In the present work, the mechanism of interaction between asphaltenes and a commercial fatty-alkylamine inhibitor was investigated by a combination of techniques. The “macro” properties, like the asphaltene precipitation onset and the amount of asphaltenes precipitated, were measured by near-infrared (NIR) and UV-vis spectroscopy, respectively, while the interaction enthalpy between asphaltenes and inhibitor was measured by isothermal titration calorimetry (ITC). Asphaltenes subfractions and derivatives were also used to identify the mechanism.
ITC indicated that only a small fraction (~6%) of asphaltenes interacts strongly with the inhibitor. The proportion of interacting species was found to be higher in irreversibly adsorbed asphaltenes subfraction. These 6% are mostly composed of acidic asphaltenes, as indicated by measurements involving ester asphaltenes. However, the measurement of precipitation onset and amounts precipitated for whole and ester asphaltenes indicated that the acid–base interaction was not the main interaction responsible for the inhibitory action. Other type(s) of interaction is/are responsible for the inhibition properties of the inhibitor, which are not detected by ITC. The nature of other interactions is not known for the moment, but it was shown that irreversibly adsorbed asphaltene fraction contains a higher concentration of the functionality (ies) responsible for the “other” type of interaction. 相似文献
This paper reports the thermal characterization of kerosene fuel-doped ionic liquid (1, 2-methylethyl 1-methyl pyrrolidinium bis(trifluoromethanesulfonyl) amide) (MEMP TFSA), an antistatic additive used in jet fuel engines. The ionic liquids (ILs) samples are prepared with the mass of 5, 10 and 15% in the kerosene fuel. These fuel samples are subjected to thermal decomposition studies at different scanning rates of 5, 10 and 15 °C min?1 using the differential scanning calorimetry (DSC) method. The onset temperatures of exothermic reactions of kerosene-doped ILs are increased from 360–465 °C, when the mass percentage of ILs increased in the kerosene fuel. The boiling point of the kerosene-doped ILs was displaced to the higher temperature when compared to the pure kerosene. This showed that the doping of antistatic additives of ILs with kerosene increased its thermal stability property than the pure kerosene fuel. The thermo-kinetic studies are also carried out using Ozawa’s Kinetic method to determine the activation energy (Ea) and pre-exponential factor (A). The FTIR analysis showed that the kerosene-doped ionic liquid forms a homogenous mixture rather than prevailing separately.
We studied the kinetics of the formation of iron oxide nanocrystals obtained from the solution-phase thermal decomposition of iron-oleate complex via the "heating-up" process. To obtain detailed information on the thermal decomposition process and the formation of iron oxide nanocrystals in the solution, we performed a thermogravimetric-mass spectrometric analysis (TG-MS) and in-situ magnetic measurements using SQUID. The TG-MS results showed that iron-oleate complex was decomposed at around 320 degrees C. The in-situ SQUID data revealed that the thermal decomposition of iron-oleate complex generates intermediate species, which seem to act as monomers for the iron oxide nanocrystals. Extensive studies on the nucleation and growth process using size exclusion chromatography, the crystallization yield data, and TEM showed that the sudden increase in the number concentration of the nanocrystals (burst of nucleation) is followed by the rapid narrowing of the size distribution (size focusing). We constructed a theoretical model to describe the "heating-up" process and performed a numerical simulation. The simulation results matched well with the experimental data, and furthermore they are well fitted to the well-known LaMer model that is characterized by the burst of nucleation and the separation of nucleation and growth under continuous monomer supply condition. Through this theoretical work, we showed that the "heating-up" and "hot injection" processes could be understood within the same theoretical framework in which they share the characteristics of nucleation and growth stages. 相似文献
Well-ordered, compact, self-assembled monolayers (SAMs) of hexyl and dodecyl diselenides have been formed on oriented (111) gold surfaces. Monolayer formation has been effected by adsorption from neat diselenides as well as millimolar solutions of diselenides in alcohol. The monolayer formation is confirmed using electrochemical quartz crystal microbalance studies. The stability and permeability of the monolayers at various temperatures have been probed using reflection absorption infrared spectroscopy (RAIRS) and electrochemistry. The RAIRS studies in the dry state show the formation of highly ordered, compact structures when adsorbed from neat compounds compared to the monolayers adsorbed in the presence of alcohol. The monolayers adsorbed from neat diselenide are quite stable as a function of temperature irrespective of the chain length. The electrochemical studies based on the blocking behavior of the monolayers toward electron transfer between a diffusing species and the electrode surface reflect the stability and the compactness of the structure. The results point out that the presence of solvent molecules during the SAM formation hinders the organization of the monolayer structure, especially in the case of short-chain diselenide monolayers. 相似文献
The interfacial properties at well-ordered short-chain alkanethiol monolayer-aqueous interfaces are probed to understand the water structure near a hydrophobic surface. Monolayers of hexanethiol on highly oriented gold substrates have been prepared by various methods such as adsorption from alcoholic solution of the thiol, adsorption from neat thiol, and potential-controlled adsorption. The compactness and crystallinity of the monolayer have been probed using reflection-absorption infrared spectroscopy (RAIRS), atomic force microscopy (AFM), quartz crystal microbalance (QCM), and electrochemical techniques. The presence of a thin layer of solvent with reduced density/dielectric constant (termed "drying transition") close to the methyl groups is identified. This is based on reduced interfacial capacitance observed in the presence of an aqueous electrolyte solution as compared to the expected value for a well-ordered monolayer-aqueous interface. Atomic force microscopy allows the determination of the variation in the dielectric constant of the solvent medium as a function of distance from the monolayer head group. The thickness of the transition layer (interphase) is found to be approximately 2 nm. The phenomenon of drying transition is not unique to water; preliminary studies indicate that formamide, which has a two-dimensional hydrogen-bonded network, shows similar characteristics. 相似文献
This work describes the application of a three-dimensional gold nanoelectrode ensembles (GNEE) for monitoring l-dopa in standards and human urine samples using flow injection analysis (FIA) with amperometric detection. Analytical results reveal that the GNEE exhibited better electrocatalytic activity than a gold disk or glassy carbon electrode. Under optimal conditions of l-dopa analysis at GNEE, the calibration plot has a linear range of 5-300 ng/mL with a coefficient of variation (CV) of 3.1% in pH 7.0 phosphate buffer saline (PBS, pH 7.0). The detection limit was 3.0 ng/mL for FIA. The high precision and sensitivity of GNEE provides a feasible means of directly determining l-dopa in urine samples. 相似文献
New photo-induced electron transfer (PET) probes OMOX and OBOX, carrying an additional binding site in the form of ‘oxadiazole nitrogen’ have been designed to evaluate binding interactions with biologically significant Li+, Na+, K+, Ca2+, Mg2+, and Zn2+ including environmentally toxic Ba2+ and Cd2+ using optical spectral techniques. While Li+, Na+, and K+ did not appreciably perturb either the absorption or emission spectra, Ba2+, Ca2+, Mg2+, Zn2+, and Cd2+ induced slight red shifts (2-8 nm) in the UV-visible spectra as well as pronounced chelation induced enhanced fluorescence (CHEF). Both OMOX and OBOX exhibited the highest CHEF in contact with the zinc ion, whereas Ba2+, Ca2+, Mg2+, and Cd2+ induced relatively less emission enhancements. OBOX, which is a poorer emitter (Φf=0.0062) than OMOX (Φf=0.015), showed highly promising 160-fold emission enhancement in the presence of Zn2+. Potential, therefore is available in OBOX to function as a selective luminescent ‘off-on’ sensor for Zn2+ in the presence of coordinatively competing Ba2+, Ca2+, Mg2+, and Cd2+ ions. 相似文献
This paper deals with the Traveling Salesman Problem (TSP) with Draft Limits (TSPDL), which is a variant of the well-known TSP in the context of maritime transportation. In this recently proposed problem, draft limits are imposed due to restrictions on the port infrastructures. Exact algorithms based on three mathematical formulations are proposed and their performance compared through extensive computational experiments. Optimal solutions are reported for open instances of benchmark problems available in the literature. 相似文献
Photonic bandgap structures can also be utilized for the realization of transformational optical devices like metamaterials. In this Letter, the possibility of cylindrical to plane wave source transformation in an open cavity formed by one dimensional photonic crystal is demonstrated. It is observed that the gap solitary wave behavior at the near-bandgap regime is fair enough to produce highly directional plane waves out of the point source placed inside the open cavity. The limitations of such a source transformation device are governed by the strength of the bandgap that decides the amplitude of the emitted plane waves. 相似文献
Optical coherence tomography (OCT) relies on interference between a polarized reference and the target reflection. Thus, it has generally been impossible to detect any unpolarized part in the signal. Here, we demonstrate a scheme that overcomes this limitation. Using a combination of heterodyning and filtering, we realize a polarization-sensitive OCT system capable of measuring the full Stokes vector, including the depolarized part. Based on such a system, we perform full Stokesmetric imaging of different layers in a porcine tendon sample. The complete 4 × 4 backscattering Muellermetric images of one layer are acquired and investigated. 相似文献