Preparación y propiedades de tensión superficial de diol monoésteres oxipropilados de ácidos grasos con un grupo terminal amido oxima

Locally produced non-edible oil, namely, rice bran oil (R.B.O.) was utilized as starting materials for preparing new nonionic surfactant. Oxypropylated diol monoesters of linoleic and rice bran oil fatty acids were prepared. Also amide oxime derivatives were obtained. Surface active properties of these compounds were measured. Under neutral condition amide eximes served as nonionic surfactants and their properties were similar to other oxypropylated monoesters.Se ha utilizado un aceite no comestible de producción local, denominado, aceite de salvado de arroz (R.B.O.) como materia prima para la preparación de nuevos tensioactivos no iónicos. Se prepararon diol monoésteres oxipropilados de ácido linoleico y ácidos grasos de aceite de salvado de arroz. También se obtuvieron los derivados de amido oxima. Se midieron las propiedades de tensión superficial de estos compuestos. Bajo condiciones neutras las amido eximas sirvieron como tensioactivos no iónicos y sus propiedades fueron similares a los de otros monoésteres oxipropilados

Validation for application of the Monte Carlo simulation code for 235U mass content verification for large size samples of nuclear materials

In this work, a new semi- absolute non-destructive assay technique has been developed to verify the mass content of 235U in the large sizes nuclear material samples of different enrichment through combination of experimental measurements and Mont Carlo calculations (version MCNP5). A good agreement was found between the calculated and declared values of the mass content of 235U of uranium oxide (UO2) samples. The results obtained from Mont Carlo calculations showed that the semi-absolute technique can be used with sufficient reliability to verify the uranium mass content in the large sizes nuclear material samples of different enrichment

Structure effect of some amine derivatives on corrosion inhibition efficiency for carbon steel in acidic media using electrochemical and Quantum Theory Methods

The structure effect on corrosion inhibition of two amines and their derivatives is the main object of this article. The first amine was 1,8-diaminooctane and its ethoxylated (50 e.o.) 1,8-diaminooctane and propoxylated (50 p.o.) 1,8-diaminooctane. The second amine is the tetraethylenepentamine and its ethoxylated (50 e.o.) and propoxylated (50 p.o.) derivatives. The investigations were carried out by open circuit potential, potentiodynamic polarization, electrochemical impedance, quantum calculations and SEM measurements. The data obtained for the first amine showed the minimum inhibition efficiency (65.5%), meanwhile the maximum inhibition efficiency was 78.9% for its propoxylated derivative. On the other hand the maximium inhibition efficiency was 91% for the second propoxylated amine. The electronic properties; HOMO and LUMO energy levels, energy gap, dipole moment, polarizability, log P, total energy, charge densities, area/molecule and hydration energy have been calculated. The inhibition efficiency was calculated theoretically using the electronic parameters. From the obtained results, there is a significant difference between the inhibition efficiency of the electronic and the inhibition efficiency experimentally. The results were discussed on the light of the chemical structure of the used inhibitors. In general, the inhibition efficiency is affected by the shape and structure of the molecule

Glycolysis of Poly(ethylene terephthalate) Catalyzed by the Lewis Base Ionic Liquid [Bmim][OAc]

The glycolysis of poly­(ethylene terephthalate) (PET) was studied using 1-butyl-3-methylimidazolium acetate ([Bmim]­[OAc]) as a catalyst. The effects of temperature, time, ethylene glycol dosage, PET amount, and [Bmim]­[OAc] dosage on the glycolysis reaction were examined. The results revealed that [Bmim]­[OAc] has a PET conversion of 100% and a bis­(2-hydroxyethyl)­terephthalate (BHET) yield of 58.2% under the optimum conditions of 1.0 g of [Bmim]­[OAc] with 20 g of ethylene glycol in the presence of 3.0 g of PET at 190 °C after 3 h of glycolysis. The ionic liquid could be reused up to six times with no apparent decrease in the conversion of PET or yield of BHET. The pH plays a major role in explaining the proposed mechanism of glycolysis using the Lewis base ionic liquid [Bmim]­[OAc]. The kinetics of the reaction was first-order with an activation energy of 58.53 kJ/mol