Characterization of cordierite based h-BN doped ceramics as an electronic substrate/circuit board material

In this study, h-BN was added to the cordierite composition obtained from zeolite, which was prepared by the determined stoichiometry to facilitate machinability and increase thermal conductivity. Sintering behavior, hardness, machinability, and thermal/electrical properties of the samples obtained by sintering the compounds at different times were investigated. Thanks to these features, it is aimed to use cordierite as an alternative material to integrated circuit substrates and electronic packaging materials. The produced samples were analyzed by X-ray diffraction analysis, examined by scanning electron microscopy, and field emission scanning electron microscopy. Afterward, thermal properties such as thermal diffusivity, thermal conductivity, and electrical properties such as electrical conductivity and dielectric permittivity were measured. The hardness and machinability of samples were investigated. Cordierite, spinel, glassy phase, and h-BN phase were detected, and it was observed that the blocky cordierite grains turned into equiaxed grains with the increase of the h-BN. According to the results obtained from the thermal conductivity test, it was seen that the h-BN additive increased the thermal conductivity value in general. In addition, it was determined that with the increase of h-BN, the hardness decreased, and the machinability properties of the samples improved.     

Electrical Properties of Lead‐Free Na1/2Bi1/2TiO3 Relaxor Ferroelectric Ceramics Doped with Hafnium or Zirconium

Ferroelectric (Na_1/2Bi_1/2)TiO₃ and its various solid solutions have been drawing special attention as a new candidate for their lead‐based counterparts. In this study, therefore, hafnium‐ or zirconium‐doped grain‐oriented (Na_1/2Bi_1/2)TiO₃ ceramics with <001>_pc orientation were fabricated by templated grain growth method using anisotropically shaped SrTiO₃ template particles. These molten salt synthesized SrTiO₃ platelets were tape cast with calcined (Na_1/2Bi_1/2)TiO₃ powders, and then sintered at 1200°C for 6 h. Texture fractions up to 70% have been obtained. Unipolar strains up to >0.25% were measured. Doped ceramics showed a “relaxor‐like” ferroelectric behavior. A broad dielectric peak with a slim hysteresis loop was present for hafnium‐ or zirconium‐doped samples. Electrostrictive coefficient of hafnium‐doped (Na_1/2Bi_1/2)TiO₃ ceramics were found to be 0.032 m⁴/C², which is much larger than that of PMN‐based electrostrictive materials. Electromechanical properties of hafnium‐ and zirconium‐doped (Na_1/2Bi_1/2)TiO₃ ceramics under electric bias were studied as well.     

Biodegradable Poly(ε‐Caprolactone)‐Based Graft Copolymers Via Poly(Linoleic Acid): In Vitro Enzymatic Evaluation

Well‐defined graft copolymers based on poly(ε‐caprolactone) (PCL) via poly(linoleic acid) (PLina), are derived from soybean oil. Poly(linoleic acid)‐g‐poly(ε‐caprolactone) (PLina‐g‐PCL) and poly(linoleic acid)‐g‐poly(styrene)‐g‐poly(ε‐caprolactone) (PLina‐g‐PSt‐g‐PCL) were synthesized by ring‐opening polymerization of ε‐caprolactone initiated by PLina and one‐pot synthesis of graft copolymers, and by ring‐opening polymerization and free radical polymerization by using PLina, respectively. PLina‐g‐PCL, PLina‐g‐PSt‐g‐PCL3, and PLina‐g‐PSt‐g‐PCL4 copolymers containing 96.97, 75.04 and 80.34 mol% CL, respectively, have been investigated regarding their enzymatic degradation properties in the presence of Pseudomonas lipase. In terms of weight loss, after 1 month, 51.5 % of PLina‐g‐PCL, 18.8 % of PLina‐g‐PSt‐g‐PCL3, and 38.4 % of PLina‐g‐PSt‐g‐PCL4 were degraded, leaving remaining copolymers with molecular weights of 16,140, 83,220 and 70,600 Da, respectively. Introducing the PLina unit into the copolymers greatly decreased the degradation rate. The molar ratio of [CL]/[Lina] dramatically decreased, from 21.3 to 8.4, after 30 days of incubation. Moreover, reduced PCL content in PLina‐g‐PSt‐g‐PCL copolymers decreased the degradation rate, probably due to the PSt enrichment within the structure, which blocks lipase contact with PCL units. Thus, copolymerization of PCL with PLina and PSt units leads to a controllable degradation profile, which encourages the use of these polymers as promising biomaterials for tissue engineering applications.     

Poly‐2‐[(4‐methylbenzylidene)amino]phenol: Investigation of thermal degradation and antimicrobial properties

A new polyphenol (poly‐2‐[(4‐methylbenzylidene)amino]phenol) (P(2‐MBAP)) containing an azomethine group was synthesized by oxidative polycondensation reaction of 2‐[(4‐methylbenzylidene)amino]phenol (2‐MBAP) with NaOCl, H₂O₂, and O₂ oxidants in an aqueous alkaline medium. The structures of 2‐MBAP and P(2‐MBAP) were characterized by UV‐vis, FT‐IR, and ¹H NMR spectra. While the monomer decomposed completely up to 350°C and 57.2% of the polymer decomposed up to 1000°C. The thermal degradation of P(2‐MBAP) was also supported by the Thermo‐IR spectra recorded in the temperature range of 25–800°C. Electrical conductivity of the polymer was observed to increase 10⁸ fold after doping with I₂. Antimicrobial activities of the P(2‐MBAP) and 2‐MBAP against Sarcina lutea, Enterobacter aerogenes, Escherichia coli, Enterococcus feacalis, Klebsiella pneumoniae, Bacillus subtilis, Candida albicans, and Saccharomyces cerevisiae were also investigated. The number average molecular weight (M_n), weight average molecular weight (M_w) and polydispersity index (PDI) of the polymers were determined by gel permeation chromatography (GPC). © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41758.     

Spray-Dried Mesoporous Hydroxyapatite–Chitosan Biocomposites

In this study, hydroxyapatite–chitosan composites with weight ratio of 1:0.1 were produced by spray-drying technique using two different inlet temperature. Besides, the effect of weight change of hydroxyapatite on composites was investigated on composites which were spray-dried in the selected temperature. Synthesized hydroxyapatite–chitosan samples were characterized using Fourier transform infrared microscopy, scanning electron microscopy, X-ray fluorescence spectroscopy, Brunauer–Emmet–Teller method, and X-ray diffraction. Particle size measurements were also performed in this content. Simulated body fluid studies were conducted on selected samples. According to results, hydroxyapatite–chitosan sample was successfully synthesized. Spray-dried mesoporous microspheres with high surface areas could be suitable for biomedical usage.     

Preparation and characterization of membranes obtained from blends of acrylonitrile copolymers with poly(vinyl alcohol)

New microfiltration and ultrafiltration membranes were obtained using acrylonitrile‐vinyl acetate copolymers in mixture with poly(vinyl alcohol) (PVA). Thus, a blend polymer solution was prepared in dimethylsulfoxide (DMSO) and used to obtain bicomponent polymer membranes by phase inversion. The rheological behavior of the DMSO polymer solutions was, mostly, dilatant at low shear gradients and pseudo plastic with quasi Newtonian tendency at higher gradients. Membranes were characterized by Fourier transform infrared spectrometry (FTIR), optical microscopy, atomic force microscopy, thermal gravimetric analysis‐differential thermal gravimetry, and pure water flux (PWF). FTIR spectra displayed the characteristic bands for acrylonitrile, vinyl acetate, and PVA. The morphology and the porosity can be tailored by the preparation conditions. PVA allows controlling the size of the pores and enables, in principle, to use the resulted membranes as supports for enzyme immobilization. PVA content influences the thermal stability. PWF values depend on the copolymer, on the content in PVA, but also on the coagulation bath composition. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41013.     

Thoughening of poly(lactic acid) with silicone rubber

In this study, poly(lactic acid) (PLA) was blended with silicone rubber (SR) to improve its impact strength and toughness by using dynamic crosslinking in the presence of peroxide during melt compounding. The SR to PLA ratio, peroxide and coagent concentrations were taken as experimental parameters. Blends were evaluated in terms of their thermal properties, tensile and impact strengths, dynamic mechanical properties, and micro‐structure. Results showed that PLA was successfully toughened with SR using dynamic crosslinking. Impact strength and energy of fracture in tensile test improved up to 4 and 10 times, respectively. On the other hand, yield strength and stiffness of blends deteriorated by the incorporation of SR. Thermal analysis pointed out that presence of SR decreased the cold crystallization temperature. It was observed from scanning electron microscopy (SEM) that the energy absorbing mechanism under impact loads in PLA/SR blends is tortuosity in the crack patterns. POLYM. ENG. SCI., 54:2029–2036, 2014. © 2013 Society of Plastics Engineers     

Removal of Cr(VI) by a chelating resin containing N-methyl-d-glucamine

The resin poly[N-(4-vinylbenzyl)-N-methyl-d-glucamine] [P(VbNMDG)] was synthesized and its performance for Cr(VI) removal was studied. This resin presented a very fast kinetic of Cr(VI) sorption following a pseudo-second order. Also, the rate-controlling step of Cr(VI) sorption performed by film diffusion in accordance with infinite solution volume model and reacted layer in accordance with unreacted core model. The column study showed a breakthrough capacity of 12.2 mg Cr/mL-resin, with an elution efficiency of 92 %. Mechanism of sorption could correspond to an electrostatic interaction followed by a complexation reaction.     

Characterization of Turkish Olive Oils by Triacylglycerol Structures and Sterol Profiles

A characterization study of Turkish monovarietal olive oils using chemical variables such as fatty acid, sn‐2 fatty acid, triacylglycerol, and sterol composition is presented. A total of 101 samples of Olea europaea L. fruits from 18 cultivars were collected for two crop years from west, south, and southeast regions of Turkey. Olives were processed to oil and olive oil samples were evaluated for their triacylglycerol structures and sterol composition. Oleic acid content ranged from 60.15 to 80.46 % of total fatty acids and represented 70.90–89.02 % of sn‐2 position triacylglycerols. Major triglycerides of oil samples were triolein, palmitodiolein, dioleolinolein, palmitooleolinolein, dipalmitoolein, and stearodiolein. Triolein values were between 24.72 and 48.64 % and compatible with the fatty acid composition. Total sterol content varied from 1,145.32 to 2,211.77 mg/kg and Edremit yagl?k stood out because of its high sterol content. A one‐way analysis of variance revealed significant differences for variables among cultivars. Principle component analysis enabled the classification of common varieties on the basis of analytical data. Sterol composition achieved more relevant discrimination than fatty acid and triglyceride composition. Classification according to geographical origin was performed by discriminant analysis.