Patent Application
20070031315
The present invention is directed to a method and apparatus for the manufacture of nitrogen trifluoride (NF.sub.3) by reacting elemental fluorine (“F.sub.2”), gaseous ammonia (“NH.sub.3”) and a molten ammonium acid fluoride (“AAF”). In the preferred embodiment, the method and apparatus concurrently produces co-product ammonium bifluoride (NH.sub.4HF, “ABF”) that is salable after removal of excess hydrogen fluoride (“HF”).
The reaction is accomplished in a static reactor without significant mechanical agitation that may contain static mixing elements and that may be configured in a closed loop. The present invention increases reaction selectivity and yield of nitrogen trifluoride while minimizing creation of undesired and unstable by-products and, simultaneously, reducing operational costs and improving control over reaction kinetics.
In the preferred embodiment, flow of reactants is accomplished without adding significant energy to the process (for mixing or pumping, for example) in excess of the energy required to remove the heat of reaction.
The rate of introduction of the reactants and the maintenance of a proper temperature along the length of the reactor controls reaction temperature. NF.sub.3 is used in many industries, for example, in semiconductor manufacturing; flat display panel cleaning; as a fluorine source in the preparation of fluorocarbons; and as an oxidizing agent for high energy fuels. NF.sub.3 has advantages over elemental fluorine and competing products in these and other applications because it is relatively inert at low temperatures, e.g., 300.degree.F. or below, and, therefore safer and more convenient to handle. Further, NF.sub.3 can safely be compressed to high pressures, e.g., 1,700 psig for shipment.
In contrast to the present invention, known methods of producing NF.sub.3 demonstrate poorer yields and are less efficient. The three principal known methods for manufacturing NF.sub.3 are as follows:
These known manufacturing methods have yields that are typically lower than those achieved by the present invention. Additionally, in contrast to the present invention, Method 1 (as currently practiced)—the most widely practiced method—suffers from greater corrosion of the reactor, and reaction kinetics that are more difficult to control, in part because the shear induced by mechanical agitation increases the surface area of gaseous reactants resulting in an increase of un-reacted F.sub.2 gas.
Moreover, in contrast to the present invention, Method 2 (electrolysis) is economically less efficient because it requires use of an electrolytic cell with nickel anodes. These anodes suffer substantial corrosion and the process, therefore, requires frequent maintenance not required by the present invention. Additionally, the energy costs for Method 2 are higher than those of the present invention and the quality of the NH.sub.3 product is lower than that of the present invention because of metal ion contaminants. Finally, use of Method 2 results in a substantial expense for nickel anodes, an expense that the present invention avoids.
Method 3 is the subject of several Japanese patent applications, but in comparison to the present invention, is difficult to control except in a lab scale because the gas-phase fluorination of NH.sub.3 is highly exothermic and reaction kinetics are more difficult to control than with a gas-liquid phase reaction such as that of the present invention. Also, previous attempts to produce NF.sub.3 by the direct fluorination method, (3), and by direct fluorination of NH.sub.3 in molten ABF resulted in yields substantially lower than those of the present invention.
Competing Chemical Reactions
The basic competing reactions are as follows:
3F.sub.2+NH.sub.3→NF.sub.3+3HF Reaction 1:
3F.sub.2+2NH.sub.3→N.sub.2+6HF Reaction 2:
4F.sub.2+2NH.sub.3→N.sub.2F.sub.2+6HF Reaction 3:
4F.sub.2+2NH.sub.3+H.sub.2O→N.sub.2O+8HF Reaction 4:
Reaction 1 is the desired reaction. Reaction 2 is most favored thermodynamically, but produces only undesirable N.sub.2 and HF. Minimizing reaction 2 requires minimizing the reaction temperature, since lower reaction temperatures favor Reaction 1. Reaction 3 produces N.sub.2F.sub.2, which is unstable and a significant safety hazard, and large quantities of undesired HF. Reaction 4 results from poor quality NH.sub.3 and F.sub.2.
Currently, the most commonly used process for producing NF.sub.3 is described in U.S. Pat. No. 5,637,285 (“the '285 patent”). As described in the '285 patent, NF.sub.3 is produced by the direct fluorination of ammonium ions by contacting gaseous F.sub.2 with a liquid phase acidic ammonium acid fluoride (NH.sub.4F·x HF where x is 2.55 or greater, and preferably greater than 2.65 or 2.85) while NH.sub.3 is separately contacted with the liquid-phase AAF to generate ammonium ions. In contrast to the present invention, this process typically gives NF.sub.3 yields of 65% to 90%, but only at an elevated mixing rate in a stirred reactor at operating temperatures of 260.degree.F. to 400.degree.F. (126.7.degree.C. to 204.4.degree.C.), preferably 260.degree.F.-320.degree.F. (126.7.degree.C. to 160.degree.C.), with lower temperatures favoring Reaction 1. The F.sub.2 is contacted with liquid phase AAF by using a specially designed sparger, having a plurality of small holes, and the contact is enhanced by mechanical agitation with a flat blade turbine.
Compared to the present invention, this process has lower selectivity and yield of NF.sub.3. In contrast to the present invention (which uses a static reactor with reactants conveyed by thermal conduction and siphon across static mixing elements with minimal, if any mechanical agitation, that is substantially self-regulating so long as proper operational temperature is maintained), the process described in the '285 patent (introduction of the F.sub.2 and NH.sub.3 through spargers with a plurality of small holes) makes reaction kinetics more difficult to control because the agitator blades induce shear and because of the large surface area of the gaseous reactants (because of the sparger design with a plurality of small holes). Additionally, in comparison to the the static reactor design of the present invention, the operational and maintenance costs of the process described in the '285 patent are higher since the process requires 5,000 to 35,000 watts/cubic meter, typically 35,000 watts/cubic meter of reactor volume for agitation in addition to the energy required to remove the heat of reaction. The sub-optimal reaction conditions of the process described in the '285 patent relative to the present invention, particularly the higher acidity of the molten AAF, which necessitates higher operating temperatures, and the use of spargers with a plurality of small holes to introduce gaseous reactants and mechanical agitation, result in the production of greater volumes of one or more undesired by-products (N.sub.2, N.sub.2F.sub.2, N.sub.2O and HF). In summary, the present invention: (i) utilizes a less acidic AAF, allowing operation at lower temperature, (ii) utilizes static mixing elements and little, if any, mechanical agitation, and, thus, avoids significant energy requirements in excess of those necessary to remove the heat of reaction and the maintenance costs of mechanical agitation, (iii) relies on thermal siphon or conduction of reactants, which provides improved control over reaction kinetics, and (iv) avoids the use of materials of construction with the potential to introduce contaminants in the product.
Similarly, Japanese patent application 2001-376685 teaches a method for producing NF.sub.3 comprised of introducing a fluorine-containing supplying material flow into contact with liquid acidic ammonium fluoride in an agitated reactor for a fixed time. In contrast, the present invention: (i) utilizes static mixing elements and little, if any, mechanical agitation, and, thus, avoids significant energy requirements in excess of those necessary to remove the heat of reaction and the maintenance costs of mechanical agitation, (ii) relies on thermal siphon or conduction of reactants, which provides improved control over reaction kinetics, and (iv) avoids the use of materials of construction with the potential to introduce contaminants in the product.
U.S. Pat. No. 5,628,894 discloses a method for the production of NF.sub.3 and hydrogen (H.sub.2) gas, starting with a molten flux including at least NH.sub.3, a metal fluoride, and HF, including the steps of: circulating the molten flux from an electrolyzer, to an ammonia solubilizer, to an NF.sub.3 reactor, to an HF solubilizer, and back to the electrolyzer; maintaining the quantity of the molten flux substantially constant by adding NH.sub.3 and a carrier gas to the NH.sub.3 solubilizer and by adding HF and a carrier gas to the HF solubilizer; producing F.sub.2 gas and H2 gas in the electrolyzer; transferring the carrier gas from at least one of the solubilizers to the NF.sub.3 reactor; mixing the F.sub.2 gas and the carrier gas and supplying the mixed gases to the NF.sub.3 reactor; reacting the F.sub.2 gas with the molten flux in the NF.sub.3 reactor to produce NF.sub.3. The present invention does not require complex apparatus such as a flux tank, HF solubilizer, ammonium solubilizer, compressor, condenser, NF.sub.3 flux loop and a fluoride flux loop. Additionally, the energy requirements of the present invention are limited to those necessary to remove the heat of reaction and no energy for electrolysis is required.
U.S. Pat. No. 6,361,679 discloses a process for producing high-purity NF.sub.3 gas by molten salt electrolysis using a nickel electrode and NH.sub.4HF as an electrolyte, wherein CF.sub.4 impurity gas entrained in a crude gas, among impurities in the nickel electrode as an anode is controlled to an amount of 400 wt % or less. In contrast, the present invention achieves comparable purity without the use of nickel or carbon electrodes and thereby avoids both metal and significant CF.sub.4 impurities. Additionally, the energy requirements of the present invention are limited to those necessary to remove the heat of reaction and no energy for electrolysis is required.
U.S. Pat. No. 6,010,605 discloses an apparatus for the production of NF.sub.3, starting with an anhydrous molten flux including NH.sub.3, a metal fluoride (AAF), and HF. The apparatus includes an electrolyzer, an NH.sub.3 solubilizer, an HF solubilizer, an NF.sub.3 reactor, two compressors, two pumps, three condensers a gas recycle loop, and, two flux loops of the same component ternary flux, but each loop with different concentration. The present invention does not require complex apparatus such as an electrolyzer, an NH.sub.3 solubilizer, an HF solubilizer, an NF.sub.3 reactor, two compressors, two pumps, three condensers a gas recycle loop, and, two flux loops and a flux tank. Additionally, the energy requirements of the present invention are limited to those necessary to remove the heat of reaction and no energy for electrolysis is required.
U.S. Pat. No. 6,183,713 discloses a method for producing NF.sub.3 by gas-solid reaction of a fluorine-containing gas with particulate solid of an ammonium complex of a metal fluoride. This method includes the steps of (a) providing a packed-bed-type vessel filled with a particulate solid of an ammonium complex of a metal fluoride; (b) introducing a fluorine-containing gas into the vessel to allow the fluorine-containing gas to flow upwardly through the vessel such that fluorine of the fluorine-containing gas is reacted with the particulate solid in the vessel, thereby to obtain a reaction gas containing NF.sub.3; and (c) separating the NF.sub.3 from the reaction gas. The present invention does not use an ammonium complex of a metal fluoride, thus avoiding potential metal impurities in the product and the present invention is conducted in liquified NH.sub.4HF with the introduction of both NH.sub.3 and F.sub.2. This provides the advantage of producing NH.sub.4HF and HF as salable co-products.
U.S. Pat. 4,091,081 discloses a method for preparing NF.sub.3 is prepared by passing F.sub.2, optionally with an inert diluent, in intimate contact with liquid phase ammonium acid fluoride, preferentially in a nickel reactor, maintained at a temperature above its melting point but below about 400.degree.F. (204.4.degree.C.) for a time sufficient to effect reaction. The intimate contact is achieved using a sparger with a plurality of small holes. Generally, NH.sub.3 is injected into the ammonium acid fluoride along with the F.sub.2 to maintain a molar ratio of by-product HF to ammonia of approximately 2.0 to 2.5. The essence of this invention is the use of the sparger with the plurality of small holes and the maintenance of a molar ratio of HF to NH.sub.3 to maintain the desired acidity of the ammonium acid fluoride and avoid formation of ammonium fluoride. In contrast, the present invention: does not employ a special sparger of the type described and, thus, avoids the materials of construction, corrosion and maintenance problems encountered with such a sparger and the difficulties in controlling reaction kinetics that result from the greater surface area of the gaseous reactant introduced using such a sparger. Additionally, in contrast to the process described in the '081 patent, the present invention employs thermal conduction and siphon to convey reactants across static mixing elements with little, if any, mechanical agitation, and, thus, avoids significant energy requirements in excess of those necessary to remove the heat of reaction and the maintenance costs of mechanical agitation. Moreover, again in contrast to the process described in the '081 patent, the present invention's reliance on thermal siphon or conduction of reactants provides improved control over reaction kinetics as long as a proper operational temperature is maintained. Finally, in contrast to the process described in the '081 patent, the present invention does not employ the use of diluents, and thereby avoids the complications and cost associated with their use.
U.S. Pat. No.4,543,242 (“the '242 patent”) discloses a synthesis of NF.sub.3 similar to that described in the '285 patent using F.sub.2 and solid (NH.sub.4).sub.3 AlF.sub.6. The asserted yield of NF.sub.3 was in the range of 65-78%, based upon F.sub.2 selectivity. The present invention does not employ metal ammonium fluoride complexes and, therefore, avoids potential metal impurities in the product.
Electrolytic processes are described in U.S. Pat. Nos. 4,804,447 and 4,975,259, Japanese patents 3550074, 3043251, 3043243, 3162588, 3037464, 3037463, and Japanese patent applications 2000-388841, 11-237912, 2000-029044, 10-278799, 10-247239, 10-232049, 10-137144, 10-141710, 09-357666, 03-211917, 03-215188, 03-215187, 02-164031, 02-110167, 02-033458, 02-033457, 01-334811, 63-014725, 62-277514 and 62-104656. Electrolytic processes require energy in excess of that necessary to remove the heat of reaction and, therefore, are less efficient in contrast to the present invention, which does not require energy substantially in excess of that necessary to remove the heat of reaction. Electrolytic processes also have the potential to introduce impurities from the anodes into the product while the present invention avoids this problem.
Gas phase reactions of ammonia and fluorine are described in Japanese patent applications 2002-131823, 2000-139846, 03-274206, 01-074107, 01-074106, 01-074105. In comparison to the present invention, direct gas phase reactions are difficult to control except in a lab scale because the gas-phase fluorination of NH.sub.3 is highly exothermic and reaction kinetics are more difficult to control than with a gas-liquid phase reaction such as that of the present invention. Many of the gas phase processes use diluents such as perfluorocarbons or helium. The present invention is preferable to such processes because it avoids the cost of diluents that do not contribute to the reaction. Also, processes that produce NF.sub.3 by direct fluorination, and by gas-phase fluorination of NH.sub.3 in the presence of ABF have yields substantially lower than those of the present invention.
U.S. Pat. No. 3,304,248 discloses a process for forming nitrogen trifluoride by passing gaseous nitrogen through a plasma arc at a temperature in excess of 1,000.degree. C. and introducing gaseous elemental fluorine into the post arc region as near the anode as possible. The molar ratio of nitrogen to fluorine during such process is maintained in excess of 0.4:1. In contrast to the '248 patent, the present invention does not employ a plasma arc and, thus, the energy requirements of the present invention are limited to those necessary to remove the heat of reaction. In comparison to the present invention, gas phase reactions are difficult to control except in a lab scale because the direct gas-phase fluorination of NH.sub.3 is highly exothermic and reaction kinetics are more difficult to control than with a gas-liquid phase reaction such as that of the present invention.
U.S. Pat. No. 3,055,817 discloses a process for producing nitrogen trifluoride by reacting hydrazoic acid gas with oxygen difluoride in the presence of actinic (ultraviolet) radiation. In contrast, the present invention avoids the use of hydrazoic acid gas, which is difficult to synthesize and unstable, and also avoids the need to synthesize or procure oxygen difluoride. Additionally, the present invention avoids the energy requirements for producing actinic radiation.
U.S. Pat. No. 4,001,380 discloses an improved process for preparing nitrogen trifluoride from by reaction with nitrosyl fluoride or chlorine trifluoride at a temperature above the boiling point of fluorine azide but below 100.degree. C. The present invention avoids the need to synthesize or procure nitrosyl fluoride or chlorine trifluoride, both of which are materially more costly than NH.sub.3 and F.sub.2.
U.S. Pat. No. 3,043,662 discloses a process for preparing nitrogen trifluoride by reacting carbon tetrafluoride or carbonyl fluoride with binary oxides of nitrogen, e.g. nitrous, nitric and nitrogen oxide. The reaction is carried out by passing the gases through an electric arc at a temperature of 2,000.degree.C. to 4,000.degree. C. for a period of 0.001 to about 2 seconds. In contrast, the present invention avoids the need to synthesize or procure carbon tetrafluoride or carbonyl fluoride and oxides of nitrogen, all of which are materially more costly than NH.sub.3 and F.sub.2. By avoiding the use of carbon tetrafluoride or carbonyl fluoride, the present invention—in contrast to the process described in the '662 patent—minimizes, or eliminates, generation of carbon trifluoride as an impurity in the product. Additionally, in contrast to the process described in the '662 patent, the present invention avoids the energy requirements for producing an electric arc and the use of costly materials of construction capable of sustaining the reaction temperatures in the electric arc process.
Japanese patent application 2003-388952 describes a method of manufacturing NF.sub.3 from a fluorine reactant and an ammonium ion source dispersed in a liquid phase reaction mixture containing one or more perfluorocarbon fluids. The present invention does not require the use of perfluorocarbon fluids and the present invention gives yields substantially higher than the 80% yield claimed for this process.
Japanese patent application 2003-029347 describes a method of producing NF.sub.3 comprised of passing a working fluid through a heat engine cycle and using mechanical energy generated by the working fluid to produce a sufficient mixing intensity inside a nitrogen trifluoride reactor. This method utilizes a working fluid vapor jet, such as hydrogen fluoride vapor jet, to impart sufficient energy to the mixing zone of the reactor in order to disperse gaseous fluorine into an ammonium acid fluoride melt. A gaseous reaction product flow, containing NF.sub.3 and the working vapor fluid, is removed from the reactor. The working fluid is then separated and recycled for reuse in the process. The present invention, by contrast, does not require a complex vapor or the separation and recycling of the liquid reaction medium.
Japanese patent application 11-030333 teaches a process to produce NF.sub.3 by introducing a gas containing F.sub.2 through the lower part of a vertical reactor filled with particles of an ammonium complex of metal fluoride such as (NH.sub.4).sub.3AlF.sub.6 in a packed layer reactor so as to allow the gas to react with the complex. The NF.sub.3 concentration is increased by partially recirculating and reintroducing the gas discharged from the reactor after removing impurities such as F.sub.2, HF, N.sub.2O. In contrast, the present invention does not require use of an ammonium complex of metal fluorides, which are more expensive than ABF or AAF. Further, it does not require successive purification and recirculation of the gas from the reaction and avoids the cost and complexity of purification apparatus, compressors and blowers for this purpose at the production stage.
A process for producing NF.sub.3 by introducing F.sub.2 gas into a perfluorocarbon liquid containing dissolved NH.sub.3 or by introducing NH.sub.3 gas into a perfluorocarbon liquid containing dissolved F.sub.2 is described in Japanese patent application 01-307243. In contrast to this process, the present invention avoids the cost of perfluorocarbon as a liquid medium and the energy requirements to maintain a liquid phase reaction and for distillation of the product from the reaction medium.
Japanese patent application 01-307242 describes a process for manufacturing NF.sub.3 by reacting a metal fluoride (e.g. CoF.sub.3, AgF.sub.2 or MnF.sub.3) and/or a metal fluoride composite salt (e.g. CoF.sub.3.KF) with NH.sub.3 and F.sub.2, preferably at 50-450.degree.C. The present invention avoids both the cost of metal fluorides or metal fluoride composite salts and the potential for metal contamination in the product.
The prior art has failed to produce NF.sub.3 in yields or efficiencies in the range achieved by the present invention. With the increased demand for NF.sub.3 for the electronics industry, a need has arisen to for greater NF.sub.3 production capacity. At the higher energy and capital costs of larger production plants, it is increasingly important to achieve the highest yields and efficiencies. The present invention achieves unexpectedly high yields and efficiencies as described in more detail to follow.
The present invention efficiently produces high yields of NF.sub.3 in a novel reactor without significant mechanical agitation in which F.sub.2 and NH.sub.3 are introduced into the reactor through conduits or nozzles into liquefied, less acidic AAF reactant (NH.sub.4F·x HF where the ratio of NH.sub.3 to HF is approximately 1:2.28-1:2.55). This maximizes Reaction 1 over the competing reactions and optimizes selectivity of the production of NF.sub.3 to the production of undesired byproducts.
Cooling can be through reactor-external coolant-carrying jacket(s) partially or totally encircling the reactor in intimate contact with exterior surfaces of the reactor, separate flow channels in intimate contact with exterior surfaces of the reactor, or internal cooling apparatus within the reactor (which may be integrated into the construction of any static mixing elements that may be used). The liquid AAF, reactants and reaction products flow, primarily by convection or thermal siphon with minimal, if any, mechanical agitation, through the reactor into one or more cooling zone(s). If more than one cooling zone is employed, the subsequent cooling zones can be of any design or configuration as would be adequate for the first cooling zone, and, subject to this condition, the design or configuration of the subsequent cooling zones may be the same as, or different from, that of the first cooling zone. The materials of construction for the cooling apparatus can include any materials compatible with the cooling media that provide sufficient heat transfer when located in intimate contact with exterior surfaces of the reactor. If the cooling apparatus is internal, the materials of construction can include any materials compatible with the reactants that provide sufficient heat transfer.
The materials of construction for the reactor can include any materials compatible with the reactants and the reactor may be configured in a closed loop, and may or may not contain static mixing element(s) or mechanical agitation of less than 5000 wafts per cubic meter of reactor volume. The optional static mixing element(s) can be formed from any material compatible with the reactants and capable of withstanding reaction conditions. There is no limit on the size of the reactor as long as the reactor is designed with sufficient cooling capacity to maintain the desired reaction temperature.
The nozzles used for the introduction of F.sub.2 and NH.sub.3 and the pipes used for withdrawal of NF.sub.3 and AAF can be formed from any material compatible with the reactants and the product and co-products. A small amount of added mechanical mixing may be utilized in accordance with the method described here in (up to about 5000 wafts per cubic meter of reactor volume) but without vigorous mixing. Any cooling media sufficient to remove the heat of reaction is satisfactory.
The rate of reactant flow is dependent upon the rate of NH.sub.3 addition to the liquid AAF, and the temperature differential, if any, on opposite sides or spaced lengths of the reactor. The rate of NH.sub.3 addition controls the molar ratio of HF to NH.sub.3 in the AAF (a molar ratio of NH.sub.3 to HF of 1:2.28-1:2.55) and the rate of consumption of F.sub.2. The reactor operates at a pressure of 4 to 5 kilograms per square centimeter.
Meanwhile, the use of static mixing element(s) increases the reaction efficiency, but lowers the flow rate (because of the hydraulic resistance posed by the static mixing element(s)). Any number of static mixing elements may be used, the only limitation on the maximum number being the hydraulic resistance to the rate of flow of the reactants. The number of static mixing element(s) is determined by balancing the hydraulic resistance with the desired flow rate to achieve optimal conversion and selectivity to NF.sub.3. The static mixing elements can be constructed using any material compatible with the reactants and the reaction conditions and, typically, will be made from a metal or alloy such as Hastelloy C, Inconel 600, Stainless steels 316 or 304, or carbon steel.
For a given rate of introduction of F.sub.2, the rate of introduction of NH.sub.3 must be regulated to maintain the specified acidity of the AAF to obtain the highest NF.sub.3 selectivity. The rate of introduction of NH.sub.3 thus controls reaction temperature and flow rate.
Experiment showing the effect on NF.sub.3 selectivity and yield of a less acidic AAF reactant (NH.sub.4·F x HF where the ratio of NH.sub.3 to HF is approximately 1:2.34-1:2.40) in the static reactor claimed in this invention versus the molar ratio of NH.sub.3 to HF used in Method 1 and the '285 patent (approximately 1:2.55 or greater, and preferably 1:2.65 or 1:2.85 or greater).
A stainless steel (SUS 316), closed loop reactor with an approximate volume of 0.616 cubic meters and 8″ inner diameter was charged with ammonium bifluoride, NH.sub.4HF.sub.2. The reactor was fitted with external cooling jackets, an F.sub.2 inlet tube at point A on the diagram (
Coolant was fed through the external cooling jackets (D to E on
NF.sub.3, together with un-reacted HF, NH.sub.3 and F.sub.2, was withdrawn from point H on
The NF.sub.3 yield is determined by gas chromatography relative to the total quantity of F.sub.2 fed to the reactor and the conversion is based on the amount of un-reacted F.sub.2 measured in the exit stream from the reactor.
Experiment showing the effect of the use of static mixers on NF.sub.3 selectivity and yield.
The reactor was designed and operated as described in Example 1, except that a number of static mixers were introduced to enhance selectivity and yield. The static mixers were placed between points A and B on
The results show that the addition of static mixers dramatically improves selectivity and yield to levels that meet or exceed those achieved by the prior art without the energy cost of agitation (up to 35,000 watts per cubic meter), and without the mechanical complexity, high corrosion rates and increased operational cost of an agitated reactor.
Experiment showing the effect on reactor diameter on NF.sub.3 selectivity and yield.
Two reactors were designed and operated as described in Example 2. One reactor had a volume of 0.616 cubic meters and an inner diameter of 8 inches, and the other had a volume of 0.231 cubic meters and an inner diameter of 3 inches. The operational parameters were as described in Examples 1 and 2. The following results were obtained:
The results show that increased reactor diameter dramatically improves selectivity and yield to levels well in excess of those achieved by the prior art.
The F.sub.2 flows into the reactor through inlet A, and the NH.sub.3 is added through inlet B, where both gaseous reactants come into contact in the liquid AAF that fills the reactor. The static mixing elements are located between inlets A and B across approximately 30%-40% of the length of the reactor.
In the preferred embodiment, the reaction vessel may be disposed horizontally, or vertically as shown in
The F.sub.2 and NH.sub.3 react with the molten, low acidity AAF within the reactor and flow, together with reaction products, including NF.sub.3, across the static mixing elements between inlets A and B.
In the preferred embodiment, cooling zones (example: D-H and F-G on
The AAF is removed from the reactor, together with excess HF, at outlet C, and the ABF is later separated from AAF and sold. The HF is separated from AAF, recovered and can be fed to an electrolytic cell to produce F.sub.2, The gaseous NF.sub.3 product is removed from the reactor at NF.sub.3 outlet H together with HF and any gaseous byproducts. The NF.sub.3 product is isolated and purified using conventional techniques.
The preferred embodiment of the method and apparatus for producing NF.sub.3 set forth in the summary above is a closed-loop, stainless steel reactor of approximately 0.616 cubic meters with an inner diameter of approximately 8 inches employing one or more static mixing elements, preferably about 8 to 10 static mixing elements, between points A and B shown on
F.sub.2 is introduced at point A on
F.sub.2 is introduced at a rate of approximately 24 kg/hr and NH.sub.3 is introduced as necessary to maintain a molar ratio of NH.sub.3 to HF of 1:2.28-1:2.46, preferably 1:2.34 to 1:2.40 and, more preferably, approximately 1:345. Coolant is fed through the external cooling jackets to maintain an operating temperature of approximately 5.degree.C. higher than the melting point of the AAF, but in all cases less than approximately 140.degree.C., preferably approximately 120.degree.C. to 137.degree.C.
The heat of reaction is removed, as necessary, from opposite sides of reactor to maintain optimal operating temperature and, if necessary, to supplement (through temperature differential) the flow of reactants, reaction products and molten AAF reaction media across the static mixing element(s). Ordinarily however, reactant flow rate is maintained by thermal conduction or siphon and controlled by the rate of NH.sub.3 addition, which is determined by the quantity necessary to maintain the desired molar ratio of NH.sub.3 to HF.
