US20060169432A1 - Method of preparing modified cellulose pulp - Google Patents
Method of preparing modified cellulose pulp Download PDFInfo
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- US20060169432A1 US20060169432A1 US11/231,016 US23101605A US2006169432A1 US 20060169432 A1 US20060169432 A1 US 20060169432A1 US 23101605 A US23101605 A US 23101605A US 2006169432 A1 US2006169432 A1 US 2006169432A1
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- arabinoxylan
- cellulose pulp
- pulp
- paper
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- 229920002678 cellulose Polymers 0.000 title claims abstract description 30
- 239000001913 cellulose Substances 0.000 title claims abstract description 30
- 238000000034 method Methods 0.000 title claims abstract description 21
- 229920000617 arabinoxylan Polymers 0.000 claims abstract description 96
- UGXQOOQUZRUVSS-ZZXKWVIFSA-N [5-[3,5-dihydroxy-2-(1,3,4-trihydroxy-5-oxopentan-2-yl)oxyoxan-4-yl]oxy-3,4-dihydroxyoxolan-2-yl]methyl (e)-3-(4-hydroxyphenyl)prop-2-enoate Chemical compound OC1C(OC(CO)C(O)C(O)C=O)OCC(O)C1OC1C(O)C(O)C(COC(=O)\C=C\C=2C=CC(O)=CC=2)O1 UGXQOOQUZRUVSS-ZZXKWVIFSA-N 0.000 claims abstract description 83
- 239000000725 suspension Substances 0.000 claims abstract description 20
- QGGOCWIJGWDKHC-FSIIMWSLSA-N (2s,3s,4r,5r)-2,4,5-trihydroxy-3-methoxy-6-oxohexanoic acid Chemical group OC(=O)[C@@H](O)[C@@H](OC)[C@H](O)[C@@H](O)C=O QGGOCWIJGWDKHC-FSIIMWSLSA-N 0.000 claims abstract description 11
- 125000000089 arabinosyl group Chemical group C1([C@@H](O)[C@H](O)[C@H](O)CO1)* 0.000 claims abstract description 8
- 239000000654 additive Substances 0.000 claims description 18
- 230000000996 additive effect Effects 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 7
- 238000007670 refining Methods 0.000 claims 1
- 229920001221 xylan Polymers 0.000 description 36
- 150000004823 xylans Chemical class 0.000 description 36
- 239000000243 solution Substances 0.000 description 26
- 239000010903 husk Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 150000004783 arabinoxylans Chemical class 0.000 description 13
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 10
- 238000002474 experimental method Methods 0.000 description 10
- 239000002023 wood Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 241001070947 Fagus Species 0.000 description 6
- 235000010099 Fagus sylvatica Nutrition 0.000 description 6
- QGGOCWIJGWDKHC-UHFFFAOYSA-N O4-Methyl-D-glucuronsaeure Natural products OC(=O)C(O)C(OC)C(O)C(O)C=O QGGOCWIJGWDKHC-UHFFFAOYSA-N 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000001556 precipitation Methods 0.000 description 6
- 230000009471 action Effects 0.000 description 5
- 230000006872 improvement Effects 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 235000018185 Betula X alpestris Nutrition 0.000 description 4
- 235000018212 Betula X uliginosa Nutrition 0.000 description 4
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 4
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 4
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 238000011534 incubation Methods 0.000 description 4
- 229920001131 Pulp (paper) Polymers 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920002488 Hemicellulose Polymers 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 238000005903 acid hydrolysis reaction Methods 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 238000000149 argon plasma sintering Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 235000009973 maize Nutrition 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000000834 fixative Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 150000004804 polysaccharides Chemical class 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 239000010414 supernatant solution Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 125000000969 xylosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)CO1)* 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
- 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
-
- 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
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
- D21H17/22—Proteins
-
- 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
- D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
- D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
Definitions
- the present invention concerns the use of arabinoxylans as additive in paper production.
- the mechanical properties of paper are influenced by a series of different parameters of a chemical and physical nature.
- Several theories to explain the tear resistance properties of paper have been suggested, most of which emphasise the special relevance of fibre-fibre bonding. Amongst the most frequently cited is the theory that includes the factors of interfibre bonding force of the bonded surface and the length of the fibre.
- xylans from the raw material wood and its secondary product pulp is discussed.
- acetyl-4-O-methylglucuronoxylan from deciduous wood and arabino-4-O-methylglucuronoxylan from coniferous wood is cited.
- the examples on the use of xylans cites Lenzing xylan. This product is obtained by alkaline extraction of beech wood pulp in the viscose process and exhibits only a low degree of polymerisation of about 35.
- a modified cellulose pulp comprising:
- an arabinoxylan comprising, on its main chain:
- the subject matter of the invention relates in part to the use of arabinoxylans as additive in paper manufacture.
- FIG. 1 is a graphical representation of plots of tear and tensile strengths of pulp samples treated with arabinoxylan
- FIG. 2 is a graphical representation of a plot of specific volume of pulp versus tensile break strength for samples of pulp treated with arabinoxylan.
- Suitable arabinoxylans are polysaccharides that are present in, for example, different annual plants and agricultural residues such as oat husks, straw or maize.
- the arabinoxylans can be obtained by different extraction techniques, e.g., with water, steam or solvents with the aid of the most different of auxiliary chemicals, as well as by enzymatic isolation and purification steps.
- alkali-extracted arabinoxylans are used, especially arabinoxylans from oat husks that can be obtained, for example, by extraction of oat husks with aqueous alkali solution, separation of the alkaline extract and subsequent precipitation of the alkaline extract in a precipitation bath of water and a water-miscible organic solvent A, with the alkaline extract not neutralised before precipitation.
- arabinoxylans from oat husks in comparison to xylans from deciduous wood and coniferous wood is that they have a comparably high number of arabinose substituents but not the 4-O-methylglucuronic acids occurring in deciduous and coniferous xylans. In comparison to xylans from pulp such as the Lenzing xylans, the arabinoxylans exhibit a much higher chain length.
- arabinoxylans are understood to be such xylans that bear 5 to 20% (w/w relative to the whole sample), preferably 7 to 15%, most preferably 8 to 13% arabinose substituents in their main chain and less than 5%, preferably less than 2%, most preferably less than 1% 4-O-methylglucuronic acid substituents (chromatographic sugar determination after acid hydrolysis).
- a further subject matter of the invention is a method for the preparation of cellulose pulps comprised of contact with a concentrated solution or suspension of an arabinoxylan with pulp or stock system that contains pulp.
- a homogeneous solution or suspension of the arabinoxylan can be achieved, for example, by intense mechanical loading such as stirring, by the effect of temperature or with the help of chemicals, preferably basic chemicals such as alkali or alkaline earth hydroxides, preferably NaOH.
- concentration of the arabinoxylan solution or suspension can be varied over a wide range of 0.1 to 40% (w/w). Preferred is the range of 0.1 to 25% (w/w), especially preferred is the range from 0.5% to 10% (w/w).
- the arabinoxylan solution or suspension can be incubated with the pulp and the desired paper auxiliaries and additives in high pulp density (solids content) of up to 20% before the pulp enters the headbox of the paper machine. Then by squeezing out the supernatant solution any unabsorbed chemicals can be used for the next batch.
- the pulp is mixed with the additives and the arabinoxylan solution or suspension in any desired sequence in the headbox, that is immediately before entry into the machine for paper production.
- the addition of the arabinoxylan in the headbox usually achieves better results than the previous incubation with the pulp.
- arabinoxylan solution or suspension is added to the pulp suspension before the refinement of the pulp fibres.
- compositions of xylans are given as % w/w relative to the whole sample, determined by chromatographic sugar determination after acid hydrolysis.
- a 4-O-methylglucuronoxylan from birch wood (no arabinose side chains, 8.8% molar ratio 4-O-methylglucuronic acid relative to xylose units, determined by 1 H NMR, DP ca. 95) was dissolved in water with heating as 5% solution.
- 20 g coniferous sulfite pulp was suspended in water and treated with the xylan solution.
- For experiments with higher amounts of xylan solution correspondingly lower amounts of water were used to suspend the pulp. After addition of the xylan suspensions the pulp density was 7.1% in each case.
- the experimental batches were each incubated for 2 h at 50° C. After incubation the pulp was filtered off through a nutsch.
- the Lenzing xylan from beech wood pulp (no arabinose side chains, 1% 4-O-methylglucuronic acid, DP ca. 35) was dissolved in water with heating as 5% solution. 20 g coniferous sulfite pulp was suspended in water and treated with the xylan solution. For experiments with higher amounts of xylan solution correspondingly lower amounts of water used to suspend the pulp. After addition of the xylan suspensions the pulp density was 7.1% in each case. The experimental batches were incubated for 2 h at 50° C. After incubation the pulp was filtered off through a nutsch.
- the pulp was refined for 2.5 min in a Jokro mill in accordance with ISO 5264-3 and laboratory sheets produced in accordance with ISO 5269-2 (rapid Köthen method). Testing for strength was carried out in accordance with ISO 1974 (DIN EN 21974).
- the tear length can be improved by more than 1000 m by the addition of arabinoxylan from oat husks compared to the reference. With this method of addition the increases in strength can be achieved with low usage of arabinoxylan.
- a cationic polyamide-epichlorhydrin resin was added as paper auxiliary and stirred into the suspension for 5 min.
- the dosage of the paper additive corresponded constantly to a charge density of 0.013 meq/g pulp in all experiments carried out.
- the respective arabinoxylan solution was added. After 5 min portioning and preparation of the laboratory sheets was carried out.
- the tear length can again be significantly increased by the addition of arabinoxylan compared to the reference. It can be clearly seen from the reference that through the use of the paper additive the strength generally lies at a higher level. In regard to the effect of the arabinoxylan a synergistic effect emerges in the interaction with the paper additive. The increases in the tear length are now up to as much as ca. 1800 m. The higher increases in strength are even effective at lower amounts of arabinoxylan than in the experiments without paper additive.
- the specific volume of the pulp is characterised by the bulk, which is plotted in FIG. 2 against the tensile breaking strength (Effect of arabinoxylan from oat husks (9.38% relative to pulp) on the bulk-tensile plot of beech sulfite pulp). It is clear that the curve for the different points of the degree of refinement is displaced to higher bulk values. In order to produce a product with the desired strength a higher sheet volume can be produced by the addition of the arabinoxylan. The increased bulk leads to an increase in the light scattering coefficients and thus to improved optical properties.
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Paper (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
Description
- The present patent application claims the right of priority under 35 U.S.C. § 119 (a)-(d) of European Patent Application No. 05 002 073.4, filed Feb. 2, 2005.
- The present invention concerns the use of arabinoxylans as additive in paper production.
- The mechanical properties of paper are influenced by a series of different parameters of a chemical and physical nature. Several theories to explain the tear resistance properties of paper have been suggested, most of which emphasise the special relevance of fibre-fibre bonding. Amongst the most frequently cited is the theory that includes the factors of interfibre bonding force of the bonded surface and the length of the fibre.
- It is generally agreed that the hemicelluloses native to the pulp improves the tear resistance and contributes to the formation of stronger fibre bonding. Depending upon the raw material and the pulping method, these hemicelluloses are modified greatly during pulp preparation and are destroyed to a considerable extent.
- The use of xylans as additive in paper manufacture is known. Thus Naterova et al. (Papir a celuloza, 41, (7-8), V23-V30, 1986) describe the addition of 2% maize xylan to packaging paper. In this way the flexural strength is increased by about 172% by the addition of 2% xylan.
- DE 44 09 372 A1, U.S. Pat. No. 5,810,972 and WO 2004/031477 A1 describe the addition of highly refined birch pulp and Lenzing xylan in the range of 0.005 to 0.14% (WO 2004/031477 A1) or 0.15 to 1.5% (U.S. Pat. No. 5,810,972, DE 44 09 372 A1) to tissue products. A positive effect of the xylans and xylan-rich, highly refined birch pulp on the softness of the tissue product and the behaviour of the paper web on the drying drum is described. The breaking strength was increased by 15 to 73% in the machine way and 17 to 90% transverse to the direction of travel. Allegedly the behaviour of the dry end was positively influence but not reported numerically, but assessed according to the experience of the paper maker.
- In the aforementioned applications the use of xylans from the raw material wood and its secondary product pulp is discussed. In particular, the use of acetyl-4-O-methylglucuronoxylan from deciduous wood and arabino-4-O-methylglucuronoxylan from coniferous wood is cited. The examples on the use of xylans cites Lenzing xylan. This product is obtained by alkaline extraction of beech wood pulp in the viscose process and exhibits only a low degree of polymerisation of about 35.
- Consequently different xylans have been investigated in respect of their attributes for the fibre properties or as paper additive. However, the work cited shows that an improvement in tear length is associated with a deterioration in other strength properties or in an unacceptable deterioration in optical properties.
- There is therefore still the requirement for a cost-effective paper additive that brings about an improvement in paper properties, in particular strength, bulk and optical properties.
- It has now been surprisingly found that the addition of arabinoxylans to pulp during paper production brings about a significant improvement in paper properties. By the use of arabinoxylan the tear length, the tear resistance and the bulk, i.e., the volume of the paper, is improved. The improvement in the bulk improves both the strength properties and the optical properties of the paper. Surprisingly a significantly greater improvement of the paper properties is achieved in comparison to other xylans such as 4-O-methylglucuronoxylans from deciduous wood or Lenzing xylans.
- In accordance with the present invention, there is provided a method of preparing a modified cellulose pulp comprising contacting,
-
- (i) an arabinoxylan, said arabinoxylan being in a form selected from the group consisting of a concentrated solution comprising arabinoxylan and a suspension comprising arabinoxylan, with
- (ii) a cellulose pulp.
- In further accordance with the present invention, there is provided a modified cellulose pulp comprising:
-
- cellulose pulp; and
- 0.1% to 40% by weight of an arabinoxylan, based on the total weight of cellulose pulp and arabinoxylan.
- There is also provided, in accordance with the present invention, an arabinoxylan comprising, on its main chain:
-
- 5 to 20% arabinose substituents; and
- less that 5% 4-O-methylglucuronic acid substituents the percent weights being based on the total weight of the arabinoxylan.
- The subject matter of the invention relates in part to the use of arabinoxylans as additive in paper manufacture.
- The features that characterize the present invention are pointed out with particularity in the claims, which are annexed to and form a part of this disclosure.
- These and other features of the invention, its operating advantages and the specific objects obtained by its use will be more fully understood from the following detailed description and accompanying drawings in which preferred embodiments of the invention are illustrated and described.
- Unless otherwise indicated, all numbers or expressions used in the specification and claims are understood as modified in all instances by the term “about.”
-
FIG. 1 is a graphical representation of plots of tear and tensile strengths of pulp samples treated with arabinoxylan; and -
FIG. 2 is a graphical representation of a plot of specific volume of pulp versus tensile break strength for samples of pulp treated with arabinoxylan. - Suitable arabinoxylans are polysaccharides that are present in, for example, different annual plants and agricultural residues such as oat husks, straw or maize. The arabinoxylans can be obtained by different extraction techniques, e.g., with water, steam or solvents with the aid of the most different of auxiliary chemicals, as well as by enzymatic isolation and purification steps. Preferably alkali-extracted arabinoxylans are used, especially arabinoxylans from oat husks that can be obtained, for example, by extraction of oat husks with aqueous alkali solution, separation of the alkaline extract and subsequent precipitation of the alkaline extract in a precipitation bath of water and a water-miscible organic solvent A, with the alkaline extract not neutralised before precipitation.
- The special feature of the arabinoxylans from oat husks in comparison to xylans from deciduous wood and coniferous wood is that they have a comparably high number of arabinose substituents but not the 4-O-methylglucuronic acids occurring in deciduous and coniferous xylans. In comparison to xylans from pulp such as the Lenzing xylans, the arabinoxylans exhibit a much higher chain length.
- Within the context of the present invention arabinoxylans are understood to be such xylans that bear 5 to 20% (w/w relative to the whole sample), preferably 7 to 15%, most preferably 8 to 13% arabinose substituents in their main chain and less than 5%, preferably less than 2%, most preferably less than 1% 4-O-methylglucuronic acid substituents (chromatographic sugar determination after acid hydrolysis).
- Arabinoxylans that are obtained by extraction of oat husks with aqueous alkaline solution with isolation of an alkaline extract and subsequent precipitation of the alkaline extract in a precipitation bath of water with a water-miscible organic solvent A with the alkaline extract not neutralised before precipitation are particularly preferred. Such arabinoxylans exhibit a chain length of at least 100 also after a possible bleaching stage. Usually the chain lengths of these arabinoxylans lie in the range 120 to 240.
- A further subject matter of the invention is a method for the preparation of cellulose pulps comprised of contact with a concentrated solution or suspension of an arabinoxylan with pulp or stock system that contains pulp.
- In one embodiment of the invention the arabinoxylan solution or suspension is added to the fibre suspension before sheet making. The action of the arabinoxylan is also carried out in combination with other paper chemicals which are added to the fibre before, after or together with the arabinoxylan. In this way the use of arabinoxylan is advantageous for the most different of products in the paper industry.
- Other normal paper chemicals are for example wet-strength agents, fillers, retention agents, fixatives, defoamers, deaerators, sizing agents, optical brighteners and colorants.
- A homogeneous solution or suspension of the arabinoxylan can be achieved, for example, by intense mechanical loading such as stirring, by the effect of temperature or with the help of chemicals, preferably basic chemicals such as alkali or alkaline earth hydroxides, preferably NaOH. The concentration of the arabinoxylan solution or suspension can be varied over a wide range of 0.1 to 40% (w/w). Preferred is the range of 0.1 to 25% (w/w), especially preferred is the range from 0.5% to 10% (w/w).
- The arabinoxylan solution or suspension can be incubated with the pulp and the desired paper auxiliaries and additives in high pulp density (solids content) of up to 20% before the pulp enters the headbox of the paper machine. Then by squeezing out the supernatant solution any unabsorbed chemicals can be used for the next batch.
- In a further embodiment of the invention the pulp is mixed with the additives and the arabinoxylan solution or suspension in any desired sequence in the headbox, that is immediately before entry into the machine for paper production. The addition of the arabinoxylan in the headbox usually achieves better results than the previous incubation with the pulp.
- In a further embodiment of the invention the arabinoxylan solution or suspension is added to the pulp suspension before the refinement of the pulp fibres.
- Usually after achieving the optimal quantities no further increase in strength and bulk is achieved by further increase in the amount of arabinoxylan in a product formulation. The optimal amount is dependent upon which other paper auxiliaries are used in the mass so that that the amount of arabinoxylan used relative to pulp can be in a wide range of 0.1% to 40% (w/w). Preferably, however, an amount between 0.5 and 10% arabinoxylan is used. Usually with the use of paper additives the optimal increase in strength is achieved at even lower arabinoxylan concentration.
- The invention is illustrated but not limited in the following by a number of embodiment examples.
- Unless otherwise stated in the following examples the compositions of xylans are given as % w/w relative to the whole sample, determined by chromatographic sugar determination after acid hydrolysis.
- An arabinoxylan from oat husks (9.5% arabinose, <1% 4-O-methylglucuronic acid, DP ca. 160) was dissolved in water with heating with formation of a 5% solution. 20 g coniferous sulfite pulp was suspended in water and treated with the xylan solution in the amounts given in Table 1. For experiments with higher amounts of xylan solution correspondingly lower amounts of water were used in each case for suspension of the pulp. After addition of the xylan suspensions the pulp density was 7.1% in each case. The experimental batches were all incubated for 2 h at 50° C. After incubation the pulp was filtered off through a nutsch.
- The pulp was refined for 2.5 min in a Jokro mill in accordance with ISO 5264-3 and laboratory sheets produced in accordance with ISO 5269-2 (rapid Köthen method). Testing for strength was carried out in accordance with ISO 1974 (DIN EN 21974).
TABLE 1 Amount of arabinoxylan in % (w/w) rel. to pulp Tear length (m) 0 2734 (reference) 7.5 3473 22.5 3935 37.5 4199 - The data in Table 1 show that in comparison with the reference pulp without xylan the pulp treated with arabinoxylan from oat husks exhibited considerably higher strength. The tear lengths increased with increasing xylan amounts. The greatest increase in tear length by addition of arabinoxylan from oat husks is 1465 m.
- A 4-O-methylglucuronoxylan from birch wood (no arabinose side chains, 8.8% molar ratio 4-O-methylglucuronic acid relative to xylose units, determined by 1H NMR, DP ca. 95) was dissolved in water with heating as 5% solution. 20 g coniferous sulfite pulp was suspended in water and treated with the xylan solution. For experiments with higher amounts of xylan solution correspondingly lower amounts of water were used to suspend the pulp. After addition of the xylan suspensions the pulp density was 7.1% in each case. The experimental batches were each incubated for 2 h at 50° C. After incubation the pulp was filtered off through a nutsch.
- The pulp was refined for 2.5 min in a Jokro mill in accordance with ISO 5264-3 and laboratory sheets produced in accordance with ISO 5269-2 (rapid Köthen method). Testing for strength was carried in accordance with ISO 1974 (DIN EN 21974).
TABLE 2 Amount of 4-O- methylglucuronoxylan in % (w/w) rel. to pulp Tear length (m) 0 2734 (reference) 7.5 2983 22.5 3126 37.5 3189 - The data in Table 2 show that the 4-O-methylglucuronoxylan from birch wood can bring about only a very small increase in strength. The action of this xylan is less that 31% of the action of arabinoxylan from oat husks.
- The Lenzing xylan from beech wood pulp (no arabinose side chains, 1% 4-O-methylglucuronic acid, DP ca. 35) was dissolved in water with heating as 5% solution. 20 g coniferous sulfite pulp was suspended in water and treated with the xylan solution. For experiments with higher amounts of xylan solution correspondingly lower amounts of water used to suspend the pulp. After addition of the xylan suspensions the pulp density was 7.1% in each case. The experimental batches were incubated for 2 h at 50° C. After incubation the pulp was filtered off through a nutsch.
- The pulp was refined for 2.5 min in a Jokro mill in accordance with ISO 5264-3 and laboratory sheets produced in accordance with ISO 5269-2 (rapid Köthen method). Testing for strength was carried out in accordance with ISO 1974 (DIN EN 21974).
- The data in Table 3 show that the “Lenzing xylan” from beech wood pulp can bring about only a very small increase in strength. The action of this xylan is less that 36% of the action of arabinoxylan from oat husks.
TABLE 3 Amount of Lenzing xylan in % (w/w) rel. to pulp Tear length (m) 0 2734 (reference) 7.5 3010 22.5 3000 37.5 3260 - An arabinoxylan (9.5% arabinose, <1% 4-O-methylglucuronic acid DP ca. 160) from oat husks was dissolved in water with heating as 5% solution. A coniferous sulfite pulp was then refined for 2.5 min. in a Jokro mill in accordance with ISO 5264-3 and laboratory sheets prepared in accordance with ISO 5269-2 (rapid Köthen method). The arabinoxylan solutions were in each case added to the pan which is used for portioning the suspension for the individual laboratory sheets. In each pan 16 g pulp were equalised in each case in a total liquid of 6.67 l with a pulp density of 0.24%. The respective amounts of arabinoxylan solution was added. After 5 min portioning and preparation of the laboratory sheets was carried out. All experiments were carried out at room temperature. Testing for strength was carried out according to ISO1974 (DIN EN 21974).
TABLE 4 Influence of arabinoxylan from oat husks on the tear length of coniferous sulfite pulp. The arabinoxylan treatment took place at a pulp density of 0.24% after refinement of the pulp. Amount of arabinoxylan % (w/w) rel. to pulp Tear length (m) Reference 2830 4.7 3759 9.4 4216 28.1 4031 - The tear length can be improved by more than 1000 m by the addition of arabinoxylan from oat husks compared to the reference. With this method of addition the increases in strength can be achieved with low usage of arabinoxylan.
- An arabinoxylan from oat husks (9.5% arabinose, <1% 4-O-methylglucuronic acid DP ca. 160) was dissolved in water with heating as 5% solution. A coniferous sulfite pulp was then refined for 2.5 min. in a Jokro mill in accordance with ISO 5264-3 and laboratory sheets prepared in accordance with ISO 5269-2 (rapid Köthen method). The xylan solutions were in each case added to the pan which is used for portioning the suspension for the individual laboratory sheets. In each pan 16 g pulp were equalised in each case in a total liquid of 6.67 l with a pulp density of 0.24%. A cationic polyamide-epichlorhydrin resin was added as paper auxiliary and stirred into the suspension for 5 min. The dosage of the paper additive corresponded constantly to a charge density of 0.013 meq/g pulp in all experiments carried out. Next the respective arabinoxylan solution was added. After 5 min portioning and preparation of the laboratory sheets was carried out.
- All experiments were carried out at room temperature. Testing for strength was carried out according to ISO1974 (DIN EN 21974).
TABLE 5 Influence of arabinoxylan from oat husks on the tear length of coniferous sulfite pulp with concomitant use of a paper additive. The arabinoxylan treatment took place at a pulp density of 0.24% after refinement of the pulp. Arabinoxylan with paper Amount of xylan additive % (w/w) rel. to pulp Tear length (m) Reference 3944 0.09 3992 0.93 4698 2.3 5486 4.7 5629 7.0 5710 9.4 5728 - The tear length can again be significantly increased by the addition of arabinoxylan compared to the reference. It can be clearly seen from the reference that through the use of the paper additive the strength generally lies at a higher level. In regard to the effect of the arabinoxylan a synergistic effect emerges in the interaction with the paper additive. The increases in the tear length are now up to as much as ca. 1800 m. The higher increases in strength are even effective at lower amounts of arabinoxylan than in the experiments without paper additive.
- An arabinoxylan from oat husks (9.5% arabinose, <1% 4-O-methylglucuronic acid, DP ca. 160) was dissolved in water with heating as 5% solution. A beech wood sulfite pulp was then refined for 2.5 min, 5 min, 10 min, 15 min and 20 min in a Jokro mill in accordance with ISO 5264-3 and laboratory sheets were prepared in accordance with ISO 5269-2 (rapid Köthen method). The arabinoxylan solutions at 9.4% (relative to pulp) were in each case added to the pan which is used for portioning the suspension for the individual laboratory sheets. In each pan 16 g pulp were equalised in each case in a total liquid of 6.67 l with a pulp density of 0.24%. 5 Min after addition of the arabinoxylan solution portioning and preparation of the laboratory sheets was carried out. All experiments were carried out at room temperature. Testing for strength was carried out according to ISO1974 (DIN EN 21974). Light scattering coefficients were determined according to Instruction SCAN C 27:76.
- The experiments showed that not only the tensile strength of the pulp was increase by arabinoxylan addition, but also the tear strength. The tear-tensile plot allows combined viewing of the tensile strength and tear strength of all samples from the refinement series (
FIG. 1 , Effect of arabinoxylan from oat husks (9.38% relative to pulp) on the tear-tensile plot of beech sulfite pulp). It is obvious that the samples show clearly better values in both strengths by the addition of the arabinoxylan such that the whole curve is displaced to a higher level. - The specific volume of the pulp is characterised by the bulk, which is plotted in
FIG. 2 against the tensile breaking strength (Effect of arabinoxylan from oat husks (9.38% relative to pulp) on the bulk-tensile plot of beech sulfite pulp). It is clear that the curve for the different points of the degree of refinement is displaced to higher bulk values. In order to produce a product with the desired strength a higher sheet volume can be produced by the addition of the arabinoxylan. The increased bulk leads to an increase in the light scattering coefficients and thus to improved optical properties. - Although the invention has been described in detail in the foregoing for the purpose of illustration, it is to be understood that such detail is solely for that purpose and that variations can be made therein by those skilled in the art without departing from the spirit and scope of the invention except as it may be limited by the claims.
Claims (10)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05002073A EP1688534A1 (en) | 2005-02-02 | 2005-02-02 | Use of Arabinoxylanes in paper production |
| EP05002073.4 | 2005-02-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20060169432A1 true US20060169432A1 (en) | 2006-08-03 |
Family
ID=34933545
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/231,016 Abandoned US20060169432A1 (en) | 2005-02-02 | 2005-09-20 | Method of preparing modified cellulose pulp |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20060169432A1 (en) |
| EP (1) | EP1688534A1 (en) |
| CA (1) | CA2586187A1 (en) |
| RU (1) | RU2007116306A (en) |
| WO (1) | WO2006081845A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040129395A1 (en) * | 2002-10-01 | 2004-07-08 | The Procter & Gamble Company | Strengthened tissue paper products comprising low levels of xylan |
| US20080128100A1 (en) * | 2002-10-01 | 2008-06-05 | Frank Rehders | Strengthened tissue paper products comprising low level of xylan |
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| US5395765A (en) * | 1991-10-18 | 1995-03-07 | Novo Nordisk A/S | Thermostable xylanase from a strain of Rhodothermus marinus |
| US5683518A (en) * | 1993-01-21 | 1997-11-04 | Moore Epitaxial, Inc. | Rapid thermal processing apparatus for processing semiconductor wafers |
| US5810972A (en) * | 1994-03-18 | 1998-09-22 | The Procter & Gamble Company | Method for the production of creped hygienic cellulose paper |
| US5834301A (en) * | 1992-03-25 | 1998-11-10 | The United States Of America As Represented By The Secretary Of Agriculture | Method of removing color from kraft wood pulps |
| US5885819A (en) * | 1993-03-10 | 1999-03-23 | Novo Nordisk A/S | Enzyme with xylanase activity |
| US5902581A (en) * | 1995-12-04 | 1999-05-11 | Genencor International, Inc. | Xylanase from acidothermus cellulolyticus |
| US20020195213A1 (en) * | 1999-03-23 | 2002-12-26 | Yoshiya Izumi | Process for producing xylooligosaccharide from lignocellulose pulp |
| US20030124192A1 (en) * | 2000-01-05 | 2003-07-03 | Fitchett Colin Stanley | Pharmaceutical compositions and their preparation |
| US20040129395A1 (en) * | 2002-10-01 | 2004-07-08 | The Procter & Gamble Company | Strengthened tissue paper products comprising low levels of xylan |
| 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 |
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| AU1437897A (en) * | 1996-01-22 | 1997-08-20 | Novo Nordisk A/S | An enzyme with xylanase activity |
| CA2301371C (en) * | 1999-03-23 | 2009-09-01 | Oji Paper Co., Ltd. | Process for bleaching lignocellulose pulp |
| FR2852202B1 (en) * | 2003-03-14 | 2006-08-11 | NEW PROCESS FOR POTENTIATING AND SIMULATION OF NATURAL DEFENSE OF PLANTS |
-
2005
- 2005-02-02 EP EP05002073A patent/EP1688534A1/en not_active Withdrawn
- 2005-09-08 CA CA002586187A patent/CA2586187A1/en not_active Abandoned
- 2005-09-08 WO PCT/EP2005/009657 patent/WO2006081845A1/en not_active Application Discontinuation
- 2005-09-08 RU RU2007116306/12A patent/RU2007116306A/en unknown
- 2005-09-20 US US11/231,016 patent/US20060169432A1/en not_active Abandoned
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|---|---|---|---|---|
| US5395765A (en) * | 1991-10-18 | 1995-03-07 | Novo Nordisk A/S | Thermostable xylanase from a strain of Rhodothermus marinus |
| US5834301A (en) * | 1992-03-25 | 1998-11-10 | The United States Of America As Represented By The Secretary Of Agriculture | Method of removing color from kraft wood pulps |
| US5683518A (en) * | 1993-01-21 | 1997-11-04 | Moore Epitaxial, Inc. | Rapid thermal processing apparatus for processing semiconductor wafers |
| US6080567A (en) * | 1993-03-10 | 2000-06-27 | Novo Nordisk A/S | Enzymes with xylanase activity from Aspergillus aculeatus |
| US5885819A (en) * | 1993-03-10 | 1999-03-23 | Novo Nordisk A/S | Enzyme with xylanase activity |
| US6197564B1 (en) * | 1993-03-10 | 2001-03-06 | Novo Nordisk A/S | Enzymes with xylanase activity from Aspergillus aculeatus |
| US6228630B1 (en) * | 1993-03-10 | 2001-05-08 | Novo Nordisk A/S | Enzymes with xylanase activity from aspergillus aculeatus |
| US5810972A (en) * | 1994-03-18 | 1998-09-22 | The Procter & Gamble Company | Method for the production of creped hygienic cellulose paper |
| US5902581A (en) * | 1995-12-04 | 1999-05-11 | Genencor International, Inc. | Xylanase from acidothermus cellulolyticus |
| US20020195213A1 (en) * | 1999-03-23 | 2002-12-26 | Yoshiya Izumi | Process for producing xylooligosaccharide from lignocellulose pulp |
| 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 |
| US20030124192A1 (en) * | 2000-01-05 | 2003-07-03 | Fitchett Colin Stanley | Pharmaceutical compositions and their preparation |
| US20040129395A1 (en) * | 2002-10-01 | 2004-07-08 | The Procter & Gamble Company | Strengthened tissue paper products comprising low levels of xylan |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040129395A1 (en) * | 2002-10-01 | 2004-07-08 | The Procter & Gamble Company | Strengthened tissue paper products comprising low levels of xylan |
| US20080128100A1 (en) * | 2002-10-01 | 2008-06-05 | Frank Rehders | Strengthened tissue paper products comprising low level of xylan |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2006081845A1 (en) | 2006-08-10 |
| EP1688534A1 (en) | 2006-08-09 |
| CA2586187A1 (en) | 2006-08-10 |
| RU2007116306A (en) | 2009-03-10 |
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