ZA200103812B - Method of producing a particle or group of particles having a coating of polymers interacting with each other. - Google Patents
Method of producing a particle or group of particles having a coating of polymers interacting with each other. Download PDFInfo
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- ZA200103812B ZA200103812B ZA200103812A ZA200103812A ZA200103812B ZA 200103812 B ZA200103812 B ZA 200103812B ZA 200103812 A ZA200103812 A ZA 200103812A ZA 200103812 A ZA200103812 A ZA 200103812A ZA 200103812 B ZA200103812 B ZA 200103812B
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- South Africa
- Prior art keywords
- particles
- particle
- polymers
- fibers
- paper
- Prior art date
Links
- 239000002245 particle Substances 0.000 title claims description 55
- 229920000642 polymer Polymers 0.000 title claims description 42
- 238000000034 method Methods 0.000 title claims description 27
- 239000011248 coating agent Substances 0.000 title claims description 6
- 238000000576 coating method Methods 0.000 title claims description 6
- 239000000835 fiber Substances 0.000 claims description 40
- 239000000945 filler Substances 0.000 claims description 16
- 125000002091 cationic group Chemical group 0.000 claims description 14
- 229920001448 anionic polyelectrolyte Polymers 0.000 claims description 4
- 239000000872 buffer Substances 0.000 claims 1
- 239000010410 layer Substances 0.000 description 19
- 125000000129 anionic group Chemical group 0.000 description 10
- 239000000126 substance Substances 0.000 description 9
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 7
- 239000001768 carboxy methyl cellulose Substances 0.000 description 7
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 7
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 7
- 229940105329 carboxymethylcellulose Drugs 0.000 description 7
- 229920006317 cationic polymer Polymers 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 229920000867 polyelectrolyte Polymers 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- 244000007835 Cyamopsis tetragonoloba Species 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 229920006318 anionic polymer Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 239000012209 synthetic fiber Substances 0.000 description 3
- 229920002994 synthetic fiber Polymers 0.000 description 3
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229920002324 Galactoglucomannan Polymers 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 229940072056 alginate Drugs 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- -1 carboxy methyl hydroxy ethyl Chemical group 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 229920000831 ionic polymer Polymers 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 229910017489 Cu I Inorganic materials 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 229940117913 acrylamide Drugs 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 229920006320 anionic starch Polymers 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000009918 complex formation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 1
- 150000001470 diamides Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 229920001746 electroactive polymer Polymers 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000005672 electromagnetic field Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000005660 hydrophilic surface Effects 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000012764 mineral filler Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- PZNOBXVHZYGUEX-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine;hydrochloride Chemical compound Cl.C=CCNCC=C PZNOBXVHZYGUEX-UHFFFAOYSA-N 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002717 polyvinylpyridine Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/16—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only modified by a particular after-treatment
- D21H11/20—Chemically or biochemically modified 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
- D21H17/63—Inorganic compounds
- D21H17/67—Water-insoluble compounds, e.g. fillers, pigments
- D21H17/69—Water-insoluble compounds, e.g. fillers, pigments modified, e.g. by association with other compositions prior to incorporation in the pulp or paper
-
- 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
- D21H17/25—Cellulose
- D21H17/26—Ethers thereof
-
- 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
- D21H17/42—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups anionic
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Inorganic Chemistry (AREA)
- Paper (AREA)
- Paints Or Removers (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Nonwoven Fabrics (AREA)
- Multicomponent Fibers (AREA)
Description
© WO 00/32702 PCT/SE99/02149
Method of producing a particle or group of particles having a coating of polymers interacting with each other
The present invention refers to a method of producing a particle or group of particles having a coating of at least two, preferably at least three, outside each other located thin layers of interacting polymers, at which the particle or group of particles is treated in consecutive steps with solutions of the interacting polymers. The particles consists at first hand of fibers or filler particles. Such a coating modifies the properties of the particles as well as the properties of the products, € g paper and nonwoven, in which the treated fibers and/or filler particles are contained.
The increased use of recovered fibers in paper production and the use of components with poorer bonding properties, such as mineral fillers, have increased the need for . more effective dry strength agents in the paper. Traditionally two different methods have been used for adding strength improving chemicals to the paper, viz. by adding chemicals at the wet end of the paper process or by surface application by means ofa size press. Wet end addition is usually more effective than surface application counted per kg utilized product. In order to maintain the addition made in the wet end in the paper sheet, wet end chemicals are mainly exclusively cationic, and for making them less sensitive to dissolved and colloidal materials and the increased concentration of electrolytes caused by the increased closing of the systems, their cationic charge is usually increased. This leads in turn to a decreased saturation adsorption of the additive chemicals to the fibers, which leads to a reduced maximum effect of the additive chemicals. This involves that there is a need both for new methods of applying strength-improving chemicals to the paper, and new chemical systems.
Besides there is an increased need for improving the opacity of the finished paper.
Since the today most frequently used strength agents contribute negatively to the opacity the need for new methods of developing strength in the paper is further reinforced.
Such a way would be to utilize size presses to a higher extent, but this would however lead to large reductions of the manufacturing capacity and the production economy since the paper has to be dried once further depending on the rewet it is exerted to in the size press.
This involves that there is a great need for new ways of treating fibers and other particles contained in the paper, such as filler particles, in the wet end of the paper machine.
Also treatment with a similar process such as size presses may be of interest if the quality of the produced paper is herewith increased in a satisfactory way, so that the above mentioned drawbacks will be of less importance.
Tt is known to build up thin multilayers of electro active polymers on an electrosta- tically charged substrate for use in optics, such as sensors, friction reduction etc. This is described in for example in Thin Solid Films, 210/211 (1992) 831-835 and in Thin
Solid Films, 244 (1994) 806-809. The substrate is herewith immersed alternatingly in diluted solutions of a polycation with an intermediate rinsing in order to remove rests of ’ the previous polyion which is not bonded to the substrate. The thickness of each deposited layer is described to be between 5-20A. There is no indication that the treated substrates could be particles, such as fibers.
In US 5,338,407 there is disclosed a method for improving the dry strength properties of paper, at which an anionic carboxy methyl guar or carboxy methyl hydroxy ethyl guar and a cationic guar is added to the furnish. These two components are either added in mixture or separately. There is no indication that the treatment is made under such conditions that a double layer is built up on the fibers with one component in one layer and the other component in the other layer.
In the US patents 5,507,914 and 5,185, 062 there are disclosed methods for improving the dewatering properties and the retention of paper by adding anionic and cationic polymers to the pulp. There is no indication that the treatment takes place under such conditions that a double- or multilayer is created on the pulp fibers with the anionic component in one layer and the cationic component in the other layer.
© WO 00/32702 PCT/SE99/02149
Dual surface treatment of filler particles with anionic and cationic polymers is disclosed in EP-A-0 850 879, WO 95/32335, US-A-4,495,245 and US-A-4,925,530. There is no indication that the treatment takes place under such controlled conditions that a double- or multilayer is created on the pulp fibers with the anionic component in one layer and the cationic component in the other layer.
The object and most important features of the invention
The object of the present invention is to provide a method for producing particles or groups of particles, especially fibers and/or filler particles, having a coating of at least two, preferably at least three, outside each other located thin layers of interacting polymers, at which the particle or group of particles is treated in consecutive steps with solutions of the interacting polymers. This has been provided by the fact that excess of the previous polymer is removed between each treatment step alternatively that the respective polymer is added only in such an amount in each step that substantially all polymer is adsorbed to the particle surface.
The particles or groups of particles may be of optional type, however fibers, € g cellulosic fibers, regenerated fibers and different types of synthetic fibers, and filler particles are mainly concerned.
The interacting polymers are preferably alternating cationic and anionic polyelectro- lytes, but they may also be so called zwitter ions.
The thickness of each of said thin layers is preferably between 3 and 100A, more preferably between 7 and 20A.
The invention further refers to a paper- or nonwoven product, which contains fibers and/or filler particles produced by the method described above.
Fig. 1 shows in the form of bar charts the tensile strength index of sheets made of cellulosic fibers with different numbers of applied polymer layers.
Fig. 2 shows in the form of bar charts the tensile strength index of paper containing different amounts of filler particles treated according to the invention.
Fig. 3 shows a tensile strength index - opacity diagram for paper containing different amounts of filler particles treated according to the invention.
Fig. 4 shows in the form of a bar chart the increase of tensile strength of paper : containing pulp fibers coated with an anionic and a cationic polymer added at the same time and added separately in six consecutive steps rinsing away the excess of polymer between each step.
According to the present invention particles or groups of particles, e g fibers or filler particles, are treated with interacting polymers in order to build up thin multilayers of the interacting polymers on the particle surface. In principle the technique described in for example above mentioned articles from Thin Solid Films is used in case alternating cationic and anionic polyelectrolytes are used as interacting polymers, with the difference that according to the invention the substrate is fibers or other particles or groups of particles.
The particles are treated in consecutive steps with solutions of the interacting polymers, ; at which the treatment time for each step is sufficient for forming a layer of the desired molecular thickness, preferably of the magnitude 5-100A. The interaction between the : particles can be in the form of electrostatic forces, at which the polymers consist of alternating cationic and anionic polyelectrolytes, or by interaction between nonionic polymers by means of ¢ g dispersion forces or hydrogen bonds. Examples of this type of interaction between nonionic polymers are adsorption of polyethylene oxide on unbleached cellulosic fibers and complex formation between polyethylene oxide and polyacrylic acid.
Tn case the interacting polymers are alternating cationic and anionic polyelectrolytes the first layer should be a cationic polymer for particles or groups of particles having an anionic surface, which for example is the case for cellulosic fibers, and vice versa.
Possible excess of the previous polyelectrolyte can be removed between every treatment step, ¢ g by rinsing with water. Alternatively the addition is controlled in such a way that no excess amount of the respective polymer is added in each step, so that substantially all polymer is adsorbed to the particle surface.
© WO 00/32702 PCT/SE99/02149
The method is based on electrostatic attraction between oppositely charged polyelectro- lytes for building the desired multilayers. By treating the fibers in consecutive steps with a solution containing polyions of opposite charge and permit these spontaneously to adsorb to the particle surface, multilayers of the stated kind are buiit up. In principle 5 all types of polyelectrolytes may be used.
Through such a treatment of particles or groups of particles, such as fibers, it is possible to make new types of surface modifications to them. By for example treating fibers with consecutive layers of hydrophobic, charged polyelectrolytes it would be possible for example to develop new types of hydrophobizing chemicals for the hydrophobization of paper. It would also be possible to build up "intelligent" surface layers on fibers, which alter the properties with temperature, pH, salt content etc. These changes could for example be based on fundamental knowledge about modern theories on interaction between polymers and surfactants.
Further applications are ion-exchanging fibers where "membranes" with ion-exchanging properties are provided on the fiber surface, wet strength agents where the added polymers are reactive with the fibers and with each other, in order to provide permanent ) bonds between the fibers and for the production of highly swelling surface layers, where the added chemicals form swollen gel structures on the fiber surface for use in absorbent hygiene products. Another possible application are new types of fibers for printing paper, where the adsorbed polymers change colour when they are exerted to an electric, magnetic or electromagnetic field. Such polymers are available today.
The fibers that are treated with the method according to the invention can be of optional kind, natural as well as synthetic fibers. Mainly cellulosic fiber are concerned. However it would be possible to treat synthetic fibers, for example for giving them a more hydrophilic surface.
Also groups of fibers or particles can be treated according to the method.
Examples of suitable anionic and cationic polyelectrolytes which may be used in the method according to the invention are given below.
Anionic polyelectrolvtes: Anionic starch with different degrees of substitution,
polystyrene sulphonate, carboxy methyl cellulose with different degrees of substitution, anjonic galactoglucomannan, polyphosphoric acid, polymethacrylic acid, polyvinyl sulphate, alginate, copolymers of acryl amide and acrylic acid or 2-acrylic amide-2- alkylpropane sulphonic acid.
Cationic polyelectrolyte: Cationic galactoglucomannan, polyvinyl amine, polyvinyl pyridine and its N-alkyl derivatives, polyvinyl pyrrolidone, chitosan, alginate, modified polyacryl amides, polydiallyl dialkyl, cationic amide amines, condensation products between dicyane diamides, formaldehyde and an ammonium salt, reaction products between epichlorhydrine, polyepichlorhydrine and ammonia, primary and secondary amines, polymers formed by reaction between ditertiary amines or secondary amines or dihaloalkanes, polyethylene imines and polymers formed by polymerisation of N- (dialkylaminoalkyl)acrylic amide monomers.
Example 1
The example below shows the increase of tensile strength of sheets made in a dynamic ’ sheet former. The pulp that is used was bleached SWK (softwood sulphate pulp) beaten in accordance with SCAN-C 18:65, diluted to 3g/! and pH adjusted to 8. PVAm : (polyvinyl amine), a cationic polymer, was added in excess and was given time to react after which the excess of polymer was washed away from the fiber suspension by means : of water. After that CMC (carboxy methyl cellulose), an anionic polymer, was added in excess, and after 10 minutes non-adsorbed polymer was removed through washing.
Admixture of PVAm and CMC was repeated in several steps. After each addition of
CMC the so called dynamic sheet former was used for making sheets having a basis weight of 80 g/m’. The sheets were tested with respect to tensile strength according to
SCAN-P 67:93. The results are shown in Table 1 below and proves clearly an improvement of tensile strength index with the number of applied polymer layers.
Table 1
LE we
"WO M/32702 PCT/SE99/02149
Foc es
EEC
The results are also shown in Fig. 1 in the drawings.
Example 2
In this example fillers for papermaking have been used which have been treated through multilayer adsorption with the same polymers as in Example 1 above, i e polyvinyl amine and carboxy methyl cellulose. Paper sheets of 30 g/m* were made in a dynamic sheet former. The sheets were tested with respect to ash content, tensile strength index and opacity. The results are shown in Table 2 below. Ash content here means the content of filler treated as above and which has been added to the paper.
Table 2 : (P=PVAm, C=CMC) (kKNmvkg)
A Cu I Lo
I LN CL 2 J
I LI EL
CE LC LN
OL CN LL LA iA LI EN LN
The results are also shown in Fig. 2 and 3. Fig. 2 shows the effect on strength in the paper containing different amounts of filler particles treated according to the invention.
Fig. 3 shows the effect on the opacity of paper when using different amounts of fillers treated according to Example 2 above.
Example 3
Two types of polymers were used: an anionic polyacryl amide (A-PAM), Percoi 155 from Ciba, and a cationic polydimethyl diallyl ammonium chloride (DMDAAC) also from Ciba. The pulp that was used was unrefined, fully bleached longfiber pulp, pH 8 in all tests. The dosing of the polymers were done in two different ways:
A) all at the same time and in this case 3.9 kg/ton A-PAM was added first and then 6.6 kg/ton polyDMDAAC was added.
B) Six layers of 1.1 kg/ton polyDMDAAC and 0.65 kg/ton A-PAM in the respective layers were added. Excess of polymer was removed between the dosings.
Handsheets were then made and the strength (tensile strength index) was measured. In
Fig. 4 the strength increase in % is shown for the two different cases. As can clearly be seen it is much more effective to add the polymers in layers in a controlled manner.
Claims (12)
1. Method of producing a particle or group of particles having a coating of at least two, preferably at least three, outside each other located thin layers of interacting polymers, at which the particle or group of particles is treated in consecutive steps with solutions of the interacting polymers, characterized in that excess of the previous polymer is removed between each treatment step alternative- ly that the respective polymer is added only in such an amount in each step that substantially all polymer is adsorbed to the particle surface.
2. Method as claimed in claim 1, characterized in that the particle is a fiber.
i 3. Method as claimed in claim 2, characterized in that the fiber is a cellulosic fiber.
4. Method as claimed in claim 2, characterized in that the fiber is a synthetic or regenerated fiber.
5. Method as claimed in claim 1, characterized 1n that the particle is a filler particle or another type of particle used in papermaking.
6. Method as claimed in any of the preceding claims, characterized in that the interacting polymers are alternating cationic and anionic polyelectrolytes or ampholytes.
7. Method as claimed in any of the preceding claims, characterized in
. PCT/SE99/02149 that each of said thin layers has a thickness of between 1 and 100A.
8. Method as claimed in any of the preceding claims, characterized in that each of said thin layers has a thickness between 7 and 20A.
9. Paper or nonwoven product, characterized in that it contains fibers, filler particles or other particles produced according to the method of any of claims 1-8.
10. A method as claimed in claim 1, substantially as herein described and illustrated.
11. A product as claimed in claim 9, substantially as herein described and illustrated.
12. A new method of producing an article, or a new product. substantially as herein described. AMENDED SHEET
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE9804123A SE521591C2 (en) | 1998-11-30 | 1998-11-30 | Method of preparing a particle having coating of interacting polymers and paper or nonwoven product containing the particles |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200103812B true ZA200103812B (en) | 2002-08-12 |
Family
ID=20413481
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200103812A ZA200103812B (en) | 1998-11-30 | 2001-05-10 | Method of producing a particle or group of particles having a coating of polymers interacting with each other. |
Country Status (14)
Country | Link |
---|---|
US (1) | US20020088579A1 (en) |
EP (1) | EP1137719B1 (en) |
JP (1) | JP2002531714A (en) |
AT (1) | ATE318289T1 (en) |
AU (1) | AU1903500A (en) |
BR (1) | BR9915750A (en) |
CO (1) | CO5121087A1 (en) |
DE (1) | DE69930005T2 (en) |
ES (1) | ES2259242T3 (en) |
HU (1) | HU225401B1 (en) |
PL (1) | PL348462A1 (en) |
SE (1) | SE521591C2 (en) |
WO (1) | WO2000032702A1 (en) |
ZA (1) | ZA200103812B (en) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
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SE0001268L (en) * | 2000-04-06 | 2001-10-07 | Sca Hygiene Prod Ab | Process for adsorbing successive thin layers of cationic and anionic polymers onto the surface of particles or groups of particles, and paper or nonwoven product containing such particles or groups of particles |
DE10315363A1 (en) * | 2003-04-03 | 2004-10-14 | Basf Ag | Aqueous slurries of finely divided fillers, process for their preparation and their use for the production of filler-containing papers |
DE10334133A1 (en) * | 2003-07-25 | 2005-02-24 | Basf Ag | Aqueous composition and its use for papermaking |
US9156990B2 (en) | 2003-12-22 | 2015-10-13 | Eka Chemicals Ab | Filler for papermaking process |
KR100585138B1 (en) * | 2004-04-08 | 2006-05-30 | 삼성전자주식회사 | Mask pattern for manufacturing semiconductor device and method of forming the same and method of manufacturing semiconductor device having fine patterns |
DK1799905T3 (en) * | 2004-10-15 | 2012-02-13 | Stora Enso Ab | Process for making paper or paperboard as well as the paper or paperboard produced according to the method |
US8778139B2 (en) * | 2004-12-17 | 2014-07-15 | Basf Aktiengesellschaft | Papers with a high filler material content and high dry strength |
US20090107645A1 (en) * | 2005-05-11 | 2009-04-30 | Stora Enso Ab | Process for the Production of a Paper and a Paper Produced According to the Process |
JP2009509702A (en) | 2005-10-05 | 2009-03-12 | エスセーアー・ハイジーン・プロダクツ・アーベー | Absorbent article with thin film containing activator |
BRPI0520628B8 (en) | 2005-10-05 | 2021-06-22 | Essity Hygiene & Health Ab | absorbent article and liquid permeable cover sheet comprising hydrophilic and hydrophobic regions |
CA2641309A1 (en) * | 2006-02-03 | 2007-08-16 | Nanopaper Llc | Functionalization of paper components with an amine-containing polymer |
JP5202857B2 (en) * | 2007-03-13 | 2013-06-05 | 古河電気工業株式会社 | Composite particles having high dispersibility and preventing non-specific adsorption, composite particle colloid, analytical reagent using the same, and method for producing composite particles |
CA2692297C (en) | 2007-07-05 | 2019-04-02 | Basf Se | Aqueous slurries of finely divided fillers, a process for their preparation and their use for the production of papers having a high filler content and high dry strength |
CA2692299C (en) * | 2007-07-05 | 2017-11-21 | Basf Se | Aqueous slurries of finely divided fillers, a process for their preparation and their use for the production of papers having a high filler content and high dry strength |
FI121999B (en) * | 2009-10-06 | 2011-07-15 | Upm Kymmene Corp | Process for making a web and web |
JP5489914B2 (en) * | 2010-08-19 | 2014-05-14 | 花王株式会社 | Method for producing hydrolytic paper and method for producing water-degradable cleaning article |
CN105612284B (en) | 2013-11-07 | 2018-01-23 | 尤妮佳股份有限公司 | Absorbent commodity Composite material and its manufacture method |
SE539914C2 (en) | 2014-04-29 | 2018-01-09 | Stora Enso Oyj | Process for making at least one layer of a paper or paperboard and a paper or paperboard made according to the process |
WO2017065800A1 (en) * | 2015-10-16 | 2017-04-20 | General Mills, Inc. | Paperboard product |
DE102021005047A1 (en) | 2021-10-08 | 2023-04-13 | Factum Consult Gmbh | Polyelectrolyte system, composition having a polyelectrolyte system and method of manufacture |
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US3770482A (en) * | 1971-01-18 | 1973-11-06 | Beatrice Foods Co | Electrostatic coating method of applying multilayer coating |
GB1505641A (en) * | 1974-04-19 | 1978-03-30 | Grace W R & Co | Process of preparing a filler composition for paper |
US4488932A (en) * | 1982-08-18 | 1984-12-18 | James River-Dixie/Northern, Inc. | Fibrous webs of enhanced bulk and method of manufacturing same |
US4495245A (en) * | 1983-07-14 | 1985-01-22 | E. I. Du Pont De Nemours And Company | Inorganic fillers modified with vinyl alcohol polymer and cationic melamine-formaldehyde resin |
GB8531558D0 (en) * | 1985-12-21 | 1986-02-05 | Wiggins Teape Group Ltd | Loaded paper |
US5244542A (en) * | 1987-01-23 | 1993-09-14 | Ecc International Limited | Aqueous suspensions of calcium-containing fillers |
DE4026978A1 (en) * | 1990-08-25 | 1992-02-27 | Bayer Ag | Coated substrates for electro=optical applications, etc. |
US5155791A (en) * | 1990-12-07 | 1992-10-13 | E. I. Du Pont De Nemours And Company | Hybrid optical waveguides for phase-matched nonlinear wavelength conversion |
IL113721A (en) * | 1994-05-20 | 1999-04-11 | Minerals Tech Inc | Dual surface treated filler material method for its preparation and use in papermaking |
US5716709A (en) * | 1994-07-14 | 1998-02-10 | Competitive Technologies, Inc. | Multilayered nanostructures comprising alternating organic and inorganic ionic layers |
GB9626941D0 (en) * | 1996-12-27 | 1997-02-12 | Ecc Int Ltd | Dispersed aqueous suspensions |
-
1998
- 1998-11-30 SE SE9804123A patent/SE521591C2/en not_active IP Right Cessation
-
1999
- 1999-11-23 DE DE69930005T patent/DE69930005T2/en not_active Expired - Lifetime
- 1999-11-23 AU AU19035/00A patent/AU1903500A/en not_active Abandoned
- 1999-11-23 ES ES99962630T patent/ES2259242T3/en not_active Expired - Lifetime
- 1999-11-23 JP JP2000585336A patent/JP2002531714A/en not_active Withdrawn
- 1999-11-23 AT AT99962630T patent/ATE318289T1/en not_active IP Right Cessation
- 1999-11-23 PL PL99348462A patent/PL348462A1/en not_active Application Discontinuation
- 1999-11-23 BR BR9915750-0A patent/BR9915750A/en not_active Application Discontinuation
- 1999-11-23 EP EP99962630A patent/EP1137719B1/en not_active Expired - Lifetime
- 1999-11-23 HU HU0104488A patent/HU225401B1/en not_active IP Right Cessation
- 1999-11-23 WO PCT/SE1999/002149 patent/WO2000032702A1/en active IP Right Grant
- 1999-11-30 CO CO99075241A patent/CO5121087A1/en unknown
-
2001
- 2001-05-10 ZA ZA200103812A patent/ZA200103812B/en unknown
- 2001-05-21 US US09/860,560 patent/US20020088579A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
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SE9804123D0 (en) | 1998-11-30 |
US20020088579A1 (en) | 2002-07-11 |
EP1137719A1 (en) | 2001-10-04 |
SE9804123L (en) | 2000-05-31 |
ES2259242T3 (en) | 2006-09-16 |
DE69930005T2 (en) | 2006-10-26 |
WO2000032702A1 (en) | 2000-06-08 |
HUP0104488A2 (en) | 2002-03-28 |
AU1903500A (en) | 2000-06-19 |
HUP0104488A3 (en) | 2003-07-28 |
BR9915750A (en) | 2001-08-28 |
DE69930005D1 (en) | 2006-04-27 |
JP2002531714A (en) | 2002-09-24 |
EP1137719B1 (en) | 2006-02-22 |
PL348462A1 (en) | 2002-05-20 |
HU225401B1 (en) | 2006-11-28 |
SE521591C2 (en) | 2003-11-18 |
CO5121087A1 (en) | 2002-01-30 |
ATE318289T1 (en) | 2006-03-15 |
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