PRIORITY CLAIM

[001] This application claims priority to Australian Provisional Patent Application 2018904898 filed on 21 December 2018, the content of which is hereby incorporated by reference in its entirety.

FIELD

[002] The present disclosure relates to methods, systems products for converting carbon dioxide to one or more small organic compounds.

BACKGROUND

[003] The production of carbon dioxide (CO2) is widely considered to be a contributing factor to global warming. This has led to the recognition that it would be highly desirable to develop new technologies to prevent the accumulation of CO2.

[004] A variety of technologies have been developed to reduce net atmospheric emissions, including its removal through processes such as scrubbing or sequestration of the gas in highly porous materials. However, another means of reducing CO2 is to convert the material into commercially useful compounds, for example, into high energy compounds such as methane which can themselves be used to generate power or into compounds that can be used in other commercial processes.

[005] Processes for converting CO2 into other commercially useful compounds are known, but these processes typically involve large amounts of input energy, rely on the use of other compounds, and/or are inefficient for large scale conversion of CO2. For example, some photo catalytic conversion systems have been developed, but these remain inefficient.

[006] Accordingly, it would be desirable to develop new processes for converting carbon dioxide into commercially useful compounds, particularly high energy compounds that may be used for generating power.

SUMMARY

[007] The present disclosure relates to methods and products for converting carbon dioxide to one or more small organic compounds.

[008] Certain embodiments of the present disclosure provide a method of converting CO2 and/or a related form thereof to one or more small organic compounds, the method comprising exposing the CO2 and/or the related form thereof to a beta particle activated high band-gap semiconductor and thereby converting the CO2 and/or the related form thereof to the one or more small organic compounds.

[009] Certain embodiments of the present disclosure provide a method of converting CO2 and/or a related form thereof to one or more small organic compounds, the method comprising exposing a high band-gap semiconductor undergoing electronic excitation by energetic beta-particles to the CO2 and/or the related form thereof and thereby converting the CO2 and/or the related form thereof to the one or more small organic compounds.

[0010] Certain embodiments of the present disclosure provide a method of converting CO2 and/or a related form thereof to one or more small organic compounds, the method comprising exposing the CO2 and/or the related form thereof to a beta particle emitting radionuclide coupled to a high band-gap semiconductor and thereby converting the CO2 and/or the related form thereof to the one or more small organic compounds.

[0011] Certain embodiments of the present disclosure provide a method of converting CO2 and/or a related form thereof to one or more small organic compounds, the method comprising exposing the CO2 and/or the related form thereof to a high band-gap semiconductor activated by beta particles from a radionuclide and thereby converting the CO2 and/or the related form thereof to the one or more small organic compounds.

[0012] Certain embodiments of the present disclosure provide a method of producing one or more small organic compounds, the method comprising using a method as described herein to convert CO2 and/or a related form thereof to the one or more small organic compounds.

[0013] Certain embodiments of the present disclosure provide a method of producing one or more small organic compounds, the method comprising exposing CO2 and/or a related form thereof to a beta particle activated high band-gap semiconductor and thereby producing the one or more small organic compounds from the CO2 and/or the related form thereof.

[0014] Certain embodiments of the present disclosure provide a method of producing one or more small organic compounds, the method comprising exposing a high band-gap semiconductor undergoing electronic excitation by energetic beta particles to CO2 and/or a related form thereof and thereby producing the one or more small organic compounds from the CO2 and/or the related form thereof.

[0015] Certain embodiments of the present disclosure provide a method of producing one or more small organic compounds, the method comprising exposing CO2 and/or a related form thereof to a beta particle emitting radionuclide coupled to a high band-gap semiconductor and thereby producing the one or more small organic compounds from the CO2 and/or the related form thereof.

[0016] Certain embodiments of the present disclosure provide a method of producing one or more small organic compounds, the method comprising exposing CO2 and/or a related form thereof to a high band-gap semiconductor activated by beta particles from a radionuclide and thereby producing the one or more small organic compounds from the CO2 and/or the related form thereof.

[0017] Certain embodiments of the present disclosure provide one or more small organic compounds produced by a method as described herein.

[0018] Certain embodiments of the present disclosure provide a system for converting CO2 and/or a related form thereof to one or more small organic compounds, the system comprising:

a source of CO2 and/or a related form thereof; a reaction container comprising a high band-gap semiconductor coupled closely with a beta particle emitting radionuclide for exposure to the CO2 and/or the related form thereof; and

means for extracting the one or more small organic compounds produced by exposure of the CO2 and/or the related form thereof to the high band-gap semiconductor and the radionuclide.

[0019] Certain embodiments of the present disclosure provide one or more small organic compounds produced by a system as described herein.

[0020] Certain embodiments of the present disclosure provide a method of activating a high band-gap semiconductor for the conversion of CO2 and/or a related form thereof to one or more small organic compounds, the semiconductor having a conduction band edge energy sufficient to enable the reduction of CO2 _, the method comprising exposing the high band-gap semiconductor to a beta particle emitting radionuclide and thereby activating the high band-gap semiconductor.

[0021] Certain embodiments of the present disclosure provide a high band-gap semiconductor activated by a method as described herein.

[0022] Certain embodiments of the present disclosure provide a radiocatalytic material comprising a high band-gap semiconductor coupled with a beta particle emitting radionuclide.

[0023] Certain embodiments of the present disclosure provide use of a radiocatalytic material as described herein for producing one or more small organic compounds from CO2 and/or a related form thereof.

[0024] Certain embodiments of the present disclosure provide a method of identifying a high band-gap semiconductor for converting CO2 and/or a related form thereof to one or more small organic compounds by beta particle activation of the semiconductor, the method comprising:

exposing CO2 and/or a related form thereof to a beta particle emitting radionuclide coupled with a candidate high band-gap semiconductor; and determining the ability of the candidate high band-gap semiconductor to convert the CO2 and/or the related form thereof to one or more small organic compounds, thereby identifying the candidate high band-gap semiconductor as a high band- gap semiconductor for converting CO2 and/or a related form thereof to one or more small organic compounds by beta particle activation of the high band-gap semiconductor.

[0025] Certain embodiments of the present disclosure provide a high band-gap semiconductor identified by a method as described herein.

[0026] Other embodiments are disclosed herein.

BRIEF DESCRIPTION OF FIGURES

[0027] Certain embodiments are illustrated by the following figures. It is to be understood that the following description is for the purpose of describing particular embodiments only and is not intended to be limiting with respect to the description.

[0028] Figure 1 shows an experimental setup for a reaction in the presence of b-emitter and a high band-gap semiconductor.

[0029] Figure 2 shows an experimental setup for non-radioactive treatments.

[0030] Figure 3 shows PTFE vessel setup using an alternative ⁸⁹ Sr methodology. PTFE lid has Swagelok fittings including pressure relief valve (right) and manual open/close valve (top). Gas manifold has pressure gauge (top), isolation valves and two way valve for introduction of CO2 and vacuum.

[0031] Figure 4 shows the setup of active experiments during CO2 loading using the alternative ⁸⁹ Sr methodology. [0032] Figure 5 shows the setup for gas sampling, showing two way inlet valve for CO2 and vacuum (left) and Tedlar bag (for gas sampling) attached to manifold (right).

DETAILED DESCRIPTION

[0033] The present disclosure relates, at least in part, to methods, systems and products for converting carbon dioxide to one or more small organic compounds.

[0034] The present disclosure is based, at least in part, on the recognition that a radiocatalysis system can be used to convert waste carbon dioxide to valuable organic compounds, such as methanol.

[0035] Without being bound by theory, it has been recognised that exposing certain high band-gap semiconductors to a flux of energetic beta particles (for example from beta particle emitting radionuclides) electronically excites the high band-gap semiconductor to an activated state capable of driving electron transfer to CO2 molecules. Accordingly, it is possible to convert carbon dioxide at electronically excited semiconductor sites where the electronic excitation creates a high reduction potential.

[0036] Certain embodiments of the present disclosure are directed to methods and products that have one or more combinations of advantages. For example, some of the advantages of some of the embodiments disclosed herein include one or more of the following: a new and/or improved method for converting CO2 into commercially useful compounds; new and/or improved methods for converting CO2 into chemical compounds that may be used to generate energy; new and/or improved methods for converting waste CO2 into commercially useful organic compounds; the ability to utilise certain radioactive waste materials to convert CO2 to small organic compounds; adding value to radioactive compounds formerly considered as waste products; converting a “green-house” compound into a source of commercially useful compounds; assisting with reducing release of CO2 into the atmosphere; a method that can potentially contribute to reducing anthropogenic climate change; a method for utilising bicarbonate and/or carbonate feedstocks to produce new commercially useful compounds; obviating the use of emissions-intensive Fh to produce certain organic compounds, thereby improving safety, providing economic benefits, and benefits to greenhouse credentials; to address one or more problems and/or to provide one or more advantages, or to provide a commercial alternative. Other advantages of certain embodiments of the present disclosure are also disclosed herein.

[0037] Certain embodiments of the present disclosure provide a method of converting CO2 to one or more small organic compounds.

[0038] The term“CO ₂ ” as used herein refers to carbon dioxide or one of its related forms, for example a form present in a solvated or solid state, such as HCO ₃ , CO ₃ ² or H ₂ CO ₃ , or a form of CO ₂ complexed with another molecule, and includes within its scope radicals and radical ions of the aforementioned chemical entities, or complexes with other molecules.

[0039] In certain embodiments, the CO2 is dissolved in an aqueous solution, CO2 in a gaseous form, for example as a gas mixed with water vapour, the use of CO2 dissolved in another solvent, or the use of liquid CO2 itself.

[0040] In certain embodiments, the method is carried out in solution. In certain embodiments, the method is carried out in an aqueous solution or a substantially aqueous solution. In certain embodiments, the method is carried out in a non-aqueous solution. In certain embodiments, the method is carried out in a solvent or a mixed solvent, such as dioxane or dioxane and water. In certain embodiments, the method is carried out in a gaseous or vapour state. Methods and apparatus for conducting reactions in the aforementioned states are known in the art.

[0041] In certain embodiments, the method is carried out under conditions where the CO2 is in the liquid state, alone or mixed with other substances. Methods and apparatus for conducting reactions in liquid CO2 are known in the art.

[0042] In certain embodiments, the present disclosure provides a method of converting CO2 and/or a related form thereof to one or more small organic compounds, the method comprising exposing the CO2 and/or the related form thereof to a beta particle activated high band-gap semiconductor and thereby converting the CO2 and/or the related form thereof to the one or more small organic compounds. [0043] In certain embodiments, the CO2 comprises one or more of waste CO2, atmospheric CO2, liquid CO2, sequestered CO2, a source of CO2 complexed with another agent, a bicarbonate, a carbonate, a carbonate ore, or a source of a related form of CO2. Other sources of CO2 are contemplated.

[0044] The term“small organic compound” as used herein refers to any compound having one or more carbon atoms and which are bonded to another carbon atom and/or to another element, such as hydrogen, oxygen or nitrogen. It will be appreciated that the term includes within its scope compounds such as carbon monoxide (CO) which is sometimes not classified as an organic compound, and also includes within its scope ions, complexes, and radicals of carbon containing compounds.

[0045] In certain embodiments, the one or more small organic compounds comprise one of more of carbon monoxide (CO), methane, H ₂ CO (formaldehyde), CH ₃ OH (methanol), HCO ₂ H (formic acid or the anion thereof), CH ₃ CHO (acetaldehyde), CH ₃ CH ₂ OH (ethanol), CH ₃ CH ₂ COOH (acetic acid or the anion thereof), CH ₃ CH ₂ CH ₂ OH (propanol), or (CH3)2CHOH (isopropanol). Other types of small organic compounds are contemplated. Methods for identifying small organic compounds are known in the art.

[0046] In certain embodiments, the method further comprises purifying or extracting the one or more small organic compounds. Methods for purifying or extracting small organic compounds are known in the art, for example distillation and condensation, or differential adsorption.

[0047] A suitable semiconductor having a high band-gap and a conduction band edge energy sufficient to enable the reduction of CO2 may be selected.

[0048] In certain embodiments, the high band-gap semiconductor has both the properties of a band-gap of at least 2.0 eV and a conduction band edge energy of -0.15 V or less (more negative than) relative to the standard hydrogen electrode. Methods are known in the art for determining the characteristics of semiconductors.

[0049] In certain embodiments, the high band-gap semiconductor has a band-gap of at least 2.6 eV. In certain embodiments, the high band-gap semiconductor has a band-gap of at least 3.1 eV. In certain embodiments, the high band-gap semiconductor has a band- gap of at least 3.2 eV. In certain embodiments, the high band-gap semiconductor has band gap of at least 3.4 eV. In certain embodiments, the high band-gap semiconductor has a band-gap in the range from 2.6 to 5.4 eV, 3.1 to 5.4 eV, 3.2 to 5.4 eV, or 3.4 to 5.4 eV.

[0050] In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -0.15 volts, with respect to the standard hydrogen electrode.

[0051 ] In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -0.4 volts with respect to the standard hydrogen electrode. In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -0.8 volts with respect to the standard hydrogen electrode. In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -2.0 volts with respect to the standard hydrogen electrode.

[0052] Examples of high band-gap semiconductors include a titanate, zirconate, molybdate, vanadate, technetate, pertechnetate, tungstate, niobate, tantalate, doped tin oxides, doped zinc oxide, a hafnate, a germanium oxide, an oxide of manganese, cobalt and iron (eg a ferrate, a manganate, a cobaltate), a chromate, a simple oxide, a sulphide, a chalcogenide and a carbon allotrope. Other types of high-band semiconductors are contemplated. High band gap semiconductors are commercially available or may be produced by a method known in the art.

[0053] In certain embodiments, the high band-gap semiconductor comprises a titanate and/or a zirconate.

[0054] In certain embodiments, the high band-gap semiconductor comprises one or more of a strontium zirconate (SrZrO,), a strontium titanate (SrTiO,) and a titanium oxide.

[0055] In certain embodiments, the high band-gap semiconductor has one or more of the following preferred characteristics: a low electron-hole-pair recombination rate; a melting point of at least 250°C; resistance to oxidation; hardness; strength; resistance to impact fracture, erosion and/or abrasion. Methods for assessing the aforementioned characteristics are known in the art.

[0056] In certain embodiments, the high band-gap semiconductor comprises a characteristic of the ability to be fabricated into a free-flowing powder form that does not self-agglomerate.

[0057] In certain embodiments, the beta particle activated high band-gap semiconductor comprises beta particle activation via emission from a radionuclide. In this regard, it will be appreciated that the radionuclide may also be a radionuclide that decays to a beta- emitting radionuclide.

[0058] In certain embodiments, the radionuclide also emits gamma (g) radiation and/or emits g radiation from one of its decay products.

[0059] In certain embodiments, the radionuclide comprises one or more of ⁹⁰ Sr, "Tc, ³ H, ¹⁴ C, ⁶³ M, ¹³⁷ CS, ¹⁴⁷ Pm, ¹⁵¹ Sm, ^121m Sn, ¹⁵⁵ Eu, ⁹³ Zr, ²¹⁰ Pb and ¹²⁶ Sn. Sources of radionuclides are known in the art, such as being obtained commercially. Methods for producing radionuclides are also known in the art. Other beta particle emitting radionuclides are contemplated.

[0060] In certain embodiments, the radionuclide has one or more of the following preferred properties: (i) the radionuclide emits b-particles with energies in the range 1 - 100 kilo electron volts (keV); (ii) the radionuclide emits b-particles at a rate governed by a half-life in the range of 1-10 years, for example ~5 years (to minimise replacement periods); and (iii) the radionuclide is an isotope of an element with tractable chemical characteristics, such that the radionuclide can be readily loaded into the high band-gap semiconductor.

[0061] It will be appreciated that a single radioactive beta decay event can cause a cascade of secondary electrons extending tens of micrometers (pm) from the original decaying atom, and each of these is potentially capable of causing excited electronic states within the high band-gap semiconductor. [0062] In certain embodiments, the radionuclide is a radionuclide that produces multiple b-particle emissions via its chain of decaying daughter radionuclides as it ultimately decays to a stable isotope/ nucleus, such as ⁹⁰ Sr and ¹²⁶ Sn.

[0063] In certain embodiments, activation of the high band-gap semiconductor comprises exposure to b-particles emitted from a radionuclide in contact with, located at a distance from, and/or coupled with the high band-gap semiconductor.

[0064] In certain embodiments the radionuclide is physically incorporated into the high band-gap semiconductor. In certain embodiments, the radionuclide is chemically incorporated into the high band-gap semiconductor.

[0065] A suitable amount of loading of the radionuclide into the high band-gap semiconductor may be selected. In certain embodiments, the high band-gap semiconductor is loaded with radionuclide in the range from 01. -100 GBq/mm ³ , 1.0-100 GBq/mm ³ , or 10-100 GBq/mm ³ . Other ranges are contemplated.

[0066] In certain embodiments, the radionuclide is proximal to the high band-gap semiconductor, physically admixed with the high band-gap semiconductor, chemically incorporated into the high band-gap semiconductor, present in a matrix of the high band- gap semiconductor, or located internally to the high band-gap semiconductor. Other arrangements are contemplated.

[0067] In certain embodiments, the high band-gap semiconductor and the radionuclide are coupled to form a radioactive catalyst. In this regard, the term“radioactive catalyst” as used herein may also be referred to as a“radiocatalytic material”.

[0068] In certain embodiments, the radioactive catalyst is in macroscopic form, for example as granules, beads, a powder, or consolidated into a porous solid form such as a frit.

[0069] In certain embodiments, the radionuclide is distributed substantially homogeneously in the high band-gap semiconductor. [0070] In certain embodiments, the radionuclide is distributed substantially heterogeneously in the high band-gap semiconductor. For example, there may be a radioactively doped zone at the centre of high band-gap semiconductor particles, with the outer rim having no radioisotope content.

[0071] In certain embodiments, the radioactive catalyst comprises the radionuclide coating all or part of the high band-gap semiconductor. In certain embodiments, the radioactive catalyst comprises the radionuclide encapsulated by the high band-gap semiconductor. In certain embodiments, the radioactive catalyst comprises the radionuclide physically admixed with the high-band gap semiconductor. In certain embodiments, the radioactive catalyst has a graded distribution of radionuclide within the high band gap semiconductor. In certain embodiments, the radioactive catalyst comprises the radionuclide loaded into the high band-gap semiconductor. In certain embodiments, the radioactive catalyst comprises the radionuclide chemically incorporated into the high band-gap semiconductor. In certain embodiments, the radioactive catalyst comprises a matrix comprising the radionuclide and the high band-gap semiconductor. Other arrangements are contemplated.

[0072] In certain embodiments, the radioactive catalyst comprises a radioactive content of 0.1 GBq/mm ³ or greater. In certain embodiments, the radioactive catalyst comprises a radioactive content of 1 GBq/mm ³ or greater. In certain embodiments, the radioactive catalyst comprises a radioactive content of 10 GBq/mm ³ or greater. In certain embodiments, the radioactive catalyst comprises a radioactive content of 100 GBq/mm ³ or greater.

[0073] In certain embodiments, the radioactive catalyst comprises a radioactivity content in the range from 0.1 - 100 GBq/mm ³ range, 1.0 - 100 GBq/mm ³ , or 10 - 100 GBq/mm ³ . Other ranges are contemplated.

[0074] In certain embodiments, the radioactive catalyst has a high surface area. In certain embodiments, the radioactive catalyst has a surface area of 1 rrrg ¹ or greater, 10 rrrg ¹ or greater, or 100 rrrg ¹ or greater. Methods for assessing surface area are known in the art. [0075] In certain embodiments, the radioactive catalyst is in a macroscopic form. In certain embodiments, the radioactive catalyst is in a porous macroscopic form.

[0076] In certain embodiments, the radioactive catalyst is porous, having sufficient open porosity to permit a reactant fluid (liquid or gas) to enter pores and/or flow through the bulk catalyst without high applied pressure.

[0077] In certain embodiments, the radioactive catalyst is a composite material. For example, a dispersion of ¹⁴ C particles (eg graphene, amorphous carbon, or diamond) in a semiconductor matrix.

[0078] In certain embodiments, the radioactive catalyst is a ceramic material. Methods for producing ceramics are known in the art.

[0079] In certain embodiments, the radioactive catalyst is a cermet material (“ceramic metal composite material”). Methods for producing such materials are known in the art.

[0080] In certain embodiments, the present disclosure provides a method of converting CO2 and/or a related form thereof to one or more small organic compounds, the method comprising exposing a high band-gap semiconductor undergoing electronic excitation by energetic beta-particles to the CO2 or the related form thereof and thereby converting the CO2 and/or the related form thereof to the one or more small organic compounds.

[0081] In certain embodiments, the present disclosure provides a method of converting CO2 and/or a related form thereof to one or more small organic compounds, the method comprising activating a high band-gap semiconductor by energetic b-particles emitted from a radionuclide and exposing the high band-gap semiconductor to the CO2 and the related form thereof, and thereby converting the CO2 and/or the related form thereof to the one or more small organic compounds.

[0082] In certain embodiments, the present disclosure provides a method of converting CO2 and/or a related form thereof to one or more small organic compounds, the method comprising exposing the CO2 and/or the related form thereof to a beta particle emitting radionuclide coupled to a high band-gap semiconductor and thereby converting the CO2 and/or the related form thereof to the one or more small organic compounds.

[0083] In certain embodiments, the present disclosure provides a method of converting CO2 and/or a related form thereof to one or more small organic compounds, the method comprising exposing the CO2 and/or the related form thereof to a beta particle emitting radionuclide in the presence of a high band-gap semiconductor and thereby converting the CO2 and/or the related form thereof to the one or more small organic compounds.

[0084] In certain embodiments, the present disclosure provides a method of converting CO2 and/or a related form thereof to one or more small organic compounds, the method comprising exposing the CO2 and/or the related form thereof to a high band-gap semiconductor activated by beta particles from a radionuclide and thereby converting the CO2 and/or the related form thereof to the one or more small organic compounds.

[0085] Certain embodiments of the present disclosure provide a method of producing one or more small organic compounds using a method as described herein to convert CO2 and/or a related form thereof to the one or more small organic compounds.

[0086] Small organic compounds are as described herein.

[0087] In certain embodiments, the present disclosure provides a method of producing one or more small organic compounds, the method comprising exposing CO2 and/or a related form thereof to a beta particle activated high band-gap semiconductor and thereby producing the one or more small organic compounds from the CO2 and/or the related form thereof.

[0088] In certain embodiments, the present disclosure provides a method of producing one or more small organic compounds, the method comprising exposing a high band-gap semiconductor undergoing electronic excitation by energetic beta particles to CO2 and/or a related form thereof and thereby producing the one or more small organic compounds from the CO2 and/or the related form thereof.

[0089] In certain embodiments, the present disclosure provides a method of producing one or more small organic compounds, the method comprising exposing CO2 and/or a related form thereof to a beta particle emitting radionuclide coupled to a high band-gap semiconductor and thereby producing the one or more small organic compounds from the CO2 and/or the related form thereof.

[0090] In certain embodiments, the present disclosure provides a method of producing one or more small organic compounds, the method comprising exposing CO2 and/or a related form thereof to a beta particle emitting radionuclide in the presence of a high band- gap semiconductor and thereby producing the one or more small organic compounds from the CO2 and/or the related form thereof.

[0091] In certain embodiments, the present disclosure provides a method of producing one or more small organic compounds, the method comprising exposing CO2 and/or a related form thereof to a high band-gap semiconductor activated by beta particles from a radionuclide and thereby producing the one or more small organic compounds from the CO2 and/or the related form thereof.

[0092] In certain embodiments, the methods further comprise purifying or extracting the one or more small organic compounds. Methods for purifying or extracting small organic compounds are as described herein. Methods for determining the extent of purification/extraction are known in the art.

[0093] Certain embodiments of the present disclosure provide one or more small organic compounds produced by a method as described herein.

[0094] Examples of small organic compounds are as described herein. In certain embodiments, the small organic compound comprises one or more of carbon monoxide, formaldehyde, methane, methanol, formic acid, acetaldehyde, ethanol, acetic acid, propanol, and isopropanol.

[0095] Methods for purifying or extracting small organic compounds are known in the art. For example, the small organic compounds may be separated and purified using processes such as distillation or differential adsorption. Other methods are contemplated.

[0096] Certain embodiments of the present disclosure provide a system for converting CO2 and/or a related form thereof to one or more small organic compounds.

[0097] In certain embodiments, the present disclosure provides a system for converting CO2 and/or a related form thereof to one or more small organic compounds, the system comprising:

a source of CO2 and/or a related form thereof; and

a reaction container comprising a high band-gap semiconductor coupled closely with a beta particle emitting radionuclide for exposure to the CO2 and/or the related form thereof.

[0098] In certain embodiments, the system further comprises a means for extracting one or more small organic compounds.

[0099] In certain embodiments, the present disclosure provides a system for converting CO2 and/or a related form thereof to one or more small organic compounds, the system comprising:

a source of CO2 and/or a related form thereof;

a reaction container comprising a high band-gap semiconductor coupled closely with a beta particle emitting radionuclide for exposure to the CO2 and/or the related form thereof; and

means for extracting one or more small organic compounds produced by exposure of the CO2 and/or the related form thereof to the high band-gap semiconductor and the radionuclide.

[00100] In certain embodiments, the present disclosure provides a system for converting CO2 and/or a related form thereof to one or more small organic compounds, the system comprising:

a source of CO2 and/or a related form thereof;

a reaction container comprising a high band-gap semiconductor and a beta particle emitting radionuclide for exposure to the CO2 and/or the related form thereof; and

means for extracting one or more small organic compounds produced by exposure of the CO2 and/or the related form thereof to the high band-gap semiconductor and the radionuclide.

[00101] In certain embodiments, the present disclosure provides a system for converting CO2 and/or a related form thereof to one or more small organic compounds, the system comprising:

a source of CO2 and/or a related form thereof;

a reaction container comprising a radioactive catalyst comprising a high band- gap semiconductor and a beta particle emitting radionuclide for exposure to the CO2 and/or the related form thereof; and

means for extracting one or more small organic compounds produced by exposure of the CO2 and/or the related form thereof to the radioactive catalyst.

[00102] In certain embodiments, the source of CO2 comprises one or more of waste CO2, atmospheric CO2, liquid CO2, sequestered CO2, CO2 complexed with another agent, a bicarbonate, a carbonate, or a carbonate ore, or a chemical compound that provides CO2. Other sources of CO2 are contemplated.

[00103] In certain embodiments, the radioactive catalyst comprises a porous solid form through which reactant fluids can pass.

[00104] In certain embodiments, the reaction container comprises the radionuclide and the high band-gap semiconductor in a granular form in a fluidised bed in which the desired chemical reactions take place. In certain embodiments, the reaction container comprises the radioactive catalyst in a granular form in a fluidised bed in which the desired chemical reactions take place.

[00105] In certain embodiments, the means for extracting small organic molecules comprises a distillation means and/or a condensing means, or differential adsorption means. Other means for extracting small organic compounds are contemplated.

[00106] In certain embodiments, the system comprises a production plant for the production of one or more small organic compounds, for example methanol.

[00107] Certain embodiments of the present disclosure provide a system for producing one or more small organic compounds from CO2 and/or a related form thereof, as described herein.

[00108] Certain embodiments of the present disclosure provide a method of producing one or more small organic compounds using a system as described herein,

[00109] Certain embodiments of the present disclosure provide one or more small organic compounds produced by a system as described herein.

[00110] Examples of small organic compounds are as described herein. In certain embodiments, the small organic compound comprises one or more of carbon monoxide, formaldehyde, methane, methanol, formic acid, acetaldehyde, ethanol, acetic acid, propanol, and isopropanol.

[00111] Certain embodiments of the present disclosure provide a method of activating a high band-gap semiconductor.

[00112] In certain embodiments, the high-band gap semiconductors are suitable for conversion of CO2 (and/or a related form thereof) to one or more small organic compounds. Other uses are contemplated.

[00113] In certain embodiments, the present disclosure provides a method of activating a high band-gap semiconductor for the conversion of CO2 and/or a related form thereof to one or more small organic compounds, the semiconductor having a conduction band edge energy sufficient to enable the reduction of CO2, the method comprising exposing the high band-gap semiconductor to a beta particle emitting radionuclide and thereby activating the high band-gap semiconductor.

[00114] In certain embodiments, the present disclosure provides a method of activating a high band-gap semiconductor for the conversion of CO2 and/or a related form thereof to one or more small organic compounds, the semiconductor having a conduction band edge energy sufficient to enable the reduction of CO2, the method comprising exposing the high band-gap semiconductor to a beta particle emitting radionuclide and thereby electronically exciting the high band-gap semiconductor to an activated state capable of driving the chemical reduction of CO2 molecules, or a related form thereof.

[00115] Certain embodiments of the present disclosure provide a high band-gap semiconductor activated by a method as described herein.

[00116] In certain embodiments, the high band-gap semiconductor has both the properties of a band-gap of at least 2.0 eV and a conduction band edge energy of -0.15 V or less (more negative than) relative to the standard hydrogen electrode.

[00117] In certain embodiments, the high band-gap semiconductor has a band-gap of at least 2.6 eV. In certain embodiments, the high band-gap semiconductor has a band-gap of at least 3.1 eV. In certain embodiments, the high band-gap semiconductor has a band- gap of at least 3.2 eV. In certain embodiments, the high band-gap semiconductor has band gap of at least 3.4 eV. In certain embodiments, the high band-gap semiconductor has a band-gap in the range from 2.6 to 5.4 eV, 3.1 to 5.4 eV, 3.2 to 5.4 eV, or 3.4 to 5.4 eV.

[00118] In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -0.15 volts, with respect to the standard hydrogen electrode.

[00119] In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -0.4 volts with respect to the standard hydrogen electrode. In certain embodiments, the high band-gap semiconductor having a conduction band edge energy of less than (more negative than) -0.8 volts with respect to the standard hydrogen electrode. In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -2.0 volts with respect to the standard hydrogen electrode.

[00120] Certain embodiments of the present disclosure provide a method of producing an activated high band-gap semiconductor. [00121] In certain embodiments, the activated high band-gap semiconductor is suitable for the conversion of CO2 and/or a related form thereof to one or more small organic compounds. Other uses are contemplated.

[00122] In certain embodiments, the present disclosure provides a method of producing an activated high band-gap semiconductor, the semiconductor having a conduction band edge energy sufficient to enable the reduction of CO2, the method comprising exposing the semiconductor to a beta particle emitting radionuclide and thereby producing the activated high band-gap semiconductor.

[00123] Certain embodiments of the present disclosure provide an activated high band- gap semiconductor produced by a method as described herein.

[00124] Certain embodiments of the present disclosure provide a radiocatalytic material comprising a high band-gap semiconductor coupled with a beta particle emitting radionuclide.

[00125] Certain embodiments of the present disclosure provide a radiocatalytic material comprising a high band-gap semiconductor loaded with a beta particle emitting radionuclide.

[00126] Radiocatalytic materials comprising a high band-gap semiconductor coupled to a beta particle emitting radionuclide are as described herein.

[00127] In certain embodiments, the radioactive catalyst material comprises a radioactive content of 0.1 GBq/mm ³ or greater. In certain embodiments, the radioactive catalyst material comprises a radioactive content of 1.0 GBq/mm ³ or greater. In certain embodiments, the radioactive catalyst material comprises a radioactive content of 10 GBq/mm ³ or greater. In certain embodiments, the radioactive catalyst comprises a radioactive content of 100 GBq/mm ³ or greater. In certain embodiments, the radioactive catalyst material comprises a radioactivity content in the range from 0.1-100 GBq/mm ³ 1.0- 100 GBq/mm ³ , or 10-100 GBq/mm ³ . Other ranges are contemplated.

[00128] Certain embodiments of the present disclosure provide a radiocatalytic material comprising a beta particle emitting radionuclide encapsulated by a high band-gap semiconductor.

[00129] Radiocatalytic materials comprising a beta particle emitting radionuclide encapsulated by a high band-gap semiconductor are as described herein.

[00130] High band-gap semiconductors and beta particle emitting radionuclides are as described herein.

[00131] In certain embodiments, the high band-gap semiconductor has both the properties of a band-gap of at least 2.0 eV and a conduction band edge energy of -0.15 V or less (more negative than) relative to the standard hydrogen electrode.

[00132] In certain embodiments, the high band-gap semiconductor has a band-gap of at least 2.6 eV. In certain embodiments, the high band-gap semiconductor has a band-gap of at least 3.1 eV. In certain embodiments, the high band-gap semiconductor has a band- gap of at least 3.2 eV. In certain embodiments, the high band-gap semiconductor has band gap of at least 3.4 eV. In certain embodiments, the high band-gap semiconductor has a band-gap in the range from 2.6 to 5.4 eV, 3.1 to 5.4 eV, 3.2 to 5.4 eV, or 3.4 to 5.4 eV.

[00133] In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -0.15 volts, with respect to the standard hydrogen electrode.

[00134] In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -0.4 volts with respect to the standard hydrogen electrode. In certain embodiments, the high band-gap semiconductor having a conduction band edge energy of less than (more negative than) -0.8 volts with respect to the standard hydrogen electrode. In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -2.0 volts with respect to the standard hydrogen electrode.

[00135] Certain embodiments of the present disclosure provide use of a radiocatalytic material as described herein for producing one or more small organic compounds from CO2 and/or a related form thereof.

[00136] In certain embodiments, the radiocatalytic material is porous in form. In certain embodiments, the radiocatalytic material is in a form comprising a particle, a granule, a bead, a powder, or a pellet.

[00137] In certain embodiments, the radionuclide is distributed substantially homogeneously within the high band-gap semiconductor.

[00138] In certain embodiments, the radionuclide is distributed substantially heterogeneously within the high band-gap semiconductor. For example, a radioactively doped zone at the centre of a radiocatalyst particle and the outer rim has no radioisotope loading.

[00139] Certain embodiments of the present disclosure provide use of a radiocatalytic material for stimulating the production of one or more small organic compounds from CO2 and/or a related form thereof.

[00140] Certain embodiments of the present disclosure provide a composition comprising a solution of dissolved CO2 and/or a related form thereof, a beta particle emitting radionuclide and a high band-gap semiconductor.

[00141] In certain embodiments, the composition is an aqueous composition, a gaseous composition or a liquid composition, including a liquid solvent or liquid gas.

[00142] Certain embodiments of the present disclosure provide a composition comprising a solution of dissolved CO2 and/or a related form thereof and a radiocatalytic material comprising a beta particle emitting radionuclide and a high band-gap semiconductor.

[00143] Certain embodiments of the present disclosure provide a method of identifying a high band-gap semiconductor for converting CO2 and/or a related form thereof to one or more small organic compounds by beta particle activation of the semiconductor. [00144] In certain embodiments, the present disclosure provides a method of identifying a high band-gap semiconductor for converting CO2 and/or a related form thereof to one or more small organic compounds by beta particle activation of the semiconductor, the method comprising:

exposing CO2 and/or a related form thereof to a beta particle emitting radionuclide coupled closely with a candidate high band-gap semiconductor; and determining the ability of the candidate high band-gap semiconductor to convert the CO2 and/or the related form thereof to one or more small organic compounds, thereby identifying the candidate high band-gap semiconductor as a high band- gap semiconductor for converting CO2 and/or a related form thereof to one or more small organic compound by beta particle activation of the semiconductor.

[00145] In certain embodiments, the high band-gap semiconductor has both the properties of a band-gap of at least 2.0 eV and a conduction band edge energy of -0.15 V or less (more negative than) relative to the standard hydrogen electrode.

[00146] In certain embodiments, the high band-gap semiconductor has a band-gap of at least 2.6 eV. In certain embodiments, the high band-gap semiconductor has a band-gap of at least 3.1 eV. In certain embodiments, the high band-gap semiconductor has a band- gap of at least 3.2 eV. In certain embodiments, the high band-gap semiconductor has band gap of at least 3.4 eV. In certain embodiments, the high band-gap semiconductor has a band-gap in the range from 2.6 to 5.4 eV, 3.1 to 5.4 eV, 3.2 to 5.4 eV, or 3.4 to 5.4 eV.

[00147] In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -0.15 volts, with respect to the standard hydrogen electrode.

[00148] In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -0.4 volts with respect to the standard hydrogen electrode. In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less (more negative than) than -0.8 volts with respect to the standard hydrogen electrode. In certain embodiments, the high band-gap semiconductor has a conduction band edge energy of less than (more negative than) -2.0 volts with respect to the standard hydrogen electrode.

[00149] Examples of candidate semiconductors include a titanate, zirconate, molybdate, vanadate, technetate, pertechnetate, tungstate, niobate, tantalate, doped tin oxides, doped zinc oxide, a hafnate, an oxide of manganese, cobalt and iron (eg a ferrate, a manganate, a cobaltate), a chromate, a germanium oxide, a simple oxide, a sulphide, a chalcogenide and a carbon allotrope. In certain embodiments, the high band-gap semiconductor comprises a titanate and/or a zirconate.

[00150] Certain embodiments of the present disclosure provide a high band-gap semiconductor for converting CO2 and/or a related form thereof to a small organic compound by beta particle activation identified by a method as described herein.

[00151] The present disclosure is further described by the following examples. It is to be understood that the following description is for the purpose of describing particular embodiments only and is not intended to be limiting with respect to the above description.

EXAMPLE 1 - Transformation of carbon dioxide to carbon products using radioactive Yttrium-90 (a b-Particle Emitter)

[00152] 1. Introduction

[00153] A proof-of-concept study was undertaken to demonstrate the conversion of carbon dioxide (CO2) to one or more small organic compounds, such as methanol, ethanol, propanol or formic acid.

[00154] Photocatalysis may be used to convert CO2 to other compounds. These type of techniques rely on light energy sources to reduce CO2 to other compounds by pairing the light energy (usually UV light) with a catalytic material to break the C=0 bond in CO2 in a H2O environment. There are a number of reaction conditions which may influence the products formed including, catalyst type, light source and pH. However, one of the key limitations of the process is the need to use a light source providing a reasonable flux of photons having an energy greater than the photocatalytic semiconductor band-gap. [00155] It was recognised that an alternative to a light source would be to utilise the energy of particles released during radioactive decay to energise the catalyst. In a proof- of-concept study, yttrium-90 ( ⁹⁰ Y) was selected as a source of beta particles, in conjunction with a strontium titanate (SrTiO,) catalyst, to investigate the transformation of CO2 to organic compounds over a 6 week period. At the end of the study, the liquid samples were analysed for the presence of various small organic compounds.

[00156] 2. Materials and Methods

[00157] (i) Reaction in Presence of b-Emitter

[00158] The proof-of-concept studies were designed around the availability and form of a special beta radiation source - a multitude of functionalised polystyrene resin microbeads (18 - 30 pm diameter) loaded with the yttrium-90 ( ⁹⁰ Y) isotope, referred to as“ ⁹⁰ Y-loaded polymer microspheres”. Such beads are available and used as a radio embolization therapy for controlling metastatic liver tumours.

[00159] The experimental arrangement involved agitating the beta-emitting resin beads together with SrTiCh semiconductor particles in a related HCO3 (bicarbonate) solution as a source of soluble carbon dioxide. Such solutions‘self buffer’ to a pH of around 8.15.

[00160] The activity of the ⁹⁰ Y used was between 1.1 and 2.2 GBq. Upon receipt of the material, the ⁹⁰ Y-loaded polymer microspheres were removed from the container and added to an Erlenmeyer flask containing a 100 mL solution of NaHCCh (40 g L ¹ ) and suspended SrTiCE powder (5 g L ¹ ). The solution was stirred at a constant speed to maintain a small vortex in the solution surface. The experimental setup is shown in Figure 1. The experiment was conducted behind a 10-mm perspex shield and the exposure dose monitored and recorded throughout the experimental period. The experiment was conducted in a radiation approved facility over a 6 week period and at the end of this period, samples were collected and filtered through 0.22 pm cellulose filters to remove the suspended materials. The gamma dose rate was monitored and recorded periodically throughout the experiment. Aqueous samples were analysed by an accredited external laboratory. [00161] (ii) Reaction in Absence of b-Emitter

[00162] Non-radioactive“blank” reaction vessels (NaHCCb only and NaHCCb plus SrTiCb) were set up as controls and used identical conditions as outlined for the ⁹⁰ Y study (Figure 2). The experiment was run in parallel with the ⁹⁰ Y experiment and samples were collected at the same time and filtered through 0.22 pm cellulose filters to remove the suspended materials. The samples were analysed by the accredited external laboratory.

[00163] 3. Results

[00164] Analyses were made for the presence of methanol (CH ₃ OH), ethanol (CH ₃ CH ₂ OH), propanol, (CH ₃ CH ₂ CH ₂ OH) and formic acid (HCOOH) in each of the three reaction environments, ie, the vessels with the beta-emitter present, and the blanks. The levels of other organic compounds - notably; methane (CH ₄ ), carbon monoxide (CO) and formaldehyde (HCHO) were not measured in this experiment, as they would have been difficult to capture in the experimental arrangement.

Table 1. Organic products identified

[00165] The assays showed that formic acid was present in all samples irrespective of the treatment (Table 1). However, treatments that did not include ⁹⁰ Y contained approximately half the formic acid concentration compared to the treatment where ⁹⁰ Y was added (Table 1). The formic acid concentration in the two treatments that did not include ⁹⁰ Y were 418 and 487 mg L ¹ , compared to a formic acid concentration of 785 mg L ¹ in the ⁹⁰ Y treatment.

[00166] The presence of ethanol and propanol was not identified in any of the treatments (Table 1), but methanol was identified in the treatment which included ⁹⁰ Y. Methanol was not identified in the other two non-radioactive beta radiation driven treatments (Table 1).

[00167] These studies demonstrate the conversion of CO2 to small organic compounds such as methanol and formate by exposing a related form of CO2 to a high band-gap semiconductor activated by a beta particle emitting radionuclide, such as ¹⁴ C, ⁹⁰ Sr, "Tc, ¾, ⁶³ Ni, ¹³⁷ Cs, ¹⁴⁷ Pm, ¹⁵¹ Sm, ^121m Sn, ¹⁵ ¾u, ⁹³ Zr, ²¹⁰ Pb and ¹²⁶ Sn.

EXAMPLE 2 - Compositions for catalytic conversion of CO2. to small organic compounds

[00168] A beta particle emitting radionuclide may be obtained from sources such as those where the radionuclide is regarded as waste or a liability, an example being nuclear industry processing facilities, where notable radionuclides are ¹⁴ C, ⁹⁰ Sr, "Tc, ¾, and ¹³⁷ Cs. These nuclides are typically isolated from aqueous process streams such as adsorbed salt species.

[00169] In one embodiment, the beta-emitting radionuclide may be exchanged for a similar cation in a high band-gap semiconductor such as strontium titanate (commercially available from chemical suppliers), using for example, an established hydrothermal process in a suitable autoclave which are known in the art. The resulting radioactive solid will be processed into a high surface area form (eg, a powder, granules, frit) such that it may be easily contacted with a solution containing dissolved CO2 to produce small organic compounds such as carbon monoxide, methane or methanol.

[00170] In another embodiment, solid titanate/zirconate semiconductors may be loaded with a beta-emitting isotope using methods such as (i) 'solvothermal' approaches in which precursor oxides are reacted together in a high temperature aqueous fluid (up to ~240°C), typically with high pH, for example using a modification of the method as described in Modeshia and Walton (2010) Chemical Society Reviews 39:4303-4325; (ii) solid state reaction approaches in which powders of precursor phases are blended together and raised to a high temperature at which desired structural transformations and consolidation take place, for example using a modification of the method as described in Fu et al. (2010) Physica Scripta T 139 : 1 -4.

[00171] In a further embodiment, solid titanate/zirconate semiconductors may be loaded with a beta-emitting isotope using high energy physical mixing approaches to transform constituent oxides into desired titanates or zirconates, which are known in the art.

[00172] In another embodiment, hollow porous strontium titanate particles containing the beta particle emitting radionuclide may be produced by adapting the method as described in Tzeng and Shih (2015) Journal of the American Ceramic Society 98(2): 386- 391. This method permits the production of porous powders with a high surface area, which may be contacted with a solution such as one containing dissolved CO2, serving as a parent fluid for the radiocatalytic production of small organic compounds such as methanol.

EXAMPLE 3- Production of small organic compounds such as methanol

[00173] The present disclosure relates to technology in which the energy of certain radioactive particles is harnessed to achieve a number of useful industrial endpoints. The study in Example 1 has demonstrated the feasibility of a radiocatalysis system for converting waste carbon dioxide to valuable organic compounds. The carbon dioxide may be, for example, waste carbon dioxide and/or a bicarbonate feedstock.

[00174] In some embodiments, the present disclosure utilises a high band-gap semiconductor into which a suitable radioactive isotope with suitable particle-emitting characteristics can be intrinsically incorporated (eg doped), such that the radioactivity content of the semiconductor is in a range, for example, in the range from 1.0 - 100 GBq /mm ³ range.

[00175] In some embodiments, the radioisotope may be distributed heterogeneously within the solid semiconductor particle, for example where the radioactively doped zone is at the centre of a particle and the outer rim has no radioisotope loading. [00176] It is envisaged that the material may be used in various physical forms, including powder, granules, or as a porous 'frit'.

[00177] The system may use a chemical reaction vessel which (i) contains physical radioactive catalyst arranged in a manner that leads to a high degree of contact between the catalyst surface and a related solution containing dissolved carbon dioxide, (ii) possesses radiation shielding measures to prevent occupational radiation doses from the static physical catalyst residing within the vessel; and (iii) delivers its outflow fluids to a supplementary organic compound separation system.

[00178] It is envisaged that the physical catalyst may be in a porous solid form through which reactant fluids can pass, or a granular form and which can be used to create a fluidised bed in which the desired chemical reactions may take place.

[00179] In some embodiments, the catalyst is selected from either or both strontium zirconate (SrZrO,) and strontium titanate (SrTiO,). These compounds are significant because they have a high band-gap (>2.0 eV), a conduction band edge energy that leads to a strong electrochemical reduction potential for excited electron hole pairs, and there is a strontium isotope ( ⁹⁰ Sr) which is has excellent beta-particle emitting properties in terms of its half-life and energy.

[00180] A proposed system for the large scale conversion of CO2 using the catalytic activity of a beta particle activated semiconductor is described below.

[00181] A solution of concentrated CO2, CO3 ² or HCO3 may be fed continuously into a reaction chamber comprising a slurry with a composition as described in Example 2, and which is mixed by constant agitation with a residence time in the order of hours, which catalytically converts the CO2 into a number of small organic compounds, including methanol.

[00182] A portion of the aqueous solution is drawn off periodically and subject to mild centrifugation and/or filtration to separate suspended solids from the solution, and the remaining aqueous solution fed into a series of distillation chambers and condensing chambers, which allows production of high grade methanol. Methods for producing methanol by distillation are known in the art, for example as described in WO 2013/110368.

EXAMPLE 4 - Use of ⁸⁹ Sr in conjunction with strontium titanate

[00183] 1. Methodology

[00184] For the non-radioactive“blank” reaction, strontium titanate (SrTiCb, 1.99 g) was added to a 250 mL PTFE vessel followed by addition of 1,4-dioxane (97 mL), MilliQ water (3 mL) and a stirrer bar. The PTFE vessel lid, modified with Swagelok fittings including a pressure relief valve and manual open/close valve, was attached to a gas manifold with a pressure gauge and connected to a CO2 gas bottle via a two way valve, as shown in Figure 3. A flow of CO2 gas was passed through the manifold and through the PTFE lid to purge the air from the PTFE vessel as it was screwed onto the lid.

[00185] Once attached to the gas manifold, the PTFE vessel was loaded with CO2 via the following method:

• CO2 added to the reaction vessel until the pressure gauge indicated 3 atm.

• CO2 inlet valve then closed.

• With stirring, CO2 dissolved in the solvent and pressure decreased, as monitored by the pressure gauge.

• When the rate of pressure decrease slowed, pressure value was recorded and CO2 valve opened to repeat the process.

[00186] In this way approximately 11 atm CO2 was added to the reaction vessel over 10 minutes, at which point the rate of pressure decrease was very slow and the system was assumed to be close to equilibrium. The valve to the vessel was then closed, CO2 in the manifold vented and the vessel disconnected from the manifold. [00187] Once loaded with CO2, the reaction vessel was placed on a stirrer plate and continued stirring (at approximately 600 rpm) for 17 days.

[00188] For the active reaction, identical reaction conditions were used, but the SrTi0 ₃ (2.1 g) was irradiated in the OPAL reactor for 9 days followed by 16 days decay. Gamma spectroscopy of the irradiated SrTi0 ₃ indicated a Sr-85 activity of 48.8 ± 4.4 MBq and hence a Sr-89 activity of 88 ± 21 MBq. The amount of CO2 gas loaded into this reaction vessel was not explicitly measured but assumed to be similar to the inactive experiment (11 atm), as the reaction vessel was equilibrated via stirring under CO2 at 3 atm for 15 min. CO2 loading was performed behind lead shielding as shown in Figure 4, and the exposure dose was monitored and recorded throughout the experimental period.

[00189] Every 3-4 days the reaction vessels were re-attached to the gas manifold and re loaded with CO2, as the pressure was observed to be dropping over time. The manifold was purged with CO2 before being opened to the reaction vessels, to prevent contamination of the headspace gas with air. The measured pressures and volumes of CO2 added at each time interval are given in Table 2.

Table 2: Measured pressure (P, atm) and amount of CO2 added (atm) over time for active and inactive experiments.

[00190] At the end of the 17 day experimental period, the headspace gas of each experiment (active and inactive) was sampled via the following method: • Reaction vessel attached to the gas manifold.

• Tedlar bag (for gas sampling) attached to right hand side of manifold (see Figure

3)·

• Manifold evacuated via vacuum pump attached to two way valve (see Figure 5).

• Reaction vessel opened to evacuated manifold, to record pressure.

• Valve to Tedlar bag opened until bag full.

• Sealed Tedlar bag removed from manifold and remaining CO ₂ overpressure vented into fumehood.

[00191] The reaction vessel lid was then opened and the slurry within allowed to settle for 1.5 h. The supernatant liquid was sampled via pipette (2 mL) and centrifuged (5000 rpm, 5 min) to remove fines.

[00192] 2. Results

[00193] Gas samples (active and inactive) were analysed for CO and CH4 by an accredited external laboratory. Liquid samples (active and inactive) were analysed for methanol, ethanol, formaldehyde and formic acid via GC-MS. GC-MS was undertaken using an Agilent GC3800 with split injection mode (10: 1), AT -WAX column with length 30 m, 0.32 mm I.D., df=0.5 pm, injection volume of 1 pL and MS1200 with electron ionisation, ionisation voltage 70 V and emission current 150 pA.

[00194] Levels of the following molecules will be determined: carbon monoxide, methane, methanol, ethanol, formaldeyde, and formic acid.

[00195] It is anticipated that the above reaction methodology will result in the production of a variety of small organic molecules.

[00196] Although the present disclosure has been described with reference to particular examples, it will be appreciated by those skilled in the art that the disclosure may be embodied in many other forms.

[00197] It is to be understood that various alterations, additions and/or modifications may be made to the parts previously described without departing from the ambit of the present disclosure, and that, in the light of the above teachings, the present disclosure may be implemented in software, firmware and/or hardware in a variety of manners as would be understood by the skilled person.

[00198] As used herein, the singular forms“a,”“an,” and“the” may refer to plural articles unless specifically stated otherwise.

[00199] Throughout this specification, unless the context requires otherwise, the word “comprise”, or variations such as“comprises” or“comprising”, will be understood to imply the inclusion of a stated element or integer or group of elements or integers but not the exclusion of any other element or integer or group of elements or integers.

[00200] All methods described herein can be performed in any suitable order unless indicated otherwise herein or clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., "such as") provided herein, is intended merely to better illuminate the example embodiments and does not pose a limitation on the scope of the claimed invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential.

[00201] The description provided herein is in relation to several embodiments which may share common characteristics and features. It is to be understood that one or more features of one embodiment may be combinable with one or more features of the other embodiments. In addition, a single feature or combination of features of the embodiments may constitute additional embodiments.

[00202] The subject headings used herein are included only for the ease of reference of the reader and should not be used to limit the subject matter found throughout the disclosure or the claims. The subject headings should not be used in construing the scope of the claims or the claim limitations.

[00203] Reference to any prior art in this specification is not, and should not be taken as, an acknowledgment or any form of suggestion that this prior art forms part of the common general knowledge in any country.

[00204] Future patent applications may be filed on the basis of the present application, for example by claiming priority from the present application, by claiming a divisional status and/or by claiming a continuation status. It is to be understood that the following claims are provided by way of example only, and are not intended to limit the scope of what may be claimed in any such future application. Nor should the claims be considered to limit the understanding of (or exclude other understandings of) the present disclosure. Features may be added to or omitted from the example claims at a later date.