High-temperature phase relations and thermodynamics in the silver-tin-sulfur system

The SnS activities in liquid Ag₂S-SnS liquid mattes were obtained at 1100 °C and 1200 °C by the dew-point method. Negative deviations were observed, and the liquid matte solutions were modeled by the Wilson equations. Part of the liquid boundaries of the Ag₂S-SnS phase diagram were derived from the model equations, yielding a eutectic temperature of 528 °C at x _SnS=0.38. The phase diagram of the pseudobinary Ag₂S-SnS was also verified experimentally by quenching samples equilibrated in evacuated and sealed silica capsules. Solubility limits of the components at the narrow-terminal solid-solution ranges were determined around the eutectic temperature. Within the Ag-Sn-S ternary system, the boundaries of the immiscibility region, together with the tie-line distributions, were established at 1200 °C. Activities of Ag, Sn, and S along the miscibility gap were calculated by utilizing the bounding binary thermodynamics, phase equilibria, and tie-lines.     

Mulberry Seed Oil: a Rich Source of δ‐Tocopherol

In the present study, mulberry seed oil (MSO) samples obtained from seeds of different mulberry varieties as well as concentrated mulberry juice production waste (mulberry pomace) were investigated. Radical scavenging capacity, tocopherol and total phenolic content of MSO were determined. It was observed that MSO contain unique amounts of δ‐tocopherol varying between 1645–2587 mg kg^?1 oil depending on the variety. The secondary tocopherol homologue was γ‐tocopherol within a concentration range of 299–854 mg kg^?1 oil. MSO exhibited a very high antioxidant capacity varying in the range of 1013–1743 and 2574–4522 mg α‐tocopherol equivalents (α‐TE) per kg of oil for 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) and freeze‐dried 2,2′‐azino‐bis (3‐ethylbenzothiazoline‐6‐sulfonic acid) (FD‐ABTS) radical cation assays, respectively. Both antioxidant capacity and total phenolic content were higher for mulberry pomace oil compared with the seed oils. Fatty acid composition of MSO was also determined, and linoleic acid was found to be the primary fatty acid (66–80 %).     

Some properties of set yoghurt made from caprine milk and bovine–caprine milk mixtures fortified by ultrafiltration or the addition of skim milk powder

Set yoghurt was produced from caprine milk (A), 70% caprine-30% bovine (B) and 50% caprine–50% bovine milk (C) mixtures, and stored for 14 days at ±4°C. Two methods of fortification, namely ultrafiltration (UF) and the addition of bovine skim milk powder (SMP), were applied to the milk mixtures. Some chemical, physical, microbiological and sensory properties of the six samples were analysed on the 1st, 7th and 14th days of storage. The effects of milk type, concentration method and storage period on the physicochemical and microbiological properties of the samples were investigated statistically.     

Enhanced mechanical and thermal properties of graphene nanoplatelets-reinforced polyamide11/poly(lactic acid) nanocomposites

The present paper aims to obtain a sustainable nanocomposite by using bio-based polyamide 11 and biodegradable poly (lactic acid) blend as matrix and graphene nanoplatelets (GNP) as nanofiller. GNP was incorporated in the PA11/PLA blend matrix in the ratio of 0.5-1-3-5-10 wt% through the twin-screw extruder. The crystallinity of PA11 in the blend, which was 12.9%, increased with the inclusion of GNP, and the highest crystallinity value was observed at 20% for the 1GNP sample. The crystallinity of PLA in the blend, which was 2.3%, increased to 4.6% with 5 wt% GNP addition. The inclusion of GNP to PA11/PLA improved the thermal degradation temperatures and increase the char residue. Also, increments were observed for storage modulus, loss modulus, and glass transition temperature of the matrix with the inclusion of GNP. The addition of GNP caused the tensile strength of the matrix to increase first and then decrease at higher amounts due to the agglomerations. 0.5–1 wt% GNP increased tensile strength by 10% and 5%, respectively. Increasing the amount of GNP to 10 wt% led to a sharp decrease in tensile strength by 24%. Overall, GNP is a suitable nanofiller to enhance the thermal and mechanical features of the PA11/PLA blend.     

Development of Degradable,pH‐Sensitive Star Vectors for Enhancing the Cytoplasmic Delivery of Nucleic Acids

The report describes the synthesis of degradable, pH‐sensitive, membrane‐destabilizing, star‐shaped polymers where copolymers of hydrophobic hexyl methacrylate (HMA) and 2‐(dimethylamino)ethyl methacrylate (DMAEMA) monomers are grafted from the secondary face of a beta‐cyclodextrin (β‐CD) core via acid‐labile hydrazone linkages using atom transfer radical polymerization. The effect of the graft's molecular weight, HMA/DMAEMA molar ratio, and the fraction of DMAEMA converted to cationic N,N,N‐trimethylaminoethyl methacrylate (TMAEMA) monomers on polymer's transfection capacity is systematically investigated. Results show that all star‐shaped polymers condense anti‐GAPDH silencing RNA (siRNA) into nanosized particles at +/‐ ratio ≤ 4:1. Star polymers with shorter (25kDa) P(HMA‐co‐DMAEMA‐co‐TMAEMA) grafts are more efficient and less cytotoxic than carriers with longer (40kDa) grafts. The results show that increasing the ratio of hydrophobic HMA monomers in graft's composition higher than 50 mole% dramatically reduces polymer's aqueous solubility and abolishes their transfection capacity. Further, retention of DMAEMA monomers in graft's composition provide a buffering capacity that enhanced the endosomal escape and transfection capacity of the polymers. These systematic studies show that β‐CD‐P(HMA‐co‐DMAEMA‐co‐TMAEMA)_4.8 polymer with a 25 kDa average graft's molecular weight and a 50/25/25 ratio of HMA/DMAEMA/TMAEMA monomers is the most efficient carrier in delivering the siRNA cargo into the cytoplasm of epithelial cancer cells.     

Modification of multiwall carbon nanotube by thiol-ene click chemistry

Thiol-ene click chemistry was used for the preparation of polystyrene grafted multiwall carbon nanotubes (MWCNTs) via the thermal initiation method. The thiol end-functional PSt (PSt-SH) was prepared by the nucleophilic substitution reaction of the bromide end groups of PSt obtained by atom transfer radical polymerization. PSt-SH grafted to the surface of the MWCNTs by thiol-ene click chemistry via the thermal initiation method.