Abstract: In this work, the condensation fraction and transition
temperature of neutral many bosonic system are studied within the
static fluctuation approximation (SFA). The effect of the potential
parameters such as the strength and range on the condensate fraction
was investigated. A model potential consisting of a repulsive step
potential and an attractive potential well was used. As the potential
strength or the core radius of the repulsive part increases, the
condensation fraction is found to be decreased at the same
temperature. Also, as the potential depth or the range of the attractive
part increases, the condensation fraction is found to be increased. The
transition temperature is decreased as the potential strength or the
core radius of the repulsive part increases, and it increases as the
potential depth or the range of the attractive part increases.
Abstract: The effect of nano Co3O4 addition on the
superconducting properties of (Bi, Pb)-2223 system was studied. The
samples were prepared by the acetate coprecipitation method. The
Co3O4 with different sizes (10-30 nm and 30-50 nm) from x=0.00 to
0.05 was added to Bi1.6Pb0.4Sr2Ca2Cu3Oy(Co3O4)x. Phase analysis by
XRD method, microstructural examination by SEM and dc electrical
resistivity by four point probe method were done to characterize the
samples. The X-ray diffraction patterns of all the samples indicated
the majority Bi-2223 phase along with minor Bi-2212 and Bi-2201
phases. The volume fraction was estimated from the intensities of Bi-
2223, Bi-2212 and Bi-2201 phase. The sample with x=0.01 wt% of
the added Co3O4 (10-30 nm size) showed the highest volume fraction
of Bi-2223 phase (72%) and the highest superconducting transition
temperature, Tc (~102 K). The non-added sample showed the highest
Tc(~103 K) compared to added samples with nano Co3O4 (30-50 nm
size) added samples. Both the onset critical temperature Tc(onset)
and zero electrical resistivity temperature Tc(R=0) were in the range
of 103-115 ±1K and 91-103 ±1K respectively for samples with added
Co3O4 (10-30 nm and 30-50 nm).
Abstract: The first and basic cause of the failure of concrete is repeated freezing (thawing) of moisture contained in the pores, microcracks, and cavities of the concrete. On transition to ice, water existing in the free state in cracks increases in volume, expanding the recess in which freezing occurs. A reduction in strength below the initial value is to be expected and further cycle of freezing and thawing have a further marked effect. By using some experimental parameters like nuclear magnetic resonance variation (NMR), enthalpy-temperature (or heat capacity) variation, we can resolve between the various water states and their effect on concrete properties during cooling through the freezing transition temperature range. The main objective of this paper is to describe the principal type of water responsible for the reduction in strength and structural damage (frost damage) of concrete following repeated freeze –thaw cycles. Some experimental work was carried out at the institute of cryogenics to determine what happens to water in concrete during the freezing transition.
Abstract: New lead-free ferroelectric relaxor ceramics were
prepared by conventional solid-state synthesis in the BaTiO3-Bi2O3-
Y2O3 systems. Some of these ceramics present a ferroelectric relaxor
with transition temperature close to room temperature. These new
materials are very interesting for applications and can replace leadbased
ceramic to prevent the toxic pollutions during the preparation
state. In the other hand, the energy band diagram shows the
potentiality of these compounds for the solar energy conversion.
Thus, some compositions have been tested successfully for H2
production upon visible light. The best activity occurs in alkaline
media with a rate evolution of about 0.15 mL g-1 mn-1 and a quantum
yield of 1% under polychromatic light.
Abstract: In this research work, poly (acrylonitrile-butadienestyrene)/
polypropylene (ABS/PP) blends were processed by melt
compounding in a twin-screw extruder. Upgrading of the thermal
characteristics of the obtained materials was attempted by the
incorporation of organically modified montmorillonite (OMMT), as
well as, by the addition of two types of compatibilizers;
polypropylene grafted with maleic anhydride (PP-g-MAH) and ABS
grafted with maleic anhydride (ABS-g-MAH). The effect of the
above treatments was investigated separately and in combination.
Increasing the PP content in ABS matrix seems to increase the
thermal stability of their blend and the glass transition temperature
(Tg) of SAN phase of ABS. From the other part, the addition of ABS
to PP promotes the formation of its β-phase, which is maximum at 30
wt% ABS concentration, and increases the crystallization temperature
(Tc) of PP. In addition, it increases the crystallization rate of PP.The
β-phase of PP in ABS/PP blends is reduced by the addition of
compatibilizers or/and organoclay reinforcement. The incorporation
of compatibilizers increases the thermal stability of PP and reduces
its melting (ΔΗm) and crystallization (ΔΗc) enthalpies. Furthermore it
decreases slightly the Tgs of PP and SAN phases of ABS/PP blends.
Regarding the storage modulus of the ABS/PP blends, it presents a
change in their behavior at about 10°C and return to their initial
behavior at ~110°C. The incorporation of OMMT to no compatibilized
and compatibilized ABS/PP blends enhances their storage modulus.
Abstract: In this work, we incorporated a quartic bond potential
into a coarse-grained bead-spring model to study lubricant adsorption
on a solid surface as well as depletion instability. The surface tension
density and the number density profiles were examined to verify the
solid-liquid and liquid-vapor interfaces during heat treatment. It was
found that both the liquid-vapor interfacial thickness and the
solid-vapor separation increase with the temperatureT* when T*is
below the phase transition temperature Tc
*. At high temperatures
(T*>Tc
*), the solid-vapor separation decreases gradually as the
temperature increases. In addition, we evaluated the lubricant weight
and bond loss profiles at different temperatures. It was observed that
the lubricant desorption is favored over decomposition and is the main
cause of the lubricant failure at the head disk interface in our
simulations.