Laser-assisted preparation of C3N4/Fe2O3/Au nanocomposite: a magnetic reusable catalyst for pollutant degradation

Clean Technologies and Environmental Policy - Assorted common contaminants namely organic dyes and nitro compounds are generated by various industries and have caused alarming problems for the...     

Experimental Investigation and optimization of Process Parameters for Shear Strength of Compound Cast Bimetallic Joints

Joining of A356 alloy and magnesium was carried out by vacuum assisted sand mold compound casting process. Microstructure at the joint interface was studied by using optical microscope, scanning electron microscope, energy dispersive X-ray spectroscopy and X-ray diffractometer. Characterization indicated that a relatively uniform joint interface was obtained. The joint interface was composed of three distinct layers containing Mg₂Al₃ on aluminum side, Mg₁₇Al₁₂?+?δ eutectic structure on magnesium side and Mg₁₇Al₁₂ as middle layer. As a result of interaction between silicon, present in A356 with magnesium, Mg₂Si compound was formed. Push out test was conducted on electronics universal testing machine to measure the shear strength across the joint interface. The important process parameters (grit size of sand paper, insert temperature, pouring temperature and vacuum pressure) were optimized to maximize the shear strength. Optimization was carried out by using response surface methodology, desirability analysis and genetic algorithm (GA) techniques. It was observed that the shear strength increased by 14.21, 8.60 and 4.80% with genetic algorithm, desirability analysis and regression model respectively. GA reported the optimal value of shear strength.     

Na2CO3-Based Sorbents Coated on Metal Foil: Post Testing Analysis

Worldwide increase in energy demand coupled with a continued reliance on fossil fuel resources have contributed to a significant increase in atmospheric levels of carbon dioxide. According to the International Energy Agency’s (IEA’s) World Energy Outlook 2010 main scenario, the projected growth in energy demand will translate into a 21 % rise in energy related CO₂ emissions between 2008 and 2035, mostly due to robust economic growth in developing countries. This quantity of greenhouse gas emissions would make it next to impossible to meet a 2 ºC goal thought to avoid the worst consequences of global climate change without additional actions. Scenarios for stabilizing climate-forcing emissions suggest atmospheric CO₂ stabilization can only be accomplished through the development and deployment of a robust portfolio of solutions, of which carbon capture and sequestration represent one component. In previous work [1], Na₂CO₃/Al₂O₃ distributed on metal foil was shown to be effective for CO₂ capture. In the current work, Na₂CO₃/Al₂O₃ prepared in the powder-form and foil-form were tested in a fixed-bed reactor and characterized by X-ray diffraction, BET surface area, Raman spectroscopy and scanning electron microscopy, before and after testing, to better understand the performance of the sorbents. The powder sorbents exhibited higher performance, in general, but one of the foil samples showed the highest performance out of all the power and foil sorbents. The same sorbent was also tested for 500 cycles to understand the long-term stability.     

Development of cost-effective noncarbon sorbents for Hg(0) removal from coal-fired power plants

Noncarbonaceous materials or mineral oxides (silica gel, alumina, molecular sieves, zeolites, and montmorillonite) were modified with various functional groups such as amine, amide, thiol, urea, and active additives such as elemental sulfur, sodium sulfide, and sodium polysulfide to examine their potential as sorbents for the removal of elemental mercury (Hg(0)) vapor at coal-fired utility power plants. A number of sorbent candidates such as amine- silica gel, urea- silica gel, thiol- silica gel, amide-silica gel, sulfur-alumina, sulfur-molecular sieve, sulfur-montmorillonite, sodium sulfide-montmorillonite, and sodium polysulfide-montmorillonite, were synthesized and tested in a lab-scale fixed-bed system under an argon flow for screening purposes at 70 degrees C and/or 140 degrees C. Several functionalized silica materials reported in previous studies to effectively control heavy metals in the aqueous phase showed insignificant adsorption capacities for Hg(0) control in the gas phase, suggesting that mercury removal mechanisms in both phases are different. Among elemental sulfur-, sodium sulfide-, and sodium polysulfide-impregnated inorganic samples, sodium polysulfide-impregnated montmorillonite K 10 showed a moderate adsorption capacity at 70 degrees C, which can be used for sorbent injection prior to the wet FGD system.     

Polyaniline salts as polymer‐based solid acid catalyst for low molecular weight poly(lactic acid)

Polymer‐based solid acid catalyst, polyaniline (PANI) salt, is used for the first time to synthesize polymer. In continuation of our work to synthesize organic chemicals using PANI‐based solid acid catalyst, in this work, polylactic acid is synthesized by the condensation polymerization of lactic acid using PANI salts. PANI salts are characterized by FTIR, FE‐SEM, and TGA analyses. Polymerization of lactic acid in xylene solvent at 140°C for 24 h with the use of very low amount of PANI catalysts gave polylactic acid (PLLA) in the order: PANI‐MSA (46%) > PANI‐TFA (33%) > PANI‐Bi(OTf)₃ (27%) > PANI‐Cu(OTf)₂ (20%) > PANI‐Yb(OTf)₃ (15%). Molecular weights of PLLA synthesized using PANI‐MSA and PANI‐TFA are found to be 4385 and 4830, respectively. This methodology gives highly crystalline polymer with mushroom cap‐like morphology. Advantage of this methodology is the use of easily synthesizable, recyclable, easily handlable, cheaper, and eco‐friendly nature of the catalyst. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41147.     

Trends of biofuel cells for smart biomedical devices

Due to the increasing demand for monitoring diseases such as rising heart rate, diabetes, and ocular disorders wearable and implantable biomedical devices seems too essential for patients not only in the hospital but also at home or during working time. Researchers mostly try to offer valuable information on the conditions of patients as non-invasive, by using comfort biomedical device with a minimum side effect. So, small and self-powered with high sensitivity biomedical devices are recommended, among different power sources that introduced for devices, biofuel cells would be produced as power source for a range of medical devices because of its capability to generate sufficient power output compared to the primary power source. The nature of the electrode reaction and the nature of the biochemical reactions are some of the important parameters that are considered for the classification of fuel cells. Enzymatic biofuel cells due to high activity at mild conditions widely applied in pacemaker; glucometer; and smart contact lenses when compared to other kinds of biofuel cells. On the other hand, short lifespan is one of important limitations in this type of biofuel cells. So, the easiest way to overcome these challenges is to apply non-enzymatic ones. Recent studies have attempted to issue novel method for fabrication of non-enzymatic biofuel cell in order to produce a new generation which are inexpensive, disposable, selective, and sensitive in properties. However, consideration of researchers to the development of self-powered biomedical devices by using body fluids or providing electricity storage is rising.     

Unprecedented Selective Oxidation of Styrene Derivatives using a Supported Iron Oxide Nanocatalyst in Aqueous Medium

Iron oxide nanoparticles supported on mesoporous silica‐type materials have been successfully utilized in the aqueous selective oxidation of alkenes under mild conditions using hydrogen peroxide as green oxidant. The supported catalyst could be easily recovered after completion of the reaction and reused several times without any loss in activity (no metal leaching observed during the reaction), constituting a facile and straightforward example of aqueous oxidation chemistry promoted by iron‐based heterogeneous systems.