Patent classifications
C07C45/83
Method for separating materials by means of an extractive distillation process
A method for separating a mixture of materials A and B by extractive distillation, using an extraction medium having a higher affinity to B than to A, collecting a liquid fraction on a collecting tray and heated and partially evaporated in a first indirect heat exchanger, collecting the resultant vapor is released into the column and a non-evaporated proportion of the liquid fraction in the sump of the column, and a series of heating, separation and cooling where partially cooled extraction medium fraction is used as heating medium for a heat exchanger.
Acoustic string instrument, and methods for manufacturing and repairing same
An acoustic string instrument includes a top plate, a back plate, and a body disposed between the top plate and the back plate. The body has a plurality of first positioning portions. At least one of the top plate or the back plate, or both has a plurality of second positioning portions. The first positioning portions are fixed to the second positioning portions corresponding to the first positioning portions.
Acoustic string instrument, and methods for manufacturing and repairing same
An acoustic string instrument includes a top plate, a back plate, and a body disposed between the top plate and the back plate. The body has a plurality of first positioning portions. At least one of the top plate or the back plate, or both has a plurality of second positioning portions. The first positioning portions are fixed to the second positioning portions corresponding to the first positioning portions.
PROCESS FOR THE SEPARATION OF FORMALDEHYDE FROM CRUDE ACRYLIC ACID
A process for purification of a crude product stream recovered from the production of acrylic acid by an aldolisation reaction is disclosed. The product stream comprises acrylic acid, formaldehyde, water, non-condensable vapours and optionally heavy by-products. The process comprises: providing the crude product stream in the vapour phase to a first separation column operated at a temperature and pressure to form an intermediate overhead stream comprising water, formaldehyde and methanol; and passing said intermediate overhead stream to a formaldehyde separation column operated at a temperature and pressure to enable a stream having a higher formaldehyde concentration than the formaldehyde concentration in the intermediate overhead stream to be formed and recovered from at or near the bottom of the formaldehyde separation column as a formaldehyde enriched stream.
PROCESS FOR THE SEPARATION OF FORMALDEHYDE FROM CRUDE ACRYLIC ACID
A process for purification of a crude product stream recovered from the production of acrylic acid by an aldolisation reaction is disclosed. The product stream comprises acrylic acid, formaldehyde, water, non-condensable vapours and optionally heavy by-products. The process comprises: providing the crude product stream in the vapour phase to a first separation column operated at a temperature and pressure to form an intermediate overhead stream comprising water, formaldehyde and methanol; and passing said intermediate overhead stream to a formaldehyde separation column operated at a temperature and pressure to enable a stream having a higher formaldehyde concentration than the formaldehyde concentration in the intermediate overhead stream to be formed and recovered from at or near the bottom of the formaldehyde separation column as a formaldehyde enriched stream.
PROCESS FOR THE RECOVERY OF KETONES AND GLYCOLS FROM FERMENTATION
A method of obtaining ketones from a fermentation process may include collecting an off-gas and a fermented broth from a fermenter, transferring the off-gas from the fermenter to a ketone recuperation module and the fermented broth to a fluid separating module, and isolating the ketones from both the off-gas and the fermented broth. The off-gas and the fermented broth may both comprise a ketone
PROCESS FOR THE RECOVERY OF KETONES AND GLYCOLS FROM FERMENTATION
A method of obtaining ketones from a fermentation process may include collecting an off-gas and a fermented broth from a fermenter, transferring the off-gas from the fermenter to a ketone recuperation module and the fermented broth to a fluid separating module, and isolating the ketones from both the off-gas and the fermented broth. The off-gas and the fermented broth may both comprise a ketone
Process for the recovery of ketones and glycols from fermentation
Methods may include obtaining ketones and glycols from a fermentation process, the method including: collecting an off-gas and/or a fermented broth from the fermenter, wherein the off-gas comprises a ketone, and wherein the fermented broth comprises one or more of glycol or ketone; and performing at least one of: transferring the off-gas from the fermenter to a ketone recuperation module; or transferring the fermented broth to a fluid separating module; and isolating one or more of: the ketone from the off-gas; and the glycol from the fermented broth.
Process for the recovery of ketones and glycols from fermentation
Methods may include obtaining ketones and glycols from a fermentation process, the method including: collecting an off-gas and/or a fermented broth from the fermenter, wherein the off-gas comprises a ketone, and wherein the fermented broth comprises one or more of glycol or ketone; and performing at least one of: transferring the off-gas from the fermenter to a ketone recuperation module; or transferring the fermented broth to a fluid separating module; and isolating one or more of: the ketone from the off-gas; and the glycol from the fermented broth.
METHOD FOR PREPARING A ß-HYDROXYKETONE
Method for preparing a -hydroxyketone having 4 to 8 carbon atoms by reacting formaldehyde with a branched or unbranched dialkyl ketone having 3 to 7 carbon atoms in the liquid phase in a reactor in the presence of a basic component at a temperature of 50 to 150 C. and a pressure of 0.2 to 10 MPa abs, in which (a) a trialkylamine having 1 to 4 carbon atoms per alkyl group is used as basic component and the reaction (b) is carried out in the presence of 1 to 25% by weight water, based on the liquid phase, and (c) at a molar ratio of trialkylamine to formaldehyde in the liquid phase of from 1 to 5.