CA1322436C - Pulp dewatering process - Google Patents
Pulp dewatering processInfo
- Publication number
- CA1322436C CA1322436C CA000594867A CA594867A CA1322436C CA 1322436 C CA1322436 C CA 1322436C CA 000594867 A CA000594867 A CA 000594867A CA 594867 A CA594867 A CA 594867A CA 1322436 C CA1322436 C CA 1322436C
- Authority
- CA
- Canada
- Prior art keywords
- pulp
- suspension
- polymer
- added
- cationic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C3/00—Pulping cellulose-containing materials
- D21C3/22—Other features of pulping processes
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/18—De-watering; Elimination of cooking or pulp-treating liquors from the pulp
-
- 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
- D21H23/76—Processes or apparatus for adding material to the pulp or to the paper characterised by choice of auxiliary compounds which are added separately from at least one other compound, e.g. to improve the incorporation of the latter or to obtain an enhanced combined effect
- D21H23/765—Addition of all compounds to the pulp
-
- 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
- D21H17/29—Starch cationic
-
- 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
-
- 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
Abstract
ABSTRACT
Pulp Dewatering Process Dry market pulp is made by shearing a cellulosic suspension and draining it through a screen to form a pulp sheet which is then dried, and the productivity of the process is increased by adding a water soluble cationic polymer before the shearing and bentonite or other suitable inorganic material after the shearing.
Pulp Dewatering Process Dry market pulp is made by shearing a cellulosic suspension and draining it through a screen to form a pulp sheet which is then dried, and the productivity of the process is increased by adding a water soluble cationic polymer before the shearing and bentonite or other suitable inorganic material after the shearing.
Description
~322~
Allied Colloids Limited 60/2863/02 Pulp Dewatering Process Paper or paper board is made by forming an aqueous cellulosic suspension (usually known as a thin stock), draining the suspension to form a sheet, and drying the sheet. The draining and drying stages are designed such that the sheet has the desired properties for the final paper or paper board and so generally involves calendering or other surface treatments to impart adequate smoothness and other performance properties to the sheet.
In order to optimise the process, it has for many years been standard practice to add various chemical additives to the suspension, and cationic polymers have been widely used for this purpose. Originally they were always natural or modified natural polymers, such as cationic starch, but synthetic cationic polymers have been widely used for man~ years. Their purpose is to act as retention aids and/or as dewatering aids and the polymer is chosen having regard to the desired property.
A retention aid serves to retain fine fibres and fine filler particles in the sheet. A dewatering aid serves to increase the rate of drainage or to increase the rate of dr~fing after drainage. These properties can be ~5 mutually conflicting and so a large amount of effort has, in recent years, been put into ways of optimising drainage and~dewatering.
The need to improve the quality of the final paper, to avoid loss of fibre or filler fines (for instance for environmental pollution reasons) and to optimise dewatering means that substantially every significant paper making process has, for many years, been operated using one or more retention and/dewatering aids.
The research into ways for improving these properties has led to the use of different materials in ~3~2~3~
the same process, including the use of sequential addition of different materials. One such process is described in U.S. 4,38~,150 and has been commercialised under the trade name Composil (trade mark ), and involves S the addition of cationic starch followed by colloidal silicic acid.
A particuarly successful process has been commercialised under the trade name Hydrocol (trade mark) and is described in EP 235893. It involves the addition of a s~nthetic cationic polymer, followed by shearing of the suspension, followed by the addition of bentonite.
It is of particular value in the production of fine papers.
The aqueous cellulosic suspensions that are used as the starting material in all these processes, and to which various retention aids and/or dewatering aids are then added, are in all instances made by pulping a fibrous cellulosic material, generally wood. The pulping involves comminution and suspension of the resultant fibres in water, and it is generally necessary to wash and filter the pulp several times. The filtering is normally effected by dxainage through a screen.
Some modern plants consist of integrated mills that serve both as pulp and paper mills, i.e.~ wood or other feedstock is converted to a pulp which is subjected to various washing and filtering stages and is finall~
diluted to a thin stock that is then drained to form the paper or paper board. In integrated mills of this type, it is unnecessary to dry the pulp at any stage, since it has to be resuspended in water at the same mill.
Accordingly the main objective is to ensure that the drainage oceurs quickly during eaeh washing and filtering stage. In praetice adequate drainage oceurs without the addition of any drainage aid and so normally no addition ~ ~, ', ' - ' - ' '' ' .
, , ~3~3~
of cationic polymers is made at the pulp end of an integrated mill, although extensive and sophisticated additions of cationic polymers are made at the paper end of the mill.
The more traditional method of making paper and board (and which is still used on a large scale worldwide) involves separatlon of the pulp-making and paper-making facilities. Thus wood or other fibrous cellulosic material is converted in a pulp mill to a dry product generally known as "dry market pulp". This dry pulp is then used as the feedstock at a paper mill to make the aqueous cellulosic suspension that is drained to make the paper or paper board. For instance the dry pulp may first be dispersed in water to form a thick stock which is then diluted to form a thin stock.
The pulping stages in the pulp mill can be generally similar to the pulping stages in an integrated mill but at the end of the washing stages it is necessary to drain the pulp and then thermally dry it. This drainage is normally conducted on a machine known as a "lap pulp machine".
It has, of course, been ~nown for many years that the drainage in this and the preceding stages could possibly be accelerated by the addition of a drainage aid but, despite the addition of sophisticated dewatering and retention systems in paper mills, ~it has not been found useful to add any such systems in pulp mills. One reason is that drainage aids may tend to reduce retention and since drainage is relatively fast in any event the disadvantage of reducing retention outweighs the advantage of accelerating drainage. Conversely, a retention aid is generally unnecessary since retention is satisfactory under normal drainage conditions. A
further disadvantage of drainage aids is that they tend to increa-e tle amount of th-r~al drying that is , ' .
" " .
~ ~2~
required. Thus they accelerate the _ree drainage but they result in the wet sheet containing a larger amount of trapped water, and so additional thermal drving is required.
The present state of the art therefore is that there is widespread use of cationic synthetic polymers (alone or with other materials) in the paper making stages but there is substantiall~ no use of cationic polymers in the pulp making stages because the application to the pulp stages of the paper making chemical technolog~ is not cost effective and ma,~ even worsen, rather than improve, the pulp making process.
Nevertheless it would, of course, be desirable to increase the rate of pulp production and, in particular, to increase the rate of production of dry market pulp and/or to reduce the amount of thermal energy that is required before drying it.
Despite the co-e~istence for many years of additive-free pulp making processes and of additive-including paper making processes, and despite all the contra-indications that warn against including additives in a pulp making process, we have now found that one particular set of additives do give a remarkable and bene~icial improvement in the production of dry market pulp.
In a pulp making process according to the invention, fibrous cellulosic material is pulped to form an aclueous suspension of cellulosic material, the suspension is subjected to one or more shear stages, the sheared suspension is drained through a screen to form a pulp sheet and the pulp sheet is dried to form a dry market pulp, and a water soluble polymer is added to the suspension before the shear stage or before one of the shear stages and an inorganic material is added to the su=pension after that shear st ge. ~he polymer is one :
:~3~2~3~
s that promotes drainage of the suspension through the screen and is selected from cationic starch and substantiall~ linear synthetic cationic polymers. The inorganic material is selected from colloidal silicic acid and ben-tonite.
The polymer can be cationic starch, as described in U.S. 4,388,150.
Preferably, however, the polymer is a substantially linear synthetic cationic polymer. It should have a molecular weight o above 500,000, preferably above abou~
1 million and often above about 5 milllon for instance in the range 10 to 30 million or more.
The pol-~mer may be a polymer of one or more ethylenically unsaturated monomers, generally acrylic monomers, that consist of or include cationic monomer.
Suitable cationic monomers are dialkvl amino alkyl~
(meth) acrylates or (meth) acrylamides, either as acid salts or, preferably, quaternary ammonium salts. The alk~l groups may each contain one to four carbon atoms and the aminoalkyl groups may contain one to eight carbon atoms. Particularly preferred are dialkylaminoethyl (meth) acrylates, dialk~laminomethyl (meth) acrvlamides and dialkyl amino-1,3-propyl (meth) acrylamides. These cationic monomers are preferably copolymerised with a non-ionic ~onomer, preferably acrylamide. Other suitable cationic polymers are polyethylene imines, polyamine epichlorohydrin polymers, other polyamines, polycyandiamide formaldehyde polymers and homopolymers or copolymers, generally ~Jith acrylamide, of monomers such as diall-~l dimethyl ammonium chloride.
The preferred polymers have an intrinsic viscosity - above 4 dl/g. Intrinsic viscosities herein are derived in standard manner from determination of solution viscosities by suspended level viscometer of solutions at 25C in 1 Molar NaCl buffered to pH about 7 using sodium phosphate.
', ' ~ . .
1322~3~
The polymer should be linear relative to the ~lobular structure o~ cationic starch. It can be wholly linear or it can be sli~htly cross lin~ed, as described in EP 202780. For instance it can be a branched product such as the polyethylene imine that is sold under the trade name Polymin SK.
In general, the molecular weight and chemical type of the polymer should be selected such that the polymer will promote drainage of the suspension through the screen. In general this means that the polymer is one that would be suitable for use as a retention or drainage aid in the production of paper.
The cationic polymer preferably has a relatively high charge densit~, for instance above 0.2, preferably at least 0.35, most preferably 0.4 to 2.5 or more, equivalents of cationic nitrogen per kilogram of polymer.
The inorganic material may be colloidal silicic acid that may be modified silicic acid as described in W086/5826, or may be other inorganic particulate material such as bentonite. Preferably the inorganic material has an extremely small particle size and thus should be of pigment size and preferably it is swellable in water.
When the polymer is cationic starch, the use of colloidal silicic acid is often preferred. When the polymer is synthetic, the preferred materials are bentonites, that is to say bentonite-type clays such as the anionic swelling clays known as sepialites, attapulgites ~and, most preferably,~ montmorillinites.
Suitable montmorillinites include Wyoming bentonite and Fullers Earth. The clays may or~ may not be chemically modified, e.g., by alkali treatment to convert calcium bentonite to alkali metal bentonite.
In general, the polymers and the~bentonites should preferably be as described in EP 235893.
.
~ 3~2~
It is important to add the bentonite or other silicate or other inorganic material after shearing, and to add the polymer before shearing. The pulp making process includes one or more shear stages, for instance cleaning, mixing and pumping stages such as are typified by centriscreens, vortex cleaners, fan pumps and mixing pumps. The polymer must be added before one of these and the bentoni~e or other inorganic material at a later stage. Generally the bentonite is added after the last shear stage and the polymer at some earlier stage, for instance just before the last shear stage. Thus the polymer may be added as the aqueous pulp leaves the penultimate shear stage or approaches the final shear stage (for instance a centriscreen or fan pump) and the bentonite or other inorganic material may be added substantially at the head box for the drainage screen.
Thus the bentonite may be added at the head box, or just prior to the head box, of the lap pulp machine, accompanied by sufficient mixing to mix the bentonite throughout the pulp, generally without applying significant shear at this stage.
This treatment prior to the lap pulp machine can have two beneficial effects. First, it can increase the rate of drainage. Second, and most important, the drained sheet can be easier to dry than when cationic polymer alone is used. As a result the pulp sheet can be passed ehrough the driers more quickly (or a thicker sheet can be passed a~ the same rate) and thus it is possible to increase the; production of the pulp mill and/or reduce the amount of thermal drying that is required, while producing a~ dry ~market pulp having suitable properties for normal paper making process.
This pulp is in the form of crude, non-calendered, sheet typically ha~ing a fibre weight of lOO to lOOO g/m2.
~' :
- '' .
-.
.
~ 3 ~
The amount of polymer that has to be added willdepend upon the nature of the pulp. It will normally be at least 0.005% and usually is at least 0.01 or 0.02%.
Although amounts above 0.1~ are usually unnecessary, larger amounts can be used ~typically 0.2%, 0.3~ or even up to, for instance, 0.5~. Preferred amounts are in the ran~e 0.02 to 0.1~ (200 to lO00 grams polymer per ton dry weight pulp).
The amount of inorganic material will be selected according to the nature of the pulp and the amount and t~ype of polymer and the type of inorganic material.
Suitable amounts, especially when the inorganic material is bentonite, are generally above 0.03% and usually above 0.1~, but amounts above 0.5% are generally unnecessary.
The preferred process uses from lO00 to 2500kg bentonite per ton dry weight of pulp.
The aqueous pulp to which the polymer is added will have been made by conventional methods from the wood or other feedstock. Deinked waste may be used to provide some of it. For instance the wood may be debarked and then subjected to grinding, chemical or heat pulping techniques, for instance to make a mechanical pulp, a thermomechanical Fulp or a chemical pulp. The pulp may have been washed and drained and rewashed with water or other aqueous ~wash liquor prior~ to reaching the final drainage stage on the lap pulp machine. The dry market pulp is generally free or substantially free of filler, but filler can be included if desired.
After ~drainage through the screen~of the lap pulp machine, the resultant wet sheet is then subjected to drying in conventional manner, for instance through a tunnel drier or over drying cyllnders, or both.
By the invention it~is possible easily to increase the production rate of dry market pulp, of constant water content, by lO to 20~ or even up to 30% or more.
:
,:
~32~3~
g The following are some examples.
ExamE~le 1 A pulp mill is operated in conventional manner to produce chemi-thermo mechanlcal pulp by conventional techniques terminating in pumping the pulp through a pump to the head boY~ of a lap pulp machine, the pulp -then being drained through the screen of this machine and taken off the screen and thermally dried to form the dry market pulp. When no polymeric or bentonite additives are included and the head box consistency is 1.42%, the mill operates at a speed of 31.1 metres per minute to produce 7.3 tonnes per hour of dried sheet weighing 566g/m2 and having a dryness after the third press of 43.8~. The steam demand is 6.6 tonnes per hour.
15In a process according to the invention, 700 grams per ton of a copolymer of 70~ by weight acrylamide 30% by weight dimethylaminoethyl acrylate methyl chloride quaternaxy salt, intrinsic viscosity lOdl/g, is added just before the pump and 2kg/ton bentonite is added at the head box. The consistency in the head box is 1.36~.
The machine runs at a speed of 83.7 metres per minute and produces 9.1 tonnes per hour of dry market pulp at 677g/m2 and having a dryness after the third press of ~6%. The steam demand is g.5 tonnes per hour. Thus the process of the invention gives an improvement in production of about 25% whilst reducing steam demand (per ton of pulp)~and increasing dryness. ~;
`When the process is repeated using hal the amount of polymer, the increased production is less, but is still more than lO~ above the process in the absence of polymer and bentonite.
Example 2 To demonstrate the effect of varying the proportions - of polymer and bentonite, a pulp of tissue fibres having a freeness value of 4iO has a speci4ied amount of polymer ~32~3~
added to it, the mlxture is subjected to high shear mixing for about one minute, bentonite is added and a standard volume of the pulp is subjected to a standard drainage evluation on a drainage tube using a standard S machine wire. The time is recorded in seconds. The value should be low.
The process is conducted using pulp A, which is a peroxide bleached chemi-thermo mechanical pulp and pulp B, which is a bleached sulphite pulp. The process is conducted with polymer C which is a copolymer having intrinsic viscosity from 8 to lOdl/g of 70% by weight acrylamide and 30% by weight dimethylaminoethyl acrylate quaternised with methyl chloride, and with polymer D
which is formed from the same monomers in a weight ratio 76:24 and has intrinsic viscosity 6 to 8.
The results are shown in the following table in which the amount of polymer and bentonite that is added is ~iven in kg/ton dry weight of pulp and the dewatering time is measured in seconds.
~: :
:~`
~1 3~2~3~
Pulp PolymerBentoniteDewateri~g Time A lC 2 45 A 1.5C 2 24 A 2C 1.5 16 A 2C 2.5 18 B 0.3D 2 20 B 0.8D 2 14 B 1.2D 2 14 B 1.6D 2 14 B O.5D 0.5 20 B 0.5D 1 18 B 0.5D 1.5 16 B O.SD 2.5 17 The benefit of the sequential addition of polymer and bentonite, relative to a process in~which no addition is made or polymer only is made, is clearly apparent from this table.
:
~ 30 :
: :
. .
'
Allied Colloids Limited 60/2863/02 Pulp Dewatering Process Paper or paper board is made by forming an aqueous cellulosic suspension (usually known as a thin stock), draining the suspension to form a sheet, and drying the sheet. The draining and drying stages are designed such that the sheet has the desired properties for the final paper or paper board and so generally involves calendering or other surface treatments to impart adequate smoothness and other performance properties to the sheet.
In order to optimise the process, it has for many years been standard practice to add various chemical additives to the suspension, and cationic polymers have been widely used for this purpose. Originally they were always natural or modified natural polymers, such as cationic starch, but synthetic cationic polymers have been widely used for man~ years. Their purpose is to act as retention aids and/or as dewatering aids and the polymer is chosen having regard to the desired property.
A retention aid serves to retain fine fibres and fine filler particles in the sheet. A dewatering aid serves to increase the rate of drainage or to increase the rate of dr~fing after drainage. These properties can be ~5 mutually conflicting and so a large amount of effort has, in recent years, been put into ways of optimising drainage and~dewatering.
The need to improve the quality of the final paper, to avoid loss of fibre or filler fines (for instance for environmental pollution reasons) and to optimise dewatering means that substantially every significant paper making process has, for many years, been operated using one or more retention and/dewatering aids.
The research into ways for improving these properties has led to the use of different materials in ~3~2~3~
the same process, including the use of sequential addition of different materials. One such process is described in U.S. 4,38~,150 and has been commercialised under the trade name Composil (trade mark ), and involves S the addition of cationic starch followed by colloidal silicic acid.
A particuarly successful process has been commercialised under the trade name Hydrocol (trade mark) and is described in EP 235893. It involves the addition of a s~nthetic cationic polymer, followed by shearing of the suspension, followed by the addition of bentonite.
It is of particular value in the production of fine papers.
The aqueous cellulosic suspensions that are used as the starting material in all these processes, and to which various retention aids and/or dewatering aids are then added, are in all instances made by pulping a fibrous cellulosic material, generally wood. The pulping involves comminution and suspension of the resultant fibres in water, and it is generally necessary to wash and filter the pulp several times. The filtering is normally effected by dxainage through a screen.
Some modern plants consist of integrated mills that serve both as pulp and paper mills, i.e.~ wood or other feedstock is converted to a pulp which is subjected to various washing and filtering stages and is finall~
diluted to a thin stock that is then drained to form the paper or paper board. In integrated mills of this type, it is unnecessary to dry the pulp at any stage, since it has to be resuspended in water at the same mill.
Accordingly the main objective is to ensure that the drainage oceurs quickly during eaeh washing and filtering stage. In praetice adequate drainage oceurs without the addition of any drainage aid and so normally no addition ~ ~, ', ' - ' - ' '' ' .
, , ~3~3~
of cationic polymers is made at the pulp end of an integrated mill, although extensive and sophisticated additions of cationic polymers are made at the paper end of the mill.
The more traditional method of making paper and board (and which is still used on a large scale worldwide) involves separatlon of the pulp-making and paper-making facilities. Thus wood or other fibrous cellulosic material is converted in a pulp mill to a dry product generally known as "dry market pulp". This dry pulp is then used as the feedstock at a paper mill to make the aqueous cellulosic suspension that is drained to make the paper or paper board. For instance the dry pulp may first be dispersed in water to form a thick stock which is then diluted to form a thin stock.
The pulping stages in the pulp mill can be generally similar to the pulping stages in an integrated mill but at the end of the washing stages it is necessary to drain the pulp and then thermally dry it. This drainage is normally conducted on a machine known as a "lap pulp machine".
It has, of course, been ~nown for many years that the drainage in this and the preceding stages could possibly be accelerated by the addition of a drainage aid but, despite the addition of sophisticated dewatering and retention systems in paper mills, ~it has not been found useful to add any such systems in pulp mills. One reason is that drainage aids may tend to reduce retention and since drainage is relatively fast in any event the disadvantage of reducing retention outweighs the advantage of accelerating drainage. Conversely, a retention aid is generally unnecessary since retention is satisfactory under normal drainage conditions. A
further disadvantage of drainage aids is that they tend to increa-e tle amount of th-r~al drying that is , ' .
" " .
~ ~2~
required. Thus they accelerate the _ree drainage but they result in the wet sheet containing a larger amount of trapped water, and so additional thermal drving is required.
The present state of the art therefore is that there is widespread use of cationic synthetic polymers (alone or with other materials) in the paper making stages but there is substantiall~ no use of cationic polymers in the pulp making stages because the application to the pulp stages of the paper making chemical technolog~ is not cost effective and ma,~ even worsen, rather than improve, the pulp making process.
Nevertheless it would, of course, be desirable to increase the rate of pulp production and, in particular, to increase the rate of production of dry market pulp and/or to reduce the amount of thermal energy that is required before drying it.
Despite the co-e~istence for many years of additive-free pulp making processes and of additive-including paper making processes, and despite all the contra-indications that warn against including additives in a pulp making process, we have now found that one particular set of additives do give a remarkable and bene~icial improvement in the production of dry market pulp.
In a pulp making process according to the invention, fibrous cellulosic material is pulped to form an aclueous suspension of cellulosic material, the suspension is subjected to one or more shear stages, the sheared suspension is drained through a screen to form a pulp sheet and the pulp sheet is dried to form a dry market pulp, and a water soluble polymer is added to the suspension before the shear stage or before one of the shear stages and an inorganic material is added to the su=pension after that shear st ge. ~he polymer is one :
:~3~2~3~
s that promotes drainage of the suspension through the screen and is selected from cationic starch and substantiall~ linear synthetic cationic polymers. The inorganic material is selected from colloidal silicic acid and ben-tonite.
The polymer can be cationic starch, as described in U.S. 4,388,150.
Preferably, however, the polymer is a substantially linear synthetic cationic polymer. It should have a molecular weight o above 500,000, preferably above abou~
1 million and often above about 5 milllon for instance in the range 10 to 30 million or more.
The pol-~mer may be a polymer of one or more ethylenically unsaturated monomers, generally acrylic monomers, that consist of or include cationic monomer.
Suitable cationic monomers are dialkvl amino alkyl~
(meth) acrylates or (meth) acrylamides, either as acid salts or, preferably, quaternary ammonium salts. The alk~l groups may each contain one to four carbon atoms and the aminoalkyl groups may contain one to eight carbon atoms. Particularly preferred are dialkylaminoethyl (meth) acrylates, dialk~laminomethyl (meth) acrvlamides and dialkyl amino-1,3-propyl (meth) acrylamides. These cationic monomers are preferably copolymerised with a non-ionic ~onomer, preferably acrylamide. Other suitable cationic polymers are polyethylene imines, polyamine epichlorohydrin polymers, other polyamines, polycyandiamide formaldehyde polymers and homopolymers or copolymers, generally ~Jith acrylamide, of monomers such as diall-~l dimethyl ammonium chloride.
The preferred polymers have an intrinsic viscosity - above 4 dl/g. Intrinsic viscosities herein are derived in standard manner from determination of solution viscosities by suspended level viscometer of solutions at 25C in 1 Molar NaCl buffered to pH about 7 using sodium phosphate.
', ' ~ . .
1322~3~
The polymer should be linear relative to the ~lobular structure o~ cationic starch. It can be wholly linear or it can be sli~htly cross lin~ed, as described in EP 202780. For instance it can be a branched product such as the polyethylene imine that is sold under the trade name Polymin SK.
In general, the molecular weight and chemical type of the polymer should be selected such that the polymer will promote drainage of the suspension through the screen. In general this means that the polymer is one that would be suitable for use as a retention or drainage aid in the production of paper.
The cationic polymer preferably has a relatively high charge densit~, for instance above 0.2, preferably at least 0.35, most preferably 0.4 to 2.5 or more, equivalents of cationic nitrogen per kilogram of polymer.
The inorganic material may be colloidal silicic acid that may be modified silicic acid as described in W086/5826, or may be other inorganic particulate material such as bentonite. Preferably the inorganic material has an extremely small particle size and thus should be of pigment size and preferably it is swellable in water.
When the polymer is cationic starch, the use of colloidal silicic acid is often preferred. When the polymer is synthetic, the preferred materials are bentonites, that is to say bentonite-type clays such as the anionic swelling clays known as sepialites, attapulgites ~and, most preferably,~ montmorillinites.
Suitable montmorillinites include Wyoming bentonite and Fullers Earth. The clays may or~ may not be chemically modified, e.g., by alkali treatment to convert calcium bentonite to alkali metal bentonite.
In general, the polymers and the~bentonites should preferably be as described in EP 235893.
.
~ 3~2~
It is important to add the bentonite or other silicate or other inorganic material after shearing, and to add the polymer before shearing. The pulp making process includes one or more shear stages, for instance cleaning, mixing and pumping stages such as are typified by centriscreens, vortex cleaners, fan pumps and mixing pumps. The polymer must be added before one of these and the bentoni~e or other inorganic material at a later stage. Generally the bentonite is added after the last shear stage and the polymer at some earlier stage, for instance just before the last shear stage. Thus the polymer may be added as the aqueous pulp leaves the penultimate shear stage or approaches the final shear stage (for instance a centriscreen or fan pump) and the bentonite or other inorganic material may be added substantially at the head box for the drainage screen.
Thus the bentonite may be added at the head box, or just prior to the head box, of the lap pulp machine, accompanied by sufficient mixing to mix the bentonite throughout the pulp, generally without applying significant shear at this stage.
This treatment prior to the lap pulp machine can have two beneficial effects. First, it can increase the rate of drainage. Second, and most important, the drained sheet can be easier to dry than when cationic polymer alone is used. As a result the pulp sheet can be passed ehrough the driers more quickly (or a thicker sheet can be passed a~ the same rate) and thus it is possible to increase the; production of the pulp mill and/or reduce the amount of thermal drying that is required, while producing a~ dry ~market pulp having suitable properties for normal paper making process.
This pulp is in the form of crude, non-calendered, sheet typically ha~ing a fibre weight of lOO to lOOO g/m2.
~' :
- '' .
-.
.
~ 3 ~
The amount of polymer that has to be added willdepend upon the nature of the pulp. It will normally be at least 0.005% and usually is at least 0.01 or 0.02%.
Although amounts above 0.1~ are usually unnecessary, larger amounts can be used ~typically 0.2%, 0.3~ or even up to, for instance, 0.5~. Preferred amounts are in the ran~e 0.02 to 0.1~ (200 to lO00 grams polymer per ton dry weight pulp).
The amount of inorganic material will be selected according to the nature of the pulp and the amount and t~ype of polymer and the type of inorganic material.
Suitable amounts, especially when the inorganic material is bentonite, are generally above 0.03% and usually above 0.1~, but amounts above 0.5% are generally unnecessary.
The preferred process uses from lO00 to 2500kg bentonite per ton dry weight of pulp.
The aqueous pulp to which the polymer is added will have been made by conventional methods from the wood or other feedstock. Deinked waste may be used to provide some of it. For instance the wood may be debarked and then subjected to grinding, chemical or heat pulping techniques, for instance to make a mechanical pulp, a thermomechanical Fulp or a chemical pulp. The pulp may have been washed and drained and rewashed with water or other aqueous ~wash liquor prior~ to reaching the final drainage stage on the lap pulp machine. The dry market pulp is generally free or substantially free of filler, but filler can be included if desired.
After ~drainage through the screen~of the lap pulp machine, the resultant wet sheet is then subjected to drying in conventional manner, for instance through a tunnel drier or over drying cyllnders, or both.
By the invention it~is possible easily to increase the production rate of dry market pulp, of constant water content, by lO to 20~ or even up to 30% or more.
:
,:
~32~3~
g The following are some examples.
ExamE~le 1 A pulp mill is operated in conventional manner to produce chemi-thermo mechanlcal pulp by conventional techniques terminating in pumping the pulp through a pump to the head boY~ of a lap pulp machine, the pulp -then being drained through the screen of this machine and taken off the screen and thermally dried to form the dry market pulp. When no polymeric or bentonite additives are included and the head box consistency is 1.42%, the mill operates at a speed of 31.1 metres per minute to produce 7.3 tonnes per hour of dried sheet weighing 566g/m2 and having a dryness after the third press of 43.8~. The steam demand is 6.6 tonnes per hour.
15In a process according to the invention, 700 grams per ton of a copolymer of 70~ by weight acrylamide 30% by weight dimethylaminoethyl acrylate methyl chloride quaternaxy salt, intrinsic viscosity lOdl/g, is added just before the pump and 2kg/ton bentonite is added at the head box. The consistency in the head box is 1.36~.
The machine runs at a speed of 83.7 metres per minute and produces 9.1 tonnes per hour of dry market pulp at 677g/m2 and having a dryness after the third press of ~6%. The steam demand is g.5 tonnes per hour. Thus the process of the invention gives an improvement in production of about 25% whilst reducing steam demand (per ton of pulp)~and increasing dryness. ~;
`When the process is repeated using hal the amount of polymer, the increased production is less, but is still more than lO~ above the process in the absence of polymer and bentonite.
Example 2 To demonstrate the effect of varying the proportions - of polymer and bentonite, a pulp of tissue fibres having a freeness value of 4iO has a speci4ied amount of polymer ~32~3~
added to it, the mlxture is subjected to high shear mixing for about one minute, bentonite is added and a standard volume of the pulp is subjected to a standard drainage evluation on a drainage tube using a standard S machine wire. The time is recorded in seconds. The value should be low.
The process is conducted using pulp A, which is a peroxide bleached chemi-thermo mechanical pulp and pulp B, which is a bleached sulphite pulp. The process is conducted with polymer C which is a copolymer having intrinsic viscosity from 8 to lOdl/g of 70% by weight acrylamide and 30% by weight dimethylaminoethyl acrylate quaternised with methyl chloride, and with polymer D
which is formed from the same monomers in a weight ratio 76:24 and has intrinsic viscosity 6 to 8.
The results are shown in the following table in which the amount of polymer and bentonite that is added is ~iven in kg/ton dry weight of pulp and the dewatering time is measured in seconds.
~: :
:~`
~1 3~2~3~
Pulp PolymerBentoniteDewateri~g Time A lC 2 45 A 1.5C 2 24 A 2C 1.5 16 A 2C 2.5 18 B 0.3D 2 20 B 0.8D 2 14 B 1.2D 2 14 B 1.6D 2 14 B O.5D 0.5 20 B 0.5D 1 18 B 0.5D 1.5 16 B O.SD 2.5 17 The benefit of the sequential addition of polymer and bentonite, relative to a process in~which no addition is made or polymer only is made, is clearly apparent from this table.
:
~ 30 :
: :
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Claims (10)
1. A pulp-making process in which fibrous cellulosic material is pulped to form an aqueous supension of cellulosic material, the suspension is subjected to one or more shear stages, the sheared suspension is drained through a screen to form a pulp sheet and the pulp sheet is dried to form a dry market pulp, and in which a water soluble polymer is added to the suspension before the shear stage or before one of the shear stages and an inorganic material is added to the suspension after that shear stage, and in which the polymer promotes drainage of the suspension through the screen and is selected from cationic starch and substantially linear synthetic cationic polymers, and the inorganic material is selected from colloidal silicic acid and bentonite.
2. A process according to claim 1 in which the polymer is a cationic substantially linear synthetic polymer having a molecular weight of 500000.
3. A process according to claim 2 in which the polymer is selected from polyethylene imine, polyamine epichlorhydrin products, polyamines, polydicyandiamide formaldehyde polymers, polymers of diallyl dimethyl ammonium chloride and polymers of acrylic monomers comprising a cationic acrylic monomer.
4. A process according to claim 2 in which the polymer is a cationic polymer having intrinsic viscosity above 4dl/g and formed from acrylic monomers comprising dialkylaminoalkyl (meth) -acrylate or -acrylamide, as acid or quaternary salt.
5. A process according to claim 2 in which the inorganic material is bentonite.
6. A process according to claim 2 in which the one or more shear stages are selected from cleaning, mixing and pumping stages comprising a centriscreen, a vortex cleaner, a fan pump or a mixing pump.
7. A process according to claim 1 in which the inorganic material is added to the suspension substantially immediately before the drainage through the screen.
8. A process according to claim 1 in which the polymer is added to the suspension and is subjected to shearing, the sheared suspension is fed to the head box of a lap pulp machine having a drainage screen, the inorganic material is added substantially at the head box, and the suspension is drained through the said screen to form the pulp sheet.
9. A process according to claim 1 in which the polymer is added in an amount of from 0.01 to 0.5% and the inorganic material is added in an amount of from 0.03 to 0.5%, based on the dry weight of suspension.
10. A pulp-making process in which fibrous cellulosic material is pulped to form an aqueous supension of cellulosic material, the suspension is subjected to one or more shear stages, selected from cleaning, mixing and pumping stages comprising a centriscreen, a vortex cleaner, a fan pump or a mixing pump and the sheared suspension is fed to the head box of a lap pulp machine having a drainage screen, and the suspension is drained through the screen to form a pulp sheet and the sheet is dried to form dry market pulp, and: in which 0.01 to 0.5%
(dry weight) of a water soluble cationic polymer is added to the suspension before the final shear stage, said polymer being selected from polyethylene imine, polyamine epichlorhydrin products, polyamines, polydicyandiamide formaldehyde polymers, polymers of diallyl dimethyl ammonium chloride and polymers of acrylic monomers comprising a cationic acrylic monomer, and 0.03 to 0.5%
(dry weight) of bentonite is added to the suspension substantially at the said head box.
(dry weight) of a water soluble cationic polymer is added to the suspension before the final shear stage, said polymer being selected from polyethylene imine, polyamine epichlorhydrin products, polyamines, polydicyandiamide formaldehyde polymers, polymers of diallyl dimethyl ammonium chloride and polymers of acrylic monomers comprising a cationic acrylic monomer, and 0.03 to 0.5%
(dry weight) of bentonite is added to the suspension substantially at the said head box.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8807445.5 | 1988-03-28 | ||
GB888807445A GB8807445D0 (en) | 1988-03-28 | 1988-03-28 | Pulp dewatering process |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1322436C true CA1322436C (en) | 1993-09-28 |
Family
ID=10634297
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000594867A Expired - Fee Related CA1322436C (en) | 1988-03-28 | 1989-03-28 | Pulp dewatering process |
Country Status (13)
Country | Link |
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US (1) | US4969976A (en) |
EP (1) | EP0335576B1 (en) |
JP (1) | JPH026684A (en) |
KR (1) | KR890014833A (en) |
AT (1) | ATE89350T1 (en) |
AU (1) | AU613464B2 (en) |
CA (1) | CA1322436C (en) |
DE (1) | DE68906452T2 (en) |
ES (1) | ES2040461T3 (en) |
FI (1) | FI92724B (en) |
GB (1) | GB8807445D0 (en) |
NO (1) | NO174723B (en) |
ZA (1) | ZA892281B (en) |
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CA1069742A (en) * | 1978-01-03 | 1980-01-15 | Edwin H. Flaherty | Pulp sheet formation |
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-
1988
- 1988-03-28 GB GB888807445A patent/GB8807445D0/en active Pending
-
1989
- 1989-03-22 EP EP89302843A patent/EP0335576B1/en not_active Revoked
- 1989-03-22 DE DE8989302843T patent/DE68906452T2/en not_active Revoked
- 1989-03-22 ES ES198989302843T patent/ES2040461T3/en not_active Expired - Lifetime
- 1989-03-22 AT AT89302843T patent/ATE89350T1/en not_active IP Right Cessation
- 1989-03-27 JP JP1074814A patent/JPH026684A/en active Pending
- 1989-03-28 KR KR1019890003910A patent/KR890014833A/en not_active Application Discontinuation
- 1989-03-28 ZA ZA892281A patent/ZA892281B/en unknown
- 1989-03-28 NO NO891302A patent/NO174723B/en unknown
- 1989-03-28 AU AU31746/89A patent/AU613464B2/en not_active Ceased
- 1989-03-28 CA CA000594867A patent/CA1322436C/en not_active Expired - Fee Related
- 1989-03-28 FI FI891466A patent/FI92724B/en not_active IP Right Cessation
- 1989-03-28 US US07/329,665 patent/US4969976A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
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ES2040461T3 (en) | 1993-10-16 |
NO891302L (en) | 1989-09-29 |
GB8807445D0 (en) | 1988-05-05 |
FI891466A0 (en) | 1989-03-28 |
DE68906452T2 (en) | 1993-09-23 |
US4969976A (en) | 1990-11-13 |
FI891466A (en) | 1989-09-29 |
EP0335576A2 (en) | 1989-10-04 |
ATE89350T1 (en) | 1993-05-15 |
KR890014833A (en) | 1989-10-25 |
ZA892281B (en) | 1990-05-30 |
FI92724B (en) | 1994-09-15 |
NO891302D0 (en) | 1989-03-28 |
DE68906452D1 (en) | 1993-06-17 |
AU3174689A (en) | 1989-09-28 |
AU613464B2 (en) | 1991-08-01 |
NO174723B (en) | 1994-03-14 |
EP0335576A3 (en) | 1990-12-19 |
JPH026684A (en) | 1990-01-10 |
EP0335576B1 (en) | 1993-05-12 |
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