BACKGROUND OF THE INVENTION Carboxymethylcellulose (CMC) is one of the most versatile and widely used cellulose ethers as a component for aqueous systems. It may act as a suspending agent, thickening agent, protective colloid, humectant, and for the control of crystallization of some other components. CMC is physiologically inert and is an anionic polyelectrolyte. The above noted characteristics makes CMC suitable for use in a wide spectrum of applications in the food, pharmaceutical, personal care, paper, building materials and construction, oilfield, and other industries.

There are many types of commercial CMCs available varying with respect to average degree of polymerization and substitution. The chemical and physical properties of the CMCs depend not only on the average degree of polymerization and substitution, but also on the overall solubility of the CMC as well as the distribution of carbomethoxy substituents along the cellulose chains.

Both smoothly and blocky substituted CMCs are well known in the art. Blocky CMCs can be produced by lowering DS and/or changing the manufacturing process. However, processes that target a blocky CMC produce CMCs with limited solubility. In many cases a substantial portion of the CMC forms a swollen gel in aqueous applications. Such gels are undesirable in many applications, such as toothpaste, where the gel structure imparts an undesirable gel appearance in the toothpaste.

US Patent Re 32,976 discloses a smoothly substituted, enzyme and salt resistant CMC which is prepared using an etherification agent which comprises at least 50% isopropyl monochloroacetate. Smoothly substituted CMCs will not provide the associative properties of the current invention. The CMCs of the present invention are prepared from monochloroacetic acid or sodium chloroacetate, not isopropyl monochloroacetate.

US Patent No. 4,579, 943 discloses a CMC that has high liquid absorbing property that is derived from regenerated cellulose, having cellulose 11 form. The CMCs are of relatively low DS (0.1-0. 64) and are substantially insoluble in water.

The CMCs of the current invention are derived from cellulose 1, not cellulose 11 or regenerated cellulose.

Publication WO 99/20657 discloses a CMC that has a tan delta of less than 1.0 at a concentration of 0.5 % under specific testing conditions. The CMC of the current invention do not have a tan delta less than 1.0 at 0.5% concentration.

The publication by G. Mann, J. Kunze, F. Loth and H-P fink of Fraunhofer Institut fur Angewandte Polymerforschung entitled"Cellulose ethers with a Block- like Distribution of the Substituents by Structure-selective Derivatization of Cellulose", Polymer, vol. 39, No. 14, pp. 3155-3165, Published 1998, discloses the preparation and testing of block-like distribution of CMC. The CMC is prepared by a step-by-step etherification reaction where a systematic carboxymethylation in alcohol-water medium is conducted while maintaining a low NaOH concentration (NaOH/AGU molar ratio < 0.6). The alkali cellulose is formed at elevated temperatures (50-70° C). It is reported that this process produces block-like cellulose ethers, including CMC, or cellulose etheresters with alternating hydrophilic and hydrophobic as well as various ionic chain segments.

The CMCs are swollen particles in water and are not substantially soluble. The CMCs of the present invention are produced at higher NaOH/AGU ratios (about 1.1 to about 1.9) and low alkali cellulose temperatures (20-30° C), and are substantially soluble in water.

There is still a need for an associative, thixotropic CMC that exhibits associative behavior both in neat solutions and in filled systems. The association would be shear reversible, which would enhance utility. Such rheology would provide high thickening efficiency, and stabilize emulsions and suspensions, yet allow processing advantages such as ease of pumping or spreading, due to the reversible shear thinning characteristics of the associative network.

SUMMARY OF THE INVENTION The present invention is related to a composition comprising CMC having a relative urea/water ratio of less than about 0.9. The relative urea ratio is defined as: Relative Viscosity in 6M Urea = Dynamic Viscosity of 1 % CMC in 6M = Dynamic Viscosity of 1 % CMC in urea 6M urea 6M urea viscosity 1. 4 cP Relative Viscosity in Water = Dynamic Viscosity of 1% CMC in = Dynamic Viscosity of 1% CMC in Water 6M urea Water viscosity 0.89 cP Relative Urea/Water Ratio = Relative Viscosity in 6M Urea Relative Viscosity in Water This invention is also directed to a process for making a CMC comprising a) reacting in an aqueous slurry of isopropyl alcohol, a source of cellulose, and about 50-80% of the stoichiometric level of alkali for a sufficient time and at a sufficient temperature to form an alkali cellulose b) adding sufficient alkali to bring the total alkali concentration to stoichiometric levels, followed by addition of the requisite amount of etherification agent, c) completing the etherification reaction and optionally, d) adjusting final molecular weight/viscosity by addition of oxidizing agents capable of degrading cellulosic chains.

This invention also comprehends the use of the CMC of the present invention in an aqueous rheology modifier system as a vehicle component of a

personal care, household care, plaint, buitaingmateriat, construction pharmaceutical, oilfield, food, paper making or paper coating composition.

BRIEF DESCRIPITION OF DRAWINGS Figure 1 shows a graph of toothpaste viscosity over time.

Figure 2 shows a graph of toothpaste viscosity overtime that has been normalized.

Figure 3 shows a graph of toothpaste structure over time.

Figure 4 shows a graph of toothpaste structure over time that has been normalized.

Figure 5 shows a graph of crushing strengths of blends of polymers.

Figure 6 shows a graph of percent drug dissolved over time.

Figure 7 shows a graph of percent drug dissolved over time.

DETAILED DESCRIPTION OF THE INVENTION A CMC has been surprisingly discovered that exhibits unique and highly desirable rheology and performance properties in end use systems.

In accordance with the present invention, the viscosity builds up not only by means conventional to CMC, but also is boosted significantly by molecular association. The association leads to network formation and gel-like rheological properties. The fact that the association is shear reversible enhances utility.

The CMCs of the present invention have been shown to lower the CMC use level needed and to provide rheology attributes unique from other CMCs available today. The unique rheology provides high thickening efficiency, and stabilizes emulsions and suspensions. The CMCs of the present invention provide significantly enhanced performance over known CMCs in aqueous systems including personal care formulations (e. g. , toothpaste, skin care, and hair care), medical care (e. g. , wound care and ostomy, ), food applications (i. e., tortillas, cake mixes, bread mixes, bread, ice cream, sour cream, pasteurized processed cheese spreads, and cheese foods), beverages (i. e. , instant cold/hot

drinks, ready to drink beverages, and fruit flavored drinks), paint systems, building and construction materials (such as joint formulations), mineral processing, oil field formulations (e. g., drilling fluids), paper making and paper coating formulations, household formulations (e. g., laundry detergents, fabric softeners), and pharmaceutical formulations.

In accordance with the present invention, when the composition is a personal care composition, it includes (a) from about 0.1 % to about 99.0 % by weight of the vehicle component and (b) at least one active personal care ingredient. Examples of the at least one active personal care ingredient are deodorant, skin coolants, emollients, antiperspirant actives, moisturizing agents, cleansing agents, sunscreen actives, hair treatment agents, oral care agents, tissue paper products, and beauty aids.

In accordance with the present invention, the composition is a household care composition, it includes (a) from about 0.1 % to about 99.0 % by weight of the vehicle component and (b) at least one active household care ingredient.

Examples of the at least one active household care ingredient are industrial grade bar, gel and liquid soap actives, all purpose cleaning agents, disinfecting ingredient, rug and upholstery cleaning actives, laundry softeners actives, laundry detergent ingredients, dishwashing detergents, toilet bowl cleaning agents and fabric sizing agents.

In addition to the ingredients conventionally used in the personal care and household care, the composition according to the present invention can optionally also include ingredients such as a colorant, preservative, antioxidant, nutritional supplements, activity enhancer, emulsifiers, viscosifying agents (such as salts, i. e., NaCI, NH4CI & KCI, water-soluble polymers, i. e., hydroxyethylcellulose, and fatty alcohols, i. e., cetyl alcohol), alcohols having 1-6 carbons, and fats and oils.

The CMCs may also be used in combination with other known rheology modifiers including, but not limited to, polysaccharides (e. g. , carrageenan, guar, hyaluronic acid, glucosaminoglycan, hydroxyethyl cellulose, hydrophobically

modified hydroxyethyl cellulose, ethyl hydmxyenyl cenmose, nydroxypropyl methylcellulose, hydroxyethyl methylcellulose, methylcellulose, cationic guar, carbomer), biopolymers (e. g. , xanthan), synthetic polymers (polyethylene glycol, polyvinylacetate, chlorohexidiene), and thickening silicas.

The use of CMC in toothpaste formulations is well known in the toothpaste industry as a binder system for toothpaste that gives the toothpaste a desirable high structure. The binder system includes CMC types with other polysaccharides, inorganic salts, cheating agents and combinations thereof.

Commercially available CMC types vary in the degree of structure they provide to the toothpaste. Highly thixotropic grades of CMC tend to render toothpaste of higher structure. These thixotropic CMC types also tend to contribute to greater post-thickening.

Cellulose gum (CMC) alone has been a traditional binder for toothpaste.

In toothpaste, CMC provides viscosity, stand-up or structure, and syneresis control. Toothpaste made with CMC is also known to have a slow rate in viscosity build up over the shelf life of the toothpaste thus not reaching a stable viscosity until after first 30 days or more. This is also called"post-thickening".

Other binders commonly used in toothpaste are carrageenan or carrageenan and xanthan together. Carrageenan and xanthan provide good stand-up, viscosity and syneresis control ; however, they tend to be more expensive alternatives as compared to CMC. Toothpaste made with carrageenan and xanthan tend to exhibit a stable viscosity rather quickly after processing and little post-thickening.

In accordance with the present invention, the CMC of the present invention can be use either alone or in combination with other polysaccharides, synthetic polymers and or salts and provide high efficiencies and enhanced performance. See the toothpaste Examples hereinafter for the demonstration of the unexpected results of the present invention.

Use of the CMCs of the present invention have allowed a use level reduction of about 40% while maintaining critical toothpaste properties such as stand-up, gloss and syneresis control. The lower use levels and/or shear thinning behavior of the CMCs may offer additional advantages to toothpaste properties such as improved flavor release, improved actives delivery, improved fluoride delivery, higher gloss, improved extrudability from the tube, and improved anti-microbial effectiveness. Potential improvements to the toothpaste manufacturing process include, but are not limited to, reduction of entrapped air during manufacturing process, improvements in mixing operations, and improvements in extrusion into tubes.

Water-based protective coating compositions (commonly referred to as paints) in which cellulose ether derivatives are conventionally used include latex paints or dispersion paints, of which the principal ingredients are film-forming lattices such as styrenebutadiene copolymers, vinyl acetate polymers and copolymers, and acrylic polymers and copolymers. Typically, they also contain opacifying pigments, dispersing agents and water-soluble protective colloids, the proportions being, by weight of the total composition, about 10 parts to about 50 parts of a latex, about 10 parts to about 50 parts of an opacifying pigment, about 0.1 part to about 2 parts of a dispersing agent, and about 0.1 part to about 2 parts of a water-soluble protective colloid.

Water soluble protective colloids conventionally used in the manufacture of latex paints (to stabilize the lattices and maintain the wet edge of a painted area longer in use) include casein, methyl cellulose, hydroxyethylcellulose (HEC), sodium carboxymethyl cellulose (CMC), polyvinyl alcohol, starch, and sodium polyacrylate. The disadvantages of the natural based cellulose ethers are that they may be susceptible to biological degradation and frequently impart poor flow and leveling properties, while the synthetic materials such as polyvinyl alcohol often lack enough thickening efficiency to maintain sag resistance. The thickening efficiency of the cellulose ethers is usually improved by increasing their molecular weight which normally is more expensive.

In accordance with the present inventi tSCMC ; PäFX preGM invention can be used in lower amounts in paints and provide unexpected high quality results. This is illustrated in the working Examples hereinafter.

The CMCs of the present invention are prepared using conventional slurry process methods. For example, isopropyl alcohol, water, and about 50-80% of the stoichiometric amount of NaOH are reacted with cellulose at a temperature of about 20°C for a sufficient time to produce alkali cellulose, about 1.5 hours.

Sufficient NaOH is added to bring the total NaOH level to or slightly above stoichiometric levels and monochloroacetic acid is added shortly after the second NaOH addition. The reaction conditions are normally to raise the temperature to about 70°C for about one to two hours to effect etherification.

The molecular weight and viscosity of the CMC can be adjusted (reduced) by addition of an oxidizing agent, such as hydrogen peroxide, subsequent to etherification. The reaction mass is then optionally cooled, excess base neutralized, if necessary, and the product is washed. This product can then be dried and ground. The critical feature of this invention is that the amount of alkali utilized to effect etherification is less than stoichiometric and that the remaining alkali is added just prior to the etherification agent. The degree of substitution of the CMC is about 0.6 to about 1.2.

In accordance with the present invention, the CMC can be differentiated from prior art CMCs by their being substantially soluble in aqueous media environments and their behavior in environments that do not favor association. It is a known fact that urea breaks up association by breaking hydrogen bonds.

The subject CMCs exhibit a viscosity decrease in the presence of urea, as determined by the relative urea ratio. The relative urea ratio is defined as: Relative Viscosity in 6M Urea = Dynamic Viscosity of 1 % CMC in 6M = Dynamic Viscosity of 1 % CMC in urea 6M urea 6M urea viscosity 1. 4 cP Relative Viscosity in Water = Dynamic Viscosity of 1 % CMC in = Dynamic Viscosity of 1 % CMC in Water 6M urea Water viscosity 0.89 cP Relative Urea/Water Ratio = Relative Viscosity in 6M Urea Relative Viscosity in Water

EXAMPLES The following examples are merely set forth for illustrative purposes, but it is to be understood that other modifications of the present invention within the skill of an artisan in the related industry can be made without departing from the spirit and scope of the invention. All percentages and parts are by weight unless specifically stated otherwise.

Example 1 Isopropyl alcohol (IPA, 696. 67g) and deionized (DI) water (76. 945g) were charged into a jacketed resin kettle reactor equipped with an air driven stirrer, stainless steel agitator, a pressure equalizing addition funnel, a reflux condenser, vacuum, nitrogen inlet and a thermocouple. A cellulose pulp (65. 0g, 6.4% moisture) was added to the reactor, the reactor was sealed, and the agitator was adjusted to obtain good mixing. The reactor was inerted and the mixture was cooled to 20°C.

Aqueous NaOH (50%, 60.92g) was slowly added to the reactor through the addition funnel, maintaining the mixture slurry temperature at 20°C. The reaction mixture was held for 1 hour at 20°C after the caustic addition was completed.

Aqueous NaOH (50%, 16. 02g) was slowly added to the reactor through the addition funnel, maintaining the mixture slurry temperature at 20°C. The reaction mixture was held for 5 minutes at 20°C after the caustic addition was completed. Monochloroacetic acid (MCA, 42. 91g) was added to the reactor through an open reactor port, maintaining a reactor slurry temperature of 20°C.

After MCA addition was completed, the reaction slurry was heated to 70°C and held for 1.5 hours. The reaction slurry was filtered and the resulting wet cake was washed three times with 565g of 80% aqueous methanol and one time with 1 OOOg of pure methanol. The resulting wet cake was broken into small particles and dried in a fluidized bed dryer for 35 minutes. (Air-dry for 5 minutes, heat-dry at 50°C for 10 minutes, and heat-dry at 70°C for an additional 20 minutes. ) The

product was ground in Retsch Grinding Mill musing a 1 mm screen. Degree of Substitution (DS) = 0.89 Example 2 Isopropyl alcohol (IPA, 696.67g) and deionized (DI) water (76.945g) were charged into a jacketed resin kettle reactor equipped with an air driven stirrer, stainless steel agitator, a pressure equalizing addition funnel, a reflux condenser, vacuum, nitrogen inlet and a thermocouple. A cellulose pulp (65. 0g, 6.4% moisture) was added to the reactor, the reactor was sealed, and the agitator was adjusted to obtain good mixing. The reactor was inerted and the mixture was cooled to 20°C.

Aqueous NaOH (50%, 60. 92g) was slowly added to the reactor through the addition funnel, maintaining the mixture slurry temperature at 20°C. The reaction mixture was held for 1 hour at 20°C after the caustic addition was completed.

Aqueous NaOH (50%, 16. 02g) was slowly added to the reactor through the addition funnel, maintaining the mixture slurry temperature at 20°C. The reaction mixture was held for 5 minutes at 20°C after the caustic addition was completed. Monochloroacetic acid (MCA, 42.91 g) was added to the reactor through an open reactor port, maintaining a reactor slurry temperature of 20°C.

After MCA addition was completed, the reaction slurry was heated to 70°C and held for 1.5 hours. 1.6 ml of 6% H202 was added to the reactor and the slurry was heated at 70°C for 30 minutes. The reaction slurry was filtered and the resulting wet cake was washed three times with 565g of 80% aqueous methanol and one time with 1000g of pure methanol. The resulting wet cake was broken into small particles and dried in a fluidized bed dryer for 35 minutes. (Air-dry for 5 minutes, heat-dry at 50°C for 10 minutes, and heat-dry at 70°C for an additional 20 minutes. ) The product was ground in Retsch Grinding Mill using a 1 mm screen. Degree of Substitution (DS) = 0.87.

Example 3 Isopropyl alcohol (IPA, 123.4 gallons), water (130. 3 bs), methanol (6.36 gallons), and NaOH (flake, 35.4 Ibs.) were charged into the reactor. The reactor was inerted and the caustic/solvent mix was cooled to about 20°C, at which time a cellulose pulp (1 081bs, 4% moisture) was added to the reactor. The agitation was adjusted to give good mixing in the slurry and the slurry was recooled to about 20°C. The reaction slurry was held for 1 hour at 20°C.

Aqueous NaOH (50%, 58. 7 Ibs.) was added to the reactor and the reaction mixture was held for 15 minutes at 20°C after the caustic addition was completed. Monochloroacetic acid (MCA, 70.5 Ibs.). IPA (9.0 gallons), dichloroacetic acid (DCA, 926. 8g) and acetic acid (79. 9g) were added to the reactor, maintaining a reactor slurry temperature of 20°C. After MCA addition was completed, the reaction slurry was heated to 70°C and held for 1 hour. 282g of 18% H202 was added to the reactor and the slurry was heated at 70°C for 60 minutes.

The reaction slurry was centrifuged and the wet cake was washed with three times with 300 gallons of 80% methanol and two times with 300 gallons 100% methanol. The material was dried in an Abbe dryer under vacuum at 80- 90°C to a moisture content of 4-6 %. The product was ground in a micropulverizer through a 0.0278 inch screen. Degree of Substitution (DS) = 0.79.

Example 4 The conditions of Example 3 were repeated. DS = 0.78 Example 5 Isopropyl alcohol (IPA, 121.9 gallons), water (130.0 Ibs), methanol (6.29 gallons), and NaOH (flake 45.6 Ibs.) were charged into the reactor. The reactor was inerted and the caustic/solvent mix was cooled to about 20°C, at which time a cellulose pulp (1081bs, 4% moisture) was added to the reactor. The agitation was adjusted to give good mixing in the slurry and the slurry was recooled to about 20°C. The reaction slurry was held for 1 hour at 20°C.

Aqueous NaOH (50%, 58. 7 bs. was aaaea to the reactor and the reaction mixture was held for 15 minutes at 20°C after the caustic addition was completed. Monochloroacetic acid (MCA, 81. 0 lbs.). IPA (9. 0 gallons), dichloroacetic acid (DCA, 1065. 9g) and acetic acid (91.9g) were added to the reactor, maintaining a reactor slurry temperature of 20°C. After MCA addition was completed, the reaction slurry was heated to 70°C and held for 1 hour.

188g of 18% H202 was added to the reactor and the slurry was heated at 70°C for 60 minutes.

The reaction slurry was centrifuged and the wet cake was washed with three times with 300 gallons of 80% methanol and two times with 300 gallons 100% methanol. The material was dried in an Abbe dryer under vacuum at 80- 90°C to a moisture content of 4-6 %. The product was ground in a micropulverizer through a 0.0278 inch screen. Degree of Substitution (DS) = 0.86.

Example 6 The conditions of Example 5 were repeated. DS = 0. 86 Example 7 Isopropyl alcohol (IPA, 121.1 gallons), water (146.0 Ibs), methanol (6.24 gallons), and NaOH (flake, 35. 4 lbs.) were charged into the reactor. The reactor was inerted and the caustic/solvent mix was cooled to about 20°C, at which time a cellulose pulp (1 081bs, 4% moisture) was added to the reactor. The agitation was adjusted to give good mixing in the slurry and the slurry was recooled to about 20°C. The reaction slurry was held for 1 hour at 20°C.

Aqueous NaOH (50%, 58.7 Ibs.) was added to the reactor and the reaction mixture was held for 15 minutes at 20°C after the caustic addition was completed. Monochloroacetic acid (MCA, 70.5 Ibs.). 4PA (9. 0 gallons), dichloroacetic acid (DCA, 926. 8g) and acetic acid (79. 9g) were added to the reactor, maintaining a reactor slurry temperature of 20°C. After MCA addition was completed, the reaction slurry was heated to 70°C and held for 1 hour. 282g

of 18% H202 was added to the reactor and the slurry was heated at 70°C for 60 minutes.

The reaction slurry was centrifuged and the wet cake was washed with three times with 300 gallons of 80% methanol and two times with 300 gallons 100% methanol. The material was dried in an Abbe dryer under vacuum at 80- 90°C to a moisture content of 4-6%. The product was ground in a micropulverizer through a 0.0278 inch screen. Degree of Substitution (DS) = 0.79.

Example 8 Isopropyl alcohol (IPA, 14 kg), water (2184g), methanol (728.8g), were charged into the reactor. The reactor was inerted and the solvent mix was cooled to about 20°C, at which time a cellulose pulp (1800 g, 3.6% moisture) was added to the reactor. The agitation was adjusted to give good mixing in the slurry, the slurry was recooled to about 20°C, and NaOH (flake, 691.4g) was added to the reactor. The reaction slurry was held for 1 hour at 20°C.

Aqueous NaOH (50%, 353. 6g) was added to the reactor and the reaction mixture was held for 15 minutes at 20°C after the caustic addition was completed. Monochloroacetic acid (MCA, 939.8g). IPA (977g), dichloroacetic acid (DCA, 27.3g) and acetic acid (2.4g) were added to the reactor, maintaining a reactor slurry temperature of 20°C. After MCA addition was completed, the reaction slurry was heated to 70°C and held for 1 hour.

The reaction slurry was filtered, and the resulting wet cake was washed three times with 12 gallons of 80% aqueous methanol, and one time with 12 gallons of 95% methanol. The material was dried in a vacuum tray dryer at 70°C to a final moisture content of 4-6%. The dried product was ground in a micropulverizer through a 0.0278 inch screen. Degree of Substitution = 0.73.

Example 9 Isopropyl alcohol (IPA, 696.67g) and deionized (DI) water (76.95g) were charged into a jacketed resin kettle reactor equipped with an air driven stirrer,

stainless steel agitator, a pressure equalizing addition tunnel, a reflux condenser, vacuum, nitrogen inlet and a thermocouple. A cellulose pulp (65. 0g, 6.8% moisture) was added to the reactor, the reactor was sealed, and the agitator was adjusted to obtain good mixing. The reactor was inerted and the mixture was cooled to 20°C.

Aqueous NaOH (50%, 60.92g) was slowly added to the reactor through the addition funnel, maintaining the mixture slurry temperature at 20°C. The reaction mixture was held for 1 hour at 20°C after the caustic addition was completed.

Aqueous NaOH (50%, 36.37g) was slowly added to the reactor through the addition funnel, maintaining the mixture slurry temperature at 20°C. The reaction mixture was held for 5 minutes at 20°C after the caustic addition was completed. Monochloroacetic acid (MCA, 42. 91g) was added to the reactor through an open reactor port, maintaining a reactor slurry temperature of 20°C.

After MCA addition was completed, the reaction slurry was heated to 70°C and held for 1.5 hours. 1.6 ml of 6% H202 was added to the reactor and the slurry was heated at 70°C for 30 minutes. The reaction slurry was filtered and the resulting wet cake was washed three times with 565g of 80% aqueous methanol and one time with 1000g of pure methanol. The resulting wet cake was broken into small particles and dried in a fluidized bed dryer for 35 minutes. (Air-dry for 5 minutes, heat-dry at 50°C for 10 minutes, and heat-dry at 70°C for an additional 20 minutes. ) The product was ground in Retsch Grinding Mill using a 1 mm screen. Degree of Substitution (DS) = 0.62. 1 % aqueous viscosity = 2200 cps.

Example 10 lsopropyl alcohol (IPA, 713.86g) and deionized (Di) water (73. 79g) were charged into a jacketed resin kettle reactor equipped with an air driven stirrer, stainless steel agitator, a pressure equalizing addition funnel, a reflux condenser, vacuum, nitrogen inlet and a thermocouple. A cellulose pulp (65. 0g, 3. 7% moisture) was added to the reactor, the reactor was sealed, and the agitator was

adjusted to obtain good mixing. The reactor was tnerteo ana tne mixture was cooled to 20°C.

Aqueous NaOH (50%, 39.98g) was slowly added to the reactor through the addition funnel, maintaining the mixture slurry temperature at 20°C. The reaction mixture was held for 1 hour at 20°C after the caustic addition was completed.

Aqueous NaOH (50%, 35.77g) was slowly added to the reactor through the addition funnel, maintaining the mixture slurry temperature at 20°C. The reaction mixture was held for 5 minutes at 20°C after the caustic addition was completed. Monochloroacetic acid (MCA, 42.25g) was added to the reactor through an open reactor port, maintaining a reactor slurry temperature of 20°C.

After MCA addition was completed, the reaction slurry was heated to 70°C and held for 1.5 hours. The reaction slurry was filtered and the resulting wet cake was washed three times with 565g of 80% aqueous methanol and one time with 1000g of pure methanol. The resulting wet cake was broken into small particles and dried in a fluidized bed dryer for 35 minutes. (Air-dry for 5 minutes, heat-dry at 50°C for 10 minutes, and heat-dry at 70°C for an additional 20 minutes. ) The product was ground in Retsch Grinding Mill using a 1 mm screen. Degree of Substitution (DS) = 0.84. 1% aqueous viscosity = 3760 cps.

Example 11 This Example illustrates the behavior of the preparations of a 1.0% CMC samples of the present invention in a 6.0 M urea solution.

The 1 % CMC solution was prepared in the following equipment: Caframo RZR1 overhead stirrer, 8-oz. glass jars, stainless steel stirring shaft with two 3-blade propellers (1.5 inch diameter), Parafilm@, deionized (DI) water, Germaben II.

A 0.50% Germaben solution was prepared by adding the Germaben II to DI water. This solution was then weighed into an 8-oz. glass jar. The solution was then stirred with an overhead stirrer, while the CMC was quickly added to

the solution. The CMC level is 1.0% of me final sample weight. CMC weight is corrected for moisture content. As the viscosity begins to increase, the speed of the stirrer was increased to the maximum rate that does not cause splashing out of the sample. The jar is covered with Parafilm while mixing to prevent evaporation of water and loss from splashing. The sample is stirred for one hour. After one hour of stirring at the highest rate, the stirring speed was decreased to a setting of 4 for one additional hour. The sample was centrifuged for approximately 5 minutes to remove trapped air.

The behavior of the samples were studied in the following equipment: Caframo RZR1 overhead stirrer, 8-oz. glass jars, stainless steel stirring shaft with two 3-blade propeller (1"diameter), Parafilm@, 6. 0M Urea (180. 18g urea diluted to 500ml) Procedure : 6. 0M urea solution was weighed into an 8-oz. glass jar. The solution was stirred with an overhead Caframo RZR1 stirrer, as the CMC was quickly added to the solution. The CMC level was 1.0% of the final sample weight. CMC weight was corrected for moisture content. As the viscosity begins to increase, the speed of the stirrer was increased to the maximum rate that does not cause splashing out of the sample. The jar was covered with Parafilm while mixing to prevent evaporation of water and loss from splashing. The sample was stirred for one hour. After one hour of stirring at the highest rate, the stirring speed was decreased to a setting of 4 for one additional hour. The sample was centrifuged for approximately 5 minutes to remove trapped air.

Table"1 1% 1% Dynamic Dynamic Water 6M Urea Relative CMC DS viscosity viscosity U/W ratio Example 8 0.73 1113 1364 0.78 Example 1 0.89 574 632 0.70 Example 2 0.87 238 288 0.77 Example 7 0. 79 762 539 0.45 Example 5 0.86 265 338 0.81 Example 3 0.79 286 355 0.79 Example 4 0.78 346 398 0.73 Example 6 0. 86 163 228 0.89 Aqualon 7LF 0.81 11 16 0. 97 Aqualon 7LF 11 17 0. 96 Aqualon 7L 0. 79 9 14 0. 97 Aqualon 7H3SF 0.97 7191 12754 1.13 Aqualon 7H3SF 0.92 2286 4179 1.16 Aqualon 7H3SF 0.88 7337 13258 1. 15 Aqualon 7H3XSF 0.89 3262 5909 1.15 Aqualon 7H3SXF 3111 4950 1.01 Aqualon 7HF 0.86 7023 11648 1.05 Aqualon 7H4F 0. 77 4875 8576 1.12 Aqualon 7M8SF 68 111 1.03 Aqualon 9M31F 0.9 260 467 1. 14 Aqualon 9M31F 0.92 577 1065 1.17 Aqualon 9M31F 0.9 539 823 0.97 Aqualon 9M31XF 282 470 1.06 Amtex 168 282 1.07 Antisol FL 300000 2852 8510 1.90 Aqualon Aquapac 7795 12583 1.03 Aqualon Aquapac 11446 19881 1.10 DKS Cellogen HE-90 100 179 1.14 DKS Cellogen HP-5HS 4417 8154 1.17 Fine Gum SA-H 463 1016 1.40 Monpac Regular 2755 5980 1.38 Novant Cekol 500T 47 68 0. 92 Novant Cekol 700 53 96 1. 16 Noviant Cekol 2000 139 246 1. 13 PAC-R 7335 11798 1.02 Tylopur C1000 P2 316 558 1.12 Walocel CRT 2000 180 285 1. 01

The flavor was mixed in the same way. Hrrer au rormuiawcornponents were together, the mixture was mixed under vacuum for 15 minutes at high speed.

The batch was then packed into 2-oz. jars and 6-oz. toothpaste tubes.

Toothpaste samples were stored for 30 days at room temperature.

Samples were equilibrated in a 25°C water bath for 4 hours prior to any tests conducted.

Viscosity was measured using a Brookfield DV-I fitted with a T-bar style spindle. A helipath stand was used to allow the spindle to sweep downward through the sample to prevent the effects of shear. Viscosity was taken every 30 seconds over 2 minutes and values were averaged.

Toothpaste consistency was measured using a rack test. The rack designed with cross bars of increasing distance apart left to right. The toothpaste tube containing the sample to be measured is fitted with a stainless orifice fitting to eliminate differences in orifice size that may occur. The tube is squeezed in a uniform manner across the rack, extruding the paste onto the rack in a ribbon. After 15 seconds it is recorded at which opening the ribbon has fallen through the opening and broken. The opening number from left to right is the value recorded as a"Cuban"value.

The toothpaste data are summarized in Table 2.

Table 2 30 day Toothpaste Polymer Viscosity Cuban Comments Example 2 137500 5 Example 1 188125 10 Example 3 146750 6 Example 4 136250 6 Example 5 120000 5 Example 6 94500 3 Example 7 125750 5 Cekol 500T 61875 2 severe Cekol 2000 25875 0 syneresis 9M31 XFGL 40125 0 syneresis 9M31 F 32500 0 syneresis

Example 14 The CMC's of the present invention in combination with other polymers exhibit decreased post thickening and structure build and enhanced initial structure in toothpaste formulations.

Viscosity is one measure of post-thickening in toothpaste. Toothpaste samples were packed into vials and the viscosity was measured using a Brookfield DV-I fitted with a T-bar style spindle. A helipath stand was used to allow the spindle to sweep downward through the sample to prevent the effects of shear. Viscosity was taken every 30 seconds over 2 minutes and values were averaged It can be seen from the data in the graph (Figure 1) that most samples exhibited a change in viscosity from the first day after processing through 30 days. When the data are normalized to the initial viscosity as 100%, the change over time is more apparent (Figure 2). Toothpaste made with combinations of Example 7 CMC with other polysaccharides or inorganic salts exhibited lower post-thickening compared to toothpaste made with Example 7 alone.

Toothpaste structure is also an important aspect. This property may be measured by force required for compression using a MTS Servo Hydraulic test system from MTS Systems Corporation, Minneapolis, MN. The instrument was fitted with a half-inch acrylic cylinder probe, toothpaste samples were packed into vials after processing and measured directly without disturbance.

It can be seen below in Table 3 that the Example 7 CMC alone or with other polysaccharides or inorganic salt produced toothpaste of similar or greater initial structure compared to toothpaste made with carrageenan and xanthan and much greater initial structure than toothpaste made with commercial CMC 9M31 F.

Peak force of compression was monitored over 30 days. It was found that most samples changed in values (Figure 3). The comparison can be made more

Example 122 Dynamic viscosities were measured using at 25°C using an RFS III strained controlled rheometer by Rheometrics using a 40 mm parallel tool geometry with the gap set at 2 mm. The samples were pre-sheared at 100s-'for 60 second upon loading to erase the loading history. The pre-shearing was followed by the steady shear experiment between 0.01 and 100s-1. Each point data is the average of clockwise and counter-clockwise rotations each with the duration of 20 sec. All samples exhibited a low shear Newtonian plateau, the average of which was used in the data analysis and further comparisons. The dynamic viscosities of the aqueous and 6M 1 % CMC solutions are summarized in Table 1. The relative urea/water ratios are also summarized in Table 1, above.

Example 13 The CMC's of the present invention exhibit enhanced thickening capabilities and syneresis control in toothpaste formulations. Calcium Carbonate Based Toothpaste formulation: Ingredient : wt. % Calcium carbonate 45.00 Sorb sorbitol (70% solids) 27.00 Distilled water 23.97 CMC Polymer (Table 2) 0.60 Sodium lauryl sulfate, 100% active powder 1.00 Sodium monofluorophosphate 0.76 Sodium benzoate 0.50 Flavor 0.55 Tetra sodium pyrophosphate 0.42 Sodium saccharin 0.20 100. 00 Standard laboratory toothpaste preparation was performed. Salts were first dissolved in part of the water and warmed for complete dissolution. The CMC was dispersed in the sorbitol, using an overhead mixer with a propeller attachment. After the CMC was well dispersed, the balance of the water was added with continued mixing until the CMC appeared dissolved. The warm salt solution was mixed into the CMC solution. This was then transferred to a 1-quart Ross double planetary mixer. The calcium carbonate was then stirred in the mixer, and after it was well dispersed, a vacuum was applied. After mixing under vacuum for 20 minutes, the sodium lauryl sulfate was mixed in without vacuum.

easily if the data are normalized to the initial structure value as 100% as shown in Figure 4. From the normalized data of Figure 4, it can be seen that toothpaste samples made with combinations of CMC of Example 7 with other polysaccharides or inorganic salt have lower structure build over time.

From the work outlined here, it can be concluded that toothpaste with high structure and low post-thickening can be made with CMCs of the present invention in combination with other polysaccharides, inorganic salts or combinations thereof.

The toothpaste formulation used in this Example was as follows : Ingredient Wt. % Sorbitol (Sorbo) 29.2 Glycerine 6 PEG 400 3 Sident 9 14 Sident 22S 16 Sodium Saccharine 0. 20 Sodium Monofluorophosphate 0.23 Sodium Benzoate 0. 20 Sodium Lauryl Sulfate 1. 20 Flavor 0. 50 Water q.s.

The different polymers used in this Example in the formulation was as follows : Formulation Polymer : wt% Polymer : wt% 1Carrageenan (THP1) 0.7 Xanthan (Rhodicare) 0.3 2 CMC Example 7 1. 0 N/A 3 CMC 9M31 F 1. 0 N/A 4CMC Example 7 0. 5 Natrosol + 330, 0. 3 5 CMC Example 7 0. 6 Natrosol 250 M 0. 6 6 CMC Example 7 0. 7 Carrageenan 0. 3 7 CMC Example 7 1. 0 Sodium Silicate 0. 5 8 CMC Example 7 0. 7 Xanthan 0 3

Table"3- Initial Toothpaste Structure Peak Force Compression from MTS Peak Force Polymer Compressitg Carageenan/Xanthan 56. 5 Example 7 51. 1 Example 7 HMHEC 78.1 Exampie 7/Na2SiO3 60. 8 Example 7 HEC 75. 1 Example 7/Carrageenan 75.3 Example 7/Xanthan 35. 0 CMC 9M31 F 14. 7

Toothpaste after 24 hours, ambient temperature.

The identity and supplier of the ingredients of this Example are as follows : Sorbitol Sorbo, 70%, USP/FCC, SPI Pharma, New Castle, DE, USA Glycerine Glycerin, USP, Spectrum Chemical, Gardena, CA, USA PEG 400 Polyethylene Glycol NF, Dow Chemical, Midland, MI, USA Silica, thickening Sident 9, Degussa, Frankfurt, Germany Silica, abrasive Sident 22S, Degussa, Franfurt, Germany Sodium Lauryl Sulfate Stepan, Northfield, IL, USA Flavor Fresh Mint, Givaudan, UK Sodium Silicate, crystalline JT Baker, reagent grade Sodium Benzoate Fisher Scientific, reagent grade Saccharine Sigma, reagent grade Sodium Fluorophosphate Alfa Aesar, Ward Hill, ME, USA Carrageenan THP1, CP Kelco, San Diego, CA, USA Xanthan Rhodicare S, Rhodia, Cranbury NJ, USA CMC 9M31 F Aqualon HM HEC Natrosol Plus 330 CS Aqualon HEC Natrosol 250 M Pharm Aqualon

Example 15 The CMC's of the present invention exhibit enhanced thickening capabilities in beverage formulations.

Beverage Example Orange Beverage-Reference Ingredients Wt % Orange Juice concentrate, 45 Brix 7.00 Sugar 40.00 Citric acid 0.05 Sodium benzoate 0.55 Water 52.14 Cellulose Gum, CMC-9M31 F 0.60

Orange Beverage-Test Example Ingredients Wt % Orange Juice concentrate, 45 Brix 7.00 Sugar 40.00 Citric acid 0.05 Sodium benzoate 0.55 Water 52.14 Polymer Example 7 0.42 Mix cellulose gum or polymer into water, allow to mix for 20 minutes.

Premix acid, preservative and sugar, add and mix 5 minutes. Add juice concentrate, mix 3 minutes.

Beverage results : Reference Test Example Viscosity, 24 hours, cps 53.0 51.0 Brookfield LV, spindle 2,30 rpm, 20s Example 16 The CMC's of the present invention exhibit enhanced thickening capabilities in food formulations.

Cake Mix and Cake Example CAKE MIX-Reference ingredients for Dry Mix % Flour wt Wt % of dry mix Bleached Cake Flour 100 40.4 Sugar 105.9 42.2 Shortening 27.2 11.0 Milk Solids Nonfat 3.7 1.5 Dextrose (l) 2. 5 1.0 Salt 2.5 1.0 Sodium Bicarbonate (2) 2.2 0.9 Sodium aluminum phosphate (3) 1.2 0.9 Vanilla Powder (4) 1.2 0.5 Butter Flavor (5) 0.3 0.1 Cellulose Gum, CMC-7HF 1.2 0.5 CAKE MIX-Test Example Ingredients for Dry Mix % Flour wt Wt % of dry mix Bleached Cake Flour 100 40.4 Sugar 105.9 42.2 Shortening 27.2 11.0 Milk Solids Nonfat 3.7 1.5 Dextrose (1) 2.5 1.0 Salt 2.5 1.0 Sodium Bicarbonate (2) 2.2 0.9 Sodium aluminum phosphate (3) 1. 2 0.9 Vanilla Powder (4) 1.2 0.5 Butter Flavor (5) 0.3 0.1 Polymer Example 9 0. 72 0. 3 (1) Arm & Hammer Baking Soda, Church & Dwight (2) Cantab Dextrose, Penford Food Ingredient Company (3) Levair, FCC Grade Sodium Aluminum Phosphate, Rhodia Food Ingredients (4) Vanilla FL Pure Pwd K, Virginia Dare (5) Butter FL N&A Pwd 685 KD, Virginia Dare Formulation for the Finished Cake-One 8-inch Layer Dry mix, g 270 Water, g 140 Whole egg, g 53 Dry ingredients were blended on mixer with paddle attachment until evenly mixed. Water and egg were added to mix and mixed on medium speed for 3 minutes. The batter was poured into a greased cake pan and baked in a moderate oven (350°F/177°C) for 30 minutes.

Cake results : Reference Test Example Batter Viscosity, cps 5660 7650 Brookfield RV, spindle 3,10 rpm, 30 s Batter density, g/100mls 111 113 Cake height, cm 3.8 3.8 Crumb cell structure even even Bake out OK OK Crumb moisture, 24 hours after bake, % 39.0 39.0 Example 17 The CMCs of the present invention exhibit efficiency by the use of reduced amounts but yet obtain corporate results with prior art materials. The film forming and viscosity properties are enhanced in food preparations.

Masa and Corn Tortilla Example

MASA-Reference Ingredients for Dry Mix % Flour wt Wt % of dry mix NCF (') 100 98.83 Sodium Benzoate 0.4 0.39 Fumaric Acid 0.3 0.29 Cellulose Gum, CMC-7H4F K 0.5 0.49 MASA-Test Example Ingredients for Dry Mix % Flour wt Wt % of dry mix NCF 100 98.63 Sodium Benzoate 0.4 0.39 Fumaric Acid 0.3 0.29 Polymer Example 10 0.3 0.29 (1) Nixtamalized corn flour, Quaker Oats Company Dry ingredients were blended on mixer with paddle attachment until evenly mixed. Water was added to mix and mixed on medium speed for 2 minutes. Dough was portioned into 50g balls and pressed on a tortilla press.

The tortillas were baked on an ungreased skillet for 1 minutes on each side.

Tortillas were cooled on a wire rack, wrapped in foil sheets and checked for pliability and reheat after 1 day.

Tortilla results : Reference Test Example Appearance after bake even blisters even blisters Pliability good roll, no cracks good roll, no cracks Reheat good puff good puff Example 18 The CMC's of the present invention exhibit enhanced tablet crushing strength without effecting drug release kinetics.

The following formulations were prepared. Total batch size 1500 3750 Tablets Material % Wt per Tab (M Example 7 7. 5 30 Klucel HXF 22. 5 90 Phenylpropanolamine 20. 0 80 Avicel PH101 49. 5 198 Magnesium Stearate 0. 5 2 Total batch size 1500 3750 Tablets Material % Wt per Tab (M@ Example 7 7. 5 30 Natrosol 250 HX 22. 5 90 Theophylline 20. 0 80 Avicel PH 101 49. 5 198 Magnesium Stearate 0. 5 2

Total batch size 1500 3750 Tablets Material % Wt er Tab (Mg) CMC 12M8 PH 7. 5 30 Klucel HXF 22. 5 90 Phenylpropanolamine 20 80 Avicel PH101 49. 5 198 Magnesium Stearate 0. 5 2 Total batch size 1500 3750 Tablets Material % Wt er Tab M CMC 12M8 PH 7. 5 30 Natrosol 250 HX 22. 5 90 Theophylline 20 80 Avicel PH101 49.5 198 Magnesium Stearate 0. 5 2

Experimental Procedures.

All ingredients were sieved through a 20 mesh screen. All ingredients except magnesium were then dry blended in a 4 quart low shear Hobart mixer for 2 minutes. Thereafter water was added at a rate of 100 g/min while using low speed stirring. A total of 500mi per 1500 g of powder was added to the

formulations containing Klucel. This was increase) to 700g for Natrosol containing formulations. The wet masses were tray dried at 60°C down to less than 2 % moisture content. Following the drying step, the granulations were milled using the Fitzpatrick Comminutor Fitzmill at 2300 rpm, knives forward.

The reduced granulation was then lubricated by addition of 0,5% magnesium stearate. This final mix was blended for 3 minutes in a V-blender.

Compactibility.

As shown in Figure 5 for both model formulations, the inclusion of Example 7 CMC in place of CMC 12M8 pH in the tablet matrix results in a significant increase in tablet crushing strength.

Drug Release Kinetics While compactibility is improved, inclusion of Example 7 CMC does not manifest in significant differences in the release kinetics when compared to 12M8 pH. This shown in figures 6 and 7 for both highly soluble drug (phenylpropanolamine) and a sparingly soluble drug (Theophylline). Additionally no differences were evident at pH 1.5 or 6.8 between the Example 7 CMC and CMC 12M8 containing formulations.

Example 19 The CMC's of the present invention exhibit enhanced thickening efficiency, enchanced high shear viscosity (ICI), improved spatter resistance and improved water resistance in paint formulations.

Model of an interior latex flat paint based on Acronal 290 D.

Position Ingredients Function Parts by weight 1. Water 230. 0 2. Calgon N wetting agent 1.5 3. Pigmentverteiler A dispersing agent 3.0 4. CA 24 preservative 3. 0 5. Agitan 280 defoamer 5.0 6. thickener rheological modifier variable pre-mix 7. Kronos 2057 pigment 198.0 8. Omyalite 90 extender 140.0 9. Durcal 5 extender 198.0 10. Talcom AT 200 extender 28.0 mill base 11. Acronal 290 D latex binder 93.0 13. butylglycol coalescing agent 20.0 14. Texanol 5.0 15. additional water 71.5 let down PVC (%) 80% NVW (%) 61% Suppliers : 2 Benckiser Knapsack GmbH 3 BASF AG 4 Biochema Schwaben-Dr. Lehmann & Co.

5 Munzing Chemie GmbH 6 Aqualon/HERCULES 7 Kronos Titan GmbH 8 Plüss Staufer SG 9 Plüss Staufer SG 10 a/s Norwegian Talc 11 BASF AG 12 Shell Nederland Chemie BV 13 Eastman Chemicals

. 1 S, ; C w I [I : THkkItMr, 5to0kS. w.. ( 4" (y-F') n1c JCi" ; ; Cti) :, *'_..."SF 'tS WaNrMfvl. , ° i BLANOSE"7M3') C O. S7' 70SO 9S « M'2S 50''600 2-3 4 BLANOS 7M31C 0. 57 7050 98 108 125 5 0 600 2-3 4 BLANOSEw 7M31C 0. 46 6750 97 103 120 4 0 600 2-3 5 BLANOSE~7M31C 0. 45 6500 97 104 iso 2 0 550 3 4 Example 7 CMC 0. 41 7550 97 107 150 1 0 600 4 3 P Rating 1) 0-10,10 = BEST 2) Water resistance test acc. Grimshaw; Omm* best

ICI Viscosity Determination: Determined using ASTM D4287-83 Krebs Stormer Viscosity Measurement: Determined using ASTM D 562 Levelling Leneta: Determined using ASTM D 4062-81 Levelling test NYPC: Determined using ASTM D 2801-69 Sag Resistance: Determined using ASTM D4400-84 Spatter Resistance-Roller : The following equipment was used to evaluate the samples : paint roller with synthetic fibers e. g. verfroller 15 cm art. nr. 32913 ex Van Vliet Kwastenfabriek wall paper (woodchip quality) e. g. Erfurt Raufaser 52 Procedure: About 200 grams of paint is taken up by the roller. Paint is applied on a woodchip wallpaper with dimensions 100 x 50 cm placed in vertical position.

Paint is applied by ten-up and down strokes with the roller. A piece of black carch paper is placed horizontally 50 cm below the bottom line of the wallpaper.

The amount of spatter that is intercepted on the black paper is compared to a series of reference charts rating from 1 to 10. A rating of 1 means severe spatter and a rating of 10 stands for completely spatter free.

Water Retention (According GRIMSHAW) Equipment used in this part of the experment is: Substrate: Whatman No. 1 circular Filter paper (diameter 12.5 cm) Clamp ring inner diameter 7.7 cm outer diameter 12.6 cm Pasteur pipette (poly ethylene disposable) Colorant : Quink parket permanent block ink Balance

Procedure 1. Mix a blend of paint/colorant thoroughly in an aluminum cup.

Depending on the viscosity the following ratio's can be chosen: Paint: colorant 50: 50 60: 40 75: 25 Total amount 4-5 grams 2. Put the filter paper between two clamp rings and fix these with paper clips.

3. Weigh the clamped filter paper and apply with a Pasteur pipette 0.5 or 1.0 gram (depending the fluidity of the colored point blob) on the center of the filter paper.

4. Allow an overnight drying at room temperature.

5. Measure with a ruler the shaded stain round the paint center on 6 different spots.

6. The average expressed in mm is a measure for the water retention. A low value means a good water retention.

7. Report the used test conditions, ratio and amount of paint as well as the increase of the stain in mm.

While this invention has been described with respect to specific embodiments, it should be understood that these embodiments are not intended to be limiting and that many variations and modifications are possible without departing from the scope and spirit of this invention.