WO2005028744A1 - Chemical activation and refining of southern pine kraft fibers - Google Patents
Chemical activation and refining of southern pine kraft fibers Download PDFInfo
- Publication number
- WO2005028744A1 WO2005028744A1 PCT/IB2004/003080 IB2004003080W WO2005028744A1 WO 2005028744 A1 WO2005028744 A1 WO 2005028744A1 IB 2004003080 W IB2004003080 W IB 2004003080W WO 2005028744 A1 WO2005028744 A1 WO 2005028744A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- pulp
- fibers
- treatment
- metal ion
- refining
- Prior art date
Links
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21B—FIBROUS RAW MATERIALS OR THEIR MECHANICAL TREATMENT
- D21B1/00—Fibrous raw materials or their mechanical treatment
- D21B1/04—Fibrous raw materials or their mechanical treatment by dividing raw materials into small particles, e.g. fibres
- D21B1/12—Fibrous raw materials or their mechanical treatment by dividing raw materials into small particles, e.g. fibres by wet methods, by the use of steam
- D21B1/14—Disintegrating in mills
- D21B1/16—Disintegrating in mills in the presence of chemical agents
-
- 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
- D21C9/007—Modification of pulp properties by mechanical or physical means
-
- 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
- D21C3/006—Pulping cellulose-containing materials with compounds not otherwise provided for
-
- 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
- D21C3/02—Pulping cellulose-containing materials with inorganic bases or alkaline reacting compounds, e.g. sulfate 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
- 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
-
- 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
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/16—Bleaching ; Apparatus therefor with per compounds
- D21C9/163—Bleaching ; Apparatus therefor with per compounds with peroxides
-
- 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
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/1026—Other features in bleaching processes
- D21C9/1036—Use of compounds accelerating or improving the efficiency of the processes
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/298—Physical dimension
Definitions
- This invention relates to papermaking and particularly to the treatment of cellulosic material preparatory to use of the treated material to manufacture paper web material.
- paper is commonly formed from wood.
- the industry divides wood used in paperrna-king into two categories; namely hardwoods and softwoods.
- Softwood fibers come from needle-bearing conifer trees such as pine, spruce, alpine fir, and Douglas fir.
- Hardwood fibers are derived from deciduous trees of various varieties.
- HW hardwood
- SW softwood
- Paper as used herein includes webs or sheets without limitation as to the size or basis weight of the web or sheet.
- HW or SW paper may be employed as "bleache board” (useful in containers for consumer products, for example) or as “container board” or “liner board” (useful in corrugated boxes, for example).
- Printability of a paper is a major consideration with respect to the end use of the paper.
- SW fibers are notoriously problematic as respects the printability of the paper produced from these fibers in that SW fiber papers tend to be inordinately porous, stiff, and must be treated specially to obtain a paper surface which is suitably printable.
- HW and SW must be subjected to specific treatments for converting the wood into a fibrous slurry employed in the formation of a paper web.
- Softwoods are more plentiful and are more readily replaceable, as by tree farming.
- Softwoods in general are less costly.
- SW fibers be substituted for HW fibers wherever possible in papermaking.
- Southern pine, or mixtures of hardwoods and softwoods, are commonly examined as possible substitutes for end products which have heretofore been manufactured using hardwoods.
- Smoothness and Formation are measures of, among other things, the printability of the paper.
- "Formation" as used as a paper characteristic usually, and herein, is a synonym for relative uniformity over a scale of some distance, e.g., 5 to 20 mm. Formation may be judged by viewing it with light from the back and other means. Both smoothness and formation are affected, among other things, fiber length, morphology and collapsibility.
- alteration of the morphology of cellulose fibers, particularly softwood fibers by (a) subjecting the fibers to a metal ion-activated peroxide treatment carried out at a pH of between about 1 and about 9, preferably between 3 and 7, and (b) subjecting the treated fibers to a refining treatment converts SW fibers to HW-like fibers in many respects.
- the metal ion-activated peroxide treatment has been noted to act on pulp cellulose and hemi-cellulose, causing oxidation and oxidative degradation of cellulose fibers.
- the chemical treatment of the pulp taken alone, is not sufficient to attain the desired modification of the morphology of the fibers, however, subsequent refining or like mechanical treatment of the chemically- treated fibers to achieve a given degree of refinement of the fibers requires dramatically less refining energy, e.g., between about 30 and 50% less energy to achieve a desired end point of refinement.
- the pulp treated in accordance with the present invention demonstrates substantially reduced fiber length or fiber length distribution, thereby enabling better uniformity of paper sheet (web) structure as measured by formation or texture.
- the treated fibers are more collapsible during sheet consolidation and result in significantly improved paper surface properties such as smoothness.
- SW fibers treated in accordance with the present invention are substantially functionally equivalent to HW fibers in regards to their usefulness in papermaking.
- the treatment of the present invention may be applied to wood chemical pulps (or pulp mixtures)having various processing histories such as pulping, bleaching or acid hydrolysis, or other combinations of processing of wood into pulp suitable for infeed to a papermaking machine.
- the present invention may be applied to pulp which has already been subjected to refining, chemical treatment, enzyme treatment, microfibrilltion, and/ or acid hydrolysis, for example, to increase the pulp freeness or improve drainage during the papermaking process and/ or to reduce the cellulose particles suspension viscosity and improving flow characteristic.
- the advantages of the present invention may be achieved employing a hypochlorite treatment at pH 3 - 9, preferably, pH 3-8 and employing hypochlorous acid as the dominate active agent, followed by subsequent refining of the treated pulp.
- either the metal ion- activated peroxide or the hypochlorous acid treatment may be applied alone to refined fibers for increased freeness/drainage, or on micro-fibrillated cellulose materials for reduced suspension viscosity.
- either embodiment may be employed as a means for controlling the viscosity of a pulp suspension at any of various locations between the initial digestion of the cellulose material to and including the feeding of the pulp suspension into a papermaking machine. This latter aspect of the present invention is applicable in the dissolution of pulp for viscose production, for example.
- the beneficial effects of the present invention are exhibited in the calendaring of a paper web or sheet formed from treated SW fibers or combinations of HW fibers and treated SW fibers.
- the present invention may be combined with a fiber fractionation process for the treatment of specific fiber fractions.
- Paper produced employing pulp treated in accordance with the present invention exhibits tear strengths at HW levels, with little material deterioration of tensile strength. Improved bonding of the fibers within the sheet is also provided due to enhanced freeness.
- Figure 1 is a graph depicting the energy savings attributable to the present invention when refining Southern Pine pulp
- Figure 2 is a graph depicting fiber length reduction achieved when treating
- FIG. 3 is a graph depicting the shifting of fiber length distribution between treated and untreated softwood pulp in accordance with the present invention.
- Figure 4 is a microphotograph depicting untreated pine fibers
- Figure 5 is a microphotograph depicting pine fibers treated in accordance with the present invention.
- Figure 6 is a graph depicting the relationship of bulk vs. smoothness of hardwood pulp, untreated pine pulp and treated pine pulp;
- Figure 7 is a graph depicting the relationship of bulk vs. freeness of the pulps depicted in Figure 6;
- Figure 8 is a graph depicting the relationship of tear vs. freeness of the pulps depicted in Figure 6;
- Figure 9 is a graph depicting bulk and smoothness relationship of untreated hardwood pulp, untreated pine pulp, and various mixtures of hardwood and softwood pulps;
- Figure 10 is a graph depicting the fiber length reduction of untreated pine pulp and pulp treated in accordance with the present invention, employing low intensity disc refining;
- Figure 11 is a graph depicting the energy savings associated with disc refining employed as a component of the present invention when processing treated and untreated pine pulp.
- Figure 12 is a graph depicting the relationship between fiber length reduction and the energy employed in refining untreated pulp and pulp treated in accordance with the present invention.
- a method for the transformation of softwood fibers, particularly Southern pine fibers, into hardwood-like fibers employs the steps of (a) subjecting a SW pulp containing cellulose and hemicellulose, to a solution containing a transitional metal ion and a peroxide at a pH of between about 1 and 9 for a time sufficient to oxidize a substantial portion of the cellulose /hemi-cellulose and to oxidatively degrade the cellulose fibers, and (b) subjecting the treated pulp to a refining operation.
- the pulp thus treated when formed into a web on a papermaking machine exhibits many hardwood-like properties such as overall formability into a web having surface properties like webs formed from hardwood fibers employing conventional papermaking techniques.
- softwood fibers obtained from coniferous trees, and particularly Southern pine trees are converted into a pulp employing the kraft process in which the fibers are treated in a heated alkaline solution to substantially separate the fibers from their lignin binder, as is well known in the art.
- Southern pine fibers are particularly suitable for treatment employing the present invention, it is recognized that fibers from other coniferous trees may be employed.
- the present invention may be advantageously employed with mixtures of SW and HW fibers, for example mixtures containing between about 50% and 90% by weight of SW pulp and between about 10% and 50% HW pulp.
- the SW pulp or mixture of SW and HW pulps prior to treatment thereof employing the present invention, may comprise pulp which has not undergone any conventional treatment of the pulp subsequent to the digestion step.
- the present invention is useful in treating pulps which, subsequent to digestion, have undergone substantially any of the commonly employed treatments of pulp such as an acid hydrolysis for removal of hexauronic acid, oxidation /bleaching employing oxygen and/or peroxide, or ozone, on the pulp and/or mechanical treatment of the pulp, ie., refining.
- the pulp or mixture of pulps, to be subjected to the method of the present invention will be a pulp(s) which has been digested and at least washed to remove black liquor.
- the pulp solution at a temperature of between about 40 and 120 degrees C, is subjected to a solution of a transitional metal-activated peroxide for between about 10 and 600 minutes.
- a higher treatment temperature will require less residence time, and vice versa.
- the treatment be done at 70-79 degrees C, with a residence time between 30-180 minutes.
- the treatment can be carried out in a bleach tower, high- density tower, re-pulper tanks, or any suitable vessel with sufficient mixing and residence time.
- the treatment solution of the present invention includes between about 0.2% and about 5% by wt. hydrogen peroxide and between about 0.002% and about 0.1% of a transitional metal ions, based on pulp.
- Iron (III) salts such as ferric chloride, or iron (II) salts such as ferrous sulfate and ferrous chloride, are especially useful as a source of the metal ions.
- Other metal ions such as copper (II), cobalt(II) may be employed.
- a trace of the transitional metal ions is required to achieve the advantageous results of the present invention, preferably between about 0.002% and about 0.01% of the metal ion.
- the pulp treatment is carried out at a pH of between about 1 and about 9, preferably a pH between about 2 and 7.
- Figure 2 shows the fiber length reduction (length-weighted average) by refining and indicates that, with catalyzed hydrogen peroxide treatment before refining, the fiber length is substantially reduced after being subsequently refined. While for comparison, the untreated pulp (control) showed little fiber length reduction by PFI refining.
- Figure 3 further illustrates the fiber length reduction as shown in Figure 2.
- Figure 3 there is demonstrated the fiber length distribution curves, with the treated vs. the untreated (control) southern pine, at the same refining. As seen, the treatment caused a significant shift of fiber length to shorter range than the control.
- Example 1 Bleached southern pine as employed in Example 1 was treated with 1% hydrogen peroxide based on pulp at pH 4, with 0.006% FE(II) as from ferrous sulfate. The treatment was carried out at the temperature of 70°C for 1 hour. The treated pulp and control were PFI refined as in Example 1. TAPPI hand sheets were then made from these pulps.
- Figure 9 plots the bulk-smoothness curve of the mixed pulp furnish (data from Table III), along with 100% pine and hardwood curves (data from Table II). It is obvious that the treated pine can be used to replace substantial amounts of hardwood pulp. The exact amount of hardwood replacement in the paper mill, however, may also be affected somewhat by the nature, type and optimization of commercial refiners.
- EXAMPLE 5 [0037] A Voith LRl Disc Refiner was used to refine bleached southern pine which had been treated with 1% hydrogen peroxide, as catalyzed by Fe(III) at pH4. The refiner specific edge load was set at 0.8 Ws/m. As seen from Table IV, Figure 10, energy saving and fiber length reduction were confirmed.
- EXAMPLE 6 [0038] A Voith LRl Disc Refiner was used to refine bleached southern pine , which had been treated with 1% hydrogen peroxide, as catalyzed by Fe(II) at pH4. The refiner specific edge load was set at 4 km.
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- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mechanical Engineering (AREA)
- Inorganic Chemistry (AREA)
- Paper (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04769444A EP1668180B1 (en) | 2003-09-23 | 2004-09-22 | Chemical activation and refining of southern pine kraft fibers |
PL04769444T PL1668180T3 (en) | 2003-09-23 | 2004-09-22 | Chemical activation and refining of southern pine kraft fibers |
NZ545801A NZ545801A (en) | 2003-09-23 | 2004-09-22 | Chemical activation and refining of southern pine kraft fibers for alteration of the morphology of cellulose fibers |
DE602004007942T DE602004007942T2 (en) | 2003-09-23 | 2004-09-22 | CHEMICAL ACTIVATION AND FINISHING OF SOUTH PINE FIBERS |
CA2539095A CA2539095C (en) | 2003-09-23 | 2004-09-22 | Chemical activation and refining of southern pine kraft fibers |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/668,387 | 2003-09-23 | ||
US10/668,387 US8262850B2 (en) | 2003-09-23 | 2003-09-23 | Chemical activation and refining of southern pine kraft fibers |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2005028744A1 true WO2005028744A1 (en) | 2005-03-31 |
Family
ID=34313471
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2004/003080 WO2005028744A1 (en) | 2003-09-23 | 2004-09-22 | Chemical activation and refining of southern pine kraft fibers |
Country Status (9)
Country | Link |
---|---|
US (6) | US8262850B2 (en) |
EP (2) | EP1668180B1 (en) |
CN (1) | CN100575597C (en) |
AT (1) | ATE368766T1 (en) |
CA (1) | CA2539095C (en) |
DE (1) | DE602004007942T2 (en) |
NZ (1) | NZ545801A (en) |
PL (1) | PL1668180T3 (en) |
WO (1) | WO2005028744A1 (en) |
Cited By (16)
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CN101240089B (en) * | 2008-03-11 | 2010-06-30 | 江苏江昕轮胎有限公司 | Rubber activity cut staple |
WO2011141692A1 (en) | 2010-05-10 | 2011-11-17 | Unilever Plc | Freeness of paper products |
US8262850B2 (en) | 2003-09-23 | 2012-09-11 | International Paper Company | Chemical activation and refining of southern pine kraft fibers |
US8282774B2 (en) | 2005-05-02 | 2012-10-09 | International Paper Company | Ligno cellulosic materials and the products made therefrom |
US9512562B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US9512237B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Method for inhibiting the growth of microbes with a modified cellulose fiber |
US9512563B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Surface treated modified cellulose from chemical kraft fiber and methods of making and using same |
US9511167B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US9617686B2 (en) | 2012-04-18 | 2017-04-11 | Gp Cellulose Gmbh | Use of surfactant to treat pulp and improve the incorporation of kraft pulp into fiber for the production of viscose and other secondary fiber products |
US9719208B2 (en) | 2011-05-23 | 2017-08-01 | Gp Cellulose Gmbh | Low viscosity kraft fiber having reduced yellowing properties and methods of making and using the same |
US9951470B2 (en) | 2013-03-15 | 2018-04-24 | Gp Cellulose Gmbh | Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same |
US10000890B2 (en) | 2012-01-12 | 2018-06-19 | Gp Cellulose Gmbh | Low viscosity kraft fiber having reduced yellowing properties and methods of making and using the same |
US10138598B2 (en) | 2013-03-14 | 2018-11-27 | Gp Cellulose Gmbh | Method of making a highly functional, low viscosity kraft fiber using an acidic bleaching sequence and a fiber made by the process |
US10151064B2 (en) | 2013-02-08 | 2018-12-11 | Gp Cellulose Gmbh | Softwood kraft fiber having an improved α-cellulose content and its use in the production of chemical cellulose products |
US10865519B2 (en) | 2016-11-16 | 2020-12-15 | Gp Cellulose Gmbh | Modified cellulose from chemical fiber and methods of making and using the same |
US11332886B2 (en) | 2017-03-21 | 2022-05-17 | International Paper Company | Odor control pulp composition |
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US8268122B2 (en) | 2005-12-02 | 2012-09-18 | Akzo Nobel N.V. | Process of producing high-yield pulp |
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WO2011088889A1 (en) * | 2010-01-19 | 2011-07-28 | Södra Skogsägarna Ekonomisk Förening | Process for production of oxidised cellulose pulp |
CA3036575A1 (en) | 2016-09-16 | 2018-03-22 | Basf Se | Methods of modifying pulp comprising cellulase enzymes and products thereof |
US10865520B2 (en) | 2017-09-18 | 2020-12-15 | International Paper Company | Method and apparatus for controlling a fiber fractionation system |
JP7113785B2 (en) * | 2019-06-07 | 2022-08-05 | ユニ・チャーム株式会社 | Method for producing softwood-derived paper pulp fiber and softwood-derived paper pulp fiber |
AT524092A2 (en) * | 2020-08-06 | 2022-02-15 | Mondi Ag | Process for manufacturing cellulosic fiber-based packaging products and cellulosic fiber-based packaging product |
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- 2004-09-22 CN CN200480027582A patent/CN100575597C/en not_active Expired - Lifetime
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- 2004-09-22 WO PCT/IB2004/003080 patent/WO2005028744A1/en active IP Right Grant
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Also Published As
Publication number | Publication date |
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US20130098571A1 (en) | 2013-04-25 |
EP1862587A2 (en) | 2007-12-05 |
CN100575597C (en) | 2009-12-30 |
US8262850B2 (en) | 2012-09-11 |
DE602004007942D1 (en) | 2007-09-13 |
ATE368766T1 (en) | 2007-08-15 |
CA2539095C (en) | 2010-08-03 |
EP1862587A3 (en) | 2010-01-27 |
CA2539095A1 (en) | 2005-03-31 |
US20160024713A1 (en) | 2016-01-28 |
NZ545801A (en) | 2010-03-26 |
DE602004007942T2 (en) | 2008-04-17 |
US20090054863A1 (en) | 2009-02-26 |
US20140000825A1 (en) | 2014-01-02 |
US20050061455A1 (en) | 2005-03-24 |
US20070119556A1 (en) | 2007-05-31 |
CN1856616A (en) | 2006-11-01 |
EP1668180B1 (en) | 2007-08-01 |
EP1668180A1 (en) | 2006-06-14 |
PL1668180T3 (en) | 2007-12-31 |
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