Separation and Speciation of Iron Ions by Using Colorimetric Hydrogels

In this study, Fe³⁺ ion selective N-(Rhodamine-6G)lactam-N'-acryloyl-ethylenediamine (RH6GAC) monomer was synthesized. Then, p(Acrylamide-co-N-(Rhodamine-6G)lactam-N'-acryloyl-ethylenediamine) (p(AAm-co-RH6GAC)) and p(2-hydroxyethyl- methacrylate-co- N-(Rhodamine-6G)lactam-N'-acryloyl-ethylenediamine) (p(HEMA-co-RH6GAC)) colorimetric hydrogels were synthesized by using acrylamide (AAm) and 2-hydroxyethylmethacrylate (HEMA) as primary monomers. FT-IR, SEM, polymerization yield and swelling characterizations were conducted for the resulting hydrogels. Then, these hydrogels were used in selective absorption of Fe³⁺ ions from aqueous media. The hydrogels, which could absorb Fe³⁺ ions selectively from a mixture of metal ions, were used as column packing material. The solutions containing Fe²⁺ and Fe³⁺ ions at different concentrations were separated at a rate of 97.7 ± 0.7%.     

UV-Induced Electrical and Optical Changes in PVC Blends

 2-Chloro-polyaniline (2-Cl-PANI) in its non-conducting (emeraldine base, EB) form, prepared by a chemical route, was dissolved together with poly-(vinylchloride) (PVC) in THF for casting into thin (10–50 μm) films. Upon exposure to UV radiation, the electrical conductivity of these films increased by more than 4 orders of magnitude (from 10⁻⁶ to 10⁻²S/cm). This is attributed to the dehydrochlorination of PVC by exposure to energetic photons and subsequent doping of 2-Cl-PANI (i.e. conversion to emeraldine salt, ES) by in situ created HCl. The doped films could be returned to their undoped form by exposure to NH₃ vapours. The UV-induced doping/NH₃ undoping cycles could be repeated several times. Various spectroscopic techniques were employed to follow the changes in the films upon exposure to UV radiation. The same photo-dehydrochlorination process has also been utilized for optical and/or lithographic purposes by preparing PVC blends containing methyl violet, and acid-base indicator dye. The photo-dehydrochlorination can be effectively sensitized by incorporating hydroquinone into the PVC blends containing methyl violet.     

Chaoticity analysis of the current through pure, hydrogenated and hydrophobically modified PEG-Si thin films under varying relative humidity

Polyethylene Glycol has an irregular current characteristic under constant voltage and slowly varying relative humidity. The current through a thin film of Gamma-isocyanatopropyltriethoxysilane added Polyethylene glycol (PEG-Si), its hydrogenated and hydrophobically modified forms, as a function of increasing relative humidity at equal time steps is analyzed for chaoticity. We suggest that the irregular behavior of current through PEG-Si thin films as a function of increasing relative humidity could best be analyzed for chaoticity using both time series analysis and detrended uctuation analysis; the relative humidity is kept as a slowly varying parameter. The presence of more then one regime is suggested by the calculation of the maximal Lyapunov exponents. Furthermore, the maximal Lyapunov exponent in each of the regimes was positive, thus confirming the presence of low dimensional chaos. DFA also confirms the presence of at least two different regimes, in agreement with the behavior of the maximal Lyapunov exponent in the time series analysis. We also suggest that the irregular behavior of the current through PEG-Si can be reduced by hydrogenating and hydrophobically modifying PEG-Si and the improvement in stability can be confirmed by our study.      

Adsorption behavior of linear and cyclic genetically engineered platinum binding peptides

Recently, phage and cell-surface display libraries have been adapted for genetically selecting short peptides for a variety of inorganic materials. Despite the enormous number of inorganic-binding peptides reported and their bionanotechnological utility as synthesizers and molecular linkers, there is still a limited understanding of molecular mechanisms of peptide recognition of and binding to solid materials. As part of our goal of genetically designing these peptides, understanding the binding kinetics and thermodynamics, and using the peptides as molecular erectors, in this report we discuss molecular structural constraints imposed upon the quantitative binding characteristics of peptides with an affinity for inorganics. Specifically, we use a high-affinity seven amino acid Pt-binding sequence, PTSTGQA, as we reported in earlier studies and build two constructs: one is a Cys-Cys constrained "loop" sequence (CPTSTGQAC) that mimics the domain used in the pIII tail sequence of the phage library construction, and the second is the linear form, a septapeptide, without the loop. Both sequences were analyzed for their adsorption behavior on Pt thin films by surface plasmon resonance (SPR) spectroscopy and for their conformational properties by circular dichroism (CD). We find that the cyclic peptide of the integral Pt-binding sequence possesses single or 1:1 Langmuir adsorption behavior and displays equilibrium and adsorption rate constants that are significantly larger than those obtained for the linear form. Conversely, the linear form exhibits biexponential Langmuir isotherm behavior with slower and weaker binding. Furthermore, the structure of the cyclic version was found to adopt a random coil molecular conformation, whereas the linear version adopts a polyproline type II conformation in equilibrium with the random coil. The 2,2,2-trifluoroethanol titration experiments indicate that TFE has a different effect on the secondary structures of the linear and cyclic versions of the Pt binding sequence. We conclude that the presence of the Cys-Cys restraint affects both the conformation and binding behavior of the integral Pt-binding septapeptide sequence and that the presence or absence of constraints could be used to tune the adsorption and structural features of inorganic binding peptide sequences.     

Metal-organic framework functionalized with deep eutectic solvent for solid-phase extraction of Rhodamine 6G in water and cosmetic products

An NH₂-MIL-53(Al)-DES(ChCl-Urea) nanocomposite was synthesized for extraction and determination of Rhodamine (Rh) 6G from environmental and cosmetic samples. The deep eutectic solvent (DES) was prepared by mixing choline chloride and urea in a mole ratio of 1:2. NH₂-MIL-53(Al)-DES(ChCl-Urea) nanocomposite was synthesized using the impregnation method at a ratio of 60:40 (w/w). The optimum conditions were determined after NH₂-MIL-53(Al)-DES(ChCl-Urea) characterization was performed. The optimum conditions were determined as pH 8, adsorbent amount of 15 mg, total adsorption-desorption time of 6 min, and enrichment factor of 20. The recovery values of the solid-phase extraction method for water and cosmetic samples under optimum conditions were between 95% and 106%. NH₂-MIL-53(Al)-DES(ChCl-Urea) nanocomposite was an economically advantageous adsorbent because of its reusability of 15 times. All analyses were performed using the ultraviolet-visible spectrophotometer. The linear range, limit of detection, and limit of quantification of the method were 100–1000, 9.80, and 32.68 μg/L, respectively. The obtained results showed that the synthesized nanocomposite is a suitable adsorbent for the determination of Rh 6G in water and cosmetic samples. The real sample applications were verified with the high-performance liquid chromatography system.     

A new solution algorithm for improving performance of ant colony optimization

This study proposes an improved solution algorithm using ant colony optimization (ACO) for finding global optimum for any given test functions. The procedure of the ACO algorithms simulates the decision-making processes of ant colonies as they forage for food and is similar to other artificial intelligent techniques such as Tabu search, Simulated Annealing and Genetic Algorithms. ACO algorithms can be used as a tool for optimizing continuous and discrete mathematical functions. The proposed algorithm is based on each ant searches only around the best solution of the previous iteration with β. The proposed algorithm is called as ACORSES, an abbreviation of ACO Reduced SEarch Space. β is proposed for improving ACO’s solution performance to reach global optimum fairly quickly. The ACORSES is tested on fourteen mathematical test functions taken from literature and encouraging results were obtained. The performance of ACORSES is compared with other optimization methods. The results showed that the ACORSES performs better than other optimization algorithms, available in literature in terms of minimum values of objective functions and number of iterations.     

Near-field light localization using subwavelength apertures incorporated with metamaterials

We report strong near-field electromagnetic localization by using subwavelength apertures and metamaterials that operate at microwave frequencies. We designed split ring resonators with distinct configurations in order to obtain extraordinary transmission results. Furthermore, we analyzed the field localization and focusing characteristics of the transmitted evanescent waves. The employed metamaterial configurations yielded an improvement on the transmission efficiency on the order of 27 dB and 50 dB for the deep subwavelength apertures. The metamaterial loaded apertures are considered as a total system that offered spot size conversion ratios as high as 7.12 and 9.11 for the corresponding metamaterial configurations. The proposed system is shown to intensify the electric fields of the source located in the near-field. It also narrows down the electromagnetic waves such that a full width at half maximum value of λ/29 is obtained.     

UV-Induced Electrical and Optical Changes in PVC Blends

Summary.  2-Chloro-polyaniline (2-Cl-PANI) in its non-conducting (emeraldine base, EB) form, prepared by a chemical route, was dissolved together with poly-(vinylchloride) (PVC) in THF for casting into thin (10–50 μm) films. Upon exposure to UV radiation, the electrical conductivity of these films increased by more than 4 orders of magnitude (from 10⁻⁶ to 10⁻²S/cm). This is attributed to the dehydrochlorination of PVC by exposure to energetic photons and subsequent doping of 2-Cl-PANI (i.e. conversion to emeraldine salt, ES) by in situ created HCl. The doped films could be returned to their undoped form by exposure to NH₃ vapours. The UV-induced doping/NH₃ undoping cycles could be repeated several times. Various spectroscopic techniques were employed to follow the changes in the films upon exposure to UV radiation. The same photo-dehydrochlorination process has also been utilized for optical and/or lithographic purposes by preparing PVC blends containing methyl violet, and acid-base indicator dye. The photo-dehydrochlorination can be effectively sensitized by incorporating hydroquinone into the PVC blends containing methyl violet. Received June 23, 2000. Accepted (revised) July 31, 2000