CA2010189C - Process for trash removal or pitch-like resin control in the paper manufacture - Google Patents
Process for trash removal or pitch-like resin control in the paper manufacture Download PDFInfo
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- CA2010189C CA2010189C CA002010189A CA2010189A CA2010189C CA 2010189 C CA2010189 C CA 2010189C CA 002010189 A CA002010189 A CA 002010189A CA 2010189 A CA2010189 A CA 2010189A CA 2010189 C CA2010189 C CA 2010189C
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- 239000010813 municipal solid waste Substances 0.000 title claims abstract description 46
- 238000000034 method Methods 0.000 title claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 239000011347 resin Substances 0.000 title description 7
- 229920005989 resin Polymers 0.000 title description 6
- 229920000642 polymer Polymers 0.000 claims abstract description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 31
- 125000002091 cationic group Chemical group 0.000 claims abstract description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 5
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 claims abstract description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 5
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims abstract description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 4
- FLCAEMBIQVZWIF-UHFFFAOYSA-N 6-(dimethylamino)-2-methylhex-2-enamide Chemical compound CN(C)CCCC=C(C)C(N)=O FLCAEMBIQVZWIF-UHFFFAOYSA-N 0.000 claims abstract 3
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 9
- 229920001131 Pulp (paper) Polymers 0.000 claims description 5
- 125000000129 anionic group Chemical group 0.000 claims description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 3
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 claims description 2
- 229940073608 benzyl chloride Drugs 0.000 claims description 2
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 claims description 2
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 claims description 2
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 claims description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000000416 hydrocolloid Substances 0.000 claims description 2
- 239000000178 monomer Substances 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- ZWAPMFBHEQZLGK-UHFFFAOYSA-N 5-(dimethylamino)-2-methylidenepentanamide Chemical compound CN(C)CCCC(=C)C(N)=O ZWAPMFBHEQZLGK-UHFFFAOYSA-N 0.000 claims 2
- 239000006227 byproduct Substances 0.000 claims 1
- 230000001747 exhibiting effect Effects 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 abstract description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 230000014759 maintenance of location Effects 0.000 description 12
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000000725 suspension Substances 0.000 description 7
- 229910000019 calcium carbonate Inorganic materials 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 229940010048 aluminum sulfate Drugs 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 235000010216 calcium carbonate Nutrition 0.000 description 4
- 229960003563 calcium carbonate Drugs 0.000 description 4
- 229910001873 dinitrogen Inorganic materials 0.000 description 4
- 238000005755 formation reaction Methods 0.000 description 4
- 239000010893 paper waste Substances 0.000 description 4
- 238000010926 purge Methods 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- 239000008399 tap water Substances 0.000 description 4
- 235000020679 tap water Nutrition 0.000 description 4
- 239000002351 wastewater Substances 0.000 description 4
- 229940037003 alum Drugs 0.000 description 3
- 238000010009 beating Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 3
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 229920002488 Hemicellulose Polymers 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000329 aluminium sulfate Inorganic materials 0.000 description 1
- 235000011128 aluminium sulphate Nutrition 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- -1 dimethylaminopropyl Chemical group 0.000 description 1
- 239000013051 drainage agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical class NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- DNHVXYDGZKWYNU-UHFFFAOYSA-N lead;hydrate Chemical compound O.[Pb] DNHVXYDGZKWYNU-UHFFFAOYSA-N 0.000 description 1
- 235000009408 lignans Nutrition 0.000 description 1
- 230000005291 magnetic effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 238000000643 oven drying Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 229960002668 sodium chloride Drugs 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- UZNHKBFIBYXPDV-UHFFFAOYSA-N trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)NCCC[N+](C)(C)C UZNHKBFIBYXPDV-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 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
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
- D21H17/44—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups cationic
- D21H17/45—Nitrogen-containing groups
- D21H17/455—Nitrogen-containing groups comprising tertiary amine or being at least partially quaternised
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paper (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Water Treatment By Sorption (AREA)
- Surgical Instruments (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
- Analysing Materials By The Use Of Radiation (AREA)
Abstract
The present invention relates to a process for trash removal or pitch control in the paper manufacture, in which process as agent for the trash removal or pitch control cationic groups containing polymers of 50 to 100%-wt.
quaternized dimethylaminopropylmethacrylamide or dimethylaminapropylmethacrylamide and 0 to 50%-wt acrylamide, acrylic acid, methacrylic acid, acrylamidomethylpropanesulfonic acid, are used, which polymers have an intrinsic viscosity of smaller than 150 ml/g. The trash removal or pitch control agent is added to the pulp flow and/or the circuit water in amounts of up to 1%-wt., relative to the dry weight of the paper manufactured.
quaternized dimethylaminopropylmethacrylamide or dimethylaminapropylmethacrylamide and 0 to 50%-wt acrylamide, acrylic acid, methacrylic acid, acrylamidomethylpropanesulfonic acid, are used, which polymers have an intrinsic viscosity of smaller than 150 ml/g. The trash removal or pitch control agent is added to the pulp flow and/or the circuit water in amounts of up to 1%-wt., relative to the dry weight of the paper manufactured.
Description
1 ~~1~1~~
D E S C R I P T I O N
The present invention relates to a process for trash removal or pitch control in the paper manufacture.
During the last decades, the paper industry succeeded in reducing considerably the specific fresh water consumption and the specific waste water amount by concentrating and closing the water circuits in the paper manufacture. Reasons for said concentration, on the one hand is to avoid loss of matter with waste water, on the other hand there are the official requirements with respect to composition and amount of waste water abducted according to the law concerning waste-water emission.
Many new problems have arisen due to this concentration of the water amount. Due to the increased portion of circuit water the temperature within the pulp system partially in-creases considerably. Thus increased slime formation may result. Higher electrolyte concentrations in the process water lead to earlier corrosion. Due to anaerobic zones within the water cycle, problems in connection with odour may arise.
However, the major problem in connection with concentrating ~U1~189 the water circuit is the enrichment of organic substances in the recycled water, the so-called trash or pitch-like res-ins. According to Auhorn "Wochenblatt fur Papierfabrikation 112, 37-48 (1984)" these matter consist of dissolved or colloidally dissolved anionic oligomers or polymers, and non-ionic hydrocolloids. They are formed in the production and processing of cellulose, wood pulp, and waste paper as lignanes or polysaccharides or oligosaccharides deriving from the hemicelluloses. Other trash originates from the anionic auxiliaries used in papermaking.
The concentration of such "water-soluble" substances con-siderably increases with increasing concentration of re-cycled water. The circuit water of paper machines is extreme-ly loaded with such trash or pitch-like resins, if wood-con-taming paper is made.
The trash impairs the paper manufacture in many respects.
They influence pulp beating due to less fiber swelling and delayed beating effect, they lead to increased sedimentation within the circuit and the pulp flow of a paper making machine.
Furthermore, deterioration of retention, drainage, sheet formation, as well as paper strength are to be observed. The efficiency of practically all chemical auxiliaries is affect-s 2~~~~8~
ed by the pitch-like resins. This is true, e.g., in case of auxiliaries for retention and drainage, wet and dry strength agents, sizing agents, defoamers, bleaching chemicals, and dyes. The trash concentration can become a limiting factor for the cycle concentration.
In former times, the addition of aluminum sulfate was common so that these problems could widely be prevented. The high adsorption capacity of the intermediate Al-complexes effects a relief of the recycled water of inorganic and organic impurities. Due to todays neutral operation, aluminum sulfa-to used as precipitation and fixing agent can no longer be employed. This also results from the fact that calcium car-bonate is presently used as coating arid filling pigment due to economic and qualitative considerations.
Due to the increased use of calcium carbonate, the produc-tion problems in processing the calcium carbonate containing coating refuse and the waste paper in the acidic range have grown considerably.
Thus the problem arose to eliminate the trash from the re-cycled water of the paper manufacturing factories with simultaneously minimizing the aluminium sulfate formerly used.
First hints to solve this problem are already known. Accord 4 2fl~0~89 ing to Arheilger and von Medvey, "Wochenblatt fur Papierfa-brikation 114, 958-961 (1986)", highly wood-containing, coated paper is produced using calcium carbonate without the addition of alum. This was achieved by adding polydiallyldi-methyl ammonium chloride (PolyDadmac) to the circuit water.
However, PolyDadmac does not seem to have all of the posi-tive characteristics as alum. For example, considerable difficulties arose in connection with combatting the forma-tion of slime, which could only be removed by the use of other agents.
Furthermore, in contrast to alum, PolyDadmac also fixed chromophoric substances in such a way that the addition of fixing agents in industrial scale lead to a decrease of whiteness of approximately 1.5 points of whiteness, which resulted in a significant increase of costs for bleaching agents.
Thus, the problem of finding substitutes for aluminum sul-fate in the elimination of trash or pitch-like resins, which do not exhibit negative side effects, still remains.
In DE-OS 36 20 065 another method is used: There special drainage, retention and flocculating agents are used, namely high molecular, water-soluble polymers of N-vinylamides, which only exhibit their efficiency in the presence of ~~1~~89 trash, which contain as accompanying substances phenolic groups containing oligomers and/or polymers of the sub-stances of wood. These special N-vinylamide-polymers thus are insensitive to pitch-like-resins which are always pres-ent in the paper manufacture in case of concentrated or closed water circuits.
It is a disadvantage of this method that trash removal does not take place, and in particular that the known commonly used agents in the paper industry, i.e., flocculating-, drainage-, and retention-agents, on the basis of cationic polymers cannot be employed.
It is accordingly an object of the present invention to perform trash removal in a simple and efficient way without having to make use of aluminum sulfate, and wherein the auxiliaries, known and proven per se, on the basis of cation-is polymers can be used as drainage-, retention-, and floccu-lating-auxiliaries without reducing their efficiency.
According to the present invention this object is achieved by the use of polymers (homopolymers and/or copolymers) on the basis of quaternized dimethylaminopropyl (meth-)acryl-amides, which polymers are added to the pulp flaw and/or to the circuit water, whereby these polymers have an intrinsic viscosity of less than 150 ml/g determined in 10%-wt 2~~0189 sodium-chloride solution.
The polymers used according to the present invention advan-tageously consist of 50 to 100-wt quaternized dimethylamino-propyl(meth-)acrylamide and 0 to 50%-wt acrylamide, acrylic acid, methacrylic acid, acrylamidomethylpropanesulfonic acid, or of mixtures of these cationic and anionic monomers.
The dimethylaminopropyl(meth)acrylamide is quaternized with the usual and known quaternizing agents, e.g., dimethyl sulfate, dimethyl carbonate, benzyl chloride, methyl chlo-ride, or ethyl bromide.
The polymers are used in an amount of 0.05 to 1~-wt, rela-tive to the dry weight of the paper produced, and in fact applied in addition to the usual auxiliaries, in that they are added to the pulp flow and/or to the circuit water. It is preferred to employ the polymer used as trash remover in an amount of 0.2 to 0.8~-wt, relative to the dry weight of the paper produced.
Advantageously the total amount of polymer added for trash removal can be distributed to several feeders.
Surprisingly, it is achieved by the polymers used according to the present invention that ~~~018~
a) the trash contained in the plant water is fixed at the paper fiber and b) the degree of whiteness of the paper such produced is not impaired by the trash adsorption.
The polymers according to the present invention employed as trash removers or pitch control agents are preferably used in neutral operation without the addition of aluminum sul-fate. However, it is possible, too, to use these products in combination with aluminum sulfate according the pseudoneu-tral operation.
The polymers used according to the present invention are of particular advantage in the paper manufacture where the water circuit is closed by more than 900.
The invention is further illustrated by the following exam-ples which are not construed as limiting:
Tf not indicated to the contrary, the parts given are always parts by weight.
8 ~~~U~B~
A) Production of the golymers Polymer 1:
250 parts of acrylamidopropyltrimethyl ammonium chloride are dissolved in 750 parts of water. A pH-value of 5.U is adjust-ed. During purging with nitrogen gas, it is heated to 75°C.
After the addition of 0.6 part of potassium peroxodisulfate polymerisation starts.
The final temperature of 90°C is achieved within 5 minutes.
After cooling, the product has a viscosity of 1050 mPa.s, the intrinsic viscosity amounts to 120 ml/g.
Polymer 2:
180 parts of acrylamidopropyltrimethyl ammonium chloride and 180 parts of acrylamidomethylpropanesulfonic acid are dis-solved one after the other in 568 parts of water. A pH of 5.0 is adjusted using 72 parts of 45o caustic soda solution.
During purging with nitrogen gas, it is heated to 75°C.
After the addition of 0.6 part of potassium peroxodisulfate polymerisation starts. The final temperature of 92°C is achieved within 10 minutes. After cooling, the product exhi-bits a viscosity of 860 mPa.s, the intrinsic viscosity amounts to 75 ml/g.
Polymer 3:
~9~0~89 200 parts of acrylamidopropyltrimethyl ammonium chloride are dissolved in 709 parts of water. After addition of 50 parts of acrylic acid, it is adjusted to pH 5.0 using 41 parts of 45% caustic soda solution. During purging with nitrogen gas, it is heated to 75°C. After the addition of 0.4 part of potassium peroxodisulfate polymerisation starts. The final temperature of 94°C is achieved within 7 minutes. After cooling, the product has a viscosity of 750 mPa.s, the in-trinsic viscosity amounts to 98 ml/g.
Polymer 4:
210 parts of methacrylam.idopropyltrimethyl ammonium chloride are dissolved in 6~8 parts of water. After addition of 90 parts of methacrylic acid, a pH of 5.0 is adjusted using 62 parts of 45% caustic soda solution. During purging with nitrogen gas, it is heated to 75°C. After the addition of 0.8 part of potassium peroxodisulfate polymerisation starts.
The final temperature of 91°C is achieved within 15 minutes.
After cooling, the product exhibits a viscosity of 890 mPa.s, the intrinsic viscosity amounts to 105 ml/g.
~(3~.~J3,~3~
Polymer 5:
210 parts of methacrylamidopropyltrimethyl ammonium chloride and 30 parts of acrylamidomethylpropanesulfonic acid are dissolved one after the other in 646 of parts water. After addition of 60 parts of acrylic acid, a pH of 5.0 is adjust-ed using 54 parts of 45% caustic soda solution. After the addition of 0.8 part of potassium peroxodisulfate polymerisa-tion starts. The final -temperature of 94°C is achieved with-in 12 minutes. After cooling, the product exhibits a viscosi-ty of 740 mPa.s, the intrinsic viscosity amounts to 88 ml/g.
As comparative polymer a polydimethyldiallyl ammonium chloride having an intrinsic viscosity of 95 ml/g was used in the examinations with respect to technical application.
B) Examinations with respect to the technical application:
As proof of the trash removal or pitch control the following methods are usual:
1. The efficiency of cationic drainage and retention agents is decreased by the anionic trash. After addition of trash remover the drainage and retention efficiency is improved and determined quantitatively.
11 ~~~.~~.~~
2. The degree of whiteness achieved in the paper is measured according to DIN 53145. A reduction of whiteness of the paper is effected by fixing certain trash or pitch-like resins and chromophores at the paper fibres.
Naturally the degree of whiteness is highest without control agents; and it is reduced by a considerably lower degree when the trash removers or pitch control agents according to the present invention are used compared with the result when using the comparative substances.
I. Pulp drainage, Schopper-Riegler-method The appartus used is described in "Zellstoff Papier, 5th edition, VEB publishers, Leipzig, pages 387-388". It was modified in such a way that both discharge ports are empty-ing into a common receiving vessel. Thus it is achieved that no longer the degree of beating but exclusively the pulp drainage is measured.
A waste paper pulp having a solids content of 45 was used.
D E S C R I P T I O N
The present invention relates to a process for trash removal or pitch control in the paper manufacture.
During the last decades, the paper industry succeeded in reducing considerably the specific fresh water consumption and the specific waste water amount by concentrating and closing the water circuits in the paper manufacture. Reasons for said concentration, on the one hand is to avoid loss of matter with waste water, on the other hand there are the official requirements with respect to composition and amount of waste water abducted according to the law concerning waste-water emission.
Many new problems have arisen due to this concentration of the water amount. Due to the increased portion of circuit water the temperature within the pulp system partially in-creases considerably. Thus increased slime formation may result. Higher electrolyte concentrations in the process water lead to earlier corrosion. Due to anaerobic zones within the water cycle, problems in connection with odour may arise.
However, the major problem in connection with concentrating ~U1~189 the water circuit is the enrichment of organic substances in the recycled water, the so-called trash or pitch-like res-ins. According to Auhorn "Wochenblatt fur Papierfabrikation 112, 37-48 (1984)" these matter consist of dissolved or colloidally dissolved anionic oligomers or polymers, and non-ionic hydrocolloids. They are formed in the production and processing of cellulose, wood pulp, and waste paper as lignanes or polysaccharides or oligosaccharides deriving from the hemicelluloses. Other trash originates from the anionic auxiliaries used in papermaking.
The concentration of such "water-soluble" substances con-siderably increases with increasing concentration of re-cycled water. The circuit water of paper machines is extreme-ly loaded with such trash or pitch-like resins, if wood-con-taming paper is made.
The trash impairs the paper manufacture in many respects.
They influence pulp beating due to less fiber swelling and delayed beating effect, they lead to increased sedimentation within the circuit and the pulp flow of a paper making machine.
Furthermore, deterioration of retention, drainage, sheet formation, as well as paper strength are to be observed. The efficiency of practically all chemical auxiliaries is affect-s 2~~~~8~
ed by the pitch-like resins. This is true, e.g., in case of auxiliaries for retention and drainage, wet and dry strength agents, sizing agents, defoamers, bleaching chemicals, and dyes. The trash concentration can become a limiting factor for the cycle concentration.
In former times, the addition of aluminum sulfate was common so that these problems could widely be prevented. The high adsorption capacity of the intermediate Al-complexes effects a relief of the recycled water of inorganic and organic impurities. Due to todays neutral operation, aluminum sulfa-to used as precipitation and fixing agent can no longer be employed. This also results from the fact that calcium car-bonate is presently used as coating arid filling pigment due to economic and qualitative considerations.
Due to the increased use of calcium carbonate, the produc-tion problems in processing the calcium carbonate containing coating refuse and the waste paper in the acidic range have grown considerably.
Thus the problem arose to eliminate the trash from the re-cycled water of the paper manufacturing factories with simultaneously minimizing the aluminium sulfate formerly used.
First hints to solve this problem are already known. Accord 4 2fl~0~89 ing to Arheilger and von Medvey, "Wochenblatt fur Papierfa-brikation 114, 958-961 (1986)", highly wood-containing, coated paper is produced using calcium carbonate without the addition of alum. This was achieved by adding polydiallyldi-methyl ammonium chloride (PolyDadmac) to the circuit water.
However, PolyDadmac does not seem to have all of the posi-tive characteristics as alum. For example, considerable difficulties arose in connection with combatting the forma-tion of slime, which could only be removed by the use of other agents.
Furthermore, in contrast to alum, PolyDadmac also fixed chromophoric substances in such a way that the addition of fixing agents in industrial scale lead to a decrease of whiteness of approximately 1.5 points of whiteness, which resulted in a significant increase of costs for bleaching agents.
Thus, the problem of finding substitutes for aluminum sul-fate in the elimination of trash or pitch-like resins, which do not exhibit negative side effects, still remains.
In DE-OS 36 20 065 another method is used: There special drainage, retention and flocculating agents are used, namely high molecular, water-soluble polymers of N-vinylamides, which only exhibit their efficiency in the presence of ~~1~~89 trash, which contain as accompanying substances phenolic groups containing oligomers and/or polymers of the sub-stances of wood. These special N-vinylamide-polymers thus are insensitive to pitch-like-resins which are always pres-ent in the paper manufacture in case of concentrated or closed water circuits.
It is a disadvantage of this method that trash removal does not take place, and in particular that the known commonly used agents in the paper industry, i.e., flocculating-, drainage-, and retention-agents, on the basis of cationic polymers cannot be employed.
It is accordingly an object of the present invention to perform trash removal in a simple and efficient way without having to make use of aluminum sulfate, and wherein the auxiliaries, known and proven per se, on the basis of cation-is polymers can be used as drainage-, retention-, and floccu-lating-auxiliaries without reducing their efficiency.
According to the present invention this object is achieved by the use of polymers (homopolymers and/or copolymers) on the basis of quaternized dimethylaminopropyl (meth-)acryl-amides, which polymers are added to the pulp flaw and/or to the circuit water, whereby these polymers have an intrinsic viscosity of less than 150 ml/g determined in 10%-wt 2~~0189 sodium-chloride solution.
The polymers used according to the present invention advan-tageously consist of 50 to 100-wt quaternized dimethylamino-propyl(meth-)acrylamide and 0 to 50%-wt acrylamide, acrylic acid, methacrylic acid, acrylamidomethylpropanesulfonic acid, or of mixtures of these cationic and anionic monomers.
The dimethylaminopropyl(meth)acrylamide is quaternized with the usual and known quaternizing agents, e.g., dimethyl sulfate, dimethyl carbonate, benzyl chloride, methyl chlo-ride, or ethyl bromide.
The polymers are used in an amount of 0.05 to 1~-wt, rela-tive to the dry weight of the paper produced, and in fact applied in addition to the usual auxiliaries, in that they are added to the pulp flow and/or to the circuit water. It is preferred to employ the polymer used as trash remover in an amount of 0.2 to 0.8~-wt, relative to the dry weight of the paper produced.
Advantageously the total amount of polymer added for trash removal can be distributed to several feeders.
Surprisingly, it is achieved by the polymers used according to the present invention that ~~~018~
a) the trash contained in the plant water is fixed at the paper fiber and b) the degree of whiteness of the paper such produced is not impaired by the trash adsorption.
The polymers according to the present invention employed as trash removers or pitch control agents are preferably used in neutral operation without the addition of aluminum sul-fate. However, it is possible, too, to use these products in combination with aluminum sulfate according the pseudoneu-tral operation.
The polymers used according to the present invention are of particular advantage in the paper manufacture where the water circuit is closed by more than 900.
The invention is further illustrated by the following exam-ples which are not construed as limiting:
Tf not indicated to the contrary, the parts given are always parts by weight.
8 ~~~U~B~
A) Production of the golymers Polymer 1:
250 parts of acrylamidopropyltrimethyl ammonium chloride are dissolved in 750 parts of water. A pH-value of 5.U is adjust-ed. During purging with nitrogen gas, it is heated to 75°C.
After the addition of 0.6 part of potassium peroxodisulfate polymerisation starts.
The final temperature of 90°C is achieved within 5 minutes.
After cooling, the product has a viscosity of 1050 mPa.s, the intrinsic viscosity amounts to 120 ml/g.
Polymer 2:
180 parts of acrylamidopropyltrimethyl ammonium chloride and 180 parts of acrylamidomethylpropanesulfonic acid are dis-solved one after the other in 568 parts of water. A pH of 5.0 is adjusted using 72 parts of 45o caustic soda solution.
During purging with nitrogen gas, it is heated to 75°C.
After the addition of 0.6 part of potassium peroxodisulfate polymerisation starts. The final temperature of 92°C is achieved within 10 minutes. After cooling, the product exhi-bits a viscosity of 860 mPa.s, the intrinsic viscosity amounts to 75 ml/g.
Polymer 3:
~9~0~89 200 parts of acrylamidopropyltrimethyl ammonium chloride are dissolved in 709 parts of water. After addition of 50 parts of acrylic acid, it is adjusted to pH 5.0 using 41 parts of 45% caustic soda solution. During purging with nitrogen gas, it is heated to 75°C. After the addition of 0.4 part of potassium peroxodisulfate polymerisation starts. The final temperature of 94°C is achieved within 7 minutes. After cooling, the product has a viscosity of 750 mPa.s, the in-trinsic viscosity amounts to 98 ml/g.
Polymer 4:
210 parts of methacrylam.idopropyltrimethyl ammonium chloride are dissolved in 6~8 parts of water. After addition of 90 parts of methacrylic acid, a pH of 5.0 is adjusted using 62 parts of 45% caustic soda solution. During purging with nitrogen gas, it is heated to 75°C. After the addition of 0.8 part of potassium peroxodisulfate polymerisation starts.
The final temperature of 91°C is achieved within 15 minutes.
After cooling, the product exhibits a viscosity of 890 mPa.s, the intrinsic viscosity amounts to 105 ml/g.
~(3~.~J3,~3~
Polymer 5:
210 parts of methacrylamidopropyltrimethyl ammonium chloride and 30 parts of acrylamidomethylpropanesulfonic acid are dissolved one after the other in 646 of parts water. After addition of 60 parts of acrylic acid, a pH of 5.0 is adjust-ed using 54 parts of 45% caustic soda solution. After the addition of 0.8 part of potassium peroxodisulfate polymerisa-tion starts. The final -temperature of 94°C is achieved with-in 12 minutes. After cooling, the product exhibits a viscosi-ty of 740 mPa.s, the intrinsic viscosity amounts to 88 ml/g.
As comparative polymer a polydimethyldiallyl ammonium chloride having an intrinsic viscosity of 95 ml/g was used in the examinations with respect to technical application.
B) Examinations with respect to the technical application:
As proof of the trash removal or pitch control the following methods are usual:
1. The efficiency of cationic drainage and retention agents is decreased by the anionic trash. After addition of trash remover the drainage and retention efficiency is improved and determined quantitatively.
11 ~~~.~~.~~
2. The degree of whiteness achieved in the paper is measured according to DIN 53145. A reduction of whiteness of the paper is effected by fixing certain trash or pitch-like resins and chromophores at the paper fibres.
Naturally the degree of whiteness is highest without control agents; and it is reduced by a considerably lower degree when the trash removers or pitch control agents according to the present invention are used compared with the result when using the comparative substances.
I. Pulp drainage, Schopper-Riegler-method The appartus used is described in "Zellstoff Papier, 5th edition, VEB publishers, Leipzig, pages 387-388". It was modified in such a way that both discharge ports are empty-ing into a common receiving vessel. Thus it is achieved that no longer the degree of beating but exclusively the pulp drainage is measured.
A waste paper pulp having a solids content of 45 was used.
3 g oven-dry pulp are diluted with tap water (350 mg/1 CaC03) to a volume of 300 ml. The fixing agent is diluted to a volume of 300 ml and the pulp suspension is added. The suspension is trasferred for three times. Subsequently, the drainage auxiliary is diluted i~o 400 ml and added to the ~~~0~~9 suspension. Then this system is trasferred once and drained in the Schopper-Riegler-apparatus.
The time for 700 ml of drain is determined.
In case of the blank reading the drainage is carried out without control agent and drainage agent; in case of the zero value the trash remover is omitted but drainage auxi-liary added.
As drainage auxiliary a 25$ cationic polyacrylamide is used.
13 ~0'g.~~.~'9 Drainage tests Schopper-Riegler (Time in seconds for 700 ml of filtrate) Drainage auxiliary (%) 0.00 0.01 0.02 0.03 blank reading. 255 zero value . 121 83 67 Trash remover1: 0.3 % 89 71 59 " 1: 0.6 % 78 65 54 Trash remover2: 0.3 % 96 76 63 " 2: 0.6 % 86 69 57 Trash remover3: 0.3 % 93 74 62 " 3: 0.6 % 82 64 57 Trash remover4: 0.3 % 92 71 61 " 4: 0.6 % 82 65 55 Trash remover5: 0.3 % 94 74 63 5: 0.6 % 83 66 56 Compa rison . 0.3 % 115 81 65 0.6 % 105 76 61 14 ~Oq.01$~
2. Determination of retention (Britt-Jar-Test) The apparatus used for the determination of the retention is described in "New methods for monitoring retention", Tappi, February 1976, vol. 59, no. 2, KW. Britt and J. E.
Unbehend. 2.5 g oven-dry pulp (90% wood pulp with 48° S.R., 10% chalk, 60% of which have a particle size of smaller than 2~m, as 71% slurry are diluted with tap water (350 mg/1 CaC03) to 400 ml volume. After addition of the trash remover, the suspension is trasferred 10 times. Subsequent-ly, the retention auxiliary is added as 0.1% solution and the suspension is trasferred thrice. After dilution with water to 500 ml, the suspension is placed into the Britt-Jar-tester and stirred at a rotation of 800 rpm for 15 seconds. Then the discharge valve is openend for 30 seconds under further stirring, and the filtrate is collected.
After filtration of the filtrate over a nutsch provided with a "Schwarzbandfilter" the accepted stock which was not subjected to retention is determined by drying. The reten-Lion is given as percentage of that portion of accepted stock which did not undergo retention to the total accepted stock.
15 i~~~~~~~
Britt-Jar-Test (Retention %) Drainage auxiliary (%) 0.00 0.02 0.03 blank reading. 48.9 zero value . 57.1 61.6 Trash remover1:0.3 % 66.5 71.3 " 1:0.6 % 69.8 75..4 Trash remover2:0.3 % 64.6 70.8 " 2:0.6 % 68.4 75.1 Trash remover3:0.3 % 64.3 70.1 ' 3:0.6 % 68.9 74.3 Trash remover4:0.3 % 65.2 69.9 " 4:0.6 % 69.2 74.8 Trash remover5:0.3 % 64.8 69.3 " 5:0.6 % 68.2 73.9 Comparison . 0.3 % 58.3 62.7 " . 0.6 % 63.9 67.3 16 2~3.~~,~~3 3. Determination of the degree of whiteness a) Sheet formation The waste paper pulp having a solids concentration of 4% is diluted with tap water in an amount of 2.5 g oven-dry to a volume of 500 ml. The trash remover or pitch control agent is added in an amount of 0.4%, relative to oven-dry pulp, as a 0.5% solution and stirred for 30 seconds with a magne-tic stirrer at 500 rpm. Subsequently, the drainage auxili-ary, a 25% cationic polyacrylamide, is added in an amount of 0.03% as 0.01% solution and stirred further for 30 seconds. 4 liters tap water are placed in the sheet former and and is made effervescing by blowing in air. The pulp suspension is now added and is drawn off after mixing.
The surfacing cartboard is applied onto the formed sheet and the sheet is drawn off from the wire. Subsequently, it is dried in the vacuum dryer for 10 minutes followed by oven-drying for 5 minutes. The zero value is obtained with-out fixing agent.
b) Measurement of whiteness Following DIN 53145 the degree of whiteness of the sheets 1 ~ ;~~3.~J9.89 thus made is determined. The measurements were carried out using the Elrepho-apparatus of Messrs. Zeiss, the filter no. 7 having calibrated against MgO.
1 s ~~1~D~.~~
Measurement of whiteness degree whiteness (o) Zero value 65.9 Trash remover1 62.8 Trash remover2 63.2 Trash remover3 62.7 Trash remover4 61.3 Trash remover5 61.9 Comparison 57.3
The time for 700 ml of drain is determined.
In case of the blank reading the drainage is carried out without control agent and drainage agent; in case of the zero value the trash remover is omitted but drainage auxi-liary added.
As drainage auxiliary a 25$ cationic polyacrylamide is used.
13 ~0'g.~~.~'9 Drainage tests Schopper-Riegler (Time in seconds for 700 ml of filtrate) Drainage auxiliary (%) 0.00 0.01 0.02 0.03 blank reading. 255 zero value . 121 83 67 Trash remover1: 0.3 % 89 71 59 " 1: 0.6 % 78 65 54 Trash remover2: 0.3 % 96 76 63 " 2: 0.6 % 86 69 57 Trash remover3: 0.3 % 93 74 62 " 3: 0.6 % 82 64 57 Trash remover4: 0.3 % 92 71 61 " 4: 0.6 % 82 65 55 Trash remover5: 0.3 % 94 74 63 5: 0.6 % 83 66 56 Compa rison . 0.3 % 115 81 65 0.6 % 105 76 61 14 ~Oq.01$~
2. Determination of retention (Britt-Jar-Test) The apparatus used for the determination of the retention is described in "New methods for monitoring retention", Tappi, February 1976, vol. 59, no. 2, KW. Britt and J. E.
Unbehend. 2.5 g oven-dry pulp (90% wood pulp with 48° S.R., 10% chalk, 60% of which have a particle size of smaller than 2~m, as 71% slurry are diluted with tap water (350 mg/1 CaC03) to 400 ml volume. After addition of the trash remover, the suspension is trasferred 10 times. Subsequent-ly, the retention auxiliary is added as 0.1% solution and the suspension is trasferred thrice. After dilution with water to 500 ml, the suspension is placed into the Britt-Jar-tester and stirred at a rotation of 800 rpm for 15 seconds. Then the discharge valve is openend for 30 seconds under further stirring, and the filtrate is collected.
After filtration of the filtrate over a nutsch provided with a "Schwarzbandfilter" the accepted stock which was not subjected to retention is determined by drying. The reten-Lion is given as percentage of that portion of accepted stock which did not undergo retention to the total accepted stock.
15 i~~~~~~~
Britt-Jar-Test (Retention %) Drainage auxiliary (%) 0.00 0.02 0.03 blank reading. 48.9 zero value . 57.1 61.6 Trash remover1:0.3 % 66.5 71.3 " 1:0.6 % 69.8 75..4 Trash remover2:0.3 % 64.6 70.8 " 2:0.6 % 68.4 75.1 Trash remover3:0.3 % 64.3 70.1 ' 3:0.6 % 68.9 74.3 Trash remover4:0.3 % 65.2 69.9 " 4:0.6 % 69.2 74.8 Trash remover5:0.3 % 64.8 69.3 " 5:0.6 % 68.2 73.9 Comparison . 0.3 % 58.3 62.7 " . 0.6 % 63.9 67.3 16 2~3.~~,~~3 3. Determination of the degree of whiteness a) Sheet formation The waste paper pulp having a solids concentration of 4% is diluted with tap water in an amount of 2.5 g oven-dry to a volume of 500 ml. The trash remover or pitch control agent is added in an amount of 0.4%, relative to oven-dry pulp, as a 0.5% solution and stirred for 30 seconds with a magne-tic stirrer at 500 rpm. Subsequently, the drainage auxili-ary, a 25% cationic polyacrylamide, is added in an amount of 0.03% as 0.01% solution and stirred further for 30 seconds. 4 liters tap water are placed in the sheet former and and is made effervescing by blowing in air. The pulp suspension is now added and is drawn off after mixing.
The surfacing cartboard is applied onto the formed sheet and the sheet is drawn off from the wire. Subsequently, it is dried in the vacuum dryer for 10 minutes followed by oven-drying for 5 minutes. The zero value is obtained with-out fixing agent.
b) Measurement of whiteness Following DIN 53145 the degree of whiteness of the sheets 1 ~ ;~~3.~J9.89 thus made is determined. The measurements were carried out using the Elrepho-apparatus of Messrs. Zeiss, the filter no. 7 having calibrated against MgO.
1 s ~~1~D~.~~
Measurement of whiteness degree whiteness (o) Zero value 65.9 Trash remover1 62.8 Trash remover2 63.2 Trash remover3 62.7 Trash remover4 61.3 Trash remover5 61.9 Comparison 57.3
Claims (10)
1. In the manufacture of paper wherein paper pulp is contacted with water and chemicals resulting in production of by-product trash comprising dissolved or colloidally dissolved anionic oligomers or polymers and non-ionic hydrocolloids, which trash is contained in the water, and the water is recycled, the method of preventing excessive build-up of the trash in the recycled water which comprises incorporating into the recycled water a polymer consisting essentially of a) 50 to 100%-wt. quaternized dimethylaminopropylacrylamide or dimethylaminopropylmethacrylamide and b) 0 to 50%-wt. acrylamide, acrylic acid, methacrylic acid, acrylamidomethylpropanesulfonic acid, or mixtures of these monomers, the polymer exhibiting an intrinsic viscosity of at most about 150 ml/g as determined in a wt. % NaCl solution.
2. The method according to claim 1, wherein the polymer is incorporated in an amount of 0.05 to 1 wt. %, relative to the dry weight of the manufactured paper.
3 . The method according to claim 1, wherein the polymer is incorporated in an amount of 0.2 to 0.8 wt. %, relative to the dry weight of the manufactured paper.
4. The method according to claim 1, wherein the dimethylaminopropylacrylamide or dimethylaminopropylmethacrylamide is quaternized with dimethyl sulfate, methyl chloride, ethyl bromide, dimethyl carbonate or benzyl chloride.
5. The method according to claim 4, wherein the polymer is incorporated in an amount of 0.2 to 0.8 wt. %, relative to the dry weight of the manufactured paper, without the addition of aluminum sulfate, the total amount of the polymer incorporated is added through a plurality of feeders, and there is also incorporated into the recycled water a known cationic paper auxiliary.
6. The method according to claim 1, wherein the total amount of the polymer incorporated is added through a plurality of feeders.
7. The method according to claim 1, wherein there is also incorporated into the recycled water a known cationic paper auxiliary.
8. The method according to claim 1, wherein the polymer is incorporated without the addition of aluminum sulfate.
9. The method according to claim 1, wherein along with the polymer there is incorporating aluminum sulfate.
10. The method according to claim 1, wherein in the papermaking process the circulation of water is closed up for more than 90%.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3905049A DE3905049A1 (en) | 1989-02-18 | 1989-02-18 | METHOD OF DEXIFICATION OF MIXTURES IN PAPER MANUFACTURE |
| DEP3905049.1-45 | 1989-02-18 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2010189A1 CA2010189A1 (en) | 1990-08-18 |
| CA2010189C true CA2010189C (en) | 2001-04-17 |
Family
ID=6374441
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002010189A Expired - Fee Related CA2010189C (en) | 1989-02-18 | 1990-02-15 | Process for trash removal or pitch-like resin control in the paper manufacture |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0384268B1 (en) |
| JP (1) | JP2854072B2 (en) |
| AT (1) | ATE106964T1 (en) |
| AU (1) | AU634208B2 (en) |
| CA (1) | CA2010189C (en) |
| DE (2) | DE3905049A1 (en) |
| DK (1) | DK0384268T3 (en) |
| ES (1) | ES2055181T3 (en) |
| FI (1) | FI100117B (en) |
| HU (1) | HUT53165A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991015260A1 (en) * | 1990-03-30 | 1991-10-17 | Alza Corporation | Device and method for iontophoretic drug delivery |
| DE4409580A1 (en) * | 1994-03-21 | 1995-09-28 | Bayer Ag | Process for fixing contaminants in papermaking |
| JP4594656B2 (en) * | 2004-06-10 | 2010-12-08 | 油化産業株式会社 | Pitch control agent |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7308872A (en) * | 1972-07-12 | 1974-01-15 | ||
| US4190491A (en) * | 1976-08-02 | 1980-02-26 | Rohm And Haas Company | Process for controlling pitch in papermaking |
| ZA774417B (en) * | 1976-08-02 | 1978-08-30 | Rohm & Haas | Method of controlling pitch |
| JPS5916563B2 (en) * | 1976-11-04 | 1984-04-16 | 日東化学工業株式会社 | Production method of water-soluble cationic polymer |
| AU8040082A (en) * | 1981-02-17 | 1982-08-26 | Calgon Corporation | Reducing deposition of resins in paper production |
| AU8039982A (en) * | 1981-02-17 | 1982-08-26 | Calgon Corporation | Reducing deposition of resins in paper production |
| US4391932A (en) * | 1982-01-22 | 1983-07-05 | Nalco Chemical Company | Polycationic latices of dimethylaminopropyl-acrylamide, and their use of as sludge dewatering agents and/or paper retention aids |
| US4444971A (en) * | 1983-07-25 | 1984-04-24 | Texaco Inc. | Acrylic and methacrylic quaternary chloromethyl ammonium chloride cationic monomers and polymers thereof |
| DE3544909A1 (en) * | 1985-12-19 | 1987-06-25 | Stockhausen Chem Fab Gmbh | ACRYLAMIDE AND DIMETHYLAMINOPROPYLACRYLAMIDE COPOLYMERS AS FLOCCANTS AND METHOD FOR THE DRAINAGE OF CLARIFYING SLUDGE USING THESE FLOCCANTS |
| DE3620065A1 (en) * | 1986-06-14 | 1987-12-17 | Basf Ag | METHOD FOR PRODUCING PAPER, CARDBOARD AND CARDBOARD |
| DE3627407C2 (en) * | 1986-08-13 | 1994-05-19 | Steinbeis Temming Papier Gmbh | Process for cleaning water circuits in pulp and paper production |
| DE3704173A1 (en) * | 1987-02-11 | 1988-08-25 | Wolff Walsrode Ag | NEW MEANS FOR PAPER PRODUCTION |
| JPS6461595A (en) * | 1987-08-28 | 1989-03-08 | Sanyo Chemical Ind Ltd | Papermaking filterability enhancer |
-
1989
- 1989-02-18 DE DE3905049A patent/DE3905049A1/en not_active Withdrawn
-
1990
- 1990-02-13 DK DK90102772.2T patent/DK0384268T3/en active
- 1990-02-13 EP EP90102772A patent/EP0384268B1/en not_active Expired - Lifetime
- 1990-02-13 AT AT90102772T patent/ATE106964T1/en not_active IP Right Cessation
- 1990-02-13 ES ES90102772T patent/ES2055181T3/en not_active Expired - Lifetime
- 1990-02-13 DE DE59005979T patent/DE59005979D1/en not_active Expired - Fee Related
- 1990-02-15 CA CA002010189A patent/CA2010189C/en not_active Expired - Fee Related
- 1990-02-16 FI FI900785A patent/FI100117B/en active IP Right Grant
- 1990-02-16 HU HU90837A patent/HUT53165A/en unknown
- 1990-02-16 AU AU49815/90A patent/AU634208B2/en not_active Ceased
- 1990-02-19 JP JP2036425A patent/JP2854072B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE59005979D1 (en) | 1994-07-14 |
| ATE106964T1 (en) | 1994-06-15 |
| FI900785A0 (en) | 1990-02-16 |
| AU4981590A (en) | 1990-08-23 |
| FI100117B (en) | 1997-09-30 |
| DK0384268T3 (en) | 1994-10-03 |
| HU900837D0 (en) | 1990-05-28 |
| AU634208B2 (en) | 1993-02-18 |
| EP0384268A1 (en) | 1990-08-29 |
| DE3905049A1 (en) | 1990-08-23 |
| HUT53165A (en) | 1990-09-28 |
| ES2055181T3 (en) | 1994-08-16 |
| JPH02259195A (en) | 1990-10-19 |
| JP2854072B2 (en) | 1999-02-03 |
| EP0384268B1 (en) | 1994-06-08 |
| CA2010189A1 (en) | 1990-08-18 |
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