CA1131159A - Method for producing improved heat transfer surface - Google Patents
Method for producing improved heat transfer surfaceInfo
- Publication number
- CA1131159A CA1131159A CA319,220A CA319220A CA1131159A CA 1131159 A CA1131159 A CA 1131159A CA 319220 A CA319220 A CA 319220A CA 1131159 A CA1131159 A CA 1131159A
- Authority
- CA
- Canada
- Prior art keywords
- tube
- foam
- heat transfer
- foam material
- metal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000012546 transfer Methods 0.000 title claims abstract description 23
- 238000004519 manufacturing process Methods 0.000 title abstract description 6
- 238000009835 boiling Methods 0.000 claims abstract description 22
- 238000000034 method Methods 0.000 claims abstract description 21
- 238000007747 plating Methods 0.000 claims abstract description 21
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 16
- 239000010439 graphite Substances 0.000 claims abstract description 16
- 239000002184 metal Substances 0.000 claims abstract description 15
- 229910052751 metal Inorganic materials 0.000 claims abstract description 15
- 238000000197 pyrolysis Methods 0.000 claims abstract description 10
- 239000011248 coating agent Substances 0.000 claims abstract description 7
- 238000000576 coating method Methods 0.000 claims abstract description 7
- 239000006261 foam material Substances 0.000 claims description 11
- 239000011148 porous material Substances 0.000 claims description 9
- 229920001247 Reticulated foam Polymers 0.000 claims description 5
- 238000009713 electroplating Methods 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 3
- 230000001464 adherent effect Effects 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims 1
- 239000006260 foam Substances 0.000 abstract description 31
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract description 26
- 229910052802 copper Inorganic materials 0.000 abstract description 23
- 239000010949 copper Substances 0.000 abstract description 23
- 239000007788 liquid Substances 0.000 abstract description 8
- 239000000758 substrate Substances 0.000 abstract description 6
- 230000006911 nucleation Effects 0.000 description 15
- 238000010899 nucleation Methods 0.000 description 15
- 239000002245 particle Substances 0.000 description 9
- 239000002826 coolant Substances 0.000 description 7
- 239000012808 vapor phase Substances 0.000 description 7
- 230000015556 catabolic process Effects 0.000 description 4
- 210000004027 cell Anatomy 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 239000012530 fluid Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 229910000365 copper sulfate Inorganic materials 0.000 description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 2
- 239000002659 electrodeposit Substances 0.000 description 2
- 230000005686 electrostatic field Effects 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000011496 polyurethane foam Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000007788 roughening Methods 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 241001593730 Acacia salicina Species 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- PTVDYARBVCBHSL-UHFFFAOYSA-N copper;hydrate Chemical compound O.[Cu] PTVDYARBVCBHSL-UHFFFAOYSA-N 0.000 description 1
- 210000001787 dendrite Anatomy 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012811 non-conductive material Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000000399 optical microscopy Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 238000004626 scanning electron microscopy Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F28—HEAT EXCHANGE IN GENERAL
- F28F—DETAILS OF HEAT-EXCHANGE AND HEAT-TRANSFER APPARATUS, OF GENERAL APPLICATION
- F28F13/00—Arrangements for modifying heat-transfer, e.g. increasing, decreasing
- F28F13/18—Arrangements for modifying heat-transfer, e.g. increasing, decreasing by applying coatings, e.g. radiation-absorbing, radiation-reflecting; by surface treatment, e.g. polishing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21C—MANUFACTURE OF METAL SHEETS, WIRE, RODS, TUBES OR PROFILES, OTHERWISE THAN BY ROLLING; AUXILIARY OPERATIONS USED IN CONNECTION WITH METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL
- B21C37/00—Manufacture of metal sheets, bars, wire, tubes or like semi-manufactured products, not otherwise provided for; Manufacture of tubes of special shape
- B21C37/06—Manufacture of metal sheets, bars, wire, tubes or like semi-manufactured products, not otherwise provided for; Manufacture of tubes of special shape of tubes or metal hoses; Combined procedures for making tubes, e.g. for making multi-wall tubes
- B21C37/15—Making tubes of special shape; Making tube fittings
- B21C37/154—Making multi-wall tubes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
- B22F3/11—Making porous workpieces or articles
- B22F3/1121—Making porous workpieces or articles by using decomposable, meltable or sublimatable fillers
- B22F3/1137—Making porous workpieces or articles by using decomposable, meltable or sublimatable fillers by coating porous removable preforms
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23P—METAL-WORKING NOT OTHERWISE PROVIDED FOR; COMBINED OPERATIONS; UNIVERSAL MACHINE TOOLS
- B23P15/00—Making specific metal objects by operations not covered by a single other subclass or a group in this subclass
- B23P15/26—Making specific metal objects by operations not covered by a single other subclass or a group in this subclass heat exchangers or the like
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
- B22F2998/10—Processes characterised by the sequence of their steps
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Electroplating Methods And Accessories (AREA)
- Laminated Bodies (AREA)
- Chemically Coating (AREA)
Abstract
METHOD FOR PRODUCING IMPROVED
HEAT TRANSFER SURFACE
ABSTRACT
The invention relates to a method of improving the heat transfer properties in boiling liquids of tubes and other surfaces by applying a very porous reticulated organic foam layer which has been precoated with graphite in contact with the tube surface, and then plating a thin metal coating on the foam substrate. Preferably, the tube is copper and the plating consists of an electroplated layer of copper which is applied over the conductive graphite coated foam. The foam is preferably in the form of a thin tape which is spirally wound about the tube. Pyrolysis of the foam after plating improves the heat transfer performance of the tube. A method for applying the graphite to the foam is also disclosed.
HEAT TRANSFER SURFACE
ABSTRACT
The invention relates to a method of improving the heat transfer properties in boiling liquids of tubes and other surfaces by applying a very porous reticulated organic foam layer which has been precoated with graphite in contact with the tube surface, and then plating a thin metal coating on the foam substrate. Preferably, the tube is copper and the plating consists of an electroplated layer of copper which is applied over the conductive graphite coated foam. The foam is preferably in the form of a thin tape which is spirally wound about the tube. Pyrolysis of the foam after plating improves the heat transfer performance of the tube. A method for applying the graphite to the foam is also disclosed.
Description
METHOD FOR PRODUCING IMPROVED
HEAT TRANSFER SURFACE
SPECIFICATION
Improved heat transfer tube technology in recent years has been highly dependent upon the improvement of two phase heat transfer, that is the transfer of thermal energy due to the phase transformation from the liquid to the vapor phase. The methods to improve this two phase heat transfer include both passive and active techniques. Passive techniques include surface treatments, roughening the surface, extending n ~O~c~o~
the surfaces, swirl flow techniques, altcrnation of surface tension, and the inclusion of additives to the coolant. Active techniques include mechanical aids, surface vibration, fluid vibration, and the addition of electrostatic fields.
In the area of treated surfaces, various materials are deposited on the heat transfer tube surfaces to promote boiling. Such materials have included Teflon, tube surface oxides, and the addition of high surface copper powder. These surface treatments improve the wettability of the surface and result in a low wall super heat which eliminates boiling curve hysteresis.
Surface roughening is a technique to provide a large number of nucleation sites on the tube surfaces. The technique involves the mechanical deformation of the surface to provide ¦ a large number of re-entrant cavities.
Extended surface tubes are produced by finning techniques which yield high external surface areas to the tube and allow very large heat transfer rates if the base temperature is in the 7rc~d~ k
HEAT TRANSFER SURFACE
SPECIFICATION
Improved heat transfer tube technology in recent years has been highly dependent upon the improvement of two phase heat transfer, that is the transfer of thermal energy due to the phase transformation from the liquid to the vapor phase. The methods to improve this two phase heat transfer include both passive and active techniques. Passive techniques include surface treatments, roughening the surface, extending n ~O~c~o~
the surfaces, swirl flow techniques, altcrnation of surface tension, and the inclusion of additives to the coolant. Active techniques include mechanical aids, surface vibration, fluid vibration, and the addition of electrostatic fields.
In the area of treated surfaces, various materials are deposited on the heat transfer tube surfaces to promote boiling. Such materials have included Teflon, tube surface oxides, and the addition of high surface copper powder. These surface treatments improve the wettability of the surface and result in a low wall super heat which eliminates boiling curve hysteresis.
Surface roughening is a technique to provide a large number of nucleation sites on the tube surfaces. The technique involves the mechanical deformation of the surface to provide ¦ a large number of re-entrant cavities.
Extended surface tubes are produced by finning techniques which yield high external surface areas to the tube and allow very large heat transfer rates if the base temperature is in the 7rc~d~ k
-2-~13~1~.9 film boiling range; however, nucleate boiling is not promoted with this type of heat transfer tube.
Surface tension devices operate on the wicking principle which relies on capillary forces while the addition of additives to the coolant affects the wettability of the coolant to the heat transfer tube.
A number of mechanical boiling aids have been proposed including rotating of the boilers themselves, the introduction of rotating plates, and the introduction of bubbles into the vicinity of the heat surface.
The purpose of vibrating either the fluid or the sur-face is to form localized nucleate boiling sites due to pressure variations in the liquid. The use of electrostatic fields im-proves mixing within the coolant and is used principally with poorly conductingor dielectric fluids.
Of the above techniques, those that promote nucleate boiling are of principal interest from a technological viewpoint.
The parameters of importance in a nucleate boiling tube-coolant - system include the specific heat of the liquid, the specific heat of the tube material, the heat transfer coefficient, the latent heat of vaporization, the thermal conductivity of the liquid and the heater tube, the geometry of the nucleation site, the temperature of the coolant, vapor, and surface, the liquid viscosity, the surface tension, and the densities of the liquid and vapor phase.
The nucleate boiling phenomenon involves two separate operations. The first of these is the nucleation of the vapor phase within the liquid while the second is the subsequent growth .,9 of the vapor phase to form bubbles within the liquid. It has been postulated that improved efficiency of heat transfer can be attained when the nucleation process does not have to be continuously redone. This nucleation process requires a large amount of superheating. Improved efficiency can be observed if the thermal energy is transferred by the growth of pre-exisit-ing vapor phase nuclei. This approach has resulted in the speci-fication of re-entrant cavities as highly effective nucleate boiling sites.
A number of patents have been issued whereby the sur-face of a heat transfer tube is mechanically altered to provide these re-entrant sites. These include U.S. Patent Numbers
Surface tension devices operate on the wicking principle which relies on capillary forces while the addition of additives to the coolant affects the wettability of the coolant to the heat transfer tube.
A number of mechanical boiling aids have been proposed including rotating of the boilers themselves, the introduction of rotating plates, and the introduction of bubbles into the vicinity of the heat surface.
The purpose of vibrating either the fluid or the sur-face is to form localized nucleate boiling sites due to pressure variations in the liquid. The use of electrostatic fields im-proves mixing within the coolant and is used principally with poorly conductingor dielectric fluids.
Of the above techniques, those that promote nucleate boiling are of principal interest from a technological viewpoint.
The parameters of importance in a nucleate boiling tube-coolant - system include the specific heat of the liquid, the specific heat of the tube material, the heat transfer coefficient, the latent heat of vaporization, the thermal conductivity of the liquid and the heater tube, the geometry of the nucleation site, the temperature of the coolant, vapor, and surface, the liquid viscosity, the surface tension, and the densities of the liquid and vapor phase.
The nucleate boiling phenomenon involves two separate operations. The first of these is the nucleation of the vapor phase within the liquid while the second is the subsequent growth .,9 of the vapor phase to form bubbles within the liquid. It has been postulated that improved efficiency of heat transfer can be attained when the nucleation process does not have to be continuously redone. This nucleation process requires a large amount of superheating. Improved efficiency can be observed if the thermal energy is transferred by the growth of pre-exisit-ing vapor phase nuclei. This approach has resulted in the speci-fication of re-entrant cavities as highly effective nucleate boiling sites.
A number of patents have been issued whereby the sur-face of a heat transfer tube is mechanically altered to provide these re-entrant sites. These include U.S. Patent Numbers
3,326,283; 3,454,081; 3,566,514; 3,881,342 and 3,906,604.
While all of the above patents propose the improvement of nucleation by the mechanical introduction of nucleation sites, they all suffer from the common characteristic of having a sm~ //
relatively ~e~ number of nucleation sites per given area of tubing surface. This limitation is imposed by the manufacturing tooling required to produce the tubes, and is an inherent limi-tation for any mechanically produced tube.
The demonstrated heat transfer capability of a tube produced with a much higher density of nucleation sitesis covered in U.S. Patent No. 3,384,154. This tube is of the treated sur-face variety mentioned above where copper powder particles are sintered to the surface of the heat exchanger tube. This pro-vides a very high density of nucleation sites on the tube sur-face and allows retention of the vapor phase throughout the open pore structure of the sintered surface. This sintered surface 11311,J9 tube, while an effective boiling surface and heat transfer tube, suffers from manufacturing difficulties. The copper powder is mixed with an organic binder and sprayed onto the tube surface for ease of handling. The coated tube is then subjected to a high temperature exposure. This decomposes the organic binder and sinters the copper particles together as well as to the base tube. The sintering temperature is stated to be about 960C.
which is about 100C. below the melting point of copper. This temperature treatment is not only difficult to do but can result in serious degradation of the mechanical properties of the base tube. The degradation problems can be minimized by utilizing alloys whose superior recrystallization and grain growth char-acteristics will reduce the amount of property degradation but such alloys introduce added cost and have lower thermal con-ductivity.
U.S. Patent 4,018,264 discloses a tube with improved nucleate boiling performance as compared to a standard finned tube which is made by initially plating the tube at high current density to form spaced dendrites or nodules which are then further plated at lower current densities and physically deformed.
It is among the objects of the present invention to provide an improved heat transfer-surface and a method of making same which will produce a very high density of nucleation sites at a relatively low cost and without affecting the properties of the base tube. These and other objects are achieved by the present invention which provides a method of providing a metal heat transfer member with a porous nucleate boiling surface comprising the steps of applying a layer of open cell reticulated organic foam material having an adherent coating of conductive graphite to the surface of the metal member and electroplating the exposed graphite coated surfaces of the reticulated foam material and the exposed surfaces of the metal member which underlie the foam material with a metal so as to form a ;~.~ .
~ .
c ~
- 11311~,9 reticulated metal surface having open cells which overlies the surface of the metal member and is firmly adhered thereto.
The foam material can be in the form of a thin strip or tape that is spirally wound around the base tube or it can be in a tubular shape which could be slipped over the tube. The foam coating can also be directly applied to the tube surface if it is foamed in such a manner as to leave open cells rather than a closed cell skin in contact with the base tube. The open celled nature of the foam allows free and easy excess of the coolant all the way to the tube surface and is more resistant to having its nucleation sites blocked by foreign objects in the plating solution than would be the case for a sintered surface tube.
The reticulated foam comprises a substrate upon which copper is plated after the foam has been made conductive. The initial step is to apply a graphite coating to the foam which will adhere sufficiently well to make the surface of the organic foam electrically conductive. Standard electroplating of copper is then used to plate the coated foam and the portions of the tube which are not contacted by the foam and to build the thick ness of the copper coating up to the point where it has structural integrity. After plating, the organic precursor can be pyrolyzed if desired.
In making experimental tubes we used a reticulated poly~rethane foam sold as Scott Industrial Foam by Scott Paper Company and having a 97~ void volume with a pore size con-trolled at 39 pores per linear cm. For the experimental tubes, strips approximately 2,54 cm wide by 1.66 mm thickness were wrapped in a spiral fashion along the length of the base tube and mechanically held in place by an elastic band during the plating n sd/ ~ 6-,9 operations. The foam was previously made conductive by drawing it through a container of finely divided graphite powder and then passing it through the roll nip of a shear mill wherein the different surface speeds of rotation of the work engaging rollers forced the graphite particles into relatively firm con-tact with the reticulated foam structure. A graphite powder having a mesh size of less than 200 sold by the Joseph Dixon Crucible Co. of Jersey City, New Jersey, under the formula number 8485 performed satisfactorily. The tube was then electroplated in an air agitated standard copper sulfate electroplating solution using a copper electrode and a DC voltage. Electroplating was continued until a sufficiently thick copper electrodeposit was formed so that the foam had sufficient strength to allow normal handling. The plating conditions were 1.65 volts and 10.0 amps for 142 minutes, resulting in a copper electrodeposit of 24.17 g for the 30.5 cm long sample tube. Measurement of the plating thickness is extremely difficult but the thickness appeared to be about 10.2 to 15.2/~m.
Heat transfer testing of an as-plated tube in Refrigerant R-ll showed a considerable improvement in the surface nucleation boiling characteristics of this tube as compared to a standard fin tube. The boiling characteristics were also superior to a commercially available nucleate boiling tube produced by mechanical means in accordance with the aforementioned U.S.
Patent No. 3,906,604. Observation of the surface boiling charac-teristics when compared with a length of tubing as produced in accordance with the aforementioned U.S. Patent No. 3,384,154 showed that nucleation on the foam surface was quite close to that produced by the sintered copper surface.
11;~11. :,,9 The efEect of pyrolysis of the polyurethane foam on surface structure and boiling characteristics was then determined. The plated foamed tube was held in a labora-tory gas flame until pyrolysis of the graphite coated poly-urethane substrate was complete. Optical and scanning electron microscopy of the remaining copper foam showed a series of very small pores along the surfaces of the skeletal copper remaining after the pyrolysis of the sub-strate. These pores varied in size with a maximum of about 50~ m in their largest dimension. The pores were probably produced by the pressure of the gases created during the pyrolysis of the organic substrate which fracture the thin plated walls which encapsulate the organic substrate.
Boiling tests of the pyrolyzed tube in the same R-ll coolan,t as used previously indicated superior performance of the pyrolyzed tube as compared to the tube before pyroly-sis. This is undoubtedly due to the large number of very tiny vapor phase nucleation sites resulting from the poro-sity due to the pyrolysis. Since the polyurethane can be pyrolyzed at temperatures in the range of 302 to 482C. it is obvious that the degradation problems which can take place at temperatures closer to the melting point of copper are of little consequence.
BRIEF DESCRIPTION OF THE _RAWINGS
FIG. 1 is a perspective view showing a thin strip of reticulated foam being wound about a plain tube;
FIG. 2 is a side view illustrating the application of graphite particles to a foam strip and the passage of the strip through a shear mill;
FIG. 3 is a side sectional view showing the tube of FIG. 1 being electroplated;
Pg/~ - 8 - }
~i 1~311I^ J9 FIG. 4 is a side yiew of a tube which has been wrapped with foam and then plated being passed over a flame to pyrolyze the foam;
FIG. 5 is a side view showing the pyrolyzed tube of FIG. 4 having its plated surface compressed in a swag-ing die.
FIG. 6 is a 100 x SEM photograph showing the tube after plating; and FIG. 7 is a 100 x SEM photograph showing the tube of FIG. 4 after being swaged.
DESCRIPTION of the PREFERRED EMBODIMENT
. . .
Referring to Fig. 1, a tube 10, preferably-of copper, is shown. The first step in providing the tube lQ with an improved nucleate boiling surface is illustrated and-com-prises the wrapping of a thin strip of reticulated poly-urethane foam 12 about the tube 10 and anchoring it thereto such as by means b ~9 of a rubber band 14. The normally non-conductive foam strip 12 is preferably precoated with graphite particles 18 in order that its surface will be conductive.
The graphite particles 18 may be applied to the foam S strip 12 in any suitable manner. One example of a suitable apparatus is shown in Fig. 2 where the foam strip 12 is drawn lor.gitudinally through a shear mill 20 after graphite particles 18 have been dropped upon it from a supply hopper 24. Excess particles fall through the foam strip 12 into a collection tray 26 from which they are recirculated to the storage hopper 24 by means of a blower 28 and a tube 30. The shear mill 20 in-cludes a pair of rolls 34, 36 which are of like diameters but which rotate at different speeds so as to exert a shearing action on the foam strip 12, thus causing the particles 18 to become attached thereto. The ratio of the speeds of surface rotation of the lower faster roll 34 to the higher slower roll 36 are approximately 3:4.
Fig. 3 illustrates a side section of a plating appa-ratus 40 in which the foam wrapped tube of Fig. 1 can be plated.
The plating apparatus 40 preferably comprises a vertical plating tank or container 41 which contains a conventional copper plating solution 42, such as one consisting of copper sulfate, sulfuric acid and water. The tube 10 and its conductive foam layer 12 comprise the cathode of the plating apparatus while the anode may comprise a copper tube 44 of larger diameter which surrounds the tube 10 and is preferably evenly spaced from it. The tube 10 is shown as being mounted on a mounting block 48 of plastic or other non-conductive material. The mounting block 48 preferably 1. ,9 includes internal passages 50 and is sealed relative to the tube 10 by an O-ring 52. An air inlet tube 56 mounted in a stopper 58 in the upper end of the tube 10 permits air from a suitable source to be carried to the bottom of the tube 10 so that it can pass through the air passages 50 and bubble up in the form of bubbles 60 through the solution 42 in the region between the tube 10 and the tubular cathode 44. The bubbles 60 agitate the plating solution 42 and provide a more uniform plating.
The cathode or tube member 10 is connected by a lead member 62 and a connector or clamp ring 64 to a battery or other DC current source 68. The anode 44 is connected with a lead member 66 to the battery 68.
Fig. 4 illustrates the step of pyrolyzing the organic foam after it has been plated with a copper surface 72 in the plating apparatus 40. The pyrolysis operation removes the foam but leaves open spaces underneath the copper plating which form pores under the copper surface 72.
Fig. 5 illustrates a preferred step whereby the py-rolyzed tube is passed through a set of swaging dyes 76 to force down the copper surface 72 so that it achieves a smaller outer diameter 72'. The swaged surface provides the advantage of a smaller outer diameter so that tubes can be spaced closer to-gether in a tube bundle.
Figs. 6 and 7 are approximately lOOx (SEM) scanning electron microscope photographs showing the surface of an ex-perimental tube produced in the apparatus of Fig. 3. In Fig.
6, the tube 10 is shown after pyrolysis and illustrates the porous nature of the plated copper surface 72. Fig. 7 illustrates l,.,C~
a portion of the same tube after swaging through a 16.3 mm diameter die 76 in the manner illustrated in Fig. 5. The swaged plated copper surface 72' is compressed so that fewer pores are visible than in Fig. 6.
While all of the above patents propose the improvement of nucleation by the mechanical introduction of nucleation sites, they all suffer from the common characteristic of having a sm~ //
relatively ~e~ number of nucleation sites per given area of tubing surface. This limitation is imposed by the manufacturing tooling required to produce the tubes, and is an inherent limi-tation for any mechanically produced tube.
The demonstrated heat transfer capability of a tube produced with a much higher density of nucleation sitesis covered in U.S. Patent No. 3,384,154. This tube is of the treated sur-face variety mentioned above where copper powder particles are sintered to the surface of the heat exchanger tube. This pro-vides a very high density of nucleation sites on the tube sur-face and allows retention of the vapor phase throughout the open pore structure of the sintered surface. This sintered surface 11311,J9 tube, while an effective boiling surface and heat transfer tube, suffers from manufacturing difficulties. The copper powder is mixed with an organic binder and sprayed onto the tube surface for ease of handling. The coated tube is then subjected to a high temperature exposure. This decomposes the organic binder and sinters the copper particles together as well as to the base tube. The sintering temperature is stated to be about 960C.
which is about 100C. below the melting point of copper. This temperature treatment is not only difficult to do but can result in serious degradation of the mechanical properties of the base tube. The degradation problems can be minimized by utilizing alloys whose superior recrystallization and grain growth char-acteristics will reduce the amount of property degradation but such alloys introduce added cost and have lower thermal con-ductivity.
U.S. Patent 4,018,264 discloses a tube with improved nucleate boiling performance as compared to a standard finned tube which is made by initially plating the tube at high current density to form spaced dendrites or nodules which are then further plated at lower current densities and physically deformed.
It is among the objects of the present invention to provide an improved heat transfer-surface and a method of making same which will produce a very high density of nucleation sites at a relatively low cost and without affecting the properties of the base tube. These and other objects are achieved by the present invention which provides a method of providing a metal heat transfer member with a porous nucleate boiling surface comprising the steps of applying a layer of open cell reticulated organic foam material having an adherent coating of conductive graphite to the surface of the metal member and electroplating the exposed graphite coated surfaces of the reticulated foam material and the exposed surfaces of the metal member which underlie the foam material with a metal so as to form a ;~.~ .
~ .
c ~
- 11311~,9 reticulated metal surface having open cells which overlies the surface of the metal member and is firmly adhered thereto.
The foam material can be in the form of a thin strip or tape that is spirally wound around the base tube or it can be in a tubular shape which could be slipped over the tube. The foam coating can also be directly applied to the tube surface if it is foamed in such a manner as to leave open cells rather than a closed cell skin in contact with the base tube. The open celled nature of the foam allows free and easy excess of the coolant all the way to the tube surface and is more resistant to having its nucleation sites blocked by foreign objects in the plating solution than would be the case for a sintered surface tube.
The reticulated foam comprises a substrate upon which copper is plated after the foam has been made conductive. The initial step is to apply a graphite coating to the foam which will adhere sufficiently well to make the surface of the organic foam electrically conductive. Standard electroplating of copper is then used to plate the coated foam and the portions of the tube which are not contacted by the foam and to build the thick ness of the copper coating up to the point where it has structural integrity. After plating, the organic precursor can be pyrolyzed if desired.
In making experimental tubes we used a reticulated poly~rethane foam sold as Scott Industrial Foam by Scott Paper Company and having a 97~ void volume with a pore size con-trolled at 39 pores per linear cm. For the experimental tubes, strips approximately 2,54 cm wide by 1.66 mm thickness were wrapped in a spiral fashion along the length of the base tube and mechanically held in place by an elastic band during the plating n sd/ ~ 6-,9 operations. The foam was previously made conductive by drawing it through a container of finely divided graphite powder and then passing it through the roll nip of a shear mill wherein the different surface speeds of rotation of the work engaging rollers forced the graphite particles into relatively firm con-tact with the reticulated foam structure. A graphite powder having a mesh size of less than 200 sold by the Joseph Dixon Crucible Co. of Jersey City, New Jersey, under the formula number 8485 performed satisfactorily. The tube was then electroplated in an air agitated standard copper sulfate electroplating solution using a copper electrode and a DC voltage. Electroplating was continued until a sufficiently thick copper electrodeposit was formed so that the foam had sufficient strength to allow normal handling. The plating conditions were 1.65 volts and 10.0 amps for 142 minutes, resulting in a copper electrodeposit of 24.17 g for the 30.5 cm long sample tube. Measurement of the plating thickness is extremely difficult but the thickness appeared to be about 10.2 to 15.2/~m.
Heat transfer testing of an as-plated tube in Refrigerant R-ll showed a considerable improvement in the surface nucleation boiling characteristics of this tube as compared to a standard fin tube. The boiling characteristics were also superior to a commercially available nucleate boiling tube produced by mechanical means in accordance with the aforementioned U.S.
Patent No. 3,906,604. Observation of the surface boiling charac-teristics when compared with a length of tubing as produced in accordance with the aforementioned U.S. Patent No. 3,384,154 showed that nucleation on the foam surface was quite close to that produced by the sintered copper surface.
11;~11. :,,9 The efEect of pyrolysis of the polyurethane foam on surface structure and boiling characteristics was then determined. The plated foamed tube was held in a labora-tory gas flame until pyrolysis of the graphite coated poly-urethane substrate was complete. Optical and scanning electron microscopy of the remaining copper foam showed a series of very small pores along the surfaces of the skeletal copper remaining after the pyrolysis of the sub-strate. These pores varied in size with a maximum of about 50~ m in their largest dimension. The pores were probably produced by the pressure of the gases created during the pyrolysis of the organic substrate which fracture the thin plated walls which encapsulate the organic substrate.
Boiling tests of the pyrolyzed tube in the same R-ll coolan,t as used previously indicated superior performance of the pyrolyzed tube as compared to the tube before pyroly-sis. This is undoubtedly due to the large number of very tiny vapor phase nucleation sites resulting from the poro-sity due to the pyrolysis. Since the polyurethane can be pyrolyzed at temperatures in the range of 302 to 482C. it is obvious that the degradation problems which can take place at temperatures closer to the melting point of copper are of little consequence.
BRIEF DESCRIPTION OF THE _RAWINGS
FIG. 1 is a perspective view showing a thin strip of reticulated foam being wound about a plain tube;
FIG. 2 is a side view illustrating the application of graphite particles to a foam strip and the passage of the strip through a shear mill;
FIG. 3 is a side sectional view showing the tube of FIG. 1 being electroplated;
Pg/~ - 8 - }
~i 1~311I^ J9 FIG. 4 is a side yiew of a tube which has been wrapped with foam and then plated being passed over a flame to pyrolyze the foam;
FIG. 5 is a side view showing the pyrolyzed tube of FIG. 4 having its plated surface compressed in a swag-ing die.
FIG. 6 is a 100 x SEM photograph showing the tube after plating; and FIG. 7 is a 100 x SEM photograph showing the tube of FIG. 4 after being swaged.
DESCRIPTION of the PREFERRED EMBODIMENT
. . .
Referring to Fig. 1, a tube 10, preferably-of copper, is shown. The first step in providing the tube lQ with an improved nucleate boiling surface is illustrated and-com-prises the wrapping of a thin strip of reticulated poly-urethane foam 12 about the tube 10 and anchoring it thereto such as by means b ~9 of a rubber band 14. The normally non-conductive foam strip 12 is preferably precoated with graphite particles 18 in order that its surface will be conductive.
The graphite particles 18 may be applied to the foam S strip 12 in any suitable manner. One example of a suitable apparatus is shown in Fig. 2 where the foam strip 12 is drawn lor.gitudinally through a shear mill 20 after graphite particles 18 have been dropped upon it from a supply hopper 24. Excess particles fall through the foam strip 12 into a collection tray 26 from which they are recirculated to the storage hopper 24 by means of a blower 28 and a tube 30. The shear mill 20 in-cludes a pair of rolls 34, 36 which are of like diameters but which rotate at different speeds so as to exert a shearing action on the foam strip 12, thus causing the particles 18 to become attached thereto. The ratio of the speeds of surface rotation of the lower faster roll 34 to the higher slower roll 36 are approximately 3:4.
Fig. 3 illustrates a side section of a plating appa-ratus 40 in which the foam wrapped tube of Fig. 1 can be plated.
The plating apparatus 40 preferably comprises a vertical plating tank or container 41 which contains a conventional copper plating solution 42, such as one consisting of copper sulfate, sulfuric acid and water. The tube 10 and its conductive foam layer 12 comprise the cathode of the plating apparatus while the anode may comprise a copper tube 44 of larger diameter which surrounds the tube 10 and is preferably evenly spaced from it. The tube 10 is shown as being mounted on a mounting block 48 of plastic or other non-conductive material. The mounting block 48 preferably 1. ,9 includes internal passages 50 and is sealed relative to the tube 10 by an O-ring 52. An air inlet tube 56 mounted in a stopper 58 in the upper end of the tube 10 permits air from a suitable source to be carried to the bottom of the tube 10 so that it can pass through the air passages 50 and bubble up in the form of bubbles 60 through the solution 42 in the region between the tube 10 and the tubular cathode 44. The bubbles 60 agitate the plating solution 42 and provide a more uniform plating.
The cathode or tube member 10 is connected by a lead member 62 and a connector or clamp ring 64 to a battery or other DC current source 68. The anode 44 is connected with a lead member 66 to the battery 68.
Fig. 4 illustrates the step of pyrolyzing the organic foam after it has been plated with a copper surface 72 in the plating apparatus 40. The pyrolysis operation removes the foam but leaves open spaces underneath the copper plating which form pores under the copper surface 72.
Fig. 5 illustrates a preferred step whereby the py-rolyzed tube is passed through a set of swaging dyes 76 to force down the copper surface 72 so that it achieves a smaller outer diameter 72'. The swaged surface provides the advantage of a smaller outer diameter so that tubes can be spaced closer to-gether in a tube bundle.
Figs. 6 and 7 are approximately lOOx (SEM) scanning electron microscope photographs showing the surface of an ex-perimental tube produced in the apparatus of Fig. 3. In Fig.
6, the tube 10 is shown after pyrolysis and illustrates the porous nature of the plated copper surface 72. Fig. 7 illustrates l,.,C~
a portion of the same tube after swaging through a 16.3 mm diameter die 76 in the manner illustrated in Fig. 5. The swaged plated copper surface 72' is compressed so that fewer pores are visible than in Fig. 6.
Claims (7)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A method of providing a metal heat transfer member with a porous nucleate boiling surface comprising the steps of applying a layer of open cell reticulated organic foam material having an adherent coating of conductive graphite to the surface of the metal member and electroplating the exposed graphite coated surfaces of the reticulated foam material and the exposed surfaces of the metal member which underlie the foam material with a metal so as to form a reticulated metal surface having open cells which overlies the surface of the metal member and is firmly adhered thereto.
2. The method of Claim 1 wherein said graphite coating is applied to said layer of foam material by a shear mill.
3. The method of Claim 1 or 2 wherein said heat trans-fer member is a tube and said layer of graphite coated foam material is applied by spirally wrapping a strip of said foam material about said tube.
4. The method of Claim 1 or 2 wherein said plating has a thickness in the range of about 10.2 to 15.2µm.
5. The method of Claim 1 wherein said metal heat transfer member is heated after it has been plated to pyrolyze the organic foam material.
6. The method of Claim 5 wherein said metal plating is made sufficiently thin that portions of it will be fractured by gases developing during pyrolysis to produce pore openings therein.
7. The method of Claim 5 wherein said heating takes place at a temperature of less than 482°C.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US05/867,858 US4136428A (en) | 1977-02-16 | 1978-01-09 | Method for producing improved heat transfer surface |
US867,858 | 1978-01-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1131159A true CA1131159A (en) | 1982-09-07 |
Family
ID=25350605
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA319,220A Expired CA1131159A (en) | 1978-01-09 | 1979-01-08 | Method for producing improved heat transfer surface |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS54101540A (en) |
CA (1) | CA1131159A (en) |
DE (1) | DE2900430C3 (en) |
ES (1) | ES476636A1 (en) |
FR (1) | FR2414081A1 (en) |
IT (1) | IT1109863B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3339584A1 (en) * | 1983-11-02 | 1985-05-15 | Wolfgang Dr.-Ing. 4630 Bochum Leiner | Device for improving the transfer of heat and material on evaporator heating surfaces and expulsion surfaces |
FR2693134B1 (en) * | 1992-07-02 | 1994-10-14 | Plastic Omnium Cie | Method for producing an externally sheathed metal tube. |
NL1020708C2 (en) * | 2002-05-29 | 2003-12-02 | Andries Meuzelaar | Device for transferring heat. |
US7776430B2 (en) * | 2004-10-21 | 2010-08-17 | Graftech International Holdings Inc. | Carbon foam tooling with durable skin |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1544002A (en) * | 1966-07-12 | 1968-10-31 | Foam Metal Ltd | Openwork material with metallic structure and process for its manufacture |
GB1238183A (en) * | 1968-03-13 | 1971-07-07 | ||
GB1242864A (en) * | 1968-05-15 | 1971-08-18 | Dunlop Holdings Ltd | Acoustical elements |
FR2026088A1 (en) * | 1968-12-13 | 1970-09-11 | Dunlop Co Ltd | Metallic foam heat transfer element |
GB1375160A (en) * | 1971-11-01 | 1974-11-27 |
-
1979
- 1979-01-08 CA CA319,220A patent/CA1131159A/en not_active Expired
- 1979-01-08 DE DE2900430A patent/DE2900430C3/en not_active Expired
- 1979-01-08 IT IT19136/79A patent/IT1109863B/en active
- 1979-01-08 ES ES476636A patent/ES476636A1/en not_active Expired
- 1979-01-08 FR FR7900346A patent/FR2414081A1/en active Granted
- 1979-01-09 JP JP171779A patent/JPS54101540A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
DE2900430C3 (en) | 1981-06-11 |
IT7919136A0 (en) | 1979-01-08 |
IT1109863B (en) | 1985-12-23 |
ES476636A1 (en) | 1980-07-01 |
DE2900430A1 (en) | 1979-07-19 |
JPS54101540A (en) | 1979-08-10 |
FR2414081B1 (en) | 1982-11-05 |
FR2414081A1 (en) | 1979-08-03 |
DE2900430B2 (en) | 1980-10-09 |
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