Dispersions and emulsions comprising a fatty acid ester to reduce viscosity

Information

  • Patent Grant
  • 5549845
  • Patent Number
    5,549,845
  • Date Filed
    Thursday, January 21, 1993
    32 years ago
  • Date Issued
    Tuesday, August 27, 1996
    28 years ago
Abstract
An emulsion or dispersion in which the continuous phase is aqueous and comprises gelatin wherein its viscosity has been reduced by addition thereto of a water-soluble protein or a surfactant which is an ester of a polyalkoxylate.
Description

This invention relates to dispersions and emulsions and, in particular, to those in which the continuous phase comprises aqueous gelatin.
The abstract of JP-A-59-072 410 describes a negative photoresist solution comprising gelatin as binder which has its viscosity and gel temperature lowered by the addition of 20 to 70 wt. % casein. Such a solution does not contain solid particles or any discontinuous liquid phase.
Photosensitive photographic silver halide materials contain silver halide/gelatin emulsions and, in many colour materials, also contain dispersions of droplets of colour couplers in high boiling coupler solvents in a continuous aqueous gelatin phase. In fact the terms emulsion and dispersion are used erroneously interchanged but their nature is well understood by the photographic chemist.
There are a number of factors which tend to increase the viscosity of such emulsions and dispersions. This often leads to undesirable effects, especially when coupled with the phenomenon of shear thinning which can occur when dispersions and emulsions are mixed, pumped or emerge from coating hoppers. Non-uniform coatings can be due to such phenomena. The present emphasis on thin layers can aggravate these problems.
Accordingly the present invention provides a means for reducing the viscosity of such emulsions and dispersions.
According to the present invention there is provided an emulsion or dispersion in which the continuous phase is aqueous and comprises gelatin wherein the viscosity of the emulsion or dispersion has been reduced by addition thereto of a water-soluble protein at a concentration of from 0.01 to 10% or a surfactant which is an ester of a polyalkoxylate.
The water-soluble protein may, for example, be casein or a caseinate salt, .alpha.-lactalbumin, .beta.-lactoglobulin, ovalbumin or conalbumin. The surfactant is preferably an ester of a polyethoxylate, especially a carboxylic ester and particularly a fatty acid ester thereof. The polyalkoxy moiety may contain 4 to 30 alkoxy units which are typically derived from ethoxy or glycidyl units. Examples of suitable fatty acids are stearic, lauric, palmitic and oleic acid. Specifically the surfactant may, for example, be from the commercially available TWEEN.TM. (Honeywell Atlas), CRILLET.TM. (Croda), or ARMOTAN.TM. (Akzo) ranges.
The addition may be made to the emulsion or dispersion before, during or after its initial formation. Preferably the addition is made as an aqueous solution of the material. The amount added is preferably from 0.1-5% and especially from 1-2%.
The emulsions may be any photographic silver halide emulsions. For example they may be any of those emulsions mentioned in Research Disclosure, December 1978, Item 17643, published by Kenneth Mason Publications Ltd., 12a North Street, Emsworth, Hants PO10 7DQ, U.K.
The dispersions may have a discontinuous phase comprising a high boiling coupler solvent and a photographic colour coupler. Information on such couplers and on methods for their dispersions are given in Sections VII and XIV, respectively, of the above Research Disclosure article.





The invention is illustrated in the following Examples. The Couplers used in the Examples are as follows: ##STR1##
EXAMPLE 1
To 10 g Samples of the following photographic coupler dispersion:
______________________________________OILCoupler (A) 151 gDibutyl phthalate 38 g2-(2-butoxyethoxy)ethyl acetate 11 gGELDry gelatin 91 gWater 638 ml10% ALKANOL XC .TM. 60.5 g2N Propionic Acid 8 ml.2N sodium hydroxide 2.4 ml______________________________________
formed by adding the oil solution to the gelatin solution and mechanically dispersing it therein, were added a range of volumes of a 10% solution of sodium caseinate solution. After standing for not less than 15 minutes the viscosities were measured on a BROOKFIELD LVT.TM. microviscometer. A similar series was prepared in which the dispersion was diluted with water only. The results are given in FIG. 1 of the accompanying drawings and show that caseinate solution lowers the viscosity much more than the control additions of water.
EXAMPLE 2
The procedure described in Example 1 was repeated with the following dispersion of a photographic colour coupler:
______________________________________OILCoupler (B) 87.4 gDibutyl phthalate 44 g2-(2-butoxyethoxy)ethyl acetate 13 gDioctylhydroquinone 8 g2,2-dimethyl-4-isopropyl-6- 37 ghydroxy-7-octyl-chromanGELDry gelatin 87.4 gWater 612 ml2N Propionic acid 5.1 ml2N NaOH 9.1 ml10% ALKANOL XC .TM. 96.2 ml______________________________________
The results are given in FIG. 2 of the accompanying drawings and show that caseinate solution lowers the viscosity much more than the control additions of water.
EXAMPLE 3
The procedure described in Example 1 was repeated with the following dispersion of a photographic colour coupler:
______________________________________OILCoupler (C) 100 gDibutyl phthalate 54 g2-(2-butoxyethoxy)ethyl acetate 8 gDioctylhydroquinone 8 gGELDry gelatin 99 gWater 698 ml2N Propionic acid 11 ml2N NaOH 5 ml10% ALKANOL XC .TM. 35 ml______________________________________
The results are given in FIG. 3 of the accompanying drawings and show that caseinate solution lowers the viscosity much more than the control additions of water.
EXAMPLE 4
Samples of the dispersion described in Example 3 were mixed with a range of weights of a 10% solution of TWEEN 60.TM. (a polyoxyethylene monostearate having 20 oxyethylene residues in the molecule). The results are shown as an additional line on FIG. 3 in which it can be seen that its viscosity-reducing effects are greater than that of sodium caseinate in Example 3.
EXAMPLE 5
To 1.0 g of Coupler (D) was added 0.5 g of a UV absober of the formula: ##STR2## 0.5 g di-n-butyl phthalate, and 0.5 g of the surfactant PETRONATE L.TM.. These components were dissolved together by heating and stirring, and the resulting oily solution was mechanically dispersed into 8.0 g of 7.8% w/w aqueous gelatin solution.
Caseinate solutions were added to 10 g samples of the above dispersion as in Examples 1-3 and the results are shown in FIG. 4. Again, the caseinate solution reduces the viscosity more than the comparative water additions.
Claims
  • 1. An emulsion or dispersion comprising a continuous phase comprising an aqueous solution of gelatin and a discontinuous phase comprising a water-immiscible solid or liquid, wherein the viscosity of said emulsion or dispersion has been reduced by addition thereto of a surfactant which is a fatty acid ester of a polyethoxylate at a concentration of from 1 to 2%.
  • 2. An emulsion or dispersion according to claim 1, wherein the fatty acid part to the ester is derived from stearic, lauric, palmitic or oleic acid.
Priority Claims (1)
Number Date Country Kind
9016473 Jul 1990 GBX
PCT Information
Filing Document Filing Date Country Kind 102e Date 371c Date
PCT/EP91/01378 7/24/1991 1/21/1993 1/21/1993
Publishing Document Publishing Date Country Kind
WO92/01971 2/6/1992
US Referenced Citations (4)
Number Name Date Kind
2401718 Young Jun 1946
3617292 Gantz Nov 1971
3762928 Williems Oct 1973
3912517 Van Poucke et al. Oct 1975
Foreign Referenced Citations (4)
Number Date Country
1173540 Feb 1959 FRX
1313700 Nov 1962 FRX
59-072410 Apr 1984 JPX
1038029 Aug 1966 GBX