Adsorption of boron from aqueous solutions using fly ash: batch and column studies

In the present paper, boron removal from aqueous solutions by adsorption was investigated. Fly ash particle size used in adsorption experiments was between 250 and 400 microm. During the experimental part of this study, the effect of parameters such as pH, agitation time, initial boron concentration, temperature, adsorbent dosage and foreign ion on boron removal were observed. In addition, adsorption kinetics, adsorption isotherm studies and column studies were made. Maximum boron removal was obtained at pH 2 and 25 degrees C. Thermodynamic parameters such as change in free energy (DeltaG degrees), enthalpy (DeltaH degrees), entropy (DeltaS degrees) were also determined. As a result of the kinetic studies, it was observed that the adsorption data conforms to the second degree kinetics model. In the isotherm studies, Langmuir and Freundlich isotherm models were applied and it was determined that the experimental data conformed to Langmuir isotherm model. Batch adsorbent capacity (q(o)) was calculated as 20.9 mg/g. The capacity value for column study was obtained by graphical integration as 46.2 mg/g. The Thomas and the Yoon-Nelson models were applied to experimental data to predict the breakthrough curves and to determine the characteristics parameters of the column useful for process design.     

Investigation of Spin State Transition of [FeC<Subscript>17</Subscript>H<Subscript>31</Subscript>N<Subscript>7</Subscript>]<Superscript>2+</Superscript> Compound by Using the Density Functional Method

The symmetry of the [FeC₁₇H₃₁N₇]²⁺ novel compound is close to octahedral which has spin crossover properties (SCO). In this study, geometrical optimization, IR vibration frequencies, and HOMO-LUMO energy differences at various temperatures of the compound were calculated by DFT. It is realised that the computed splitting energies and splitting free enthalpies together with the mole fraction of HS state are compatible with the experiment.     

Effect of high valency cations on the (BiPb)2Sr2Ca3Cu4O12+δ compounds

We have produced the (BiPb)₂V _x Sr₂Ca₃Cu_4−y Ti _y O_12+δ compounds by a melt-quenching method. For two different sintering times (185 and 192 hours), the effects of vanadium adding and Ti doping on the structure have been investigated by electrical resistance, scanning electron micrographs (SEM), XRD patterns and magnetic hysteresis loop measurements. It has been found that the high-T _c superconducting phase, (2223), is formed in the samples annealed at 845 ^○C for 185 and 192 h, with concentration x=0.2 and y=0.05. However, with increasing Ti doping the (2223) phase gradually transforms into the (2212) phase. The hysteresis loop areas decrease with increasing Ti concentration and sintering time. Our data have indicated that the critical current, J _c , decreases with increasing magnetic field.     

Further experimental considerations on poly(dihalophenylene oxide)

The decomposition of copper(II) 2,6-dibromo-4-chlorophenoxide in acetonitrile yields poly(dihalophenylene oxide). ¹H NMR study revealed that 1,4-catenation was favoured over 1,2-catenation, leading to higher linearity in the structure.     

Cyclopolymerization of cinnamate ester derivatives of alkyl α-(hydroxymethyl) acrylates

Summary Three new monomers for cyclopolymerization were synthesized using phase transfer catalysis of ethyl -(chloromethyl) acrylate (ECMA), t-butyl -(bromomethyl) acrylate (TBBMA) and isobornyl -(bromomethyl)acrylate (IBBMA) with cinnamic acid sodium salt. Bulk and solution polymerization at 70–80°C using AIBN gave soluble cyclopolymers with Mn=13650 and Mw=36540 for the ethyl ester, Mn=47700 and Mw=86900 for the t-butyl ester and Mn=3500 and Mw=4650 for the isobornyl ester monomer. The ester polymerizabilities decreased with increasing substituent bulkiness. FTIR spectra showed ca 30 to 93% cyclic units depending on the concentration of the monomer used in polymerizations. DSC thermograms showed that alkyl group size had little effect on Tg's, with values of 151°C, 156°C, and 164°C for the ethyl, t-butyl and isobornyl esters, respectively.