Investigation of long-term engine oil performance using lab-based artificial ageing illustrated by the impact of ethanol as fuel component

The effect of ethanol and its combustion products on the lubrication system is not very well understood. In this paper, a novel lab-based artificial ageing method for the evaluation of engine oils for bio-fuelled automotives and the results thereof are presented. Artificial ageing of three fully formulated engine oils with addition of ethanol, acetaldehyde, and acetic acid was carried out. The oil formulations chosen represent a consequent series of optimisation steps based on the engine oil performance in terms of preservation of typical oil parameters, e.g. base reserve and oxidation, observed during the artificial ageing procedure. It was shown that ethanol as well as acetaldehyde has almost no effect on the oil degradation especially in the case that advanced additive technology was used. On the contrary, acetic acid significantly affected the formulated oil showing influence on the detergent chemistry and even caused sludge formation. The use of the novel artificial ageing method proved to clearly differentiate the impact of the respective compounds added with the possibility to simulate enhanced stress conditions without the need of time-consuming and expensive engine bench tests. Hence, the novel setup offers valuable input for the formulation and the pre-selection of future engine oils suitable for bio-fuel.     

Highly efficient blue organic light-emitting diodes using quantum well-like multiple emissive layer structure

In this study, the properties of blue organic light-emitting diodes (OLEDs), employing quantum well-like structure (QWS) that includes four different blue emissive materials of 4,4′-bis(2,2′-diphenylyinyl)-1,1′-biphenyl (DPVBi), 9,10-di(naphth-2-yl)anthracene (ADN), 2-(N,N-diphenyl-amino)-6-[4-(N,N-diphenyl amine)styryl]naphthalene (DPASN), and bis(2-methyl-8-quinolinolate)-4-(phenyl phenolato) aluminum (BAlq), were investigated. Conventional QWS blue OLEDs composed of multiple emissive layers and charge blocking layer with lower highest occupied molecular orbital (HOMO)-lowest unoccupied molecular orbital (LUMO) energy level, and devices with triple emissive layers for more significant hole-electron recombination and a wider region for exciton generation were designed. The properties of triple emissive layered blue OLEDs with the structure of indium tin oxide (ITO) /N,N′-diphenyl-N,N′-bis(1-naphthyl-phenyl)-(1,1′-biphenyl)-4,4′-diamine (NPB) (700 Ǻ)/X (100 Ǻ)/BAlq (100 Ǻ)/X (100 Ǻ)/4,7-diphenyl-1,10-phenanthroline (Bphen) (300 Ǻ)/lithium quinolate (Liq) (20 Ǻ)/aluminum (Al) (1,200 Ǻ) (X = DPVBi, ADN, DPASN) were examined. HOMO-LUMO energy levels of DPVBi, ADN, DPASN, and BAlq are 2.8 to 5.9, 2.6 to 5.6, 2.3 to 5.2, and 2.9 to 5.9 eV, respectively. The OLEDs with DPASN/BAlq/DPASN QWS with maximum luminous efficiency of 5.32 cd/A was achieved at 3.5 V.     

含水固形物干燥脱水蒸汽再利用专利技术工艺及设备

在无机盐产品生产过程中,中间产品和副产品通常需要进行干燥,文章对含水固形物干燥脱水蒸汽再利用工艺及设备进行了论述。并就干燥脱水蒸汽再利用专利工艺及设备对节省能源消耗进行了分析。     

Multilayer emulsions as delivery systems for controlled release of volatile compounds using pH and salt triggers

Multilayer oil-in-water (M-O/W) emulsions were compared to primary oil-in-water (P-O/W) emulsions as carriers for volatile organic compounds (VOCs) under various environmental conditions (pH and salt). The M-O/W emulsion consisted of soy oil coated with β-lactoglobulin (βLG) and pectin layers. The release of VOCs with different physiochemical properties from aqueous solutions and emulsion systems was measured using static and dynamic headspace methods. The partition coefficients (K) calculated by the phase ratio variation (PRV) method, showed different volatile release profiles between the emulsion types. An increase in VOC release was found for the unstable P-O/W emulsion at pH 5, whereas M-O/W emulsions were stable at the same pH and retained the hydrophobic VOCs. Hydrophobic interactions and hydrogen bonds with the secondary dense layer of pectin may be responsible for the improved retention. Increasing pH and ionic strength acts as a VOC release trigger to detach the pectin from the interface. The release rates from initial dynamic curves support the results under equilibrium conditions. The results of this study demonstrate the capability of using M-O/W emulsions for controlled release of VOCs, as well as an alternative system to create stable emulsions with similar VOC release profiles.     

Measurement of Micro Kinetics of Hydrogenation in Liquid Phase Using Raman Spectroscopy

Hydrogenation of liquid organic hydrogen carriers is usually carried out in liquid phase. To measure the kinetics of this hydrogenation, an experimental setup using in situ Raman spectroscopy for analysis of the reaction mixture is proposed. With this setup it is possible to perform hydrogenation reactions at temperatures of up to 573 K and pressures up to 25 MPa. For validation of the experimental setup the hydrogenation of 1‐octene was measured in liquid phase. The reaction progress can be monitored in detail by Raman spectroscopy. To determine kinetic parameters from the experimental data, two modeling approaches were applied: a classic kinetic model and a thermodynamic kinetic model. The results were compared to literature data.     

Ultrafine particles generated from coloring with scented markers in the presence of ozone

High concentrations of ultrafine particles (UFPs) have been previously reported during school art activities. This is possibly due to secondary organic aerosols (SOAs) formed from reactions between ozone and volatile organic compounds emitted from art products. Four brands of markers, three scented and one unscented, were tested inside a stainless steel chamber at eight different ozone concentrations between 0 and 300 ppb. Out of the 32 tested markers, only the lemon‐ and orange‐scented markers from one brand reacted with ozone to form UFPs. Limonene, pinene, and several other terpenes were identified as ingredients of ink in SOA‐forming markers. Coloring with one lemon‐scented marker for 1 min without ozone generated on average approximately 26 ± 4 ppb of limonene inside the chamber. At 150 ppb ozone, using one lemon marker for 1 min formed on average 7.7 × 10¹⁰ particles. The particle size distribution indicated an initial mode of 15 nm which grew to 40 nm. At 50 ppb ozone and below, no significant SOA formation occurred. The number of particles formed is moderately correlated with the mass of ink used (R² = 0.68). Based on these data, scented markers are not likely a strong source of SOA under normal indoor ozone levels.     

Degradation mechanisms in Li‐ion batteries: a state‐of‐the‐art review

One of the most prominent energy storage technologies which are under continuous development, especially for mobile applications, is the Li‐ion batteries due to their superior gravimetric and volumetric energy density. However, limited cycle life of Li‐ion batteries inhibits their extended use in stationary energy storage applications. To enable wider market penetration of Li‐ion batteries, detailed understanding of the degradation mechanisms is required. A typical Li‐ion battery comprised of an active material, binder, separator, current collector, and electrolyte, and the interaction between these components plays a critical role in successful operation of such batteries. Degradation of Li‐ion batteries can have both chemical and mechanical origins and manifests itself by capacity loss, power fading or both. Mechanical degradation mechanisms are associated with the volume changes and stress generated during repetitive intercalation of Li ions into the active material, whereas chemical degradation mechanisms are associated with the parasitic side reactions such as solid electrolyte interphase formation, electrolyte decomposition/reduction and active material dissolution. In this study, the main degradation mechanisms in Li‐ion batteries are reviewed. Copyright © 2017 John Wiley & Sons, Ltd.     

Study on inorganic oxidants assisted sonocatalytic degradation of Resazurin dye in presence of β-SnWO4 nanoparticles

This work presents about the study of inorganic oxidants assisted sonocatalytic degradation of Resazurin (RZ) dye in the presence of β-SnWO₄ nanoparticles. The catalysts were synthesized via a surfactant free sonochemical method. Physical properties of the as-prepared β-SnWO₄ nanoparticles were analyzed by XRD and FE-SEM. The dispersion property and particle size were analyzed by Zeta potential and Particle size analyzer. The degradation of RZ was analyzed in the presence and absence of common oxidants such as PMS (peroxymonosulfate) and H₂O₂ (hydrogen peroxide). The result shows that the RZ was first mineralized to Resorufin and it was degraded to simple molecule in the presence of β-SnWO₄. 75% of degradation efficiency was achieved in presence of β-SnWO₄, while in addition of H₂O₂ and PMS, the efficiency was increased up to 93% and 85% respectively. Our results will pave a new opening in degradation of poisonous dye using inorganic common oxidants.     

分析水对无烟煤挥发分测定产生的影响

根据GB／T212-2008《煤的工业分析方法》中的规定，在测定挥发分时，通过实验对比，无烟煤中水分随着煤的变质程度加深而呈规律性变化。从泥炭、褐煤、烟煤到年轻无烟煤水分逐渐减少，从年轻无烟煤到老年无烟煤的水分又逐渐增加。由于煤中水分过高和煤的氧化增重，导致挥发分测定值产生负值，影响挥发分的测定结果。