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
  • 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
  • D21C9/08—Removal of fats, resins, pitch or waxes; Chemical or physical purification, i.e. refining, of crude cellulose by removing non-cellulosic contaminants, optionally combined with bleaching
  • D21C9/086—Removal of fats, resins, pitch or waxes; Chemical or physical purification, i.e. refining, of crude cellulose by removing non-cellulosic contaminants, optionally combined with bleaching with organic compounds or compositions comprising organic compounds
• • 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
  • D21H21/02—Agents for preventing deposition on the paper mill equipment, e.g. pitch or slime control

Definitions

• This invention relates to the control of pitch on equipment surfaces which are in contact with an aqueous pulp suspension in paper making machines, and more particularly to a method for controlling or inhibiting the deposition of pitch onto paper making equipment surfaces in papermaking processes which use natural pulp.
• Pitch is known to accumulate at various points in the papermaking system. For example, pitch deposits have been known to block the paper machine felts and thus hinder drainage of the paper web. Pitch can adhere to the wires or drying cylinders causing it to pick holes in the paper. It may also deposit on press rolls, dryer fabric or other like equipment surfaces which come into direct or indirect contact with the aqueous pulp suspension, paper sheet or paper machine felts. In fact, all paper machine fabrics and many of the rolls which contact the fabrics or paper sheet will, from time to time, accumulate pitch deposits.
• Natural pulp refers to an aqueous pulp suspension which is obtained by kraft processes, sulfite processes, semichemical processes, groundwood processes and the like, and excludes those aqueous pulp suspensions which are derived from secondary fiber.
• Also provided in accordance with the present invention is a novel composition which is useful for inhibiting the deposition of pitch onto equipment surfaces in pulp and papermaking equipment comprising certain water-soluble, non-ionic surfactants having a pitch dispersant value between 1 and 3, and a water-soluble cationic polymer in a weight ratio of surfactant:polymer in the range 50:1 to 1:1.
• the present invention is directed to a novel composition and method for inhibiting the deposition of pitch onto pulp and papermaking equipment surfaces which are in contact with a natural pulp which comprises applying to the equipment surfaces a water-soluble, non-ionic surfactant having a pitch dispersant value between 1 to 3 and a water-soluble cationic polymer, in amounts effective to inhibit the deposition of pitch.
• Pitch dispersant values refer to the ability of a compound to disperse natural pitch particles in an aqueous solution. Pitch dispersant values are considered to be an important feature of the compositions of this invention because it allows the cationic polymeric agents to effectively remove pitch deposits from pulp and papermaking equipment surfaces.
• Suitable non-ionic surfactants for use in this generally include non-ionic surfactants which are water soluble or water dispersible, act as detergents and/or stabilizers for oil-in-water emulsions, and are capable of lowering surface and interfacial tension. More particularly, suitable nonionic surfactants for use in this invention have pitch dispersant values between 1 and 3, preferably between 1 and 2, as determined by the following Pitch Dispersant Test: into a beaker, add 1 to 5 grams of tall oil pitch, 1 to 2 grams of the nonionic surfactant to be evaluated, and blend until the mixture is homogenous. Add 10 to 20 ml of deionized water with continuous stirring. The pitch dispersant value of the nonionic surfactant is rated as follows:
• the nonionic surfactants of this invention will have a Pitch Dispersant Value of between 1 and 3 which generally corresponds to a % emulsified pitch in the range of 100% to 50%, preferably from 100% to 75% and most preferably from 100% to 90%.
• non-ionic surfactants having the above-specified pitch dispersant values, are effective for controlling pitch deposits derived from natural pulp.
• the non-ionic surfactants of this invention inhibit pitch deposition by reducing the surface tension of the water with respect to the pitch particles thereby freeing them to adhere more easily to the cationic polymers which adhere to the pulp fibers and are thus removed from the papermaking system.
• nonionic surfactants exhibit pitch dispersant values from 1 to 3, and surprisingly, those nonionic surfactants that do possess pitch dispersant values from 1 to 3 are only effective for treating pitch derived from natural pulp. That is, the use of cationic polymers alone was effective for treating sticky material derived from secondary fiber pulps whereas, pitch deposits derived from natural pulp required the use of the nonionic surfactants of this invention.
• Preferred water-soluble, non-ionic surfactants for use in this invention include, but are not limited to detergent type surfactants having good wetting ability such as alkyl phenols including nonyl phenols, or octyl phenols, ethoxylated dialkyl phenols which are commercially available from Rhone-Poulenc under the trademark Igepal DM, secondary alcohol ethoxylates which are commercially available from Union Carbide under the trademark Tergitol, block copolymers of alkylene oxides which are commercially available from BASF under the trademark Tetronic, and alkylphenoxypolyethoxyalkanols which are commercially available from Rohm and Haas under the trademark Triton X-100, and the like, and mixtures thereof. It is especially preferred that the non-ionic surfactants of this invention be non-foaming or defoaming type surfactants and that they be approved for use in food and drug type applications.
• the present invention is of general applicability as regards the precise nature of the cationic polymer, and a considerable variety of different cationic polymers can be used, provided of course that they maintain their cationic charge in the system.
• Use of polyethylenimines is considered to be within this invention, as is use of various other polymeric materials containing amino groups such as those produced in accordance with the procedure disclosed in U.S. Patent Nos. 3,250,664, 3,642,572, 3,893,885 or 4,250,299; but it is generally preferred to use protonated or quaternary ammonium polymers.
• polymers include polymers obtained by reaction between an epihalohydrin and one or more amines, and polymers derived from ethylenically unsaturated monomers which contain a quaternary ammonium group.
• the cationic polymers of this invention also include dicyandiamideformaldehyde condensates. Polymers of this type are disclosed in U.S. Patent No. 3,582,461, which is incorporated herein in its entirety. Either formic acid or ammonium salts, and most preferably both formic acid or ammonium chloride, may also be included as polymerization reactants.
• dicyandiamideformaldehyde condensates have a tendency to agglomerate on felts and the like, even in the presence of cationic surfactants.
• One dicyandiamide-formaldehyde type polymer is commercially available as Tinofix QF from Ciba Geigy Chemical Ltd. of Ontario, Canada and contains as its active ingredient about 50 weight percent of a polymer believed to have a molecular weight between about 20,000 and 50,000.
• quaternary ammonium polymers which are derived from epihalohydrins and various amines are those obtained by reaction of epichlorohydrin with at least one amine selected from the group consisting of dimethylamine, ethylene diamine, and polyalkylene polyamine. Triethanolamine may also be included in the reaction. Examples include those polymers obtained by reaction between a polyalkylene polyamine and epichlorohydrin, as well as those polymers obtained by reaction between epichlorohydrin, dimethylamine, and either ethylene diamine or a polyalkylene polyamine.
• a typical amine which can be employed is N,N,N',N'tetramethylethylene-diamine as well as ethylene diamine used together with dimethylamine and triethanolamine. Polymers of this type include those having the formula: where n is from 0-500, although, of course, other amines can be employed.
• the preferred cationic polymers of this invention also include those made by reacting dimethylamine, diethylamine, or methylethylamine, preferably either dimethylamine or diethylamine, with an epihalohydrin, preferably epichlorohydrin.
• Polymers of this type are disclosed in U.S. Patent No. 3,738,945, and Canadian Patent No. 1,096,070, which are incorporated herein in their entirety.
• Such polymers are commercially available as Agefloc A-50, Agefloc A-50HV, and Agefloc B-50 from CPS Chemical Co., Inc. of New Jersey, U.S.A.
• Typical cationic polymers which can be used in the present invention and which are derived from ethylenically unsaturated monomers include homo- and copolymers of vinyl compounds such as vinyl pyridine and vinyl imidazole which may be quaternized with, say, a C1 to C18 alkyl halide, a benzyl halide, especially a chloride, or dimethyl or diethyl sulphate, or vinyl benzyl chloride which may be quaternized with, say, a tertiary amine of formula NR1R2R3 in which R1, R2 and R3 are independently lower alkyl, typically of 1 to 4 carbon atoms, such that one of R1, R2, and R3 can be C1 to C18 alkyl; allyl compounds such as diallyldimethyl ammonium chloride; or acrylic derivatives such as dialkyl aminomethyl(meth)acrylamide which may be quaternized with, say, a C1 to C18 alkyl halide
• These monomers may be copolymerized with a (meth)acrylic derivative such as acrylamide, an acrylate or methacrylate C1 - C18 alkyl ester or acrylonitrile or an alkyl vinyl ether, vinyl pyrrolidone, or vinyl acetate.
• a (meth)acrylic derivative such as acrylamide, an acrylate or methacrylate C1 - C18 alkyl ester or acrylonitrile or an alkyl vinyl ether, vinyl pyrrolidone, or vinyl acetate.
• Such polymers typically contain 10-100 mol % of recurring units of the formula: and 0-90 mol % of recurring units of the formula: in which R1 represents hydrogen or a lower alkyl radical, typically of 1-4 carbon atoms, R2 represents a long chain alkyl group, typically of 8 to 18 carbon atoms, R3, R4 and R5 independently represent hydrogen or a lower alkyl group while X represents an anion, typically a halide ion, a methosulfate ion, an ethosulfate ion or 1/n of a n-valent anion.
• quaternary ammonium polymers derived from an unsaturated monomer include the homo-polymer of diallyldimethylammonium chloride which possesses recurring units of the formula:
• this polymer should be regarded as "substantially linear” since although it contains cyclic groupings, these groupings are connected along a linear chain and there is no crosslinking.
• a particularly preferred such polymer is poly(dimethylbutenyl) ammonium chloride bis-(triethanol ammonium chloride).
• polystyrene resin Another class of polymer which can be used and which is derived from ethylenically unsaturated monomers includes polybutadienes which have been reacted with a lower alkyl amine and some of the resulting dialkyl amino groups are quaternized. In general, therefore, the polymer will possess recurring units of the formula: in the molar proportions a:b:c:d, respectively, where R represents a lower alkyl radical, typically a methyl or ethyl radical. It should be understood that the lower alkyl radicals need not all be the same. Typical quaternizing agents include methyl chloride, dimethyl sulfate and diethyl sulfate.
• Varying ratios of a:b:c:d may be used with the amine amounts (b+c) being generally from 10-90% with (a+c) being from 90%-10%.
• These polymers can be obtained by reacting polybutadiene with carbon monoxide and hydrogen in the presence of an appropriate lower alkyl amine.
• cationic polymers which are capable of interacting with anionic macromolecules and/or sticky material in papermaking pulp may also be used within the scope of this invention.
• cationic tannin derivatives such as those obtained by a Mannich-type reaction of tannin (a condensed polyphenolic body) with formaldehyde and an amine, formed as a salt, e.g. acetate, formate, hydrochloride or quaternized, as well as polyamine polymers which have been crosslinked, such as polyamideamine/polyethylene polyamine copolymers crosslinked with, say, epichlorohydrin.
• Natural gums and starches which are modified to include cationic groups are also considered useful.
• the molecular weight of the most useful polymers of this invention is generally between about 2,000 and about 3,000,000, although polymers having molecular weights below 2,000 and above 3,000,000 may also be used with some success.
• molecular weight of the polymer used is at least about 10,000, and is most preferably at least about 20,000.
• molecular weight of the polymer used is about 300,000 or less, and is most preferably about 50,000 or less.
• the polymers most preferably have a molecular weight within the range of about 20,000 to 50,000. Mixtures of these polymers may also be used.
• the polymers and surfactants of this invention may advantageously be supplied as liquid compositions comprising aqueous solutions of the polymer and/or surfactant.
• Polymer concentrations in the compositions may range from the relatively dilute solutions having polymer concentrations suitable for continuous application, up to the solubility or gelling limits of the polymer, but generally the compositions are relatively concentrated for practical shipping and handling purposes.
• the liquid compositions may comprise additional materials which further the dissolution of the polymers so as to allow more concentrated compositions.
• alkoxyethanols such as butoxyethyanol.
• Aqueous compositions suitable for shipping and handling will generally contain between 5 and 50 weight percent, active, of the cationic polymer of this invention.
• nonionic surfactants of this invention may be supplied as compositions separate from the cationic polymer compositions and then either applied to the equipment surfaces separately (e.g. by using separate shower systems) or mixed prior to application, it is preferred to provide aqueous compositions comprising the nonionic surfactant and the cationic polymer.
• the weight ratio of surfactant to polymer is such combined compositions is generally between about 50:1 to 1:50.
• the weight ratio of surfactant to polymer in the aqueous composition is between about 10:1 and about 1:1, especially where oils may potentially be present; and is most preferably about 1:1 for general application, although excess surfactant (e.g. a weight ratio of 1.1:1, or more) may be considered most suitable in the event oils might be present.
• the most appropriate treatment dosage depends on such system factors as the amount of pitch particles present in the aqueous pulp suspension, and whether cleaning is continuous or periodic.
• liquid compositions comprising relatively high concentrations of a polymer of the invention (for example, 50%) may be employed at full strength (100% as the liquid composition), for example by spraying the undiluted liquid composition directly onto the felts.
• the compositions may be advantageously diluted at the treatment location with clean fresh water or other aqueous liquid. Where necessary for water economy, a good quality process water may be adequate for dilution.
• the advantages of this invention can be realized at application concentrations as low as 2 ppm of the polymer, especially where continuous treatment is practiced, and, as explained further below, sufficient surfactant to inhibit a build-up of deposits derived from the applied cationic polymer component.
• continuous treatment is not practical and treatment with the cationic polymers and surfactants of this invention may be periodic.
• aqueous solutions of the polymer and surfactant may be sprayed on the equipment surfaces until the equipment surfaces are satisfactorily conditioned and the spray may then be discontinued until supplemental conditioning is needed to further inhibit the build-up of deposits.
• Equipment surfaces which may be advantageously treated in accordance with this invention generally include any solid surface or screen surfaces having porous openings in the range of 30 mesh to 250 mesh such as the forming wires, press rolls or thickener equipment such as Decker wire, gravity couch roll thickener, disk filters and related equipment parts where pitch deposits are prone to form.
• Two grades of kraft linerboard were manufactured on a fourdriner paper machine.
• the first grade was manufactured with 100% natural kraft fiber.
• the second grade was manufactured with 100% secondary fiber.
• the additives used in the process were alum, rosin size and a polyacrylamide retention aid to improve first pass retention.

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Citations (4)

• 1993
  • 1993-11-23 AU AU51828/93A patent/AU5182893A/en not_active Abandoned
  • 1993-11-24 EP EP93250323A patent/EP0599440A1/en not_active Withdrawn
  • 1993-11-24 CA CA 2109866 patent/CA2109866A1/en not_active Abandoned
  • 1993-11-25 JP JP31908393A patent/JPH07305289A/ja active Pending
  • 1993-11-25 BR BR9304830A patent/BR9304830A/pt not_active Application Discontinuation

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