US3398047A - Pitch prevention by addition of ligand and organic sulfonate - Google Patents
Pitch prevention by addition of ligand and organic sulfonate Download PDFInfo
- Publication number
- US3398047A US3398047A US402628A US40262864A US3398047A US 3398047 A US3398047 A US 3398047A US 402628 A US402628 A US 402628A US 40262864 A US40262864 A US 40262864A US 3398047 A US3398047 A US 3398047A
- Authority
- US
- United States
- Prior art keywords
- pitch
- acid
- pulp
- composition
- ligand
- 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
- 239000003446 ligand Substances 0.000 title description 15
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 title description 10
- 230000002265 prevention Effects 0.000 title description 4
- 239000011295 pitch Substances 0.000 description 49
- 239000000203 mixture Substances 0.000 description 32
- 239000002253 acid Substances 0.000 description 21
- 239000000123 paper Substances 0.000 description 21
- 238000000151 deposition Methods 0.000 description 19
- 230000008021 deposition Effects 0.000 description 19
- 239000000463 material Substances 0.000 description 15
- 235000000346 sugar Nutrition 0.000 description 15
- 150000003839 salts Chemical class 0.000 description 14
- 238000000034 method Methods 0.000 description 13
- 239000000126 substance Substances 0.000 description 12
- 150000007513 acids Chemical class 0.000 description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- 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 6
- -1 alkaline earth metal salts Chemical class 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 239000000080 wetting agent Substances 0.000 description 6
- 229920001732 Lignosulfonate Polymers 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical class O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
- 229930006000 Sucrose Chemical class 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000005720 sucrose Chemical class 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- URDCARMUOSMFFI-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(2-hydroxyethyl)amino]acetic acid Chemical compound OCCN(CC(O)=O)CCN(CC(O)=O)CC(O)=O URDCARMUOSMFFI-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 3
- 229940106681 chloroacetic acid Drugs 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 125000003107 substituted aryl group Chemical group 0.000 description 3
- 150000003871 sulfonates Chemical class 0.000 description 3
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 3
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical class OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000002738 chelating agent Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229960001484 edetic acid Drugs 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000002655 kraft paper Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 159000000001 potassium salts Chemical class 0.000 description 2
- 229920005552 sodium lignosulfonate Polymers 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 229940048842 sodium xylenesulfonate Drugs 0.000 description 2
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- XNCSCQSQSGDGES-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]propyl-(carboxymethyl)amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)C(C)CN(CC(O)=O)CC(O)=O XNCSCQSQSGDGES-UHFFFAOYSA-N 0.000 description 1
- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
- DNIDAYOSPDNUKP-UHFFFAOYSA-N 3-(2-phenylethenyl)benzene-1,2-diamine Chemical compound NC1=CC=CC(C=CC=2C=CC=CC=2)=C1N DNIDAYOSPDNUKP-UHFFFAOYSA-N 0.000 description 1
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N Biguanide Chemical compound NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 description 1
- 229940123208 Biguanide Drugs 0.000 description 1
- FCKYPQBAHLOOJQ-UHFFFAOYSA-N Cyclohexane-1,2-diaminetetraacetic acid Chemical compound OC(=O)CN(CC(O)=O)C1CCCCC1N(CC(O)=O)CC(O)=O FCKYPQBAHLOOJQ-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- WQZGKKKJIJFFOK-IVMDWMLBSA-N D-allopyranose Chemical class OC[C@H]1OC(O)[C@H](O)[C@H](O)[C@@H]1O WQZGKKKJIJFFOK-IVMDWMLBSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric Acid Chemical class [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 229920005550 ammonium lignosulfonate Polymers 0.000 description 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004984 aromatic diamines Chemical class 0.000 description 1
- 125000005228 aryl sulfonate group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229920005551 calcium lignosulfonate Polymers 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical group 0.000 description 1
- 150000001734 carboxylic acid salts Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 239000011323 chemical pitch Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 210000000038 chest Anatomy 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000002153 concerted effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000008121 dextrose Chemical class 0.000 description 1
- 125000005594 diketone group Chemical group 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- ZZGUZQXLSHSYMH-UHFFFAOYSA-N ethane-1,2-diamine;propanoic acid Chemical compound NCCN.CCC(O)=O.CCC(O)=O ZZGUZQXLSHSYMH-UHFFFAOYSA-N 0.000 description 1
- IFQUWYZCAGRUJN-UHFFFAOYSA-N ethylenediaminediacetic acid Chemical compound OC(=O)CNCCNCC(O)=O IFQUWYZCAGRUJN-UHFFFAOYSA-N 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- XKUKSGPZAADMRA-UHFFFAOYSA-N glycyl-glycyl-glycine Natural products NCC(=O)NCC(=O)NCC(O)=O XKUKSGPZAADMRA-UHFFFAOYSA-N 0.000 description 1
- 108010067216 glycyl-glycyl-glycine Proteins 0.000 description 1
- 150000003977 halocarboxylic acids Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 150000002690 malonic acid derivatives Chemical class 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 230000018984 mastication Effects 0.000 description 1
- 238000010077 mastication Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000005031 sulfite paper Substances 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 150000004044 tetrasaccharides Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 150000004043 trisaccharides Chemical class 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/09—Sulfur-containing 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
- 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
- D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
- D21H17/23—Lignins
-
- 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
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/02—Agents for preventing deposition on the paper mill equipment, e.g. pitch or slime control
Definitions
- the instant invention is concerned with an improvement in the making of paper. More specific-ally, the present invention relates to a method of preventing deposition of pitch and other precipitants which commonly occur in pulp and paper mill systems.
- pitch deposits are one which has been found to manifest itself at practically all points in numerous pulp and paper mill operations at one time or another. Quite often it is found that deposits particularly occur at a point in the system shortly after a high degree of de-fibering or after a point of stock dilution. Generally the pitch is released from the pulp in the form of small water-insoluble particles. These particles subsequently agglomerate and deposit upon the fibers and any available surface in the pulp and paper mill system which they contact.
- a number of methods of pitch control are employed to combat the just-discussed problem. This includes the use of pitch solvents, polyphosphates, talc, clays, etc. While these have met with some measure of success, in many instances proper pitch control cannot be effected even with benefit of one or more of the above or other additive chemicals employed in the papermaking operation. It would therefore be of benefit to the papermaking art if a composition could be discovered which had excellent activity in controlling pitch deposition. Moreover, if a single composition could be devised which could be usefully employed to inhibit pitch depositions in both pulp and paper mill systems of varying types, such additive would find ready acceptance in the paper field. In view of the above, it therefore becomes an object of the invention to provide an improved papennaking process.
- a more specific object of the invention is to provide a method of preventing deposition of pitch and other deposits in pulp and paper mill systems by application of a single extremely effective paper additive composition.
- Still another object of the invention is to provide a chemical composition compatible with an aqueous pulp stream which is effective in preventing pitch deposition at economical dosages without fear of deleterious sideeffects.
- the invention lies in treating a pulp being processed in either of said systems with a pitch control composition in at least an amount sufficient to substantially inhibit the pitch deposition.
- the pitch control material should include an organic polydentate ligand and an organic sulfonate.
- the organic polydentate ligand material is one which is normally characterized as possessing the ability to form chelate structures.
- Preferred for use in the invention are multidentate chelating agents which have threeeight donor atoms. These materials are well-known and their structures need little elaboration.
- Two treatises dealing with a number of organic polydentate ligands are Chemistry of the Coordination Compounds by J. C. Bailar, Jr., Reinhold Publishing Corporation, 1956 and Chelating Agents and Metal Chelates by F. P. Dwyer and D. P. Mellor, Academic Press, 1964.
- Preferred polydentate ligands for use in the instant invention include ethylenediamine, glycol, glycerol, mannitol, sorbitol, mono-, di-, and triethanol amines; oxalate and malonate salts; salicylic, lactic, citric, glycollic and tartaric acids; iminodiacetic acid, glycine, nitrilotriacetic acid, ethylenediamine-tetraacetic acid and salts thereof; diketones as acetylacetone, propylenediamine, stilbenediamine, aromatic diamines, biguanide, substituted quinolines, phthalocyanines, porphins, triglycine, etc.
- aminopolycarboxylic acids and sugar acids.
- aminopolycarboxylic acids the following are illustrative: ethylenediaminediacetic acid, ethylenediaminedipropionic acid, ethylenediaminetetraacetic acid, 1,2 propylenediaminetetraacetic acid, 1,2 cyclohexanediaminetetraacetic acid, -N- hydroxyethylethylenediaminetriacetic acid.
- Salts of the above listed acids or other polyaminocarboxylic acids work equally well in the invention.
- Alkali metal and alkaline earth metal salts are most preferred to ⁇ form carboxytlate materials.
- Partial salts that is, amino acids only partly neutralized to varying degrees, may likewise be employed without loss of activity in prevention of pitch deposition.
- the trisodium salt of N-hydroxyethylethylene diaminetriacetic acid is most preferred.
- sugar acid or salt of a sugar acid is a sugar compound, and more particularly a sugar acid or salt of a sugar acid.
- sugar acids are carbohydrates having carboxylic acid function to a greater or lesser degree.
- Preferred sugar acids or salts are those in which there is at least one carboxylic group or carboxylic salt group per molecule.
- these sugar acids or salts have three or more carbon atoms in the molecule.
- Representative types are sodium heptogluconate, sodium salt of glycoxyacetic acid, various wood sugars and their salts removed from a cook liquor obtained in pulping of wood such as soft woods, carboxylic acids or acid salts of glucose, allose, dextrose, sucrose, etc.
- Mono-, di-, tri-, and tetra saccharides having some free carboxyl character or carboxylic salt function may all be usefully employed.
- Preferred substances are sodium heptogluconate, and the so dium salt of glucoxyacetic acid.
- sugar acid is derived from reaction of a sugar, such as sucrose, and a halocarboxylic acid or acid salt such as chloroacetic acid or sodium chloroacetiate, it is preferred that a molar ratio of acid or acid salt to sugar of from 1:1 to 4.1 be employed.
- EXAMPLE I 15.20 parts of sucrose, 4.50 parts of chloroacetic acid and 3.80 parts of 50% sodium hydroxide were added together and allowed to react at about room temperature while mixing was effected. The strong base was present to neutralize any hydrochloric acid formed in the reaction between the chloroacetic acid and sucrose. The resultant product can be used directly as one of the components of the compositions of the invention.
- the other component used in making up the pitch control compositions of the invention is an organic sulfonate.
- organic sulfonate these materials are well-known products of commerce. Both alkyl and aryl sulfonates as well as alkaryl sulfonate substances may be employed.
- petroleum sulfonates are a useful class.
- Particularly preferred organic sulfonates are water-soluble lignosulfonates, substituted aryl sulfonates and naphthalene sulfonates.
- water-soluble lignosulfonates derived as by-products in the manufacture of sulfite pulp where wood is cooked with calcium bisulfite-magnesium bisulfite-sulfur dioxide liquor.
- the lignin is converted to lignosulfonic acid which is thereafter converted to a solid salt product such as calcium lignosulfonate, ammonium lignosulfonate, potassium lignosulfate, sodium lignosulfonate, etc.
- Preferred naphthalene sulfonates are those materials which contain one or more sulfonated naphthalene nuclei.
- water-soluble naphthalene sulfonates which can be used in accordance with the invention are polymethylene-bis-naphthalene sulfonate, the sodium or potassium salts thereof, and alkyl naphthalene sulfonates or the sodium or potassium salts thereof in which the alkyl group contains about 1-12 carbon atoms.
- Other preferred sulfonates are substituted aryl sulfonates such as sodium xylene sulfonate.
- the organic polydentate ligand and organic sulfonate are preferably present as set out in Composition I below:
- composition I Percent by weight Ligand -80 Sulfonate -90
- a more preferred composition of the invention includes the respective components in the following proportion:
- composition II Percent by Weight Ligand 10-60 Sulfonate 40-90
- a non-ionic wetting agent be employed along with the above described components.
- Preferred classes of non-ionic materials are the alkyl substituted ethoxylated phenols and polyalkoxylated aliphatic substances.
- Other suitable non-ionics wetting agents are the wellknown Pluronic materials which are block copolymers of propylene and ethylene oxide and are described in U.S. Patent 2,674,619.
- Pluronic materials which are block copolymers of propylene and ethylene oxide and are described in U.S. Patent 2,674,619.
- the pitch control compositions of the invention may be applied in solid admixture with or without non-ionic wetting agent or in form of an aqueous solution.
- a combination of water and polar organic solvents may be used as the solvating medium.
- Materials such as alcohols, acetone, dimethyl formamide, sulfoxides, etc. may be employed, as Well as host of other polar organics.
- Preferred organic solvating materials are methanol, ethanol, and isopropyl alcohol.
- the respective components which make up the composition of the invention may be added to the pulp or paper mill system separately or in combination. It is greatly preferred that the chemical pitch control agents be added in the form of a single composition, and more preferably in solvent media.
- Composition III Component: Percent by weight Sodium lignosulphonate 30.0 Sugar acid (primarily sodium salt of glucoheptonic acid-34-38% solids) 30.0 Isopropyl alcohol 9.0 Water 31.0
- composition IV Sodium xylene sulfonate 25.0 Isopropyl alcohol 15.0 Water 30.0 Polyalkoxylated aliphatic base 20.0 Trisodium salt of N-hydroxyethylethylenediaminetriacetic acid 10.0
- the pitch control compositions of the invention may be added to either a pulp or paper mill and are particularly necessary at any point where physical mastication of fiber takes place. At these points release of pitch substances is more prevalent.
- the additive combination may be added in the pulp mill at points such as at the grinders, blow-pits, washers, chests, showers, blending and/or storage tanks etc.
- the pitch control compositions may be incorporated into the pulp stream at the heaters and refiners.
- the composition of the invention may be added to the headboxes, repulpers following washers, lines, etc. Occurrence of pitch is particularly noticed on the Fourdrinier wire and wet press felts.
- application of the pitch control composition at any point in the stream prior to formation of the wet web itself assists in preventin formation of pitch at the just mentioned areas.
- the pitch control agents of the invention may be employed in any type of pulp and paper mill system designed to produce a wide variety of paper products.
- pitch control chemical comprising ligand and sulfonate per ton of pulp (dry weight) gives effective control. More preferably 0.05-10 lbs. per ton are employed.
- the materials are particularly desirable for control of pitch in groundwood and sulfite mills.
- the invention is not limited to the particular type of pulp and paper mill under treatment.
- Composition IV was here tested in a midwestern tissue mill using groundwood, blended sulfite and waste paper furnish. Before application a pitch problem occurred in the machine area on the wires and the felts. Composition IV was fed at a level of 1 pound per ton to the heaters with excellent results. The wires were run about 30 days before any cleaning whatsoever was necessary when the proper pitch control program was carried out employing Composition IV.
- composition of the invention while particularly effective in preventing pitch deposition also control deposition of other materials of varying type whether they occur in form of lumps, stringers, beards, ropes, etc.
- pitch control agents of the invention are useful in preventing deposits of a number of types, including microbiological slimes, fibrous materials and hydrated fines, chemical substances such as alumina, silica, clay, starch, titanium dioxide, and barium salts, calcareous deposits, resinous materials, iron, etc.
- a method of preventing the deposition of pitch and other deposits in pulp and paper mill systems of the til type wherein pulp is masticated and then formed into a sheet which comprises the step of feeding to such systems at a point prior to sheet formation from 0.01 to 20 lbs. of a pitch control composition per ton of pulp on a dry weight basis, said pitch control composition consisting of the following components:
- (B) from 2090% by weight of an organic sulfonate from the group consisting of: lignosulfonates, substituted aryl sulfonates and naphthalene sulfonates.
- component (A) is present in an amount ranging from 10 by weight and component (B) is present in an amont ranging from 40-90% by weight.
- said pitch-control composition additionally contains a non-ionic wetting agent.
- non-ionic wetting agent is a polyalkoxylated aliphatic compound.
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Description
United States Patent 3,398,047 PITCH PREVENTION BY ADDITION OF LIGAND AND ORGANIC SULFONATE Raymond J. Michalski, Riverdale, Ill., assignor to Nalco Chemical Company, Chicago, 11]., a corporation of Delaware No Drawing. Filed Oct. 8, 1964, Ser. No. 402,628 7 Claims. (Cl. 162-48) ABSTRACT OF THE DISCLOSURE This invention deals with treating pulp and paper mill systems to prevent the deposition of pitch in such systems. This is achieved by treating these systems with a composition consisting of a blend of a ligand and an organic sulfonate.
The instant invention is concerned with an improvement in the making of paper. More specific-ally, the present invention relates to a method of preventing deposition of pitch and other precipitants which commonly occur in pulp and paper mill systems.
Recently, the problem of occurrence of deposits of various substances upon equipment employed in pulp and paper mill systems has assumed a position of increasing importance and as well has become more difficult to control. Such deposits generally result in offgrade production, increased maintenance costs, decreased production because of breaks, requirement of more frequent washups, and excessive raw material usage.
One of the most serious problems causing one or more of the above undesirable results in deposition of pitch upon paper and pulp mill equipment, transfer lines, storage tanks, etc. This problem has become more prevalent and burdensome of late due to increased utilization of lower grade pulps from pulp wood of high pitch content. With usage of green pulp woods, pitch deposition becomes increasingly ditficult to handle, resulting in overfrequent shutdowns and loss of production.
The problem of pitch deposits is one which has been found to manifest itself at practically all points in numerous pulp and paper mill operations at one time or another. Quite often it is found that deposits particularly occur at a point in the system shortly after a high degree of de-fibering or after a point of stock dilution. Generally the pitch is released from the pulp in the form of small water-insoluble particles. These particles subsequently agglomerate and deposit upon the fibers and any available surface in the pulp and paper mill system which they contact.
A number of methods of pitch control are employed to combat the just-discussed problem. This includes the use of pitch solvents, polyphosphates, talc, clays, etc. While these have met with some measure of success, in many instances proper pitch control cannot be effected even with benefit of one or more of the above or other additive chemicals employed in the papermaking operation. It would therefore be of benefit to the papermaking art if a composition could be discovered which had excellent activity in controlling pitch deposition. Moreover, if a single composition could be devised which could be usefully employed to inhibit pitch depositions in both pulp and paper mill systems of varying types, such additive would find ready acceptance in the paper field. In view of the above, it therefore becomes an object of the invention to provide an improved papennaking process.
A more specific object of the invention is to provide a method of preventing deposition of pitch and other deposits in pulp and paper mill systems by application of a single extremely effective paper additive composition.
Still another object of the invention is to provide a chemical composition compatible with an aqueous pulp stream which is effective in preventing pitch deposition at economical dosages without fear of deleterious sideeffects.
Other objects will appear hereinafter.
In accordance with the invention, a new and improved method of preventing deposition of pitch and other deposits in pulp and paper mill systems has been discovered. In its broadest aspects, the invention lies in treating a pulp being processed in either of said systems with a pitch control composition in at least an amount sufficient to substantially inhibit the pitch deposition. The pitch control material should include an organic polydentate ligand and an organic sulfonate. By applying these materials in concerted action, surprising efficiency in prevention of pitch deposition is noted.
The organic polydentate ligand material is one which is normally characterized as possessing the ability to form chelate structures. Preferred for use in the invention are multidentate chelating agents which have threeeight donor atoms. These materials are well-known and their structures need little elaboration. Two treatises dealing with a number of organic polydentate ligands are Chemistry of the Coordination Compounds by J. C. Bailar, Jr., Reinhold Publishing Corporation, 1956 and Chelating Agents and Metal Chelates by F. P. Dwyer and D. P. Mellor, Academic Press, 1964.
Preferred polydentate ligands for use in the instant invention include ethylenediamine, glycol, glycerol, mannitol, sorbitol, mono-, di-, and triethanol amines; oxalate and malonate salts; salicylic, lactic, citric, glycollic and tartaric acids; iminodiacetic acid, glycine, nitrilotriacetic acid, ethylenediamine-tetraacetic acid and salts thereof; diketones as acetylacetone, propylenediamine, stilbenediamine, aromatic diamines, biguanide, substituted quinolines, phthalocyanines, porphins, triglycine, etc.
Greatly preferred ligands are aminopolycarboxylic acids and sugar acids. Among the aminopolycarboxylic acids the following are illustrative: ethylenediaminediacetic acid, ethylenediaminedipropionic acid, ethylenediaminetetraacetic acid, 1,2 propylenediaminetetraacetic acid, 1,2 cyclohexanediaminetetraacetic acid, -N- hydroxyethylethylenediaminetriacetic acid.
Salts of the above listed acids or other polyaminocarboxylic acids work equally well in the invention. Alkali metal and alkaline earth metal salts are most preferred to {form carboxytlate materials. Partial salts, that is, amino acids only partly neutralized to varying degrees, may likewise be employed without loss of activity in prevention of pitch deposition. Among the just-named materials the trisodium salt of N-hydroxyethylethylene diaminetriacetic acid is most preferred.
Another class of greatly preferred polydentate ligands is a sugar compound, and more particularly a sugar acid or salt of a sugar acid. These sugar acids are carbohydrates having carboxylic acid function to a greater or lesser degree. Preferred sugar acids or salts are those in which there is at least one carboxylic group or carboxylic salt group per molecule. Generally, these sugar acids or salts have three or more carbon atoms in the molecule. Representative types are sodium heptogluconate, sodium salt of glycoxyacetic acid, various wood sugars and their salts removed from a cook liquor obtained in pulping of wood such as soft woods, carboxylic acids or acid salts of glucose, allose, dextrose, sucrose, etc. Mono-, di-, tri-, and tetra saccharides having some free carboxyl character or carboxylic salt function may all be usefully employed. Preferred substances are sodium heptogluconate, and the so dium salt of glucoxyacetic acid.
If the sugar acid is derived from reaction of a sugar, such as sucrose, and a halocarboxylic acid or acid salt such as chloroacetic acid or sodium chloroacetiate, it is preferred that a molar ratio of acid or acid salt to sugar of from 1:1 to 4.1 be employed.
The following example illustrates preparation of a typical sugar acid useful in the invention to inhibit pitch deposition.
EXAMPLE I 15.20 parts of sucrose, 4.50 parts of chloroacetic acid and 3.80 parts of 50% sodium hydroxide were added together and allowed to react at about room temperature while mixing was effected. The strong base was present to neutralize any hydrochloric acid formed in the reaction between the chloroacetic acid and sucrose. The resultant product can be used directly as one of the components of the compositions of the invention.
The other component used in making up the pitch control compositions of the invention is an organic sulfonate. Again, these materials are well-known products of commerce. Both alkyl and aryl sulfonates as well as alkaryl sulfonate substances may be employed. For example, petroleum sulfonates are a useful class. Particularly preferred organic sulfonates are water-soluble lignosulfonates, substituted aryl sulfonates and naphthalene sulfonates.
Particularly preferred are water-soluble lignosulfonates derived as by-products in the manufacture of sulfite pulp where wood is cooked with calcium bisulfite-magnesium bisulfite-sulfur dioxide liquor. In this process the lignin is converted to lignosulfonic acid which is thereafter converted to a solid salt product such as calcium lignosulfonate, ammonium lignosulfonate, potassium lignosulfate, sodium lignosulfonate, etc.
Preferred naphthalene sulfonates are those materials which contain one or more sulfonated naphthalene nuclei. Examples of water-soluble naphthalene sulfonates which can be used in accordance with the invention are polymethylene-bis-naphthalene sulfonate, the sodium or potassium salts thereof, and alkyl naphthalene sulfonates or the sodium or potassium salts thereof in which the alkyl group contains about 1-12 carbon atoms. Other preferred sulfonates are substituted aryl sulfonates such as sodium xylene sulfonate.
When used in combination to control the deposition of pitch, the organic polydentate ligand and organic sulfonate are preferably present as set out in Composition I below:
Composition I Component: Percent by weight Ligand -80 Sulfonate -90 A more preferred composition of the invention includes the respective components in the following proportion:
Composition II Component: Percent by Weight Ligand 10-60 Sulfonate 40-90 In a specific embodiment of the invention, it is preferred that a non-ionic wetting agent be employed along with the above described components. Preferred classes of non-ionic materials are the alkyl substituted ethoxylated phenols and polyalkoxylated aliphatic substances. Other suitable non-ionics wetting agents are the wellknown Pluronic materials which are block copolymers of propylene and ethylene oxide and are described in U.S. Patent 2,674,619. For a more comprehensive and detailed list of various non-ionic wetting agents that may be used, reference may be made to the publication, Detergents and Emulsifiers to Date by John W. McCutcheon, John W. McCutcheon, Inc., 1963.
The pitch control compositions of the invention may be applied in solid admixture with or without non-ionic wetting agent or in form of an aqueous solution. In some instances a combination of water and polar organic solvents may be used as the solvating medium. Materials such as alcohols, acetone, dimethyl formamide, sulfoxides, etc. may be employed, as Well as host of other polar organics. Preferred organic solvating materials are methanol, ethanol, and isopropyl alcohol.
Again, the respective components which make up the composition of the invention may be added to the pulp or paper mill system separately or in combination. It is greatly preferred that the chemical pitch control agents be added in the form of a single composition, and more preferably in solvent media.
Illustrative solutions of pitch control reagents are given as follows:
Composition III Component: Percent by weight Sodium lignosulphonate 30.0 Sugar acid (primarily sodium salt of glucoheptonic acid-34-38% solids) 30.0 Isopropyl alcohol 9.0 Water 31.0
Composition IV Sodium xylene sulfonate 25.0 Isopropyl alcohol 15.0 Water 30.0 Polyalkoxylated aliphatic base 20.0 Trisodium salt of N-hydroxyethylethylenediaminetriacetic acid 10.0
The pitch control compositions of the invention may be added to either a pulp or paper mill and are particularly necessary at any point where physical mastication of fiber takes place. At these points release of pitch substances is more prevalent.
Thus the additive combination may be added in the pulp mill at points such as at the grinders, blow-pits, washers, chests, showers, blending and/or storage tanks etc.
In the paper mill the pitch control compositions may be incorporated into the pulp stream at the heaters and refiners. Likewise, the composition of the invention may be added to the headboxes, repulpers following washers, lines, etc. Occurrence of pitch is particularly noticed on the Fourdrinier wire and wet press felts. Thus, application of the pitch control composition at any point in the stream prior to formation of the wet web itself assists in preventin formation of pitch at the just mentioned areas.
Again, the pitch control agents of the invention may be employed in any type of pulp and paper mill system designed to produce a wide variety of paper products. Generally, 0.01-20 lbs. of pitch control chemical comprising ligand and sulfonate per ton of pulp (dry weight) gives effective control. More preferably 0.05-10 lbs. per ton are employed. The materials are particularly desirable for control of pitch in groundwood and sulfite mills. However, it is understood that the invention is not limited to the particular type of pulp and paper mill under treatment.
In order to illustrate the efiicacy of the invention, the following examples are given by way of illustration. It is understood, of course, that the invention is not limited thereto.
EXAMPLE II In this test a paper mill located in the northwest area of the country was treated with Composition IV whose chemical make-up was outlined above. The mill was engaged in making napkin on a Fourdrinier machine operating at pH 7-8. Total hardness of the water was 195 ppm. The tray water temperature was -90 F. The stock furnish was primarily bleached sulfite with some bleached kraft. Previously, a pitch control program employing 2.5 pounds of prior art pitch control material per ton of pulp added to the beater had been unsuccessful. Particularly, pitch control problems occurred by way of deposit build-up on the table rolls, wire return rolls, and wire itself. Also, pitch deposition occurred on the press roll doctor blades and in the head box. Composition IV at a level of 0.25-.5 pound per ton added to the beater gave excellent results and substantially inhibited pitch deposition in all areas.
EXAMPLE III At a southern unbleached kraft mill, Composition IV was fed continuously to .the secondary fan pump at a level of 0.25 pound per ton. The secondary head box was maintained completely free of deposits. Heretofore, no pitch control chemical tested had been effectual.
' EXAMPLE IV Composition IV was here tested in a midwestern tissue mill using groundwood, blended sulfite and waste paper furnish. Before application a pitch problem occurred in the machine area on the wires and the felts. Composition IV was fed at a level of 1 pound per ton to the heaters with excellent results. The wires were run about 30 days before any cleaning whatsoever was necessary when the proper pitch control program was carried out employing Composition IV.
It was also noted that the composition of the invention while particularly effective in preventing pitch deposition also control deposition of other materials of varying type whether they occur in form of lumps, stringers, beards, ropes, etc. More particularly, the pitch control agents of the invention are useful in preventing deposits of a number of types, including microbiological slimes, fibrous materials and hydrated fines, chemical substances such as alumina, silica, clay, starch, titanium dioxide, and barium salts, calcareous deposits, resinous materials, iron, etc.
The invention is hereby claimed as follows:
1. A method of preventing the deposition of pitch and other deposits in pulp and paper mill systems of the til type wherein pulp is masticated and then formed into a sheet which comprises the step of feeding to such systems at a point prior to sheet formation from 0.01 to 20 lbs. of a pitch control composition per ton of pulp on a dry weight basis, said pitch control composition consisting of the following components:
(A) from 10-80% by weight of a ligand from the group consisting of: polyaminocarboxylic acids, sugar acids, and salts thereof; and
(B) from 2090% by weight of an organic sulfonate from the group consisting of: lignosulfonates, substituted aryl sulfonates and naphthalene sulfonates.
2. The method of claim 1 wherein component (A) is present in an amount ranging from 10 by weight and component (B) is present in an amont ranging from 40-90% by weight.
3. The method of claim 1 wherein said lignosulfonate is an alkali metal lignosulfonate.
4. The method of claim 1 wherein said sugar acid is sodium heptogluconate.
5. The method of claim 1 wherein said ligand is the trisodium salt of N-hydroxyethylethylenediaminetriacetic acid.
6. The method of claim 1 wherein said pitch-control composition additionally contains a non-ionic wetting agent.
7. The method of claim 6 wherein said non-ionic wetting agent is a polyalkoxylated aliphatic compound.
References Cited UNITED STATES PATENTS 2,753,309 7/1956 Figdor 162190X 3,071,504 1/1963 Dunklin 162-199 3,256,140 6/1966 Poschmann 162190 OTHER REFERENCES Brauns: The Elimination of Pitch Trouble, Pulp and Paper of Canada, pp. 333-336, September 1932.
DONALL H. SYLVESTER, Primary Examiner.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US402628A US3398047A (en) | 1964-10-08 | 1964-10-08 | Pitch prevention by addition of ligand and organic sulfonate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US402628A US3398047A (en) | 1964-10-08 | 1964-10-08 | Pitch prevention by addition of ligand and organic sulfonate |
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| Publication Number | Publication Date |
|---|---|
| US3398047A true US3398047A (en) | 1968-08-20 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US402628A Expired - Lifetime US3398047A (en) | 1964-10-08 | 1964-10-08 | Pitch prevention by addition of ligand and organic sulfonate |
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| Country | Link |
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| US (1) | US3398047A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3630830A (en) * | 1969-06-30 | 1971-12-28 | Eastman Kodak Co | Method for surface sizing of paper |
| US3896046A (en) * | 1972-09-07 | 1975-07-22 | Key Chemicals Inc | Composition for controlling pitch in paper manufacture |
| US4715931A (en) * | 1987-03-24 | 1987-12-29 | Betz Laboratories, Inc. | Process for inhibiting aluminum hydroxide deposition in papermaking felts |
| US4861429A (en) * | 1988-07-29 | 1989-08-29 | Betz Laboratories, Inc. | Process for inhibiting white pitch deposition in papermaking felts |
| US4895622A (en) * | 1988-11-09 | 1990-01-23 | Betz Laboratories, Inc. | Press felt conditioner for neutral and alkaline papermaking systems |
| US4995944A (en) * | 1988-09-16 | 1991-02-26 | Dearborn Chemical Company Ltd. | Controlling deposits on paper machine felts using cationic polymer and cationic surfactant mixture |
| US5167767A (en) * | 1991-03-25 | 1992-12-01 | Betz Paperchem, Inc. | Paper mill press felt conditioner |
| WO2017007614A1 (en) | 2015-07-07 | 2017-01-12 | Solenis Technologies, L.P. | Methods for inhibiting the deposition of organic contaminants in pulp and papermaking systems |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2753309A (en) * | 1951-10-27 | 1956-07-03 | Pioneer Chemical Works Inc | Defoaming agents |
| US3071504A (en) * | 1958-05-12 | 1963-01-01 | Us Movidyn Corp | Paper mill boil out methods and compositions |
| US3256140A (en) * | 1961-05-03 | 1966-06-14 | Basf Ag | Flotation of paper fibers |
-
1964
- 1964-10-08 US US402628A patent/US3398047A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2753309A (en) * | 1951-10-27 | 1956-07-03 | Pioneer Chemical Works Inc | Defoaming agents |
| US3071504A (en) * | 1958-05-12 | 1963-01-01 | Us Movidyn Corp | Paper mill boil out methods and compositions |
| US3256140A (en) * | 1961-05-03 | 1966-06-14 | Basf Ag | Flotation of paper fibers |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3630830A (en) * | 1969-06-30 | 1971-12-28 | Eastman Kodak Co | Method for surface sizing of paper |
| US3896046A (en) * | 1972-09-07 | 1975-07-22 | Key Chemicals Inc | Composition for controlling pitch in paper manufacture |
| US4715931A (en) * | 1987-03-24 | 1987-12-29 | Betz Laboratories, Inc. | Process for inhibiting aluminum hydroxide deposition in papermaking felts |
| US4861429A (en) * | 1988-07-29 | 1989-08-29 | Betz Laboratories, Inc. | Process for inhibiting white pitch deposition in papermaking felts |
| US4995944A (en) * | 1988-09-16 | 1991-02-26 | Dearborn Chemical Company Ltd. | Controlling deposits on paper machine felts using cationic polymer and cationic surfactant mixture |
| US4895622A (en) * | 1988-11-09 | 1990-01-23 | Betz Laboratories, Inc. | Press felt conditioner for neutral and alkaline papermaking systems |
| US5167767A (en) * | 1991-03-25 | 1992-12-01 | Betz Paperchem, Inc. | Paper mill press felt conditioner |
| WO2017007614A1 (en) | 2015-07-07 | 2017-01-12 | Solenis Technologies, L.P. | Methods for inhibiting the deposition of organic contaminants in pulp and papermaking systems |
| US10253214B2 (en) | 2015-07-07 | 2019-04-09 | Solenis Technologies, L.P. | Methods for inhibiting the deposition of organic contaminates in pulp and papermaking systems |
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