Patent classifications
C07C253/10
Process for removing cations from an isophoronenitrile product mixture
Cations are removed from a substance stream that is produced during the production of isophoronenitrile with the help of a cation exchanger.
Process for removing cations from an isophoronenitrile product mixture
Cations are removed from a substance stream that is produced during the production of isophoronenitrile with the help of a cation exchanger.
Process for removing cations from an isophoronenitrile product mixture
Cations are removed from a substance stream that is produced during the production of isophoronenitrile with the help of a cation exchanger.
Methods of making halogenated fluorinated ether-containing compounds
Described herein are three methods for making halogenated fluorinated ether-containing compounds using a fluorinated olefin or hexafluoropropylene oxide.
Methods of making halogenated fluorinated ether-containing compounds
Described herein are three methods for making halogenated fluorinated ether-containing compounds using a fluorinated olefin or hexafluoropropylene oxide.
Methods of making halogenated fluorinated ether-containing compounds
Described herein are three methods for making halogenated fluorinated ether-containing compounds using a fluorinated olefin or hexafluoropropylene oxide.
Nickel form for preparation of catalytic nickel-ligand complexes
A novel nickel particulate form is provided that efficiently forms a zero-valent nickel complex with a phosphorus-containing ligands in an organic liquid to form a hydrocyanation catalyst. Particles in the nickel particulate form comprise nickel crystallites. For example, the nickel particulate form can have a BET Specific Surface Area of at least about 1 m.sup.2/gm; an average crystallite size less than about 20-25 nm, the nickel particulate form can have at least 10% of the crystallites in the nickel form can have can have a diameter (C10) of less than about 10 nm, and/or there are on average at least about 10.sup.15 surface crystallites per gram nickel. A ratio of BET SSA to C50 for the nickel particulate form can be at least about 0.110.sup.9 m/gm and preferably at least about 0.410.sup.9 m/gm. Methods of preparation and use are also provided.
Nickel form for preparation of catalytic nickel-ligand complexes
A novel nickel particulate form is provided that efficiently forms a zero-valent nickel complex with a phosphorus-containing ligands in an organic liquid to form a hydrocyanation catalyst. Particles in the nickel particulate form comprise nickel crystallites. For example, the nickel particulate form can have a BET Specific Surface Area of at least about 1 m.sup.2/gm; an average crystallite size less than about 20-25 nm, the nickel particulate form can have at least 10% of the crystallites in the nickel form can have can have a diameter (C10) of less than about 10 nm, and/or there are on average at least about 10.sup.15 surface crystallites per gram nickel. A ratio of BET SSA to C50 for the nickel particulate form can be at least about 0.110.sup.9 m/gm and preferably at least about 0.410.sup.9 m/gm. Methods of preparation and use are also provided.
Nickel form for preparation of catalytic nickel-ligand complexes
A novel nickel particulate form is provided that efficiently forms a zero-valent nickel complex with a phosphorus-containing ligands in an organic liquid to form a hydrocyanation catalyst. Particles in the nickel particulate form comprise nickel crystallites. For example, the nickel particulate form can have a BET Specific Surface Area of at least about 1 m.sup.2/gm; an average crystallite size less than about 20-25 nm, the nickel particulate form can have at least 10% of the crystallites in the nickel form can have can have a diameter (C10) of less than about 10 nm, and/or there are on average at least about 10.sup.15 surface crystallites per gram nickel. A ratio of BET SSA to C50 for the nickel particulate form can be at least about 0.110.sup.9 m/gm and preferably at least about 0.410.sup.9 m/gm. Methods of preparation and use are also provided.
Composition for improved nickel-ligand solubility
In the hydrocyanation reaction of butadiene proceeding through pentenenitriles to adiponitrile, catalysis by complexes of zerovalent nickel with bidentate phosphorus-based ligands of the NiL.sub.2A type wherein L.sub.2 is a bidentate ligand and A is an unsaturated compound, can be rate-limited by the solubility of the catalytic complex. The present invention concerns solvent compositions for the nickel-ligand complex comprising mixtures of unsaturated nitriles that provide for increased metal solubility, particularly in the absence of a Lewis acid promoter, resulting in higher hydrocyanation reaction rates in an industrial-scale process for production of important nylon manufacturing intermediates. The mixed nitrile solvent compositions can include mixtures of pentenenitriles and/or methylbutenenitriles. The mixtures of mixed unsaturated nitriles can be, at least in part, from recycle streams from the hydrocyanation reaction for which the nickel-bidentate ligand complexes are used as catalysts.