Redox-responsive degradable PEG cryogels as potential cell scaffolds in tissue engineering

A Michael addition strategy involving the reaction between a maleimide double bond and amine groups is investigated for the synthesis of cryogels at subzero temperature. Low-molecular-weight PEG-based building blocks with amine end groups and disulfide-containing building blocks with maleimide end groups are combined to synthesize redox-responsive PEG cryogels. The cryogels exhibit an interconnected macroporous morphology, a high compressive modulus and gelation yields of around 95%. While the cryogels are stable under physiological conditions, complete dissolution of the cryogels into water-soluble products is obtained in the presence of a reducing agent (glutathione) in the medium. Cell seeding experiments and toxicologic analysis demonstrate their potential as scaffolds in tissue engineering.     

A quintic B-spline finite-element method for solving the nonlinear Schr?dinger equation

The nonlinear Schr?dinger equation is numerically solved using the collocation method based on quintic B-spline interpolation functions. The efficiency and robustness of the proposed method are demonstrated by standard test problems, such as a one-soliton solution, interaction of two solitons, and formation of a soliton. This method is compared with both the analytical and numerical techniques in the computational section.     

A comparison of electromigration failure of metal lines with fracture mechanics

Atoms constructing an interconnecting metal linein a semiconductor device are transported by electron flowin high density.This phenomenon is called electromigration,which may cause the line failure.In order to characterize theelectromigration failure,a comparison study is carried outwith some typical phenomena treated by fracture mechanicsfor thin and large structures.An example of thin structures,which have been treated by fracture mechanics,is silica optical fibers for communication systems.The damage growth ina metal line by electromigration is characterized in comparison with the crack growth in a silica optical fiber subjectedto static fatigue.Also a brief comparison is made betweenthe electromigration failure and some fracture phenomena inlarge structures.     

Accuracy of the Sampling Moiré Method and its Application to Deflection Measurements of Large-Scale Structures

Measuring accurate displacement distributions for large-scale structures is an important issue and a very challenging task. Recently, a simple and accurate phase measurement technique called sampling moiré method [Exp Mech 50–4:501–508, (2010)] has been developed for small-displacement distribution measurements. In this method, the phase distribution of moiré fringes can be analyzed from a single grating image by simultaneously performing down-sampling image processing and intensity-interpolation to generate multiple phase-shifted moiré fringe images. In addition, the phase of the original grating can also be obtained from the phase of the moiré fringe by adding the phase of the sampling grating. In this study, the measurement accuracy of the sampling moiré method was analyzed through computer simulations and a displacement measurement experiment. Four factors of the sampling moiré method were investigated, including the sampling pitch, the order of the intensity-interpolation, random noise, and the form of grating. The results show that determining the optimal sampling pitch is an important factor for obtaining better results but it is not critical. In addition, a practical application of the sampling moiré method is presented that involves a deflection measurement on a 10-meter-long crane. The experimental results demonstrate that submillimeter deflections of the crane can be successfully detected.     

Eco‐friendly Sensors Developed by Herbal Based Silver Nanoparticles for Electrochemical Detection of Mercury (II) Ion

In our study, the single‐use & eco‐friendly electrochemical sensor platform based on herbal silver nanoparticles (AgNPs) was developed for detection of mercury (II) ion (Hg²⁺). For this purpose, the surface of pencil graphite electrode (PGE) was modified with AgNPs and folic acid (FA), respectively. The concentrations of AgNPs and FA were firstly optimized by differential pulse voltammetry (DPV) to obtain an effective surface modification of PGE. Each step at the surface modification process was characterized by using cyclic voltammetry (CV) and electrochemical impedence spectroscopy (EIS). The limit of detection (LOD) for Hg²⁺ was estimated and found to be 8.43 μM by CV technique. The sensor presented an excellent selectivity for Hg²⁺ against to other heavy metal ions such as Ca²⁺, Cd²⁺, Cr³⁺, Cu²⁺, Mg²⁺, Ni²⁺, Pb²⁺, Zn²⁺, Co²⁺ and Mn²⁺. Moreover, a rapid, selective and sensitive detection of Hg²⁺ was successfully performed in the samples of tap water within 1 min.     

Supramolecular Coordination of Pb2+ Defects in Hybrid Lead Halide Perovskite Films Using Truxene Derivatives as Lewis Base Interlayers

Truxene derivatives, due to their molecular structure and properties, are good candidates for the passivation of defects when deposited onto hybrid lead halide perovskite thin films. Moreover, their semiconductor characteristics can be tailored through the modification of their chemical structure, which allows-upon light irradiation- the interfacial charge transfer between the perovskite film and the truxene molecules. In this work, we analysed the use of the molecules as surface passivation agents and their use in complete functional solar cells. We observed that these molecules reduce the non-radiative carrier recombination dynamics in the perovskite thin film through the supramolecular complex formation between the Truxene molecule and the Pb²⁺ defects at the perovskite surface. Interestingly, this supramolecular complexation neither affect the carrier recombination kinetics nor the carriers collection but induced noticeable hysteresis on the photocurrent vs voltage curves of the solar cells under 1 sun illumination.     

Degradation of substituted phenols with different oxygen sources catalyzed by Co(II) and Cu(II) phthalocyanine complexes

Research on substituted phenol degradations has received substantial attention. In this work, effective Co(II) and Cu(II) phthalocyanine complexes as catalysts were studied to degrade toxic phenols to harmless products. The effect of various process parameters, such as initial concentration of phenol, catalyst, oxygen sources, and temperature on the degradation reaction was investigated to achieve maximum degradation efficiency. The catalytic activities of Co(II) and Cu(II) phthalocyanines were evaluated for oxidation of phenolic compounds such as p-nitrophenol, o-chlorophenol, 2,3-dichlorophenol, and m-methoxyphenol. Co(II) phthalocyanine displayed good catalytic performance in degradation of 2,3-dichlorophenol to 2,3-dichlorobenzaldehyde and 2,3-dichloro-1,4-benzoquinone with the highest TON and TOF values within 3?h at 50?°C. The fate of catalyst during the degradation process was followed by UV–Vis spectroscopy.     

A theoretical study on calculation of absolute hydration enthalpies for some univalent ions

Using the total radius of alkaline fluorides and sodium halides and their experimental total enthalpy values, absolute hydration enthalpies of sodium and fluoride ions ( and ) were previously calculated. Also, by the help of data of sodium and fluoride ions for all alkaline metal ions and halides absolute hydration enthalpies were determined.

In-situ Study on the Fatigue Process of Metals by HVEM

In-situ fatigue test on pre-fatigued aluminum single crystals and also in-situ tensile test of pre-fatigued copper-2 at.% aluminum alloy single crystals were carried out in an HVEM. In the Al crystals, forward and backward motion of dislocations, change of cell structures, formation of voids and crack propagation were directly observed in-situ by an HVEM under alternating stress. In the Cu-Al crystals, it was observed that slip occurred only in the part of the persistent slip bands during in-situ tensile deformation in an HVEM.     

A new high‐performance blue to transmissive electrochromic material and use of silver nanowire network electrodes as substrates

Synthesis of a novel, high‐performance blue to transmissive switching electrochromic material is described. The polymer (P1) was prepared by both electrochemical ( P1E ) and chemical ( P1C ) means from the corresponding monomer. The electrochemically synthesized polymer ( P1E ) revealed 64% optical contrast change (on ITO) in the visible region and very fast switching times of 0.32 s (coloration) and 0.90 s (bleaching). On the other hand, the chemically synthesized, solution processable polymer ( P1C ) also showed a high optical contrast value (49%, on ITO) with very fast switching times of 0.86 s for coloration and 0.57 s for bleaching. These high optical contrast values coupled with fast switching times place these materials along with high‐performance blue to transmissive electrochromic polymers. Significantly, these improved characteristics were achieved by side chain engineering of a known, inferior blue to transmissive polymer, PBEBT. Towards fabrication of flexible electrochromic devices, the performance of P1C was also tested on silver nanowire network electrodes. Even though the full potential of the material could not be demonstrated, a good optical contrast of 24% was achieved using these electrodes. Under the same potential range allowed by silver nanowire network electrodes, P1C on ITO showed an optical contrast of 30%. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 1680–1686