Liquid Oxygen Compatible Biodegradable Dye Penetrant and Method of Dye

This invention relates to an improved liquid oxygen (LOX) compatible biodegradable dye penetrant composition and method for non-destructively testing material specimens to locate and identify surface voids, cracks or defects, prior to contacting such parts with liquid oxygen. The invention is especially concerned with a novel generally easily water washable, stable and sensitive dye penetrant composition of the above type having the characteristics of being able to disclose a wide range of defective conditions in parts, employing as solvent or vehicle essentially a biodegradable nonionic surfactant in the form of certain ethoxylated alcohols, and mixtures thereof, and incorporating an additive to render the composition compatible with liquid oxygen (LOX); and to a method utilizing such dye penetrant composition for non-destructive testing of parts subsequently contacted with liquid oxygen.

Dye penetrants are highly useful materials for nondestructive testing of metal work piece surfaces. In many important and expensive mechanical devices, it is necessary to inspect every metal component of the system for structural defects, prior to final fabrication, Dye penetrants are particularly useful in descreasing inspection processing time and can be highly sensitive in detecting micro-defects in metal components of aluminum, steel, nickel, titanium and the like.

In known penetrant inspection methods for rapid location and evaluation of surface flaws or cracks in test bodies or parts, a dye penetrant composition, preferably containing a fluorescent dye, and which will penetrate the openings of the surface cracks or flaws in the part, is applied to the surface of the test body, and the excess penetrant composition is removed from the surface of the body. A developer composition may then be applied to the part surface, which acts as a wick and causes the liquid penetrant containing the fluorescent dye, which was retained in the cracks or surface flaws, to be drawn up out of the surface defects by capillary action. The part is then exposed to appropriate lighting conditions, such as invisible fluorescigenous light, and the location of the surface flaws is revealed by the emission of visible fluorescent light by the penetrant dye which was retained in the cracks or flaws after the penetrant composition was removed from the surface of the part.

For best efficiency, particularly for the detection and location of minute surface cracks and flaws, as well as intermediate size and gross cracks, it is necessary that the dye penetrant composition have high sensitivity.

In addition, stability of the penetrant solution is essential without the necessity for carefully balancing the various liquid components of a dye penetrant solution in order to obtain efficient penetration of the solution into the cracks and flaws of a part, dye solubility, wetting action and washability control.

An additional criterion has recently developed also with respect to dye penetrant solutions and compositions. Generally, dye penetrant solutions presently being used and containing solvents and wetting agents present a disposal problem in that they are substantially non-biodegradable, that is, they are very difficult to decompose by bacteria in sewage disposal plants. Hence the necessity for the development of dye penetrant solutions and compositions which are biodegradable, that is which employ dye solvents and carriers which are biodegradable, and are readily available despite the petrochemical shortage, has attained considerable importance.

In my above copending application Ser. No. 444,433 there is disclosed a novel dye penetrant which has improved washability and sensitivity characteristics, and which is biodegradable, containing as the vehicle for the dye, certain biodegradable nonionic ethoxylated alcohols.

Further, where the parts to be inspected are to be later subjected to contact with LOX or a like strong oxidizer, it is particularly desirable that the inspection system, and the dye pentrants used in inspection do not increase the danger or sensitivity of the mechanical components to reaction with such strong oxidizers including LOX. For example, a large rocket propellant motor may use LOX, or a like strong oxidizer, in the rocket propellant. It is quite important under these circumstances that the LOX not be reactive with any traces or residues of the inspection dye penetrant which may remain in the cracks or defects of the inspected propellant tanks or other components, fabricated from inspected metal stock after cleaning.

In my U.S. Pat. No. 3,753,647 there is disclosed a liquid dye penetrant which is compatible with liquid oxygen and which comprises N-methyl-2-pyrrolidone, a mixture of a ketone and wetting agents, a fluorescent dye and a halocarbon. Although such dye penetrant composition has been found effective, it has the disadvantages of requiring a multiplicity of dye carriers or solvents, with proper balance thereof necessary to provide a desired sensitivity, and the composition is not biodegradable.

Accordingly, an object of the present invention is the provision of a readily water washable biodegradable dye penetrant solution or composition which is of simple formulation and which does not require the use of mixtures of conventional solvents and wetting agents, and which is formed of an essentially single or sole nonionic surfactant, and which is highly stable, has excellent sensitivity and is essentially nonflammable and non-toxic. A particular object of the invention is to provide a dye penetrant solution of the above noted type, and which incorporates an additive which eliminates the hazard of traces of dye penetrant reacting explosively with liquid oxygen or other strong oxidizers, substantially without affecting the biodegradability or sensitivity of the dye penetrant. A still further object is the provision of procedure employing such novel biodegradable and LOX safe dye penetrant composition for inspection of cracks, flaws and metallurgical conditions in metal structural components which are later to be placed in contact with liquid oxygen.

It has now been found that the above objects and advantages can be accomplished according to the invention, and an improved LOX and gaseous oxygen compatible liquid dye penetrant, having good sensitivity for detection of cracks and defects in metal surfaces, and which is biodegradable, is provided by employing as a solvent or carrier for the dye, e.g. fluorescent dye, certain biodegradable nonionic surfactants comprised of certain ethoxylated linear alcohols, of the type disclosed in my above copending application Ser. No. 444,433, separately or in admixture, and a halocarbon solvent, which is volatile at room temperature. The halocarbon is a nonflammable liquid which is relatively non-toxic, resistant to hydrolysis in contact with water, and is inexpensive. The biodegradable nonionic surfactant employed essentially as the sole solvent or carrier for the dye preferably comprises ethoxylates of a mixture of linear secondary aliphatic alcohols having linear alkyl chains of from 11 to 15 carbon atoms, and an average of from 3 to 12 moles of ethylene oxide.

The dye penetrant composition of the invention contains a large or major proportion of the halocarbon, and upon application of the composition to a part surface, for example, the metal components of a rocket motor system which employs LOX as an oxidizer in rocket liquid propellants, it has been found that the halocarbon rapidly volatilizes and the organic residue in the cracks and flaws of the part or component following inspection thereof, does not react chemically or explosively, with the liquid or gaseous oxygen in contact with the metal surfaces of the rocket motor system. On the other hand, in the absence of such halocarbon in the dye penetrant composition, such residue can react violently with liquid oxygen.

In addition, due to the rapid and substantially complete volatility of the halocarbon following application of the penetrant to a part surface, the biodegradability of the remaining dye penetrant, in the absence of the halocarbon, is not altered or affected, and moreover, the initial presence of the halocarbon in the dye penetrant does not affect the sensitivity of the dye penetrant following removal of the halocarbon.

The nonionic biodegradable solvents or carriers which can be employed as substantially the sole vehicle for the dye of the LOX compatible dye penetrant compositions according to the present invention are ethoxylates of a mixture of linear secondary aliphatic alcohols, with the hydroxyl groups randomly distributed, the linear aliphatic hydrophobic portion of such alcohols being a mixture of alkyl chains containing in the range from 10 to 17 carbon atoms, preferably from 11 to 15 carbon atoms, and containing an average of from 3 to 12 moles of ethylene oxide.

The above particularly preferred class of nonionic biodegradable surfactant employed as carrier for the dye penetrant of the invention is a mixture of compounds which can be represented by the formula: ##STR1## where n is in the range from 9 to 13, and m is an average of 3 to 12.

Although preferably each of the above-defined surfactants is formed of a mixture of two or more linear alkyl hydrophobic chains ranging from C.sub.11 to C.sub.15, as noted below, the surfactant can contain a single such chain formed from a single secondary aliphatic alcohol of the types described below.

The linear alkyl hydrophobic portion of the above defined surfactant is a mixture of C.sub.11 to C.sub.15 linear alkyl chains, and can be derived from a mixture of C.sub.11 to C.sub.15 aliphatic secondary alcohols, for example the secondary undecyl, dodecyl, tridecyl, tetradecyl and pentadecyl alcohols. The hydrophilic portion of the surfactant is a polyoxyethylene chain randomly attached to any carbon atom of the linear alkyl hydrophobic chains, other than to the terminal carbon atoms thereof, through an ether linkage. It will accordingly be understood that the specific carbon atom in the alkyl hydrophobic chains to which the hydrophilic polyoxyethylene chain is attached will become a ##STR2## Such hydrophilic polyoxyethylene chain is generally expressed in terms of an average number of moles of ethylene oxide.

Illustrative examples of biodegradable nonionic surfactant of the types defined in the above formula are those consisting of a mixture of ethoxylates of from 11 to 15 carbon atoms in the aliphatic hydrophobic chain, and which have an average of 3, 5, 7, 9 and 12 moles of ethylene oxide, respectively, as the hydrophil.

Materials corresponding to these five examples of biodegradable nonionic surfactants are marketed, respectively as:

In each case of the Tergitol S series of surfactants listed above, the number to the left of the S indicates a hydrophobic aliphatic chain of from 11 to 15 carbon atoms derived from a mixture of alcohols on C.sub.11 to C.sub.15 backbone chains, and the number to the right of the S designates the average number of moles of ethylene oxide as the hydrophil. Thus for example, Tergitol 15-S-5 is a mixture of liner aliphatic alcohols in the C.sub.11 to C.sub.15 range ethoxylated with an average of 5 moles of ethylene oxide. All of these commercially marketed Tergitol S series of surfactants are water soluble except for Tergitol 15-S-3, which is essentially water insoluble. Mixtures of these materials can also be employed in providing the dye penetrant of the invention, such as a mixture of the above Tergitols 15-S-5 and 15S-3; a mixture of 15-S-3 and 15-S-9; and a mixture of 15-S-5 and 15-S-9.

The above preferred class of nonionic biodegradable surfactants employed as carrier or vehicle for the dye of the penetrant solution according to the invention, are prepared by reacting an alcohol or mixture of alcohols, with the desired proportion of ethylene oxide, in the presence of an alkaline catalyst, such as potassium hydroxide. The ethylene oxide may be added to the alcohol or mixture of alcohols in one continuous step or it may be added in several steps. The products thus produced possess random distribution of oxyethylene groups, as noted above.

Another process for preparing the above nonionic surfactants in the form of ethoxylates of linear secondary aliphatic alcohols, is described in U.S. Pat. No. 2,870,220.

Although Tergitol 15-S-3 is essentially water insoluble and is usually employed in combination with the other members of the Tergitol S series noted above, such as Tergitol 15-S-15, dye penetrant compositions according to the invention containing Tergitol 15-S-3 alone, can be employed. However, Tergitol 15-S-3 has its greatest utility for production of dye penetrants having high sensitivity according to the invention, when employed in combination with the other water washable and water soluble Tergitols such as Tergitol 15-S-5 and Tergitol 15-S-9. Also, particularly effective dye penetrants are provided according to the invention employing a combination or mixture of the above Tergitols 15-S-5 and 15-S-9, and to which there can be added optionally Tergitol 15-S-3, as described in my above copending application Ser. No. 521,730.

The halocarbon additive incorporated in the dye penetrant composition for rendering the subsequent halocarbon-free residues thereof LOX safe or compatible, is a nonflammable liquid volatile at room temperature, and which preferably has a boiling temperature below 260.degree. F at ambient pressure, and is non-toxic, nonflammable, resistant to hydrolysis and functions as a solvent for the dye penetrant components, including the ethoxylated nonionic surfactant and the dye. Examples of halocarbon solvents which can be employed include 1-bromo-1-difluoro-2-bromo-2-difluoro ethane, 1-dichloro-1-fluoro-2-chloro-2-difluoro ethane, 1-dichloro-1-fluoro-2-dichloro-2-fluoro ethane, 1,1,1,-trichloroethane, trichloroethylene and tetrachloroethylene. Also, there can be employed as halocarbon solvent certain of the Freons such as Freon TF, which is 1,1,2-trichloro-1,2,2-trifluoroethane, Freon MF, which is trichlorofluoromethane, and Freon FE, which is bromotrifluoromethane.

Any suitable dye generally employed in dye penetrant compositions can be incorporated into the nonionic oxyalkylated alcohol surfactants described above for producing the dye penetrant compositions employed in the invention process. Preferably, however, a fluoroescent dye is employed for this purpose. The ethoxylated surfactant vehicle for the dye is compatible therewith and has the ability to dissolve either small or relatively large amounts of the dye and to hold a high concentration of dye in solution while providing good resolution and clarity of the dye trace in the cracks and flaws.

As previously noted, the dye penetrant solution employed according to the invention preferably contain a fluorescent dye. Various types of fluoroescent dyes can be employed including for example the dye marketed as Fluorol 7GA as well as other fluorescent dyes such as those marketed as Calcofluor Yellow, Azosol Brilliant Yellow 6GF; Rhodanine B, Rhodanine 6 GDN, Calcofluor White RW, Blancophor While AW, Auramine and Eosine G, and water soluble fluorescent dyes such as Blancophor FFG.

The dye penetrant composition employed according to the invention alternatively can contain non-fluorescent or daylight type dyes such as azo type dyes, e.g., xyleneazo-beta-naphthol, Mefford No. 322 dye, believed to be o-toluene-azoxyleneazo-beta-naphthol, and the azo dyes marketed as Oil Red "O" and Sudan Red. These dyes conveniently can be employed where daylight or white light is only available, and particularly where the surface of the body to be detected contains relatively gross cracks. However, it is preferred to employ fluorescent dyes having greater sensitivity or detectability as result of the high contrast obtained by the fluorescent indications.

The amount of dye which is incorporated into the ethoxylated alcohol surfactant or carrier to produce the dye penetrant composition of the invention, can range from about 0.1 to 15, preferably about 0.5 to about 10, parts of the dye, or mixtures thereof, per 100 parts of the ethoxylated alcohol surfactant, by weight. In preparing the dye penetrant composition employed according to the invention, the dye is simply added to the ethoxylated alcohol carrier, in the desired proportion. The resulting dye penetrant composition has both high and low temperature stability.

The amount of halocarbon solvent added to the dye penetrant constitutes a major proportion of the resulting solution. Generally, the dye penetrant including the above nonionic surfactant and dye, is diluted with halocarbon in a proportion ranging from about 10 to about 40, preferably about 15 to about 25, parts of the halocarbon solvent to 1 part of dye penetrant, consisting of the sum of the other components, that is ethoxylated alcohol surfactant or surfactants, and dye, by volume, with an optimum ratio of 20 to 1 of halocarbon to the sum of the other components, by volume. It is preferred to employ a ratio of halocarbon to the sum of the other components not greater than about 30 to 1, by volume, since use of halocarbon in excess of the above noted 30 to 1 ratio results in some decrease in performance and in penetrant sensitivity.

Typical dye penetrant compositions to which halocarbon solvent can be added according to the invention are as follows:

Illustrative examples of the LOX compatible dye penetrant composition of the invention incorporating varying proportions of halocarbon such as 1,1,1-trichloroethane, into the typical dye penetrant composition A of Table 1 above, are set forth in Table 2 below.

The effectiveness or LOX compatibility of the dye penetrants of the invention is illustrated by comparative impact test measurements which determine the compatibility of the dye penetrant compositions with liquid oxygen. The following is an example of such test measurements.

In National Aeronautics and Space Administration specification MSFC-SPEC-106 criteria and a method is established for determining the compatibility and impact sensitivity of materials with liquid and gaseous oxygen. Employing this test procedure, and utilizing the liquid dye penetrant composition I above, and containing 1,1,1-trichloroethane as halocarbon, impact sensitivity tests were conducted. In these tests individual, clean, anodized aluminum 6061-I6 discs, 11/16 inch diameter were respectively soaked in the liquid dye penetrant. The discs were then allowed to drain for 15 minutes and were tested in an impact tester of the type described in the aove specification. 20 specimen discs each coated with penetrant were impact tested at 72 ft.-lbs. impact, while the discs were immersed at the bottom of a precooled test cup containing liquid oxygen. If the material being tested is not compatible with liquid oxygen it will immediately explode, flash or burn. The penetrant samples were reported to be compatible with LOX at 72 ft-lbs impact if there were no audible explosions, no visible flash in a darkened room, and no discoloration of the aluminum specimen discs or evidence of disc charring.

The subject dye penetrant, composition I did not react during the required 20 impact drops at 72 ft-lbs. and successfully passed the impact test with LOX.

To further explore the margin of safety of this dye penetrant, composition I, the impact was raised to 80 ft-lbs., in excess of the standard 72 ft-lbs. requirements. Again the penetrant did not react during the 20 impact drops required, and successfully passed the test.

It is noted that the dye penetrant composition I employed in this test procedure, and incorporating composition A of Table 1 above, had a substantial amount of dye which is capable of reaction with LOX, yet by incorporating the halocarbon into such composition it successfully passed the LOX compatibility test as noted above.

The same test procedure was carried out as in the case of Example 1 above, using the standard 20 impact drops at 72 ft-lbs, employing the dye penetrant composition A of Table 1 above, alone, and in the absence of any halocarbon.

The results showed 17 reactions occurred out of the 20 drops. Thus, dye penetrant composition A did not pass the test and hence is not LOX compatible.

If desired, a developer composition can be employed in conjunction with the halocarbon-containing dye penetrant composition of the invention. When employed, a dry powder or non-aqueous (volatile solvent base) developer composition can be employed, provided that when the latter type developer is employed sufficient time is given to permit evaporation of the solvent. Thus, any developer of the above types can be utilized provided they are LOX compatible, so that any remaining developer residue is non-reactive with liquid oxygen. In each case, the developer composition contains a light colored powder, forming a coating which contrasts with the color of the dye in the penetrant and which acts as a wick or blotter, and causes liquid penetrant containing the dye, e.g. fluorescent dye, which was retained in the cracks or surface flaws, to be drawn up out of the surface defects by capillary action and to "bleed" through the powder. Preferred developer compositions for use in conjunction with the dye penetrant composition according to the invention, are those described in my U.S. Pat. No. 3,803,051, which is a dry powder developer containing fumed alumina, fumed silica, fumed titanium dioxide and talc, and in my U.S. Pat. No. 3,748,469, and which is a wet non-aqueous developer composition consisting essentially of isopropyl alcohol, talc and glycol monobutyl ether. The descriptions of such developer compositions contained in the above patents are incorporated herein by reference.

The dye penetrant composition employed in the invention process, employing the above biodegradable nonionic ethoxylated alcohol surfactants can be tailored to have varying degrees of sensitivity for detection of the smallest microcracks to gross cracks in a part surface by generally varying the amount of dye incorporated, and also by selecting particular surfactants or combinations thereof.

In the method for detecting cracks and flaws in the surface of an object employing the LOX compatible dye penetrant composition of the invention, such dye penetrant is applied to the part surface in any suitable manner, as by spraying. Upon application of the dye penetrant to the surface of the test part, the halocarbon solvent evaporates very rapidly, e.g. within about 2 to about 5 seconds, although in some instances this may require a period up to about 5 minutes, and the excess dye penetrant composition is readily removed from the object surface by water washing, e.g. by application of a water spray or a sprayed mixture of air and water, or by wiping with a water moistened cloth. The dye penetrant compositions hereof, particularly these containing the above Tergitols 15-S-5 to 15-S-9, generally have excellent wetability and practically instantaneous washability with water without removing dye penetrant from the cracks and defects on the part surface, followed by drying the part surface.

If desired, a developer composition of the types noted above can then be applied to the part surface followed by removal of excess developer, as by means of an air blast. The part is then viewed under suitable lighting conditions, employing black light or fluorescent illumination when the dye penetrant contains a fluorescent dye.

Following inspection of the part and incorporation thereof into a device such as the propellant tanks of a rocket motor which uses liquid oxygen, any thin remaining residue of dye penetrant on the part surface or in any surface defects such as cracks, is now rendered inactive or inert with respect to LOX. Thus, it is believed that the halocarbon solvent in some unknown manner functions to deactivate such dye penetrant residue remaining on the surface and in the surface cracks of the part. However, as previously noted, unexpectedly the use of the halocarbon solvent in the dye penetrant does not affect the biodegradability of the dye penetrant following evaporation of the solvent, and does not affect the sensitivity of the dye penetrant. Examples showing these results are set forth below.

Where it is desired to employ a relatively insoluble nonionic surfactant in the dye penetrant composition, such as Tergitol 15-S-3 noted above, alone or in substantial proportion in admixture with another water soluble Tergitol such as Tergitol 15-S-5, in order to obtain high sensitivity, the post emulsifiable dye penetrant inspection method of my above copending application Ser. No. 535,262 can be employed. According to such procedure, the dye penetrant composition containing the biodegradable ethoxylated nonionic surfactant, such as Tergitol 15-S-3 as carrier, and diluted with halocarbon solvent according to the invention, can be applied as by dipping or spraying, preferably the latter to a test part, and the solvent evaporated, e.g. in about 1 to 5 seconds, followed by treatment of the penetrant covered part as by spraying, with an emulsifier containing as an essential component biodegradable nonionic surfactants of the same general class as employed as carrier for the dye in the dye penetrant composition, but having greater water solubility, such as Tergitol 15-S-9. In such postemulsifiable process, the ethoxylated nonionic surfactant in the dye penetrant can have an average value for m in the formula above of about 3 to 4, and the ethoxylated nonionic surfactant in the emulsifier can have an average value for m of about 5 to 12. In order to render the dye penetrant residue compatible with liquid oxygen, in this post emulsifiable procedure the emulsifier must also contain halocarbon solvent as above defined in combination with the above surfactant, e.g. Tergitol 15-S-9. Thus, in the emulsifier, such surfactant is diluted with the above halocarbon in the same proportions as the dye penetrant composition, namely about 10 to about 40, preferably about 15 to about 25, parts of halocarbon solvent to 1 part of nonionic surfactant, by volume.

The halocarbon in the emulsifier is then allowed to evaporate, leaving a thin film of emulsifier over the initially applied penetrant. After a dwell time of about 1 to 5 minutes, the resulting emulsified penetrant is then removed from the surface of the part as by spraying with water, without dislodging the dye penetrant from the surface cracks and thus entrapping the penetrant therein, and the part surface is then dried and inspected under suitable light, e.g. ultraviolet light. If desired, a developer also can be employed following removal of the emulsified penetrant from the part surface.

The following are examples of practice of the invention.

A test panel of 2014 aluminum and containing microcracks uniformly distributed over the panel was divided by a groove into two equal test areas for test comparison purposes.

The fluorescent dye penetrant composition I of Table 2 above was applied as by spraying, to 1/2 of the surface of the test panel. Almost instantaneously, that is in a matter of 2 or 3 seconds, the halocarbon solvent evaporated, and a water wash was then applied as by an air-water spray over the coating of the dye penetrant composition I on the test panel, causing almost instantaneous washing away of the dye penetrant on the surface of the panel without dislodging the dye penetrant from the surface cracks and thus entrapping the penetrant therein. The part surface was then dried with an air blast. The washed dye penetrant removed from the part surface was biodegradable.

The procedure above was repeated, by applying the dye penetrant composition A of Table 1 above, containing no halocarbon, to the other half of the test panel surface, followed by application of a water wash under the same conditions noted above for removal of excess dye penetrant, and finally followed by drying with an air blast.

Inspection of the two penetrant treated surfaces of the test panel under ultraviolet or fluorescent light, revealed fluorescent indications from numerous readily defined microcracks therein, the fluorescent indications on both sides of the test panel being in substantially equivalent concentration, with substantially the same brightness and sensitivity or optical intensity on both sides of the test panel.

This example shows that the halocarbon containing dye penetrant composition of the invention, following removal of the volatile halocarbon solvent, has essentially the same sensitivity or ability to disclose cracks and defects in a part surface, and the same biodegradability, as in the case of the dye penetrant composition free of halocarbon, yet the former has the substantial advantage of being LOX compatible.

The procedure of Example 3 was repeated except that in each case, following removal of excess dye penetrant from the part surface, both halves of the test panel surface were covered with a powder developer having the following composition, according to my above U.S. Pat. No. 3,083,051.

The above developer was permitted to dwell over the surface of the test panel for a period of about 2 minutes.

Excess developer composition was then carefully removed from the surface of the test panel by means of a gentle air blast.

Both areas of the panel were then placed under fluorescent or ultraviolet illumination and it was again observed that a substantially equal concentration of fluorescent indications was revealed on each of the adjacent surfaces of the test panel, with substantially equivalent fluorescent brightness and sensitivity in both areas of the test specimen.

The procedure of Example 3 was repeated except employing in place of composition I, composition II of Table 2 above, having a dilution, or solvent concentration, in the proportion of 30 parts of 1,1,1-trichloroethane to 1 part of dye penetrant composition A, by volume.

Substantially the same results were obtained as in Example 3, namely substantially equivalent concentration of fluorescent indications of cracks on both sides of the test specimen, with substantially equal brightness and sensitivity of the fluorescent indications on both test areas of the panel.

A fluorescent dye penetrant composition is prepared by diluting a composition containing 100 parts biodegradable Tergitol 15-S-3 as carrier, and 5 parts Calcofluor White RW and 1.5 parts Fluorol 7 G A, by weight, with 1,1,1-trichloroethane, in a proportion of 20 parts of the halocarbon to 1 part of the sum of the other components, by volume.

The resulting dye penetrant composition is applied by spraying to a chromium-plated brass test panel containing microcracks closely distributed over its entire surface.

After the halocarbon evaporates, the dye penetrant covered surface is sprayed with an emulsifier containing biodegradable Tergitol 15-S-9 surfactant, diluted with 20 parts of 1,1,1-trichloroethane per 1 part of surfactant by volume. The emulsifier is allowed to dwell on the initially applied penetrant for a period of about 1 minute.

The test panel containing the emulsified penetrant, following evaporation of solvent, is then sprayed with water applied by an air-water spray over the dye penetrant-emulsifier coating, causing instantaneous washing away of the emulsified dye penetrant on the surface of the panel without dislodging the dye penetrant from the surface cracks and thus entrapping the penetrant therein, and the surface is dried by an air blast.

The test panel is then covered with a powder developer as described in Example 4.

Excess developer composition is then removed from the surface of the test panel by means of a gentle air blast.

The panel is then placed under black light (fluorescent) illumination and the above treated surface of the panel viewed in such illumination, revealing sharp and brilliant fluorescent indications from the numerous readily defined microcracks in the panel. The dye penetrant residue is compatible with liquid oxygen.

From the foregoing, it is seen that the invention provides a highly effective substantially biodegradable water washable dye penetrant composition whose residue is compatible with liquid oxygen, and consisting essentially of a single carrier for the dye, which is preferably fluorescent, in the form of certain biodegradable ethoxylated alcohols, diluted with a substantial proportion of a volatile, non-toxic and nonflammable halocarbon, which permits substantially instantaneous removal of halocarbon solvent by evaporation following application of the dye penetrant composition to a part surface, leaving an organic residue in the cracks or defects, which is non-reactive with liquid oxygen, followed by rapid removal of excess dye penetrant in a single wash operation, and further processing of the part surface in the conventional manner for viewing under suitable, e.g. fluorescent, lighting conditions, to obtain high brilliance, definition and resolution of the dye traces from cracks and flaws in the part surface, equivalent in this respect to the results obtained employing the same dye penetrant but in the absence of the halocarbon.

Since various changes and modifications of the invention will occur to and can be made readily by those skilled in the art without departing from the invention concept, the invention is not to be taken as limited except by the scope of the appended claims.