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US2465346A - Dedusting process and product thereof - Google Patents

Dedusting process and product thereof Download PDF

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US2465346A
US2465346A US494847A US49484743A US2465346A US 2465346 A US2465346 A US 2465346A US 494847 A US494847 A US 494847A US 49484743 A US49484743 A US 49484743A US 2465346 A US2465346 A US 2465346A
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soap
particles
dust
product
hygroscopic
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US494847A
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John W Bodman
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Lever Brothers Co
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Lever Brothers Co
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D9/00Compositions of detergents based essentially on soap
    • C11D9/04Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
    • C11D9/06Inorganic compounds
    • C11D9/08Water-soluble compounds
    • C11D9/10Salts
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0039Coated compositions or coated components in the compositions, (micro)capsules
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/06Powder; Flakes; Free-flowing mixtures; Sheets

Definitions

  • This invention relates to improvements in the manufacture of soaps and more particularly to powdered, granulated or comminuted soaps substantially devoid of objectionable finely divided soap dust particles; the invention relates also to methods of manufacturing such soaps.
  • Granulated or powdered soaps usually are formed in one of three well-known ways, namely, grinding, in which dried soap is comminuted and reduced to a powdered condition; spray-cooling, wherein a hot liquid soap that is capable of crystallizing is sprayed into a current of cooling air; and spray-drying, wherein a hot liquid or semi-liquid soap or soap mix is sprayed into a current of heated drying gas to evaporate a portion of the water and cause the soap to solidify as particles, or wherein soap is heated under pressure and flashed into cool air at lower pressure.
  • Spray dried soaps may be either hollow or porous fragile particles.
  • Soaps of these types are usually packaged in cardboard cartons and are sold to the consuming public in this convenient form. While such soaps are highly desirable from the standpoint of ease in solubility and convenience in use, when they reach the consumer they contain a quantity of finely divided soap particles. A material proportion of this dust or fines is capable of being air home. The portion of the dust capabe of being air borne is usually released upon opening the carton and pouring the soap therefrom. It is this air borne soap dust that has been found in many cases to irritate the membranes of the nose and throat, causing coughing and sneezing.
  • the dust particles or fines also have a tendency to lump together on the surface of the water and resist solution. This characteristic of comminuted or powdered soap products has long been recognized in the industry and attempts have been made to eliminate the dust or at least materially reduce the quantity in the product. i
  • Dust formed during the process of. manufacture could be made relatively unobjectionable in the final product by an efficient dedusting process after manufacture and prior to packaging.
  • One of the principal causes of dust in the packaged product is the disintegration of the particles after the product is packaged. This may be.
  • a soap product such as, for examp'e, a spray-dried soap, may consist of more or less spherical globules, each having one or more voids therein.
  • a moisture content of between 10 percent to 20 percent is normally present in typical forms of ranulated soaps at the time they are manufactured and packaged. This moisture content is sufficient to render the particles somewhat plastic and resistant to shattering. As long as this moisture content is maintained at substantially its initial amount, there is little tendency for the soap to form dust. However, if the soap dries, as is often the case, the pasticity of the particles is then reduced.
  • the dried and friable particles Upon being subjected to shock or abrasion, the dried and friable particles will break or shatter and thus form additional quantities of dust. Low moisture content also impedes any tendency towards a reag gregation of the fines into larger agglomeratcs.
  • loss of moisture permits a migratlm 9f fillers or builders in the soap, such as sodium carbonate, sodium sulfate and sodium silicate, toward the surfaces of the particles where they deposit as crust or groups of crystas. These crystals are separable by abrasion from the larger particles as dust.
  • this form of dust is of a particularly irritatlng nature.
  • My invention may be utilized to overcome and avoid at least some, and preferably all, of the disadvantages and difilculties of the typ indicated above, as well as others, in comminuted friable substances, and for preserving and im-. proving such substances, particularl those of the type of soap.
  • the invention may preferably beutilized to substantially reduce the tendency of granulated or powdered soaps or other such friable substances to disintegrate or change their physical state with consequentdust formation.
  • the invention may also be preferably utilized to maintain the moisture content of soap particles substantially constant despite'variations in relative humidity so as to minimize and prevent the drying out of the soap particles with a resultant undesirable formation of dust.
  • the individual soap particles or granules after they are formed, may be coated with a material that functions primaril because of its hygroscopic nature and which. normally withdraws moisture from the atmosphere and thus prevents a migration or diffusion of the moisture from the interior of the soap particles.
  • the invention may be utilized material in many cases also may act to bind dust particles to each other or to the larger particles. These dust particles may be present in the soap initially or may be formed if the soap is subj ect to unusual conditions.
  • the polyhydric alcohols are desirable compounds to use as coating materials to eliminate dust. These compounds assist in maintaining a definite water concentration in the soap inasmuch as under normal humidity conditions they will withdraw moisture fromv the atmosphere. This moisture will compensate for any that is lost by evaporation, or if more is withdrawn it will penetrate into the soap particles and improve their plasticity. Even under dry conditions moisture will only diffuse from the soap until a balance is reached between the atmospheric humidity and the ability of the polyhydric alcohol to withdraw moisture from the air.
  • Th organic and inorganic phosphates such as, for example, dipotassium phosphate or potassium methyl or ethyl phosphate, also are satisfactory hygroscopic coating materials.
  • Dipotassium phosphate is very effective at relative humidities in excess of about 30 percent. For example at 50 percent relative humidity, dipotassium phosphate will carry about 40 percent of water, which is adequate to maintain it in the form of an oily or mobile liquid. However, below about 30 percent relative humidity, it will dry out to a crystalline solid. Therefore, it is less suitable for use in treating soap which will be exposed to very low humidities.
  • Alkyl phos phates having the formula MRHP-O4, in which M is an alkali metal and R is an alkyl group, therefore, are particularly suitable for use as coating agents for granulated soap under all conditions of relative humidity.
  • the above mentioned compounds also cause any dust particles to aggregate into larger particles or adhere to large soap granules. They also minimize the formation of static charges and thus reduce the tendency of any small soap particles to remain-in suspension.
  • hygroscopic materials such as potassiumcarbonate, potassium silicate, disodium phosphate and calcium or magnesium chloride.
  • Other hygroscopic materials which also function as wetting agents maybe used since these materials contribute to the plasticity of the soap particles because of their wetting nature and strengthen the bond between aggregates of fines and between the fines and the particles of normal size.
  • I-Iygroscopic substances or those which themselves may be conductors have the additional chracteristic of preventing the formation of static charges on the soap particles for the reason that they render the surfaces of the particles conductive, and thus reduce the tendency of the dust to remain in suspension in air.
  • Such substances which might be used for this purpose would include, for example, glycerin, dipotassium phosphate, sodium potassium ethyl phosphate, triethanolamine ethyl phosphate, glycerin and dipotassium phosphate, glycerin and sodium potassium ethyl phosphate, glycerin and potash coconut oil soap, water-soluble sulfonated oils and lithium chloride.
  • coating compositions should be present in sufficient proportion to obtain the desired results and yet not in such proportion that they will cause lumping and formation of aggregates of such size that the characteristic of rapid dissolving, which is desirable in granulated soaps, is materially reduced.
  • the amount of the hygroscopic material to be employed will depend upon the hygroscopic character of the material selected, the nature of the soap, the climatic conditions where the product is to be used, etc. Soaps made from certain fatty acids and alkalies and having certain fillers and builders have different degrees of natural plasticities and water retentivity. This fact coupled with the different hygroscopic character of various materials makes it difficult to state any range applicable to all of the hygroscopic materials, When glycerin is used, for example, an amount of about 0.5% to 6.0% based on the weight of the soap, is preferable. It is believed that in view of the generic disclosure and the specific example, one skilled in the art would readily be able to determine the amount to be used in any particular instance, depending upon the particular soap to be treated and the use to which it is to be put.
  • An embodiment of my invention that is of particular importance is the use of calcium chloride as a hygroscopic agent.
  • a calcium compound to soap or to water in which soap is to be used would be thought of as objectionable because it is the calcium which causes hardness in water. This is normally thought to be a disadvantage and calcium is an ingredient sought to be eliminated.
  • the amount of calcium chloride to be added to the surface of the soap particles as a hygroscopic material to preserve the moisture content may be so small as not to interfere seriously with the increase in hardness properties.
  • the amount of calcium chloride to be applied to the soap may be within the range of 0.25% to 1.0% based upon the weight of the soap.
  • the soap When the soap is made with tetrasodium pyrophosphate as a builder, it is desirable to have an amount of calcium present in the water as this increases the detergent properties. In soft water districts if the amount of calcium in the water is not sufficient it may be added to secure this effect.
  • calcium chloride may be added to the soap not only to prevent dusting but also as a convenient way of introducing the necessary calcium into the wash water,
  • the hygroscopic material is applied to the surface of the particles as distinguished from an ingredient that is admixed with the soap composition before it is dried.
  • the hygro scopic material would not have an opportunity to exert its hygroscopic character to any marked extent.
  • the soap particle dries, the moisture first leaves the outer surface and it is the outer surface which driesfirst. The moisture from the interior then migrates through the particle to the outer surface.
  • the outer surface can be kept moist as a result of the hygroscopic material, there will be no tendency for the normal moisture on the interior to leave the particles.
  • hygroscopic material since it is only the surface of the particle which is in contact with the air from which moisture could be absorbed by hygroscopicity, there is no point in having the hygroscopic material at any point other than on the outside surface of the soap particles. Th hygroscopic material may be applied more or less uniformly over the surface of the soap particles and it may be applied more or less spotted or continuously over the surface. Since the hygroscopic agents will, for the greater part, be watersoluble, there is no objection to a continuous coating on the surface of the particles, although a partially spotted coating may be suflicient to keep the soap particles plastic with the coating of this amount and nature.
  • the hygroscopic material may be soluble in the soap or not. If not, it has the advantage that it will not tend to diffuse into the soap particles and will not require such a large quantity of material. On the other hand, the materials which penetrate tend to keep the entire mass of the soap particle plastic.
  • the coating materials may be applied to soap particles in various ways, and at any convenient time between the formation of the soap particles and the packaging step,
  • the coating materials are preferably atomized and the soap particles allowed to fall through the atomized coating material. It is desirable to maintain the finest possible mist or fog of the material to be applied so that the most effective application can be made and even the finest of the dust particles forced into contact with the treating material. It has been found that a series of repeating treatments is effective in obtaining a desirable" dust-free product.
  • the coating composition may be applied by spraying in a rotary drum through which the soap particles are tumbled.
  • the major portion of the soap particles treated will, for the most part, vary in particle size from about 20 to mesh. They may be coated completely or partially with a single coating composition or a blend, simultaneously or in separate stages, as already-described. Any fine, objectionable, dust-likematerial will be. coated and will tend-to bond with the larger particles or with otherfi'ne material-to'fonn aggregates of a size larger than the: average size; of the dust particles. This will be the case not only with disintegrate-d or finesoap particles, but also with any dust formed as a result of the migrationor separation of the ingredients ordinarily present in the soap composition, suchas the hydrating salts,
  • dust particles of a mesh of 140 or smaller are undesirable in the final product and are considered as dust. It has been found that dust particles of about 400mesh or smaller, as calculated on the bases of formulas for standard screens, will be air borne under conditions of relatively low air movement. These air borne particles might average 50 microns in size and smaller. They are, therefore, particularly undesirable as they can readily move into contact with the membrane of the nasal passages to cause irritation. Larger particles than 400 mesh may be air-borne under conditions of increased air movement and for the same reason should be rendered innocuous.-
  • the present invention has resulted in. the production of a. novel dustless type. of granular or comminuted soap product and that a simple process has been provided for obtaining such dustless soap granules. It will be understood that the present process can be. applied to any of the usual types of-granulated or powdered soaps in order to overcome their objectionable dusting characteristics and that by means of thep-rocessshrinkage in packaging or in weigh-t may be largely avoided.
  • a process of treating granulated water soluble soap to'prevent substantially the formaticn of dust therein comprising applying to the particles of soap a superficial coating, of a hygroscopic alkaline earth metal chloride in an amount to inhibit dehydration of the soap and the formation of soap dust.
  • partic1es,,-but not to. increase greatly the hardness properties. ofth water when the soap is used in ordinary concentrations for laundry.
  • a Water soluble soap product comprising granulated soap particles. having on at least a portion of. their surfaces at superficial coating of a hygroscopic alkaline earth metal chloride in an amount to inhibit dehydration of the soap particles and dusting of the-soap product, but not to increase. greatly the hardness properties of the water when the soap product is used in ordinary concentrations in laundry.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
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  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)

Description

Patented Mar. 29, 1949 DEDUSTING PROCESS AND PRODUCT THEREOF John W. Bodman, Winchester, Mass, assignor to Lever Brothers Company, a corporation of Maine No Drawing. Application July 15, 1943, Serial No. 494,847
9 Claims.
This invention relates to improvements in the manufacture of soaps and more particularly to powdered, granulated or comminuted soaps substantially devoid of objectionable finely divided soap dust particles; the invention relates also to methods of manufacturing such soaps.
Granulated or powdered soaps usually are formed in one of three well-known ways, namely, grinding, in which dried soap is comminuted and reduced to a powdered condition; spray-cooling, wherein a hot liquid soap that is capable of crystallizing is sprayed into a current of cooling air; and spray-drying, wherein a hot liquid or semi-liquid soap or soap mix is sprayed into a current of heated drying gas to evaporate a portion of the water and cause the soap to solidify as particles, or wherein soap is heated under pressure and flashed into cool air at lower pressure. Spray dried soaps may be either hollow or porous fragile particles.
Soaps of these types are usually packaged in cardboard cartons and are sold to the consuming public in this convenient form. While such soaps are highly desirable from the standpoint of ease in solubility and convenience in use, when they reach the consumer they contain a quantity of finely divided soap particles. A material proportion of this dust or fines is capable of being air home. The portion of the dust capabe of being air borne is usually released upon opening the carton and pouring the soap therefrom. It is this air borne soap dust that has been found in many cases to irritate the membranes of the nose and throat, causing coughing and sneezing.
The dust particles or fines also have a tendency to lump together on the surface of the water and resist solution. This characteristic of comminuted or powdered soap products has long been recognized in the industry and attempts have been made to eliminate the dust or at least materially reduce the quantity in the product. i
The attempts to overcome this difficulty have led to improvements in spray-drying processes, by means of which the soap is formed into more or less rounded and discrete individual granues. Such granules are small enough to dissolve readily, but also large enough to minimize greatly the disadvantages of the so-called dusting. The factors affecting the size and character of the soap granules produced in a spray-drying process are well known. For example, fine partices can be puffed to above dust size if high temperatures and other conditions are employed. However, large puffing generally is not desirable, for in doing this t the fine particles, the total product ill is bulked to such a large degree that in general there is present too small an amount of soap in any given volume, and the product does not have desirabie sudsing properties. Furthermore, large puffing creates thin walled particles more susceptible to breakage, thus tending to increase the dust content of the product.
In spite of the exact control now possible, there is still generally an objectionable amount of dusty material in the product at the time the customer uses it. A proportion of "fines unavoidably results from the commercial manufacturing processes. Dust formed during the process of. manufacture could be made relatively unobjectionable in the final product by an efficient dedusting process after manufacture and prior to packaging. One of the principal causes of dust in the packaged product is the disintegration of the particles after the product is packaged. This may be.
because of conditions of storing and handling before or after the carton or package is opened for use.
Attempts to remove finely divided material of dust size by screening before packing have not been successful, however, for the reason that screens of sufiicient fineness to allow separation of the dust become clogged, and, at best, remove only a part of the dust. Even assuming that a screening process removes the dust formed during the production of the soap, it cannot remove the dust which is formed in the package.
The formation of dust in the package results, in part, from disintegration of the soap particles during handling and is increased by drying out of the soap. A soap product such as, for examp'e, a spray-dried soap, may consist of more or less spherical globules, each having one or more voids therein. A moisture content of between 10 percent to 20 percent is normally present in typical forms of ranulated soaps at the time they are manufactured and packaged. This moisture content is sufficient to render the particles somewhat plastic and resistant to shattering. As long as this moisture content is maintained at substantially its initial amount, there is little tendency for the soap to form dust. However, if the soap dries, as is often the case, the pasticity of the particles is then reduced. Upon being subjected to shock or abrasion, the dried and friable particles will break or shatter and thus form additional quantities of dust. Low moisture content also impedes any tendency towards a reag gregation of the fines into larger agglomeratcs. In addition, loss of moisture permits a migratlm 9f fillers or builders in the soap, such as sodium carbonate, sodium sulfate and sodium silicate, toward the surfaces of the particles where they deposit as crust or groups of crystas. These crystals are separable by abrasion from the larger particles as dust. In the case of the more alkaline fillers, suchas sodium carbonate or sodium silicate, this form of dust is of a particularly irritatlng nature. There is also a tendency for the dust to remain in suspension in the air because of the presence of static charges of like sign on the particles. Such electrical dispersing charges may be created as a resu't of friction between the particles and the package during handling. The presence of adequate moisture content in the particles, however, largely eliminates the effects of static electricity. The breaking up or di integration of the roap particles also has the undesirabe effect of reducing the apparent volume of t e soap in the cartons. This creates an adverse psychological effect upon the user when the package of soap is opened, inasmuch as it would appear as if less than the full quantity of soap were present in the package.
It has been suggested that drying out of the soap particles might be avo ded by packaging the granulated soap in moisture-proof containers. While this increases the cost of packaging, it will, of course, prevent drying of the soap as long as the package is uno ened, but inasmuch as the entire contents of the soap package ordinarily is not used immediately after opening the package, the remainder of the soap will dry out readily upon standing in a dry place, and objectionable dust will be formed.
My invention may be utilized to overcome and avoid at least some, and preferably all, of the disadvantages and difilculties of the typ indicated above, as well as others, in comminuted friable substances, and for preserving and im-. proving such substances, particularl those of the type of soap. In this connection the invention may preferably beutilized to substantially reduce the tendency of granulated or powdered soaps or other such friable substances to disintegrate or change their physical state with consequentdust formation. The invention may also be preferably utilized to maintain the moisture content of soap particles substantially constant despite'variations in relative humidity so as to minimize and prevent the drying out of the soap particles with a resultant undesirable formation of dust. to minimize 'or eliminate dust particles present in a soap product, for example, by maintaining the soap in an undried form so as to retain the strength of the soap. particles; consequently there is little or no tendencyfor the soap, particles to" disintegrate or change their state. Under some circumstances the surface of the larger particles may hold the fines attached thereto or the fines may be held together through a cohesive action.
I have subsequently set forth preferred examples and illustrations of how my process may preferably be practiced to produce desirable Products.
In accordance with the present invention the individual soap particles or granules, after they are formed, may be coated with a material that functions primaril because of its hygroscopic nature and which. normally withdraws moisture from the atmosphere and thus prevents a migration or diffusion of the moisture from the interior of the soap particles. 'The hygroscopic The invention may be utilized material in many cases also may act to bind dust particles to each other or to the larger particles. These dust particles may be present in the soap initially or may be formed if the soap is subj ect to unusual conditions.
' Of the materials which have been used in treating granulated soap, the polyhydric alcohols, are desirable compounds to use as coating materials to eliminate dust. These compounds assist in maintaining a definite water concentration in the soap inasmuch as under normal humidity conditions they will withdraw moisture fromv the atmosphere. This moisture will compensate for any that is lost by evaporation, or if more is withdrawn it will penetrate into the soap particles and improve their plasticity. Even under dry conditions moisture will only diffuse from the soap until a balance is reached between the atmospheric humidity and the ability of the polyhydric alcohol to withdraw moisture from the air. Under conditions such that the relative humidity is as low as 30 percent, it has been found that polyhydric alcohols, such as glycerin, ethylene glycol, diethylene glycol, sorbitol and mannitol, are satisfactory for preventing the dusting of the soap. I
Th organic and inorganic phosphates, such as, for example, dipotassium phosphate or potassium methyl or ethyl phosphate, also are satisfactory hygroscopic coating materials. Dipotassium phosphate is very effective at relative humidities in excess of about 30 percent. For example at 50 percent relative humidity, dipotassium phosphate will carry about 40 percent of water, which is adequate to maintain it in the form of an oily or mobile liquid. However, below about 30 percent relative humidity, it will dry out to a crystalline solid. Therefore, it is less suitable for use in treating soap which will be exposed to very low humidities. The presence of an alkyl group, such as an ethyl or methyl group, in place of one of the alkali metal ions, results in compounds which will retain their fluidity at extremely low humidities. Alkyl phos phates, having the formula MRHP-O4, in which M is an alkali metal and R is an alkyl group, therefore, are particularly suitable for use as coating agents for granulated soap under all conditions of relative humidity.
The above mentioned compounds also cause any dust particles to aggregate into larger particles or adhere to large soap granules. They also minimize the formation of static charges and thus reduce the tendency of any small soap particles to remain-in suspension.
Other hygroscopic materials may be used such as potassiumcarbonate, potassium silicate, disodium phosphate and calcium or magnesium chloride. Other hygroscopic materials which also function as wetting agents maybe used since these materials contribute to the plasticity of the soap particles because of their wetting nature and strengthen the bond between aggregates of fines and between the fines and the particles of normal size.
I-Iygroscopic substances or those which themselves may be conductors have the additional chracteristic of preventing the formation of static charges on the soap particles for the reason that they render the surfaces of the particles conductive, and thus reduce the tendency of the dust to remain in suspension in air.: Such substances which might be used for this purpose would include, for example, glycerin, dipotassium phosphate, sodium potassium ethyl phosphate, triethanolamine ethyl phosphate, glycerin and dipotassium phosphate, glycerin and sodium potassium ethyl phosphate, glycerin and potash coconut oil soap, water-soluble sulfonated oils and lithium chloride.
The various materials mentioned may be used alone or in any admixture.
These coating compositions should be present in sufficient proportion to obtain the desired results and yet not in such proportion that they will cause lumping and formation of aggregates of such size that the characteristic of rapid dissolving, which is desirable in granulated soaps, is materially reduced.
It is desirable to prevent excess quantities of the coating material from impinging upon the soap particles in order to prevent them from sticking or lumping together and interfering with their normally free-flowing properties. Since the coating material is applied only to the surface of the particles, very small quantities are required. This makes the process particularly economical and achieves results that would be prohibitive from the standpoint of cost if the material were incorporated within the soap before it was placed in granular form.
The amount of the hygroscopic material to be employed will depend upon the hygroscopic character of the material selected, the nature of the soap, the climatic conditions where the product is to be used, etc. Soaps made from certain fatty acids and alkalies and having certain fillers and builders have different degrees of natural plasticities and water retentivity. This fact coupled with the different hygroscopic character of various materials makes it difficult to state any range applicable to all of the hygroscopic materials, When glycerin is used, for example, an amount of about 0.5% to 6.0% based on the weight of the soap, is preferable. It is believed that in view of the generic disclosure and the specific example, one skilled in the art would readily be able to determine the amount to be used in any particular instance, depending upon the particular soap to be treated and the use to which it is to be put.
It will be understood that a greater or less amount of the coating composition referred to may be used, depending on the character and physical characteristics of the granulated soap treated. Greater amounts of these coating compositions may be used, although this increases the cost of treating the soap.
An embodiment of my invention that is of particular importance is the use of calcium chloride as a hygroscopic agent. Normally the addition of a calcium compound to soap or to water in which soap is to be used would be thought of as objectionable because it is the calcium which causes hardness in water. This is normally thought to be a disadvantage and calcium is an ingredient sought to be eliminated. It is, nevertheless, surprising that the amount of calcium chloride to be added to the surface of the soap particles as a hygroscopic material to preserve the moisture content may be so small as not to interfere seriously with the increase in hardness properties. For example, the amount of calcium chloride to be applied to the soap may be within the range of 0.25% to 1.0% based upon the weight of the soap. When this soap is used in water in a concentration of 0.4%, which is an ordinary concentration for laundry, the amount of calcium introduced into the wash water as a result of using the treated soap will increase the hardness of water only about 16 parts per million. This is very small considering the fact that hard water ordinarily runs as high as 100 to 500 parts per million in the hard water districts. The percentage increase is relatively small.
When the soap is made with tetrasodium pyrophosphate as a builder, it is desirable to have an amount of calcium present in the water as this increases the detergent properties. In soft water districts if the amount of calcium in the water is not sufficient it may be added to secure this effect. In accordance with this invention calcium chloride may be added to the soap not only to prevent dusting but also as a convenient way of introducing the necessary calcium into the wash water,
It is characteristic of the invention that the hygroscopic material is applied to the surface of the particles as distinguished from an ingredient that is admixed with the soap composition before it is dried. In the latter case, the hygro scopic material would not have an opportunity to exert its hygroscopic character to any marked extent. As the soap particle dries, the moisture first leaves the outer surface and it is the outer surface which driesfirst. The moisture from the interior then migrates through the particle to the outer surface. Thus if the outer surface can be kept moist as a result of the hygroscopic material, there will be no tendency for the normal moisture on the interior to leave the particles. Furthermore, since it is only the surface of the particle which is in contact with the air from which moisture could be absorbed by hygroscopicity, there is no point in having the hygroscopic material at any point other than on the outside surface of the soap particles. Th hygroscopic material may be applied more or less uniformly over the surface of the soap particles and it may be applied more or less spotted or continuously over the surface. Since the hygroscopic agents will, for the greater part, be watersoluble, there is no objection to a continuous coating on the surface of the particles, although a partially spotted coating may be suflicient to keep the soap particles plastic with the coating of this amount and nature.
The hygroscopic material may be soluble in the soap or not. If not, it has the advantage that it will not tend to diffuse into the soap particles and will not require such a large quantity of material. On the other hand, the materials which penetrate tend to keep the entire mass of the soap particle plastic.
The coating materials may be applied to soap particles in various ways, and at any convenient time between the formation of the soap particles and the packaging step, The coating materials are preferably atomized and the soap particles allowed to fall through the atomized coating material. It is desirable to maintain the finest possible mist or fog of the material to be applied so that the most effective application can be made and even the finest of the dust particles forced into contact with the treating material. It has been found that a series of repeating treatments is effective in obtaining a desirable" dust-free product. Also, the coating composition may be applied by spraying in a rotary drum through which the soap particles are tumbled.
The major portion of the soap particles treated will, for the most part, vary in particle size from about 20 to mesh. They may be coated completely or partially with a single coating composition or a blend, simultaneously or in separate stages, as already-described. Any fine, objectionable, dust-likematerial will be. coated and will tend-to bond with the larger particles or with otherfi'ne material-to'fonn aggregates of a size larger than the: average size; of the dust particles. This will be the case not only with disintegrate-d or finesoap particles, but also with any dust formed as a result of the migrationor separation of the ingredients ordinarily present in the soap composition, suchas the hydrating salts,
It has been found that in general dust particles of a mesh of 140 or smaller are undesirable in the final product and are considered as dust. It has been found that dust particles of about 400mesh or smaller, as calculated on the bases of formulas for standard screens, will be air borne under conditions of relatively low air movement. These air borne particles might average 50 microns in size and smaller. They are, therefore, particularly undesirable as they can readily move into contact with the membrane of the nasal passages to cause irritation. Larger particles than 400 mesh may be air-borne under conditions of increased air movement and for the same reason should be rendered innocuous.-
From the foregoing it Will be apparent that the present invention has resulted in. the production of a. novel dustless type. of granular or comminuted soap product and that a simple process has been provided for obtaining such dustless soap granules. It will be understood that the present process can be. applied to any of the usual types of-granulated or powdered soaps in order to overcome their objectionable dusting characteristics and that by means of thep-rocessshrinkage in packaging or in weigh-t may be largely avoided.
This application is a continuation-in-part of my'pending application Serial No. 351,111, filed August 3, 1940, now Patent No. 2 329,694.
It will be understood that coating compositions similar to but other than those mentioned specifically above may be used without departing from the invention.- Therefore, the forms of the invention described above should be considered as illustrative and not as limiting the scope of the following claims. I a
I claim: v
l. A process of treating granulated water soluble soap to'prevent substantially the formaticn of dust therein, comprising applying to the particles of soap a superficial coating, of a hygroscopic alkaline earth metal chloride in an amount to inhibit dehydration of the soap and the formation of soap dust. partic1es,,-but; not to. increase greatly the hardness properties. ofth water when the soap is used in ordinary concentrations for laundry. 1
2. The process of. claim. 1 in whichthe. soap particles are spray dried, and the alkaline earth metal chloride. which is applied is calcium chloride. i
3. The process of claim 2 in which the calcium chloride is applied to the surface of the soap particles by spraying.
4. The process of claim 3 in. which the amount of calcium chloride applied is within the range of 0.25% to 1%, based on the weight of the soap. 5-. A Water soluble soap product comprising granulated soap particles. having on at least a portion of. their surfaces at superficial coating of a hygroscopic alkaline earth metal chloride in an amount to inhibit dehydration of the soap particles and dusting of the-soap product, but not to increase. greatly the hardness properties of the water when the soap product is used in ordinary concentrations in laundry.
6. The product of claim 5 in which the granulated soap particles are spray dried.
7. The product of claim 6 in which the alkaline earth metal chloride is calcium chloride.
8. The product of claim 7 in which the amount of calcium chloride is 0.25% to 1%.,
9. The product of claim 8 in which the soap particles contain tetrasodium pyrophosphate as a-builder. 1
- JOHN W. BQDMAN;
REFERENCES CITED The following references are of record'in the file of this patent: v
UNITED STATES PATENTS Number Name Date 1,692. 996 Richardson Nov. 27, 1928 1,853,151 Segur 1 Apr. 12, 1932 2,013,667 OBrien Sept. 10,1935 2,093,927 Preston Sept. 21, 1937 2,104,619 Lehmann Jan..4, 1938 2,174,450 Segura Sept. 26, 1939 2,183.173 Segura Dec. 12, 1939 2,183,337 Perkins Dec. 12, 1939 2.293350 Martin Aug. 18, 1942 2,298,650 Samaras et al. Oct. 13, 1942 2,307,253 Yee Jan. 5, 1943 2,326 984 Tomlin Aug.- 17, 1943 2,329,694 Bodman Sept. 21, 1943 Certificate of Correction Patent No. 2,465,346. March 29, 1949.
JOHN W. BODMAN It is hereby certified that errors appear in the printed specification of the above numbered patent requiring correction as follows:
Column 2, line 24, for packing read packaging; column 8, line 44, list of references cited, before the patent number 2,093,927 insert the following- 2,080,583 Haas Feb. 11, 1986 and that the said Letters Patent should be read with these corrections therein that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 4th day of October, A. D. 1949.
THOMAS F. MURPHY,
Assistant Oommz'esz'oner of Patents.
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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2730507A (en) * 1952-01-28 1956-01-10 Swift & Co Method of making dustless soap powder
US2759823A (en) * 1954-07-26 1956-08-21 Eastman Kodak Co Preparation of fixing powders
DE1000122B (en) * 1955-09-10 1957-01-03 Phil Willy Weiss Dipl Ing Dr Detergents, cleaning agents, soaking agents and dishwashing detergents with a low bulk weight
US2776943A (en) * 1951-05-14 1957-01-08 Procter & Gamble Treatment of soap particles
DE1037050B (en) * 1954-11-20 1958-08-21 Richard Huttenlocher Dr washing powder
US2982736A (en) * 1961-05-02 Method of preparedg washing
US2990336A (en) * 1959-10-16 1961-06-27 Permanent Hair Waving Corp Process of hair waving and preparation therefor
US3112274A (en) * 1959-11-24 1963-11-26 Procter & Gamble Process for making a bleach composition
US3130166A (en) * 1957-05-16 1964-04-21 United States Borax Chem Granular soap compositions containing carbamide
US4704221A (en) * 1986-10-22 1987-11-03 The Procter & Gamble Company Granular detergents which contain high levels of anionic surfactant that forms a middle-phase, surface treated with a water soluble cationic surfactant
US10287171B2 (en) 2016-05-05 2019-05-14 Rec Silicon Inc Tumbling device for the separation of granular polysilicon and polysilicon powder

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US1692996A (en) * 1925-12-10 1928-11-27 Emma D Richardson Method for protecting granular substances and resulting product
US1853151A (en) * 1930-05-12 1932-04-12 American Soap & Glycerine Prod Treating fruit
US2013667A (en) * 1935-09-10 Process of making metallic soaps
US2093927A (en) * 1935-05-08 1937-09-21 Procter & Gamble Soap builder of reduced alkalinity
US2104619A (en) * 1936-07-02 1938-01-04 Pennsylvania Salt Mfg Co Noncaking smoked salt and method of making the same
US2174450A (en) * 1938-09-12 1939-09-26 Jefferson Island Salt Mining C Method for treating rock and evaporated salt
US2183173A (en) * 1938-12-22 1939-12-12 Jefferson Island Salt Mining C Method of treating salt and resulting product
US2183337A (en) * 1937-01-09 1939-12-12 American Smelting Refining Process of inhibiting dusting of arsenious oxide and product thereof
US2293350A (en) * 1940-04-25 1942-08-18 Monsanto Chemicals Stabilization of fatty acid derivatives
US2298650A (en) * 1938-01-05 1942-10-13 Monsanto Chemicals Particulate detergent composition
US2307253A (en) * 1940-10-22 1943-01-05 Claude R Wickard Process for the production of noncaking fertilizer materials
US2326984A (en) * 1941-12-04 1943-08-17 Monsanto Chemicals Thiuram sulphides
US2329694A (en) * 1940-08-03 1943-09-21 Lever Brothers Ltd Dedusting process and the product thereof

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2013667A (en) * 1935-09-10 Process of making metallic soaps
US1692996A (en) * 1925-12-10 1928-11-27 Emma D Richardson Method for protecting granular substances and resulting product
US1853151A (en) * 1930-05-12 1932-04-12 American Soap & Glycerine Prod Treating fruit
US2093927A (en) * 1935-05-08 1937-09-21 Procter & Gamble Soap builder of reduced alkalinity
US2104619A (en) * 1936-07-02 1938-01-04 Pennsylvania Salt Mfg Co Noncaking smoked salt and method of making the same
US2183337A (en) * 1937-01-09 1939-12-12 American Smelting Refining Process of inhibiting dusting of arsenious oxide and product thereof
US2298650A (en) * 1938-01-05 1942-10-13 Monsanto Chemicals Particulate detergent composition
US2174450A (en) * 1938-09-12 1939-09-26 Jefferson Island Salt Mining C Method for treating rock and evaporated salt
US2183173A (en) * 1938-12-22 1939-12-12 Jefferson Island Salt Mining C Method of treating salt and resulting product
US2293350A (en) * 1940-04-25 1942-08-18 Monsanto Chemicals Stabilization of fatty acid derivatives
US2329694A (en) * 1940-08-03 1943-09-21 Lever Brothers Ltd Dedusting process and the product thereof
US2307253A (en) * 1940-10-22 1943-01-05 Claude R Wickard Process for the production of noncaking fertilizer materials
US2326984A (en) * 1941-12-04 1943-08-17 Monsanto Chemicals Thiuram sulphides

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2982736A (en) * 1961-05-02 Method of preparedg washing
US2776943A (en) * 1951-05-14 1957-01-08 Procter & Gamble Treatment of soap particles
US2730507A (en) * 1952-01-28 1956-01-10 Swift & Co Method of making dustless soap powder
US2759823A (en) * 1954-07-26 1956-08-21 Eastman Kodak Co Preparation of fixing powders
DE1037050B (en) * 1954-11-20 1958-08-21 Richard Huttenlocher Dr washing powder
DE1000122B (en) * 1955-09-10 1957-01-03 Phil Willy Weiss Dipl Ing Dr Detergents, cleaning agents, soaking agents and dishwashing detergents with a low bulk weight
US3130166A (en) * 1957-05-16 1964-04-21 United States Borax Chem Granular soap compositions containing carbamide
US2990336A (en) * 1959-10-16 1961-06-27 Permanent Hair Waving Corp Process of hair waving and preparation therefor
US3112274A (en) * 1959-11-24 1963-11-26 Procter & Gamble Process for making a bleach composition
US4704221A (en) * 1986-10-22 1987-11-03 The Procter & Gamble Company Granular detergents which contain high levels of anionic surfactant that forms a middle-phase, surface treated with a water soluble cationic surfactant
US10287171B2 (en) 2016-05-05 2019-05-14 Rec Silicon Inc Tumbling device for the separation of granular polysilicon and polysilicon powder

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