Proposed is a high-yield simultaneous conversion method for a hydrogen source and a carbon dioxide source. The method significantly increases a yield of a formate through conversion of carbon dioxide. To this end, a carbon dioxide source and a hydrocarbon containing one or more hydroxy groups undergo a simultaneous conversion reaction in the presence of a solvent containing one or more alcohols and having a pH of 10 to 14.

The present invention discloses a photocatalytic process and methodology for the preparation of acetic acid by a hydrocarboxylation reaction of methanol using carbon dioxide under visible light irradiation. Importantly, the reaction occurred under ambient temperature and pressure condition using a readily available household LED lamp in the presence of a transition metal based molecular photocatalyst, homogeneous as well as supported to semiconductor support and a CO.sub.2-philic solvent without adding any external electron and proton donors.

The present invention discloses a photocatalytic process and methodology for the preparation of acetic acid by a hydrocarboxylation reaction of methanol using carbon dioxide under visible light irradiation. Importantly, the reaction occurred under ambient temperature and pressure condition using a readily available household LED lamp in the presence of a transition metal based molecular photocatalyst, homogeneous as well as supported to semiconductor support and a CO.sub.2-philic solvent without adding any external electron and proton donors.

The present invention discloses a photocatalytic process and methodology for the preparation of acetic acid by a hydrocarboxylation reaction of methanol using carbon dioxide under visible light irradiation. Importantly, the reaction occurred under ambient temperature and pressure condition using a readily available household LED lamp in the presence of a transition metal based molecular photocatalyst, homogeneous as well as supported to semiconductor support and a CO.sub.2-philic solvent without adding any external electron and proton donors.

The present invention generally relates to processes for purification, recovery, and conversion of chlorophenol salts (e.g., 2,5-dichlorophenol and salts thereof). In various aspects, the present invention is related to removing one or more impurities from chlorophenol salt-containing process streams and/or recovering chlorophenol salts from process streams for use of the recovered chlorophenol elsewhere in an integrated process. Process streams that may be treated in accordance with the present invention include those incorporating one or more chlorophenol salts in a feed mixture and also those where one or more chlorophenol salts are present in a product or by-product stream of an integrated process. For example, conversion processes of the present invention are suitable as one piece of an integrated process for producing 3,6-dichloro-2-methoxybenzoic acid (dicamba) or a salt or ester thereof or a process for producing 2,4-dichlorophenoxyacetic acid (2,4-D) or a salt or ester thereof. The present invention further relates to processes for preparation, purification, and recovery of intermediates formed in integrated processes utilizing chlorophenol salts such as 2,5-dichlorophenol as starting material, including the intermediate 3,6-dichlorosalicylic acid (3,6-DCSA) formed during preparation of dicamba from 2,5-dichlorophenol.

The present invention generally relates to processes for purification, recovery, and conversion of chlorophenol salts (e.g., 2,5-dichlorophenol and salts thereof). In various aspects, the present invention is related to removing one or more impurities from chlorophenol salt-containing process streams and/or recovering chlorophenol salts from process streams for use of the recovered chlorophenol elsewhere in an integrated process. Process streams that may be treated in accordance with the present invention include those incorporating one or more chlorophenol salts in a feed mixture and also those where one or more chlorophenol salts are present in a product or by-product stream of an integrated process. For example, conversion processes of the present invention are suitable as one piece of an integrated process for producing 3,6-dichloro-2-methoxybenzoic acid (dicamba) or a salt or ester thereof or a process for producing 2,4-dichlorophenoxyacetic acid (2,4-D) or a salt or ester thereof. The present invention further relates to processes for preparation, purification, and recovery of intermediates formed in integrated processes utilizing chlorophenol salts such as 2,5-dichlorophenol as starting material, including the intermediate 3,6-dichlorosalicylic acid (3,6-DCSA) formed during preparation of dicamba from 2,5-dichlorophenol.

A process for producing functionalized organic molecules having 1 to 3 carbon atoms. The method includes the step of contacting carbon dioxide as the only gas, or a gas mixture that includes carbon dioxide and methane, in the presence of water, with a catalyst that includes permanently polarized hydroxyapatite.

A process for producing functionalized organic molecules having 1 to 3 carbon atoms. The method includes the step of contacting carbon dioxide as the only gas, or a gas mixture that includes carbon dioxide and methane, in the presence of water, with a catalyst that includes permanently polarized hydroxyapatite.

A method including collecting exhaust gas comprising carbon dioxide (CO.sub.2) at a wellsite to provide a collected exhaust gas, separating CO.sub.2 from the collected exhaust gas to provide a separated CO.sub.2, and forming formic acid utilizing at least a portion of the separated CO.sub.2. At least a portion of the formic acid can be utilizing in a wellbore servicing fluid (e.g., a fracturing fluid) introduced downhole via a wellbore. The exhaust gas can be produced during a wellbore servicing operation at the or another wellbore. A system for carrying out the method is also provided.

A method including collecting exhaust gas comprising carbon dioxide (CO.sub.2) at a wellsite to provide a collected exhaust gas, separating CO.sub.2 from the collected exhaust gas to provide a separated CO.sub.2, and forming formic acid utilizing at least a portion of the separated CO.sub.2. At least a portion of the formic acid can be utilizing in a wellbore servicing fluid (e.g., a fracturing fluid) introduced downhole via a wellbore. The exhaust gas can be produced during a wellbore servicing operation at the or another wellbore. A system for carrying out the method is also provided.