Acrylonitrile‐butadiene‐styrene nanocomposites filled with nanosized alumina

A polymer nanocomposite was produced by acrylonitrile‐butadiene‐styrene (ABS) and α‐alumina was prepared through sol‐gel process using aluminum nitrate and citric acid. The particle size was analyzed by X‐ray diffraction and scanning electron microscopy (SEM) studies. The nanocomposites were characterized through tensile strength, Young's modulus, strain% at break, flexural strength, flexural modulus, and impact strength. The ABS/Al₂O₃ nanocomposites are found to have slightly higher Young's modulus, but lower tensile strength, strain% at break, flexural and impact strength than the virgin ABS. But its flexural modulus increases with increasing Al₂O₃ content in ABS matrix. The d‐spacing was calculated in nanocomposites to evaluate the interaction between Al₂O₃ and ABS. The particle distributions in nanocomposites were studied by SEM. The fractured surfaces of tensile test samples were also examined through SEM and show that the ductile fracture of ABS is converted to brittle fracture with addition of Al₂O₃. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers     

On the Growth and Microstructure of Carbon Nanotubes Grown by Thermal Chemical Vapor Deposition

Carbon nanotubes (CNTs) were deposited on various substrates namely untreated silicon and quartz, Fe-deposited silicon and quartz, HF-treated silicon, silicon nitride-deposited silicon, copper foil, and stainless steel mesh using thermal chemical vapor deposition technique. The optimum parameters for the growth and the microstructure of the synthesized CNTs on these substrates are described. The results show that the growth of CNTs is strongly influenced by the substrate used. Vertically aligned multi-walled CNTs were found on quartz, Fe-deposited silicon and quartz, untreated silicon, and on silicon nitride-deposited silicon substrates. On the other hand, spaghetti-type growth was observed on stainless steel mesh, and no CNT growth was observed on HF-treated silicon and copper. Silicon nitride-deposited silicon substrate proved to be a promising substrate for long vertically aligned CNTs of length 110–130 μm. We present a possible growth mechanism for vertically aligned and spaghetti-type growth of CNTs based on these results.     

Development of Iron-based Closed-Cell Foams by Powder Forging and Rolling

In the present investigation, an attempt has been made to develop in situ sandwich Fe-based foams using powder forging and rolling. Several metal carbonates are first studied by thermo gravimetric analysis to find out their suitability to be used as foaming agent for iron-based foams. Barium carbonate is found to be the most promising foaming agent among other suitable options studied such as SrCO₃, CaCO₃, MgCO₃, etc. The effects of process parameters such as precursor composition, sintering temperature, foaming temperature and time, and content of foaming agent have been studied. The microstructural characteristics of the sintered precursor have been studied by means of optical and scanning electron microscopy. It was found that a good pore structure can be obtained using 2-3% C in Fe and 3% BaCO₃ as foaming agent and by foaming at around 1350 °C for 3-6 min.     

Mechanically driven phase transformation in single phase Al62.5Cu25Fe12.5 quasi-crystals: Effect of milling intensity

In this work the effect of mechanical milling on the structure, thermal stability and hardness of single phase Al_62.5Cu₂₅Fe_12.5 icosahedral quasi-crystals has been investigated for different milling intensities. The results indicate that, irrespective of the milling intensity used, the quasi-crystals transform to a body-centered cubic (bcc) phase during milling. This transformation starts when the grain size of the QC phase is about 10 nm, which represents the critical grain size initiating the phase transformation. Upon heating the milled powder displays grain growth of the bcc phase at low temperatures, followed by transformation to the original icosahedral QC phase at higher temperatures. The phase transformations occurring during milling and subsequent annealing have a remarkable effect on the indentation hardness, which can be tuned within a wide range (7–10 GPa) as a function of the volume fractions of the different phases. This suggests that a composite material with optimized mechanical properties can be produced by appropriate thermo-mechanical treatments.     

Early‐stage oxidation behavior of Co‐rich high‐temperature alloys

The long‐term oxidation performance of an alloy is critically linked to the early‐stage oxidation behavior of high‐temperature alloys. This study investigates early‐stage oxidation behavior in terms of oxidation kinetics, scale evolution, and residual stresses developed within a scale of the commercially available cobalt‐rich alloys: HAYNES® 188, 6B, 25, and HR‐160® and a newly developed nitride‐dispersion strengthened NS‐163® alloy (HAYNES®, HR‐160®, NS‐163® are registered trademarks of Haynes International, Inc). Short‐term isothermal oxidation exposures were conducted in flowing air at 982 °C for durations of 1–50 h. Oxidation kinetics was assessed by weight‐change behavior, which showed that 188 alloy exhibited the lowest weight‐gain, while for similar times HR‐160 alloy underwent weight‐loss. SEM/EDS analysis was performed to characterize oxides formed in these alloys, while stresses developed in the oxides of different alloys were measured using synchrotron X‐ray radiation. The results in this paper clearly demonstrated the effects of alloy composition on the scale evolution and the amount of stresses developed in oxides.     

Blends of cardanol-based epoxidized novolac resin and CTBN for application in surface coating: a study on thermal,mechanical, chemical,and morphological characteristics

Blend samples of cardanol-based epoxidized novolac resin and different weight percentages of carboxyl-terminated butadiene acrylonitrile (CTBN) were developed and cured with stoichiometric amounts of aliphatic amine. The formation of various products during the curing of blend samples has been studied by Fourier-transform infrared spectroscopy. The dynamic differential scanning calorimeter scans showed that the pure epoxies and their blend samples with CTBN cured in the temperature range of 100–150°C. The blend sample containing 15 wt% CTBN showed the least cure time (at 120°C) among all other blend samples. Upon evaluation, it was found that blend samples exhibit better properties compared to pure epoxy resin in terms of increase in impact strength and elongation-at-break of the casting and gloss, scratch hardness, adhesion, and flexibility of the film. The improvement in these properties indicates that the rubber modified resin would be more durable than the epoxy based on cardanol. Chemical and morphological properties of the formulated resins were also determined. The thermal stability of the blend samples containing 15 wt% CTBN in epoxy resin was the highest among all other prepared systems. The blend morphology, studied by scanning electron microscope, showed the presence of precipitated discrete rubber particles, which dispersed throughout the epoxy matrix—i.e., they revealed the presence of two-phase morphological features.     

Identification of Natural Products as Potential Pharmacological Chaperones for Protein Misfolding Diseases

Defective protein folding and accumulation of misfolded proteins is associated with neurodegenerative, cardiovascular, secretory, and metabolic disorders. Efforts are being made to identify small-molecule modulators or structural-correctors for conformationally destabilized proteins implicated in various protein aggregation diseases. Using a metastable-reporter-based primary screen, we evaluated pharmacological chaperone activity of a diverse class of natural products. We found that a flavonoid glycoside ( C-10 , chrysoeriol-7-O-β-D-glucopyranoside) stabilizes metastable proteins, prevents its aggregation, and remodels the oligomers into protease-sensitive species. Data was corroborated with additional secondary screen with disease-specific pathogenic protein. In vitro and cell-based experiments showed that C-10 inhibits α-synuclein aggregation which is implicated in synucleinopathies-related neurodegeneration. C-10 interferes in its structural transition into β-sheeted fibrils and mitigates α-synuclein aggregation-associated cytotoxic effects. Computational modeling suggests that C-10 binds to unique sites in α-synuclein which may interfere in its aggregation amplification. These findings open an avenue for comprehensive SAR development for flavonoid glycosides as pharmacological chaperones for metastable and aggregation-prone proteins implicated in protein conformational diseases.     

CO2 Hydrogenation over Ru-NPs Supported Amine-Functionalized SBA-15 Catalyst: Structure–Reactivity Relationship Study

Catalysis Letters - We gave an effective protocol to support Ru NPs on amine-functionalized SBA-15 mesoporous silica to catalyze the CO2 hydrogenation reaction. The amine groups present in the...     

On the computer simulation of the P–C isotherms of ZrFe2 type hydrogen storage materials

This paper deals with computer simulation of the P–C isotherms of some ZrFe₂ type (Zr(Fe_1−xCr_x)₂, Zr_1−xTi_xFe_1.4Cr_0.6, Zr_1−2xMm_xTi_xFe_1.4Cr_0.6 : x00.4) of hydrogen storage materials. A feasible mathematical model has been developed to simulate the P–C isotherms. The randomized variables in the model applied for simulating the P–C isotherms of the above-mentioned ZrFe₂ type hydrogen storage materials correspond to change in enthalpy (ΔH) and entropy (ΔS) of hydride formation. Several ZrFe₂ type materials as in above have been synthesized and their P–C isotherms, enthalpy and entropy change has been evaluated experimentally in order to have input data for simulation. A special software was developed to simulate the P–C isotherms using the said model. A close match between the experimentally observed and simulated P–C isotherms for the above said ZrFe₂ type alloys has been obtained.     

Modeling mineral phase change chemistry of groundwater in a rural-urban fringe

This research paper aims to determine the genetic origin of the chemical elements in groundwater. It deals with the results of physicochemical parameters, to evaluate the hydro-geochemistry of groundwater in rural-urban fringe of district Bareilly, India. Pre- and post-monsoon sampling has been carried out, which reveals inter-seasonal variability effect on the hydro-geochemical processes. Geochemical modeling especially computation of saturation index was undertaken using the WATEQ4F model. Majority of samples fall in the category of undersaturation, which further suggests that groundwater still has potential to dissolve more minerals. Chemical categorizations of groundwater samples were performed with the help of the Aquachem model. Grouping of groundwater on the Piper diagram reveals a common composition and origin. In most of the area, water facies is of Ca(2+)-HCO(3)(-) type in both the seasons. It also indicates that in pre-monsoon, ion exchange is the dominant process, whereas in post-monsoon, both ion exchanges as well as reverse ion exchanges are reported in the groundwater of the study area.