EFFICIENCY OF A CONTROLLED-CYCLE EXTRACTOR

Experimental studies were performed with a 4.0 in. (10.2 cm.) diameter extraction column containing ten dualflow type trays and operated in a controlled cycling mode. The systems methyl isobutyl ketone/acetic acid/water and toluene/acetone/water were used. The overall stage efficiency was found to be a function of the ratio of the volume of a phase transferred during a cycle to the volume of that phase held up on the tray, of the feed-to-solvent ratio, and of the phase throughput rates. A non-equilibrium model was developed to represent the experimental data. For the HIBK/acetic acid/water system, overall stage efficiencies were in the range of 30 to 38 percent, corresponding to HETS values of 0.46 to 0.55 meters. For the toluene/acetone/water system, overall stage efficiencies were in the range of 20 to 31 percent, corresponding to HETS values of 0.55 to 0.95 meters.     

Polymer electrolyte membranes from fluorinated polyisoprene-block-sulfonated polystyrene: Structural evolution with hydration and heating

Small-angle neutron scattering (SANS) and ultra-small-angle X-ray scattering (USAXS) have been used to study the structural changes in fluorinated polyisoprene/sulfonated polystyrene (FISS) diblock copolymers as they evolved from the dry state to the water swollen state. A dilation of the nanometer-scale hydrophilic domains has been observed as hydration increased, with greater dilation occurring in the more highly sulfonated samples or upon hydration at higher temperatures. Furthermore, a decrease in the order in these phase separated structures is observed upon swelling. The glass transition temperatures of the fluorinated blocks have been observed to decrease upon hydration of these materials, and at the highest hydration levels, differential scanning calorimetry (DSC) has shown the presence of tightly bound water. A precipitous drop in the mechanical integrity of the 50% sulfonated materials is also observed upon exceeding the glass transition temperature (T_g), as measured by dynamic mechanical analysis (DMA).     

Review on carbon-derived,solid-state,micro and nano sensors for electrochemical sensing applications

The aim of this review is to summarize the most relevant contributions in the development of electrochemical sensors based on carbon materials in the recent years. There have been increasing numbers of reports on the first application of carbon derived materials for the preparation of an electrochemical sensor. These include carbon nanotubes, diamond like carbon films and diamond film-based sensors demonstrating that the particular structure of these carbon material and their unique properties make them a very attractive material for the design of electrochemical biosensors and gas sensors.Carbon nanotubes (CNT) have become one of the most extensively studied nanostructures because of their unique properties. CNT can enhance the electrochemical reactivity of important biomolecules and can promote the electron-transfer reactions of proteins (including those where the redox center is embedded deep within the glycoprotein shell). In addition to enhanced electrochemical reactivity, CNT-modified electrodes have been shown useful to be coated with biomolecules (e.g., nucleic acids) and to alleviate surface fouling effects (such as those involved in the NADH oxidation process). The remarkable sensitivity of CNT conductivity with the surface adsorbates permits the use of CNT as highly sensitive nanoscale sensors. These properties make CNT extremely attractive for a wide range of electrochemical sensors ranging from amperometric enzyme electrodes to DNA hybridization biosensors. Recently, a CNT sensor based fast diagnosis method using non-treated blood assay has been developed for specific detection of hepatitis B virus (HBV) (human liver diseases, such as chronic hepatitis, cirrhosis, and hepatocellular carcinoma caused by hepatitis B virus). The linear detection limits for HBV plasma is in the range 0.5–3.0 µL^? 1 and for anti-HBVs 0.035–0.242 mg/mL in a 0.1 M NH₄H₂PO₄ electrolyte solution. These detection limits enables early detection of HBV infection in suspected serum samples. Therefore, non-treated blood serum can be directly applied for real-time sensitive detection in medical diagnosis as well as in direct in vivo monitoring.Synthetic diamond has been recognized as an extremely attractive material for both (bio-) chemical sensing and as an interface to biological systems. Synthetic diamond have outstanding electrochemical properties, superior chemical inertness and biocompatibility. Recent advances in the synthesis of highly conducting nanocrystalline-diamond thin films and nano wires have lead to an entirely new class of electrochemical biosensors and bio-inorganic interfaces. In addition, it also combines with development of new chemical approaches to covalently attach biomolecules on the diamond surface also contributed to the advancement of diamond-based biosensors. The feasibility of a capacitive field-effect EDIS (electrolyte-diamond-insulator-semiconductor) platform for multi-parameter sensing is demonstrated with an O-terminated nanocrystalline-diamond (NCD) film as transducer material for the detection of pH and penicillin concentration. This has also been extended for the label-free electrical monitoring of adsorption and binding of charged macromolecules. One more recent study demonstrated a novel bio-sensing platform, which is introduced by combination of a) geometrically controlled DNA bonding using vertically aligned diamond nano-wires and b) the superior electrochemical sensing properties of diamond as transducer material. Diamond nano-wires can be a new approach towards next generation electrochemical gene sensor platforms.This review highlights the advantages of these carbon materials to promote different electron transfer reactions specially those related to biomolecules. Different strategies have been applied for constructing carbon material-based electrochemical sensors, their analytical performance and future prospects are discussed.     

Estimates of alcohol use and clinical treatment needs among homosexually active men and women in the U.S. population.

Concerns about dysfunctional alcohol use among lesbians and gay men are longstanding. The authors examined alcohol use patterns and treatment utilization among adults interviewed in the 1996 National Household Survey on Drug Abuse. Sexually active respondents were classified into 2 groups: those with at least 1 same-gender sexual partner (n?=?194) in the year prior to interview and those with only opposite-gender sexual partners (n?=?9,714). The authors compared these 2 groups separately by gender. For men, normative alcohol use patterns or morbidity did not differ significantly between the 2 groups. However, homosexually active women reported using alcohol more frequently and in greater amounts and experienced greater alcohol-related morbidity than exclusively heterosexually active women. Findings suggest higher risk for alcohol-related problems among lesbians as compared with other women, perhaps because of a more common pattern of moderate alcohol consumption. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Nanometric bimetallic sulfides prepared via thermal decomposition of Ni and Fe heteropolymolybdate emulsions

NiMo and FeMo nanometric particles were prepared by thermal decomposition of water in oil emulsions, where the aqueous phase was a solution of iron or nickel heteropolymolybdates. Decomposition experiments were carried out at 573 K and 70 Bar of hydrogen, with carbon disulfide added to the emulsions. Solids were characterized by X ray diffraction, confocal microscopy and BET surface area. Thiophene hydrodesulfurization was performed in a continuous flow microreactor at 553 K and 1.0 Bar. Particles with diameters between 370 and 560 nm were obtained, and thiophene HDS was in the order NiMoS > MoS ≈ FeMoS > NiS > FeS. The feasibility of using thermal decomposition of emulsions to obtain nanometric bimetallic sulfides particles was shown.     

Simulation of global solar radiation based on cloud observations

A stochastic model for simulating global solar radiation on a horizontal surface has been developed for use in power systems reliability calculations. The importance of an appropriate model for global solar radiation has increased with the increased use of photovoltaic power generation. The global solar radiation shows not only regular yearly and daily variations but also a random behaviour. The yearly and daily variations can be described in a deterministic way while the random behaviour has a high correlation with the state of the atmosphere. The astronomic effects can easily be described mathematical with only some minor simplifications but the atmospheric effects are more complicated to describe. The transmittivity of solar radiation in the atmosphere depends on various factors, e.g. humidity, air pressure and cloud type. By using cloud observations as input for the simulations, the local meteorological conditions can be accounted for. The model is usable for any geographical location if cloud observations are available at the location or at locations with similar climatological conditions. This is especially useful for development countries where long-term solar radiation measurement can be hard to obtain. Cloud observations can be performed without any expensive equipment and have been a standard parameter for many years throughout the world. Standard observations are done according to the Oktas-scale. It is the interval between observations that sets the resolution of the simulation: the observations are normally only every hour or every third hour. The model can easily be combined with cloud coverage simulations, has been proposed, for a more general model. For some calculations higher resolution may be needed. This can be obtained by including a stochastic model for the short-term variations and simple model has been proposed. Errors and limitations of the model are estimated and discussed.     

Nonlinear coupling between thermal mass and natural ventilation in buildings

An ideal naturally ventilated building model that allows a theoretical study of the effect of thermal mass associating with the non-linear coupling between the airflow rate and the indoor air temperature is proposed. When the ventilation rate is constant, both the phase shift and fluctuation of the indoor temperature are determined by the time constant of the system and the dimensionless convective heat transfer number. When the ventilation rate is a function of indoor and outdoor air temperature difference, the thermal mass number and the convective heat transfer air change parameter are suggested. The new thermal mass number measures the capacity of heat storage, rather than the amount of thermal mass. The analyses and numerical results show that the non-linearity of the system does neither change the periodic behaviour of the system, nor the behaviour of phase shift of the indoor air temperature when a periodic outdoor air temperature profile is considered. The maximum indoor air temperature phase shift induced by the direct outdoor air supply without control is 6 h.