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
  • D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
  • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
  • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
  • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
• • 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
  • D21H17/03—Non-macromolecular organic compounds
  • D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
  • D21H17/14—Carboxylic acids; Derivatives 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
  • D21H17/03—Non-macromolecular organic compounds
  • D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
  • D21H17/18—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only forming new compounds in situ, e.g. within the pulp or paper, by chemical reaction with itself, or other added substances, e.g. by grafting on the 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
  • D21H17/20—Macromolecular organic compounds
  • D21H17/33—Synthetic macromolecular compounds
  • D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • D21H17/54—Synthetic 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
  • D21H17/56—Polyamines; Polyimines; Polyester-imides

Definitions

• This invention relates to the sizing of cellulose paper substrates. More particularly this invention provides new combinations of materials which are very effective as sizing agents, especally under neutral and alkaline conditions of papermaking.
• Much of the cellulosic paper produced at the present time is prepared under acid conditions, that is, with pulp slurries having pHs in the range of from about 4.5 to 5.5.
• acid conditions that is, with pulp slurries having pHs in the range of from about 4.5 to 5.5.
• economical sizing is being accomplished using commercially available rosin size formulations and papermakers alum which are added into the pulp slurries used to make the paper.
• papermakers have been trying to develop methods .for manufacturing paper under alkaline pH conditions.
• this invention provides a sizing combination of ingredients which are particularly useful for sizing textiles and paper products.
• the sizing combinations comprise a mixture of (1) one or more higher alkyl propiolate or higher alkyl acrylate compounds, or mixtures of such propiolates and acrylates and (2) a polyalkyleneimine or a poly (N-methylalkyleneimine), or mixtures thereof having from 2 to 3 carbon atoms in each alkylene moiety.
• This combination type of sizing operation provided for by this invention is particularly surprising in view of the substantially lowering sizing eifectiveness demonstrated by the alkyl propiolates alone and the complete absence of sizing by the polyalkyleneimine and/ or poly(N-methylalkyleneimine) component when used alone.
• the alkyl propiolate or alkyl acrylate to polyalkyleneimine or po1y(N-methylalkyleneimine) polymer weight ratios may range from about 1:10 to about :1, although we prefer to use them in a weight ratio of about 1:1 to 1:3.
• the preferred method of applying the sizing materials to the cellulosic substrate is to add to an aqueous dispersion of the pulp used to make the cellulosic paper sheet or article an emulsion of the alkyl propiolate or alkyl acrylate and the polyalkyleneimine or poly (N-methylalkyleneimine) in a mixing vessel and then to form sheets or webs from the treated aqueous pulp slurry in the United States Patent 0 ice conventional manner.
• the alkyl propiolate or alkyl acrylate and the polyalkyleneimine or poly(N-methylalkyleneimine) may be mixed into one emulsion prior to adding them to the aqueous pulp slurry or the two components may be added separately.
• Optimum results are obtained when the pH of the treated pulp slurry is adjusted to the basic pH range, preferably at from about 7 to 10. With the higher alkyl acrylates, substantial sizing is lost as pH is lowered much below about 7.
• the alkyl propiolates are not as sensitive to pH and form effective sizing agents when used with the polyalkyleneimines or poly(N-methylalkyleneimine) at pHs ranging from about 4.8 and higher.
• the alkyl acrylates are also more sensitive to the use of alum in the papermaking process. As the alum content increases, the effectiveness of the alkyl acrylates diminishes.
• the alkyl acrylates in combination with the polyalkyleneimines or poly(N-methylalkyleneimines) provide a high degree of sizing in the basic pH range where no or little alum is being used.
• the alkyl propiolates may be used with the polyalkyleneimines and poly(N-methylalkyleneimine) even in the presence of alum. Use of more than about 3% alum, based on the dry pulp used reduces the sizing effectiveness of these materials somewhat, especially in the acid pH papermaking range.
• Effective sizing of cellulosic substrates may also be accomplished by dipping the cellulosic paper into dilute aqueous emulsions or organic solvent solutions of the alkyl propiolate and/or the alkyl acrylate and the polyalkyleneimine or poly(N-methylalkyleneimine). Papers and textiles in general, including those from synthetic polymeric fibers may also be sized with these materials by spraying them on the surface of the substrate being sized.
• the hard sizing is developed with the preferred alkyl propiolates, such as C C alkyl propiolates and with polyethyleneimines in the normal drying operation of papermaking.
• the paper may be cured at room temperature for a few days or at relatively elevated temperature say -110 C. for from 10 to minutes to enhance the speed of the sizing action.
• the alkyl propiolates, and methods fpr preparing them are described in U.S. Patent 3,100,794.
• the alkyl propiolates having from 8 to about 12 carbon atoms in the alkyl group are used, they should be used in concentrations of at least about 0.3 to 1.0% by weight based on the dry weight of the material being sized.
• Alkyl propiolates having about 12 carbon atoms and higher may be used in lower concentration down to about 0.05 concentration, based on the substrate, especially if higher quantities of the polyalkyleneimines are used.
• the preferred unsaturated esters are the alkyl propiolates having from 16 to about 20 carbon atoms.
• the propiolate ingredient may be one compound or may be a mixture of compounds.
• the higher alkyl acrylates having from 8 to 30 carbon atoms may be prepared in a similar manner to that described above in preparing the propiolic acid esters in U.S. Patent 3,100,794.
• the preferred alkyl acrylates are those having from about 16 to about 20 carbon atoms.
• the polyalkyleneimines used in this invention are the polymerization products of ethyleneimine or derivatives thereof. Those used in this invention are those having from 2 to 3 carbon atoms in each alkylene group which are water soluble. Such products are described, for example, in U.S. Patent 2,182,306.
• the poly(N-methylalkyleneimines) are the polymerization products of N- methylethyleneimine, N-methylpropyleneimine, or mixtures thereof.
• Example 1 This example illustrates the use of the preferred combination of sizing ingredients in what we call the wet-end method of application.
• a typical alkyl propiolate, or acrylate e.g., 0.75 g. of octadecyl propiolate was dissolved in a suitable organic solvent such as xylene or dimethylbenzyl alcohol.
• the resulting propiolate solution was emulsified with 20 ml. of 0.1% aqueous hexadecyltrimethyl-ammonium bromide.
• Cellulose pulp used to make paper was slurried with water to give 2% pulp solids and then refined to 480520 Canadian Standard Freeness.
• the chosen polyalkyleneimine e.g., polyethyleneirnine
• An amount of this 1% polyethyleneimine solution equivalent to the desired weight percent of the polyethyleneimine based on the dry pulp was added to the pulp slurry and stirred.
• the pH of the treated aqueous pulp slurry was adjusted to the desired test pH, usually 5, 7, or 9 and then a quantity of the propiolate or acrylate aqueous emulsion was added to the pulp slurry to give 1% (or other test concentration of the chemical or chemicals being evaluated) based on the dry cellulose pulp.
• Handsheets are prepared from the treated pulp slurries thus obtained on a Noble and Wood machine and the dried paper sheets obtained are tested for the amount of water repellancy (sizing) possessed by the sheet by floating a sample of the treated paper sheet on a standard ink bath having a pH of 1.5, and observing the time (in seconds) needed for the first traces of a blue coloration to appear on the observed surface of the test sample.
• a high number of seconds is an indication of hard sizing of the paper by the added chemicals.
• a moderate degree of sizing (10 to 500 seconds) is desired; slack sizing is evidenced by a moderately high number of seconds of resistance to ink penetration. Resistance levels of under about 10 seconds are taken as an indication of no or minimal sizing efiectiveness of the added chemical or combination of chemicals.
• pH of pulp slurry percent HOP-CHO Example 3 This example illustrates the use of mixtures of alkyl propiolates and polyalkyleneimines as effective sizing agents.
• a standard bleached Gatineau sulfite pulp refined to a Canadian Standard Freeness of 500120 ml. as a 2% pulp solids aqueous slurry of pH 9 was treated with a 1% aqueous emulsion of a 50:50 molar mixture of the indicated alkyl propiolates in an amount suflicient to provide varying weight percents of the mixture based on the dry pulp.
• the treated pulp was m'ured 15 minutes and then polyethyleneimine was added in quantity sufiicient to provide varying Weight percents thereof based on the dry weight of the pulp used.
• Cellulosic paper sized with a combination of (1) at least one member of the group consisting of an alkyl acrylate having from 16 to 20 carbon atoms in the alkyl group and an alkyl propiolate having from 8 to about 20 carbon atoms in the alkyl group and (2) at least one member of the group consisting of a poly-N-methylalkyleneimine and polyalkyleneimine having from 2 to 3 carbon atoms in each alkylene group thereof.
• alkyl propiolate (1) is used and is a mixture of two or more alkyl propiolates having from 8 to 20 carbon atoms in each alkyl group, and component (2) is a polyalkyleneimine which is a polyethyleneimine.
• component (1) is an alkyl propiolate and is octadecyl propiolate and component (2) is a polyalkyleneimine which is a polyethyleneimine.
• a method for preparing sized cellulosic paper which comprises mixing with an aqueous cellulosic pulp slurry being used to prepare paper therefrom an aqueous dispersion of (1) at least one member of the group consisting of an alkyl acrylate having from 16 to 20 carbon atoms in the alkyl group and an alkyl propiolate having from 8 to 20 carbon atoms in the alkyl groups thereof, also mixing with said aqueous pulp slurry with (2) at least one member of the group consisting of polyalkyleneimines and poly(N-methylalkyleneimines) having from 2 to 3 carbon atoms in the alkylene groups in concentrations sufiicient to provide at least about 0.05% by weight of component (1) and at least about 0.15% by weight of component (2) based on the weight of the dry pulp, and then forming the treated aqueous pulp slurry thus obtained into paper.
• component (1) is an alkyl propiolate and is used as a mixture of alkyl propiolates having from 8 to about 20 carbon atoms in the alkyl groups thereof and component (2) is a polyalkyleneimine having from 2 to 3 carbon atoms in each alkylene group.
• component (1) is an alkyl propiolate and is octadecyl propiolate and component (2) is a polyalkyleneimine and is polypropyleneimine.
• a composition comprising (1) at least one member of the group consisting of alkyl acrylate having from 16 to 20 carbon atoms in the alkyl group and alkyl propiolates having from 8 to about 20 carbon atoms in the alkyl group and (2) at least one member of the group consisting of polyalkylenepolyimines and poly(N-methylalkyleneimines) having from 2 to 3 carbon atoms in the alkylene groups thereof.
• component (l) is an alkyl propiolate and component (2) is a polyalkyleneimine and said components (1) and (2) are present in Weight ratios of from about 1:10 to about 10:1 of alkyl propiolate to polyalkyleneimine.
• component (1) is an alkyl propiolate and is a mixture of alkyl propiolates having from 8 to 20 carbon atoms in the alkyl groups of each molecule and component (2) is a polyalkyleneimine and is a polyethyleneimine.
• composition as described in claim 9 wherein the alkyl propiolate is octadecyl propiolate and the polyalkyleneimine is a polyethyleneirnine.

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• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Textile Engineering (AREA)
• Paper (AREA)
• Joining Of Glass To Other Materials (AREA)

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Citations (3)

• 1965
  • 1965-10-21 US US500209A patent/US3461029A/en not_active Expired - Lifetime
• 1966
  • 1966-10-20 DE DE19661546267 patent/DE1546267A1/de active Pending
  • 1966-10-20 NO NO165250A patent/NO115695B/no unknown
  • 1966-10-20 FI FI662758A patent/FI44749C/fi active
  • 1966-10-20 SE SE14345/66A patent/SE315790B/xx unknown
  • 1966-10-20 FR FR80813A patent/FR1517784A/fr not_active Expired
  • 1966-10-21 GB GB47289/66A patent/GB1128085A/en not_active Expired
• 1969
  • 1969-06-30 US US837959A patent/US3574053A/en not_active Expired - Lifetime

Patent Citations (3)

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