US1717483A - Textile material and method of treating the same - Google Patents

Textile material and method of treating the same Download PDF

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US1717483A
US1717483A US639219A US63921923A US1717483A US 1717483 A US1717483 A US 1717483A US 639219 A US639219 A US 639219A US 63921923 A US63921923 A US 63921923A US 1717483 A US1717483 A US 1717483A
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textile material
salts
rare earth
water
thorium
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Clarence B White
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VIVATEX PROCESSES Inc
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423Amino-aldehyde resins
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S8/00Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/12Wave energy treatment of textiles

Definitions

  • the invention has for its chief object the treatment of textile material, under which term is included not only woven fabrics but also all other kinds of fabrics including knitted fabrics, netted fabrics, and also threads, yarns, fibers and various associations thereof.
  • Another objectof the invention is to produce a water repellent textile material which will retain its water repellency after repeated washings with either soap and water or hydrocarbon solvents such as gasoline, naphtha or equivalent materials such as carbon tetrachloride, acetone, alcohol, ether and the like or various combinations of such materials or treatments.
  • a further object of the invention is to roduce a textile material which is less absor ent than ordinary textile materials and which will therefore take up'less atmospheric moisture and will accordingly be more highly, resistant to the injurious influences of atmospheric gases and moisture.
  • Still further object is to produce a textile material which will be less subject'to shrinking.
  • thorium and other rare earth elements As equivalents of thorium and other rare earth elements referred to hereinbefore, at least as regards making textile material repellent to mildew and other fungus growths, I desire to include uranium, actinium, and degradation products, such as radium, m'esothorium, radiothorium, and polonium. Textile material impregnated with salts or other'compounds of these sub- .stances or in combination with other elements the tendency to form colloidal precipitates or compounds as carriers, are notably reionized field inimical to bacterial life and in,
  • the second step of the process may consist in drying the impregnated textile material. This is in many cases important since if the material is not dry, there may not be as good a union of the metal bases with the fiber of the textile material, and hence the precipitate when formed may separate from the textile material.
  • the third step of the process consists in converting the metal salts or other compounds of the rare earth metals, into a water-insoluble and apparently colloidal state, by means of appropriate precipitants.
  • the fourth step of the process consists preferably in washing the textile material in water orother liquid to remove the soluble salts, especially salts constituting the by-products of the precipitation reaction.
  • the fifth step of the process consists in drying the washed fabric, and subjecting the same to a sufficient amount of heat or pressure, or both, to produce the insolubilization of the rare earth metal compound. While the preferred mode of carrying out this invention involves these five steps, itv may not require anylong period of time for the accomplishment of the results stated, it being well known that webs of fabric may be passed through several dipping or impregnating baths, precipitating baths, washing baths, and 'calendering machines. as a continuous process.
  • the textile material can also be impregnated with compounds of various metals-,capable of producing colored precipitates,'such as iron salts, chromium salts, nickel salts, cobalt "salts, copper salts, lead salts.
  • compounds of various metals-,capable of producing colored precipitates such as iron salts, chromium salts, nickel salts, cobalt "salts, copper salts, lead salts.
  • this can be accomplished by impregnation with a lead or copper com ound
  • the salts of these metals can be mixe with the salt of the rare earth compound used in the first step or the treatment with the salts of these metals may be effected separately, either after or before the other treatment.
  • Normal thorium nitrate is anextremely soluble, hygroscopic, 'deliquescent, crystalline salt.
  • the same description applies to the normal chlorid. Both have a tendency to attack textile'fibers, especiall when the temperature is comparatively igh. Moreover, on account of their strongly deliquescent character it is almost impossible to-dry them unless the temperature'be high or a vacuum chamber be used. Both of these conditions introduce technical complications.
  • Thorium nitrate solution also dissolves the carbonate of thorium, the acetate of thorium, the formate of thorium, the chlorid, or mixtures of any or all of these. making highly complex' double salts, all of which have a gelatinous rather thana crystalline tendency.
  • the preferred impregnating bath for the first step is a solution of thorium sub nitrate, say of about 20 per cent strength, or if desired, a solution containing about 16 per cent of sub-nitrate and 4 per cent of chlorid.
  • the textile material may remain in contact with the solution for any desired length of time, it being of course preferred that the liquid should thoroughly permeate the interstices and pores of the material.
  • the impregnation may also be effected, in some cases, by an operation similar to that used in printing fabrics; as for example by passing the material between rollers which are coated or wet with the impregnating solution.
  • the material is then dried, for example by being subjected to the action of a series of steam heated calender rolls, these rolls furnishing both the necessary heat and pressure.
  • the drying temperature need not be higher than 100 C. It may be stated that complete dryness is scarcely ever, if at all, necessary. In many cases the material may contain suflicient moisture to make it appreciably damp to the touch, as would be the case if subjected to firm squeezing between unheated rolls.
  • the textile material then passes to a bath of precipitating agent.
  • the precipitating bath may be mamtamed' at ordinary atmospheric temperature, or at a lower or higher temperature. Even a b011- ing temperature, 100 0., does not (materially, if at all).diminish the mildew repellency; and a high temperature, especially with zirconium and thorium compounds, is distinctly favorable in the direction of imparting resistance to acids. Some compounds of these metals for example zirconium and thorium hydroxids) precipitated hot are almost insoluble in acids, even strong hydrochloric, but are readily soluble therein if precipitated cold.
  • insoluble tungstate, stannate, molybdate or phosphate of the metals referred to, in or upon the text le material confers a certain resistance to' flame, making the material less inflammable.
  • the concentration of the precipitating bath is also a matter of some importance, dilute solutions being preferable.
  • caustic soda as the precipitating material
  • I preferably employ a solution of about 5-10 per cent strength, which keeps the precipitate in a highly colloidal and strongly adherent condition in which it is held .tenaciously by the textile material under treatment.
  • the length of time that the goods remain in the precipitating bath will vary, depending upon the thickness of the goods. Ordinarily the goods may remain in the precipitating bath about the same length of time which they remained in the first impregnating bath.
  • I employ gaseous ammonia (NH as the precipitating bath, better results being obtained in many cases by the use of the gas than by the use of liquid ammonia.
  • the precipitate is denser, and more repellent to water.
  • the gas may be used at ordinary temperature and pressure, and may or may not be diluted with air, as most convenient under the circumstances.
  • the goods may, if desired, then pass between calendering rollers. which may be heated.
  • the textile material then passes into a washing bath containing water or other suitable washing fluid in which the by-prodnets of the reaction are removed.
  • This washin g fluid may contain soap, as I have observed in some cases a marked tendency for the precipitated compound to be converted thereby into a strongly repellent fatty acid compound.
  • The, textile material then passes again through wringing rollsand hot calendering rolls, for the complete insolubilization of the precipitate carried thereby.
  • ' earth'metals ' (cerium, lanthanum, and didymium) can be employed alone or in mixtures', or compounds of thorium together with compounds of one or more of the other rare earth metals, can be used, these being em-l ployed alone or with other metal compounds,
  • Thorium or other rare earth metal compound preferably subnitrate or acetate t '1O Zirconium compound, preferably acetate 5 Water 8
  • the following baths are well adapted to impart radio-active properties to the textile material:
  • temperatures should not be used which are capable of materially injuring -thefiber of the textile material, by seriously weakening the same.
  • these drying operations are conducted at temperatures about 100 C., or but slightly above, so as not to reduce the strength of the textile material.
  • temperatures about 100 C., or but slightly above, so as not to reduce the strength of the textile material.
  • temperatures of about 100 C. in the final drying operation, it appears that the hydroxids of the rare earth elements are in dant for forming insoluble lakes with dye-.
  • the textile material may be passed continuously or step-by-step between (and preferably in contact with) a pair or several pairs of electrodes while immersed in or wet with the impregnating bath, the elec trodes being connected to the appropriate poles or terminals of a suitable source of current.
  • a voltage of from 6 to 8 volts (preferably) may be em loyed.
  • the amperage used is determined c iefiy'by economical factors, and in general should not be so-high as to waste current in the form of heat reduced by resistance losses .in the bath.
  • the electrolytic method may be used in conjunction w1th the chemical method, either before or after the same.
  • the second treatment may impart or increase the external water re ellency of the fabric, by which is meant the ifliculty of-being wetted.
  • Textile material inherently capable of supporting mildew and like fungous growth, ered resistant thereto and a so repellent to water and resistant to attack by aelds, by impregnationwith a rare earth metal compound which is insoluble in alkaline solutions.
  • repellent to such action and also repe lent to water and resistant to attack by acids which comprises impregnating the material with a solution of a subnitrate of a rare earth metal,removin excess liquid from the material, treating t e partially dried material with a reagent capable of converting the said salt into a compound insoluble in alkaline solutions, washing the material to remove any soluble compounds present, and thereafter drying the material. 6.
  • Process of rendering textile material repellent to fungous growth and to water, and resistant to attack by acids whichcomprises impregnating the material with a dilute solution of a rare earth metal compound, treating the impregnated material with a reagent adapted to precipitate the rare earth metal compound in a colloidal form which is insoluble in hydrocarbons and alkaline solutions, and thereafter drying the material.
  • Process of rendering textile material repellent to fungous growth and to water, and resistant to attack by acids which comrises imprelgnating the material with a diute relative y cold solution of a rare earth metal salt, treating the impregnated material with a precipitant adapted to convert the rare earthmetal salt into a colloidal form and thereafter drying the textile material --under pressure whereby tate is rendered substantially insoluble in the colloidal precipih drocarbons and alkali solutions and resistant to attack by acids.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)

Description

Patented June 18, 1929. v
,; UNITED STATES PATENT OFFICE:
CLARENCE 3. WHITE, OF MONTCLAIR, NEW JERSEY, ASSIGNOB, BY IESNE ASSIGN- MENTS, TO VIVATEX PROCESSES, INC., OF NEW JERSEY.
OF LODI, NEW JERSEY, A. CORPORATION TEXTILE MATERIAL AND METHOD OF TREATING THE SAME.
. No Drawing. Application filed May I5,
The invention which forms the subject of the presentapplication, a continuation, in
- part, of my earlier applicationSerial No.
544,944, filed March 18, 1922, relates to waterproofed and preserved textile material and to methods of preparing the same. The invention has for its chief object the treatment of textile material, under which term is included not only woven fabrics but also all other kinds of fabrics including knitted fabrics, netted fabrics, and also threads, yarns, fibers and various associations thereof. Another objectof the invention is to produce a water repellent textile material which will retain its water repellency after repeated washings with either soap and water or hydrocarbon solvents such as gasoline, naphtha or equivalent materials such as carbon tetrachloride, acetone, alcohol, ether and the like or various combinations of such materials or treatments.
A further object of the invention is to roduce a textile material which is less absor ent than ordinary textile materials and which will therefore take up'less atmospheric moisture and will accordingly be more highly, resistant to the injurious influences of atmospheric gases and moisture. still further object is to produce a textile material which will be less subject'to shrinking. It is also another important object of the invention to produce a textile material which Willbe repellent, that is, resistant, to mildew and other fungus growths. It also frequently is an object of the invention, to producea textile material which will combine the feature of water repellency with the feature .of possessing a completely-fast color, especially in the case of fabrics which are 'dyed with a mineral color or a pigment, as for example the familiar khaki. I
The objects above enumerated are accomplished in the present case by the use of compounds of the rare earth group of metals and the expression rare earth as-used herein is intended to include the elements zirconium, titanium and thorium, which latter element seems to possess some points of superiority over the others of the group. These metals 1923. Serial No. 639,219.
possess the property of precipitating in a particular physical condition, if the operation is properly conducted. When dilute or cold solutions are treated, one of such solutions including a salt of an element of the rare earths, if the operation is conducted in the cold or with relatively dilute solutions,
exists to a high degree. In the case of .thorium compounds, particularly from cold and dilutesolutions, the tendency is to produce j elly-like rather than slimy precipitates, these jelly-like precipitates being, under certain conditions,capable'of forming within the jected to heat, especially with simultaneous subjection to pressure, while intimately a'ssociatedwith the fiber, the more or less colloidal precipitates'are converted into a form in which they are not readily attackable by acids or alkalis. This phenomenon is very noticeable, whether weak or very dilute acids, organic or inorganic are employed, or whether relatively strong and usually active, acids are used. As equivalents of thorium and other rare earth elements referred to hereinbefore, at least as regards making textile material repellent to mildew and other fungus growths, I desire to include uranium, actinium, and degradation products, such as radium, m'esothorium, radiothorium, and polonium. Textile material impregnated with salts or other'compounds of these sub- .stances or in combination with other elements the tendency to form colloidal precipitates or compounds as carriers, are notably reionized field inimical to bacterial life and in,
a measure capable of inhibiting its growth.
Some of these substances, notably radium, mesothorium and rad1othor1um,are of course costly, but they are intensely radioactive and hence can be used in quantities small enough vto make theiremployment practicable with suitable carriers, among which may be mentioned salts of the rare earths, zircomum, aluminum, etc. In addition to their radloactive properties, many of the salts and othercompounds of thorium and uranium, employed as herein described, for example, impart marked water repellency, and by their use one may create a fabric which is water repellent without material loss of porosity,
and which at the same time, by reason of thematerial with metallic salts of the kind re-' ferred to, namely, solutions of salts of the rare earth metals, as above described. The second step of the process may consist in drying the impregnated textile material. This is in many cases important since if the material is not dry, there may not be as good a union of the metal bases with the fiber of the textile material, and hence the precipitate when formed may separate from the textile material. The third step of the process consists in converting the metal salts or other compounds of the rare earth metals, into a water-insoluble and apparently colloidal state, by means of appropriate precipitants. The fourth step of the process consists preferably in washing the textile material in water orother liquid to remove the soluble salts, especially salts constituting the by-products of the precipitation reaction. The fifth step of the process consists in drying the washed fabric, and subjecting the same to a sufficient amount of heat or pressure, or both, to produce the insolubilization of the rare earth metal compound. While the preferred mode of carrying out this invention involves these five steps, itv may not require anylong period of time for the accomplishment of the results stated, it being well known that webs of fabric may be passed through several dipping or impregnating baths, precipitating baths, washing baths, and 'calendering machines. as a continuous process.
For the production of colored effects, the textile material can also be impregnated with compounds of various metals-,capable of producing colored precipitates,'such as iron salts, chromium salts, nickel salts, cobalt "salts, copper salts, lead salts. Also if it is desired to render the product more resistantpr repellent to mildew, fungous decay and dismtegration, or the like, this can be accomplished by impregnation with a lead or copper com ound, The salts of these metals can be mixe with the salt of the rare earth compound used in the first step or the treatment with the salts of these metals may be effected separately, either after or before the other treatment.
For most purposes, the salts of thorium are found to give especially satisfactory results.
Normal thorium nitrate is anextremely soluble, hygroscopic, 'deliquescent, crystalline salt. The same description applies to the normal chlorid. Both have a tendency to attack textile'fibers, especiall when the temperature is comparatively igh. Moreover, on account of their strongly deliquescent character it is almost impossible to-dry them unless the temperature'be high or a vacuum chamber be used. Both of these conditions introduce technical complications.-
If a small quantity of an ammonium saltthe nitrate or chlorid, as the case may be-- be added, the solubility is greatly decreased, the salt becomes highly crystalline, and can be easily dried at normal temperatures. No great amount of ammonia is necessary, as little as 2 per cent producing a satisfactory effeet. This deportment characteristic not only of thorium, but also of cerium and most others of the rare earths, and is a marked feature of lanthanum and of the didymium complex. In a way the addition of ammonium, which addition apparently gives rise to the formation of a double saltof the rare earth and ammonium, does away to a large extent with the tendering action of the salt on fabrics, and also largely eliminates the difliculty in drying.
here is, however, a still better series of compounds, viz the sub-acid or basic salts of thorium dissolves large quantities of the hydroxid of thorium forming a basic nitrate, or at least a solution of the hydroxid in the nitrate. The former is probably, the true explanation because of the marked change in characteristics. The solution no-longer crystallize's, nor does the dried, more or less gumlike product absorb moisture, and moreover is easily dried at low temperatures. Its reactions to precipitants differ from what one finds in the case of the normalsalt. Thorium nitrate solution'also dissolves the carbonate of thorium, the acetate of thorium, the formate of thorium, the chlorid, or mixtures of any or all of these. making highly complex' double salts, all of which have a gelatinous rather thana crystalline tendency.
,Also it will dissolve salts of other metals,
make admirable impregnating solutions for textile fabrics. What has been said in this connection of the nitrate is also true of the chlorid, although in less measure. Others of the rare earths exhibit the same general tendency. The preferred impregnating bath for the first step is a solution of thorium sub nitrate, say of about 20 per cent strength, or if desired, a solution containing about 16 per cent of sub-nitrate and 4 per cent of chlorid. The textile material may remain in contact with the solution for any desired length of time, it being of course preferred that the liquid should thoroughly permeate the interstices and pores of the material. With goods which are not very heavy, say like ordinary heavy sheeting, one minute or so in the impregnating bath is ample time to allow complete permeation of the liquid, into the pores of the material. The impregnation may also be effected, in some cases, by an operation similar to that used in printing fabrics; as for example by passing the material between rollers which are coated or wet with the impregnating solution. The material is then dried, for example by being subjected to the action of a series of steam heated calender rolls, these rolls furnishing both the necessary heat and pressure. The drying temperature need not be higher than 100 C. It may be stated that complete dryness is scarcely ever, if at all, necessary. In many cases the material may contain suflicient moisture to make it appreciably damp to the touch, as would be the case if subjected to firm squeezing between unheated rolls. The textile material then passes to a bath of precipitating agent.
As a precipitant any compound may be used which is capable of precipitating the rare earth metal in-a closely adherent and preferably colloidal condition on the textile material. Among these the ones preferred are, in the order named. ammonia, ammonium hydroxid and salts, and alkali metal hydrates. Others that may be named are cyanids and other salts of the alkali metals, such as sulfids, fluorids, phosphates, oxalates (and oxalic acid), flue-silicates, tungstates, stannates, titanates. molybdates, silicates, salicylates, benzoates, phenolates, and borates. Anilin and pyrodin may be used. also salicyclic, benzoic, hydrofluoric, phosphoric,-fluosilycic, phenolic, and boric acid. For Water repellency as well as mildew repellency I prefer ammonium, sodium or potassium hydroxid, or sodium or potassium cyanid. Among reagents which give more or'less soluble precipitates (which are, however, repellent to mildew) are phosphates of the alkali metals. It is seen that the choice of the precipitating agent is much wider than in processes in which aluminum, titanium or zirconium compounds are employed. I have observed that when alkali metal sulfids are used as the precipitating agents, they do not, in eneral, form sulfids of the rare earth metal, ut hydroxids.
The precipitating bath may be mamtamed' at ordinary atmospheric temperature, or at a lower or higher temperature. Even a b011- ing temperature, 100 0., does not (materially, if at all).diminish the mildew repellency; and a high temperature, especially with zirconium and thorium compounds, is distinctly favorable in the direction of imparting resistance to acids. Some compounds of these metals for example zirconium and thorium hydroxids) precipitated hot are almost insoluble in acids, even strong hydrochloric, but are readily soluble therein if precipitated cold. Other compounds, for example thorium and other rare earth phosphates, hypophosphates, fiuorids and oxalates, are practically insoluble in dilute acids even when precipitated cold. In general, rare earth metal, zirconium, and uranium, compounds, such as phosphates, fluorids, oxalatcs, hypophosphates, and fluosilicates, precipitated by the corresponding precipitants,
impart measurable protection against weak acids, as do other compounds when strongly dried. Moreover, the presence of insoluble tungstate, stannate, molybdate or phosphate of the metals referred to, in or upon the text le material, confers a certain resistance to' flame, making the material less inflammable.
The concentration of the precipitating bath is also a matter of some importance, dilute solutions being preferable. When using, say, caustic soda as the precipitating material, I preferably employ a solution of about 5-10 per cent strength, which keeps the precipitate in a highly colloidal and strongly adherent condition in which it is held .tenaciously by the textile material under treatment. The length of time that the goods remain in the precipitating bath will vary, depending upon the thickness of the goods. Ordinarily the goods may remain in the precipitating bath about the same length of time which they remained in the first impregnating bath. Preferably, however, I employ gaseous ammonia (NH as the precipitating bath, better results being obtained in many cases by the use of the gas than by the use of liquid ammonia. The precipitate is denser, and more repellent to water. The gas may be used at ordinary temperature and pressure, and may or may not be diluted with air, as most convenient under the circumstances.
The goods may, if desired, then pass between calendering rollers. which may be heated. The textile material then passes into a washing bath containing water or other suitable washing fluid in which the by-prodnets of the reaction are removed. This washin g fluid may contain soap, as I have observed in some cases a marked tendency for the precipitated compound to be converted thereby into a strongly repellent fatty acid compound. i
The, textile material then passes again through wringing rollsand hot calendering rolls, for the complete insolubilization of the precipitate carried thereby. Y
' earth'metals '(cerium, lanthanum, and didymium) can be employed alone or in mixtures', or compounds of thorium together with compounds of one or more of the other rare earth metals, can be used, these being em-l ployed alone or with other metal compounds,
such as those above referred to for producing mineral dyeings, increased resistance to mildew or fungous growths andthe like; These compounds can also be employed with compounds of Y titanium, aluminum, zirconiumv and the hke which themselves have some water-proofing effects. As examples of other impregnating baths the following may be noted, the figures given being per cents:
Thorium, cerium, lanthanum or didymium salt or salts (preferably nitrate or chlorid, or both) of one or more of these metals Iron salt or salts .40 Chromium salt or salts 40 Water, sufficient to make'a per cent solution. v
Cerium, didymium' (neodymium) or lanthanum acetate, or a mixture of two or more 15 .Water 85 Thorium nitrate or acetate 15 Water 85 Cerium and thorium acetates, with or without aluminum acetate 15 Water 85 v Cerium, lanthanum and didymium acetates 20 Iron acetate 30' Water 50 Cerium, lanthanum and didymium ace-' tates 10 Chromium acetate -r 10 Iron acetate .30 Water 50 Thorium and aluminum acetates 15 Copper acetate 0.5 Water 84.5
Thorium or other rare earth metal compound, preferably subnitrate or acetate t '1O Zirconium compound, preferably acetate 5 Water 8 The following baths are well adapted to impart radio-active properties to the textile material:
Aluminum and uranium compounds (each 5 per cent) 10 Rare earth compound 5 Water 85 Thorium compound 5 Other rare earth compound 10 Water 85 -Uranium -compound 5 Bare earthcompound; 10 Water. 85*
Actinium, radium or mesothorium, 1 part in 250,000 of the earrierused.
In the drying operation after the first step of the process, and also in the later drying operation, following the washing step, it is lmportant that temperatures should not be used which are capable of materially injuring -thefiber of the textile material, by seriously weakening the same. In the preferred form of the process these drying operations are conducted at temperatures about 100 C., or but slightly above, so as not to reduce the strength of the textile material. In the use 7 .of temperatures of about 100 C., in the final drying operation, it appears that the hydroxids of the rare earth elements are in dant for forming insoluble lakes with dye-.
stuffs, and, as before stated, for the purpose of imparting water repellency, but they have part at'least dehydrated with the formation always suffered from the disadvantage of being easily removed by alkalis, for example,
alkali soap solutions, the reason being apparently that owing to the acidic character of ts, oxid, aluminum reacts with the alkali v to form soluble compounds with the alkali metals, as for example sodium or potassium aluminate. The difli'culty just mentioned can be overcome in large measure by using the aluminum compound in connection or in combination with compounds of the rare 7 earth 'metals,in which case the rare earth or other compound appears to occlude or cover up the aluminum salt or salts in such manner that, while not destroying the distinctive character thereof, nevertheless renders it difficult to leach out'because of the difficulty of establishing actual contact of the alkalin solution with the aluminum compound so occluded or covered in the rare earth matrix.
' Because of its open and absorbent character itihas always been a matter of extreme difiiculty to render bleached fabric effectively water repellent, and it has therefore required such a large quantity of repellent ma terial to accomplish the desired end-that the uality and character of the fabric itself have e uently been impaired by the treatment a p ied. By a preliminary treatment b w ich the internal pores of the bleached fab- I ric are filled with insoluble and difiicultly recal methods of effecting purpose the textile material may be passed continuously or step-by-step between (and preferably in contact with) a pair or several pairs of electrodes while immersed in or wet with the impregnating bath, the elec trodes being connected to the appropriate poles or terminals of a suitable source of current. A voltage of from 6 to 8 volts (preferably) may be em loyed. The amperage used is determined c iefiy'by economical factors, and in general should not be so-high as to waste current in the form of heat reduced by resistance losses .in the bath. of the current is to decompose the salt the metallic radical moving toward the cathode but being converted into the hydroxid. There also appears to be a tendency for the current to force the finely pores of the fa ric by a process of cataphoresis or electrical osmosis. In some cases the electrolytic method may be used in conjunction w1th the chemical method, either before or after the same. In either case the second treatment may impart or increase the external water re ellency of the fabric, by which is meant the ifliculty of-being wetted.
I am aware that incandescent gas mantles have been made by impregnating textile fabren ric with rare earth metal oxides, and I do not claim such articles, which have no utility until burned or incinerated, but what claim is:
1. Textile material inherently capable of supporting mildew and like fungous growth, ered resistant thereto and a so repellent to water and resistant to attack by aelds, by impregnationwith a rare earth metal compound which is insoluble in alkaline solutions.
2. Textile material as described in the preceding claim, which is also impregnated with divided hydroxid into the an insoluble metallic compound imparting 4. Textile material impregnated with an insoluble rare earth metal compound and with a mildew-proofing metallic compound, said material being unincinerated.
5. Process of rendering textile material,
inherently capable of supporting mildew and like fungous growth, repellent to such action and also repe lent to water and resistant to attack by acids, which comprises impregnating the material with a solution of a subnitrate of a rare earth metal,removin excess liquid from the material, treating t e partially dried material with a reagent capable of converting the said salt into a compound insoluble in alkaline solutions, washing the material to remove any soluble compounds present, and thereafter drying the material. 6. Process of rendering textile material repellent to fungous growth and to water, and resistant to attack by acids, whichcomprises impregnating the material with a dilute solution of a rare earth metal compound, treating the impregnated material with a reagent adapted to precipitate the rare earth metal compound in a colloidal form which is insoluble in hydrocarbons and alkaline solutions, and thereafter drying the material. Process of rendering textile material repellent to fungous growth and to water, and resistant to attack by acids, which comrises imprelgnating the material with a diute relative y cold solution of a rare earth metal salt, treating the impregnated material with a precipitant adapted to convert the rare earthmetal salt into a colloidal form and thereafter drying the textile material --under pressure whereby tate is rendered substantially insoluble in the colloidal precipih drocarbons and alkali solutions and resistant to attack by acids.
8. Textile material repellent to fun ous growth, resistant to attack by acids, and repellent to .water, by impregnation with a hydroxid of a rare earth metal.
In testimony whereof I hereto afiix my signature.
CLARENCE B. WHITE.
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2482816A (en) * 1943-06-08 1949-09-27 Nat Lead Co Method of waterproofing textiles with zirconyl compounds
US2525049A (en) * 1946-08-22 1950-10-10 Du Pont Cellulose titanate film production
US2567184A (en) * 1948-01-06 1951-09-11 Borden Co Hardening casein artificial fibers with titanium, zirconium or tin salts
US2614025A (en) * 1948-04-26 1952-10-14 Ici Ltd Formaldehyde and uranyl salt treatment of protein filaments
US2766032A (en) * 1943-11-16 1956-10-09 Meister George Impregnated crucible
US2785041A (en) * 1953-12-07 1957-03-12 Du Pont Process of flameproofing and rot-proofing cellulosic materials by applying acidic solutions of antimony, zirconium and titanium and neutralizing with ammonia gas
DE975801C (en) * 1937-09-29 1962-09-27 Bayer Ag Process for impregnating textiles with aqueous dispersions of paraffin or waxes containing metal salts in a single bath process
US3446656A (en) * 1964-12-30 1969-05-27 Us Agriculture Zirconium compounds as algaecides
US3484271A (en) * 1965-06-25 1969-12-16 Riegel Paper Corp Two step in situ reaction for producing coated paper webs

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE975801C (en) * 1937-09-29 1962-09-27 Bayer Ag Process for impregnating textiles with aqueous dispersions of paraffin or waxes containing metal salts in a single bath process
US2482816A (en) * 1943-06-08 1949-09-27 Nat Lead Co Method of waterproofing textiles with zirconyl compounds
US2766032A (en) * 1943-11-16 1956-10-09 Meister George Impregnated crucible
US2525049A (en) * 1946-08-22 1950-10-10 Du Pont Cellulose titanate film production
US2567184A (en) * 1948-01-06 1951-09-11 Borden Co Hardening casein artificial fibers with titanium, zirconium or tin salts
US2614025A (en) * 1948-04-26 1952-10-14 Ici Ltd Formaldehyde and uranyl salt treatment of protein filaments
US2785041A (en) * 1953-12-07 1957-03-12 Du Pont Process of flameproofing and rot-proofing cellulosic materials by applying acidic solutions of antimony, zirconium and titanium and neutralizing with ammonia gas
US3446656A (en) * 1964-12-30 1969-05-27 Us Agriculture Zirconium compounds as algaecides
US3484271A (en) * 1965-06-25 1969-12-16 Riegel Paper Corp Two step in situ reaction for producing coated paper webs

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