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US2839526A - Water-soluble carboxyalkyl cellulose derivative and method of manufacture - Google Patents

Water-soluble carboxyalkyl cellulose derivative and method of manufacture Download PDF

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US2839526A
US2839526A US478932A US47893254A US2839526A US 2839526 A US2839526 A US 2839526A US 478932 A US478932 A US 478932A US 47893254 A US47893254 A US 47893254A US 2839526 A US2839526 A US 2839526A
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fibrous
carboxyalkyl cellulose
cellulose derivative
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Jr Herbert C Miller
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Hercules Powder Co
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B11/00Preparation of cellulose ethers
    • C08B11/20Post-etherification treatments of chemical or physical type, e.g. mixed etherification in two steps, including purification

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  • This invention relates to the conversion of fibrous water-soluble carboxyalkyl cellulose ethers, particularly sodium carboxymethylcellulose, into free-flowing granu lar powder form.
  • water-soluble salts of carboxyalkyl cellulose in fibrous form are easily prepared by an etherification reaction between cellulose fibers, sodium hydroxide and a carboxyalkylating agent in the presence of an amount of aqueous alcohol such that upon completion of the etherification reaction, the resulting cellulose ether prodnot is obtained as a mass of loose moist fibers having a fiber form similar to that of the starting cellulose.
  • the crude product may either be neutralized and dried directly, or it may be neutralized and then washed free of byproduct salts with a suitable aqueous alcohol and then dried. In either case the product retains substantially the fibrous form of the starting cellulose through the subsequent processing steps.
  • fibrous forms of carboxyalkyl cellulose derivatives are converted into free-fiowing substantially granular powder forms thereof by agitating a loose fibrous mass comprising a water-soluble carboxyalkyl cellulose derivative moist with an aqueous alcohol and containing water and alcohol in such proportions that the mass would normally dry to a loose fibrous product, simultaneously introducing thereto a dispersed stream of aqueous fluid until the amount of water introduced is sufficient to form with the aqueous alcohol present in the mass an active solvent for the carboxyalkyl cellulose derivative, said active solvent containing at least about 67.5% by weight of water, maintaining the total liquid content in the mass below about 4 parts by weight based on the dry weight of the carboxyalkyl cellulose derivative, continuing agitation until the fibrous structure of the mass is substantially destroyed and the carboxyalkyl cellulose derivative is converted into a mass of separate, discrete gel particles, discontinuing agitation while the mass is still substantially in the form of separate, discrete gel particles
  • a number of methods are also known for converting fibrous forms of water-soluble cellulose others, including carboxyalkyl cellulose derivatives such as sodium carboxymethylcellulose, into free-flowing granular powders after they have been purified and/or dried ready for use. It is also known to add limited amounts of water,
  • EXAMPLE 1 A series of runs was made employing as starting material a commercial grade of sodium carboxymethylcellulose known as Hercules CMC-70-High. This material had a degree of substitution of 0.68-0.78 carboxymethyl radical per glucose anhydride unit, and a viscosity of 1300-2500 .cps. in a 1% aqueous solution. This material was prepared and purified in accordance with the procedure set forth in U. S. Patent 2,517,577. The resulting product was a dry loose mass of fibers having substantially Table 1 PHYSICAL PROPERTIES OF FIBROUS CMO Bulk Flow No. Solution Dust Run No. Density, (6 mm.) Time Loss,
  • Flow number is the number of times required to assist the flow of 50 g. OMC through a funnel with a 4 mm. opening until the tunnel is empty.
  • EXAMPLE 2 A series of runs was made employing as starting material sodium carboxymethylcellulose reacted in the same manner as that employed in Example 1. However, in this series of runs the fibrous material was converted to a granular form in accordance with my copending application as hereinbefore described, purified, and then classified after drying. The moist gels formed by the conversion flowed freely through the processing equipment and were easily purified. The physical properties of the granular classified sodium carboxymethylcellulose (CMC) thus produced are given in Table II.
  • Flow number is the number of times required to assist the flow of 50 g. 0M0 through a funnel with a 4 mm. opening until the funnel is empty.
  • EXAMPLE 3 A series of tests was made to demonstrate the relative segregation of fibrous and granular, classified, sodium carboxymethylcellulose (CMC). For this test, the fibrous product of Example 1 was compared to the granular, classified product of Example 2 by thoroughly blending equal parts of the products with sugar and placing in 8 ounce cylindrical glass jars. The blends were then subjected to gentle agitation for 90 minutes and were then separated into equal portions from the top and bot tom of the containers. The results of these tests are given in Table III.
  • the conversion of the fibrous material to the granular form should be substantially complete with not more than of fibrous particles present in the total converted mass. Since conversion of the fibrous material to the granular form ordinarily involves a densification step, the granular classified product normally has a somewhat higher bulk density than the fibrous product. This will be seen with reference to Tables I and II where the average bulk density, of the fibrous and granular productswas 0.45 g./cc. and 0.56 g./cc., respectively.
  • Bulk density is relatively unimportant in determining product quality with the exception that coarse grains of very high bulk density tend to hydrate and dissolve much less rapidly than less dense grains of the same size. It has been found that a bulk density range of from about 0.30 to about 1.0 g../cc. gives very satisfactory results.
  • the range of operability in respect to classification of the converted product is substantially 100% through a U. S. standard series sieve No. 12 with not more than about 20% through a U. S. standard series sieve No. 100.
  • the optimum range from a product standpoint appears to be 100% through a sieve No. 40 with 100% retained on a sieve No. 100.
  • such narrow particle size distribution is not feasible in commercial production and products of 100% through a sieve No. 20 with 90% retained on a sieve No. 100 have been found satisfactory.
  • this invention is suitable for processing any fibrous water-soluble.
  • carboxyalkylcellulose derivative including by way of example, any of the alkalimetal or ammonium salts of carboXyrnethyl-, carboxyetl1yl-, carboxypropyl-, carboxymethyl hydroxyethyl-, carboxyethyl hydroXyethyl-celluloses, and the like.
  • the cellulose derivative may be in the form of the crude product still containing by-product salts such as sodium chloride and sodium glycolate, partially purified, or purified. In order to obtain the greatest benefit in end product, it is preferred to apply the process of this invention to purified water-soluble carboxyalkyl cellulose derivatives. Purified derivatives do not contain any substantial amount of by-product salts which to some extent contribute to improved water solubility.
  • Drying of the gels after conversion as herein set forth follows conventional practice with respect to drying times, temperatures, drying equipment, and the like.
  • the moist or wet gels may be classified by suitable wet screening equipment to give the end product classification desired, it is preferred to dry the product to a volatile content below about 5% by weight and then classify. Since the dried product is inthe form of a free-flowing granular powder, it may be classified directly without further treatment.
  • the water-soluble products produced in accordance with this invention are readily and rapidly dissolved in Water and find a wide application of improved use where other water-soluble gums have heretofore been employed.
  • the products of this invention are especially efficacious in compounding stabilizers for various frozen comestibles,

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Description

WATER-SOLUBLE CARBOXYALKYL CELLULOSE DERIVATIVE AND METHOD OF MANUFAC- TURE Herbert C. Miller, Jr., Hopewell, Va., assignor t Hercules Powder Company, Wilmington, Del., a corporation of Delaware No Drawing. Application December 30, 1954 Serial No. 478,932
4 Claims. (Cl. 260-232) This invention relates to the conversion of fibrous water-soluble carboxyalkyl cellulose ethers, particularly sodium carboxymethylcellulose, into free-flowing granu lar powder form.
It is known that water-soluble salts of carboxyalkyl cellulose in fibrous form, particularly sodium carboxymethylcellulose, are easily prepared by an etherification reaction between cellulose fibers, sodium hydroxide and a carboxyalkylating agent in the presence of an amount of aqueous alcohol such that upon completion of the etherification reaction, the resulting cellulose ether prodnot is obtained as a mass of loose moist fibers having a fiber form similar to that of the starting cellulose. Following the etherification reaction the crude product may either be neutralized and dried directly, or it may be neutralized and then washed free of byproduct salts with a suitable aqueous alcohol and then dried. In either case the product retains substantially the fibrous form of the starting cellulose through the subsequent processing steps.
Although it is highly advantageous and desirable to carry out the etherification reaction while maintaining the product in the fibrous form, there are certain disadvantages in the fibrous form of the ether during subsequent processing, particularly purification and/or drying, and in a number of important uses for the cellulose ether. These difiiculties stem largely from the fact that the fibrous form of the ether tends to cling together and form fiber aggregates. Such aggregates impede flow through the processing equipment and are quite bulky. Moreover, when the fibrous form of carboxyalkyl cellu-. lose derivatives is added to water to prepare a solution of the product, there is a marked tendency for the fiber aggregates to cling together rather than disperse uniformly through the dissolving medium so that each individual fiber can be simultaneously swollen and dissolved by the water. These aggregates become gelled on the outside and persist as gel lumps in the solution, requiring displaced from the insufiicient to destroy the fibrous character of the ether, to sodium carboxymethylcellulose moist with aqueous alcohol of such composition that the cellulose ether would normally dry to a dry fluffy product, to change its original characteristics so that upon being subjected to mechanical comminution it is converted into a product of improved flowability with any desired particle size. While these methods have been fairly successful in overcoming the disadvantages of the fibrous form of these cellulose ethers in their ultimate uses, none of these methods overcome the processing difiiculties inherent in the fibrous form of these cellulose others during purification and/ or drying.
However, the processing difiiculties referred to above have been overcome in accordance with the process set forth in my copending application Serial No. 364,960, filed June 29, 1953.
In accordance with my copending application, fibrous forms of carboxyalkyl cellulose derivatives are converted into free-fiowing substantially granular powder forms thereof by agitating a loose fibrous mass comprising a water-soluble carboxyalkyl cellulose derivative moist with an aqueous alcohol and containing water and alcohol in such proportions that the mass would normally dry to a loose fibrous product, simultaneously introducing thereto a dispersed stream of aqueous fluid until the amount of water introduced is sufficient to form with the aqueous alcohol present in the mass an active solvent for the carboxyalkyl cellulose derivative, said active solvent containing at least about 67.5% by weight of water, maintaining the total liquid content in the mass below about 4 parts by weight based on the dry weight of the carboxyalkyl cellulose derivative, continuing agitation until the fibrous structure of the mass is substantially destroyed and the carboxyalkyl cellulose derivative is converted into a mass of separate, discrete gel particles, discontinuing agitation while the mass is still substantially in the form of separate, discrete gel particles and before said gels coalesce into doughy masses, and drying the gels thus formed to obtain a free-flowing substantially granular powder. In a preferred embodiment the active solvent containing at least about 67.5 water by weight is gels with aqueous alcohol containing less than about 40 0 water by weight prior to drying the gels.
In a specific embodiment of my copending application inordinately long periods of very vigorous agitation to completely break up the gel lumps and obtain a homogeneous solution. Unfortunately, mechanical disintegration of the fibrous product does not destroy the fibrous structure although it reduces the length of the fibers, and the resulting comminuted fibrous material still exhibits the above-mentioned disadvantages of the fibrous form. Additionally, the material in fibrous form has undesirable properties in that it is dusty in handling and tends to segregate badly in dry blends.
A number of methods are also known for converting fibrous forms of water-soluble cellulose others, including carboxyalkyl cellulose derivatives such as sodium carboxymethylcellulose, into free-flowing granular powders after they have been purified and/or dried ready for use. It is also known to add limited amounts of water,
converted into free-flowing substantially granular powder forms thereof by agitating a loose fibrous mass comprising a water-soluble carboxymethylcellulose derivative containing from about 0.5 to about 1.5 parts by weight, based on said carboxymethylcellulose derivative, of an aqueous alcohol containing not more than about 40% of water by weight, simultaneously introducing thereto a dispersed stream of aqueous fluid until the amount of water introduced is suflicient to raise the water content of the aqueous alcohol present in the fibrous mass to at least about 67.5 by weight and suificient to form with the aqueous alcohol present in the mass an active solvent for the carboxymethylcellulose derivative, maintaining the total liquid contentin the mass below about 4 parts by weight based on the dry weight of the carboxymethylcellulose derivative, continuing agitation until the fibrous structure of the mass is substantially destroyed and the carboxymethylcellulose derivative is converted into a mass of separate, discrete gel particles, discontinuing agitation while the mass is still substantially in the form of separate, discrete gel particles and before said gels coalesce into doughy masses, and drying the gels thus formed to obtain a free-flowing substantially granular powder.
It has been discovered that in order to obtain watersoluble carboxyalkyl .cellulose derivatives possessing a combination of outstanding desirable characteristics such as freedom from dust, quick solution rate, freedom of segregation in dry blends, and freedom from lumping in making solutions, it is first necessary to convert fibrous carboxyalkyl cellulose derivative into gel particles which upon drying are granular in contrast to the original fibrous form and then classifying the gel particles or granular material within critical limits. More specifically, in accordance with this invention, in processes for converting water-soluble fibrous carboxyalkyl cellulose derivative into substantailly free-flowing powder, there is provided the improvement which comprises converting the fibrous carboxyalkyl cellulose derivative into gel particles and classifying the gel particles to obtain in dry form 100% through a U. S. standard series sieve No. 12 with not more than about through a U. S. standard series sieve No. 100, whereby the product so converted, dried and classified in addition to being a free-flowing substantially granular powder is quickly soluble in water and substantially dust-free. The preferred procedure for converting the fibrous carboxyalkyl cellulose derivative into gel particles is that of my copending application since the procedure has been found particularly efiicacious when employed for the conversion step in the present invention.
The following examples are presented in illustration of this invention. It is to be understood, however, that the examples are purely illustrative and are not to be construed as a limitation of the invention.
EXAMPLE 1 A series of runs was made employing as starting material a commercial grade of sodium carboxymethylcellulose known as Hercules CMC-70-High. This material had a degree of substitution of 0.68-0.78 carboxymethyl radical per glucose anhydride unit, and a viscosity of 1300-2500 .cps. in a 1% aqueous solution. This material was prepared and purified in accordance with the procedure set forth in U. S. Patent 2,517,577. The resulting product was a dry loose mass of fibers having substantially Table 1 PHYSICAL PROPERTIES OF FIBROUS CMO Bulk Flow No. Solution Dust Run No. Density, (6 mm.) Time Loss,
g./cc. (Min) Percent 1 Flow number is the number of times required to assist the flow of 50 g. OMC through a funnel with a 4 mm. opening until the tunnel is empty.
2 A 6 mm. tunnel was used for the fibrous CMC since flow numbers for all samples were over 100 using the 4 turn. funnel.
3 Weight percent of CMC lost when tunneling 50 g. 0M0 from one containerto another.
NorE.The method for assisting flow 01 a sample of CMC through the tunnels consisted in thrusting a stiff wire about 7 inches long and 0.07 inch diameter down through the sample in the funnel and then withdrawing it. One such thrust and withdrawal constituted one assist.
EXAMPLE 2 A series of runs was made employing as starting material sodium carboxymethylcellulose reacted in the same manner as that employed in Example 1. However, in this series of runs the fibrous material was converted to a granular form in accordance with my copending application as hereinbefore described, purified, and then classified after drying. The moist gels formed by the conversion flowed freely through the processing equipment and were easily purified. The physical properties of the granular classified sodium carboxymethylcellulose (CMC) thus produced are given in Table II.
Table II PHYSICAL PROPERTIES OF GRANULAR, CLASSIFIED GMO Bulk Flow 1 Solution Dust 1 Sieve Classification, Percent Retained Run Density, No. (4 Time Loss, on No. g./cc. mm.) (min.) Percent 20 30 40 80 100 Pan 0. 53 3 2.1 0.26 0.8 13. 5 28.8 45. 2 3. 7 8.8 0.63 0 4. 1 0.02 0.4 4. 4 26. 6 63. 5 2. 5 2. 6 0.58 0 4. 1 0.26 0 15. 6 31. 9 38. 6 2. 3 11.6 0. 51 4 4.1 0.12 0 27.3 40.2 30.1 0.8 1. 6 0.62 1 3. 6 0.12 0. 1 7. 4 23. 3 54. 4 4. 4 10.4 0. 55 0 2. 8 O. 10 0 18. 6 34. 2 42. 0 1. 7 3. 5 0.40 4. 5 0.02 0.2 33. 5 40. 4 23.1 0.7 2.1 0. 58 0 1. 7 0 0 24. 4 55. 2 3. 6 1G. 8 0. 66 0 3. 2 0.06 0 0. 4 27. 4 57. 3 3. 5 11.4 0.59 O 2. 3 0. 16 0 0 30. 2 57. 5 3. 2 9. 1 0.62 0 1. 6 0 0.3 44. 1 50. 5 1. 8 3. 3 0.41 0 1. 3 0.20 0 0.1 56.8 39. 4 0.8 2. 9 0.62 0 2. 9 0.24 0 0 27. 5 58.6 3. 3 10. 6 0. 59 0 2. 7 0.20 0 0.2 30. 8 52. 5 3. 5 13.0
1 Flow number is the number of times required to assist the flow of 50 g. 0M0 through a funnel with a 4 mm. opening until the funnel is empty.
2 Weight percent of CMC lost when tunneling 50 g. CMC from one container to another.
EXAMPLE 3 A series of tests was made to demonstrate the relative segregation of fibrous and granular, classified, sodium carboxymethylcellulose (CMC). For this test, the fibrous product of Example 1 was compared to the granular, classified product of Example 2 by thoroughly blending equal parts of the products with sugar and placing in 8 ounce cylindrical glass jars. The blends were then subjected to gentle agitation for 90 minutes and were then separated into equal portions from the top and bot tom of the containers. The results of these tests are given in Table III.
Table III RELATIVE SEGREGATION OF FIBROUS AND GRANULAR, CLASSIFIED CMG With reference to the above examples and tables, it is evident that the improvement in processing in acordance with this invention is quite outstanding in yielding granular, classified products having significant commercial advantage over those heretofore available to the art. For example, the improvement in free-flowing characteristics is of value in a number of handling operations, such as pouring from containers, unloading from bins, and dry blending with other materials. The improvement in solution time is quite important. The fibrous products of Example 1 had an average solution time value of 9.5 minutes While the granular, classified products of Exam ple 2 had an average value of only 2.9 minutes. Moreover, the data presented relative to solution time were obtained by a controlled laboratory test Where only a small quantity of material was used. This test was conducted as follows:
Measure 300 ml. of water into a 600 ml. beaker. Heat to 65 C. and agitate slowly, so as to form a vortex of about /2 inch. Weigh 1.5 g. of the carboxyalkylcellulose product to be tested and pour into vortex in l to 2 seconds. Start stop watch simultaneously with addition of said product to water. Continue agitation until complete solution of said product. Complete solution may be determined more readily by placing a polaroid glass and a light behind the solution. Stop the watch as soon as said product is completely in solution, andrecord the elapsed time as solution time.
In commercial practice, where large quantities of material are dissolved in water the lumping tendency of fibrous material is still more pronounced and solution times are increased proportionately. The granular, classified material made in accordance with this invention, however, disperses readily and therefore dissolves in several minutes under conditions which in some instances require several hours for fibrous or finely pulverized material. The relative freedom from dusting is quite important in economy of use and handling where it will be observed that the dust lost for the fibrous material averaged 3.8% while that of the granular, classified material made in accordance with this invention averaged only 0.15%.
With reference to the foregoing, it is evident that there are several factors which will influence conditions for most satisfactory operation of the invention in which the actual requirements are determined by the processing sequence and finished products desired. In general, the conversion of the fibrous material to the granular form should be substantially complete with not more than of fibrous particles present in the total converted mass. Since conversion of the fibrous material to the granular form ordinarily involves a densification step, the granular classified product normally has a somewhat higher bulk density than the fibrous product. This will be seen with reference to Tables I and II where the average bulk density, of the fibrous and granular productswas 0.45 g./cc. and 0.56 g./cc., respectively. Bulk density is relatively unimportant in determining product quality with the exception that coarse grains of very high bulk density tend to hydrate and dissolve much less rapidly than less dense grains of the same size. It has been found that a bulk density range of from about 0.30 to about 1.0 g../cc. gives very satisfactory results.
The range of operability in respect to classification of the converted product is substantially 100% through a U. S. standard series sieve No. 12 with not more than about 20% through a U. S. standard series sieve No. 100. The optimum range from a product standpoint appears to be 100% through a sieve No. 40 with 100% retained on a sieve No. 100. However, such narrow particle size distribution is not feasible in commercial production and products of 100% through a sieve No. 20 with 90% retained on a sieve No. 100 have been found satisfactory.
It will be appreciated that this invention. is suitable for processing any fibrous water-soluble. carboxyalkylcellulose derivative including by way of example, any of the alkalimetal or ammonium salts of carboXyrnethyl-, carboxyetl1yl-, carboxypropyl-, carboxymethyl hydroxyethyl-, carboxyethyl hydroXyethyl-celluloses, and the like. The cellulose derivative may be in the form of the crude product still containing by-product salts such as sodium chloride and sodium glycolate, partially purified, or purified. In order to obtain the greatest benefit in end product, it is preferred to apply the process of this invention to purified water-soluble carboxyalkyl cellulose derivatives. Purified derivatives do not contain any substantial amount of by-product salts which to some extent contribute to improved water solubility.
Drying of the gels after conversion as herein set forth follows conventional practice with respect to drying times, temperatures, drying equipment, and the like. Although the moist or wet gels may be classified by suitable wet screening equipment to give the end product classification desired, it is preferred to dry the product to a volatile content below about 5% by weight and then classify. Since the dried product is inthe form of a free-flowing granular powder, it may be classified directly without further treatment.
The water-soluble products produced in accordance with this invention are readily and rapidly dissolved in Water and find a wide application of improved use where other water-soluble gums have heretofore been employed. The products of this invention are especially efficacious in compounding stabilizers for various frozen comestibles,
particularly in compounding stabilizers for ice cream. This application is a continuation-impart of my co- I pending application Serial No. 364,960, filed June 29 1953, now U. 8. Patent 2,715,124 which issued August 9, 1955.
What I claim and desire to protect by Letters Patent is:
1. In a process for converting fibrous carboxyalkyl cellulose derivatives into free-flowing substantially granular powder which comprises agitating a loose fibrous mass comprisinga water-soluble carboxyalkyl cellulose derivative moist with an aqueous alcohol and containing water and alcohol in such proportions that the mass would normally dry to a loose fibrous product, simultaneously introducing thereto a dispersed stream of aqueous fluid until the amount of water introduced is sufficient to form with the aqueous alcohol present in the mass an active solvent for the carboxyalkyl cellulose derivative, said active solvent containing at least about 67.5% by weight of Water, maintaining the total liquid content in the mass below about 4 parts by weight based on the dry weight of the carboxyalkyl cellulose derivative, continuing agitation until the fibrous structure of the mass is substan- 7 tially destroyed and the carboxyalkyl cellulose derivative is converted into a mass of separate, discrete gel particles, discontinuing agitation While the mass is still substantially'in the form of separate, discrete gel particles and before said gels coalesce into doughy masses: the improvement-which comprises classifying the gel particles to obtain in dry form substantially 100% through a U. S. standard series sieve No. 12 with not more than about 20% through a U. S. standard series sieve No. 100, whereby the product so converted, dried and classified in addition to being a free-flowing substantially granular powder is quickly soluble in water and substantially dust-free.
2. In a process for converting fibrous carboxyalkyl cellulose derivatives into free-flowing substantially granular powder which comprises agitating a loose fibrous mass comprising a water-soluble carboxyalkyl cellulose derivative moist with an aqueous alcohol and containing water and alcohol in such proportions that the mass would normally dry to a loose fibrous product, simultaneously introducing thereto a dispersed stream of aqueous fluid until the amount of water introduced is sufiicient to form with the aqueous alcohol present in the mass an active solvent for the carboxyalkyl cellulose derivative, said active solvent containing at least about'67.5% by weight of water, maintaining the total liquid content in the mass below about 4 parts by weight based on the dry weight of the carboxyalkyl cellulose derivative, continuing agitation until the fibrous structure of the mass is substantially destroyed and the carboxyalkyl cellulose derivative is converted into a mass of separate, discrete gel particles, discontinuing agitation while the mass is still substantially in the form of separate, discrete gel particles and before said gels coalesce into doughy masses, and drying the gels thus formed to obtain a free-flowing substantially granular powder: the improvement which comprises classifying the powder to obtain substantially 100% through a U. S. standard series sieve No. 12 with not more than about 20% through a U. S. standard series sieve No. 100, whereby the product so converted, dried and classified in addition to being a free-flowing substantially granular powder is quickly soluble in water and substantially dust-free.
3. In a process for converting fibrous carboxyrnethylcellulose into free-flowing substantially granular powder which comprises agitating a loose fibrous mass comprising water-soluble carboxymethylcellulose moist with an aqueous alcohol and containing water and alcohol in such proportions that the mass would normally dry 'to a loose fibrous product, simultaneously introducing thereto a dispersed stream of aqueous fiuid until the amount of r water introduced is suflicient to form with the aqueous a lcohol present in the mass an active solvent for the carboxymethylcellulose, said active solvent containing at least about 67.5% by weight of water, maintaining the total liquid content in the mass below about 4 parts by weight based on the dry weight of the carboxymethylcellulose, continuing agitation until the fibrous structure of the mass is substantially destroyed and the carboxymethylcellulose is converted into a mass of separate, discrete gel particles, discontinuing agitation while the mass is still substantially in the form of separate, discrete gel particles and before said gels coalesce into doughy masses: the improvement which comprises classifying the gel particles to obtain in dry form substantially 100% through a U. S; standard series sieve No. 12 with not more than about 20% through a U. S. standard series sieve No. 100, whereby the product so converted, dried and classified in addition to being a free-flowing substantially granular powder is quickly soluble in water and substantially dust-free.
4. In a process for converting fibrous carboxymethylcellulose into free-flowing substantially granular powder which comprises agitating a loose fibrous mass comprising water-soluble carboxymethylcellulose moist with an aqueous alcohol and containing water and alcohol in such proportions that the mass would normally dry to a loose fibrous product, simultaneously introducing thereto a dispersed stream of aqueous fluid until the amount of water introduced is sufiicient to form with the aqueous alcohol present in the mass an active solvent for the carboxymethylcellulose, said active solvent containing at least about 67.5% by Weight of water, maintaining the total liquid content in the mass below about 4 parts by weight based'on the dry weight of the carboxymethylcellulose, continuing agitation until the fibrous structure of the mass is substantially destroyed and the carboxymethylcellulose is converted into a mass of separate, discrete gel particles, discontinuing agitation while the mass is still substantially in the form of separate, discrete gel particles and before said gels coalesce into doughy masses, and drying the gels thus formed toobtain a free-flowing substantially granular powder: the improvement which comprises classifying the powder to obtain substantially 100% through a U. S. standard series sieve No. 12 with not more than about 20% through a U. S. standard series sieve No. 100, whereby the product so converted, dried and classified in addition to being a free-flowing substantially granular powder is quickly soluble in water and substantially dust-free.
References Cited in the tile of this patent UNITED STATES PATENTS nlnran PATENT orrncn @ERHIFMATE @t no 15 EEMN Patent No, 23339526 June 17, 1958 of Herbert GD Miller Jr It is herebg} certified that error appears in the printed specification of the above numbered patent requiring correction and that the said Letters Patent should read as corrected helom Colwnn 3, line 3, for "It has been" read It now heen column. 4 Table II, under the heading "Sieve Classifioatiom Percent Retained on fi under the subheading "2O" first line thereof for "03'' read O Signed and sealed this 26th day of August 1958,
(SEAL) fittest:
KARL Ho AXLINE n i a FH UIEHIMWLT WATFSMN Atteating @fifioer Commissioner of

Claims (1)

1. IN A PROCESS FOR CONVERTING FIBROUS CARBOXYALKYL CELLULOSE DERIVATIVES INTO FREE-FLOWING SUBSTANTIALLY GRANULAR POWDER WHICH COMPRISES AGITATING A LOOSE FIBROUS MASS COMPRISING A WATER-SOLUBLE CARBOXYALKYL CELLULOSE DERIVATIVE MOIST WITH AN AQUEOUS ALCOHOL AND CONTAINING WATER AND ALCOHOL IN SUCH PROPORTIONS THAT THE MASS WOULD NORMALLY DRY TO A LOOSE FIBROUS PRODUCT, SIMULTANEOUSLY INTRODUCING THERETO A DISPERSED STREAM OF AQUEOUS FLUID UNTIL THE AMOUNT OF WATER INTRODUCED IS SUFFICIENT TO FORM WITH THE AQUEOUS ALCOHOL PRESENT IN THE MASS AN ACTIVE SOLVENT FOR THE CARBOXYALKYL CELLULOSE DERIVATIVE, SAID ACTIVE SOLVENT CONTAINING AT LEAST ABOUT 67.5% BY WEIGHT OF WATER, MAINTAINING THE TOTAL LIQUID CONTENT IN THE MASS BELOW ABOUT 4 PARTS BY WEIGHT BASED ON THE DRY WEIGHT OF THE CARBOXYALKYL CELLULOSE DERIVATIVE, CONTINUING AGITATION UNTIL THE FIBROUS STRUCTURE OF THE MASS IS SUBSTANTIALLY DESTROYED AND THE CARBOXYALKYL CELLULOSE DERIVATIVE IS CONVERTED INTO A MASS OF SEPARATE, DISCRETE GEL PARTICLES, DISCONTINUING AGITATION WHILE THE MASS IS STILL SUBSTANTIALLY IN THE FORM OF SEPARATE, DISCRETE GEL PARTICLES AND BEFORE SAID GEL COALESCE INTO DOUGHY MASSES: THE IMPROVEMENT WHICH COMPRISES CLASSIFYING THE GEL PARTICLES TO OBTAIN IN DRY FORM SUBSTANTIALLY 100% THROUGH A U.S. STANDARD SERIES SIEVE NO. 12 WITH NOT MORE THAN ABOUT 20% THROUGH A U.S. STANDARD SERIES SIEVE NO. 100, WHEREBY THE PRODUCT SO CONVERTED, DRIED AND CLASSIFIED IN ADDITION TO BEING A FREE-FLOWING SUBSTANTIALLY GRANDULAR POWDERIS QUICKLY SOLUBLE IN WATER AND SUBSTANTIALLY DUST-FREE.
US478932A 1954-12-30 1954-12-30 Water-soluble carboxyalkyl cellulose derivative and method of manufacture Expired - Lifetime US2839526A (en)

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US3360440A (en) * 1966-04-13 1967-12-26 Haab Walter Cold water reconstitutable microbiological medium, process for preparation and use, ad product
US3394127A (en) * 1964-09-30 1968-07-23 Du Pont Densification of carboxymethyl cellulose
DE3245794A1 (en) * 1981-12-10 1983-06-23 NL Industries, Inc., 10020 New York, N.Y. METHOD FOR PRODUCING AN ALKALINE METAL SALT OF CARBOXYMETHYLCELLULOSE
US4689408A (en) * 1985-05-14 1987-08-25 Hercules Incorporated Method of preparing salts of carboxymethylcellulose
WO1988002375A1 (en) * 1986-09-24 1988-04-07 Bp Chemicals Limited Improvement in the preparation of cellulose ethers
US20220273840A1 (en) * 2021-01-14 2022-09-01 Soane Materials Llc Absorbent fibrous composites and resulting high performance products

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US2331864A (en) * 1942-03-20 1943-10-12 Dow Chemical Co Method of preparing powdered cellulose ethers quickly soluble in cold water
US2331865A (en) * 1942-03-20 1943-10-12 Dow Chemical Co Method of preparing cold-watersoluble powdered cellulose ethers
US2517577A (en) * 1946-12-10 1950-08-08 Hercules Powder Co Ltd Preparation of carboxyalkyl ethers of cellulose
US2607772A (en) * 1949-12-21 1952-08-19 Ici Ltd Production of powdery products comprising carboxymethyl cellulose
US2618018A (en) * 1948-10-22 1952-11-18 British Celanese Treatment of fibrous cellulose derivatives to render them more easily powdered
US2631943A (en) * 1947-08-15 1953-03-17 Ciba Ltd Process for the manufacture of a pulverulent alkyl cellulose coated upon a pulverulent carrier
US2667480A (en) * 1950-07-05 1954-01-26 Du Pont Manufacture of cellulose ether
US2667482A (en) * 1950-02-09 1954-01-26 Ici Ltd Production of water-soluble salts of certain cellulose derivatives of improved physical form

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US2331864A (en) * 1942-03-20 1943-10-12 Dow Chemical Co Method of preparing powdered cellulose ethers quickly soluble in cold water
US2331865A (en) * 1942-03-20 1943-10-12 Dow Chemical Co Method of preparing cold-watersoluble powdered cellulose ethers
US2517577A (en) * 1946-12-10 1950-08-08 Hercules Powder Co Ltd Preparation of carboxyalkyl ethers of cellulose
US2631943A (en) * 1947-08-15 1953-03-17 Ciba Ltd Process for the manufacture of a pulverulent alkyl cellulose coated upon a pulverulent carrier
US2618018A (en) * 1948-10-22 1952-11-18 British Celanese Treatment of fibrous cellulose derivatives to render them more easily powdered
US2607772A (en) * 1949-12-21 1952-08-19 Ici Ltd Production of powdery products comprising carboxymethyl cellulose
US2667482A (en) * 1950-02-09 1954-01-26 Ici Ltd Production of water-soluble salts of certain cellulose derivatives of improved physical form
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3394127A (en) * 1964-09-30 1968-07-23 Du Pont Densification of carboxymethyl cellulose
US3360440A (en) * 1966-04-13 1967-12-26 Haab Walter Cold water reconstitutable microbiological medium, process for preparation and use, ad product
DE3245794A1 (en) * 1981-12-10 1983-06-23 NL Industries, Inc., 10020 New York, N.Y. METHOD FOR PRODUCING AN ALKALINE METAL SALT OF CARBOXYMETHYLCELLULOSE
US4689408A (en) * 1985-05-14 1987-08-25 Hercules Incorporated Method of preparing salts of carboxymethylcellulose
WO1988002375A1 (en) * 1986-09-24 1988-04-07 Bp Chemicals Limited Improvement in the preparation of cellulose ethers
EP0265088A1 (en) * 1986-09-24 1988-04-27 Union Carbide Benelux N.V. Improvement in the preparation of cellulose ethers
US4918180A (en) * 1986-09-24 1990-04-17 Union Carbide Chemicals And Plastics Company, Inc. Preparation of cellulose ethers
US20220273840A1 (en) * 2021-01-14 2022-09-01 Soane Materials Llc Absorbent fibrous composites and resulting high performance products
US12064524B2 (en) * 2021-01-14 2024-08-20 Soane Materials Llc Absorbent fibrous composites and resulting high performance products

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