US2602757A - Method and composition for producing silver coatings - Google Patents

Method and composition for producing silver coatings Download PDF

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US2602757A
US2602757A US20117A US2011748A US2602757A US 2602757 A US2602757 A US 2602757A US 20117 A US20117 A US 20117A US 2011748 A US2011748 A US 2011748A US 2602757 A US2602757 A US 2602757A
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silver
solution
mold
spray
lower aliphatic
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Morris S Kantrowitz
Earl J Gosnell
General Bernard
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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C18/00Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
    • C23C18/16Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
    • C23C18/31Coating with metals
    • C23C18/42Coating with noble metals
    • C23C18/44Coating with noble metals using reducing agents
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C18/00Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
    • C23C18/16Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
    • C23C18/18Pretreatment of the material to be coated
    • C23C18/20Pretreatment of the material to be coated of organic surfaces, e.g. resins
    • C23C18/28Sensitising or activating
    • C23C18/285Sensitising or activating with tin based compound or composition

Definitions

  • This invention relates to the production of silver coatings on surfaces and to new reducin compositions adapted to the deposition of silver from silver salt solutions. More particularly, this invention relates to the production of electrically conductive surfaces on wax or plastic electrotype molds or other non-conducting type surfaces. Still more particularly, this invention relates to the production of continuous silver coatings on wax or plastic electro-type molds by the spray method, i. e., the method wherein a spray of a silver complex solution is co-mingled with a spray of a reducer composition.
  • a silver solution such as, for example, silver ammonio nitrate, otherwise known as ammoniacal silver nitrate, is intermingled with a. suitable reducing agent such as, for example, formaldehyde, as disclosed in United States Letters Patent No. 2,400,518 to Kreber et al., or alternatively, hydrazine compounds or glyoxal, as disclosed in United States Letters Patent No. 2,363,354 to William Peacock, and the mixture is immediately contacted with the surface to be coated with silver.
  • a suitable reducing agent such as, for example, formaldehyde, as disclosed in United States Letters Patent No. 2,400,518 to Kreber et al., or alternatively, hydrazine compounds or glyoxal, as disclosed in United States Letters Patent No. 2,363,354 to William Peacock
  • the invention has for an object theproduction of adherent bright coatings of silver on any desired sub-surface such as, for example, electro-type molds of wax or plastic materials.
  • Another object is the provision of a novel reducing composition which permits substantially instantaneous reduction of silver, and
  • ther object is the production ,of a synergistic reducer composition adapted for the bright deposition of metallic silver from solutions of silver complexes;
  • Other and further objects will be apparent as the ensuing description proceeds.
  • a continuous bright adherent coating of silver is produced on a surface by first sensitizing said surface by treatment with asolution of a stannous salt and thereafter contacting the thus-sensitized surface with a mixture of a silver complex solution and a re ducer solution, said reducer solution comprising a lower aliphatic aldehyde admixed with a-lower alkylol amine.
  • the silver complex solution such as, for example, ammoniacal silver nitrate solution, is intermixed in the spray form witha reducer solution containing a lower aliphatic aldehyde admixed with a low-er alkylol amine.
  • an electrotype mold of wax, resin, or other plastic material is cleaned and sensitized by treatment with an alcoholic solution of stannous chloride or other stannous salt.
  • the residual stannous salt solution is then rinsed off and the surface is ready to receive the deposit of the silver coating.
  • An ammoniacal silver nitrate solution is preparedand then, separately, a reducer solution is prepared containing the synergistic mixture of a lower aliphaticaldehydewith a lower alkylol amine, as more fully described hereinafter.
  • the preferred spray apparatus, of the Barnes type, for example, is then charged and the twin sprays, one of silver solution and one of reducer solution, are impinged and simultaneously intermixed and brought in contact with 3. the surface of the electrotype mold or other object to be silvered.
  • the apparatus is operated similarly to the operation of the well-known paint spray gun to provide a uniform coating.
  • the spray apparatus is turned off and the th-us-silvered mold or other object is rinsed off and is complete and ready for use.
  • the silver deposit is employed as one electrode and additionally plated in the usual electroplating 'bath.
  • Suitable surfaces or objects for coating with silver in accordance with this invention include glass, metal,'varlous waxes capable of being molded, and the natural'and synthetic rubbers and resins or mixtures of thforegolng, forexample, Objects made of parafiin wax or othergwaxe's such as ozokerlte, montan-wax, carnaubaand other similar wax objects, as well as objects made of polyamides of the nylon type, many of the polymerized vinyl resins such as vinyl chloride, vinyl acetate, polystyrene, polymerized acrylates, methacrylates, polymerized silicones, co polymers, inter-polymers and mixtures of the foregoing, cellulose esters and ethers, urea-formaldehyde polymer, phenol formaldehyde resins, and mixtures of co-polymers and inter-polymers of the same, together with fillers, plasticizers, and other softening and modifying agents.
  • Any surface having a relatively impervious surface or made of relatively impervious material can readily be coated with silver in accordance with this invention.
  • superior results have been achieved employing a vinyl acetate-vinyl chloride co-polymer sold to the trade as "Vinylite by the Carbide and Carbon Chemicals Corporation.
  • Suitable silver salts for employment in accordance with this invention include many of the silver salts and their complexes which are readily reducible in solution to liberate native silver, such as, for example, ammoniacal silver chloride, ammoniacal silver sulphate, and, preferably, ammoniacal silver nitrate solution.
  • Other readily reducible compounds of silver can likewise be employed.
  • ammoniacal silver nitrate can be readily prepared,
  • the silver salt solution for reduction in accordance with this invention can be prepared in any suitable way, such as, for example, by
  • stannous chloride dissolved in a suitable lower ,aliphatic alcohol, preferably isopropyl alcohol,
  • the plastic or other object to be coated can be sponged,.wiped, rinsed or otherwise treated so as to sensitize the surface thereof for the acceptance and retention of metallic silver, while simultaneously the surface is adequately cleaned to provide a tenaciously adherent and continuously uniform coating of silver upon subsequent deposition. While isopropyl alcohol is preferred for reasons of economy and convenience, ethanol,
  • methanol, normalv propanol and similar lower aliphatic alcohols can be employed.
  • concentration of stannous chloride-inthe isopropanol or other selected alcohol is chosen.
  • chloride sensitization of this invention entirely overcomes the drastic cleaning procedures heretofore considered necessary while at the same time providing a continuous and tenaciously adherent deposit of metallic silver on highly polished glass, plastic or wax and other surfaces whichit is'desired to coat. No roughening" or other abrasion treatments of the object to be treated are required.
  • the reducing solution employed in accordance with this invention is a truly synergistic com position in that the combined solution of an aliphatic aldehyde with a lower alkylol amine possesses reducing properties which are a great deal stronger and infinitely superior to the reduction of metallic silver achieved by the sum of, either of the component.
  • Suitable lower aliphatic aldehydes for employment, in the reducing solution of this invention include acetaldehyde, propionaldehyde and, preferably, formaldehyde or glyoxal.
  • Other suitable water soluble monoor di-aldehydes can be employed. but as stated, it is preferred to employ glyoxal or formaldehyde.
  • glyoxal is preferred in that it operates in a highly satisfactory manner while at the same time is much more convenient for workmen to handle.
  • the glyoxal or other selected aldehyde is mixed with water and with the selected lower alkylol amine to make the finished reducing composition.
  • Suitable lower alkylol amines for employment in accordance with this invention include morpholine, ethylmonoethanolamine, ethyldiethanolamine, diethylethanolamine, 'monoethanolamine, diethanolamine, and preferably, triethanolamine.
  • Triethanolamine constitutes a preferred lower alkylol amine for employment in accordance with this invention since it is inexpensive, yields somewhat better silver films than the others, provides a more neutral reducer solu; tion when mixed with the selected aldehyde, and apparently has a greater stabilizingaction on the finished reducing solution when admixed with glyoxal or other selected lower aliphatic composition for employment inaccordance with this invention, the glyoxal or other selected lower aliphatic aldehyde is mixed with a suitable quantity of water and thereafter the desired quantity of triethanolamine or other selected lower alkylolamine, is incorporated in the solution. The order of mixing is unimportant to'the final composition, however.
  • a suitable quantity of lower aliphatic'aldehyde in the reducer c'o u position is from 1% to by weight, although it' is preferred to employ a somewhat more restricted proportion of formaldehyde, glyoxal or other lower aliphatic aldehyde, preferably within about 0.5% to 5.0% by weight of the total amount of reducer solution.
  • a suitable quantity of triethanol amine or other lower alkylol amine for admixture with the solvent and the glyoxal or other lower aliphatic aldehyde is from .02 to 2.0% by weight of lower alkyl amine such as triethanolamine.
  • the quantity of alkylol amine in the reduced composition is maintained within the more restricted range of from about 0.5 to 1.0% by weight based on the total composition.
  • An electro-type mold made of a co-polymer of vinyl acetate with vinyl chloride is suitably impressed in the customary fashion. Thereafter, the plastic mold is rinsed thoroughly with a 1% by weight solution of stannous chloride in isopropanol.
  • the thus cleaned and sensitized mold is rinsed with water and then exposed to an air-mixed spray of silver ammonio nitrate designated as solution A below, while concurrently mixing therewith in air a liquid spray of the reducing agent designated as solution B and prepared as described below.
  • the mixed spray is directed against the surface of the mold until there results a bright adherent continuous metallic silver deposit having a thickness of about 150 10- longer continued spraying produces a proportionately thicker film.
  • Solution A is prepared by dissolving 2 ounces of silver nitrate in about one-half gallon of water, then adding aqueous ammonia until the precipitate which first forms is redissolved and thereafter diluting the resulting mixture to a total volume of one gallon.
  • Solution B is prepared by dissolving nine fluid ounces of 37% formaldehyde solution in about one gallon of water, adding thereto sufficient triethanolamine to make 0.6% by weight of finished solution.
  • the formaldehyde component can be replaced by adding 2 by volume of a 30% glyoxal concentrated solution to one gallon of the diluted triethanolamine solution.
  • immersion coating can likewise be employed 'forsuch uses as, for exampleythe' silvering of mirrors'or the like. lt has been observed that the silver-coating in accordancewith this invention provides substantially complete freedom from the-usual commonly occurring pinholing.
  • adherent deposit of silver shows substantially no tendency to flake off during deposition, rinsing or other subsequent operations. This holds true even when extremely thick deposits are applied to highly polished surfaces.
  • a synergistic reducer composition for the bright deposition of continuous silver coatings of controlled thickness from silver complex solutions which comprises an aqueous solution of from about 0.5 to 1.0% by weight of triethanolamine admixed with about 0.5 to 5.0% of a lower aliphatic aldehyde selected from the group consisting of formaldehyde and glyoxal.
  • a synergistic reducer composition for the bright deposition of continuous silver coatings of controlled thickness from silver complex solutions which comprises an aqueous solution of from about 0.5 to 5.0% of glyoxal admixed with from about 0.5 to 1.0% by weight of triethanolamine.
  • steps which comprise first sensitizing such a mold by treating with a lower aliphatic alcohol solution of a stannous compound and then spraying the thus-sensitized mold with an aqueous solution of silver ammonio nitrate while co-mingling with said first spray a reducer spray solution comprising an aqueous synergistic mixture of about 0.5 to 1.0% by weight of triethanolamine having admixed therewith about 0.5 to 5.0% of a lower aliphatic aldehyde selected from the group consisting of formaldehyde and glyoxal, and then continuing said comingled spray treatment until a continuous adherent bright deposit of metallic silver of electrotype thickness is produced on said mold.
  • a process for the rapid production of a continuous bright adherent coating of silver on a surface of an electro-type mold which comprises first sensitizing said surface by treatment with a lower aliphatic alcoholic stannous chloride solution, and thereafter contacting said sensitized surface with an aqueous mixture of ammoniacal silver nitrate solution and aqueous reducing solution, said reducing solution comprising from about 0.5 to 5.0% by weight of formaldehyde and from about 0.5 to 1.0% by weight of tri ethanolamine.

Description

Patented July 8, 1952 METHOD AND COMPOSITION FOR PRODUC- ING SILVER COATINGS Morris S. Kantrowitz, Earl J. Gosnell, and
Bernard General, Washington; D. C.
No Drawing. Application April e, 1948, r
Serial No. 20 ,117" 1 5 claims? (Cl. 117-4 7 I (Granted under the act amended April 30, 1928; 370 0.
The invention described herein maybe manufactured and used by or for. the Government of the United States for governmental purposes without the payment to us of any royalty thereon in accordance with the provisions'of the Act of April 30, 1928 (Ch. 460, 45 Stat. L. 467).
This invention relates to the production of silver coatings on surfaces and to new reducin compositions adapted to the deposition of silver from silver salt solutions. More particularly, this invention relates to the production of electrically conductive surfaces on wax or plastic electrotype molds or other non-conducting type surfaces. Still more particularly, this invention relates to the production of continuous silver coatings on wax or plastic electro-type molds by the spray method, i. e., the method wherein a spray of a silver complex solution is co-mingled with a spray of a reducer composition.
Heretofore, surfaces or objects have been silvered by conjointly spraying against or impinging on said surfaces a co-mingled spray of a reducing agent with a silver complex solution in conventional apparatus such as that disclosed in United States Letters Patent No. 625,733, issued on May 30, 1899, to one Albert Barnes. By this technique, a silver solution such as, for example, silver ammonio nitrate, otherwise known as ammoniacal silver nitrate, is intermingled with a. suitable reducing agent such as, for example, formaldehyde, as disclosed in United States Letters Patent No. 2,400,518 to Kreber et al., or alternatively, hydrazine compounds or glyoxal, as disclosed in United States Letters Patent No. 2,363,354 to William Peacock, and the mixture is immediately contacted with the surface to be coated with silver.
These methods, while reasonably satisfactory for some purposes, suffer from several disadvantages, as, for example, the deposition of the silver is relatively slow, the surfaces to be coated must first be subjected to an exhaustive cleaning treatment, in many cases, the resulting silver film is full of pinholes or tends to flake off during deposition and subsequent rinsing, particularly on surfaces which are highly polished, and also, the noxious chemicals which are employ-ed are expensive and difiicult to obtain. One alternative to these methods, heretofore proposed in United States Letters Patent No. 1,989,764, is the employment of various ethanol amines as reducing agents. These ethanol amine reducing agents suffer from the serious disadvantage of necessitating the employment of high temperatures before they have any substantially effective action iTMmh 3,, i883f as and even then a very great length of time is necessary for the treatment, so long in fact .as to preclude the utilization of the Barnes'spray technique above mentioned.
Accordingly, the invention has for an object theproduction of adherent bright coatings of silver on any desired sub-surface such as, for example, electro-type molds of wax or plastic materials. Another object is the provision of a novel reducing composition which permits substantially instantaneous reduction of silver, and
at the same time, provides a continuous adherent coating of a thickness which .can be controlled substantially to any desired degree. Still a fur-. ther object is the production ,of a synergistic reducer composition adapted for the bright deposition of metallic silver from solutions of silver complexes; Other and further objects will be apparent as the ensuing description proceeds.
These objects are accomplished in accordance with this invention wherein a continuous bright adherent coating of silver is produced on a surface by first sensitizing said surface by treatment with asolution of a stannous salt and thereafter contacting the thus-sensitized surface with a mixture of a silver complex solution and a re ducer solution, said reducer solution comprising a lower aliphatic aldehyde admixed with a-lower alkylol amine. In one preferred embodiment, the silver complex solution such as, for example, ammoniacal silver nitrate solution, is intermixed in the spray form witha reducer solution containing a lower aliphatic aldehyde admixed with a low-er alkylol amine. Certain specific proportions of the chemicals employed have been found to yield superior'results in practice, as will be more fully described hereinafter.
In general, the-operating steps in carrying'out this invention are simply and easily carried out.
For example, an electrotype mold of wax, resin, or other plastic material is cleaned and sensitized by treatment with an alcoholic solution of stannous chloride or other stannous salt. The residual stannous salt solution is then rinsed off and the surface is ready to receive the deposit of the silver coating. An ammoniacal silver nitrate solution is preparedand then, separately, a reducer solution is prepared containing the synergistic mixture of a lower aliphaticaldehydewith a lower alkylol amine, as more fully described hereinafter. The preferred spray apparatus, of the Barnes type, for example, is then charged and the twin sprays, one of silver solution and one of reducer solution, are impinged and simultaneously intermixed and brought in contact with 3. the surface of the electrotype mold or other object to be silvered. The apparatus is operated similarly to the operation of the well-known paint spray gun to provide a uniform coating.
'I'hereupon, the spray apparatus is turned off and the th-us-silvered mold or other object is rinsed off and is complete and ready for use. In the electro-type mold, the silver deposit is employed as one electrode and additionally plated in the usual electroplating 'bath.
Suitable surfaces or objects for coating with silver in accordance with this invention include glass, metal,'varlous waxes capable of being molded, and the natural'and synthetic rubbers and resins or mixtures of thforegolng, forexample, Objects made of parafiin wax or othergwaxe's such as ozokerlte, montan-wax, carnaubaand other similar wax objects, as well as objects made of polyamides of the nylon type, many of the polymerized vinyl resins such as vinyl chloride, vinyl acetate, polystyrene, polymerized acrylates, methacrylates, polymerized silicones, co polymers, inter-polymers and mixtures of the foregoing, cellulose esters and ethers, urea-formaldehyde polymer, phenol formaldehyde resins, and mixtures of co-polymers and inter-polymers of the same, together with fillers, plasticizers, and other softening and modifying agents. Any surface having a relatively impervious surface or made of relatively impervious material can readily be coated with silver in accordance with this invention. For electro-type work, superior results have been achieved employing a vinyl acetate-vinyl chloride co-polymer sold to the trade as "Vinylite by the Carbide and Carbon Chemicals Corporation.
Suitable silver salts for employment in accordance with this invention include many of the silver salts and their complexes which are readily reducible in solution to liberate native silver, such as, for example, ammoniacal silver chloride, ammoniacal silver sulphate, and, preferably, ammoniacal silver nitrate solution. Other readily reducible compounds of silver can likewise be employed. However, it has been found that ammoniacal silver nitrate can be readily prepared,
is stable and relatively inexpensive, and it is therefore preferred.
The silver salt solution for reduction in accordance with this invention, can be prepared in any suitable way, such as, for example, by
dissolving the desired quantity of silver nitrate in water, thereafter adding ammonium hydroxide until the precipitate which first forms is just redissolved and then diluting to the desired final concentration. While a wide range of concentrations can be successfully employed, it has been found that an ammoniacal silver solution complex containing about two and one-half ounces of silver nitrate per gallon of finished solution, is entirely satisfactory. Greater concentrations up to ten ounces per gallon can be employed but are wasteful of silver, while lower concentrations tend to yield thinner films. In general, a silver nitrate concentration of from one to five ounces of silver nitrate per gallon of finished ammoniacal silver nitrate solution is preferred.
Before coating the surface with silver, it is highly desirable to sensitize the surface by treatment with a solution of a stannous salt. In this invention, an entirely effective cleaning of the surface to be coated is achieved simultaneously with sensitization by rinsing the plastic or other surface to be coated with an alcoholic solution of stannous chloride or other stannous s tion of a selected stannous salt, for example.
stannous chloride, dissolved in a suitable lower ,aliphatic alcohol, preferably isopropyl alcohol,
the plastic or other object to be coated can be sponged,.wiped, rinsed or otherwise treated so as to sensitize the surface thereof for the acceptance and retention of metallic silver, while simultaneously the surface is adequately cleaned to provide a tenaciously adherent and continuously uniform coating of silver upon subsequent deposition. While isopropyl alcohol is preferred for reasons of economy and convenience, ethanol,
methanol, normalv propanol and similar lower aliphatic alcohols can be employed. Preferably, the concentration of stannous chloride-inthe isopropanol or other selected alcohol, is chosen...
to be approximately 1%. At this concentration, an entirely satisfactory sensitization is secured, the solubility limits of the stannous saltin the alcohol are not exceeded, undesired hydrolysis is obviated since no aqueous medium is required, and the use of auxiliary wetting and penetrating agents is eliminated. The alcoholic stannous.
chloride sensitization of this invention entirely overcomes the drastic cleaning procedures heretofore considered necessary while at the same time providing a continuous and tenaciously adherent deposit of metallic silver on highly polished glass, plastic or wax and other surfaces whichit is'desired to coat. No roughening" or other abrasion treatments of the object to be treated are required.
The reducing solution employed in accordance with this invention, is a truly synergistic com position in that the combined solution of an aliphatic aldehyde with a lower alkylol amine possesses reducing properties which are a great deal stronger and infinitely superior to the reduction of metallic silver achieved by the sum of, either of the component. Suitable lower aliphatic aldehydes for employment, in the reducing solution of this invention, include acetaldehyde, propionaldehyde and, preferably, formaldehyde or glyoxal. Other suitable water soluble monoor di-aldehydes can be employed. but as stated, it is preferred to employ glyoxal or formaldehyde. Of these latter two, glyoxal is preferred in that it operates in a highly satisfactory manner while at the same time is much more convenient for workmen to handle. The glyoxal or other selected aldehyde is mixed with water and with the selected lower alkylol amine to make the finished reducing composition.
Suitable lower alkylol amines for employment in accordance with this invention include morpholine, ethylmonoethanolamine, ethyldiethanolamine, diethylethanolamine, 'monoethanolamine, diethanolamine, and preferably, triethanolamine. Triethanolamine constitutes a preferred lower alkylol amine for employment in accordance with this invention since it is inexpensive, yields somewhat better silver films than the others, provides a more neutral reducer solu; tion when mixed with the selected aldehyde, and apparently has a greater stabilizingaction on the finished reducing solution when admixed with glyoxal or other selected lower aliphatic composition for employment inaccordance with this invention, the glyoxal or other selected lower aliphatic aldehyde is mixed with a suitable quantity of water and thereafter the desired quantity of triethanolamine or other selected lower alkylolamine, is incorporated in the solution. The order of mixing is unimportant to'the final composition, however. A suitable quantity of lower aliphatic'aldehyde in the reducer c'o u position is from 1% to by weight, although it' is preferred to employ a somewhat more restricted proportion of formaldehyde, glyoxal or other lower aliphatic aldehyde, preferably within about 0.5% to 5.0% by weight of the total amount of reducer solution.
A suitable quantity of triethanol amine or other lower alkylol amine for admixture with the solvent and the glyoxal or other lower aliphatic aldehyde is from .02 to 2.0% by weight of lower alkyl amine such as triethanolamine. Preferably however, for superior results the quantity of alkylol amine in the reduced composition is maintained within the more restricted range of from about 0.5 to 1.0% by weight based on the total composition.
In the practice of this invention the following example is illustrative, without, however, being by way of limitation:
An electro-type mold made of a co-polymer of vinyl acetate with vinyl chloride is suitably impressed in the customary fashion. Thereafter, the plastic mold is rinsed thoroughly with a 1% by weight solution of stannous chloride in isopropanol. The thus cleaned and sensitized mold is rinsed with water and then exposed to an air-mixed spray of silver ammonio nitrate designated as solution A below, while concurrently mixing therewith in air a liquid spray of the reducing agent designated as solution B and prepared as described below. The mixed spray is directed against the surface of the mold until there results a bright adherent continuous metallic silver deposit having a thickness of about 150 10- longer continued spraying produces a proportionately thicker film. The spraying is then discontinued and the resulting silver coated electro-type mold is rinsed in water and is ready for the customary electro-plating procedure. Upon electro-plating, it Was found that a highly satisfactory electrically conductive surface was formed which showed no tendency to rupture during initial current surge.
Solution A is prepared by dissolving 2 ounces of silver nitrate in about one-half gallon of water, then adding aqueous ammonia until the precipitate which first forms is redissolved and thereafter diluting the resulting mixture to a total volume of one gallon. Solution B is prepared by dissolving nine fluid ounces of 37% formaldehyde solution in about one gallon of water, adding thereto sufficient triethanolamine to make 0.6% by weight of finished solution. Alternatively, the formaldehyde component can be replaced by adding 2 by volume of a 30% glyoxal concentrated solution to one gallon of the diluted triethanolamine solution.
It will be clear from the foregoing that there has been provided a highly desirable silver coating method and synergistic reducing composition for use therein which does not require the employment of heat or any other complicated procedure for its use. The silver deposition, in accordance with this invention, occurs substantially instantaneously and apparently is independent of the temperatures employed. No tedious and expensive cleaning procedures. are necessary in accordance with this'inventiomand acontinuous highly-adherent silver coating is produced whose thickness can be varied at the will of the operator by merely spraying for-av longer or shorter'ti'me.
While we preferv to employ the spray coating technique, immersion coating can likewise be employed 'forsuch uses as, for exampleythe' silvering of mirrors'or the like. lt has been observed that the silver-coating in accordancewith this invention provides substantially complete freedom from the-usual commonly occurring pinholing.
One of the very important advantages of this invention is that the adherent deposit of silver shows substantially no tendency to flake off during deposition, rinsing or other subsequent operations. This holds true even when extremely thick deposits are applied to highly polished surfaces.
It will be apparent from the foregoing that various changes in the details disclosed will occur to one skilled in the art and, therefore, various changes can be made without departing from the spirit and scope of this invention.
What we claim is:
l. A synergistic reducer composition for the bright deposition of continuous silver coatings of controlled thickness from silver complex solutions which comprises an aqueous solution of from about 0.5 to 1.0% by weight of triethanolamine admixed with about 0.5 to 5.0% of a lower aliphatic aldehyde selected from the group consisting of formaldehyde and glyoxal.
2. A synergistic reducer composition for the bright deposition of continuous silver coatings of controlled thickness from silver complex solutions which comprises an aqueous solution of from about 0.5 to 5.0% of glyoxal admixed with from about 0.5 to 1.0% by weight of triethanolamine.
3. In a process for the production of an electrically conductive surface on a plastic electrotype mold, the steps which comprise first sensitizing such a mold by treating with a lower aliphatic alcohol solution of a stannous compound and then spraying the thus-sensitized mold with an aqueous solution of silver ammonio nitrate while co-mingling with said first spray a reducer spray solution comprising an aqueous synergistic mixture of about 0.5 to 1.0% by weight of triethanolamine having admixed therewith about 0.5 to 5.0% of a lower aliphatic aldehyde selected from the group consisting of formaldehyde and glyoxal, and then continuing said comingled spray treatment until a continuous adherent bright deposit of metallic silver of electrotype thickness is produced on said mold.
4. A process for the rapid production of a continuous bright adherent coating of silver on a surface of an electro-type mold which comprises first sensitizing said surface by treatment with a lower aliphatic alcoholic stannous chloride solution, and thereafter contacting said sensitized surface with an aqueous mixture of ammoniacal silver nitrate solution and aqueous reducing solution, said reducing solution comprising from about 0.5 to 5.0% by weight of formaldehyde and from about 0.5 to 1.0% by weight of tri ethanolamine.
5. In a process for the production of an electrically conductive surface on a plastic electrotype mold, the steps of first sensitizing such a mold by rinsing with a lower aliphatic alcohol 2,602,757 v r y 7 8 7 solution of stannous chloride, and then spraying 4 the thus sensitized plastic mold with an aqueous REFERENCES CITED solution of silver ammonio nitrate while 00- The foliewmg e c s are of record in the mingling with said first spray a reducer spray file 0f thls petenti solution comprising an aqueous synergistic mix- 5 UNITED STATES PATENTS ture of about 0.5 to 5.0% by weight of glyoxal and from about 0.5 to 1.0% by weight of triethanolgf gfi De 3 amine and continuing said co-mingled spray 1941438 Ki i "5- 1933 treatment until a continuous adherent bright 1989764 r 1935 deposit of metallic silver of electro-type thick- 10 e sner e 2,184,053 Muehler Dec. 19, 1939 ness is produced on. said mold.
s W s Aug. 15, 2,363,354 Peacock Nov. 21, 194i EARL J. GOSNELL. BERNARD GENERAL.

Claims (1)

  1. 3. IN A PROCESS FOR THE PRODUCTION OF AN ELECTRICALLY CONDUCTIVE SURFACE ON A PLASTIC ELECTROTYPE MOLD, THE STEPS WHICH COMPRISE FIRST SENSITIZING SUCH A MOLD BY TREATING WITH A LOWER ALIPHATIC ALCOHOL SOLUTION OF A STANNOUS COMPOUND AND THEN SPRAYING THE THUS-SENSITIZED MOLD WITH AN AQUEOUS SOLUTION OF SILVER AMMONIO NITRATE WHILE CO-MINGLING WITH SAID FIRST SPRAY A REDUCER SPRAY SOLUTION COMPRISING AN AQUEOUS SYNERGISTIC MIXTURE OF ABOUT 0.5 TO 1.0% BY WEIGHT OF TRIETHANOLAMINE HAVING ADMIXED THERETWITH ABOUT 0.5 TO 5.0% OF A LOWER ALIPHATIC ALDEHYDE SELECTD FROM THE GROUP CONSISTING OF FORMALDEHYDE AND GLYOXAL, AND THEN CONTINING SAID COMINGLED SPRAY TREATMENT UNTIL A CONTINUOUS ADHERENT BRIGHT DEPOSIT OF METALLIC SILVER OF ELECTROTYPE THICKNESS IS PRODUCED ON SAID MOLD.
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Cited By (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2759845A (en) * 1954-10-25 1956-08-21 Metropolitan Mirror And Glass Processes of precipitating copper from copper sulfate solutions and precipitating media for so doing
US2764502A (en) * 1954-11-26 1956-09-25 Emerson & Cuming Inc Method of treating resinous materials to improve their adhesion characteristics
US2871139A (en) * 1955-12-08 1959-01-27 Wein Samuel Silvering process and materials
US2872346A (en) * 1956-05-21 1959-02-03 Miller Adolph Metal plating bath
US2879175A (en) * 1953-10-23 1959-03-24 Ericsson Telefon Ab L M Method for producing a silver coating on a non metallic material
US2915406A (en) * 1958-03-03 1959-12-01 Int Nickel Co Palladium plating by chemical reduction
US2934460A (en) * 1958-03-31 1960-04-26 Union Carbide Corp Method for impregnating a carbonaceous brush with silver
US2996408A (en) * 1958-03-31 1961-08-15 Gen Electric Copper plating process and solution
US3012906A (en) * 1958-08-15 1961-12-12 Gen Aniline & Film Corp Metallized plastics and methods for making same
US3075855A (en) * 1958-03-31 1963-01-29 Gen Electric Copper plating process and solutions
US3091554A (en) * 1960-07-01 1963-05-28 American Viscose Corp Oxidation resistant cellulosic pellicle and process for the manufacture thereof
US3093509A (en) * 1959-09-28 1963-06-11 Wein Samuel Process for making copper films
US3119709A (en) * 1956-09-28 1964-01-28 Atkinson Lab Inc Material and method for electroless deposition of metal
US3135046A (en) * 1960-09-30 1964-06-02 Corning Glass Works Method of forming metallic films on glass
US3274419A (en) * 1962-01-23 1966-09-20 Dow Chemical Co Flexible electroluminescent lamp having transparent metal-coated strands as the light transmitting electrode
DE1268471B (en) * 1963-09-09 1968-05-16 Photocircuits Corp Chemical gold plating bath
US3397963A (en) * 1964-04-04 1968-08-20 Bayer Ag Reducing agent
US3425946A (en) * 1966-08-26 1969-02-04 William M Emons Jr Electroless plating composition
US3489602A (en) * 1965-05-25 1970-01-13 Hughes Aircraft Co Method of impregnating porous tungsten and resulting article
US3877965A (en) * 1970-09-28 1975-04-15 Rohm & Haas Conductive nylon substrates and method of producing them
US4139660A (en) * 1963-07-16 1979-02-13 Bernhard Joos Method for increasing solid surface tension
US4144361A (en) * 1977-07-06 1979-03-13 Nathan Feldstein Methods for applying metallic silver coatings
DE3242649C1 (en) * 1982-11-18 1984-05-03 Glasplakatefabrik Offenburg Fritz Borsi KG, 7600 Offenburg Method of producing a silver mirror
US5395651A (en) * 1989-05-04 1995-03-07 Ad Tech Holdings Limited Deposition of silver layer on nonconducting substrate
US20030157264A1 (en) * 2000-10-06 2003-08-21 Carl Hutchinson Bath and method of electroless plating of silver on metal surfaces
US6716895B1 (en) 1999-12-15 2004-04-06 C.R. Bard, Inc. Polymer compositions containing colloids of silver salts
US20040116551A1 (en) * 1999-12-15 2004-06-17 Terry Richard N. Antimicrobial compositions containing colloids of oligodynamic metals
US7820284B2 (en) 2001-12-03 2010-10-26 C.R. Bard Inc. Microbe-resistant medical device, microbe-resistant polymeric coating and methods for producing same
US20140205859A1 (en) * 2013-01-22 2014-07-24 Andre Reiss Electroless silvering ink

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US1741477A (en) * 1926-01-02 1929-12-31 Radio Patents Corp Method of metallizing the surfaces of insulating bands
US1941438A (en) * 1931-09-15 1933-12-26 Kiefer Karl Process for metallizing with reflecting highly polished surface celluloid in sheets and any other form by chemical means
US1989764A (en) * 1934-01-03 1935-02-05 Meltsner Max Process and composition for the production of reflecting surfaces
US2184053A (en) * 1939-03-29 1939-12-19 Eastman Kodak Co Stable compositions useful in the compounding of photographic developers
US2355933A (en) * 1941-04-12 1944-08-15 Cohan Epner Co Inc Process of metal plating
US2363354A (en) * 1939-11-16 1944-11-21 Libbey Owens Ford Glass Co Method of making mirrors

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Publication number Priority date Publication date Assignee Title
US1741477A (en) * 1926-01-02 1929-12-31 Radio Patents Corp Method of metallizing the surfaces of insulating bands
US1941438A (en) * 1931-09-15 1933-12-26 Kiefer Karl Process for metallizing with reflecting highly polished surface celluloid in sheets and any other form by chemical means
US1989764A (en) * 1934-01-03 1935-02-05 Meltsner Max Process and composition for the production of reflecting surfaces
US2184053A (en) * 1939-03-29 1939-12-19 Eastman Kodak Co Stable compositions useful in the compounding of photographic developers
US2363354A (en) * 1939-11-16 1944-11-21 Libbey Owens Ford Glass Co Method of making mirrors
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Cited By (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2879175A (en) * 1953-10-23 1959-03-24 Ericsson Telefon Ab L M Method for producing a silver coating on a non metallic material
US2759845A (en) * 1954-10-25 1956-08-21 Metropolitan Mirror And Glass Processes of precipitating copper from copper sulfate solutions and precipitating media for so doing
US2764502A (en) * 1954-11-26 1956-09-25 Emerson & Cuming Inc Method of treating resinous materials to improve their adhesion characteristics
US2871139A (en) * 1955-12-08 1959-01-27 Wein Samuel Silvering process and materials
US2872346A (en) * 1956-05-21 1959-02-03 Miller Adolph Metal plating bath
US3119709A (en) * 1956-09-28 1964-01-28 Atkinson Lab Inc Material and method for electroless deposition of metal
US2915406A (en) * 1958-03-03 1959-12-01 Int Nickel Co Palladium plating by chemical reduction
US2934460A (en) * 1958-03-31 1960-04-26 Union Carbide Corp Method for impregnating a carbonaceous brush with silver
US2996408A (en) * 1958-03-31 1961-08-15 Gen Electric Copper plating process and solution
US3075855A (en) * 1958-03-31 1963-01-29 Gen Electric Copper plating process and solutions
US3012906A (en) * 1958-08-15 1961-12-12 Gen Aniline & Film Corp Metallized plastics and methods for making same
US3093509A (en) * 1959-09-28 1963-06-11 Wein Samuel Process for making copper films
US3091554A (en) * 1960-07-01 1963-05-28 American Viscose Corp Oxidation resistant cellulosic pellicle and process for the manufacture thereof
US3135046A (en) * 1960-09-30 1964-06-02 Corning Glass Works Method of forming metallic films on glass
US3274419A (en) * 1962-01-23 1966-09-20 Dow Chemical Co Flexible electroluminescent lamp having transparent metal-coated strands as the light transmitting electrode
US4139660A (en) * 1963-07-16 1979-02-13 Bernhard Joos Method for increasing solid surface tension
DE1268471B (en) * 1963-09-09 1968-05-16 Photocircuits Corp Chemical gold plating bath
US3397963A (en) * 1964-04-04 1968-08-20 Bayer Ag Reducing agent
US3489602A (en) * 1965-05-25 1970-01-13 Hughes Aircraft Co Method of impregnating porous tungsten and resulting article
US3425946A (en) * 1966-08-26 1969-02-04 William M Emons Jr Electroless plating composition
US3877965A (en) * 1970-09-28 1975-04-15 Rohm & Haas Conductive nylon substrates and method of producing them
US4144361A (en) * 1977-07-06 1979-03-13 Nathan Feldstein Methods for applying metallic silver coatings
DE3242649C1 (en) * 1982-11-18 1984-05-03 Glasplakatefabrik Offenburg Fritz Borsi KG, 7600 Offenburg Method of producing a silver mirror
US5395651A (en) * 1989-05-04 1995-03-07 Ad Tech Holdings Limited Deposition of silver layer on nonconducting substrate
US5747178A (en) * 1989-05-04 1998-05-05 Adtech Holding Deposition of silver layer on nonconducting substrate
US5965204A (en) * 1989-05-04 1999-10-12 Ad Tech Holdings Limited Deposition of silver layer on nonconducting substrate
US6224983B1 (en) 1989-05-04 2001-05-01 Ad Tech Holdings Limited Deposition of silver layer on nonconducting substrate
US7179849B2 (en) 1999-12-15 2007-02-20 C. R. Bard, Inc. Antimicrobial compositions containing colloids of oligodynamic metals
US6716895B1 (en) 1999-12-15 2004-04-06 C.R. Bard, Inc. Polymer compositions containing colloids of silver salts
US20040116551A1 (en) * 1999-12-15 2004-06-17 Terry Richard N. Antimicrobial compositions containing colloids of oligodynamic metals
US20090293882A1 (en) * 1999-12-15 2009-12-03 C.R. Bard, Inc. Antimicrobial compositions containing colloids of oligodynamic metals
US8034454B2 (en) 1999-12-15 2011-10-11 C.R. Bard, Inc. Antimicrobial compositions containing colloids of oligodynamic metals
US6869637B2 (en) * 2000-10-06 2005-03-22 Atotech Deutschland Gmbh Bath and method of electroless plating of silver on metal surfaces
US20030157264A1 (en) * 2000-10-06 2003-08-21 Carl Hutchinson Bath and method of electroless plating of silver on metal surfaces
US7820284B2 (en) 2001-12-03 2010-10-26 C.R. Bard Inc. Microbe-resistant medical device, microbe-resistant polymeric coating and methods for producing same
US20140205859A1 (en) * 2013-01-22 2014-07-24 Andre Reiss Electroless silvering ink
US9663667B2 (en) * 2013-01-22 2017-05-30 Andre Reiss Electroless silvering ink

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