Investigation on bonding quality of beech wood (Fagus orientalis L.) veneer during high temperature drying and aging

In the present study, the effects of high drying temperature and UV light induced aging on bonding quality of plywood manufactured from untreated and treated veneer layers were investigated. Rotary cut veneers with dimensions of 500 mm×500 mm×2 mm produced from beech (Fagus orientalis Lipsky) log were selected for topochemical, chemical and mechanical analyses. The veneer sheets were oven-dried at 100°C and 180°C after the peeling process. Afterwards, the surfaces were exposed to artificial UV irradiation in an UV chamber for 24 h, 48 h and 72 h representing natural sun irradiation of 2, 4 and 6 months, respectively. Topochemical distribution of lignin and phenolic extractives of the treated and untreated veneers was investigated on a cellular level using UV microspectrophotometry (UMSP). For the chemical characterization of accessory compounds high performance liquid chromatography (HPLC) was used. Furthermore, the shear and bending strengths of plywood manufactured from the treated samples are determined in order to study the bonding quality. The UV microscopic detection shows that after high drying temperature and aging treatment, lignin condensation occurs. With increasing drying temperature and aging duration, more phenolic extractives are situated in parenchyma cells and vessel lumens which can be proved by increased absorbance at 278 nm. The HPLC analysis of the treated tissue showed distinct signals of polymerized compounds such as catechin and 2,6-dimethoxybenzoquinone which are chromophoric compounds in discolored beech wood. The mechanical properties of plywood showed that with increasing drying temperature up to 180°C does not negatively affect shear and bending strengths of samples. After exposure of the veneers to UV irradiation (especially 6 months), decreasing shear and bending strengths of plywood samples can be observed.     

Data-driven Distributionally Adjustable Robust Chance-constrained DG Capacity Assessment

Moving away from fossil fuels towards renewable sources requires system operators to determine the capacity of distribution systems to safely accommodate green and distributed generation（DG）. However, the DG capacity of a distribution system is often underestimated due to either overly conservative electrical demand and DG output uncertainty modelling or neglecting the recourse capability of the available components. To improve the accuracy of DG capacity assessment, this paper proposes a distributionally adjustable robust chance-constrained approach that utilises uncertainty information to reduce the conservativeness of conventional robust approaches. The proposed approach also enables fast-acting devices such as inverters to adjust to the real-time realisation of uncertainty using the adjustable robust counterpart methodology. To achieve a tractable formulation, we first define uncertain chance constraints through distributionally robust conditional value-at-risk（CVa R）, which is then reformulated into convex quadratic constraints. We subsequently solve the resulting large-scale, yet convex, model in a distributed fashion using the alternating direction method of multipliers（ADMM）. Through numerical simulations, we demonstrate that the proposed approach outperforms the adjustable robust and conventional distributionally robust approaches by up to 15% and 40%, respectively, in terms of total installed DG capacity.     

Reaction of methyltrans-2,3-epoxyhexadecanoate with urea: Synthesis of long chain fatty 2-oxazolidones

Methyltrans-2,3-epoxyhexadecanoate on refluxing with urea in dimethylformamide (DMF) afforded isomeric 4(5)-tridecyl-5(4)-carbomethoxy-cis-2-oxazolidone (II), 5-tridecylmethylene hydantoin (II) and 2-hydroxy-3-carbamidohexadecanoic acid (III). Presented at the 4th Convention of the Indian Council of Chemists at Uttar Pradesh, India, December 1984.     

The antioxidant activity of amino acids in two vegetable oils

Of 27 amino acids studied, most had some antioxidant activity when added in aqueous solution to either safflower oil or a mixture of sunflower and cottonseed oil (active oxygen and storage methods). Cysteine-HCl, glutamic acid-HCl (in the mixture), and glutamic acid-HCl (in safflower oil) behaved as prooxidants. When added as a solid, most amino acids were ineffective. The protection factors of these amino acids were less than 1.3 in safflower oil with methionine, proline, lysine and cysteine providing the highest activ-ity. In the oil mixture (which had a higher metal content) lysine, arginine, glutamic acid, methionine, and hydroxyproline were anti-oxidant with protection factors of up to 1.85. Chelation of metals by amino acids was presumably responsible for the antioxidant activity. The increase in cysteine concentration up to 1% has more than doubled the protection factor in Bint oil (compared with the 0.01% level), whereas with some other amino acids the increase was either small or slight.     

A polyamide-silica composite prepared by the sol-gel process

Summary A new kind of organic-inorganic hybrid composite was prepared by means of the sol-gel process. The polymer employed was a mixed-isomer aromatic polyamide having good solubility and thermal stability. The silica constituting the inorganic phase was produced by the hydrolysis and condensation of tetramethoxysilane. The bonding between the phases involved aminophenyl-trimethoxysilane, in which the amino group can react with the phthaloyl chloride end-capped polymer, and the methoxysilane groups undergo hydrolysis. The composition of these composites was varied by changing the linear polymer chain length and relative amount of tetramethoxysilane. The gelation time was found to range from a few minutes to several days. Thermogravimetric analyses showed that decomposition starts at approximately 450 °C. Thin films cast from materials having a relatively high silica content were opaque and rigid, but those with low silica content were flexible and transparent.     

Effect of Rare-Earth Additives on Electromechanical Properties of Modified Lead Titanate Ceramics

The influence of rare-earth additives, such as La, Nd, Sm, and Gd, and poling conditions on the electromechanical properties of (Pb_{1−3 x /2}Ln _x )(Ti_0.98Mn_0.02)O₃ compositions, x = 0.04–0.12, were investigated. The type and amount of additive were found to affect the lattice anisotropy, dielectric constant, and electromechanical properties. A large electromechanical anisotropy ( k _t / k _p ) could be obtained in 10 mol% Sm-modified and 8 mol% Gd-modified lead titanate ceramics, and seemed to correlate to a low Poisson's ratio.     

Quantitative preparation of long chain thioethers from an oxo-trans-2-enoic ester and a 9,12-dioxo-trans-10-enoic acid

Branched-chain thioethers have been prepared from methyl 4-oxo-trans-2-hexadecenoate and 9,12-dioxo-trans-10-octadecenoic acid. The reagents involved in these preparations were mercaptoacetic and mercaptopropionic acids. The yields of these thioethers are almost quantitative.