Stability and activity of carbon nanofiber-supported catalysts in the aqueous phase reforming of ethylene glycol

Nickel, cobalt, copper and platinum nanoparticles supported on carbon nano-fibers were evaluated with respect to their stability, catalytic activity and selectivity in the aqueous phase reforming of ethylene glycol (230 C, autogenous pressure, batch reactor). The initial surface-specific activities for ethylene glycol reforming were in a similar range but decreased in the order of Pt (15.5 h1 ) >Co(13.0 h1 ) >Ni(5.2 h1 ) while the Cu catalyst only showed low dehydrogenation activity. The hydrogen molar selectivity decreased in the order of Pt (53%)>Co(21%)>Ni (15%) as a result of the production of methane over the latter two catalysts. Over the Co catalyst acids were formed in the liquid phase while alcohols were formed over Ni and Pt. Due to the low pH of the reaction mixture, especially in the case of Co (as a result of the formed acids), significant cobalt leaching occurs which resulted in a rapid deactivation of this catalyst. Investigations of the spent catalysts with various techniques showed that metal particle growth is responsible for the deactivation of the Pt and Ni catalysts. In addition, coking might also contribute to the deactivation of the Ni catalyst.     

Relationship between polymer creep curves and stress-strain diagrams

For polymers whose () diagram has the form of a monotonically increasing curve the creep rate is monotonically damped with time. If, however, the stress-strain diagram has a maximum, the creep curve becomes stepped: after first slowing, the creep sharply accelerates, and then slows down again. The strains corresponding to characteristic points on the stress-strain curves coincide with those corresponding to singular points on the creep curves.A. F. Ioffe Physicotechnical Institute, Academy of Sciences of the USSR, Leningrad. Translated from Mekhanika Polimerov, Vol. 4, No. 5, pp. 787–792, September–October, 1968.     

Creep of linear unoriented polymers in tension,compression, and torsion

The creep of polymethyl methacrylate, polystyrene, and polyethylene in tension, compression, and torsion has been investigated over a broad interval of temperature below the glass transition point. It is shown that the creep criterion changes depending on the temperature. This is associated with changes in molecular mobility.A. F. Ioffe Physicotechnical Institute, Academy of Sciences of the USSR, Leningrad. Translated from Mekhanika Polimerov, No. 1, pp. 24–28, January–February, 1970.