1,755 research outputs found

    Study of the effect of pH, salinity and DOC on fluorescence of synthetic mixtures of freshwater and marine salts

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    In order to provide support for the discussion of the fate of organic matter in estuaries, a laboratory simulation was performed by changing freshwater ionic strength, pH and organic matter content. The change in spectroscopic characteristics caused by variations in salinity, pH and organic matter concentration in the filtered samples was observed by UV-Vis and fluorescence spectroscopy. The increase in emission fluorescence intensity of dissolved organic matter (DOM) due to increasing salinity (in the range 0 to 5 g l−1) is affected by the pH of the samples. The emission fluorescence intensity at the three maxima observed in the fluorescence spectra, is linearly correlated with dissolved organic carbon (DOC) concentration at several salinity values in the same sample. The increase in organic matter concentration caused a shift in the emission peak wavelength at 410 nm for several salinity values.We concluded that it is necessary to take into account the influence of salinity and pH on emission fluorescence of dissolved organic matter if it is to be used as a tracer in estuarine or near shore areas

    Chemical changes of heat treated pine and eucalypt wood monitored by FTIR

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    A hardwood, Eucalyptus globulus Labill., and a softwood Pinus pinaster Aiton., were heat treated at temperatures between 170 and 210ÂșC in an oven and in an autoclave. The samples were pre-extracted with dichloromethane, ethanol and water and ground prior to Fourier Transform Infrared (FTIR) spectroscopic analysis. The heat treatment caused significant changes in the chemical composition and structure of wood, in lignin and polysaccharides. Hemicelluloses were the first to degrade as proved by the initial decrease of the 1730 cm-1 peak due to the breaking of acetyl groups in xylan. Hardwood lignin changed more than softwood lignin, with a shift of maximum absorption from 1505 cm-1 to approximately 1512 cm-1 due to decrease of methoxyl groups, loss of syringyl units or breaking of aliphatic side-chains. The macromolecular structure becomes more condensed and there is a clear increase of non-conjugated (1740 cm-1) in relation to conjugated groups (1650 cm-1). However, the changes induced by the thermal treatment are difficult to monitor by FTIR spectroscopy due to the different chemical reactions occurring simultaneously.info:eu-repo/semantics/publishedVersio

    Stacking effect via solvent polarity differences in micellar electrokinetic chromatography with aqueous-organic background electrolyte

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    In this manuscript, a new stacking mode for micellar electrokinetic chromatography with anionic micelles and neutral analytes was investigated. The variation in the velocity of the analytes between the sample and the separation zones, needed for stacking effects, was obtained by using solvents with different polarities, the concentration of salts and micelles being identical between the two zones. Whereas a pure aqueous solvent was used in the injection zone, up to 30% ACN was used in the separation zone. In such conditions, higher interactions between the analyte and the micelles are obtained in the sample zone than in the separation zone, this due to the presence of the organic solvent. As the velocity of neutral analyte depends on its interactions with the moving micelles, its speed will drop when crossing two distinct zones where in the second zone its interactions with the micelles are lower than in the outgoing zone. This will induce a stacking effect. This approach was validated using a background electrolyte in the separation zone made with 10 mM disodium hydrogen phosphate, 15 mM sodium dodecyl sulphate and 15% ACN. The three triazines (simazine, atrazine, and terbuthylazine), used as test analytes, were dissolved in 10 mM disodium hydrogen phosphate, 15 mM sodium dodecyl sulphate and either 15 or 0% ACN. A stacking factor of around 2 was obtained injecting the sample in 0% ACN rather than 15% ACN. This was in accordance with the theoretical values predicted measuring the effective mobilities in both zonesCOMPETE/QREN/UE and PTDC/QUI-QUI/116156/2009 and SFRH / BPD / 30548 / 200

    Hybrid membrane/PSA processes for CO2/N-2 separation

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    New integrated schemes combining membrane permeation and pressure swing adsorption (PSA) have been developed for gas separation. By using the membrane as a pre-bulk separation unit and coupling it to the intrinsically dynamic periodic operation of the PSA, the separation performance of the hybrid scheme is enhanced with respect to that of die two stand-alone units. Instead of constant-composition regular feed, the PSA is fed with a mixture which is progressively enriched in the more adsorbed component during the pressurization and high-pressure adsorption steps of the cycle. This results in sharper concentration fronts. The hybrid scheme detailed here has been applied successfully to the bulk separation of an 30:70 mol% CO2/N-2 mixture over activated carbon. Process performance is reported in terms of product recovery and purity at cyclic steady state. Numerical simulations were validated by experimental work on a composite membrane and a laboratory-scale PSA unit. For the examples studied, product purity and recovery for the hybrid process were increased by 23% and 58% for CO2, and by 14% and 5% for N-2, compared to an equivalent stand-alone PSA.publishersversionpublishe

    Carbon Materials Derived from Cyano-Based IL@ZIF-8 Composites for CO2 Sorption Separation Systems

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    Additionally, this work was partially supported by the Asso- ciate Laboratory for Green Chemistry, LAQV, which is funded by national funds from FCT/MCTES (LA/P/00 08/2020) .The sorption capacity and selectivity of pre- and post-carbonized cyano-based metal-organic framework (MOF) composite materials (cyano-based IL@ZIF-8) were investigated for the first time. The influence of the ionic liquid (IL) loading and number of cyano groups in the IL anion on a materials gas sorption separation performance was studied. Sorption-desorption equilibrium isotherms of CO2, CH4, and N2 were measured at 303 K in the ZIF-8, cyano-based IL@ZIF-8 composites and their derived carbon materials. The IL loading did not significantly affect the gas uptake of the carbon materials, while for the composites its main contribution was on the increase of the selectivity. The number of cyano groups in the anion played a key role in the sorption capacity and selectivity performance as it directly affects the N content and textural properties. The carbon material obtained from ZIF-8 (C_ZIF-8) precursor showed the best sorption capacity for all gases, just being surpassed by the C_15%[C6MIM][B(CN)4]@ZIF-8 carbon up to 1 bar. In terms of selectivity performance, carbons based on [C6MIM][B(CN)4]@ZIF-8 composites revealed to be equally or more selective than C_ZIF-8, increasing up to 65% between 0 and 1 bar depending on the mixture. The composites produced and their respective carbons demonstrated a promising application as sorbents for post-combustion CO2 separation systems.publishersversionpublishe

    Sulfated Polysaccharides in Marine Sponges: Extraction Methods and Anti-HIV Activity

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    The extraction, fractionation and HIV-1 inhibition potential of polysaccharides extracted from three species of marine sponges, Erylus discophorus, Cliona celata and Stelletta sp., collected in the Northeastern Atlantic, is presented in this work. The anti-HIV activity of 23 polysaccharide pellets and three crude extracts was tested. Crude extracts prepared from Erylus discophorus specimens were all highly active against HIV-1 (90 to 95% inhibition). Cliona celata pellets showed low polysaccharide content (bellow 38.5%) and almost no anti-HIV activity (<10% inhibition). Stelletta sp. pellets, although quite rich in polysaccharide (up to 97.3%), showed only modest bioactivity (<36% HIV-1 inhibition). Erylus discophorus pellets were among the richest in terms of polysaccharide content (up to 98%) and the most active against HIV-1 (up to 95% inhibition). Chromatographic fractionation of the polysaccharide pellet obtained from a specimen of Erylus discophorus (B161) yielded only modestly active fractions. However, we could infer that the active molecule is most probably a high molecular weight sulfated polysaccharide (>2000 kDa), whose mechanism is possibly preventing viral attachment and entry (fusion inhibitor)

    Electromagnetic hybrid active-passive vehicle suspension system

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    The suspension systems currently in use can be classified as passive, semi-active and active. The passive suspension systems are the most commonly used due to their low price and high reliability. However, this system can not assure the desired performance from a modem suspension system An important improvement of the suspension performance is achieved by the active systems. Nevertheless, they are only used in a very reduced number of automobile models because they are expensive and complex. Another disadvantage of active systems is the relatively high energy consumption. The use of electromagnetic linear actuators is an alternative for the implementation of active suspensions. Moreover, this solution has the advantage of the suspension energy recovery. In spite of the materials development, the electromagnetic actuators are yet expensive to produce. In this paper it is proposed an hybrid suspension system which combines the simplicity of the passive dampers with the performance of an electromagnetic active suspension. Maintaining the passive damper, it is possible to keep the performance of the active suspension, but using a smaller electromagnetic actuator

    Permanent-magnets linear actuators applicability in automobile active suspensions

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    Significant improvements in automobile suspension performance are achieved by active systems. However, current active suspension systems are too expensive and complex. Developments occurring in power electronics, permanent magnet materials, and microelectronic systems justifies analysis of the possibility of implementing electromagnetic actuators in order to improve the performance of automobile suspension systems without excessively increasing complexity and cost. In this paper, the layouts of hydraulic and electromagnetic active suspensions are compared. The actuator requirements are calculated, and some experimental results proving that electromagnetic suspension could become a reality in the future are shown
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