US20040107871A1 - Aluminum trihydrate containing slurries - Google Patents
Aluminum trihydrate containing slurries Download PDFInfo
- Publication number
- US20040107871A1 US20040107871A1 US10/629,300 US62930003A US2004107871A1 US 20040107871 A1 US20040107871 A1 US 20040107871A1 US 62930003 A US62930003 A US 62930003A US 2004107871 A1 US2004107871 A1 US 2004107871A1
- Authority
- US
- United States
- Prior art keywords
- slurry
- ath
- slurries
- aluminum trihydrate
- titanium dioxide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000002002 slurry Substances 0.000 title claims abstract description 177
- RREGISFBPQOLTM-UHFFFAOYSA-N alumane;trihydrate Chemical compound O.O.O.[AlH3] RREGISFBPQOLTM-UHFFFAOYSA-N 0.000 title claims abstract description 20
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 139
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract description 66
- 239000004408 titanium dioxide Substances 0.000 claims abstract description 56
- 239000002245 particle Substances 0.000 claims abstract description 35
- AZJYLVAUMGUUBL-UHFFFAOYSA-A u1qj22mc8e Chemical compound [F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O=[Si]=O.O=[Si]=O.O=[Si]=O.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 AZJYLVAUMGUUBL-UHFFFAOYSA-A 0.000 claims abstract description 28
- 239000002270 dispersing agent Substances 0.000 claims abstract description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000004927 clay Substances 0.000 claims abstract description 19
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000003139 biocide Substances 0.000 claims abstract description 17
- 230000003115 biocidal effect Effects 0.000 claims abstract description 15
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- 238000000576 coating method Methods 0.000 claims description 21
- 239000011347 resin Substances 0.000 claims description 15
- 229920005989 resin Polymers 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 12
- 239000011248 coating agent Substances 0.000 claims description 11
- 230000008569 process Effects 0.000 claims description 8
- 235000013305 food Nutrition 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 3
- 239000000203 mixture Substances 0.000 abstract description 34
- 239000000123 paper Substances 0.000 abstract description 26
- 239000011087 paperboard Substances 0.000 abstract description 10
- 230000000052 comparative effect Effects 0.000 description 29
- 239000000049 pigment Substances 0.000 description 26
- 239000007787 solid Substances 0.000 description 26
- 239000008367 deionised water Substances 0.000 description 12
- 229910021641 deionized water Inorganic materials 0.000 description 12
- 229940094522 laponite Drugs 0.000 description 11
- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 11
- 239000003153 chemical reaction reagent Substances 0.000 description 10
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 9
- 229920002125 Sokalan® Polymers 0.000 description 6
- 239000000440 bentonite Substances 0.000 description 6
- 229910000278 bentonite Inorganic materials 0.000 description 6
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 6
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 6
- 229910000271 hectorite Inorganic materials 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 239000004606 Fillers/Extenders Substances 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 238000000518 rheometry Methods 0.000 description 4
- 150000004684 trihydrates Chemical class 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- RNFNDJAIBTYOQL-UHFFFAOYSA-N chloral hydrate Chemical compound OC(O)C(Cl)(Cl)Cl RNFNDJAIBTYOQL-UHFFFAOYSA-N 0.000 description 3
- -1 for example Chemical compound 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 230000008570 general process Effects 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 239000003002 pH adjusting agent Substances 0.000 description 3
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 239000006254 rheological additive Substances 0.000 description 3
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000000149 argon plasma sintering Methods 0.000 description 2
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- 150000007529 inorganic bases Chemical class 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- XJUNLJFOHNHSAR-UHFFFAOYSA-J zirconium(4+);dicarbonate Chemical compound [Zr+4].[O-]C([O-])=O.[O-]C([O-])=O XJUNLJFOHNHSAR-UHFFFAOYSA-J 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
- 229940043276 diisopropanolamine Drugs 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 239000011268 mixed slurry Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/71—Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes
- D21H17/74—Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes of organic and inorganic material
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/37—Polymers of unsaturated acids or derivatives thereof, e.g. polyacrylates
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/63—Inorganic compounds
- D21H17/67—Water-insoluble compounds, e.g. fillers, pigments
- D21H17/675—Oxides, hydroxides or carbonates
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/63—Inorganic compounds
- D21H17/67—Water-insoluble compounds, e.g. fillers, pigments
- D21H17/68—Water-insoluble compounds, e.g. fillers, pigments siliceous, e.g. clays
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/38—Coatings with pigments characterised by the pigments
- D21H19/385—Oxides, hydroxides or carbonates
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
Definitions
- U.S. Pat. 5,824,145 discloses a photodurable titanium dioxide slurry which comprises at least 78% titanium dioxide particles and at least 3% alumina particles along with a dispersant, which can include polyacrylates, alcoholamines, citric acid, and the like with a pH of about 6.0 to9.0.
- Example 1 The process of Example 1 was repeated, using larger amounts of the comparative clays, with compositions provided in Table 3. All clays were first hydrated in deionized water for 30 minutes. Example 2 took 10 minutes to bring ATH into solutions whereas the comparative examples took 12-15 minutes, with comparative example G needing additional water. Properties of the slurries are provided in Table 4.
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Paper (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Abstract
The present invention relates to Aluminum trihydrate slurries comprising aluminum trihydrate particles, an acrylic dispersant, citric acid, synthetic hectorite clay, optionally a compound to adjust pH, a biocide and water. These slurries may be mixed with titanium dioxide slurries to produce a stable slurry blends useful in paper and paper-board applications.
Description
- This invention relates to aqueous high solids slurries comprising aluminum trihydrate and blends of such slurries comprising titanium dioxide slurries for use in paper, coatings and plastic applications, especially for use in indirect food-contact paper.
- Aluminum trihydrate (ATH) can be used as a filler to produce coatings for paper and paperboard. Because of the relative high cost of titanium dioxide (TiO2), paper mills often replace or extend titanium dioxide with less expensive pigment alternatives, such as ATH, calcium carbonate, kaolin clays and the like. The extender may reduce or eliminate the need for the more expensive white titanium dioxide pigment.
- Typically pigments and fillers are introduced into papermaking processes in the form of aqueous slurries. Commercial slurries of ATH are available, but they typically contain organic chemicals that are not compliant with United States Food and Drug Administration (FDA) regulations 21 C.F.R. 176.170 and 21 C.F.R. 176.180 for use in paper with indirect food contact. Even if a paper product is not intended for indirect use with food, paper manufacturers do not typically separate their lines for food and non-food use.
- For a slurry to be useful in paper and paper-board applications, the paper manufacturer must be able to pump the slurry from storage into the paper furnish or into the coating make-up area. Pigment slurries at high percent solids are desired to reduce drying energy and increase production rates through the paper coater dryer. High solids slurries combined with low viscosity also improve the flow through the coater to avoid coating scratches and streaks on the final coated paper surface. In order for an ATH slurry to be considered useable as an extender pigment filler or for blending with TiO2 slurry, the ATH pigment solids content should be greater than 50 wt. % and preferably 67.5 wt. % or higher. At such high solids content the available ATH slurries often have unacceptably high viscosities for either indirect use or use as a slurry to be blended with TiO2 slurries.
- U.S. Pat. 4,376,655 discloses aqueous titanium dioxide slurries comprising ATH and kaolin clays. The ratio of TiO2 to alumina is between 1000:1 and 2000:1. The ATH useful can either be a 9-10% aqueous slurry or a 50-55% dried gel. Preferably the dried gel contains occluded carbonates.
- U. S. Pat. 5,015,334 discloses a dispersable colloidal silica material, which is a clay, including Laponite® brand synthetic hectorite clays, associated with an anionic organic polymer for use as a retention agent in papermaking.
- U.S. Pat. 5,171,631 discloses a titanium dioxide pigment/ATH extender/spacer pigment composition comprising 70-98% titanium dioxide by volume and 2-30% ATH by volume wherein the ATH has a similar median particles size as the titanium dioxide. Typically the median particle size of the titanium dioxide is 0.2 to 0.3 microns. The ATH has a median particle size within ±20% compared to the titanium dioxide particle size. An example of a coating composition comprising the pigments was prepared with titanium dioxide and ATH and contained a cellulosic thickener, associative thickener, propylene glycol, nonionic surfactant, neutralizer defoamer, coalescing agent and biocide, in water at a solids content of 3.23%.
- U.S. Pat. 5,342,485 discloses use of ATH with improved whiteness in papermaking to reduce costs relative to using solely TiO2. This patent discusses use of ATH in slurries at 15-30% solids.
- U.S. Pat. 5,571,379 discloses a composition comprising hectorite clay, acrylic polymer and other additives commonly used in the manufacture of paper or paperboard, including fillers and pigments such as TiO2. There is no disclosure of use with ATH or of hectorite clay reducing the viscosity of an aqueous slurry of TiO2 or ATH.
- U. S. Pat. 5,676,748 discloses an aqueous slurry for use as providing filler for paper and paperboard products comprising 1 to 30 wt. % solids of mineral particles with a distribution of coarse (>0.5 microns) and fine particles (<0.2 microns) and an anionic acrylic dispersing agent and a cationic flocculating agent. However, slurry of the minerals may be up to 70-76% solids that must be diluted for use, for example, at a paper mill. Examples are limited to kaolin clays.
- U.S. Pat. 5,824,145 discloses a photodurable titanium dioxide slurry which comprises at least 78% titanium dioxide particles and at least 3% alumina particles along with a dispersant, which can include polyacrylates, alcoholamines, citric acid, and the like with a pH of about 6.0 to9.0.
- U. S. Pat. 6,387,500 discloses coating formulations for paper and paperboards comprising aqueous slurries of titanium dioxide pigment with extender pigments, which include ATH and calcined clay, and dispersants, which include acrylates. There is no mention of combining with synthetic hectorite clay to improve viscosity and rheology.
- Therefore, there remains a need to decrease the cost of opacity in paper and paper-board applications. There is a need to provide an ATH slurry with improved viscosity and rheological properties. There is a need to find suitable ATH slurry compositions that are of suitable viscosities for use in paper applications including FDA compliant and non-FDA compliant compositions. There is also a need for ATH slurry compositions compatible with titanium dioxide slurries that are stable at suitable viscosities and are FDA compliant for indirect food contact. The present invention meets these needs.
- The present invention provides aluminum trihydrate slurries comprising (a) at least 50% by weight of the slurry of dispersed aluminum trihydrate particles having an average particle size of at least 0.5 micron; (b) a dispersant comprising an acrylic dispersing resin, and optionally citric acid; (c) a rheology modifier consisting of a synthetic hectorite clay; (d) optionally a compound to adjust pH; (e) a biocide; and (f) water.
- The present invention further provides aluminum trihydrate/rutile titanium dioxide slurry blends comprising (a) at least 50% by weight of the slurry of dispersed aluminum trihydrate particles having an average particle size of at least 0.5 micron; (b) a dispersant comprising an acrylic dispersing resin, and optionally citric acid; (c) a rheology modifier consisting of a synthetic hectorite clay; (d) optionally a compound to adjust pH; (e) a biocide; and (f) water. Preferably the slurry blend comprises from 75 to 50 wt. % TiO2 to 25 to 50 wt. % ATH.
- Still further the present invention provides a process for making paper comprising mixing pulp and an ATH/rutile TiO2 slurry blend wherein (a) at least 50% by weight of the slurry of dispersed aluminum trihydrate particles having an average particle size of at least 0.5 micron; (b) a dispersant comprising an acrylic dispersing resin, and optionally citric acid; (c) a rheology modifier consisting of a synthetic hectorite clay; (d) optionally a compound to adjust pH; (e) a biocide; and (f) water.
- The present invention provides aluminum trihydrate slurries which are particularly useful in coatings, paper and paperboard applications. Such slurries typically have greater than 67% ATH pigment solids and are useful for blending as extender pigments with TiO2 slurry for use in paper and coating applications.
- Surprisingly, incorporating a synthetic hectorite clay, provides a superior ATH slurry in terms of viscosity and rheological properties as well as improved storage stability by (1) enhancing dispersant(s) effectiveness and reducing viscosity of the ATH slurry; (2) improving wet-in, that is, reducing time needed to incorporate solid pigment particles of ATH into an aqueous slurry and (3) inhibiting low shear settling of 1 micron and larger ATH particles.
- ATH useful in the present invention is known as pigmentary grade and is characterized by a surface area of from 400 to 1100 m2/g, preferably about 700 m2/g. Preferably it has an average particle size of at least 0.5 micron, and may have an upper limit on particle size as high as 10 microns. Preferably the average particle size is from about 0.50 to 2.0 microns.
- It should be recognized that for any given particulate ATH, the particles will be of range of sizes, and the ATH may be characterized by an average particle size and a particle size distribution. Particle size selection in formulating a suitable ATH influences overall slurry properties. For example, particles are smaller than 0.25 microns cause viscosity problems; while particles that are larger than 2.0 microns may lead to settling problems. Pigment grade (pigmentary) ATH is commercially available, for example the Alcoa, Inc. branded product Hydral® 710 and the Alcan, Inc branded GenBrite® 700 product and other ATH products sold as solids, and having a particle size typically about 1 micron.
- The ATH slurry of the present invention has an ATH solids content of at least 50% by weight, and up to about 70% by weight, preferably about 67-68% by weight.
- The viscosities of the ATH slurries of the present invention as well as for the viscosities of commercial products were measured using either a Brookfield instrument or Tappi methods known in the art and described in more detail hereinbelow.
- Water used in the preparation of the ATH slurries of this invention is preferably deionized. That is, the water has been passed through an ion exchange column to remove unwanted ions that may affect the stability and other properties of the slurries. Preferably the metal ion content should provide an electrical resistance less than 0.05 micro-ohm-cm electrical resistivity as measured using ASTM method D 1125.
- The ATH slurry of the present invention is stabilized with an acrylic polymer dispersant comprising an acrylic dispersing resins and citric acid. Examples of suitable acrylic dispersing resins include polymers of acrylic acid, especially acrylic acid polymer salts, and particularly, sodium polyacrylate resins, which are commercially available. To satisfy FDA requirements for compliance, the molecular weight of this dispersant should conform to FDA standards set forth in 21 C.F.R. 176.170. Also, the amount of dispersant present in the slurry may be limited to a specific value or range of values required to meet the FDA standards. For uses other than FDA compliant uses, it is not necessary to restrict the level of acrylic dispersant, and the dispersant may be used at any level necessary to achieve optimal stabilization. FDA standards for compliance are provided in 21 C.F.R. 176.170 and 21 C.F.R. 176.180 which are incorporated herein by reference.
- Prior to the compositions of the present invention, ATH slurries could not be made that were FDA compliant and, at the same time, having viscosity and rheology properties suitable for use in paper applications. In addition to the selection of the acrylic dispersing resin, for FDA compliant slurries, it is preferred to use a combination of an acrylic dispersing resin with citric acid, for example, sodium polyacrylate and citric acid. Surprisingly the presence of citric acid improves the wet-in of the ATH into the slurry during pigment loading and seems to codisperse the ATH resulting in a lowering of the slurry viscosity. When citric acid is added, it is preferably added in an amount less than 0.1 wt % based on dry weight of ATH. The range os citric acid useful in the present invention is from about 0.05% to about 0.5%. More than about 0.5 wt. % citric acid results in quick settling of the slurry forming a compact and hard heel in a storage container. At least 0.05 wt % is needed to enhance the rate of dry ATH wet in during the dispersing process, but about 0.1 wt % is preferred amount.
- ATH slurry compositions of the present invention include a synthetic hectorite. Synthetic hectorite has the formula:
- [MgwLixSi8O20H4−yFy]2−
- wherein w=3to6; x=0 to 3; y=0 to 4; z=12−2w−x, wherein the negative lattice charge is balanced by counterions, and wherein the counterions are selected from the group consisting of Na+, K+, NH4 +, Li+, Mg2+, Ca2+, Ba2+, N(CH3)4 +, and mixtures thereof.
- Synthetic hectorite resembles natural clay mineral hectorite and is a layered hydrous magnesium silicate, which is free from natural clay impurities. Synthetic hectorite is commercially available, for example, from Southern Clay Products, Inc., and includes the brands Laponite®; Lucenite SWN®, Laponite S®, Laponite XL®, Laponite RD® and Laponite RDS® of synthetic hectorite. The present inventors have discovered that unlike other clays commonly present in papermaking slurries comprising ATH, the synthetic hectorite provides the dual benefits of enhancing the rheology of the ATH slurries while as reducing the viscosity during shear.
- In the ATH slurries of this invention, the synthetic hectorite is present in an amount from 0.1 up to about 1%, preferably about 0.3% by weight of the total slurry formulation. Surprisingly it has been found that when synthetic hectorite clay, is present in an aqueous ATH slurry, the viscosity of the slurry is dramatically reduced. This is surprising since synthetic hectorite is known to produce thickened liquids or gels, and, is commonly used to increase viscosity for water-based slurries and paints, The synthetic hectorite, in contrast, natural clays are ineffective at reducing the viscosity and providing rheological benefits in an ATH slurry. In fact, such clays increase viscosity as a function of the amount present.
- Frequently, it may be necessary to adjust the pH to the desired pH range. An amine is generally used for this purpose. Typical amines suitable for use in the present invention include amines, especially alcohol amines, such as 2-amino-2-methyl-1-propanol (“AMP”) and monoisopropanolamine (“MIPA”). Other suitable amines include 1-amino-2-ethanol, 2-amino-1-ethanol, 1-amino-2-propanol, diethanolamine, diisopropanolamine, and 2-methylamino-1 -ethanol.
- While other alkaline additives may be used, such as inorganic bases, care should be taken to avoid possible interference such as metal ion interference with the dispersant selection. When used, the selected amine or inorganic base is typically present in the slurry at an amount to maintain the pH of the product slurry in the range of 8.5 to 11, preferably 9 to 9.5.
- For FDA compliance when using MIPA, the permissible concentration range is from 0.01 up to 0.25% based on total slurry formulation level, with a typical level of 0.14%.
- Any commercially available biocide can be used in the slurry of this invention. Preferably the biocide used is identified as FDA compliant or is present in the slurry in a concentration not more than is FDA compliant for indirect food contact. Examples of such biocides include, but are not limited to: 1,2-benzisothiazolin-3-one, Proxel GXL,i available from Avecia, Inc., 2-bromo-2-nitro-1,3-propanediol, glutaraldehyde, and 3,5-dimethyl-1,3,5-,2H-tetrahydrothiadiazine-2-thione. The amount of biocide in an ATH slurry of the present invention is typically in the range of 50 to 500 ppm, based on the weight of the slurry solids. Preferably, the amount of biocide is about 400 ppm in an ATH slurry. Typically the amount of biocide in a blended ATH/ TiO2 slurry of the present invention is in the range of 25 to 250 ppm, based on the weight of the slurry solids. Preferably the amount of biocide is about 100 ppm in a blended ATH/ TiO2 slurry.
- Advantageously, rutile titanium dioxide may be combined with the ATH slurry of the present invention to provide a mixed ATH/ TiO2 slurry blend to provide a slurry having comparable to a commercial anatase slurry, but at a reduced TiO2 concentration. Such mixed slurries are useful for providing at least comparable opacity in paper and paper-board applications at a competitive cost than anatase TiO2 slurries. When an ATH slurry is blended with a rutile titanium dioxide slurry, for best results, each slurry should be a high solids slurry. For example, preferably the ATH slurry will have a solids level of at least 67.5 wt. %. The titanium dioxide slurry may have a solids content from 50 wt. % to as high as 92 wt. %. A particularly useful rutile titanium dioxide slurry has a solids content of 71 wt. %. Suitable rutile titanium dioxide slurries for use in blending with a high solids ATH slurry include any stable high solids rutile slurries with compatible dispersants and other components. An example of a rutile titanium dioxide slurry particularly suitable for use with the ATH slurries of this invention is a titanium dioxide slurry prepared using dilatant grinding, especially those produced by the process of U. S. Pat. 5,563,793, the teachings of which are hereby incorporated by reference.
- When a rutile titanium dioxide slurry is combined with the ATH slurry of this invention, a preferred slurry blend comprises about 75% titanium dioxide and about 25% ATH slurry on a pigment weight basis. The titanium dioxide content may be higher, with conversely lower amounts of ATH. As the titanium dioxide content of the slurry is increased, the opacity achieved at a given slurry concentration is increased, but there is the corresponding increase in the cost of a slurry. An ATH/rutile TiO2 blended slurry composition having about 75 wt. % TiO2 and 25 wt. % ATH provides opacity and brightness equal to a conventional (100%) anatase TiO2 slurries used in paper and paperboard manufacture. Similar blends of ATH slurries and TiO2 slurries are also useful for coatings, such as architectural and paper coatings, and other applications, including plastics.
- The ATH slurries of the present invention are high solids slurries comprising at least 50% by weight ATH, and up to 70% by weight ATH, preferably 67-68% ATH. The ATH slurries have good stability. The ATH slurries have a low grit content, that is, less than 0.01% unbrushed grit. The high solids ATH slurries of this invention have low viscosity. Viscosity is measured using a Brookfield viscometer. The viscosity of the high solids ATH slurries is less than 1500 Cps at 20 rpm, using a #3 spindle, preferably less than 1000 Cps and more preferably in the range of 200 to 800 Cps, measured at room temperature and 68% solids. The ATH slurries of this invention are pumpable. “Pumpable” is defined herein as having a Hercules viscosity of less than 125 cps, and preferably less than 100 as measured using a Hercules High Shear Viscometer with an “A” bob, a spring setting of 50,000 dynes/cm and 500 rpm shear rate.
- The ATH/ TiO2 slurry blend of this invention is useful in paper and paper-board applications. The present invention provides a process for making paper comprising mixing pulp and a slurry comprising ATH and rutile TiO2 pigment particles to form a stock and dewatering and drying the stock to form a sheet wherein the slurry comprises (a) at least 50% by weight of dispersed ATH pigmentary particles having an average particle size of at least 0.5 micron; (b) a dispersant comprising an acrylic dispersing resin, and optionally citric acid; (c) a synthetic hectorite clay; (d) optionally a compound to adjust pH; (e) a biocide; and (f) water. Preferably the slurry comprises from 75 to about 50% by weight of rutile TiO2 and from 25 to about 50% ATH.
- Various test methods were employed to characterize the ATH slurries and ATH/ TiO2 blended slurries of this invention. The pH of the slurries were measured using a Beckman model 200 pH meter and a Corning flat surface combination wRJ electrode. Brookfield viscosity was measured using a standard Brookfield Digital Viscometer, model RTVTD-II, available from Brookfield Engineering Company.
- Tappi standard test method T646 was used as the procedure for determination of the low- and high shear viscosity of slurry pigments. Pigment rheology test conditions used an “A” or an “E” bob over a shear range of 0-4400 rpm, and a 50,000 dyne/cm spring setting for low viscosity slurries and a 100,000 dyne /cm spring setting for high viscosity slurries. The Hercules Hi Shear Viscometer is available from Kaltec Scientific Instrument, Inc.
- The slurries of this invention were prepared using a labscale Dispermat model AE5C high-speed disperser, HSD, equipped with a 60 mm Cowles blade. All slurry preparations were performed in a cylindrical stainless steel vessel measuring 4 inches in diameter and 6 inches high. To a high speed disperser was added deionized water and Laponite RD® brand synthetic hectorite, in the amounts provided in the tables, corresponding to the examples, with stirring for 30 minutes at low speed (approx. 200 to 400 rpm) to achieve adequate hydration. Reagent for pH adjustment (such as monoisopropanolamine) as well as dispersants and biocides were slowly added and mixed for 10 minutes at low speed until uniform. ATH was then added slowly and mixed at high speed (approx. 1800 to 2000 rpm) for 15 minutes. Additional deionized water was added followed by mixing for 10 minutes at low speed to achieve adequate uniformity.
- The General Process was followed with the compositions provided in Table 1. Synthetic hectorite clay and comparative clays, which are natural clays, (were first hydrated in deionized water using an air mixer for 30 minutes. The acrylic dispersing resin was 602N Alcosperse® brand sodium polyacrylate available from National Starch and Chemical Company, Berkely, Calif. Example 1 took 5 minutes to incorporate ATH into the slurry, while the other samples took much longer (9-10 minutes). Properties of the slurries produced are provided in Table 2.
TABLE 1 Amounts for Reagents for Example 1 and Comparative Examples A-D, in grams Tradename, if Examples Reagent applicable A B 1 C D Aluminum GenBrite ® 675 675 675 675 675 trihydrate Dispersants Alcosperse ® 12.5 12.5 12.5 12.5 12.5 602, 45% Bentonite Bentolite ® WH 0.5 0 0 0 0 Bentonite Permont ® 0 1 0 0 0 SX 10 Synthetic Laponite RD ® 0 0 1.5 0 0 Hectorite Bentonite Bentolite ® L10 0 0 0 0.5 0 Deionized water, 257 256.5 256 257 257.5 initial Deionized water 55 55 55 55 55 (let down) -
TABLE 2 Properties of Example 1 and Comparative Examples A-D Examples Measurement A B 1 C D Brookfield viscosity 9000/5 8160/5 2460/3 9500/5 7000/3 10 rpm/spindle 1 day Brookfield viscosity 5500/5 4920/5 1540/3 5700/5 4010/3 20 rpm/spindle 1 day Brookfield viscosity 1750/5 1400/5 548/3 1700/5 1200/4 100 rpm/spindle 1 day pH 10.15 10.2 10.18 10.16 10.31 Hercules viscosity 1 Too Too 74.5 Too 114.6 day RT* viscous viscous viscous - As can be seen from Table 2, only the synthetic hectorite clay formed a stable aqueous slurry containing the ATH. The comparative clays all formed very viscous, non-pumpable mixtures. The viscosities of slurries containing the comparative clays were higher than the viscosity of the slurry containing ATH alone.
- The process of Example 1 was repeated, using larger amounts of the comparative clays, with compositions provided in Table 3. All clays were first hydrated in deionized water for 30 minutes. Example 2 took 10 minutes to bring ATH into solutions whereas the comparative examples took 12-15 minutes, with comparative example G needing additional water. Properties of the slurries are provided in Table 4.
TABLE 3 Amounts for Reagents for Example 2 and Comparative Examples E-G, in grams Tradename, if Examples Reagent applicable E F 2 G Aluminum GenBrite ® 675 675 675 675 trihydrate Dispersants Alcosperse ® 602, 12.5 12.5 12.5 12.5 45% Bentonite Bentolite ® WH 3 0 0 0 Bentonite Permont ® SX 10 0 3 0 0 Synthetic Hectorite Laponite RD ® 0 0 3 0 Bentonite Bentolite ® L10 0 0 0 3 Deionized water, 254.5 254.5 254.5 254.5 initial Deionized water 55 55 55 55 (let down) -
TABLE 4 Properties of Example 2 and Comparative Examples A-D Examples Measurement E F 2 G Brookfield viscosity 10 rpm/ 35000/7 5840/3 1920/3 12000/5 spindle 1 day Brookfield viscosity 20 rpm/ 31200/7 3820/3 1230/3 7800/5 spindle 1 day Brookfield viscosity 100 rpm/ 11000/7 1700/4 470/3 2230/5 spindle 1 day PH 10.08 9.95 10.04 9.62 Hercules viscosity 1 day Too Too 66.9 112.7 RT* viscous viscous - As can be seen from Table 4, even with higher amounts of the comparative clays, there was no improvement in viscosity relative to that observed with the synthetic hectorite clay. Furthermore, higher levels of the comparative clays resulted in higher viscosities than those in Table 2.
- The General Process was followed with the compositions provided in Table 5. Examples 3 and 4 both have the synthetic hectorite whereas Comparative Examples H-I do not. In addition, Example 4 uses less of the acrylic dispersing resin than Example 12 and has citric acid present. Note that the resulting combination when all starting reagents had been added resulted in a pH of 9.81, thus, no pH modifier was used. Properties of the slurries produced are provided in Table 6.
TABLE 5 Amounts for Reagents for Examples 3-4 and Comparative Examples H-I, in grams Tradename, Example Reagent if applicable H 3 I 4 Aluminum GenBrite ® 675 675 675 675 trihydrate 700 Dispersants Alcosperse ® 12.5 12.5 3.6 3.6 602, 45% Citric acid 0 0 1 1 pH adjuster MIPA 0 0 1.4 1.4 Synthetic Laponite RD ® 0 3 0 3 hectorite Deionized water, 267.5 254.5 269 266 initial Deionized water 45 55 50 50 (let down) -
TABLE 6 Properties of Examples 3-4 and Comparative Examples H-I Examples Measurement H 3 I 4 Brookfield viscosity 10 rpms/spindle 1 day RT 11220/6 2130/3 7000/3 1120/3 Brookfield viscosity 20 rpms/spindle 1 day RT 6700/6 1350/3 4580/3 830/3 Brookfield viscosity 100 rpms/spindle 1 day RT 1900/6 490/3 1500/3 392/3 pH - day of preparation 9.82 9.81 9.37 9.37 Hercules viscosity 1 day RT* 89.8 74.5 133.7 66.9 Brookfield viscosity 7 days RT 10 rpms/spindle 12600/6 2130/3 7340/4 1080/3 Brookfield viscosity 7 days RT 20 rpms/spindle 7950/6 1350/3 4760/4 780/3 Brookfield viscosity 7 days RT 100 rpms/spindle 2420/6 502/3 1670/4 390/3 pH - 7 days RT 10.1 10.18 9.85 9.75 Hercules viscosity day 7 RT 156.6 64.9 212.0 105.0 Brookfield viscosity 7 days 140 F 10 rpms/spindle 2750/6 2810/3 16500/4 1590/3 Brookfield viscosity 7 days 140 F 20 rpms/spindle 16300/6 1770/3 9750/5 1220/3 Brookfield viscosity 140 F 7 days 100 rpms/spindle 4420/6 653/3 3190/5 580/3 pH - 7 days 140 F 10.29 10.22 9.83 9.76 Hercules viscosity day 7 140 F 206.3 53.5 194.8 76.4 - As can be seen from Table 6, the presence of the synthetic hectorite in the slurry of ATH, GenBrite® 700 brand ATH, significantly reduced the viscosity of the slurries, comparing Examples 3 and 4 with Comparative Examples H and I, respectively. In addition, when less acrylic dispersing resin is used (in order to comply with FDA standards), but is used in combination with citric acid, there is reduction in viscosity and rheology, compared to Example 3 in which the slurry contains more acrylic dispersant, but does not contain any citric acid.
- The process of Examples 3 and 4 and Comparative Examples H and I was repeated, using a different commercial ATH sample, with compositions provided in Table 7. Properties of the slurries produced are provided in Table 8.
TABLE 7 Amounts for Reagents for Examples 5-6 and Comparative Examples J-K, in grams Tradenames Examples Reagent if applicable J 5 K 6 Aluminum Hydral ® 710 675 675 675 675 trihydrate flash dried Dispersants Alcosperse ® 12.5 12.5 3.6 3.6 602, 45% Citric acid 0 0 1 1 pH adjuster MIPA 0 0 1.4 1.4 Synthetic Laponite 0 3 0 3 hectorite RD ® Deionized water, 252.5 239.5 269 266 initial Deionized water 60 70 50 50 (let down) -
TABLE 8 Properties of Examples 5-6 and Comparative Examples J-K Ex- amples Examples Examples Examples Measurement J 5 K 6 Brookfield viscosity 10 4640/3 1770/3 7700/5 1940/3 rpms/spindle 1 day RT Brookfield viscosity 20 3140/3 1100/3 6540/5 1330/3 rpms/spindle 1 day RT Brookfleld viscosity 100 1550/3 416/3 2480/5 560/3 rpms/spindle 1 day RT pH - day of preparation 10.38 10.4 9.82 9.88 Hercules viscosity 1 day 84.0 49.7 154.7 95.5 RT* Brookfield viscosity 7 days 5300/6 1900/3 8500/5 1950/3 RT 10 rpms/spindle Brookfield viscosity 7 days 3580/3 1230/3 5750/5 1380/3 RT 20 rpms/spindle Brookfield viscosity 7 1480/5 450/3 2400/5 679/3 days RT 100 rpms/spindle pH - 7 days RT 10.55 10.54 9.71 10.1 Brookfield viscosity 7 days 12000/5 2580/3 12000/5 2820/3 140 F 10 rpms/spindle Brookfield viscosity 7 days 7750/5 1660/3 8000/3 2090/3 140 F 20 rpms/spindle Brookfield viscosity 140 F 2560/5 628/3 2750/5 1040/4 7 days 100 rpms/spindle pH - 7 days 140 F 10.39 10.43 9.94 10.13 - As can be seen from Table 7, the synthetic hectorite, Laponite RD®, in the aqueous slurry of ATH, Hydral® 710 flash dried, significantly reduced the viscosity of the slurries, comparing Examples 5 and 6 with Comparative Examples J and K. The viscosities of the slurries decrease when the synthetic hectorite is added, comparing Example 5 with Comparative Example J and comparing Example 6 with Comparative Example K. The viscosities of the slurries containing the citric acid are comparable to the slurries not containing citric acid, but overall containing a much higher concentration of dispersants. That is, the viscosity of the slurry of Example 6 was nearly equal to the viscosity of the slurry of Example 5 although the slurry of Example 6 contained substantially less dispersant.
- An ATH slurry was prepared according to Example 4 using GenBrite® 700 brand ATH on a 250-gallon high speed disperser. The ATH slurry was blended with a rutile titanium dioxide slurry prepared according to U.S. Pat. 5,693,753, using MIPA as a dispersant, at a ratio, based on the weight of the dry pigment, of 75 parts TiO2 to 25 parts ATH. Table 9 provides the properties of the slurries and slurry blend.
TABLE 9 Properties of starting ATH, TiO2 and ATH/TiO2 blended slurries. Brookfield Viscosity Hercules wt. (@100 rpm, #4 Spindle, High Shear Slurry pH % Solids 25° C.) (Cp) Viscosity (Cp) Rutile TiO2 9.0 71.1 118 16.8* 75/25 Blend 8.8 70.48 104 22.3* ATH 8.8 68.2 228 54.4** - Relative optical density (OD) test, as described in U.S. Pat. 6,040,913, was used to compare the light scattering efficiency of the pigment slurries described in Example 7. The higher the relative optical density number, the better the light scattering efficiency.
- Total transmission for each of a series of pigment slurries was measured using a 1- cm path length cell on a Hunter Ultrascan™ spectrophotometer (available from HunterLab, Reston, Va.) equipped with an integrating sphere to provide analysis of total transmittance. Measurements were recorded at wavelength of 700 nm.
- Table 10 provides the relative OD of the specified pigment slurries using a rutile TiO2 slurry prepared according to according to U.S. Pat. 5,693,753, using AMP as a dispersant, as the standard. Comparisons are made with the rutile TiO2 slurry prepared in Example 7, the ATH slurry prepared in Example 7, the blended ATH/TiO2 slurry prepared in Example 7 and two commercial anatase titanium dioxide slurries, T-4000 and A-2000, available from Millenium Chemicals, Inc.
TABLE 10 Relative Scattering Efficiency based on Relative Optical Pigment Density divided by Concentration measured at 700 nm. Relative Scattering Slurry Efficiency Rutile TiO2 prepared with AMP 1.00 Example 7 Rutile TiO2 prepared with 1.12 MIPA Example 7 ATH/TiO2 blend 0.86 T-4000 0.86 T-2000 0.80 Example 7 ATH 0.05 - As can be seen from Table 10, the ATH/TiO2 slurry blend of this invention has OD numbers equivalent to or better than the comparative commercial anatase slurries.
- The ATH/TiO2 slurry blend from Example 7 was used to make coatings for a coated recycle paper -board application across a range of ATH/TiO2 pigment blend additions showing that the slurry blend of the present invention may be used as the titanium dioxide containing component of a paper coating. The coatings were made using the raw materials and formulations provided in Table 11. Following the order of raw material addition listed in Table 11, a Cowles mixer was first used at high shear to make the pigment grind, then at low shear to make the coating reduction. The coatings were then drawn down on a pre-coated recycle board using either a 10 or 12 point rod to achieve the target coat weight of 3.5 lb/1000 ft2, and air dried. The coated board Examples were then calendered to achieve the target 75° gloss of 50, and pH of 8.5±0.3 at the target coat weight. The coating formulation, make-down, and coating application were typical for the coated recycle board market. The properties of the Examples are provided in Table 12.
TABLE 11 Raw Materials and Order of Addition for Examples 9-11. Order of Example 9 Example 10 Example 11 Raw Material Addition (parts) (parts) (parts) Clays Kaolin clay (a) 2 71 67 63 Calcined kaolin 3 10 10 10 clay (b) ATH/TiO2 slurry 4 19 23 27 blend from Example 7 Binders Modified styrene- 6 18 18 18 butadiene latex (c) Soy polymer (d) 5 4 4 4 Lubricant Calcium stearate (e) 7 0.3 0.3 0.3 Dispersant Low molecular 1 0.1 0.1 0.1 weight polyacrylate (f) Thickener Ammonium 8 0.4 0.4 0.4 zirconium carbonate (g) Water Total Parts 122.8 122.8 122.8 -
TABLE 12 Coating Data for Examples 9-11. Brookfield Ex- Parts Coating Coat- Spin- Viscosity ample Example % ing dle cps @ cps @ Temp. No. 7 Solids pH # 20 rpm 100 rpm ° F. 9 19 58.29 8.70 5 7000 2430 72 10 23 58.03 8.73 5 3450 2300 72 11 27 58.30 8.77 5 5700 2010 72 - The properties for the above coatings made with Example 7 in Table 12 are well within typical range for a Coated Recycle Board mill. The coatings were drawn down on a precoated basesheet with the properties listed in Table 13. Comparative Example L is pre-coated basesheet.
TABLE 13 Coated Recycle Board Properties Coating #- Parts Coating TAPPI Example Example 7 % Solids Brightness L* a* b* K + N 75° Gloss Comparative — — 65.12 84.82 0.31 0.90 37 — Example L Example 9 19 58.29 78.98 91.47 −0.49 0.79 17 52 Example 10 23 58.03 79.87 91.72 −0.50 0.63 18 53 Example 11 27 58.30 80.28 91.89 −0.47 0.47 19 52 - As can be seen from Table 13, the target TAPPI Brightness of 80 and the target 75° loss of greater than 50 were achieved by using the blended ATH/ TiO2 slurry of Example 7 in the top coat. The color (L*, a*, and b*) and the IGT pick strength were also well within typical performance for a coated recycle board application. Data reported was measured using standard Tappi methods.
Claims (7)
1. An aqueous slurry comprising pigmentary aluminum trihydrate, aluminum trihydrate slurries comprising:
(a) at least 50% by weight of the slurry of dispersed aluminum trihydrate particles having an average particle size of at least 0.5 micron;
(b) a dispersant comprising an acrylic dispersing resin, and optionally citric acid;
(c) a synthetic hectorite clay;
(d) optionally a compound to adjust pH;
(e) a biocide; and
(f) water.
2. The slurry of claim 1 wherein the slurry is FDA compliant for indirect food contact.
3. The slurry of claim 1 comprising at 67-68% by weight dispersed aluminum trihydrate pigmentary particles.
4. A blended slurry comprising an aqueous slurry of pigmentary rutile titanium dioxide particles and an aqueous pigmentary aluminum trihydrate slurry comprising:
(a) at least 50% by weight of dispersed aluminum trihydrate pigmentary particles having an average particle size of at least 0.5 micron;
(b) a dispersant comprising an acrylic dispersing resin, and optionally citric acid;
(c) a synthetic hectorite clay;
(d) optionally a compound to adjust pH;
(e) a biocide; and
(f) water.
5. The slurry of claim 4 wherein the weight percentage of the rutile titanium dioxide slurry is from about 75 to about 50% and the weight percentage of the aluminum trihydrate slurry is from about 25 to about 50%.
6. A process for making paper comprising mixing pulp and the slurry of claim 5 to form a stock and dewatering and drying the stock to form a sheet.
7. A paper coating having as the titanium dioxide containing component an aqueous slurry of pigmentary rutile titanium dioxide particles and an aqueous pigmentary aluminum trihydrate slurry comprising:
(a) at least 50% by weight of dispersed aluminum trihydrate pigmentary particles having an average particle size of at least 0.5 micron;
(b) a dispersant comprising an acrylic dispersing resin, and optionally citric acid;
(c) a synthetic hectorite clay;
(d) optionally a compound to adjust pH;
(e) a biocide; and
(f) water.
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/629,300 US20040107871A1 (en) | 2002-08-09 | 2003-07-28 | Aluminum trihydrate containing slurries |
JP2004527873A JP2005535749A (en) | 2002-08-09 | 2003-08-06 | Slurry containing aluminum trihydrate |
EP03785037A EP1551926A1 (en) | 2002-08-09 | 2003-08-06 | Aluminum trihydrate containing slurries |
PCT/US2003/024848 WO2004015015A1 (en) | 2002-08-09 | 2003-08-06 | Aluminum trihydrate containing slurries |
CA002495096A CA2495096A1 (en) | 2002-08-09 | 2003-08-06 | Aluminum trihydrate containing slurries |
CNA038188635A CN1675318A (en) | 2002-08-09 | 2003-08-06 | Aluminum trihydrate containing slurries |
TW092121848A TW200413605A (en) | 2002-08-09 | 2003-08-08 | Aluminum trihydrate containing slurries |
US11/605,982 US7476272B2 (en) | 2002-08-09 | 2006-11-29 | Aluminum trihydrate containing slurries |
Applications Claiming Priority (2)
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US40221402P | 2002-08-09 | 2002-08-09 | |
US10/629,300 US20040107871A1 (en) | 2002-08-09 | 2003-07-28 | Aluminum trihydrate containing slurries |
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US11/605,982 Continuation US7476272B2 (en) | 2002-08-09 | 2006-11-29 | Aluminum trihydrate containing slurries |
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US20040107871A1 true US20040107871A1 (en) | 2004-06-10 |
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US11/605,982 Expired - Fee Related US7476272B2 (en) | 2002-08-09 | 2006-11-29 | Aluminum trihydrate containing slurries |
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US11/605,982 Expired - Fee Related US7476272B2 (en) | 2002-08-09 | 2006-11-29 | Aluminum trihydrate containing slurries |
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US (2) | US20040107871A1 (en) |
EP (1) | EP1551926A1 (en) |
JP (1) | JP2005535749A (en) |
CN (1) | CN1675318A (en) |
CA (1) | CA2495096A1 (en) |
TW (1) | TW200413605A (en) |
WO (1) | WO2004015015A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060260509A1 (en) * | 2005-04-22 | 2006-11-23 | Evers Glenn R | Compositions for enhanced paper brightness and whiteness |
Families Citing this family (6)
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US20040107871A1 (en) * | 2002-08-09 | 2004-06-10 | Defeo Maureen A. | Aluminum trihydrate containing slurries |
WO2013142352A1 (en) | 2012-03-20 | 2013-09-26 | The Research Foundation Of State University Of New York | Flocculation of lignocellulosic hydrolyzates |
US9951196B2 (en) * | 2012-10-24 | 2018-04-24 | J.M. Huber Corporation | Cationic polyoxometalate-coated alumina trihydrate dispersants |
US9896366B2 (en) * | 2014-02-26 | 2018-02-20 | Ecolab Usa Inc. | Alternative additives to enhance slurry dewatering |
EP3356480B1 (en) * | 2015-09-30 | 2021-01-06 | Dow Global Technologies LLC | Shelf-stable aqueous composition and process of making the same |
KR102613596B1 (en) * | 2018-01-29 | 2023-12-13 | 이시하라 산교 가부시끼가이샤 | Titanium dioxide aqueous dispersion and method for producing the same |
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Also Published As
Publication number | Publication date |
---|---|
WO2004015015A1 (en) | 2004-02-19 |
TW200413605A (en) | 2004-08-01 |
CA2495096A1 (en) | 2004-02-19 |
US20070068643A1 (en) | 2007-03-29 |
EP1551926A1 (en) | 2005-07-13 |
CN1675318A (en) | 2005-09-28 |
JP2005535749A (en) | 2005-11-24 |
US7476272B2 (en) | 2009-01-13 |
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Legal Events
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AS | Assignment |
Owner name: E.I. DU PONT DE NEMOURS AND COMPANY, DELAWARE Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:DEFEO, MAUREEN A.;EVERS, GLENN RICHARD;MCINTYRE, PATRICK F.;REEL/FRAME:014218/0962;SIGNING DATES FROM 20031210 TO 20031215 |
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STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |