US3250322A - Corrosive fluid heat exchanger - Google Patents

Corrosive fluid heat exchanger Download PDF

Info

Publication number
US3250322A
US3250322A US343267A US34326764A US3250322A US 3250322 A US3250322 A US 3250322A US 343267 A US343267 A US 343267A US 34326764 A US34326764 A US 34326764A US 3250322 A US3250322 A US 3250322A
Authority
US
United States
Prior art keywords
fluid
heat exchange
silicon carbide
bores
exchange element
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 - Lifetime
Application number
US343267A
Inventor
Jr James W Mccrary
Iii Robert C Post
John J Aylwin
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Texas Instruments Inc
Original Assignee
Texas Instruments Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Texas Instruments Inc filed Critical Texas Instruments Inc
Priority to US343267A priority Critical patent/US3250322A/en
Priority to US418572A priority patent/US3391016A/en
Application granted granted Critical
Publication of US3250322A publication Critical patent/US3250322A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F28HEAT EXCHANGE IN GENERAL
    • F28FDETAILS OF HEAT-EXCHANGE AND HEAT-TRANSFER APPARATUS, OF GENERAL APPLICATION
    • F28F7/00Elements not covered by group F28F1/00, F28F3/00 or F28F5/00
    • F28F7/02Blocks traversed by passages for heat-exchange media
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/80After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
    • C04B41/81Coating or impregnation
    • C04B41/85Coating or impregnation with inorganic materials
    • C04B41/87Ceramics
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F28HEAT EXCHANGE IN GENERAL
    • F28FDETAILS OF HEAT-EXCHANGE AND HEAT-TRANSFER APPARATUS, OF GENERAL APPLICATION
    • F28F21/00Constructions of heat-exchange apparatus characterised by the selection of particular materials
    • F28F21/02Constructions of heat-exchange apparatus characterised by the selection of particular materials of carbon, e.g. graphite

Definitions

  • the present invention contemplates a heat exchange element for use in oxidizing and other corrosive environments which is comprised of a body forming a fluid passageway for the corrosive fluid having walls which are coated by a uniform layer of fluidimpervious material which is predominantly beta silicon carbide.
  • the invention contemplates a heat exchange element comprised of graphite having a thermal coefficient of expansion approximately matching the thermal coefficient of expansion of the impervious layer of predominantly silicon carbide such that the element may be used over a wide range of temperatures without rupturing the fluid tight silicon carbide layer. More specifically, the graphite body has a coeflicient of thermal expansion'of about 4.0 to 5.4 1O- in./in./ C.
  • the present invention also contemplates a novel proc ment in a chamber, heating the element, and introducing a hydrogen stream containing silicon and carbon into the chamber in such a manner that the process stream will pass over the surface of the article at a relatively high rate to increase the rate of deposition and thereby form a bulk coating on the surface of the article which is predominately silicon carbide and is essentially fluid-impervious silicon carbide which may have traces of free silicon or carbon as a second phase.
  • the coatings are impervious to H at temperatures as high as 1500 C.
  • the hydrogen stream is introduced in such a manner as to pass through the fluid passageways in the article as the article is rotated and heated.
  • Another specific aspect of the invention entails heating the element by radiant energy and rotating the element so as to attain uniform heating and a uniform coating of silicon carbide.
  • the present invention further contemplates a novel system for carrying out the process comprised generally of a reaction chamber, support means for rotating the substrate body, heating means for heating the body as it is rotated, and nozzle means for introducing a process stream into the reaction chamber so as to impinge upon the substrate and pass through the bores, if any, through the substrate.
  • the substrate is heated by a radiant energysource disposed below the substrate and a portion of the process stream is introduced below the substrate body such that thermal convection currents will tend to circulate the process stream within the reaction chamber.
  • an important object of the present invention is to provide a heat exchange element which will handle oxidizing and other corrosive fluids without deleterious effects on the element.
  • Another object of the invention is to provide a heat exchange element of the type described which will also have an extremely hard surface and which may therefore be used to handle highly abrasive fluids.
  • Yet another object of the present invention is to provide a heat exchange element of the type described having good thermal conductivity.
  • Still another object of the present invention is to provide a heat exchange element of the type described which may be used over a wide temperature range.
  • a still further object of the present invention is to provide a heat exchange assembly for handling fluids which tend to oxidize or otherwise corrode graphite and most metals.
  • FIGURE 1 is a somewhat schematic sectional view of a heat exchanger, constructed in accordance with the present invention.
  • FIGURE 2 is a side view, partially in section, of a heat exchange element of the device of FIGURE 1;
  • FIGURE 3 is a sectional view taken substantially on lines 3-3 of FIGURE 2;
  • FIGURE 4 is a schematic drawing of a process system constructed in accordance with the present invention which also serves to illustrate the process of the present invention.
  • FIG. 10 an exemplary heat exchange assembly employing heat exchange elements coated in accordance with the present invention is indicated generally by the reference numeral 10.
  • the exemplary heat exchanger 16 illustrated in FIGURE 1 is of the type described in its various aspects in US. Patents Nos. 2,721,730 and 2,821,369. A brief description of this exemplary heat exchanger follows.
  • the heat exchanger comprises a metal cylindrical shell 12, the upper and lower ends of which are covered generally by the plates 14 and 16, respectively.
  • the lower end of the cylindrical shell 12 rests on an anular flange 18 and is received within a second annular flange 20.
  • the lower plate 16 and the annular flanges 13 and 20 are fastened together by bolts 22.
  • a plurality of elements 24, 25, 23, 30, and 32 and 34 constructed in accordance with the present invention are stacked within the shell 12.
  • Each of the elements is preferably fabricated of graphite and is coated with fluidimpervious silicon carbide of the type hereafter described in greater detail for protecting the elements and the assembly from oxidation or otherwise corrosive action.
  • the lower header element 24 has a necked portion 36 which is received within an aperture in the lower plate 16 and a downward-facing annular shoulder 33 which rests on the upper face of the plate 16.
  • the header element 24 also has a diameter 40 which is closely received within the annular flange 18.
  • a suitable seal 42 is provided at the junction between the lower header member 24, the lower plate 16 and the annular flange 18.
  • An multichannel fluid passageway 44 extends through the header element 24.
  • the heat exchange elements 26, 28, 30, and 32 are I doughnut-shaped and are stacked upon the lower header element 24 and will hereafter be described in greater detail.
  • the upper header element 34 is substantially identical to the lower header element 24 and is stacked on the uppermost heat exchange element 32.
  • the header element 34 has a neck portion 46, which is received within an aperture in the upper plate 14, and an annular shoulder 48 which abuts against the lower face of the plate 14.
  • a multichannel fluid passageway 49 extends through the header element 34.
  • the periphery of the header element 34 is received within an inwardly projecting annular flange 50 formed at the upper end of the cylindrical shell 12 and within an annular washer 52.
  • An annular O-ring seal 54 is clamped between the washer 52 and the flange 50 to provide a peripheral seal around the header element 34.
  • An annular spacer 55 is disposed between the washer 52 and the plate 14.
  • a plurality of bolts 56 extend through the suitable aperatures in the upper plate 14 and are connected to the lower annular flange 20 so as to clamp the stack of elements including the header element 34, the heat ex change elements 26, 28, 30, and 32, and the lower header element 24 tightly together.
  • the heater exchange elements 26, 28, 30, and 32 are of identical construction and each is comprised for a doughnut-shaped body of heat exchange material substantially as shown in FIGURES 2 and 3.
  • the heater exchange element 26 is illustrated in FIG- URES 2 and 3 and has an outer annular wall 60 and an inner annular wall 62.
  • a plurality of generally radial bores 64 extending between and intersecting the inner and outer walls 60 and 62 to provide for fluid communication therebetween.
  • the element 26 also has upper and lower faces 66 and 68.
  • a plurality of axial bores provides fluid communication between the upper and lower faces 66 and 63 but do not intersect the radial bores 64.
  • the center portions of the upper and lower faces 66 and 68 are preferably concave, substantially as illustrated in FIGURE 2
  • the upper face 66 is bounded by inner and outer annular gasket grooves 72 and 74
  • the lower face 68 is bounded by inner and outer gasket grooves 76 and 78.
  • the corrosive fluid enters through a multichannel passageway 44 in the lower header 24, for example, and passes through the bores 70 of the successive heat exchange elements'26, 28, 30, and 32, then exists through the multichannel passageway 49 in the upper header 34, substantially as indicated by the arrow 92.
  • the annular spaces formed between the adjacent heat exchange elements by the concave faces 66 and 68 form mixing chambers which assist in agitating the fluid and promoting heat exchange.
  • the Teflon sealing rings 79 in the annular grooves restrict the corrosive fluid to the upper and lower faces of the heat 7 exchange elements and to the axial bores 70.
  • the other fluid enters the shell 12 through a flanged conduit 80.
  • An annular baflie 82 is provided between the heat exchange elements 30 and 32 to insure that the incoming fluid passes radially inwardly through the radial bores 64 into the interior of the heat exchange element 32.
  • a disc-shaped batfle 84 is disposed between the heat exchange elements 28 and 30 to direct the fluid outwardly through the radial bores 64 of the heat exchange element 30.
  • a second annular baflie 86 is disposed between the elements 26 and 28 to direct the fluid back through the radial bores of the heat exchange element 28 into the interior of the element. Then the fluid passes stantially as indicated by the arrow 90.
  • the corrosive fluid is confined exclusively to the interior of the header elements 24 and 34 and the heat exchange elements 26, 28, 30, and 32.
  • the surfaces. of the header elements 24 and 34 and the surfaces of heat exchange elements 26, 23, 30, and 32 are uniformly coated with dense, fluid-impervious, beta crystalline, silicon carbide which may have traces of free silicon or free carbon atoms as hereinafter described in greater detail.
  • the silicon carbide by reason of its chemical properties and impervious nature, protects the base material of the elements from oxidation and corrosion.
  • the silicon carbide is also extremely hard and protects the elements from abrasive wear such as would be caused by solids entrained in the fluids.
  • the header and heat exchange elements are preferably fabricated from graphite having a coefficient of thermal expansion in the range from about 4.0)(10- to about 54x10 in./in./ C., and preferably about 4.5 X 10- in./in./C.
  • the elements may be comprised of tungsten or molybdenum coated with silicon carbide.
  • the fluid-impervious coat of silicon carbide may be appliedto each of the elements by a process carried out in the novel system illustrated schematically in FIGURE 4.
  • the system is comprised of a reaction chamber which may be provided with suitable insulation (not illustrated) in order to efficiently and conveniently maintain a high and uniform temperature within the chamber.
  • the chamber 100 may also be provided with some suitable access means such as a bolted flange connection between the top and bottom halves of the chamber.
  • a suitable support means 102 comprises three relatively sharp spikes 104 and supports the graphite body of the element 28. The spikes 104 contact a minimum area of the element and space the remainder of the support means 102 away from the lower surface of the element.
  • the support means 102 has a shaft 106 which extends through and is rotatably journaled in the bottom of the chamber 100.
  • a suitable drive is connected to the shaft 106 for rotating the shaft and therefore the element 28 about its longitudinal axis which, as illustrated, is vertically disposed.
  • a resistive heating element 108 is disposed beneath and axially spaced from the element 28.
  • the resistive heating element 103 is connected to a suitable variable current source 110.
  • the heating element 108 preferably has a generally round configuration corresponding to that of the element 28 so as .to promote uniform heating of the element.
  • a system for injecting reactants into the chamber 100 includes a hydrogen pressure tank 112 and a materials container 114.
  • a conduit 116 interconnects the hydrogen tank 112 and the proportioning valve 118.
  • a second conduit extends from the valve 118 to a point within the materials container 114.
  • the end of the conduit 120 within the container 114 extends below the surface of the liquid in the container so as to bubble the hydroen through the material and entrain vapors of the material in the hydrogen.
  • a conduit 122 extends from the container 114 to a second valve 124.
  • a bypass conduit 126 extends from the proportioning valve 118 to the conduit 122.
  • a pair of fan shaped nozzles 128 and 132 are connected to valve 124 by conduits 130 and 134, respectively.
  • the location of the nozzles 128 and 132 is an important aspect of the present invention.
  • the nozzle 128 is so positioned as to direct the process stream into the adjacent radial bores 64 of the element 28 as the element is rotated about its longitudinal axis as hereafter described in greater detail.
  • the nozzle 132 is so positioned as to direct the process stream through the axial bores 70 of the element 28 then adjacent the nozzle. Additional nozzles may be provided as desired to direct the process stream across the surface of the substrate body.
  • An exhaust conduit 136 having a valve 138 removes the proces steam from the chamber 100.
  • the process of the present invention is an improvement over the process described in US. application S.N. 68,767, entitled Novel Vapor Deposition Process and Product, filed by William A. Santini, Jr., on November 14, 1960.
  • a gaseous stream containing hydrogen, silicon and carbon in an appropriate ratio is introduced into the reaction zone in which is located a heated substrate.
  • the carrier gas of the process stream is hydrogen and the flow conditions and geometry of the reaction zone are chosen with reference to the heated substrate such that the process stream flows about the heated substrate to form a minimum thickness quiescent zone through which a relatively high rate of diffusion occurs to produce the rapid codeposition of silicon and carbon atoms onto the surface of the heated substrate.
  • the proportion of atoms of silicon and carbon that are deposited can be controlled to yield a ma terial which is substantially stoichiometric silicon carbide or may be silicon carbide having either carbon or silicon atoms as a second phase.
  • the process provides a diffusion controlled, surface catalyzed reaction in which molecules of the reactants move across the thin quiescent zone existing adjacent the surface of the heated substrate by virtue of a relatively high diffusion gradient. The molecules, upon reaching the surface of the substrate, are degraded to yield free silicon and carbon atoms which subsequently react to form a coat of silicon carbide.
  • hydrogen favors the formation of silicon atoms and this can be employed to control the proportion of silicon and carbon atoms formed.
  • methyltrichlorosilane is used to supply the silicon and carbon atoms in the hydrogen carrier gas and form the process stream.
  • the heating element 108 is resistively heated by current from the source 110.
  • the heat exchange element 28 is then rotated by the drive means connected to the shaft 106 at a relatively slow rate of from about 0.5 to rpm. As the heat exchange element 28 is rotated, it is uniformly heated by radiant energy from the heating element 108 to a temperature of from about 900 C. to about 1500" C.
  • a suitable heat sensing means such as an optical pyrometer (not illustrated) may be used to determine the temperature of the substrate heat exchange element 28 and automatically control the current to the heating element to maintain a preset temperature.
  • the valve 118 provides a means for controlling the ratio of hydrogen to methyltrichlorosilane in the process stream.
  • the mol ratio of the hydrogen to the methyltrichlorosilane should be from about 50:1 to about 4:1.
  • the ratios between the hydrogen and methyltrichlorosilane may be determined by a thermal conductivity cell.
  • the flow rate of the process stream may be monitored by suitable flow meters and controlled by the valve 124. As the process stream leaves the valve 124, it is divided and passes through the nozzles 128 and 132 and is directed into the reaction chamber 100 onto the hot heat exchange element 28.
  • the process stream injected from the nozzle 128 tends to pass through the radial bores 64 of the element 28 as the element is rotated and the bores become generally aligned with the nozzle.
  • the process stream of the nozzle 132 is directed through the axial bores 70 of the element 28 as the element is rotated and the respective bores become generally aligned with the nozzle.
  • the process materials are exhausted through the conduit 136 and the valve 138.
  • the rotation of the element 28 is necessary in order to assure that the exchange element 28 is evenly heated by radiant energy from the element 108 and also to insure that the process stream penetrates the generally radial bores 64 and the axial bores 70 uniformly around the perpihery of the annular body of the heat exchange element.
  • the rotation feature is particularly advantageous when the bores 64 and 70 are of relatively small diameter.
  • a heat exchange element with bores 64 and 70 as small'as A" in diameter has successfully been coated with silicon carbide in accordance with this invention.
  • the process stream is caused to flow through the bores.
  • a relatively high flow velocity should be established (by employing a suitable feed rate) to insure that the quiescent zone is relatively thin and that the diffusion rate is relatively high so that the carbon and silicon atoms will be deposited on the surface at a sufficien-tly high rate to prevent the formation of large crystals and produce a dense bulk coat of beta silicon carbide which is essentially fluid-impervious.
  • the process fluids tend to be stagnant within the bores such that little deposition takes place.
  • a substantially uniform coat of silicon carbide is formed over the entire surf-ace of the heat exchange element 28 including the interior surfaces of the radial bores 64 and the axial bores 70.
  • the silicon carbide coat is formed by the mechanism previously explained in which the methyltrichlorosilane is decomposed to produce free atoms of silicon and carbon at the surface of the element 28 by virtue of a diffusion controlled, surface catalyzed reaction.
  • the silicon carbide coatings have ranged from stoichiometrically pure silicon carbide to silicon carbide having as much as 0.89% free carbon or as much as 36.5% free silicon as a second phase element, depending upon the excess materials present and the amount.
  • the compressive strength of the materials produced by the process ranges from about 31X 10 to about 55 X 10 p.s.i.
  • the modulus of elasticity ranges from about 45 X 10 to about 50x10 p.s.i.
  • the coefficient of thermal expansion ranges from about 40x10" to about 5.4 10- in./in./ C. when tested in temperature range of 10 to 810 C.
  • the Knoop hardness of the material determined by utilizing a 1000 gram load and ranges from about 988 to about 2900.
  • the resistivity of the material ranges from 0.005 to about 4 ohm-centimeters.
  • the density determined on a water di-splacement'basis and ranges from 2.59 to 3.28 grams per cc. The material was checked for thermal shock and no appreciable adverse eflect resulted when material at 1000 C. was plunged into water at room temperature.
  • the silicon carbide source may be single compounds, such as dimethyldichlorosilane, trimethylchlorosilane, tetramethylsilane and other aliphatic and aromatic substituted halogenated silanes.
  • the silicon atoms and carbon atoms may be supplied in separate compounds.
  • the carbon atoms may be supplied by compounds such as methane, ethane, propane, benzene, toluene, xylene, ethylene, propylene, and other aliphatic and aromatic hydrocarbons
  • the silicon atoms may be supplied by compounds, for example, such as silicon tetrachloride, silicon tetrabromide, silicon tetraiodide, or any one or more of mono-, di-, and tri-, chloro-, bromo-, and iodo-silane.
  • the heat exchange element is highly resistant to oxidation and other corrosive fluids because of the chemical properties of silicon carbide, has good thermal conductivity due to the thermal properties of graphite and the silicon carbide, can be utilized at very high temperatures in high thermal gradients for maximum efliciency due to the stability of the silicon carbide at high temperature and the substantially matching coelficients of thermal expansion of the graphite and silicon carbide.
  • the silicon carbide coat is extremely hard so that the heat exchange element may be used under severe abrasive conditions and still have a long service life.
  • the novel process and novel system for carrying out the process insure that the relatively large heat exchange element will be uniformy heated and that the process stream will uniformly enter the multitude of small bores, thereby insuring that the body of substrate material is uniformly coated with silicon carbide. Due to the fact that the process stream is impinged directly upon the surface of the substrate and passed through the bores at a considerable velocity, the quiescent zone necessarily established adjacent the surface is reduced in thickness such that diffusion of the carbon and silicon atoms to the surface occurs at a relatively high rate due to the concentration gradient across the quiescent zone. Further, the rapidly flowing process stream constantly makes additional carbon and silicon atoms available so that a dense bulk coat of fluid-impervious silicon carbide is formed over that portion of the surface exposed to the stream.
  • the process stream nozzles are located so as to pass the process stream over substantially the entire surface of the substrate body at one time or another as the relatively large substrate body is rotated.
  • the process of this invention is particularly suited for (though not limited to) commerical operation-at pressures between atmospheric pressure and about 5 p.s.i.g. thereby avoiding the necessity for complex and expensive gas exhausting equipment and the concomitant safety hazards normally associated with operating hydrogen at reduced pressures.
  • a heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid comprising:
  • thermally conductive body having a fluid passageway extending therethrough, the walls of the fluid passageway being coated by dense, essentially fluidimpervious silicon carbide.
  • thermoly conductive body is comprised of molybdenum.
  • a heat exchange element for transferring thermal energy between at least one corrosive fluid and anotherfluid comprising:
  • a graphite body having a plurality of separate fluid passageways extending therethrough for passing the corrosive fluid and for passing the other fluid while maintaining the fluids separated, the graphite body having a continuous coat of dense, fluid-impervious material comprised essentially of beta silicon carbide over all areas where the corrosive fluid contacts the body.
  • a heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid comprising:
  • a body of graphite having a first pair of opposite faces and a second pair of opposite faces, a first set of bores extending between the first pair of opposite faces for transmitting fluid therethrough, a second set of bores extending between the second pair of opposite faces for transmitting fluid therethrough, and a coat of material over the outer surface of at least one set of bores and the associated faces comprised essentially of fluid-impervious silicon carbide.
  • a heat exchange element for transferringthermal energy between at least one corrosive fluid and another fluid comp-rising:
  • the coat of material covers at least the end surfaces and the surfaces formed by said second set of generally axially extending bores.
  • the coat of material covers the entire surface of the body including the surfaces formed by said first and second sets of bores and said coating in beta silicon carbide.
  • a heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid comprising a body having a plurality of separate fluid passageways extending therethrough for passing the corrosive fluid and for passing the other fluid while maintaining the fluids separated, the body having a continuous coat of dense, fluid-impervious material comprised essentially of silicon carbide substantially over all areas where the corrosive fluid contacts the body and said body being formed of thermally conductive material having a coeflicient of thermal expansion approximating that of said coat of silicon carbide.
  • a heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid comprising a graphite body having a fluid passageway extending therethrough, the walls of the fluid passageway being coated by dense, essentially fluid-impervious silicon carbide.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)

Description

May 10, 1966 J. w. M CRARY, JR., ETAL 3,250,322
CORROSIVE FLUID HEAT EXCHANGER Filed Feb. 7, 1964 2 Sheets-Sheet 1 INVENTORS UAMas MA M C/PAEYfl/Z, 05927" 6; #05 127;
(/OZA/ Q1 AYL 317v ATTOP VE'Y United States Patent Ofi ice 3,250,322 Patented May 10, 1966 3,258,322 CORROSIVE FLUID HEAT EXCHANGER James W. McCrary, Jr., Richardson, and Robert C. Post 111, and John .7. Aylwin, Dallas, Tex., assignors to Texas Instruments Incorporated, Dallas, Tex., a corporation of Delaware Filed Feb. 7, 1964, Ser. No. 343,267 13 Claims. (Cl. 165133) This invention relates to heat exchangers, and more particularly, but not by way of limitation, relates to an improved heat exchange element and assembly for handling an oxidizing or otherwise corrosive fluid.
It is desirable in many commercial processes to transfer thermal energy between a noncorrosive fluid and an oxidizing or otherwise corrosive fluid. For example, processes utilizing hydrochloric acid, nitric acid, various chrome plating solutions, molten materials and the like may often be performed more economically by the use of a heat exchanger provided the heat exchanger has an economical operating life and can handle the corrosive fluid without contaminating the fluid. Heat exchangers having various corrosion resisting elements such as glass and tantalum have been proposed for these applications but are not wholly satisfactory for various reasons. Graphite elements have been employed for some corrosive fluid applications, but are generally unsuitable under oxidation conditions such as described above.
The present invention contemplates a heat exchange element for use in oxidizing and other corrosive environments which is comprised of a body forming a fluid passageway for the corrosive fluid having walls which are coated by a uniform layer of fluidimpervious material which is predominantly beta silicon carbide. In particular, the invention contemplates a heat exchange element comprised of graphite having a thermal coefficient of expansion approximately matching the thermal coefficient of expansion of the impervious layer of predominantly silicon carbide such that the element may be used over a wide range of temperatures without rupturing the fluid tight silicon carbide layer. More specifically, the graphite body has a coeflicient of thermal expansion'of about 4.0 to 5.4 1O- in./in./ C.
The present invention also contemplates a novel proc ment in a chamber, heating the element, and introducing a hydrogen stream containing silicon and carbon into the chamber in such a manner that the process stream will pass over the surface of the article at a relatively high rate to increase the rate of deposition and thereby form a bulk coating on the surface of the article which is predominately silicon carbide and is essentially fluid-impervious silicon carbide which may have traces of free silicon or carbon as a second phase. The coatings are impervious to H at temperatures as high as 1500 C.
In accordance with a more specific aspect of the invention, the hydrogen stream is introduced in such a manner as to pass through the fluid passageways in the article as the article is rotated and heated. Another specific aspect of the invention entails heating the element by radiant energy and rotating the element so as to attain uniform heating and a uniform coating of silicon carbide.
The present invention further contemplates a novel system for carrying out the process comprised generally of a reaction chamber, support means for rotating the substrate body, heating means for heating the body as it is rotated, and nozzle means for introducing a process stream into the reaction chamber so as to impinge upon the substrate and pass through the bores, if any, through the substrate. In accordance with more specific aspects of the invention, the substrate is heated by a radiant energysource disposed below the substrate and a portion of the process stream is introduced below the substrate body such that thermal convection currents will tend to circulate the process stream within the reaction chamber.
Therefore, an important object of the present invention is to provide a heat exchange element which will handle oxidizing and other corrosive fluids without deleterious effects on the element.
Another object of the invention is to provide a heat exchange element of the type described which will also have an extremely hard surface and which may therefore be used to handle highly abrasive fluids.
Yet another object of the present invention is to provide a heat exchange element of the type described having good thermal conductivity.
Still another object of the present invention is to provide a heat exchange element of the type described which may be used over a wide temperature range.
A still further object of the present invention is to provide a heat exchange assembly for handling fluids which tend to oxidize or otherwise corrode graphite and most metals.
Many additional objects and advantages of this invention will be evident to those skilled in the art from the following detailed description and drawings, wherein:
FIGURE 1 is a somewhat schematic sectional view of a heat exchanger, constructed in accordance with the present invention;
FIGURE 2 is a side view, partially in section, of a heat exchange element of the device of FIGURE 1;
FIGURE 3 is a sectional view taken substantially on lines 3-3 of FIGURE 2; and
FIGURE 4 is a schematic drawing of a process system constructed in accordance with the present invention which also serves to illustrate the process of the present invention.
Referring now to the drawings, an exemplary heat exchange assembly employing heat exchange elements coated in accordance with the present invention is indicated generally by the reference numeral 10. The exemplary heat exchanger 16 illustrated in FIGURE 1 is of the type described in its various aspects in US. Patents Nos. 2,721,730 and 2,821,369. A brief description of this exemplary heat exchanger follows. The heat exchanger comprises a metal cylindrical shell 12, the upper and lower ends of which are covered generally by the plates 14 and 16, respectively. The lower end of the cylindrical shell 12 rests on an anular flange 18 and is received within a second annular flange 20. The lower plate 16 and the annular flanges 13 and 20 are fastened together by bolts 22.
A plurality of elements 24, 25, 23, 30, and 32 and 34 constructed in accordance with the present invention are stacked within the shell 12. Each of the elements is preferably fabricated of graphite and is coated with fluidimpervious silicon carbide of the type hereafter described in greater detail for protecting the elements and the assembly from oxidation or otherwise corrosive action. The lower header element 24 has a necked portion 36 which is received within an aperture in the lower plate 16 and a downward-facing annular shoulder 33 which rests on the upper face of the plate 16. The header element 24 also has a diameter 40 which is closely received within the annular flange 18. A suitable seal 42 is provided at the junction between the lower header member 24, the lower plate 16 and the annular flange 18. An multichannel fluid passageway 44 extends through the header element 24.
The heat exchange elements 26, 28, 30, and 32 are I doughnut-shaped and are stacked upon the lower header element 24 and will hereafter be described in greater detail. The upper header element 34 is substantially identical to the lower header element 24 and is stacked on the uppermost heat exchange element 32. The header element 34 has a neck portion 46, which is received within an aperture in the upper plate 14, and an annular shoulder 48 which abuts against the lower face of the plate 14. A multichannel fluid passageway 49 extends through the header element 34. The periphery of the header element 34 is received within an inwardly projecting annular flange 50 formed at the upper end of the cylindrical shell 12 and within an annular washer 52. An annular O-ring seal 54 is clamped between the washer 52 and the flange 50 to provide a peripheral seal around the header element 34. An annular spacer 55 is disposed between the washer 52 and the plate 14. A plurality of bolts 56 extend through the suitable aperatures in the upper plate 14 and are connected to the lower annular flange 20 so as to clamp the stack of elements including the header element 34, the heat ex change elements 26, 28, 30, and 32, and the lower header element 24 tightly together.
The heater exchange elements 26, 28, 30, and 32 are of identical construction and each is comprised for a doughnut-shaped body of heat exchange material substantially as shown in FIGURES 2 and 3. Specifically, the heater exchange element 26 is illustrated in FIG- URES 2 and 3 and has an outer annular wall 60 and an inner annular wall 62. A plurality of generally radial bores 64 extending between and intersecting the inner and outer walls 60 and 62 to provide for fluid communication therebetween. The element 26 also has upper and lower faces 66 and 68. A plurality of axial bores provides fluid communication between the upper and lower faces 66 and 63 but do not intersect the radial bores 64. The center portions of the upper and lower faces 66 and 68 are preferably concave, substantially as illustrated in FIGURE 2 The upper face 66 is bounded by inner and outer annular gasket grooves 72 and 74, and the lower face 68 is bounded by inner and outer gasket grooves 76 and 78. When the elements 26, 28, 30, and 32 and the header elements 24 and 34 are stacked in the heat exchange assembly 10, the annular grooves of the abutting elements mate to form annular cavities which receive Teflon (a trademark of E. I. du Pont de Nemours Company for a tetrafluoroethylene polymer) or other suitable sealing rings 79 as can be seen in FIGURE 1. For high temperature application ground joint seals between elements may be substituted for the sealing rings.
In the operation of the device, the corrosive fluid enters through a multichannel passageway 44 in the lower header 24, for example, and passes through the bores 70 of the successive heat exchange elements'26, 28, 30, and 32, then exists through the multichannel passageway 49 in the upper header 34, substantially as indicated by the arrow 92. The annular spaces formed between the adjacent heat exchange elements by the concave faces 66 and 68 form mixing chambers which assist in agitating the fluid and promoting heat exchange. The Teflon sealing rings 79 in the annular grooves restrict the corrosive fluid to the upper and lower faces of the heat 7 exchange elements and to the axial bores 70.
The other fluid enters the shell 12 through a flanged conduit 80. An annular baflie 82 is provided between the heat exchange elements 30 and 32 to insure that the incoming fluid passes radially inwardly through the radial bores 64 into the interior of the heat exchange element 32. A disc-shaped batfle 84 is disposed between the heat exchange elements 28 and 30 to direct the fluid outwardly through the radial bores 64 of the heat exchange element 30. A second annular baflie 86 is disposed between the elements 26 and 28 to direct the fluid back through the radial bores of the heat exchange element 28 into the interior of the element. Then the fluid passes stantially as indicated by the arrow 90.
It will be noted that the corrosive fluid is confined exclusively to the interior of the header elements 24 and 34 and the heat exchange elements 26, 28, 30, and 32. As previously mentioned, the surfaces. of the header elements 24 and 34 and the surfaces of heat exchange elements 26, 23, 30, and 32 are uniformly coated with dense, fluid-impervious, beta crystalline, silicon carbide which may have traces of free silicon or free carbon atoms as hereinafter described in greater detail. The silicon carbide, by reason of its chemical properties and impervious nature, protects the base material of the elements from oxidation and corrosion. The silicon carbide is also extremely hard and protects the elements from abrasive wear such as would be caused by solids entrained in the fluids. The header and heat exchange elements are preferably fabricated from graphite having a coefficient of thermal expansion in the range from about 4.0)(10- to about 54x10 in./in./ C., and preferably about 4.5 X 10- in./in./C. However, in accordance with the broader aspects of the invention, the elements may be comprised of tungsten or molybdenum coated with silicon carbide.
The fluid-impervious coat of silicon carbide may be appliedto each of the elements by a process carried out in the novel system illustrated schematically in FIGURE 4. The system is comprised of a reaction chamber which may be provided with suitable insulation (not illustrated) in order to efficiently and conveniently maintain a high and uniform temperature within the chamber. The chamber 100 may also be provided with some suitable access means such as a bolted flange connection between the top and bottom halves of the chamber. A suitable support means 102 comprises three relatively sharp spikes 104 and supports the graphite body of the element 28. The spikes 104 contact a minimum area of the element and space the remainder of the support means 102 away from the lower surface of the element. The support means 102 has a shaft 106 which extends through and is rotatably journaled in the bottom of the chamber 100. A suitable drive is connected to the shaft 106 for rotating the shaft and therefore the element 28 about its longitudinal axis which, as illustrated, is vertically disposed.
A resistive heating element 108 is disposed beneath and axially spaced from the element 28. The resistive heating element 103 is connected to a suitable variable current source 110. The heating element 108 preferably has a generally round configuration corresponding to that of the element 28 so as .to promote uniform heating of the element.
A system for injecting reactants into the chamber 100 includes a hydrogen pressure tank 112 and a materials container 114. A conduit 116 interconnects the hydrogen tank 112 and the proportioning valve 118. A second conduit extends from the valve 118 to a point within the materials container 114. The end of the conduit 120 within the container 114 extends below the surface of the liquid in the container so as to bubble the hydroen through the material and entrain vapors of the material in the hydrogen. A conduit 122 extends from the container 114 to a second valve 124. A bypass conduit 126 extends from the proportioning valve 118 to the conduit 122. A pair of fan shaped nozzles 128 and 132 are connected to valve 124 by conduits 130 and 134, respectively. The location of the nozzles 128 and 132 is an important aspect of the present invention. The nozzle 128 is so positioned as to direct the process stream into the adjacent radial bores 64 of the element 28 as the element is rotated about its longitudinal axis as hereafter described in greater detail. The nozzle 132, on the other hand, is so positioned as to direct the process stream through the axial bores 70 of the element 28 then adjacent the nozzle. Additional nozzles may be provided as desired to direct the process stream across the surface of the substrate body. An exhaust conduit 136 having a valve 138 removes the proces steam from the chamber 100.
The process of the present invention is an improvement over the process described in US. application S.N. 68,767, entitled Novel Vapor Deposition Process and Product, filed by William A. Santini, Jr., on November 14, 1960. In the present process, a gaseous stream containing hydrogen, silicon and carbon in an appropriate ratio is introduced into the reaction zone in which is located a heated substrate. The carrier gas of the process stream is hydrogen and the flow conditions and geometry of the reaction zone are chosen with reference to the heated substrate such that the process stream flows about the heated substrate to form a minimum thickness quiescent zone through which a relatively high rate of diffusion occurs to produce the rapid codeposition of silicon and carbon atoms onto the surface of the heated substrate. The proportion of atoms of silicon and carbon that are deposited can be controlled to yield a ma terial which is substantially stoichiometric silicon carbide or may be silicon carbide having either carbon or silicon atoms as a second phase. The process provides a diffusion controlled, surface catalyzed reaction in which molecules of the reactants move across the thin quiescent zone existing adjacent the surface of the heated substrate by virtue of a relatively high diffusion gradient. The molecules, upon reaching the surface of the substrate, are degraded to yield free silicon and carbon atoms which subsequently react to form a coat of silicon carbide. In the reaction, hydrogen favors the formation of silicon atoms and this can be employed to control the proportion of silicon and carbon atoms formed.
In accordance with a specific aspect of the invention, methyltrichlorosilane is used to supply the silicon and carbon atoms in the hydrogen carrier gas and form the process stream. The heating element 108 is resistively heated by current from the source 110. The heat exchange element 28 is then rotated by the drive means connected to the shaft 106 at a relatively slow rate of from about 0.5 to rpm. As the heat exchange element 28 is rotated, it is uniformly heated by radiant energy from the heating element 108 to a temperature of from about 900 C. to about 1500" C. A suitable heat sensing means such as an optical pyrometer (not illustrated) may be used to determine the temperature of the substrate heat exchange element 28 and automatically control the current to the heating element to maintain a preset temperature.
After the heat exchange element 28 has been uni formly heated to the desired temperature, some hydrogen from the pressure tank 112 is passed through the proportioning valve 118 into the container 114 where methyltrichlorosilane vaporis entrained in the hydrogen. The hydrogen-methyltrichlorosilane vapors then pass through the conduit 122 and are reunited before the valve 124 with pure hydrogen bypassed through the conduit 126 by the proportioning valve 118. Thus the valve 118 provides a means for controlling the ratio of hydrogen to methyltrichlorosilane in the process stream. The mol ratio of the hydrogen to the methyltrichlorosilane should be from about 50:1 to about 4:1. The ratios between the hydrogen and methyltrichlorosilane may be determined by a thermal conductivity cell. The flow rate of the process stream may be monitored by suitable flow meters and controlled by the valve 124. As the process stream leaves the valve 124, it is divided and passes through the nozzles 128 and 132 and is directed into the reaction chamber 100 onto the hot heat exchange element 28. The process stream injected from the nozzle 128 tends to pass through the radial bores 64 of the element 28 as the element is rotated and the bores become generally aligned with the nozzle. Similarly, the process stream of the nozzle 132 is directed through the axial bores 70 of the element 28 as the element is rotated and the respective bores become generally aligned with the nozzle. The process materials are exhausted through the conduit 136 and the valve 138.
It will be noted that the rotation of the element 28 is necessary in order to assure that the exchange element 28 is evenly heated by radiant energy from the element 108 and also to insure that the process stream penetrates the generally radial bores 64 and the axial bores 70 uniformly around the perpihery of the annular body of the heat exchange element. The rotation feature is particularly advantageous when the bores 64 and 70 are of relatively small diameter. For example a heat exchange element with bores 64 and 70 as small'as A" in diameter has successfully been coated with silicon carbide in accordance with this invention. Thus as each set of bores passes the respective nozzles, the process stream is caused to flow through the bores. As the process stream passes through the bores, a relatively high flow velocity should be established (by employing a suitable feed rate) to insure that the quiescent zone is relatively thin and that the diffusion rate is relatively high so that the carbon and silicon atoms will be deposited on the surface at a sufficien-tly high rate to prevent the formation of large crystals and produce a dense bulk coat of beta silicon carbide which is essentially fluid-impervious. As the bores rotate away from the nozzle, the process fluids tend to be stagnant within the bores such that little deposition takes place. As the process is carried out, a substantially uniform coat of silicon carbide is formed over the entire surf-ace of the heat exchange element 28 including the interior surfaces of the radial bores 64 and the axial bores 70. The silicon carbide coat is formed by the mechanism previously explained in which the methyltrichlorosilane is decomposed to produce free atoms of silicon and carbon at the surface of the element 28 by virtue of a diffusion controlled, surface catalyzed reaction.
In order to afford a better understanding of the silicon carbide coating, specific properties of silicon carbide coatings produced by the present process will now be presented. A relatively wide range of process variables including the mol ratios, process stream flow rate and therefore flow velocities, temperature of the substrate, and duration of the run will vary the thickness and physical and chemical properties of the silicon carbide coat within the following ranges. Runs have been conducted using hydrogen flow rates of 20 liters per minute to liters per minute depending upon the system. Duration of the runs have been varied from 0.05 to 8.7 hours at temperatures from 1180 C. to 1450 C. Silicon carbide coatings having thicknesses from 3 to mils have been produced. The silicon carbide coatings have beta crystalline structure, are very dense and, most important of all, are essentially fluid-impervious. The silicon carbide coatings have ranged from stoichiometrically pure silicon carbide to silicon carbide having as much as 0.89% free carbon or as much as 36.5% free silicon as a second phase element, depending upon the excess materials present and the amount. The compressive strength of the materials produced by the process ranges from about 31X 10 to about 55 X 10 p.s.i. The modulus of elasticity ranges from about 45 X 10 to about 50x10 p.s.i. The coefficient of thermal expansion ranges from about 40x10" to about 5.4 10- in./in./ C. when tested in temperature range of 10 to 810 C. The Knoop hardness of the material determined by utilizing a 1000 gram load and ranges from about 988 to about 2900. The resistivity of the material ranges from 0.005 to about 4 ohm-centimeters. The density determined on a water di-splacement'basis and ranges from 2.59 to 3.28 grams per cc. The material was checked for thermal shock and no appreciable adverse eflect resulted when material at 1000 C. was plunged into water at room temperature.
Although methyltrichlorosilane was specified in the above described example, it will be appreciated that various other materials can be employed to furnish the silicon and carbon without departing from the teachings of the invention. For example, the silicon carbide source may be single compounds, such as dimethyldichlorosilane, trimethylchlorosilane, tetramethylsilane and other aliphatic and aromatic substituted halogenated silanes. Also, the silicon atoms and carbon atoms may be supplied in separate compounds. For example, the carbon atoms may be supplied by compounds such as methane, ethane, propane, benzene, toluene, xylene, ethylene, propylene, and other aliphatic and aromatic hydrocarbons, and the silicon atoms may be supplied by compounds, for example, such as silicon tetrachloride, silicon tetrabromide, silicon tetraiodide, or any one or more of mono-, di-, and tri-, chloro-, bromo-, and iodo-silane.
From the above detailed description of preferred embodiments of the present invention, it will be evident that a novel heat exchange element, a novel process for manufactoring the heat exchange element, and a novel system for carrying out the process have been described. The heat exchange element is highly resistant to oxidation and other corrosive fluids because of the chemical properties of silicon carbide, has good thermal conductivity due to the thermal properties of graphite and the silicon carbide, can be utilized at very high temperatures in high thermal gradients for maximum efliciency due to the stability of the silicon carbide at high temperature and the substantially matching coelficients of thermal expansion of the graphite and silicon carbide. The silicon carbide coat is extremely hard so that the heat exchange element may be used under severe abrasive conditions and still have a long service life.
The novel process and novel system for carrying out the process insure that the relatively large heat exchange element will be uniformy heated and that the process stream will uniformly enter the multitude of small bores, thereby insuring that the body of substrate material is uniformly coated with silicon carbide. Due to the fact that the process stream is impinged directly upon the surface of the substrate and passed through the bores at a considerable velocity, the quiescent zone necessarily established adjacent the surface is reduced in thickness such that diffusion of the carbon and silicon atoms to the surface occurs at a relatively high rate due to the concentration gradient across the quiescent zone. Further, the rapidly flowing process stream constantly makes additional carbon and silicon atoms available so that a dense bulk coat of fluid-impervious silicon carbide is formed over that portion of the surface exposed to the stream. The process stream nozzles are located so as to pass the process stream over substantially the entire surface of the substrate body at one time or another as the relatively large substrate body is rotated. Advantageously the process of this invention is particularly suited for (though not limited to) commerical operation-at pressures between atmospheric pressure and about 5 p.s.i.g. thereby avoiding the necessity for complex and expensive gas exhausting equipment and the concomitant safety hazards normally associated with operating hydrogen at reduced pressures.
Although several preferred embodiments of the invention have been described in detail, it is to be understood that various changes, substitutions and alterations can be made therein without departing from the spirit and scope of the invention as defined by the appended claims.
What is claimed is:
1. A heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid comprising:
a thermally conductive body having a fluid passageway extending therethrough, the walls of the fluid passageway being coated by dense, essentially fluidimpervious silicon carbide. 2. A heat exchange element for transferring thermal energy between at least one corrosive fluid and another 5 fluid as defined in claim 1 wherein the thermally conductive body has a coefficient of thermal expansion in the range from about 4.0 l to about 5.4 1() in./in./ C.
3. A heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid as defined in claim 1 wherein the thermally conductive body is comprised of tungsten.
4. A heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid as defined in claim 1 wherein the thermally conductive body is comprised of molybdenum.
5. A heat exchange element for transferring thermal energy between at least one corrosive fluid and anotherfluid comprising:
a graphite body having a plurality of separate fluid passageways extending therethrough for passing the corrosive fluid and for passing the other fluid while maintaining the fluids separated, the graphite body having a continuous coat of dense, fluid-impervious material comprised essentially of beta silicon carbide over all areas where the corrosive fluid contacts the body.
6. A heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid as defined in .claim 5 wherein the graphite body has a coeflicient of thermal expansion of about 4.5 in./in./ C.
7. A heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid comprising:
a body of graphite having a first pair of opposite faces and a second pair of opposite faces, a first set of bores extending between the first pair of opposite faces for transmitting fluid therethrough, a second set of bores extending between the second pair of opposite faces for transmitting fluid therethrough, and a coat of material over the outer surface of at least one set of bores and the associated faces comprised essentially of fluid-impervious silicon carbide.
8. A heat exchange element for transferringthermal energy between at least one corrosive fluid and another fluid comp-rising:
a circular body of graphite having a longitudinal axis,
a pair of opposite concentric faces, a pair of opposed end faces, a first set of bores in the body intersecting and extending transversely to said faces provid-. ing fluid communication between the concentric faces, a second set of generally axially extending bores providing fluid communication between the end faces, and a coat of material over at least one set of bores and the associated faces comprised essentially of fluid-impervious silicon carbide.
9. A heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid as defined in claim 8 wherein:
the coat of material covers at least the end surfaces and the surfaces formed by said second set of generally axially extending bores.
10. A heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid as defined in claim 8 wherein:
the coat of material covers the entire surface of the body including the surfaces formed by said first and second sets of bores and said coating in beta silicon carbide.
11. A heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid comprising a body having a plurality of separate fluid passageways extending therethrough for passing the corrosive fluid and for passing the other fluid while maintaining the fluids separated, the body having a continuous coat of dense, fluid-impervious material comprised essentially of silicon carbide substantially over all areas where the corrosive fluid contacts the body and said body being formed of thermally conductive material having a coeflicient of thermal expansion approximating that of said coat of silicon carbide.
12. A heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid comprising a graphite body having a fluid passageway extending therethrough, the walls of the fluid passageway being coated by dense, essentially fluid-impervious silicon carbide.
13. A heat exchange element for transferring thermal energy between at least one corrosive fluid and another fluid as defined in claim 12 wherein said silicon carbide coating is beta silicon carbide.
References Cited by the Examiner UNITED STATES PATENTS 2,479,540 8/ 1949 Osterberg 117106 10 2,611,585 9/1952 Boling 165-164 2,650,801 9/1953 Collito 165164 2,721,730 10/1955 Clause 61; a1 16588 2,726,072 12/ 1955 Hermann 165133 X 2,821,369 1/1958 Hilliard 165159 2,849,860 9/1958 Lowe 1581 2,914,424 11/ 1959 Murray 117-106 2,941,962 6/ 1960 Van Der Beck 23208 X 3,100,688 8/1963 Dess 23-208 FOREIGN PATENTS 1,078,019 5/1964 France.
285,151 2/ 1928 Great Britain.
866,813 5/1961 Great Britain.
901,176 7/ 1962 Great Britain.
OTHER REFERENCES Refractories," published by General Refractories Co., copyright 1959, page 64 relied on.
FREDERICK L. MATTESON, 111., Primary Examiner.
CHARLES SUKALO, Examiner.

Claims (1)

1. A HEAT EXCHANGER ELEMENT FOR TRANSFERRING THERMAL ENERGY BETWEEN AT LEAST ONE CORROSIVE FLUID AND ANOTHER FLUID COMPRISING: A THERMALLY CONDUCTIVE BODY HAVING A FLUID PASSAGEWAY EXTENDING THERETHROUGH, THE WALLS OF THE FLUID PASSAGEWAY BEING COATED BY DENSE, ESSENTIALLY FLUIDIMPREVIOUS SILICON CARBIDE.
US343267A 1964-02-07 1964-02-07 Corrosive fluid heat exchanger Expired - Lifetime US3250322A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US343267A US3250322A (en) 1964-02-07 1964-02-07 Corrosive fluid heat exchanger
US418572A US3391016A (en) 1964-02-07 1964-10-16 Silicon carbide coating on graphite bores of heat exchanger

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US343267A US3250322A (en) 1964-02-07 1964-02-07 Corrosive fluid heat exchanger

Publications (1)

Publication Number Publication Date
US3250322A true US3250322A (en) 1966-05-10

Family

ID=23345387

Family Applications (1)

Application Number Title Priority Date Filing Date
US343267A Expired - Lifetime US3250322A (en) 1964-02-07 1964-02-07 Corrosive fluid heat exchanger

Country Status (1)

Country Link
US (1) US3250322A (en)

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3604523A (en) * 1970-06-01 1971-09-14 Dresser Ind Silicon carbide seal for an earth boring bit
US4044825A (en) * 1975-01-06 1977-08-30 Commissariat A L'energie Atomique Heat exchanger for high temperature
FR2496245A1 (en) * 1980-12-17 1982-06-18 Przed Projektowania Heat exchanger using vertical stack of carbon blocks - where each block has large number of holes for heat exchange between two fluids, esp. for cooling acid
US4617232A (en) * 1982-04-15 1986-10-14 Kennecott Corporation Corrosion and wear resistant graphite material
US4621017A (en) * 1982-04-15 1986-11-04 Kennecott Corporation Corrosion and wear resistant graphite material and method of manufacture
US5362228A (en) * 1991-11-04 1994-11-08 Societe Europeenne De Propulsion Apparatus for preheating a flow of gas in an installation for chemical vapor infiltration, and a densification method using the apparatus
US5422088A (en) * 1994-01-28 1995-06-06 Hemlock Semiconductor Corporation Process for hydrogenation of tetrachlorosilane
US5906799A (en) * 1992-06-01 1999-05-25 Hemlock Semiconductor Corporation Chlorosilane and hydrogen reactor
US20040173597A1 (en) * 2003-03-03 2004-09-09 Manoj Agrawal Apparatus for contacting gases at high temperature
US20110032512A1 (en) * 2008-06-19 2011-02-10 University Of Florida Research Foundation, Inc. Floating-element shear-stress sensor
DE102010030780A1 (en) * 2010-06-30 2012-01-05 Sgl Carbon Se Heat transfer element for a heat exchanger, method for producing a heat transfer element for a heat exchanger, heat exchangers and Nachrüstverfahren for a heat exchanger
US20120328503A1 (en) * 2011-06-21 2012-12-27 Scott Fahrenbruck Apparatus and Methods for Conversion of Silicon Tetrachloride to Trichlorosilane
DE102014205001A1 (en) 2014-03-18 2015-09-24 Wacker Chemie Ag Process for the preparation of trichlorosilane
US9222733B2 (en) 2011-02-03 2015-12-29 Memc Electronic Materials S.P.A. Reactor apparatus and methods for reacting compounds
DE102018217204A1 (en) * 2018-10-09 2020-04-09 Zf Friedrichshafen Ag Temperature control device and test bench arrangement
US20210129621A1 (en) * 2018-11-02 2021-05-06 Sumitomo Riko Company Limited Internal heat exchanger
US11262142B2 (en) * 2016-04-26 2022-03-01 Northrop Grumman Systems Corporation Heat exchangers, weld configurations for heat exchangers and related systems and methods

Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB285151A (en) * 1926-11-11 1928-02-13 Cecil Wheatley Stancliffe Improvements relating to apparatus for the heating and cooling of fluids
US2479540A (en) * 1942-12-29 1949-08-16 American Optical Corp Method of coating by vacuum distillation
US2611585A (en) * 1948-03-30 1952-09-23 Heat X Changer Co Inc Heat exchanger
US2650801A (en) * 1949-10-11 1953-09-01 Michael B Collito Heat exchanger
FR1078019A (en) * 1952-06-03 1954-11-15 Lorraine Carbone Improvements to heat exchange processes and apparatus
US2721730A (en) * 1952-04-22 1955-10-25 Lorraine Carbone Heat exchanger
US2726072A (en) * 1948-12-23 1955-12-06 Dynamit Nobel Ag Device for absorbing gases by liquids, especially for use in connection with the production of hydrochloric acid
US2821369A (en) * 1952-10-14 1958-01-28 Lorraine Carbone Heat exchangers
US2849860A (en) * 1955-10-17 1958-09-02 Norton Co Rocket motor with recrystallized silicon carbide throat insert
US2914424A (en) * 1958-02-24 1959-11-24 Little Inc A Vapor phase corrosion inhibition
US2941962A (en) * 1958-02-17 1960-06-21 Carborundum Co Silicon carbide resistor bodies
GB866813A (en) * 1958-04-08 1961-05-03 Power Jets Res & Dev Ltd Improvements relating to the production of dense bodies of silicon carbide
GB901176A (en) * 1957-08-13 1962-07-18 Carborundum Co Method of making refractory bodies
US3100688A (en) * 1961-10-04 1963-08-13 Union Carbide Corp Foamed silicon carbide

Patent Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB285151A (en) * 1926-11-11 1928-02-13 Cecil Wheatley Stancliffe Improvements relating to apparatus for the heating and cooling of fluids
US2479540A (en) * 1942-12-29 1949-08-16 American Optical Corp Method of coating by vacuum distillation
US2611585A (en) * 1948-03-30 1952-09-23 Heat X Changer Co Inc Heat exchanger
US2726072A (en) * 1948-12-23 1955-12-06 Dynamit Nobel Ag Device for absorbing gases by liquids, especially for use in connection with the production of hydrochloric acid
US2650801A (en) * 1949-10-11 1953-09-01 Michael B Collito Heat exchanger
US2721730A (en) * 1952-04-22 1955-10-25 Lorraine Carbone Heat exchanger
FR1078019A (en) * 1952-06-03 1954-11-15 Lorraine Carbone Improvements to heat exchange processes and apparatus
US2821369A (en) * 1952-10-14 1958-01-28 Lorraine Carbone Heat exchangers
US2849860A (en) * 1955-10-17 1958-09-02 Norton Co Rocket motor with recrystallized silicon carbide throat insert
GB901176A (en) * 1957-08-13 1962-07-18 Carborundum Co Method of making refractory bodies
US2941962A (en) * 1958-02-17 1960-06-21 Carborundum Co Silicon carbide resistor bodies
US2914424A (en) * 1958-02-24 1959-11-24 Little Inc A Vapor phase corrosion inhibition
GB866813A (en) * 1958-04-08 1961-05-03 Power Jets Res & Dev Ltd Improvements relating to the production of dense bodies of silicon carbide
US3100688A (en) * 1961-10-04 1963-08-13 Union Carbide Corp Foamed silicon carbide

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3604523A (en) * 1970-06-01 1971-09-14 Dresser Ind Silicon carbide seal for an earth boring bit
US4044825A (en) * 1975-01-06 1977-08-30 Commissariat A L'energie Atomique Heat exchanger for high temperature
FR2496245A1 (en) * 1980-12-17 1982-06-18 Przed Projektowania Heat exchanger using vertical stack of carbon blocks - where each block has large number of holes for heat exchange between two fluids, esp. for cooling acid
US4617232A (en) * 1982-04-15 1986-10-14 Kennecott Corporation Corrosion and wear resistant graphite material
US4621017A (en) * 1982-04-15 1986-11-04 Kennecott Corporation Corrosion and wear resistant graphite material and method of manufacture
US5362228A (en) * 1991-11-04 1994-11-08 Societe Europeenne De Propulsion Apparatus for preheating a flow of gas in an installation for chemical vapor infiltration, and a densification method using the apparatus
US5906799A (en) * 1992-06-01 1999-05-25 Hemlock Semiconductor Corporation Chlorosilane and hydrogen reactor
US5422088A (en) * 1994-01-28 1995-06-06 Hemlock Semiconductor Corporation Process for hydrogenation of tetrachlorosilane
DE19502550B4 (en) * 1994-01-28 2005-06-30 Hemlock Semiconductor Corp., Hemlock Improved process for the hydrogenation of tetrachlorosilane
US20040173597A1 (en) * 2003-03-03 2004-09-09 Manoj Agrawal Apparatus for contacting gases at high temperature
US20110032512A1 (en) * 2008-06-19 2011-02-10 University Of Florida Research Foundation, Inc. Floating-element shear-stress sensor
US8879052B2 (en) * 2008-06-19 2014-11-04 University Of Florida Research Foundation, Inc. Floating-element shear-stress sensor
DE102010030780A1 (en) * 2010-06-30 2012-01-05 Sgl Carbon Se Heat transfer element for a heat exchanger, method for producing a heat transfer element for a heat exchanger, heat exchangers and Nachrüstverfahren for a heat exchanger
US9222733B2 (en) 2011-02-03 2015-12-29 Memc Electronic Materials S.P.A. Reactor apparatus and methods for reacting compounds
US9644902B2 (en) 2011-02-03 2017-05-09 Memc Electronic Materials, S.P.A. Methods for reacting compounds
US20120328503A1 (en) * 2011-06-21 2012-12-27 Scott Fahrenbruck Apparatus and Methods for Conversion of Silicon Tetrachloride to Trichlorosilane
US9217609B2 (en) * 2011-06-21 2015-12-22 Gtat Corporation Apparatus and methods for conversion of silicon tetrachloride to trichlorosilane
DE102014205001A1 (en) 2014-03-18 2015-09-24 Wacker Chemie Ag Process for the preparation of trichlorosilane
US11262142B2 (en) * 2016-04-26 2022-03-01 Northrop Grumman Systems Corporation Heat exchangers, weld configurations for heat exchangers and related systems and methods
US11768040B2 (en) 2016-04-26 2023-09-26 Northrop Grumman Systems Corporation Aerospace structures comprising heat exchangers, and related heat exchangers and apparatuses
DE102018217204A1 (en) * 2018-10-09 2020-04-09 Zf Friedrichshafen Ag Temperature control device and test bench arrangement
US20210129621A1 (en) * 2018-11-02 2021-05-06 Sumitomo Riko Company Limited Internal heat exchanger
US11865894B2 (en) * 2018-11-02 2024-01-09 Sumitomo Riko Company Limited Internal heat exchanger for a vehicular air conditioning system

Similar Documents

Publication Publication Date Title
US3391016A (en) Silicon carbide coating on graphite bores of heat exchanger
US3250322A (en) Corrosive fluid heat exchanger
US4539933A (en) Chemical vapor deposition apparatus
KR880000472B1 (en) Chemical vapor deposition apparatus
US6797069B2 (en) Gas driven planetary rotation apparatus and methods for forming silicon carbide layers
US3460510A (en) Large volume semiconductor coating reactor
US7851019B2 (en) Method for controlling the sublimation of reactants
US9053935B2 (en) Chemical vapor deposition with elevated temperature gas injection
CN101203633B (en) Device for introducing reaction gases into a reaction chamber and epitaxial reactor which uses said device
US7596305B2 (en) Method and apparatus for preparing vaporized reactants for chemical vapor deposition
US6569250B2 (en) Gas-driven rotation apparatus and method for forming silicon carbide layers
JPH06206718A (en) Extra-high purity silicon carbide and high temperature semiconductor processing device produced by said silicon carbide
US6045617A (en) Method for CVD surface coating and CVD reactor system
US4547404A (en) Chemical vapor deposition process
US2810365A (en) Apparatus for resistor film deposition
US2781251A (en) Quench for furnace type reactors
US3496010A (en) Machining silicon coating prior to vapor deposition of silicon carbide
EP0586651A1 (en) Treatment chamber
JP3450033B2 (en) Heat treatment equipment
JPS6357775A (en) Cvd thin film forming device
KR940007175Y1 (en) Low pressure cvd apparatus of wafer
US2880078A (en) Apparatus for converting hydrocarbons
US2719873A (en) Means and method for converting hydrocarbons
JP2775837B2 (en) Chemical vapor deposition equipment
JPS61202424A (en) Chemical vapor deposition equipment