Patent classifications
B01D3/38
Method and apparatus for steam separation of pyrolysis oils
Method and apparatus for processing pyrolysis oil from vehicular tires and effecting a steam distillation for separation of the pyrolysis oil to create a lighter fraction which may be subjected to fractional distillation and a heavy fraction which is usable as a fuel oil.
Method and apparatus for steam separation of pyrolysis oils
Method and apparatus for processing pyrolysis oil from vehicular tires and effecting a steam distillation for separation of the pyrolysis oil to create a lighter fraction which may be subjected to fractional distillation and a heavy fraction which is usable as a fuel oil.
METHOD OF IMPROVED PRODUCTION OF RECONSTITUTE ESSENTIAL OILS
The present invention relates to the field of perfumery, that is, the art or process of making a fragrant substance be it natural or synthetic.
The present invention discloses a method of obtaining a better reconstituted essential oil NNO+ comprising the steps of: a) adding the reconstituted essential oil with distilled water; b) refluxing the mixture of step (a); c) resting the mixture of step (b); d) separation of essential oil and water from the mixture of step (c); e) allowing the solution of step (d) to stand for maturation of the reconstituted essential oil NNO+.
PROCESS FOR OBTAINING AROMATICS AND AROMATIC STREAM
The present invention addresses to a process for the production of aromatic compounds from streams containing linear chains with 5 to 18 carbon atoms, of fossil or renewable origin, and application in the field of catalytic cracking aiming at a regenerator operation at much lower temperature, between 480° C. and 620° C., preferably the temperature should be between 500° C. and 600° C. The coked catalyst generated by the cracking of light streams with low potential for delta coke generation can have the combustion effected at a lower temperature. The regeneration temperature must be at least 40° C. and at most 100° C. higher than the reaction temperature, keeping the catalyst circulation high to maintain the energy balance in the reaction section. The minimum regeneration temperature can be ensured by installing an air preheating furnace before entering the regenerator and passing through the air distributor inside the regenerator. The used catalyst must contain zeolite with pores of intermediate size. Such conditions greatly favor the production of aromatics and the octane rating of the produced naphtha.
PROCESS FOR OBTAINING AROMATICS AND AROMATIC STREAM
The present invention addresses to a process for the production of aromatic compounds from streams containing linear chains with 5 to 18 carbon atoms, of fossil or renewable origin, and application in the field of catalytic cracking aiming at a regenerator operation at much lower temperature, between 480° C. and 620° C., preferably the temperature should be between 500° C. and 600° C. The coked catalyst generated by the cracking of light streams with low potential for delta coke generation can have the combustion effected at a lower temperature. The regeneration temperature must be at least 40° C. and at most 100° C. higher than the reaction temperature, keeping the catalyst circulation high to maintain the energy balance in the reaction section. The minimum regeneration temperature can be ensured by installing an air preheating furnace before entering the regenerator and passing through the air distributor inside the regenerator. The used catalyst must contain zeolite with pores of intermediate size. Such conditions greatly favor the production of aromatics and the octane rating of the produced naphtha.
METHODS FOR OBTAINING COMPOUNDS FROM A PLANT OR FUNGUS MATERIAL, RESPECTIVE COMPOSITIONS, AND USES THEREOF
Disclosed herein is a method for obtaining compounds and compositions from plant and fungus materials by thermal treatment, affinity capture, filtration, and release through multi-phasic transitions between gas, solid, and liquid states. The compounds of interest are obtained by manipulating the temperature and pressure of the heating chamber. The compounds in gas phase are passed through an affinity medium which captures the compounds of interest in either solid or liquid phase by exposing the compound of interest to the localized micro-affinity environment of the medium. The compounds are separated from the medium using direct competition with solvent or buffers optimized for the specific chemical properties of compounds.
Edible oil refining
The present invention relates to a process for improving the quality of edible oils or fats and in the process an edible oil is passed through an oil refining equipment consisting of a stripping column with packing and not more than one oil collection tray. It further relates to the use of the refining equipment consisting of a stripping column with packing and not more than one oil collection tray, for degrading, decomposing or breaking down oxidation products of triglycerides, diglycerides, monoglycerides and/or fatty acids.
Edible oil refining
The present invention relates to a process for improving the quality of edible oils or fats and in the process an edible oil is passed through an oil refining equipment consisting of a stripping column with packing and not more than one oil collection tray. It further relates to the use of the refining equipment consisting of a stripping column with packing and not more than one oil collection tray, for degrading, decomposing or breaking down oxidation products of triglycerides, diglycerides, monoglycerides and/or fatty acids.
Plant and process for concentrating tartaric acid
A plant for concentrating a tartaric acid solution includes a first and a second evaporation unit arranged in series, a pump for feeding a diluted tartaric acid solution into the first evaporation unit, a barometric condenser placed downstream of the second evaporation unit, and a system for feeding a first low-temperature vapor into the first evaporation unit. A process for concentrating tartaric acid includes providing a plant according to the above description, performing a first concentration, by evaporation, of the diluted tartaric acid solution, inside the first evaporation unit, and performing a second concentration, by evaporation, of the partially concentrated tartaric acid solution from the first evaporation unit, inside the second evaporation unit. The plant and process for concentrating tartaric acid have the advantages of ensuring low energy consumption, allowing concentration of solutions tending to crystallization, and allowing the continuous measurement of the tartaric acid concentration to be concentrated.
Plant and process for concentrating tartaric acid
A plant for concentrating a tartaric acid solution includes a first and a second evaporation unit arranged in series, a pump for feeding a diluted tartaric acid solution into the first evaporation unit, a barometric condenser placed downstream of the second evaporation unit, and a system for feeding a first low-temperature vapor into the first evaporation unit. A process for concentrating tartaric acid includes providing a plant according to the above description, performing a first concentration, by evaporation, of the diluted tartaric acid solution, inside the first evaporation unit, and performing a second concentration, by evaporation, of the partially concentrated tartaric acid solution from the first evaporation unit, inside the second evaporation unit. The plant and process for concentrating tartaric acid have the advantages of ensuring low energy consumption, allowing concentration of solutions tending to crystallization, and allowing the continuous measurement of the tartaric acid concentration to be concentrated.