Kinetics of microwave‐assisted polymerization of ϵ‐caprolactone

The kinetics of polymerization of ?‐caprolactone (CL) in bulk was studied by irradiating with microwave of 350 W and frequency of 2.45 GHz with different cycle‐heating periods (30–50 s). The molecular weight distributions were determined as a function of reaction time by gel permeation chromatography. Because the temperature of the system continuously varied with reaction time, a model based on continuous distribution kinetics with time/temperature‐dependent rate coefficients was proposed. To quantify the effect of microwave on polymerization, experiments were conducted under thermal heating. The polymerization was also investigated with thermal and microwave heating in the presence of zinc catalyst. The activation energies determined from temperature‐dependent rate coefficients for pure thermal heating, thermally aided catalytic polymerization, and microwave‐aided catalytic polymerization were 24.3, 13.4, and 5.7 kcal/mol, respectively. This indicates that microwaves increase the polymerization rate by lowering the activation energy. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1450–1456, 2004     

Investigation of the effect of functionalized carbon nanotube and graphene oxide in guar gum-based mixed matrix membrane for gas separation application

The present study deals with preparing mixed matrix membranes (MMMs), a new polysaccharide-based natural polymer used as a matrix with functionalized carbon nanotubes (FCNTs) and graphene oxide (GO) used as an inorganic filler. This work identified the effect of the inorganic fillers (FCNTs or GO) with naturally occurring polymer for gas separation. The incorporation of fillers improves the gas separation performance of MMMs. In GG/FCNTs MMMs, the selectivities of CO₂/N₂ and CO₂/H₂ were enhanced by 55.24% and 57.89%, respectively. Moreover, in GG/GO MMMs, the selectivities of CO₂/N₂ and CO₂/H₂ were improved by 99.50% and 50%, respectively. The membrane was characterized by scanning electron microscopy (SEM) and Fourier-transform infrared spectroscopy (FTIR). The SEM analysis of GG/GO MMMs reveals layered structure, and GG/FCNTs MMMs create passages to transport gases. The Universal testing machine (UTM) is used to analyze the mechanical properties of pristine and modified membranes.     

White light emission from Eu co-activated Ca2Gd8Si6O26:Dy nanophosphors by solvothermalsynthesis

Ca₂Gd₈(SiO₄)₆O₂ (CGS) nanophosphors with different concentrations of single-doped Dy³⁺ ions and co-doped Dy³⁺/Eu³⁺ ions were prepared by a solvothermal synthesis. Very fine particles in the nanometer range could be achieved by this method, as evidenced by transmission electron microscope measurements. The hexagonal phase of the oxyapatite structure was confirmed by X-ray diffraction patterns. The energy transfer between Eu³⁺ and Dy³⁺ ions was investigated by photoluminescence excitation and emission properties. These phosphors had absorption bands in the UV and NUV region, which are suitable for the emission wavelength of UV or NUV light-emitting diodes (LEDs). With increasing the Eu³⁺ ion concentration, the emission peak intensity corresponding to the ⁵D₀→⁷F₂ transition increased and the yellow (⁴F_9/2→⁶H_13/2) emission intensity also increased compared to the blue (⁴F_9/2→⁶H_15/2) emission intensity due to the increased energy transfer between Dy³⁺ to Eu³⁺ ions. Thus, the Eu³⁺ ions compensated the red emission component of the Dy³⁺ doped CGS nanophosphors. Such phosphors are expected to have potential applications for NUV based white LEDs.     

High‐Performance Nanocomposites of Sodium Carboxymethylcellulose and Graphene Oxide

High‐performance nanocomposites of NaCMC with GO are produced by solution casting. FESEM images reveal a good homogeneous dispersion of GO in the NaCMC matrix. The composite formation is facilitated by H‐bonding interaction between GO and NaCMC. T_g of the composites increases with increasing GO concentration. The storage modulus (G′) exhibits a maximum 174% increase over NaCMC at 1 wt% GO. The mechanical properties of the composites exhibit highest increase of tensile stress and Young's modulus of 188 ± 4% and 154 ± 11%, respectively, for 1 wt% GO. Analysis of Young's modulus (E_y) data using the Halpin‐Tsai equation suggests that the E_y data are close to the unidirectional orientation at >0.5 wt% GO, indicating more efficient load transfer at these compositions.

     

Study on glass transition temperature and mechanical properties of cadmium sulfide/polystyrene nanocomposites

The cadmium sulfide/polystyrene (CdS/PS) nanocomposites with concentration (0, 2, 4, 6, and 8) wt% of CdS nanoparticles were prepared by solution casting method and characterized through fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM) measurements. The particle size of nanoparticles is found to be around 15 nm. Glass transition and mechanical behavior of CdS/PS nanocomposites were investigated using dynamic mechanical analyzer (DMA). The mechanical properties such as Young's modulus and tensile strength were determined at room, as well as at elevated temperatures through their stress–strain curves. The result shows that glass transition temperature (T_g) is shifted toward the higher temperature after the addition of CdS nanoparticles. The mechanical properties increased at low wt% loading of CdS nanoparticles and decreased for higher wt% loading of CdS nanoparticles. It was also found that mechanical properties decline with increase in the temperature. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

COMPARISON AND VALIDATION OF OHM AND SCEM MEASUREMENTS FOR A FULL-SCALE COAL-FIRED POWER PLANT

Mercury emission measurements were performed at a 250 MW coal-fired power plant using the Ontario Hydro method (OHM) and semi-continuous emission monitors (SCEM). Flue gas sampling was performed at the inlet of the air preheater and at the outlet of the electrostatic precipitator. The results indicated that there is some agreement between the OHM and SCEM measurements on the total mercury species. However, the SCEM results were not always in good agreement with the OHM measurements on the elemental mercury species. These discrepancies in elemental mercury concentrations are probably the result of the differences in the location of the SCEM and OHM probes, the temperature difference between the SCEM sampling probe and the flue gas, and the nonuniformities in mercury concentration over the flue gas duct cross section. The other factor that contributed to the deviation between the SCEM and OHM measurement results is the sampling method: the SCEM measurements were performed at a single point while the OHM probe was traversed over multiple points over the duct cross section and the results were averaged. The effect of the SCEM sampling probe temperature was investigated by designing a sampling probe that could be heated to the sampled flue gas temperatures. This resulted in improvements in the accuracy of the elemental mercury measurements by the SCEM system.     

Modeling of the Extraction Equilibrium of Copper from Sulfate Solutions with Acorga M5640

The extraction equilibrium of copper from sulfate media with the aldoxime Acorga M5640 in ShellSol D70 has been investigated. The distribution results were interpreted by taking into account the nonideality of the aqueous phase. The activity of copper and hydrogen ions in the target systems CuSO₄/H₂SO₄/Na₂SO₄ and CuSO₄/H₂SO₄/Fe₂(SO₄)₃/ZnSO₄ were calculated through the speciation of the aqueous solutions and by applying the Pitzer model. The experimental pH values were found in good agreement with the predicted pH values. A model considering the dimerization of the aldoxime extractant was proposed to predict the distribution ratio and the copper loading isotherms. The extraction constant at infinite dilution and the apparent dimerization constant were evaluated from the experimental data and were found to be 10^{3.06 ± 0.07} and 51 ± 9 M^?1, respectively, at 25°C.     

Use of Surfactants to Enhance the Removal of PAHs from Soil

The efficiency of soil remediation is often limited by the low aqueous solubility of Polycyclic Aromatic Hydrocarbons, PAHs. Surfactants can then be used to enhance the removal of PAHs from soils. The dissolution of pure solid deposit of benzo(a)pyrene, B(a)P, has shown that cationic surfactants are the most efficient to increase the aqueous solubility of B(a)P, when compared to neutral or anionic surfactants. In this paper we compare by using soil suspension washings, the efficiency of two surfactants (i) a cationic surfactant, the benzyldimethyl dodecylammonium bromide, BDDA, and (ii) a neutral one, the t-octylphenoxypolyethoxy ethanol, triton X-100. The losses of surfactant, by adsorption on soil or precipitation, were measured together with the release of B(a)P, chosen as a model molecule, representative of all the PAHs. The efficiency of surfactants used in blend was then compared to the efficiency of surfactants alone.     

ADSORPTIVE TREATMENT OF CYANIDE-BEARING WASTEWATER: A PROSPECT FOR SUGAR INDUSTRY WASTE

The biosorption of cyanide ions from aqueous solution by bagasse was studied in a batch adsorption system with pH, contact time, cyanide ion concentration, metal ion concentration, and adsorbent dosage as variables. XRD, FT-IR spectroscopy, CHN, proximate, ultimate, and TG/DTG thermal analyses were used for the characterization of bagasse. The biosorption capacities and rates of biosorption of cyanide ions onto bagasse were evaluated. The Langmuir and Freundlich adsorption models were applied to describe the isotherms and isotherm constants. Biosorption isothermal data were interpreted by the Langmuir model followed by the Freundlich model with maximum adsorption capacity of 98% of cyanide ion on bagasse. The kinetic experimental data were properly correlated with the first- and second-order kinetic model.