WO1997030210A1 - Procede de blanchiment de pate haut rendement - Google Patents
Procede de blanchiment de pate haut rendement Download PDFInfo
- Publication number
- WO1997030210A1 WO1997030210A1 PCT/FI1997/000108 FI9700108W WO9730210A1 WO 1997030210 A1 WO1997030210 A1 WO 1997030210A1 FI 9700108 W FI9700108 W FI 9700108W WO 9730210 A1 WO9730210 A1 WO 9730210A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- bleaching
- pulp
- process according
- peroxide
- terized
- Prior art date
Links
- 238000004061 bleaching Methods 0.000 title claims abstract description 69
- 238000000034 method Methods 0.000 title claims abstract description 29
- 239000002738 chelating agent Substances 0.000 claims abstract description 39
- 150000002978 peroxides Chemical class 0.000 claims abstract description 36
- 229910001385 heavy metal Inorganic materials 0.000 claims abstract description 15
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims abstract description 8
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims abstract description 6
- 150000004697 chelate complex Chemical class 0.000 claims abstract description 3
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims abstract description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 24
- 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 24
- 229910052783 alkali metal Inorganic materials 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 11
- -1 alkali metal salt Chemical class 0.000 claims description 10
- 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 8
- 229960001484 edetic acid Drugs 0.000 claims description 8
- PQHYOGIRXOKOEJ-UHFFFAOYSA-N 2-(1,2-dicarboxyethylamino)butanedioic acid Chemical compound OC(=O)CC(C(O)=O)NC(C(O)=O)CC(O)=O PQHYOGIRXOKOEJ-UHFFFAOYSA-N 0.000 claims description 5
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 3
- 229960003330 pentetic acid Drugs 0.000 claims description 3
- VKZRWSNIWNFCIQ-UHFFFAOYSA-N 2-[2-(1,2-dicarboxyethylamino)ethylamino]butanedioic acid Chemical group OC(=O)CC(C(O)=O)NCCNC(C(O)=O)CC(O)=O VKZRWSNIWNFCIQ-UHFFFAOYSA-N 0.000 claims description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric Acid Chemical compound [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 2
- WSHYKIAQCMIPTB-UHFFFAOYSA-M potassium;2-oxo-3-(3-oxo-1-phenylbutyl)chromen-4-olate Chemical compound [K+].[O-]C=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 WSHYKIAQCMIPTB-UHFFFAOYSA-M 0.000 claims description 2
- 150000004965 peroxy acids Chemical class 0.000 claims 3
- CNJLMVZFWLNOEP-UHFFFAOYSA-N 4,7,7-trimethylbicyclo[4.1.0]heptan-5-one Chemical compound O=C1C(C)CCC2C(C)(C)C12 CNJLMVZFWLNOEP-UHFFFAOYSA-N 0.000 claims 2
- DPZHKLJPVMYFCU-UHFFFAOYSA-N 2-(5-bromopyridin-2-yl)acetonitrile Chemical compound BrC1=CC=C(CC#N)N=C1 DPZHKLJPVMYFCU-UHFFFAOYSA-N 0.000 claims 1
- PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical compound NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 229910001882 dioxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 229910052723 transition metal Inorganic materials 0.000 claims 1
- 150000003624 transition metals Chemical class 0.000 claims 1
- 229920001131 Pulp (paper) Polymers 0.000 abstract description 42
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 26
- VKZRWSNIWNFCIQ-WDSKDSINSA-N (2s)-2-[2-[[(1s)-1,2-dicarboxyethyl]amino]ethylamino]butanedioic acid Chemical group OC(=O)C[C@@H](C(O)=O)NCCN[C@H](C(O)=O)CC(O)=O VKZRWSNIWNFCIQ-WDSKDSINSA-N 0.000 description 20
- 239000011734 sodium Substances 0.000 description 19
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000002474 experimental method Methods 0.000 description 12
- 150000007513 acids Chemical class 0.000 description 9
- 239000000835 fiber Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 235000019353 potassium silicate Nutrition 0.000 description 8
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 8
- 238000005406 washing Methods 0.000 description 8
- 239000011575 calcium Substances 0.000 description 7
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 239000007844 bleaching agent Substances 0.000 description 6
- 229910052791 calcium Inorganic materials 0.000 description 6
- 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 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 229940050410 gluconate Drugs 0.000 description 5
- 239000011572 manganese Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 4
- 239000013522 chelant Substances 0.000 description 4
- 239000003599 detergent Substances 0.000 description 4
- 230000001627 detrimental effect Effects 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000008139 complexing agent Substances 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000009897 hydrogen peroxide bleaching Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 230000009916 joint effect Effects 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- 159000000003 magnesium salts Chemical class 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 159000000001 potassium salts Chemical class 0.000 description 2
- 238000004076 pulp bleaching Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011122 softwood Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 102100031260 Acyl-coenzyme A thioesterase THEM4 Human genes 0.000 description 1
- 101500002332 Aplysia californica Proline-rich mature peptide Proteins 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 229940120146 EDTMP Drugs 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical group OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- 101000638510 Homo sapiens Acyl-coenzyme A thioesterase THEM4 Proteins 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- XDDGVTBJYGSVPM-DBRKOABJSA-N [(2r,3s,4r,5r)-5-(4-carbamoyl-1,3-thiazol-2-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate Chemical compound NC(=O)C1=CSC([C@H]2[C@@H]([C@H](O)[C@@H](COP(O)(O)=O)O2)O)=N1 XDDGVTBJYGSVPM-DBRKOABJSA-N 0.000 description 1
- YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910001430 chromium ion Inorganic materials 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- NFDRPXJGHKJRLJ-UHFFFAOYSA-N edtmp Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CCN(CP(O)(O)=O)CP(O)(O)=O NFDRPXJGHKJRLJ-UHFFFAOYSA-N 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/16—Bleaching ; Apparatus therefor with per compounds
- D21C9/163—Bleaching ; Apparatus therefor with per compounds with peroxides
-
- 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
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/1026—Other features in bleaching processes
- D21C9/1042—Use of chelating agents
Definitions
- the invention relates to a process for the bleaching of a high yield pulp, wherein the pulp is pretreated before peroxide bleaching and/or is treated in connection with peroxide bleach ⁇ ing with a chelating agent in order to bind into a chelate complex the heavy metals present in the pulp.
- high yield pulps are meant above all mechanical pulps the bleaching of which differs from the bleaching of chemical pulps in that the aim is to avoid delignification.
- the yield of pulp is maintained at a high level.
- the aim in bleaching is to ren ⁇ der colorless the color-producing components (chromophoric groups) present in lignin.
- the chelating carried out in connec ⁇ tion with the bleaching of mechanical pulps differs from the pretreatment carried out in connection with the bleaching of chemical pulps. In the latter case the complexes formed in the chelating are removed by a wash.
- no wash is carried out in the pretreatment; instead, the pretreated pulp is compressed to the consistency used in bleaching, in which case only a small proportion of the metal complexes are removed from the pulp.
- mechanical pulps also com ⁇ prise recycled fibers, from which only printing ink is removed, not lignin.
- Mechanical pulps can be divided into two principal categories, pure mechanical pulps and chemi-mechanical pulps. These pulps can further be divided into subcategories so that mechanical pulps include stone groundwood (SGW), pressure groundwood (PGW), refiner mechanical pulp (RMP), thermomechanical pulp (TMP) and others such as TRMP and PRMP. Respectively, the chemi-mechanical pulps include low-sulfonated pulps (chemi- thermomechanical pulp CTMP and BCTMP), chemically modified pulps (OPCO) and high-sulfonated pulps (CMP, UHYS).
- Mechanical pulps are used in the making of, for example, news ⁇ print, magazine paper and porous paper grades (tissue papers). Certain highly bleached chemi-mechanical pulps (BCTMP grades) are also used in bleached printing papers to replace chemical pulp.
- BCTMP grades highly bleached chemi-mechanical pulps
- Hydrogen peroxide is used for the bleaching of mechanical pulps and of recycled fiber which contains paper fiber made from mechanical pulps.
- the bleaching conditions must be rendered such that the hydro ⁇ gen peroxide will not dissociate.
- Heavy metals catalyze the dissociation of hydrogen peroxide and peroxy compounds.
- the ions the most detrimental in terms of bleaching are manganese (Mn) , iron (Fe) and copper (Cu).
- other heavy metals such as chromium ions (Cr), etc., have a detrimental effect on the consumption of peroxy compounds.
- Detrimental heavy metals originate in the pulp, the treatment waters and the pulp-treatment apparatus.
- heavy metals are bound by using agents which chelate metal ions, for example poly- aminocarboxylic acids.
- agents which chelate metal ions for example poly- aminocarboxylic acids.
- EDTA ethylene diamine tetra-acetic acid and its salts
- DTPA diethylene triamine penta-acetic acid and its salts
- DTMPA diethylene triamine pentame hylenephosphonic acid
- the bleaching of mechanical pulps and recycled fiber is common ⁇ ly carried out with hydrogen peroxide at a high pH.
- Magnesium sulfate and waterglass are added during the bleaching step in order to stabilize the peroxide.
- Many hypotheses have been presented regarding the stabilizing effect of the above- mentioned compounds.
- the stabilizing effect of waterglass is probably based on waterglass surrounding the hydroxides, oxy- hydroxides and oxides formed under alkaline conditions when iron precipitates, thus inactivating the catalytic surfaces of these solids.
- biodegradable chelating agents At least in part with biodegradable chelating agents which do not contain nitrogen.
- the bleaching of recycled fibers can often also be carried out using reducing agents such as dithionite, and peroxide bleach ⁇ ing is not always necessary. Hydrogen peroxide is used more in the slushing of recycled pulp than in actual bleaching. For this reason the treatment of recycled fiber involves the same problems as regards the stability of hydrogen peroxide.
- EDTA and DTMPA are regarded as non-biodegradable.
- DTPA is poor ⁇ ly biodegradable.
- Biodegradable complexing agents have been developed for deter ⁇ gent builders. They must at the same time have softening action on water, i.e. they must bind calcium ions and magnesium ions.
- One such sequestering agent is ethylenediamine disuccinic acid (EDDS). This compound has three stereoisomers.
- ISA 2,2'-imino- disuccinic acid
- ISA 2,2'-imino- disuccinic acid
- the use of this compound in alkaline detergents is disclosed in EP patent application 509 382.
- the patent application mentions the use of 2,2'-iminodisuccinic acid as a stabilizer of peroxide compounds, in particular in alkaline detergent compositions which contain hydrogen peroxide and its derivatives.
- DE patent application 4 340 043 discloses the use of ISA as a bleaching agent in the bleaching of groundwood.
- the purpose of ISA is the stabilization of hydrogen peroxide, and the examples show that at a pH of 10 it is a better stabilizer of hydrogen peroxide than is DTPA.
- biodegradable ethylenediamine disuccinic acid (EDDS) or 2,2'-iminodisuccinic acid (ISA), and their alkali metal salts can be used successfully as a chelat ⁇ ing agent.
- the object of the present invention is to eliminate the adverse effects of heavy metals in the bleaching of high yield pulps.
- the aim is to provide for use a biodegradable chelating agent which yields a good bleaching result.
- hydroxy ⁇ carboxylic acids can be used successfully as chelating agents together with nitrogen-containing chelating agents in bleach ⁇ ing.
- Hydroxycarboxylic acids are not efficient binders of heavy metals.
- they chelate well calcium and mag ⁇ nesium.
- Citric acid for example, has been used instead of phosphates in phosphate-free detergents and cleansing agents, which are required to bind calcium and magnesium.
- the usability of the chelating process according to the invention is based specifically on the joint effect of chelating agents of dif ⁇ ferent types.
- the pH the most preferable in terms of bleaching is approx. 5-5.5.
- aminopolycarboxylic acids are replaced with the above-mentioned hydroxycarboxylic acids, the chelating can be carried out at a higher pH.
- the usable pH range is 6-8, most preferably pH 6.5-7.5.
- the procedure according to the invention is advantageous, since the nitrogen-containing chelating agent can in part be replaced with a biodegradable chelating agent which does not contain nitrogen.
- the characteristics of the invention are given in the accom ⁇ panying claims.
- nitrogen-containing chelating agents can be replaced with compounds, known per se, having the general formula I
- n 1-8, is 0-2n, p is 0-n, q is 0-2,
- R- ⁇ is COOH
- R 2 is H, CH 2 OH or COOH.
- carboxylic acids, hydroxycarboxylic acids, polyhydroxycarboxylic acids and hydroxypolycarboxylic acids according to Formula I such as citric acid, tartaric acid, lactic acid, pimelic acid, glutamic acid, glucoheptonic acid, ascorbic acid, glycolic acid, glutaric acid, adipic acid, succinic acid or malonic acid, can be used as replacement che ⁇ lating agents.
- the process according to the invention can be used in the pre ⁇ treatment of mechanical pulps and/or in the actual bleaching.
- the process is suitable for the treatment of all mechanical pulps, such as stone groundwood, pressure groundwood, refiner mechanical pulp, thermomechanical pulp, chemi-mechanical refiner pulp and chemi-mechanical pulp.
- the process is also suitable for the bleaching of recycled fiber and textile fiber.
- the process can be used both in single-step and in two-step peroxide bleaching of mechanical pulp.
- the treatment is also suitable for mechanical pulp bleaching in which dithionite or formadine sulfinic acid bleaching is used instead of peroxide in some step.
- the compounds according to Formula I may be added already to the impregnation liquor, whereby the efficacy of the bleaching can be improved.
- the treatment may be performed on pulps obtained from various fiber raw materials, such as softwood or hardwood.
- the pH control of the acid chelating step can be carried out using conventional mineral acids, such as sulfuric acid, sulfur dioxide or an aqueous solution thereof, carbon dioxide, or organic acids such as formic acid and acetic acid.
- mineral acids such as sulfuric acid, sulfur dioxide or an aqueous solution thereof, carbon dioxide, or organic acids such as formic acid and acetic acid.
- nitrogen-containing, phosphorus-free chelating agents are preferably used, whereby environmental problems due to phosphorus are avoided.
- chelating agents include ethylenediamine-N,N'-disuccinic acid (EDDS), its various isomers and its alkali metal salts such as sodium and potassium salts, and its earth-alkali metal salts such as calcium and magnesium salts, 2,2'-iminodisuccinic acid (ISA), its various isomers and its alkali metal salts such as sodium and potassium salts, and its earth-alkali metal salts such as calcium and magnesium salts.
- EDDS ethylenediamine-N,N'-disuccinic acid
- ISA 2,2'-iminodisuccinic acid
- ISA 2,2'-iminodisuccinic acid
- its various isomers and its alkali metal salts such as sodium and potassium salts
- earth-alkali metal salts such as calcium and magnesium salts.
- Usable chelating agents also include, among polyaminocarboxylic acids, ethylenediamine tetra-acetic acid (EDTA) and its salts, and diethylenetriamine penta-acetic acid (DTPA) and its salts.
- EDTA ethylenediamine tetra-acetic acid
- DTPA diethylenetriamine penta-acetic acid
- Chelating agents within the scope of the invention are those which in addition to nitrogen also contain phosphorus, such as polyaminomethylene phosphonic acids or biodegradable aminoalkane diphosphonic acids, the use of which in the bleaching of pulp is known per se from WO applica ⁇ tion publication 95/12029.
- Some specific examples of these chelating agents are, among aminoalkane phosphonic acids, 4- morpholinomethylene-1,1-diphosphonic acid (MMDPA) and its salts, among alkane diphosphonic acids, 1-hydroxyethylene di ⁇ phosphonic acid (HEDPA) and its salts, and, among aminopoly- methylene phosphonic acids, aminotrimethylene phosphonic acid and its salts, ethylene diamine tetramethylene phosphonic acid and its salts, and diethylene triamine pentamethylene phos ⁇ phonic acid (DTMPA) and its salts.
- MMDPA 4- morpholinomethylene-1,1-diphosphonic acid
- HEDPA 1-hydroxyethylene di ⁇ phosphonic acid
- DTMPA diethylene triamine pentamethylene phos ⁇ phonic acid
- washing experi ⁇ ments were first performed on a chemical pulp.
- the success of bleaching is not dependent solely on the efficacy of the che ⁇ lating of heavy metals, but the chelating results can be re ⁇ lodged as giving a guideline.
- the best pH range for metal removal can be sought by means of washing experiments. With the help of washing experiments carried out on the same pulp at the same pH it is possible to compare the efficacies in the chelat ⁇ ing of metal ions by different chelating agents.
- Table 1 shows that a water wash is without effect as regards the chelating of metals.
- citric acid used alone does not remove heavy metals.
- Citric acid chelates only earth-alkali metals, which is not desirable in terms of bleaching. This indicates that a good chelating result is achieved through the joint effect of nitrogen-containing chelating agents and, for example, citric acid.
- a commercial TMP having an initial brightness of 55 % ISO was bleached with peroxide by pretreating it first with chelates for 30 minutes at a consistency of 10 % and a temperature of 60 °C.
- the dose of chelates was 1.5 kg/metric ton of pulp.
- the pH in the pretreatment was 6.5.
- the peroxide bleaching was carried out at a temperature of 70 °C and a consistency of 15 % for 60 minutes.
- the doses of waterglass and alkali are shown in accompanying Table 2. Table 2
- Refiner mechanical pulp was bleached by pretreating it first at the same consistency, at the same temperature and for the same time as in Example 2.
- the dose of the chelating agents was 2 kg/metric ton of pulp.
- the pH in the pretreatment was approx. 6-6.5.
- the conditions of the peroxide bleaching are shown in Table 3.
- the final pH of the bleaching was approx. 8.5 in all the experiments. Residual peroxide was determined from the bleaching filtrate.
- Refiner mechanical pulp was bleached with hydrogen peroxide by pretreating it fir ⁇ t at a consistency of 10 % at 60 °C.
- the chelating agents were dosed at a rate of 2 kg/metric ton of pulp, both in the pretreatment and in the bleaching.
- the pH was 6-6.5.
- the peroxide bleaching was carried out at 70 °C, at a consistency of 15 %, for 60 min. The results of the experiments are shown in Table 4.
- Citric acid kg/tp 1
- Citric acid kg/tp 1
- Refiner mechanical pulp was bleached with hydrogen peroxide at 70 °C, at a consistency of 15 %, for 60 min.
- the results of the experiments are shown in Table 5.
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Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU17975/97A AU1797597A (en) | 1996-02-19 | 1997-02-19 | Process for bleaching of a high yield pulp |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FI960758A FI115641B (fi) | 1996-02-19 | 1996-02-19 | Korkeasaantomassojen valkaisumenetelmä |
FI960758 | 1996-02-19 |
Publications (1)
Publication Number | Publication Date |
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WO1997030210A1 true WO1997030210A1 (fr) | 1997-08-21 |
Family
ID=8545487
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FI1997/000108 WO1997030210A1 (fr) | 1996-02-19 | 1997-02-19 | Procede de blanchiment de pate haut rendement |
Country Status (3)
Country | Link |
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AU (1) | AU1797597A (fr) |
FI (1) | FI115641B (fr) |
WO (1) | WO1997030210A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6103686A (en) * | 1997-07-16 | 2000-08-15 | Nippon Shokubai Co. Ltd. | Chelating composition |
US6590120B1 (en) | 1998-03-09 | 2003-07-08 | Kemira Chemicals Oy | Methods for the preparation of an N-bis-[2-(1,2-dicarboxy-ethoxy)-ethyl]amine derivative and products of the methods and their uses |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0141355A1 (fr) * | 1983-10-21 | 1985-05-15 | Benckiser-Knapsack GmbH | Procédé pour blanchir une pulpe de bois broyé |
WO1988006202A1 (fr) * | 1987-02-12 | 1988-08-25 | Kubat Josef | Methode amelioree de decoloration au peroxyde |
GB2206903A (en) * | 1987-06-26 | 1989-01-18 | Sandoz Ltd | Stabilisers for peroxide-containing bleaching liquors |
WO1994003553A1 (fr) * | 1992-08-01 | 1994-02-17 | The Procter & Gamble Company | Composition de blanchiment peroxy stabilisee a l'acide ethylenediamine-n,n'-disuccinique |
DE19528843A1 (de) * | 1995-08-04 | 1997-02-06 | Cht R Beitlich Gmbh | Verfahren zur Stabilisierung von alkalischen peroxidenthaltenden Bleichflotten für die Bleiche von Zellstoffen und anderen Faserstoffen |
-
1996
- 1996-02-19 FI FI960758A patent/FI115641B/fi not_active IP Right Cessation
-
1997
- 1997-02-19 WO PCT/FI1997/000108 patent/WO1997030210A1/fr active Application Filing
- 1997-02-19 AU AU17975/97A patent/AU1797597A/en not_active Abandoned
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0141355A1 (fr) * | 1983-10-21 | 1985-05-15 | Benckiser-Knapsack GmbH | Procédé pour blanchir une pulpe de bois broyé |
WO1988006202A1 (fr) * | 1987-02-12 | 1988-08-25 | Kubat Josef | Methode amelioree de decoloration au peroxyde |
GB2206903A (en) * | 1987-06-26 | 1989-01-18 | Sandoz Ltd | Stabilisers for peroxide-containing bleaching liquors |
WO1994003553A1 (fr) * | 1992-08-01 | 1994-02-17 | The Procter & Gamble Company | Composition de blanchiment peroxy stabilisee a l'acide ethylenediamine-n,n'-disuccinique |
DE19528843A1 (de) * | 1995-08-04 | 1997-02-06 | Cht R Beitlich Gmbh | Verfahren zur Stabilisierung von alkalischen peroxidenthaltenden Bleichflotten für die Bleiche von Zellstoffen und anderen Faserstoffen |
WO1997006303A1 (fr) * | 1995-08-04 | 1997-02-20 | Cht R. Beitlich Gmbh | Procede de stabilisation de bains de blanchiment alcalins contenant des peroxydes pour le blanchiment de pates de cellulose et d'autres substances fibreuses |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6103686A (en) * | 1997-07-16 | 2000-08-15 | Nippon Shokubai Co. Ltd. | Chelating composition |
EP0892040A3 (fr) * | 1997-07-16 | 2001-01-03 | Nippon Shokubai Co., Ltd. | Compositions chélatantes |
US6590120B1 (en) | 1998-03-09 | 2003-07-08 | Kemira Chemicals Oy | Methods for the preparation of an N-bis-[2-(1,2-dicarboxy-ethoxy)-ethyl]amine derivative and products of the methods and their uses |
Also Published As
Publication number | Publication date |
---|---|
FI960758A0 (fi) | 1996-02-19 |
FI960758L (fi) | 1997-08-20 |
FI115641B (fi) | 2005-06-15 |
AU1797597A (en) | 1997-09-02 |
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