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
  • D21H19/00—Coated paper; Coating material
  • D21H19/36—Coatings with pigments
  • D21H19/38—Coatings with pigments characterised by the pigments
  • D21H19/385—Oxides, hydroxides or carbonates
• • D—TEXTILES; PAPER
  • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
  • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
  • D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
  • D21H21/50—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by form
  • D21H21/52—Additives of definite length or shape

Definitions

• This invention relates to suspensions of calcium carbonate pigments, to paper coating compositions formed from such suspensions and to coated paper made using said coating compositions, and to a paper-making process which includes the recycling of coated paper.
• calcium carbonate pigments which have been treated to have specified particle size and surface area characteristics, can be anionically dispersed in water to form high solids paper coating compositions for gravure printing papers (GB-A-2139606A).
• a high solids, aqueous suspension of a particulate calcium carbonate pigment characterised in that the particulate calcium carbonate pigment has a specific surface area, as measured by the BET N 2 method, of less than 7.5m 2 g -1 , and a particle size distribution such that not more than 1% by weight of the particles have an equivalent sperical diameter (esd) larger than 10 microns, at least 65% by weight of the particles have an equivalent sperical diameter smaller than 2 microns and not more than 10% by weight of the particles have an equivalent spherical diameter smaller than 0.25 microns; and in that the particulate calcium carbonate pigment is cationically dispersed with a dispersing agent which is a combination of a cationic polyelectrolyte and an anionic polyelectrolyte, with the cationic electroyte being used in an amount sufficient to render the pigment particles cationic.
• a dispersing agent which is a combination of a cationic polyelectrolyt
• a paper coating composition which has a solids content of at least 45% by weight, characterised in that it comprises a high solids, aqueous suspension according to the present invention, and a non-ionic or cationic adhesive.
• a process for making paper which includes the step of recycling coated paper that has been reduced to a fibrous, recyclable state and then incorporated into a paper-making composition, characterised in that the coated paper is a paper which has been coated with a coating composition according to the invention.
• a cationically dispersed, high solids, aqueous suspension of a calcium carbonate pigment in accordance with the present invention has very good rheological properties.
• a cationic aqueous suspension, or slurry, having a given viscosity and prepared in accordance with the present invention can have a higher solids content than a slurry in which the calcium carbonate pigment has a broader particle size distribution.
• a high solids, aqueous suspension according to the present invention should preferably have a solids content of at least 60% by weight solids.
• the calcium carbonate pigment when ground to a particulate mass, exists in the form of regular, approximately spherical particles having a low mean particle aspect ratio.
• the calcium carbonate may be in any form, natural or synthetic. Particularly preferred is ground marble, although precipitated calcium carbonate (PCC) and chalk are operable.
• the calcium carbonate pigment employed in the present invention should have a specific surface area, as measured by the BET N 2 method, which is less than about 6.5m 2 g -1 , but preferably is at least 2m 2 g -1 .
• a calcium carbonate material is ground, before dispersion, to the desired particle size distribution.
• the grinding conditions can be adjusted in a manner known per se to produce pigments having varying particle size distributions.
• Ground marble for use in the present invention is preferably formed by first crushing batches of marble in aqueous suspension in the absence of a chemical dispersing agent using a particulate grinding medium. Further size reduction can be achieved by dewatering the suspension of ground marble, for example by filtration in the absence of a flocculating agent, and then drying the pigment, and pulverising the dried product in a conventional mill.
• the particles of the pigment may be readily dispersed using a dispersing agent, in accordance with the invention, comprising a combination of an anionic polyelectrolyte and a cationic polyelectrolyte, the cationic polyelectrolyte being used in an amount sufficient to render the particles cationic.
• chalk particles when in a raw state, do not carry a positive charge, because of natural anionic species absorbed to the particle surface, and the chalk particles should be subjected to vigorous agitation in order to strip off such anionic species and render the particles capable of being effectively dispersed at high solids using the combination of an anionic polyelectrolyte and cationic polyelectrolyte.
• the raw pigment is received as a filter cake having a relatively high solids content.
• the dispersing agent in order to provide a dispersed high solids slurry (45-80% by weight solids) which may then be subjected to vigorous mixing.
• the particulate calcium carbonate pigment is dispersed with a combination of an anionic polyelectrolyte and a cationic polyelectrolyte, with the cationic electroyte being used in an amount sufficient to render the pigment particles cationic.
• the amount of cationic polyelectrolyte used is in the range of from about 0.01% to about 1.5% by weight, based on the dry weight of calcium carbonate, and the amount of anionic polyelectroyte used is such that the weight ratio of the cationic polyelectrolyte to anionic polyelectroyte is in the range of from about 2:1 to about 20:1.
• the anionic polyelectrolyte is a water-soluble vinyl polymer, an alkali metal or ammonium salt thereof or an alkali metal or ammonium salt of polysilicic acid.
• the anionic polyelectrolyte is a poly(acrylic acid), a poly(methacrylic acid), a substituted poly(acrylic acid) or a substituted poly(methacrylic acid), or an alkali metal or ammonium salt of any of these acids.
• the substituted poly(acrylic acid) may be a partially sulphonated polymer.
• An especially effective anionic polyelectrolyte is an alkali metal or ammonium salt of a copolymer of acrylic acid and a sulphonic acid derivative of acrylic acid, in which the proportion of the sulphonic acid derivative monomer is preferably from 5% to 20% of the total number of monomer units.
• the number average molecular weight of the anionic polyelectrolyte is preferably at least 500, but preferably no greater than 100,000.
• the amount used is generally in the range of from about 0.01% to about 0.5% by weight based on the weight of dry pigment, and preferably is in the range of from about 0.1 to 0.2% by weight.
• the cationic polyelectrolyte may be a water-soluble substituted polyolefin containing quaternary ammonium groups.
• the quaternary ammonium groups may be in the linear polymer chain or may be in branches of the polymer chain.
• the number average molecular weight of the substituted polyolefin is preferably at least 1500 but preferably no greater than 1,000,000, and is more preferably in the range of from 50,000 to 500,000.
• the quantity required is generally in the range of from about 0.01% to about 1.5% by weight based on the weight of dry pigment.
• Advantageous results have been obtained when the substituted polyolefin is a poly(diallyl di(hydrogen or lower alkyl)ammonium salt).
• the lower alkyl groups which may be the same or different, may have, for example, up to four carbon atoms and each is preferably methyl.
• the ammonium salt may be, for example, a chloride, a bromide, an iodide, HSO 4 - , CH 3 SO 4 - or nitrite.
• the salt is a chloride.
• the cationic polyelectrolyte is poly(diallyl dimethyl ammonium chloride).
• the water-soluble substituted polyolefin may be the product of copolymerising epichlorohydrin and an aliphatic secondary amine, said product having the formula in which R and R', which may be the same of different, are each hydrogen or a lower alkyl group having from one to four carbon atoms, preferably methyl or ethyl and X is Cl - , Br - , I - , HSO 4 - , CH 3 SO 4 - or nitrite.
• the preferred number average molecular weight of this epichlorohydrin product is in the range of from 50,000 to 300,000.
• the cationic polyelectrolyte may be a water-soluble organic compound having a plurality of basic groups and preferably having a number average molecular weight of at least 10,000 but preferably no greater than 1,000,000. Most preferably, the number average molecular weight is at least 50,000.
• These water-soluble organic compounds may be described as polyacidic organic bases, and are preferably compounds of carbon, hydrogen and nitrogen only and are free of other functional groups, such as hydroxy or carboxylic acid groups, which would increase their solubility in water and thus increase the likelihood of their being desorbed from the mineral in an aqueous suspension.
• the organic compound is polyethyleneimine (PEI) having a number average molecular weight in the range 50,000 to 1,000,000.
• PEI polyethyleneimine
• a further example of a water-soluble organic compound which may be employed is a polyethylene diamine which may be a copolymer of ethylene diamine with an ethylene dihalide or with formaldehyde.
• the cationic polyelectrolyte is employed in an amount sufficient to render the mineral particles cationic.
• the zeta potential of the particles will normally be at least +20mV after treatment, typically in the range of from +30 to +40 mV and usually no greater than +50 to +60mV. These potentials have been measured using a dilute (0.02 weight %) solids suspension using a supporting electrolyte of potassium chloride (10 -4 M) with a "Pen Kem Laser Z" meter.
• the ratio, by weight, of cationic polyelectrolyte to anionic polyelectrolyte used is generally in the range of from about 2:1 to about 20:1, and preferably is in the range of from 2:1 to 10:1.
• the calcium carbonate pigment is preferably mixed with the anionic polyeletrolyte before mixing with the cationic polyelectrolyte. This appears to enable a more fluid suspension to be obtained at a higher solids concentration.
• Aqueous suspensions of the present invention should preferably be subjected to vigorous mixing before or after dispersion of the pigment.
• the vigorous mixing should be sufficient to impart at least 10kJ energy per kg of the inorganic material, but preferably no more than about 50kJ per kg.
• the amount of energy input will be in the range of from 18-36kJ per kg of the inorganic material.
• the high solids aqueous suspension of the present invention can be "made down" into a paper coating composition by dilution (if necessary) to a solids concentration of at least 45% by weight and by addition of an adhesive, which should be non-ionic or cationic in nature.
• an adhesive which should be non-ionic or cationic in nature.
• Such adhesives contrast with the anionic adhesives which are normally used in paper coating compositions in which the pigment is anionic.
• cationic casein and cationic starch adhesives can be used as well as cationic or non-ionic latices.
• Such cationic and non-ionic adhesives are readily commercially available.
• the particular cationic or non-ionic adhesive used will depend, for example, on the printing process to be used, e.g. offset lithography requires the adhesive to be water-insoluble.
• the amount of adhesive should preferably be of the order of from 7 to 25% by weight, based on the weight of pigment whilst, for gravure printing paper, the adhesive should be used in an amount of 4-15% by weight, based on the weight of pigment.
• the precise quantity of adhesive required will depend upon the nature of the adhesive and the material being coated, but this can readily be determined by the person skilled in the art.
• the paper coating composition may also include other conventional paper coating composition adjuvants such as an insolubilising agent (e.g. a melamine formaldehyde resin), a lubricant such as calcium stearate and a catalyst to catalyze cross-linking of the cationic latex if present: a suitable such catalyst is sodium bicarbonate.
• an insolubilising agent e.g. a melamine formaldehyde resin
• a lubricant such as calcium stearate
• the quantities of these adjuvants required are known to those skilled in the art.
• a full discussion of the constituents of paper coating compositions and of the methods of applying such compositions to paper is given in Chapter XIX, Volume III of the second edition of the book by James P. Casey entitled “Pulp and Paper: Chemistry and Technology”.
• a further discussion is given in
• the paper coating compositions of the invention can be used in a method of coating a sheet member using normal paper coating machinery and under normal paper coating conditions.
• coated paper which is obtained using coating compositions of the present invention is particularly suitable for use in a recycling process which includes the step of reducing the paper into a fibrous recyclable state and incorporating said fibre in a paper-making composition.
• a coated paper which is made using a coating composition of the present invention is of advantage when it is employed as "broke", or recycled paper, as part of a paper-making composition.
• Such a paper-making composition may include conventional paper-making pulp, such as a bleached sulphite pulp.
• the broke fibre and the conventional pulp will be employed in a ratio of from 10:90 to 60:40.
• a filler for instance a calcium carbonate filler and also a retention aid.
• broke fibre will include a proportion of calcium carbonate pigment from the coating, it is possible to reduce the amount of calcium carbonate filler employed to give a total quantity of filler in the range of from 5 to 20 percent by weight of the total paper-making composition.
• the weight of dried broke added (fibre and filler) should preferably be in the range of from about 5 to 30 percent by weight of fibre.
• the broke fibre employed is derived from a coated paper in accordance with the present invention
• the amount of retention aid employed in the paper making composition can be reduced.
• a ground marble having a broad particle size distribution gives approximately 4 units lower solids for a given rheology when cationically dispersed.

Landscapes

• Paper (AREA)
• Glass Compositions (AREA)
• Pigments, Carbon Blacks, Or Wood Stains (AREA)
• Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
• Silicates, Zeolites, And Molecular Sieves (AREA)
• Colloid Chemistry (AREA)
• Crystals, And After-Treatments Of Crystals (AREA)
• Coloring Foods And Improving Nutritive Qualities (AREA)
• Disintegrating Or Milling (AREA)

Applications Claiming Priority (3)

Publications (2)

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• 1990
  • 1990-12-04 GB GB9026362A patent/GB2251254B/en not_active Expired - Fee Related
• 1991
  • 1991-11-28 BR BR919107142A patent/BR9107142A/pt not_active Application Discontinuation
  • 1991-11-28 WO PCT/GB1991/002110 patent/WO1992010609A1/en active IP Right Grant
  • 1991-11-28 CA CA002088515A patent/CA2088515A1/en not_active Abandoned
  • 1991-11-28 EP EP91920520A patent/EP0560813B1/en not_active Expired - Lifetime
  • 1991-11-28 JP JP4500472A patent/JP2919970B2/ja not_active Expired - Lifetime
  • 1991-11-28 ES ES91920520T patent/ES2104735T3/es not_active Expired - Lifetime
  • 1991-11-28 AT AT91920520T patent/ATE157415T1/de not_active IP Right Cessation
  • 1991-11-28 DK DK91920520.3T patent/DK0560813T3/da active
  • 1991-11-28 AU AU89399/91A patent/AU654514B2/en not_active Ceased
  • 1991-11-28 DE DE69127458T patent/DE69127458T2/de not_active Expired - Fee Related
• 1993
  • 1993-03-31 NO NO931216A patent/NO300021B1/no not_active IP Right Cessation
  • 1993-05-31 FI FI932475A patent/FI932475A0/fi unknown

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