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
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J3/00—Processes of treating or compounding macromolecular substances
  • C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
  • C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
  • C08J3/07—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media from polymer solutions
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L93/00—Compositions of natural resins; Compositions of derivatives thereof
  • C08L93/04—Rosin
• • 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
  • D21H21/14—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 function or properties in or on the paper
  • D21H21/16—Sizing or water-repelling agents
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2393/00—Characterised by the use of natural resins; Derivatives thereof
  • C08J2393/04—Rosin
• • 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
  • D21H17/07—Nitrogen-containing 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
  • D21H21/50—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
• • 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
  • D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
  • D21H23/04—Addition to the pulp; After-treatment of added substances in the pulp
• • 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
  • D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
  • D21H23/22—Addition to the formed paper
  • D21H23/24—Addition to the formed paper during paper manufacture

Definitions

• This invention relates to the emulsification and stabilization of dispersions of rosin by using alkanolamine salts of rosin. Such dispersions are useful in the manufacture of sized paper and paperboard.
• Soluble rosin salts are surface active materials which generally makes them useful as emulsifiers.
• the sodium salts of rosin were used to stabilize the first dispersed rosin sizing agents that were developed (see, for example, Davison, U.S. Pat. No. 3,565,755). Unfortunately, the stability of these products was not great. They were shear sensitive and the particles settled over time; sediment that collected at the bottom of tanks was difficult to remove.
• alkanolamine salts of rosin are known to be emulsifying agents.
• Alkanolamines and long-chain fatty acids react at room temperature to give neutral alkanolamine soaps, which are waxy, noncrystalline materials with widespread commercial applications as emulsifiers.”
• Analogous statements about the alkanolamine salts of rosin are not apparent in the literature.
• German Temporary Patent #1,131,348 Japanese.
• rosin shall include “rosin” per se and “rosin adducts” unless otherwise indicated.
• stable dispersions of rosin can be made by combining an organic phase of rosin with water that contains a defined amount of alkanolamine, and passing the mixture through a homogenizer.
• the alkanolamine is believed to react with resin to form an alkanolamine salt of the resin, which serves to stabilize the dispersion.
• the final product is a stable dispersion with low viscosity and uniform mean particle size, usually of 0.3 to 1.5 microns. These dispersions are physically stable on storage as shown by viscosity measurement and have good pump (shear) stability.
• composition aspect of this invention is a rosin sizing composition that is an aqueous and oil emulsion of rosin stabilized with an alkanolamine rosin salt.
• the process aspect of the invention is a process for preparing an oil-in-water emulsion, which comprises
• Stable dispersions of rosin can be made by combining an organic phase of rosin with an aqueous phase that contains a defined amount of alkanolamine, and passing the mixture through a homogenizer.
• the organic phase can simply be molten rosin, or it can be a solution of the rosin in an organic solvent such as methylene chloride. If the organic phase is the molten phase, homogenization must be carried out at elevated temperature and pressure. The product is then cooled to ambient temperature through a heat exchanger. If the organic phase is a solution of rosin in an organic solvent, the homogenization can be carried out at ambient temperature and pressure. The solvent must then be stripped from the emulsion, leaving a stable dispersion of the rosin.
• an organic solvent such as methylene chloride
• the rosin component can be any of the commercially available types of rosin such as wood rosin, gum rosin, tall oil rosin, and mixtures thereof, in their crude or refined state.
• rosin such as wood rosin, gum rosin, tall oil rosin, and mixtures thereof
• Partially or substantially completely hydrogenated rosins and polymerized rosins, as well as rosins that have been treated to inhibit crystallization, such as by heat treatment or reaction with formaldehyde, can be used as the rosin component as well as mixtures thereof.
• the “rosin adduct” useful in this invention is the reaction product of rosin and an acidic compound containing the
• ⁇ , ⁇ -unsaturated polybasic organic acids and their known anhydrides specific examples of which include fumaric acid, maleic acid, acrylic acid, maleic anhydride, itaconic acid, itaconic anhydride, citraconic acid and citraconic anhydride.
• the amount of acidic compound employed will be that amount which will provide fortified rosin containing from about 1 to about 16% by weight of adducted acidic compound based on the weight of the fortified rosin. Best results are obtained at levels of about 3-8%
• the aqueous phase is a solution of the alkanolamine in water. Because the alkanolamine is reacting with the rosin to form a salt, there is a limit to the amount of alkanolamine that can be used in this process. If the level of salt is too high, the dispersion is not stable.
• the alkanolamine can be for example triethanol amine, diethanolamine, diisopropanolamine, and the like.
• the preferred amount of alkanolamine is the amount sufficient to generate about 0.0033 to 0.011 moles alkanolamine salt (reaction product of alkanolamine and a resin acid) per 100 grams aqueous phase, or in the case of triethanolamine, 1.5-5 wt % of the triethanolamine salt based on aqueous phase.
• the organic phase and the aqueous phase containing the alkanolamine aqueous phase are combined to form a coarse oil in water emulsion referred to as the premix.
• the premix is homogenized to form a stable oil in water emulsion.
• the alkanolamine salts of the rosin serve as the emulsifying agent for the emulsion. Any of the appropriate homogenization techniques can be used, from an ultra-sonic probe to a Gaulin homogenizer.
• the final product is a stable dispersion of the rosin stabilized with the alkanolamine salt of rosin or rosin adduct.
• the particles comprising the dispersed phase are relatively small, with a mean particle size of about 0.3 to 1.5 micron.
• the product is of relatively low viscosity, ⁇ 50 cps, with good physical stability.
• the product is shear stable, as indicated by a lab pump stability test.
• additives such as defoamers, biocides and other preservatives, can be added to the stable dispersion of the present invention in amounts and using techniques known to those in the papermaking industry.
• the agents of this invention can be applied as internal paper sizing agents or surface sizing agents.
• Internal sizing involves adding the sizing agent to the paper pulp slurry before sheet formation, while surface sizing involves immersion of the paper in the sizing agent or spraying the sizing agent on the paper, followed by drying at elevated temperatures in accordance with known drying techniques.
• the present invention is useful in sizing paper materials such as, for example, linerboard and food packaging board.
• the amount used is based on the desired sizing requirements of the paper mill, depending upon the required degree of sizing, the grade of paper, the type of pulp furnish used to make the paper, and other factors well known and easily determined empirically by those skilled in the art. In general, the least amount of sizing agent is used to obtain the desired sizing specifications.
• the rosin sizing compositions can be used with papermaker's alum or other equivalent aluminum compounds (e.g. polyaluminum chloride, PAC).
• the aluminum compound is applied as a separate component to the pulp when a dispersion of the current invention is used as an internal size or when it is applied as an external, surface size.
• the amount of aluminum compound to be used is determined based on the type, the grade of paper being treated, the amount of sizing agent being applied, and other factors well known to those skilled in the art.
• HST Hercules Size Test
• TAPPI Test Method T530 om-96 The Hercules Size Test
• This method employs an aqueous dye solution as the penetrant to permit optical detection of the liquid front as it moves through the paper sheet.
• the apparatus determines the time required for the reflectance of the sheet surface not in contact with the penetrant to drop to a predetermined percentage of its original reflectance. All HST testing data reported measure the seconds to 80% reflection with 20% formic acid ink unless otherwise noted.
• the use of formic acid ink is a more severe test than neutral ink and tends to give faster test times. High HST values are better than low values.
• the amount of sizing desired depends upon the kind of paper being made and the system used to make it.
• Particle size was determined using a Malvern Mastersizer Microplus using procedures recommended by the manufacturer.
• Viscosity was determined at 25° C. by means of a Brookfield Viscometer, LV Series, using a No. 1 spindle at 60 rpm.
• the sizing efficacy of the rosin dispersions was determined on a pilot paper machine using a pulp furnish that is a blend of recycled medium (70%) and European old corrugated container (30%) with a Canadian standard freeness of 376 cc.
• the water for dilutions was adjusted to contain 50 ppm hardness and 25 ppm alkalinity.
• a pilot scale papermachine designed to simulate a commercial Fourdrinier was used, including stock preparation, refining and storage.
• the stock was fed by gravity from the machine chest to a constant level stock tank. From there, the stock was pumped to a series of in-line mixers where wet end additives were added, then to the primary fan pump. The stock was diluted with white water at the fan pump to about 0.2% solids. Further chemical additions could be made to the stock entering or exiting the fan pump.
• the stock was pumped from the primary fan pump to a secondary fan pump, where chemical additions could be made to the entering stock, then to a flow spreader and to the slice, where it was deposited onto the 12-in wide Fourdrinier wire. Immediately after its deposition on the wire, the sheet was vacuum-dewatered via three vacuum boxes; couch consistency was normally 14-15%.
• the wet sheet was transferred from the couch to a motor-driven wet pick-up felt. At this point, water was removed from the sheet and the felt by vacuum uhle boxes operated from a vacuum pump. The sheet was further dewatered in a single-felted press and left the press section at 38-40% solids.
• a 160 g/sq m (98 lb/3000 ft2 ream) sheet was formed and dried on seven dryer cans to 5% moisture (dryer can surface temperatures were 85 C) and passed through a single nip of a 5-nip, 6 roll calendar stack at 40 pli.
• Fumaric acid 174.08 parts at 99% solids, was reacted, at elevated temperatures, with Chinese gum rosin, 2700 parts.
• the fumaric acid dissolved in the molten rosin and reacted therewith to provide a reaction product.
• the reaction product after substantially all the fumaric acid had reacted with the gum rosin, was allowed to cool to room temperature (about 23 C).
• the product was a mixture comprised of unreacted rosin and rosin-fumaric acid reaction product or adduct.
• the reaction product contained 6% by weight fumaric acid, substantially all of which had been reacted.
• a solution was prepared by dissolving 750 parts of reaction product from Example 1 in 893.93 parts of methylene chloride. The solution was thoroughly mixed with an aqueous solution prepared by dissolving 11.22 parts (98%) triethanol amine in 930 parts water to provide a coarse oil-in-water emulsion. The triethanol amine reacted with some of the carboxyl groups of the rosin and/or rosin-fumaric acid adduct to produce a salt thereof which acted to stabilize the system. The coarse emulsion was passed through a commercial homogenizer at a pressure of 3000 psi. The product was an oil-in-water emulsion of good stability.
• Substantially all methylene chloride was removed from the oil-in-water emulsion by distillation at reduced pressure to provide an aqueous dispersion which was passed through a paint filter.
• the aqueous suspension after passage through the filter, had a solids content of 42.6% and a viscosity of 8 cps.
• the aqueous suspension was comprised of suspended particles having diameters from about 0.05 micron to about 1.5 microns, with a mean average of 0.33 micron.
• a solution was prepared by dissolving 123.32 parts of reaction product from Example 1 in 147 parts of methylene chloride. The solution was thoroughly mixed with an aqueous solution prepared by dissolving 2.68 parts (98%) triethanol amine in 233.86 parts water to provide a coarse oil-in-water emulsion. The triethanol amine reacted with some of the carboxyl groups of the rosin and/or rosin-fumaric acid adduct to produce a salt thereof which acts to stabilize the system. The coarse emulsion was homogenized using a lab sonicator. The product was an oil-in-water emulsion of excellent stability.
• aqueous dispersion which was passed through a paint filter.
• the aqueous suspension after passage through the filter, had a solids content of 36.61, a mean particle size of 0.29 um, and a viscosity of 7 cps.
• Example 3 was repeated, except 4.56 parts triethanol amine were added to water in preparation of the aqueous phase.
• the oil-in-water emulsion was homogenized without incident, but failed during removal of the methylene chloride with substantially all of the rosin separating from the aqueous phase.
• Example 3 was repeated, except the aqueous phase was prepared by simply adjusting the pH of 230 parts water to 12.5 using 11.15 parts of a 4% aqueous solution of sodium hydroxide.
• the aqueous suspension contained 34.96% total solids had a mean particle size of 0.34 micron and a viscosity of 6 cps.
• the test used in the lab to predict pump stability measures the time for the back-pressure on a screen placed in a recirculation loop to build-up to a predetermined level. Longer times correspond to better pump stability.
• a Masterflex peristaltic pump, Model 7564-10 with head 7016 was used at a pump speed of 5, on a 0-10 scale.
• the tubing was set up to pass through a constant temperature bath to maintain the temperature of the product being tested at a constant temperature.
• a 100 mesh screen was used in the recirculation loop. The products are filtered through a 325 mesh screen before testing.
• Example 3 The dispersions of Examples 3 and 5 were evaluated using this lab test. The test was run at 27 ⁇ 1 C. With the dispersion of Example 5, based on Davison's patent, the pump test reached the cut-off level after only 120 minutes, whereas the dispersion of this invention, Example 3, pumped for the full duration of the test, 360 minutes, without building sufficient back-pressure to stop the test.
• Example 1 was repeated, except 205.28 parts fumaric acid was added and tall oil rosin was used in place of the Chinese gum rosin to give a reaction product containing 7% fumaric acid, substantially all of which had reacted. This reaction product is then used in the preparation of an aqueous suspension as outlined in Example 3. The final product had total solids of 35.55% and a mean particle size of 0.26 micron. It had a viscosity of 6 cps., and after 4 weeks of aging the viscosity was still 6 cps.
• Example 1 was repeated, except 172.34 parts maleic anhydride were used in place of fumaric acid to form a reaction product containing 6% maleic anhydride, substantially all of which had reacted.
• This reaction product was then used in the preparation of an aqueous suspension as outlined in Example 3.
• the final product had total solids of 45.41% and a mean particle size of 0.34 micron.
• the viscosity was 10 cps as made and was still 10 cps after 4 weeks of aging.
• Sizing efficiency was measured using the pilot laboratory paper machine described above.
• the sizing agent was added, with alum at the inlet of the primary fan pump.
• Alum was added at a level of 0.75%. No other chemical additives were used.
• the headbox pH was adjusted to 7, trimming with caustic if needed.
• Example 3 0.073 4 0.1 13 0.2 89
• Example 5 0.073 5 0.1 14 0.2
• Hi-pHase 35 0.073 4 0.1 12 0.2
• Hi-pHase ® 35 is a dispersion of rosin commercially available from Hercules Incorporated. This shows Example 3 (of invention) sizes as well as prior art Example 5 and Hi-pHase ®.

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Dispersion Chemistry (AREA)
• Paper (AREA)

Priority Applications (4)

Applications Claiming Priority (1)

Related Child Applications (1)

Publications (1)

Family

ID=39684834

Family Applications (2)

Family Applications After (1)

Country Status (3)

Families Citing this family (2)

Citations (7)

Family Cites Families (7)

• 2007
  • 2007-02-12 US US11/705,345 patent/US20080190577A1/en not_active Abandoned
• 2008
  • 2008-02-08 US US12/069,377 patent/US7854800B2/en active Active
  • 2008-02-11 WO PCT/US2008/001824 patent/WO2008100492A2/en not_active Ceased
  • 2008-02-12 TW TW097104895A patent/TWI444521B/zh active

Patent Citations (7)

Also Published As

Similar Documents

Legal Events