Anthocyanins characterization of 15 Iranian pomegranate (Punica granatum L.) varieties and their variation after cold storage and pasteurization

Anthocyanins (ACs) are phenolic compounds that are distributed widely in fruits and vegetables. Apart from imparting color to plants, ACs also have an array of health-promoting benefits. In this research, the amounts of major ACs of 15 pomegranate (Punica granatum L.) varieties obtained from Yazd province were determined. The major ACs detected in the studied varieties were as follows: delphinidin 3-glucoside (2.19–16.29 mg/L), delphinidin 3,5-diglucoside (2.36–63.07 mg/L), pelargonidin 3-glucoside (0.26–1.36 mg/L), pelargonidin 3,5-diglucoside (0.01–8.11 mg/L), cyanidin 3-glucoside (5.78–30.38 mg/L), and cyanidin 3,5-diglucoside (4.39–166.32 mg/L). The effect of storage time of unprocessed and pasteurized juices on ACs content of four selected varieties was also studied. Average degradation percentage of each AC was between 23.0 and 83.0% during 10 days at 4 °C. Moreover, in pasteurized juices average degradation of ACs was 42.8 ± 0.5% after 10 weeks storage at 4 °C.     

Efficient biodegradation of naphthalene by a newly characterized indigenous Achromobacter sp. FBHYA2 isolated from Tehran Oil Refinery Complex

A bacterial strain, FBHYA2, capable of degrading naphthalene, was isolated from the American Petroleum Institute (API) separator of the Tehran Oil Refinery Complex (TORC). Strain FBHYA2 was identified as Achromobacter sp. based on physiological and biochemical characteristics and also phylogenetic similarity of 16S rRNA gene sequence. The optimal growth conditions for strain FBHYA2 were pH 6.0, 30 °C and 1.0% NaCl. Strain FBHYA2 can utilize naphthalene as the sole source of carbon and energy and was able to degrade naphthalene aerobically very fast, 48 h for 96% removal at 500 mg/L concentration. The physiological response of Achromobacter sp., FBHYA2 to several hydrophobic chemicals (aliphatic and aromatic hydrocarbons) was also investigated. No biosurfactant was detected during bacterial growth on any aliphatic/aromatic hydrocarbons. The results of hydrophobicity measurements showed no significant difference between naphthalene- and LB-grown cells. The capability of the strain FBHYA2 to degrade naphthalene completely and rapidly without the need to secrete biosurfactant may make it an ideal candidate to remediate polycyclic aromatic hydrocarbon (PAH)-contaminated sites.     

Forecasting Home Sales in the Four Census Regions and the Aggregate US Economy Using Singular Spectrum Analysis

Accurate forecasts of home sales can provide valuable information for not only, policy makers, but also financial institutions and real estate professionals. Given this, our analysis compares the ability of two different versions of singular spectrum analysis (SSA) methods, namely recurrent SSA (RSSA) and vector SSA (VSSA), in univariate (UV) and multivariate (MV) frameworks, in forecasting seasonally unadjusted home sales for the aggregate US economy and its four census regions (Northeast, Midwest, South and West). We compare the performance of the SSA-based models with classical and Bayesian variants of the autoregressive (AR) and vector AR models. Using an out-of-sample period of 1979:8–2014:6, given an in-sample period of 1973:1–1979:7, we find that the UVVSSA is the best performing model for the aggregate US home sales, while the MV versions of the RSSA is the outright favorite in forecasting home sales for all the four census regions. Our results highlight the superiority of the nonparametric approach of the SSA, which in turn, allows us to handle any statistical process: linear or nonlinear, stationary or non-stationary, Gaussian or non-Gaussian.     

Enhanced oil recovery from carbonate reservoirs by spontaneous imbibition of low salinity water

An experimental study was performed to investigate the impact of low salinity water on wettability alteration in carbonate core samples from southern Iranian reservoirs by spontaneous imbibition. In this paper, the effect of temperature, salinity, permeability and connate water were investigated by comparing the produced hydrocarbon curves. Contact angle measurements were taken to confirm the alteration of surface wettability of porous media. Oil recovery was enhanced by increasing the dilution ratio of sea water, and there existed an optimum dilution ratio at which the highest oil recovery was achieved. In addition, temperature had a very significant impact on oil recovery from carbonate rocks. Furthermore, oil recovery from a spontaneous imbibition process was directly proportional to the permeability of the core samples. The presence of connate water saturation inside the porous media facilitated oil production significantly. Also, the oil recovery from porous media was highly dependent on ion repulsion/attraction activity of the rock surface which directly impacts on the wettability conditions. Finally, the highest ion attraction percentage was measured for sodium while there was no significant change in pH for all experiments.     

Simultaneous Determination of Pentaerythritol Tetranitrate and 2,4,6‐Trinitrotoluene by High Performance Thin Layer Chromatography and Partial Least Squares Regression (PLSR) Method

High performance thin layer chromatography (HPTLC) has been used for the simultaneous determination of pentaerythritol tetranitrate (PETN) and 2,4,6‐trinitrotoluene (TNT). With this aim, the spots were developed on silica gel 60 F₂₅₄ layers with petroleum ether–acetone (2 : 1 v/v). Both PETN and TNT compounds were separated from other constituent materials, and were developed at the same speed, by this solvent system. Then ultraviolet (UV) spectra of these materials were recorded with TLC‐scanner3 of CAMAG Company, and partial least squares regression‐2 (PLSR‐2) method was applied for the calibration and quantitative determination of these materials. The figure of merit (FOM) of this method was determined, and the method was applied for the analysis of an artificial sample.     

Numerical modeling of thawing in frozen rocks of underground mines caused by backfilling

The thawing effect due to backfilling in permafrost mining rocks is investigated. The heat transfer equation in rock and backfill is obtained by considering the effect of phase change, heat generation due to cement hydration and temperature dependent material properties. The governing equations are solved using a finite volume numerical method and the phase change phenomenon is modeled based on the manipulation of specific heat, thermal conductivity and density of rock and backfill. The harmonic mean method was employed to handle the change of thermal properties. The effects of different influential parameters such as cement content of backfill, water content of rock and backfill, thermal conductivity of rock and filling material, and the number of adjacent stopes are investigated. Eventually, using the resulting temperature and phase field, a new parameter regarded as the radius of thawing, is introduced.     

The evaluation of autothermal methane reforming for hydrogen production over Ni/CeO2 catalysts

Nanocrystalline Ni/CeO₂ catalysts with various loadings of Ni (10, 15, 20, and 25%) were synthesised by a facile solvent deficient precipitation method for methane autothermal reforming process. The characterisation techniques such as XRD, BET, TPH, H₂-TPR were carried out on fresh and spent samples to investigate the catalytic properties of the Ni/CeO₂. On the basis of characterisation results, the 20% Ni/CeO₂ performs the best activity among the catalysts with different Ni contents. The optimal reaction conditions for autothermal methane reforming has been investigated by evaluating the effect of reaction parameters including the reactivity temperature, the gas hourly space velocity (GHSV) and H₂O/CH₄ (S/C) and O₂/CH₄ (O/C) molar ratios. The stability of 20 wt% Ni/CeO₂ catalyst at 700 °C is examined for 20 h on-stream reaction. It reveals that the methane conversion starts a graduate decrease trend from the second 10 h, which is found to be because of the sintering of Ni nanoparticles by TPH and BET analysis.     

Steady-state and dynamic desorption of organic vapor from activated carbon with electrothermal swing adsorption

A new method to achieve steady-state and dynamic-tracking desorption of organic compounds from activated carbon was developed and tested with a bench-scale system. Activated carbon fiber cloth (ACFC) was used to adsorb methyl ethyl ketone (MEK) from air streams. Direct electrothermal heating was then used to desorb the vapor to generate select vapor concentrations at 500 ppmv and 5000 ppmv in air. Dynamic-tracking desorption was also achieved with carefully controlled yet variable vapor concentrations between 250 ppmv and 5000 ppmv, while also allowing the flow rate of the carrier gas to change by 100%. These results were also compared to conditions when recovering MEK as a liquid, and using microwaves as the source of energy to regenerate the adsorbent to provide MEK as a vapor or a liquid.     

Roles of Li+ and Zr4+ cations in the catalytic performances of Co(1-x)M(x)Cr(2)O(4) (M = Li, Zr; x = 0-0.2) for methane combustion

Co(1-x)M(x)Cr(2)O(4) (M = Li, Zr; x = 0-0.2) catalysts were prepared via the citric acid method and investigated for catalytic combustion of methane. Substitution at tetrahedral (A) sites with monovalent (Li) or tetravalent (Zr) metal ions led to a decrease or increase of the catalytic activity, respectively. The Co(0.95)Zr(0.05)Cr(2)O(4) catalyst proved to be the most active and its catalytic activity reached 90% of methane conversion at 448 °C, which dropped by 66 °C compared with that of the undoped CoCr(2)O(4) catalyst. XRD and Raman results indicated that lithium or zirconium substitution could modify the spinel structure and electronic properties. For lithium-doped catalysts, oxygen deficiency and a strong surface enrichment in lithium and chromium were detected. Zirconium substitution enhanced the reducibility of zirconium-doped catalysts and decreased the strength constant of both the Co-O band and the Cr-O band, which may contribute to the catalytic activity toward methane combustion. In addition, the prevalent catalytic combustion activity of the zirconium-substituted catalysts could be explained by their higher concentration of suprafacial, weakly chemisorbed oxygen.