Friction coefficient and wear resistance of a modified polypropylene impregnated with different oils

The aim of the study was to determine the changes in the sliding friction coefficient and wear mechanism of PP impregnated by oils with respect to the unmodified PP under dry sliding conditions. The study showed that the impregnation of the PP clearly influenced the wear rate of PP and its friction coefficient. During the test, the wear behavior of the unmodified and impregnated polypropylenes was investigated using ASTM G77-98 standard wear test equipment in which the specimens were worn by counter sample made by steel 100Cr6. The recording program of the test system enabled the visualization and registration of the following parameters: specimen rotation and load value, linear wear of specimen, friction coefficient, and temperature of specimen and environment. The wear of the specimens was evaluated by weight loss and their wear mechanisms were investigated using scanning electron microscopy. The predominant wear mechanism between a polymer and steel was adhesion. However, at the high sliding velocity, when a higher temperature was generated, the predominant mechanism of wear was thermal wear. Impregnation of PPs moved the thermal wear into the higher sliding velocity values and caused better resistance of the PPs to melting and plastic flow. The most important finding of this investigation was that impregnation of PPs improved their tribological properties at a low value of load represented by the sliding velocity.     

The Use of Reverse Osmosis in the Removal of PAHs from Municipal Landfill Leachate

Polycyclic aromatic hydrocarbons (PAHs) are relatively well-known organic pollutants and due to their carcinogenic and mutagenic properties their presence in the environment still attracts a lot of attention.

According to literature reports and own research, PAHs presence in wastewaters is common. It was confirmed that PAHs are the components of municipal landfill leachate. Membrane techniques are one of the most interesting ways of removing PAHs from leachate.

The purpose of this article is to monitor PAHs concentration changes during the membrane (reverse osmosis - RO) leachate treatment processes. In the first stage of testing leachates were filtrated on the sand bed (pre-filtration). After the pre-filtration they were directed to the membrane module for the main filtration.

Sixteen PAHs listed by EPA were analyzed. The results with information on PAHs concentration in leachate samples were presented using HPLC with fluorescence detection (FLD). The changes in PAHs concentration were determined in leachate samples before and after pre-filtration as well as after RO. The decrease of PAHs concentration in the samples was observed after these processes. The total concentration of 16 PAHs in raw municipal landfill leachates amounted to 23.64–26.95 μg/L. The research confirmed the high efficiency in removal of PAHs while using a reverse osmosis (59–72%). Including the pre-filtration, the overall level of removed PAHs reached 81–86%. The average PAHs concentration after pre-filtration and RO was in the 4.46–4.99 μg/L range. The municipal landfill leachate with a high concentration of PAHs should be cleaned before it is discharged into the environment.     

Synthesis,spectroscopic characterisation,and potential application of dyes containing a carbostyril skeleton as sensors for thiols

Several dyes based on a carbostyril skeleton were synthesised and characterised using proton nuclear magnetic resonance spectroscopy and electron ionisation mass spectrometry. Their basic spectroscopic properties, such as absorption and emission spectra, were also measured. The behaviour of the obtained dyes in the absence and presence of thiol amino acids and other compounds under various conditions were studied. These dyes contain various moieties in the structure, acting as Michael acceptors. Results show that the studied compounds have the potential to act as colorimetric sensors for thiols, but the benzothioazolium dyes are less effective than dicyanoethylene derivatives.     

Microstructure and properties of friction stir welded aluminium alloys

Aluminium alloy 7136 belongs to the Al–Zn–Mg–Cu group of aluminium alloys strengthened by precipitation. These alloys offer very good properties, i.e. high strength combined with good corrosion resistance, which makes them suitable for aerospace applications. The limited range of applications of these alloys is due to problems associated with their welding. The Al–Zn–Mg–Cu alloys are classified as non-weldable. The aim of this study was to determine the quality and properties of friction stir welded (FSW) joints of alloy 7136-T76. This article presents the results of a detailed study into the microstructure and mechanical properties of FSW welds. The paper demonstrates that the FSW method is suitable for joining Al–Zn–Mg–Cu alloys. The FSW joints are of good quality and high mechanical properties. Tests of joints created at various tool rotation speeds have shown that joints of suitable quality, in terms of microstructure and properties, can be obtained for a relatively wide range of process parameters. The tool rotation speeds applied during the welding process did not have a significant influence on the quality of the welds.     

Microstructure study of poly(isobutyl acrylate) and poly(<Emphasis Type="Italic">sec</Emphasis>-butyl acrylate) by incremental analysis of <Superscript>13</Superscript>C NMR spectra

Microstructure of poly(isobutyl acrylate) (PiBuA) and poly(sec-butyl acrylate) (PsBuA), prepared by free radical and anionic polymerization, was investigated by ¹³C NMR spectroscopy. The carbonyl signal in the 100 MHz ¹³C NMR spectra of both homopolymers provided sufficient resolution to perform detailed analysis of distribution of configurational sequences at the pentad/heptad level. Application of Bernoulli and first order Markov statistics to determine probabilities of configurational sequences and incremental calculation to estimate chemical shifts of the individual sequences allowed for positive simulation of carbonyl signals.     

Optimization of subtractive-transformative hybrid processes supported by the technological heredity concept

This paper presents the optimization procedure of a hybrid removal-forming type process based on the minimum energy consumption and demanded surface roughness which is supported by the analysis of transformation of the surface and sublayer properties termed as the technological heredity. The experimental investigation covers an alloy steel hardened to 35 HRC and 55 HRC which was initially turned using coated carbide and CBN tools and subsequently burnished to produce surfaces with Ra roughness parameter of about 0.15 μm. The modifications of the initial surface profiles, microstructure and microhardness of the sublayer were determined and relevant technological limits are selected.     

Nonlinear Absorption of Submicrometer Grain‐Size Cobalt‐Doped Magnesium Aluminate Transparent Ceramics

Transparent cobalt‐doped magnesium aluminate spinel (Co:MgAl₂O₄) ceramics with a submicrometer grain size were prepared by spark plasma sintering. For the first time, the nonlinear absorption of Co:MgAl₂O₄ transparent ceramics was experimentally demonstrated. Both ground state absorption (σ_GSA) and excited state absorption (σ_ESA) were estimated using the solid‐state slow saturable absorber model based on absorption saturation measurements performed at 1.535 μm. σ_GSA and σ_ESA for 0.03 at.% Co:MgAl₂O₄ were found to be 4.1 × 10^?19 cm² and 4.0 × 10^?20 cm², respectively. In the case of 0.06 at.% Co:MgAl₂O₄ ceramics, σ_GSA = 2.6 × 10^?19 cm² and σ_ESA= 5.3 × 10^?20 cm² were determined.     

Origin of Violet‐Blue Emission in Ti‐Doped Gahnite

ZnAl₂O₄ doped with Ti⁴⁺ (2%) was synthesized by the hydrothermal method at 220°C at pressure of 25 bars. An average grain size of the as‐prepared sample was 3 nm, the samples with biggest grain size were obtained after annealing at 300°C, 500°C, 600°C, 700°C, and 900°C, diameter of the latter was about 33 nm. IR spectroscopy indicated that ZnAl₂O₄ was partially inverted. The degree of the inversion decreases with increase in the annealing temperature but increases with increasing Ti⁴⁺ content. Absorption and emission spectra as well as emission decay profiles were recorded at 300 and 77 K. The observed spectra are due to charge‐transfer O^2??Ti⁴⁺ transitions. Color of the emission depends on the nanocrystal size and with increase in its diameter changes from violet to blue, accordingly the absorption bands exhibit redshift. The calculations based on Density Functional Theory confirmed the experimental results. 3d electrons of titanium ions form the bottom of the ZnAl₂O₄:Ti⁴⁺ conduction band, oxygen, aluminum or zinc vacancies create additional levels in the gahnite energy band gap. It was also found that in ZnAl₂O₄ aluminum or zinc vacancy induces magnetism with relatively high magnetic moment close to 1 μ_B per vacancy.     

Elaboration of small‐diameter vascular prostheses—Selection of appropriate sterilisation method

The aim of study is the elaboration of semi‐biodegradable, multilayered tubular structures as substitutes for the reconstruction of small diameter vascular prostheses (<6 mm). The inert external layer of the prostheses will be fabricated via the melt electrospinning of poly (l ‐lactide‐co‐glycolide) (PLGA). The middle layer will be constructed from polypropylene (PP); the first prototype will be produced via melt electrospinning and the second using the melt blowing technique. The general aim of this stage of the research is the selection of a sterilisation technique that is appropriate for semi‐biodegradable, multilayered tubular structures. For this purpose, single tubular structures created via the melt electrospinning of PLGA or PP and melt blown tubular structures of PP were elaborated. The influence of steam, ethylene‐oxide (EO), and radiation sterilisation techniques on the elaborated microstructure of tubular structures was analyzed during this study. The effect of each sterilisation technique was evaluated using differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy/energy‐dispersive X‐ray spectroscopy analysis (SEM/EDS). The changes in average molecular weight (M_w) and crystallinity index (CI) of the PLGA tubular structures after EO and steam sterilisation were evaluated. The EO and steam sterilisation resulted in the complete destruction of PLGA tubular structures. Only the radiation sterilisation (accelerated electrons) did not influence on PLGA tubular structures morphology as well as thermal and chemical properties. FTIR and SEM/EDS analysis indicated that no changes in the chemical properties of PP tubular structures after each sterilisation occurred. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40812.     

Enzymatically Modified Fats Based on Mutton Tallow and Rapeseed Oil Suitable for Fatty Emulsions

The aim of this work was to develop a new fat by enzymatic interesterification of mutton tallow with rapeseed oil. It was assumed that by inducing hydrolysis of fats by addition of water to the enzymatic preparation (8, 10, 15 wt%) natural emulsifiers would be produced in the reaction environment. Fat blends obtained from the enzymatic reactions were evaluated as a fat base for emulsion systems. It was found that the fat resulting from interesterification in the presence of Lipozyme RM IM (immobilized lipase from Rhizomucor miehei, Novozymes Bagsvaerd, Denmark) with 15 wt% of water possessed the highest content of polar fraction (MAG and DAG), and served as the most suitable blend for emulsification, producing emulsions that exhibited the highest stability.