Grafting of ion-imprinted polymers on the surface of silica gel particles through covalently surface-bound initiators: a selective sorbent for uranyl ion

A new ion imprinted polymer coated silica gel sorbent has been prepared using the radical "grafting from" polymerization method through surface-bound azo initiators for selective uranyl uptake. The introduction of azo initiator onto the silica surface was achieved by the reaction of surface amino groups with 4,4'-azobis(4-cyanopentanoic acid chloride). The grafting step was then carried out in a stirred solution of initiator-modified silica particles in the presence of uranyl ion and functional and cross-linking monomers. The prepared sorbent was characterized using FT-IR spectroscopy, scanning electron microscopy (SEM), elemental analysis (EA), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and BET adsorption isotherm analysis. The influence of the uranyl concentration, pH, and flow rate of solution on the grafted polymer affinity has been investigated. Maximum uptake of uranyl ion was observed at a pH 3.0. The rebinding behavior of the sorbent has been successfully described by the Langmuir-Freundlich isotherm. The dynamic column capacity of sorbent and enrichment factor for uranyl ion were 52.9 +/- 3.4 micromol g(-1) and 52, respectively. It was found that imprinting results in increased affinity of the sorbent toward uranyl ion over strong competitor metal ions such as Fe(III) and Th(IV). The sorbent was repeatedly used and regenerated for 3 months without any significant decrease in polymer binding affinities. Finally the sorbent was applied to the preconcentration and determination of uranyl ion in real water samples.     

Highly selective and sensitive voltammetric sensor based on modified multiwall carbon nanotube paste electrode for simultaneous determination of ascorbic acid,acetaminophen and tryptophan

A carbon-paste electrode modified with multiwall carbon nanotubes (MWCNTs) was used for the sensitive and selective voltammetric determination of ascorbic acid (AA) in the presence of 3,4-dihydroxycinnamic acid (3,4-DHCA) as mediator. The mediated oxidation of AA at the modified electrode was investigated by cyclic voltammetry (CV), chronoamperommetry and electrochemical impedance spectroscopy (EIS). Also, the values of catalytic rate constant (k), and diffusion coefficient (D) for AA were calculated. Using square wave voltammetry (SWV), a highly selective and simultaneous determination of AA, acetaminophen (AC) and tryptophan (Trp) has been explored at the modified electrode. The modified electrode displayed strong function for resolving the overlapping voltammetric responses of AA, AC and Trp into three well-defined voltammetric peaks. In the mixture containing AA, AC and Trp, the three compounds can well separate from each other with potential differences of 200, 330 and 530 mV between AA and AC, AC and Trp and AA and Trp, respectively, which was large enough to determine AA, AC and Trp individually and simultaneously.     

Influence of the Polyvinyl Pyrrolidone Concentration on Particle Size and Dispersion of ZnS Nanoparticles Synthesized by Microwave Irradiation

Zinc sulfide semiconductor nanoparticles were synthesized in an aqueous solution of polyvinyl pyrrolidone via a simple microwave irradiation method. The effect of the polymer concentration and the type of sulfur source on the particle size and dispersion of the final ZnS nanoparticle product was carefully examined. Microwave heating generally occurs by two main mechanisms: dipolar polarization of water and ionic conduction of precursors. The introduction of the polymer affects the heating rate by restriction of the rotational motion of dipole molecules and immobilization of ions. Consequently, our results show that the presence of the polymer strongly affects the nucleation and growth rates of the ZnS nanoparticles and therefore determines the average particle size and the dispersion. Moreover, we found that PVP adsorbed on the surface of the ZnS nanoparticles by interaction of the C–N and C=O with the nanoparticle’s surface, thereby affording protection from agglomeration by steric hindrance. Generally, with increasing PVP concentration, mono-dispersed colloidal solutions were obtained and at the optimal PVP concentration (5%), sufficiently small size and narrow size distributions were obtained from both sodium sulfide and thioacetamide sulfur sources. Finally, the sulfur source directly influences the reaction mechanism and the final particle morphology, as well as the average size.     

A novel water perm-selective membrane dual-type reactor concept for Fischer-Tropsch synthesis of GTL (gas to liquid) technology

The present study proposes a novel configuration of Fischer-Tropsch synthesis (FTS) reactors in which a fixed-bed water perm-selective membrane reactor is followed by a fluidized-bed hydrogen perm-selective membrane reactor. This novel concept which has been named fixed-bed membrane reactor followed by fluidized-bed membrane reactor (FMFMDR) produces gasoline from synthesis gas. The walls of the tubes of a fixed-bed reactor (water-cooled reactor) of FMFMDR configuration are coated by a high water perm-selective membrane layer. In this new configuration, two membrane reactors instead of one membrane reactor are developed for FTS reactions. In other words, two different membrane layers are used. In order to investigate the performance of FMFMDR, a one-dimensional heterogeneous model is taken into consideration. The simulation results of three schemes named fluidized-bed membrane dual-type reactor (FMDR), FMFMDR and conventional fixed-bed reactor (CR) are presented. They have been compared in terms of temperature, gasoline and CO₂ yields, H₂ and CO conversions and the water permeation rate through the membrane layer. Results show that the gasoline yield in FMFMDR is higher than the one in FMDR. The FMFMDR configuration not only decreases the undesired product such as CO₂ but also produces more gasoline.     

Synthesis,characterization and TL properties of SrSO_4:Dy,Tb nanocrystalline phosphor

SrSO4:Dy,Tb nanocrystalline with crystalline size in the range of 44–54 nm was prepared by co-precipitation method followed by thermal treatment and characterized by X-ray diffraction(XRD), scanning electron microscopy(SEM), energy dispersive X-ray spectroscopy(EDX) and UV-visible spectrometry. Our results provided direct evidence of incorporation of impurities into nanocrystalline SrSO4. The thermoluminescence(TL) properties of SrSO4:Dy,Tb nanocrystalline pellets irradiated with gamma rays at different doses were studied. The TL glow curve of SrSO4:Dy,Tb nanocrystalline pellets had a prominent peak at around 490 K and a small peak at around 430 K. The major peak in the TL glow curve was almost resolved from other peaks, which was analyzed using Chen's peak shape method to determine the TL kinetic parameters such as activation energy, E and kinetic order, b. The intensity of main dosimetric peak of SrSO4:Dy,Tb nanocrystalline pellets at around 490 K increased linearly with the increase in gamma dose. The TL response was linear in the range of 0.1–7 kGy. These properties made it a candidate as a dosimeter to be used for estimating the high dose of gamma rays.     

Recent advantages in the metal (bulk and nano)-catalyzed S-arylation reactions of thiols with aryl halides in water: a perfect synergy for eco-compatible preparation of aromatic thioethers

Transition-metal-catalyzed C–S cross-coupling reactions comprise one of the most efficient methods for the synthesis of biologically and synthetically important aryl sulfide derivatives. Among the various solvents used in this cross-coupling reaction (ionic liquids, water, organic, and aqueous biphasic solvents), neat water have attracted notable interest in recent years due to its properties such as non-toxicity, non-flammability, renewability, and widely availability compared with other solvents. Since several catalytic systems for this green synthesis of aryl sulfides have been reported from 2007 to present, a comprehensive review on this interesting field seems to be timely. In this study, we discuss the most representative and interesting reports on the synthesis of aryl sulfides via metal-catalyzed cross-coupling of thiols with aryl halides in water. Mechanistic aspects of the reactions are considered and discussed in detail.     

Microwave Absorption Properties of Polyaniline/Carbonyl Iron Composites

In this work, carbonyl iron (CI) containing polya- niline composites (PANI+CI) were prepared via in-situ polymerization of aniline in an aqueous solution containing different amounts of CI as the magnetic filler for the micro- wave absorbers. The incorporation of the magnetic powder to the PANI matrix was confirmed by X-ray diffraction (XRD), IR and SEM. Synthesized PANI+CI composite particles were subsequently added to an epoxy resin matrix to produce related R-PANI+CI composites. Study of thermal properties by thermogravimetric analysis revealed enhanced thermal stability of the composites. The electromagnetic-absorbing properties were studied by measuring the reflection loss in the frequency range of 8.0 to 12.0 GHz. The experimental results indicated that the electromagnetic wave absorbing properties of PANI+CI composites are dependent on the PANI/CI weight ratio. The good reflection loss of the composite at the optimum PANI/CI weight ratio of 1:6 suggests its potential applicability as a good radar absorber.     

FORCE TRANSDUCER MODELING OF RECTANGULAR,V–SHAPED,AND DAGGER CANTILEVER PROBES BASED ON ATOMIC FORCE MICROSCOPY

Real-time monitoring of the nano-particle manipulation process by atomic force microscope (AFM) is almost impossible since the manipulator of the AFM is used as either the imaging or manipulation tool at a given instant. As one approach to this problem, researchers scan the area where the target particle exists, before and after the nano-manipulation. Thus, by using some fixed reference features, the new relative position of the particle is obtained from the images. However, this imaging is offline, and unexpected problems during nano-manipulation process cannot be detected. In this article, force transducer of the AFM rectangular, V-shaped, and dagger cantilevers, which convert the three-dimensional deflections measured by the detection system to corresponding three-dimensional force, are modeled and compared. So there would be a feedback from the real-time force system during nano-manipulation process, which can be utilized for better understanding and reliable handling of nano-particles. Furthermore, the manipulation forces are affected directly by spring constants of cantilever. Hence, the cantilever is the most significant and sensitive component of the AFM. Therefore, variations of the lateral, longitudinal, and normal spring constants of the mentioned cantilever for different geometrical parameters are analyzed and discussed.     

Variants in the PPARGC1A Gene may Influence the Effect of Fat Intake on Resting Metabolic Rate in Obese Women

Recent studies have shown that dietary intake and genetic variants play a decisive role in the risk of obesity. Therefore, this study was designed to examine the interaction between dietary fat and PPARGC1A polymorphisms on the level of resting metabolic rate (RMR). We enrolled 288 Iranian overweight and obese women in this cross‐sectional study. We sequenced the 648 b.p. DNA in Exon 8 of PPARGC1A gene. We analyzed the two single‐nucleotide polymorphisms, namely rs11290186 and rs2970847, in this region. All participants were assessed for RMR, dietary intake, and body composition. This study demonstrated that total cholesterol and insulin levels were positively associated with T allele carriers of rs2970847. Moreover, the A‐deletion allele carrier of the rs11290186 genotype had higher triacylglycerol and insulin concentrations. The current study revealed that, after adjustment for energy intake, the AA genotype of PPARGC1A (rs11290186) had a direct association with polyunsaturated fatty acids and linoleic acid intakes. Another important finding in our study was that there was an interaction seen between fat and saturated fatty acids intake with the PPARGC1A genotypes. Women with fat intakes of more than 30% of calorie intake per day and the A‐deletion genotype had a lower RMR and RMR/fat free mass (FFM). It seems that the PPARGC1A polymorphisms lead to the downregulation of insulin signaling and subsequently insulin resistance. In addition, the interactions between the PPARGC1A polymorphisms (rs11290186) and the level of dietary fat intake probably can have an effect on RMR and RMR/FFM in obese women.