Abstract: A method for removing thiophene and thiophene compounds from liquid fuel includes contacting the liquid fuel with an adsorbent which preferentially adsorbs the thiophene and thiophene compounds. The adsorption takes place at a selected temperature and pressure, thereby producing a non-adsorbed component and a thiophene/thiophene compound-rich adsorbed component. The adsorbent includes either a metal or a metal ion that is adapted to form ?-complexation bonds with the thiophene and/or thiophene compounds, and the preferential adsorption occurs by ?-complexation. A further method includes selective removal of aromatic compounds from a mixture of aromatic and aliphatic compounds.

Abstract: A method for removing thiophene and thiophene compounds from liquid fuel includes contacting the liquid fuel with an adsorbent which preferentially adsorbs the thiophene and thiophene compounds. The adsorption takes place at a selected temperature and pressure, thereby producing a non-adsorbed component and a thiophene/thiophene compound-rich adsorbed component. The adsorbent includes either a metal or a metal cation that is adapted to form ?-complexation bonds with the thiophene and/or thiophene compounds, and the preferential adsorption occurs by ?-complexation. A further method includes selective removal of aromatic compounds from a mixture of aromatic and aliphatic compounds.

Abstract: A method for removing thiophene and thiophene compounds from liquid fuel includes contacting the liquid fuel with an adsorbent which preferentially adsorbs the thiophene and thiophene compounds. The adsorption takes place at a selected temperature and pressure, thereby producing a non-adsorbed component and a thiophene/thiophene compound-rich adsorbed component. The adsorbent includes either a metal or a metal cation that is adapted to form ?-complexation bonds with the thiophene and/or thiophene compounds, and the preferential adsorption occurs by ?-complexation. A further method includes selective removal of aromatic compounds from a mixture of aromatic and aliphatic compounds.

Abstract: A method for removing thiophene and thiophene compounds from liquid fuel includes contacting the liquid fuel with an adsorbent which preferentially adsorbs the thiophene and thiophene compounds. The adsorption takes place at a selected temperature and pressure, thereby producing a non-adsorbed component and a thiophene/thiophene compound-rich adsorbed component. The adsorbent includes either a metal or a metal ion that is adapted to form ?-complexation bonds with the thiophene and/or thiophene compounds, and the preferential adsorption occurs by ?-complexation. A further method includes selective removal of aromatic compounds from a mixture of aromatic and aliphatic compounds.

Abstract: A method for removing thiophene and thiophene compounds from liquid fuel includes contacting the liquid fuel with an adsorbent which preferentially adsorbs the thiophene and thiophene compounds. The adsorption takes place at a selected temperature and pressure, thereby producing a non-adsorbed component and a thiophene/thiophene compound-rich adsorbed component. The adsorbent includes either a metal or a metal cation that is adapted to form &pgr;-complexation bonds with the thiophene and/or thiophene compounds, and the preferential adsorption occurs by &pgr;-complexation. A further method includes selective removal of aromatic compounds from a mixture of aromatic and aliphatic compounds.

Abstract: CuY and AgY zeolites as selective sorbents for desulfurization of liquid fuels. Thiophene and benzene were used as the model system, and vapor phase isotherms were measured. Compared with NaY, CuY and AgY adsorbed significantly larger amounts of both thiophene and benzene at low pressures. It is hypothesized that this is due to &pgr;-complexation with Cu+ and Ag+. On a per-cation basis, more thiophene was adsorbed by Cu+ than by Ag+, e.g., 0.92 molecule/Cu+ versus 0.42 molecule/Ag+ at 2×10−5 atm and 120° C. Molecular orbital calculations confirmed the relative strengths of &pgr;-complexation: thiophene>benzene and Cu+>Ag+. The experimental heats of adsorption for &pgr;-complexation are in qualitative agreement with theoretical predictions. The invention further comprises a process and sorbents for removal of aromatics from hydrocarbons.

Abstract: CuY and AgY zeolites as selective sorbents for desulfurization of liquid fuels. Thiophene and benzene were used as the model system, and vapor phase isotherms were measured. Compared with NaY, CuY and AgY adsorbed significantly larger amounts of both thiophene and benzene at low pressures. It is hypothesized that this is due to &pgr;-complexation with Cu+ and Ag+. On a per-cation basis, more thiophene was adsorbed by Cu+ than by Ag+, e.g., 0.92 molecule/Cu+ versus 0.42 molecule/Ag+ at 2×10−5 atm and 120° C. Molecular orbital calculations confirmed the relative strengths of &pgr;-complexation: thiophene>benzene and Cu+>Ag+. The experimental heats of adsorption for &pgr;-complexation are in qualitative agreement with theoretical predictions. The invention further comprises a process and sorbents for removal of aromatics from hydrocarbons.

Abstract: CuY and AgY zeolites as selective sorbents for desulfurization of liquid fuels. Thiophene and benzene were used as the model system, and vapor phase isotherms were measured. Compared with NaY, CuY and AgY adsorbed significantly larger amounts of both thiophene and benzene at low pressures. It is hypothesized that this is due to &pgr;-complexation with Cu+ and Ag+. On a per-cation basis, more thiophene was adsorbed by Cu+ than by Ag+, eg. 0.92 molecule/Cu+ versus 0.42 molecule/Ag+ at 2×10−5 atm and 120° C. Molecular orbital calculations confirmed the relative strengths of &pgr;-complexation: thiophene>benzene and Cu+>Ag+. The experimental heats of adsorption for &pgr;-complexation are in qualitative agreement with theoretical predictions. The invention further comprises a process and sorbents for removal of aromatics from hydrocarbons.