Improving the performance of an active carbon-nitrogen adsorption cryocooler by thermal regeneration

Thermodynamic analysis was done on single and two stage active carbon nitrogen adsorption cryocoolers to study the effect of thermal regeneration on the performance. Heat regeneration within compressors operating in the same temperature range is considered. From the analysis done on 80 K cooler and 117.5 K cooler, it is found that dramatic efficiency improvement is possible with the use of compressor heat regeneration techniques.     

Natural rubber–isotactic polypropylene thermoplastic blends

Thermoplastic elastomers, prepared by melt blending of natural rubber (NR) and isotactic polypropylene (PP) through a dynamic vulcanization technique, were developed during the later 1970s. However, they have certain drawbacks due to thermal degradation and higher molecular weight of NR. In the study reported here, NR was masticated to different levels prior its addition to isotactic polypropylene to improve the flow properties and to reduce the incompatibility resulting from molecular weight mismatch of NR/PP thermoplastic blends. Mixing energy curves of uncrosslinked blends and those of dynamically vulcanized blends crosslinked using different cure systems were compared. The mixing energy curves of blends containing NR of different molecular weight (M _n) and two grades of PP (injection and film grades) were also compared. Technological and processing properties of the dynamically vulcanized (sulphur and peroxide cure systems) and unvulcanized blends were compared with those of the samples containing unmasticated NR. The results indicated that a number average molecular weight in the range 4 × 10⁵ for NR increased the procoessability without significantly affecting the technological properties of NR/PP thermoplastic blends. Among the three cure systems studied Luperox 101 and dicumyl peroxide gave better technological properties than the sulphur‐cured samples. Two antioxidants, viz. quinoline (TDQ) and imidazole (MBI) type, were tried in NR/PP blends. It was found that TDQ imparts better aging resistance compared to MBI. The improvement in processability due to the reduction in molecular weight of natural rubber by mastication is more noticeable in the case of peroxide vulcanized blends compared to sulphur vulcanized samples. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 2063–2068, 2004     

Dispersion and Setting of Powder Suspensions in Concentrated Aqueous Urea Solutions for the Preparation of Porous Alumina Ceramics with Aligned Pores

Highly concentrated alumina powder suspensions have been prepared in aqueous urea solutions of concentrations in the range 200–360 g/100 mL using an ammonium poly(acrylate) dispersant at 80°C. The dispersant concentration for the suspension viscosity minimum in the urea solutions is higher than that in water due to the higher processing temperature. The urea solutions having higher dielectric constant than that of water offer higher interparticle potential that resulted in better dispersion of the powder as evidenced from the lower viscosity and yield stress of the suspensions. The decrease in temperature increased the suspension viscosity and the suspension formed a strong gel when cooled to room temperature due to the crystallization of urea. The minimum urea solution concentration for a 55 vol% alumina suspension to form a dimensionally stable gel is 240 g/100 mL. The compressive strength and Young's modulus of the gels increased with the increase in urea solution concentration. The alumina ceramics prepared by the urea removal followed by sintering at 1500°C had porosity in the range 28–36 vol% with the rectangular rod‐shaped aligned pores.     

Synthesis of Nanocrystalline Lanthanum Strontium Manganite Powder by the Urea–Formaldehyde Polymer Gel Combustion Route

Nanocrystalline lanthanum strontium manganite (LSM) powder has been synthesized by combustion of a transparent gel obtained by the polymerization of methylol urea and urea in a solution containing La³⁺, Sr²⁺, and Mn²⁺ (LSM ions). Chemistry of the transparent urea–formaldehyde (UF) polymer gel formation and structure of the gel have been proposed such that the LSM ions act in between the growing UF polymer chains by interacting through NH, OH, and CO groups by co-ordination and prevent polymer self-assembly through inter-chain hydrogen bonding as evidenced from infrared spectrum. Thermally stable structures formed by the decomposition of UF polymer below 300°C undergo combustion in the presence of nitrate oxidant in a temperature range from 350°–450°C. A perovskite LSM phase has been formed by self-sustained combustion of the dried gel initiated with little kerosene. The powder obtained after deagglomeration and calcination at 600°C for 2 h has a D ₅₀ value of 0.19 μm, and the particles are aggregates of crystallites 10–25 nm in size.     

Low‐Density Open Cellular Silicon Carbide Foams from Sucrose and Silicon Powder

Open cellular SiC foams with low densities were prepared by thermo‐foaming and setting (130°C–150°C) of silicon powder dispersions in molten sucrose followed by pyrolysis and reaction sintering at 1500°C. The bubbles generated in the dispersion by water vapor produced by the –OH condensation was stabilized by the adsorption of silicon particles on the air‐molten sucrose interface. The composition of a sucrose‐silicon powder mixture for producing SiC foam without considerable unreacted carbon was optimized. The sucrose in the thermo‐foamed silicon powder dispersion leaves 24 wt% carbon during the pyrolysis. The sintering additives such as alumina and yttria promoted the silicon‐carbon reaction. SiC nanowires with diameters in the range of 35–55 nm and length >10 μm observed on the cell walls as well as in the fractured strut region were grown by both vapor–liquid–solid and vapor–solid mechanisms. Large SiC foam bodies without crack could be prepared as the total shrinkage during pyrolysis and reaction sintering was only ~30 vol%. The relatively low compressive strength (0.06–0.41 MPa) and Young's modulus (14.9–24.2 MPa) observed was due to the large cell size (1.1–1.6 mm) and high porosity (93%–96%).     

Carbon nanostructure grown using bi-metal oxide as electrocatalyst support for proton exchange membrane fuel cell

A novel carbon nanostructure grown by catalytic chemical vapour deposition technique has been applied as an electrocatalyst support for oxygen reduction reaction in proton exchange membrane fuel cell. The growth of carbon nanostructure (CNS) is carried over a low cost bi-metal oxide catalyst (Fe–Sn–O) synthesized by sol–gel technique. Platinum nanoparticle decoration on Fe–Sn–O incorporated CNS (CNS-FSO) is performed by ethylene glycol reduction method. The structural as well as morphological analysis confirms the formation of CNS-FSO and platinum decoration on CNS-FSO. The electrochemically active surface area (ECSA) of platinum decorated CNS-FSO (Pt/CNS-FSO) is 68 m² g⁻¹, as revealed from cyclic voltammetry. Polarization studies are carried out at different temperatures (40 °C, 50 °C and 60 °C) to exploit the oxygen reduction reaction activity of Pt/CNS-FSO. A maximum power density of 449 mW cm⁻² (without back pressure) at 60 °C shows the potential of this novel CNS-FSO as an electrocatalyst support in proton exchange membrane fuel cell.     

Larvicidal activity of green synthesized silver nanoparticles using Excoecaria agallocha L. (Euphorbiaceae) leaf extract against Aedes aegypti

Green synthesis of silver nanoparticles (AgNPs) using plant extracts has been achieved by eco‐friendly reducing and capping agents. The present study was conducted to evaluate the larvicidal efficacies of AgNPs synthesized using aqueous leaf extracts of Excoecaria agallocha against dengue vector, Aedes aegypti. The 3^rd and 4^th instar larvae of A. aegypti were exposed to various concentrations of aqueous extracts of E. agallocha, synthesized AgNPs and also crude solvent extracts (methanol and chloroform) for 24 h. The formation of AgNPs using aqueous leaf extracts was observed after 30 min with a characteristic colour change. The results recorded from UV‐Vis spectrum, XRD, FTIR, EDX, SEM and HR‐TEM were used to characterize and confirm the biosynthesis of AgNPs. The highest larvicidal efficacy of synthesized AgNPs was observed against 3^rd instar larvae at LC₅₀ 4.65 mg/L, LC₉₀ 14.17 mg/L and 4^th instar larvae with a concentration of LC₅₀ 6.10 mg/L, LC₉₀ 15.64 mg/L. A significant larvicidal activity was also observed with crude methanolic extracts against 3^rd instar larvae at a concentration LC₅₀ 41.74 mg/L, LC₉₀ 123.61 mg/L and 4^th instar larvae at a concentration of LC₅₀ 52.06 mg/L, LC₉₀ 166.40 mg/L as compared to the chloroform extract.Inspec keywords: silver, nanoparticles, nanofabrication, microorganisms, cellular biophysics, organic compounds, ultraviolet spectra, visible spectra, X‐ray diffraction, Fourier transform infrared spectra, X‐ray chemical analysis, scanning electron microscopy, transmission electron microscopyOther keywords: larvicidal activity, green synthesised silver nanoparticles, Excoecaria agallocha L. leaf extract, Aedes aegypti, plant extracts, capping agents, larvicidal efficacies, aqueous leaf extracts, excoecaria agallocha, dengue vector, Aedes aegypti, aegypti, aqueous extraction, E. agallocha, crude solvent extracts, methanol, chloroform, characteristic colour change, ultraviolet‐visible spectrum, X‐ray diffraction, Fourier‐transform infrared spectroscopy, EDX, scanning electron microscopy, high‐resolution transmission electron microscopy, AgNP biosynthesis, larvicidal efficacy, third instar larvae, instar larvae, crude methanolic extracts, chloroform extraction, time 24 h     

Preparation of a Porous Cermet SOFC Anode Substrate by Gelcasting of NiO–YSZ Powders

A porous NiO–YSZ substrate for anode-supported solid oxide fuel cells has been prepared by gelcasting of NiO–YSZ powders using urea–formaldehyde monomers, followed by humidity-controlled drying, binder removal, and sintering of the gelled bodies. The gelled bodies had sufficient strength to remove even 2-mm-thick samples from the mold immediately after gelation. A gelcast NiO–YSZ sample sintered at 1450°C for 2 h showed an open porosity of ∼53 vol%, and the porosity increased to ∼58% upon reduction with hydrogen. Pore sizes measured on the scanning electron microscopy photomicrograph of NiO–YSZ and Ni–YSZ cermet substrates are in the range of 2–5 μm. Urea–formaldehyde polymer, present in a high amount (∼13 wt%) in the gelcast body, acts as a template for pores.     

Scanning electron microscopy studies on tensile,tear and abrasion failure of thermoplastic elastomers

The tensile strength, tear resistance and abrasion resistance of four different types of commercial thermoplastic elastomers have been studied and their fracture surfaces examined by scanning electron microscopy. Thermoplastic polyurethane (TPU) showed elastic deformation under tensile fracture, whereas in 1,2 polybutadiene (1,2 PB) the fracture was initiated by craze formation and propagated by tear failure. Styrene-isoprene-styrene block copolymer (K1107) showed ductile type failure whereas in styrene-butadiene-styrene block copolymer containing a higher proportion of styrene and silica filler (K5152), the fracture occurred by shearing action. The tear failure surfaces of the thermoplastic elastomers showed different fracture patterns which could be correlated with the tear strength of the materials. The tear fracture surface of 1,2 PB showed stick-slip tear lines and that of TPU had a broad tear path with vertical striations. The fracture surfaces of K5152 and K1107 had the characteristics of laminar tearing and uninterrupted continuous tearing processes, respectively. The abrasion resistance of the samples was in the order TPU>1,2 PB>K5152, which was manifested through the type of ridge patterns formed on the abraded surfaces. Abraded surfaces of TPU, 1,2 PB and K5152 showed closely spaced stable ridges, widely spaced ridges bridged by elongated fibrils and highly deformed ridges, respectively.     

Shigella and the fluorinated quinolones

An 8-year-old girl presented with marked shortening of the right forearm due to destruction of both the radius and ulna secondary to neonatal osteomyelitis. A one-bone forearm operation was performed to achieve a stable forearm. Two years later, the one-bone forearm was lengthened for 6 months by callus distraction (callotasis) achieving 12 cm of extra length. The patient was last followed up at the age of 16. The appearance and functional outcome of the right upper limb had been improved and she was independent in all activities of daily living.