US3800033A

US3800033A - Hair control compositions and method of use

Info

Publication number: US3800033A
Application number: US00313077A
Authority: US
Inventors: R Flawn; M Nearn; P Petter
Original assignee: Lever Brothers Co
Current assignee: CPPD Inc A CORP OF
Priority date: 1971-12-08
Filing date: 1972-12-07
Publication date: 1974-03-26
Anticipated expiration: 1991-03-26
Also published as: AU4964072A; IE36981L; FR2162563A1; SE394946B; AU462765B2; DE2259515A1; PH11066A; BE792261A; FI55441B; LU66590A1; ZA728586B; AT328621B; IN137892B; ATA1033272A; CA975298A; IT999517B; DK132204B; JPS4862951A; CH578869A5; FR2162563B1

Abstract

A hair control preparation, particularly an aerosol hairspray, comprises a solution of a film-forming resin and a normally solid plasticiser for the resin which gradually volatilises from the resin after the hair control preparation has been applied to the hair, the weight ratio of resin to volatile plasticiser being from 1:2 to 20:1.

Description

United States Patent Flawn et al.

HAIR CONTROL COMPOSITIONS AND METHOD OF USE Inventors: Richard Edwin Flawn, Shepperton; Malcolm Richard Neam, Camberley; Peter John Petter, Maidenhead, all of England Assignee: Lever Brothers Company, New

York, NY.

Filed: Dec. 7, 1972 Appl. No.1 313,077

Foreign Application Priority Data Dec. 8, 1971 Great Britain 56968/71 U.S. Cl..l 424/47, 424/71 Int. Cl A6lk 7/10 Field of Search 424/71, 47

[56] References Cited UNITED STATES PATENTS 3,400,198 9/1968 Lang 424/71 3,723,616 3/1973 Erlemann et a1. 424/71 Primary Examiner-Sam Rosen Attorney, Agent, or Firm-Louis F. Kline, Jr.

[ 5 7] ABSTRACT 8 Claims, No Drawings HAIR CONTROL COMPOSITIONS AND METHOD OF USE This invention relates to hair preparations, and more particularly to hair control preparations for holding the hair in a desired configuration. Preparations of this .kind include hair setting lotions and hairsprays, the

hairsprays, who use the productsfrequently find thatthe resin deposited on the hair tends to build up despite brushing of the hair between applications and that as a consequence the hair becomes progressively more difficult to comb and brush out. Furthermore, this accu-' 1 mulation of resin gives the hair an unnatural feel. One

can, of course, mitigate this disadvantage by applying less resin to the hair, but this, however, results in less hold being obtained.

1n the work leading up ,to the present invention we found that the resins which have the better hair retaining properties are those which. are relatively flexible whereas those which are the more easily combed or brushed out of the hair'are the more brittle resinsaln other words, those resins having the lower glass transition temperatures (Tg) have the better hold characteristics and those of higher glass transition temperatures have the better comb-out properties.

We have now discovered that improved hair control preparations can be formulated by including along with resin a resin-modifying agent which is normally solid (i.e.', is solid at 20 C) and which softens the resin and improves its initial holding properties but which over a relatively shortperiod of time, say within hours, volatilises from the hairwhereby the resin is gradually converted into a form in which it is more easily combed out of the hair.

Accordingly the invention provides a hair control preparation comprising a solution of a film-forming resin and a normally solid material which plasticises the resin and which gradually volatilises from the resin after applying the preparation to the hair, the weight ratio of resin to volatile plasticiser being from 1:2 to :1.

An advantage of the invention is that by the use of the volatile plasticiser one can improve the initial holding properties of the resin (matching that obtainable with acornparable or even greater amount of a softer resin) and produce a resin deposit which develops over a period of time an improved ease of removal as the plasticiser volatilises from the hair. From another aspect, the use of a volatile plasticiser in accordance with the invention permits one to improve the initial hold properties of a hair preparation without increasing the amount of the resin in the preparation: an increase in the amount of the resin would result in more resin being applied to the hair with the consequence that the hair would be more difficult to comb out.

The film-forming resins used in preparations in accordance with the invention desirably have glass transition temperatures (Tg) of at least 20 C. The use of the Tg is a common way of characterising resins and is described for example by Burrell, H in Official Digest, 34, 131 (1962). It can be determined by the technique known as Differential Thermal Analysis (see, for example, the method of Keavney, JJ and Eberlin, EC in J.Appl.Polymer Sci., 3 47 (1960). A high Tg is an indication of the brittleness of a resin.'ln accordance with our finding that the more brittle the resin the more easily it is combed out of the hair,the preferred resins used in hair compositions of this invention are those having a Tg of at least 35 C and usually no more than 150 C.

Compatible Volatile Resin Plasticisers LUVlSKOL VA 28l propionamide (a copolymer containing benzoic acid 20% vinyl pyrrolidone and salicylic acid vinyl acetate having menthol a Tg value of 42C and thymol supplied as a 50% solution in isopropanol) methyl-Lnaphthylketone LUVISKOL VA 37E propionamide (a copolymer containing benzoic acid 30% vinyl pyrrolidone and salicylic acid 70%'vinyl acetate having hexachloroethane a Tg value of 65C and benzophenone supplied as a 50% solution in ethanol A copolymer containing propionamide about 43% rnethacrylic acetamide acid and about 57% hexachloroethane methyl acrylate having benzo'phenone a Tg value of 95C We have also found that propionamide is also a suitable volatile plasticiser for use with the following reslnSZ Resin Tg Value" "C Bina 405, an acrylic ester amide copolymer containing carboxyl groups National Starch Resyn 28-1310, a copolymer of vinyl acetate and crotonic acid Aristotlex C, a copolymer of vinyl acetate and crotonic acid VEM 640 M48, a vinyl terpolymer containing ester, acrylic and carboxyl groups (supplied as a 48% solution in ethanol) Gantrez ES 225, a copolymer of methyl vinyl ether and monoethyl ester of maleic acid (supplied as a 50% solution in ethanol) Gantrez ES 335-l, a copolymer of methyl vinyl ether and monoisopropyl ester of maleic acid (supplied as a 50% solution in isopropanol) Gantrez ES 435, a copolymer of methyl vinyl ether and monobutyl ester of maleic acid (supplied as a 50% solution in isopropanol) as determined by the Keavney et al. method) 3 The vapour pressures at a temperature of 25 C and at a pressure of 760 mm Hg of the volatile plasticisers referred to above are as follows:

Vapour Pressure estimated values It is to be understood that the invention is not limited solely to the resin/volatile plasticiser combinations specifically referred to above. Some experimentation may be necessary in order to select other suitable combinations of resin and normally solid volatile plasticiser for use in the present invention. A plasticiser for one resin is not necessarily suitable for plasticising another resin. For instance, benzophenone, when used with resins obtained by copolymerising vinyl pyrrolidone with no more than an equal amount of vinyl acetate (and with certain other water-soluble resins) is reported in British Patent Specification No. 868,879 to result in a stiffening of the resin (i.e., the opposite of a plasticising effeet).

The film-forming resin and the volatile plasticiser are both present in the hair preparation as a solution in a mutually suitable solvent. As an example, the solvent can be a volatile organic solvent such as an alcohol, especially ethanol, isopropanol or 2-methoxyethanol: methylene chloride is also a suitable volatile organic solvent.

The weight ratio of film-forming resin to volatile plasticiser in the hair preparation according to the invention is from 1:2 to :1. By appropriate choice of the ratio of resin to plasticiser and of the content of resin in the solution, it is possible to obtain hair preparations which differ widely in their properties.

- At low resimplasticiser ratios, the difference between the degree ofhold exerted by the hair preparation initially and that exerted when the majority of the plasticiser has volatilised is quite marked, whereas at-high resinzplasticiser ratios the difference between the initial hold and the hold at a later time is less marked.

The preferred weight ratio of film-forming resin to volatile plasticiser is from 1:1 to 10:1.

The amount of resin present in the solution will depend on the degree of hold the product is intended to produce and will usually be from 1 to 10 percent by weight of the solution.

The hair preparation is preferably in the form of an aerosol hairspray. In this case the solvent, especially one of those previously exemplified, the film-forming resin and the volatile plasticiser will be present in an aerosol dispenser together with a suitable aerosol propellant, usually a liquefied normally gaseous substance. Commonly used propellants are trichlorofluoromethane (propellant l 1) and dichlorodifluoromethane (propellant 12) but others may be employed. Suitable propellants and propellant mixtures 4 for use with hairsprays are well known tothose in the art.

Aerosol hairspray preparations in accordance with the invention will comprise concentrate and propellant in the usual ratios, generally from about 2:1 to 1:5 with the concentrate having typically-the following composition:

% by weight Resin 1 to 10 Volatile plasticiser 0.05 to 10 Perfume 0.3 to 1 Solvent balance to In aerosol hairsprays, the amount by weight of resin based on the total weight of hairspray is usually from 0.5 to 4.0 percent.

In further embodiments of the hair control preparation of the invention other than those based on an aerosol formulation, the preparation may simply be in the form of a solution of the resin and plasticiser in the solvent, for example in the weight proportions as set out for the above concentrate. In other product forms, particularly for hair setting-lotions, an aqueous alcoholic solvent can be used. In certain other cases it might also be possible to use water as the solvent, although the presence of a volatile organic solvent is preferred to give a quick drying product. Other conventional ingredients can be incorporated, if desired, for example a denaturant for ethanol.

, In accordance with a further aspect of the invention, a process is provided for treating human hair to impart hold to a desired style and subsequently to facilitate the brush out property of the hair as the hold diminishes by applying to the hair a hair control preparation of the type defined herein.

Examples of hair control preparations in accordance with the invention will now be described. Percentages are by weight.

EXAMPLE 1 A hairspray of lotion was prepared having the following composition:

Luviskol VA 3715 (50% solution in ethanol) 6.0 Propionamide 0.6 Perfume 0.5 Denaturant 0.2 Industrial methylated spirit to 100.0

' 1 EXAMPLE 2 An aerosol hairspray was prepared having the following composition:

EXAMPLE 3 An aerosol hairspray was prepared having the following composition:

5 Luviskol VA 37E (50% solution in ethanol) 4.0 Benzoic acid 0.4 Perfume 0.2 Denaturant 0.1 Industrial methylated spirit 35.3 Propellant 11 39.0 Propellant 12 to 100.0

-Continued Perfume 0.20 2-methoxyethanol 6.00 Methylene chloride 36.21 Propellant 11 27.50 Propellant 12 to 100.00

The following Tests illustrate in vitro and in vivo experiments where hair control preparations according to the invention were applied to hair and certain properties of the hair were evaluated over a period of a few hours as the plasticiser volatilised from the resin. In two EXAMPLE 4 An aerosol hairspray was prepared having the follow- 15 ing composition:

2-amino-2-methyl-l-propancil is present as a neutralizing a en tqtthsr s o-r .3

EXAMPLE 6 An aerosol hairspray was prepared having the follow- 4 ing composition:

experiments, control data where a plasticiser was omitted from the hair preparation is also provided for comparison.

TEST 1 The following experiment showed the variation with time of the resistance to combing of hair switches when sprayed with an aerosol hairspray of the following composition: I

Copolymer 2.0 Plasticiser 0.4 Industrial methylated spirit 37.6 Propellant l1 39.0 Propellant 12 to 100.0

Containing about 43% of methacrylic acid and about 57% of methyl acrylate switches of 28 cms' length, prepared from untreated Italian hair fitted with clips at each end were sprayed with the above aerosol hairspray for a predetermined time so that the same amount of resin was sprayed onto each switch. After various intervals of time four of the switches were taken and each switch drawn through a comb five times and an average combining resistance value determined for the switches. In

this experiment, the comb used was one which had a r strain gauge transducer cemented. onto the back of it and the varying resistance produced by varying strains on the gauge as the hair travelled through the comb was processed electronically. During the determination of the combing resistance value, the hair switches were in a cabinet maintained at a temperature of 23 C and a Propionamide 0.24 Farms 20 relative humidity of 35 percent. Denawyam (H0 The combing resistance values given below have Industrial methylated spirit 38.26 b d n Propellant 11 9, een correcte to a ow for any variation in resistance Propellant 12 to 100.00' to combing of the untreated switches, so that the values iven are a measure in em irica u r EXAMPLE 7 g p l mts, of the 111C ease in work required to comb the hair due to the applied An aerosol hairspray was prepared having the followh i ing composition: The above test procedure was carried out on a number of compositions containing different plasticisers National Starch Resyn 28-1310 2.00 and the results are gwen m Table 2 2 1 We have found that the hold of the hair as udged by Propionamide (140 users correlates well with the combing resistance.

TABLE 1 Time of Measurement Combing Resistance value of Combing Resistance Plasticiser Benzophenone Hexachloroethane Acetamide Propionamide 1 hour after spraying 195 195 225 130 2 hours after spraying 180 175 150 3 hours after spraying 170 145 95 4 hours after spraying 160 1 10 85 125 105 80 5 hours after spraying TEST- 2 A similar test was carried out with an aerosol hairspray of the following composition and the results are given in Table II.

Luviskol 37E (50% solution in ethanol) 4.0 Plasticiser 0.4 Perfume 0.2 lndustrial methylated spirit 35.4 Propellant l 1 39.0 Propellant 12 to 100.0

A similar comparison of the results for products B and C showed the preferences as set out in Table lVb.

TABLE II Time of Measurment Combing Resistance Value of Combing Resistance Plasticiser Propionamide Hexachloroethane Benzoic Acid Salicylic Acid 1 hour after spraying 170 180 114 256 2 hours after spraying 166 155 I10 200 3 hours after spraying 164 130 107 145 5 hours after spraying 160 82 92 132 8 hours after spraying 92 85 54 120 TEST 3 TABLE lVb A further test, similar to those described above, was a performed to demonstrate the effect on combing resiszzg i g tance at two hourly intervals after spraying of variation in the resinzplasticiser ratio. The test products used had Hlding PR B C Lack of stiffness B l in 100 following formula- Ease of brushing B 1 in 20 Z Stickiness after brushing B l in 10 Copolymer used in Test 1 Propionamide 2.4 ldt'l th1td"t 37.6 ,f "}i y e 393 Thus the addition of propionamide to a lightly hold- Propellant 1; to 100.0 ing resin allowed the superior hold of the control (product C) tobe matched while retaining the superior The results are given In Table 111- case of brushing and feel after brushing of the lighter holding resin (in product B).

TABLE III 40 TEST 5' Combing Resistance Value ResinzPlasticiser after (wt. ratio) 2 hours 4 hours 6 hours For a comparative product containing 2.4 percent of the resin and no plasticiser, the combing resistance value was constant with time at 88 units.

TEST 4 Two experimental hairsprays, one containing 2.4 percent of Luviskol VA 37E solution (Product A), the other containing 2.4 percent of Luviskol VA 37E solution together with 0.24 percent of propionamide (product B), were compared with a commercial hairspray containing 2.25 percent of National Starch Resyn 28-1310 (product C) in a user panel test involving 80 women. All the women used each of the three products for a two week period, at the end of which they completed a questionnaire on the performance of the hairspray.

Comparison of the results for products A and C showed the preferences as set out in Table [Va The following experiment was performed to investigate the loss by volatilisation of propionamide from a film of Luviskol VA 37E resin plasticized with this .,vg l atile material.

TABLE V Time of Analysis by weight of propionamide after spraying present in resin sample 30 mins 14.9 50 mins 6.7 mins 4.1 mins 2.3 20 hours 0.5

What is claimed is: 1. A hair control preparation for imparting hold to the hair yet enabling the hair subsequently to be easily brushed out as the hold diminishes, said hair control preparation comprising a solution of i. from about 1 percent to about percent by weight of a film-forming resin having a glass transition temperature of from about 20 C to about 150 C,

ii. a plasticiser for the resin which is a solid and which has a vapour pressure at a temperature of 25 C and a pressure of 760 mm Hg of from about 0.0000] mm to 2 mm Hg, and which gradually volatilises from the resin thereby diminishing the hold property of the preparation, after applying the preparation to the hair, and the weight ratio of film-forming resin to volatile plasticiser being from 2. The hair control preparation as claimed in claim 1, wherein the resin is a copolymer of vinyl pyrrolidone and vinyl acetate containing at least 70 percent by weight of vinyl acetate.

3. The hair control preparation as claimed in claim 1, wherein the resin is a copolymer of vinyl acetate and crotonic acid. v

4. The hair control preparation as claimed in claim 2, wherein the volatile plasticiser is propionamide.

5. The hair control preparation as claimed in claim 2, wherein the volatile plasticiser is selected from the group consisting of benzoic acid and salicylic acid.

6. The hair control preparation as claimed in claim 3, wherein the volatile plasticiser is propionamide.

7. The hair control preparation as claimed in claim 1, additionally comprising an aerosol propellant.

8. A process for treating human hair to impart hold to a desired style and subsequently to facilitate the brush-out property of the hair as the hold diminishes, which process includes the step of applying to the hair a hair control preparation as claimed in claim 1.

Claims

2. The hair control preparation as claimed in claim 1, wherein the resin is a copolymer of vinyl pyrrolidone and vinyl acetate containing at least 70 percent by weight of vinyl acetate.
3. The hair control preparation as claimed in claim 1, wherein the resin is a copolymer of vinyl acetate and crotonic acid.
4. The hair control preparation as claimed in claim 2, wherein the volatile plasticiser is propionamide.
5. The hair control preparation as claimed in claim 2, wherein the volatile plasticiser is selected from the group consisting of benzoic acid and salicylic acid.
6. The hair control preparation as claimed in claim 3, wherein the volatile plasticiser is propionamide.
7. The hair control preparation as claimed in claim 1, additionally comprising an aerosol propellant.
8. A process for treating human hair to impart hold to a desired style and subsequently to facilitate the brush-out property of the hair as the hold diminishes, which process includes the step of applying to the hair a hair control preparation as claimed in claim 1.