Introducing a novel integrated NGL recovery process configuration (with a self-refrigeration system (open–closed cycle)) with minimum energy requirement

In this study a novel process configuration for recovery of hydrocarbon liquids from natural gas is proposed. The required refrigeration in this configuration is obtained by a self-refrigeration system (open–closed cycle). High performance of the multi-stream heat exchangers, high recovery levels of the hydrocarbon liquids and low required compression power (in the internal refrigeration section) are three of most important characteristic of the proposed configuration. The effects of the mixed self-refrigerant flow rate and pressure on the performance of the process are discussed. Various values for feed composition are tested and the results show that the process can work efficiently with different feeds. In order to analyze the need of external refrigeration by a close or open cycle that is related to the composition of the inlet gas, a configuration with external refrigeration is designed the manner that it is similar with the purposed configuration in the separation section.     

Investigation of the catalytic activity of LaBO3 (B = Ni, Co, Fe or Mn) prepared by the microwave-assisted method for hydrogen evolution in acidic medium

LaBO₃ (B = Ni, Co, Fe and Mn) were prepared by microwave-assisted citrate method. The electrocatalytic activity toward hydrogen evolution reaction (HER) was investigated. XRD characterization showed that pure perovskite crystals were indeed formed. SEM images showed that changing the type of the B-site metal ion affected the morphology of the prepared perovskites. The influence of the type of B-cation on the catalytic activity toward hydrogen evolution was studied and the order of the electrocatalytic activity was LaFeO₃ > LaCoO₃ > LaNiO₃ > LaMnO₃, that was related to the calculated values of the activation energy 51.61, 45.37, 41.15 and 55.05 kJ mol⁻¹ for LaBO₃ (B = Ni, Co, Fe and Mn), respectively. The reaction order and the reaction mechanism for all the prepared perovskites were identified. In addition, the effect of the partial substitution at the B-site in LaNi_{1 − x}Co_xO₃ was also studied. It was found that among ternary perovskites, the catalytic activity of LaNiO₃ decreased by increasing the fraction of doped-Co.     

Bond Strength of a Silicone Soft Lining Material to Poly(methyl methacrylate) Resin Treated with Maleic Anhydride and its Terpolymers

This study investigated the effectiveness of surface treatment of Poly (methyl methacrylate) (PMMA) denture base resin on tensile bond strength between PMMA/silicone-based soft liner. A total of 25 specimens were fabricated and assigned into five groups (n = 5). The surfaces of PMMA were treated with maleic anhydride, maleic anhydride-styrene-vinyl-acetate, n-butylmaleate-styrene-vinyl-acetate, or n-pentamaleate-styrene-vinyl-acetate prior to Primo adhesive primer application and silicone liner placement. The Primo adhesive primer on applied group untreated dentuse base resin served as control. The tensile test was performed using a universal testing machine. Fractured surfaces were observed under Scanning Electron Microscopy (SEM) and spectroscopic interpretation of the interfaces was done by Fourier Transform Infrared (FTIR). Test results showed that surface treatment increased interfacial strength giving the highest value for n-butylmaleate-styrene-vinyl acetate treated group. SEM micrographs revealed that the specimens with n-butylmaleate-styrene-vinyl-acetate and n-penta maleate-styrene-vinyl-acetate terpolymers underwent cohesive failure. FTIR analysis indicated secondary interactions such as hydrogen bonding, possibly on acrylic resin surfaces, caused by the use of maleic anhydride and its terpolymers, and the adhesive.     

STEM nanoanalysis of Au/Pt/Ti-Si3N4 interfacial defects and reactions during local stress of SiGe HBTs

Nanoscaled materials are attractive building blocks for hierarchical assembly of functional nanodevices, which exhibit diverse performances and simultaneous functions. We innovatively fabricated semiconductor nano-probes of tapered ZnS nanowires through melting and solidifying by electro-thermal process; and then, as-prepared nano-probes can manipulate nanomaterials including semiconductor/metal nanowires and nanoparticles through sufficiently electrostatic force to the desired location without structurally and functionally damage. With some advantages of high precision and large domain, we can move and position and interconnect individual nanowires for contracting nanodevices. Interestingly, by the manipulating technique, the nanodevice made of three vertically interconnecting nanowires, i.e., diode, was realized and showed an excellent electrical property. This technique may be useful to fabricate electronic devices based on the nanowires' moving, positioning, and interconnecting and may overcome fundamental limitations of conventional mechanical fabrication.     

Effect of filler dispersion degree on the Joule heating stimulated recovery behaviour of nanocomposites

Composites based on highly branched ethylene-1-octene copolymer (EOC) and carbon black (CB) with different dispersion degree of CB were prepared. The method of the online measured electrical conductance/resistance was used to monitor the change of the electrical conductance/resistance of the composites during the preparation processes, i.e. mixing and cross-linking. It was found that the kinetics of thermally stimulated shape-memory recovery of CB filled EOC is strongly influenced by the filler dispersion degree, which actually affects the heat transfer in the composites. Using a special arrangement of experiments the Joule heating stimulated shape-memory behaviour was quantified. CB dispersion degree and related electrical resistivity determine the extent of the Joule heating stimulated shape-memory behaviour. Composite collected at the maximum in the online measured conductance–time characteristics showed the best shape-memory effect owing to the highest electrical conductivity in the solid state. The CB filled EOC showed a negative thermal coefficient of resistivity (NTC) effect, which accelerates the temperature increase and shape-memory recovery of the composites when applying a voltage.     

Cyanoethylation of Hydroxyethyl Cellulose: Preparation and Characterization

Commercial hydroxyethyl cellulose (HEC) was cyanoethylated with acrylonitrile in nonaqueous medium in the presence of sodium hydroxide under a variety of conditions. Variables studied included the amount of acrylonitrile and the reaction temperature. The reaction was proved by NMR and its extent was measured by determining the nitrogen content. The physical properties of the obtained derivatives—i.e., the electric properties and the apparent viscosity at various rates of shear—were investigated. It was found that the extent of reaction was increased by increasing the amount of acrylonitrile as well as the reaction temperature. The products were water soluble and their apparent viscosity increased with increasing nitrogen content. The same holds true for the dielectric constant and dielectric loss.     

Modeling reaction kinetics of rigid polyurethane foaming process

A theoretical model was developed to simulate the polyurethane foaming process for a rigid foam. In the model, multiple ordinary differential equations were solved by MATLAB and the model was able to predict temperature profiles by inputting foam recipe information. This initial study on foam modeling focusses on reaction kinetic parameters that were fitted to experimental temperature data as a function of time. The modeling was able to accurately model temperature profiles of single‐polyol polyurethane formulations and was able to accurately predict temperature profiles of mixtures based on pure component kinetic parameters. A primary goal of this work is to expedite the ability to develop new foam formulations by simulation—especially for incorporation of new bio‐based polyols into formulations. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 1131‐1138, 2013