ABSTRACT
The dielectric properties of Cymbopogon nardus, Eucalyptus sp., Piper aduncum and Piper hispidinervum were investigated as a function of frequency and temperature, using dry plant matter and its mixtures with water at different concentrations. This was followed by the extraction of essential oils performed with microwave heating in single-mode and multimode cavities with a variable power 6.0 kW generator operating at 2.45 GHz. The dielectric properties of the dry plant matter changed markedly with increasing water content, exhibiting high loss factors and small penetration depths. Due to the high level of absorption, even with low water contents, microwave-assisted extraction (MAE) showed better green performance employing lower plant matter/water ratios (1 : 2 or 1 : 4) and applying shorter extraction times compared with conventional hydrodistillation (HD). Using the single-mode MAE reactor, in the case of Cymbopogon nardus, for a plant matter/water ratio of 1 : 4 the energy efficiency was 1.78 g kW-1 h-1, applying 0.3 kW for 16.7 min. By way of comparison, for the same extraction time using HD, the corresponding efficiency was only 0.50 g kW-1 h-1. In experiments with citronella using multimode MAE, the best energy efficiency of 2.53 g kW-1 h-1 was obtained with a plant matter/water ratio of 1 : 2 applying 1.8 kW of power for 30 min. Single and multimode MAE experiments showed optimum conditions with lower water content. Thus, greater amounts of material can be processed in a shorter time, in accordance with the ideals of a green chemistry. The resulting extractions showed an energy efficiency up to 27 times greater compared with conventional HD, applying the same extraction time.
ABSTRACT
Microwave heating technology is dependent on the dielectric properties of the materials being processed. The dielectric properties of H2SO4, H3PO4, ClSO3H, and H3CSO3H were investigated in this study using a vector network analyzer in an open-ended coaxial probe method at various temperatures. Phosphoric and sulfuric acids presented higher loss tangents in the frequency range 0.3-13 GHz, reflecting greater mobility of the ions and counterions. The acids were employed as catalysts in microwave-assisted homogeneous transesterification reactions for the production of methylic and ethylic biodiesel. The effects of catalyst concentration, alcohol to oil molar ratio, and irradiation time on biodiesel conversions were investigated. The results showed a significant reduction in the reaction time for microwave-assisted transesterification reactions as compared to times for conventional heating. Also, despite its higher loss tangent, it was observed that H3PO4 leads to lower conversion to biodiesel, which can be explained by its lower carbonyl protonation capacity.
ABSTRACT
A new possibility for estimating the octanol/water coefficient (log P) was investigated using only one descriptor, the semi-empirical electrotopological index (I(SET)). The predictability of four octanol/water partition coefficient (log P) calculation models was compared using a set of 131 aliphatic organic compounds from five different classes. Log P values were calculated employing atomic-contribution methods, as in the Ghose/Crippen approach and its later refinement, AlogP; using fragmental methods through the ClogP method; and employing an approach considering the whole molecule using topological indices with the MlogP method. The efficiency and the applicability of the I(SET) in terms of calculating log P were demonstrated through good statistical quality (r > 0.99; s < 0.18), high internal stability and good predictive ability for an external group of compounds in the same order as the widely used models based on the fragmental method, ClogP, and the atomic contribution method, AlogP, which are among the most used methods of predicting log P.
Subject(s)
Octanols/chemistry , Organic Chemicals/chemistry , Water/chemistry , Models, Chemical , Quantitative Structure-Activity RelationshipABSTRACT
The semi-empirical electrotopological index, I(SET,) used for QSRR models, was developed and optimized to describe the chromatographic retention of saturated esters on the five different stationary phases (SE-30, OV-7, DC-710, OV-225 and XE-60). The simple linear regressions between the retention indices and the proposed index were of good statistical quality, high internal stability and good predictive ability for external groups, especially for the stationary phase with low polarity, showing that the specific molecular interactions occur on highly polar phases. For the esters, the interactions between the molecules and the stationary phase are slowly increased relative to hydrocarbons due to the charge redistribution that occurs in the presence of the heteroatom. These facts were included in the calculation of I(SET) through a small increase in the SET(i) values for heteroatoms and the carbon atoms attached to them. The increase in the SET(i) values originates from the dipole moment of the whole molecule and an equivalent local dipole moment related to the net charges of the atoms belonging to the functional group and the carbon atoms attached to them. The polarity of the stationary phases, indicated by the retention polarity (P(R)) given by Tarján, is reflected in the intercept of the equations obtained for each stationary phase. Thus, a single combined QSRR model was generated with a satisfactory predictive quality, including a parameter that represents the polarity retention of all stationary phases studied.
Subject(s)
Esters/chemistry , Models, Chemical , Molecular Structure , Quantitative Structure-Activity Relationship , Regression AnalysisABSTRACT
Semi-empirical molecular orbital calculations at AM1 level were done with the aim to investigate the structure-activity relationships of antispasmodic activities of ten 2-(X-benzyloxy)-4,6-dimethoxyacetophenones with X = H, 4'-F, 4'-NO2, 4'-CH3, 4'-Cl, 3',4'-(CH3)2, 4'-OCH3, 4'-Br, 4'-OCH2C6H5, and 4'-C(CH3)3, against acetylcholine-induced contraction of the guinea pig ileum. The most significant quantum chemical descriptors for this series of compounds were the net atomic charges, nucleophilic and electrophilic frontier electron density, HOMO and LUMO orbitals, and reactivity indices. While no significant correlations were found employing molecular parameters such as heat of formation, dipole moment, molecular polarizability, and so on, good correlations were obtained using the reactivity indices of HOMO and LUMO orbitals at specific atoms of the molecules. These results indicate that the spatial distribution of HOMO and LUMO orbitals over these specific atoms play an important role for an increase of biological activity.
