Friction and wear behaviors of reciprocatingly extruded Al–SiC composite

This study focuses on the friction and wear behaviors of reciprocatingly extruded Al–SiC composites. To increase the strength of metal matrix composites and refine the grains of the matrix some deformation processes can be applied, such as reciprocating extrusion (RE). For this reason, RE was carried out on a 6061 Al matrix by a SiC (20 μm) reinforced composite one. The billets were extruded under a pressure of 17.5 MPa at 573 K with a 10:1 extrusion ratio. The reciprocating extrusions were carried out by using up to 15 passes.     

Hyperbranched homo and thermoresponsive graft copolymers by using ATRP‐macromonomer initiators

Macromonomer initiators behave as macro cross‐linkers, macro initiators, and macromonomers to obtain branched and cross‐linked block/graft copolymers. A series of new macromonomer initiators for atom transfer radical polymerization (MIM‐ATRP) based on polyethylene glycol (M_n = 495D, 2203D, and 4203D) (PEG) were synthesized by the reaction of the hydroxyl end of mono‐methacryloyl polyethylene glycol with 2‐bromo propanoyl chloride, leading to methacryloyl polyethylene glycol 2‐bromo propanoyl ester. Poly (ethylene glycol) functionalized with methacrylate at one end was reacted with 2‐bromopropionyl chloride to form a macromonomeric initiator for ATRP. ATRP was found to be a more controllable polymerization method than conventional free radical polymerization in view of fewer cross‐linked polymers and highly branched polymers produced from macromonomer initiators as well. In another scenario, ATRP of N‐isopropylacrylamide (NIPAM) was initiated by MIM‐ATRP to obtain PEG‐b‐PNIPAM branched block/graft copolymers. Thermal analysis, FTIR, ¹H NMR, TEM, and SEM techniques were used in the characterization of the products. They had a thermo‐responsive character and exhibited volume phase transition at ～ 36°C. A plasticizer effect of PEG in graft copolymers was also observed, indicating a lower glass transition temperature than that of pure PNIPAM. Homo and copolymerization kinetics were also evaluated. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Electrochemical determination of urea using a gold nanoparticle-copolymer coated-enzyme modified gold electrode

A new amperometric urea biosensor based on gold nanoparticle embedded poly(propylene-co-imidazole) was developed for the determination of urea. The urease adsorbed on the polymeric film catalyzed the hydrolysis of urea to ammonium and bicarbonate ions and the ammonium was then electrooxidized on the gold electrode with the aid of gold nanoparticles at +0.2?V versus Ag/AgCl using differential pulse voltammetry. The biosensor provided a linear current response to urea concentration from 0.1 to 30?mM, a detection limit of 36?µM, a relative standard deviation of 2.43% (n?=?18), and excellent storage stability, as the current decrease was only 3% after 75 days. The operation of the biosensor was evaluated by the analysis of municipal sewage wastewater collected from the inlet pipe of the treatment plant of Zonguldak City in Turkey. The effects of possible interferants were also characterized.     

Ultrasonic testing to measure the stress statement of steel parts

This paper presents an efficient method for stress measurement propagation. Pulse-echo method are used as stress measurement method on railway wheels. Hard service conditions and brake failures can lead to dangerous stress on the railway wheels. Stress measurements so important for wheels. Especially wheel expose to severe drag braking conditions in freight service. Residual stresses can significantly reduce the engineering properties and fatigue life of materials such as railway components. The paper presents results of stress state investigation of ER7 steel. Finally, the article briefly discusses how to adopt the pulse-echo method to railway wheels. Reducing cost of residual stress measurement investigated.

     

Preparation and characterization of thermosensitive submicron particles for gene delivery

In this study, a new thermosensitive material was proposed as a carrier for gene delivery. The thermosensitive submicron particles were synthesized by the dispersion copolymerization of N-isopropylacylamide (NIPA) with a relatively new, cationic comonomer, N-3-dimethylaminopropylmethacrylamide (DMAPM) with higher ionization ability with respect to the commonly used cationic comonomers. To achieve particle sizes smaller than 1 microm, suitable for gene delivery, the total monomer concentration in the dispersion copolymerization was kept at a sufficiently low level. The size of poly(NIPA-co-DMAPM) particles was determined as 454 nm, by AFM in dry state. The poly(NIPA-co-DMAPM) particles showed both temperature and pH sensitivity in the aqueous media.The plasmid DNA adsorption onto the thermosensitive cationic particles was investigated at different temperatures and pHs. The adsorbed amount of plasmid DNA onto the particles was significantly increased by the introduction of cationic comonomer. The equilibrium plasmid DNA adsorptions up to 13 mg/g dry particles were achieved at physiological pH. Approximately 36% w/w of adsorbed plasmid could be desorbed from the cationic nanolatex. The results of biocompatibility studies performed with mouse fibroblast cells showed the suitability of thermosensitive cationic particles for intended application.     

Solid-Phase Microextraction and Determination of Tin Species in Beverages and Food Samples by Using Poly (ε-Caprolactone-b-4-Vinyl Benzyl-g-Dimethyl Amino Ethyl Methacrylate) Polymer in Syringe System: a Multivariate Study

A new solid-phase microextraction (SPμE) procedure has been developed for separation and preconcentration of Sn ions by using graphite furnace atomic absorption spectrometry (GFAAS). This technique is based on the complexation of Sn(IV) ions with 1-(2-pyridylazo)-2-naphthol (PAN). The poly (ε-caprolactone-b-4-vinyl benzyl-g-dimethyl amino ethyl methacrylate) polymer (PCL vacr) was used as an adsorbent, and it was loaded in micropipette tip of syringe system. Sn(IV) ions were adsorbed on polymer at pH 6. Different experimental conditions were optimized such as pH, amount of complexing agent, and amount of adsorbent. The detection limit (LOD), limit of quantification, preconcentration factor (PF), and relative standard deviation (RSD) were found as 4.5 ng L^?1, 13.5 ng L^?1, 100, and 3.3%, respectively. Certified reference materials were used to confirm the accuracy of the investigated procedure, and the procedure was successfully practiced for determination of entire concentration of tin within beverages and different food samples.     

Recovery of boric acid from ulexite by leaching with hydrochloric acid derived from waste chlorine gas and froth flotation

A process for producing boric acid from ulexite and the recovery of the product by flotation is described. It was found that the degree of conversion of ulexite to boric acid decreased with rising HCl concentration. The undissolved mineral, together with other impurities such as clays, could be depressed by Quebracho, Orzan-S, Daxad-23 or starch, the first two being more effective. Concentrates assaying 97.1% H₃BO₃ were obtained without resorting to recrystallisation of the product. No flotation reagents other than the above-mentioned were necessary for the process.     

Effect of metal ions on the molecular weight distribution of humic substances derived from municipal compost: ultrafiltration and size exclusion chromatography with spectrophotometric and inductively coupled plasma-MS detection

The effect of metal ions (Co, Cu, Ni, Pb, Zn) on the molecular weight distribution of humic substances (HSs) obtained from compost is studied. We believe this is the first of this type of study applied in this way to humic substances. Size exclusion chromatography is coupled with two on-line detection systems (spectrophotometric and ICPMS) to study the binding of metal ions by humic substances leached from compost. ICPMS provided highly specific, sensitive, and multielement analytical information that enabled obtaining direct experimental evidence for the participation of metal ions in molecular size distributions of humic compounds. The compost extract or its high molecular weight fraction (>5,000) was put in contact with EDTA or citrate ions, thereby competing with HSs for binding metals. The experiments were carried out by varying the pH maintained by Tris-HCl or CAPS buffer (pH 8.0 and 10.3) and keeping the ionic strength constant. The elution profile of humic substances using UV/ visible detection was compared with those from ICPMS detection of Co, Cu, Ni, Pb, and Zn in the same chromatographic runs. The results obtained suggested that both bridging between small molecules and complexation/ chelation by individual molecules are involved in metal ion binding to humic substances. The use of ICPMS to study the role of metal ions in aggregation/disassociation of humic substances proposed in this work is promising. Coupling element-specific detection with SEC or other separation systems allows better understanding of the mobility and bioaccessibility of elemental species in the environment and further elucidation of the dissolved humic structure.     

Synthesis and thermal characterization of macromonomeric azo initiator containing poly(ε-caprolactone): Styrene and methyl methacrylate copolymerization

Macromonomeric azo initiator containing biodegradable poly(ε-caprolactone, (PCL) was synthesized by the condensation reaction of PCL with 4,4′-azobis(4-cyanopentanoyl chloride) and methacryloyl chloride. This macromonomeric azo initiator (MIM–PCL) was further used in the polymerization of styrene (St) or methylmethacrylate (MMA) via a radical initiated process at 60°C in bulk in order to obtain polystyrene (PS)-b-PCL or poly(methyl methacrylate) (PMMA)-b-PCL crosslinked block copolymers. Thermal decomposition kinetics of MIM–PCL and its copolymers were studied by using thermogravimetric analysis and differential scanning calorimetry (DSC). DSC traces of MIM–PCL showed two different exotherms, at 98 and 127°C. The first exotherm, observed at 98°C, was due to the polymerization of the terminal methacrylic groups; the other was due to the exothermic decomposition of azo groups of MIM–PCL. PCL-b-PS and PCL-b-PMMA crosslinked block copolymers showed single glass transition temperatures due to the compatibility of the crosslinked block segments. The polymer–solvent interaction parameter of PCL in chloroform was determined by vapor pressure osmometry to be 0.1 for the PCL–chloroform system at 30°C. The average molecular weights between junction points of crosslinked homo PCL were calculated by using the Flory–Rehner equation. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68: 1149–1157, 1998     

Uniaxial tensile and structural properties of poly(vinyl alcohol) films: The influence of heating and film thickness

Poly(vinyl alcohol) as pure or composite materials is widely used in the food and textile industries, andbiomedical applications due to some important properties such as uniaxial tensile, biocompatibility, and noncarcinogenicity. Investigation of the influence of the film thickness and heating on the uniaxial tensile, spectroscopic, and surface properties of PVA films investigated in this study is quite important for improving the properties of such materials and their applicability in different conditions. In this study, with the influence of heating, a necking behavior was observed at around 2% for thin films and 4–9% strain for thicker PVA films for which a kind of transition point at around 1–2% strain was observed. The mechanical strength of PVA films, strain at break, and Young's modulus were enhanced greatly as the temperature increased from 80 to around 110 °C, and then most of them decreased. The degree of crystallinity increased linearly with the heat temperature from around 36–40%. Although PVA thin films obtained a very smooth surface structure after being heated at 80 °C, with increasing heat temperature, the surface roughness of both thin and thick PVA films increased and the PVA thin films obtained more degraded film surface. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44915.