The present invention generally relates to methods and systems relating to the selection of substrates comprising crystalline templates for the controlled crystallization of molecular species. In some embodiments, the methods and systems allow for the controlled crystallization of a molecular species in a selected polymorphic form. In some embodiments, the molecular species is a small organic molecule (e.g., pharmaceutically active agent).

The present invention generally relates to methods and systems relating to the selection of substrates comprising crystalline templates for the controlled crystallization of molecular species. In some embodiments, the methods and systems allow for the controlled crystallization of a molecular species in a selected polymorphic form. In some embodiments, the molecular species is a small organic molecule (e.g., pharmaceutically active agent).

Methods of making reduced derivatives of hydroxymethyl furfural using metal catalysts are described. The derivatives may have tetrahydrofuran or furan nucleus with alkoxymethyl ether or ester moieties on the 5′ carbon and methanol on the 2′ carbon. Suitable metal catalyst include Raney nickel, a nickel catalyst with a zirconium promoter, a chromite catalyst with a barium, a palladium catalyst, such as palladium on carbon, or a ruthenium catalyst. Also provided are a new class of compounds, which are n-alkoxy hexane diols (i.e., 1,2 or 1,5 hexane diol ethers) and methods of making the same by reduction of furan or tetrahydrofuran derivatives.

Methods of making reduced derivatives of hydroxymethyl furfural using metal catalysts are described. The derivatives may have tetrahydrofuran or furan nucleus with alkoxymethyl ether or ester moieties on the 5′ carbon and methanol on the 2′ carbon. Suitable metal catalyst include Raney nickel, a nickel catalyst with a zirconium promoter, a chromite catalyst with a barium, a palladium catalyst, such as palladium on carbon, or a ruthenium catalyst. Also provided are a new class of compounds, which are n-alkoxy hexane diols (i.e., 1,2 or 1,5 hexane diol ethers) and methods of making the same by reduction of furan or tetrahydrofuran derivatives.

A process for preparing a drag reducing polymer which is to be added to a liquid hydrocarbon. The liquid hydrocarbon has an asphaltene content of at least about 3 weight percent and an API gravity of less than about 26°. The drag reducing polymer can comprise the residues of a monomer having at least one heteroatom. Treatment of the liquid hydrocarbon with the drag reducing polymer allows a reduction in pressure drop associated with turbulent flow of the liquid hydrocarbon through a conduit.

A process for preparing a drag reducing polymer which is to be added to a liquid hydrocarbon. The liquid hydrocarbon has an asphaltene content of at least about 3 weight percent and an API gravity of less than about 26°. The drag reducing polymer can comprise the residues of a monomer having at least one heteroatom. Treatment of the liquid hydrocarbon with the drag reducing polymer allows a reduction in pressure drop associated with turbulent flow of the liquid hydrocarbon through a conduit.

The present disclosure provides an additive and a method for terminating polymerization and/or reducing viscosity of polymer solution. The additive comprises a carboxylic acid, an alcohol, a salt chosen from alkali metal salts, alkaline earth metal salts, ammonium salts, and any combination thereof, and optionally, water. The method of the present disclosure comprises adding the additive according to present disclosure into a polymer solution and mixing the resulting mixture. The additive of the present disclosure can terminate living polymer chain ends efficiently and can destroy catalytic active centers and can substantially reduce the viscosity of a polymer solution.

The present disclosure provides an additive and a method for terminating polymerization and/or reducing viscosity of polymer solution. The additive comprises a carboxylic acid, an alcohol, a salt chosen from alkali metal salts, alkaline earth metal salts, ammonium salts, and any combination thereof, and optionally, water. The method of the present disclosure comprises adding the additive according to present disclosure into a polymer solution and mixing the resulting mixture. The additive of the present disclosure can terminate living polymer chain ends efficiently and can destroy catalytic active centers and can substantially reduce the viscosity of a polymer solution.

The present disclosure provides dimeric fluorosurfactants related methods and ink-jet inks incorporating such fluorosurfactants. As such, an ink-jet ink can comprise a liquid vehicle; a non-ionic fluorosurfactant dimer having the structure CF.sub.3(CF.sub.2).sub.x(CH.sub.2).sub.y(CR.sub.2CR.sub.2O).sub.z-A-(OCR.sub.2CR.sub.2).sub.a(CH.sub.2).sub.b(CF.sub.2).sub.cCF.sub.3, where R is independently H or methyl, A is a bridging unit containing aliphatic or aromatic functionality, x is 3 to 18, y is 0 to 8, z is 0 to 100, a is 0 to 100, b is 0 to 8, and c is 3 to 18; and a colorant.

An object is to provide dispersion containing lipid peptide type compound useful as low molecular weight gelator, such as lipid dipeptide and lipid tripeptide, and dissolution accelerator capable of dissolving the lipid peptide type compound at lower temperature and more easily. It is also an object to provide dispersion that can form hydrogel by simpler method and under milder condition (low temperature) and from which gel can be obtained as gel having high thermal stability, and provide method for forming the gel. Dispersion including: a lipid peptide type compound in which peptide portion formed by repetition of at least two or more identical or different amino acids is bonded to lipid portion including C.sub.10-24 aliphatic group; dissolution accelerator having, in molecules thereof, hydrophilic portion and hydrophobic portion, the hydrophilic portion having betaine structure; and water; and method for producing hydrogel by use of the dispersion.