CA2329028C - A process for the production of paper - Google Patents
A process for the production of paper Download PDFInfo
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- CA2329028C CA2329028C CA002329028A CA2329028A CA2329028C CA 2329028 C CA2329028 C CA 2329028C CA 002329028 A CA002329028 A CA 002329028A CA 2329028 A CA2329028 A CA 2329028A CA 2329028 C CA2329028 C CA 2329028C
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- process according
- suspension
- organic polymer
- drainage
- cationic organic
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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
- D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
- D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
- D21H23/04—Addition to the pulp; After-treatment of added substances in the pulp
- D21H23/06—Controlling the addition
- D21H23/08—Controlling the addition by measuring pulp properties, e.g. zeta potential, pH
-
- 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
- D21H21/06—Paper forming aids
- D21H21/10—Retention agents or drainage improvers
-
- 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
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/14—Secondary fibres
-
- 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
- D21H17/01—Waste products, e.g. sludge
-
- 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
- D21H17/24—Polysaccharides
-
- 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
- D21H17/24—Polysaccharides
- D21H17/28—Starch
-
- 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
- D21H17/24—Polysaccharides
- D21H17/31—Gums
- D21H17/32—Guar or other polygalactomannan gum
-
- 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
- D21H17/37—Polymers of unsaturated acids or derivatives thereof, e.g. polyacrylates
- D21H17/375—Poly(meth)acrylamide
-
- 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
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/63—Inorganic compounds
- D21H17/67—Water-insoluble compounds, e.g. fillers, pigments
- D21H17/68—Water-insoluble compounds, e.g. fillers, pigments siliceous, e.g. clays
-
- 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
- D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
- D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
- D21H23/04—Addition to the pulp; After-treatment of added substances in the pulp
- D21H23/06—Controlling the addition
- D21H23/08—Controlling the addition by measuring pulp properties, e.g. zeta potential, pH
- D21H23/10—Controlling the addition by measuring pulp properties, e.g. zeta potential, pH at least two kinds of compounds being added
Landscapes
- Paper (AREA)
- Polarising Elements (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Abstract
The invention relates to a process for the production of paper from a suspension containing cellulosic fibres, and optional fillers, which comprises adding to the suspension a drainage and retention aid comprising a cationic organic polymer, forming and dewatering the suspension on a wire, wherein the cationic organic polymer has an aromatic group and the suspension which is dewatered on the wire has a conductivity of at least 2.0 mS/cm. The invention further relates to a process for the production of paper from a suspension containing cellulosic fibres, and optional fillers, comprising adding to the suspension a drainage and retention aid comprising a cationic organic polymer having an aromatic group, forming and dewatering the suspension on a wire to obtain a wet web of paper and white water, recirculating the white water and optionally introducing fresh water to form a suspension containing cellulosic fibres, and optional fillers, to be dewatered, wherein the amount of fresh water introduced is less than 30 tons per ton of dry paper produced.
Description
A process for the production of paper This invention relates to papermaking and more specifically to a process for the production of paper in which a cationic organic polymer having an aromatic group is added to a papermaking stock. The process provides improved drainage and retention.
Background In the papermaking art, an aqueous suspension containing cellulosic fibres, and optional fillers and additives, referred to as stock, is fed into a headbox which ejects the stock onto a forming wire. Water is drained from the stock through the forming wire so that a wet web of paper is formed on the wire, and the web is further dewatered and dried in the drying section of the paper machine. Water obtained by dewatering the stock, referred to as white water, which usually contains fine particles, e.g. fine fibres, fillers and additives, is normally recirculated in the papermaking process. Drainage and retention aids are conventionally introduced into the stock in order to facilitate drainage and increase adsorption of fine particles onto the cellulosic fibres so that they are retained with the fibres on the wire. Cationic organic polymers like cationic starch and cationic acrylamide-based polymers are widely used as drainage and retention aids.
These polymers can be used alone but more frequently they are used in combination with other polymers and/or with anionic microparticulate materials such as, for example, anionic inorganic particles like colloidal silica, colloidal aluminium-modified silica and bentonite.
U.S. Patent Nos. 4,980,025; 5,368,833; 5,603,805; 5,607,552; and 5,858,174; as well as International Patent Application WO 97/18351 disclose the use of cationic and amphoteric acrylamide-based polymers and anionic inorganic particles as stock additives in papermaking. These additives are among the most efficient drainage and retention aids now in use. Similar systems are disclosed in European Patent Application No.
805,234.
It has, however, been observed that the performance of drainage and retention aids comprising cationic organic polymers deteriorates when used in stocks with high levels of salt, i.e. high conductivity, and dissolved and colloidal substances. Higher dosages of cationic polymer are normally required in such stocks but usually the drainage and retention effect obtained is still not entirely satisfactory.
These problems are noticeable in paper mills where white water is extensively recirculated with the introduction of only low amounts of fresh water into the process, thereby further increasing the accu-mulation of salts and colloidal materials in the white water and the stock to be dewatered.
The Invention According to the present invention it has been found that improved drainage and retention can be obtained in stocks containing high levels of salt (high conductivity) and colloidal materials and/or in papermaking processes with a high degree of white water
Background In the papermaking art, an aqueous suspension containing cellulosic fibres, and optional fillers and additives, referred to as stock, is fed into a headbox which ejects the stock onto a forming wire. Water is drained from the stock through the forming wire so that a wet web of paper is formed on the wire, and the web is further dewatered and dried in the drying section of the paper machine. Water obtained by dewatering the stock, referred to as white water, which usually contains fine particles, e.g. fine fibres, fillers and additives, is normally recirculated in the papermaking process. Drainage and retention aids are conventionally introduced into the stock in order to facilitate drainage and increase adsorption of fine particles onto the cellulosic fibres so that they are retained with the fibres on the wire. Cationic organic polymers like cationic starch and cationic acrylamide-based polymers are widely used as drainage and retention aids.
These polymers can be used alone but more frequently they are used in combination with other polymers and/or with anionic microparticulate materials such as, for example, anionic inorganic particles like colloidal silica, colloidal aluminium-modified silica and bentonite.
U.S. Patent Nos. 4,980,025; 5,368,833; 5,603,805; 5,607,552; and 5,858,174; as well as International Patent Application WO 97/18351 disclose the use of cationic and amphoteric acrylamide-based polymers and anionic inorganic particles as stock additives in papermaking. These additives are among the most efficient drainage and retention aids now in use. Similar systems are disclosed in European Patent Application No.
805,234.
It has, however, been observed that the performance of drainage and retention aids comprising cationic organic polymers deteriorates when used in stocks with high levels of salt, i.e. high conductivity, and dissolved and colloidal substances. Higher dosages of cationic polymer are normally required in such stocks but usually the drainage and retention effect obtained is still not entirely satisfactory.
These problems are noticeable in paper mills where white water is extensively recirculated with the introduction of only low amounts of fresh water into the process, thereby further increasing the accu-mulation of salts and colloidal materials in the white water and the stock to be dewatered.
The Invention According to the present invention it has been found that improved drainage and retention can be obtained in stocks containing high levels of salt (high conductivity) and colloidal materials and/or in papermaking processes with a high degree of white water
2 closure when using a drainage and retention aid comprising a cationic organic polymer having an aromatic group. More specifically, the present invention relates to a process for the production of paper from a suspension containing cellulosic fibres, and optional fillers, which comprises adding to the suspension a drainage and retention aid comprising a cationic organic polymer, forming and dewatering the suspension on a wire, the process being characterised in that the cationic organic polymer has an aromatic group and the suspension being dewatered on the wire has a conductivity of at least 2.0 mS/cm. The present invention also relates to a process as described in the pre-characterising clause above, the process being further characterised in that it comprises forming and dewatering the suspension on a wire to obtain a wet web containing cellulosic fibres, or paper, and white water, recirculating the white water and optionally introducing fresh water to form a suspension containing cellulosic fibres, and optional fillers, to be dewatered to form paper, wherein the cationic organic polymer has an aromatic group and the amount of fresh water introduced is less than 30 tons per ton of dry paper produced.
The invention thus relates to a process as further defined in the claims.
The present invention results in improved drainage and/or retention when using stocks having high contents of salt, and thus having high conductivity levels, and colloidal materials. The present invention also results in improved drainage andlor retention when applied to papermaking processes with extensive white water recirculation and limited fresh water supply andlor processes using fresh water having high salt contents, in particular salts of di- and multivalent cations like calcium. Hereby the present invention makes it possible to increase the speed of the paper machine and to use lower dosages of additives to give a corresponding drainage and/or retention effect, thereby leading to an improved papermaking process and economic benefits.
The cationic organic polymer having an aromatic group according to this invention, herein also referred to as "main polymer", is capable of functioning as a drainage and retention aid {agent). The term "drainage and retention aid", as used herein, refers to one or more components (aids, agents, or additives) which, when being added to a stock, give better drainage and/or retention than is obtained when not adding the said one or more components. Accordingly, the main polymer provides improved drainage and/or retention, either when used alone or when used in conjunction with one or more additional stock additives. The main polymer can be linear, branched or cross-linked, e.g. in the form of a microparticulate material. Preferably the main polymer is water-soluble or water-dispersable. The aromatic group of the main polymer can be present in the polymer backbone or, preferably, it can be a pendent group attached to or extending from the polymer backbone or be present in a pendent group that is attached to or extending
The invention thus relates to a process as further defined in the claims.
The present invention results in improved drainage and/or retention when using stocks having high contents of salt, and thus having high conductivity levels, and colloidal materials. The present invention also results in improved drainage andlor retention when applied to papermaking processes with extensive white water recirculation and limited fresh water supply andlor processes using fresh water having high salt contents, in particular salts of di- and multivalent cations like calcium. Hereby the present invention makes it possible to increase the speed of the paper machine and to use lower dosages of additives to give a corresponding drainage and/or retention effect, thereby leading to an improved papermaking process and economic benefits.
The cationic organic polymer having an aromatic group according to this invention, herein also referred to as "main polymer", is capable of functioning as a drainage and retention aid {agent). The term "drainage and retention aid", as used herein, refers to one or more components (aids, agents, or additives) which, when being added to a stock, give better drainage and/or retention than is obtained when not adding the said one or more components. Accordingly, the main polymer provides improved drainage and/or retention, either when used alone or when used in conjunction with one or more additional stock additives. The main polymer can be linear, branched or cross-linked, e.g. in the form of a microparticulate material. Preferably the main polymer is water-soluble or water-dispersable. The aromatic group of the main polymer can be present in the polymer backbone or, preferably, it can be a pendent group attached to or extending from the polymer backbone or be present in a pendent group that is attached to or extending
3 from the polymer backbone (main chain). Suitable aromatic (aryl) groups include those comprising a phenyl group, optionally substituted, a phenylene group, optionally substituted, and a naphthyl group, optionally substituted, for example groups having the general formulae -C6H5, -C6H4 , -CsH3-, and -C6Hz-, e.g. in the form of phenylene (-C6H4-), xylylene (-CH2-CsH4-CHZ-), phenyl (-C6H5), benzyl (-CH2-C6H5), phenethyl (-CHzCH2-C6H5), and substituted phenyl (for example -C6H4-Y, -CsH3Y2, and -C6HZY3) where one or more substituents (Y) attached to the phenyl ring can be selected from hydroxyl, halides, e.g. chloride, nitro, and hydrocarbon groups having from 1 to 4 carbon atoms.
The main polymer can be selected from homopolymers and copolymers prepared from one or more monomers comprising at least one monomer having an aromatic group, suitably an ethyfenically unsaturated monomer, and the main polymer is suitably a vinyl addition polymer. The term "vinyl addition polymer", as used herein, refers to a polymer prepared by addition polymerization of one or more vinyl monomers or ethyienically unsaturated monomers which include, for example, acrylamide-based and acrylate-based monomers. Suitable main polymers include cationic vinyl addition polymers obtained by polymerizing a cationic monomer or a monomer mixture comprising a cationic monomer represented by the general formula (I):
CHZ = C - R, RZ (I) O=C-A,-B,-N+-Q X-l wherein R, is H or CH3; Rz and R3 are each or, preferably, an alkyl group having from 1 to 3 carbon atoms, usually 1 to 2 carbon atoms; A, is O or NH; B, is an alkylene group having from 2 to 8 carbon atoms, suitably from 2 to 4 carbon atoms, or a hydroxy propylene group;
Q is a substituent containing an aromatic group, suitably a phenyl or substituted phenyl group, which can be attached to the nitrogen by means of an alkylene group usually having from 1 to 3 carbon atoms, suitably 1 to 2 carbon atoms, and preferably Q is a benzyl group (- CH2- CsHs); and X- is an anionic counterion, usually a halide like chloride. Examples of suitable monomers represented by the general formula (I) include quaternary monomers obtained by treating dialkylaminoalkyl (meth)acrylates, e.g.
dimethylaminoethyl (meth)-acrylate, diethylaminoethyl (meth)acrylate and dimethylaminohydroxypropyl (meth)acrylate, and dialkylaminoalkyl (meth)acrylamides, e.g. dimethylaminoethyl (meth)acrylamide, diethylaminoethyl (meth)acrylamide, dimethylaminopropyl (meth)acrylamide, and diethyl-aminopropyl (meth)acrylamide, with benzyl chloride. Preferred cationic monomers of the
The main polymer can be selected from homopolymers and copolymers prepared from one or more monomers comprising at least one monomer having an aromatic group, suitably an ethyfenically unsaturated monomer, and the main polymer is suitably a vinyl addition polymer. The term "vinyl addition polymer", as used herein, refers to a polymer prepared by addition polymerization of one or more vinyl monomers or ethyienically unsaturated monomers which include, for example, acrylamide-based and acrylate-based monomers. Suitable main polymers include cationic vinyl addition polymers obtained by polymerizing a cationic monomer or a monomer mixture comprising a cationic monomer represented by the general formula (I):
CHZ = C - R, RZ (I) O=C-A,-B,-N+-Q X-l wherein R, is H or CH3; Rz and R3 are each or, preferably, an alkyl group having from 1 to 3 carbon atoms, usually 1 to 2 carbon atoms; A, is O or NH; B, is an alkylene group having from 2 to 8 carbon atoms, suitably from 2 to 4 carbon atoms, or a hydroxy propylene group;
Q is a substituent containing an aromatic group, suitably a phenyl or substituted phenyl group, which can be attached to the nitrogen by means of an alkylene group usually having from 1 to 3 carbon atoms, suitably 1 to 2 carbon atoms, and preferably Q is a benzyl group (- CH2- CsHs); and X- is an anionic counterion, usually a halide like chloride. Examples of suitable monomers represented by the general formula (I) include quaternary monomers obtained by treating dialkylaminoalkyl (meth)acrylates, e.g.
dimethylaminoethyl (meth)-acrylate, diethylaminoethyl (meth)acrylate and dimethylaminohydroxypropyl (meth)acrylate, and dialkylaminoalkyl (meth)acrylamides, e.g. dimethylaminoethyl (meth)acrylamide, diethylaminoethyl (meth)acrylamide, dimethylaminopropyl (meth)acrylamide, and diethyl-aminopropyl (meth)acrylamide, with benzyl chloride. Preferred cationic monomers of the
4 general formula (I) include dimethylaminoethylacrylate benzyl chloride quaternary salt and dimethylaminoethylmethacrylate benzyl chloride quaternary salt.
The main polymer can be a homopolymer prepared from a cationic monomer having an aromatic group or a copolymer prepared from a monomer mixture comprising a cationic monomer having an aromatic group and one or more copolymerizabie monomers.
Suitable copolymerizable non-ionic monomers include monomers represented by the general formula (II):
CH2 = C - R4 RS (II) O=C-AZ-BZ-N
Rs wherein R4 is H or CH3; R5 and Rs are each H or a hydrocarbon group, suitably alkyl, having from 1 to 6, suitably from 1 to 4 and usually from 1 to 2 carbon atoms; Az is O or NH; BZ is an alkylene group of from 2 to 8 carbon atoms, suitably from 2 to 4 carbon atoms, or a hydroxy propylene group or, alternatively, A and B are both nothing whereby there is a single bond between C and N (O=C-NRSRs). Examples of suitable copolymerizable monomers of this type include (meth)acrylamide; acrylamide-based monomers like N-alkyl (meth)acrylamides and N,N-dialkyl (meth)acrylamides, e.g. N-n-propylacrylamide, N-isopropyl (meth)acrylamide, N-n-butyl (meth)acrylamide, N-isobutyl {meth)acrylamide and N-t-butyl (meth)acrylamide; and dialkylaminoalkyl (meth)acrylamides, e.g.
dimethylamino-ethyl (meth)acrylamide, diethylaminoethyl (meth)acrylamide, dimethylaminopropyl (meth)acrylamide and diethylaminopropyl (meth)acrylamide; acrylate-based monomers like dialkylaminoalkyl (meth)acrylates, e.g. dimethylaminoethyl (meth)acrylate, diethylamino-ethyf (meth)acrylate, t-butylaminoethyl (meth)acrylate and dimethylaminohydroxypropyl acrylate; and vinylamides, e.g. N-vinylformamide and N-vinylacetamide.
Preferred copolymerizable non-ionic monomers include acrylamide and methacrylamide, i.e.
(meth)acrylamide, and the main polymer is preferably an acrylamide-based polymer.
Suitable copolymerizable cationic monomers include the monomers represented by the general formula (111):
CHz=C-R, RB (III) O=C-As-B3-N+-R,o X_ wherein R, is H or CH3; Re, R9 and R,o are each H or, preferably, a hydrocarbon group, suitably alkyl, having from 1 to 3 carbon atoms, usually 1 to 2 carbon atoms;
A3 is O or NH;
The main polymer can be a homopolymer prepared from a cationic monomer having an aromatic group or a copolymer prepared from a monomer mixture comprising a cationic monomer having an aromatic group and one or more copolymerizabie monomers.
Suitable copolymerizable non-ionic monomers include monomers represented by the general formula (II):
CH2 = C - R4 RS (II) O=C-AZ-BZ-N
Rs wherein R4 is H or CH3; R5 and Rs are each H or a hydrocarbon group, suitably alkyl, having from 1 to 6, suitably from 1 to 4 and usually from 1 to 2 carbon atoms; Az is O or NH; BZ is an alkylene group of from 2 to 8 carbon atoms, suitably from 2 to 4 carbon atoms, or a hydroxy propylene group or, alternatively, A and B are both nothing whereby there is a single bond between C and N (O=C-NRSRs). Examples of suitable copolymerizable monomers of this type include (meth)acrylamide; acrylamide-based monomers like N-alkyl (meth)acrylamides and N,N-dialkyl (meth)acrylamides, e.g. N-n-propylacrylamide, N-isopropyl (meth)acrylamide, N-n-butyl (meth)acrylamide, N-isobutyl {meth)acrylamide and N-t-butyl (meth)acrylamide; and dialkylaminoalkyl (meth)acrylamides, e.g.
dimethylamino-ethyl (meth)acrylamide, diethylaminoethyl (meth)acrylamide, dimethylaminopropyl (meth)acrylamide and diethylaminopropyl (meth)acrylamide; acrylate-based monomers like dialkylaminoalkyl (meth)acrylates, e.g. dimethylaminoethyl (meth)acrylate, diethylamino-ethyf (meth)acrylate, t-butylaminoethyl (meth)acrylate and dimethylaminohydroxypropyl acrylate; and vinylamides, e.g. N-vinylformamide and N-vinylacetamide.
Preferred copolymerizable non-ionic monomers include acrylamide and methacrylamide, i.e.
(meth)acrylamide, and the main polymer is preferably an acrylamide-based polymer.
Suitable copolymerizable cationic monomers include the monomers represented by the general formula (111):
CHz=C-R, RB (III) O=C-As-B3-N+-R,o X_ wherein R, is H or CH3; Re, R9 and R,o are each H or, preferably, a hydrocarbon group, suitably alkyl, having from 1 to 3 carbon atoms, usually 1 to 2 carbon atoms;
A3 is O or NH;
5 PCT/SE99/00677 B3 is an alkylene group of from 2 to 4 carbon atoms, suitably from 2 to 4 carbon atoms, or a hydroxy propylene group, and X- is an anionic counterion, usually methylsulphate or a halide like chloride. Examples of suitable cationic copolymerizable monomers include acid addition salts and quaternary ammonium salts of the dialkylaminoalkyl (meth)acrylates and 5 dialkylaminoalkyl (meth)acrylamides mentioned above, usually prepared using acids like HCI, HZS04, etc., or quaternizing agents like methyl chloride, dimethyl sulphate, etc.; and diallyldimethylammonium chloride. Preferred copolymerizable cationic monomers include dimethylaminoethyl (meth)acrylate methyl chloride quaternary salt and diallyldimethyl-ammonium chloride. Copolymerizable anionic monomers like acrylic acid, methacrylic acid, various sulfonated vinyl addition monomers, etc. can also be employed and, preferably, in minor amounts.
The main polymer according to this invention can be prepared from a monomer mixture generally comprising from 1 to 99 mole%, suitably from 2 to 50 mole%
and preferably from 5 to 20 mole% of cationic monomer having an aromatic group, preferably represented by the general formula (I), and from 99 to 1 mole%, suitably from 98 to 50 mole%, and preferably from 95 to 80 mole% of other copolymerizable monomers which preferably comprises acrylamide or methacrylamide ((meth)acrylamide), the monomer mixture suitably comprising from 98 to 50 mole% and preferably from 95 to 80, mole% of (meth)acrylamide, the sum of percentages being 100.
The main polymer can also be selected from polymers prepared by condensation reaction of one or more monomers containing an aromatic group. Examples of such monomers include toluene diisocyanates, bisphenol A, phthalic acid, phthalic anhydride, etc., which can be used in the preparation of cationic polyurethanes, cationic polyamide-amines, etc.
Alternatively, or additionally, the main polymer can be a polymer subjected to aromatic modification using an agent containing an aromatic group. Suitable modifying agents of this type include benzyl chloride, benzyl bromide, N-(3-chloro-2-hydroxypropyl)-N-benzyl-N,N-dimethylammonium chloride, and N-(3-chloro-2-hydroxypropyl) pyridinium chloride. Suitable polymers for such an aromatic modification include vinyl addition polymers. If the polymer contains a tertiary nitrogen which can be quaternized by the modifying agent, the use of such agents usually results in that the polymer is rendered cationic. Alternatively, the polymer to be subjected to aromatic modification can be cationic, for example a cationic vinyl addition polymer.
Usually the charge density of the main polymer is within the range of from 0.1 to
The main polymer according to this invention can be prepared from a monomer mixture generally comprising from 1 to 99 mole%, suitably from 2 to 50 mole%
and preferably from 5 to 20 mole% of cationic monomer having an aromatic group, preferably represented by the general formula (I), and from 99 to 1 mole%, suitably from 98 to 50 mole%, and preferably from 95 to 80 mole% of other copolymerizable monomers which preferably comprises acrylamide or methacrylamide ((meth)acrylamide), the monomer mixture suitably comprising from 98 to 50 mole% and preferably from 95 to 80, mole% of (meth)acrylamide, the sum of percentages being 100.
The main polymer can also be selected from polymers prepared by condensation reaction of one or more monomers containing an aromatic group. Examples of such monomers include toluene diisocyanates, bisphenol A, phthalic acid, phthalic anhydride, etc., which can be used in the preparation of cationic polyurethanes, cationic polyamide-amines, etc.
Alternatively, or additionally, the main polymer can be a polymer subjected to aromatic modification using an agent containing an aromatic group. Suitable modifying agents of this type include benzyl chloride, benzyl bromide, N-(3-chloro-2-hydroxypropyl)-N-benzyl-N,N-dimethylammonium chloride, and N-(3-chloro-2-hydroxypropyl) pyridinium chloride. Suitable polymers for such an aromatic modification include vinyl addition polymers. If the polymer contains a tertiary nitrogen which can be quaternized by the modifying agent, the use of such agents usually results in that the polymer is rendered cationic. Alternatively, the polymer to be subjected to aromatic modification can be cationic, for example a cationic vinyl addition polymer.
Usually the charge density of the main polymer is within the range of from 0.1 to
6.0 meqvlg of dry polymer, suitably from 0.2 to 4.0 and preferably from 0.5 to 3Ø
WO 99!55965 PCT/SE99/00677 The weight average molecular weight of synthetic main polymers is usually at least about 500,000, suitably above about 1,000,000 and preferably above about 2,000,000.
The upper limit is not critical; it can be about 50,000,000, usually 30,000,000 and suitably 25,000,000.
The main polymer of this invention may be in any state of aggregation such as, for example, in solid form, e.g. powders, in liquid form, e.g. solutions, emulsions, dispersions, including salt dispersions, etc. Examples of suitable main polymers for use in this invention include those described in U.S. Patent Nos. 5,169,540; 5,708,071; and European Patent Applications 183,466; 525,751 and 805,234. When being added to the stock, the main polymer is suitably in liquid form, e.g. in the form of an aqueous solution or dispersion.
The main polymer can be added into the stock to be dewatered in amounts which can vary within wide limits depending on, inter alia, type of stock, salt content, type of salts, filler content, type of filler, point of addition, etc. Generally the main polymer is added in an amount that give better retention than is obtained when not adding it. The main polymer is usually added in an amount of at least 0.001 %, often at least 0.005% by weight, based on dry stock substance, whereas the upper limit is usually 3% and suitably 1.5% by weight.
In a preferred embodiment of this invention, the main polymer is used in conjunction with an additional stock additive, thereby forming a drainage and retention aid comprising two or more components, usually referred to as drainage and retention aids. The term "drainage and retention aids", as used herein, refers to two or more components (aids, agents or additives) which, when being added to a stock, give better drainage andlor retention than is obtained when not adding the components.
Examples of suitable stock additives of this type include anionic microparticulate materials, e.g.
anionic organic particles and anionic inorganic particles, water-soluble anionic vinyl addition polymers, low molecular weight cationic organic polymers, aluminium compounds, and combinations thereof. In a preferred aspect of this embodiment, the main polymer is used in conjunction with an anionic microparticulate material, notably with anionic inorganic particles. In another preferred aspect of this embodiment, the main polymer is used in conjunction with anionic inorganic particles and a low molecular weight cationic organic polymer. In yet another preferred aspect of this embodiment, the main polymer is used in conjunction with anionic inorganic particles and an aluminium compound.
Anionic inorganic particles that can be used according to the invention include anionic silica-based particles and clays of the smectite type. It is preferred that the anionic inorganic particles are in the colloidal range of particle size. Anionic silica-based particles, i.e. particles based on Si02 or silicic acid, are preferably used and such particles are usually WO 99/559b5 PCT/SE99/00677
WO 99!55965 PCT/SE99/00677 The weight average molecular weight of synthetic main polymers is usually at least about 500,000, suitably above about 1,000,000 and preferably above about 2,000,000.
The upper limit is not critical; it can be about 50,000,000, usually 30,000,000 and suitably 25,000,000.
The main polymer of this invention may be in any state of aggregation such as, for example, in solid form, e.g. powders, in liquid form, e.g. solutions, emulsions, dispersions, including salt dispersions, etc. Examples of suitable main polymers for use in this invention include those described in U.S. Patent Nos. 5,169,540; 5,708,071; and European Patent Applications 183,466; 525,751 and 805,234. When being added to the stock, the main polymer is suitably in liquid form, e.g. in the form of an aqueous solution or dispersion.
The main polymer can be added into the stock to be dewatered in amounts which can vary within wide limits depending on, inter alia, type of stock, salt content, type of salts, filler content, type of filler, point of addition, etc. Generally the main polymer is added in an amount that give better retention than is obtained when not adding it. The main polymer is usually added in an amount of at least 0.001 %, often at least 0.005% by weight, based on dry stock substance, whereas the upper limit is usually 3% and suitably 1.5% by weight.
In a preferred embodiment of this invention, the main polymer is used in conjunction with an additional stock additive, thereby forming a drainage and retention aid comprising two or more components, usually referred to as drainage and retention aids. The term "drainage and retention aids", as used herein, refers to two or more components (aids, agents or additives) which, when being added to a stock, give better drainage andlor retention than is obtained when not adding the components.
Examples of suitable stock additives of this type include anionic microparticulate materials, e.g.
anionic organic particles and anionic inorganic particles, water-soluble anionic vinyl addition polymers, low molecular weight cationic organic polymers, aluminium compounds, and combinations thereof. In a preferred aspect of this embodiment, the main polymer is used in conjunction with an anionic microparticulate material, notably with anionic inorganic particles. In another preferred aspect of this embodiment, the main polymer is used in conjunction with anionic inorganic particles and a low molecular weight cationic organic polymer. In yet another preferred aspect of this embodiment, the main polymer is used in conjunction with anionic inorganic particles and an aluminium compound.
Anionic inorganic particles that can be used according to the invention include anionic silica-based particles and clays of the smectite type. It is preferred that the anionic inorganic particles are in the colloidal range of particle size. Anionic silica-based particles, i.e. particles based on Si02 or silicic acid, are preferably used and such particles are usually WO 99/559b5 PCT/SE99/00677
7 ..
supplied in the form of aqueous colloidal dispersions, so-called sols.
Examples of suitable silica-based particles include colloidal silica and different types of polysilicic acid. The silica-based sols can also be modified and contain other elements, e.g. aluminium andlor boron, which can be present in the aqueous phase and/or in the silica-based particles. Suitable silica-based particles of this type include colloidal aluminium-modified silica and aluminium silicates. Mixtures of such suitable silica-based particles can also be used.
Drainage and retention aids comprising suitable anionic silica-based particles are disclosed in U.S. Patent Nos. 4,388,150; 4,927,498; 4,954,220; 4,961,825; 4,980,025; 5,127,994;
5,176,891;
5,368,833; 5,447,604; 5,470,435; 5,543,014; 5,571,494; 5,573,674; 5,584,966;
5,603,805;
5,688,482; and 5,707,493.
Anionic silica-based particles suitably have an average particle size below about 50 nm, preferably below about 20 nm and more preferably in the range of from about 1 to about 10 nm. As conventional in silica chemistry, the particle size refers to the average size of the primary particles, which may be aggregated or non-aggregated. The specific surface area of the silica-based particles is suitably above 50 mZ/g and preferably above 100 m2lg.
Generally, the specific surtace area can be up to about 1700 mZlg and preferably up to 1000 mZlg. The specific surface area can be measured by means of titration with NaOH in known manner, e.g. as described by Sears in Analytical Chemistry 28(1956):12, and in U.S. Patent No. 5,176,891. The given area thus represents the average specific surface area of the particles.
In a preferred embodiment of the invention, the anionic inorganic particles are silica-based particles having a specific surface area within the range of from 50 to 1000 m2lg, preferably from 100 to 950 mzlg. Sols of silica-based particles these types also encompass modified sots like aluminium-containing silica-based sots and boron-containing silica-based sots. Preferably, the silica-based particles are present in a sol having an S-value in the range of from 8 to 45%, preferably from 10 to 30%, containing silica-based particles with a specific surface area in the range of from 300 to 1000 m2lg, suitably from 500 to 950 mzlg, and preferably from 750 to 950 m2lg, which sols can be modified with aluminium andJor boron as mentioned above. For example, the particles can be surface-modified with aluminium to a degree of from 2 to 25% substitution of silicon atoms. The S-value can be measured and calculated as described by Iler & Dalton in J. Phys.
Chem.
60(1956), 955-957. The S-value indicates the degree of aggregate or microgel formation and a lower S-value is indicative of a higher degree of aggregation.
In yet another preferred embodiment of the invention, the silica-based particles are selected from poiysilicic acid and modified polysilicic acid having a high specific surface area, suitably above about 1000 m2lg. The specific surface area can be within the range of from 1000 to 1700 m2lg and preferably from 1050 to 1600 m2/g. The sots of modified polysilicic acid can contain other elements, e.g. aluminium andlor boron, which can be present in the aqueous phase and/or in the silica-based particles. In the art, polysilicic acid is also referred to as polymeric silicic acid, polysilicic acid microgel, polysilicate and polysilicate microgel, which are all encompassed by the term polysilicic acid used herein.
Aluminium-containing compounds of this type are commonly also referred to as poly-aluminosilicate and polyaluminosilicate microgel, which are both encompassed by the terms colloidal aluminium-modified silica and aluminium silicate used herein.
Clays of the smectite type that can be used in the process of the invention are known in the art and include naturally occurring, synthetic and chemically treated materials.
Examples of suitable smectite clays include montmorillonite/bentonite, hectorite, beidelite, nontronite and saponite, preferably bentonite and especially such bentonite which after swelling preferably has a surface area of from 400 to 800 mz/g. Suitable clays are disclosed in U.S. Patent Nos. 4,753,710; 5,071,512; and 5,607,552 Anionic organic particles that can be used according to the invention include highly cross-linked anionic vinyl addition polymers, suitably copolymers comprising an anionic monomer like acrylic acid, methacrylic acid and sulfonated or phosphonated vinyl addition monomers, usually copolymerized with nonionic monomers like (meth)acrylamide, alkyl (meth)acrylates, etc. Useful anionic organic particles also include anionic condensation polymers, e.g. melamine-sulfonic acid sots. Water-soluble anionic vinyl addition polymers that can be used according to the invention include copolymers comprising an anionic monomer like acrylic acid, methacrylic acid and sulfonated vinyl addition monomers, usually copolymerized with nonionic monomers like acrylamide, alkyl acrylates, etc., for example those disclosed in U.S. Patent Nos. 5,098,520 and 5,185,062, Low molecular weight (hereinafter LMW) cationic organic polymers that can be used according to the invention include those commonly referred to and used as anionic trash catchers (ATC). ATC's are known in the art as neutralizing and/or fixing agents for detrimental anionic substances present in the stock and the use thereof in combination with drainage andlor retention aids often provide further improved drainage and/or retention.
The LMW cationic organic polymer can be derived from natural or synthetic sources, and preferably it is an LMW synthetic polymer. Suitable organic polymers of this type include LMW highly charged cationic organic polymers such as polyamines, polyamidoamines, polyethyleneimines, homo- and copolymers based on diallyldimethyl ammonium chloride, (meth)acrylamides and (meth)acrylates. In relation to the molecular weight of the main polymer, the molecular weight of the LMW cationic organic polymer is preferably lower; it is suitably at least 2,000 and preferably at least 10,000. The upper limit of the molecular weight is usually about 700,000, suitably about 500,000 and usually about 200,000.
Aluminium compounds that can be used according to the invention include alum, aluminates, aluminium chloride, aluminium nitrate and polyaluminium compounds, such as polyaluminium chlorides, polyaluminium sulphates, polyaluminium compounds containing both chloride and sulphate ions, polyaluminium silicate-sulphates, and mixtures thereof.
The polyaluminium compounds may also contain other anions than chloride ions, for example anions from sulfuric acid, phosphoric acid, organic acids such as citric acid and oxalic acid.
Components of drainage and retention aids according to the invention can be added to the stock in conventional manner and in any order. When using drainage and retention aids comprising a main polymer and an anionic microparticulate material, notably anionic inorganic particles, it is preferred to add the main polymer to the stock before adding the microparticulate material, even if the opposite order of addition may be used. It is further preferred to add the main polymer before a shear stage, which can be selected from pumping, mixing, cleaning, etc., and to add the anionic particles after that shear stage. When using an LMW cationic organic polymer or an aluminium compound, such components are preferably introduced into the stock prior to introducing the main polymer, optionally used in conjunction with an anionic microparticulate material.
Alternatively, the LMW cationic organic polymer and the main polymer can be introduced into stock essentially simultaneously, either separately or in admixture, for example as disclosed in U.S. Patent No. 5,858,174. The LMW cationic organic polymer and the main polymer are preferably introduced into the stock prior to introducing an anionic microparticulate material.
The drainage and retention aids) according to the invention can be added to the stock to be dewatered in amounts which can vary within wide limits depending on, inter alia, type and number of components, type of stack, salt content, type of salts, filler content, type of filler, point of addition, degree of white water closure, etc. Generally the aids) are added in amounts that give better drainage andlor retention than is obtained when not adding the components. The main polymer is usually added in an amount of at least 0.001%, often at least 0.005% by weight, based on dry stock substance, and the upper limit is usually 3% and suitably 1.5% by weight. Similar amounts are suitable for water-soluble anionic vinyl addition polymers, if used. When using an anionic microparticulate material in the process, the total amount added is usually at least 0.001 % by weight, often at least 0.005% by weight, based on dry substance of the stock, and the upper limit is usually 1.0%
and suitably 0.6% by weight. When using anionic silica-based particles, the total amount added is suitably within the range of from 0.005 to 0.5% by weight, calculated as Si02 and based on dry stock substance, preferably within the range of from 0.01 to 0.2%
by weight.
When using an LMW cationic organic polymer in the process, it can be added in an amount 5 of at least 0.05%, based on dry substance of the stock to be dewatered.
Suitably, the amount is in the range of from 0.07 to 0.5%, preferably in the range from 0.1 to 0.35%.
When using an aluminium compound in the process, the total amount introduced into the stock to be dewatered depends on the type of aluminium compound used and on other effects desired from it. It is for instance well known in the art to utilize aluminium 10 compounds as precipitants for rosin-based sizing agents. The total amount added is usually at least 0.05%, calculated as AIz03 and based on dry stock substance. Suitably the amount is in the range of from 0.5 to 3.0%, preferably in the range from 0.1 to 2.0%.
The process of this invention is preferably used in the manufacture of paper from a suspension containing cellulosic fibers, and optional fillers, i.e. a stock, which has a high conductivity. Usually, the conductivity of the stock that is dewatered on the wire is at least 2.0 mSlcm, suitably at least 3.5 mS/cm, preferably at least 5.0 mS/crn and most preferably at least 7.5 mS/cm. Conductivity can be measured by standard equipment such as, for example, a WTUV LF 539 instrument supplied by Christian Berner. The values referred to above are suitably determined by measuring the conductivity of the cellulosic suspension that is fed into or present in the headbox of the paper machine or, alternatively, by measuring the conductivity of white water obtained by dewatering the suspension. High conductivity levels mean high contents of salts (electrolytes), where the various salts can be based on mono-, di- and multivalent cations like alkali metals, e.g. Na+
and K+, alkaline earths, e.g. Ca2+ and Mg2+, aluminium ions, e.g. AI3+, AI(OH)2+ and polyaluminium ions, and mono-, di- and multivalent anions like halides, e.g., CI-, sulfates, e.g. SOa2-and HS04 , carbonates, e.g. C032- and HC03 , silicates and lower organic acids. The invention is particularly useful in the manufacture of paper from stocks having high contents of salts of di- and multivalent cations, and usually the content of di- and multivalent cations is at least 200 ppm, suitably at least 300 pm and preferably at least 400 ppm. The salts can be derived from the stock preparation stage, i.e. from the materials used to form the stock, e.g.
water, celfulosic fibres and fillers, in particular in integrated mills where a concentrated aqueous fibre suspension from the pulp mill normally is mixed with water to form a dilute suspension suitable for paper manufacture in the paper mill. The salt may also be derived from various additives introduced into the stock, from the fresh water supplied to the process, etc. Further, the content of salts is usually higher in processes where white water is extensively recirculated, which may lead to considerable accumulation of salts in the water circulating in the process.
The present invention further encompasses papermaking processes where white water is extensively recirculated (recycled), i.e. with a high degree of white water closure, for example where from 0 to 30 tons of fresh water are used per ton of dry paper produced, usually less than 20, suitably less than 15, preferably less than 10 and notably less than 5 tons of fresh water per ton of paper. Recirculation of white water obtained in the process suitably comprises mixing the white water with cellulosic fibres and/or optional fillers to form a suspension to be dewatered; preferably it comprises mixing the white water with a suspension containing cellulosic fibres, and optional ~Ilers, before the suspension enters the forming wire for dewatering. The white water can be mixed with the suspension before, between, simultaneous with or after introducing the components of drainage and retention aids, if used; and before, simultaneous with or after introducing the main polymer. Fresh water can be introduced in the process at any stage; for example, it can be mixed with celluiosic fibres in order to form a suspension, and it can be mixed with a suspension containing cellulosic fibres to dilute it so as to form the suspension to be dewatered, before, simultaneous with or after mixing the stock with white water and before, between, simultaneous with or after introducing the components of drainage and retention aids, if used; and before, simultaneous with or after introducing the main polymer.
Further additives which are conventional in papermaking can of course be used in combination with the additives) according to the invention, such as, for example, dry strength agents, wet strength agents, optical brightening agents, dyes, sizing agents like rosin-based sizing agents and cellulose-reactive sizing agents, e.g. ketene dimers and succinic anhydrides, etc. The cellulosic suspension, or stock, can also contain mineral fillers of conventional types such as, for example, kaolin, china clay, titanium dioxide, gypsum, talc and natural and synthetic calcium carbonates such as chalk, ground marble and precipitated calcium carbonate.
The process of this invention is used for the production of paper. The term "paper", as used herein, of course include not only paper and the production thereof, but also other cellulosic fibre-containing sheet or web-like products, such as for example board and paperboard, and the production thereof. The process can be used in the production of paper from different types of suspensions of cellulose-containing fibres and the suspensions should suitably contain at least 25% by weight and preferably at least 50% by weight of such fibres, based on dry substance. The suspension can be based on fibres from chemical pulp such as sulphate, sulphite and organosolv pulps, mechanical pulp such as thermomechanical pulp, chemo-thermomechanical pulp, refiner pulp and groundwood pulp, from both hardwood and softwood, and can also be based on recycled fibres, optionally from de-inked pulps, and mixtures thereof.
The invention is further illustrated in the following Examples which, however, are not intended to limit the same. Parts and % relate to parts by weight and % by weight, respectively, unless otherwise stated.
Example 1 (Comparison) Drainage performance was evaluated by means of a Dynamic Drainage Analyser (DDA), available from Akribi, Sweden, which measures the time for draining a set volume of stock through a wire when removing a plug and applying vacuum to that side of the wire opposite to the side on which the stock is present.
The furnish used was based on 70% by weight of pulp of bleached birch/pine sulphate (60/40) refined to 200°CSF and 30% by weight of ground marble.
Stock volume was 800 ml, consistency 0.3% and pH about 8.
Conductivity of the stock was adjusted to 0.47 mS/cm by addition of sodium sulphate. The stock was stirred in a baffled jar at a speed of 1500 rpm throughout the test and chemicals additions were conducted as follows: i) adding cationic polymer to the stock following by stirring for 30 seconds, ii) adding anionic inorganic particles to the stock followed by stirring for 15 seconds, iii) draining the stock while automatically recording the drainage time.
The polymers used for in the test series were P1) a cationic copolymer prepared by polymerisation of acrylamide (90 mole%) and acryloxyethyldimethylbenzylammonium chloride (10 mole%) and having an average molecular weight of about 6,000,000;
and P2) a cationic copolymer prepared by polymerisation of acrylamide (90 mole%) and acryloxyethyltrimethylammonium chloride (10 mole%) and having an average molecular weight of about 6,000,000. The polymers P1 and P2 were dissolved in water and used as 0.1 % aqueous solutions.
The anionic inorganic particles used were silica-based particles of the type disclosed in U.S. Patent No. 5,368,833. The sol had an S-value of about 25%
and contained silica particles with a specific surface area of about 900 m2lg which were surface-modified with aluminium to a degree of 5%. The silica-based particles were added in an amount of 1.0 kglton, calculated as SiOz and based on dry stock system.
Table 1 shows the drainage time at various dosages of P1 and P2, calculated as dry polymer on dry stock system.
Table 1 Test Polymer SiOz ConductivityDewatering No. Dosage Dosage time [s]
[kg/t] [kglt] [mSlcm] P1 P2 1 0 0 0.47 18.4 18.4 2 1 1 0.47 12.5 10.6 3 1.5 1 0.47 6.9 5.6 4 2 1 0.47 4.9 4.3 Example 2 (Comparison) Dewatering and retention effect was evaluated by means of the DDA used in Example 1 in combination with a nephelometer. First pass retention was evaluated by measuring the turbidity of the filtrate, the white water, obtained by draining the stock.
The furnish used was based on 56% by weight of peroxide bleached TMPISGW
pulp (80/20), 14% by weight of bleached birch/pine sulphate pulp (60140) refined to 200° CSF and 30% by weight of china clay. To the stock was added 40 g/I
of a colloidal fraction, bleach water from an SC mill, filtrated through a 5 ~.m screen and concentrated with an OF filter, cut off 200,000. Stock volume was 800 ml, consistency 0.14%
and pH
was adjusted to 4.0 using dilute sulphuric acid. The conductivity was adjusted by addition of calcium chloride (60 ppm Ca2+), magnesium sulphate (18 ppm Mgz+) and sodium bicarbonate (134 ppm HC03 ).
The polymers and anionic inorganic particles according to Example 1 were similarly used in this test series. Two dosages of polymers were used, 1 kg/t and 2 kg/t, respectively, calculated as dry polymer on dry stock system. Table 2 shows the dewatering and retention effect at various dosages of silica-based particles, calculated as Si02 and based on dry stock system.
Table 2 TestPolymer Si02 ConductivityDewatering Turbidity No. dosage Dosage time [NTU]
[s]
[kglt] [kglt] [mSlcm] P1 P2 P1 P2 1 1 0 1.375 21.2 18.7 63 55 2 1 1 1.375 17.2 16.1 67 60 3 1 2 1.375 21.2 18.6 66 57 4 2 0 1.375 15.2 14.2 47 45 5 2 1 1.375 11 9.9 47 47 6 2 2 1.375 11.4 10.8 45 50 Examale 3 In this test series, the dewatering and retention effect was evaluated according to the procedure descibed in Example 2.
The furnish used was the same as used in Example 2. Stock volume was 800 ml and pH about 7. The conductivity was adjusted by addition of calcium chloride, thus simulating a very high electrolyte content and a high degree of white water closure.
The polymers and anionic inorganic particles according to Example 1 were similarly used in this test series.
Table 3 shows the dewatering and retention effect at various dosages of silica-based particles, calculated as Si02 and based on dry stock system.
Table 3 TestPolymer Si02 ConductivityDewatering Turbidity time No. Dosage Dosage [s] [NTU]
(kglt] [kglt] [mSlcm] P1 P2 P1 P2 990 ppm Ca2+
1 2 0 5.5 14.2 19.2 42 64 2 2 1 5.5 10.8 13.9 41 43 3 2 2 5.5 7.7 9.5 35 36 4 2 3 5.5 7.3 8.9 32 39 1300 ppm Ca2+
5 2 0 7.0 16.2 23.0 46 50 6 2 1 7.0 10.0 17.1 40 45 7 2 2 7.0 7.5 13.6 36 44
supplied in the form of aqueous colloidal dispersions, so-called sols.
Examples of suitable silica-based particles include colloidal silica and different types of polysilicic acid. The silica-based sols can also be modified and contain other elements, e.g. aluminium andlor boron, which can be present in the aqueous phase and/or in the silica-based particles. Suitable silica-based particles of this type include colloidal aluminium-modified silica and aluminium silicates. Mixtures of such suitable silica-based particles can also be used.
Drainage and retention aids comprising suitable anionic silica-based particles are disclosed in U.S. Patent Nos. 4,388,150; 4,927,498; 4,954,220; 4,961,825; 4,980,025; 5,127,994;
5,176,891;
5,368,833; 5,447,604; 5,470,435; 5,543,014; 5,571,494; 5,573,674; 5,584,966;
5,603,805;
5,688,482; and 5,707,493.
Anionic silica-based particles suitably have an average particle size below about 50 nm, preferably below about 20 nm and more preferably in the range of from about 1 to about 10 nm. As conventional in silica chemistry, the particle size refers to the average size of the primary particles, which may be aggregated or non-aggregated. The specific surface area of the silica-based particles is suitably above 50 mZ/g and preferably above 100 m2lg.
Generally, the specific surtace area can be up to about 1700 mZlg and preferably up to 1000 mZlg. The specific surface area can be measured by means of titration with NaOH in known manner, e.g. as described by Sears in Analytical Chemistry 28(1956):12, and in U.S. Patent No. 5,176,891. The given area thus represents the average specific surface area of the particles.
In a preferred embodiment of the invention, the anionic inorganic particles are silica-based particles having a specific surface area within the range of from 50 to 1000 m2lg, preferably from 100 to 950 mzlg. Sols of silica-based particles these types also encompass modified sots like aluminium-containing silica-based sots and boron-containing silica-based sots. Preferably, the silica-based particles are present in a sol having an S-value in the range of from 8 to 45%, preferably from 10 to 30%, containing silica-based particles with a specific surface area in the range of from 300 to 1000 m2lg, suitably from 500 to 950 mzlg, and preferably from 750 to 950 m2lg, which sols can be modified with aluminium andJor boron as mentioned above. For example, the particles can be surface-modified with aluminium to a degree of from 2 to 25% substitution of silicon atoms. The S-value can be measured and calculated as described by Iler & Dalton in J. Phys.
Chem.
60(1956), 955-957. The S-value indicates the degree of aggregate or microgel formation and a lower S-value is indicative of a higher degree of aggregation.
In yet another preferred embodiment of the invention, the silica-based particles are selected from poiysilicic acid and modified polysilicic acid having a high specific surface area, suitably above about 1000 m2lg. The specific surface area can be within the range of from 1000 to 1700 m2lg and preferably from 1050 to 1600 m2/g. The sots of modified polysilicic acid can contain other elements, e.g. aluminium andlor boron, which can be present in the aqueous phase and/or in the silica-based particles. In the art, polysilicic acid is also referred to as polymeric silicic acid, polysilicic acid microgel, polysilicate and polysilicate microgel, which are all encompassed by the term polysilicic acid used herein.
Aluminium-containing compounds of this type are commonly also referred to as poly-aluminosilicate and polyaluminosilicate microgel, which are both encompassed by the terms colloidal aluminium-modified silica and aluminium silicate used herein.
Clays of the smectite type that can be used in the process of the invention are known in the art and include naturally occurring, synthetic and chemically treated materials.
Examples of suitable smectite clays include montmorillonite/bentonite, hectorite, beidelite, nontronite and saponite, preferably bentonite and especially such bentonite which after swelling preferably has a surface area of from 400 to 800 mz/g. Suitable clays are disclosed in U.S. Patent Nos. 4,753,710; 5,071,512; and 5,607,552 Anionic organic particles that can be used according to the invention include highly cross-linked anionic vinyl addition polymers, suitably copolymers comprising an anionic monomer like acrylic acid, methacrylic acid and sulfonated or phosphonated vinyl addition monomers, usually copolymerized with nonionic monomers like (meth)acrylamide, alkyl (meth)acrylates, etc. Useful anionic organic particles also include anionic condensation polymers, e.g. melamine-sulfonic acid sots. Water-soluble anionic vinyl addition polymers that can be used according to the invention include copolymers comprising an anionic monomer like acrylic acid, methacrylic acid and sulfonated vinyl addition monomers, usually copolymerized with nonionic monomers like acrylamide, alkyl acrylates, etc., for example those disclosed in U.S. Patent Nos. 5,098,520 and 5,185,062, Low molecular weight (hereinafter LMW) cationic organic polymers that can be used according to the invention include those commonly referred to and used as anionic trash catchers (ATC). ATC's are known in the art as neutralizing and/or fixing agents for detrimental anionic substances present in the stock and the use thereof in combination with drainage andlor retention aids often provide further improved drainage and/or retention.
The LMW cationic organic polymer can be derived from natural or synthetic sources, and preferably it is an LMW synthetic polymer. Suitable organic polymers of this type include LMW highly charged cationic organic polymers such as polyamines, polyamidoamines, polyethyleneimines, homo- and copolymers based on diallyldimethyl ammonium chloride, (meth)acrylamides and (meth)acrylates. In relation to the molecular weight of the main polymer, the molecular weight of the LMW cationic organic polymer is preferably lower; it is suitably at least 2,000 and preferably at least 10,000. The upper limit of the molecular weight is usually about 700,000, suitably about 500,000 and usually about 200,000.
Aluminium compounds that can be used according to the invention include alum, aluminates, aluminium chloride, aluminium nitrate and polyaluminium compounds, such as polyaluminium chlorides, polyaluminium sulphates, polyaluminium compounds containing both chloride and sulphate ions, polyaluminium silicate-sulphates, and mixtures thereof.
The polyaluminium compounds may also contain other anions than chloride ions, for example anions from sulfuric acid, phosphoric acid, organic acids such as citric acid and oxalic acid.
Components of drainage and retention aids according to the invention can be added to the stock in conventional manner and in any order. When using drainage and retention aids comprising a main polymer and an anionic microparticulate material, notably anionic inorganic particles, it is preferred to add the main polymer to the stock before adding the microparticulate material, even if the opposite order of addition may be used. It is further preferred to add the main polymer before a shear stage, which can be selected from pumping, mixing, cleaning, etc., and to add the anionic particles after that shear stage. When using an LMW cationic organic polymer or an aluminium compound, such components are preferably introduced into the stock prior to introducing the main polymer, optionally used in conjunction with an anionic microparticulate material.
Alternatively, the LMW cationic organic polymer and the main polymer can be introduced into stock essentially simultaneously, either separately or in admixture, for example as disclosed in U.S. Patent No. 5,858,174. The LMW cationic organic polymer and the main polymer are preferably introduced into the stock prior to introducing an anionic microparticulate material.
The drainage and retention aids) according to the invention can be added to the stock to be dewatered in amounts which can vary within wide limits depending on, inter alia, type and number of components, type of stack, salt content, type of salts, filler content, type of filler, point of addition, degree of white water closure, etc. Generally the aids) are added in amounts that give better drainage andlor retention than is obtained when not adding the components. The main polymer is usually added in an amount of at least 0.001%, often at least 0.005% by weight, based on dry stock substance, and the upper limit is usually 3% and suitably 1.5% by weight. Similar amounts are suitable for water-soluble anionic vinyl addition polymers, if used. When using an anionic microparticulate material in the process, the total amount added is usually at least 0.001 % by weight, often at least 0.005% by weight, based on dry substance of the stock, and the upper limit is usually 1.0%
and suitably 0.6% by weight. When using anionic silica-based particles, the total amount added is suitably within the range of from 0.005 to 0.5% by weight, calculated as Si02 and based on dry stock substance, preferably within the range of from 0.01 to 0.2%
by weight.
When using an LMW cationic organic polymer in the process, it can be added in an amount 5 of at least 0.05%, based on dry substance of the stock to be dewatered.
Suitably, the amount is in the range of from 0.07 to 0.5%, preferably in the range from 0.1 to 0.35%.
When using an aluminium compound in the process, the total amount introduced into the stock to be dewatered depends on the type of aluminium compound used and on other effects desired from it. It is for instance well known in the art to utilize aluminium 10 compounds as precipitants for rosin-based sizing agents. The total amount added is usually at least 0.05%, calculated as AIz03 and based on dry stock substance. Suitably the amount is in the range of from 0.5 to 3.0%, preferably in the range from 0.1 to 2.0%.
The process of this invention is preferably used in the manufacture of paper from a suspension containing cellulosic fibers, and optional fillers, i.e. a stock, which has a high conductivity. Usually, the conductivity of the stock that is dewatered on the wire is at least 2.0 mSlcm, suitably at least 3.5 mS/cm, preferably at least 5.0 mS/crn and most preferably at least 7.5 mS/cm. Conductivity can be measured by standard equipment such as, for example, a WTUV LF 539 instrument supplied by Christian Berner. The values referred to above are suitably determined by measuring the conductivity of the cellulosic suspension that is fed into or present in the headbox of the paper machine or, alternatively, by measuring the conductivity of white water obtained by dewatering the suspension. High conductivity levels mean high contents of salts (electrolytes), where the various salts can be based on mono-, di- and multivalent cations like alkali metals, e.g. Na+
and K+, alkaline earths, e.g. Ca2+ and Mg2+, aluminium ions, e.g. AI3+, AI(OH)2+ and polyaluminium ions, and mono-, di- and multivalent anions like halides, e.g., CI-, sulfates, e.g. SOa2-and HS04 , carbonates, e.g. C032- and HC03 , silicates and lower organic acids. The invention is particularly useful in the manufacture of paper from stocks having high contents of salts of di- and multivalent cations, and usually the content of di- and multivalent cations is at least 200 ppm, suitably at least 300 pm and preferably at least 400 ppm. The salts can be derived from the stock preparation stage, i.e. from the materials used to form the stock, e.g.
water, celfulosic fibres and fillers, in particular in integrated mills where a concentrated aqueous fibre suspension from the pulp mill normally is mixed with water to form a dilute suspension suitable for paper manufacture in the paper mill. The salt may also be derived from various additives introduced into the stock, from the fresh water supplied to the process, etc. Further, the content of salts is usually higher in processes where white water is extensively recirculated, which may lead to considerable accumulation of salts in the water circulating in the process.
The present invention further encompasses papermaking processes where white water is extensively recirculated (recycled), i.e. with a high degree of white water closure, for example where from 0 to 30 tons of fresh water are used per ton of dry paper produced, usually less than 20, suitably less than 15, preferably less than 10 and notably less than 5 tons of fresh water per ton of paper. Recirculation of white water obtained in the process suitably comprises mixing the white water with cellulosic fibres and/or optional fillers to form a suspension to be dewatered; preferably it comprises mixing the white water with a suspension containing cellulosic fibres, and optional ~Ilers, before the suspension enters the forming wire for dewatering. The white water can be mixed with the suspension before, between, simultaneous with or after introducing the components of drainage and retention aids, if used; and before, simultaneous with or after introducing the main polymer. Fresh water can be introduced in the process at any stage; for example, it can be mixed with celluiosic fibres in order to form a suspension, and it can be mixed with a suspension containing cellulosic fibres to dilute it so as to form the suspension to be dewatered, before, simultaneous with or after mixing the stock with white water and before, between, simultaneous with or after introducing the components of drainage and retention aids, if used; and before, simultaneous with or after introducing the main polymer.
Further additives which are conventional in papermaking can of course be used in combination with the additives) according to the invention, such as, for example, dry strength agents, wet strength agents, optical brightening agents, dyes, sizing agents like rosin-based sizing agents and cellulose-reactive sizing agents, e.g. ketene dimers and succinic anhydrides, etc. The cellulosic suspension, or stock, can also contain mineral fillers of conventional types such as, for example, kaolin, china clay, titanium dioxide, gypsum, talc and natural and synthetic calcium carbonates such as chalk, ground marble and precipitated calcium carbonate.
The process of this invention is used for the production of paper. The term "paper", as used herein, of course include not only paper and the production thereof, but also other cellulosic fibre-containing sheet or web-like products, such as for example board and paperboard, and the production thereof. The process can be used in the production of paper from different types of suspensions of cellulose-containing fibres and the suspensions should suitably contain at least 25% by weight and preferably at least 50% by weight of such fibres, based on dry substance. The suspension can be based on fibres from chemical pulp such as sulphate, sulphite and organosolv pulps, mechanical pulp such as thermomechanical pulp, chemo-thermomechanical pulp, refiner pulp and groundwood pulp, from both hardwood and softwood, and can also be based on recycled fibres, optionally from de-inked pulps, and mixtures thereof.
The invention is further illustrated in the following Examples which, however, are not intended to limit the same. Parts and % relate to parts by weight and % by weight, respectively, unless otherwise stated.
Example 1 (Comparison) Drainage performance was evaluated by means of a Dynamic Drainage Analyser (DDA), available from Akribi, Sweden, which measures the time for draining a set volume of stock through a wire when removing a plug and applying vacuum to that side of the wire opposite to the side on which the stock is present.
The furnish used was based on 70% by weight of pulp of bleached birch/pine sulphate (60/40) refined to 200°CSF and 30% by weight of ground marble.
Stock volume was 800 ml, consistency 0.3% and pH about 8.
Conductivity of the stock was adjusted to 0.47 mS/cm by addition of sodium sulphate. The stock was stirred in a baffled jar at a speed of 1500 rpm throughout the test and chemicals additions were conducted as follows: i) adding cationic polymer to the stock following by stirring for 30 seconds, ii) adding anionic inorganic particles to the stock followed by stirring for 15 seconds, iii) draining the stock while automatically recording the drainage time.
The polymers used for in the test series were P1) a cationic copolymer prepared by polymerisation of acrylamide (90 mole%) and acryloxyethyldimethylbenzylammonium chloride (10 mole%) and having an average molecular weight of about 6,000,000;
and P2) a cationic copolymer prepared by polymerisation of acrylamide (90 mole%) and acryloxyethyltrimethylammonium chloride (10 mole%) and having an average molecular weight of about 6,000,000. The polymers P1 and P2 were dissolved in water and used as 0.1 % aqueous solutions.
The anionic inorganic particles used were silica-based particles of the type disclosed in U.S. Patent No. 5,368,833. The sol had an S-value of about 25%
and contained silica particles with a specific surface area of about 900 m2lg which were surface-modified with aluminium to a degree of 5%. The silica-based particles were added in an amount of 1.0 kglton, calculated as SiOz and based on dry stock system.
Table 1 shows the drainage time at various dosages of P1 and P2, calculated as dry polymer on dry stock system.
Table 1 Test Polymer SiOz ConductivityDewatering No. Dosage Dosage time [s]
[kg/t] [kglt] [mSlcm] P1 P2 1 0 0 0.47 18.4 18.4 2 1 1 0.47 12.5 10.6 3 1.5 1 0.47 6.9 5.6 4 2 1 0.47 4.9 4.3 Example 2 (Comparison) Dewatering and retention effect was evaluated by means of the DDA used in Example 1 in combination with a nephelometer. First pass retention was evaluated by measuring the turbidity of the filtrate, the white water, obtained by draining the stock.
The furnish used was based on 56% by weight of peroxide bleached TMPISGW
pulp (80/20), 14% by weight of bleached birch/pine sulphate pulp (60140) refined to 200° CSF and 30% by weight of china clay. To the stock was added 40 g/I
of a colloidal fraction, bleach water from an SC mill, filtrated through a 5 ~.m screen and concentrated with an OF filter, cut off 200,000. Stock volume was 800 ml, consistency 0.14%
and pH
was adjusted to 4.0 using dilute sulphuric acid. The conductivity was adjusted by addition of calcium chloride (60 ppm Ca2+), magnesium sulphate (18 ppm Mgz+) and sodium bicarbonate (134 ppm HC03 ).
The polymers and anionic inorganic particles according to Example 1 were similarly used in this test series. Two dosages of polymers were used, 1 kg/t and 2 kg/t, respectively, calculated as dry polymer on dry stock system. Table 2 shows the dewatering and retention effect at various dosages of silica-based particles, calculated as Si02 and based on dry stock system.
Table 2 TestPolymer Si02 ConductivityDewatering Turbidity No. dosage Dosage time [NTU]
[s]
[kglt] [kglt] [mSlcm] P1 P2 P1 P2 1 1 0 1.375 21.2 18.7 63 55 2 1 1 1.375 17.2 16.1 67 60 3 1 2 1.375 21.2 18.6 66 57 4 2 0 1.375 15.2 14.2 47 45 5 2 1 1.375 11 9.9 47 47 6 2 2 1.375 11.4 10.8 45 50 Examale 3 In this test series, the dewatering and retention effect was evaluated according to the procedure descibed in Example 2.
The furnish used was the same as used in Example 2. Stock volume was 800 ml and pH about 7. The conductivity was adjusted by addition of calcium chloride, thus simulating a very high electrolyte content and a high degree of white water closure.
The polymers and anionic inorganic particles according to Example 1 were similarly used in this test series.
Table 3 shows the dewatering and retention effect at various dosages of silica-based particles, calculated as Si02 and based on dry stock system.
Table 3 TestPolymer Si02 ConductivityDewatering Turbidity time No. Dosage Dosage [s] [NTU]
(kglt] [kglt] [mSlcm] P1 P2 P1 P2 990 ppm Ca2+
1 2 0 5.5 14.2 19.2 42 64 2 2 1 5.5 10.8 13.9 41 43 3 2 2 5.5 7.7 9.5 35 36 4 2 3 5.5 7.3 8.9 32 39 1300 ppm Ca2+
5 2 0 7.0 16.2 23.0 46 50 6 2 1 7.0 10.0 17.1 40 45 7 2 2 7.0 7.5 13.6 36 44
8 2 3 7.0 7.7 11.7 34 44 1930 ppm Ca2+
9 2 0 10.0 18.7 22.0 44 58
10 2 1 10.0 11.6 23.3 39 52
11 2 2 10.0 8.2 15.8 36 53
12 2 3 10.0 8.0 15.4 41 47 Example 4 In this test series, the dewatering effect was evaluated with a "Canadian Standard Freeness Tester" which is the conventional method for characterising drainage according to SCAN-C 21:65. All additions of chemicals were made in a "Britt Dynamic Drainage Jar" with blocked outlet at a stirring speed of 1000 rpm during 45 seconds according to the procedure of Example 1 and the stock system was then transferred to the Freeness apparatus. Here the smallest hole in the bottom of the Freeness tester was blocked and the time for 400 ml of furnish to filtrate through the screen was measured.
The stock was taken from a closed mill using waste paper. Consistency was 0.14%, conductivity 8.0 mS/cm and pH about 7. Table 4 shows the dewatering effect at various dosages of silica-based particles, calculated as Si02 and based on dry stock system Table 4 Test Polymer SiOz ConductivityDewatering No. dosage Dosage time [s]
[kglt] [kglt] [mSlcm] P1 P2 1 0.6 0 8.0 100.4 103.2 2 0.6 0.25 8.0 66.4 92.5 3 0.6 0.5 8.0 58.3 85.8 4 0.6 0.75 8.0 50.0 76.0 5 0.6 1 8.0 44.6 79.2 5 Example 5 In this test series, the dewatering effect was evaluated as in Example 3, except that both sodium acetate (550 ppm Na') and calcium chloride (1300 ppm Ca2') was used to adjust the conductivity.
The polymers and anionic inorganic particles according to Example 1 were 10 similarly used in this test series.
Table 5 shows the dewatering effect at various dosages of silica-based particles, calculated as Si02 and based on dry stock system.
Table 5 Test Polymer Si02 ConductivityDewatering No. dosage dosage time [s]
[kglt] [kglt] [mSlcm] P1 P2 1 2 1 2.5 16.1 18.2 2 1 3 10.0 10.7 14.7 3 2 3 10.0 6.8 13.5 4 3 3 10.0 5.3 14.0 5 2 1 10.0 9.7 20.4 6 2 2 10.0 7.9 14.8 15 Example 6 In this test series, the dewatering and retention effect was evaluated as in Example 3, using a combination of sodium acetate (550 ppm Na+) and calcium chloride (1300 ppm Ca2+) to adjust the conductivity.
The polymers according to Example 1 were similarly used in this test series.
The anionic microparticulate material used was hydrated suspension of powdered Na bentonite in water. The bentonite had a surface charge of about 0.33 meq/g and a swelling ability of 41 ml (2 g}. The bentonite particles were added in an amount of 8.0 kg/ton, calculated as dry bentonite on dry stock system Table 6 shows the dewatering and retention effect at various dosages of P1 and P2, calculated as dry polymer on dry stock system.
Table 6 TestPolymer Bentonote ConductivityDewatering Turbidity No. Dosage dosage time [NTU]
[s]
[kglt] [kglt] [mSlcm] P1 P2 P1 P2 1 1 8 10.0 13.6 18.5 41 47 2 2 8 10.0 10.8 20.6 29 41 3 3 8 10.0 8.48 24.8 20 36 4 4 8 10.0 7.42 26.6 18 36 Example 7 In this test series, the dewatering effect was evaluated as in Example 6, except that sodium chloride was used to adjust the conductivity.
The polymers and bentonite according to Example 6 were similarly used in these tests. The bentonite particles were added in an amount of 8.0 kg/ton, calculated as dry bentonite on dry stock system. Table 7 shows the dewatering and retention effect at various dosages of P1 and P2, calculated as dry polymer on dry stock system.
Table 7 Test Polymer BentoniteConductivityDewatering time No. Dosage dosage [s]
[kglt] [kglt] [mSlcm] P1 P2 550 ppm Na+
1 2 8 2.5 15.3 17.5 2 3 8 2.5 11.9 14.1 3 4 8 2.5 8.6 9.8 4 5 8 2.5 6.8 8.2 3320 ppm Na+
5 2 8 10.0 12.7 15.5 6 3 8 10.0 9.4 12.5 7 4 8 10.0 6.9 10.9 8 5 8 10.0 5.6 10.0 Example 8 In this test series, the dewatering effect was ealuated as in Example 3, except that zink chloride was used to adjust the conductivity. The polymers and anionic inorganic particles according to Example 1 were similarly used in these tests.
Table 8 shows the results of the dewatering tests at various dosages of silica-based particles, calculated as as Si02 and based on dry stock system.
Table 8 Test Polymer SiOZ ConductivityDewatering No. Dosage dosage time Is]
[kglt] [kglt] [mSlcm] P1 P2 700 ppm Zn2+
1 2 0 2.4 13.6 22.7 2 2 1 2.4 7.9 8.5 3 2 2 2.4 5.5 5.6 1400 ppm Znz+
4 2 0 4.5 18.0 28.0 2 2 4.5 8.3 11.4
The stock was taken from a closed mill using waste paper. Consistency was 0.14%, conductivity 8.0 mS/cm and pH about 7. Table 4 shows the dewatering effect at various dosages of silica-based particles, calculated as Si02 and based on dry stock system Table 4 Test Polymer SiOz ConductivityDewatering No. dosage Dosage time [s]
[kglt] [kglt] [mSlcm] P1 P2 1 0.6 0 8.0 100.4 103.2 2 0.6 0.25 8.0 66.4 92.5 3 0.6 0.5 8.0 58.3 85.8 4 0.6 0.75 8.0 50.0 76.0 5 0.6 1 8.0 44.6 79.2 5 Example 5 In this test series, the dewatering effect was evaluated as in Example 3, except that both sodium acetate (550 ppm Na') and calcium chloride (1300 ppm Ca2') was used to adjust the conductivity.
The polymers and anionic inorganic particles according to Example 1 were 10 similarly used in this test series.
Table 5 shows the dewatering effect at various dosages of silica-based particles, calculated as Si02 and based on dry stock system.
Table 5 Test Polymer Si02 ConductivityDewatering No. dosage dosage time [s]
[kglt] [kglt] [mSlcm] P1 P2 1 2 1 2.5 16.1 18.2 2 1 3 10.0 10.7 14.7 3 2 3 10.0 6.8 13.5 4 3 3 10.0 5.3 14.0 5 2 1 10.0 9.7 20.4 6 2 2 10.0 7.9 14.8 15 Example 6 In this test series, the dewatering and retention effect was evaluated as in Example 3, using a combination of sodium acetate (550 ppm Na+) and calcium chloride (1300 ppm Ca2+) to adjust the conductivity.
The polymers according to Example 1 were similarly used in this test series.
The anionic microparticulate material used was hydrated suspension of powdered Na bentonite in water. The bentonite had a surface charge of about 0.33 meq/g and a swelling ability of 41 ml (2 g}. The bentonite particles were added in an amount of 8.0 kg/ton, calculated as dry bentonite on dry stock system Table 6 shows the dewatering and retention effect at various dosages of P1 and P2, calculated as dry polymer on dry stock system.
Table 6 TestPolymer Bentonote ConductivityDewatering Turbidity No. Dosage dosage time [NTU]
[s]
[kglt] [kglt] [mSlcm] P1 P2 P1 P2 1 1 8 10.0 13.6 18.5 41 47 2 2 8 10.0 10.8 20.6 29 41 3 3 8 10.0 8.48 24.8 20 36 4 4 8 10.0 7.42 26.6 18 36 Example 7 In this test series, the dewatering effect was evaluated as in Example 6, except that sodium chloride was used to adjust the conductivity.
The polymers and bentonite according to Example 6 were similarly used in these tests. The bentonite particles were added in an amount of 8.0 kg/ton, calculated as dry bentonite on dry stock system. Table 7 shows the dewatering and retention effect at various dosages of P1 and P2, calculated as dry polymer on dry stock system.
Table 7 Test Polymer BentoniteConductivityDewatering time No. Dosage dosage [s]
[kglt] [kglt] [mSlcm] P1 P2 550 ppm Na+
1 2 8 2.5 15.3 17.5 2 3 8 2.5 11.9 14.1 3 4 8 2.5 8.6 9.8 4 5 8 2.5 6.8 8.2 3320 ppm Na+
5 2 8 10.0 12.7 15.5 6 3 8 10.0 9.4 12.5 7 4 8 10.0 6.9 10.9 8 5 8 10.0 5.6 10.0 Example 8 In this test series, the dewatering effect was ealuated as in Example 3, except that zink chloride was used to adjust the conductivity. The polymers and anionic inorganic particles according to Example 1 were similarly used in these tests.
Table 8 shows the results of the dewatering tests at various dosages of silica-based particles, calculated as as Si02 and based on dry stock system.
Table 8 Test Polymer SiOZ ConductivityDewatering No. Dosage dosage time Is]
[kglt] [kglt] [mSlcm] P1 P2 700 ppm Zn2+
1 2 0 2.4 13.6 22.7 2 2 1 2.4 7.9 8.5 3 2 2 2.4 5.5 5.6 1400 ppm Znz+
4 2 0 4.5 18.0 28.0 2 2 4.5 8.3 11.4
Claims (19)
1. A process for the production of paper from a suspension containing cellulosic fibres, comprising adding to the suspension a drainage and retention aid comprising a cationic organic polymer, forming and dewatering the suspension on a wire, characterised that the cationic organic polymer has an aromatic group and that the suspension which is dewatered on the wire has a conductivity of at least 2.0 mS/cm.
2. A process according to claim 1, characterised in that the amount of any fresh water introduced is less than 30 tons per ton of dry paper produced.
3. A process according to claim 1, characterised in that the process further comprises dewatering the suspension on a wire to obtain a wet web of paper and white water, recirculating the white water to form a suspension containing cellulosic fibres to be dewatered, and introducing fresh water in an amount of less than 20 tons per ton of dry paper produced.
4. A process according to claim 1, 2 or 3, characterised in that the suspension additionally contains fillers.
5. A process according to claim 1, 2, 3 or 4, characterised in that fresh water is introduced in the formation of the suspension.
6. A process according to claim 1, 2, 3, 4 or 5, characterised in that the suspension which is dewatered on the wire has a conductivity of at least 5.0 mS/cm.
7. A process according to claim 1, 2, 3, 4, 5 or 6, characterised in that less than tons of fresh water is introduced per ton of dry paper produced.
8. A process according to claim 1, 2, 3, 4, 5, 6 or 7, characterised in that the cationic organic polymer is a vinyl addition polymer comprising in polymerized form one or more monomers comprising at least one monomer having an aromatic group.
9. A process according to any one of claims 1 to 8, characterised in that the cationic organic polymer is an acrylamide-based polymer.
10. A process according to any one of claims 1 to 9, characterised in that the cationic organic polymer comprises in polymerized form a cationic monomer having an aromatic group represented by the general formula (I):
wherein R1, is H or CH3, R2 and R3 are each an alkyl group having from 1 to 3 carbon atoms, A1 is O or NH, B1 is an alkylene group of from 2 to 4 carbon atoms or a hydroxy propylene group, Q is benzyl, and X- is an anionic counterion.
wherein R1, is H or CH3, R2 and R3 are each an alkyl group having from 1 to 3 carbon atoms, A1 is O or NH, B1 is an alkylene group of from 2 to 4 carbon atoms or a hydroxy propylene group, Q is benzyl, and X- is an anionic counterion.
11. A process according to any one of claims 1 to 10, characterised in that the cationic organic polymer has a weight average molecular weight of at least 1,000,000.
12. A process according to any one of claims 1 to 11, characterised in that the cationic organic polymer is prepared from a monomer mixture comprising from 5 to 20 mole% of cationic monomer having an aromatic group and from 95 to 80 mole%
of other copolymerizable monomers.
of other copolymerizable monomers.
13. A process according to any one of claims 1 to 12, characterised in that the drainage and retention aid further comprises anionic inorganic particles.
14. A process according to claim 13, characterised in that the anionic inorganic particles are selected from the group consisting of silica-based particles and bentonite particles.
15. A process according to claim 13 or 14, characterised in that the anionic inorganic particles are selected from aluminium-modified silica-based particles.
16. A process according to any one of claims 1 to 15, characterised in that the drainage and retention aid further comprises a low molecular weight cationic organic polymer.
17. A process according to any one of claims 1 to 16, characterised in that the drainage and retention aid further comprises an aluminium compound.
18. A process according to any one of claims 1 to 17, characterised in that the suspension which is dewatered on the wire has a content of di- and multivalent cations of at least 200 ppm.
19. A process according to any one of claims 1 to 18, characterised in that the suspension comprises recycled fibres.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
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| US8325398P | 1998-04-27 | 1998-04-27 | |
| US60/083,253 | 1998-04-27 | ||
| EP98850067A EP0953680A1 (en) | 1998-04-27 | 1998-04-27 | A process for the production of paper |
| EP98850067.4 | 1998-04-27 | ||
| PCT/SE1999/000677 WO1999055965A1 (en) | 1998-04-27 | 1999-04-26 | A process for the production of paper |
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| CA002329191A Expired - Fee Related CA2329191C (en) | 1998-04-27 | 1999-04-26 | A process for the production of paper |
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| JP (3) | JP4307721B2 (en) |
| CN (3) | CN1155754C (en) |
| AT (3) | ATE243281T1 (en) |
| AU (3) | AU748735B2 (en) |
| BR (3) | BR9909947A (en) |
| CA (3) | CA2329027C (en) |
| CZ (3) | CZ301092B6 (en) |
| DE (3) | DE69908938T2 (en) |
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| ES (3) | ES2196815T3 (en) |
| ID (3) | ID27899A (en) |
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| KR100403839B1 (en) * | 1998-04-27 | 2003-11-01 | 악조 노벨 엔.브이. | A process for the production of paper |
| US6417268B1 (en) | 1999-12-06 | 2002-07-09 | Hercules Incorporated | Method for making hydrophobically associative polymers, methods of use and compositions |
| US6846384B2 (en) | 2000-08-07 | 2005-01-25 | Akzo Nobel N.V. | Process for sizing paper |
| CA2418424C (en) * | 2000-08-07 | 2008-10-28 | Akzo Nobel N.V. | A process for the production of paper |
| GB0019415D0 (en) * | 2000-08-09 | 2000-09-27 | Ciba Spec Chem Water Treat Ltd | Noval monomers, polymers thereof and the use of the polymers |
| WO2002025013A1 (en) | 2000-09-20 | 2002-03-28 | Akzo Nobel N.V. | A process for the production of paper |
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1998
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