AU2004201151B2 - Coating compositions - Google Patents
Coating compositions Download PDFInfo
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- AU2004201151B2 AU2004201151B2 AU2004201151A AU2004201151A AU2004201151B2 AU 2004201151 B2 AU2004201151 B2 AU 2004201151B2 AU 2004201151 A AU2004201151 A AU 2004201151A AU 2004201151 A AU2004201151 A AU 2004201151A AU 2004201151 B2 AU2004201151 B2 AU 2004201151B2
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- starch
- composition
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- 239000008199 coating composition Substances 0.000 title claims description 39
- 239000000203 mixture Substances 0.000 claims description 181
- 229920002472 Starch Polymers 0.000 claims description 142
- 235000019698 starch Nutrition 0.000 claims description 133
- 239000008107 starch Substances 0.000 claims description 129
- 239000000123 paper Substances 0.000 claims description 117
- 235000013312 flour Nutrition 0.000 claims description 85
- 238000000034 method Methods 0.000 claims description 73
- 235000018102 proteins Nutrition 0.000 claims description 65
- 108090000623 proteins and genes Proteins 0.000 claims description 65
- 102000004169 proteins and genes Human genes 0.000 claims description 65
- 238000000576 coating method Methods 0.000 claims description 53
- 108010064851 Plant Proteins Proteins 0.000 claims description 50
- 235000021118 plant-derived protein Nutrition 0.000 claims description 50
- 239000011248 coating agent Substances 0.000 claims description 47
- 239000003513 alkali Substances 0.000 claims description 37
- 239000007787 solid Substances 0.000 claims description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 33
- 230000003647 oxidation Effects 0.000 claims description 30
- 238000007254 oxidation reaction Methods 0.000 claims description 30
- 238000004519 manufacturing process Methods 0.000 claims description 25
- 241000196324 Embryophyta Species 0.000 claims description 24
- 240000008042 Zea mays Species 0.000 claims description 23
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 23
- 235000021307 Triticum Nutrition 0.000 claims description 21
- 241000209140 Triticum Species 0.000 claims description 21
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 21
- 235000009973 maize Nutrition 0.000 claims description 21
- 238000010438 heat treatment Methods 0.000 claims description 18
- 235000007319 Avena orientalis Nutrition 0.000 claims description 11
- 244000075850 Avena orientalis Species 0.000 claims description 11
- 240000005979 Hordeum vulgare Species 0.000 claims description 11
- 235000007340 Hordeum vulgare Nutrition 0.000 claims description 11
- 235000007238 Secale cereale Nutrition 0.000 claims description 11
- 235000013339 cereals Nutrition 0.000 claims description 11
- 239000011087 paperboard Substances 0.000 claims description 11
- 235000019714 Triticale Nutrition 0.000 claims description 10
- 241000228158 x Triticosecale Species 0.000 claims description 10
- 240000003183 Manihot esculenta Species 0.000 claims description 9
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 claims description 9
- 239000011111 cardboard Substances 0.000 claims description 9
- 239000007800 oxidant agent Substances 0.000 claims description 9
- 241000209056 Secale Species 0.000 claims description 8
- 235000012054 meals Nutrition 0.000 claims description 8
- 239000000470 constituent Substances 0.000 claims description 6
- 239000010440 gypsum Substances 0.000 claims description 6
- 229910052602 gypsum Inorganic materials 0.000 claims description 6
- 240000006394 Sorghum bicolor Species 0.000 claims description 5
- 235000011684 Sorghum saccharatum Nutrition 0.000 claims description 5
- 230000009969 flowable effect Effects 0.000 claims description 5
- 229920001685 Amylomaize Polymers 0.000 claims description 4
- 244000061456 Solanum tuberosum Species 0.000 claims description 4
- 235000002595 Solanum tuberosum Nutrition 0.000 claims description 4
- 239000004464 cereal grain Substances 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 235000007558 Avena sp Nutrition 0.000 claims description 3
- 239000002245 particle Substances 0.000 claims description 3
- 239000011369 resultant mixture Substances 0.000 claims description 3
- 239000002131 composite material Substances 0.000 claims description 2
- 229940100486 rice starch Drugs 0.000 claims 2
- 102100035353 Cyclin-dependent kinase 2-associated protein 1 Human genes 0.000 claims 1
- 239000002023 wood Substances 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 35
- 238000012360 testing method Methods 0.000 description 29
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 13
- 239000000243 solution Substances 0.000 description 12
- 238000010411 cooking Methods 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
- 239000002002 slurry Substances 0.000 description 9
- 229940100445 wheat starch Drugs 0.000 description 9
- 230000001965 increasing effect Effects 0.000 description 8
- 108010068370 Glutens Proteins 0.000 description 7
- 235000021312 gluten Nutrition 0.000 description 7
- 229920000856 Amylose Polymers 0.000 description 5
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- -1 alkali metal sulfites Chemical class 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 150000002978 peroxides Chemical class 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000004513 sizing Methods 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 239000013530 defoamer Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000004160 Ammonium persulphate Substances 0.000 description 3
- 102100028717 Cytosolic 5'-nucleotidase 3A Human genes 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 3
- 235000019395 ammonium persulphate Nutrition 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 3
- 102000013142 Amylases Human genes 0.000 description 2
- 108010065511 Amylases Proteins 0.000 description 2
- 208000000659 Autoimmune lymphoproliferative syndrome Diseases 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 241000219745 Lupinus Species 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 108010055615 Zein Proteins 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000011790 ferrous sulphate Substances 0.000 description 2
- 235000003891 ferrous sulphate Nutrition 0.000 description 2
- 235000011868 grain product Nutrition 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 235000019426 modified starch Nutrition 0.000 description 2
- 238000010979 pH adjustment Methods 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000004296 sodium metabisulphite Substances 0.000 description 2
- 235000010262 sodium metabisulphite Nutrition 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- ZKQDCIXGCQPQNV-UHFFFAOYSA-N Calcium hypochlorite Chemical compound [Ca+2].Cl[O-].Cl[O-] ZKQDCIXGCQPQNV-UHFFFAOYSA-N 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- 235000019759 Maize starch Nutrition 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 206010029350 Neurotoxicity Diseases 0.000 description 1
- 238000013494 PH determination Methods 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 206010044221 Toxic encephalopathy Diseases 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920002494 Zein Polymers 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 230000007815 allergy Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 101150099875 atpE gene Proteins 0.000 description 1
- 101150018639 atpFH gene Proteins 0.000 description 1
- 101150048329 atpH gene Proteins 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- FDYSSWYQRTVFIS-UHFFFAOYSA-N buta-1,3-diene 3-phenylprop-2-enoic acid Chemical compound C=CC=C.C(=O)(O)C=CC1=CC=CC=C1 FDYSSWYQRTVFIS-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000000837 carbohydrate group Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical group 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
- 239000003054 catalyst Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000012669 compression test Methods 0.000 description 1
- 238000004320 controlled atmosphere Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- 230000006240 deamidation Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 229910001448 ferrous ion Inorganic materials 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000007431 microscopic evaluation Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 230000007135 neurotoxicity Effects 0.000 description 1
- 231100000228 neurotoxicity Toxicity 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 229910001456 vanadium ion Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000005019 zein Substances 0.000 description 1
- 229940093612 zein Drugs 0.000 description 1
Landscapes
- Paper (AREA)
Description
19- 3-04; 4;09 612 93645173 7/ 37
AUSTRALIA
PATENTS ACT 1990 COMPLETE SPECIFICATION Kr- NAME OF APPLICANT(S):: George Weston Foods Limited r-- ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys Level 10, 10 Barrack StreetSydney, New South Wales, Australia, 2000 INVENTION TITLE: Coating compositions The following statement is a full description of this invention, including the best method of performing it known to me/us:- 5102 COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 m 1S- 3-04. 4!09 B 12 93645173 it S/ 37 COATING COMPOSITIONS Field of the Invention This invention is directed to coating compositions, in particular paper coating compositions, processes for the production of paper coating compositions, and treated paper and other products.
Background of the Invention Paper may be strengthened by means of adding stength agents in the paper making process, for example into the funish at what is known as the wet end of a paper machine or as a coating at the size press unit or coater, which is situated at the dry end of the paper machine. Various types of starches are used in both applications, viz: cationic or amphoterc starches for wet end addition and oxidised or acid modified starches at the size press. Another means of adding starch to strengthen paper is to spray a starch slurry between the plys on multiwire paper machines. Casein and/or latexes have also been used at the coating end of paper machines particularly in conjunction with pigments to improve opacity, whiteness and strength.
Starch is oxidised under acid conditions in order to obtain the necessary starch hydrolysis and viscosity reduction as required in the paper industry- Starches used in paper coating compositions, whether gelatinised, hydrolyzed, oxidised or otherwise modified, exhibit sporadic unpredictable behaviour which typically results in inconsistent coating properties associated with batch variability. For example, starch prepared from water damaged wheat may give low viscosity coatings when subject to oxidation.
Starch is an extensively chemically purified product obtained from various agro-industrial crops, including maize, potato, wheat and tapioca. For example, maize starch may be prepared from maize by steeping the maize in sodium metabisuiphite to soften protein constituents. The steeped maize is then passed through a roller mill to separate protein, wet miilied or ground into a starch slurry, screened to remove fibre, and then flash dried.
COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04; 4:09 612 93645173 9/ 37 t1WmatGC S7UOI22tVI FZ ;;4e-1f34 -2- Starch production involves significant energy use and waste production, and is accordingly a costly processed product.
in an attempt to overcome the problems of gelatinised, hydrolysed and modified starch, Bassie et al (US Patent No. 6,517,625) describes aqueous dispersions for coating paper stock which comprise 20 to 45% by weight of a filler such as clay, calcium carbonate, talc, ungelled starch or mixtures thereof, and from 16 to 18% wheat gluten. The gluten of Bassie is reduced to cleave some of the disulfide bonds using an acidic reducing agent such as alkali metal sulfites, alkali metal bisulfites, alkali metal metabisulfites, sulfur dioxide, mercaptan and cysteine. Sodium hydroxide is added to a an aqueous solution of the gluten and then the reducing agent is added. The next step is the addition of granular starch, that is ungelatinised starch, to the dispersion. The finished composition has a pH in the range 9-12 such as pH of 9.5-11. The use of a reducing agent such as sodium metabisulphite in Bassi el al raises allergy concerns associated with sodium metabisulphite or other reducing agent residues. The costs involved in providing purified components and subsequent reduction processes according to Bassie el al are not associated with improved processes for the preparation of paper nor does it ensure the paper prepared has improved strength or durability. Furthermore, pHs above 9 in final compositions such as those described by Bassi el al disadvantageously affects paper properties, particularly paper strength.
Wheat flour has also been proposed for use as an additive at the beginning stages of paper production, particularly addition to wet pulp in the uncooked form. Retention of flour in these proposals was often less than 60%/ w/w, which was uneconomic.
It has also been proposed to use cooked flour at the sizing step of manufacture of paper.
However, the insoluble gluten results in fouling of the paper production equipment- A further problem with these proposals is that the gluten content causes a gummy finish in the resultant paper.
US Patent 6,022,450 (Van Kessel et al) dcscribes methods for manufacturing paper or cardboard from a fibre matrix and flour comprising subjecting the flour to a deamidation COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04: 4:09 612 93645173 10/ 37 -3reaction and/or partial hydrolysis degradation treatment. Flour is mixed with ammoniun persulphate under acidic conditions, achieved for example by the addition of acetic acid or citric acid. Flour degradation may also be carried out according to Van Kessel et al by treatment with amylase enzymes, or combinations of amylase enzymes with ammonium persulphate.
In comparative testing with conventional starch coatings, Van Kessel et al found that the performance properties of paper treated according to their methods were either equivalent to those properties conferred by conventional starch coating, or somewhat less effective.
For example burst and breaking strength of paper treated according to the methods of Van Kesse] et a) were respectively 13% and 17% less effective than standard starch coating treatments.
A large number of different types of paper size compositions have been developed in attempts to increase the strength and durability of paper, and to improve printability, opacity and whiteness. For example, US Patents Nos. 5,122,568 and 5,139,614 teach the use of styrene acrylic copolymers for enhancing sizing and ink print contrast. US Patent No. 3,562,102 discloses amine reaction products of alkyl glycidyl mixed esters for use in sizing paper substrates. US Patent No. 4,294,704 describes paper and paperboard coating compositions which contain aqueous latex binders of synthetic polymers, such as styrenebutadiene copolymers, carboxyl styrene-butadiene copolymers and the like in order to provide improved dry and wet tear resistance. US Patent No. 6,494,990 describes coating compositions based on hydrophilic polyacrylimides and various copolymers. Issues of expense and health concerns of such compositions arise. For example, polyacrylimides have been associated with neurotoxicity.
There remains a need for low cost, high performance, non-noxious paper coating compositions.
This invention has particular applicability to the end stages of paper production, for example the size press coating stage, as well as other stages of paper, paperboard and cardboard production, as well as the production of other products. Coating compositions COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 P %WPDOCSCRN"XLSpm' 2233441 ncw clans do.4flAnY9/(X 00 -4e, also find use as adhesives. This invention thus has application in the adhesive field, for example in gummed tape manufacture, and as an additive to gypsum board to improve bonding of the liner to the gypsum core.
Summary of the Invention SSurprisingly it has been found that alkali oxidation of protein and starch mixtures and (-i cooking to give viscosity reduction gives rise to highly advantageous coating Scompositions, having particular application as paper coatings. These coatings have been found to increase the strength and durability of paper.
Disclosed herein is an aqueous coating composition which comprises an alkali oxidised aqueous gelatinised starch/protein mixture, said composition having a viscosity from about 1 to about 100 centapoise (cps), preferably from about 5 to about 80, more preferably about 5 to about 60 cps, and an alkali pH from about pH 7.5 to about pH 9, preferably from about pH 7.8 to about pH 8.8.
In a first aspect, the present invention provides a process for the production of a coating composition which comprises the steps of: oxidising a mixture which comprises at least one plant protein and starch, in water at an alkaline pH; and heating the mixture concomitantly with oxidation or subsequent to oxidation to provide a composition with a viscosity from I to 100 centapoise, and a pH from pH 7.5 to pH 9.
In a second aspect, the present invention provides a process for the production of a coating composition which comprises the steps of forming a mixture of a plant protein and plant starch in water, said mixture comprising solids in an amount between 3% w/w and w/w, oxidising the mixture with an oxidising agent at alkaline pH and heating the oxidised mixture at a temperature between 70'C and 150 0 C until the viscosity is lowered to 1 to 100 centapoise.
P 1WPDOCSkCRNNX\SpcI ~223144 nm cl eans do.4P/2(XJ8 00 The pH of the solution is generally from pH 7.5 to pH 9 at the completion of the process.
SWhere the pH at the completion of the process is outside this range, appropriate pH adjustment is made.
Preferably in the process the alkaline pH is from about pH 8 to about pH 13, more preferably from about pH 9 to about pH 12. Preferably the solids content of the composition is from about 3% w/w to about 30%w/w, more preferably about 5% w/w to Sabout 30% w/w. Preferably the protein content of the composition is from about 4% w/w to about 50% w/w, more preferably 6% w/w to about 50% w/w, and especially 8% w/w to about 25% w/w of solids.
In a third aspect, the present invention provides a composition for coating paper when obtained by the process of the first aspect.
In a fourth aspect, the present invention provides a process for coating paper comprising the step of applying a composition according to the third aspect to paper.
In a fifth aspect, the present invention provides a process for coating paper which comprises the steps: preparing a composition for coating by a process according to the first aspect; and applying the composition to paper.
Also disclosed herein is a process for increasing the strength and durability of paper which comprises applying to the surface of paper an aqueous coating composition which comprises an alkali oxidised gelatinised starch/protein mixture, said composition having a viscosity between 1 and 100 cps, and a pH from about pH 7.5 to about pH 9.
Further disclosed herein is an adhesive composition which comprises an alkali oxidised gelatinised starch/protein mixture, said composition having a viscosity between about 1 and about 100 cps, and a pH from about pH 7.5 to about pH 9.
P PDOCSXCRNXLSpcm\I2233441 nem clarns dmc4A0/1(W)9 -6- In a sixth aspect, the present invention provides a paper coated with an aqueous coating composition which comprises an alkali oxidised gelatinised starch/protein mixture, said composition having a viscosity from 1 to 100 centapoise, and a pH between pH 7.5 and pH 9.
In a seventh aspect, the present invention provides an aqueous composition for coating paper or paper board which comprises an alkali oxidised gelatinised starch and protein mixture, said composition having a viscosity from 1 to 100 centapoise (cps), and a pH from pH 7.5 to pH 9.
The protein employed in the invention is plant protein, which includes protein derivable from plants.
Preferably the solids content of the composition is about 3% w/w to about 50%, more preferably about 3% w/w to about 30% w/w, especially about 5% w/w to about 30% w/w.
Preferably the protein content of the composition is from about 4% w/w to about 50% w/w of solids, more preferably about 6% w/w to about 50% w/w, especially about 8% w/w to about 25 %w/w of solids.
Preferably the starch and protein mixture is flour, or other milled or crushed grain products. Preferably the composition may be used to treat paper, for example as a paper size or paper coating composition. The compositions of the present invention dramatically increase paper strength, for example as measured by the Ring Crush test.
Preferably the aqueous coating composition in accordance with the seventh aspect of this invention comprises a mixture of starch and plant protein in water having a solids content of 3% w/w to 30% w/w, a protein content of 4% w/w to 50% w/w of the total solids, a viscosity of about 1 to about 100 centapoise, and a pH from about pH 7.5 to about pH 9, wherein the starch is gelatinised and both the starch and protein in the mixture are alkali P 4WPDOCS\CR M1Spe l 221344) nme claims doc-4tD9/)8 00 0- 6aoxidised at a pH from about pH 8 to about pH 13, for about 5 to about 30 minutes at a temperature of about 70 0 C to about 150 0
C.
In an eighth aspect, the present invention provides an aqueous coating composition which comprises a mixture of starch and plant protein in water having a solids content between 3% w/w and 30% w/w, a protein content between 4% w/w and 50% w/w, a viscosity of 1 to 100 centapoise, and a pH from pH 7.5 to pH 9, wherein the starch is gelatinised and both Sthe starch and protein in the mixture are alkali oxidised at a pH from pH 8 to pH 13.
In a ninth aspect, the present invention provides a process for coating paper which comprises the step of applying a composition according to the seventh aspect to paper, paperboard or cardboard.
In a tenth aspect, the present invention provides a fibreboard comprising an alkali oxidised and gelatinised starch/protein mixture incorporated within the fibreboard.
In an eleventh aspect, the present invention provides a process for the production of fibreboard, which comprises forming a mixture of plant protein and plant starch in water, oxidising the mixture with an oxidising agent at alkali pH at 25 0 C to 50 0 C for 5-30 minutes or up to 24-48 hours, mixing the alkali oxidised mixture with the fibreboard constituents, followed by heating the resultant mixture which is formed into sheets in an oven at a temperature between 50 0 C and 150°C for 20 to 150 minutes.
Detailed Description of the Invention Thus the invention provides a process for the production of a coating composition which comprises the steps: oxidising a mixture which comprises at least one plant protein and starch, in water at an alkaline pH; and P.%WPDOC RN\Xt'SpccU 2233441 nm clims doc4/M9RI28 00
O
CD
q to -6bheating the mixture concomitantly with oxidation or subsequent to oxidation to provide a composition with a viscosity from 1 to 100 centapoise, and a pH from pH to pH 9.
The invention also provides compositions for coating paper, paperboard or cardboard obtainable by the process that is, produced by the above process.
The process provides a flowable aqueous coating composition for coating paper, paperboard or cardboard, which comprises an oxidised mixture comprising starch and protein, wherein said mixture is gelatinised and the composition has a pH from pH 7.5 to pH 9 and a viscosity from 1 to 100 centapoise.
Coating compositions according to the present invention may be used to treat paper, for example as a size composition. The compositions of the invention impart strength and durability to paper, and may also improve paper printability. Paper strength, as determined IS- 3-04; 4:09 812 93645173 14/ 37 Piu7Dac,'aRswnC122I1thIhW.4-1 -7by the standard Ring Crush test (TAPPI test T822 OM-89), is advantageously increased by over 20% using the compositions of the invention.
The coating compositions may be used in coating techniques known to persons skilled in the art, for example, employing a roller coater, blade coater or wire-wound rod coater.
In its broadest aspect, this invention is concerned in a first aspect with a coating composition, in particular a paper coating composition, which comprises an alkali oxidised aqueous gelatinised starch/protein mixture, said composition having a viscosity from about 1 to about 100 cps, and a pH from about pH 7 to about pH 9.
Gelatinised in the context of the application will be understood to mean that the material does not exhibit bifringence when subjected to polarised light and a nichol prism. Starch is gelatinised starch granules ruptured) when heated at a temperature above its natural gel point (about 7PC). Granular starch on microscopic analysis shows discrete starch granules which exhibit biflingence when subject to polarised light.
The protein may comprise plant proteins from wheat, rye, sorghum, triticale, maize, oats, barley, or other plant source. The preferred plant proteins are those capable of forming disulfide bonds on oxidation and include, for example, gluten, glutenen and zein. Plant proteins may be a mixture of one or more plant proteins. For example, the plant protein may be a zein protein from maize or plant protein from other cereals, or a mixture of plant proteins. The plant protein may comprise plant proteins extracted from plant material according to methods well known in the art. They include the extraction of gluten from wheat flour by means of washing a flour dough gently with copious amounts of water to remove the starch and leaving the protein in a gummy mass which is then dried to a powder in a ring dryer. This process in known as the Martin process and is described in US patent No. 3, 119, 719. Alternatively, low water content extraction can be used, such as the process known to those skilled in the art as the Rasio process.
The starch component may comprise a plant starch from wheat, sorghum, triticalc, maize, oats, barley (including waxy and high amylose starches), tapioca, potato, sago or rye. Any plant starch may be used in the invention, including waxy and high amylose versions of COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04; 4:09 612 93645173 15/ 37 -8cereal plants particularly wheat starch, corn starch and tapioca starch. Wheat starch comprises both large and fine starch particles, both or either of which would be suitable for this use. Also starch extracted from waxy maize or other waxy grains may be used in implementing the invention.
Plant proteins and plant starches may be mixed together to give a mixture of plant starch and plant protein. Generally, the resulting mixture contains from about 4% w/w to about w/w plant protein or up to as much as 50% plant protein, with the remainder comprising plant starch. r.
Preferably, the starch/protein mixture is flour, that is flour produced by milling grain, such as cereal grains. Protein levels in the grains may range from about 2% w/w to about w/w, preferably from about 5% w/w to about 18% w/w. Flours may be produced from high or low amylose content grains, or grains having intermediate anylose content. High amylose starch generally contains in the order of 50 to 70/ w/w amylose, whilst a low amylose starch generally contains in the order of 40% amylose or less. Examples of flours, which may be used in this invention, include wheat flour, sorghum flour, triticale flour, maize flour, oat flour, barley flour and rye flour. Other milled or crushed grain products such as meals (for example corn meal), grits (for example corn grits) or other plant protein/starch products may be used in this invention. Protein levels in such flours generally range from about 2 to about 20%. Plant protein may be added to flour to increase total protein levels, for example up to 50%. The plant protein may be from the same grain from which the flour was produced, or another plant protein.
Flour or other starch/protein mixtures may be mixed with water to give a solids content of from about 3% w/w to about 501/6 w/w, preferably 3% w/w to about 30% w/w and especially about 5% w/w to about 30%/ w/w. Such a mixture is generally in the form of a slurry or paste. The slurry of flour and water is readily oxidised using a conventional oxidising agent, for example as used in the oxidation of starch or flour, including a peroxide such as hydrogen peroxide, sodium hypochlorite, calcium hypochlorite or sodium perborate under alkaline conditions. The mixture may be agitated, for example by mixing during the oxidation. Alkali oxidation of flour/water mixtures may be conducted at a COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04* 4:09 19- -04:4:0 612 93645173 16/ 37 -9reaction temperature of about 25-50*'C, preferably about 30 to 45 0 C, for about 5-30 minutes, preferably about 6 to 20 minutes, prior to cooking to assist the oxidation process.
Alternatively, as mentioned below oxidation and cooking are conducted at the same time, that is, simultaneously (ic concomitantly).
Oxidation of flour and water mixturs, or for that matter any plant protein and plant starch mixture in water, is carried out under alkali conditions according to this invention, forp example at a pH from about 8 to about 13, preferably a pH of about pH 9 to about pH 12.7 The pH is adjusted to this range by the addition of alkali, such as sodium hydroxide, potassium hydroxide or other alkali. Oxidation may be carried out in the presence of metal catalysts, such as vanadium, ferrous or copper ions. Levels of addition are from about to looppm. Whilst not wishing to be bound by theory it is believed that under these conditions, it is carbohydrate groups in flour, for example in starch, which in particular undergo oxidation. Protein is also oxidised. Oxidation is generally carried out from about 5 to about 150 minutes, preferably about 6 to about 120 midnutes, until a viscosity of from about 1 to aboutl0O cps, preferably about 5 to about 80 cps, is achieved when cooked (heated) as set out below.
Alkali oxidised flour or other starch/protein mixtures are heated so as to reduce viscosity of the aqueous compositions to about 1 to about 100 cps, preferably about 5 to about cps. For example, heating at a temperature of about 50 to about l5m*C, preferably about to about 1450C, for about 5 to about 150 minutes, preferably about 6 to about 120 minutes, will reduce the viscosity of the composition to within the desired range. The alkali oxidised mixtures may be heated in a batch cooker, for example to about 95 0 C, or via a jet cooker (for example up from about 140rC to about 150T C) whereby the starch component is reduced in viscosity to the desired level. The alkali and oxidant may also be directly injected into the flour slurry or other starch/flour mixture immediately prior to entering the jet cooker, so that the oxidation and heating step are carried out at the same time. Protein within the composition remains in solution, and in combination with gelatinised starch is found to enhance the strength benefit of the composition when coated onto paper. Advantageously the compositions of the invention are flowable, aqueous compositions, which facilitates use of the compositions.
COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04: 4:09 612 93645173 1 7/ 37 Alkali oxidised aqueous starch/protein mixtures having a viscosity from about I to about 100 cps, preferably about 5 to about 80 cps, have a pH generally in the range from about PH 7.5 to about 9 at the completion of heating. The pH is more preferably within the range of about pH 7.5 to about 8.7, such as about pH 7.8 to about 8.7.
The compositions may include a range of additives that can be used to facilitate protein solubility including acetates (for example about 1-2% in flour), urea (for example about 3in flow), sodium benzoate (for example about 1-2% in flour), detergents, such as sodiumt dodecyl sulfate (for example about 0.01-0.02% in flour), alkalis, such sodium, potassium or calcium hydroxide (fbr example about 0.5 to 1.5% in flour) and gums (for example about 0.05-0.1% in flow), including gums possessing carboxylic acid end groups, for example xanthan gum and guar gum etc.
The composition may include one or more antifoaming agents, for example, silicon or oil based defoamers at an amount from about 0.005% w/w to about 0. 1% w/w, preferably about 0.05% w/w to about 0.1% w/w. It may also be necessary to filter the sizing agent to remove fibre.
The coating composition may be dried, for example in a ring dryer or other standard dryer, such as those used far drying starch. The dried material is readily reconstituted in water., In accordance with another aspect of this invention there is provided a process for the production of a coating composition, for example a paper coating composition, which comprises the steps of forming a mixture of a plant protein and plant starch in water, preferably having from about 3% w/w to about 50% wlw solids content, oxidising the mixture with an oxidising agent at alkl~ine pH and heating the oxidised mixture at a temperature from about 70"C to about 15WC until the viscosity is lowered to from about I to about 100 cps. The pH of the solution is generally from about pH 7.5 to about pH 9 at the completion of the process. Where the pH at the completion of the process is outside this rang;, appropriate pH adjustment is made. Preferably the alkaline pH at which oxidation is conducted is from about pH 8 to about pH 13, especially from about pH 9 to COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 IS- 3-04; 4:09 19- -04:4±0 612 93645173 IS/ 37 about pH 12. Preferably the solids content of the composition is from about 3% w/w to about 30%, especially about 5% w/w to about 30%/ w/w. Preferably the protein content of the composition is from about 4% w/w to about 50% w/w of solids, The process according to the invention is simple to cary out, and is readily implemented in paper mills or other commercial settings.
Whilst not wishing to be bound by theory it is thought that the alkaline oxidations results; in the formation of disulfide bonds which are destroyed in earlier parts of the processing, and which in contrast to the teaching of US 6, 517, 625 are believed by the inventors to be advantageous to the properties of the composition contained.
The coating composition of the present invention may be applied to paper or a paperboard, such as linerboard or corrugating medium, according to methods well known in the art for the application of size compositions, for example, in a size process roller or blade coater.
For example, the compositions may be utilised in a paper making machine, for example for use as a coating at the size press unit or coater. The advantageous properties of the compositions according to the present invention minimise the problems of the machines being tbuled or becoming blocked, and therefore reduces the amount of a time and costs lost as a result of these problems.
For the purpose of this invention, reference to paper includes all grades of paper as well as boards such as cardboard. Further examples of paper include recycled and non-recycled paper, kraft paper, high quality printing paper, plasterboard liners, cardboard or other fibreboard, photographic papers, and magazine paper.
In accordance with another aspect this inven tion relates to paper, coated with a coating composition as herein described. The paper is coated with an aqueous coating composition which comprises an alkali oxidised aqueous gelatinised starch/protein mixture, having a viscosity between about I and about 100 centapoise (cps) and a pH from about pH 7.5 to about pH 9.
COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04; 4:09 612 33645173 419/ 37 12- The amount of protein/starch solution applied to the paper depends on the desired strength requirements. Levels of from about 2% w/w dry coating on fibre and up to about 301/ w/w dry coating on fibre may be applied, particularly if high pigment levels are present in the coating.
The alkali oxidised aqueous gelatinised starch/protein mixtures having a viscosity from about 1 and about 100 cps, for example where the starch/protein mixture is flour, may be used as an adhesive composition, for example in the production of adhesive tapes such as gummed tape manufacture and in other industrial uses requiring adhesive properties.
In accordance with another aspect of the invention, there is provided a fibreboard, such as plasterboard or composite board or particle board, comprising an alal oxidised and gelatinised starch/protein mixture incorporated within the board.
Processes for the production of fibreboards, for example plasterboard, comprise the steps of forming a mixture of plant protein and plant starch in water, preferably having from, about 5-50% w/w solids content, oxidising the mixture with an oxidising agent at alkali pH, at about 25 0 C to about 50"C for up to 24-48 hours, preferably for about 5-30 minutes, mixing the alkali oxidised mixture with the fibreboard constituents, such as gypsum, air and wax emulsion followed by heating the resultant mixture which may be formed into sheets in an oven at a temperature of about 500C to about 150 3 C for about 20 to about 150 minutes. The starch in the plant starch/plant protein mixture is gelatinised under these conditions. Preferably the alkali pH is from about pH 8 to about pH 13, especially about pH 9to about pH 12.
Viscosity is conventionally measured between 5-12% w/w solids whilst the mixture is hot, for example at about The invention also extends to use of the compositions previously defined above for the manufacture or treatment of paper and particularly for preparing paper with increased the strength and/or durability in comparison to untreated paper.
COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04: 4:09 612 93645173 20/ 37 P:W FCQCRrflNeO 2U1 U Iild- MWI -13- This invention will now be described with reference to the following non-limiting examples.
EXAMPLES
Example I
I--
Test solutions of three size coatings were prepared using wheat starch, ASW (Australian Standard White Wheat) flour (10.1% protein) and TPF (high protein flour of 13.1% protein).
U
The wheat starch was shunied with water to give a 10% dry solids solution and w/w axnmonimn persulphate was added prior to cooking at 950C for minutes. The pH before cooking was 6.0. After cooking the pH was 2.1, and this was adjusted to 5.2 with I N NaOH solution and the solids were checked with a refractometer A Brookfield viscosity was measured at 80'C (waterbath) and found to be 27.5 cps (No. 1 spindle at 20 rpm).
The ASW flour (protein 10.1%) was slurried with water at 400(C to give a 10-11 dry solids mixture and I N NaOH solution was added to adjust the pH to 11.5.
2.6% of a 30% hydrogen peroxide solution was also added. This mixture was allowed to stand at 40C for 30 minutes before being cooked at 95'C for minutes. The solution was then placed in a waterbath at 80'C and its viscosity checked with a Brookfield viscometer and found to be 17.5 cps (No. 1 spindle at rpm). A pH determination gave a pH of 8.7 and solids were 11.0 The HPF (13.1 protein flour) was prepared in the seme manner as above and also placed in a waterbath at It was found to have a pH of 9.2, solids of 11.8% and a viscosity of 17.5 ups.
Sample Preparation An untreated (ic unsized) sample of corrugating medium having a basis weight of 122 gsm (grams per square metre), was out into strips ready for coating at two application levels COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 IS- 3-04* 4:09 19 3-4 4:0 2 9 36 45 1 73 4$ 2 1/ 3 7 -14using two different sizes of wire wound rods. After coating with the 80"C size solutions, the paper samples were dried in an oven at 11I000 for 20 minutes. The samples were then placed in a controlled atmosphere room for a further 24 hours to condition prior to being sent to a paper testing laboratory for strength testing. They were also weighed carefully to calculate the exact coating application rate. The tests performed included Ring Crush, burst and concora.
These tests measure paper strength, and are well established standard tests conducted according to TAPPI (the leading technical association for the worldwide pulp, paper and converting industry) test standards. Ring Crush, burst and concora and tests are carried out according to the respective TAPPI tests T822 OM-89, T403 QM-02 and T8O8. The Ring Crush test is a compression test and predicts box compression properties, as well as paper strength and durability. The burst test is a test of tensile strength of paper and cardboard.
Coacora is a test used to estimate flat crush resistance, particularly of corrugated board.
Results are shown in Table 1.
Results To enable a viable comparison to be nmade, the results were recalculated in terms of percent strength increase for each one percent of coating pickup. Figs. 1, 2 and 3 show the strength gains for each type of size coating.
The results clearly demonstrate that oxidised flour is considerably more effective than oxidised wheat starch and fur-ther, that this increase improves as the protein increases in the flour.
COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04; 4:09 612 93645173 22/ 37 PrAUVOCIManSAlIMIniIIttAwfIWii Table 1 Paper Rod No. Percent Coating Burst Concora Ringcrush Comments sample Used dry Type Kg/sq.cm (CMT) (RCT) No. coating Kgf Kgf Al 25 8.54 Starch 2.57 A2 25 8.25 Starch 18.72 13.79 Bl 10 6.36 Starch 2.32 B2 10 7.0 Starch 17.34 15.96 C1 25 8.15 ASW 2.71 C2 25 7.76 ASW 19.05 16.88 D1 10 6.0 ASW 2.16 Defect in one test D2 10 6.93 ASW 19.23 15.30 El 25 7.48 HPF 2.64 E2 25 9.1 HPF 19.84 15.37 F1 10 6.86 HPF 2.55 F2 10 7.04 HPF 13.87 18.26* One test only G 0 1.66 15 1_(defect) G 0 0 1.66 14.45 10.62 Summary of Results RCT (Ring Crush) (percent increase in RCT per percent application) Kgf Starch 5.4 ASW Flour HPF 7.56 Compared to the control starch the ASW flour and HPF flour compositions respectively increased RCT by 29.6% and Burst (percent increase in burst per percent application) Kg/cm 2 Starch 6.34 ASW Flour 7.76
HPF
7.96 Compared to control starch the ASW flour and HPF flour compositions respectively increased burst by 22.4% and 26%.
COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04; 4:09 612 93645173 23/ 37 MfWrnGCcEiUaJiggI LSo cc.Iwfmt/f -16- Concora (CMT) (percent increase in CMT per percent application) Starch ASW Flour
HPF
3.2 4.4 4.1 Compared to control starch ASW flour and HPF flour compositions respectively increase CMT by 37.5% and 28.1%.
U
The Ring Crush test in particular has been found to be an excellent indicator of paper strength.
Example 2 Coating compositions prepared from various grain flours were tested and paper strength determination carried out.
I.
Method The following slurries were made up and cooked to coat paper of the type 120 gins recycled corrugating medium. The papers were dried and trimmed for evaluation: Paste 1. Wheat starch 10% dsb (Dry solids Basis) Starch 57 g, water 438 g, NaOH 4.5 g, H 2 O% 2 g, and an oil based defoamer 1 ml.
Paste 2. ASW flour 10% dsb ASW flour 57 g, water 436 g, NaOH 7.2 g, H202 2 g and an oil based defoamer 1 ml.
Paste 3. Maize meal 10% dsb Maize meal 57 g, water 430 g, NaOH 13 g, H202 2 g, and an oil based defoamer 1 ml.
All slunrry pH was adjusted to 11.5 except for Paste 3, where pH was adjusted to 11.7 with additional NaOH.
All slurries were cooked using a Viscoamylograph (80°C for 10 minutes at 7.0% w/w solids).
COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04; 4:09 612 93645173 24/ 37 -17- Viscosity, solids and pH were measured after the cooking and coated onto sheets, preweighed and cut.
Summary of results Table 2. Paste results Paste pH Viscosity (cP) Solids Paste 1 9.2 62.5 9.8 Paste 2 9 32.5 Paste 3 8.5 22.5 The Ring Crush was carried out on the coated paper. Test results are set out in the table below. The test results for the Paste 2 and Paste 3 were averaged.
Table 3. Table of paper results Paste Ring Crush Test Percent increase per pick up Paste 1. Wheat 1 Starch Paste 2. ASW flour 3 Paste 3. Maize meal 3.1 These results show that compositions prepared from wheat and maize meal were particularly effective compared to wheat starch.
Example 3 The following pastes were cooked in the Viscoamylograph, then coated onto paper of the type 120 gms recycled corrugated medium.
1. Promax (High protein flour) 10% dsb with 2 gm HzO2 at pH 11.
2. ASW flour- 10% dsb with 11% lupin protein with 2 gm H20z2 at pH 11, 3. ASW flour- 10% dsbwith2 gmH2Oz atpH 11- COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04; 4:09 612 93845173 25/ 37 PWDONI'RSSfumantlllo..-tw*M4 18 4. Tapioca starch 10% dsb with 1% ammonium peroxide on starch at pH 6. The pfl dropped on cooking to pH 2, and was adjusted to pH 5 with NaOH.
Final viscosity (after cooking), pH and solids were measured before paper coating. Three papers for each paste were coated and dried to work out the pick up rate for each paste.
The coated papers were tested for Ring Crush.
Summary of Results Table 4. Paper coating trial 0 Paste Final Brix° Viscosity Paper GSM coating on description pH cP number on the paper paper 8.3 10.5 17.5 Al 10.02 7.6 Promax flour A2 9.1 with A3 7.4 5.8 Hydrogen Ave. 6.63 5.1 peroxide ASW 8.5 11.5 22.5 Bi 10.05 7.7 10% Lupin B2 9.3 7.2 prot With B3 9.0 6.9 Hydrogen Ave. 7.69 5.91 peroxide ASW 8.2 10.8 35 C1 9.1 7.1 flour with C2 9.0 6.9 Hydrogen C3 9.1 7 peroxide Ave. 8.03 6.18 5 11.5 12.5 D1 12.7 Tapioca D2 11.3 starch with D3 9.7 7.4 APS Ave. 11.23 8.47 Paste description Ring Crush Test (Kg f) AR per 1% pick up Promax flour with 0.641 Hydrogen peroxide ASW 10% Lupin 0.562 prot. With Hydrogen peroxide ASW flour with 0.610 Hydrogen peroxide Tapioca starch 0.347 with APS COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04; 4:09 6 12 93645173 26/ 37 -19- In this experiment increases in Ring Crush values are measured with reference to untreated paper. These results show that increased paper strength is achieved with each composition.
Results obtained for tapioca starch cooked with Al'S on the acid side that is in the pH range about 2 to about 6 as a control highlights the surprising and most advantageous benefits obtained using the composition of the invention. For example, Paste 1 increased paper strength by more than 80% when compared to the control starch of Paste 4. Example 4 A trial under factory conditions was conducted on a recycled paper machine running 100 r G3SM (grams per square meter) corrugating medium.
aprearatin 3 batches of the following coating composition were prepared as follows: 379 1 water (recycled, pHl 6.6) 0.7 kg ferrous sulphate kg dry sodium hydroxide 144 kg 9.9% protein wheat flour 0.01 kg an oil based defoamer The above blend was thoroughly stirred to remove lumps and a dilute solution of hydrogen peroxide was injected just prior to entering a jet cooker which raised the temperature to 1420C, after which dilution water was added to give a size solution of 7.2% cdry solids, viscosity of 30 cps (at 8m*C, 7.0% w/w solids) and a pH of 8.4. This solution was pumped to the size press recirculation system where it was further diluted to 4.3% solids with extra water. The paper machine was operated at 750 MPM (metres per minute). The paper produced was tested for Ring Crush and short span compression.
The next reel of paper was rim using a standard wheat starch size at 5.8% solids, and comparative strength tests were then conducted. When a calculation was made to offset the difference in solids content of the two sizes, the modified flour size showed an increase in Ring Crush +20.2% and short span compression of +51.1% compared to the standard starch composition.
COMS ID No: SMBI-00672818 Received by IF' Australia: Time 18:08 Date 2004-03-19 IS- 3-04; 4:09 1 612 93645173 27/ 37 The reel of paper produced using the composition of the invention was cut into smaller reels and run as medium on a corrugator machine at 200 MPM without problem.
In terms of a financial benefit to the paper mill this showed a 29% reduction in sizing cost when allowing for the cost difference between flour and starch, and a 20% reduction in usage to provide a paper with a similar Ring Crush value.
Example Pastes were made up at 8% solids and coated onto paper and tested for paper strength (Ring Crush test) in accordance with Example 2.
Paste 1. Wheat starch 45.6 g, ammonium persulphate 0.46 g and water 453.9 g (at 300C).
Paste 2. ASW flour (10.2% protein), 45.9 g, ammonium persulphate 0.46 g, and water 453.6 g (at Paste 3. ASW flour 45.9 g, NaOH (IM) 11 g, H202 1.8 g, water 441.3 g (at 3rC).
Cooking was carried out at 95°C for 10 minutes.
Summan' of Results Table 5. Results on cooked pastes COMS ID No: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-03-19 197 3-04; 4.09 19- 612 93645173 28/ 37 -21- Table 6. Test results Paste king Crush Test Paste I (erc-entk 'erl%picku Paste 17.8 Paste 2 5.65 Paste 3 11.52 Coating 2, unlike coatings 1 (conventional starch) and 3 (in accordance with the invention) cloudy with Precipitated protein material.
This experiment demonstrates that acid ammninum porsuiphate (APS) treated flour (coating 2) confers 28% less paper stregth than starch treated under the same conditions (coating 1) as tested by the Ring Crush test. Flour treated according to the present invention (coating being oxidised and cooked under alkali conditions, increased paper strength by 46% over the acid ALPS starch coating, and by 74% over the acid APS flour coating (coating This is a most advantageous and unexpected result.
Oxidation of starh with ALPS under acid conditions reflects the prevailing conditions for starch oxidation used in the paper industry. Acid oxidation with both Al'S and H20O2 are used in the paper coating industry to achieve a combined acid thinning and oxidation of the starch.
Coating 2 was prepare according to Example I of US Patent 6,022,450 and the results obtained demonstrate the disadvantages of such compositions compared to conventional starch compositions used in the paper coating field.
Example 6 Plasterboard Droduction The following slurry was prepared: 270 g water (250C) 171.8 g 9.7% protein wheat flour COMS 10 No: SMSI-0072818 Received by IP Australia: Time 18:08 Date 2004-03-19 19- 3-04; 4.09 3-4 40 12 93645173 29/ 37 22 g calcium hydroxide (to pH 11.-7) 0.05 g ferrous sulphate 22.45 g 30% hydrogen peroxide This was allowed to react for 24 hours at 25 0 C after which 1 g of sodium thiosuiphate was added to mop up any unreacted peroxide and the pH was adjusted to 9.0 using 1 M sulphuric acid.
An alkaline fluidity test confinned that at a result of 74.7 ml the product was suitable as a starch replacement in the manufacture of plasterboard. The modified flour slurry was mixed into gypsum and the boards produced were heated in an oven at 130*C which gelled the starch in the flour. The liner to gypsum bonding was found to be as good as that produced when oxidised starch was used.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", or variations such as "comprises" or"comprising", will be understood to fimply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.
The reference to any prior art in this specification is not, and should not be taken as an acknowledgment or any form of suggestion that that prior art forms part of the commnon general knowledge in Australia- COMS IDNo: SMBI-00672818 Received by IP Australia: Time 18:08 Date 2004-3-19
Claims (47)
1. A process for the production of a coating composition which comprises the steps of: oxidising a mixture which comprises at least one plant protein and starch, in Swater at an alkaline pH; and S(b) heating the mixture concomitantly with oxidation or subsequent to oxidation to provide a composition with a viscosity from 1 to 100 centapoise, and a pH from pH 7.5 to pH 9.
2. A process of claim 1, wherein the composition is a flowable aqueous paper coating composition.
3. A process of claim 1 or claim 2, wherein the mixture comprises solids in an amount between 3% w/w and 50% w/w.
4. A process of any one of claims 1 to 3, wherein the heating is performed at a temperature between 70 0 C and 150 0 C. A process of any one of claims 1 to 4, wherein the composition comprises an alkali oxidised mixture of gelatinised starch and protein with a viscosity from 1 to 100 centapoise, and a pH from pH 7.5 to pH 9.
6. A process for the production of a coating composition which comprises the steps of forming a mixture of a plant protein and plant starch in water, said mixture comprising solids in an amount between 3% w/w and 50% w/w, oxidising the mixture with an oxidising agent at alkaline pH and heating the oxidised mixture at a temperature between 70 0 C and 150°C until the viscosity is lowered to 1 to 100 centapoise. P %WPDOCSCRMNNXL\Spm%1221344I ,-cla d- I .(rnn 00 0 -24- r/ 7. A process of claim 6, wherein the composition comprises an alkali oxidised t mixture of gelatinised starch and protein with a viscosity from 1 to 100 centapoise, and a pH from pH 7.5 to pH 9.
8. A process of any one of claims 1 to 7, wherein the alkaline pH is from pH 8 to pH
13. 9. A process of claim 8, wherein the alkaline pH is from pH 9 to pH 12. 10. The process of any one of claims 1 to 9, wherein said plant protein is selected from the group consisting of wheat, rye, triticale, maize, oats, and barley protein. 11. The process of any one of claims 1 to 9, wherein said plant protein is a mixture of two or more different plant proteins selected from the group consisting of wheat, rye, triticale, maize, oats, and barley proteins. 12. The process of any one of claims 1 to 11, wherein said starch is a plant starch selected from the group consisting of wheat, rye, sorghum, triticale, maize, oats, barley, tapioca, potato, sago and rice starch. 13. The process of any one of claims 1 to 12, wherein said starch is selected from waxy starch and high amylose starch.
14. The process of any one of claims 1 to 13, wherein said mixture of plant protein and starch comprises between 4% w/w and 50% w/w plant protein. The process of any one of claims 1 to 14, wherein said mixture of plant protein and starch is selected from the group consisting of flour, meal, grits and milled or crushed cereal grains. PI\WPDOCSXCR"NXL\Spcc3I223344 nw claims doc1/39/2008 00 O CD tq c, tt o
16. The process of claim 15, wherein the mixture is a flour selected from the group consisting of wheat flour, rye flour, triticale flour, maize flour, oat flour and barley flour.
17. The process of claim 16, wherein said flour comprises protein in an amount between 2% and
18. The process of any one of claims 1 to 17, wherein an additional plant protein is added to the flour to increase protein level.
19. The process of claim 18, wherein said additional plant protein is from the same grain from which the flour was produced, or is a plant protein from another plant species.
20. The process of any one of claims 4 to 19, wherein the mixture of starch and protein comprises solids in an amount between 3% w/w and 50% w/w.
21. The process of any one of claims 1 to 20, wherein said oxidation is conducted at a temperature between 25 0 C and 50 0 C for 5 to 30 minutes prior to subsequent heating for 5 to 150 minutes at a temperature between 50 0 C and 150°C until the viscosity of the composition is from 1 to 100 centapoise.
22. The process of any one of claims 1 to 21, wherein said composition is dried in a dryer to a flowable particulate state.
23. The process of any one of claims 1 to 22, wherein the oxidation and heating are conducted concomitantly.
24. A composition for coating paper when obtained by a process as defined in any one of claims 1 to 23. PA PDOCSkCRNXL\Spc(\ I 22l44l nm claim, d-lIAn(I/EN 00 O 0 -26- A process for coating paper comprising the step of applying a composition as defined in claim 24 to paper.
26. A process for coating paper which comprises the steps: preparing a composition for coating by a process as defined in any one of 0claims 1 to 23; and S(b) applying the composition to paper.
27. A product when obtained by the process defined in claim 26.
28. A paper coated with an aqueous coating composition which comprises an alkali oxidised gelatinised starch/protein mixture, said composition having a viscosity from 1 to 100 centapoise, and a pH between pH 7.5 and pH 9.
29. An aqueous composition for coating paper or paper board which comprises an alkali oxidised gelatinised starch and protein mixture, said composition having a viscosity from 1 to 100 centapoise (cps), and a pH from pH 7.5 to pH 9.
30. A composition of claim 29, wherein the viscosity is from 5 to 80 centapoise.
31. A composition of claim 30, wherein the viscosity is from 5 to 60 centapoise.
32. A composition of any one of claims 29 to 31, wherein the pH is from pH 7.8 to pH 8.8.
33. A composition of any one of claims 29 to 32, wherein said protein is a plant protein selected from the group consisting of wheat, rye, triticale, maize, oats, and barley protein. P \WPDOCS\CRNNXL\SpccI 2233441 new claims doc.IA912()8 00 0 -27- CD C) 34. A composition of any one of claims 29 to 32, wherein the protein is a mixture of t two or more different plant proteins selected from the group consisting of wheat, rye, triticale, maize, oats, and barley protein.
35. A composition of any one of claims 29 to 34, wherein said starch comprises a plant starch.
36. A composition of any one of claims 29 to 35, wherein said starch is a plant starch selected from the group consisting of wheat, rye, sorghum, triticale, maize, oats, barley, tapioca, potato, sago and rice starch.
37. A composition of any one of claims 29 to 36, wherein said starch is selected from waxy starch and high amylose starch.
38. A composition of any one of claims 29 to 37, wherein said gelatinised starch and protein mixture comprises between 6% w/w and 50% w/w plant protein.
39. A composition of claim 38, wherein said gelatinised starch and protein mixture comprises between 8% w/w and 25% w/w plant protein. The composition of any one of claims 29 to 39, wherein said starch and protein mixture is selected from the group consisting of flour, meal, grits and milled or crushed cereal grains.
41. The composition of claim 40, wherein said cereal grains are selected from the group consisting of wheat, rye, triticale, maize, oat and barley grains.
42. The composition of claim 40, wherein said flour comprises protein in an amount between 2% and 20% w/w. P WPDOCSCRN XIASpcc\1223344 nm clims doc.IA)912{8 00 O 0 -28-
43. The composition of any one of claims 40 to 42, wherein an additional plant protein t is added to the flour to increase protein level.
44. The composition of claim 43, wherein said additional plant protein is from the same grain from which the flour was produced, or is a plant protein from another 0 plant species. The composition of any one of claims 29 to 44, wherein said alkali oxidised aqueous gelatinised starch/protein mixture comprises solids in an amount between 3% w/w and 50% w/w.
46. The composition of any one of claims 29 to 45, wherein said alkali oxidised aqueous gelatinised starch/protein mixture is obtained by oxidising a plant starch and plant protein mixture with an oxidising agent under alkaline conditions and heating the oxidised mixture at a temperature between 70 0 C and 150 0 C until the viscosity is from 1 to 100 centapoise.
47. The composition of claim 46, wherein oxidation is conducted at a temperature between 25 0 C and 50 0 C for 5 to 30 minutes prior to heating for 5 to 150 minutes at a temperature between 50 0 C and 150 0 C until the viscosity of the composition is from 1 to 100 centapoise.
48. The composition of claim 46 or claim 47, wherein oxidation is carried out under conditions of heating for a period of 5 to 150 minutes at a temperature between 50 0 C and 150°C until viscosity of the composition is from 1 to 100 centapoise.
49. The composition of claim 46, wherein oxidation and heating are conducted concomitantly.
50. The composition of any one of claims 29 to 49 which is dried in a dryer to a flowable particulate state. P %WPDOCSCRN\NXL\SpmcI221344I newclaisdoc-1/9flfX 00 O 0 -29-
51. An aqueous coating composition which comprises a mixture of starch and plant protein in water having a solids content between 3% w/w and 30% w/w, a protein content between 4% w/w and 50% w/w, a viscosity of 1 to 100 centapoise, and a pH from pH 7.5 to pH 9, wherein the starch is gelatinised and both the starch and Sprotein in the mixture are alkali oxidised at a pH from pH 8 to pH 13.
52. A process for coating paper which comprises the step of applying a composition as defined in any one of claims 29 to 51 to paper, paperboard or cardboard.
53. A product when obtained by the process of claim 52.
54. A fibreboard comprising an alkali oxidised and gelatinised starch/protein mixture incorporated within a fibreboard. The fibreboard according to claim 54, wherein said fibreboard is selected from the group consisting of plasterboard, composite board, and particleboard.
56. A process for the production of fibreboard, which comprises forming a mixture of plant protein and plant starch in water, oxidising the mixture with an oxidising agent at alkali pH at 25°C to 50 0 C for 5-30 minutes or up to 24-48 hours, mixing the alkali oxidised mixture with the fibreboard constituents, followed by heating the resultant mixture which is formed into sheets in an oven at a temperature between 50 0 C and 150 0 C for 20 to 150 minutes.
57. The process of claim 56, wherein said fibreboard constituents are selected from the group consisting of gypsum, wood particles, and fibrous constituents.
58. The process of claim 56, wherein the mixture of plant protein and plant starch in water comprises solids in an amount between 3% w/w and 50% w/w. P PDOCSTCRMNXLSp=3I2233441 nmctaims doc I OMMSE
59. A process for the production of a coating composition, said process being substantially as hereinbefore described with reference to the examples.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2004201151A AU2004201151B2 (en) | 2003-03-21 | 2004-03-19 | Coating compositions |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2003901311A AU2003901311A0 (en) | 2003-03-21 | 2003-03-21 | Coating compositions |
| AU2003901311 | 2003-03-21 | ||
| AU2004900984A AU2004900984A0 (en) | 2004-02-26 | Coating compositions | |
| AU2004900984 | 2004-02-26 | ||
| AU2004201151A AU2004201151B2 (en) | 2003-03-21 | 2004-03-19 | Coating compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2004201151A1 AU2004201151A1 (en) | 2004-10-07 |
| AU2004201151B2 true AU2004201151B2 (en) | 2008-09-25 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2004201151A Ceased AU2004201151B2 (en) | 2003-03-21 | 2004-03-19 | Coating compositions |
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| Country | Link |
|---|---|
| AU (1) | AU2004201151B2 (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000058085A1 (en) * | 1999-03-31 | 2000-10-05 | Penford Corporation | Packaging and structural materials comprising potato peel waste |
-
2004
- 2004-03-19 AU AU2004201151A patent/AU2004201151B2/en not_active Ceased
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000058085A1 (en) * | 1999-03-31 | 2000-10-05 | Penford Corporation | Packaging and structural materials comprising potato peel waste |
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| AU2004201151A1 (en) | 2004-10-07 |
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