Classifications

• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
  • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
  • C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
  • C03C17/40—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal all coatings being metal coatings

Definitions

• a mirror is made by depositing silver on a glass plate by chemical reduction of silver nitrate, covering the silver film with a protective copper layer deposited from a copper sulfate solution by means of a finely divided less noble metal, and by passivating the copper coating by contact with a solution of chromic acid, a chromate, or a dichromate.
• the invention relates to mirrors having a reflecting silver surface protected by a copper coating, and particularly to an improvement in minors whose copper coating is formed by reduction of a copper sulfate solution by means of a metal less noble than copper.
• a reflecting silver film is readily deposited on plate glass, transparent plastic, or other solid, inert, transparent substrates by contacting a surface of the substrate with a solution of a silver salt containing a reducing agent. A more uniform and better adhering deposit is obtained if the surface to be coated is first activated. Although the silver film so produced is very thin, it is mechanically and optically adequate for a second surface mirror when protected by a coating of metallic copper.
• Copper coatings can be formed by electrodeposition but a simpler chemical deposition method has been disclosed by Meth in US. Pats. No. 2,664,363, 2,720,487, and 2,768,944.
• a copper layer having a thickness of 200 or even more is formed on the silver film by contact with a copper sulfate solution in which a metal less noble than copper is dispersed. The deposition rate is highest if the copper is deposited from an acidic solution.
• Silver mirrors covered with a copper layer by the chemical method outlined above have been found to corrode more readily than otherwise similar mirrors in which the copper coating is formed by electrodeposition. Even relatively heavy copper coatings produced by the above chemical method are prone to fonn corrosion pits even when carefully rinsed to remove all soluble electrolytes from the copper surface. Corrosion is even more rapid if the copper coating is not rinsed with extreme care.
• Copper coatings as thin as 40 p. adequately protect a mirror of the invention against corrosion if passivated by the chromating treatment. Rinsing before or after the treatment is not critical nor even useful.
• test i atmospheric corrosion tests of mirrors of the type described and accelerated tests of varying severity which will be referred to hereinafter as test i, test II, and test III.
• test l the exposed copper surface of the finished mirror is sprayed with distilled water for a few seconds and dried.
• test ll the copper coating is left in contact with a 30 g./l. sodium chloride solution for 48 hours at room temperature.
• test III the copper surface is covered for five minutes with a filter paper freshly impregnated with an aqueous solution of 60 gJl. sodium chloride, l g./l. potassium ferricyanide, and L2 ml./l. concentrated ammonium hydroxide solution.
• the corrosion behavior of the mirror in the atmosphere can be predicted with good accuracy from the number of pin holes visible in the reflecting silver surface under a low power microscope.
• EXAMPLE I A glass plate was thoroughly cleaned and ultimately rinsed with distilled water. A surface of the plate was then activated by brief contact with a 0.3% solution of stannous chloride. It was then silvered by pouring a freshly prepared 2:] mixture of a silver salt solution and of a reducing solution over the plate at a rate of 5 ml. per dm. glass surface.
• the silver salt solution contained 23 g./l. silver nitrate and 36 g./l. ammonium hydroxide.
• the reducing solution contained l0 g./l. cane sugar and 1.4 g./l. tartaric acid.
• the silver layer formed had a thickness of 55 m It was coated with copper by simultaneous spraying with a solution of g./l.
• the freshly copper-coated solution was not rinsed with water but was directly dipped for five seconds in a solution of 0.5 g./l. chromium trioxide or chromic acid. After withdrawal from the chromating solution, the finished mirror was airdried without rinsing. lts appearance was not affected by the chromating treatment.
• EXAMPLE 2 A carefully cleaned glass plate was activated by contact with a 0.1% solution of stannous chloride and silvered by flooding at a rate of 5 rnL/dm. with a freshly prepared 2:1 mixture of a silver salt solution prepared from 18 g./l. silver nitrate, 32 g./l. ammonium hydroxide, and I4 g./l. sodium hydroxide, and a reducing solution containing 10 g./l. cane sugar and L4 g./l. tartaric acid.
• the silver film produced had a thickness of 50 u. it was then sprayed simultaneously with 30 mlJdm. each of an aqueous solution containing I20 g./l.
• a thoroughly cleaned and rinsed glass plate was activated with a 0.05% stannous chloride solution and thereafter silvered by flooding with a 2:1 mixture of a silver salt solution containing 20 g./l. silver nitrate, 35 g./l. ammonium hydroxide, and 15 g./l. sodium hydroxide, with a reducing solution of 10 g./l. cane sugar and 1.4 g. tartaric acid.
• the silver film produced had an average thickness of 54 m it was coated with I20 m copper by simultaneous spraying with 40 ml. per drn. each of a solution containing l g./l. CuSO,.5HB20 and I g./l.
• ammonium persulfate and of dispersion of 9.3 g. zinc powder (passing a 300 mesh screen) in one liter water.
• the freshly deposited copper coating was not washed, but the mirror was dipped at once for three seconds in a solution of sodium chromate containing 2 g./l. CrO, equivalent. lt withstood all corrosion tests as described in examples I and 2.
• the copper coating turned black upon 2 days exposure to the corrosive atmosphere.
• Activating treatments with nucleating agents other than stannous chloride are well known to those skilled in the art and may be substituted for the specifically disclosed method without affecting the results achieved.
• stannous chloride it should be present in the activating solution in a preferred concentration of 0.01 to l.0 percent.
• the silvering of glass and plastics is a well developed art.
• the silver film need not be deposited by chemical reduction of a silver salt from its aqueous solution but may be formed by vacuum deposition in a known manner. If an ammoniacal silver nitrate solution provides the silver salt in the reduction method, the concentration of silver nitrate should be about 5 to 25 g./l., and that of ammonium hydroxide to to 50 g./l. Equivalent amounts of other silver salts may be substituted for the nitrate.
• the reducing agent should be used in an amount sufficient to precipitate from the solution approximately to 60% of the silver present therein as a soluble compound.
• Rochelle salt, saccharides other than sucrose, and formaldehyde are merely representative of the wide range of reducing agents which have been used for the same purpose heretofore, and are equally applicable in the method of this invention.
• cadmium, nickel, cobalt and chromium may be substituted for the zinc and iron powders described in the examples. It has further been found that the same or closely similar effects are produced by tungsten powder, molybdenum powder, or manganese powder, and by finely dispersed alloys of the several metals mentioned. About 6 to 12 grams of the fine metal powders can be kept adequately dispersed in a liter of water by mechanical agitation. The concentration of the metal dispersion is chosen so that it may be sprayed on the silver surface at a rate of 20 to 60 mLIdm.
• the copper sulfate solution may contain 50 to 240 g./l. copper sulfate crystals (CuSO,5H,O) and should contain 5 to 20 grams of an acidic solution agent.
• CuSO,5H,O copper sulfate crystals
• the use of sulfuric and and they may of all the adphosphoric acid has been disclosed in the above-identified patents, but tartaric acid, oxalic acid, formic acid and many other acids varying in their dissociation rate between the values for sulfuric acid and the mentioned organic acids have been found similarly effective. Good results have also been obtained with acidic salts, ammonium persulfate being par ticularly useful in producing good mirrors with a minimum thickness of copper.
• the ratio of copper sulfate and reducing metal in the mixture applied to the silver surface should be such that the copper sulfate is present in an amount five to ten times the equivalent of the reducing metal. Thus, a large excess of copper sulfate remains in the solution after the reducing metal is completely spent.
• a copper layer 45 to 100 mg. is quickly formed, and heavier coatings may be prepared, as has been shown above.
• the chromating solution may contain chromic acid or soluble chromates or dichromates.
• the alkali metal and ammonium chromates and dichromates are most conveniently available and are preferred when free chromic acid is not used.
• concentrations between 0.0! and g./l. chromium trioxide, or the corresponding amount of chromate or dichromate concentrations of less than 0.1 g./l. are too slow to be practical, and nothing is gained by increasing the concentration beyond 20 g./l. while drag-out losses of CrO values are unnecessarily increased.
• the chromating solution should be free from significant amounts of strong acids such as sulfuric acid, hydrochloric acid, or nitric acid.
• the concentration of strong mineral acid, if any, should be not more than to make the chromating solution 0.01 N with respect to the acid. Nitric acid is particularly detrimental when present in excessive amounts.
• the necessary time of contact between the copper deposit and the chromating solution is short, one second being generally adequate. While there does not seem to be a critical upper limit to the chromating time, nothing is accomplished by extending the chromating treatment beyond a few seconds, and the copper layer may be attacked by the more concentrated chromium oxide, chromate, or dichromate solutions. The treatment should therefore not usually be prolonged beyond 300 seconds.
• the method of application may be chosen freely, dipping and spraying being usually most convenient. Spraying with 5 to 50 ml. ⁇ dm. is normally preferred.
• the copper coating may be washed with water prior to chromating and also after chromating, but the washing is not necessary and only adds to the cost of the method.
• the freshly deposited copper layer may be chromated at once while still wet with the mixture employed in forming the copper deposit.
• a method of making a mirror in which a smooth surface of a solid, inert, transparent substrate is silvered, and the silver film on the substrate is further coated with a protective layer of copper by reduction of an acidic copper sulfate solution by means of a finely divided metal less noble than copper, the improvement which comprises contacting the exposed surface of said protective layer with a dilute aqueous solution essentially consisting of water and of chromic acid, a water-soluble chromate, or a water-soluble dichromate, at ambient temperature, said solution containing an amount of chromium equivalent to 0.01 to 80 grams per literchromium trioxide, and said exposed surface being contacted with said aqueous solution for not substantially less than one second.
• said exposed surface being contacted with said aqueous solution after the coating of said silver film with said protective layer without intermediate rinsing of the exposed surface with water.
• aqueous solution being a solution of an alkali metal salt or of an ammonium salt of chromic or dichromic acid.

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• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Geochemistry & Mineralogy (AREA)
• Materials Engineering (AREA)
• Organic Chemistry (AREA)
• Chemical Treatment Of Metals (AREA)
• Surface Treatment Of Glass (AREA)

Applications Claiming Priority (1)

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Cited By (4)

• 1968
  • 1968-10-31 BE BE723176D patent/BE723176A/xx unknown
  • 1968-11-20 DE DE19681810030 patent/DE1810030A1/de active Pending
  • 1968-11-20 FR FR1604274D patent/FR1604274A/fr not_active Expired
  • 1968-11-27 GB GB56192/68A patent/GB1192100A/en not_active Expired
  • 1968-12-23 US US786419A patent/US3615882A/en not_active Expired - Lifetime

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