GB665083A - Production of stable concentrated aqueous emulsions - Google Patents

Production of stable concentrated aqueous emulsions

Info

Publication number
GB665083A
GB665083A GB30482/49A GB3048249A GB665083A GB 665083 A GB665083 A GB 665083A GB 30482/49 A GB30482/49 A GB 30482/49A GB 3048249 A GB3048249 A GB 3048249A GB 665083 A GB665083 A GB 665083A
Authority
GB
United Kingdom
Prior art keywords
water
urea
butanol
formaldehyde
dissolved
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.)
Expired
Application number
GB30482/49A
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.)
BASF Schweiz AG
Original Assignee
Ciba AG
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 Ciba AG filed Critical Ciba AG
Publication of GB665083A publication Critical patent/GB665083A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/02Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
    • C08J3/03Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
    • 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
    • C09K23/00Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
    • C09K23/017Mixtures of compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2361/00Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
    • C08J2361/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Treatment And Processing Of Natural Fur Or Leather (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Colloid Chemistry (AREA)

Abstract

Concentrated emulsions which may subsequently be diluted with water or organic solvents are prepared by incompletely distilling off water and solvent from an oil-in-water emulsion such as described in Specification 645,023 in which the internal phase consists of an easily emulsifiable solution in a water-immiscible solvent, preferably an alcohol, of a water-insoluble hardenable condensate obtained from formaldehyde, a substance of amide character such as urea, thiourea, guanidine, biuret, dicyandiamide or melamine, and a water-immiscible alcohol, and of which the external phase consists of an aqueous solution containing, in addition to one protein as, such casein or gelatine, urea, thiourea or a mixture thereof. Suitable alcohols are butyl, amyl, hexyl, cyclohexanol or benzyl alcohol. The distillation is preferably effected under reduced pressure with vigorous agitation; if desired, water or a different organic solvent may be added before, during, or after distillation. Softening agents, filling materials, waxes and pigments may be added to the organic solvent constituting the inner phase, which solvent may be aliphatic or cyclic hydrocarbons, higher alcohols, ethers, esters, ketones or nitrobenzene. Additions to the aqueous phase may be emulsifying agents, softeners such as glycerine or polyglycol, hardening catalysts, filling or matting agents, pigments or buffers. Examples relate to the distillation of emulsions containing as the internal phase urea-formaldehyde-butanol resin, dissolved in butanol, an urea-formaldehyde condensate etherified with butanol and free from uncombined butanol and dissolved in metaxylene or a mixture of monochlorobenzene and ethyl alcohol, a melamine formaldehyde butanol resin dissolved in butanol, a urea/thiourea formaldehyde condensate modified with cyclohexanol, and a urea-formaldehyde condensate modified with 2-ethylhexanol dissolved in a mixture of 2-ethylhexanol and toluene. Specifications 597,390 and 650,977 also are referred to.ALSO:Concentrated emulsions which may subsequently be diluted with water or emulsified with organic solvents are prepared by incompletely distilling off water and solvent from an oil in water emulsion such as described in Specification 645,023 in which the internal phase consists of an easily emulsified solution in a water immiscible organic solvent, preferably an alcohol, of a water insoluble hardenable condensate obtained from formaldehyde, a substance of amide character such as urea, thiourea, guanidine, biuret, dicyandiamide or melamine and a water immiscible alcohol, and of which the external phase consists of an aqueous solution containing in addition to one protein such as acid casein or gelatine, urea, thiourea or a mixture thereof. Suitable alcohols are butyl, amyl, hexyl cyclohexanol or benzyl alcohol. The distillation is preferably effected under reduced pressure with vigorous agitation and if desired, water or a different organic solvent may be added before, during, or after distillation. Softening agents, filling materials, waxes and pigments may be added to the organic solvent constituting the inner phase, which solvent may be aliphatic or cyclic hydrocarbons, higher alcohols, ethers, esters, ketones or nitrobenzene. Additions to the aqueous phase may be emulsifying agents, softeners such as glycerine or polyglycol, hardening catalysts, filling or matting agents, pigments and buffers. Examples relate to the distillation of emulsions containing the internal phase urea-formaldehyde butanol resin dissolved in butanol, an urea-formaldehyde condensate etherified with butanol freed from uncombined butanol and dissolved in metaxylene, or a mixture of monochlorobenzene and ethyl alcohol, a melamine formaldehyde butanol resin dissolved in butanol, an urea/thiourea formaldehyde condensate modified with cyclohexanol, and an urea formaldehyde condensate modified with 2-ethylhexanol dissolved in a mixture of 2-ethylhexanol and toluene. Specifications 597,390, [Group IV], and 650,977 also are referred to.
GB30482/49A 1948-12-02 1949-11-28 Production of stable concentrated aqueous emulsions Expired GB665083A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH665083X 1948-12-02

Publications (1)

Publication Number Publication Date
GB665083A true GB665083A (en) 1952-01-16

Family

ID=4527222

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30482/49A Expired GB665083A (en) 1948-12-02 1949-11-28 Production of stable concentrated aqueous emulsions

Country Status (2)

Country Link
CH (1) CH272265A (en)
GB (1) GB665083A (en)

Also Published As

Publication number Publication date
CH272265A (en) 1950-12-15

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