SE461652B - Skumreglerande, ph-kaenslig alkylaminpolyeter - Google Patents
Skumreglerande, ph-kaenslig alkylaminpolyeterInfo
- Publication number
- SE461652B SE461652B SE8304339A SE8304339A SE461652B SE 461652 B SE461652 B SE 461652B SE 8304339 A SE8304339 A SE 8304339A SE 8304339 A SE8304339 A SE 8304339A SE 461652 B SE461652 B SE 461652B
- Authority
- SE
- Sweden
- Prior art keywords
- foam
- range
- polyether
- paper
- flotation
- Prior art date
Links
- 150000003973 alkyl amines Chemical class 0.000 title claims description 17
- 239000006260 foam Substances 0.000 title description 80
- 229920000570 polyether Polymers 0.000 claims description 35
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- -1 poly (oxyethylene) chain Polymers 0.000 claims description 15
- 229920000642 polymer Polymers 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 229920001451 polypropylene glycol Polymers 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
- 125000001165 hydrophobic group Chemical group 0.000 claims description 3
- 239000000835 fiber Substances 0.000 description 50
- 238000000034 method Methods 0.000 description 47
- 239000000463 material Substances 0.000 description 44
- 239000003795 chemical substances by application Substances 0.000 description 41
- 238000005188 flotation Methods 0.000 description 36
- 239000000123 paper Substances 0.000 description 34
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 29
- 230000008569 process Effects 0.000 description 29
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- 238000004042 decolorization Methods 0.000 description 24
- 239000004094 surface-active agent Substances 0.000 description 23
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- 230000035945 sensitivity Effects 0.000 description 18
- 239000002002 slurry Substances 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 16
- 238000005187 foaming Methods 0.000 description 16
- 238000003860 storage Methods 0.000 description 16
- 238000005406 washing Methods 0.000 description 16
- 239000002736 nonionic surfactant Substances 0.000 description 14
- 150000001412 amines Chemical class 0.000 description 12
- 230000000694 effects Effects 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 239000000976 ink Substances 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- 235000011121 sodium hydroxide Nutrition 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 230000008901 benefit Effects 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- 239000001913 cellulose Substances 0.000 description 8
- 229920002678 cellulose Polymers 0.000 description 8
- 230000002209 hydrophobic effect Effects 0.000 description 8
- 239000002609 medium Substances 0.000 description 8
- 239000000344 soap Substances 0.000 description 8
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical class [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 7
- 230000008859 change Effects 0.000 description 7
- 239000012535 impurity Substances 0.000 description 7
- 238000007639 printing Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 239000002657 fibrous material Substances 0.000 description 6
- 239000003973 paint Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 230000001105 regulatory effect Effects 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 239000000543 intermediate Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 230000009467 reduction Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 206010061592 cardiac fibrillation Diseases 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 230000002600 fibrillogenic effect Effects 0.000 description 4
- 239000003292 glue Substances 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 230000003068 static effect Effects 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003377 acid catalyst Substances 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000356 contaminant Substances 0.000 description 3
- 230000001419 dependent effect Effects 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000011118 potassium hydroxide Nutrition 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 229920003043 Cellulose fiber Polymers 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 2
- 229940073608 benzyl chloride Drugs 0.000 description 2
- 238000005574 benzylation reaction Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 238000005352 clarification Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000007046 ethoxylation reaction Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 150000002924 oxiranes Chemical class 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 230000005588 protonation Effects 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- RXBXBWBHKPGHIB-UHFFFAOYSA-L zinc;diperchlorate Chemical compound [Zn+2].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O RXBXBWBHKPGHIB-UHFFFAOYSA-L 0.000 description 2
- BHKKSKOHRFHHIN-MRVPVSSYSA-N 1-[[2-[(1R)-1-aminoethyl]-4-chlorophenyl]methyl]-2-sulfanylidene-5H-pyrrolo[3,2-d]pyrimidin-4-one Chemical compound N[C@H](C)C1=C(CN2C(NC(C3=C2C=CN3)=O)=S)C=CC(=C1)Cl BHKKSKOHRFHHIN-MRVPVSSYSA-N 0.000 description 1
- JRBAVVHMQRKGLN-UHFFFAOYSA-N 16,16-dimethylheptadecan-1-amine Chemical compound CC(C)(C)CCCCCCCCCCCCCCCN JRBAVVHMQRKGLN-UHFFFAOYSA-N 0.000 description 1
- WHQOKFZWSDOTQP-UHFFFAOYSA-N 2,3-dihydroxypropyl 4-aminobenzoate Chemical compound NC1=CC=C(C(=O)OCC(O)CO)C=C1 WHQOKFZWSDOTQP-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- 241001482108 Alosa pseudoharengus Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- 101100298295 Drosophila melanogaster flfl gene Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 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
- MPCRDALPQLDDFX-UHFFFAOYSA-L Magnesium perchlorate Chemical compound [Mg+2].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O MPCRDALPQLDDFX-UHFFFAOYSA-L 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 102100038239 Protein Churchill Human genes 0.000 description 1
- 101150030723 RIR2 gene Proteins 0.000 description 1
- 101100478214 Schizosaccharomyces pombe (strain 972 / ATCC 24843) spo6 gene Proteins 0.000 description 1
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical compound CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 125000005265 dialkylamine group Chemical group 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 239000008396 flotation agent Substances 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- QVRFMRZEAVHYMX-UHFFFAOYSA-L manganese(2+);diperchlorate Chemical compound [Mn+2].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O QVRFMRZEAVHYMX-UHFFFAOYSA-L 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- PXSXRABJBXYMFT-UHFFFAOYSA-N n-hexylhexan-1-amine Chemical compound CCCCCCNCCCCCC PXSXRABJBXYMFT-UHFFFAOYSA-N 0.000 description 1
- ZBJVLWIYKOAYQH-UHFFFAOYSA-N naphthalen-2-yl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(C=CC=C2)C2=C1 ZBJVLWIYKOAYQH-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- ZLQBNKOPBDZKDP-UHFFFAOYSA-L nickel(2+);diperchlorate Chemical compound [Ni+2].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O ZLQBNKOPBDZKDP-UHFFFAOYSA-L 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920000867 polyelectrolyte Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- RPDAUEIUDPHABB-UHFFFAOYSA-N potassium ethoxide Chemical compound [K+].CC[O-] RPDAUEIUDPHABB-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- SYXYWTXQFUUWLP-UHFFFAOYSA-N sodium;butan-1-olate Chemical compound [Na+].CCCC[O-] SYXYWTXQFUUWLP-UHFFFAOYSA-N 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/01—Organic compounds containing nitrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/0043—Organic compounds modified so as to contain a polyether group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2618—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen
- C08G65/2621—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen containing amine groups
- C08G65/2624—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen containing amine groups containing aliphatic amine groups
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/42—Ethers, e.g. polyglycol ethers of alcohols or phenols
- C09K23/46—Ethers of aminoalcohols
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C5/00—Other processes for obtaining cellulose, e.g. cooking cotton linters ; Processes characterised by the choice of cellulose-containing starting materials
- D21C5/02—Working-up waste paper
- D21C5/022—Chemicals therefor
-
- 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
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/53—Polyethers; Polyesters
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/64—Paper recycling
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Toxicology (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Medicinal Chemistry (AREA)
- Paper (AREA)
- Polyethers (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/406,885 US4483741A (en) | 1982-08-10 | 1982-08-10 | Low-foaming, pH sensitive, alkylamine polyether surface active agents and methods for using |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| SE8304339D0 SE8304339D0 (sv) | 1983-08-09 |
| SE8304339L SE8304339L (sv) | 1984-02-11 |
| SE461652B true SE461652B (sv) | 1990-03-12 |
Family
ID=23609770
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8304339A SE461652B (sv) | 1982-08-10 | 1983-08-09 | Skumreglerande, ph-kaenslig alkylaminpolyeter |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4483741A (fr) |
| JP (2) | JPH0633599B2 (fr) |
| AU (1) | AU1469483A (fr) |
| BR (1) | BR8304283A (fr) |
| CA (1) | CA1220490A (fr) |
| DE (2) | DE3347906C2 (fr) |
| ES (1) | ES524824A0 (fr) |
| FI (1) | FI75003C (fr) |
| FR (1) | FR2531719B1 (fr) |
| GB (1) | GB2125058B (fr) |
| IT (1) | IT1172280B (fr) |
| NO (1) | NO160086C (fr) |
| SE (1) | SE461652B (fr) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4483741A (en) * | 1982-08-10 | 1984-11-20 | Economics Laboratory, Inc. | Low-foaming, pH sensitive, alkylamine polyether surface active agents and methods for using |
| SE439787B (sv) * | 1984-03-19 | 1985-07-01 | Berol Kemi Ab | Sett att reducera missfergning och/eller klibbighet vid upparbetning av avfallspapper |
| DE3416043C2 (de) * | 1984-04-30 | 1986-12-04 | Akzo Gmbh, 5600 Wuppertal | Verwendung von Carbonsäureestern oder Polyäthern bei der Herstellung von Papier, insbesondere von trocken- oder naßgekreppten Papieren |
| CA1321449C (fr) * | 1988-03-02 | 1993-08-24 | Cheng-I Chen | Procede de production de pate kraft pour papier |
| DE3928599A1 (de) * | 1989-08-30 | 1991-03-07 | Henkel Kgaa | Verfahren zur altpapieraufbereitung in gegenwart polyalkylenoxidketten- und stickstoffhaltiger verbindungen |
| EP0478505A3 (en) * | 1990-09-26 | 1993-09-01 | Sandoz Ltd. | De-inking process |
| US5302245A (en) * | 1991-04-02 | 1994-04-12 | Vps Technology Partnership | Integrated wastepaper treatment process |
| US5417808A (en) * | 1991-08-30 | 1995-05-23 | Lion Corporation | Deinking composition for flotation and deinking method |
| JP2593032B2 (ja) * | 1992-02-07 | 1997-03-19 | 新技術事業団 | 両末端ヘテロ官能性ポリエーテル並びに該ポリエーテルを製造する方法及び重合開始剤 |
| US5314580A (en) * | 1992-07-08 | 1994-05-24 | Mauvin Material & Chemical Processing Limited | Process for the removal of ink, resin, and adhesive residues from paper, textile fabrics and solid surfaces |
| US5414123A (en) * | 1992-09-11 | 1995-05-09 | Thiokol Corporation | Polyether compounds having both imine and hydroxyl functionality and methods of synthesis |
| JP2627043B2 (ja) * | 1993-02-26 | 1997-07-02 | ライオン株式会社 | 脱墨剤及び該脱墨剤を用いたフローテーションによる脱墨方法 |
| US5582681A (en) * | 1994-06-29 | 1996-12-10 | Kimberly-Clark Corporation | Production of soft paper products from old newspaper |
| US6001218A (en) * | 1994-06-29 | 1999-12-14 | Kimberly-Clark Worldwide, Inc. | Production of soft paper products from old newspaper |
| US6074527A (en) * | 1994-06-29 | 2000-06-13 | Kimberly-Clark Worldwide, Inc. | Production of soft paper products from coarse cellulosic fibers |
| EP0819190B1 (fr) | 1995-04-05 | 2002-02-13 | Kao Corporation | Procede de desencrage |
| US5744065A (en) * | 1995-05-12 | 1998-04-28 | Union Carbide Chemicals & Plastics Technology Corporation | Aldehyde-based surfactant and method for treating industrial, commercial, and institutional waste-water |
| US5744064A (en) * | 1995-05-12 | 1998-04-28 | Union Carbide Chemicals & Plastics Technology Corporation | Ketone-based surfactant and method for treating industrial, commerical, and institutional waste-water |
| JP2958269B2 (ja) * | 1996-06-03 | 1999-10-06 | 花王株式会社 | 脱墨方法 |
| JP3405888B2 (ja) * | 1996-09-25 | 2003-05-12 | 花王株式会社 | 脱墨方法 |
| JP3262517B2 (ja) * | 1996-10-02 | 2002-03-04 | 花王株式会社 | 脱墨方法 |
| US6296736B1 (en) | 1997-10-30 | 2001-10-02 | Kimberly-Clark Worldwide, Inc. | Process for modifying pulp from recycled newspapers |
| ATE268212T1 (de) | 1998-03-16 | 2004-06-15 | Nalco Co | Bei recycling von behandelten behältern nützliche verunreinigungs-dispergierungsmittel |
| US6113738A (en) * | 1998-03-16 | 2000-09-05 | Nalco Chemical Company | Use of additives to breakdown and stabilize wax during fiber recycle |
| US6387210B1 (en) | 1998-09-30 | 2002-05-14 | Kimberly-Clark Worldwide, Inc. | Method of making sanitary paper product from coarse fibers |
| US6281268B1 (en) * | 1999-12-20 | 2001-08-28 | Eastman Kodak Company | Process for making an ink jet ink |
| US6544383B2 (en) * | 2000-08-07 | 2003-04-08 | Kao Specialties Americas | Flotation deinking process |
| US6784146B1 (en) | 2000-10-27 | 2004-08-31 | Kemira Chemicals, Inc. | Deinking method and composition for wastepaper |
| DE10223279A1 (de) * | 2002-05-24 | 2003-12-04 | Basf Ag | Hydrophob modifizierte Vinylamin- oder Ethylenimineinheiten enthaltende Polymere, Verfahren zur ihrer Herstellung und ihre Verwendung als Retentionsmittel |
| US7897010B2 (en) * | 2006-01-09 | 2011-03-01 | Kemira Chemicals, Inc. | Method for deinking pulp using premixed hydrophobically modified calcium carbonate particles |
| US7862685B2 (en) * | 2006-01-09 | 2011-01-04 | Kemira Chemicals, Inc. | Method for deinking pulp using premixed hydrophobically modified calcium carbonate particles |
| US8815051B2 (en) | 2006-06-12 | 2014-08-26 | Thiele Kaolin Company | Deinking of waste paper |
| US8052837B2 (en) * | 2006-06-12 | 2011-11-08 | Thiele Kaolin Company | Deinking of waste paper |
| RU2467804C2 (ru) * | 2007-06-12 | 2012-11-27 | Акцо Нобель Н.В. | Коллектор для флотации глинистых минералов из калийных руд |
| EA018960B1 (ru) * | 2008-11-26 | 2013-12-30 | Акцо Нобель Н.В. | Смесь собирателей для флотации глинистых минералов из калийных руд |
| US8317973B2 (en) | 2009-11-11 | 2012-11-27 | Kemira Chemical, Inc. | Polyester surfactants for deinking |
| PL2758485T3 (pl) | 2011-09-23 | 2017-05-31 | Dow Global Technologies Llc | Zastosowanie rozpuszczalnych w dwutlenku węgla niejonowych środków powierzchniowo czynnych do ulepszonego odzyskiwania ropy naftowej |
| CN104084086B (zh) * | 2014-07-17 | 2016-01-13 | 天津悦泰石化科技有限公司 | 用于车用尿素溶液的表面活性剂及其制备方法和用途 |
| WO2016079167A1 (fr) * | 2014-11-21 | 2016-05-26 | Akzo Nobel Chemicals International B.V. | Collecteur pour la flottation par moussage de minéraux argileux à partir de minerais de potasse |
| US11447914B2 (en) | 2017-12-07 | 2022-09-20 | Thiele Kaolin Company | Removal of stickies in the recycling of paper and paperboard |
| CN111073623A (zh) * | 2019-12-27 | 2020-04-28 | 西安三业新材料股份有限公司 | 一种用于气田的缓溶型排泡剂 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA538842A (fr) * | 1957-03-26 | R. Jackson Donald | Melanges de detersifs de composes de polyoxyethylene-polyoxypropylene conjugees | |
| CA538843A (fr) * | 1957-03-26 | Wyandotte Chemicals Corporation | Melanges de composes nouveaux de polyoxyalkylene | |
| US2673882A (en) * | 1954-03-30 | Mixed higher polyoxyalkylene | ||
| GB754679A (en) * | 1953-07-29 | 1956-08-08 | Rohm & Haas | Improvements in or relating to polyoxyalkylated tert.-carbinamines |
| US2674619A (en) * | 1953-10-19 | 1954-04-06 | Wyandotte Chemicals Corp | Polyoxyalkylene compounds |
| US2871266A (en) * | 1957-01-07 | 1959-01-27 | Rohm & Haas | Tert-carbinamines |
| US3118000A (en) * | 1959-08-10 | 1964-01-14 | Rohm & Haas | Polyoxyalkylene surface-active agents |
| US3117999A (en) * | 1959-08-10 | 1964-01-14 | Rohm & Haas | Tert-carbinamine polyoxyalkylene surface-active agents |
| NL254761A (fr) * | 1959-08-10 | |||
| US3822178A (en) * | 1971-08-11 | 1974-07-02 | Wright Chem Corp | Process for repulping waxed paper using a water soluble nonionic emulsifier |
| DE2243340C2 (de) * | 1972-04-26 | 1983-08-25 | Great Eastern Packing & Paper Stock Corp., Richmond, Va. | Verwendung eines äthoxylierten aliphatischen Mono-Ols oder Diols zum umweltschonenden Entfärben von bedrucktem Abfallpapier |
| DE2412785B2 (de) * | 1974-03-16 | 1981-07-16 | Bayer Ag, 5090 Leverkusen | Verfahren zum Weißtönen stickstoffhaltiger Fasermaterialien und Fasermaterialien aus Cellulose |
| JPS5184905A (fr) * | 1975-01-24 | 1976-07-24 | Kao Corp | |
| SE403611B (sv) * | 1975-09-05 | 1978-08-28 | Berol Kemi Ab | Forfarande for framstellning av en reaktionsprodukt mellan en epoxid och en organisk forening innehallande reaktivt vete i nervaro av viss angiven katalysator |
| JPS5331804A (en) * | 1976-09-03 | 1978-03-25 | Asahi Denka Kogyo Kk | Process for decolorizing printed ink on high grade used paper at low temperature |
| GB1596281A (en) * | 1977-02-21 | 1981-08-26 | Ici Ltd | Dispersions |
| GB1566770A (en) * | 1977-12-28 | 1980-05-08 | Kuraray Co | Etherification of polyocyalkylene compounds |
| DE2903150A1 (de) * | 1979-01-27 | 1980-08-07 | Henkel Kgaa | Verfahren zum deinken von bedrucktem altpapier |
| JPS5725489A (en) * | 1980-07-23 | 1982-02-10 | Nippon Oils & Fats Co Ltd | Deinking agent of used paper |
| JPS5729691A (en) * | 1980-07-25 | 1982-02-17 | Honshu Paper Co Ltd | Removal of sticky substance of waste paper pulp of corrugated board |
| US4483741A (en) * | 1982-08-10 | 1984-11-20 | Economics Laboratory, Inc. | Low-foaming, pH sensitive, alkylamine polyether surface active agents and methods for using |
-
1982
- 1982-08-10 US US06/406,885 patent/US4483741A/en not_active Expired - Lifetime
-
1983
- 1983-05-19 AU AU14694/83A patent/AU1469483A/en not_active Abandoned
- 1983-05-20 CA CA000428585A patent/CA1220490A/fr not_active Expired
- 1983-06-22 DE DE3347906A patent/DE3347906C2/de not_active Expired
- 1983-06-22 DE DE3322330A patent/DE3322330C2/de not_active Expired
- 1983-06-23 FR FR8310399A patent/FR2531719B1/fr not_active Expired
- 1983-07-06 IT IT4862783A patent/IT1172280B/it active
- 1983-08-04 JP JP14309783A patent/JPH0633599B2/ja not_active Expired - Lifetime
- 1983-08-09 GB GB08321359A patent/GB2125058B/en not_active Expired
- 1983-08-09 BR BR8304283A patent/BR8304283A/pt unknown
- 1983-08-09 SE SE8304339A patent/SE461652B/sv not_active IP Right Cessation
- 1983-08-09 ES ES524824A patent/ES524824A0/es active Granted
- 1983-08-09 NO NO832855A patent/NO160086C/no unknown
- 1983-08-09 FI FI832859A patent/FI75003C/fi not_active IP Right Cessation
-
1992
- 1992-07-14 JP JP18711492A patent/JPH0759796B2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| GB2125058A (en) | 1984-02-29 |
| NO160086B (no) | 1988-11-28 |
| FI75003C (fi) | 1988-04-11 |
| AU1469483A (en) | 1984-02-23 |
| DE3322330C2 (de) | 1986-08-07 |
| SE8304339L (sv) | 1984-02-11 |
| JPH0633599B2 (ja) | 1994-05-02 |
| SE8304339D0 (sv) | 1983-08-09 |
| FI832859A (fi) | 1984-02-11 |
| JPS5953532A (ja) | 1984-03-28 |
| FR2531719B1 (fr) | 1987-05-22 |
| DE3347906C2 (de) | 1987-04-16 |
| IT8348627A0 (it) | 1983-07-06 |
| ES8502747A1 (es) | 1985-01-16 |
| BR8304283A (pt) | 1984-03-20 |
| JPH0759796B2 (ja) | 1995-06-28 |
| GB8321359D0 (en) | 1983-09-07 |
| NO160086C (no) | 1989-03-08 |
| ES524824A0 (es) | 1985-01-16 |
| GB2125058B (en) | 1986-06-04 |
| FI832859A0 (fi) | 1983-08-09 |
| CA1220490A (fr) | 1987-04-14 |
| IT1172280B (it) | 1987-06-18 |
| JPH05209384A (ja) | 1993-08-20 |
| FI75003B (fi) | 1987-12-31 |
| DE3322330A1 (de) | 1984-02-16 |
| US4483741A (en) | 1984-11-20 |
| NO832855L (no) | 1984-02-13 |
| FR2531719A1 (fr) | 1984-02-17 |
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