GB2028364A - Aerosol Preparations - Google Patents

Aerosol Preparations Download PDF

Info

Publication number
GB2028364A
GB2028364A GB7927810A GB7927810A GB2028364A GB 2028364 A GB2028364 A GB 2028364A GB 7927810 A GB7927810 A GB 7927810A GB 7927810 A GB7927810 A GB 7927810A GB 2028364 A GB2028364 A GB 2028364A
Authority
GB
United Kingdom
Prior art keywords
propellant
preparation according
aerosol
weight
aerosol preparation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB7927810A
Other versions
GB2028364B (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CHEMSICO Inc
Original Assignee
CHEMSICO Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by CHEMSICO Inc filed Critical CHEMSICO Inc
Publication of GB2028364A publication Critical patent/GB2028364A/en
Application granted granted Critical
Publication of GB2028364B publication Critical patent/GB2028364B/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/30Materials not provided for elsewhere for aerosols
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/02Emulsion paints including aerosols
    • C09D5/021Aerosols
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
    • C10M2201/042Carbon; Graphite; Carbon black halogenated, i.e. graphite fluoride
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • C10M2203/022Well-defined aliphatic compounds saturated
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • C10M2203/024Well-defined aliphatic compounds unsaturated
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/04Well-defined cycloaliphatic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/046Hydroxy ethers
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/02Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
    • C10M2211/022Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/06Perfluorinated compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/08Amides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/08Amides
    • C10M2215/082Amides containing hydroxyl groups; Alkoxylated derivatives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/28Amides; Imides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/10Phosphatides, e.g. lecithin, cephalin
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04Siloxanes with specific structure
    • C10M2229/041Siloxanes with specific structure containing aliphatic substituents
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/30Refrigerators lubricants or compressors lubricants
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/32Wires, ropes or cables lubricants
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/34Lubricating-sealants
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/36Release agents or mold release agents
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/38Conveyors or chain belts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/40Generators or electric motors in oil or gas winning field
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/42Flashing oils or marking oils
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/44Super vacuum or supercritical use
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/50Medical uses
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/04Aerosols

Landscapes

  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Cosmetics (AREA)
  • Medicinal Preparation (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

An aerosol preparation for providing a continuous film upon dispensing comprises an active ingredient, a propellant, an auxiliary solvent for the propellant, water and cocodiethanolamide as a dispersal agent.

Description

SPECIFICATION Aerosol Preparations The invention relates to aerosol preparations.
Heretofore, there have been innumerable, unsuccessful efforts to develop an aerosol emulsion for providing a continuous, uninterrupted film or coating, whether for decorative or protective purposes, such as with paints, various types of finishes, lubricants, etc., wherein water constitutes the continuous or external phase. With present day knowledge, oil-in-water emulsions have proved inadequate for such purposes as the same are productive of foams which may be basically of two types, that is, the conventional foams, such as, for producing shaving lather, and the sprayable foams used with window cleaners, starch sprays, bathtub cleaners, oven cleaners and the like.But such foams recognizedly are physically quite distinct from a consistent, unbroken film as the same are extremely porous with developed geometric structures determined by the surfactant used, and are hence incapable of film formation.
Correspondingly, the water-in-oil aerosol emulsions wherein oil is the continuous phase and the water the dispersed phase, have proved equally unproductive of a thin, uninterrupted film with such being used to produce non-foaming sprays, such as, room deodorants, and the like where a mist-like distribution within a space or volume is sought. Thus, neither type of emulsion has been found amenable to aerosolization for the creation of a nonbroken coating upon the particular surface to be treated, and foremost with respect to water borne active ingredients.
The present accepted incapacity of aerosols to be useful with water based coating agents, such as, for example, latex paints, has been an especial problem of long standing. With present technology, aerosols that reauire a smooth finish or film on spraying, such as paints, silicone, or the like have utilized solvents other than water as the vehicle. Typical of such solvents are hydrocarbons, sucn as aromatics, aliphatics, chlorinateds, fluorinateds and the like, wherein, in most instances, the propellant is generally soluble in such solvents and may be considered chemically as part of the solvent active mixture.Thus, in effect, resort has necessarily been made to a single phase system or solution wherein the active ingredient, such an an oil-based paint, is dissolved within a suitable solvent other than water, as oarticularly, within a wide range of compatible organic solvents. However, the utilization of such solvents or carriers has involved inherent peril factors, as for example, the high risk hazard in that aerosol paint is extremely flammable by reason of the incorporated solvent; and the majority of the commercially used and available solvents have low threshold limit values that are intensified by the atomization process of the selected aerosol.
Furthermore, most of these solvents have undesired ecological consequences in bringing about a further depletion of fossil fuel resources, as well as being uneconomical in light of the continual rise in cost therefor. Additionally, these solvents consistently cause unpleasant and even obnoxious odors.
Accordingly, to the present time there has been no means for aerosilizing agents for providing an unbroken film wherein water is utilized as the solvent so that water based paints, among other coating or finishing agents have had to be applied through means other than aerosols, since neither the utilization of emulsions or of single phase systems have proved efficacious.
There has, therefore, been a continuing effort to solve this problem as such would eliminate immediately the recognized and reluctantly accepted hazards of using aerosol systems with respect to oil based paints, among others.
Therefore, it is an object of the present invention to provide an aerosol preparation which is water based and is productive of an uninterrupted, continuous film and which eliminates all of the various hazards associated with the dispensing of aerosolized ingredients carried in the requisite organic solvents or vehicles.
It is another object of the present invention to provide a preparation of the character stated which is capable of producing a continuous film from a broad spectrum of film and coating agents, such as water-base paints, lubricants, sealants, mold releases, protective coatings, waxes, and the like.
It is a still further object of the present invention to provide a preparation of the character stated which upon dispensing provides a continuous film as distinguished from the foams and sprays heretofore attained by aerosolization of emulsions which are nonproductive of corrosion; which are not fundamentally flamable or toxic so that circumscription as to usage is eliminated thereby presenting a breadth of application hitherto unknown in the aerosol field.
It is a still further object of the present invention to provide a preparation of the character stated which has a substantially indefinite shelf life; merely requiring a degree of agitation prior to each application regardless of the transpired interval between dispensing.
It is another object of the present invention to provide a preparation of the character stated which may be most economically produced; there being no necessity of complex instrumentatioh and equipment for formulation as the same may be accomplished in accordance with well known production techniques; and which may be charged to individual containers and subjected to the preferred propellant with presently, generally utilized equipment.
Another object of the present invention is to provide a preparation of the type stated which is extremely effective in use; which has demonstrated a remarkable versatility in being adapted for accommodating a most extensive range of varied film-producing agents, so as to be endowed with a unique neo-universatility; and which preparation may be most economically produced and sold; and with the films developed thereby being tenacious, durable, and proof against rupture, scuffing or the like through the normal intended usage peculiar to the particular film.
The present invention contemplates the development of an aerosol preparation which through its unusual characteristics is both physically and chemically distinct from the customary aerosol emulsions, as well as from the single phase solutions as heretofore used for film formation by oil based paints and the like. The system of the present preparation does embody generally immiscible phases, one of which may be considered a water phase, and the other an active ingredient phase, which phases are normally clearly defined, sharply distinct, and separated. The active ingredient of the active ingredient phase is the agent to be provided in film or coating form and which phase also embodies a liquefied propellant or compressed gas propellant, or combinations thereof, together with a conventional solvent suitable for controlling the evaporation rate of the propellant.However, there is also, and most critically, provided within the active ingredient phase a predetermined quantity of what might be referred to as a dispersal agent, being soluble in both of said phases but in different degrees.
The preparation will thus in its normal state be unhomogenized with the two phases being sharply separated. The separation from a visual standpoint might be likened unto "creaming" as such occurs in various types of emulsions.
When the preparation is to be utilized, immediately prior to dispensing, the same is agitated and then substantially instantaneously dispensed, with the dispensed material being a transitory mixture.
As applied the dispensed matter will present a continuous film upon the applied surface, uninterrupted by any type of lacunae, pores or geometric formations so that a coating with desired thickness and entirely continuous is developed. As indicated, the present invention has been proved to be fully successful with water based paints, as well as numerous other film producing agents, none of which have been heretofore discovered to be amenable to film distribution by aerosolization. Although the constituents of the preparation will be discussed in greater detail below, attention is directed to the unique dispersal agent which is critical for the development of aerosol preparations of this invention.It has been found that cocodiethanolamide*, which has been heretofore recognized as an emulsifier, possesses certain unexpected and surprising properties when used in a predetermined proportionality in the two phase system of the present invention. It has been discovered that providing cocodiethanolamide in an amount approximating .5% by weight of the system or preparation will react with the water phase and the active ingredient phase to bring about what is generally considered an unstable emulsion, that is, wherein the phases tend to separate, but are capable of being brought into relative stability by agitation, and upon spraying the phases separate and revert to their constituent components whereby the active ingredient does not produce a continuous film but one which is highly irregular and interrupted, typical of the results obtained to the present time when water based solvents are utilized in aerosol form.
If the proportionality of the cocodiethanolamide is increased as within the range of immediately above .5% to approximately 2.5% by weight, a resulting stable emulsion is developed and thus the cocodiethanolamide acts in the expected manner of an emulsifying agent, as in a water-in-oil emulsion, so that upon dispensing of such a preparation containing such proportionality, a discontinuous broken film is presented despite the fact that the emulsion is stable. In its generally normal state the emulsion gives a visual appearance of a homogeneous, pasty character, consistent with its being considered stable.Thus, the foregoing merely underscores that cocodiethanolamide as used in the aforesaid proportion with the active ingredients of the preparations of this invention, serves in its characteristic function as an emulsifying agent and with the resultant dispersant being expectedly of a character unlike a continuous film.
However, if the quantity of cocodiethanolamide is increased beyond 2.5%, as within the specific range of 2.5 to 10% by weight, the system looses its stability so that a separation immediately develops which, at first glance, would bear a seeming resemblance to the unstable emulsion incorporating a .5% by weight of said agent as above described. Despite any visual similarity between the phase separations of the unstable emulsion and the preparation incorporating in excess of 2.5% by weight of cocodiethanolamide, such generally corresponding phases are quite different both chemically and physically.It is suggested that the preparation with the greater quantity of cocodiethanolamide has become a dispersion, that is atypical of traditional technology having, as stated, the immiscibility of the *A preparation of this compound which is fully effective for the purpose of this invention is offered commercially by Clintwood Chemical Company of Chicago, Illinois under the trademark CLINDROL 101-CG and constitutes an amber liquid having a congealing point of approximately 60C and with a specific gravity at 250C of .99. The free or unreacted fatty acid, as lauric, 3%-4% maximum and the pH 1% dispersion is between 8 and 9. This commercial compound is stated to possess solubility in alcohols, glycols, ketones, esters, aromatic and aliphatic carbons and chlorinated solvents, while also being dispersible in water at low concentrations of 1 to 2%. It is stated to become soluble at higher concentrations and with a 10% solution being quite viscous approximating a gel.
two phases being sharply defined. Without any intention of limitation, the preparation herein will be referred to as a "dispersion" merely to facilitate exposition. The agitation prior to dispensation merely promotes a momentary intermixture so that upon discharge the dispersion characteristics control as distinguished from the emulsion characteristics which would be overriding if the cocodiethanolamide was 2.5% or below. A continuous film is promoted by the dispersion as distinguished from the discontinuous character of the dispensing of an emulsion.
As developed more fully hereinbelow, the preferred effective range of cocodiethanolamide for aerosol preparations of the present invention is 2.5 to 3.5% by weight. However, research has demonstrated that additionai amounts up to 10% by weight bring about no diminution in the character and quality of the developed film. However, above 109/0 it has been discovered that the applied coating develops and undesirable thickness of a generally lumpy character so that beyond such limit a continuous, unbroken film is no longer achievable.
This crucial, unexpected action caused by the cocodiethanolamide is all the more apparent when one recognizes that the use of emulsifying agents in emulsions cause a predictive response. It is recognized that there are numerous factors which contribute to the relative stability or instability of a particular emulsion but generally when the emulsifier is below a predetermined proportionality the associated emulsion will be in an unstable state with the phases separated. As the emulsifier is added, the emulsion becomes relatively stable, with the phases intermixing to present a homogeneous appearance; and further addition of the emulsifier generally has no effect upon the stability of the emulsion.But with the present invention the further addition of cocodiethanolamide beyond substantially 2.5% by weight of the system brings about a destruction of the erstwhile stability so that if a stable emulsion did exist, one would necessarily expect that the further addition of the cocodiethanolamide would be without effect. As pointed out, this unusual and surprising action of this particular agent supports the view that the system is no longer an emulsion with all of the various accepted emulsion characteristics but becomes a dispersion, with the cocodiethanolamide manifestly ceasing to act as an emulsifying agent. Therefore, the crucialness of this agent to preparations formed in accordance with this disclosure is apparent. It should be fully understood that no other compound has been found to possess the requisite properties despite extensive investigatory efforts.
Active ingredients peculiarly adapted for incorporation in aerosol preparations of the present invention are water insoluble and comprehend the active phase of waterbase paints commonly referred to as latex paints, exemplary of which are acrylic emulsions, vinyl emulsions, vinyl copolymer acetate emulsions, alkyd emulsions and polyurethane emulsions; mold release and lubricating agents, as for instance, silicones, namely the alkyl polysiloxanes and polyorganosiloxanes; lecithin and other soya or animal fat derivatives; stearates, telefluoromers, as Teflon*; also synthetic lubricants, such as, butoxylated and ethoxylated glycols; as well as polybutene used for transmission belt dressing, etc.; and various common greases, such as lithium stearate, calcium stearate, petrolatum, aluminum naphthenate, and the like for utilization as lubricant coatings; moreover, mineral seal oil, as both a penetrant and a lubricant, às well as petroleum based hydrocarbon oils and synthetic oils are amenable to incorporation in preparations of the present invention. A further category of active ingredients would be constituted of the waxes, including animal waxes, such as beeswax and stearic acid; vegetable waxes, such as carnauba, bayberry and candellila, as well as the various artificial or synthetic waxes as obtained from distillation of paraffin base petroleum.The foregoing enumerated types and examples of active ingredients for forming constituents of aerosol preparations of this invention is not meant to be exhaustive but merely indicative of the comprehensive range of compounds which by virtue of the uniqueness of this invention may now be aerosolized in water borne systems to provide a continuous film which was heretofore deemed impossible through such aerosolization. All these compositions are of the type wherein the intended usage or purpose requires an unbroken coating.
Accordingly, the range of treatments is infinite when it is recognized that such preparations can provide lubrication, mold release, adhesives, sealants, water displacement sprays, wax coatings, polymeric finishes, such as for floors and like surfaces; inks and dyes; asphaltic undercoatings, polyurethane coatings, and paints.
The particular propellants embodied in aerosol preparations of the present invention are of generally accepted types, that is liquefied, such as, hydrocarbons or halocarbons, as fluorocarbons, and blends of the same, or compressed gases, or combinations of liquefied and compressed gases. The selection of the foregoing is dependent upon desired characteristics relating to evaporation rate, solubility, economics, pressure, and safety. The well known fluorocarbon 12 and fluorocarbon 114 are exemplary of halocarbon propellants equally useful. Generally the hydrocarbon propellants are liquefied petroleum gases, such as propane, butane and isobutane, such being more popular at the present time than the halocarbons due to the possible environmental efforts thereof.
Also, compressed gas propellants, such as carbon dioxide, nitrogen, nitrous oxide, and dimethyl ether may be used with the same facility as with other aerosol preparations but with attention, of course, directed to such considerations as stability and pressure requirements for selection determination.
*TEFLON is a trademark of E. I. DuPont De Nemours s Co., Inc. for tetrafluoroethylene resins.
It is to be understood that the choice of propellant in the present invention is dictated by the same considerations as in aerosol preparations generally and, thus, the precise propellant does not form a part of the present invention.
In order to appropriately control the properties of the selected propellant, a wide range of organic auxiliary solvents for the propellants are used, all as in accordance with known technology. Such solvents are used to control the evaporation rate of the propellant, avoiding rupture of the finish applied, and which evaporation rate may also be controlled by selecting a combination of solvents that will dry in time with the active ingredients.Included among such solvents are those which have heretofore been widely known in the aerosol field, such as aromatic hydrocarbons, examples of which are benzene, toluene, xylene, commercial solvents which flash at 1000 and 1500; aliphatics, and aliphatic petroleum napthas,~such as heptane, hexane, kerosene, lacquer diluent, napthol spirits, mineral seal oil, mineral spirits, odorless mineral spirits, deodorized kerosene, pentane, petroleum ether, Stoddard solvent, textile spirits, VM8P naptha, isoparaffinic hydrocarbons, as well as mixtures and blends thereof.
Another general class of auxiliary solvents are the chlorinated hydrocarbons; among the more commonly used are carbon tetrachloride; 1,1 1-trichlorethane, methylene chloride and perchlorethylene.
In addition to the foregoing, which is not meant to suggest an exhaustive compilation of suitable auxiliary solvents, there may be included tetra hydrofuran and 2-nitropropane. As indicated above, and as is implicit in the involved chemistry, the choice of solvents is made in accordance with well known considerations, such as, as indicated, evaporation rate control, compatability with the particular active ingredient, etc. Further, it is understood that such solvents may be intermixed or blended to produce a desired resultant characteristic. The blending of heptane and hexane is but illustrative in that a blend of the same would dry somewhat slower than hexane alone but faster than heptane if used alone.
The choice of auxiliary solvent is dictated by the same general considerations as in the field of aerosols and, hence, the precise auxiliary solvent does not form a part of the present invention.
Aerosol preparations having the properties of the present invention have the following general formula wherein liquefied propellants, namely the hydrocarbons and halocarbons are used: Percent by Weight Active Ingredient Approx. .1% to 50% Propellant Approx. 5% to 30% Dispersal Agent: Cocodiethanolamide 2.5% to 10% Auxiliary Solvent 10% to 25% Water Approx. 1 1% to 70% In those preparations wherein compressed gas constitutes the propellant, the general formulation will be as follows: Percent by Weight Active Ingredient Approx..1% to Approx. 50% Propellant 2% to 5% Dispersal Agent: Cocodiethanolamide 2.5% to 10% Auxiliary Solvent 10% to 25% Water Approx. 30% to 73% In those preparations wherein the propellant is constituted of a combination of the liquefied and compressed gases, the general formula will be as follows: Percent by Weight Active Ingredient Approx. . 1% to Approx. 50% Propellant: Liquefied 2% to 30% Gaseous . 1% to 5% Dispersal Agent: Cocodiethanolamide 2.5% to 10% Auxiliary Solvent 10% to 25% Water Approx. 10% to 75% The application of these formulations will become more intelligible as a study is made of specific formulae hereinbelow. However, it will be observed that the range of cocodiethanolamide is quite defined, all as fully discussed hereinabove; and that the proportionality of the propellant and the auxiliary solvents therefor also fall within well acknowledged ranges. Solvents therefor also fall within well acknowledged ranges. Solvents within an amount less than 10% by weight have not demonstrated the capacity to act efficaciously with the propellant and, similarly, levels above 25% appear to have an adverse effect upon the action of the propellant and also increase the potential hazard of flammability.An appreciation of the relative length of ranges with respect to the embodied water and the active ingredient may conceivably be more effectively understood when one considers these two components jointly so that the same in combination will constitute, on average, roughly 70 or slightly more percent by weight of the entire system wherein liquefied propellants are utilized. In compressed gas systems the combined water and active ingredients may jointly constitute as much as 85% by weight of the system.
Example I An aerosol preparation for providing a continuous paint coating may be formulated as follows: Percent by Weight Active Ingredient Latex Paint 49.9% Propellant 70% Isobutane/ 30% Propane 20% Dispersal Agent Cocodiethanolamide 2.8% Auxiliary Solvent Isoparaffinic Hydrocarbon 1 6% Water 11.3% The foregoing constitutes a general formulation useful with all of the well known water base paints. It will be observed that essentially 61.2% by weight of the formula is comprised of the water and the water-base paint which provide the appropriate viscosity and hiding characteristics essential for a pleasing, continuous, uninterrupted finish. The isoparaffinic hydrocarbon is relatively odorless and flashes off at a temperature that will not rupture the finish as evaporation occurs.One particular commercial preparation of this solvent is identified by the trademark ISOPAR L of Exxon Corporation.
As indicated above, the isobutanepropane mixture provides a suitable pressure for dispensing but, manifestly, other propellants are equally effective, such as fluorocarbon 1 2 and combinations of fluorocarbons 12 and 114 and others. Nevertheless this unique formulation will permit attaining an unbroken film which may have desired thickness which has not been heretofore achieved in the field of aerosols.
Example lI(a) The following exemplifies the constitution of an aerosol preparation in accordance with the present invention useful in the field of mold release: Percent by Weight Active Ingredient Alkyl Polysiloxane 4% Propellant 70% Isobutane/ 30% Propane 20% Dispersal Agent Cocodiethanolamide 3% Auxiliary Solvent Isoparaffinic Hydrocarbon 20% Water 53% This formula exemplifies a paintable silicone mold release preparation wherein the active ingredient, although constituting, seemingly, a small percentage of the formula, attains with the water present a continuous film for promoting ready mutual release of mold components.As a matter of interest the isoparaffinic hydrocarbon in this preparation may be of a type promoting a higher or faster evaporation rate and one commercial form thereof is identified by the trademark ISOPAR C, being a product of Exxon Corporation.
As revelatory of the range of propellants and solvents which may be useful with preparations of the present invention, a similar silicone mold release may incorporate the following constituents: Percent by Weight Active Ingredient Dimethyl Polysiloxane 2.5% Propellant Carbon Dioxide 4% Dispersal Agent Cocodiethanolamide 3% Auxiliary Solvent Hexane 20% Water 70.5% In this particular formulation, it is to be observed that the propellant is a compressed gas, in this instance, carbon dioxide. Thus, such is set forth to demonstrate the efficiency of the present preparations wherein either a liquefied propellant or compressed gas propellant is involved.
Example lI(b) The preceding example sets forth formulae for release agents wherein silicone is the active ingredient. However, release agents utilizing other than silicone as the release agent may be equally prepared by this invention. One such formula is as follows: Percent by Weight Active Ingredient Lecithin 2.5% Propellant Dichlorodifluoromethane 20% Dispersal Agent Cocodiethanolamide 3% Auxiliary Solvent Mineral Spirits 1 5% Water 59.5% Another example of such preparation is:: Percent by Weight Active Ingredient Lecithin 2.5% Propellant Difluoroethane 5.0% Dispersal Agent Cocodiethanolamide 3% Auxiliary Solvent Chlorothene 1 5% Water 59.5% Pressure Depressant n-Butane 1 5% The foregoing discloses the utilization of a pressure depressant, in this case, n-Butane, for bringing about a resultant pressure within the appropriate range in view of the normally excessive pressure of difluoroethane. Thus, the usual hydrocarbons and halocarbons may be used in association with depressants where required.
Example Ill The present invention is also productive of a silicone lubricant which may be aerosolized and provide the desired finish or film to the treated surface. An example of such preparation is as follows: Percent by Weight Active Ingredient Dimethyl Polysiloxane .1% Propellant 70% Isobutane/ 30% Propane 20% Dispersal Agent Cocodiethanolamide 3% Auxiliary Agent Isoparaffinic Hydrocarbon 20% Water 56.9% Another related formula for providing a silicone film as for lubrication and as particularly for belt rejuvenation is as follows:: Percent by Weight Active Ingredient Dimethyl Polysiloxane 2% Propellant Propane 15% Dimethyl Ether 5% Dispersal Agent Cocodiethanolamide 2.5% Auxiliary Solvent Methylene Chloride 15.1% Kerosene 8.2% Water 52.5% This formulation is of interest as revealing the incorporation of a mixture of propellants namely, propane and dimethyl ether, as well as a mixture of auxiliary solvents namely, methylene chloride and kerosene, preferably deodorized, which are productive of a desired drying time and avoidance of an adverse odor.
A still further formulation useful for providing a silicone film as a lubrication and wherein the propellant is a combination of liquefied and compressed gases, is as follows: Percent by Weight Active Ingredient Dimethyl Polysiloxane 5% Propellant Liquefied: propane 5% Gaseous: carbon dioxide 1% Dispersal Agent Cocodiethanolamide 2.5% Auxiliary Solvent Isoparaffinic Hydrocarbon 20% Water 66.5% Example IV The formula of this example is merely illustrative of the proportionality of the components for bringing about a continuous film as used for a dressing upon belts of various types, such as transmissions and the like: : Percent by Weight Active Ingredient Polybutene 10% Propellant 70% Isobutane/ 30% Propane 20% Dispersal Agent Cocodiethanolamide 3% Auxiliary Solvent Isoparaffinic Hydrocarbon 20% Water 47% Example V As developed hereinbelow, aerosol preparations produced in accordance with the present invention are also fully competent to provide a continuous film of grease to serve for lubricating a preselected surface, the provision of which further highlights the uniqueness of this invention and the provision through aerosolization in water borne systems of a surface coating which had not been believed capable of accomplishment to the present time.A representative formula is as follows: Percentby Weight Active Ingredient Lithium Grease 109/0 Propellant 60% Fluorocarbon 12 40% Fluorocarbon 114 30% Dispersal Agent Cocodiethanolamide 3% Auxiliary Solvent 50% Hexane 50% Heptane 10% Water 47% Example VI As the above disclosure impliedly indicates, the present invention is also adapted for dispensing a water-displacement/penetrant which will produce an unbroken film and an illustrative formulation for such purpose is as follows:: Percent by Weight Active Ingredient Mineral Seal Oil 10% Colloidal Graphite Dis persion 0.5% Ethylene glycol mono butyl ether 1% Propellant Isobutane 20% Dispersal Agent Cocodiethanolamide 3% Auxiliary Solvent Odorless Mineral Spirits 10% Water ' 55.5% In the foregoing exampre, it will be seen that the active ingredient may have certain components mixed therein to endow the same with properties which serve a particular application and thus demonstrate the versatility of this invention.
Example VII Another preparation productive of this development is one whereby a wax may be aerosolized and thus expeditiously and yet fully efficaciously provide the needed uninterrupted finish to the applied surface. The utilization of waxes for preserving and protecting various surfaces is indeed well recognized, being useful on surfaces of all character, whether metal, wood, leather or the like.One such formulation is as follows: Percent by Weight Active Ingredient Paraffin Wax 5% Propellant 70% Isobutane/ 30% Propane 20% Dispersal Agent Cocodiethanolamide 2.5% Auxiliary Solvent Isoparaffinic Hydrocarbon 15% Water 57.5% Another such formulation is: Percent by Weight Active Ingredient Paraffin Wax 5% Propellant Liquefied: isobutane 5% Gaseous: carbon dioxide 2% Dispersal Agent Cocodiethanolamide 2.5% Auxiliary Solvent Mineral Spirits 20% Water 65.5 Further examples of the broad range of waxes which can be dispensed for film formation of this invention are outlined in an illustrative fashion hereinabove.
Another type of preparation wherein wax constitutes the active ingredient as in a formulation referred to generically as leaf polish, is as follows: Percent by Weight Active Ingredient Carnauba Wax Emulsion 50% Propellant Nitrous Oxide 4% Dispersal Agent Cocodiethanolamide 3.5% Auxiliary Solvent Acetone 12.5% Water 30% This particular formula also exemplifies the utilization of the compressed gas propellant, nitrous oxide.
Example VIII Another formulation demonstrative of the incorporation of a propellant comprised of a combination of liquefied and compressed gases, within the scope of the present invention, is as follows: Percent by Weight Active Ingredient Ethoxylated Linear alcohol 2.5% Propellant Liquefied: propane 2.0% Gaseous: nitrogen .. 1% Dispersal Agent Cocodiethanolamide 3% Auxiliary Solvent Mineral Spirits 20% Water 72.4% The foregoing formulation is exemplary of the adaptability of the present invention for use with detergents and cleaning agents as the above formula is particularly useful in cleaning the white sidewalls of automotive tires.
Example IX The present invention has proved highly utilitarian for dispensing of weatherstrip caulking, thus demonstrating the remarkable versatility of this invention. The following formulation is illustratively typical: Percent by Weight Active Ingredient Latex Filler 40% Propellant Liquefied: Isobutane Gaseous: Nitrous Oxide 1% Dispersal Agent Cocodiethanolamide 3% Auxiliary Solvent Isoparaffinic Hydrocarbon 20% Water 11% In studying the foregoing formulae it will be appreciated that there has been no indication of the inclusion of customary preservatives and anti-corrosion agents; the use of which would be pursuant to the usual considerations and in keeping with customary techniques.
The formulations herewith submitted serve to demonstrate the broad range of active ingredients that may be incorporated in preparations of this invention for continuous film formation. It is understood that all of the various propellants and auxiliary solvents set forth in the foregoing as examples are equally effective as are the corresponding components set forth in the specific examples which merely establish the effectiveness of the present invention for myriad purposes.
It is to be observed that in the majority of the foregoing formulations hydrocarbons and halocarbons are the propellants most widely used. Compressed gas propellants are, as shown, fully useful with the present preparations but with the selectivity thereof being based upon usual considerations. Effective levels for nitrogen, have been found to be about 120 psig (approximately 2%) and for carbon dioxide approximately 50 to 90 psig (from approximately 2.5 to 5%). Nitrogen, although fully effective, has limited usage in view of the fact that the pressure requirements are too great for commercially available containers. Carbon dioxide would be the propellant of choice if stability studies for each application would demonstrate the lack of formation of carbonic acid.As pointed out hereinabove, the propellants useful in the present invention may be constituted of combinations of the liquefied and compressed gas types which are equally effective and are in many instances economyproducing.
The production of aerosol preparations conforming to the present invention may be effected in most facile manners, all in accordance with known procedures; with all involved steps being undertaken under normal ambient conditions and thus obviating the necessity of environmentally controlled conditions.
One such procedure is:- the active ingredient phase is first prepared by incorporating the particular ingredient in the indicated proportion, together with the selected auxiliary solvent and the required amount of cocodiethanolamide. As thus prepared, the active ingredient phase is subjected to agitation which is continued until a solution is formed. Then during continued agitation the prescribed quantity of water is blended in and agitation is maintained to effect an intermixture of the phases. The ultimate dispensing container is then filled in accordance with present technology, with the intermixture which has been maintained in an agitated state to the point of filling.Substantially instantaneously upon discontinuance of the agitation, the water phase and the active ingredient phase will separate and remain in such separated state pending subsequent agitation immediately prior to dispensing. Thus, the procedure for developing any of the myriad formulations embodying the present invention is accomplished in an econmical manner, being fully suitable for high volume production, and all in accordance with common practices so as to obviate expenditure for complex, costly equipment or the maintenance of close tolerance conditions.
Immediately prior to a proposed usage, the container for the particular preparation is manually agitated by the user which brings about a transitory mixture of the two phases being, in essence, a quick or most temporary dispersion in which state the discharge occurs. Upon discontinuing discharging the phases promptly separate into the normal, basically two phase condition and remain in such state pending subsequent discharge. Thus, the shelf life of aerosol preparations as developed herein is most extensive since the cyclic mixing and separation as developed through use and through non-use has no deleterious effect upon the ingredients and the phases so that regardless of the passage of time the continuous film produced by this invention is assured.

Claims (22)

Claims
1. An aerosol preparation comprising an active ingredient, a propellant, an auxiliary solvent for the propellant, water and cocodiethanolamide as a dispersal agent.
2. An aerosol preparation according to claim 1 in which the cocodiethanolamide comprises from 2.5% to 10% of the weight of the preparation.
3. An aerosol preparation according to claim 1 or claim 2 in which the active ingredient is water insoluble.
4. An aerosol preparation according to any preceding claim in which the auxiliary solvent comprises from 10% to 25% of the weight of the preparation.
5. An aerosol preparation according to any preceding claim in which the auxiliary solvent is an aromatic hydrocarbon, an aliphatic hydrocarbon, an aliphatic petroleum naptha, an isoparaffinic hydrocarbon, a chlorinated hydrocarbon or a mixture of two or more thereof.
6. An aerosol preparation according to any preceding claim in which the active ingredient comprises from 0.1% to 50% of the weight of the preparation.
7. An aerosol preparation according to any preceding claim in which the active ingredient is the active phase of a water-base paint, a wax, a grease, a polysiloxane, an alkyl polysiloxane, an alkyl polyorganosiloxane, polybutene, a petroleum based hydrocarbon oil or a synthetic oil.
8. An aerosol preparation according to any preceding claim in which the propellant is a liquified gas.
9. An aerosol preparation according to any preceding claim in which the propellant comprises from 5% to 30% of the weight of the preparation.
10. An aerosol preparation according to any preceding claim in which the active ingredient and the water jointly comprise more than 50% of the weight of the preparation.
11. An aerosol preparation according to any preceding claim in which the water comprises from 11% to 70% of the weight of the preparation.
12. An aerosol preparation according to any of claims 1 to 7 in which the propellant is a compressed gas.
13. An aerosol preparation according to claim 12 in which the propellent comprises from 2% to 5% of the weight of the preparation.
14. An aerosol preparation according to claim 12 or claim 13 in which the water comprises from 30% to 73% of the weight of the preparation.
1 5. An aerosol preparation according to any of claims 1 to 7 in which the propellant is a combination of a liquified gas and a compressed gas.
1 6. An aerosol preparation according to claim 1 5 in which the liquefied gas propellant comprises from 2% to 30% of the weight of the preparation and the compressed propellant gas comprises from 0.1% to 5% by weight of the preparation.
1 7. An aerosol preparation according to claim 1 5 or claim 1 6 in which the water comprises from 10% to 75% of the weight of the preparation.
1 8. An aerosol preparation according to any of claims. 1 to 11 or claims 1 5 to 1 7 in which the liquified gas is a liquified hydrocarbon, a liquified halocarbon, a mixture of liquified hydrocarbons, a mixture of liquified halocarbons, or a mixture of at least one liquified hydrocarbon and at least one liquified halocarbon.
1 9. An aerosol preparation according to any of claims 12 to 1 7 in which the propellant is compressed nitrogen, nitrous oxide, carbon dioxide or dimethyl ether.
20. An aerosol preparation according to any preceding claim in which the active ingredient, the propellant and the auxiliary solvent form a first phase, the water forms a second phase, the two phases are normally separate, and the cocodiethanolamide is soluble in both phases.
21. An aerosol preparation according to claim 20 in which the two phases are miscible upon agitation to create a transitory dispersion.
22. An aerosol preparation substantially as described herein with reference to any one of the Examples. ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
GB7927810A 1978-08-09 1979-08-09 Aerosol preparations Expired GB2028364B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US93221178A 1978-08-09 1978-08-09
US5873279A 1979-07-23 1979-07-23

Publications (2)

Publication Number Publication Date
GB2028364A true GB2028364A (en) 1980-03-05
GB2028364B GB2028364B (en) 1982-12-01

Family

ID=26737977

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7927810A Expired GB2028364B (en) 1978-08-09 1979-08-09 Aerosol preparations

Country Status (12)

Country Link
AU (1) AU528160B2 (en)
BR (1) BR7905092A (en)
CA (1) CA1125457A (en)
CH (1) CH644148A5 (en)
DE (1) DE2932301A1 (en)
FR (2) FR2433039A1 (en)
GB (1) GB2028364B (en)
IT (1) IT1218878B (en)
MX (1) MX152716A (en)
NL (1) NL174063C (en)
PT (1) PT70045A (en)
YU (1) YU192479A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0031531A2 (en) * 1979-12-14 1981-07-08 Frank Scotti Composition suitable for preparing a cellular foam, a method of caulking and insulating, and aerosol container containing said composition
EP0033792A1 (en) * 1980-02-07 1981-08-19 United Industries Corporation Aerosol preparation
US4597895A (en) * 1984-12-06 1986-07-01 E. I. Du Pont De Nemours And Company Aerosol corrosion inhibitors
US4604226A (en) * 1985-03-22 1986-08-05 E. I. Du Pont De Nemours And Company Aerosol corrosion inhibitors
EP0375010A1 (en) * 1988-12-07 1990-06-27 Mobacc B.V. Aerosol paint
US4968735A (en) * 1984-12-05 1990-11-06 Page Edward H Aerosol water based paint
WO1995009056A1 (en) * 1993-09-29 1995-04-06 Union Carbide Chemicals & Plastics Technology Corporation Methods for the spray application of water-borne coatings with compressed fluids
US5988455A (en) * 1994-12-16 1999-11-23 The Sherwin-Williams Company Latex aerosol paint products
WO2001098065A1 (en) * 2000-06-20 2001-12-27 Pennzoil-Quaker State Company Tire sealer and inflating composition and method of use

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4384661A (en) 1982-04-07 1983-05-24 Page Edward H Aerosol water-based paint compositions
US4381066A (en) 1982-05-10 1983-04-26 Page Edward H Polymeric foam caulking compositions
DE3347742A1 (en) * 1983-12-30 1985-07-11 IG Sprühtechnik GmbH, 7867 Wehr Deodorising spray
DE4132176C2 (en) * 1991-09-27 1997-03-13 Ig Spruehtechnik Gmbh Metered aerosols with isobutane as propellant

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2524590A (en) * 1946-04-22 1950-10-03 Carsten F Boe Emulsion containing a liquefied propellant gas under pressure and method of spraying same
US2907664A (en) * 1956-05-16 1959-10-06 Easy Glitter Wax Co Self-spraying wax polish and method for its production
US3092555A (en) * 1958-04-21 1963-06-04 Roy H Horn Relatively collapsible aerosol foam compositions
FR1439945A (en) * 1965-03-17 1966-05-27 Poitevine De Conditionnement S Improvements with aerosol cans
DE1617049A1 (en) * 1965-06-30 1971-02-11 Colgate Palmolive Co Aerosol mixture, in particular aerosol shaving cream
US3929492A (en) * 1971-11-26 1975-12-30 Johnson & Son Inc S C Surface treating compositions
DE2613410A1 (en) * 1975-03-31 1976-10-21 Risdon Mfg Co Non-corrosive water-based antiperspirant compsn - consisting of a continuous aq phase within a non aq carrier fluid
GB1578331A (en) * 1976-02-18 1980-11-05 Unilever Ltd Aerosol compositions

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0031531A2 (en) * 1979-12-14 1981-07-08 Frank Scotti Composition suitable for preparing a cellular foam, a method of caulking and insulating, and aerosol container containing said composition
EP0031531A3 (en) * 1979-12-14 1982-01-13 Frank Scotti Composition suitable for preparing a cellular foam, a method of caulking and insulating, and aerosol container containing said composition
EP0033792A1 (en) * 1980-02-07 1981-08-19 United Industries Corporation Aerosol preparation
US4968735A (en) * 1984-12-05 1990-11-06 Page Edward H Aerosol water based paint
US4597895A (en) * 1984-12-06 1986-07-01 E. I. Du Pont De Nemours And Company Aerosol corrosion inhibitors
US4604226A (en) * 1985-03-22 1986-08-05 E. I. Du Pont De Nemours And Company Aerosol corrosion inhibitors
EP0375010A1 (en) * 1988-12-07 1990-06-27 Mobacc B.V. Aerosol paint
WO1995009056A1 (en) * 1993-09-29 1995-04-06 Union Carbide Chemicals & Plastics Technology Corporation Methods for the spray application of water-borne coatings with compressed fluids
US5988455A (en) * 1994-12-16 1999-11-23 The Sherwin-Williams Company Latex aerosol paint products
WO2001098065A1 (en) * 2000-06-20 2001-12-27 Pennzoil-Quaker State Company Tire sealer and inflating composition and method of use
EP1167002A1 (en) * 2000-06-20 2002-01-02 Pennzoil-Quaker State Company Tire sealer and inflating composition and method of use

Also Published As

Publication number Publication date
FR2531973B1 (en) 1987-06-12
FR2531973A1 (en) 1984-02-24
DE2932301C2 (en) 1990-07-12
NL7906057A (en) 1980-02-12
YU192479A (en) 1983-09-30
FR2433039B1 (en) 1983-12-16
AU528160B2 (en) 1983-04-14
PT70045A (en) 1979-09-01
AU4967579A (en) 1980-02-14
CA1125457A (en) 1982-06-15
CH644148A5 (en) 1984-07-13
DE2932301A1 (en) 1980-02-21
NL174063B (en) 1983-11-16
IT1218878B (en) 1990-04-24
MX152716A (en) 1985-10-21
NL174063C (en) 1984-04-16
IT7924973A0 (en) 1979-08-08
BR7905092A (en) 1980-07-29
FR2433039A1 (en) 1980-03-07
GB2028364B (en) 1982-12-01

Similar Documents

Publication Publication Date Title
US4439343A (en) Aerosol preparation
US4439342A (en) Aerosol preparation
US2524590A (en) Emulsion containing a liquefied propellant gas under pressure and method of spraying same
GB2028364A (en) Aerosol Preparations
US4198313A (en) Propellant compositions for aerosols
US4439344A (en) Water dispersions
US3929492A (en) Surface treating compositions
US2907664A (en) Self-spraying wax polish and method for its production
US3395028A (en) Wax composition and method for making the same
US7053124B2 (en) Aerosol delivery systems
EP0503004A1 (en) Post-foaming shaving gels.
CA1089609A (en) Powdered solid aerosol composition and method of manufacture
US4365028A (en) Coating composition
JPH08302375A (en) Light lubricant and method of using it
US4655959A (en) Preparation of non-flammable aerosol propellant microemulsion system
CA1066836A (en) Aerosol latex paint containing imidazoline surfactants
US5397384A (en) Furniture polish composition
US5085849A (en) d-Limonene containing space or room aerosol deodorant
JPH07233001A (en) Aerosol composition
WO1981002023A1 (en) Aerosol preparation
EP0033791B1 (en) Preparations containing cocodiethanolamide
EP0033792B1 (en) Aerosol preparation
US4647309A (en) Waterborne firm coating for temporary protection of parts, providing controlled lubrication during assembly
US5653789A (en) Water base conditioner for acrylic wood flooring
BR112018068940B1 (en) AEROSOL PAINT BASED ON A LATEX EMULSION AND METHOD FOR MAKING AN AEROSOL PAINT BASED ON A LATEX EMULSION

Legal Events

Date Code Title Description
727 Application made for amendment of specification (sect. 27/1977)
727A Application for amendment of specification now open to opposition (sect. 27/1977)
727B Case decided by the comptroller ** specification amended (sect. 27/1977)
SP Amendment (slips) printed
PCNP Patent ceased through non-payment of renewal fee

Effective date: 19960809