Optimized preparation of alumina based fillers for tuning composite properties

Alumina based particles were prepared from aluminium chloride hydroxide as starting material by sol-gel technique. One series of particles was doped with ferrous oxide. Both series of particles were calcinated at three different temperatures: 700?°C, 800?°C and 900?°C. Poly(methyl methacrylate), PMMA, was used as a matrix and two different types of alumina based particles were added into the matrix to form the composites. All composites consisted of 3?wt% of alumina based particles. The aim of this study was to examine whether and how the temperature of particle calcination affects the microhardness and mechanical properties of the composite. The particles were characterized by the X-ray diffraction (XRD) and physical absorption methods. The morphology of the composites was examined using a field emission scanning electron microscope (FESEM). The microhardness of composites was measured using a traditional Vickers hardness (HV) method. The mechanical characteristics of obtained composites were determined using tensile test and impact testing.     

Studies of structure in carbonized composites from a phenolic resin and oxidized PAN fibres using chromic acid as an etchant

Composites have been prepared from a phenolic resin (49 vol%) and oxidized PAN fibres (51vol%) with heat treatment to 423, 573, 873, 973, 1073 and 1173 K. Optical and scanning microscopy of polished surfaces indicate a fusing of these two materials into a homogeneous matrix. However, SEM of samples etched with chromic acid shows that the identity of materials is preserved. Initially the resin is less reactive than the PAN fibres. Upon carbonization, the carbon from the resin and the PAN have approximately equal reactivities. Enhanced etching occurs at the curved interfaces of the two carbons. The transverse sections of PAN fibres, HTT>973 K exhibit selective etching suggesting the existence of skin/core components in the fibre. It is the more graphitic components of the skin region which are oxidized preferentially.     

Fate of ivermectin residues in ewes' milk and derived products

The fate of ivermectin (IVM) residues was studied throughout the processing of daily bulk milk from 30 ewes (taken up to 33 d following subcutaneous administration of 0.2 mg IVM/kg b.w.) in the following milk products: yoghurt made from raw and pasteurized milk; cheese after pressing; 30- and 60-day ripened cheese; and whey, secondary whey and whey proteins obtained after cheese-making (albumin cheese). The concentration of the H2B1a component of IVM was analysed in these dairy products using an HPLC method with fluorescence detection. The mean recovery of the method was, depending on the matrix, between 87 and 100%. Limits of detection in the order of only 0.1 microg H2B1a/kg of product were achieved. Maximum concentrations of IVM were detected mostly at 2 d after drug administration to the ewes. The highest concentration of IVM was found on day 2 in 60-day ripened cheese (96 microg H2B1a/kg cheese). Secondary whey was the matrix with the lowest concentration of IVM (<0.6 microg H2B1a/ kg). Residue levels fell below the limits of detection between day 5 (for secondary whey) and day 25 (for all cheese samples). In the matrices investigated, linear correlations between daily concentrations of IVM, milk fat and solid content were evident. During yoghurt production, fermentation and thermal stability of IVM was observed. During cheese production, approximately 35% of the IVM, present in the raw (bulk) milk samples, was lost. From the results it was concluded that the processing of ewes' milk did not eliminate the drug residues under investigation. The consequences of IVM in the human diet were discussed. Milk from treated animals should be excluded from production of fat products like cheese for longer after treatment with IVM than for lower fat products.     

Transformations of mercury in the terrestrial isopod Porcellio scaber (Crustacea)

The biological cycle of mercury in the terrestrial isopod Porcellio scaber was investigated. Testing the possibility of in vivo Hg(2+) methylation was divided into two methodologically different parts. Firstly, concentrations of total mercury and MeHg in isopods P. scaber and their environment from a Hg-unpolluted area were measured by the use of validated methods (CV AAS, CV AFS). The data obtained show that the percentage of MeHg in leaves, soil and faeces was less than 1%. In contrast, the percentage of MeHg in gut and hepatopancreas was increased to 14 and 77%, respectively, indicating methylation of Hg(2+) in the gut and its further accumulation in glands. To confirm this assumption, the second methodology was applied-a radiotracer technique with 203Hg(2+) of high specific activity. There are few radiotracer techniques for Hg-methylation assays; for our work we chose the method of Czuba et al. which includes alkaline leaching of Hg species, their extraction into dithizone-toluene, followed by specific separation of Hg dithizonates by thin-layer chromatography and gamma counting. All steps of the analytical protocol were checked and optimised by the use of aqueous solutions of 203Hg(2+) and Me(203)Hg(+). The most important finding was that cleaning-up the extract through a florisil column is not appropriate, because the column retains different percentages of Hg(2+) and MeHg(+) and consequently affects the accuracy of the final result. This optimised protocol was then applied to Hg transformation studies in the terrestrial isopod P. scaber. Leaching Hg species from P. scaber fed with 203Hg(2+) or Me(203)Hg(+) dosed food was completely efficient only at elevated temperatures. Preliminary results of methylation/demethlytion studies are rather variable but they show that both processes (Hg(2+)<-->MeHg(+)) take place in the isopod P. scaber. Additionally, an assessment of the mass balance of Hg in isopods P. scaber exposed to 203Hg(2+) indicates that volatile Hg species are also formed.     

Fully-Naphthalenoid Hydrocarbons and their Conjugation Modes

Abstract

A fully-naphthalenoid hydrocarbon (FUN) is a benzenoid hydrocarbon whose all π-electrons can be (formally) grouped into disjoint naphthalene-units. The cyclic conjugation in FUNs is studied by means of the energy-effects of their various cycles. It is found that the dominant conjugation modes in FUNs are those involving the 6- and 10-membered cycles of the “full” naphthalene fragments. The cycles belonging to the “empty” domains of a FUN have significantly smaller energy-effects.     

The synthesis and structural study of two benzothiazolyl azo dyes: X-ray crystallographic and computational study of azo–hydrazone tautomerism

The synthesis, FT-IR, ¹H and ¹³C NMR characterisation, as well as crystal and molecular structure determined by single-crystal X-ray diffraction data, of two azo dyes derived from 6-aminobenzothiazole: 6-[(4-N,N-dimethylaminophenyl)diazenyl]benzothiazole and 6-[(2-hydroxy-1-naphthyl)diazenyl]benzothiazole are reported. Both dyes are essentially planar with the exclusion of methyl groups in 6-[(4-N,N-dimethylaminophenyl)diazenyl]benzothiazole, which exibits 100% E-configuration in terms of orientation of the substituents about the central azo linkage. Single-crystal X-ray study of 6-[(2-hydroxy-1-naphthyl)diazenyl]benzothiazole was undertaken to established whether the hydrazone or azo tautomer was present in the solid state as well as any potential shift in tautomeric equilibrium imparted by temperature variation (296 and 100 K). Density functional theory calculations revealed that the hydrazone tautomer was more stable than the azo tautomer and that the tautomeric equilibrium was shifted towards the hydrazone form at lower temperature.     

Potentials and economic viability of small grain residue use as a source of energy in Serbia

One of the numerous challenges awaiting Serbia in the process of European integration is the increase in use of renewable sources of energy. The reason for such an increase is not merely a formal acceptance of European goals but the high energy import dependence, a relatively developed agricultural sector, with insufficiently exploited potentials of biomass, accompanied by an ever-growing awareness of the need for establishing long-lasting sustainable development. Serbia has a relatively undeveloped livestock sector which can absorb a limited portion of the biomass produced. Additionally, insufficient awareness on the part of farmers and the preconception of the low cost-effectiveness of biomass utilisation for the purpose of energy production are factors which, unsurprisingly, contribute to the current practice of burning the largest portion of the biomass produced on site, which is economically and ecologically unacceptable. This paper analyses the amounts of biomass available in Serbia and the prospects of its economically viable utilisation. The cost analysis conducted indicates that the energy obtained from small rectangular straw bales (the most widespread way of utilisation), is less costly by 28%, than the energy obtained from coal, whereas the energy obtained from round bales is cheaper by 34%. Sensitivity analysis has shown that the results obtained are relatively resistant to price changes in the most important inputs. The sensitivity is higher towards the efficiency of the machinery used; therefore, insistent efforts should be made for creating conditions where the introduction of more up-to-date technical solutions, already existing in developed countries, will become feasible.     

Salting-out in Aqueous Solutions of Ionic Liquids and K3PO4: Aqueous Biphasic Systems and Salt Precipitation

The salting-out effect produced by the addition of potassium phosphate, K₃PO₄ to aqueous solutions of water-miscible ionic liquids, viz. 1-ethyl-3-methylimidazolium ethyl sulfate, 1-butyl-3-methylimidazolium methyl sulfate, or 1-alkyl-3-methylimidazolium chloride (alkyl = butyl, octyl or decyl) is investigated. The effects are analyzed using both the corresponding temperature–composition pseudo-binary and composition ternary phase diagrams. Different regions of liquid-liquid and solid-liquid phase demixing are mapped. The phase behavior is interpreted taking into account the complex and competing nature of the interactions between the ionic liquid, the inorganic salt and water. In the case of solutions containing 1-octyl- or 1-decyl-3-methylimidazolium chloride, the smaller magnitude of the salting-out effects is explained in terms of the possibility of self-aggregation of the ionic liquid.     

Interaction of the cubic boron nitride with the gas phase of chrome iodides

Translated from Poroshkovaya Metallurgiya, No. 3(327), pp. 90–92, March, 1990.