B01J20/282

Bisphenol Hypersorbents for Enhanced Detection of, or Protection From, Hazardous Chemicals
20220258126 · 2022-08-18 ·

The invention relates to strong hydrogen-bond acidic sorbents. The sorbents may be provided in a form that limits or eliminates intramolecular bonding of the hydrogen-bond acidic site between neighboring sorbent molecules, for example, by providing steric groups adjacent to the hydrogen-bond acidic site. The hydrogen bond site may be a phenolic structure based on a bisphenol architecture. The sorbents of the invention may be used in methods for trapping or detecting hazardous chemicals or explosives.

Bisphenol Hypersorbents for Enhanced Detection of, or Protection From, Hazardous Chemicals
20220258126 · 2022-08-18 ·

The invention relates to strong hydrogen-bond acidic sorbents. The sorbents may be provided in a form that limits or eliminates intramolecular bonding of the hydrogen-bond acidic site between neighboring sorbent molecules, for example, by providing steric groups adjacent to the hydrogen-bond acidic site. The hydrogen bond site may be a phenolic structure based on a bisphenol architecture. The sorbents of the invention may be used in methods for trapping or detecting hazardous chemicals or explosives.

ISOLATION AND ANALYSIS OF TERPENES
20220291099 · 2022-09-15 ·

In accordance with embodiments of the present invention, a terpene-rich sample is prepared for terpene analysis using liquid chromatography via an extraction method that takes little time, uses minimal external equipment, and permits direct injection of extracted terpenes into a liquid chromatography instrument for analysis. An embodiment of the invention involves preparing a terpene-containing sample for analysis by liquid chromatography by liquid extraction; heating the liquid extract in a vial that contains a filter medium or solvent; collecting the terpenes in the medium by the vapor pressure forced through the filter from heating; and eluting the collected terpenes into a vial or directly into a chromatography injector.

SEPARATION OF BACL2 FROM CACL2 BRINE SOLUTION
20220281754 · 2022-09-08 · ·

The present invention relates to a process for separating BaCl.sub.2 from a CaCl.sub.2 brine solution.

SEPARATION OF BACL2 FROM CACL2 BRINE SOLUTION
20220281754 · 2022-09-08 · ·

The present invention relates to a process for separating BaCl.sub.2 from a CaCl.sub.2 brine solution.

Bisphenol Hypersorbents for Enhanced Detection of, or Protection From, Hazardous Chemicals
20220241750 · 2022-08-04 ·

The invention relates to strong hydrogen-bond acidic sorbents. The sorbents may be provided in a form that limits or eliminates intramolecular bonding of the hydrogen-bond acidic site between neighboring sorbent molecules, for example, by providing steric groups adjacent to the hydrogen-bond acidic site. The hydrogen bond site may be a phenolic structure based on a bisphenol architecture. The sorbents of the invention may be used in methods for trapping or detecting hazardous chemicals or explosives.

Bisphenol Hypersorbents for Enhanced Detection of, or Protection From, Hazardous Chemicals
20220241750 · 2022-08-04 ·

The invention relates to strong hydrogen-bond acidic sorbents. The sorbents may be provided in a form that limits or eliminates intramolecular bonding of the hydrogen-bond acidic site between neighboring sorbent molecules, for example, by providing steric groups adjacent to the hydrogen-bond acidic site. The hydrogen bond site may be a phenolic structure based on a bisphenol architecture. The sorbents of the invention may be used in methods for trapping or detecting hazardous chemicals or explosives.

Bisphenol Hypersorbents for Enhanced Detection of, or Protection From, Hazardous Chemicals
20220250032 · 2022-08-11 ·

The invention relates to strong hydrogen-bond acidic sorbents. The sorbents may be provided in a form that limits or eliminates intramolecular bonding of the hydrogen-bond acidic site between neighboring sorbent molecules, for example, by providing steric groups adjacent to the hydrogen-bond acidic site. The hydrogen bond site may be a phenolic structure based on a bisphenol architecture. The sorbents of the invention may be used in methods for trapping or detecting hazardous chemicals or explosives.

Bisphenol Hypersorbents for Enhanced Detection of, or Protection From, Hazardous Chemicals
20220250032 · 2022-08-11 ·

The invention relates to strong hydrogen-bond acidic sorbents. The sorbents may be provided in a form that limits or eliminates intramolecular bonding of the hydrogen-bond acidic site between neighboring sorbent molecules, for example, by providing steric groups adjacent to the hydrogen-bond acidic site. The hydrogen bond site may be a phenolic structure based on a bisphenol architecture. The sorbents of the invention may be used in methods for trapping or detecting hazardous chemicals or explosives.

POROUS NANOSHEETS FOR EFFECTIVE ADSORPTION OF SMALL MOLECULES AND VOLATILE ORGANIC COMPOUNDS
20220219993 · 2022-07-14 ·

Disclosed herein is a material suitable for the adsorption, storage and release of volatile organic compounds comprising: a porous thin film layer formed from nanosheets of one or more MXenes.