1000 resultados para Ph


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La presente investigación tiene como objetivo determinar la concentración de pH en las hojas de 17 cultivares clónales de Spondias purpurea L, ubicado en el Arboretum Alain Meyrat de la Universidad Nacional Agraria, la metodología utilizada consistió en la recolección del material vegetativo de las cuales se seleccionaron 20 hojas de cada cultivar clonal en buen estado (sanas, verdes y completas). Se procedió medir con ayuda de una balanza el peso verde de las hojas separando los foliolos y el raquis la cuales se rotularon con el nombre de cada cultivar clonal. Para determinar la concentración pH de cada cultivar se recortó los foliolos y el raquis utilizando 3 g de cada muestra, se macera con un mortero hasta obtener materia molida. Una vez macerado los 3 g de cada muestra se determina la solubilidad de las hojas, haciendo uso de solventes como el agua (H₂0), benceno (C₆H₆), etanol (CH₃-CH₂-0H), y tetracloruro de carbono (CCL₄), para ello se utilizó 3 ml de cada solvente. Se empleó el uso de un pHmetro para determinar la concentración de pH de las muestras combinadas con los solventes y pH de la muestra sin solvente. Se obtuvo que el pH del cultivar San franciscano posee mayor contenido de acidez empleando los solventes químicos y el raquis seco para elaborar infusiones, por el contrario las infusiones con los foliolos secos del cultivar Cocer se obtuvo la mayor concentración de acidez

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Growth of giant salvinia ( Salvinia molesta Mitchell) under different pH regimes was examined at the Lewisville Aquatic Ecosystem Research Facility (LAERF) in Lewisville, Texas.(PDF has 5 pages.)

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Endothall has been used as an aquatic herbicide for more than 40 years and provides very effective weed control of many weeds. Early research regarding the mechanism-of-action of endothall contradicts the symptomology normally associated with the product. Recent studies suggest endothall is a respiratory toxin but the mechanism-of-action remains unknown. To further elucidate the activity of endothall, several endothall formulations were evaluated for their effects on ion leakage, oxygen consumption and photosynthetic oxygen evolution from hydrilla shoot tips. The influence of pH, buffering and divalent cations was also evaluated. (PDF contains 6 pages.)

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The Alliance for Coastal Technology (ACT) convened a workshop on the in situ measurement of dissolved inorganic carbon species in natural waters in Honolulu, Hawaii, on February 16, 17, and 18, 2005. The workshop was designed to summarize existing technologies for measuring the abundance and speciation of dissolved inorganic carbon and to make strategic recommendations for future development and application of these technologies to coastal research and management. The workshop was not focused on any specific technology, however, most of the attention of the workshop was on in situ pC02 sensors given their recent development and use on moorings for the measurement of global carbon fluxes. In addition, the problems and limitations arising from the long-term deployment of systems designed for the measurement of pH, total dissolved inorganic carbon (DIC), and total alkalinity (TA) were discussed. Participants included researchers involved in carbon biogeochemistry, industry representatives, and coastal resource managers. The primary questions asked during the workshop were: I. What are the major impediments to transform presently used shipboard pC02 measurement systems for use on cost-eficient moorings? 2. What are the major technical hurdles for the in situ measurement of TA and DIC? 3. What specific information do we need to coordinate efforts for proof of concept' testing of existing and new technologies, inter-calibration of those technologies, better software development, and more precise knowledge quantzjjing the geochemistry of dissolved inoeanic carbon species in order to develop an observing system for dissolved inorganic carbon? Based on the discussion resulting from these three questions, the following statements were made: Statement No. 1 Cost-effective, self-contained technologies for making long-term, accurate measurements of the partial pressure of C02 gas in water already exist and at present are ready for deployment on moorings in coastal observing systems. Statement No. 2 Cost-effective, self-contained systems for the measurement of pH, TA, and DIC are still needed to both fully define the carbonate chemistry of coastal waters and the fluxes of carbon between major biogeochemical compartments (e.g., air-sea, shelf-slope, water column-sediment, etc.). (pdf contains 23 pages)

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Temperature-sensitive poly(N-isopropylacrylamide) (PNIPA) nanohydrogels were synthesized by nanoemulsion polymerization in water-in-oil systems. Several cross-linking degrees and the incorporation of acrylic acid as comonomer at different concentrations were tested to produce nanohydrogels with a wide range of properties. The physicochemical properties of PNIPA nanohydrogels, and their relationship with the swelling-collapse behaviour, were studied to evaluate the suitability of PNIPA nanoparticles as smart delivery systems (for active packaging). The swelling-collapse transition was analyzed by the change in the optical properties of PNIPA nanohydrogels using ultraviolet-visible spectroscopy. The thermodynamic parameters associated with the nanohydrogels collapse were calculated using a mathematical approach based on the van't Hoff analysis, assuming a two-state equilibrium (swollen to collapsed). A mathematical model is proposed to predict both the thermally induced collapse, and the collapse induced by the simultaneous action of two factors (temperature and pH, or temperature and organic solvent concentration). Finally, van't Hoff analysis was compared with differential scanning calorimetry. The results obtained allow us to solve the problem of determining the molecular weight of the structural repeating unit in cross-linked NIPA polymers, which, as we show, can be estimated from the ratio of the molar heat capacity (obtained from the van't Hoff analysis) to the specific heat capacity (obtained from calorimetric measurements).

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12 samples (6 original samples and 6 diluted samples) were analysed by 14 WEFTA laboratories for their pH values in an inter-laboratory comparison exercise. As a result it can be stated that the majority of participating laboratories could determine the pH values very exactly. The pH values obtained are ranging only little around the calculated mean (less than 0.1 pH unit). It could also be demonstrated that the participating institutes could analyse both, pH values in fishery products and aqueous salt solutions. However, also in this exercise a number of outliers and deviating values have been detected. Therefore it is of utmost importance to calibrate the pH electrodes in regular intervals and to maintain them carefully. Intra-laboratory comparison measurements are recommended to detect weak points.

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Adsorption of aqueous Pb(II) and Cu(II) on α-quartz was studied as a function of time, system surface area, and chemical speciation. Experimental systems contained sodium as a major cation, hydroxide, carbonate, and chloride as major anions, and covered the pH range 4 to 8. In some cases citrate and EDTA were added as representative organic complexing agents. The adsorption equilibria were reached quickly, regardless of the system surface area. The positions of the adsorption equilibria were found to be strongly dependent on pH, ionic strength and concentration of citrate and EDTA. The addition of these non-adsorbing ligands resulted in a competition between chelation and adsorption. The experimental work also included the examination of the adsorption behavior of the doubly charged major cations Ca(II) and Mg(II) as a function of pH.

The theoretical description of the experimental systems was obtained by means of chemical equilibrium-plus-adsorption computations using two adsorption models: one mainly electrostatic (the James-Healy Model), and the other mainly chemical (the Ion Exchange-Surface Complex Formation Model). Comparisons were made between these two models.

The main difficulty in the theoretical predictions of the adsorption behavior of Cu(II) was the lack of the reliable data for the second hydrolysis constant(*β_2) The choice of the constant was made on the basis of potentiometric titratlons of Cu^(2+)

The experimental data obtained and the resulting theoretical observations were applied in models of the chemical behavior of trace metals in fresh oxic waters, with emphasis on Pb(II) and Cu(II).

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Azken urte hauetan industriak izan duen garapenak, onura asko ekarri ditu, hala nola, bizi maila eta kalitatea gora egin dute. Baina dena ez dira alde onak, izan ere, prozesu honek, kutsagarriak eta oso konplexuak diren hondakinak sortu ditu. Kutsadura hau ez du soilik oreka ekologikoa n kalte egiten, izan ere, kutsadura hau dagoen guneetan ere eragin handia dauka. Hori dela eta , ingurumenaren babesa gero eta garrantzi handiagoa hartzen ari da. Horretarako, industriak sortzen dituen hondakinen tratamendurako prozesuetan, inbertsio ekonomiko handiak egin behar dira. Hau ez da soilik legea betetzeko egin behar, baizik eta, indus tria merkatuan dagoen konpetentzian toki on bat lortzeko oso garrantzitsua da. Jariakinen tratamenduaren xedea dituzten araztegiak duten arazo printzipala, jariakin hauetan dauden metal astunen presentzia da. Metal hauek, araztegi hauetan ematen diren pro zesu biologikoen zai ltasuna bermatzen dute eta animali, landare eta giza osasunean efektu toxikoak izaten dituzte. Baimenduta dauden kontzentrazioen limitea betetzeko, industriak normalean isurketan egin baino lehen, aurretratamendu bat egitera behartuta ikusten dira, toxikoak diren edo oso oldarkorrak diren produktuak kentzeko. Adibidez, Industria Hidrometalurgiakoak , oso kontzentrazio baxuetan metal astunak isurtzen ditu, baina kantitate hauek baimenduta daude, industria hau erabiltzen dituen emari handiak direla eta. Normalean hondakin industrialetatik kanpora isurt zen diren metal astunak , kontzentrazio baxuetan eg ot en dira . Honek, errentagarritasun positiboa du ten araztegi tekniken aplikazioa ahalbideratzen du. Kutsadura hau sortzen dituzten prozesu industrial mota asko existitzen direnez, metal hauek, oso diluituak dauden disoluzioetatik banatu behar dira. Horretara ko, metal baliotsuen errekuperazioa eta isurketa industrialaren legeak betetzea bermatzen duten, banaketa prozesuak sortu behar izan d ira. Jarraian, helburu hau duten teknika batzuk azaltzen dira