A method for reducing nitrates, nitrites, and/or hydroxylamine in water using a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex. The method includes dissolving a copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex in water having an excess amount of nitrates, nitrites, and/or hydroxylamine therein. The dissolved copper(II) tetra-substituted fluorinated pinacolate ligand pre-catalyst complex in the water is subjected to electrochemical reduction to form a homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex. The homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex reduces the nitrates, nitrites, and/or hydroxylamine in the water to compounds with nitrogen in a lower oxidation state with the homogeneous reduced copper tetra-substituted fluorinated pinacolate ligand catalyst complex.

Ethylene oligomerization catalysts include a solid support having surface hydroxyl groups on a surface of the solid support. Functional groups attached to the solid support through at least one covalent bond and coordinated with at least one catalytically active transition metal. Individual functional groups are attached to the solid support as products of condensation reactions of at least one hydrolysable group of precursor ligands with a corresponding surface group of the solid support. The precursor ligands have a general formula (Ph.sub.2P).sub.2N—R.sup.1-A, where R.sup.1 is C.sub.1-C.sub.40 hydrocarbylene or C.sub.1-C.sub.40 heterohydrocarbylene; and A is a hydrolysable group selected from trialkoxysilyl, halosilyl, carboxylates, esters, phosphonates, amines, imines, thiols, thiocarboxylates, or halides.

Provided herein are heterogeneous catalysts suitable for use in carbonylation reactions, including the production of acrylic acid from ethylene oxide and carbon monoxide on an industrial scale. The production may involve various unit operations, including, for example: a beta-propiolactone production system configured to produce beta-propiolactone from ethylene oxide and carbon monoxide; a polypropiolactone production system configured to produce polypropiolactone from beta-propiolactone; and an acrylic acid production system configured to produce acrylic acid with a high purity by thermolysis of polypropiolactone.

The invention discloses a visible light responsive titanium dioxide nanowire/metal organic skeleton/carbon nanofiber membrane and preparation method and application thereof. A CNF (Carbon Nano Fiber)/TiO.sub.2 nano-wire/MIL-100 (represented as CTWM) membrane material is prepared and an MIL-100 material is used for adsorbing waste gas to enhance the photocatalytic effect of titanium dioxide on the membrane material; a CNF/TiO.sub.2/MIL-100 membrane catalyst sufficiently utilizes the adsorption capability of MIL-100 on the waste gas, the photocatalytic degradation performance of the TiO.sub.2 and high electrical conductivity of CNF to effectively prolong the service life of photoelectrons and promote the photocatalytic activity of the photoelectrons.

Arene-immobilized Ru(II)TsDPEN Noyori-Ikariya catalysts anchored to silica through the coordinated η6-arene are provided. The catalysts efficiently catalyze many reactions, including the asymmetric transfer hydrogenation of ketones to alcohols.

The invention relates to heterogeneous catalysts comprising an organo-ruthenium complex immobilized to an aluminum-modified inorganic oxide by a chemical bond between a tetra-coordinated aluminum atom on a surface of the aluminum-modified inorganic oxide and an amino or imino nitrogen of the organo-ruthenium complex, methods of preparing the heterogeneous catalysts including immobilizing the organo-ruthenium complex to a tetra-coordinated aluminum atom on a surface of an inorganic oxide by reacting an amino or imino nitrogen of the organo-ruthenium complex and an aluminum-modified inorganic oxide, followed by a defined heat treatment, as well as methods for producing hydrogen from formic acid using the heterogeneous catalysts.

The invention relates to a material in the form of a cellular solid monolith consisting of an inorganic oxide polymer. Said monolith comprises macropores which have an average size d.sub.A of 4 μm to 50 μm, mesopores that have an average size d.sub.E of 20 to 30 Å, and micropores which have an average size d.sub.1 of 5 à 10 Å, said pores being interconnected. The inorganic oxide polymer has organic groups R of formula —(CH.sub.2).sub.n—R.sup.1, wherein 0≤n≤5, and R.sup.1 is selected from among a thiol group, a pyrrole group, an amino group having one or more optional, optionally substituted alkyl, alkylamino, or aryl substituents, an alkyl group, or a phenyl group optionally having an alkyl-type substituent R.sup.2. The disclosed material can be used as a substrate for a metal catalyst and for decontaminating liquid or gaseous media.

The present invention provides, inter alia, a multidentate ligand having the structure of: ##STR00001## Also provided are methods of preparing metal complexes from the multidentate ligand, and the metal complexes prepared by such methods. Further provided are catalysts comprising such metal complexes, and various uses of such catalysts.

The present invention provides a method for preparing 1,5-pentanediol via hydrogenolysis of tetrahydrofurfuryl alcohol. The catalyst used in the method is prepared by supporting a noble metal and a promoter on an organic polymer supporter or an inorganic hybrid material supporter, wherein the supporter is functionalized by a nitrogen-containing ligand. When the catalyst is used in the hydrogenolysis of tetrahydrofurfuryl alcohol to prepare 1,5-pentanediol, a good reaction activity and a high selectivity can be achieved. The promoter and the nitrogen-containing ligand in the supporter are bound to the catalyst through coordination, thereby the loss of the promoter is significantly decreased, and the catalyst has a particularly high stability. The lifetime investigation of the catalyst, which has been reused many times or used continuously for a long term, suggests that the catalyst has no obvious change in performance, thus reducing the overall process production cost.

A 3D structure of the graphite-titanium-nanocomposite complex and a method of preparing the graphite-titanium-nanocomposite complex are disclosed. The Graphite-titanium-nanocomposite complex includes a metal core associated with the two phases, amine functionalized graphite, and amine functionalized titanium. The method of preparation includes amine functionalizing of graphite and titanium with coupling agents to produce amine functionalized titanium and graphite, further mixing with a metal ion solution for synthesizing an ion complex. Trisodium citrate solution and sodium borohydride solution is added to the ion complex to prepare a 3D structure of the graphite-titanium-nanocomposite complex, employed as a catalyst.