The shear bond strength of repaired high-viscosity bulk-fill resin composites with different adhesive systems and resin composite types

This study compared the effect of different adhesive systems and composite resins on the shear bond strength (SBS) of repaired high-viscosity bulk-fill composites(Tetric EvoCeram Bulk Fill) and investigated failure modes. One hundred twenty cylindrical bulk-fill composite blocks (diameter 5?mm) were fabricated and thermocycled for 5000 cycles (5–55?°C). Specimens were roughened by diamond bur and divided into 8 groups (n?=?15). Bulk-fill blocks were repaired with the same material or nanohybrid composite resin(Tetric EvoCeram Nanohybrid) (diameter 3?mm) using different adhesive systems:Tetric N-Bond Universal (TSE);37% phosphoric acid etching?+?Tetric N-Bond Universal (TER); Clearfil SE Bond (CSE); 37% phosphoric acid etching?+?Adper^TMSingle Bond 2(SB). After repair procedures, all specimens were thermocycled again. The shear bond strengths were measured for all specimens using a universal test machine (crosshead speed of 1?mm/min). Cohesive strengths of bulk-fill composites were measured and described as control group. Debonded surfaces were observed with a stereomicroscope under 10x magnification to determine mode of failure. The SBS data of all groups was statistically analyzed by two-way ANOVA and Bonferroni correction test (p?<?0.05). The specimens repaired with bulk-fill composites showed significantly higher SBS values (25.86?±?5.74, 27.05?±?4.93, 24.49?±?6.95MPa) than those with nanohybrid composites (20.41?±?3.70, 22.08?±?6.37, 18.74?±?6.40?MPa) for TER,CSE,SB, respectively (p?<?0.05). There were no significant differences in SBS according to the type of adhesive systems for both repair materials (p?>?0.05). The predominant mode of failure was a mixed type in the restorative material except for the ones repaired with nanohybrid composites using Adper^TMSingle Bond 2. High-viscosity bulk-fill composites could be successfully repaired with the same materials. SBS of repaired bulk-fill composites reached cohesive strength for all tested groups.     

The effect of innovation on productivity: evidence from Turkish manufacturing firms

This paper systematically explores the effects of firms’ innovation activities on their productivity changes for Turkish manufacturing firms, differentiating between different typologies of innovation. We employ endogenous switching methodology, controlling for endogeneity and selection bias issues, as well as analysing counterfactual scenarios. The main finding of the study points to firm heterogeneity in terms of propensity both to innovate and to benefit from innovation activities. Our results indicate that all types of innovation activity have positive effects on the productivity of firms when compared with non-innovating firms. We find robust evidence for the differential impact of innovation on firm productivity across different innovation types. Further, this relationship alters across different phases of the economy with respect to the 2008 financial crisis.     

Preparation and thermal properties of Alkoxy Silane functionalized polyether sulfone/well‐defined poly(trimethoxysilyl) propyl methacrylate‐based hybrid materials

In this study, novel polyethersulfone (PES) and poly(trimethoxysilyl) propyl methacrylate (PMPS) containing hybrid materials were prepared. PES was functionalized with trimethoxysilane groups by UV‐induced grafting reaction. PMPS was synthesized by atom transfer radical polymerization. In the followed process, the functionalized PES mixed with different amount of PMPS, thermally treated to promote sol–gel crosslinking process to prepare the PES‐based hybrid materials. The trimethoxysilane grafted PES chains are covalently bonded with the well‐defined trimethoxysilane groups of PMPS. The chemical structure of the prepared PES and PMPS is confirmed by Fourier transform infrared analysis. The morphology of the hybrids was investigated by scanning electron microscopy. The results of thermogravimetric analysis show that the thermal stability of the hybrid materials was significantly affected with the addition of PMPS. POLYM. ENG. SCI., 58:1346–1352, 2018. © 2017 Society of Plastics Engineers     

Macroanatomic,light, and electron microscopic examination of pecten oculi in the seagull (Larus canus)

The present study was conducted to determine macroanatomic characteristic as well as light and electron microscopic examination (SEM) of pecten oculi and totally 20 bulbus oculi belonging to 10 seagulls (Larus canus) were used. Pecten oculi formations consisted of 18 to 21 pleats and their shape looked like a snail. Apical length of the pleats forming pecten oculi were averagely measured as 5.77 ± 0.56 mm, retina‐dependent base length was 9.01 ± 1.35 mm and height was measured as 6.4 ± 0.62 mm. In pecten oculi formations which extend up to 1/3 of the bulbus oculi, two different vascular formations were determined according to thickness of the vessel diameter. Among these, vessels with larger diameters which are less than the others in count were classified as afferent and efferent vessels, smaller vessels which are greater in size were classified as capillaries. Furthermore, the granules which were observed intensely in apical side of the pleats of pecten oculi were observed to distribute randomly along the plica.     

Removal of copper ions from aqueous solutions by kaolinite and batch design

The removal of copper ions from aqueous solutions by kaolinite was investigated by using a batch-type method. Effects of factors such as pH, ionic strength, temperature, acid-activation and calcination on copper adsorption were investigated. The uptake of copper was determined from changes in concentration as measured by atomic absorption spectrometry. The extent of copper adsorption increased with increasing pH and temperature and with decreasing ionic strength, acid-activation and calcination temperature. The Langmuir and Freundlich adsorption models were used to determine the isotherm parameters associated with the adsorption process. The results provide support for the adsorption of copper ions onto kaolinite. Thermodynamic parameters indicated the endothermic nature of copper adsorption on kaolinite. The experimental results were applied a batch design. As a result, the kaolinite may be used for removal of copper ions from aqueous solutions.     

Production of hydrogen over bimetallic Pt–Ni/δ-Al2O3: I. Indirect partial oxidation of propane

Indirect partial oxidation (IPOX) of propane was studied over bimetallic 0.2 wt.% Pt–15 wt.% Ni/δ-Al₂O₃ catalyst in the 623–743 K temperature range. The unreduced and reduced forms of the catalyst were characterized by ESEM–EDAX and X-ray diffraction (XRD). In the IPOX tests, the effects of steam to carbon ratio (S/C), carbon to oxygen ratio (C/O₂) and residence time (W/F (g_cat h/mol HC)) on the hydrogen production activity, selectivity and product distribution were studied in detail. The effect of temperature program applied (increasing from 623 to 743 K, ITP; decreasing from 743 to 623 K, DTP) during reaction was also tested. The results showed that the Pt–Ni bimetallic system has superior performance characteristics compared to the monometallic catalysts reported in literature. The reason is thought to be the utilization of the catalyst particles as micro heat exchangers during IPOX; the heat generated by Pt sites during exothermic total oxidation (TOX) being readily transferred through the catalyst particles acting as micro heat exchangers to the Ni sites, which promote endothermic steam reforming (SR). The optimal conditions were found as S/C = 3, C/O₂ = 2.70 and W/F = 0.51 g_cat h/mol HC for IPOX of propane on the basis of high hydrogen productivity and selectivity between 623 and 748 K for the experimental conditions tested. The thermo-neutral points obtained showed the sustainability of reaction in terms of energy.     

Catalytic effect of potassium carbonate on carbothermic production of hexagonal boron nitride

Effect of potassium carbonate addition on the carbothermic formation of hexagonal boron nitride (hBN) was investigated by keeping the K₂CO₃ added B₂O₃+C mixtures in nitrogen atmosphere at 1400 °C for 40–160 min. K₂CO₃ amount was varied in the range of 10–60 wt% of the B₂O₃+C mixture. Products were subjected to XRD and quantitative analyses, SEM and TEM observations, and particle size measurement. Amount of hBN increased considerably with K₂CO₃ addition; also particle size and crystallinity improved. Catalytic role of K₂CO₃ was suggested as forming a potassium borate melt in which hBN particles form, in addition to carbothermic formation reaction. Effect of K₂CO₃ on increasing the hBN amount decreased when it was used over 40%. This was attributed to the rapid evaporation of the formed potassium borate liquid.     

Dehydration,Water Vapor Adsorption and Desorption Behavior of Zn[B3O3(OH)5] · H2O and Zn[B3O4(OH)3]

The dehydration behaviors of two different hydrated zinc borate species, Zn[B₃O₃(OH)₅] · H₂O and Zn[B₃O₄(OH)₃], which are industrially important flame retardants, were studied by thermal gravimetric(TG) analysis and in situ diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy. Dehydration onset temperatures of Zn[B₃O₃(OH)₅] · H₂O and Zn[B₃O₄(OH)₃] were 129 and 320°C, respectively, at a 10°C/min ramp rate. A very small amount of boric acid was volatilized in addition to water vapor when both samples were heated at 250°C. A significant amount of water vapor was adsorbed by Zn[B₃O₃(OH)₅] · H₂O from air at 25°C. However, Zn[B₃O₄(OH)₃] adsorbed a very small amount of water under the same conditions. Both zinc borates did not have a tendency to cake during storage.