Abstract: A method of separating a Fischer-Tropsch catalyst from the output slurry of a Fischer-Tropsch bubble column reactor, where the slurry comprises Fischer-Tropsch catalyst particles and liquid hydrocarbon product is disclosed. The method comprises contacting a compressed hydrocarbon solvent (e.g., a supercritical hydrocarbon solvent, or liquid hydrocarbon solvent which may be at near supercritical conditions) with the output slurry at a temperature and pressure where the liquid hydrocarbon product is soluble in the solvent to form a concentrated slurry phase containing the catalyst particles, and an enriched solvent phase containing liquid hydrocarbon product. This contacting step is then followed by the step of separating the concentrated slurry from the enriched solvent. Apparatus for carrying out the method of the invention is also disclosed.

Abstract: A method of separating a Fischer-Tropsch catalyst from the output slurry of a Fischer-Tropsch bubble column reactor, where the slurry comprises Fischer-Tropsch catalyst particles and liquid hydrocarbon product is disclosed. The method comprises contacting a compressed hydrocarbon solvent (e.g., a supercritical hydrocarbon solvent, or liquid hydrocarbon solvent which may be at near supercritical conditions) with the output slurry at a temperature and pressure where the liquid hydrocarbon product is soluble in the solvent to form a concentrated slurry phase containing the catalyst particles, and an enriched solvent phase containing liquid hydrocarbon product. This contacting step is then followed by the step of separating the concentrated slurry from the enriched solvent. Apparatus for carrying out the method of the invention is also disclosed.

Abstract: Competitive and sandwich-type immunodiagnostic assays can be configured by use of liposomes carrying detectible markers (e.g., fluorophores) or catalysts thereof (e.g., enzymes) on the outer liposome surface. The liposome also contains at least one antigen or antibody allowing it to bind to a complementary, immobilized antibody or antigen on a support.

Abstract: Surfactants bound to a ligand and dissolved in a single phase aqueous solution form a precipitate when a multivalent antiligand is added to the solution. This invention can be used in an affinity precipitation test procedure (and kit) for detecting the presence or absence of a multivalent antiligand in a sample suspected of containing the multivalent antiligand, in an affinity precipitation inhibition test procedure (and kit) for detecting the presence or absence of a target ligand in a sample suspected of containing the target ligand, and in a process for separating a multivalent antiligand from a crude material containing the multivalent antiligand.

Abstract: Surfactants bound to a ligand and dissolved in a single phase aqueous solution form a precipitate when a multivalent antiligand is added to the solution. This invention can be used in an affinity precipitation test procedure (and kit) for detecting the presence or absence of a multivalent antiligand in a sample suspected of containing the multivalent antiligand, in an affinity precipitation inhibition test procedure (and kit) for detecting the presence or absence of a target ligand in a sample suspected of containing the target ligand, and in a process for separating a multivalent antiligand from a crude material containing the multivalent antiligand.

Abstract: A chromatography apparatus incorporating an improved means for connecting the ligand to the solid support is disclosed. The apparatus comprises a chamber containing a solid support. The solid support is a hydrophobic support. The apparatus includes chromatography surfactants bonded to the solid support. The surfactants comprise a polar group, a hydrophobic functional group substituted on the polar group, and a chromatographic functional group substituted on the polar group. The hydrophobic group is hydrophobically adsorbed to the solid support so that the chromatographic functional group is bound to the solid support and available for binding to compounds which selectively bind thereto. Compositions for and methods of making the foregoing are disclosed.The chromatographic functional group is a ligand for affinity chromatography, an ionogenic group for ion exchange chromatography, or a hydrophobic group for hydrophobic chromatography.

Abstract: A method of extracting a compound specifically bound by a ligand from a crude solution containing the compound is disclosed. The method comprises providing a multiplicity of liposomes having the ligand bound to the surface thereof, and mixing the liposomes with the crude solution so that the ligand binds to the compound to be extracted. The liposomes are then separated from the crude solution and the compound to be extracted recovered from the liposomes.