AU714243B2 - Glass fiber separators for batteries - Google Patents
Glass fiber separators for batteries Download PDFInfo
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- AU714243B2 AU714243B2 AU35139/97A AU3513997A AU714243B2 AU 714243 B2 AU714243 B2 AU 714243B2 AU 35139/97 A AU35139/97 A AU 35139/97A AU 3513997 A AU3513997 A AU 3513997A AU 714243 B2 AU714243 B2 AU 714243B2
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- AU
- Australia
- Prior art keywords
- percent
- fibers
- separator
- glass
- glass fibers
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- 239000003365 glass fiber Substances 0.000 title claims description 113
- 239000000835 fiber Substances 0.000 claims description 67
- 239000000463 material Substances 0.000 claims description 55
- 239000001913 cellulose Substances 0.000 claims description 41
- 229920002678 cellulose Polymers 0.000 claims description 41
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 23
- -1 polyethylene Polymers 0.000 claims description 12
- 239000003792 electrolyte Substances 0.000 claims description 9
- 239000002002 slurry Substances 0.000 claims description 9
- 229920000728 polyester Polymers 0.000 claims description 7
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 230000002209 hydrophobic effect Effects 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- 229920002994 synthetic fiber Polymers 0.000 claims description 6
- 239000012209 synthetic fiber Substances 0.000 claims description 6
- 229920003002 synthetic resin Polymers 0.000 claims description 5
- 239000000057 synthetic resin Substances 0.000 claims description 5
- 238000003860 storage Methods 0.000 claims description 4
- 239000004743 Polypropylene Substances 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- 239000004816 latex Substances 0.000 claims description 3
- 229920000126 latex Polymers 0.000 claims description 3
- 229920001155 polypropylene Polymers 0.000 claims description 3
- 240000005020 Acaciella glauca Species 0.000 claims description 2
- 241000218645 Cedrus Species 0.000 claims description 2
- 235000003499 redwood Nutrition 0.000 claims description 2
- 229920002972 Acrylic fiber Polymers 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 21
- 238000000034 method Methods 0.000 description 19
- 239000000203 mixture Substances 0.000 description 14
- 230000035699 permeability Effects 0.000 description 14
- 239000000123 paper Substances 0.000 description 12
- 239000011148 porous material Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000000377 silicon dioxide Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- 239000002655 kraft paper Substances 0.000 description 8
- 239000002253 acid Substances 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 238000002459 porosimetry Methods 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 238000007792 addition Methods 0.000 description 5
- 229920001131 Pulp (paper) Polymers 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 230000006798 recombination Effects 0.000 description 4
- 238000005215 recombination Methods 0.000 description 4
- 241000282346 Meles meles Species 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 239000013055 pulp slurry Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- SBMYBOVJMOVVQW-UHFFFAOYSA-N 2-[3-[[4-(2,2-difluoroethyl)piperazin-1-yl]methyl]-4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound FC(CN1CCN(CC1)CC1=NN(C=C1C=1C=NC(=NC=1)NC1CC2=CC=CC=C2C1)CC(=O)N1CC2=C(CC1)NN=N2)F SBMYBOVJMOVVQW-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 240000000907 Musa textilis Species 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- 229920006387 Vinylite Polymers 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000007596 consolidation process Methods 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/409—Separators, membranes or diaphragms characterised by the material
- H01M50/431—Inorganic material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/06—Lead-acid accumulators
- H01M10/12—Construction or manufacture
- H01M10/121—Valve regulated lead acid batteries [VRLA]
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/489—Separators, membranes, diaphragms or spacing elements inside the cells, characterised by their physical properties, e.g. swelling degree, hydrophilicity or shut down properties
- H01M50/494—Tensile strength
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/409—Separators, membranes or diaphragms characterised by the material
- H01M50/431—Inorganic material
- H01M50/434—Ceramics
- H01M50/437—Glass
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/409—Separators, membranes or diaphragms characterised by the material
- H01M50/44—Fibrous material
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Inorganic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Cell Separators (AREA)
- Secondary Cells (AREA)
Description
WO 98/00875 PCT/US97/11579 1
TITLE
GLASS FIBER SEPARATORS FOR BATERIES BACKGROUND OF THE INVENTION FIELD OF THE INVENTION The present invention relates generally to the field of batteries and, more specifically, to separators containing glass fibers which are positioned between the positive and negative plates of batteries and to a method for producing such separators. As is subsequently discussed in more detail, separators containing glass fibers are well known.
Long before glass fiber separators, however, cedar veneers were used as a separator material, and were replaced by microporous, hard rubbery separators and cellulose separators impregnated with resins.
DESCRIPTION OF THE PRIOR ART Valve regulated ("sealed" "recombinant") lead acid (VRLA) batterics are known; they usually comprise a plurality of positive and negative plates, as in a prismatic cell, or layers of separator and positive and negative electrodes wound together, as in a "jelly roll" cell. The plates are arranged so that they alternatc, negative positive negative, etc., with separator material and paste separating each plate from adjacent plates. The separator, which, typically, is a mat of glass fibers, is an inert material; it stores battery acid, applies a force to paste-grid interfaces, and provides low electric resistance. In addition, in VRLA batteries, there are innumerable gas channels in the separator material through which oxygen can migrate from the positive electrode, when generated there, to the negative electrode where it can be recombined with hydrogen, according to the oxygen cycle. One of the most important functions of a separator in a VRLA battery is to force the paste into contact with the plates, and cause a pressure between the plates.
Glass fiber separator material, typically, is produced commercially on paper making equipment including fourdrinier machines and rotoformers, inclined fourdrinier machines and extended wire rotoformers. In the production of separator made of glass fibers for VRLA batteries, it is preferred that no organic material be added to a furnish from which separator sheets are made; the entanglement of individual fibers serves to maintain the sheet in a cohesive structure, and water glass, which sometimes forms on the fiber surfaces, serves as a binder. Organic binders, however, tend to decrease the ability WO 98/00875 PCTfUS97/11579 2 of a separator to wick acid, and to decrease the amount of acid a separator can hold. A great deal of work has been directed to modifying the glass fiber furnish from which separators are produced to improve battery performance and/or lower the cost of the separator. Some of the work has entailed the addition of synthetic fibers for various reasons, such as the use of thermoformable plastic fibers so that the separator can be heat sealed on its edges to envelop a plate. Other work, which pertains to the field of this invention, has been directed to the use of filler, silica, to provide separators which are comparable to all glass fiber separators, at a lower cost. Separators made from glass fibers to which cellulose has been added and polyolefin fibers to which cellulose has been added have also been suggested. Prior art patents are discussed below.
US Patent No. 4,465,748 (Harris) discloses glass fiber sheet material for use as a separator in an electrochemical cell, and made from 5 to 35 percent w/w of glass fibers less than 1 rtm in diameter; the patent also discloses a glass fiber sheet for such use wherein there are fibers of a continuous range of fiber diameters and lengths, and most of the fibers are not over 5 mm in length.
US patent No. 4,216,280, (Kono et discloses glass fiber sheet material for use as a plate separator in a battery, and made from 50 to 95 percent w/w of glass fibers less than 1 [tm in diameter and 50 to 5 percent w/w of coarser glass fibers. The coarser glass fibers, the reference says, have a fiber diameter larger than 5 ,um, preferably larger than 10 Ftm, and it is advantageous for some of the coarser fibers to have diameters of 10 Rm to 30 rtm.
US Patent No. 4,205,122 (Minra et al) discloses a battery separator of reduced electric resistance comprising a self supporting, non woven mat consisting essentially of a mixture of olefinic resin fibers having a coarseness of from 4 to 13 decigrex and olefinic resin fibers having a coarseness of less than 4 decigrex, the latter fibers being present in an amount of not less than 3 parts by weight per 100 parts by weight of fibers; up to about 600 parts by weight of inert filler materials per 100 parts by of fibers can also be used. The battery separator is produced by subjecting a suitable aqueous dispersion to a sheet-forming operation, drying the resulting wet, non-woven mat, and heat treating the dried mat at a temperature ranging from a point 200 lower than the melting point of the aforementioned fibers to a point about 50' higher than the melting point.
WO 98/00875 PCT/US97/11579 3 US Patent No. 4,216,281 (O'Rell et al.) discloses a separator material produced from a furnish containing 30 to 70 percent w/w of polyolefin synthetic pulp, 15 to percent w/w of a siliceous filler and 1 to 35 percent w/w of "long" fibers which can be polyester fibers, glass fibers, or a mixture of the two. Cellulose in an amount up to about 10 percent w/w is disclosed as an optional ingredient of the furnish.
US Patent No. 4,363,856 (Waterhouse) discloses a separator material made from a furnish composed of polyolefin pulp fibers and glass fibers, and names polyester staple fibers, polyolefin staple fibers and cellulose pulp fibers as alternative constituents of the furnish.
US Patent No. 4,387,144 (McCallum) discloses a battery separator having a low electrical resistance after extended use which is made by thermal consolidation and thermal embossing of a paper web formed from a furnish containing a synthetic pulp the fibrils of which are filled with an inorganic filler, the web incorporating a wetting agent which is preferably an organic sulphonate, and organic succinate, or phenol ethoxylate.
US patent No. 4,373,015 (Peters et discloses sheet material for use as a separator in a battery, and "comprising organic polymeric fibers"; both of the examples of the reference describe the sheet material as "short staple fiber polyester matting about 0.3 mm thick", and indicate that the polyester fibers range from about 1 |tm to about 6 utm in diameter.
Sheet separators for use in conventional (not valve regulated) batteries and comprising both glass fibers and organic fibers are disclosed in all of the following US patents: No. 4,529,677 (Bodendorf); No. 4,363,856 (Waterhouse); and No. 4,359,511 (Strzempko).
US patent No. 4,367,271, Hasegawa, discloses storage battery separators composed of acrylic fibrils in an amount of up to about 10 percent w/w, balance glass fibers.
Japanese patent document 55/146,872 discloses a separator material comprising glass fibers (50-85 percent w/w) and organic fibers (50-15 percent w/w).
US patent No. 4,245,013, Clegg et al., discloses a separator made by overlaying a first sheet of fibrous material including polyethylene fibers with a second sheet of fibrous material including polyethylene and having a synthetic pulp content higher than the first sheet.
US Patent No. 4,908,282, Badger, discloses a separator comprising a sheet made from first fibers which impart to the sheet an absorbency greater than 90% and second WO 98/00875 PCTIUS97/11579 4 fibers which impart to the sheet an absorbency less than 80% wherein the first and second fibers are present in such proportions that the sheet has an absorbency of from 75 to This patent discloses that fine glass fibers have a high absorbency, that coarse glass fibers have a low absorbency, and that hydrophobic organic fibers have an extremely low absorbency, and that, when this separator is saturated with electrolyte, unfilled voids remain so that gas can transfer from plate to plate for recombination. The disclosure of Badger is incorporated herein by reference.
US Patent No. 5,091,275 (Brecht et al.) discloses a glass fiber separator which expands when exposed to electrolyte. The separator comprises glass fibers which are impregnated with an aqueous solution of colloidal silica particles and a sulfate salt. The separator is produced by forming a paper making web of glass fibers, impregnating the web with the aqueous mixture of silica and the salt, lightly compressing the impregnated web to remove some of the aqueous solution, partially drying the web, compressing the web to a final thickness and completing the drying of the web. The web is preferably compressed to a thickness which is less than the distance between plates in a given cell, so that insertion of an assembled cell stack into a case is facilitated. When electrolyte is added to the case, the salt dissolves in the electrolyte and the separator expands to provide good contact between the plates and the separators. According to the patent, the silica contributes to the recombination performance of cells incorporating the pre-compressed separator. The silica also contributes a great deal of stiffness to the separator, so much so that the separator may be characterized as rigid.
It has been determined that the production of battery separator by paper-making techniques from a furnish of glass fibers and silica powder leads to problems which are caused by variations in the concentration of the silica powder in the furnish. Typical glass fiber furnishes have a liquid content exceeding 98 percent w/w. In the course of making separator sheets, most of the water is removed from the furnish in the first few feet of a screen on which the furnish is cast. The water, known as white water, is recycled and winds up back in the headbox of the machine. If the furnish is composed exclusively of glass fibers, virtually none of the fibers pass through the wire and wind up in the white water. However, furnishes comprising glass fibers and silica powder do not fare so well.
In the absence of a retention aid, significant amounts of silica powder from such furnishes do pass through the paper making wire and wind up in the white water. Left unchecked, WO 98/00875 PCT/US97/11579 this phenomenon causes the concentration of silica powder in the furnish to increase, undesirably changing the properties of the furnish. Heretofore, the problem of silica powder and the like passing through a paper making wire has been avoided through the use of binders as retention aids.
US patent No. 2,477,000 discloses a synthetic fiber paper produced from fibrillae and fibers made by methods wherein a solution of the fiber is extruded through very small orifices (spinnerets) and then the extruded solution is allowed to congeal either in a precipitating bath or by evaporation of the solvent or by temperature changes (see column 2, lines 25 and following). The patent says that fibers of cellulose acetate, cellulose nitrate, regenerated cellulose from viscose, "Vinylite (a synthetic resin made by polymerization of vinyl compounds), Aralac (a fibrous product made from skim milk casein), and spun glass" which range in length from V/ inch to 1 inch and in diameter from 12-80 microns and fibrillae preferably derived from flax, Manila hemp, caroa or hemp can be used to make the paper. At least 90 percent of the fibrillae should be from 0.0015 to 0.0025 inch in length and from 0.0000027 to 0.0000044 inch in width.
BRIEF DESCRIPTION OF THE INSTANT INVENTION The instant invention is based upon the discovery that comparatively small additions of wood pulp, if beaten or refined to a sufficient degree to produce a highly fibrillated cellulose fiber, to a glass fiber furnish suitable for use in making battery separator material, cause surprisingly high increases in some of the strength properties of separator made from the furnish, improve the cut through resistance of a separator made from the furnish, and have a unique characteristic in that they hold a greater proportion of acid introduced thereunto when the separator is subsequently compressed.
In addition, the separator is repulpable, in the sense that it can be used as a constituent of a glass fiber which is used to produce "new" separator; furthermore, batteries made from glass fiber separator material which contains comparatively small amounts of wood pulp which has been beaten or refined to a sufficient degree, have remarkably long service lives, as indicated by their performance in cycling tests. In general, the pulp slurry should WO 98/00875 PCT/US97/11579 6 be beaten or refined to a Canadian freeness not greater than about 650 cc, or to an equivalent freeness by other measurement techniques, and a remarkable increase in tensile strength is achieved when the pulp is beaten or refined to a Canadian freeness not greater than about 120 cc, or to an equivalent freeness by other measurement techniques.
BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a plot of the percent w/w of added cellulose in glass fiber separator material according to the invention vs. the liters per second of air flowing through the separator material under test conditions that are subsequently described herein.
Fig. 2 is a plot of tensile strength, both machine direction ("Tensile, MD") and cross direction ("Tensile, vs. percent w/w of added cellulose in glass fiber battery separator according to the invention.
Fig. 3 is a plot of percent of initial capacity vs. number of test cycles for a battery according to the invention and for a control battery.
Figs. 4 through 9 are plots of thickness (the values plotted are 1000 times the thickness of the separator in mm) vs. load and rebound thickness vs. load for five glass fiber separator materials according to the invention and a control, where rebound thickness is 1000 times the thickness of a separator material in mm after that separator has been subjected to a load and the load has been reduced to 0.55 pounds per square inch (3.79 KPa); the data in Figs. 4 through 9 are for dry separator material.
Figs. 10 through 15 are plots similar to those of Figs. 4 through 9, showing thickness vs. load and rebound thickness vs. load for the five glass fiber separator materials according to the invention and for the control, but arc based on data where, before testing, each of the separator materials had been wet with seven times its weight of sulfuric acid having a specific gravity of 1.286.
Figs. 16 and 17 are plots similar to Figs. 4 and 5, differing in that interpolated points are plotted in the former, so that successive points along the X axis represent equal increments of cellulose content, while experimental values are plotted in the latter and, as a consequence, as is subsequently explained herein, successive points along the X axis do not always represent equal increments of cellulose content.
DEFINITIONS
Subsequently herein, the term "percent v/v" means percent by volume; the term "percent w/w" and the symbol mean percent by weight; the term "wire", as applied to WO 98/00875 PCT/US97/11579 7 a paper making machine, means the surface of the machine on which a furnish is cast in producing paper, and can be, for example, the screen of a Fourdrinier machine or the vacuum drum of a rotoformer machine; pore sizes reported herein, unless otherwise indicated, are in microns, and are determined by the first bubble method or by liquid porosimetry, Coulter; all temperatures are in and the following abbreviations have the meanings indicated: [tm micron or microns; mg=milligram or milligrams; g=gram or grams; kg=kilogram or kilograms; l=liter or liters; ml=milliliter or milliliters; cc=cubic centimeter or cubic centimeters; pcf=pound per cubic foot or pounds per cubic foot; m=meter or meters; cm=centimeter or centimeters; mm=millimeter or millimeters; m=meter or meters; mil=inch x 10 or inches x 10 (multiply times 25.4 to convert to mm); KPa=pressure in thousands of Newtons per square meter; psi=pounds per square inch (multiply times 6.89 to convert to KPa); and KN=force in thousands of Newtons.
EXAMPLE 1 Glass fiber separator hand sheets were produced in a laboratory apparatus by depositing a furnish on a wire or screen, and draining the furnish. The apparatus comprised a tank with a screen in the bottom, a drain below the screen, a valve which opened and closed the drain, and a hand paddle which was moved back and forth to simulate the movement of a furnish in commercial papermaking apparatus and establish a "machine direction" parallel to the direction of paddle movement. The furnish was produced by charging to the tank acidified water, pH 2.7, and solids composed of 74.5 percent w/w Schuller 206 glass fibers, average fiber diameter 0.76 rim, 12.8 percent w/w Evanite 610 glass fibers, nominal fiber diameter 2.6 lim, and 12.8 percent w/w /2 inch glass fibers, nominal fiber diameter 13 p[m, stirring for about a minute, charging to the tank a kraft pulp slurry which had a Canadian freeness of 57cc and a consistency of 1.235 percent, and stirring for an additional 2 minutes. The composition in the mixer, after the pulp addition, contained 73 percent w/w Schuller 206 glass fibers, 12.5 percent w/w Evanite 610 glass fibers, 12.5 percent w/w A20-BC-/2 inch glass fibers and 2 percent w/w pulp fibrils. The furnish and the pulp were stirred for about two minutes, after which the valve was opened so that the water drained through the screen while the separator was retained on the screen. The furnish contained enough glass fibers to produce a separator having a grammage of 30 g/m 2 at a thickness of 0.15 mm. The separator hand sheet was heated in a drying oven to about 1500 for 30 minutes. Two WO 98/00875 PCT/US97/11579 8 separator sheets produced as described above were tested and various data, summarized below, were collected (the data are averages of the determinations on the two sheets).
Frazier permeability, in the following data and elsewhere herein, is in L/sec/m 2 20 mm The tests, instruments and apparatus used to determine various properties in Example 1 and elsewhere herein are described in a publication entitled BCI/RBSM Standard Test Methods, Battery Council International (the disclosure of this publication is incorporated herein by reference).
Grammage (g/m 2 36.7 Thickness, mm (under a load of 10.34 KPa): 0.15 Tensile, MD (Newtons/m): 363 Tensile, CD (Newtons/m): 275 Elongation, MD (percent of total): 1.3 Elongation, CD (percent of total): 1.4 Pore Size-first bubble method, .m Frazier Permeability 98 Pore size-liquid porosimetry, Coulter, pm minimum 5.1 maximum 18.5 mean "Frazier Permeability" values reported herein were determined using Frazier Permeability tester 91A (TAPPI T2510M-85).
"Wicking", as reported above and subsequently herein, was determined by the procedure described in U.S. patent No. 5,225,298, column 7, lines 20 and following, using water instead of sulfuric acid as there described; the test is known as the Japanese Industrial Standard method.
The composition of the Schuller 206 glass fibers used in Example 1 and in subsequent Examples vary slightly from time to time. Mean values, in percent w/w, WO 98/00875 PCT/US97/11579 9 calculated from data furnished by Schuller for the period when the examples were carried out are given below: SiO, 65.40 Na2O 16.11 A120 3 2.99 KO 0.69 CaO 5.88 B,0 3 5.31 MgO 2.79 F, 1.02 Schuller also indicates that the glass contains FeO,, TiO 2 ZrO 2 Cr 2 SrO, BaO, MnO, ZnO, LiO, SO3 and Pb in amounts less than 0.1%.
The nominal composition of the Evanite 610 glass fibers used in Example 1 and in subsequent Examples varies, in percent w/w, within the following ranges: SiO, 60.0 69.0 3 3.0 CaO 5.0 MgO 2.5 NaO 8.0 12.0 KO 0.5 BA0 3 0.02 F, 0.0 ZnO <0.04 Fe,0 3 <0.02 The A20-BC-V2 inch glass fibers used in the procedure described above and in other procedures described herein are commercially available from Schuller under the indicated designation.
Glass fiber separator sheets according to the invention were produced on a pilot plant paper making machine by depositing a furnish on an advancing wire, through which water from the furnish drained. The furnish was produced in a mixer from acidified water, pH 2.7, and solids composed of Schuller 206 glass fibers, Schuller 210X glass fibers, nominal fiber diameter 3.0 um and the same composition as the 206 fibers, and /2 inch glass fibers. The furnish was stirred in the mixer for about one minute, after which time a kraft pulp slurry which had a Canadian freeness of 57cc and a consistency of 1.235 percent was added to the furnish in the mixer. The composition in the mixer, after the pulp addition, contained about 7 parts by weight of Schuller 206 glass fibers, about 1 part WO 98/00875 PCT/US97/11579 by weight of each of Schuller 210 glass fibers, A20-BC- 1 2 inch glass fibers, and about 0.6 part by weight of pulp fibrils. The furnish and the pulp were stirred for about two minutes, after which time the pulp-containing furnish was charged to the headbox of the pilot plant machine. An addition of 0.6 part by weight of pulp fibrils from red wood pulp that had been beaten to a Canadian freeness less than 100 cc was then made to the material in the headbox, and the furnish which resulted was flowed onto the advancing wire to produce a separator having a grammage of 30 g/m 2 at a thickness of 0.15 mm.
The separator was ultimately heated in a drying oven to about 150" for 30 minutes. The separator had a loss on ignition a little over 12 percent w/w, indicating a total pulp content of about 12 percent w/w. The procedure described in this paragraph constitutes the best mode presently contemplated by the inventors with respect to the production of battery separator material according to the invention.
Cells according to the invention were made using the separator material produced in the pilot plant paper machine as described above, and were subjected to life testing in comparison with batteries made using conventional, all glass separators, but otherwise identical. Battery capacity after each cycle, as a percentage of initial capacity, is set forth in Table I, below (the control battery test was terminated after 7 cycles): WO 98/00875 PCT/US97/11579 Table I Number of cycles Capacity, percent of initial According to invention Control 1 113.5 103.6 2 115.6 93.6 3 111.9 76.0 4 109.3 53.4 107.4 34.0 6 105.3 25.1 7 103.6 20.9 8 101.7 9 100.0 98.6 11 97.2 12 95.5 13 93.7 14 90.1 87.6 16 86.1 17 80.0 18 74.9 19 74.0 67.3 The data in Table I are presented graphically in Fig. 3, which was computer generated by entering the foregoing data for the battery of the invention and for the control after cycles 1 through 7, but entering zero for the percent of initial capacity after cycles 8 through EXAMPLES 2-6 Glass fiber separator hand sheets were also produced from other furnishes which contained varying amounts of kraft pulp that had been beaten to a consistency of 0.9906 percent and a Canadian freeness of 57cc. The furnishes also contained the previously identified Schuller 206, 210X and A20-BC-1/ 2 inch glass fibers. The hand sheets were produced in a laboratory apparatus by depositing a furnish on a wire or screen, and draining the furnish. The apparatus comprised a tank with a screen in the bottom, a drain below the screen, a valve which opened and closed the drain, and paddles which were WO 98/00875 PCTIUS97/11579 12 moved back and forth to simulate the movement of a furnish in commercial papermaking apparatus and establish a "machine direction" parallel to the direction of paddle movement. The furnish and the pulp were stirred for about two minutes, after which the valve was opened so that the water drained through the screen while the separator was retained on the screen. The furnish that was charged contained enough glass fibers to produce a separator having a grammage of 30 g/m 2 at a thickness of 0.15 mm. The separator hand sheet was heated in a drying oven to about 1500 for 30 minutes. The final compositions, in percent w/w, of representative ones of the furnishes and the properties of the hand sheets that were produced are set forth in Table II, below, where, as in other tables herein, unless otherwise indicated, tensile strength is in pounds per inch of width of the separator (multiply times 0.175 to convert to kilonewtons per meter), elongation is in percent, stiffness is "Gurley Stiffness" in mg, pore sizes arc in um, electrical resistance is in ohms per square inch of the separator, and loss on ignition is in percent w/w. The compositions of the furnishes are given in the following table: Composition of Example Example Example Example Example furnish 2 3 4 5 6 210 X 79 77 73 70 /2 10 10 10 10 inch fibers 206 10 10 10 10 Cellulose 1 3 7 10 WO 98/00875 PCT/US97/11579 13 Table II Property Example Example Example Example Example 2 3 4 5 6 grammage, 119.9 121.7 119.3 119.9 119.4 g/m 2 Thickness, mm (10.34 KPA) 0.765 0.850 0.653 0.620 0.591 KPa) 0.726 0.753 0.644 0.590 0.570 Tensile, Newtons/m MD 71.7 135.0 135.7 139.2 149.5 CD 84.7 117.8 108.9 125.4 130.2 Elongation Percent MD 1.37 2.00 1.96 2.08 2.13 CD 1.83 1.67 1.61 1.70 1.92 Frazier Permeability 65.7 50.2 13.4 5.9 n.d.
Wicking mm 83 89 104 153 247 Stiffness, mg MD 3800 3900 5200 4300 3200 CD 3100 3500 3900 3500 3000 Pore Sizefirst Bubble Method, zm 16.5 16.0 20.1 21.6 24.0 Electrical 0.002 0.003 0.009 0.011 0.014 Resistance LOI,% 3.3 5.2 9.0 12.5 18.1 Pore sizeliquid Porosimetry Coulter, 'um Min 5.570 5.386 3.734 2.628 1.697 Max 42.24 42.24 26.07 17.80 12.43 Mean 8.875 8.507 5.753 4.425 3.497 In the foregoing table and in subsequent tables the entry means not determined, in the cases of Examples 6 and 11, because the porosity was too low for a determination of Frazier Permeability.
Control glass fiber separator hand sheets were produced by the same method from a furnish which was composed of 80 percent w/w of Schuller 210X glass fibers, WO 98/00875 PCTIUS97/11579 14 percent w/w of A20-BC-2 inch glass fibers and 10 percent w/w Schuller 206 glass fibers. The average test results for two control sheets are set forth in Table III, below: Table III Grammage, g/m 2 117.1 Thickness, mm (10.34 KPA) 0.857 g/m 2 KPa) 0.717 g/m 2 Tensile, Newtons per M MD 10.8 CD 11.0 Elongation, MD 0.70 CD 1.21 Frazier Permeability 178.4 Wicking 62 mm Stiffness, mg MD 980 CD 655 Pore Size-first bubble Method, Rim 11.0 Pore size-liquid porosimetry, Coulter, p.m Min 6.86 Max 65.97 Mean 12.98 Electrical n.d.
Resistance LOI, 0.31 Thickness in mm x 1000 of samples of the hand sheets produced as described in Examples 2 through 6 and of the control sheets was also determined under various loads, both in an as produced condition and after having been wet with 7 times its dry weight of sulfuric acid, specific gravity 1.286. All thicknesses reported herein were determined by the method described in U.S. patent No.5,336,275. The example numbers are column headings in Table IV, below, and thicknesses (the values reported are measured thicknesses in mm x 1000) when the samples were in the as produced condition, at WO 98/00875 PCT/US97/11579 applied loads in KPa indicated in the left column, are set forth under the identifying headings: Table IV Applied Load, Control Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 KPa 3.79 38 36.5 31 28.5 26 27 6.06 35 30.5 26 25.5 23 22 9.51 29.5 27.5 23 23.5 21 19.5 13.71 25.5 25.5 21 22.5 20 18.5 17.57 22 23.5 20 21.5 19 17.5 23.98 20 22.5 18.5 20 19 17 28.87 19 21.5 17.5 19.5 18 16.5 42.65 16.5 19 16.5 18.5 17 15.5 "Rebound" thicknesses in mm x 1000 (after the excess of the load above 3.79 KPa was removed from each "as produced" sample) are given in Table V, under headings which give the load that was applied, and from which each sample "rebounded"; the values reported are 1000 x thicknesses in mm at the loads indicated in the left column of the table: Table V Applied Control Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 Load, KPa 6.06 36 33.5 28.5 27.5 24.5 26.5 9.51 33.5 30.5 29 26.5 23.5 25.5 13.71 31.5 29.5 27 25.5 22.5 26 17.57 29.5 28.5 25.5 25.5 22.5 26 23.98 29 27.5 25 25.5 22.5 28.87 28 27.5 25 24.5 22 23.5 42.65 27 27 24 24.5 22 23 The data in Tables IV and V are presented graphically in computer generated Figs.
4 through 9 of the drawings, where the loads are shown in psi, and successive points along the X axis, which are equally spaced from one another, represent 0.55 psi (3.79KPa), 0.88 psi (6.06 KPa), 1.38 psi (9.51 KPa), 1.99 psi (13.71 KPa), 2.55 psi (17.57 KPa), 3.48 psi (23.98 KPa), 4.19 psi (28.87 KPa), and 6.19 psi (42.65 KPa). Accordingly, WO 98/00875 PCTIUS97/11579 16 Figs. 4 through 9 are skewed in the sense that, for example, a given distance between the first and second points represents a change from 0.55 psi (3.79 KPa) to 0.88 psi (6.06 KPa), while the same distance between the last two points represents a change from 4.19 psi (28.87 KPa) to 6.19 psi (42.65 KPa). In order to represent the data from the control sheets and from Example 2 in a more nearly conventional plot, thickness and rebound thickness (in mm x 1000) were calculated by interpolation from the experimental data for loads of 0.69 psi (4.75 KPa), 1.19 psi (8.20 KPa), 1.69 psi (11.64 KPa), 2.19 psi (15.09 KPa), 2.69 psi (18.53 KPa), 3.19 (21.98 KPa), 3.69 psi (25.42 KPa). 4.69 psi (32.31 KPa), 5.19 psi (35.76 KPa), and 5.69 psi (39.20 KPa). These and the experimental values (in mm x 1000) at 4.19 psi (28.86 KPa) and at 6.19 psi (42.65 KPa) are set forth in Tables VI and VII, respectively: Table VI Applied Load, Control, Example 2, Control, Example 2, KPa thickness thickness Rebound Rebound 4.75 36.7 34 8.20 31.6 28.6 34.8 32 11.64 28.0 26.7 32.3 15.09 24.3 24.8 30.5 29.6 18.53 22.8 23.8 29.5 28.4 21.98 20.6 22.8 29.2 28.4 25.42 20.3 22.7 28.7 27.5 28.86 30 22.5 28 27.5 32.31 19.2 21.7 27.8 27.4 35.76 18.3 20.8 27.5 27.3 39.20 17.4 20.2 27.3 27.2 42.65 16.5 19 27 27 The data from Table VI are presented graphically in Figs. 16 and 17, which are computer generated plots using loads in KPa. It will be noted that the curves of Figs.
16 and 17 are similar in shape to those of the corresponding curves of Figs. 4 and which is deemed to indicate that valid conclusions can be reached from the skewed curves.
Thickness and rebound thickness measurements were also made on the separator materials of Examples 2 through 6 and the controls after the materials had been wet WO 98/00875 PCT/US97/11579 17 with sulfuric acid having a specific gravity of 1.286. The applied loads in KPa are given in the left hand column of Table VII, below, and thicknesses are set forth under the headings which identify the samples; the reported thicknesses are 1000 times the measured thicknesses of the separator in mm: Table VII Applied Control Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 load, KPa 3.79 36 20.5 28 29 27.5 27.5 6.06 31.5 27 26 26 25 24.5 9.51 28.5 24 23 24 22 22.5 13.91 26.5 22.5 21 22.5 20.5 20.5 17.57 24 21.5 20 21.7 19.5 19 23.98 20.5 20.5 19 20 19 17.5 28.87 19 19.5 18 19 18 16.5 42.65 17.5 17.5 16.5 17.5 16.5 15.5 "Rebound" thicknesses (after the excess of the load above 3.79 KPa was removed from each sample that had been wet with sulfuric acid) are given in Table VIII, below, adjacent entries in the left hand column which give the load that was applied, and from which each sample "rebounded"; the values reported are 1000 x measured thicknesses in mm): Table VIII Applied Control Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 load,KPa 6.06 32.5 27.5 26.5 27.5 27 25.5 9.51 31 25.5 25.5 26.5 25 24.5 13.91 29 25.5 25 25 25 23.5 17.57 27.5 25.5 25 25 25 23.5 23.98 24.5 24.5 24 25 24.5 23.5 28.87 24 24.5 24 25 24 22.5 42.65 23.5 24.5 24 24.5 24.5 22.5 WO 98/00875 PCT/US97/11579 18 The data from Tables VII and VIII are plotted in Figs. 10 through 15, where loads are in KPa. The data of Tables IV, V, VII and VIII and Figs. 4-15 indicate that the separator materials of Examples 2 through 6, above, all have sufficient resiliency that they can be compressed between the plates of a lead acid battery, and that their major surfaces will be urged against the adjacent plates with sufficient force for the battery to perform satisfactorily.
EXAMPLES 7-11 Glass fiber separator hand sheets were also produced by the method described in Example 1 from other furnishes which contained varying amounts of kraft pulp that had been beaten to a consistency of 0.9906 percent and a Canadian freeness of 57cc, and were then dipped in a latex, 3 percent w/w solids. The final compositions, in percent w/w, of representative ones of the furnishes are set forth in Table IX, below, and the properties of separators produced from the furnishes are set forth in Table X, below, where thickness of the separator material is in mm: Table IX of Furnish 7 8 9 10 11 210 X 79 77 73 70 10 10 10 10 V2 inch fibers 206 10 10 10 10 Cellulose 1 3 7 10 ,oe, WO 98/00875 PCTIUS97/11579 19 Table X Property Example Example Example Example Example 7 8 9 10 11 grammage 121.6 121.9 127.5 123.1 122.7 g/m 2 Thickness, mm (10.34 KPa) 0.792 0.778 0.750 0.742 0.603 KPa) 0.760 0.745 0.720 0.698 0.585 Tensile Newtons/m MD 93.0 120.6 139.2 152.3 168.8 CD 80.6 102.0 122.0 139.2 158.5 Elongation, Percent MD 1.8 2.3 1.9 2.3 1.9 CD 1.5 2.1 2.0 2.1 Frazier 8.97 5.08 1.39 0.918 n.d.
Permeability Wicking mm 225 184 253 261 391 Stiffness, mg MD 2500 3400 4300 4700 4600 CD 2200 2800 3900 3900 3700 Pore Size- 16.8 16.1 19.4 20.5 25.4 First Bubble Method, p.m Pore sizeliquid Porosimetry Coulter, p.m Min 5.283 4.726 3.427 2.285 1.092 Max 46.54 40.89 27.52 21.73 11.88 Mean 9.550 7.881 5.839 4.902 2.920 LOI, 6.7 8.4 12.7 17.1 21.3 EXAMPLES 12-16 Still other glass fiber separator hand sheets were produced by the method described in Example 1 from substantially the furnish of Examples 7-11 which contained various small amounts of kraft pulp that had been beaten to a consistency of 1.235 percent and a Canadian freeness of 57cc. The final compositions, in percent w/w, WO 98/00875 PCT/US97/11579 of representative ones of the furnishes are set forth in Table XI, below, and their properties are set forth in Table XII, below, where thickness is in mm: Table XI Composition Example Example Example Example Example of Furnish 12 13 14 15 16 210 X 77 79 79/4 791/2 79 10 10 10 10 V2 inch fibers 206 10 10 10 10 Cellulose 3 1 /4 Table XII Property Example Example Example Example Example 12 13 14 15 16 grammage 118.4 115.6 117.2 116.4 116.3 g/m 2 Thickness, mm (10.34 KPa) 0.757 0.751 0.778 0.774 0.797 KPa) 0.662 0.694 0.716 0.703 0.722 Tensile Newtons/m MD 49.5 25.3 23.8 20.0 18.5 CD 43.8 20.2 20.7 20.0 2.54 Percent Elongation MD 8.41 5.75 6.58 6.68 7.82 CD 8.23 6.48 6.06 6.13 8.89 Frazier 129.6 175.2 175.2 186.4 200.8 Permeability Wicking mm 74 76 72 67 62 Surface area 0.6874 0.6114 0.6603 0.6513 0.7030 Corr. 9.9970 9.9962 9.9991 9.9962 9.9970 Pore sizeliquid Porosimetry, Coulter, ptm Min 6.050 5.941 7.050 6.496 7.589 Max 44.71 50.49 62.08 70.13 78.26 Mean 10.65 12.04 12.32 12.59 12.17 LOI 0.46 1.56 1.28 0.89 0.75 WO 98/00875 PCT/US97/11579 Control glass fiber separator hand sheets were produced by the same method from a furnish which was composed of 80 percent w/w of Schuller 210X glass fibers, percent w/w of A-20-BC V2 inch glass fibers and 10 percent w/w Schuller 206 glass fibers. The test results, average of two, are set forth in Table XIII, below, where thickness is in mm: Table XIII grammage, g/m 2 113.7 Thickness, mm (10.34 KPa) 0.742 KPa) 0.600 Tensile Newtons/m MD 10.1 CD 11.0 Elongation, MD 0.96 CD 1.27 Frazier 222.4 Permeability Wicking mm 62 The data concerning Frazier permeability from Table X (Examples 12 through 16) and from Table XI (for the corresponding controls) are presented graphically in Fig.
1, which is a computer generated plot of Frazier permeability (called CFM on the drawing) vs. cellulose content. It will be noted that Fig. 1 has points on the X axis for 1.25, 1.5, 1.75. 2.0, 2.25, 2.5 and 2.75 percent pulp. To cause the plot to show these points, for which there was no experimental data, Frazier permeability was calculated for each, of these pulp contents by interpolation between the experimental values at percent and at 3.0 percent. The experimental and calculated data input to generate Fig.
2 are set forth below: WO 98/00875 PCT/US97/11579 Percent w/w cellulose 0.0 0.25 0.75 1.25 (Calc) (Calc) 1.75 (Calc) (Calc) 2.25 (Calc) (Calc) 2.75 (Calc) Frazier 27.8 25.05 23.25 21.9 21.85 21.14 20.44 19.73 19.03 18.32 17.61 16.91 16.2 Permeability The data concerning tensile strength from Table XII and from Table XIII are presented graphically in Fig. 2, which is composed of two computer generated plots of tensile strength in pounds per inch (machine direction, in one case, and cross direction in the other) vs. cellulose content. It will be noted that Fig. 2 has points on the X axis for 1.25, 1.5, 1.75. 2.0. 2.25, 2.5 and 2.75 percent pulp. To cause the plot to show these ordinate points, for which there was no experimental data, tensile strength in both directions was calculated for each of these pulp contents by interpolation between the experimental values at 1.0 percent and at 3.0 percent. The experimental and calculated data input to generate Fig. 2 are set forth below: WO 98/00875 PCTUS97/11579 23 Percent w/w cellulose Tensile, MD (Pounds per inch) 0.0 1.46 0.25 2.685 2.90 0.75 2.455 3.63 1.25 (Calc) 4.07 (Calc) 4.52 1.75 (Calc) 4.96 2.0 (Calc) 5.41 2.25 (Calc) 5.85 (Calc) 6.29 2.75 (Calc) 6.74 7.18 Percent w/w cellulose Tensile, CD (Pounds per inch) 0.0 1.55 0.25 2.54 2.72 0.75 3.005 2.93 1.25 (Calc) 3.36 (Calc) 3.79 1.75 (Calc) 4.22 2.0 (Calc) 4.65 2.25 (Calc) 5.07 (Calc) 5.50 2.75 (Calc) 5.93 6.36 If the calculated data were not plotted, the computer generated plot would move the point representing 3.0 percent w/w pulp to the left to the point which represents 1.25 percent w/w pulp in Fig. 2, so that the curves would rise sharply from tensile strengths of 1.93 and 3.63 at 1.0 percent w/w pulp to tensile strengths of 6.36 and 7.10 at percent w/w pulp, but the distance along the X axis from 1.0 to 3.0 would be the same as the distance from 0.75 to EXAMPLES 17-24 Still other glass fiber separator hand sheets were produced by the method described in Example 1 from furnishes containing 35 parts by weight of 206 glass WO 98/00875 PCT/IJS97/11579 24 fibers, 65 parts by weight of 210 glass fibers and about 1-2 parts by weight of kraft pulp that had been beaten to various Canadian freenesses. The Canadian freeness of representative ones of the furnishes and various properties of the separators produced therefrom are set forth in Table XIV, below, where thickness is in mm. Because of the small size of the samples and lack of uniformity of the furnishes, the loss on ignition of the hand sheets is the best indication of the cellulose content of the furnish from which it was produced. A hand sheet containing no cellulose can be expected to have a loss on ignition of about V2%.
Table XIV Property Example Example Example Example 17 18 19 Canadian Freeness 660 548 420 225 Grammage 147 143 141 143 g/m 2 Thickness, mm 10 KPa 0.96 0.92 0.88 0.89 KPa 0.84 0.81 0.82 0.88 KPa 0.79 0.70 0.70 0.68 Average total 1.8 2.3 2.3 1.9 tensile, pounds per inch 0 Average 2.2 2.4 2.8 2.1 elongation, Loss on ignition, 1.6 1.3 2.0 1.7 Average Tensile 0.0122 0.0161 0.0163 0.0133 g/m 2 WO 98/00875 PCTIUS97/11579 Table XIV (continued) Property Example Example Example Example 21 22 23 24 Canadian Freeness 120 40 30 Grammage 143 142 137 146 g/m 2 Thickness, mm KPa 0.97 0.91 0.94 0.92 KPa 0.84 0.80 0.82 0.82 KPa 0.73 0.70 0.70 0.72 Average total 2.4 2.5 3.0 tensile, pounds per inch Average 2.2 2.3 2.3 elongation, Loss on ignition, 1.8 1.5 1.8 2.6 Average Tensile 0.0133 0.0176 0.0219 0.0308 g/m 2 EXAMPLES 25-32 Still other glass fiber separator hand sheets were produced by the method described in Example 1 from furnishes containing 35 parts by weight of 206 glass fibers, 65 parts by weight of 210 glass fibers and 3-5 parts by weight of kraft pulp that had been beaten to various Canadian freenesses. The Canadian freeness of representative ones of the furnishes and various properties of the separators produced therefrom are set forth in Table XV, below, where thickness is in mm: Table XV Property Example Example Example Example 26 27 28 Canadian Freeness 660 548 420 225 Grammage 148 144 138 141 g/m 2 Average total 2.6 3.0 2.7 2.8 tensile, pounds per inch Average 1.9 2.5 3.1 2.2 elongation, Loss on ignition, 3.5 3.7 3.8 Average Tensile 0.0176 0.0208 0.0196 0.0199 g/m 2 WO 98/00875 PCT/US97/11579 26 Table XV (continued) Property Example Example Example Example 29 30 31 32 Canadian Freeness 120 40 30 Grammage 141 140 141 141 g/m 2 Average total 3.5 3.5 5.1 tensile, pounds per inch Average 1.9 2.0 2.1 elongation, Loss on ignition, 4.5 3.6 3.6 4.1 Average Tensile 0.0248 0.0250 0.0362 0.0496 g/m 2 EXAMPLES 33-40 Still other glass fiber separator hand sheets were produced by the method described in Example 1 from furnishes containing 35 parts by weight of 206 glass fibers, 65 parts by weight of 210 glass fibers and 9 to 11 parts by weight of kraft pulp that had been beaten to various Canadian freeness. The Canadian freeness of representative ones of the furnishes and various properties of the separators produced therefrom are set forth in Table XIV, below, where thickness is in mm: Table XVI Property Example Example Example Example 33 34 35 36 Canadian Freeness 660 548 420 225 Grammage 148 146 140 145 g/mn Average total 2.5 3.8 4.5 5.1 tensile, pounds per inch Average 2.1 2.1 2.1 elongation, Loss on ignition, 11.3 11.5 8.7 10.0 Average Tensile 0.0169 0.0261 0.0319 0.0364 g/m 2 WO 98/00875 PCT/US97/11579 Table XVI (continued) Property Example Example Example Example 37 38 39 Canadian Freeness 120 40 30 Grammage 138 144 140 150 g/m 2 Average total 6.9 7.8 9.0 13.3 tensile, pounds per inch Average 2.0 2.3 1.8 2.2 elongation, Loss on ignition, 12.0 10.6 11.5 11.0 Average Tensile 0.0500 0.0542 0.0643 0.0887 g/m 2 WO 98/00875 PCT/US97/11579 28 As has been indicated above, a remarkable increase in tensile strength is achieved when separator material according to the invention is produced using pulp that has been beaten or refined to a Canadian freeness not greater than about 120 cc. This increase is illustrated by the data of Examples 17 through 40 concerning tensile strength of separator materials according to the instant invention produced from furnishes containing varying amounts of wood pulp which had been refined to several different Canadian freenesses. The data concerning average tensile strength in g/m 2 vs. Canadian freeness are presented graphically in charts A, B and C, below. Chart A is a plot of the indicated data from Examples 17 through 24; Chart B is a plot of the indicated data from Examples 25 through 32; and Chart C is a plot of the indicated data from Examples 33 through WO 98/00875 PCT/US97/11579 4 4 k 4~~ 0 100 200 30 40 Canadian Freeness 500 600 700 Chart A :i :4.4 i..
f" 0 100 200 300 400 500 600 Canadian Freeness Chart B 444i: .:4i 44 444 4444 0 100 200 300 400 Canadian Freeness 500 600 700 Chart C WO 98/00875 PCTfUS97/11579 It has been found that the separator material produced as described in each of the foregoing Examples can be charged to conventional papermaking apparatus, and "repulped", either as the sole source for glass fibers and cellulose fibrils or supplemented with additional glass fibers and cellulose fibrils to produce a furnish which can be deposited on the moving wire of paper making apparatus as described above to produce separator material. As a consequence, there is no need for any of the separator material according to the instant invention to be scrapped; instead, it can be recycled. Further, separator material according to the instant invention has improved puncture strength than otherwise identical separator material which does not contain cellulose fibrils; as a consequence, increased yields of acceptable lead acid batteries having expanded metal or continuous cast grids can be achieved.
As has been explained above, separator material made from first fibers which impart to the sheet an absorbency greater than 90% and second fibers which impart to the sheet an absorbency less than 80% wherein the first and second fibers are present in such proportions that the sheet has an absorbency of from 75 to 95%, when saturated with electrolyte, still has unfilled voids so that gas can transfer from plate to plate for recombination. Such separator material can be produced according to the instant invention by adding to a slurry containing, in suitable proportions, first fibers which impart to the sheet an absorbency greater than 90% and second fibers which impart to the sheet an absorbency less than 80%, from 0.2 percent w/w to 20 percent w/w of a slurry of cellulose fibrils having a Canadian freeness sufficiently low that a separator material produced from the resulting slurry has a tensile strength greater than an otherwise identical separator where glass fibers having an average diameter greater than 1 [tm replace the cellulose fibrils. Preferably, the fibers which impart to the sheet an absorbency less than 80% include both relatively coarse glass fibers and hydrophobic organic fibers. Polyethylene, polypropylene, acrylic and polyester fibers are examples of preferred hydrophobic organic fibers.
A preferred separator according to the invention having an absorbency (as defined in the above identified Badger patent, of from 75 to 95% which, when saturated with electrolyte, still has unfilled voids so that gas can transfer from plate to plate for recombination contains 33.6 parts by weight Schuller 206 glass fibers or an equivalent, 50.4 parts by weight Schuller 210X fibers or an equivalent, 11 parts by weight Schuller inch glass fibers or equivalent, and 5 parts by weight of polyethylene fibers, and, in addition, from 0.2 percent w/w to 20 percent w/w of cellulose fibrils from a WO 98/00875 PCT/US97/11579 31 slurry having a Canadian freeness sufficiently low that the separator material has a tensile strength greater than an otherwise identical separator where glass fibers having an average diameter greater than 1 tm replace the cellulose fibrils.
It will be appreciated that various changes and modifications can be made from the specific details of the invention as described above without departing from the spirit and scope thereof as defined in the attached claims.
Claims (8)
1. A glass fiber separator material comprising a mass of intermeshed glass fibers substantially all of which have a fiber diameter not greater than about 20 tm, and at least percent w/w of which have a fiber diameter less than 1 tm, and, distributed through the glass fibers, from 0.2 percent w/w to 20 percent w/w of cellulose fibrils from a slurry having a Canadian freeness not greater than 650cc.
2. A glass fiber separator material as claimed in claim 1 wherein the cellulose fibrils have a Canadian freeness not greater than about 120cc.
3. A glass fiber separator material as claimed in claim 2 wherein the cellulose 1 o fibrils are impregnated with a solidified, synthetic resin.
4. A glass fiber separator material as claimed in claim 3 wherein the solidified synthetic resin with which the cellulose fibrils are impregnated is a solidified, synthetic latex. A glass fiber separator material as claimed in claim 2 wherein the cellulose 15 fibrils are redwood fibrils or cedar fibrils.
6. A glass fiber separator material as claimed in claim 2 wherein the cellulose fibrils are from a slurry which has a Canadian freeness not greater than 100cc.
7. A glass fiber separator material as claimed in claim 2 wherein the cellulose fibrils adjacent one of the two opposed major surfaces are impregnated with a solidified synthetic resin, while the cellulose fibrils adjacent the other of the two opposed major surfaces are not so impregnated.
8. A glass fiber separator material as claimed in claim 7 wherein the solidified synthetic resin with which the cellulose fibrils are impregnated is a solidified, synthetic latex. 0000 5 S 00 S S
555. SO S. S 25 9. A glass fiber separator material as claimed in claim 2 wherein there are also *@ooS hydrophobic synthetic fibers in the mass of glass fibers, the synthetic fibers are intermeshed with the glass fibers and with one another, and the size distribution of the glass fibers and the proportions of glass and synthetic fibers are such that the separator has an absorbency for a sulfuric acid electrolyte of from 75 percent v/v to 95 percent v/v. 30 10. A glass fiber separator material as claimed in claim 9 wherein the hydrophobic synthetic fibers include polyethylene fibers, polypropylene fibers, acrylic fibers or polyester fibers. 11. A glass fiber separator material comprising a mass of intermeshed glass fibers substantially all of which have a fiber diameter not greater than about 20tm, and at least 5 percent w/w of which have a fiber diameter less than 1 tm, and, distributed through the glass fibers, from 0.2 percent w/w to 20 percent w/w of cellulose fibrils from a slurry having a Canadian freeness bot greater than 650, and sufficiently low that a battery made with the separator has a service life, when cycled, at least 10 percent greater than an otherwise identical separator where glass fibers having an average diameter greater than 1 tm replace the cellulose fibrils. [N:/Iibc]00152:bmv 12. A glass fiber separator material as claimed in claim 2 wherein there are also hydrophobic side by side or shell-core bicomponent fibers which include polyethylene, polypropylene, acrylic or polyester materials. 13. A glass fiber separator material, substantially as hereinbefore described with reference to any one of the Examples. 14. A sealed lead/sulfuric acid recombinant storage battery comprising a plurality of lead plates in a closed case, a fibrous sheet plate separator between adjacent ones of said plates, and a body of a sulfuric acid electrolyte absorbed by each of said separators and maintained in contact with each of the adjacent ones of said plates, each of said lo separator sheets comprising a mass of intermeshed glass fibers substantially all of which have a fiber diameter not greater than about 20gm, and at least 5 percent w/w of which have a fiber diameter less than lgm, and, distributed through the glass fibers, from 0.2 percent w/w to 20 percent w/w of cellulose fibrils from a slurry having a Canadian freeness not greater than 650cc, and sufficiently low that the separator material has a S 15 tensile strength greater than an otherwise identical separator where glass fibers having an S average diameter greater than 1gm replace the cellulose fibrils. A sealed lead/sulfuric acid recombinant storage battery comprising a plurality S• of lead plates in a closed case, a fibrous sheet plate separator between adjacent ones of said plates, and a body of a sulfuric acid electrolyte absorbed by each of said separators and maintained in contact with each of the adjacent ones of said plates, each of said separator sheets comprising a mass of intermeshed glass fibers substantially all of which have a fiber diameter not greater than about 20gm, and at least 5 percent w/w of which have a fiber diameter less than 1lm, and, distributed through the glass fibers, from 0.2 percent w/w to 20 percent w/w of cellulose fibrils from a slurry having a Canadian freeness not greater than 650cc, and sufficiently low that the battery has a service life, when cycled, at least 10 percent greater than a battery made with an otherwise identical separator where glass fibers having an average diameter greater than lgm replace the cellulose fibrils. S•16. A sealed lead/sulfuric acid recombinant storage battery, substantially as 30 hereinbefore described with reference to any one of the Examples. Dated 29 January, 1999 Hollingsworth Vose Company Patent Attorneys for the Applicant/Nominated Person SPRUSON FERGUSON '[N:/bc00152:bmv I '[N:/Iibc]00152:bnv
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2115496P | 1996-07-01 | 1996-07-01 | |
| US60/021154 | 1996-07-01 | ||
| PCT/US1997/011579 WO1998000875A1 (en) | 1996-07-01 | 1997-06-30 | Glass fiber separators for batteries |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU3513997A AU3513997A (en) | 1998-01-21 |
| AU714243B2 true AU714243B2 (en) | 1999-12-23 |
Family
ID=21802651
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU35139/97A Ceased AU714243B2 (en) | 1996-07-01 | 1997-06-30 | Glass fiber separators for batteries |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0913006A4 (en) |
| JP (1) | JP2000513865A (en) |
| KR (1) | KR100420052B1 (en) |
| CN (1) | CN1190857C (en) |
| AU (1) | AU714243B2 (en) |
| BR (1) | BR9710134A (en) |
| CA (1) | CA2260005C (en) |
| CZ (1) | CZ288888B6 (en) |
| TW (1) | TW396652B (en) |
| WO (1) | WO1998000875A1 (en) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6072693A (en) * | 1998-11-02 | 2000-06-06 | Asahi Glass Company Ltd. | Electric double layer capacitor and separator therefor |
| US7159805B2 (en) | 2002-03-25 | 2007-01-09 | Evanite Fiber Corporation | Methods of modifying fibers |
| US6929858B2 (en) | 2002-03-25 | 2005-08-16 | Squannacook Technologies Llc | Glass fibers |
| JP2004335367A (en) * | 2003-05-09 | 2004-11-25 | Sanyo Electric Co Ltd | Lithium secondary battery |
| CN104584270B (en) * | 2012-08-22 | 2017-07-18 | 达拉米克有限责任公司 | The battery separator with immersing hydrogels non-woven fabric for lead-acid battery |
| US20140272535A1 (en) * | 2013-03-15 | 2014-09-18 | Hollingsworth & Vose Company | Three-region battery separator |
| US10062887B2 (en) * | 2013-10-08 | 2018-08-28 | Johns Manville | Battery electrode plate reinforcement mat having improved wettability characteristics and methods of use therefor |
| US10177360B2 (en) * | 2014-11-21 | 2019-01-08 | Hollingsworth & Vose Company | Battery separators with controlled pore structure |
| PL3352247T3 (en) * | 2015-09-15 | 2021-05-31 | Kuraray Co., Ltd. | Alkaline battery separator |
| US10135051B2 (en) | 2016-12-15 | 2018-11-20 | Hollingsworth & Vose Company | Battery components comprising fibers |
| CN106848154B (en) * | 2017-02-09 | 2019-03-26 | 重庆伟业电源材料有限公司 | A kind of glass fibre separator and preparation method thereof for battery |
| CN108598346A (en) * | 2018-04-16 | 2018-09-28 | 南京林业大学 | The AGM partition boards and its production method of elastic stability |
| JP6506448B1 (en) * | 2018-05-25 | 2019-04-24 | 日本板硝子株式会社 | Lead battery separator |
| CN108807825B (en) * | 2018-08-31 | 2020-08-21 | 深圳市星源材质科技股份有限公司 | Coating liquid for lithium ion battery, lithium ion battery diaphragm and lithium ion battery |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4216280A (en) * | 1977-09-19 | 1980-08-05 | Yuasa Battery Company Limited | Glass fiber separator for storage batteries |
| US4363856A (en) * | 1980-06-30 | 1982-12-14 | Texon Inc. | Battery separator material |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2734095A (en) * | 1956-02-07 | Plate separator for storage batteries | ||
| US4216281A (en) * | 1978-08-21 | 1980-08-05 | W. R. Grace & Co. | Battery separator |
| US4265985A (en) * | 1978-08-21 | 1981-05-05 | W. R. Grace & Co. | Lead acid battery with separator having long fibers |
| IT1132217B (en) * | 1980-07-22 | 1986-06-25 | Montedison Spa | PROCEDURE FOR THE MANUFACTURE OF SEPARATORS FOR BATTERIES OF SULFURIC ACID ACCUMULATORS |
| JPS5973842A (en) * | 1982-10-20 | 1984-04-26 | Matsushita Electric Ind Co Ltd | Separator for sealed lead-acid batteries |
| JPH0732007B2 (en) * | 1987-03-11 | 1995-04-10 | 日本板硝子株式会社 | Storage battery separator |
| JP2762446B2 (en) * | 1987-03-11 | 1998-06-04 | 日本板硝子株式会社 | Storage battery separator |
| JPH0422061A (en) * | 1990-05-17 | 1992-01-27 | Nippon Sheet Glass Co Ltd | Separator for storage battery |
-
1997
- 1997-06-30 WO PCT/US1997/011579 patent/WO1998000875A1/en not_active Ceased
- 1997-06-30 BR BR9710134A patent/BR9710134A/en not_active Application Discontinuation
- 1997-06-30 CA CA002260005A patent/CA2260005C/en not_active Expired - Fee Related
- 1997-06-30 CZ CZ19984369A patent/CZ288888B6/en not_active IP Right Cessation
- 1997-06-30 JP JP10504455A patent/JP2000513865A/en not_active Ceased
- 1997-06-30 AU AU35139/97A patent/AU714243B2/en not_active Ceased
- 1997-06-30 EP EP97931533A patent/EP0913006A4/en not_active Withdrawn
- 1997-06-30 CN CNB971961611A patent/CN1190857C/en not_active Expired - Fee Related
- 1997-06-30 KR KR10-1998-0710803A patent/KR100420052B1/en not_active Expired - Fee Related
- 1997-07-01 TW TW086109292A patent/TW396652B/en not_active IP Right Cessation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4216280A (en) * | 1977-09-19 | 1980-08-05 | Yuasa Battery Company Limited | Glass fiber separator for storage batteries |
| US4363856A (en) * | 1980-06-30 | 1982-12-14 | Texon Inc. | Battery separator material |
Also Published As
| Publication number | Publication date |
|---|---|
| AU3513997A (en) | 1998-01-21 |
| CA2260005C (en) | 2004-04-06 |
| CZ436998A3 (en) | 1999-06-16 |
| CN1190857C (en) | 2005-02-23 |
| CZ288888B6 (en) | 2001-09-12 |
| CN1224535A (en) | 1999-07-28 |
| KR20000022372A (en) | 2000-04-25 |
| TW396652B (en) | 2000-07-01 |
| BR9710134A (en) | 1999-08-10 |
| EP0913006A1 (en) | 1999-05-06 |
| EP0913006A4 (en) | 2001-08-08 |
| KR100420052B1 (en) | 2004-07-12 |
| JP2000513865A (en) | 2000-10-17 |
| CA2260005A1 (en) | 1998-01-08 |
| WO1998000875A1 (en) | 1998-01-08 |
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