EP0805898A1 - Papier contenant des amidons inhibes thermiquement - Google Patents

Papier contenant des amidons inhibes thermiquement

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Publication number
EP0805898A1
EP0805898A1 EP96903665A EP96903665A EP0805898A1 EP 0805898 A1 EP0805898 A1 EP 0805898A1 EP 96903665 A EP96903665 A EP 96903665A EP 96903665 A EP96903665 A EP 96903665A EP 0805898 A1 EP0805898 A1 EP 0805898A1
Authority
EP
European Patent Office
Prior art keywords
starch
flour
inhibited
starches
thermally
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP96903665A
Other languages
German (de)
English (en)
Inventor
Daniel B. Solarek
Roger Jeffcoat
Kimberly A. Koltai
Chung-Wai Chiu
Eleanor Schiermeyer
David J. Thomas
Manish B. Shah
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
National Starch and Chemical Investment Holding Corp
Original Assignee
National Starch and Chemical Investment Holding Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by National Starch and Chemical Investment Holding Corp filed Critical National Starch and Chemical Investment Holding Corp
Publication of EP0805898A1 publication Critical patent/EP0805898A1/fr
Withdrawn legal-status Critical Current

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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
    • D21H17/20—Macromolecular organic compounds
    • D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/24—Polysaccharides
    • D21H17/28—Starch

Definitions

  • This invention relates to paper and its manufacture using starches or flours.
  • Heat/moisture treatment and annealing of starches and/or flours are taught in the literature and distinguished by the amount of water present. "Annealing” involves slurrying a granular starch with excess water at temperatures below the starch's or flour's gelatinization temperature. "Heat/moisture- treatment” involves a semi-dry treatment at temperatures below the starch's or flour's gelatinization temperature, with no added moisture and with the only moisture present being that normally present in a starch granule (which is typically 10% or more) .
  • the process of the '829 patent involves dry heating flour or wheat to a point at which substantially all of the gluten is rendered non-retainable in a washing test and then blending the treated flour or wheat with untreated flour or wheat to provide a blend having superior strength.
  • the improvement of the '897 patent is continuing the dry heating, without, however, gelatinizing the starch, for a considerable time beyond that necessary to render all of the gluten non- retainable.
  • “Dry-heating” excludes heating in a steam atmosphere or an atmosphere containing considerable quantities of water vapor which would tend to gelatinize the starch.
  • the wheat or flour may contain the usual amount of moisture, preferably not greater than 15%.
  • the heat treatment may exceed 7 hours at 77-93°C (170-200°F) , e.g., 8 to 14 hours at 82°C (180 ⁇ F) or 6 hours at 100°C (212°F) .
  • GB 530.226 (accepted Dec. 6, 1940) discloses a method for drying a starch cake containing about 40-50% water with hot air or another gas at 149°c (300°F) or above without gelatinizing the starch.
  • the starch cake is disintegrated by milling it to a finely divided state prior to drying.
  • GB-595.552 discloses treatment of starch, more particularly a corn starch, which involves drying the starch to a relatively low moisture content of 1-2%, not exceeding 3%, and subsequently dry heating the substantially moisture-free starch at 115-126°C for 1 to 3 hours.
  • the treatment is intended to render the starch free from thermophilic bacteria.
  • the starch should not be heated longer than necessary to effect the desired sterilization.
  • U.S. 3.490.917 discloses a process for preparing a non-chlorinated cake flour suitable for use in cakes and sponges having a high sugar to flour ratio.
  • the starch or a flour in which the gluten is substantially or completely detached from the starch granules is heated to a temperature of from 100-140 ⁇ C and then cooled.
  • the conditions are selected so that dextrinization does not occur, e.g., about 15 minutes at 100-ll5°C and no hold and rapid cooling at the higher temperatures.
  • the heat treatment should be carried out under conditions which allow the water vapor to escape. The reduction in moisture content due to the heat treatment depends upon the temperature employed.
  • the moisture content is reduced from 10-12% to 8-9%, by weight, while at medium and high temperatures the moisture content is typically reduced to 7% or less.
  • the moisture is allowed to reach moisture equilibrium with the atmosphere.
  • the gelatinization temperature of the heat treated starch or flour is approximately 0.5-l ⁇ C higher than that of a comparable chlorinated flour or starch.
  • the heating can be carried out in many ways, including heating in a hot air fluidized bed.
  • U.S. 3.578.497 discloses a process for non-chemically improving the paste and gel properties of potato starch and imparting a swelling temperature as much as -7 to - 1°C (20 to 30°F) higher.
  • a concentrated suspension (20- 40% dry solids) at a neutral pH (5.5-8.0, preferably 6- 7.5) is heated either for a long time at a relatively low temperature or for a short time at successively higher temperatures.
  • the suspension is first heated at a temperature below the incipient swelling temperature of the particular batch of starch being treated (preferably 49°C - 120°F). Then the temperature is gradually raised until a temperature well above the original swelling temperature is attained.
  • U.S. 3.977.897 discloses a method for preparing non- chemically inhibited amylose-containing starches. Both cereal and root starches can be inhibited, but the inhibition effects are more observable with root starches. Amylose-free starches, such as waxy corn starch, show no or very slight inhibition. The Brabender viscosity of cooked pastes derived from the treated starch was used to determine the inhibition level.
  • Inhibition was indicated by a delayed peak time in the case of the treated corn starch, by the lack of a peak and a higher final viscosity in the case of the treated achira starch, and by the loss of cohesiveness in the case of the treated tapioca starch.
  • the granular starch is suspended in water in the presence of salts which raise the starch's gelatinization temperature so that the suspension may be heated to high temperatures without causing the starch granules to swell and rupture yielding a gelatinized product.
  • the preferred salts are sodium, ammonium, magnesium or potassium sulfate; sodium, potassium or ammonium chloride; and sodium, potassium or ammonium phosphate. About 10-60 parts of salt are used per 100 parts by weight of starch.
  • the suspension is heated at 50-100°C, preferably 60-90°C, for about 0.5 to 30 hours.
  • the pH of the suspension is maintained at about 3-9, preferably 4-7. Highly alkaline systems, i.e., pH levels above 9 retard inhibition.
  • U.S. 4.013.799 discloses heating a tapioca starch above its gelatinization temperature with insufficient moisture (15 to 35% by total weight) to produce gelatinization.
  • the starch is heated to 70-130°C for l to 72 hours.
  • the starch is used as a thickener in wet, pre-cooked baby foods having a pH below about 4.5.
  • U.S. 4.303.451 discloses a method for preparing a pregelatinized waxy maize starch having improved flavor characteristics reminiscent of a tapioca starch.
  • the starch is heat treated at 120-200°C for 15 to 20 minutes.
  • the pregelatinized starch has gel strength and viscosity characteristics suitable for use in pudding mixes.
  • U.S. 4.303.452 (issued Dec. 1, 1981 to Ohira et al.) discloses smoking a waxy maize starch to improve gel strength and impart a smoky taste.
  • the pH of the starch is raised to pH 9-11 before smoking.
  • the preferred water content of the starch during smoking is 10-20%.
  • Chiu discloses instant gelling tapioca and potato starches which are non-granular and which have a reduced viscosity. Unmodified potato and tapioca starches do not normally gel.
  • the starches of the patent are rendered non-granular and cold-water-dispersible by forming an aqueous slurry of the native starch at a pH of about 5-12 and then drum-drying the slurry.
  • the starches are rendered gelling by heat treating the drum-dried starch for about 1.5 to 24 hours at 125-180 ⁇ C to reduce the viscosity to within defined Brabender viscosity limitations.
  • U.S. 4.491.483 discloses subjecting a semi-moist blend of a granular starch with at least 0.25 wt. % of a fatty acid surfactant and sufficient water (about 10-40 wt. %) to a heat-moisture treatment at from about 50-120°C, followed by drying to about 5-15 wt. %, preferably 10 wt. %, moisture.
  • the heat-moisture treated starch-surfactant product is characterized by a hot water dispersibility of from about 60-100% and a higher pasting temperature than the granular starch from which it is derived.
  • the treatment takes place in a closed container so that the moisture can be maintained at a constant level.
  • the preferred conditions are 3 to 16 hours at 60-90°C. Degradation and dextrinization reactions are undesirable as they destroy the thickening ability of the starch.
  • the use of conditions, such as, e.g., 35% moisture at 90°C for 16 hours results in reduced paste viscosity. It is believed the presence of the surfactant during the treatment permits formation of a complex within the partially swollen starch matrix with straight chain portions of the starch molecules. The limited moisture environment allows complex formation without gelatinization.
  • Japanese Patent Publication No. 61-254602. discloses a wet and dry method for heating waxy corn starch and derivatives thereof to impart emulsification properties.
  • the wet or dry starch is heated at 100-200°C, preferably 130-150°C, for 0.5 to 6 hours.
  • the water content is 10%, preferably 5%, or less.
  • the water content is 5 to 50%, preferably 20-30%.
  • the pH is 3.5-8, preferably 4-5.
  • Chemical Crosslinking of Starches and Flours are chemically modified with difunctional reagents such as phosphorus oxychloride, sodium trimetaphosphate, adipic anhydride, acetic anhydride and epichlorohydrin to produce chemically crosslinked starches having excellent tolerance to processing variables such as heat, shear, and pH extremes.
  • difunctional reagents such as phosphorus oxychloride, sodium trimetaphosphate, adipic anhydride, acetic anhydride and epichlorohydrin to produce chemically crosslinked starches having excellent tolerance to processing variables such as heat, shear, and pH extremes.
  • Such chemically crosslinked starches also referred to as "inhibited starches” provide a desirable smooth texture and possess viscosity stability throughout processing operations and normal shelf life.
  • unmodified starches particularly waxy-based starches.
  • Papermakin ⁇ Papermaking is a process of forming an aqueous slurry of pulp or wood cellulosic fibers, introducing the fibers onto a screen or wire to form an interlocking mat and to allow the water to drain through the screen or wire, squeezing the mat between rollers, drying it, and processing it into a dry roll or sheets.
  • starch has been used in papermaking processes in a solubilized form so that the starch molecules are accessible for bonding to the cellulosic fibers.
  • Starch retention on cellulosic fibers is increased by making the starch cationic or amphoteric. Both starch and cellulosic fibers are anionic. Attracted to the negatively charged cellulosic fiber, and also to any of the common negatively charged fillers added to the wet end system, the cationic or amphoteric starch increases fiber-to-fiber and fiber-to-filler bonding, promoting a high degree of filler retention as well as strength.
  • This invention is directed to paper comprising, as an additive, a starch or flour that is thermally inhibited.
  • the starches and flours may be non- pregelatinized granular starches and flours or pregelatinized granular or nongranular starches and flours.
  • the starches or flours are thermally inhibited to impart the functionality previously provided by chemical crosslinking with a multifunctional crosslinking agent.
  • the thermally-inhibited starches and flours can be used wherever starches are conventionally used in paper manufacture, for example, as wet end additives, coatings, and sizes.
  • the starch is derivatized with cationic, anionic, non-ionic, or amphoteric substituents.
  • anionic or non-ionic starches are typically used in combination with cationic or amphoteric starches.
  • the starches and flours are thermally inhibited, without the addition of chemical reagents, in a heat treatment process that results in the starch or flour becoming and remaining inhibited.
  • the starches and flours are referred to as “inhibited” or “thermally- inhibited (abbreviated "T-I") .
  • T-I thermalally- inhibited
  • T-I thermally- inhibited
  • These thermally- inhibited starches and flours are dispersed and/or cooked in water, they exhibit the textural and viscosity properties characteristic of a chemically-crosslinked starch.
  • the starch granules are more resistant to viscosity breakdown. This resistance to breakdown results in what is subjectively considered a non-cohesive or "short” textured paste, meaning that the gelatinized starch or flour tends to be salve-like and heavy in viscosity rather than runny or gummy.
  • thermally-inhibited starches and flours are non-pregelatinized granular starches or flours
  • the starches or flours exhibit an unchanged or reduced gelatinization temperature.
  • most annealed and heat/moisture treated starches show an increased gelatinization temperature.
  • Chemically- crosslinked starches show an unchanged gelatinization temperature. It is believed the overall granular structure of the thermally-inhibited starches and flours has been altered.
  • the starches and flours that are substantially completely thermally inhibited will resist gelatinization.
  • the starches and flours that are highly inhibited will gelatinize to a limited extent and show a continuing rise in viscosity but will not attain a peak viscosity.
  • the starches and flours that are moderately inhibited will exhibit a lower peak viscosity and a lower percentage breakdown in viscosity compared to the same starch that is not inhibited.
  • the starches and flours that are lightly inhibited will show a slight increase in peak viscosity and a lower percentage breakdown in viscosity compared to the same starch that is not inhibited.
  • the starches and flours are inhibited by a process which comprises the steps of dehydrating the starch or flour until it is anhydrous or substantially anhydrous and then heat treating the anhydrous or substantially anhydrous starch or flour at a temperature and for a period of time sufficient to inhibit the starch or flour.
  • substantially anhydrous means containing less than 1% moisture by weight.
  • the dehydration may be a thermal dehydration or a non-thermal dehydration such as alcohol extraction or freeze drying.
  • An optional, but preferred, step is adjusting the pH of the starch or flour to neutral or greater prior to the dehydration step.
  • the amount of thermal inhibition required will depend on the reason the starch or flour is included in the paper, as well as the particular processing conditions used to prepare the paper. Paper pulps prepared with the thermally-inhibited starches and flours will possess viscosity stability, and process tolerance such as resistance to heat, acid and shear. In addition, the viscosity of the jet-cooked thermally-inhibited starches is lower than the viscosity of jet-cooked chemically-crosslinked starches. This lower viscosity is a significant processing advantage. Depending on the extent of the heat treatment, various levels of inhibition can be achieved. For example, lightly inhibited, higher viscosity products with little breakdown, as well as highly inhibited, low viscosity products with no breakdown, can be prepared by the thermal inhibition processes described herein.
  • a thermally-inhibited, cationic, anionic, amphoteric, or non-ionic starch or flour is added to the wet end of the papermaking system.
  • a non-pregelatinized starch or flour is used, it is preferably cooked, e.g., by jet cooking, before addition.
  • non-pregelatinized granular starch or flour will be thermally inhibited to a level such that, when the starch or flour is dispersed in water at 5% solids at 95°C, it will show a breakdown from peak viscosity in the range of 15-65%, preferably 25-45%.
  • the thermally-inhibited starches and flours can be derived from any native source.
  • a "native" starch or flour is one as it is found in nature in unmodified form.
  • Typical sources for the starches and flours are cereals, tubers, roots, legumes and fruits.
  • the native source can be corn, pea, potato, sweet potato, banana, barley, wheat, rice, sago, amaranth, tapioca, sorghum, waxy maize, waxy tapioca, waxy rice, waxy barley, waxy potato, waxy sorghum, starches having an amylose content of 40% or greater and the like.
  • Preferred starches are waxy starches, potato, tapioca and corn.
  • the thermal inhibition process may be carried out prior to or after other starch or flour reactions are used to modify starch or flour.
  • the starches may be modified by conversion (i.e., acid-, enzyme-, and/or heat-conversion) , oxidation, phosphorylation, etherification (e.g., by reaction with propylene oxide), esterification (e.g., by reaction with acetic anhydride or octenylsuccinic anhydride) , and/or chemical crosslinking (e.g., by reaction with phosphorus oxychloride or sodium tri etaphosphate) .
  • the flours may be modified by bleaching or enzyme conversion.
  • Native granular starches have a natural pH of about 5.0-6.5.
  • acid hydrolysis i.e., degradation
  • This degradation impedes or prevents inhibition. Therefore, the dehydration conditions need to be chosen so that degradation is avoided. Suitable conditions are dehydrating at low temperatures and the starch's natural pH or dehydrating at higher temperatures after increasing the pH of the starch to neutral or above.
  • neutral covers the range of pH values around pH 7 and is meant to include from about pH 6.5-7.5. A pH of at least 7 is preferred. More preferably, the pH is 7.5- 10.5. The most preferred pH range is above 8 to below 10.
  • the non-pregelatinized granular starch or flour is typically slurried in water or another aqueous medium, in a ratio of 1.5 to 2.0 parts of water to 1.0 part of starch or flour, and the pH is raised by the addition of any suitable base.
  • Buffers such as sodium phosphate, may be used to maintain the pH if needed.
  • a solution of a base may be sprayed onto the powdered starch or flour until the starch or flour attains the desired pH, or an alkaline gas such as ammonia can be infused into the starch or flour.
  • the slurry is then either dewatered and dried, or dried directly, typically to a 2-15% moisture content.
  • the starches or flours can be pregelatinized prior to or after the thermal inhibition process using methods known in the art.
  • the amount of pregelatinization, and consequently, whether the starch will display a high or a low initial viscosity when dispersed in water, can be regulated by the pregelatinization procedure used, as is known in the art.
  • the resulting pregelatinized starches are useful in applications where cold-water-soluble or cold-water- dispersible starches are used.
  • Pregelatinized granular starches and flours have retained their granular structure but lost their polarization crosses. They are pregelatinized in such a way that a majority of the starch granules are swollen, but remain intact. Exemplary processes for preparing pregelatinized granular starches are disclosed in U.S. 4.280.851 (issued July 28, 1981 to E. Pitchon et al.),
  • Pregelatinized non-granular starches and flours have also lost their polarization crosses and have become so swollen that the starches have lost their granular structure and broken into fragments. They can be prepared according to any of the known physical, chemical or thermal pregelatinization processes that destroy the granule such as drum drying, extrusion, or jet-cooking. See U.S. 1.516.512 (issued Nov. 25, 1924 to R.W. G. Stutzke) ; U.S. 1.901.109. (issued March 14, 1933 to W. Maier) ; US. 2.314.459 (issued March 23, 1943 to A.A.
  • the pH is adjusted by slurrying the pregelatinized granular starch or flour in water in a ratio of 1.5-2.0 parts to 1.0 part starch, and optionally, the pH is adjusted to neutral or greater.
  • the slurry is simultaneously pregelatinized and dried and the dried, starch or flour is thermally inhibited. If the thermal inhibition process is performed first, the starch or flour is slurried in water, the pH of the starch or flour is adjusted to neutral or greater, and the starch or flour is dried to about 2-15% moisture. The dried starch or flour is then dehydrated and heat treated.
  • the inhibited starch or flour is reslurried in water, optionally pH adjusted, and simultaneously pregelatinized and dried.
  • the pH is raised by slurrying the starch or flour in water at 30-40% solids and adding a sufficient amount of a solution of a base until the desired pH is reached.
  • the starch or flour is slurred at 6-10% solids in water and the pH is adjusted to the desired pH by adding a sufficient amount of a solution of a base until the desired pH is reached.
  • Suitable bases for use in the pH adjustment step include, but are not limited to, sodium hydroxide, sodium carbonate, tetrasodium pyrophosphate, ammonium orthophosphate, disodium orthophosphate, trisodium phosphate, calcium carbonate, calcium hydroxide, potassium carbonate, and potassium hydroxide, and any other bases approved for use under the applicable regulatory laws.
  • the preferred base is sodium carbonate. It may be possible to use bases not approved provided they can be washed from the starch or flour so that the final product conforms to good manufacturing practices for desired end use.
  • a thermal dehydration is carried out by heating the starch or flour in a heating device for a time and at a temperature sufficient to reduce the moisture content to less than 1%, preferably 0%.
  • the temperatures used are 125°C or less, more preferably 100- 120 ⁇ C.
  • the dehydrating temperature can be lower than
  • Representative processes for carrying out a non-thermal dehydration include freeze drying or extracting the water from the starch or flour using a solvent, preferably a hydrophilic solvent, more preferably a hydrophilic solvent which forms an azeotropic mixture with water (e.g., ethanol) .
  • a solvent preferably a hydrophilic solvent, more preferably a hydrophilic solvent which forms an azeotropic mixture with water (e.g., ethanol) .
  • the starch or flour (about 4-5% moisture) is placed in a Soxhlet thimble which is then placed in a Soxhlet apparatus.
  • a suitable solvent is placed in the apparatus, heated to its reflux temperature, and refluxed for a time sufficient to dehydrate the starch or flour. Since during the refluxing the solvent is condensed onto the starch or flour, the starch or flour is exposed to a lower temperature than the solvent's boiling point. For example, during ethanol extraction the temperature of the starch is only about 40-50 ⁇ C even though ethanol's boiling point is about 78°C. When ethanol is used as the solvent, the refluxing is continued for about 17 hours.
  • the extracted starch or flour is removed from the thimble, spread out on a tray, and the excess solvent is allowed to flash off.
  • the time required for ethanol to flash off is about 20-30 minutes.
  • the dehydrated starch or flour is immediately placed in a suitable heating apparatus for the heat treatment.
  • a suitable heating apparatus for the heat treatment for a commercial scale dehydration any continuous extraction apparatus is suitable.
  • the starch or flour (4-5% moisture) is placed on a tray and put into a freeze dryer.
  • a suitable bulk tray freeze dryer is available from FTS Systems of Stone Ridge, New York under the trademark Dura-Tap.
  • the freeze dryer is run through a programmed cycle to remove the moisture.
  • the temperature is held constant at about 20°C and a vacuum is drawn to about 50 milliTorr (mT) .
  • the starch or flour is removed from the freeze dryer and immediately placed into a suitable heating apparatus for the heat treatment. After it is dehydrated, the starch or flour is heat treated for a time and at a temperature sufficient to inhibit the starch or flour.
  • the preferred heating temperatures are greater than about 100°C.
  • the upper limit of the heat treating temperature is about 200°C. Typical temperatures are
  • the temperature selected will depend upon the amount of inhibition desired and the rate at which it is to be achieved.
  • the time at the final heating temperature will depend upon the level of inhibition desired. When a conventional oven is used, the time ranges from 1 to 20 hours, typically 2 to 5 hours, usually 3.5 to 4.5 hours. When a fluidized bed is used, the times range from 0 minutes to 20 hours, typically 0.5 to 3.0 hours. Longer times are required at lower temperatures to obtain more inhibited starches.
  • the thermal dehydrating and heat treating steps will be continuous and accomplished by the application of heat to the starch or flour beginning from ambient temperature.
  • the moisture will be driven off during the heating and the starch will become anhydrous or substantially anhydrous.
  • the peak viscosities are higher than the peak viscosities of starches heated for longer times, although there will be greater breakdown in viscosity from the peak viscosity. With continued heat treating, the peak viscosities are lower, but the viscosity breakdowns are less.
  • starches with a wide range of inhibition can be obtained by the thermal inhibition process
  • the preferred starches for use in papermaking will have a level of inhibition which results in the starch, after dispersion in an aqueous medium, having a balance of both intact granules and solubilized starch molecules.
  • the process may be carried out as part of a continuous process involving the extraction of the starch from a plant material.
  • the source of the starch or flour, the initial pH, the dehydrating conditions, the heating time and temperature, and the equipment used are all interrelated variables that affect the amount of inhibition.
  • the heating steps may be performed at normal pressures, under vacuum or under pressure, and may be accomplished by conventional means known in the art.
  • the preferred method is by the application of dry heat in dry air or in an inert gaseous environment.
  • the heat treating step can be carried out in the same apparatus in which the thermal dehydration occurs. Most conveniently the process is continuous with the thermal dehydration and heat treating occurring in the same apparatus, as when a fluidized bed reactor is used.
  • the dehydrating and heat treating apparatus can be any industrial ovens, conventional ovens, microwave ovens, dextrinizers, dryers, mixers and blenders equipped with heating devices and other types of heaters, provided that the apparatus is fitted with a vent to the atmosphere so that moisture does not accumulate and precipitate onto the starch or flour.
  • the preferred apparatus is a fluidized bed.
  • the apparatus is equipped with a means for removing water vapor, such as, a vacuum or a blower to sweep air or the fluidizing gas from the head-space of the fluidized bed.
  • Suitable fluidizing gases are air and nitrogen. For safety reasons, it is preferable to use a gas containing less than 12% oxygen.
  • Superior inhibited starches having high viscosities with low percentage breakdown in viscosity are obtained in shorter times in the fluidized bed reactor than can be achieved using other conventional heating ovens or dryers.
  • the starches or flours may be inhibited individually or more than one may be inhibited at the same time. They may be inhibited in the presence of other materials or ingredients that would not interfere with the thermal inhibition process or alter the properties of the starch or flour product.
  • thermally-inhibited starches and flours can be used wherever starches and flours are conventionally used in papermaking, e.g., as wet end additives, sizes, or coatings.
  • fillers or pigments When used as wet end additives, they increase the dry strength and the retention of fillers or pigments and minimize or overcome strength losses due to the incorporation of fillers. They are usually added as an aqueous dispersion which is prepared by cooking a thermally-inhibited non-pregelatinized granular starch or flour or dispersing a thermally-inhibited pregelatinized starch or flour.
  • Converted starches as well as starch ethers and starch esters, are useful as surface sizing agents, or coatings for providing barriers for water vapor, grease, and solvents.
  • Non-converted starches are useful as thickeners in surface sizings.
  • Cationic starches are useful as flocculants for suspensions or inorganic or organic matter having a negative charge. When used as surface sizes, they provide pick-up and penetration for inks and the like. When used as coatings, they act as water vapor, grease, and solvents barriers.
  • Cationization of starch can be carried out by well known chemical reactions with reagents containing primary, secondary, tertiary or quaternary amines attached through an ether or ester linkage, as disclosed, for example, in Solarek. "Cationic Starches”.
  • Typical cationic and cationogenic groups include the diethylaminoethyl ether groups introduced by reaction with 2-diethylaminoethylchloride hydrochloride or 3-(trimethyl ammonium chloride)-2-hydroxypropyl ether groups introduced by reaction with 3-chloro-2- hydroxypropyl trimethylammonium chloride. See, U.S. 2.813.093 (issued November 12, 1957 to Caldwell, et al.) for reactions with dialkylaminoalkyl halides to introduce tertiary amino groups which can then quaternized to ammonium groups; U.S.
  • Converted starches containing cationic or cationogenic groups and sulfo-succinate groups, useful as pigment retention aids, are described in U.S. 4.029.544 (issued June 14, 1977 to Jarowenko et al.). Amphoteric starches are also useful herein.
  • Anionic starches are prepared by substitution with anionic groups such as those discussed above according to the procedures previously disclosed for preparing amphoteric starches but without the use of cationic reagents.
  • anionic or non-ionic starches When anionic or non-ionic starches are used in the papermaking process, they are used in conjunction with cationic additives, such as a synthetic polymer containing the residues of cationic monomers or a cationic or amphoteric starch.
  • the anionic or nonionic starch may be thermally inhibited in combination with a cationic or amphoteric starch, and this thermally inhibited starch blend used as an additive in the papermaking.
  • Aldehyde-containing starches, useful as strength aids starches, are described in U.S. 4.675.394 (issued June 23, 1987 to Jobe et al.), the disclosure of which is incorporated herein by reference.
  • a granular starch is recovered by filtration, optionally washed with water to remove any residual salts, and dried.
  • the granular starch products may also be drum- dried, jet-cooked and spray-dried, or gelatinized and isolated by alcohol precipitation or freeze drying to form non-granular products. If the starch derivative is non-granular, it may be purified by dialysis to remove residual salts and isolated by alcohol precipitation, freeze drying, or spray drying.
  • the amount of a substituent on the starch is defined as the degree of substitution (DS) which means the average number of substituent groups per anhydroglucose unit of the starch molecule.
  • the degree of substitution can be varied, although generally a degree of substitution (DS) from about 0.005 to 0.2, and preferably from about 0.01 to 0.05, will be used. Higher degrees of substitution may be used, but this makes the starch more costly and difficult to make, and therefore, is not economically attractive.
  • the starch When the starch is to be used in the wet end system of papermaking, it is derivatized, optionally pregelatinized, and then thermally inhibited. It may then be subjected again to controlled gelatinization. Jet cooking provides a continuous process for gelatinizating the starch. It is well known in the art. By varying the temperature, pressure, flow rate, solids content of the starch slurry, and equipment configuration (e.g.. haffles and mixers) it is possible to provide gelatinization conditions where a proportion of the thermally-inhibited starch granules will hydrate and partially swell without fragmenting and a portion of the granules will disperse and solubilize.
  • equipment configuration e.g. haffles and mixers
  • Gelatinization and dispersion of the starch occurs in a very short period of time, from a few seconds to a few minutes.
  • Suitable conditions are temperatures of about 90-165°C, preferably about 100-160°C, more preferably about 105- 122°C, and an applied back pressure f at least 5 psi, preferably about 5-20 psi, although the pressure can be as high as 100 psi.
  • the starch concentration in the cooking chamber should be at least 3%, preferably from 3-7% solids.
  • the derivatized and thermally-inhibited starches may be effectively added to pulp prepared from any type and combination of cellulosic fibers and/or synthetic fibers.
  • Cellulosic materials include bleached and unbleached sulfate (kraft) , bleached and unbleached sulfite, bleached and unbleached soda, neutral sulfite, semi-chemical, chemiground wood, and ground wood.
  • Synthetic fibers include polyamides, polyesters, rayon and polyacrylic resins, as well as fibers from minerals, such as asbestos and glass. Viscose rayon or regenerated cellulose fibers can also be used for the pulp.
  • Inert mineral fillers such as, clay, titanium dioxide, talc, calcium carbonate, calcium sulfate, and diatomaceous earths, rosin, and other additives commonly introduced into paper, such as, dyes, pigments, sizing additives, alum, and anionic retention aids, may be added to the pulp or furnish.
  • the amount of thermally-inhibited starch that is added to the wet end or paper pulp will be an effective amount, typically from about 0.05-5%, preferably from about 0.1-2%, by weight based on the dry weight of the pulp.
  • the thermally- inhibited starch is added to a simple alkaline papermaking system (i.e., one containing mainly pulp, alum and starch) , or to a microparticle colloidal papermaking system.
  • Suitable microparticles for inclusion in the alkaline systems include colloidal silica, bentonite and anionic alum, which are usually incorporated in amounts of at least 0.001%, more typically about 0.01-1% by weight based on the weight of dry pulp. Further description of such microparticle inorganic materials may be found in U.S. 4.388.150 (issued June 14, 1983 to Batelson et al.); U.S. 4.643.801 (issued February 17, 1987 to Johnson); U.S. 4.753.710 (issued June 28, 1988 to Holroyd et al.); and U.S. 4.913.775 (issued April 3, 1990 to Holroyd et al.).
  • Peak where Peak is the peak viscosity in Brabender Units and is the viscosity after holding at 95°C for 30 minutes.
  • starches and flours used were granular and were provided by National Starch and Chemical Company of Bridgewater, New Jersey.
  • the controls for the test samples were from the same native sources as the test samples, were unmodified or modified in the same manner as the test samples, and were at the same pH, unless otherwise indicated.
  • the pH of the samples was raised by slurrying the starch or flour in water at 30-40% solids and adding a sufficient amount of a 5% sodium carbonate solution until the desired pH was reached. Measurements of pH, either on samples before or after the thermal inhibition steps, were made on samples consisting of one part starch or flour to four parts water.
  • the starch or flour was slurred at 6-10% solids in water and the pH was adjusted to the desired pH by adding a sufficient amount of 5% sodium carbonate solution until the desired pH was reached. Except where a conventional oven or dextrinizer is specified, the test samples were dehydrated and heat treated in a fluidized bed reactor, model number FDR-100, manufactured by Procedyne Corporation of New Brunswick, New Jersey. The cross-sectional area of the fluidized bed reactor was 0.05 sq meter.
  • the starting bed height was 0.3-0.8 meter, but usually 0.77 meter.
  • the fluidizing gas was air except where otherwise indicated.
  • the gas was used at a velocity of 5-15 meter/min.
  • pregelatinized granular starches were being heat treated, the gas was used at a velocity of 15- 21 meter/min.
  • the side walls of the reactor were heated with hot oil, and the fluidizing gas was heated with an electric heater.
  • the samples were loaded into the reactor and then the fluidizing gas was introduced, or the samples were loaded while the fluidizing gas was being introduced. No difference was noted in the samples in the order of loading. Unless otherwise specified, the samples were brought from ambient temperature up to no more than 125°C until the samples became anhydrous and were further heated to the specified heat treating temperatures. When the heating temperature was 160°C, the time to reach that temperature was less than three hours.
  • the moisture level of the samples at the final heating temperature was 0%, except where otherwise stated. Portions of the samples were removed and tested for inhibition at the temperatures and times indicated in the tables.
  • the VISCO ⁇ Amylo ⁇ GRAPH records the torque required to balance the viscosity that develops when a starch slurry is subjected to a programmed heating cycle.
  • the record consists of a curve tracing the viscosity through the heating cycle in arbitrary units of measurement termed Brabender Units (BU) .
  • BU Brabender Unit
  • the starch slurry is heated rapidly to 92°C and held for 10 minutes.
  • the peak viscosity and viscosity ten minutes after peak viscosity were recorded in Brabender Units (BU) .
  • the percentage breakdown in viscosity ( ⁇ 2%) was calculated according to the formula:
  • Peak where "peak” is the peak viscosity in Brabender units, and "(peak + 10')” is the viscosity in Brabender Units at ten minutes after peak viscosity. If no peak viscosity was reached, i.e., the data indicate a rising (ris.) curve or a flat curve, the viscosity at 92°C and the viscosity at 30 minutes after attaining 92°C were recorded.
  • Characterization of a thermally-inhibited starch is made more conclusively by reference to a measurement of its Brabender viscosity after it is dispersed in water and gelatinized.
  • the cycle passes through the initiation of viscosity, usually at about 60- 70°C, the development of a peak viscosity in the range of 67-95°C, and any breakdown in viscosity when the starch is held at an elevated temperature, usually 92-95°C.
  • Inhibited starches will show a Brabender curve different from the curve of the same starch that has not been inhibited (hereinafter the control starch) .
  • an inhibited starch will attain a peak viscosity somewhat higher than the peak viscosity of the control, and there may be no decrease in percentage breakdown in viscosity compared to the control.
  • the peak viscosity and the breakdown in viscosity decrease.
  • the rate of gelatinization and swelling of the granules decreases, the peak viscosity disappears, and with prolonged cooking the Brabender trace becomes a rising curve indicating a slow continuing increase in viscosity.
  • starch granules no longer gelatinize, and the Brabender curve remains flat.
  • the pregelatinized thermally-inhibited starch to be tested was slurried in a sufficient amount of distilled water to give a 4.6% anhydrous solids starch slurry at pH 3 as follows: 132.75 g sucrose, 26.55 g starch, 10.8 g acetic acid, and 405.9 g water were mixed for three minutes in a standard home Mixmaster at setting #1.
  • the slurry was then introduced to the sample cup of a Brabender VISCO/Amylo/GRAPH fitted with a 350 cm/gram cartridge and the viscosity measured as the slurry was heated to 30 ⁇ C and held for 10 minutes. The viscosity at 30°C and 10 minutes after hold at 30°C were recorded.
  • the viscosity data at these temperatures are a measurement of the extent of pregelatinization. The higher the viscosity at 30 ⁇ C, the grater the extent of granular swelling and hydration during the pregelatinization process.
  • Heating was continued to 95°C and held at that temperature for 10 minutes.
  • thermally-inhibited starch is made more conclusively by reference to a measurement of its viscosity after it is dispersed in water and gelatinized using the instrument described above.
  • the level of viscosity when dispersed in cold water will be dependent on the extent to which the starch was initially cooked out during the pregelatinization process. If the granules were not fully swollen and hydrated during pregelatinization, gelatinization will continue when the starch is dispersed in water and heated. Inhibition was determined by a measurement of the starch viscosity when the starch was dispersed at 4.6% solids in water at pH 3 and heated to 95 ⁇ C.
  • the resulting Brabender traces will be as follows: for a highly inhibited that the starch, the trace will be a flat curve, indicating that the starch is already very swollen and is so inhibited starch it is resisting any further gelatinization or the trace will be a rising curve, indicating that further gelatinization is occurring at a slow rate and to a limited extent; for a less inhibited starch, the trace will he a dropping curve, indicating that some of the granules are fragmenting, but the overall breakdown in viscosity will be lower than that for a non-inhibited control or the trace will show a second peak but the breakdown in viscosity will be lower than that for a non-inhibited control.
  • the pregelatinized starch had a low initial cold viscosity, meaning it was not highly cooked out in the pregelatinization process and
  • Brabender traces will be as follows: for a highly inhibited starch, the trace will be a rising curve, indicating that further gelatinization is occurring at a slow rate and to a limited extent; for a less inhibited starch, the trace will show a peak viscosity as gelatinization occurs and then a drop in viscosity, but with a lower percentage breakdown in viscosity than for a non-inhibited control.
  • the resulting Brabender traces will be as follows: for a highly inhibited starch the trace will be flat, indicating that the starch is so inhibited that it is resisting any further gelatinization or the trace will be a rising curve, indicating that further gelatinization is occurring at a slow rate and to a limited extent; for a less inhibited starch, the trace will show a dropping curve, but the overall breakdown in viscosity from the peak viscosity will be lower than that for a non- inhibited control.
  • the crosslinked, thermally-inhibited cationic and amphoteric starches (23.0 g) to be tested was combined with 30 ml of an aqueous solution of citric acid monohydrate (prepared by diluting 210.2 g of citric acid monohydrate to 1000 ml in a volumetric flask) and sufficient water was added to make the total charge weight 460.0 g.
  • the slurry is added to the cooking chamber of the Brabender VISCO amylo GRAPH fitted with a 700 cm/gram cartridge and rapidly heated from room temperature to 95 ⁇ C.
  • the peak viscosity (highest viscosity observed) and the viscosity after 30 minutes at 95 ⁇ C were recorded.
  • the percentage breakdown in viscosity ( ⁇ 2%) was calculated according to the formula
  • Peak Characterization of Inhibition bv Cooks A dry blend of 7 g of starch or flour (anhydrous basis) and 14 g of sugar were added to 91 ml of water in a Waring blender cup at low speed, then transferred to a cook-up beaker, allowed to stand for 10 minutes, and then evaluated for viscosity, color, clarity and texture. Some of the granular non-pregelatinized starch samples were tested for pasting temperature and/or gelatinization temperature using the following procedures.
  • Rapid Visco Analyzer This test is used to determine the onset of gelatinization, i.e., the pasting temperature. The onset of gelatinization is indicated by an increase in the viscosity of the starch slurry as the starch granules begin to swell.
  • a 5 g starch sample (anhydrous basis) is placed in the analysis cup of a Model RVA-4 Analyzer and slurried in water at 20% solids. The total charge is 25 g.
  • the cup is placed into the analyzer, rotated at 160 rpm, and heated from an initial temperature of 50 ⁇ C up to a final temperature of 80°C at a rate of 3°C/minute.
  • a plot is generated showing time, temperature, and viscosity in centipoises (cP) .
  • the pasting temperature is the temperature at which the viscosity reaches 500 cP. Both pasting temperature and pasting time are recorded.
  • Differential Scanning Calorimetrv This test provides a quantitative measurement of the enthalapy ( H) of the energy transformation that occurs during the gelatinization of the starch granule. The peak temperature and time required for gelatinization are recorded.
  • a Perkin-Elmer DSC-4 differential scanning calorimeter with data station and large volume high pressure sample cells is used.
  • the cells are prepared by weighing accurately 10 mg of starch (dry basis) and the appropriate amount of distilled water to approximately equal 40 mg of total water weight (moisture of starch and distilled water) . The cells are then sealed and allowed to equilibrate overnight at 4°C before being scanned at from 25-150 ⁇ C at the rate of 10°C/minute. An empty cell is used as the blank.
  • Brookfield Viscometer Procedure Test samples are measured using a Model RVT Brookfield Viscometer and the appropriate spindle (the spindle is selected based on the anticipated viscosity of the material) .
  • the test sample usually a cooked starch paste, is placed in position and the spindle is lowered into the sample to the appropriate height.
  • the viscometer is turned on and the spindle is rotated at a constant speed (e.g., 10 or 20 rpm) for at least 3 revolutions before a reading is taken. Using the appropriate conversion factors, the viscosity (in centipoises) of the sample is recorded.
  • a sample of 500 ml of 0.5 wt. % by weight pulp stock was placed in the jar and agitated at about 800 rpm.
  • Alum at 0.25 wt. % of the of the dry fiber in the pulp stock, was added and mixed at 400 rpm for one minute and then the mixing was increased to 1000 rpm.
  • the starch at 0.75 wt. % of the dry fiber, was then added and mixing was continued for another minute.
  • Colloidal silica was added at 0.15 wt. % of the dry fiber and the sample was mixed for another minute.
  • a 100 ml sample was collected by removing the clamp.
  • the sample was acidified with 5 N hydrochloric acid to solubilize the calcium carbonate and then filtered onto tared filter paper to recover the fine solids.
  • a standard water hardness titration was run by adding Eriochrome Black "T" indicator and titrating with 0.1 N of the disodium salt (EDTA) ethylene diamine tetra-acetic acid, disodium salt) standard solution to a blue endpoint, using a calibrated burette.
  • EDTA disodium salt
  • TPSF turbulent pulse sheet former
  • Furnish (200 ml) at 0.5% consistency was diluted to one liter with water and added to the TPSF to simulate a 80 lb/3330 sq ft fine paper grade.
  • the following were then added to the furnish in the order recited and mixed for 30 seconds at 1000 rpm after each addition: alum (0.25 wt. % of dry fiber used in the pulp stock), starch (0.75 wt. % dry fiber), colloidal silica (0.15 wt. % dry fiber).
  • the conditions for the paper formation were: air pressure of 20 in.
  • the thermally-inhibited starches and flours are referred to as " ⁇ -I” starches and flours and the conditions used for their preparation (i.e., pH to which the starch is adjusted and heat treatment temperature and time at that temperature are included in parenthesis - (pH; temperature/hoId time at that temperature) . All pH adjustments are done with sodium carbonate unless specified otherwise. Unless otherwise specified, the thermally-inhibited starches and flours referred to as "granular" starches are non-pregelatinized granular starches and flours.
  • the moisture indicated is the moisture of the starch before the dehydration and heat treating steps. As indicated above, as the starches were brought from ambient temperature up to the heating temperature, the starches became anhydrous or substantially anhydrous.
  • This example illustrates the preparation of the starches of this invention from a commercial granular waxy maize base starch by the heat treatment process of this invention. Processing conditions and their effects on viscosity and texture of waxy maize starch are set forth in the Tables below.
  • anhydrous solids of starch dispersed in water was heated rapidly to 50°C, then the heat was increased by 1.5°C per minute to 95°C, and held for 20 minutes.
  • EXAMPLE 2 This example illustrates that a variety of granular starches may be processed by the method of this invention to provide a non-cohesive thickener with properties similar to chemically crosslinked starches.
  • Waxy — — 0 Rice Control a. Tapioca starch samples were commercial granular starch obtained from National starch and Chemical Company, Bridgewater, New Jersey. Waxy barley starch samples were commercial granular starch obtained from AIKo, Finland. Waxy rice starch samples were commercial granular starch obtained from Mitsubishi Corporation, Japan. b. Samples were cooked by slurring 7.5 g of starch at 12% moisture in 100 mis of water and heating the starch slurry for 20 minutes in a boiling water bath. TABLE IV - Process Variables
  • Control a. V.O. hybrid starch samples were granular starches obtained from National Starch and Chemical Company,
  • non-cohesive, heat-stable starch thickener may be prepared from waxy barley, V.O. hybrid, tapioca and waxy rice starches by the process of this invention.
  • the amount of inhibition (non-cohesive, thickening character in cooked aqueous dispersion) increased with increasing time of heat treatment.
  • EXAMPLE 3 This example illustrates the effects of temperature, the pH, and starch moisture content on the viscosity and texture of the treated starch.
  • Samples (900 g) of a commercial granular waxy maize starch obtained from National Starch and Chemical Company, Bridgewater, New Jersey) were placed in a 10" x 15" x 0.75" aluminum tray and heated in an oven at 180 * C for 15, 30, 45 and 60 minutes. The pH of the starch was not adjusted and remained at about 5.2 during the heating process. Sample viscosity and texture were evaluated by the method of Example 1.
  • a combination of selected factors including the pH, moisture content and the type of native starch, determine whether a desirable, non-cohesive, heat-stable starch thickener is produced by the process of this invention.
  • the data shows that inhibited anhydrous or substantially anhydrous samples can be obtained at heat treating temperatures between 100-200°C, with more inhibition obtained at higher temperatures or at longer times at lower temperatures.
  • the starch samples heated at 200°C were highly inhibited (rising curves) or completely inhibited (no gelatinization) .
  • Samples of a high amylose starch (Hylon V - 50% amylose) at its natural pH and pH 9.5 were evaluated for the effect of the high amylose content on inhibition.
  • the starches were thermally-inhibited at 160°C in the fluidized bed for the indicated time. Due to the high levels of amylose, it was necessary to use a pressurized Visco/amylo/Graph (C.W. Brabender, Ralphensack, NJ) to obtain Brabender curves. Samples were slurried at 10% starch solids, heated to 120°C, and held for 30 minutes. The results are shown below:
  • EXAMPLE 6 This example shows the preparation of pregelatinized granular, thermally-inhibited waxy maize starches. The pregelatinization step was carried out prior to the thermal inhibition. The fluidized bed described previously was used.
  • Starch slurries (30-40% solids) , pH adjusted to 6, 8, and 10, were pregelatinized in a pilot size spray drier (Type-1-KA#4F, from APV Crepaco, Inc., Dryer
  • the spray nozzle had the following configuration: fluid cap, 251376, and air cap, 4691312.
  • the resulting high and low viscosity pregelatinized granular starches were dehydrated and heat treated at the temperature and time indicated.
  • the thermally-inhibited starches were evaluated for inhibition using the Brabender procedure previously described.
  • This example describes the preparation of thermally-inhibited pregelatinized granular starches from additional starch bases as well as a waxy maize starch.
  • the granular starches were adjusted to the indicated pH, pregelatinized using the procedure previously described, and heat treated in an oven at 140 ⁇ C for the indicated time.
  • the cook evaluation and Brabender results are shown below.
  • thermally-inhibited pregelatinized granular starches can be prepared using other starch bases and that for non-cohesive starches longer times and/or higher pHs are required when an oveno rather than a fluidized bed is used for the dehydration and heat treatment.
  • EXAMPLE 8 This example shows the preparation of pregelatinized, non-granular starches which were pregelatinized by drum-drying and then thermally inhibited. Samples of waxy maize, tapioca and potato starches, at pH 6, 8, and 10, were pregelatinized by drum-drying. The samples were placed in a 140°C oven, dehydrated to anhydrous, and heat treated at 140°C for the indicated times.
  • Viscosity (B.U.I
  • This example shows the preparation of another pregelatinized non-granular starch which was jet-cooked, spray-dried, and then thermally inhibited.
  • a granular high amylose starch (50% amylose) was jet-cooked and spray-dried using the continuous coupled jet-cooking/spray-drying process described in U.S. 5.131.953 and then thermally inhibited for 8 hours at 140 ⁇ C.
  • the jet-cooking/spray-drying conditions used were as follows: slurry - pH 8.5-9.0; cook solids - 10%; moyno setting - about 1.5; cooking temperature - about 145°C; excess steam - 20%; boiler pressure - about 85 psi; back pressure - 65 psi; spray-dryer - Niro dryer; inlet temperature - 245°C; outlet temperature - 115°C; atomizer - centrifugal wheel.
  • the pregelatinized non- granular starch was adjusted to pH 8.7 and dehydrated and heat treated for 8 hours in an oven at 140°C. The characteristics of the resulting thermally-inhibited starches are set out below.
  • thermally-inhibited waxy maize starches can be prepared by drum drying the starches prior to thermal inhibition.
  • the resulting non- granular thermally-inhibited drum-dried starches are compared with the non-granular thermally-inhibited waxy maize starches prepared by the continuous coupled jet- cooking and spray-drying process used in Example 8 and with granular thermally-inhibited starches prepared by the dual atomization/spray drying process described in U.S. 4.280.251 (which was used in Example 6) .
  • the conditions used for the oven dehydration and heat treatment were 8 hours at 140°C.
  • Control 100 1010 1080 340 170 84 T-I 360 950 970 860 650 33
  • results show that after 8 hours heat treatment at 140°C all the pregelatinized thermally- inhibited starches showed much less breakdown. The results also show that a higher degree of inhibition along with a higher peak viscosity can be obtained if the starch granules are completely disrupted as by drum drying or jet cooking.
  • EXAMPLE 11 This example shows that a granular starch can be dehydrated by ethanol extraction and that a better tasting starch is obtained.
  • a granular waxy maize starch was slurried in 1.5 parts water based on the weight of the starch and adjusted to pH 7 and 9.5 with 5% sodium carbonate, held for 30 minutes, filtered, and dried on a tray to a moisture content of about 5-6% moisture.
  • the starch having the pH of 5.3 was a native starch which was not pH adjusted.
  • the dried pH 5.3, pH 7.0, and pH 9.5 starches were each separated into two samples.
  • One sample was dried on trays in a forced draft oven at 80°C overnight to thermally dehydrate the starch to ⁇ l% (0%) moisture.
  • the other sample was placed in a Soxhlet extractor and allowed to reflux overnight (about 17 hours) with anhydrous ethanol (boiling point 78.32 ⁇ C).
  • the ethanol-extracted sample was placed on paper so that the excess alcohol could flash off which took about 30 minutes.
  • the ethanol-extracted starch was a free flowing powder which was dry to the touch.
  • the oven-dehydrated starches and ethanol-extracted starches were placed on trays in a forced draft oven and heated for 3, 5, and 7 hours at 160°C.
  • T-I starches The thermally-inhibited (T-I) starches and the controls were evaluated using the Brabender Procedure previously described was used. The results are shown below:
  • EXAMPLE 12 Granular tapioca, corn, and waxy rice starches and waxy rice flour were adjusted to pH 9.5, dehydrated in an oven and by extraction with ethanol, and heat treated at 160°C for the indicated time. They were evaluated for Brabender viscosity using the procedure previously described. The Brabender results are shown below. Viscosity (BUI).
  • Waxy Rice (PH 9.5 and 160°C1
  • EXAMPLE 13 This example compares ethanol extracted granular waxy maize starches and oven-dehydrated granular waxy maize starches heat treated in an oven for 5 and 7 hours at 160°C at the same pH, i.e., pH 8.03.
  • the thermally-inhibited starches were slurried at 6.6% solids (anhydrous basis), pH adjusted to 6.0-6.5, and then cooked out in a boiling water bath for 20 minutes. The resulting cooks were allowed to cool and then evaluated for viscosity, texture, and color.
  • Ethanol 7 hours mod. heavy non- mod. tan to heavy cohesive, smooth * Slightly darker than ethanol-dehydrated samples.
  • EXAMPLE 15 This example shows that thermal inhibition reduced the gelatinization temperature of the granular waxy maize starches.
  • the gelatinization temperature of an untreated waxy maize, a thermally-inhibited (T-I) waxy maize (pH adjusted and not pH adjusted) , and chemically-crosslinked (X-linked) waxy maize starches were determined by Differential Scanning Calorimetry.
  • the starches were thermally dehydrated and heat treated in an oven for the indicated time and temperature.
  • the results show that there was a significant reduction in peak gelatinization temperature of the thermally inhibited (T-I) starches.
  • the heat treatment reduced the enthalpy ( H) from 4.3 cal/g for the unmodified starch to 2.8 - 2.9 cal/g for the thermally- inhibited starch.
  • the chemically crosslinked (X-linked) starches are essentially identical to the unmodified waxy starch in peak temperature (72-74°C vs. 74°C) and enthalpy (4.2-4.4 vs 4.3 cal/g).
  • the reduced gelatinization temperature and decrease in enthalpy suggest that the overall granular structure has been altered by the dehydration and heat treatment.
  • EXAMPLE 16 This example shows that the thermal inhibition may begin as early as 110°C (230 ⁇ F) , that it is substantially noticeable at 160° (320°F) , and that the gelatinization is unchanged or reduced.
  • Granular waxy maize starches were pH adjusted to 7.0 and 9.5 and dehydrated and heat treated using air having a Dew point below 9.4°C (15°F) in the fluidized bed previously described at the indicated temperature and time. The Brabender and DSC results are shown below.
  • EXAMPLE 17 This example shows the correlation between the RVA pasting temperature and time and DSC peak gelatinization temperature and time and the reduction in Brabender viscosity breakdown for various granular starch bases and for granular waxy maize starches dehydrated by various methods including heating, ethanol extraction, and freeze drying.
  • the base starches were unmodified.
  • the starches were all adjusted to pH 9.5 before dehy-dration.
  • the ethanol-extracted and freeze-dried controls were pH adjusted and dehydrated but not heat treated.
  • the dehydrated starches were all heat treated in an oven at 160°C for the indicated time except for the starches chemically crosslinked with sodium trimetaphosphate (STMP) which were heat treated at 160°C for the indicated time in the fluidized bed previously described.
  • STMP sodium trimetaphosphate
  • EXAMPLE 19 A granular waxy maize starch which had been lightly crosslinked with 0.04% phosphorous oxychloride was thermally-inhibited. The granular starch was jet- cooked and spray-dried using the coupled continuous jet- cooking/spray-drying process and conditions described in Example 8. The spray-dried starch was oven dehydrated and heat treated for 8 hours at 140°C.
  • This example shows the thermal inhibition of converted starches.
  • Samples of waxy maize and tapioca starch were slurried in 1.5 parts water. The slurries were placed in a 52 * C water bath, with agitation, and allowed to equilibrate for one hour. Concentrated hydrochloric acid (HC1) was added at 0.8% on the weight of the samples. The samples were allowed to convert at 52°C for one hour. The pH was then adjusted to 5.5 with sodium carbonate, then to pH 8.5 with sodium hydroxide. The samples were recovered by filtering and air drying (approximately 11% moisture) . The starches in 50g amounts were placed in an aluminum tray, covered and placed into a forced draft oven at 140°C for 5.5 hours. The starches were evaluated for inhibition.
  • HC1 Concentrated hydrochloric acid
  • PO propylene oxide
  • Waxv Maize (7% PO and natural PH at 160°C1 Control — 1420 395 72 160 0 1030 380 63 34 37 46 45 47 48
  • EXAMPLE 21 A converted hydroxypropylated waxy maize starch (25 WF starch reacted with 2% propylene oxide) was adjusted to pH 9.5 and thermally inhibited using the fluidized bed previously described. Samples were taken at 110 ⁇ C, 125 ⁇ C, and l40 ⁇ C, all for 0 minutes.
  • the thermally-inhibited starch samples were cooked in tap water at 88-93'C (190-200'F) bath temperature for 30-60 minutes to yield solutions having a Brookfield viscosity of approximately 3000 cps. The viscosity stability at room temperature was evaluated. The control was a hydroxy-propylated waxy maize starch which was not thermally-inhibited. The results are tabulated below.
  • Waxy Maize (1% AC O and natural pH at 160 e C) Control — 1480 490 87 0 1170 560 — — 52
  • This example shows the preparation and use of a thermally-inhibited cationic starch in a simple papermaking system and a microparticle papermaking system.
  • a granular waxy corn starch 1000 g was slurried in 1500 cc water, 175 g of 4% sodium hydroxide were added, and the slurry was heated to 40°C.
  • One hundred (100) g of a 50% aqueous solution of 3-chloro-2- hydroxypropyl trimethyl ammonium chloride was added while maintaining the pH at 11.5 by adding 4% sodium hydroxide. The mixture was allowed to react overnight at 40°C.
  • the slurry was adjusted to pH 6.5 with hydrochloric acid, filtered, washed and air dried to about 8-15% moisture.
  • the degree of substition was of 0.04.
  • a portion of the above cationic starch derivative was chemically crosslinked with 0.01 wt. % of epichlorohydrin at 40°C for 16 hours, neutralized to pH 6.0, filtered, water washed (2 parts water per part of starch) , and air dried to about 8-15% moisture.
  • a portion of the above chemically-crosslinked, cationic starch was thermally inhibited by adjusting the pH to 9.5 with a 5% solution of sodium carbonate, spray- drying without gelatinization to between 3-15% moisture, and thermally dehydrating and heat treating the cationic, chemically-crosslinked granular starch in the fluidized bed previously described.
  • the starch samples Prior to addition to the papermaking furnish, the starch samples were slurried at 4-6% solids and cooked in a mini-jet cooker (scaled down jet cooker to simulate a commercial jet cooker) at a temperature of 105-122°C and an applied back pressure of 5-20 psi using controlled live steam.
  • the mini-jet cooker had a cooking chamber capacity or volume of 5.0 ml.
  • the starch was passed through the cooking chamber at a flow rate of about 130 ml/min with a retention time of about 2.3 seconds.
  • a standard papermaking furnish was prepared using a pulp stock which comprised an aqueous slurry of bleached hardwood kraft pulp (BHWK) and bleached softwood kraft pulp (BSWK) .
  • the pulp stock (80 wt. % BHWK and 20 wt. % BSWK) was refined in an aqueous solution to about 400 CSF (Canadian Standard Freeness) and a pH of 7.8-8.2.
  • the pulp stock contained precipitated calcium carbonate filler (30% by weight of fiber) with 8-10 wt. % fiber fines and 37-42 wt. % total fines.
  • T-I 160°C for 120 min.
  • the very lightly inhibited starch 120°C for 0 min. was better than the non-inhibited control in dry hand strength and drainage resistance and as good as the control in calcium carbonate retention.
  • the lightly inhibited starches 125 ⁇ C for 15 min. and 130°C for 0 min. were better than the non-thermally inhibited control in calcium carbonate retention, dry bond strength, drainage resistance.
  • the highly inhibited starches 160 ⁇ C were unsatisfactory in both calcium carbonate retention and dry bond strength. The samples of starches were tested for
  • T-I (160°C for 0 min.) 1900 T-I (160°C for 30 min.) ⁇ 60
  • thermally-inhibited starches are much lower in viscosity ( ⁇ 60 to 1900 cps) than the thermally-inhibited chemically crosslinked starch (3650 cps.). This is a significant advantage in papermaking since the pulp slurrier must be pumped.
  • a Brabender analysis run on the starch which thermally inhibited at 160°C for 120 minutes. It showed a percentage breakdown of 2%.
  • EXAMPLE 24 A cationic waxy maize starch was prepared using sufficient 3-chloro-2-hydroxypropyl trimethyl ammonium chloride to give about 0.30-0.36% bound nitrogen as quaternary ammonium groups.
  • the cationic starches were thermally inhibited in the fluidized bed previously described at the indicated temperature and time.
  • the thermally-inhibited cationic starches were cooked at 4% solids, a temperature of 104°C (220°F) , a pressure of 20 psi, and pump speed of 3.1 in the mini-jet cooker previously described.
  • the cooked starches were evaluated in two alkaline retention systems using a standard 80/20 hardwood:softwood bleached Kraft pulp (pH 7.8) with 30% calcium carbonate.
  • the microparticle system contained 5 lbs./ton alum, 15 lbs./ton starch, and 3 lbs./ton silica.
  • the polymer system contained 10 lbs./ton alum, 15 lbs./ton starch, and 1 lb./ton of a 33% emulsion of polyacrylamide (Nalco 625) as a retention aid.
  • a non- thermally inhibited cationic starch was used as the control. The results are shown below.
  • Control 31.1 100 49.1 100 T-I (130°C 59.1 120 for 0 min.) T-I (130 ⁇ C 43.7 150 54.8 112 for 15 min.)
  • T-I 140°C 41.1 132 57 116 for 0 min.
  • T-I 140 ⁇ C 24.1 77 42 86 for 15 min.
  • EXAMPLE 25 This example shows the use of thermally- inhibited cationic and amphoteric waxy maize starches in alkaline fine papers.
  • the cationic waxy maize starch was prepared as above.
  • amphoteric waxy maize starch was prepared by reacting a granular anionic waxy maize starch containing about 0.08-0.12% bound phosphate (provided by reaction with a sufficient amount of sodium tripolyphosphate) with a sufficient amount of 3-chloro-2- hydroxpropyl trimethyl ammonium chloride to give about 0.25-0.32% bound nitrogen.
  • the cationic and amphoteric starches were adjusted to pH 9.5 and dehydrated and heat treated in the fluidized bed previously described for the indicated time at the indicated temperature.
  • the thermally-inhibited starches were jet cooked as previously described and evaluated in the microparticle paper making system containing 5 lbs./ton alum, 15 lbs./ton starch, and 3 lbs./ton silica and in a polymer system containing 10 lbs./ton alum, 15 lbs./ton starch, and 1 lb./ton of an anionic polyacrylamide (Nalco 625) as a retention aid.
  • the calcium carbonate retention data for the cationic starches are shown below.
  • a non-thermally- inhibited cationic starch was used as the control.
  • the calcium carbonate retention data for the amphoteric starches are shown below. A non-thermally- inhibited amphoteric starch was used as the control.
  • Control 31.1 100 49.1 100 T-I (110 ⁇ C 34.6 Ill 42 86 for 15 min. )

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Abstract

On incorpore à un raffiné des amidons et des farines inhibés thermiquement, de préférence des amidons cationiques ou amphotères éventuellement chimiquement réticulés, et faisant principalement office d'additifs finaux humides. On inhibe l'amidon ou la farine en les déshydratant pour obtenir un produit anhydre ou déshydraté puis en traitant l'amidon ou la farine déshydraté(e) pendant une période et une température suffisantes pour inhiber l'amidon ou la farine et augmenter la stabilité de sa viscosité une fois dispersé(e) dans l'eau. La déshydratation peut être thermique ou non (exemple, par extraction à l'alcool ou lyophilisation). Le pH de l'amidon ou de la farine est, de préférence, de zéro ou plus avant la déshydratation.
EP96903665A 1995-01-24 1996-01-24 Papier contenant des amidons inhibes thermiquement Withdrawn EP0805898A1 (fr)

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US37771895A 1995-01-24 1995-01-24
US377718 1995-01-24
PCT/US1996/000999 WO1996023104A1 (fr) 1995-01-24 1996-01-24 Papier contenant des amidons inhibes thermiquement

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JP (1) JPH10505139A (fr)
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US6210475B1 (en) * 1999-09-03 2001-04-03 Bayer Corporation Use of hydroxyalkylated starches for improved emulsification of sizing agents
EP1103655A1 (fr) * 1999-11-25 2001-05-30 Coöperatieve Verkoop- en Productievereniging van Aardappelmeel en Derivaten 'AVEBE' B.A. Procédé de fabrication du papier
EP1176255A1 (fr) * 2000-07-24 2002-01-30 The Dow Chemical Company Utilisation de dispersions d'amidon comme liant dans des compositions pour couchage et procédé pour la préparation des dispersions d'amidon
EP1176254A1 (fr) 2000-07-24 2002-01-30 The Dow Chemical Company Utilisation de dispersions d'amidon reticulé dans la fabrication du papier
US20030173045A1 (en) * 2002-03-18 2003-09-18 Philip Confalone Liquid starch dispersions for coated paper and paperboard
FR2855840B1 (fr) * 2003-06-06 2006-09-01 Roquette Freres Composition a base d'amidon modifie, issu de legumineuses, destinee a l'ennoblissement du papier
CN1968968B (zh) 2004-06-16 2010-05-26 卡吉尔股份有限公司 阳离子交联蜡状淀粉制品及其制备方法和在纸制品中的用途
DE102007050839A1 (de) * 2007-10-24 2009-04-30 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Kohlehydratbasierende Additive mit Klebeeffekt für wässrige Feuer- und Brandsschutzmittel, deren Herstellung und Verwendung
CN102660893B (zh) * 2012-04-26 2014-12-24 金东纸业（江苏）股份有限公司 施胶液及其制备方法,应用该施胶液的涂布纸
JP6122108B2 (ja) * 2012-06-29 2017-04-26 アグラナ シュタルケ ゲゼルシャフト ミット ベシュレンクテル ハフツング 熱抑制されたデンプン及びデンプン粉
CN104452448A (zh) * 2013-09-12 2015-03-25 金东纸业（江苏）股份有限公司 淀粉表面施胶液生产工艺及淀粉表面施胶液
EA035369B1 (ru) 2014-06-02 2020-06-03 Эйнево Текнолоджиз, Ллс Модифицированный крахмал и способы его получения и использования
EP3380577A4 (fr) 2015-11-23 2019-04-17 Tethis, Inc. Particules revêtues et leurs procédés de production et d'utilisation
ES2850358T3 (es) * 2016-10-13 2021-08-27 Stichting Wageningen Res Almidones alimentarios modificados de manera no química
WO2018200460A1 (fr) * 2017-04-24 2018-11-01 Structured I, Llc Procédé de réduction de peluches de tissus et de serviettes
JP2023541114A (ja) 2020-09-14 2023-09-28 エコラボ ユーエスエー インコーポレイティド プラスチック由来の合成原料のための低温流動性添加剤
CN112812195A (zh) * 2021-01-19 2021-05-18 钟卫华 一种制备改性淀粉的复合工艺
CN113529478A (zh) * 2021-05-26 2021-10-22 冠宏化工（扬州）有限公司 一种改善纸张爆线的助剂及其应用
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CA2211372A1 (fr) 1996-08-01
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JPH10505139A (ja) 1998-05-19
AU4767496A (en) 1996-08-14
BR9607562A (pt) 1999-09-08

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