Galactitol hexa stearate and galactitol hexa palmitate as novel solid-liquid phase change materials for thermal energy storage

Galactitol has a melting point of 187.41 °C and a fusion enthalpy of 401.76 J g⁻¹. Its melting temperature is not suitable for many thermal energy storage applications although it has good latent heat storage capacity compared to the several traditional phase change materials (PCMs). The galactitol also has high supercooling degree as about 72 °C. These unfavorable properties limit the usage potential of galactitol in thermal energy storage applications. However, the phase change temperature and supercooling degree of galactitol can be reduced to a reasonable value and therefore its feasibility for energy storage systems can be increased. For this aim, in this study, galactitol hexa stearate (GHS) and galactitol hexa palmitate (GHP) were prepared as novel solid-liquid PCM by means of esterification reaction of the galactitol with palmitic acid and stearic acid. The GHP and GHS esters were characterized chemically using FT-IR and ¹H NMR techniques. By using DSC analysis method, the melting temperature and latent heat value of the PCMs were determined as 31.78 °C and 201.66 J g⁻¹ for GHP ester and 47.79 °C and 251.05 J g⁻¹ for GHS ester. Thermal cycling test showed that the prepared PCMs had good thermal reliability after thermal 1000 melting-freezing cycles. Thermogravimetric analysis (TGA) results revealed that the PCMs have good thermal stability over their working temperatures. In addition, thermal conductivity of the prepared PCMs was increased as about 26.3% for GHP and 53.3% for GHS by addition of 5 wt.% expanded graphite. Based on all results it can be concluded that the prepared GHP and GHS esters can be considered as promising solid-liquid PCMs for many energy storage applications such as solar energy storage, indoor temperature controlling in buildings, production of smart textile and insulation clothing due to their good energy storage properties.     

Thermodynamic and economic optimization of a MCFC-based hybrid system for the combined production of electricity and hydrogen

In this paper, a biogas fuelled power generation system is considered. The system is based on a molten carbonate fuel cell (MCFC) stack integrated with a micro gas turbine for electricity generation, coupled with a pressure swing absorption system (PSA) for hydrogen production.     

Fracture toughness of alumina/lanthanum titanate laminate composites with a weak interface

Layers of lanthanum titanate (La₂Ti₂O₇) and α-alumina (α-Al₂O₃) were employed to form a layered composite in order to improve the fracture toughness of monolithic alumina. The composites were produced by two different processing methods. In the first, individually presintered pellets of α-Al₂O₃ and La₂Ti₂O₇ were stacked together and hot-forged. In the second, tape cast molten salt La₂Ti₂O₇ and dense α-Al₂O₃ were stacked together and hot-forged. The forged composite samples were investigated by optical microscopy, scanning electron microscopy (SEM), Vickers indentation and three-point bending. During the hot-forging process, an interphase, aluminum titanate (Al₂TiO₅) was found to form as a result of the reaction between α-Al₂O₃ and La₂Ti₂O₇. The flexural strength and the fracture toughness of the resulting laminate composites were found to be 320 MPa and 7.1 MPa m^1 / 2, respectively. Indentation experiments showed that the newly formed Al₂TiO₅ at the interface is sufficiently weak to promote crack deflection and hence increase the fracture energy and mechanical properties of the composite.     

Comparison of the Effects of Statins on A549 Nonsmall-Cell Lung Cancer Cell Line Lipids Using Fourier Transform Infrared Spectroscopy: Rosuvastatin Stands Out

Statins are commonly prescribed antilipidemic and anticholesterol class of drugs. In addition to their major role, they have been found to have anticancer effects on in vitro, animal and clinical studies. The aim of this study was to investigate the effects of six different statins (rosuvastatin, pravastatin, simvastatin, lovastatin, fluvastatin, and atorvastatin) on A549 cancer cells lipids by Fourier transform infrared (FTIR) spectroscopy. Proliferation tests were carried out to detect the half-maximal inhibitory concentrations (IC₅₀) of each statin on A549 cells. The IC₅₀ values were 50 μM for simvastatin, 150 μM for atorvastatin and pravastatin, and 170 μM for fluvastatin, 200 μM for rosuvastatin and lovastatin on A549 cells. No correlation was found between the antiproliferative effects of the statins and lipid-lowering effect. The cells were treated with IC₅, IC₁₀, and IC₅₀ values of each statins concentration and lipid extracts were compared using FTIR spectroscopy. The results indicated that different statins had different effects on the lipid content of A549 cells. The FTIR spectra of the lipid exctracts of statin-treated A549 cells indicated that the value of hydrocarbon chain length, unsaturation index, oxidative stress level, and phospholipid containing lipids increased except for rosuvastatin-treated A549 cells. In addition, rosuvastatin significantly lowered cholesterol ester levels. In conclusion, the contrasting effects of rosuvastatin should be further investigated.     

Determination of Phthalate Residues in Different Types of Yogurt by Gas Chromatography-Mass Spectrometry and Estimation of Yogurt-Related Intake of Phthalates

Phthalates are potential endocrine-disrupting chemicals, found widely in the environment, and commonly used to make plastics softer and more flexible. Little information is available about the presence of phthalates in yogurt products sold on the world market. This study aimed to develop a sensitive GC-MS method for the determination of selected phthalates in yogurt and residue levels in fruit yogurts together with the packaging materials and to estimate a yogurt-related exposure to phthalates in the Turkish population. Acetonitrile extraction followed by cleanup procedures using different adsorbents yielded relatively clean extracts. The presence as the percent of selected phthalates tested—dibutyl phthalate (DBP), diethylhexyl phthalate (DEHP), dimethyl phthalate (DMP), diethyl phthalate (DEP), di-n-octyl phthalate (DNOP), and benzyl butyl phthalate (BBP)—were determined as 76, 70, 70, 54, 20, and 8% of the samples, respectively, for the phthalates, ranging from <LOQ to 1640 μg/kg. The highest concentrations were found in cherry yogurt among the fruit yogurts, while banana and pineapple yogurts contained the least. The results indicate that the estimated daily intakes for phthalates were below tolerable daily intakes.     

Characterization of N, N′-bis-2-(1-hydoxy-4-methylpentyl)-3, 4, 9, 10-perylene bis (dicarboximide) sensitized nanocrystalline TiO2 solar cells with polythiophene hole conductors

We have fabricated solid-state, dye-sensitized nanocrystalline TiO₂ solar cells (DSSC) based on perylene derivative dye, N,N′-bis-2-(1-hydoxy-4-methylpentyl)-3,4,9,10-perylene bis (dicarboximide) (HMPER) with two different polythiophenes as hole conductors; i.e. poly (3-octyl thiophene) (P3OT) and poly (3-hexyl thiophene) (P3HT), respectively. HMPER adsorbs strongly to the surface of nanocrystalline TiO₂ and inject electrons into TiO₂ conduction band upon absorption of light. Polythiophene derivatives are well-known materials as hole conductors in solid-state dye-sensitized solar cells. We obtained quite similar results with P3OT and P3HT yielding a short-circuit current density of around 80 μA/cm² and open-circuit voltage of around 0.7 V at 80 mW/cm² AM 1.5 light intensity. The results are compared with Ru-535 TBA-sensitized nc-TiO₂ cells prepared by using the same polythiophene derivatives.     

Effects of pore morphology and size on antimicrobial activity of chitosan/poly(ethylene glycol) diacrylate macromer semi‐IPN hydrogels

The objective of this study was to obtain antibacterial active chitosan/poly(ethylene glycol) diacrylate macromere (CS/PEGM) semi‐IPN hydrogels near a neutral pH level by changing their pore size and morphology. These hydrogels were prepared from CS and PEGM with different molecular weights in the presence of pore‐forming agents, poly (ethylene glycol) (PEG) or sodium bicarbonate (NaHCO₃), by using two different initiator system, namely chemical or UV. A combination of CS with PEG or NaHCO₃ in the presence of PEGM could be able to create desired pore formation in both initiator systems. The antibacterial activity of hydrogels changed with the molecular weight (g/mol) of PEGM in the order 2000>400>8000. A chemical initiation system was found more suitable than the UV initiation system for antibacterial activity. Hydrogels showing the highest antibacterial activity on Staphylococcus aureus and Escherichia coli have medium or distributed pore size and interconnected pores. Hydrogels prepared with PEGM (M_n: 2000 g/mol) were proposed for antibacterial wound dressing and soft tissue regeneration applications owing to their antibacterial activity and elastic modulus. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42707.     

Eco-friendly approach on wool pretreatment and effect on the wool structure and dyeability

This research investigated the effect of various proteolytic enzymatic pretreatment on morphological and chemical features and the dyeability properties of wool fibres. Scoured merino wool fibres are treated with protease, papain, trypsin, and pepsin in specified conditions. Each enzyme activity measurement was provided by appropriate methods such as Bradford, BAPNA (N-benzoyl-1-arginine-p-nitroanilide), and BSA (Bovine Serum Albumin). Enzymatic processes were carried out for 24 h in the incubator set at 40°C, 100 rpm, and specified pH with 1 mg/ml enzyme concentration. Whiteness index (Stensby) and yellowness index (ASTM D 1925) were examined after enzymatic pretreatment. Pepsin and trypsin-treated wool fibres showed the highest whiteness index as 61.3 and 61.1, respectively whilst untreated wool fibres had 52.2. Fourier-transform infrared (FTIR) analysis revealed the increase in the intensity of amide-related bands and hydroxyl bands after enzymatic treatment. Scanning electron microscopy (SEM) photomicrographs manifested the cuticle layer is partially removed in enzyme-treated fibres. Elemental identification was provided by SEM–energy-dispersive X-ray spectroscopy (EDX). It appears that the sulphur bonds decreased after the treatment and the pepsin-treated fibres have fewer bonds of all. To examine the damage to the structure, photomicrographs were taken using fluorescence and light microscopes. The alkali solubility test (ASTM D1283) was also conducted to compare different enzyme types. Wool fibres were dyed in 2.0% concentration with reactive dyestuff. Dyeability and colorimetric features of fibres were measured by a spectrophotometer. The washing fastness test showed that all the samples have good results and the colour change after washing was better in enzyme-treated samples (grade 5) compared to untreated wool fibres (grade 4–5).