METHOD AND APPARATUS PROVIDING HIGH PURITY DIATOMIC MOLECULES OF HYDROGEN ISOTOPES

Abstract

An electrochemical hydrogen isotope recycling apparatus for recycling an isotope of hydrogen includes an electrochemical recycling unit, the unit comprising: an anode; a cathode; and an isotope-treated, proton exchange membrane operatively disposed between the anode and cathode, the isotope-treated, proton exchange membrane having heavy water containing the isotope of hydrogen therein, the device configured to receive a feedstream containing the isotope of hydrogen. A process by which high purity hydrogen isotope products are produced using an electrochemical membrane process in which all conventional water containing components are pre-processed using a heavy water containing the isotope of hydrogen.

Claims

1. An electrochemical hydrogen isotope recycling apparatus for recycling an isotope of hydrogen, comprising: an electrochemical recycling unit, the unit comprising: an anode; a cathode; and an isotope-treated, proton exchange membrane operatively disposed between the anode and cathode, the isotope-treated, proton exchange membrane having heavy water (D.sub.2O or T.sub.2O) containing the isotope of hydrogen therein, the device configured to receive a feedstream containing the isotope of hydrogen.

2. The apparatus of claim 1, further comprising a humidifier or saturator, the humidifier or saturator in fluid communication with and disposed upstream of the unit configured to humidify the feedstream with heavy water containing the isotope of hydrogen, wherein the humidifier or saturator comprises an isotope-treated, proton exchange membrane having heavy water containing the isotope of hydrogen therein, the saturator in fluid communication with and disposed downstream of the unit configured to capture the heavy water containing the isotope of hydrogen evolved from the cathode.

3. The apparatus of claim 1, further comprising a dehumidifier in fluid communication with and disposed downstream of the unit, wherein the dehumidifier comprises a cold trap, adsorbent, polymer membrane, ceramic membrane, film, palladium separator, or even pressure swing absorption unit, wherein the dehumidifier comprises an isotope-treated, proton exchange membrane having heavy water containing the isotope of hydrogen therein

4. The apparatus of claim 1, wherein the isotope is deuterium or tritium.

5. The apparatus of claim 1, wherein the isotope-treated, proton exchange membrane comprises a perfluorosulfonic acid membrane.

6. The apparatus of claim 1, wherein the anode or the cathode or an interfacial layer associated with one or both of them comprises an ionomer or other water-containing layer having the heavy water containing the isotope of hydrogen therein.

7. The apparatus of claim 1, further comprising a heavy water generator to produce heavy water utilized in the apparatus.

8. The apparatus of claim 1, wherein the cathode is configured for active or passive heavy water circulation, wherein the cathode is actively flooded with heavy water.

9. The apparatus of claim 1, further comprising a pre-filter trap configured to receive an incoming mixed gas flowstream comprising a gas that includes the gas comprising the isotope of hydrogen and at least one other gas, wherein the pre-filter trap is configured to capture the at least one other gas, further comprising a circulation pump in fluid communication with a cathode inlet and a reservoir containing the heavy water, the pump configured to pump the heavy water to the cathode inlet, the reservoir also in fluid communication with a cathode outlet and configured to receive the heavy water evolved at the cathode outlet, further comprising a reservoir containing the heavy water having an outlet disposed above and in fluid communication with a cathode inlet and configured to a supply the heavy water to the cathode inlet, the reservoir having an inlet disposed in a head space of the reservoir in fluid communication with a cathode outlet configured to receive the heavy water evolved at the cathode outlet by a bubble lift method.

10. A process by which high purity hydrogen isotope products are produced using a proton exchange apparatus utilizing heavy water (D.sub.2O or T.sub.2O) and in which all conventional water containing components of the apparatus are pre-processed using a heavy water containing the isotope of hydrogen of the products to exchange hydrogen for the isotope of hydrogen.

11. The process of claim 10, wherein the proton exchange apparatus comprises a proton exchange membrane or an electrochemical pump comprising a proton exchange membrane, wherein the proton exchange membrane comprises a perfluorosulfonic acid membrane, wherein the proton exchange apparatus generates heavy water, and the heavy water generated from the apparatus regardless of whether it is the anode, cathode, or any fluid stream, is recovered by a water recovery technology, including but not limited to methods such as cold traps, adsorbents, pressure swing adsorbers, temperature swing adsorbers, enthalpy exchange units, enthalpy wheels, metal-based separators such as palladium membranes, or the like.

12. The process of claim 10, wherein the process comprises exposing components of the proton exchange apparatus that are configured for proton exchange to the heavy water.

13. The process of claim 10, wherein the proton exchange apparatus comprises a heavy water humidifier upstream of a heavy water electrochemical unit, and the process comprises feeding the gaseous isotope comprising the heavy water (D.sub.2 or T.sub.2) from the heavy water humidifier to the heavy water electrochemical stack, wherein the proton exchange apparatus comprises a heavy water saturator downstream of a heavy water electrochemical unit, and the process comprises receiving the gaseous isotope comprising the heavy water (D.sub.2 or T.sub.2) from the heavy water electrochemical stack to the heavy water humidifier, wherein the proton exchange apparatus comprises a pressure swing adsorber downstream of the cathode that is configured to adsorb the heavy water evolved from the cathode, and wherein the pressure swing adsorber is configured to recycle the heavy water or water vapor within the process, wherein the recycled heavy water or water vapor is recycled to a heavy water humidifier or saturator or to the anode.

14. The process of claim 10, wherein anode and cathode exhaust or outlet streams contain heavy water (D.sub.2O or T.sub.2O), whereby the heavy water is recovered at the anode and cathode by a water recovery system.

15. The process of claim 10, wherein the proton exchange apparatus comprises a heavy water generator, and wherein the heavy water generator produces heavy water for utilization by other components of the proton exchange apparatus, wherein the cathode is actively flooded with the heavy water, wherein the cathode is passively flooded with the heavy water by a bubble lift method.

16. The process of claim 15, wherein the proton exchange apparatus further comprises a circulation pump in fluid communication with a cathode inlet and a reservoir containing the heavy water, the pump configured for pumping the heavy water to the cathode inlet, the reservoir also in fluid communication with a cathode outlet and configured to receive the heavy water evolved at the cathode outlet, wherein the proton exchange apparatus further comprises a reservoir containing the heavy water having an outlet disposed above and in fluid communication with a cathode inlet and configured to a supply the heavy water to the cathode inlet, the reservoir having an inlet disposed in a head space of the reservoir in fluid communication with a cathode outlet configured to receive the heavy water evolved at the cathode using the bubble lift method.

17. The process of claim 1, wherein the apparatus further comprises a prefilter trap that is configured to receive an incoming mixed gas flowstream comprising a gas that includes the gas comprising the isotope of hydrogen and at least one other gas, wherein the process further comprises capturing the at least one other gas.

18. A hydrogen isotope recycling apparatus for recycling an isotope of hydrogen, comprising: a proton exchange unit, the unit comprising: an anode; a cathode; and an isotope-treated proton exchange medium operatively disposed between the anode and cathode, the isotope-treated proton exchange medium having heavy water (D.sub.2O or T.sub.2O) containing the isotope of hydrogen therein, the device configured to receive a feedstream containing the isotope of hydrogen.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0012] Other features, advantages and details appear, by way of example only, in the following detailed description of embodiments, the detailed description referring to the drawings in which:

[0013] FIG. 1 is a schematic illustration of a hydrogen separation process; and

[0014] FIG. 2 is a flow diagram of an embodiment of a recycling apparatus and method as described herein;

[0015] FIG. 3 is a flow diagram of a second embodiment of a recycling apparatus and method as described herein;

[0016] FIG. 4 is a flow diagram of a third embodiment of a recycling apparatus and method as described herein;

[0017] Appendix A is a copy of U.S. Pat. No. 8,663,448, which is incorporated herein by reference in its entirety; and

[0018] Appendix B is a copy of U.S. Pat. No. 8,734,632, which is incorporated herein by reference in its entirety.

DESCRIPTION OF THE EMBODIMENTS

[0019] The following description is merely exemplary in nature and is not intended to limit the present disclosure, its application or uses. It should be understood that throughout the drawings, corresponding reference numerals indicate like or corresponding parts and features.

[0020] The invention is based on the discovery that processing any of the three isotopes of hydrogen in the presence of second isotope of hydrogen (or third), yields an impure recycled product (mixture) from an isotopic composition perspective beyond that found in nature. In other words, it has been found that processing D.sub.2, deuterium (.sup.2H) in the presence of H.sub.2, hydrogen (.sup.1H), i.e., no neutrons, results in a recycled product gas with a mixture of .sup.1H and .sup.2H isotopes of hydrogen. Such identifications are routinely performed by analytical laboratories using mass spectrometry as well as other established hydrogen analysis techniques.

[0021] A process and electrochemical recycling device to recycle hydrogen or any of its isotopes H (hydrogen), D (deuterium), or T (tritium), from any device, application, or process that is hydrogen or hydrogen isotope intensive is disclosed. The device and process provide a new way to reclaim and recycle isotopes of hydrogen, specifically deuterium. This new method may also apply to processing tritium. In order to recycle a heavy (neutron containing) hydrogen species, such as deuterium and tritium, and to meet the purification requirements of the recycled species, it is necessary to understand exchange rates of hydrogen with deuterium or tritium or with their respective ionic forms (proton or a deuteron or a triton) can impact product purity. Hydrogen and its isotopes (deuterium and/or tritium) can exchange with themselves in any given process. This is necessary to understand because in addition to the proton exchange mechanism in the perfluorosulfonic acid membrane or other electrolytes used in electrochemical recycling units, any proton containing molecule, including water must be considered. Water is especially important as it is a requirement to support such ionic transport. If conventional H.sub.2O is used, it is likely that a hydrogen ion, i.e., a proton, from the water will exchange with a deuteron or D.sup.+ or triton or T.sup.+ containing molecule. Thereby forming all permutations of H.sub.2, D.sub.2, and H.sub.2O and D.sub.2O, in the case of deuterium, or all permutations of H.sub.2, T.sub.2, and H.sub.2O and T.sub.2O, in the case of tritium, and further permutations of both in the case where both are present, including H.sub.2, D.sub.2, T.sub.2, HD.sub.2, HT.sub.2, DT.sub.2, and H.sub.2O, D.sub.2O, T.sub.2O. HDO, DTO. For example, H.sub.2O in the presence of deuterium may become HDO, and in the presence of tritium may become HTO, and in the presence of both may become any of the preceding or TDO, HDO. This exchange process is well defined in liquid water, heavy or not. The issue is one of purity. If a high D and/or T content is required, then the exchange mechanism with an H must be overcome or engineered around. Preventing a mixed HD or HDO, or HT or HTO species from forming is key to providing a separated, high purity D.sub.2 or T.sub.2 gas stream. Ancillary sub-systems required to support the electrochemical process in the stack must also be deuterium or tritium intensive.

[0022] This invention solves this problem and will allow for the separation and recycling of D.sub.2 or T.sub.2 without imparting H.sup.+ ions or hydrogen containing molecules originating from water in the various sub-systems of the electrochemical system

[0023] In order to recycle a heavy hydrogen species in an industrial application, for example deuterium, and to meet the purification requirements of the application for the recycled species, it is necessary to understand the exchange rates of hydrogen with deuterium or with their respective ionic forms (proton or a deuteron). Hydrogen and its isotopes can exchange amongst themselves in any given chemical process. Exchange means a statistical swapping of the atoms amongst the different isotopes. This is important because, as shown in FIG. 1 and described in the electrochemical processes mentioned above, water, a hydrogen containing molecule, is a requirement for facilitating the transport of hydrogen or hydrogen isotopes from one side of the separator, the input side (anode), to the product or output side (cathode) of the process. Furthermore, in membrane-based electrochemical separation, as well as in liquid acid based separation methods, the H.sub.2 or D.sub.2 or T.sub.2, or mixed species mentioned above, regardless of the number of neutrons, is electrocatalytically oxidized to its constituent cations. For example, H.sub.2, once in contact with the catalyst at the anode (FIG. 1), the two hydrogen atoms covalently bonded together as H.sub.2, are separated into two H.sup.+ cations, commonly referred to as protons in the case of .sup.1H hydrogen. It is such cations of the hydrogen isotope that are transported across the separator of the electrochemical purification device. In membrane cells, this is typically the ionic transport membrane, e.g., a perfluorosulfonic acid membrane such as Nafion, a product of E.I. DuPont. Other membrane suppliers exist and other versions of transport membranes exist, all behaving essentially the same way. In other types of cells, it can be liquid phosphoric acid (mixture of phosphoric acid H.sub.3PO.sub.4, and water, H.sub.2O). If conventional (.sup.1H) H.sub.2O is used, a proton (H.sup.+) from the water will exchange with a deuteron or D.sup.+ containing molecule. This then allows for the formation of all permutations of H.sub.2, D.sub.2, and H.sub.2O and D.sub.2O. For example, H.sub.2O may become HDO and H.sub.2 may become DH if exposed to D.sub.2. This exchange process is well defined in liquid water, heavy or not.

[0024] The issue is one of purity in that some applications must utilize one specific isotope. If a high D content is required, then the exchange mechanism with a H must be overcome or the process engineered to prevent mixing. Preventing a mixed HD or HDO species from forming is key to providing a separated, high purity D.sub.2 product gas stream, or for that matter, any isotope of hydrogen. The layering of ion exchange membranes separated by cell hardware, hereafter referred to as the stack, as well as any ancillary sub-system required to support the electrochemical process must also contain deuterium if deuterium is called for in high purity in the process.

[0025] As mentioned above, it is also important that the critical components of the system, including the separator, namely those that employ or contain hydrogen or hydrogen compounds that are capable of proton exchange (e.g., water or hydrocarbon compounds), must also contain the desired isotope of the desired purity separated product gas. In the case of Nafion as mentioned above, all water and all protons in the as-received membrane (which contains hydrogen and hydrogen compounds that are in the membrane) must be replaced with deuterium containing molecules prior to use. The same is true for tritium-based processes. If phosphoric acid is used as the proton exchange medium in the separation process, H.sub.3PO.sub.4 must also be replaced by using D.sub.3PO.sub.4, as an example.

[0026] If the predetermined product gas or gas output is specified to be a defined mixture of H and D (or T), then knowing the proper ratios prior to use can be calculated and the proper concentrations of each utilized in the proton exchange system and components, such as the electrochemical apparatuses and methods described herein.

[0027] Referring to FIGS. 2-4, the problem solved by this invention is that the newly developed apparatuses and processes or methods will allow for the separation and recycling of D.sub.2 without imparting H.sup.+ ions or hydrogen containing molecules originating from water (containing .sup.1H) in any of the various sub-systems of the electrochemical system. It also includes molecules of the materials employed in the apparatuses and methods, including the proton exchange membranes of the separator.

[0028] The apparatuses and methods of the present invention solve the problem of the inability to provide relatively pure D.sub.2 from a (.sup.1H, H.sub.2O) proton exchange membrane electrochemical cell used in the recycling device.

[0029] The apparatuses and methods of the present invention also apply to electrochemical compression applications, as well as water electrolysis applications if heavy hydrogen or water is present.

[0030] Advantageously, this invention in the devices and processes described herein provides the ability to obtain relatively pure D.sub.2 from a water-centric (H.sub.2O) proton exchange membrane electrochemical cell used in the recycling device, which has not been possible previously.

[0031] Gas is normally graded to a specified purity. For instance, 99%, 99.9%, 99.99%, etc. Where higher purity may be required for more sensitive applications in which impurities can have a negative impact on process conditions. In the case of heavy hydrogen isotopes (deuterium, tritium), isotopic purity may be specified. This refers to the fraction of the gas that is not entirely pure and contains lighter or higher isotope impurities. For instance, semiconductor grade deuterium from one supplier is listed as better than 99.999% chemical purity (referring to non-isotope impurities) and better than 99.75% isotopic purity (referring to impurities such as HD and H.sub.2).

[0032] The effectiveness of a separation process involving chemical species is partly dependent on the process mechanics itself. For example, in an electrochemical separation device, a gas phase species such as molecular hydrogen (H.sub.2) is oxidized to protons and electrons at a catalyst interface. Though other gases can be present and must be separated from the H.sub.2 gas stream, there can be other molecular species that can be imparted into the product stream from the electrochemical process itself. One well known impurity is water, H.sub.2O. The water is part of the proton exchange membrane transport mechanism in polymeric proton exchange membrane materials, such as perfluorosulfonic acid-based membranes. Water facilitates low resistance ionic transport as the proton hops from one ionic site to another within the membrane. The water is incorporated into the membranes in the pretreatment of the membrane phase. The water solvates (hydrates) the ionic groups and also can hydrogen bond to other sites within the polymeric chain of a given membrane. In the case of perfluorosulfonic acid-based membranes, the water solvates (hydrates) the ionic sulfonic acid groups and also can hydrogen bond to other sites within the polymeric chain. One well known example of such a membrane material is DuPont's Nafion series of ion exchange membranes of the perfluorosulfonic acid family. These perfluorosulfonic acid membranes have utility in water electrolyzers, fuel cells, chlor-alkali operations, to name a few. They can also be used in an electrochemical pump. The chemistry of an electrochemical pump is shown in FIG. 1. In this depiction, the water in the membrane is conventional H.sub.2O, but the depiction is also applicable to D.sub.2O and T.sub.2O with suitable membranes, including Nafion, as described herein.

[0033] The water that exits the membrane with the gas phase species of interest can be removed downstream of the electrochemical cell by conventional methods such as a cold trap, adsorbents, membrane or ceramic membranes and films, palladium separators, or even pressure swing absorption processes (PSA). In many cases the reclaimed water is desired as it can be reused in the process and therefore is beneficial to the overall efficiency of the electrochemical pump.

[0034] There is an exchange rate between hydrogen atoms or ions in hydrogen-intensive gases and solutions, meaning if a hydrogen atom of one molecule comes in contact with a second molecule which also contains a hydrogen atom, there can be a swapping effect, or exchange mechanism, by which the two hydrogen atoms or ions switch host molecules. This exchange mechanism takes place at rapid rates in liquid water. In the case of an ion exchange membrane used for proton transport applications as described above, the proton or hydrogen ion may exchange with another proton in the water that is required to make the membrane functional by humidifying it to reduce transport (ionic) resistance. The exchanged hydrogen may come from a water (H.sub.2O) molecule or it may come from another gaseous H.sub.2 molecule or another H.sup.+ as it is driven through the membrane in the electrochemical process. The chemical formula for an example of such a reaction (Rxn 1) is:

H(1)H(2)+H(3)H(4).fwdarw.H(3)H(1)+H(2)H(4)(Rxn 1)

or any other combination thereof. The numbers in brackets only are present to represent or label a specific hydrogen atom. If any other isotope of hydrogen is present, it can be inserted into any form of reaction 1, thereby eventually forming any or all permutations of H.sub.2, HD, HT, and DT.

[0035] In the invention described below, and where there are combinations of hydrogen isotopes, such as a hydrogen, deuterium, or tritium, the exchange process may become significant and impact the desired product. For example, if H.sub.2 and D.sub.2 are present together as homonuclear diatomic molecules, after a period of time there will be a combination of H.sub.2, D.sub.2, and HD molecules. This exchange effect also takes place with water molecules such as H.sub.2O, and D.sub.2O, resulting in H.sub.2O, D.sub.2O, and DHO, and the results are analogous in the case of tritium. It can also take place between gases and liquids. For example H.sub.2O and D.sub.2 will result in all combinations of H and D molecules, including DHO and DH. Furthermore, there is a high likelihood that even if H.sub.2O remains as H.sub.2O, that the H itself has exchanged with another H containing molecule. This happens with hydrogen and all hydrogen isotopes, H, D, and T.

[0036] In addition to gas or liquid phase isotope exchange, evolution of gas at the cathode of the electrochemical pump combines any available proton (H.sup.+, D.sup.+, T.sup.+) with another proton. Gas will evolve made up from any combination of available ionized isotopes.

[0037] The invention relates to the processing of hydrogen isotopes, including deuterium and tritium. In a separation and recycling process requiring high purities of deuterium or tritium relative to protons (H.sup.+), the problem of conventional water-based proton exchange membranes such as Nafion, with a deuterium atom or ion, results in a DH or a DHO species, and the case of tritium atom or ion, results in a TH or a THO species. If the predetermined input gas and output gas flows are D.sub.2 or T.sub.2, these species are considered impurities. If the product specification calls for high purities of D.sub.2 (or T.sub.2), and minimal H, then the conventional H.sub.2O containing membrane separation and transport mechanism in such electrochemical cells will contaminate the desired deuterium product. Separation of D (or T) from H after the fact is extremely complex and expensive. And considering the expense of deuterium (or tritium) molecules alone, it is desirable to maintain the high deuterium (or tritium) content of the process, including ancillary sub-systems including the humidification process used to provide water to the ion exchange membrane in the stack if such a humidifier is required.

[0038] The invention is specific to a deuterium or tritium separation process in which D.sub.2 or T.sub.2 in the gas phase is separated from a second or third, or more, other gas phase species using the electrochemical membrane process. In this invention, it was advantageously discovered that the membrane must be pretreated with deuterated water (D.sub.2O) for deuterium separation, and tritiated water (T.sub.2O) for tritium separation, also referred to as heavy water or super heavy water, respectively, prior to use. The humidifier, regardless of the method of humidification, if required, must also be pretreated by using heavy water, and furthermore there must be a D.sub.2O or T.sub.2O condensation or adsorption process downstream of the electrochemical process so as to recycle the expensive heavy water. The heavy water deuterated (or tritiated) system must be utilized on the anode stream in an electrochemical pump, or on the anode and cathode streams of a fuel cell or a water electrolyzer if high purity deuterium or tritium products are required. Furthermore we found that all components in the electrochemical separation device capable of proton exchange must be rehydrated with heavy water in the case of deuterium, and super heavy water in the case of tritium. Liquid water of proper isotope and isotopic purity may also be utilized in the cathode of an electrochemical pump for membrane hydration.

[0039] Presented in FIG. 2 is a process by which deuterium, or tritium, or any other isotope of hydrogen can be processed if high purity products are desired. In the process dry gas from which hydrogen (or isotope) enters the system (labeled as D.sub.2 Rich Mixed Gas Stream Inlet). The gas is humidified using the appropriate form of water to avoid isotopic contamination (saturator). The humidified gas then enters the anode of the electrochemical pump where electrons are stripped from the gas and conducted away from the anode. The appropriate ionic form of the hydrogen isotope then passes through an ion conducting separator to the cathode. Electrons are supplied to the cathode where they combine with deuterons (D.sup.+) in the case of deuterium processing, to form a new molecular gas molecule of D.sub.2. The gas then exits the cathode. Gas exiting the cathode may contain high levels of water (Cl). This humid cathode gas may then be dried using conventional methods in order to provide a dry product gas (e.g. Pressure Swing Absorption (PSA)). Water plays an integral role in the electrochemical process, leading to the potential for isotopic exchange. Maintaining high isotopic purity requires that the appropriate isotope of water be used for hydration when operating with a specific isotopic of hydrogen gas. For instance D.sub.2O with D.sub.2, H.sub.2O with H.sub.2, T.sub.2O with T.sub.2, etc. One aspect of this invention includes approaches to capture and reuse heavy waters. Another aspect includes pre-treatment of various components so as to avoid isotopic contamination.

[0040] As stated above, and a surprising outcome of generating single isotope product gas, using the most commonly used separator as an example (Nafion), the electrochemical pump membrane must be pretreated with D.sub.2O in the case of deuterium separation (or T.sub.2O if tritiated). In this step the ionic form of Nafion or its equivalent, must be hydrated with D.sub.2O. The process can occur at the time of the membrane fabrication, once the membrane is in the ionic, or sulfonic acid form. If done at the time of ionization of the sulfonyl fluoride moiety attached to the perfluorosulfonic acid membrane, the complexity of the chemistry and handling of the polymer in the presence of D.sub.2O would be great, leading to a high expense. It is more attractive to treat the membrane once it is in its sulfonic acid form and hydrated with conventional water. In this case the conventional water will be rehydrated with deuterated, or heavy water, or tritiated, or super heavy water. This can be done regardless of whether the polymer is in the form of pellets or already fabricated into sheets. To do so would involve conventional rehydration methods such as soaking the membrane in D.sub.2O until the H.sub.2O is reduced to desired (low) levels. Soaking at elevated temperature may be performed as well. Once in deuterated form the membrane can be handled as before.

[0041] It is important to point out that the ability to generate a high purity hydrogen isotope is not expected to be purer or exceed that what is commonly found in nature in the case of a hydrogen mixed gas stream, and in the case of a D.sub.2 or T.sub.2 mixed gas stream, is not expected to be purer or exceed the purity of the isotope found in the mixed gas stream. It is also imperative that all elements of the membrane and membrane electrode layers be treated with D.sub.2O (or T.sub.2O) if there are any conventional water species in such a layer. For example, as small strands of perfluorosulfonic acid can be used as a membrane extender in the electrode layer (referred to as ionomer), this material also will have to be treated with D.sub.2O. Any other species or layer, including any hydrated interfacial layer which has a water content must be pretreated. This would also apply to liquid acid electrochemical separators where any water or .sup.1H species would have to be ion exchanged with the desired isotope.

[0042] Also presented in FIG. 2 above is a membrane humidifier. As perfluorosulfonic acid membranes must have water to function, the water of the humidifier and also the water feed supplied to the humidifier must also be D.sub.2O or T.sub.2O. This is also true of any water-centric humidifier membrane. Sometimes a perfluorosulfonic acid membrane is used within the humidifier. Such a humidifier would also require pretreatment in order to achieve high isotopic purity at process startup. Other membrane forms (beside perfluorosulfonic acid) that require hydration for proper operation would also require pretreatment.

[0043] The high cost of isotopic pure water may require the capture and reuse of process water entrained in the anode and or cathode gas exhaust streams. Purification processes such as adsorption beds (pressure swing adsorption, temperature swing adsorption, enthalpy wheels, palladium membranes, cold traps, and enthalpy exchange membranes for example) may be used to capture water. These processes can be integrated such that any water captured can be redirected to the water system and or the gas system prior to the anode chamber of the electrochemical pump. For instance, FIG. 2 shows a two-column pressure swing adsorption (PSA) unit with the regeneration waste stream directed back to the anode between an enthalpy exchange unit and a humidifier. FIG. 2 also shows the use of an enthalpy exchange unit for the purpose of reclaiming water from the anode exhaust gas and directing it to the anode inlet gas. These are just two examples of how water may be reclaimed and reused.

[0044] Another aspect of this invention is the formation of heavy water in process. A second part or aspect of this invention is that D.sub.2O (or T.sub.2O) can be formed on site as part of the apparatuses or methods described herein with the desired isotopic phase of hydrogen. Specifically, any separated D.sub.2 or T.sub.2 can be combined with oxygen to form the heavy water of the desired isotope phase to be used in the process. As the gas to be recycled or reused was previously vented, any excess gas not recovered by the electrochemical process can be converted to the heavy water phase and therefore considered an advantage in the process using heavy water. See balanced chemical reaction 2 (Rxn 2).

2D.sub.2+O.sub.2=2D.sub.2O(Rxn2)

[0045] It is pointed out the above is only an example. If a different membrane is used, all hydrogen, protons, or related hydrogen sources must be replaced by the desired isotopic phase. This includes water as well. This example can be extended to include phosphoric acid-based electrochemical processes, potassium hydroxide or its analogs, other acid based systems, as well as any solid state conductor.

EXAMPLES

[0046] Tests were performed to investigate isotopic exchange within an electrochemical pump. The pump and humidifier were pre-treated with D.sub.2O and used to pump D.sub.2. High isotopic purity was observed in gas exiting or being output from the electrochemical pump. Upon switching from using a D.sub.2O pretreated humidifier to a H.sub.2O humidifier a rapid increase in H was observed in gas exiting the pump. This demonstrated how readily isotopes are exchanged within the electrochemical device and supporting sub-systems.

[0047] Use of the appropriate isotopic form of water is required in order to maintain high isotopic purity of products evolving from electrochemical devices.

[0048] Referring now to FIG. 2, an embodiment of a hydrogen isotope recycling apparatus 10 for recycling or reclaiming an isotope of hydrogen 8 (e.g. D or T) is disclosed. The apparatus is configured to receive a gas stream 6 that is rich in a diatomic molecule of an isotope of hydrogen (e.g. D.sub.2 or T.sub.2, or possibly also D.sub.2O or T.sub.2O). In one embodiment, the gas stream 6 may comprise only the diatomic molecule of the isotope of hydrogen being utilized. In other embodiments, the gas stream 6 is a mixed gas stream and includes one or more other gaseous constituents (e.g. N.sub.2). The isotope rich gas stream or flow, including the mixed gas stream, may comprise a gas constituent outflow of any industrial process, including in one embodiment a heat treatment or annealing furnace or processing oven, such as a semiconductor device fabrication or annealing furnace, or a furnace or oven used as part of the manufacture or heat treatment of fiber-optic materials, or in the manufacture of pharmaceuticals, or any industrial process where treatment with a gaseous isotope of hydrogen provides enhanced characteristics to the material or materials being treated thereby and which includes a gas constituent outflow of the isotope of hydrogen. The hydrogen isotope recycling apparatus 10 shown in FIG. 2 includes a proton exchange unit 12. The proton exchange unit 12 may be any suitable proton exchange unit, including those of the types described herein, which in one embodiment is an electrochemical proton exchange unit 20 as described herein.

[0049] The proton exchange unit 12 includes an anode 14, a cathode 16, and an isotope-treated proton exchange medium 18 operatively disposed between and in conductive electrical contact with the anode and cathode, the isotope-treated proton exchange medium comprising heavy water (D.sub.2O or T.sub.2O) containing the isotope of hydrogen therein, the device configured to receive a feedstream 6 containing the isotope of hydrogen. The hydrogen isotope recycling apparatus 10 is configured to receive the gas feedstream 6 at an inlet 22, provide the diatomic molecule of the hydrogen isotope to the anode 14 of the proton exchange unit 12 where the ions of the isotope are transported through the proton exchange medium 18, such as the electrochemical proton exchange membrane 20, to the cathode 16 where the reaction shown in FIG. 1 and described herein produces the gaseous diatomic molecule of the hydrogen isotope under pressure. Thus, the hydrogen isotope recycling apparatus 10 produces a compressed gas of the hydrogen isotope being recycled or reclaimed, which is available for reintroduction as an input into the process from which it was an outflow, or for any other purpose.

[0050] As may be understood from FIG. 1-4 and the description herein, various components of the hydrogen isotope recycling apparatus 10 utilize water. Advantageously, the hydrogen isotope recycling apparatus 10 utilizes or produces heavy water (D.sub.2O) or super heavy water (T.sub.2O) in the various components comprising a part thereof, such as the proton exchange medium 18, including the electrochemical proton exchange membrane 20, and in which all conventional water containing components of the apparatus are pre-processed using a heavy (or super heavy) water containing the isotope of hydrogen of the products to exchange hydrogen for the isotope of hydrogen. As will be appreciated, the hydrogen isotope recycling apparatus 10 may, in different embodiments as shown in FIGS. 2-4, incorporate a number of different components to support the function of the apparatus, but all of the components and chemical processes occurring therein that are utilized to handle or treat the feedstream 6 or output flow 24, and that have the capability of hydrogen exchange as described herein due to the materials of the component, the chemicals utilized, or the chemical processes involved will utilize hydrogen isotope-substituted materials, including chemical feedstocks (e.g. D.sub.2O or T.sub.2O). In this way, contamination of the isotope contained in the feedstream 6 is avoided resulting in a compressed gas output flow 24 of the isotope of interest having a high purity. The compressed output flow 24 may be provided in any suitable output pressure in a range from 0-X psi, where X may be any amount compatible with the pressure handling capabilities of the components of the apparatus 10. If a pressure vessel is utilized, then the pressure may be up to the handling capabilities of the pressure vessel, and may include up to 12,000 psi, and more particularly up to 6,000 psi, and still more particularly up to 4000 psi. In one example, the range is from 500 to 12,000 psi, and more particularly 1000 to 6000 psi, and even more particularly 1,000 to 4,000 psi.

[0051] In one embodiment, the proton exchange apparatus is an electrochemical hydrogen isotope recycling apparatus for recycling an isotope of hydrogen, comprising: an electrochemical recycling unit, the unit comprising: an anode 14; a cathode 16; and an isotope-treated, water-based proton exchange membrane 20 operatively disposed between the anode and cathode, the isotope-treated, water-based proton exchange membrane having heavy water (D.sub.2O or T.sub.2O) containing the isotope of hydrogen therein, the device configured to receive a feedstream containing the isotope of hydrogen. In one embodiment, the isotope-treated, water-based proton exchange membrane 20 comprises a perfluorosulfonic acid membrane 21. In another embodiment, the anode 14 or the cathode 16 or an interfacial layer associated with one or both of them comprises an ionomer or other water-containing layer 15 having the heavy water containing the isotope of hydrogen therein.

[0052] In the embodiment of FIG. 2, the apparatus 10 also includes a pre-filter trap 28 configured to receive an incoming mixed gas flowstream 6 comprising a gas that includes the gas comprising the isotope of hydrogen, and which may in certain embodiments of the process, include at least one other gas, wherein the pre-filter trap is configured to capture the at least one other gas. The at least one other gas may also be vented from the trap through the conduit and pressure regulator shown to the outlet for the mixed gas flowstream shown.

[0053] In the embodiment of FIG. 2, the apparatus 10 also includes a humidifier or saturator 30, the humidifier or saturator in fluid communication with and disposed upstream of the proton exchange unit 12 (e.g. electrochemical recycling unit 13) and is configured to humidify the feedstream 6 with heavy water containing the isotope of hydrogen. In one embodiment, the humidifier or saturator 30 comprises an isotope-treated, water-based proton exchange membrane 32 having heavy water containing the isotope of hydrogen therein. The saturator 30 also contains heavy water 34.

[0054] In the embodiment of FIG. 2, the apparatus 10 further comprises a dehumidifier 36 in fluid communication with and disposed downstream of the proton exchange unit 12. In various embodiments, the dehumidifier 36 comprises a cold trap, adsorbent, polymer membrane, ceramic membrane, film, palladium separator, or a pressure swing absorption unit 38 (FIG. 2). The dehumidifier is configured to remove heavy water, particularly water vapor, evolved from the proton exchange unit 12. The dehumidifier 36, including pressure swing absorption unit 38, is configured to remove heavy water vapor from the output flow to provide a dry output flow 24. The dehumidifier 36, including pressure swing absorption unit 38, is also configured to be selectively and periodically purged to remove the accumulated heavy water, which may include liquid heavy water and/or heavy water vapor, for recirculation and reuse anywhere within the apparatus 10, including to the saturator 30 as flow 40. In one embodiment, the dehumidifier 36 may comprises an isotope-treated, water-based proton exchange membrane having heavy water containing the isotope of hydrogen therein.

[0055] As used herein, it will be understood that gas and liquid flows are necessarily communicated in associated conduits, and that their flow may be controlled by various valves, pressure relief valves and pressure regulators. It will also be understood that these associated conduits may also include water traps that are adapted to capture condensation of heavy water vapors that may occur within the associated conduits, and that such water traps may also include outlet conduits 42 to return accumulated heavy water to any component of the apparatus where the same may be reused or stored for reclamation, including to a heavy water reservoir 44.

[0056] Referring now to FIG. 3, a second embodiment of the proton exchange apparatus 10 is illustrated. Elements labeled with the same element numbers have the same purpose and function as in the embodiments of FIGS. 2 and 4, and vice versa. In addition, elements or components found in the other embodiments (FIGS. 2 and 4) may be incorporated into the embodiment of FIG. 3 as options. In addition, in the embodiment of FIG. 3, the proton exchange apparatus 10 also includes a heavy water generator 46 to produce heavy water utilized in the apparatus. In this embodiment, the heavy water generator 46 is in fluid communication with an enthalpy exchange drier 48, which may be used to add or remove heat from the flow received from the generator, and may be utilized to provide liquid heavy water or heavy water vapor to other components of the apparatus. For example, in this embodiment the heavy water generator 46 is also in fluid communication the heavy water saturator and configured to provide a flow 54 of heavy water to the saturator. In this embodiment, the heavy water generator 46 utilizes the diatomic molecules of the isotope gas (D.sub.2 or T.sub.2) evolved at the anode 14 outlet 50 and chemically reacts it with a flow of 0.sub.2 52 to produce heavy water or super heavy water, respectively. It will be understood that in various other embodiments a heavy water generator may be incorporated into the apparatus at any location that provides a source or flow of the diatomic molecules of the isotope gas (D.sub.2 or T.sub.2). In addition, the D.sub.2 or T.sub.2 could be from a make-up source (i.e. supplied directly and not from a process flow stream. Also, in some embodiments the source of oxygen may be air rather than a flow of O.sub.2.

[0057] Referring now to FIG. 4, a third embodiment of the proton exchange apparatus 10 is illustrated. Elements labeled with the same element numbers have the same purpose and function as in the embodiments of FIGS. 2 and 3, and vice versa. In addition, elements or components found in the other embodiments (FIGS. 2 and 3) may be incorporated into the embodiment of FIG. 4 as options. In addition, in the embodiment of FIG. 4 includes a heavy water saturator 56 in fluid communication with and disposed downstream of the unit 12 configured to capture the heavy water containing the isotope of hydrogen evolved from the cathode 16. In various embodiments, the cathode 16 is configured for active or passive heavy water circulation and the heavy water saturator 56 may be incorporated to capture heavy water evolved from the cathode and/or provide a source of supply for circulation of heavy water at the cathode 16. In one embodiment, the cathode 16 comprises an actively flooded cathode 58. In this embodiment, the apparatus 10 also includes an optional circulation pump 60 in fluid communication with a cathode inlet 62 and a reservoir 64 and/or saturator 56 containing the heavy water, the pump 60 configured to actively pump the heavy water to the cathode inlet, the reservoir 64 and/or saturator 56 also in fluid communication with a cathode outlet 66 and configured to receive the heavy water evolved at the cathode outlet. In another alternate embodiment, the apparatus 10 the cathode comprises a passively flooded cathode. In this embodiment, the apparatus 10 further comprises a reservoir 64 and/or saturator 56 containing the heavy water having an outlet 68 disposed above and in fluid communication with a cathode inlet 62 and configured to a supply the heavy water to the cathode inlet, the reservoir having an inlet 70 disposed in a head space of the reservoir and/or saturator in fluid communication with the cathode outlet 66 and configured to receive the heavy water evolved at the cathode outlet by a bubble lift method. The cathode bubble lift and method requires the outlet of the D.sub.2O reservoir to be raised higher than the electrochemical stack such that the cathode side of the stack is fully submerged under water and ensuring that the cathode ports are oriented with the inlet at the bottom and outlet at the top. When gas is evolved on the cathode, bubbles form lifting slugs of D.sub.2O up to the phase separation head space of the D.sub.2O reservoir. This method can be used to passively circulate D.sub.2O for membrane hydration and cell stack cooling.

[0058] While the invention has been described with reference to exemplary embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the invention without departing from the essential scope thereof. Therefore, it is intended that the invention not be limited to the particular embodiments disclosed, but that the invention will include all embodiments falling within the scope of the application.