Chitosan-polyvinyl alcohol-sulfonated polyethersulfone mixed-matrix membranes as methanol-barrier electrolytes for DMFCs

Chitosan (CS)-polyvinyl alcohol (PVA) cross-linked with sulfosuccinic acid (SSA) and modified with sulfonated polyethersulfone (SPES) mixed-matrix membranes are reported for their application in direct methanol fuel cells (DMFCs). Polyethersulfone (PES) is sulfonated by chlorosulfonic acid and factors affecting the sulfonation reaction, such as time and temperature, are studied. The ion-exchange capacity, degree of sulfonation, sorption, and proton conductivity for the mixed-matrix membranes are investigated. The mixed-matrix membranes are also characterised for their mechanical and thermal properties. The methanol-crossover flux across the mixed-matrix membranes is studied by measuring the mass balance of methanol using the density meter. The methanol cross-over for these membranes is found to be about 33% lower in relation to Nafion-117 membrane. The DMFC employing CS-PVA-SPES mixed-matrix membrane with an optimum content of 25 wt % SPES delivers a peak power-density of 5.5 mW cm-2 at a load current-density of 25 mA cm-2 while operating at 70 degrees C. (C) 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012

Stiffness- and wettability-dependent myoblast cell compatibility of transparent poly(vinyl alcohol) hydrogels

This study reports the in vitro compatibility of muscle cells (C2C12 mouse myoblast cell line) with the transparent poly(vinyl alcohol) (PVA) hydrogels and the results are explained on the basis of surface wettability, crystallinity, and nanoscale elastic stiffness property. Nanoindentation was carried out with a maximum load of 100 mu N for all the hydrogel compositions and the properties such as elastic stiffness, hardness and total work done during indentation were computed. The difference in cell viability as well as adhesion of cultured myoblast cells on the investigated hydrogel substrates were discussed in reference to the difference in the nanoscale elastic properties, crystallinity, and surface wettability. An important result has been that both elastic stiffness and surface wettability synergistically influence myoblast viability/adhesion on PVA hydrogels. (c) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2013.

Influence of nature of support on the catalytic activity of supported molybdenum-oxo species in benzyl alcohol conversion

Supported catalysts containing 15 wt.% of molybdenum have been prepared by the incipient wetness impregnation method. CaO, MgO, Al2O3, Zr(OH)4 and Al(OH)3 have been used as supports for the preparation of supported Mo catalysts. Characterisation of all the materials prepared has been carried out through BET surface area measurement, X-ray diffractometry and FT-IR spectroscopy. Catalytic activity measurements have been carried out with reference to structure-sensitive benzyl alcohol conversion in the liquid phase. The percentage conversion of benzyl alcohol to benzaldehyde and toluene varied over a large range depending on the support used for the preparation of catalysts, indicating the importance of the support on catalytic activity of Mo catalysts. Al(OH)3 has been found to be the best support for molybdenum among all the supports used. Support–metal interaction (SMI) has been found to play an important role in determining the catalytic activity of supported catalysts.

Microwave Spectroscopic and Atoms in Molecules Theoretical Investigations on the ArPropargyl Alcohol Complex: ArHO, Ar, and ArC Interactions

The structure of the Arpropargyl alcohol (ArPA) complex is determined from the rotational spectra of the parent complex and its two deuterated isotopologues, namely ArPA-D(OD) and ArPA-D(CD). The spectra confirm a geometry in which PA exists in the gauche form with Ar located in between OH and CCH groups. All a, b and c types of transitions show small splitting due to some large-amplitude motion dominated by COH torsion, as in the monomer. Splittings in a- and b-type transitions are of the order of a few kilohertz, whereas splitting in the c-type transitions is relatively larger (0.92.6 MHz) and decreases in the order ArPA>ArPA-D(CD)>ArPA-D(OD). The assignments are well supported by ab initio calculations. Atoms in molecules (AIM) and electrostatic potential calculations are used to explore the nature of the interactions in this complex. AIM calculations not only reveal the expected OHAr and Ar interactions in the Argauche-PA complex, but also novel CAr (of CH2OH group) and OHAr interactions in the Artrans-PA complex. Similar interactions are also present in the Armethanol complex.

Flexible poly(vinyl alcohol-co-ethylene)/modified MMT moisture barrier composite for encapsulating organic devices

Flexible, nano-composite moisture barrier films of poly(vinyl alcohol-co-ethylene) with surface modified montmorillonite fabricated by solution casting were used to encapsulate organic devices. The composite films were characterized by FTIR, UV-visible spectroscopy and SEM imaging. Thermal and mechanical properties of the composite films were studied by DSC and UTM. Calcium degradation test was used to determine the transmission rate of water vapour through the composite films, which showed a gradual reduction from similar to 0.1 g m(-2) day(-1) to 0.0001 g m(-2) day(-1) with increasing modified montmorillonite loading in the neat copolymer. The increase in moisture barrier performance is attributed to the decreased water vapour diffusivity due to matrix-filler interactions in the composite. The accelerated aging test was carried out for non-encapsulated and encapsulated devices to evaluate the efficiency of the encapsulants. The encapsulated devices exhibited longer lifetimes indicating the efficacy of the encapsulant.

Stability of fluctuating and transient aggregates of amphiphilic solutes in aqueous binary mixtures: Studies of dimethylsulfoxide, ethanol, and tert-butyl alcohol

In aqueous binary mixtures, amphiphilic solutes such as dimethylsulfoxide (DMSO), ethanol, tertbutyl alcohol (TBA), etc., are known to form aggregates (or large clusters) at small to intermediate solute concentrations. These aggregates are transient in nature. Although the system remains homogeneous on macroscopic length and time scales, the microheterogeneous aggregation may profoundly affect the properties of the mixture in several distinct ways, particularly if the survival times of the aggregates are longer than density relaxation times of the binary liquid. Here we propose a theoretical scheme to quantify the lifetime and thus the stability of these microheterogeneous clusters, and apply the scheme to calculate the same for water-ethanol, water-DMSO, and water-TBA mixtures. We show that the lifetime of these clusters can range from less than a picosecond (ps) for ethanol clusters to few tens of ps for DMSO and TBA clusters. This helps explaining the absence of a strong composition dependent anomaly in water-ethanol mixtures but the presence of the same in water-DMSO and water-TBA mixtures. (C) 2013 AIP Publishing LLC.

Fluctuating micro-heterogeneity in water-tert-butyl alcohol mixtures and lambda-type divergence of the mean cluster size with phase transition-like multiple anomalies

Water-tert-butyl alcohol (TBA) binary mixture exhibits a large number of thermodynamic and dynamic anomalies. These anomalies are observed at surprisingly low TBA mole fraction, with x(TBA) approximate to 0.03-0.07. We demonstrate here that the origin of the anomalies lies in the local structural changes that occur due to self-aggregation of TBA molecules. We observe a percolation transition of the TBA molecules at x(TBA) approximate to 0.05. We note that ``islands'' of TBA clusters form even below this mole fraction, while a large spanning cluster emerges above that mole fraction. At this percolation threshold, we observe a lambda-type divergence in the fluctuation of the size of the largest TBA cluster, reminiscent of a critical point. Alongside, the structure of water is also perturbed, albeit weakly, by the aggregation of TBA molecules. There is a monotonic decrease in the tetrahedral order parameter of water, while the dipole moment correlation shows a weak nonlinearity. Interestingly, water molecules themselves exhibit a reverse percolation transition at higher TBA concentration, x(TBA) approximate to 0.45, where large spanning water clusters now break-up into small clusters. This is accompanied by significant divergence of the fluctuations in the size of largest water cluster. This second transition gives rise to another set of anomalies around. Both the percolation transitions can be regarded as manifestations of Janus effect at small molecular level. (C) 2014 AIP Publishing LLC.

Thermal Decomposition of Propargyl Alcohol: Single Pulse Shock Tube Experimental and ab Initio Theoretical Study

Thermal decomposition of propargyl alcohol (C3H3OH), a molecule of interest in interstellar chemistry and combustion, was investigated using a single pulse shock tube in the temperature ranging from 953 to 1262 K. The products identified include acetylene, propyne, vinylacetylene, propynal, propenal, and benzene. The experimentally observed overall rate constant for thermal decomposition of propargyl alcohol was found to be k = 10((10.17 +/- 0.36)) exp(-39.70 +/- 1.83)/RT) s(-1) Ab initio theoretical calculations were carried out to understand the potential energy surfaces involved in the primary and secondary steps of propargyl alcohol thermal decomposition. Transition state theory was used to predict the rate constants, which were then used and refined in a kinetic simulation of the product profile. The first step in the decomposition is C-O bond dissociation, leading to the formation of two important radicals in combustion, OH and propargyl. This has been used to study the reverse OH propargyl radical reaction, about which there appears to be no prior work. Depending on the site of attack, this reaction leads to propargyl alcohol or propenal, one of the major products at temperatures below 1200 K. A detailed mechanism has been derived to explain all the observed products.

Rotational spectra of propargyl alcohol dimer: A dimer bound with three different types of hydrogen bonds

Pure rotational spectra of the propargyl alcohol dimer and its three deuterium isotopologues have been observed in the 4 to 13 GHz range using a pulsed-nozzle Fourier transform microwave spectrometer. For the parent dimer, a total of 51 transitions could be observed and fitted within experimental uncertainty. For two mono-substituted and one bi-substituted deuterium isotopologues, a total of 14, 17, and 19 transitions were observed, respectively. The observed rotational constants for the parent dimer A = 2321.8335(4) MHz, B = 1150.4774(2) MHz, and C = 1124.8898(2) MHz] are close to those of the most stable structure predicted by ab initio calculations. Spectra of the three deuterated isotopologues and Kraitchman analysis positively confirm this structure. Geometrical parameters and ``Atoms in Molecules'' analysis on the observed structure reveal that the two propargyl alcohol units in the dimer are bound by three different types of hydrogen bonds: O-H center dot center dot center dot O, O-H center dot center dot center dot pi, and C-H center dot center dot center dot pi. To the best of our knowledge, propargyl alcohol seems to be the smallest molecule forming a homodimer with three different points of contact. (C) 2014 AIP Publishing LLC.

Estudio florístico del estado actual del bosque ripario en la microcuenca el Coyote, Condega, Estelí

La presente investigación fue realizada en la micro cuenca el Coyote ubicada en el municipio de Condega Departamento de Estelí, como parte del convenio de la Universidad Nacional Agraria con el proyecto CARE/MARENA/P IMCHAS, con el fin de mejorar las condiciones ambientales de la micro cuenca. La intención de la investigación fue evaluar la composición florística del bosque ripario de la parte alta, media y baja de la micro cuenca donde se desarrolló en tres etapas: re conocimiento del área, realización del inventario forestal y diagnóstico de la vegetación arbórea. La metodología que se utilizó en dicho estudio fue la aplicación de un inventario forestal con un área muestreada de 0.24 ha (inventario sis temá tico con par celas de 0.01 ha cada una, con un a intensidad de muestreo 0.08 %. La composición florística existente en el bosque la conforman un total de 66 individuos mayores a los 10cm de DAP equivalentes a 31 especies arbóreas, y 18 familias botánicas, sobresaliendo la Fabaceae (5), Mimosaceae (5) y Anacardiaceae (3 especies). En las clases diamétricas la mayoría de los individuos se encuentran en la categoría diamétrica de 10 - 19.9 (clases 1) siendo la parte alta el sitio que más árboles posee con (66.66 arb ha - 1 ) y la parte media con 20.83 arb ha - 1 la parte alta con el m enor número de árboles 8.33 arb ha - 1 en la categoría de 20 - 39.9 (clase 2 y 3), donde el mayor número de individuos se encuentran en la parte baja de la microcuenca con 66.66 arb ha - 1 y la parte me dia con 20.83 arb ha - 1 , la parte alta con el men or número de árboles 8.33 arb ha - 1 . Las categorías silviculturales el mayor porcentaje de árboles presentan fuste recto sin daño evidente (categoría 1), distribuidos de la siguiente manera 13.64 % en la parte alta, 10.61 % en la parte media y 16.67 % en la parte baja. En la categoría de iluminación vertical plena el may or porcentaje de árboles se encuentra en la (categoría 2), distribuidos para la parte alta y la parte media el 4.55% y la parte baja con el 13.64% . Encontramos en la parte baja el 18.18% de árboles sin lianas (categorí a 1), observándose para la parte media el 10.61% y la parte alta el 15.15%, en esta misma categoría. En cuanto a la vigorosidad de los árboles en el bosque ripario la parte baja de la microcuenca tiene el mayor porcentaje con 17.67%, con buen follaje y buena vitalidad aparente, sin daño que afecte su crecimiento (categoría 1), seguida de la parte alta con 13.64% y la parte media con 12.12%. La regeneración natural e n (área muestr eada 0.024 ), consiguiente fue de 541.7 plantas ha - 1 , representada por 10 familias botánicas (Euphorbiaceae, Sterculiaceae, Anacardiaceae, Rutaceae, Mimosaceae, Fagaceae, Myrtaceae, Arecaceae, Verbenaceae y Bignonaceae).

Influencia de la cobertura del dosel en los daños por herbivorismo en una plantacion de enriquecimiento en el bosque seco secundario de Nandaime, Granada

El objetivo fue evaluar el establecimiento de tres especies forestales de valor comercial, Swietenia humilis, Cedrela odorata y Pachira quinata, como medida de enriquecimiento del bosque seco secundario de Nandaime, como medida de enriquecimiento del bosque seco. Se establecieron tres parcelas cuadradas con área de 625 m² (25 m x 25 m) y un espaciamiento de 3 m x 3 m entre plantas y líneas. Se plantaron 15 plantas por especie para un total de 45 individuos por parcelas, cada parcela con un porcentaje de cobertura de dosel correspondiente a: 0 a 20%, 20 a 50% y 50% a más. Las variables medidas fueron sobrevivencia, daños por insectos. Se obtuvo un porcentaje general de sobrevivencia de 53%, C. odorata es la especie que presentó valores más bajos (0%) en la cobertura0 a 20% y mayor de 50, los principales daños causados fueron notorios en los meses secos al final del período evaluado, principalmente en la cobertura mayor a 50%. Con los resultados obtenidos de las tres especies evaluadas se concluye que las especies P. quinata y Swietenia humilis, pueden utilizarse en plantaciones de enriquecimiento forestal con cobertura inferior al a 50% mientras C. odorata siempre y cuando se establezca un sistema de monitoreo y control de agentes de agentes que incrementan el riesgo de mortalidad de la especie.

Análisis espacial y multitemporal de la cobertura y uso del suelo con base en imágenes de satélites en la subcuenca Río Dipilto, Nueva Segovia, Nicaragua (1993, 2000, 2011)

La cuantificación del cambio de uso del suelo presenta aún altos niveles de incertidumbre, lo que repercute por ejemplo en la estimación de las emisiones de CO 2 . En este estudio se desarrollaron métodos, basados en imágenes de satélite y trabajo de campo, para estimar la tasa de cambio de la cobertura y uso del suelo, y las emisiones de CO 2 en la subcuenca río Dipilto, Nueva Segovia. La superficie de los tipos de vegetación se determinó con imágenes Landsat. Se utilizaron datos de carbono de nueve parcelas de muestreo en bosque de pino que fueron correlacionadas, para establecer un modelo de regresión lineal con el objetivo de estimar el Stock de Carbono. La sobreposición y algebra de mapas se utilizó para el escenario de emisiones de CO 2 . El análisis con imágenes de los años 1993, 2000 y 2011 reveló que durante es tos 18 años la velocidad a la que se perdieron los bosques latifoliados cerrado fue variable. Durante los primeros 7 años (1993 a 2000) se registró un aumento de 99.95 ha , que corresponde a una tasa de deforestación de - 1.45 % anual. Durante los últimos once años (2000 a 2011) esta cantidad cambió totalmente, ya que se eliminaron 331.76 h a , que corresponde a una tasa de deforestación anual de 3.41 %. Finalmente considerando el periodo de análisis, se transformaron más de 232.01 h a por año, correspondiente a u na tasa de deforestación anual de 1.55 %. La imagen de 2011 demostró que las reservas o Stock de C oscila entre 40 - 150 t/ha. Este intervalo de valores fue estimado por un modelo de regresión con razonable ajuste (R2 = 0.73 ), cuyas variables independientes fueron la reflectancia de las distintas bandas como índices de vegetación e infrarrojo cercano. Las pérdidas de C se estimaron en intervalos 1 - 191 t/h a en 20.76% del área. El 32.85% del área se mantuvo estable y 46.39% ganancias de 1 - 210 t/ha. La combinación de imágenes de resolución espacial media como son las de la serie Landsat para definir trayectorias de cambio de la cobertura del suelo, es una opción viable para la solución de interrogantes relacionadas con el cambio climático, tales como la estimación de las emisiones de CO 2 derivadas del cambio de uso del suelo.