Application of thermal ultrasound-assisted liquid–liquid micro-extraction coupled with HPLC-UV for rapid determination of synthetic phenolic antioxidants in edible oils

A simple, fast, and reliable liquid–liquid micro-extraction (LLME) method assisted by thermal ultrasound approach was developed for simultaneous determination of synthetic phenolic antioxidants (SPAs) in edible oils by high-performance liquid chromatography equipped with ultraviolet detector (HPLC-UV). The synthetic antioxidants were propyl gallate (PG), butylated hydroxyanisole (BHA), tert-butylhydroquinone (TBHQ), and butylated hydroxyltoluene (BHT). The best extraction conditions were observed were methanol/acetonitrile (1:1, v/v) as the solvent, ultrasound at 4 min, and a temperature of 40°C. The linearity of the calibration curves for the optimum conditions were R² > 0.989 for all of the SPAs in a range from 1–200 μg ml⁻¹. Relative standard deviation (RSD %) for five analysis was in range of 2.83% to 4.21%. Limit of detection (LOD) and limit of quantification (LOQ) were obtained in range of 0.012–0.06 and 0.04–0.2 μg g⁻¹, respectively. With regard to recovery, a range of 91%–116% was calculated for the spiked edible oils.     

Multi carrier energy systems and energy hubs: Comprehensive review,survey and recommendations

In this paper, the multi carrier energy (MCE) systems are reviewed from different point of views including mathematical models, integrated components and technologies, uncertainty management, planning objectives, environmental pollution, resilience, and robustness. The basic of MCE systems is formed by combination of cooling, heating and power (CCHP). The natural gas and electricity are the main inputs to MCE systems and the cooling, heating, and electricity are the common outputs. The regular energy converters in the MCE systems are combined heat and power (CHP), gas boiler, absorption-electrical chillers, power to gas (P2G) and fuel-cell. The generic energy storages are electrical, heating, cooling, hydrogen, carbon dioxide (CO₂) and hydro systems.     

Rheological and thermal stability of novel weak gels based on sulfonated polyacrylamide/scleroglucan/chromium triacetate

The present study deals with weak gels based on sulfonated polyacrylamide (SPA)/scleroglucan (SC)/Cr³⁺ with an exceptional thermal stability in electrolyte media. The rheological results showed that on increasing the SC concentration the shear viscosity and storage modulus of the SPA/SC/Cr³⁺ system were increased and the dependence of the storage modulus on frequency became weaker. The yield stress of the SPA/SC/Cr³⁺ system was higher than that of the corresponding SPA/SC system. The thermochemical stability increased with increasing relaxation time. The SPA/SC/Cr³⁺ semi‐interpenetrating network exhibited the lowest viscosity loss in electrolyte media; therefore this system may be a potential candidate for enhanced oil recovery applications. © 2016 Society of Chemical Industry     

Structure–property relationships in ternary polymer blends with core–shell inclusions: revisiting the critical role of the viscosity ratio

Structure–property relationship in typical polypropylene/polycarbonate/poly[styrene-b-(ethylene-co-butylene)-b-styrene] (PP/PC/SEBS) ternary blends containing maleated SEBS (SEBS-g-MAH) was investigated. Three grades of PC with different melt viscosities were used, and changes in blend morphology from PC/SEBS core–shell particles partially surrounded by SEBS-g-MAH to inverse SEBS/PC core–shell particles in PP matrix were observed upon varying the viscosity ratio of PC to SEBS. It was found that the viscosity ratio completely controls the size of the core–shell droplets and governs the type, population, and shape of the dispersed domains, as evidenced by rheological, mechanical, and thermomechanical behavioral assessments. Dynamic mechanical analysis of samples with common (PC–SEBS) and inverse (SEBS–PC) core–shell particles revealed that they show completely different behaviors: blends containing PC–SEBS presented a higher storage and loss modulus, while blends containing SEBS–PC exhibited a lower β-transition temperature. Moreover, ternary blends with PC cores showed the highest Young’s modulus values and the lowest impact strength, due to the different fracture modes of the blends containing PC–SEBS and SEPS–PC core–shell droplets, which present debonding and shell-fracture mechanisms, respectively. Morphological observations of blends with high-molecular-weight PC demonstrated the presence of detached droplets and rods of PC in the PP matrix, along with composite core–shell and rod-like particles. Micrographs of the fracture surfaces confirmed the proposed mechanisms, given the presence of stretched (debonded) PC (SEBS) cores encapsulated by SEBS (PC), which require more (less) energy to achieve fracture. The correlation between the mechanical and morphological properties proves that decreasing core diameter and shell thickness has positive effects on the impact strength but decreases the Young’s modulus.     

Compatibilization mechanisms of nanoclays with different surface modifiers in UCST blends: Opposing effects on phase miscibility

The effects of organically modified and pristine nanoclays on the kinetics of thermodynamic equilibrium state attainment for semicrystalline binary blends of polyethylene (PE)/ethylene-vinyl acetate copolymer (EVA) have been investigated. Due to the non-equilibrium compatibilization mechanism, intercalated organoclay results in a slower rate of phase miscibility change at lower annealing temperatures, thereby worsening the PE/EVA compatibility state. In contrast to poorly dispersed pristine nanoclay, the homogeneous state is obtained at higher or equal rates by adding organoclay at higher annealing temperatures because of the dominant role of nanofiller equilibrium compatibilization mechanism. Phase diagrams of these UCST blends determined by a dynamic method shifts to higher temperatures by the incorporation of nanofillers and the unexpected reduction in miscibility window area is much more noticeable for nanocomposites having highly restricted molecular movements. This can verify that dynamic methods lose their efficiency for measuring the equilibrium phase diagram of polymer blends containing nanoparticles.     

A strategic planning model for natural gas transmission networks

The design and development of natural gas transmission pipeline networks are multidisciplinary problems that require various engineering knowledge. In this problem, the type, location, and installation schedule of major physical components of a network including pipelines and compressor stations are decided upon over a planning horizon with least cost goal and subject to network constraints. Practically, this problem has been viewed as a conceptual design case and not as an optimization problem that tries to select the best design option among a set of possible solutions. Consequently, conceptual design approaches are usually suboptimal and work only for short-run development planning. We propose an integrated nonlinear optimization model for this problem. This model provides the best development plans for an existing network over a long-run planning horizon with least discounted operating and capital costs. A heuristic random search optimization method is also developed to solve the model. We show the application of the model through a simple case study and discuss how non-economic objectives may also be incorporated into model.     

Estimation of flame parameters for flame bending process

In this paper a new analytical solution is applied to study heat transfer during forming of plates by flame bending process. Produced heat flux with flame, is modeled with normal Gaussian distribution, which moves along predefined paths on plate. Mild steel with constant thermal properties is as selected material. Results of the thermal analyses by this method show good agreement in comparison with experimental data. This method is properly applicable to estimate of flame parameters that are input parameters for thermo-mechanical simulation of the process. Reasonable accuracy of the results and diminishing of model dependency and CPU time required for thermal analyses are the advantages of this solution for the process study.     

Dielectric coefficient and density of subcooled liquid hydrogen

Here we present precision dielectric coefficient measurements of subcooled equilibrium liquid hydrogen in the temperature range from 15 to 23 K and under pressures up to 1 MPa. The measurements were performed using a three-terminal flat plate capacitor and a single-frequency, ultra-precision capacitance bridge. These results are combined with the previously published data to express the dielectric coefficient in the form of the Clausius-Mossotti relation with a new correlation. The results reported in this paper are expected to be especially useful for capacitance-based measurements involving fluid hydrogen such as liquid level, mass gauging and void fraction measurements in two phase flow. Also, a new equation of state gives the density as a function of pressure and temperature for the subcooled liquid phase.     

Upper Bounds on the Partial Correlation of PN Sequences

Upper bounds on the worst case autocorrelation and the worst case cross correlation of linear PN sequences of the same period are obtained. The value of the worst case correlation curve at some specific points is found and using interpolation methods a smooth curve fitting to the correlation curve is formulated.     

Reverse iodine transfer polymerization of vinyl acetate and vinyl benzoate: synthesis and characterization of homo‐ and copolymers

Homo‐ and copolymers of vinyl esters including vinyl acetate (VAc) and vinyl benzoate (VBz) were synthesized via the reverse iodine transfer radical polymerization technique. Polymerization was carried out in the presence of iodine as the in situ generator of the transfer agent and 2,2′‐azobis(isobutyronitrile) as the initiator at 70 °C. Reverse iodine transfer radical homopolymerization of VAc and VBz led to conversions of 76 and 57%, number‐average molecular weights of 8266 and 9814 g mol^?1 and molecular weight distributions of 1.58 and 1.49, respectively. The microstructure of the synthesized polymers was investigated in detail using gel permeation chromatography, ¹H NMR, ¹³C NMR and distortionless enhancement of polarization transfer (135° decoupler pulse) techniques. Relatively narrow molecular weight distribution and controlled and predictable trend of molecular weight versus conversion were observed for the synthesized polymers, showing that reverse iodine transfer radical homo‐ and copolymerization of VAc and VBz proceeded with controlled characteristics. Results of molecular weight and its distribution along with the ¹H NMR spectra recorded for homo‐ and copolymers indicated that side reactions can occur during the course of polymerization with a significant contribution when VAc, even in a small amount, was present in the reaction mixture. This can result in polymer chains with aldehyde dead end and broadening of the molecular weight distribution. © 2015 Society of Chemical Industry