hydrocarbon chain (including polysaccharides) into groups typical of oxidized cellulose, such as carboxylic acid, carbox- ylate, aldehyde and ketone groups, the last two even in hydrated form.
- a mediating catalyst is usually needed, such catalysts being known to a person skilled in the art.
- azaadamantane-N-oxyl (AZADO) and 2,2,6,6-tetramethylpiperidine-1 -oxyl (TEMPO) radicals may be mentioned as examples of such oxidation mediating catalysts, which have been tested and found to be useful in the invention.
- TEMPO and AZADO catalysts can be used alternatively or together. It is also possible to select catalyst according to desired properties of the resulting product.
- AZADO is more powerful but less specific oxidation catalyst when compared to TEMPO.
- TEMPO catalyst favors oxidation of O6 * and thus it is preferred over AZADO when high aspect ratio of fibrils is a wished property.
- AZADO oxidation processes can be carried out faster and with less catalyst. Resulting fibrils have a lower aspect ratio than after using TEMPO catalyst. This is a favored property when lower viscosity of the product is desired.
- the aspect ratio affects the rheological properties, but potentially also the strength of materials, so that higher aspect ratio gives in general higher viscosity and higher strength enhancement.
- TEMPO or AZADO any known derivate thereof with useful catalytic activity may be used, 1 -methyl-AZADO being mentioned as an example.
- alkali hypochlorite such as NaCIO.
- Alkali bromide e.g. NaBr, is suitably added as a cocatalyst.
- chlo- rine dioxide and chlorite salts can be used either instead or together with hypochlorite.
- stoichiometric oxidants can also be selected among following chemicals: peroxodisulfate and peroxomonosulfate salts, organic peroxyacids and their salts, perborate salts, percarbonate salts, hydrogen peroxide and organic peroxides, urea peroxide, molecular oxygen and ozone.
- Beside bromide salts some other suitable co-catalysts are tungstate salts, vanadate salts, molybdate salts, manganate salts, silver salts, laccase, horseradish peroxidase, copper ligands, manganese ligands, cobalt ligands, tertiary amines and quaternary ammonium salts. It should be noticed that all co- catalyst are not suitable with all stoichiometric oxidants.
- Tungstate, vanadate, molybdate, manganate salts and horseradish peroxidase are especially suita- ble with hydrogen peroxide and other peroxide releasing compound, whereas laccase, copper ligands and cobalt ligands are preferable with molecular oxygen.
- Optimal temperature and pH are also depending on the practiced oxidation system. Generally, the oxidation is carried out between the ranges of tempera- ture 0 to 80 °C and pH 2 to 14. In specific cases it is beneficial to first mix stoichiometric oxidant and possibly co-oxidant with the pulp at temperature between 0 to 20 °C, and after this start the oxidation by increasing the temperature between 20 to 80 °C and preferably adding the mediator.
- the oxidant, the cocatalyst and the mediating catalyst can be added to the pulp suspension in any order.
- an oxidant such as alkali hypochlorite and eventual cocatalyst such as alkali bromide are added to the suspension, followed by addition of the mediating catalyst such as AZADO or TEMPO.
- the mediating catalyst such as AZADO or TEMPO.
- alkali such as NaOH
- alkali is advantageously added at the oxidation step for setting the pH to a range of 9 to 12, preferably to 10 to 1 1 , and most preferably to about 10.
- the oxidized pulp may be washed for removal of the chemicals, in particular AZADO or TEMPO as used, which may bring the pulp suspension to the low consistency range of 10 wt-% or less.
- the washed and diluted suspension is then subjected to homogenization so as to obtain the final MFC product.
- the pulp is homogenized at a consistency of at most 5 wt-%, more preferably in a range of 3 to 4 wt-%.
- the final MFC production can alternatively be carried out by extruded or (twin-screw) kneader at consistencies at least 10 wt- %, preferably at least 15 wt-%, more preferably between 20 to 30 wt-%.
- the water-content can also be varied during the treatment by simultaneously adding water in the extruder or kneader to facilitate the fibril hydration and separation.
- the pulp used for the invention may be chemical pulp or mechanical, dissolving pulp or recycled pulp, recycled paper or side flows from pulp and paper mills. Even use of cellulosic pulp of non-wood origin, for example bamboo or bagasse is possible.
- the pulp is obtained from a chemical kraft pulping process without intermediate drying.
- Naturally also MFC, nanocellulose or microcrystalline cellulose can be used as a starting material.
- Starting material can also be composed of various pulp sources.
- the pulp may be pretreated in order to increase the surface area.
- the pulp is first disintegrated mechanically, e.g. by milling, and brought to a consistency of at least 15 wt-%. Any known method can be used, e.g. centrifugation or pressing.
- the starting cellulosic material has a low lignin content of less than 5 wt-% of lignin of the dry content, preferably less than 3 wt-% lignin of the dry content, more preferably less than 2 wt-% lignin of the dry content.
- the starting cellulosic pulp has very low lignin content of 0.01 to 1 wt-% or even 0.01 to 0.5 wt-% of the mass dry content.
- the MFC product obtained by the invention is gel-like and suitably used for regulating viscosity, for production of films, or as an additive for composite materials.
- At least 50 %, preferably at least 80 % of the fibrils in the product have dimensions in the fibril length and diameter ranges as defined above for MFC.
- a particular goal of the invention is to increase the viscosity of a suspension of the final MFC product.
- a suspension of MFC, preferably aqueous, having a high viscosity is achieved by way of oxidation of pulp at a consistency of at least 12 wt-%, preferably at least 15 wt-%, and most preferably at least 20 wt-% according to the invention, as opposed to lower consistencies as conventionally applied.
- a MFC product obtained in connection with testing the invention was turned to a slurry of a low consistency of about 1 wt- % for measurement of the viscosity. Highly increased viscosities could be measured for the MFC produced according to the invention, as compared to MFC obtained through oxidation at a lower consistency.
- oxidation of pulp at consistencies of 12 wt-% or 15 wt-% yield aqueous MFC suspensions, which at a consistency of 1 wt-% have viscosities of at least 2500 cp or at least 3500 cp, respectively, as measured at rotation speed of 5 rpm with spindle Vane 71 .
- the high viscosity obtained by means of the invention is very desirable in view of various uses of the MFC suspension, especially as a thickening agent in cosmetics, foods, personal care products as well as oil drilling slurries, emulsion paints, textile printing pastes and paper coating pastes.
- the increased viscosity of the MFC suspension is believed to be due not only to improved separation of fibrils but also to an increased aspect ratio, i.e. the ratio of fibril length to fibril diameter, of the final MFC product. Increased aspect ratio is apt to improve the strength properties of MFC.
- Example 1 (comparative). Low-consistency oxidation (cellulose con- sistency 5 %)
- reagent solution Sodium bromide (2 g, purity 99%) was dissolved in ion-exchanged water (3000 ml) and after this 148.9 g of aqueous so- dium hypochlorite (10 wt-% solution) was added to this solution. The pH of the solution was adjusted to 10.2 with 1 M HCI.
- TEMPO oxidation TEMPO (0.312 g) was dissolved in 278 ml of ion- exchanged water. The solution was added into the pulp suspension and the oxidation reaction was maintained for 90 minutes. Finally, 10 ml ethanol was added to eliminate the unreacted hypochlorite.
- reagent solution Sodium bromide (2 g, purity 99%) and Na 2 CO 3 ⁇ 10 H 2 O (28.6 g, purity 98 %) were dissolved in ion-exchanged water (200 ml). The pH of the solution was then adjusted to 10.2 with sodium bicarbonate. This solution was mixed with 148.9 g of aqueous sodium hypochlorite (10 wt-% solution, pH adjusted to 10.2 with 1 M HCI). The final pH was confirmed to be 10.2.
- Mixing of reagent solution with pulp 572.7 g of never-dried softwood kraft pulp (35 wt-% consistency) was placed in a dough mixer and the previously described reagent solution was added into pulp. After this the pulp was mixed for 90 minutes to evenly disperse sodium hypochlorite and sodium bromide.
- TEMPO oxidation TEMPO (0.312 g) was dissolved in 78 ml of ion-exchanged water. The solution was added into the pulp and the oxidation reaction was maintained for 90 minutes. Finally, 10 ml ethanol was added to eliminate the unreacted hypochlorite.
- the resulting fibrous material was washed three times with 2 I of 40 w-% iso- propanol solution on a Buhner funnel to remove salts.
- the cellulose cake was thereafter diluted to 3 wt-% consistency and fibrillated using a fluidizer from Microfluidics Microfluidizer M-1 10EH-30.
- the used chambers during the cycles were the following (for cycle 1 ) first chamber 400 ⁇ and second chamber 200 ⁇ and for (cycles 2 and 3)first chamber 200 ⁇ and second chamber 100 ⁇ .
- Viscosities with five different rotation speeds, 0.5 , 5, 10, 50 and 100 rpm were determined and are shown in Table 1 .
- Example 1 shows clearly lower viscosities with all rotation speeds compared to Example 2.
- the light microscopy images show that this is due to much poorer fibrillation of the pulp during fluidisation.
- reagent solution 22.8 g aqueous sodium hypochlorite (10 w-% solution) was diluted with ion-exchanged water (17.7 ml) and the pH of the so- lution was adjusted to 10.2 with 1 M HCI.
- Mixing of reagent solution with pulp 59.5 g never-dried kraft pulp (-42 wt-% consistency) was mixed with the reaction solution and the pulp suspension was mixed with laboratory stirring device for 90 minutes to evenly disperse sodium hypochlorite. After this, 25 ml of sodium bicarbonate /sodium carbonate buffer solution (5 wt-% solution, pH 10.2) was added and the pulp was further mixed another 90 minutes.
- reagent solution 22.8 g aqueous sodium hypochlorite (10 wt-% solution) was mixed with ion-exchanged water (17.7 ml) containing 0.16 g sodium bromide. The pH of the solution was adjusted to 10.2 with 1 M HCI.
- pulp was diluted to 2 % consistency with ion-exchanged water and homogenized with Ultra Turrax device. Clear disruption of fiber structure oc- curred by this treatment.
- reagent solution 137 g aqueous sodium hypochlorite (10 wt-% solution) was mixed with ion-exchanged water (25 ml) containing 0.16 g sodium bromide. The pH of the solution was adjusted to 10.2 with 1 M HCI.
- Mixing of reagent solution with pulp 238 g never-drid kraft pulp (-42 wt-% consistency) was mixed with the reaction solution and the pulp suspension was mixed with Hobart pulper for 90 minutes to evenly disperse sodium hypochlorite and sodium. After this, 95 ml of sodium bicarbonate /sodium carbonate buffer solution (5 wt-% solution, pH 10.2) was added and the pulp was further mixed another 90 minutes.
- pulp was diluted to 2 wt-% consistency with ion-exchanged water and homogenized with Ultra Turrax device. A complete disruption of fiber structure occurred by this treatment.
- Viscosities with two different rotation speeds 10 and 100 rpm were determined and are shown in Table 2.
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AU2014291934A AU2014291934B2 (en) | 2013-07-16 | 2014-07-11 | A method of producing oxidized or microfibrillated cellulose |
EP14825900.5A EP3022357B1 (en) | 2013-07-16 | 2014-07-11 | A method of producing oxidized or microfibrillated cellulose |
CN201480050764.XA CN105531419A (en) | 2013-07-16 | 2014-07-11 | A method of producing oxidized or microfibrillated cellulose |
CA2918182A CA2918182C (en) | 2013-07-16 | 2014-07-11 | A method of producing oxidized or microfibrillated cellulose |
KR1020167003709A KR102241616B1 (en) | 2013-07-16 | 2014-07-11 | A method of producing oxidized or microfibrillated cellulose |
US14/905,463 US20160153144A1 (en) | 2013-07-16 | 2014-07-11 | A method of producing oxidized or microfibrillated cellulose |
NZ715965A NZ715965A (en) | 2013-07-16 | 2014-07-11 | A method of producing oxidized or microfibrillated cellulose |
BR112016000996-7A BR112016000996B1 (en) | 2013-07-16 | 2014-07-11 | METHOD OF PRODUCTION OF OXIDIZED OR MICROFIBRILLATED CELLULOSE |
JP2016526669A JP6498193B2 (en) | 2013-07-16 | 2014-07-11 | Process for producing oxidized or microfibrillated cellulose |
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Also Published As
Publication number | Publication date |
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NZ715965A (en) | 2020-07-31 |
EP3022357A1 (en) | 2016-05-25 |
EP3022357A4 (en) | 2017-03-15 |
US20160153144A1 (en) | 2016-06-02 |
AU2014291934B2 (en) | 2018-03-22 |
CA2918182A1 (en) | 2015-01-22 |
BR112016000996A2 (en) | 2017-07-25 |
CA2918182C (en) | 2021-11-09 |
AU2014291934A1 (en) | 2016-02-11 |
KR20160033149A (en) | 2016-03-25 |
CN113355936A (en) | 2021-09-07 |
CN105531419A (en) | 2016-04-27 |
JP2016531975A (en) | 2016-10-13 |
BR112016000996B1 (en) | 2021-11-23 |
EP3022357B1 (en) | 2019-01-16 |
JP6498193B2 (en) | 2019-04-10 |
FI20135773L (en) | 2015-01-17 |
KR102241616B1 (en) | 2021-04-19 |
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