The present disclosure relates to cannabinoid-containing product for human consumption having an improved taste profile and to methods of manufacturing same. The present disclosure also relates to a process for making a cannabinoid-containing product for human consumption, comprising the following steps extraction of a cannabinoid and waxes from cannabis plant material with carbon dioxide under supercritical conditions to obtain an extract containing the cannabinoid and waxes, adding an emulsifier to the extract containing the cannabinoid and waxes to make a cannabinoid-containing emulsion for human consumption.

Apparatuses, methods, and systems for extraction, isolation, purification, and conversion of various cannabinoids, and modifications of whole-plant hemp extracts therewith are presented. A method for preparing a whole-plant hemp extract based product includes extracting cannabinoids from plant materials, such as one or more hemp varieties of Cannabis sativa. The method also includes separating and purifying CBD from the extracted cannabinoids, converting purified CBD to Δ9-THC and Δ8-THC and concurrently converting Δ9-THC to CBN, purifying and separating the CBN, and combining the purified CBN with a whole-plan hemp extract. Products and supplements related to the method are also described.

Apparatuses, methods, and systems for extraction, isolation, purification, and conversion of various cannabinoids, and modifications of whole-plant hemp extracts therewith are presented. A method for preparing a whole-plant hemp extract based product includes extracting cannabinoids from plant materials, such as one or more hemp varieties of Cannabis sativa. The method also includes separating and purifying CBD from the extracted cannabinoids, converting purified CBD to Δ9-THC and Δ8-THC and concurrently converting Δ9-THC to CBN, purifying and separating the CBN, and combining the purified CBN with a whole-plan hemp extract. Products and supplements related to the method are also described.

A chloride salt eliminator system and method for removal of chloride salt from glycol circulated through a reboiler in natural gas dehydration, in a continuous process, close to the wellhead. Hot glycol from the reboiler is pumped into a salt eliminator unit having independently replaceable filter elements which trap chloride salts which are not soluble in hot glycol and pass clean glycol for return to the reboiler.

A chloride salt eliminator system and method for removal of chloride salt from glycol circulated through a reboiler in natural gas dehydration, in a continuous process, close to the wellhead. Hot glycol from the reboiler is pumped into a salt eliminator unit having independently replaceable filter elements which trap chloride salts which are not soluble in hot glycol and pass clean glycol for return to the reboiler.

The present disclosure discloses a method for preparing 2,5-dimethylphenol by selective catalytic conversion of lignin, relates to the technical field of chemistry, and includes the following steps: mixing lignin, a catalyst, and ethanol, and then carrying out a catalytic conversion reaction of lignin under the gaseous supercritical conditions of ethanol; and cooling the reaction product by quenching after the completion of reaction, and then subjecting it to separation and extraction to obtain 2,5-dimethylphenol. The catalyst comprises a modified sepiolite carrier, an active metal Mo, and auxiliary agents Zr and Fe. The process of the present disclosure is simple, and the prepared catalyst is a solid catalyst, which avoids problems of difficult recovery, serious environmental pollution and equipment corrosion caused by the use of homogeneous organic acid-base catalysts.

The present disclosure discloses a method for preparing 2,5-dimethylphenol by selective catalytic conversion of lignin, relates to the technical field of chemistry, and includes the following steps: mixing lignin, a catalyst, and ethanol, and then carrying out a catalytic conversion reaction of lignin under the gaseous supercritical conditions of ethanol; and cooling the reaction product by quenching after the completion of reaction, and then subjecting it to separation and extraction to obtain 2,5-dimethylphenol. The catalyst comprises a modified sepiolite carrier, an active metal Mo, and auxiliary agents Zr and Fe. The process of the present disclosure is simple, and the prepared catalyst is a solid catalyst, which avoids problems of difficult recovery, serious environmental pollution and equipment corrosion caused by the use of homogeneous organic acid-base catalysts.

The present disclosure discloses a method for preparing 2,5-dimethylphenol by selective catalytic conversion of lignin, relates to the technical field of chemistry, and includes the following steps: mixing lignin, a catalyst, and ethanol, and then carrying out a catalytic conversion reaction of lignin under the gaseous supercritical conditions of ethanol; and cooling the reaction product by quenching after the completion of reaction, and then subjecting it to separation and extraction to obtain 2,5-dimethylphenol. The catalyst comprises a modified sepiolite carrier, an active metal Mo, and auxiliary agents Zr and Fe. The process of the present disclosure is simple, and the prepared catalyst is a solid catalyst, which avoids problems of difficult recovery, serious environmental pollution and equipment corrosion caused by the use of homogeneous organic acid-base catalysts.

The present disclosure discloses a method for preparing 2,5-dimethylphenol by selective catalytic conversion of lignin, relates to the technical field of chemistry, and includes the following steps: mixing lignin, a catalyst, and ethanol, and then carrying out a catalytic conversion reaction of lignin under the gaseous supercritical conditions of ethanol; and cooling the reaction product by quenching after the completion of reaction, and then subjecting it to separation and extraction to obtain 2,5-dimethylphenol. The catalyst comprises a modified sepiolite carrier, an active metal Mo, and auxiliary agents Zr and Fe. The process of the present disclosure is simple, and the prepared catalyst is a solid catalyst, which avoids problems of difficult recovery, serious environmental pollution and equipment corrosion caused by the use of homogeneous organic acid-base catalysts.

In alternative embodiments, provided are methods for extracting essential oils, phytochemicals and pharmaceutically active components such as terpenes, phytochemicals and pharmaceutically active components from biomass or any plant materials. In alternative embodiments, provided are methods for making synthetic formulations comprising biomass-derived plant materials using essential oils, phytochemicals and pharmaceutically active components isolated by methods as provided herein. In alternative embodiments, provided are synthetic biomass-derived formulations and plant materials using essential oils, phytochemicals and pharmaceutically active components isolated by methods as provided herein.