NZ230427A - Process for dewatering cellulose pulp on a wire - Google Patents

Process for dewatering cellulose pulp on a wire

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Publication number
NZ230427A
NZ230427A NZ230427A NZ23042789A NZ230427A NZ 230427 A NZ230427 A NZ 230427A NZ 230427 A NZ230427 A NZ 230427A NZ 23042789 A NZ23042789 A NZ 23042789A NZ 230427 A NZ230427 A NZ 230427A
Authority
NZ
New Zealand
Prior art keywords
colloid
process according
anionic
cationic
aluminate
Prior art date
Application number
NZ230427A
Inventor
Hans Erik Johansson
Original Assignee
Eka Nobel Ab
Priority date (The priority date 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 date listed.)
Filing date
Publication date
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=20373187&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NZ230427(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Eka Nobel Ab filed Critical Eka Nobel Ab
Publication of NZ230427A publication Critical patent/NZ230427A/en

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Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/46Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/54Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/34Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/41Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
    • D21H17/44Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups cationic
    • D21H17/45Nitrogen-containing groups
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/63Inorganic compounds
    • D21H17/67Water-insoluble compounds, e.g. fillers, pigments
    • D21H17/68Water-insoluble compounds, e.g. fillers, pigments siliceous, e.g. clays

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Paper (AREA)
  • Diaphragms For Electromechanical Transducers (AREA)
  • Making Paper Articles (AREA)
  • Polarising Elements (AREA)
  • Electronic Switches (AREA)

Abstract

A method for the production of paper by forming and dewatering a suspension of cellulose containing fibres on a wire. The forming and dewatering takes place in the presence of an anionic, inorganic colloid, an aluminate and a cationic synthetic polymer. The process gives improved dewatering and improved retention of fines and optional fillers.

Description

New Zealand Paient Spedficaiion for Paient Number £30427 230 4 27! NO DRAWINGS , -T< «• Priority Date(s): Complete Specification Filed: •.?: A*?. Qhs: ?£«£&/&>.>lit,• • • - Publication Date: £? JUN 691 P.O." Journal. No: J \b*b N.Z. No.
NEW ZEALAND Patents Act 1953 COMPLETE SPECIFICATION A PROCESS FOR THE PRODUCTION OF PAPER We, EKA NOBEL AB, a Swedish company, of S-445 01 Surte, Sweden do hereby declare the invention, for which we pray that a patent nay be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement (Followed by 1A) 230 427' lA A process for the production of paper The present invention relates to a process for the production of paper utilizing an improved retention- and dewatering system. More particularly the invention relates to the use of a combination of a cationic synthetic polymer, an anionic inorganic colloid and aluminate as retention- and dewatering system in papermaking.
It is previously known to use combinations of cat-ionic retention agents and inorganic colloids as retention-and dewatering agents in the production of paper. The European patent application 0218674 discloses the use of polyacrylamide in combination with anionic silica sols as binders and retention agents. It is assumed that the colloidal particles of the sols with their strong charges produce a cross-linking of the polymeric retention agents and that very good retention and dewatering effect is obtained through this. From the British patent 2015614 it is further known to use polymeric cationic retention agents in combination with poly alum i num compounds. It is further known from the US patent 4,643,801 to use a combination of a cationic starch, an anionic silica sol and an anionic high molecular weight polymer, particularly an anionic polyacrylamide, as a binder in papermaking. The three component system according to the US patent can be used with additional aluminum compounds, such as alum, sodium aluminate or polyhydroxyaluminum chloride.
According to the present invention it has been found that the retention- and dewatering effect in papermaking is improved if an aluminate is used in combination with cationic, synthetic polymer and an anionic inorganic colloid. As the dewatering effect is increased the speed of the papermachine can be increased and, further, less water will have to be dried off in the drying section of the paper machine.
The present invention thus . relates to a process for the production of paper by forming and dewatering a suspension of cellulose containing fibres, and optionally fillers, on a wire whereby the forming and dewatering takes m . ■ 25QA77 2 place in the presence of em anionic inorganic colloid AYfinHing polymeric silicic acid with, a specific surface area of at least 1050 nfVg, an aluminate and a cationic synthetic polymer.
The three components can be added to the fibre stock in arbitrary order. The best effect is obtained if the 5 aluminate is added to the stock first, followed by addition v of cationic synthetic polymer and then the anionic inor ganic colloid. A considerable improvement, in comparison with known technique, is obtained also when the anionic inorganic colloid is first added to the stock and the 10 cationic polymer and the aluminate are added subsequently, in any order. Separate addition of the three respective components is preferred although it is possible to pre-mix two of the components before the addition.
As cationic synthetic polymers for use according to 15 the present invention such cationic, organic nitrogen containing polymers which are conventionally used as retention agents and/or wet strength agents in papermaking are suitable. Particularly suitable are cationic polyacryl-amides, polyethyleneimines, poly ami ne resins and polyamido-20 amine resins etc. Polyamine resins and polyamidoamine resins are suitably used in their epichl orohydrine modified form. Other cationic synthetic polymers which can also be used are the cationic melamine-formaldehyde and urea— formaldehyde wet strength resins. The amount of the cat-25 ionic synthetic polymer should suitably be within the range of from 0.01 to 3 per cent by weight, preferably within the range of from 0.03 to 2 per cent by weight, based on dry fibres and optional fillers.
/ " The anionic inorganic colloids which are used are • per se previously known for use in papermaking. As examples of such colloids can be mentioned montmorillonite, ben— tonite, titanyl sulphate sols, silica sols, aluminum modified silica sols or aiiim-inum silicate sols. The terms colloid anfl colloidal indicate very smal 1 particles. The 35 particles of the anionic substances should suitably have a specific surface area above 50 m2/g, more suitably above 100 m2/g, preferably within the range of 50 to 1000 m2/g. Silica based collwidj ul u Qii^flgeretred anionic inor- r PAT^*-1' — 17 MAY 19-1 | ' —1 230427 3 gaiiic colloid.
Particularly suitable silica based colloids are the silica sols with, colloidal particles as disclosed in the European patent 41056, which is hereby incorporated by reference in this application, and the aluminum containing silica sols which are disclosed in the European patent application 0218674, which likewise is incorporated by reference. The colloidal silica in the sols should preferably have a specific surface area of 50 to 1000 m2/g and more preferably of about 100 to 1000 m2/g, and the best results have been obtained when the specific surface area has been about 300 to 700 m2/g. It has been found that the colloidal silica particles should suitably have a particle size below 20 nm and preferably from about 10 down to about 1 nm (a colloidal silica particle having a specific surface area of about 550 m2/g corresponds to an average particle size of about 5 nm). Good results are obtained with the mentioned silica sols in the form of an alkali stabilized sol which contains about 2 to 60 per cent by weight of SiC>2, preferably from about 4 to 30 per cent by weight of S102. The silica sol can be stabilized with alkali in a molar ratio of Si02:M20 of from 10:1 to 300:1, preferably 15:1 to 100:1 (M is an ion from the group Na, K, Li and NH4). As mentioned above good results are obtained using colloidal particles which have at least a surface layer of aluminum silicate or aluminum modified silica sol, so that' the surface groups of the particles contain silicon and aluminum atoms in a ratio of from 9.5:0.5 to 7.5:2.5 and the given surfaces and particle sizes also apply to these sols. Silica sols which fulfil the above given specific- . ations sure available commercially, eg from Eka Nobel AB.
The amount of anionic colloid which is added to the stock should suitably be within the range of from 0.005 to 2 per cent by weight, preferably from 0.01 to 0.4 per cent by weight, based on dry cellulose fibres and optional fillers. The concentration of the colloid, preferably colloidal silica, in the sol added to the stock is not • critical. Prom a practical point of view it is suitable 230427 © o © 4 that the sols at the addition to the stock have a concentration of from 0.05 to 5.0 per cent by weight.
Aluminate refers to alkali aluminate which per se is well-known for use in paper production, particularly for 5 hydrophobing with rosin. Sodium aluminate (Na2Al204) is preferably used, but potassium aluminate can of course also be used even if is less advantageous from an economical point of view. The amount of aluminate can vary within wide limits. The addition of aluminate to the stock is suitably 10 made in the form of aqueous solutions and the concentration in the solutions is not critical but is adjusted with regard to practical considerations. According to the invention it has been found that already very <=amal i amounts of aluminate, with regard to the amount of anionic inor-15 ganic colloid, give considerable improvements in the dewatering effect. An improvement is obtained already at a weight ratio aluminate, calculated as AI2O3, to inorganic colloid of 0.01:1. The upper limit is not critical. However, no improvements worth mentioning are obtained when 20 the ratio of aluminate to inorganic colloid exceeds 3:1. The ratio is suitably within the range of from 0.02:1 to 1.5:1 and preferably from 0.05:1 to 0.7:1. The given ratios all relate to weight ratio between aluminate, calculated as AI2O3, and the inorganic colloid.
The improved retention- and dewatering effect with the system of the invention is obtained over a broad pH range for the stock. The pH can be within the range from about 4 to about 10. The pH is suitably above 5 and preferably within the range of from 6 to 9. If the desired pH is 30 not reached by the addition of the aluminate solution, which in itself is alkaline, the pH of the stock can be adjusted for example by addition of sodium hydroxide. If alkaline buffering fillers are used, for example chalk, a suitable pH is normally reached without adjustments. Other 35 fillers than chalk can of course also be used, but then care has to be taken so that the pH of the stock is kept within the above given limits.
At paper production according to the invention 230427 mineral fillers of conventional types can be used, for example kaolin, titanium dioxide, gypsum, chalk and talcum. The term "mineral filler" is herein used to include, in addition to these fillers, also wollastonite and glass fibres and also mineral low density fillers, such as expanded perlite. The mineral filler is usually added in the form of an aqueous slurry in conventional concentrations used for such fillers. The filler can optionally be treated before the addition to the stock with components of the dewatering- and retention- system of the invention, for example by treatment with the cationic synthetic polymer and the aluminate or the inorganic colloid, whereafter the remaining component is added to the stock.
The three-component system of the invention can be used at production of paper from different types of stocks of cellulose containing fibres. The stocks should suitably contain at least 50 per cent by weight of cellulose containing fibres. The three-component system can for example be used for stocks of fibres from chemical pulp, such as sulphate and sulphite pulp, thermomechanical pulp, refiner pulp and groundwood pulp from as well hardwood as softwood. It can of course also be used for stocks from recycled fibres. The terms paper and papermaking, which are used herein do of course not only include paper and its production, but also other cellulose fibre containing sheet or web form products, such as pulp sheet, board and cardboard and their production.
The process according the invention can be carried out in per se known manner and with other additions to the fibre stock, such as sizing agents etc.
The invention is further illustrated in the following examples wherein parts and per cent relate to parts by weight and per cent by weight Tin!ess otherwise stated.
Example 1 In the following tests the dewatering effect was investigated by means of a "Canadian Freeness Tester", which is the usual method for characterizing the dewatering capability according to SCAN-C 21:65. 230427 6 The stock was based on bleached birch/pine sulphate pulp (60:40) and contained 30 per cent by weight of chalk. The pH of the stock was 8.5 and CSF was 300 ml.
In the table amounts for the chemical additions refer to ton dry stock system (fibres+fillers). The anionic colloid was an alkali stabilized silica sol with a specific surface area of 500 m2/g. The cationic synthetic polymer was a cationic polyacrylamide of medium cationicity sold by Allied Colloids under the name Percol 292. The sodium a Tumi nate was added in the form of a 0.025% aqueous solution and the given amounts of aluminate are expressed as kg AI2O3. The additions of chemicals were made to l 1 diluted stock (about 0.3%) with intervals of 15 seconds under agitation in the order aluminate, cationic polymer, inorganic colloid. The flocked stock was transferred to the freeness apparatus and measurements were made 15 seconds after the last addition. The water which is collected is a measurement of the dewatering effect and is expressed in ml Canadian Standard Freeness (CSF). The water obtained in the tests using the three components was very clear and this shows that a good retention of the fines material to the flocks had also been obtained.
Test AI2O3 Cationic Anionic CSF No. kq/t polymer kq/t Colloid kq/t ml 1 - - — 300 2 - 0.3 - 370 3 - 0.6 - 385 4 - 0.9 . - 390 0.15 - — 290" 6 0.15 0.3 — 350 7 - - 1.0 295 8 0.15 — 1.0 290 9 - 0.3 0.5 420 - 0.3 1.0 430 11 - 0.3 1.5 440 12 0.075 0.3 0.5 495 13 0.15 0.3 1.0 520 14 0.225 0.3 1.5 515 o 2304 2 Test AI2O3 Cationic Anionic CSF No. kq/t polymer kq/t Colloid kq/t ml - 0.6 0.5 425 16 - 0.6 1.0 490 5 17 - 0.6 1.5 510 C18 0.075 0.6 0.5 495 19 0.15 0.6 1.0 570 0.225 0.6 1.5 585 As evident also use of very small amounts of alumi- nate gives a considerably improved dewatering effect for the system of cationic polymer and anionic colloid. The corresponding effect of the aluminate is not obtained if it is used in combination with only cationic polymer or only anionic colloid.
Example 2 This example corresponded entirely to example 1 with the only difference that other cationic synthetic polymers were used. These were A) an epichlorohydrine modified polyamidoamine resin sold by Hercules Inc. under the name 20 Kymene 557 H and B) a modified polyamine resin sold by Hercules Inc. under the name Delfloc-50. 0 Test AI2O3 Cat.
Polymer Anionic CSF No. kq/t type;kq/t Colloid kq/t ml 1 - - 300 2 - A; 0.6 305 3 - A; 1.2 315 4 - A; 2.4 315 - A; 1.2 0.5 325 6 - A; 1.2 1.0 330 7 - A; 1.2 1.5 310 8 0.075 A; 1.2 0.5 360 9 0.15 A; 1.2 1.0 390 0.225 A; 1.2 1.5 410 11 0.30 A; 1.2 2.0 395 12 - B; 1.2 290 13 - B; 1.2 1.5 280 14 0.225 B; 1.2 1.5 335 2304 Example 3 In this example a groundwood stock was used which did not contain any fillers. To the stock 0.5 g/1 of Na2S04 • IOH2O had been added to give an ion strength 5 corresponding to the one under large scale conditions. The cationic polymer was the same polyacrylamide as in Example 1. The anionic colloid was an aluminum modified, 15% alkali stabilized, silica sol where the surface of the colloidal particles had been modified with 9% aluminum atoms and the 10 surface area of the particles was 500 m2/g. The order of addition was sodium aluminate, cationic polymer followed by anionic colloid. Tests were made both with a stock pH of 6 and a stock pH of 7.5 whereby the pH had been adjusted with diluted H2SO4 and diluted NaOH respectively.
Test AI2O3 Cationic Anionic CSF NO kq/t polymer kq/t colloid kq/t ml PH 6.0 1 - - - 120 2 - 0.3 - 190 3 - 0.6 - 220 4 — 0.9 1.2 - 250 6 - 0.6 0.5 275 7 - 0.6 1.0 305 8 - 0.6 • r-4 300 9 0.075 0.6 0.5 325 0.15 0.6 1.0 345 11 0.225 0.6 1.5 350 PH 7.5 12 - 0.6 - 220 13 - 0.6 0.5 245 14 - 0.6 1.0 270 - 0.6 1.5 275 16 0.075 0.6 0.5 295 17 0.15 0.6 1.0 325 18 0.225 0.6 1.5 340 19 - 0.9 1.5 310 0.225 0.9 1.5 370

Claims (11)

o 230427 Example 4 In these tests a groundwood stock with addition of 0.5 g/1 of NajSO^.IOH2O was vised as in Example 3. The pH of the stock was 6.5 and the added chemicals were sodium aluminate, a cationic polyethylene imine sold by BASF under the name Polyrain SK and an anionic colloid which was a bentonite colloid having a specific surface area of from about 400 to 800 m2/g in water. 10 Test AI2O3 Cationic Anionic CSF No. kq/t polymer kq/t colloid kq/t ml 1 — - — 120 2 — 0.3 - 175 3 - 0.6 — 230 4 — 0.9 - 300 5 — 1.2 — 310 6 — 0.6 0.5 260 7 - 0.6 1.0 280 8 — 0.9 1.0 340 9 0.075 0.6 0.5 295 10 0.15 0.6 1.0 335 11 0.15 0.9 1.0 390 15 20 0 230427 WHA&TwS CLAIM IS: , ' 10
1. A process for the production of paper by forming apf? dewatering a suspension of cellulose containing fibres on a wire, characterized in that the forming and dewatering 5 takes place in the presence of an anionic inorganic colloid excluding polymeric silicic acid with a specific surface area of at least 1050m2/g, an aluminate and a cationic synthetic polymer.
2. A process according to claim 1, characterized in that the anionic colloid is a silica based colloid.
3. A process according to claim 1 or 2, characterized 10 in that the colloid is a silica sol, a silica sol with particles having at least a surface layer of aluminum silicate or an aluminum modified silica sol.
4. A process accord g to claim 1, 2 or 3, characterized in that the particles of the colloid have a speci- 15 fic surface area within the range of from 50 to 1000 m2/g.
5. A process according to claim 3, characterized in that the particle size of the colloid is 20 nm at the most.
6. A process according to claim 1, characterized in that the cationic synthetic polymer is a cationic poly- 20 acrylamide, polyethyleneimine, polyamine or polyamidoamine.
7. A process according to any of the preceding claims, characterized in that the aluminate is added to the fibre suspension before the anionic inorganic colloid and the cationic synthetic polymer. 25
8. A process according to any of claims 1, 2, 3, 4 or 5, characterized in that the amount of anionic inorganic colloid is within the range of from 0.005 to 2 per cent by weight, based on dry fibres and optioned, fillers.
9. A process according to cl aim 1 or 6, characterized 30 in that the amount of cationic synthetic polymer is within the range of from 0.01 to 3 per cent by weight, based on dry fibres and optional fillers.
10. A process according to claim 1, characterized in that the weight ratio of aluminate, calculated as AL2O3, to 35 anionic inorganic colloid is within the range of from 0.01:1 to 3:1.
11. A process according to claim 1 substantially as herein described or exemplify 1 EKA NOBS
NZ230427A 1988-09-01 1989-08-25 Process for dewatering cellulose pulp on a wire NZ230427A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE8803065A SE467627B (en) 1988-09-01 1988-09-01 SET ON PAPER MAKING

Publications (1)

Publication Number Publication Date
NZ230427A true NZ230427A (en) 1991-06-25

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ID=20373187

Family Applications (1)

Application Number Title Priority Date Filing Date
NZ230427A NZ230427A (en) 1988-09-01 1989-08-25 Process for dewatering cellulose pulp on a wire

Country Status (13)

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EP (1) EP0357574B1 (en)
JP (1) JP2521539B2 (en)
AT (1) ATE99010T1 (en)
AU (1) AU605997B2 (en)
BR (1) BR8904283A (en)
CA (1) CA1334324C (en)
DE (1) DE68911626T2 (en)
ES (1) ES2048323T3 (en)
FI (1) FI90448C (en)
NO (1) NO171567C (en)
NZ (1) NZ230427A (en)
PT (1) PT91611B (en)
SE (1) SE467627B (en)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4795531A (en) * 1987-09-22 1989-01-03 Nalco Chemical Company Method for dewatering paper
US4927498A (en) * 1988-01-13 1990-05-22 E. I. Du Pont De Nemours And Company Retention and drainage aid for papermaking
SE500367C2 (en) * 1989-11-09 1994-06-13 Eka Nobel Ab Silica soles and process for making paper
ATE162249T1 (en) * 1991-07-02 1998-01-15 Eka Chemicals Ab METHOD FOR PRODUCING PAPER
DE4437118A1 (en) * 1994-10-05 1996-04-11 Technocell Dekor Gmbh & Co Kg Base paper for decorative coating systems
US5846384A (en) * 1995-06-15 1998-12-08 Eka Chemicals Ab Process for the production of paper
SE9502184D0 (en) * 1995-06-15 1995-06-15 Eka Nobel Ab A process for the production of paper
US5595630A (en) * 1995-08-31 1997-01-21 E. I. Du Pont De Nemours And Company Process for the manufacture of paper
SE9504081D0 (en) * 1995-11-15 1995-11-15 Eka Nobel Ab A process for the production of paper
JP3785322B2 (en) * 1999-05-04 2006-06-14 アクゾ ノーベル エヌ.ブイ. Silica-based sol
US7169261B2 (en) 1999-05-04 2007-01-30 Akzo Nobel N.V. Silica-based sols
US6379501B1 (en) 1999-12-14 2002-04-30 Hercules Incorporated Cellulose products and processes for preparing the same
CN1287046C (en) 2002-04-03 2006-11-29 星光Pmc株式会社 Method for producing paper and agent for improving yield
FI121119B (en) 2003-04-15 2010-07-15 Kemira Oyj Procedure for making paper
US8245359B2 (en) 2006-12-28 2012-08-21 Tokyo Kinzoku Industry Co., Ltd. Clip
CN103556532B (en) * 2013-10-31 2016-01-20 东莞理文造纸厂有限公司 A kind of retention aid for paper making and preparation method thereof

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE8403062L (en) * 1984-06-07 1985-12-08 Eka Ab PAPER MANUFACTURING PROCEDURES
SE451739B (en) * 1985-04-03 1987-10-26 Eka Nobel Ab PAPER MANUFACTURING PROCEDURE AND PAPER PRODUCT WHICH DRAINAGE AND RETENTION-IMPROVING CHEMICALS USED COTTONIC POLYACRYLAMIDE AND SPECIAL INORGANIC COLLOID
SE8701252D0 (en) * 1987-03-03 1987-03-25 Eka Nobel Ab SET FOR PAPER MAKING
US4795531A (en) * 1987-09-22 1989-01-03 Nalco Chemical Company Method for dewatering paper
US4927498A (en) * 1988-01-13 1990-05-22 E. I. Du Pont De Nemours And Company Retention and drainage aid for papermaking
SE461156B (en) * 1988-05-25 1990-01-15 Eka Nobel Ab SET FOR PREPARATION OF PAPER WHICH SHAPES AND DRAINAGE OWN ROOMS IN THE PRESENCE OF AN ALUMINUM SUBSTANCE, A COTTONIC RETENTION AND POLYMER SILICON ACID

Also Published As

Publication number Publication date
AU605997B2 (en) 1991-01-24
NO171567B (en) 1992-12-21
FI90448C (en) 1994-02-10
ATE99010T1 (en) 1994-01-15
EP0357574A2 (en) 1990-03-07
PT91611B (en) 1995-05-31
SE8803065L (en) 1990-03-02
CA1334324C (en) 1995-02-14
FI894075A0 (en) 1989-08-30
DE68911626D1 (en) 1994-02-03
NO893500L (en) 1990-03-02
JPH0299692A (en) 1990-04-11
JP2521539B2 (en) 1996-08-07
NO893500D0 (en) 1989-08-31
BR8904283A (en) 1990-04-17
SE8803065D0 (en) 1988-09-01
DE68911626T2 (en) 1994-04-07
FI90448B (en) 1993-10-29
PT91611A (en) 1990-03-30
ES2048323T3 (en) 1994-03-16
EP0357574A3 (en) 1991-10-23
AU4084089A (en) 1990-03-29
SE467627B (en) 1992-08-17
NO171567C (en) 1993-03-31
EP0357574B1 (en) 1993-12-22
FI894075A (en) 1990-03-02

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