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Desorption Isotherms (desorption + isotherm)
Selected AbstractsDEHYDRATION CHARACTERISTICS OF PAPAYA (CARICA PUBENSCENS): DETERMINATION OF EQUILIBRIUM MOISTURE CONTENT AND DIFFUSION COEFFICIENTJOURNAL OF FOOD PROCESS ENGINEERING, Issue 5 2009R. LEMUS-MONDACA ABSTRACT This study determined the drying kinetics behavior of papaya at different temperatures (40, 50, 60, 70 and 80C). Desorption isotherms were determined at 5, 20 and 50C over a relative humidity range of 10,95%. The Guggenheim, Anderson and de Boer models were found to be suitable for description of the sorption data. The samples reached equilibrium moisture of 0.10 ± 0.01 g water/g dry matter. Fick's second law model was used to calculate the effective diffusivity (6.25,24.32 × 10 - 10 m2/s). In addition, experimental data were fitted by means of seven mathematical models. The kinetic parameters and the diffusion coefficient were temperature-dependent and were evaluated by an Arrhenius-type equation. The modified Page model obtained the best-fit quality on experimental data according to statistical tests applied. PRACTICAL APPLICATIONS The main utility of this study is the application of both different empirical models and the diffusional model in tropical fruits' dehydration, which can be considered a basis for a very accurate estimation of drying time and the optimization of the same process. Two newly mathematical models are proposed in this study, through which a good fit on the data of experimental moisture content was achieved. The study of drying of papaya cultivated in Chile engages a great technological interest, because this product is widely used in the development of different products such as candying, canning, juice, syrup and marmalade. In addition, papayas cultivated in Chile, along with other tropical fruits cultivated in Brazil, Colombia and the Caribbean, have become especially important in the exportations of these countries. The major markets for these products include the U.S.A., the European Community and Asia. [source] EFFECTS OF THERMAL AND ELECTROTHERMAL PRETREATMENTS ON HOT AIR DRYING RATE OF VEGETABLE TISSUEJOURNAL OF FOOD PROCESS ENGINEERING, Issue 4 2000WEI-CHI WANG ABSTRACT Cylindrical samples of carrot, potato and yam were dried in a hot-air dehydrator after preheating to 50C or 80C by three different heating methods (conventional, microwave and ohmic). The results showed that enhancement of drying rate increased with pretreatment temperature. Ohmic pretreatment increased the drying rate more than conventional and microwave heating. Desorption isotherms showed that in the low aw range, desorption data of preheated and raw materials were similar. However, the isotherms of preheated samples shifted when aw was high, which indicated that thermal pretreatments altered the structure, and apparently, the water distribution within these materials. For all samples, ohmic pretreatment showed stronger influences on isotherms than microwave heating, while the pretreatment effect of conventional heating was only observed for potato tissue. [source] Microporous Metal,Organic Frameworks with High Gas Sorption and Separation Capacity,ADVANCED FUNCTIONAL MATERIALS, Issue 8 2007Y. Lee Abstract The design, synthesis, and structural characterization of two microporous metal,organic framework structures, [M(bdc)(ted)0.5]·2,DMF·0.2,H2O (M,=,Zn (1), Cu (2); H2bdc,=,1,4-benzenedicarboxylic acid; ted,=,triethylenediamine; DMF: N,N -dimethylformamide) is reported. The pore characteristics and gas sorption properties of these compounds are investigated at cryogenic temperatures, room temperature, and higher temperatures by experimentally measuring argon, hydrogen, and selected hydrocarbon adsorption/desorption isotherms. These studies show that both compounds are highly porous with a pore volume of 0.65 (1) and 0.52,cm3,g,,1 (2). The amount of the hydrogen uptake, 2.1,wt,% (1) and 1.8,wt,% (2) at 77,K (1,atm; 1,atm,=,101,325,Pa), places them among the group of metal,organic frameworks (MOFs) having the highest H2 sorption capacity. [Zn(bdc)(ted)0.5]·2,DMF·0.2,H2O adsorbs a very large amount of hydrocarbons, including methanol, ethanol, dimethylether (DME), n -hexane, cyclohexane, and benzene, giving the highest sorption values among all metal,organic based porous materials reported to date. In addition, these materials hold great promise for gas separation. [source] Synthesis and modification of zeolite NaA adsorbents for separation of hydrogen and methaneASIA-PACIFIC JOURNAL OF CHEMICAL ENGINEERING, Issue 5 2009Yanna Liu Abstract To improve the adsorption capacity of zeolite A, two kinds of zeolite NaA with submicron and hierarchical structure were prepared. The XRD patterns indicated that both synthesized products were pure zeolite with LTA-type framework. The SEM images and laser particle size analysis showed that the particle size of submicron zeolite NaA was about 240 nm. The TEM and N2 adsorption/desorption isotherms proved the existence of mesopores in the hierarchical zeolite NaA. The adsorption capacities of single component CH4 or H2 on zeolite SrA adsorbents, obtained by Sr2+ ion-exchange of submicron and hierarchical zeolite NaA, and commercial zeolite 5A adsorbent were measured by the static volume method at 25 °C and pressures up to 1 MPa. The results show that both prepared zeolite SrA adsorbents have higher adsorption capacities of CH4 and ideal separation factors of CH4/H2 than commercial zeolite 5A, and the submicron zeolite SrA has the largest adsorption capacity of CH4 and ideal separation factor of CH4/H2. Copyright © 2009 Curtin University of Technology and John Wiley & Sons, Ltd. [source] APPLICATION OF DISCRETE MODELING APPROACH TO FLUIDIZED BED YEAST DRYINGJOURNAL OF FOOD PROCESS ENGINEERING, Issue 2010F. DEBASTE ABSTRACT Yeast drying is widely used to ease transport and conservation. In this work, baker's yeast drying in fluidized bed is modeled using a pore network model. Classical balanced equations at the reactor scale are coupled with the pore network for the grain, which takes into account diffusion in the gas phase, transport by liquid film in partially saturated region and pressure gradient effects in the liquid phase. The porous structure to be applied in the model is obtained using environmental scanning electron microscopy. Simulations are validated on a thermogravimetric analysis experiment. The model is then applied to fluidized bed drying for which experimental results obtained on a laboratory pilot are available. Finally, the model results are compared to those of a simplified receding front model. PRACTICAL APPLICATIONS The presented model allows simulation of Saccharomyces cerevisiae fluidized bed drying. Taking into account transport phenomena in the grain offers the opportunity to predict drying rate without the use of a desorption isotherm. Moreover, the model predicts roughly the critical humidity. Therefore, the model can be used for scale-up, design and optimization of dryer including the effect of changes in yeast granulation. [source] Permselective and Preconcentration Properties of a Surfactant-Intercalated Clay Modified ElectrodeELECTROANALYSIS, Issue 22 2006E. Ngameni Abstract This work is focused on the voltammetric examination of the ion exchange properties of a smectite type clay, before and after its modification by the replacement of its native interlamellar cations (Na+, K+, Ca2+) by hexadecyltrimethylammonium cations (HDTMA+). The raw clay and its organically modified form were first characterized by X-ray diffraction (XRD) and N2 adsorption,desorption isotherms (BET method) that confirmed the modification via an intercalation process. These materials were subsequently coated onto glassy carbon surfaces, and the resulting modified electrodes were evaluated for the uptake of [Ru(NH3)6]3+ and [Fe(CN)6]3, ions used as redox probes. Some experimental parameters affecting the incorporation of the probes within the film, including the ionic strength, the surfactant loading and the solution pH are thoroughly examined, in order to highlight the mechanism of the process. The possibility of using the surfactant-intercalated clay modified electrode as an electrochemical sensor for [Fe(CN)6]3, is also evaluated. [source] In Situ Synthesis, Characterization of SiPMo-X, and Different Catalytic Properties of SiPMo-X and SiPW-XEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 15 2006Chunfeng Shi Abstract SBA-15 frameworks with encapsulated Keggin type heteropolyacids (HPAs) were synthesized in situ under strongly acidic conditions (pH,<,0). During the hydrolysis of tetraethyl orthosilicate (TEOS), a P- and a Mo source were added into the initial sol,gel system to form Keggin type HPAs. The texture of the final products was studied by the N2 adsorption,desorption isotherms and transmission electron microscopy (TEM), and their structure was systematically characterized by X-ray diffraction (XRD), UV/Vis diffuse reflectance- (DRS), infrared- (IR), and 31P magic angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy. Characterization results suggest that the samples show very ordered hexagonal mesostructure, and the HPAs that are incorporated into the framework of meso-silica are insoluble during catalysis. Results of catalytic tests indicate that the materials demonstrated catalytic activity comparable with or even surpassing those of the bulk HPAs in catalytic tests implementing chemical reactions of bulky molecules (1,3,5-triisopropylbenzene cracking, esterification of benzoic acid with tert -butyl alcohol, and 2,3,6-trimethylphenol hydroxylation with H2O2). Additionally, some other properties, such as easy separation and stability when recycled, ensure their potential applications in the chemical industries. Here, we report not only the in situ synthesis and characterization of SiPMo-X, but also the difference in the catalytic properties of SiPMo-X and SiPW-X. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source] High-Zirconium-Content Nano-Sized Bimodal Mesoporous SilicasEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 13 2006David Ortiz de Zárate Abstract Silica-based nanoparticulated bimodal mesoporous materials with high Zr content (43 , Si/Zr , 4) have been synthesized by a one-pot surfactant-assisted procedure from a hydroalcoholic medium using a cationic surfactant (CTMABr = cetyltrimethylammonium bromide) as structure-directing agent, and starting from molecular atrane complexes of Zr and Si as hydrolytic inorganic precursors. This preparative technique allows optimization of the dispersion of the Zr guest species in the silica walls. The bimodal mesoporous nature of the final high surface area nano-sized materials is confirmed by XRD, TEM, and N2 adsorption,desorption isotherms. The small intraparticle mesopore system (with pore sizes around 2,3 nm) is due to the supramolecular templating effect of the surfactant, while the large mesopores (around 12,24 nm) have their origin in the packing voids generated by aggregation of the primary nanometric mesoporous particles. The basicity of the reaction medium seems to be a key parameter in the definition of this last pore system. The effects induced by the progressive incorporation of Zr atoms on the mesostructure have been examined, and the local environment of the Zr sites in the framework has been investigated by UV/Vis spectroscopy. Observations based on the consequences of post-treatments of the as-synthesized materials with HCl/ethanol mixtures corroborate that the atrane method leads to Zr-rich materials showing enhanced site accessibility and high chemical homogeneity throughout the pore walls. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source] Sorption Isotherm and Calorimetric Behavior of Amorphous/Crystalline Raffinose-Water SystemsJOURNAL OF FOOD SCIENCE, Issue 4 2000H.A. Iglesias ABSTRACT: The water adsorption and desorption isotherms at 27 °C of initially amorphous raffinose over a range of relative humidity of 11% to 97% have been determined. Upon adsorption, the isotherm exhibited a "quasi" plateau, and the moisture content at this plateau was found to be very close to the amount required to form the crystalline raffinose pentahydrate (R.5 H2O). Crystallization of raffinose (R.5 H2O) during water adsorption at 52% and 58% RH was indicated by differential scanning calorimetry (DSC); both thermograms showed an endothermal peak of melting corresponding to R.5H2O. The results of the crystallization kinetics at 52% and 58% RH indicated that the time to assess the stable physical state in a sugar system for a given external condition has to be properly defined and depends on the (T-Tg) value. [source] Methane hydrate equilibria in silica gels with broad pore-size distributionsAICHE JOURNAL, Issue 2 2002Duane H. Smith Equilibrium pressures for the dissociation of methane hydrates confined in silica gel pores of nominal radii 7.5, 5.0 and 3.0 nm were measured over a wide temperature range, and were observed to be higher than those for bulk methane hydrate. A model is presented that allows the pore radius involved in each equilibrium to be determined from these data, so that the model exactly reproduces the experimental equilibrium pressure. Based on this model, pore volume distributions were reconstructed and found to be in good agreement with those obtained from nitrogen desorption isotherms, indicating that hydrate formed nearly uniformly in the available pores. [source] Pore-system characteristics of pavement seam materials of urban sitesJOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 1 2006Thomas Nehls Abstract The original light-brown sandy seam filling of pavements in urban areas turns dark and changes its properties by the time due to various inputs of urban dust. Deposited Corg inputs do mostly not have natural characteristics but are man-made, e.g., diesel dust. Thus, properties of the seam material are not predictable from experiences with forest or agricultural soils. Semiperviously sealed urban areas are sites of contaminant deposition as well as groundwater recharge. For an assessment of the resulting groundwater-contamination risk in these areas, the properties of the seam material, which influences transport processes, must be known. The aim of this study was to investigate the pore-system build-up, which includes size distribution and fractal character in the seam material of urban sites. The investigated samples were taken from pavements adjacent to roads in Berlin and Warsaw. The micropore parameters (nanometer range) were characterized using water-vapor desorption isotherms, mesopore parameters (micrometer range) were estimated from mercury-intrusion porosimetry and macropore parameters (millimeter range) from water-retention curves. Particle density, dry bulk density, and particle-size distribution were measured using standard methods. Volumes of micro- and mesopores as well as particle densities and dry bulk densities correlated with Ctot contents. However, no such relation was found for macropore volumes. Compared to the original sandy seam filling, the altered seam material shows significantly higher Corg contents and higher amounts of micro- and mesopores. Therefore, the available water capacity increases by 0.05,0.11,m3,m,3, as compared to the original sandy seam filling. Compared to natural sandy soils having similar Corg contents, the seam material shows similar macropore volumes, but the volume of mesopores and micropores is a few times smaller. That is mainly because of the particulate character of the organic matter. [source] Preparation and applications of novel cross-linked fluoroalkyl end-capped oligomeric nanocomposites possessing aromatic siloxane segments as core unitsPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 12 2009Yuki Goto Abstract Fluoroalkyl end-capped N,N -dimethylacrylamide oligomer and N -(1,1-dimethyl-3-oxobutyl)acrylamide oligomer were reacted with phenylene- and biphenylene-bridged ethoxysilanes under alkaline conditions to yield cross-linked fluoroalkyl end-capped oligomeric composites possessing aromatic siloxane segments as core units. These isolated fluorinated composite powders were found to be nanometer size-controlled fine particles with a good dispersibility and stability in water and organic solvents. Nitrogen adsorption,desorption isotherms confirmed the presence of micropores in these nanocomposites; the micropore size estimated by the HK method was 0.7,0.8,nm. Interestingly, fluorinated nanocomposites possessing a higher micropore volume ratio were found to exhibit a selective encapsulation ability of fullerene into their composite cores. These fluorinated nanocomposites were also applied to the surface modification of poly(methyl methacrylate) film, resulting in a good oleophobicity imparted by fluorine on the surface. In addition, fluorescence emission was visibly observed only from the modified PMMA film surface treated with fluorinated nanocomposites possessing biphenylene units when irradiated by light. Copyright © 2009 John Wiley & Sons, Ltd. [source] Size-Tunable Highly Luminescent SiO2 Particles Impregnated with Number-Adjusted CdTe NanocrystalsCHEMPHYSCHEM, Issue 4 2010Ping Yang Dr. Abstract Highly luminescent SiO2 particles impregnated with CdTe nanocrystals (NCs) are prepared by a sol,gel procedure. Partial ligand exchange from thioglycolic acid to 3-mercaptopropyltrimethoxysilane (MPS) on the NCs enables retention of the initial photoluminescence (PL) efficiency of the NCs in water, while the simultaneous addition of a poor solvent (ethanol) results in regulated assembly of the NCs through condensation of hydrolyzed MPS. The SiO2 particles thus prepared have, for example, a diameter of 16 nm and contain three NCs each. The PL efficiency of these particles is 40,%, while the initial efficiency is 46,% in a colloidal solution. The redshift and narrowed spectral width in PL observed after impregnation indicate that the concentration of NCs in these nearly reaches the ultimate value (on the order of 1021 particles per liter). The porosity of these particles is investigated by means of N2 adsorption,desorption isotherms. Due to the SiO2 shell, these particles have higher stability in phosphate-buffered saline buffer solution than the initial NCs. Their potential use for labeling in bio-applications is investigated by conjugating biotinylated immunoglobulin G to them by using streptavidin maleimide as linker. Successful conjugation is confirmed by electrophoresis in agarose gel. This preparation method is an important step towards fabricating intensely emitting biocompatible SiO2 particles impregnated with semiconductor NCs. [source] Evaluation of hydrate-screening methodsJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 7 2008Yong Cui Abstract The purpose of this work is to evaluate the effectiveness and reliability of several common hydrate-screening techniques, and to provide guidelines for designing hydrate-screening programs for new drug candidates. Ten hydrate-forming compounds were selected as model compounds and six hydrate-screening approaches were applied to these compounds in an effort to generate their hydrate forms. The results prove that no screening approach is universally effective in finding hydrates for small organic compounds. Rather, a combination of different methods should be used to improve screening reliability. Among the approaches tested, the dynamic water vapor sorption/desorption isotherm (DVI) method and storage under high humidity (HH) yielded 60,70% success ratios, the lowest among all techniques studied. The risk of false negatives arises in particular for nonhygroscopic compounds. On the other hand, both slurry in water (Slurry) and temperature cycling of aqueous suspension (TCS) showed high success rates (90%) with some exceptions. The mixed solvent systems (MSS) procedure also achieved high success rates (90%), and was found to be more suitable for water-insoluble compounds. For water-soluble compounds, MSS may not be the best approach because recrystallization is difficult in solutions with high water activity. Finally, vapor diffusion (VD) yielded a reasonably high success ratio in finding hydrates (80%). However, this method suffers from experimental difficulty and unreliable results for either highly water-soluble or water-insoluble compounds. This study indicates that a reliable hydrate-screening strategy should take into consideration the solubility and hygroscopicity of the compounds studied. A combination of the Slurry or TCS method with the MSS procedure could provide a screening strategy with reasonable reliability. © 2007 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 97:2730,2744, 2008 [source] Interaction of water with different cellulose ethers: a Raman spectroscopy and environmental scanning electron microscopy studyJOURNAL OF PHARMACY AND PHARMACOLOGY: AN INTERNATI ONAL JOURNAL OF PHARMACEUTICAL SCIENCE, Issue 6 2005P. M. Fechner Different non-ionic cellulose ethers like methyl cellulose (MC), hydroxypropyl cellulose (HPC) and hydroxypropylmethyl cellulose (HPMC) were investigated. The characterization of the cellulose ethers was carried out by thermogravimetry and sorption/desorption isotherms. Differences in the properties of the cellulose ether films were described by time-dependent contact angle measurements. Changes in molecular structure of the raw materials, gels and films caused by water contact were studied using Raman spectroscopy. Differences between the substitution types and changes due to the gel or film formation were observed. An environmental scanning electron microscopy (ESEM) technique was used to distinguish the morphological behaviour of the cellulose ether films in contact with water. Based on in-situ ESEM experiments, the swelling and drying behaviour of the various stages of cellulose ether films (film-hydrated film-dried film) were quantified by using image analysis. 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