EP0227623B1 - Use of alkylamine salts as viscosity regulating substance - Google Patents
Use of alkylamine salts as viscosity regulating substance Download PDFInfo
- Publication number
- EP0227623B1 EP0227623B1 EP86850427A EP86850427A EP0227623B1 EP 0227623 B1 EP0227623 B1 EP 0227623B1 EP 86850427 A EP86850427 A EP 86850427A EP 86850427 A EP86850427 A EP 86850427A EP 0227623 B1 EP0227623 B1 EP 0227623B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkyl amine
- use according
- alkyl
- mix
- coating
- 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.)
- Expired - Lifetime
Links
- 230000001105 regulatory effect Effects 0.000 title claims description 3
- -1 alkylamine salts Chemical class 0.000 title description 3
- 239000000126 substance Substances 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims abstract description 52
- 238000000576 coating method Methods 0.000 claims abstract description 28
- 150000003973 alkyl amines Chemical class 0.000 claims abstract description 26
- 239000011248 coating agent Substances 0.000 claims abstract description 26
- 239000002253 acid Substances 0.000 claims abstract description 20
- 150000003839 salts Chemical class 0.000 claims abstract description 15
- 150000001875 compounds Chemical class 0.000 claims abstract description 6
- 238000002156 mixing Methods 0.000 claims abstract description 5
- 239000005995 Aluminium silicate Substances 0.000 claims description 15
- 235000012211 aluminium silicate Nutrition 0.000 claims description 15
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 4
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 3
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- 229940071106 ethylenediaminetetraacetate Drugs 0.000 claims description 3
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 claims description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 3
- 239000010452 phosphate Substances 0.000 claims description 3
- FWMPHTYMAJRSIS-HSNKUXOKSA-N (2R,3S,4S,5S)-2,3,4,5,6,8-hexahydroxy-6-(2-hydroxyethyl)octanoic acid Chemical compound C(CO)C(CCO)([C@H]([C@H]([C@@H]([C@H](C(=O)O)O)O)O)O)O FWMPHTYMAJRSIS-HSNKUXOKSA-N 0.000 claims description 2
- KFHHPVVJLXPHJL-UPHRSURJSA-N (z)-4-hydroperoxy-4-oxobut-2-enoic acid Chemical compound OOC(=O)\C=C/C(O)=O KFHHPVVJLXPHJL-UPHRSURJSA-N 0.000 claims description 2
- WUBBRNOQWQTFEX-UHFFFAOYSA-M 4-aminosalicylate(1-) Chemical compound NC1=CC=C(C([O-])=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-M 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 claims description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 claims description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 claims description 2
- 229910002651 NO3 Inorganic materials 0.000 claims description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 2
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 claims description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- 229940072107 ascorbate Drugs 0.000 claims description 2
- 235000010323 ascorbic acid Nutrition 0.000 claims description 2
- 239000011668 ascorbic acid Substances 0.000 claims description 2
- 229940001468 citrate Drugs 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims description 2
- 229940001447 lactate Drugs 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 229940039748 oxalate Drugs 0.000 claims description 2
- 229940075930 picrate Drugs 0.000 claims description 2
- OXNIZHLAWKMVMX-UHFFFAOYSA-M picrate anion Chemical compound [O-]C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-M 0.000 claims description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 claims description 2
- 229960001860 salicylate Drugs 0.000 claims description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims description 2
- 229910021653 sulphate ion Inorganic materials 0.000 claims description 2
- 229940095064 tartrate Drugs 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims 4
- 239000001175 calcium sulphate Substances 0.000 claims 2
- 235000011132 calcium sulphate Nutrition 0.000 claims 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 239000010440 gypsum Substances 0.000 description 13
- 229910052602 gypsum Inorganic materials 0.000 description 13
- 239000001768 carboxy methyl cellulose Substances 0.000 description 9
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 8
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 8
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 8
- 229940105329 carboxymethylcellulose Drugs 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 5
- 239000002270 dispersing agent Substances 0.000 description 5
- 239000004816 latex Substances 0.000 description 4
- 229920000126 latex Polymers 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical group CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- VJROPLWGFCORRM-UHFFFAOYSA-N 2-methylbutan-1-amine Chemical compound CCC(C)CN VJROPLWGFCORRM-UHFFFAOYSA-N 0.000 description 1
- GELMWIVBBPAMIO-UHFFFAOYSA-N 2-methylbutan-2-amine Chemical compound CCC(C)(C)N GELMWIVBBPAMIO-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
- 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 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-L L-tartrate(2-) Chemical compound [O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O FEWJPZIEWOKRBE-JCYAYHJZSA-L 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N N-butylamine Natural products CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- DUJHUESDNVWCBZ-UHFFFAOYSA-N [acetyloxy(2-hydroxyethyl)amino] acetate Chemical compound CC(=O)ON(CCO)OC(C)=O DUJHUESDNVWCBZ-UHFFFAOYSA-N 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- PASHVRUKOFIRIK-UHFFFAOYSA-L calcium sulfate dihydrate Chemical compound O.O.[Ca+2].[O-]S([O-])(=O)=O PASHVRUKOFIRIK-UHFFFAOYSA-L 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 150000004683 dihydrates Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- BMFVGAAISNGQNM-UHFFFAOYSA-N isopentylamine Chemical compound CC(C)CCN BMFVGAAISNGQNM-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- IGEIPFLJVCPEKU-UHFFFAOYSA-N pentan-2-amine Chemical compound CCCC(C)N IGEIPFLJVCPEKU-UHFFFAOYSA-N 0.000 description 1
- PQPFFKCJENSZKL-UHFFFAOYSA-N pentan-3-amine Chemical compound CCC(N)CC PQPFFKCJENSZKL-UHFFFAOYSA-N 0.000 description 1
- 229940100684 pentylamine Drugs 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 150000003139 primary aliphatic amines Chemical class 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 150000005619 secondary aliphatic amines Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229940086542 triethylamine Drugs 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
- 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
- D21H19/46—Non-macromolecular organic compounds
-
- 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
- D21H19/38—Coatings with pigments characterised by the pigments
- D21H19/40—Coatings with pigments characterised by the pigments siliceous, e.g. clays
Definitions
- the present invention relates to the use of acid addition salts of alkyl amines for regulating the viscosity of paper coating mixes when blending such mixes.
- the object of the present invention is to enable the interchange of coating mixes in continuous paper coating processes without substantial change in the viscosity of said mixes at the transition from one mix to the other and/or the mixing of the mixes one with the other.
- Paper is coated by applying an extremely thin layer of coating mix to a paper web.
- the purpose of the coating is to improve the properties of the paper, particularly with regard to uniformity of surface, and its ability to accept inks, lacquers etc. from the printing press.
- Such mixes today comprise finely ground kaolin, dispersant, and water, or chalk, dispersant, water.
- Mixes have also been proposed, and prepared that comprises calcium sulphate dihydrate (gypsum), dispersant and water. It has also been found, however, that when switching from a gypsum mix to a kaolin mix the viscosity of the combined mixes is much higher than that of a single mix, which renders the system inoperable.
- DE-A1-1 696 193 discloses the use of polyvinylalcohol as a binding agent in satin white-based coating mixtures, whereby an amine, alkali or ammoniumsalt of a polycarboxylic acid is used as an impart useable viscosity to the formulation.
- the polycarboxylic acids used are particularly those being of high molecular weight, such as sodium polyacrylate, sodium polyvinyl sulphonate, and sodium carboxy methyl cellulose.
- EP-A2-0 004 062 discloses aqueous dispersions of polymers, particularly on the basis of vinylpolymers, whereby salts of primary, secondary and tertiary aliphatic amines are used as dispersing agents.
- the acid addition salt is prepared by reaction with sulphuric acid, phosphoric acid, hydrochloric acid, nitric acid, perchloric acid, aliphatic, alicyclic, aromatic and heterocyclic carboxylic and sulphonic acids.
- such salts are hydrochlorides, sulphate, hydrogen sulphate, phosphate, hydrogen phosphate, nitrate, formiate, acetate, propionate, succinate, glycolate, gluconate, heptonate, lactate, tartrate, citrate, oxalate, ascorbate, maleate, hydroxy maleate, bensoate, p-amino bensoate, p-hydroxy bensoate, salicylate, p-amino salicylate, picrate, diethylene triamine pentaacetate (DTPA), ethylene diamine tetraacetate (EDTA), nitrilo triacetate (NTA), hydroxy ethyl imino diacetate, bis(hydroxyethyl)gluconate.
- DTPA diethylene triamine pentaacetate
- EDTA ethylene diamine tetraacetate
- NTA nitrilo triacetate
- the alkyl amines used in the group preferably comprise primary alkyl amines, such as methyl amine, ethyl amine, propyl amine, 1-methyl ethyl amine, butyl amine, 1-methyl propyl amine, 2-methyl propyl amine, pentyl amine, 3-methyl butyl amine, 2-methyl butyl amine, 1-ethyl propyl amine, 1-methyl butyl amine, 1,1-dimethyl ethyl amine, 1,1-dimethyl propyl amine, although they may also comprise secondary, tertiary and quarternary alkyl amines, such as dimethyl amine, diethyl amine, triethyl amine, tetramethyl amine.
- primary alkyl amines such as methyl amine, ethyl amine, propyl amine, 1-methyl ethyl amine, butyl amine, 1-methyl propyl amine, 2-methyl propy
- the product is prepared by mixing a solution of an alkyl amine with a solution of an acid which will react to form the intended acid addition salt. It is irrelevant in this respect whether one solution is added to the other, or vice versa.
- the respective solutions may have the form of a concentrate or a solvent solution of the compound concerned.
- the ratio of amine to acid is from 1 to 4, depending upon the degree of substitution desired.
- the reaction between alkyl amine and acid takes place instantaneously, whereafter the product can be filtered off (when the reaction takes place in a non-dissolving solvent) or can be used direct, in solution.
- a further gypsum based mix was prepared from 100 parts dry gypsum, 1.5 parts CMC, 9 parts latex DOW 685, NaOH to pH 8.5 and water, there being obtained a mix with DS 64.4%, viscosity 950 cps.
- Various amines according to the aforegoing were added to 400 g of the kaolin mix thus prepared, in the quantities set forth in Table 1, whereafter 30.1 g of the gypsum mix were added and the viscosity of the resultant mixture was measured. The viscosity was also measured after adding the amine.
- the results obtained when adding the gypsum based mix are set forth in the right column of Table 1 below.
- the present invention has also been tested on a semi-industrial scale in an apparatus having a volume of 25 litres.
- the apparatus comprised a machine tank having a volumetric filling capacity of 15 litres, a filter, and a buffer tank provided with an outlet leading to the machine tank and to the "coating station", i.e. the apparatus simulated the coating of a paper web by taking out 1 litre of mix per minute.
- the volume circulated was 7 litres and the flow rate 10 litres per minute.
- the system was filled with a mix 1. Whereafter the mix was pumped around the system, and "coating commenced".
- Table 2 The results set forth in Table 2 were obtained when testing a conventional kaolin coating mix (mix 2), 100 parts of kaolin, 0.35 parts Dispex R N40, -'1.2 parts of CMC FFS, and 9 parts of latex DOW 685, DS 56-59%, pH 8.5-9, and a gypsum-based coating mix (mix 1) comprising 100 parts of dry gypsum dihydrate, 1.5 parts of CMC, and 9 parts of DOW 685, DS 60-65%, pH 8.5-9, without further addition of a compound according to the present invention.
- a conventional kaolin coating mix (mix 2), 100 parts of kaolin, 0.35 parts Dispex R N40, -'1.2 parts of CMC FFS, and 9 parts of latex DOW 685, DS 56-59%, pH 8.5-9
- a gypsum-based coating mix (mix 1) comprising 100 parts of dry gypsum dihydrate, 1.5 parts of CMC, and 9 parts of DOW 685, DS 60
- Table 3 discloses the results obtained when adding to mix 1 (the gypsum mix) 0.4 parts of propyl amine phosphate, calculated as amine.
- kaolin-based mix By kaolin-based mix is meant-here and in the aforegoing, a mix in which the pigment fraction contains more than 50% kaolin. Kaolin mixes that contain 60% kaolin and 40% gypsum are thus known in the art.
- chalk-based mixes is meant a mix that contains more than 50% chalk
- gypsum-based mixes is meant a mix that contains more than 50% gypsum.
- the pigment fraction need not be totally based on one pigment.
- DS means dry substance
- Dow Latex is a polymer, whereby Dow Latex 685 is a carboxylated styrene-butadiene
- DISPEX R N40 is a sodium salt of polycarboxylic acid
- CMC is carboxymethyl cellulose, where CMC FF5 has an extra low viscosity level determined to 35-55 mPa - s at 25°C and a concentration of 4% dry matter.
Landscapes
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paper (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Radiation-Therapy Devices (AREA)
- Medicines Containing Plant Substances (AREA)
- Paints Or Removers (AREA)
Abstract
Description
- The present invention relates to the use of acid addition salts of alkyl amines for regulating the viscosity of paper coating mixes when blending such mixes.
- The object of the present invention is to enable the interchange of coating mixes in continuous paper coating processes without substantial change in the viscosity of said mixes at the transition from one mix to the other and/or the mixing of the mixes one with the other.
- Paper is coated by applying an extremely thin layer of coating mix to a paper web. The purpose of the coating is to improve the properties of the paper, particularly with regard to uniformity of surface, and its ability to accept inks, lacquers etc. from the printing press. Such mixes today comprise finely ground kaolin, dispersant, and water, or chalk, dispersant, water. Mixes have also been proposed, and prepared that comprises calcium sulphate dihydrate (gypsum), dispersant and water. It has also been found, however, that when switching from a gypsum mix to a kaolin mix the viscosity of the combined mixes is much higher than that of a single mix, which renders the system inoperable.
- Due to the complexity of paper machines it is not convenient to stop production in order to clean the coating equipment. It is also necessary, however, to be able to switch from one type of mix to another without stopping production in order to satisfy demands for paper with different coatings.
- Various systems have been tested, inter alia with variation of the dispersant, although without success.
- DE-A1-1 696 193 discloses the use of polyvinylalcohol as a binding agent in satin white-based coating mixtures, whereby an amine, alkali or ammoniumsalt of a polycarboxylic acid is used as an impart useable viscosity to the formulation. The polycarboxylic acids used are particularly those being of high molecular weight, such as sodium polyacrylate, sodium polyvinyl sulphonate, and sodium carboxy methyl cellulose.
- EP-A2-0 004 062 discloses aqueous dispersions of polymers, particularly on the basis of vinylpolymers, whereby salts of primary, secondary and tertiary aliphatic amines are used as dispersing agents.
- It has now surprisingly been found possible to solve this problem in a simple and efficient manner by means of the present invention which to this end proposes the use of compounds which comprise an acid addition salt of an alkyl amine having 1-5 carbon atoms in the alkyl chain, preferably 2-4 carbon atoms and still more preferably 3-4 carbon atoms.
- Part of the alkyl amine is present as an acid addition salt. The acid addition salt is prepared by reaction with sulphuric acid, phosphoric acid, hydrochloric acid, nitric acid, perchloric acid, aliphatic, alicyclic, aromatic and heterocyclic carboxylic and sulphonic acids. In this regard, such salts are hydrochlorides, sulphate, hydrogen sulphate, phosphate, hydrogen phosphate, nitrate, formiate, acetate, propionate, succinate, glycolate, gluconate, heptonate, lactate, tartrate, citrate, oxalate, ascorbate, maleate, hydroxy maleate, bensoate, p-amino bensoate, p-hydroxy bensoate, salicylate, p-amino salicylate, picrate, diethylene triamine pentaacetate (DTPA), ethylene diamine tetraacetate (EDTA), nitrilo triacetate (NTA), hydroxy ethyl imino diacetate, bis(hydroxyethyl)gluconate.
- Further characteristics are set forth in the following claims.
- The alkyl amines used in the group preferably comprise primary alkyl amines, such as methyl amine, ethyl amine, propyl amine, 1-methyl ethyl amine, butyl amine, 1-methyl propyl amine, 2-methyl propyl amine, pentyl amine, 3-methyl butyl amine, 2-methyl butyl amine, 1-ethyl propyl amine, 1-methyl butyl amine, 1,1-dimethyl ethyl amine, 1,1-dimethyl propyl amine, although they may also comprise secondary, tertiary and quarternary alkyl amines, such as dimethyl amine, diethyl amine, triethyl amine, tetramethyl amine.
- The product is prepared by mixing a solution of an alkyl amine with a solution of an acid which will react to form the intended acid addition salt. It is irrelevant in this respect whether one solution is added to the other, or vice versa.
- The respective solutions may have the form of a concentrate or a solvent solution of the compound concerned.
- The ratio of amine to acid is from 1 to 4, depending upon the degree of substitution desired.
- In the process of adding one solution to the other, care is taken to ensure that the alkyl amine does not boil, by a suitable control of temperature.
- The reaction between alkyl amine and acid takes place instantaneously, whereafter the product can be filtered off (when the reaction takes place in a non-dissolving solvent) or can be used direct, in solution.
- 33.6 kg of citric monohydrate were dissolved in 30 I of water. 36 I (25.9 kg) of n-propyl amine were then added carefully to the solution, while stirring and cooling the system. The temperature was maintained beneath 45°C. The resultant product, (n-propylamine)3-citrate remained in solution in the water phase.
- The following systems were.prepared in a similar manner:
-
- A series of experiments was conducted on the basis of the above substances, in which there was prepared a first kaolin mix comprising 100 parts of dry kaolin, 50 parts of water, 0.35 parts of 100%-DispexR and NaOH. The pH of the mix was 8.5. A suspension was then prepared over a period of one hour, by adding to the mix 9 parts of DOW 685,1.2 parts of CMC (carboxy methyl cellulose) and water to a viscosity of about 1500 cps, dry solids (DS) content 5558%. Peripheral data concerning different starting kaolin mixes is given in Table 1 below, left column.
- A further gypsum based mix was prepared from 100 parts dry gypsum, 1.5 parts CMC, 9 parts latex DOW 685, NaOH to pH 8.5 and water, there being obtained a mix with DS 64.4%, viscosity 950 cps. Various amines according to the aforegoing were added to 400 g of the kaolin mix thus prepared, in the quantities set forth in Table 1, whereafter 30.1 g of the gypsum mix were added and the viscosity of the resultant mixture was measured. The viscosity was also measured after adding the amine. The results obtained when adding the gypsum based mix are set forth in the right column of Table 1 below.
- The present invention has also been tested on a semi-industrial scale in an apparatus having a volume of 25 litres. The apparatus comprised a machine tank having a volumetric filling capacity of 15 litres, a filter, and a buffer tank provided with an outlet leading to the machine tank and to the "coating station", i.e. the apparatus simulated the coating of a paper web by taking out 1 litre of mix per minute. The volume circulated was 7 litres and the flow rate 10 litres per minute. The system was filled with a mix 1. Whereafter the mix was pumped around the system, and "coating commenced". Subsequent to emptying the machine tank, by consecutive simulated "coating" procedures, such that about 10 litres of mix 1 remained, the system was refilled with mix 2, this mix being intended to replace mix 1 without interrupting circulation and while continuing the "coating" process. Samples were taken from the combined mixture of mixes 1 and 2 at 30 second intervals, in order to determine the viscosity, pH, and in some cases also DS and the ratio of mix 1 to mix 2 in the combined coating mixture.
- The results set forth in Table 2 were obtained when testing a conventional kaolin coating mix (mix 2), 100 parts of kaolin, 0.35 parts DispexR N40, -'1.2 parts of CMC FFS, and 9 parts of latex DOW 685, DS 56-59%, pH 8.5-9, and a gypsum-based coating mix (mix 1) comprising 100 parts of dry gypsum dihydrate, 1.5 parts of CMC, and 9 parts of DOW 685, DS 60-65%, pH 8.5-9, without further addition of a compound according to the present invention.
-
- In a further test, mix 1 and mix 2 were mixed together in different proportions, while carefully stirring the system for one minute. The viscosity of the combined mixture was determined in accordance with the Brookfield technique (30 s 100 rpm). In this test, a study was made of a mixture between a gypsum-based mix according to the above (mix 1) and a kaolin mix (mix 2) with a synthetic thickener, DS 55% and Viscosity mPas. The results are given in Tables 4 and 5 below.
- It is evident from the above that the viscosity of the coating mixture is stabilized very effectively when an alkyl amine acid addition salt according to the aforesaid is used.
- It has been found that when using the alkyl amine acid addition salt, an acceptable result is achieved even when only a part of the alkyl amine exists in the form of such an acid addition salt.
- A satisfactory result can also be obtained by adding each of the salt components, i.e. alkyl amine and acid, separately, to the coating mix.
- By kaolin-based mix is meant-here and in the aforegoing, a mix in which the pigment fraction contains more than 50% kaolin. Kaolin mixes that contain 60% kaolin and 40% gypsum are thus known in the art.
- By chalk-based mixes is meant a mix that contains more than 50% chalk, while by gypsum-based mixes is meant a mix that contains more than 50% gypsum. Thus the pigment fraction need not be totally based on one pigment.
- In the above the abbreviation DS means dry substance; Dow Latex is a polymer, whereby Dow Latex 685 is a carboxylated styrene-butadiene; DISPEXR N40 is a sodium salt of polycarboxylic acid; CMC is carboxymethyl cellulose, where CMC FF5 has an extra low viscosity level determined to 35-55 mPa - s at 25°C and a concentration of 4% dry matter.
Claims (11)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT86850427T ATE55107T1 (en) | 1985-12-09 | 1986-12-08 | USE OF ALKYLAMINE SALTS AS VISCOSITY REGULATOR. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8505811 | 1985-12-09 | ||
| SE8505811A SE451470B (en) | 1985-12-09 | 1985-12-09 | APPLICATION OF AN ACID ADDITION SALT OF AN ALKYLAMINE FOR REGULATING THE VISCOSITY OF PAPER COATING METHODS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0227623A1 EP0227623A1 (en) | 1987-07-01 |
| EP0227623B1 true EP0227623B1 (en) | 1990-08-01 |
Family
ID=20362396
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP86850427A Expired - Lifetime EP0227623B1 (en) | 1985-12-09 | 1986-12-08 | Use of alkylamine salts as viscosity regulating substance |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0227623B1 (en) |
| AT (1) | ATE55107T1 (en) |
| DE (1) | DE3673144D1 (en) |
| ES (1) | ES2016568B3 (en) |
| FI (1) | FI864771A7 (en) |
| SE (1) | SE451470B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8252143B2 (en) | 2004-06-22 | 2012-08-28 | Akzo Nobel N.V. | Filler for paper making process |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL1778916T3 (en) * | 2004-06-22 | 2016-10-31 | Filler for paper making process |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1150561A (en) * | 1965-07-14 | 1969-04-30 | Kurashiki Rayon Kk | Coating Compositions for High Grade Paper |
| DE1696193B2 (en) * | 1966-04-07 | 1974-07-04 | Farbwerke Hoechst Ag, Vormals Meister Lucius & Bruening, 6000 Frankfurt | Satin white coating slips with good viscosity stability |
| DE2810348A1 (en) * | 1978-03-10 | 1979-09-20 | Hoechst Ag | AQUEOUS PLASTIC DISPERSION BASED ON VINYL POLYMERS |
-
1985
- 1985-12-09 SE SE8505811A patent/SE451470B/en not_active IP Right Cessation
-
1986
- 1986-11-24 FI FI864771A patent/FI864771A7/en not_active Application Discontinuation
- 1986-12-08 EP EP86850427A patent/EP0227623B1/en not_active Expired - Lifetime
- 1986-12-08 AT AT86850427T patent/ATE55107T1/en not_active IP Right Cessation
- 1986-12-08 ES ES86850427T patent/ES2016568B3/en not_active Expired - Lifetime
- 1986-12-08 DE DE8686850427T patent/DE3673144D1/en not_active Expired - Fee Related
Non-Patent Citations (1)
| Title |
|---|
| CHEMICAL ABSTRACTS, vol. 25, no. 1, Jan 1931; A.NYSSENS: " The identification of aliphatic amines", pp. 69-70 * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8252143B2 (en) | 2004-06-22 | 2012-08-28 | Akzo Nobel N.V. | Filler for paper making process |
| US8828188B2 (en) | 2004-06-22 | 2014-09-09 | Akzo Nobel N.V. | Filler for paper making process |
| US9657441B2 (en) | 2004-06-22 | 2017-05-23 | Akzo Nobel N.V. | Filler for paper making process |
Also Published As
| Publication number | Publication date |
|---|---|
| ATE55107T1 (en) | 1990-08-15 |
| FI864771A0 (en) | 1986-11-24 |
| SE8505811D0 (en) | 1985-12-09 |
| FI864771L (en) | 1987-06-10 |
| SE451470B (en) | 1987-10-12 |
| EP0227623A1 (en) | 1987-07-01 |
| ES2016568B3 (en) | 1990-11-16 |
| DE3673144D1 (en) | 1990-09-06 |
| FI864771A7 (en) | 1987-06-10 |
| SE8505811L (en) | 1987-06-10 |
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