A composition of matter is provided comprising hierarchically ordered crystalline microporous material having well-defined long-range mesoporous ordering of cubic symmetry. The composition possesses mesopores having walls of crystalline microporous material and a mass of mesostructure between mesopores of crystalline microporous material. Long-range ordering is defined by presence of secondary peaks in an X-ray diffraction (XRD) pattern and/or cubic symmetry observable by microscopy.

The invention relates to a process for the metathesis of olefins implemented with a catalyst comprising a mesoporous matrix and at least the elements molybdenum and silicon, said elements being incorporated into said matrix by means of at least two precursors of which at least one precursor contains molybdenum and at least one precursor contains silicon.

The invention relates to a process for the metathesis of olefins implemented with a catalyst comprising a mesoporous matrix and at least the elements molybdenum and silicon, said elements being incorporated into said matrix by means of at least two precursors of which at least one precursor contains molybdenum and at least one precursor contains silicon.

The present invention relates to a supported catalyst that can be used to produce a carbon nanotube aggregate with high bulk density, a method for preparing the supported catalyst, a carbon nanotube aggregate produced using the supported catalyst, and a method for producing the carbon nanotube aggregate. According to the present invention, the bulk density of the carbon nanotube aggregate is easily controllable. Therefore, the carbon nanotube aggregate is suitable for use in various fields.

The present invention relates to a supported catalyst that can be used to produce a carbon nanotube aggregate with high bulk density, a method for preparing the supported catalyst, a carbon nanotube aggregate produced using the supported catalyst, and a method for producing the carbon nanotube aggregate. According to the present invention, the bulk density of the carbon nanotube aggregate is easily controllable. Therefore, the carbon nanotube aggregate is suitable for use in various fields.

A catalyst composition for the production of carbon nanotubes (CNT) with controlled morphology is disclosed. The catalyst is represented by formula [(M.sub.xMn.sub.y)Mo.sub.z][binary metal oxide].sub.(100(x+y+z)), where x is in the range 1 to 25 wt %, y is in the range 0.1 to 20 wt %, and z is in the range 0.0 to 10 wt %. Further M represents either iron or cobalt or nickel along with manganese and molybdenum supported on binary metal oxides comprising of boron, magnesium, aluminum, silicon, calcium, barium, and combination thereof. The CNT morphology can be tailor-made with the plural combination of nature of metal and promoters in appropriate proportions. The process yields the CNT with bulk density in the range of 0.01 to 0.20 g/cc, diameter in the range of 5 to 30 nm and purity greater than 95 wt %.

A catalyst composition for the production of carbon nanotubes (CNT) with controlled morphology is disclosed. The catalyst is represented by formula [(M.sub.xMn.sub.y)Mo.sub.z][binary metal oxide].sub.(100(x+y+z)), where x is in the range 1 to 25 wt %, y is in the range 0.1 to 20 wt %, and z is in the range 0.0 to 10 wt %. Further M represents either iron or cobalt or nickel along with manganese and molybdenum supported on binary metal oxides comprising of boron, magnesium, aluminum, silicon, calcium, barium, and combination thereof. The CNT morphology can be tailor-made with the plural combination of nature of metal and promoters in appropriate proportions. The process yields the CNT with bulk density in the range of 0.01 to 0.20 g/cc, diameter in the range of 5 to 30 nm and purity greater than 95 wt %.

Redox catalysts having surface medication, methods of making redox catalysts with surface modification, and uses of the surface modified redox catalysts are provided. In some aspects, the redox catalysts include a core oxygen carrier region such as CaMnO.sub.3, BaMnO.sub.3-, SrMnO.sub.3-, Mn.sub.2SiO.sub.4, Mn.sub.2MgO.sub.4-, La.sub.0.8Sr.sub.0.2O.sub.3-, La.sub.0.8Sr.sub.0.2FeO.sub.3-, Ca.sub.9Ti.sub.0.1Mn.sub.0.9O.sub.3-, Pr.sub.6O.sub.11-, manganese ore, or a combination thereof; and an outer shell having an average thickness of about 1-100 monolayers surrounding the outer surface of the core region. The outer shell can include, for example a salt selected such as Li.sub.2WO.sub.4, Na.sub.2WO.sub.4, K.sub.2WO.sub.4, SrWO.sub.4, Li.sub.2MoO.sub.4, Na.sub.2MoO.sub.4, K.sub.2MoO.sub.4, CsMoO.sub.4, Li.sub.2CO.sub.3, Na.sub.2CO.sub.3, K.sub.2CO.sub.3, or a combination thereof.

According to the present invention, a composite including amorphous iron molybdate islands, shows a smaller island size and a uniform distribution of islands compared with a conventional composite including crystalline islands, and thus has a higher specific surface area, thereby exhibiting excellent activity as a catalyst.

According to the present invention, a composite including amorphous iron molybdate islands, shows a smaller island size and a uniform distribution of islands compared with a conventional composite including crystalline islands, and thus has a higher specific surface area, thereby exhibiting excellent activity as a catalyst.