US2865785A - Methods of coating catalyst carriers - Google Patents
Methods of coating catalyst carriers Download PDFInfo
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- US2865785A US2865785A US499589A US49958955A US2865785A US 2865785 A US2865785 A US 2865785A US 499589 A US499589 A US 499589A US 49958955 A US49958955 A US 49958955A US 2865785 A US2865785 A US 2865785A
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- carrier
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- 238000000034 method Methods 0.000 title claims description 38
- 239000003054 catalyst Substances 0.000 title claims description 22
- 238000000576 coating method Methods 0.000 title claims description 21
- 239000011248 coating agent Substances 0.000 title claims description 18
- 239000000969 carrier Substances 0.000 title description 15
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 62
- 229910052697 platinum Inorganic materials 0.000 claims description 30
- 229910052751 metal Inorganic materials 0.000 claims description 17
- 239000002184 metal Substances 0.000 claims description 17
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 16
- 230000003197 catalytic effect Effects 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 9
- 229910052763 palladium Inorganic materials 0.000 claims description 8
- 238000000354 decomposition reaction Methods 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 3
- 230000008018 melting Effects 0.000 claims description 2
- 238000002844 melting Methods 0.000 claims description 2
- 239000003863 metallic catalyst Substances 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 28
- 239000002737 fuel gas Substances 0.000 description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000000446 fuel Substances 0.000 description 8
- CLSUSRZJUQMOHH-UHFFFAOYSA-L platinum dichloride Chemical compound Cl[Pt]Cl CLSUSRZJUQMOHH-UHFFFAOYSA-L 0.000 description 7
- 238000000151 deposition Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- 150000003058 platinum compounds Chemical class 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 3
- 229910003446 platinum oxide Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 230000001464 adherent effect Effects 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 150000002940 palladium Chemical class 0.000 description 2
- 150000002941 palladium compounds Chemical class 0.000 description 2
- 150000003839 salts Chemical group 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- QZPSXPBJTPJTSZ-UHFFFAOYSA-N aqua regia Chemical compound Cl.O[N+]([O-])=O QZPSXPBJTPJTSZ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- -1 platinum compound palladium compound Chemical class 0.000 description 1
- KGRJUMGAEQQVFK-UHFFFAOYSA-L platinum(2+);dibromide Chemical compound Br[Pt]Br KGRJUMGAEQQVFK-UHFFFAOYSA-L 0.000 description 1
- NWAHZABTSDUXMJ-UHFFFAOYSA-N platinum(2+);dinitrate Chemical compound [Pt+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O NWAHZABTSDUXMJ-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003252 repetitive effect Effects 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
- B01J23/44—Palladium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/86—Catalytic processes
- B01D53/864—Removing carbon monoxide or hydrocarbons
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
- B01J23/42—Platinum
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0215—Coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/03—Precipitation; Co-precipitation
Definitions
- Catalyst-coated carriers of the type to which I have reference have just recently been developed for use in household incinerators to burn the odorous olf gases of incineration at temperatures far below those normally required for their combustion.
- My assignees co-pending applications Serial Nos. 488,888 and 488,889 setforth in detail the construction of the catalyst units which are employed, and describe the carriers for the platinum or palladium coatings which serve as the catalytic agents.
- One of the foremost objects of the instant invention is accordingly to provide a coatingvor metallizing process wherein the steps or stages of treatment in the process can be very rapidly ⁇ performed in a highly reliable and efficient mannerwhile the carriers are traveling on conveyor means which passes them continuously through the neces-- sary processing apparatus.
- Another object of the invention is to provide an improved method of the type outlined which is capable of producing coatings of greater thickness and comprisinga greater percentage of free catalytic metal in an uncombined state than has heretofore been possible.
- a further object of the invention is to provide an irnproved method of coating a catalyst on catalyst carriers which securely lodges the metal on the carrier in a manner to provide a surface which has a tine grained texture.
- Another object of the inventionris to provide a method or process such as described which provides a coating of uniform thickness and density on the entire surface of the carrier and docs not leave uncoated areas which have no catalyzing value.
- a further object of the invention is to provide a method or process such as described which requires only very simple and inexpensive processing apparatus which can be very readily set up to form a relatively compact production line.
- Another object of the invention is to provide a metallizing process which does not require the use of a flux such as would provide the problem of uniformly dispersing the ⁇ same in a mixture with the metal over the carrier, and
- the process comprises the steps of cleaning the carrier, applying an aqueous solution of a suitable platinum or palladium compound, to the carrier, firing the carrier in a fuel ame which is surrounded by non-combusted fuel vapors whose burning may be catalyzed, and
- Fig. l is a schematic view showing apparatus for coating saddle type carrier members.
- Fig. 2 is a similar view showing apparatus for coating a carrier strip which can later be cut into ribbons of the desired length.
- a numeral lll in Fig. l designates a hopper which may be continuously supplied with saddle type berl carriers C.
- These carriers which are fully described in the instant assignees co-pending application, Serial No. 488,888, may be formed of a suitable ceramic or metallic material and I have found Alundurn saddles to be particularly well adapted to the process which I will now describe.
- the hopper 1t will deposit the saddles preferably one at a time on a perforate or screen conveyor 1l traveling in the direction indicated over a cleaning ame 12 which may be provided by a conventional fuel gas burner. Actually what so that, while they are still very hot they are not.
- the solution 1S in the tank 13 may comprise an aqueous platinum chloride solution whose platinum content is 20 to 25 grams per liter of solution and may be prepared in various ways or purchased in salt form.
- One method of preparing such a solution which I have found satisfactory is to dissolve a measured weight of scrap platinum in a measured volume of aqua regia solution to produce platinum chloride and platinum nitrate which may then be evaporated to the point where the solids begin to separate out. Distilled water may then be added to form a solution wherein the platinum is in the proportion indicated above. If the platinum chloride solution which is substantially forty percent platinum is provided in salt form, fifty grams of it can be immediately dissolved in a small volume of warm distilled water and thence further distilled water may be added to make up the liter of solution.
- Such a solution will contain approximately 2O grams by weight of platinum. It should be including platinum lluoride, platinum bromide, platimiml nitrate or the like. Further, where it is desired to provide a palladium coating instead of a platinum coating, a suitable palladium salt could be employed. The preparation of the solution might be identical to provide an aqueous solution in which the palladium content was 2() grams per liter.a Still a further alternative in providing a catalyst solution might be to provide a mixture of platinum and palladium salts diluted so that their combined metallic content was approximately 20 grams per liter of solution.
- the burner which produces the flame may be a conventional Mekker or Fisher grid-type fuel gas burner' which has air blown in at the bottom thereof. Best results are obtained if the burner is disposed at a slight angle relative to the plane of the conveyor 16. While it is thought that other gascous, liquid, or solid hydrocarbon fuels may also be employed with good results, l have found that particularly good Aresults are obtained with a bottled gas fuel whose constituents are propane in the amount of S6 percent and butane in the amount of 14 percent. Such a fuel will produce a normal flame whose heat is in the range l555 F. to l730 F. or 846 C.
- the fuel used must be capable of producing a ame which heats the saddles to a white heat and is enough above the platinum chloride decomposition temperature of 581 C. and platinum oxide decomposition temperature of 555 C. to tix the separated platinum to the saddles, but below the temperature of l755 C. at which platinum melts.
- the fuel gases which are not primarily combusted because they are heavier than air hover around the ame and carrier, and in effect function as a iiuxing agent to prevent the formation of an appreciable amount of platinum oxide.
- the platinum coating will comprise an almost pure, iirmly fused, dense deposition of free platinum. This deposit and succeeding deposits, will in fact be approximately 80% pure platinum with the remainder platinum oxide. It is thought that the fuel gas employed should contain a relatively high percentage of propane or one of its homologs since these fuels will so readily catalytically oxidize in the presence of platinum or palladium to provide the high temperatures which 4 achieve the rapid and complete reduction of the metallic compounds.
- Fig. 2 I have shown a process which is identical except that the coating is tired on a continuously moving strip of metal S which is unwound from a reel 25 and passes through various stages in the process to a windup reel Z6.
- the surface of the metal strip may be roughened prior to commencing the operation by etching it.
- Means for driving the tape at a relatively slow rate are not shown, however it will be appreciated that such are well known.
- Similar numerals to the numerals used in Fig. l are applied to the tanks and burner ames in Fig. 2 and it should be apparent that the coating process is identical with that previously described.
- the tanks are, it will he noted, U-shaped rather than rectilinear, and idler rollers must be provided to direct the path of the tape.
- the coating thus applied to the tape will be so firmly lodged thereon that cutting of the tape into ribbons suitable for use in the catalytic unit described in the previously mentioned application No. 488,889 can be accomplished Without chipping the coating or
- Both carriers are provided with roughened surfaces prior to metallizing to enhance the depositing action.
- the saddles may be formed of a special mix which provides a rough rather than glazed surface or may be sandblasted.
- the metal ribbon may be etched or sandblasted.
- a process for coating a rough surface catalyst car rier with metallic catalyst selected from the group consisting of platinum, palladium, a combination of platinum and palladium, and compounds thereof comprising the steps of applying a tiame reducible catalyst compound in solution to the rough surface of the carrier to coat the carrier, and firing the coated carrier in an open ame which contacts the carrier to reduce catalyst compound to free catalytic metal and tix free catalytic metal to the carrier; said flame heating the coated carrier at temperatures above the decomposition temperature of the catalyst compound and below the melting point of the free catalytic metal.
- a process for coating a rough surface catalyst carrier with platinum comprising the steps of applying a flame reducible platinum compound in solution to the rough surface'of the carrier to coat the carrier and firing the coated carrier in an open flame to reduce platinum compound to .free platinum metal and ix free platinum metal to the carrier; said flame heating the coated carrer at a temperature from 581 C. to 1755 C.
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Description
H. L. COLES METHODS OF COATING CATALYST CARRIERS Dec. Z3, 1958 Filed April 6, 1955 INVENTOR. .Her/rg Cole BY TTORNEYS METHUDS F CA'HNG CATALYST CARS Henry L. Coles, Houghton, Mich., assignor to Calcinator Corporation, Bay City, Mich., a corporation of Michigan Application April 6, 1955, Serial No. 499,589 Claims. (Cl. 117-46) This invention relates to a method of coating catalyst carriers. l
Catalyst-coated carriers of the type to which I have reference have just recently been developed for use in household incinerators to burn the odorous olf gases of incineration at temperatures far below those normally required for their combustion. My assignees co-pending applications Serial Nos. 488,888 and 488,889 setforth in detail the construction of the catalyst units which are employed, and describe the carriers for the platinum or palladium coatings which serve as the catalytic agents. Various methods of depositing the catalytic agents in combined or free state have been suggested, however no one has to my knowledge discovered a process as simple and practical as the one to be outlined wherein the catalytic agents themselves are thought to promote their deposition to such an extent that the process can be used to coat carriers of a designated shape in an amazingly rapid and efficient manner with very simple and inexpensive equipment. Obviously, when concerned with the problem of mass producing incinerators containing catalytic units at a price which is well within the range of the average householder and which is competitive with incinerators without catalytic units it is important to develop a process which' is as etcient and economical as possible. This is particularly true in View of the relatively high cost of the catalyst metals concerned since any wasting of the metals in the process adds appreciably to the cost of manufacture.
One of the foremost objects of the instant invention is accordingly to provide a coatingvor metallizing process wherein the steps or stages of treatment in the process can be very rapidly` performed in a highly reliable and efficient mannerwhile the carriers are traveling on conveyor means which passes them continuously through the neces-- sary processing apparatus.
Another object of the invention is to provide an improved method of the type outlined which is capable of producing coatings of greater thickness and comprisinga greater percentage of free catalytic metal in an uncombined state than has heretofore been possible.
A further object of the invention is to provide an irnproved method of coating a catalyst on catalyst carriers which securely lodges the metal on the carrier in a manner to provide a surface which has a tine grained texture.
Another object of the inventionris to provide a method or process such as described which provides a coating of uniform thickness and density on the entire surface of the carrier and docs not leave uncoated areas which have no catalyzing value.
A further object of the invention is to provide a method or process such as described which requires only very simple and inexpensive processing apparatus which can be very readily set up to form a relatively compact production line.
Another object of the invention is to provide a metallizing process which does not require the use of a flux such as would provide the problem of uniformly dispersing the `same in a mixture with the metal over the carrier, and
ICC
further does not require the use of a stabilizing agent to maintain a metal powder in suspension.
Briefly, the process comprises the steps of cleaning the carrier, applying an aqueous solution of a suitable platinum or palladium compound, to the carrier, firing the carrier in a fuel ame which is surrounded by non-combusted fuel vapors whose burning may be catalyzed, and
epeating the steps of applying the solution and ring the carrier until a firmly adhering coating of metal in a practically pure state is deposited on the carrier in the desired thickness.
With the above and other objects in view, the present invention consists in the combination and arrangement of parts hereinafter more fully described, illustrated in the accompanying drawing, and more particularly pointed out in the appended claims, it being understood that equivalent changes may be made in the various elements which comprise the invention without departing from the spirit thereof or the scope of the appended claims.
In the drawings:
Fig. l is a schematic view showing apparatus for coating saddle type carrier members.
Fig. 2 is a similar view showing apparatus for coating a carrier strip which can later be cut into ribbons of the desired length. i
Referringnow more particularly to the accompanying drawing wherein I have shown preferred apparatus forl carrying out the process a numeral lll in Fig. l designates a hopper which may be continuously supplied with saddle type berl carriers C. These carriers, which are fully described in the instant assignees co-pending application, Serial No. 488,888, may be formed of a suitable ceramic or metallic material and I have found Alundurn saddles to be particularly well adapted to the process which I will now describe.
The hopper 1t) will deposit the saddles preferably one at a time on a perforate or screen conveyor 1l traveling in the direction indicated over a cleaning ame 12 which may be provided by a conventional fuel gas burner. Actually what so that, while they are still very hot they are not.
visibly so and will in fact be just below red heatY temperature.
The solution 1S in the tank 13 may comprise an aqueous platinum chloride solution whose platinum content is 20 to 25 grams per liter of solution and may be prepared in various ways or purchased in salt form. One method of preparing such a solution which I have found satisfactory is to dissolve a measured weight of scrap platinum in a measured volume of aqua regia solution to produce platinum chloride and platinum nitrate which may then be evaporated to the point where the solids begin to separate out. Distilled water may then be added to form a solution wherein the platinum is in the proportion indicated above. If the platinum chloride solution which is substantially forty percent platinum is provided in salt form, fifty grams of it can be immediately dissolved in a small volume of warm distilled water and thence further distilled water may be added to make up the liter of solution. Such a solution will contain approximately 2O grams by weight of platinum. It should be including platinum lluoride, platinum bromide, platimiml nitrate or the like. Further, where it is desired to provide a palladium coating instead of a platinum coating, a suitable palladium salt could be employed. The preparation of the solution might be identical to provide an aqueous solution in which the palladium content was 2() grams per liter.a Still a further alternative in providing a catalyst solution might be to provide a mixture of platinum and palladium salts diluted so that their combined metallic content was approximately 20 grams per liter of solution. In the description to follow the solution will be described, for convenience sake only, as a platinum chloride solution contaimng 2O grams per liter of platinum, however it is to be borne in mind that the solution could well be another soluble platinum compound solution, a soluble palladium compound solution, or a combined platinum compound palladium compound solution.
From the tank the saddles travel on the partially submerged perforate conveyor over a flame 16 which plays directly on them from below. The burner which produces the flame may be a conventional Mekker or Fisher grid-type fuel gas burner' which has air blown in at the bottom thereof. Best results are obtained if the burner is disposed at a slight angle relative to the plane of the conveyor 16. While it is thought that other gascous, liquid, or solid hydrocarbon fuels may also be employed with good results, l have found that particularly good Aresults are obtained with a bottled gas fuel whose constituents are propane in the amount of S6 percent and butane in the amount of 14 percent. Such a fuel will produce a normal flame whose heat is in the range l555 F. to l730 F. or 846 C. to 940 C. in any event the fuel used must be capable of producing a ame which heats the saddles to a white heat and is enough above the platinum chloride decomposition temperature of 581 C. and platinum oxide decomposition temperature of 555 C. to tix the separated platinum to the saddles, but below the temperature of l755 C. at which platinum melts.
While it is thought that other gases, artificial or natural, may be employed as the fuel, it has definitely been ohserved that entirely unexpected results are obtained when the saddles are heated to the desired temperature in an open atmosphere by a flame which plays on the saddles rather than in a muflie furnace or the like. When saddles were tired in a muie furnace it was discovered that less than half as much platinum was provided on a given carrier and the same was not adherent and was easily rubbed or flaked olf. Apparently, the presence of excess air and non-combusted fuel gases which are not primarily combusted, but may be secondarily combusted, are necessary to the process to achieve the startlingly firmly adherent coating of greater thickness which is produced. Under these conditions the catalyst which is initially deposited on the saddles in the primary reduction of the platinum chloride thereon promotes the reaction on its own surface to provide a very rapid reduction of the remaining nonreduced platinum chloride or oxide. This sudden reduction which is of maior proportions considering the relatively small percentage of platinum which is primarily deposited makes it possible to move the saddles continuously past the ame, although at a relatively slow rate of travel. It is brought about by the catalytic oxidation of the previously non-combusted gases and continuously issuing fuel gas which raises the flame temperature to between ll0O to 1600 C. and firmly fixes the platinum to the carriers. The fuel gases which are not primarily combusted because they are heavier than air hover around the ame and carrier, and in effect function as a iiuxing agent to prevent the formation of an appreciable amount of platinum oxide. Thus, the platinum coating will comprise an almost pure, iirmly fused, dense deposition of free platinum. This deposit and succeeding deposits, will in fact be approximately 80% pure platinum with the remainder platinum oxide. It is thought that the fuel gas employed should contain a relatively high percentage of propane or one of its homologs since these fuels will so readily catalytically oxidize in the presence of platinum or palladium to provide the high temperatures which 4 achieve the rapid and complete reduction of the metallic compounds.
After the saddles leave the flame they are carried on' the conveyor to a second tank 17 containing a like platinum solution 13. A conveyor 19 partially submerged therein carries them to a second iiame 2t) of identical makeup where the fuel gases are again catalytically oxidized and another layer of virtually free platinum is fused to the carriers.
Thereafter the steps are once more repeated, the conveyor 19 carrying the saddles C to a third tank 2l and a conveyor 22 which conveys them over a iiamc 23, and nally deposits them in a storage bin 24. In traveling to the bin and thereafter the saddlesy are air cooled` The platinum coated on will be approximately 1.2 grams per liter of 3A inch berl saddles.
In Fig. 2 I have shown a process which is identical except that the coating is tired on a continuously moving strip of metal S which is unwound from a reel 25 and passes through various stages in the process to a windup reel Z6. The surface of the metal strip may be roughened prior to commencing the operation by etching it. Means for driving the tape at a relatively slow rate are not shown, however it will be appreciated that such are well known. Similar numerals to the numerals used in Fig. l are applied to the tanks and burner ames in Fig. 2 and it should be apparent that the coating process is identical with that previously described. The tanks are, it will he noted, U-shaped rather than rectilinear, and idler rollers must be provided to direct the path of the tape. The coating thus applied to the tape will be so firmly lodged thereon that cutting of the tape into ribbons suitable for use in the catalytic unit described in the previously mentioned application No. 488,889 can be accomplished Without chipping the coating or loosening it.
Plainly, either saddle type carriers or ribbons which are prepared in this manner may be very etiiciently employed in the catalytic oxidation of the smoke and odorous gases which are normally the by products of garbage incineration and are presently commonly expelled to atmosphere.
Both carriers are provided with roughened surfaces prior to metallizing to enhance the depositing action. The saddles may be formed of a special mix which provides a rough rather than glazed surface or may be sandblasted. The metal ribbon may be etched or sandblasted.
When traveling on the conveyor the approximate speed of a saddle carrier is such that it remains in the ame about two minutes. Two repetitive depositions as shown and described are desirable and the amount deposited is about the same in each deposition.
It is to be understood that the foregoing descriptive matter and drawings are in all cases to be interpreted as merely illustrating the principles of the invention rather than as limiting the scope thereof, and I contemplate that various equivalent substitutions and changes within the Vscope of the appended claims may be made in the process described to achieve similar results.
I claim:
' l. A process for coating a rough surface catalyst car rier with metallic catalyst selected from the group consisting of platinum, palladium, a combination of platinum and palladium, and compounds thereof, said process comprising the steps of applying a tiame reducible catalyst compound in solution to the rough surface of the carrier to coat the carrier, and firing the coated carrier in an open ame which contacts the carrier to reduce catalyst compound to free catalytic metal and tix free catalytic metal to the carrier; said flame heating the coated carrier at temperatures above the decomposition temperature of the catalyst compound and below the melting point of the free catalytic metal.
2.` The process of claim 1 wherein catalyst compoundv is applied to the carrier in an aqueous solution and free catalytic metal is fixed to the carrier by fusion.
3. The process of claim 2 wherein the llame is created by the burning of a fuel gas in which propane is the major constituent and the solution includes 20 to 25 grams of catalyst per liter of solution.
4. A process for coating a rough surface catalyst carrier with platinum comprising the steps of applying a flame reducible platinum compound in solution to the rough surface'of the carrier to coat the carrier and firing the coated carrier in an open flame to reduce platinum compound to .free platinum metal and ix free platinum metal to the carrier; said flame heating the coated carrer at a temperature from 581 C. to 1755 C.
5. The process of claim 4 wherein platinum compound is applied to the carrier in an aqueous solution and free platinum is fixed to the carrier by fusion.
6. The process of claim 5 wherein the carrier is Alundum.
7. The process of claim 6 wherein the solution includes 20 to 25 grams of platinum per liter of solution and the flame is created by the burning of a fuel gas in which propane is the major constituent.
8. The process of claim 7 wherein the steps of applying the solution to the carrier to coat the carrier and tiring the coated carrier are repeated.
9. The process of claim 8 wherein the steps are repeated twice.
10. The process of claim 7 wherein the rough surface carrier is heated white hot before the platinum compound solution is applied to the carrier.
References Cited in the le of this patent UNITED STATES PATENTS 1,010,914 Howell Dec. 5, 1911 1,940,934 Bennett et al Dec. 26, 1933 2,197,792 Erickson Apr. 23, 1940 2,328,101 Rosenblatt Aug. 31, 1943 2,498,003 Peterson Feb. 21, 1950 2,623,860 Haensel Dec. 30, 1952 OTHER REFERENCES Scotts Standard Methods of Chemical Analysis, fifth edition, volume 1 (Van Nostrand Co., 1939), pages 1107- 1 109.
Claims (1)
1. A PROCESS FOR COATING A ROUGH SURFACE CATALYST CARRIER WITH METALLIC CATALYST SELECTED FROM THE GROUP CONSISTING OF PLATINUM, PALLADIUM, A COMBINATION OF PLATINUM AND PALLADIUM, AND COMPOUNDS THEREOF, SAID PROCESS COMPRISING THE STEPS OF APPLYING A FLAME REDUCIBLE CATALYST COMPOUND IN SOLUTION TO THE ROUGH SURFACE OF THE CARRIER TO COAT THE CARRIER, AND FIRING THE COATED CARRIER IN AN OPEN FLAME WHICH CONTACTS THE CARRIER TO REDUCE CATALYST COMPOUND TO FREE CATALYTIC METAL AND FIX FREE CATALYTIC METAL TO THE CARRIER; SAID FLAME HEATING THE COATED CARRIER AT TEMPERATURES ABOVE THE DECOMPOSITION TEMPERATURE OF THE CATALYST COMPOUND AND BELOW THE MELTING POINT OF THE FREE CATALYTIC METAL.
Priority Applications (1)
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US499589A US2865785A (en) | 1955-04-06 | 1955-04-06 | Methods of coating catalyst carriers |
Applications Claiming Priority (1)
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US499589A US2865785A (en) | 1955-04-06 | 1955-04-06 | Methods of coating catalyst carriers |
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US2865785A true US2865785A (en) | 1958-12-23 |
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US499589A Expired - Lifetime US2865785A (en) | 1955-04-06 | 1955-04-06 | Methods of coating catalyst carriers |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3177131A (en) * | 1959-04-27 | 1965-04-06 | Ici Ltd | Method for the production of platinum coated titanium anodes |
US3370973A (en) * | 1964-12-28 | 1968-02-27 | Ibm | Activation of glass for electroless metal deposition of uniform thick metal films |
US3867311A (en) * | 1973-05-21 | 1975-02-18 | Nalco Chemical Co | Method of making catalytically impregnated ceramic burning pads |
US4589367A (en) * | 1984-10-01 | 1986-05-20 | Empire Enterprises, Inc. | System for automatically painting pencils |
US4724428A (en) * | 1986-07-07 | 1988-02-09 | Emhart Industries, Inc. | Thermocouple jacket monitor |
US4863893A (en) * | 1986-08-06 | 1989-09-05 | Engelhard Corporation | Low temperature light off ammonia oxidation |
US5310580A (en) * | 1992-04-27 | 1994-05-10 | International Business Machines Corporation | Electroless metal adhesion to organic dielectric material with phase separated morphology |
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US1010914A (en) * | 1908-04-03 | 1911-12-05 | Gen Electric | Machine for treating filaments. |
US1940934A (en) * | 1931-03-16 | 1933-12-26 | Catalyst Research Corp | Method of making supported catalysts |
US2197792A (en) * | 1937-12-06 | 1940-04-23 | John A Erickson | Coal spraying chute |
US2328101A (en) * | 1941-01-28 | 1943-08-31 | Baker & Co Inc | Method of providing adherent metal coatings on surfaces |
US2498003A (en) * | 1946-08-19 | 1950-02-21 | Corning Glass Works | Method of coloring glass |
US2623860A (en) * | 1951-04-12 | 1952-12-30 | Universal Oil Prod Co | Method of manufacturing platinum-containing catalyst |
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Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
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US1010914A (en) * | 1908-04-03 | 1911-12-05 | Gen Electric | Machine for treating filaments. |
US1940934A (en) * | 1931-03-16 | 1933-12-26 | Catalyst Research Corp | Method of making supported catalysts |
US2197792A (en) * | 1937-12-06 | 1940-04-23 | John A Erickson | Coal spraying chute |
US2328101A (en) * | 1941-01-28 | 1943-08-31 | Baker & Co Inc | Method of providing adherent metal coatings on surfaces |
US2498003A (en) * | 1946-08-19 | 1950-02-21 | Corning Glass Works | Method of coloring glass |
US2623860A (en) * | 1951-04-12 | 1952-12-30 | Universal Oil Prod Co | Method of manufacturing platinum-containing catalyst |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3177131A (en) * | 1959-04-27 | 1965-04-06 | Ici Ltd | Method for the production of platinum coated titanium anodes |
US3370973A (en) * | 1964-12-28 | 1968-02-27 | Ibm | Activation of glass for electroless metal deposition of uniform thick metal films |
US3867311A (en) * | 1973-05-21 | 1975-02-18 | Nalco Chemical Co | Method of making catalytically impregnated ceramic burning pads |
US4589367A (en) * | 1984-10-01 | 1986-05-20 | Empire Enterprises, Inc. | System for automatically painting pencils |
US4724428A (en) * | 1986-07-07 | 1988-02-09 | Emhart Industries, Inc. | Thermocouple jacket monitor |
US4863893A (en) * | 1986-08-06 | 1989-09-05 | Engelhard Corporation | Low temperature light off ammonia oxidation |
US5310580A (en) * | 1992-04-27 | 1994-05-10 | International Business Machines Corporation | Electroless metal adhesion to organic dielectric material with phase separated morphology |
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