Enhanced hydrogen production with photo‐induced phase transformation and cocatalyst loading

In this study, reduced graphene oxide (RGO)‐Cd_{(1 ? x)}Zn_xS nanocomposites have been synthesized with the solvothermal method in one pot. Moreover Pt, Ru, and Rh nanoparticles have been loaded on the RGO‐Cd_{(1 ? x)}Zn_xS nanocomposites as cocatalysts with the aim of increasing the photocatalytic (PC) performance for hydrogen evolution reaction. The structure of Cd_{(1 ? x)}Zn_xS blend transforms from cubic to hexagonal structure during the PC hydrogen evolution reaction (PCHER) at the room temperature. This photo‐induced phase transformation (PIPT) enhances not only the hydrogen evolution rate, but also the stability of the photocatalysts. Interestingly, RGO triggers the PIPT process only during the PCHER under solar light illumination. On the other hand, the loading of Pt, Ru, and Rh cocatalysts do not affect the PIPT process. However, they enhance the PC and photoelectrochemical (PEC) hydrogen production activity of RGO‐Cd_{(1 ? x)}Zn_xS photocatalyst. PEC performance increases about 5.5 times when Pt (5%) and RGO are added to the Cd_0.60Zn_0.40S catalyst. RGO‐Cd_0.60Zn_0.40S including 1.5% Rh photocatalyst reaches a remarkable PC hydrogen production rate of 135 μmolh^?1 with QE of 23.3% at 460 nm. Therefore, Rh cocatalyst appears as a good alternative to Pt.     

A novel UV‐cured interpenetrating organic–inorganic hybrid polymer network based phase change materials (IPN‐PCM)

The purpose of this paper is to introduce a novel UV‐cured interpenetrating polymer networked phase change materials (IPN‐PCMs), on which no article has been found in the so far published research. Maleated castor oil (MCO) was synthesized via maleinization reaction of castor oil with maleic anhydride. Organic–inorganic hybrid interpenetrating polymer networked (IPN) materials containing both cationic and radical sections and IPN‐PCMs containing tetradecanol, hexadecanol, and octadecanol were prepared. The chemical structure of MCO and organic–inorganic hybrid IPN‐PCMs were determined by using Fourier Transform Infrared Spectroscopy (FT‐IR). Differential scanning calorimetry (DSC) was used for examining the phase‐change behaviors of the materials. Thermal stability was investigated by thermogravimetric analysis (TGA). Moreover, the surface formation of the specimen was investigated by scanning electron microscopy (SEM). In conclusion, our study proved that because of their high latent heat storage scope and high thermal stability, the obtained organic–inorganic hybrid IPN‐PCMs could be used as thermal energy storage materials. POLYM. ENG. SCI., 58:870–875, 2018. © 2017 Society of Plastics Engineers     

Efficacy of multi-mode adhesive systems on dentin wettability and microtensile bond strength of resin composite

Purpose: To evaluate the wetting ability and the microtensile bond strength of adhesive systems in various depths of dentin. Materials and Method: 48 extracted human molars cut in half in buccolingual direction. Buccal and lingual surfaces were used to obtain deep (n = 48) and superficial (n = 48) dentin. Groups were divided into 4 subgroups: Self-etch (CSE), etch&rinse (SB), multi-mode self-etch (SAU) and multimode etch&rinse (EAU) adhesive systems. 3 consecutive contact-angle measurements were obtained: T0- 3 μl drop of distilled water on dentin; T1-Droplet of the adhesive; T2- Distilled water after polymerization of the adhesive. After composite build-ups, microtensile measurements were performed. Contact angle data were analysed with analysis of variance for repeated measures. Bond strength data were analyzed by repeated measures analysis of variance, comparisons were made according to the logarithmic values (p < 0.05). Results: The difference between groups was not significant regardless of dentin depth for all measurements (p < 0.05). All groups except CSE enhanced the wetting ability of the adhesive but reduced the wetting ability of distilled water after application of the adhesive (p < 0.05). Regarding adhesive systems, the groups showed no significant difference between bond strengths to various depths of dentin except SAU (p > 0.05); in SAU, bond strength to deep dentine were significantly higher than superficial dentin (p < 0.05). Regarding adhesives’ bond strength, CSE showed significantly greater values than the other groups (p < 0.05). Conclusion: The cavity depth does not affect the bonding ability for all adhesive systems; self-etch adhesive systems might be a better choice since different adhesives may influence the wetting ability and microtensile bond strength of the dentin substrates.     

Removal of trivalent chromium from water using low-cost natural diatomite

Trivalent chromium was removed from the artificial wastewater using low-cost diatomite in batch and continuous systems. In batch system, four different sizes and five different amount of sorbent were used. The effect of the temperature on sorption was evaluated with using three different temperatures. As a result of the experiments, 85% of the trivalent chromium was removed from the wastewater in conditions of using 1.29 mm grain material at 30 °C temperature for 60 min in batch system but chromium removal was 82% at 30 °C temperature for 22 min and 97% from the wastewater at 30 °C temperature for 80 min in continuous system. Also, the equilibrium adsorption isotherms have been analyzed by Langmuir and Freundlich models. The Langmuir isotherms have the highest correlation coefficients. Langmuir adsorption isotherm constants corresponding to adsorption capacity, q₀, were found to be 28.1, 26.5 and 21.8 mg Cr³⁺/g diatomite at 15, 30 and 45 °C, respectively. Adsorption process was an exothermic process as a result of thermodynamic parameters calculations. The kinetic data of the sorption showed that the pseudo second-order equation was the more appropriate, which indicate that the intraparticle diffusion is the rate-limiting factor.     

Synthesis and Photopolymerizations of New Crosslinkers for Dental Applications

Summary: Five new crosslinkers for use in dental composites were synthesized. Four are based on TBHMA: 1 via reaction of TBBr and Bisphenol A; 2 by hydrolysis of t‐butyl groups of the first monomer to give a diacid derivative; 3 by conversion of the first monomer to an amide derivative using benzyl amine; 4 by conversion of the first monomer to amide derivative using APTES. The AHM‐based monomer 5 was synthesized from the Michael addition of APTES to AHM. The photopolymerization behaviors of the synthesized monomers with Bis‐GMA, TEGDMA and HEMA were investigated using photodifferential scanning calorimetry at 40 °C using DMPA as photoinitiator. The polymerization rates and degrees of conversion for mixtures of any of the monomers 1 – 4 with Bis‐GMA:TEGDMA were found to be similar to Bis‐GMA:TEGDMA, higher than Bis‐GMA:HEMA, and also higher than mixtures with Bis‐GMA:HEMA. The incorporation of TBHMA‐based monomers into the conventional resin mixture (Bis‐GMA and TEGDMA) reduced the polymerization shrinkages. Monomer 5 and its mixtures polymerized much faster and to higher degrees of conversion than the other investigated systems, however, this system exhibited the largest volume shrinkage.

Structures of some of the new crosslinkers synthesized.     

Transition probabilities and radiative lifetimes of levels in F I

The electric dipole transition probabilities and the lifetimes of excited levels have been calculated using the weakest bound electron potential model theory (WBEPMT) and the quantum defect orbital theory (QDOT) in atomic fluorine. In the calculations, many of transition arrays included both multiplet and fine-structure transitions are considered. We employed Numerical Coulomb Approximation (NCA) wave functions and numerical non-relativistic Hartree-Fock (NRHF) wave functions for expectation values of radii in determination of parameters. The necessary energy values have been taken from experimental energy data in the literature. The calculated transition probabilities and lifetimes have been compared with available theoretical and experimental results. A good agreement with results in literature has been obtained. Moreover, some transition probability and the lifetime values not existing in the literature for some highly excited levels have been obtained using these methods.     

The expression of anger amongst Turkish taxi drivers

The present study tested the four factor structure of the DAX on a sample of Turkish taxi drivers and the relationship these factors had with a number of other variables. Confirmatory Factor Analysis found that the data broadly fit the four factor solution of the DAX. These factors included three aggressive expressions: Verbal Aggressive Expression; Personal Physical Aggressive Expression; Use of a Vehicle to Express anger, and one Adaptive/Constructive factor. Driving experience was negatively related to the three types of aggressive expression. The Total Aggressive Expression was positively related to annual mileage and preferred driving speed, but negatively related to age and experience. The present research also found that the three aggressive types of anger expression were significantly related to potentially crash related conditions, such as losing control of the vehicle, loss of concentration and near-misses. However, none of the DAX factors was significantly related to either minor or major crashes.     

The effect of aggregation on the nonlinear optical absorption performance of indium and gallium phthalocyanines in a solution and co-polymer host

The nonlinear optical properties (NLO) of Pcs can be modified by substituting different metal atoms into the ring or altering peripheral and axial functionalities. In this study, nonlinear optical absorption properties of tetra-substituted gallium and indium phthalocyanine complexes both in solution and polymeric film have been investigated by open aperture Z-scan measurements with nanosecond pulses at 532 nm. All investigated compounds exhibited reverse saturable absorption for both solution and film experiments. The investigated compounds in the solution showed better nonlinear optical absorption properties than polymeric films. The observed nonlinear optical absorption differences depending on the aggregation are discussed using the ultrafast dynamics and decay processes of excited states found from femtosecond pump-probe spectroscopy with white light continuum experiments.