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
  • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
  • D21H17/62—Rosin; 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
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31844—Of natural gum, rosin, natural oil or lac
  • Y10T428/31848—Next to cellulosic
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31971—Of carbohydrate
  • Y10T428/31993—Of paper

Definitions

• the present invention relates to paper making and, in particular, the paper sizing art and provides high free-rosin sizing agents based on rosin, which can be retained on cellulosic fibres by the use of a polyamine and which will give the desired sizing effect, irrespective of the presence of alum or other precipitating or flocculating agents.
• the paper sizing agents of the invention also have the advantage that they can be added to paper stock which has a pH in the range of4 to 10.
• the high free-rosin sizing agents of this invention may alternatively be added to the paper sheet at any convenient situtation, after its formation and before it is fully dried. They may also be added in admixture with other commonly used substances for the surface treatment of paper, either at the size press or at a coating apparatus. When high free-rosin sizing agents, made in accordance with the present disclosure, are added to the surface of the paper sheet, no polyamine retention aid is required. Optimum results may be obtained when using a combination of various methods of application, as explained below.
• Conventional high free-rosin sizing agents are known to consist of an aqueous dispersion of rosin or fortified rosin, which may be partly saponified by means of a metal base such as caustic soda or caustic potash and may also contain a protective colloid such as casein.
• Other conventional sizing agents are known to consist of fortified rosins which are substantially fully saponified with a metal base. All of these conventional sizing agents depend, for their sizing effect, upon the addition of aluminium sulphate to the paper stock.
• paper sizing agents of the rosin dispersion type can be prepared by incorporating into the rosin a volatile base, for example ammonia, monomethylamine, dimethylamine, trimethylamine, monoethylamine, diethylaminc, triethylaminc, monopropyla mine, dipropylamine, monoisopropylamine, diisopropylamine, ethyl propyl amine, ethyl butylamine, di-secbutylamine, dimethyl isobutylamine, monoethanolamine, diethanolamine, tricthanolamine, N, N- dimcthyl ethanolamine, morpholine, N-methyl morpholine, N-ethyl morpholine or other amines, or mixtures thereof, which will volatilize at temperatures up to 140C whether or not in the presence of water, in place of the metal base used in conventional rosin dispersion sizing agents, and when the paper size is added to the paper stock
• any of the polyamine type retention aids conventionally used in the paper-making art may be used.
• retention aids of the polyamine type, and the preparation thereof are described in the US. Pat. Nos. 3,406,139 and 3,527,719. These retention aids are water-soluble nitrogen-containing polymers, or water-soluble salts thereof, having a molecular weight of at least about 5,000 up to about 10,000,000
• One class of such polymers has an exclusively carbon atom backbone chain to which there are directly attached a plurality of nitrogenous rings of the Formula I:
• A is an alkylene group having 2 to 3 carbon atoms, of which at least two extend in a chain between the adjacent N atoms, and
• R is selected from the group consisting of H, C C alkyl groups, hydroxy-substituted C C alkyl groups, and groups of the formula (ANH),H wherein A is as defined above and x is an integer having a value of l to 4.
• polymers in which the nitrogenous rings of Formula I are connected to the polymer chain through a phenylene group or through an ester or amide linkage.
• Such polymers have repeating units of Formula II:
• R is selected from the group consisting of H, C l C alkyl groups, phenyl, C alkaryl, and
• n is an integer having a value of l to 2
• Y is selected from the group consisting of phenylene
• Z is a C, C alkylene group.
• Polymers containing units of Formula Il may be made water soluble by converting them to the salt form with any organic or inorganic acid or acid salt, for example: hydrochloric acid, sulfuric acid, p-toluenesulfonic acid, or sodium bisulfate.
• organic or inorganic acid or acid salt for example: hydrochloric acid, sulfuric acid, p-toluenesulfonic acid, or sodium bisulfate.
• suitable polyamine type retention aids are: the sodium bisulfate salt of a 2-vinyl-2-imidazoline polymer, obtained by reaction of ethylenediamine with a polyacrylonitrile having a molecular weight of about 18,000; the sodium bisulfate salt of a polymer of 2-isopropenyl-imidazoline-2, obtained by reacting ethylenediamine on a polymethacrylonitrile having a molecular weight of about 15,000; a polymer of 2-vinyl 3,4,5,6 -tetrahydropyrimidine obtained by reacting trimethylenediamine on a polyacrylonitrile having a molecular weight of about 30,000; the hydrochloric acid salt of a polymer of 2-vinyl-4-methyl-2- imidazoline, obtained by the reaction of l, 2- diaminopropane on a polyacrylonitrile having a molecular weight of about 15,000; a homopolymer of 2-vinyl- Z-imidazoline obtained
• a modified rosin is made by reacting an alpha, beta unsaturated mono or dicarboxylic acid or anhydride with a rosin and then making an aqueous rosin dispersion.
• the preparation of the modified, or fortified, rosin essentially requires a reaction of the DielsAlder type, in which the alpha, beta unsaturated mono-or dicarboxylic acid or anhydride combines with the conjugated double bond system present in the rosin.
• the other ingredients used in the preparation of the desired modified rosin reaction product may comprise any rosin which includes colophony and may consist of tall oil rosin, wood rosin or gum rosin, in their crude state or in their refined state, or a number of derivatives thereof.
• a rosin including colophony may be diluted by the addition of more economical materials, for example crude tall oil, distilled tall oil, hydrocarbon resins and waxes of various types or other suitable diluents.
• hydrocarbon resins useful in the sizing compositions of the present invention are those conventionally used in the paper sizing art. They are noncrystalline thermoplastic hydrocarbon resins of straight chain and cycloaliphatic structure and essentially free from aromatic groups, having ring-and-ball softening points from 45C to 150C, and molecular weights of from 350 to 2,000. Preferred hydrocarbon resins are those having a ring-and-ball softening point in the range 100l02C and a molecular weight of approximately 1400. Suitable examples are the resins sold by Esso Pctroleum Co. under the tradename Escorcz 1 102B, and by Imperial Chemical Industries under the tradename Imprez 100,
• Paraffin waxes and microcrystalline waxes are preferred, and fully refined paraffin wax having a melting point range of 60 65C is particularly preferred.
• the improved paper sizing agent of this invention may be prepared in the following general manner, which may be taken as being by way of an example.
• tall oil rosin or other rosins which have a tendency to crystallise should be treated at elevated temperatures with formaldehyde or paraformaldehyde in the presence of an acid catalyst, for example p-toluene-sulphonic acid, in a manner well-known to those skilled in the art), and a calculated quantity of an alpha,beta-unsaturated carboxylic acid or anhydride, preferably maleic anhydride, is added to the molten heated rosin and allowed to react therewith to produce the desired modified rosin.
• an acid catalyst for example p-toluene-sulphonic acid
• the product will normally have a maximum softening point of 92C (according to the Ring and Ball method of determining softening points of resinic materials). It may be advantageous to use rosins having a lower softening point where the paper size is to be used on a paper-making machine having drying cylinder temperatures lower than normal in order to ensure sintering of the rosin.
• This modified rosin need not be used immediately in the preparation of the sizing agent and is sufficiently stable to enable it to be stored until required.
• a dispersing and stabilising agent is then prepared in a separate vessel by dissolving a measured quantity of a protective colloid (for example, casein) and a measured quantity of a volatile base (for example, 0.880 ammonia) in water.
• a protective colloid for example, casein
• a volatile base for example, 0.880 ammonia
• protective colloid there may be used, casein, gelatine, glue, soybean protein, zein, or other protective colloid well known to those skilled in the art, or mixtures thereof. Casein is preferred.
• Suitable volatile bases include ammonia, and amines which will volatilize at temperatures up to C whether or not in the presence of water, as previously explained. Mixtures of amines, or mixtures of ammonia and one or more of a suitable amine may also be employed. Ammonia is preferred as a volatile base.
• the quantity of volatile base used is sufficient to solubilize the protective colloid, but is limited to an amount to ensure that at least 90% of the modified ros
• the next step in the manufacture of the sizing agent is to add quickly, to the molten rosin, the prepared dis persing and stabilising agent, making use of high speed stirring or other intensive agitation of the mixture, during and after addition.
• the solids content of the resultant aqueous rosin. dispersion can then be adjusted by adding a calculated quantity of water thereto.
• Cold water may be used for this purpose and, at the same time, for cooling the dispersion.
• a small quantity of a microbicide or bactericide may be added before the dilution water.
• a microbicide or bactericide Any of the water-soluble or water-dispersible microbicides or bactericides known to those skilled in the art for the preservation of proteinaceous material may be used.
• suitable microbicides are phenols, chlorinated phenols, benzoic acid, salicylic acid, formaldehyde, organomercurial compounds, sodium phenylphenate, and the, beta-hydroxyethylpyridinium salt of Z-mercaptobenzothiazole.
• Example I describes the preparation of a modified rosin
• Examples 11 V the preparation of the sizing agent
• Examples Vl 1X methods of sizing paper, using the sizing agent are set out in the following examples, of which Example I describes the preparation of a modified rosin; Examples 11 V the preparation of the sizing agent; and Examples Vl 1X methods of sizing paper, using the sizing agent.
• the modified rosin so formed may be immediately used for the manufacture of the rosin dispersion sizing agent, or may be allowed to cool for storage.
• EXAMPLE 11 560 kg of a modified rosin, for instance the product made in accordance with Example 1, was melted in a heated vessel, fitted with a stirring mechanism suitable for intensively agitating its contents, and the molten rosin was stirred at approximately 300 revolutions per minute.
• the temperature of the rosin was adjusted to 100C.
• the emulsifying and stabilising agent was prepared in a separate vessel, by adding 14 kg of casein to 75 l water, heated to 30 to 60C, followed by the addition of 10 kg of 0.880 ammonia.
• This dispersing and stabilising agent was then added to the molten rosin as quickly as possible and the intensive agitation was continued for a further minutes, at the end of which time 0.5 kg of sodium o-phenylphenate was added.
• the resulting dispersion was then diluted with cold water until a solids content of 45% was reached.
• EXAMPLE I11 390 kg. of a modified rosin, made in accordance with the procedure of Example 1, was melted in a heated vessel fitted with a stirring mechanism suitable for intensively agitating its contents, and the molten rosin was stirred at approximately 300 revolutions per minute. 170Kg. of a molten hydrocarbon resin, Escorez 1 102B (Esso Petroleum Co.), was added to the modified rosin.
• the temperature of the rosin mixture was adjusted to
• the emulsifying and stabilising agent was prepared in a separate vessel, by adding 14Kg. of casein to 75 liters water, heated to 30C to 60C, followed by the addition of Kg. of 0.880 ammonia. This dispersing and stabilising agent was then added to the molten rosin as quickly as possible, and the intensive agitation was continued for a further five minutes, at the end of which EXAMPLE IV 500 Kg. of a modified rosin, for instance the product made in accordance with Example I, was melted in a heated vessel, fitted with a stirring mechanism suitable for intensively agitating its contents, and the molten rosin was stirred at approximately 300 revolutions per minute.
• the temperature of the rosin was adjusted to 100C.
• the emulsifying and stabilising agent was prepared in a separate vessel, by adding 14Kg. of casein to liters water, heated to 30C to 60C, followed by the addition of 10Kg. of 0.880 ammonia.
• the emulsifying and stabilising agent was added to the molten rosin and the intensive agitation was continued for 5 minutes.
• 60 Kg. of a fully refined paraffin was (melting point 60C 65C) was melted in a heated vessel and brought to a temperature of C and added to the dispersed rosin mixture, and the intensive agitation continued for a further five minutes, at the end of which time 0.5Kg. of sodium o-phenyl-phenate was added.
• the resulting dispersion was then diluted with cold water until a solids content of 45% was reached.
• EXAMPLE V A preferred method of incorporation wax into the emulsion would be to mix with suitable agitation an anionically stabilised wax emulsion with an emulsion prepared as illustrated in Example 11.
• EXAMPLE Vl Bleached sulphite pulp was beaten and refined in a normal paper machine system and an MG paper of 38 gm/m was manufactured from it on a normal MG paper machine. 7
• a coating mixture consisting of a 6% solution of starch and containing 1% calcium carbonate and 0.5% of the sizing agent referred to in Example I was added to the surface of the paper sheet at a size press.
• the resulting paper sheet when tested by the Cobb method gave a degree of sizing of 17-18 g.s.m.
• EXAMPLE Vlll A sizing dispersion agent made according to Example Ill was applied by a spray apparatus to a paper sheet during its formation on the wire of a paper making machine. No other chemical additives were present. 1.25% by weight (based on the dry fiber) of the sizing dispersion agent was added. The degree of sizing according to the Cobb method was 25 g.s.m.
• EXAMPLE IX A paper stock was prepared in the laboratory from bleached sulphite pulp, without any other additions, and was made into sheet.
• a rosin dispersion sizing agent made according to Example 1] above was applied to one surface of the sheets and, after drying, the sheets were tested according to the Cobb test procedure, giving the following results:
• the rosin-based paper sizing agent of the invention gives highly saitsfactory products. both when the sizing agent is added to the paper stock with a polyamine retention aid or when the sizing agent is applied to unsized sheeted stock in the absence of a retention aid.
• An agent for sizing paper without the use of aluminum sulfate which comprises a stable aqueous dispersion of rosin fortified by reaction with an alpha, beta unsaturated carboxylic acid or anhydride, a protective colloid, and a volatile base, at least 90% of said fortified rosin being unsaponified.
• a sizing agent as in claim 1 which also comprises a minor amount of a microbicide.
• a sizing agent as in claim 1 wherein the dispersion also comprises up to 90% by weight, based on the weight of fortified rosin, of a hydrocarbon resin.
• a sizing agent as in claim 1 wherein the dispersion also comprises up to by weight, based on the weight of fortified rosin, of paraffin wax.
• a method for the preparation of a paper sizing 'agent which comprises forming a stable dispersion by the addition of an aqueous dispersing and stabilizing agent to molten fortified rosin while agitating the rosin; said dispersing and stabilizing agent comprising water, a protective'colloid, and a volatile base; said fortified rosin comprising the reaction product of rosin and an alpha, beta-unsaturated carboxylic acid or anhydride.
• the protective colloid is casein
• the volatile bases is ammonia
• the rosin is tall oil rosin.
• a method for the preparation of sized paper in the absence of aluminum sulfate which comprises applying a stable aqueous dispersion of fortified rosin to the surface of a paper sheet and drying the paper sheet; said dispersion comprising water, a protective colloid, a volatile base and fortified rosin, said fortified rosin being at least unsaponified.

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• 1973
  • 1973-01-22 GB GB314573A patent/GB1444751A/en not_active Expired
• 1974
  • 1974-01-17 NO NO740141A patent/NO145280B/no unknown
  • 1974-01-21 ES ES422482A patent/ES422482A1/es not_active Expired
  • 1974-01-21 FR FR7401894A patent/FR2214738B1/fr not_active Expired
  • 1974-01-21 AT AT49974*#A patent/AT334197B/de not_active IP Right Cessation
  • 1974-01-21 IT IT47830/74A patent/IT1008722B/it active
  • 1974-01-21 CH CH76474A patent/CH588526A5/xx not_active IP Right Cessation
  • 1974-01-21 SE SE7400752A patent/SE417115C/xx unknown
  • 1974-01-21 BR BR74418A patent/BR7400418D0/pt unknown
  • 1974-01-21 DK DK31474AA patent/DK142119B/da not_active IP Right Cessation
  • 1974-01-21 CA CA190,729A patent/CA1030706A/fr not_active Expired
  • 1974-01-22 BE BE140072A patent/BE810037A/fr not_active IP Right Cessation
  • 1974-01-22 DE DE2402926A patent/DE2402926C2/de not_active Expired
  • 1974-01-22 ZA ZA740462A patent/ZA74462B/xx unknown
  • 1974-01-22 NL NL7400867A patent/NL7400867A/xx not_active Application Discontinuation
  • 1974-01-22 IE IE131/74A patent/IE38880B1/xx unknown
  • 1974-01-22 US US435561A patent/US3906142A/en not_active Expired - Lifetime
  • 1974-10-15 ES ES431016A patent/ES431016A1/es not_active Expired
• 1980
  • 1980-03-21 US US06/132,505 patent/US4323425A/en not_active Expired - Lifetime

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