Patent classifications
C07C41/36
Method for purifying glycol used as a hydrate inhibitor
The invention concerns a purification method comprising: providing a flow comprising a glycol, monovalent ions and multivalent ions; treating this flow with ion exclusion chromatography comprising: injecting the flow into a chromatographic unit comprising an ion exchange stationary phase; injecting an eluent into the chromatographic unit; collecting a fraction at the outlet of the chromatographic unit; the collected fraction being enriched with glycol and depleted of monovalent ions and multivalent ions relative to the flow. The invention also concerns an installation adapted to implement this method, and its application to the regeneration of an anti-hydrate agent.
Method for purifying glycol used as a hydrate inhibitor
The invention concerns a purification method comprising: providing a flow comprising a glycol, monovalent ions and multivalent ions; treating this flow with ion exclusion chromatography comprising: injecting the flow into a chromatographic unit comprising an ion exchange stationary phase; injecting an eluent into the chromatographic unit; collecting a fraction at the outlet of the chromatographic unit; the collected fraction being enriched with glycol and depleted of monovalent ions and multivalent ions relative to the flow. The invention also concerns an installation adapted to implement this method, and its application to the regeneration of an anti-hydrate agent.
Ion exchange resins, purification methods and methods of making ionic resins
An ion exchange resin comprises a crosslinked resin and a salt covalently bonded to a carbon of the resin, wherein the salt comprises a first non-metallic cation and a first counteranion, wherein the first counteranion comprises a second non-metallic cation and a thiosulfate counteranion, and wherein the ion exchange resin is essentially free of metals. The ion exchange resin finds particular use in the removal of impurities from solutions that are useful in the manufacture of semiconductor devices.
Ion exchange resins, purification methods and methods of making ionic resins
An ion exchange resin comprises a crosslinked resin and a salt covalently bonded to a carbon of the resin, wherein the salt comprises a first non-metallic cation and a first counteranion, wherein the first counteranion comprises a second non-metallic cation and a thiosulfate counteranion, and wherein the ion exchange resin is essentially free of metals. The ion exchange resin finds particular use in the removal of impurities from solutions that are useful in the manufacture of semiconductor devices.
Ion exchange resins, purification methods and methods of making ionic resins
An ion exchange resin comprises a crosslinked resin and a salt covalently bonded to a carbon of the resin, wherein the salt comprises a first non-metallic cation and a first counteranion, wherein the first counteranion comprises a second non-metallic cation and a thiosulfate counteranion, and wherein the ion exchange resin is essentially free of metals. The ion exchange resin finds particular use in the removal of impurities from solutions that are useful in the manufacture of semiconductor devices.
Intermolecular reaction of propargyl ethers with dimethylfuran in the presence of gold(I) complexes
The present invention relates to a method of preparing ortho substituted phenols from 2,5-dimethylfuran and propargyl ethers in the presence of a gold(I) complex. It is particularly advantageous to use 2,5-dimethylfuran as this offers an ecological beneficial synthesis of said ortho substituted phenols.
Intermolecular reaction of propargyl ethers with dimethylfuran in the presence of gold(I) complexes
The present invention relates to a method of preparing ortho substituted phenols from 2,5-dimethylfuran and propargyl ethers in the presence of a gold(I) complex. It is particularly advantageous to use 2,5-dimethylfuran as this offers an ecological beneficial synthesis of said ortho substituted phenols.
Intermolecular reaction of propargyl ethers with dimethylfuran in the presence of gold(I) complexes
The present invention relates to a method of preparing ortho substituted phenols from 2,5-dimethylfuran and propargyl ethers in the presence of a gold(I) complex. It is particularly advantageous to use 2,5-dimethylfuran as this offers an ecological beneficial synthesis of said ortho substituted phenols.
METHODS OF PURIFYING INDUSTRIAL GAS STREAMS
Processes for removing a sulfide or a degradation product thereof from in a gas dehydration system are disclosed along with corresponding gas dehydration systems. The processes and systems include contacting a stream comprising the sulfide or a degradation product thereof with an anionic resin to remove at least a portion of the sulfide or a degradation product thereof from the stream. The processes and systems can also be used in the removal of mercury from gas dehydration systems.
METHODS OF PURIFYING INDUSTRIAL GAS STREAMS
Processes for removing a sulfide or a degradation product thereof from in a gas dehydration system are disclosed along with corresponding gas dehydration systems. The processes and systems include contacting a stream comprising the sulfide or a degradation product thereof with an anionic resin to remove at least a portion of the sulfide or a degradation product thereof from the stream. The processes and systems can also be used in the removal of mercury from gas dehydration systems.