Estudo da atividade de água em co-produtos da indústria de sucos: sementes de maracujá, casca de laranja e cascas de manga

Pós-graduação em Engenharia e Ciência de Alimentos - IBILCE

Influence of alternative drying aids on water sorption of spray dried mango mix powders: a thermodynamic approach

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Adsorção de cádmio em Latossolos sob vegetação de mata nativa e cultivados

Heavy metals are found naturally in soils at low concentrations, but their content may be increased by human activity, making them one of the barriers in management of tropical soils. These chemical elements can be found in the composition of organic and inorganic fertilizers, insecticides, fungicides, mine tailings, and urban waste, and may cause serious damage to the environment and human health. Thus, adsorption studies are essential in assessing the behavior of heavy metals in the soil. The objective of this study was to evaluate the influence of soil chemical, particle size, and mineralogical properties on adsorption of cadmium (Cd), evaluated by Langmuir and Freundlich models, in Latossolos (Oxisols) with or without human activity. Soil samples were collected from the surface layer, 0.00-0.20 m, and chemical, particle size, and mineralogical analyzes were performed. In the adsorption study, concentrations of 0, 5, 25, 50, 100, 200, 300, and 400 mu g L-1 of Cd were used in the form of Cd(NO3)(2). The empirical mathematical models of Langmuir and Freundlich were used for construction of adsorption isotherms. Data were analyzed by means of multivariate statistical techniques, Cluster Analysis and Principal Component Analysis. The data from the adsorption experiment showed a good fit to the Langmuir and Freundlich models. Soils with a lower goethite/hematite ratio and greater cation exchange capacity and pH, showed higher maximum adsorption capacity of Cd.

Porous silica matrix obtained from pyrex class by hydrothermal treatment: Characterization and nature of the porosity

A novel porous silica matrix has been prepared from Pyrex glass, using hydrothermal treatment under saturated-steam condition. This process makes it possible to obtain, in one step, a silica support formed of a homogeneously distributed and interconnected macropore microstructure. The new matrix contains silanol groups that can be used in reactions of surface modification to provide a hybrid material and a selective macrofiltration membrane, and also it can improve chemical inertness. The porous matrix is noncrystalline as obtained and, after thermal treatment at temperatures higher than 950degreesC, exhibits an X-ray pattern characteristic of alpha-cristobalite and low volume contraction. The present samples were characterized by scanning electron microscopy, mercury intrusion porosimetry, nitrogen adsorption-desorption isotherms, infrared spectroscopy, X-ray powder diffractometry, atomic absorption, and high-resolution solid-state nuclear magnetic resonance. The results present a new way of producing a macroporous silica matrix.

Preparation of a clay-modified carbon paste electrode based on 2-thiazoline-2-thiol-hexadecylammonium sorption for the sensitive determination of mercury

A montmorillonite from Wyoming-USA was used to prepare an organo-clay complex, named 2-thiazoline-2-thiol-hexadecyltrimethylammonium-clay (TZT-HDTA-clay), for the purpose of the selective adsorption of the heavy metals ions and possible use as a chemically modified carbon paste electrode (CMCPE). Adsorption isotherms of Hg 2+, Pb 2+, Cd 2+, Cu 2+, and Zn 2+ from aqueous solutions as a function of the pH were studied at 298 K. Conditions for quantitative retention and elution were established for each metal by batch and column methods. The organo-clay complex was very selective to Hg(II) in aqueous solution in which other metals and ions were also present. The accumulation voltammetry of Hg(II) was studied at a carbon paste electrode chemically modified with this material. The mercury response was evaluated with respect to the pH, electrode composition, preconcentration time, mercury concentration, cleaning solution, possible interferences and other variables. A carbon paste electrode modified by TZT-HDTA-clay showed two peaks: one cathodic peak at about 0.0 V and an anodic peak at 0.25 V, scanning the potential from -0.2 to 0.8 V (0.05 M KNO 3 vs. Ag/AgCl). The anodic peak at 0.25 V presents excellent selectivity for Hg(II) ions in the presence of foreign ions. The detection limit was estimated as 0.1 μg L -1. The precision of determination was satisfactory for the respective concentration level. 2005 © The Japan Society for Analytical Chemistry.

Structure of copper complexes adsorbed on a silica gel surface chemically modified with benzimidazole

Silica gel having a particle size between 0.2 and 0.05 mm and a specific surface area, S BET = 473 m 2 g -1, was chemically modified with benzimidazole. Adsorption isotherms of CuX 2 (X = Cl, Br or ClO 4) from ethanol and acetone solutions were studied at 298 K. The metal is bonded to the surface through the free nitrogen atom of the attached benzimidazole. The average number of ligands co-ordinated to the central metal ion was shown to depend on the solid surface loading by the solute. At low loading the electronic and ESR spectral parameters indicated that the copper ion is in a distorted-tetragonal symmetry field.

Estudo da adsorção de níquel (II) e zinco (II) em soluções aquosas por lama vermelha natural e ativada: influência do PH, isotermas, cinética e termodinâmica

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Adsorção de cádmio e chumbo em solução aquosa por lama vermelha natural e com diferentes ativações

Pós-graduação em Engenharia Civil e Ambiental - FEB

Materiais derivados de hidróxidos duplos lamelares: síntese, caracterização e aplicação em adsorção e processos avançados de oxidação

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Estudo da utilização de serragem de madeira como adsorvente para o tratamento de efluentes têxteis

The Brazilian textile industry has been a highlight in the global economy. Connected with this high economic performance there is the water consumption and the generation of great volumes of wastewater which present high concentrations of dyes and chemical substances. One of the main techniques used in the treatment of textile effluents is adsorption, which has the activated carbon as the main adsorbent. Recently, studies have been developed to find alternative materials to activated carbon and exhibiting good adsorption capacity of dyes. The aim of this work is to study the potential of sawdust as adsorbent of low cost to remove the dye Direct Green 26. The results of this type of dye removal were obtained through the study of adsorption isotherms obtained by spectrophotometry in the UV-visible region analyzed by the Langmuir model. Finally, a comparison was made of these results with those of other adsorbents. Results showed that the average removal of dye, using sawdust, was 78.8% for an initial concentration of 500mg / L and the maximum adsorption capacity of 119mg / g. These results demonstrate the great potential of sawdust as an adsorbent for the dye Direct Green 26.

Removal of Pb2+ from aqueous solutions using two Brazilian rocks containing zeolites

The removal of Pb2+ from aqueous solution by two Brazilian rocks that contain zeolites-amygdaloidal dacite (ZD) and sandstone (ZS)-was examined by batch experiments. ZD contains mordenite and ZS, stilbite. The effects of contact time, concentration of metal in solution and capacity of Na+ to recover the adsorbed metals were evaluated at room temperature (20A degrees C). The sorption equilibrium was reached in the 30 min of agitation time. Both materials removed 100% of Pb2+ from solutions at concentrations up to 50 mg/L, and at concentrations larger than 100 mg/L of Pb2+, the adsorption capacity of sandstone was more efficient than that of amygdaloidal dacite due to the larger quantities and the type of zeolites (stilbite) in the cement of this rock. All adsorbed Pb2+ was easily replaced by Na+ in both samples. The analysis of the adsorption models using nonlinear regression revealed that the Sips and the Freundlich isotherms provided the best fit for the ZS and ZD experimental data, respectively, indicating the heterogeneous adsorption surfaces of these zeolites.

Application of succinylated sugarcane bagasse as adsorbent to remove methylene blue and gentian violet from aqueous solutions - Kinetic and equilibrium studies

In a previous work, succinylated sugarcane bagasse (SCB 2) was prepared from sugarcane bagasse (B) using succinic anhydride as modifying agent. In this work the adsorption of cationic dyes onto SCB 2 from aqueous solutions was investigated. Methylene blue, MB, and gentian violet, GV, were selected as adsorbates. The capacity of SCB 2 to adsorb MB and GV from aqueous single dye solutions was evaluated at different contact times, pH, and initial adsorbent concentration. According to the obtained results, the adsorption processes could be described by the pseudo-second-order kinetic model. Adsorption isotherms were well fitted by Langmuir model. Maximum adsorption capacities for MB and GV onto SCB 2 were found to be 478.5 and 1273.2 mg/g, respectively. (C) 2011 Elsevier Ltd. All rights reserved.

Funktionalisierte Latexpartikel

In der vorliegenden Arbeit wurden unter Verwendung neuer auf der Isophthalsäure basieren-der polymerisierbaren Tensiden carboxylfunktionalisierte Latexpartikel hergestellt, charakte-risiert und funktionalisiert. Im ersten Teil dieser Arbeit wurden 5-(10-Undecenyloxy)isophthalsäure (ISA-Vinyl), 5-(11-(4-Vinylphenoxy)undecyloxy)isophthal-säure (ISA-Sty), 5-(11-(2-Prop-1-enyl)phenoxy)undecyloxy)isophthalsäure (ISA-Pr), 5-(11-(1-Methacryloxy)undecylen)isophthalsäure (ISA-Met) und 5-(10-(3-Methylbut-3-enyl)oxy-1-oxydecylen)isophthalsäure (ISA-Bu) hergestellt. Die Surfmere wurden mit Styrol bzw. mit n-Butylacrylat copolymerisiert. ISA-Bu und ISA-Pr weisen während der Copolymerisation mit Styrol fast ideale Verläufe der Zeit/Umsatz-Kurven auf. Bei der Copolymerisation von ISA-Bu bzw. ISA-Vinyl mit n-Butylmethacrylat wurden ähnliche Ergebnisse erhalten. Die Carboxylgruppen an der Partikeloberfläche wurden mit Halogenderivaten verestert oder mit primären Aminen amidiert. Die funktionalisierten Partikel wurden mit der Polyelektrolyt-titration und konduktometrischen Titration, der IR- und UV-Spektroskopie, der Transmissi-onselektronenmikroskopie, der Fluoreszenzkorrelationsspektroskopie charakterisiert. Es konnte gezeigt werden, dass die Reaktanden kovalent an der Partikeloberfläche gebunden sind. Die Polymerpartikel wurden bei der Herstellung von Immunoassays genutzt. Die Adsorpti-onsisothermen zeigten, dass eine hohe Menge an Rinderserumalbumin an die Partikeloberflä-che physikalisch gebunden werden kann. In dieser Arbeit wurde ein einfaches Immunoassay hergestellt mit Biotin – Avidin als Modellsystem hergestellt. Die Surfmere wurden zur Stabilisierung von Miniemulsionen für die Miniemulsionspolymeri-sation genutzt. Im Laufe dieser Arbeit konnten mit dieser Methode Rylenfarbstoffe in Po-lystyrolpartikel stabilisiert werden.

Laboruntersuchungen zur Aufnahme atmosphärischer Spurengase auf statischen und wachsenden Eisoberflächen

Der erste Teil dieser Arbeit befaßt sich mit der Adsorption von H2O2 auf nicht-wachsendem Eis. Die Experimente wurden in einem zylindrischen Strömungsreaktor mit massenspektrometrischer Detektion (Elektronenstoß und chemische Ionisation) ausgeführt. Die Daten einer zuvor bereits am Max Planck-Institut für Chemie (Mainz) von Dr. N. Pouvesle ausgeführten Laborstudie zur Adsorption von H2O2 auf Eis bei 203 bis 233 K wurden im Rahmen der vorliegenden Arbeit durch Coadsorptionsexperimente mit Ameisensäure und Verwendung unterschiedlicher Ionisationsmodi validiert. Zusätzlich wurde eine Korrelation der Langmuir-Konstanten und der Kondensationsenthalpie für H2O2 und andere Moleküle durchgeführt, welche die Ergebnisse der MPI-Studie ebenfalls stützt. Die Ergebnisse belegen, daß die Aufnahme von H2O2 in Eiswolken um bis zu 3 Größenordnungen höher ist als bisher angenommen. Anhand dieser Erkenntnisse wurde die atmosphärische Relevanz der Adsorption von H2O2 auf Eis in der oberen Troposphäre neu bewertet. Der zweite Teil der Arbeit widmet sich der Aufnahme verschiedener organischer Verbindungen (Ethanol, 1-Butanol, Ameisensäure, Trifluoressigsäure) und HCl auf Eis während dieses wächst. Der hierfür erstmals in Betrieb genommene Eiswachstumsreaktor wurde zunächst durch Messung der Adsorptionsisotherme von Ethanol und Butanol und Berechnung der Adsorptionsenthalpien aus experimentellen Daten evaluiert. Im Anschluß wurden die Ergebnisse der Wachstumsexperimente der oben aufgeführten Verbindungen vorgestellt, wobei jedoch nur Trifluoressigsäure und HCl eine erhöhte Aufnahme zeigen. Der Aufnahmekoeffizient g_trapp von HCl wurde bei Temperaturen zwischen 194,3 und 228 K und HCl-Gasphasenkonzentrationen von 6,4x10^9 bis 2,2x10^11 cm^-3 gemessen und war unter den untersuchten Bedingungen proportional zu Eiswachstumsgeschwindigkeit x und antikorreliert zum Bedeckungsgrad theta und der Eistemperatur T. Der vom wachsenden Eis aufgenommene Fluß von HCl-Molekülen war positiv mit x und negativ mit T korreliert, während theta keinen Einfluß hatte. Anhand der erzielten Resultate wurde eine Parametrisierung für g_trapp entwickelt, mit der die Aufnahme künftig in Abhängigkeit von x, T und [HCl]_gas leicht berechnet werden kann, beispielsweise in globalen Modellsimulation der troposphärischen Chemie. Abschließend wurden die Ergebnisse mit einem von Kärcher et al. (2009) entwickelten semiempirischen Modell verglichen und für die offenen Parameter des Modells wurden aus den experimentellen Daten ebenfalls Parametrisierungen entwickelt.

Characterization of a Coal Fly Ash-Cement Slurry by the Absolute Foam Index

This dissertation established a standard foam index: the absolute foam index test. This test characterized a wide range of coal fly ash by the absolute volume of air-entraining admixture (AEA) necessary to produce a 15-second metastable foam in a coal fly ash-cement slurry in a specified time. The absolute foam index test was used to characterize fly ash samples having loss on ignition (LOI) values that ranged from 0.17 to 23.3 %wt. The absolute foam index characterized the fly ash samples by absolute volume of AEA, defined as the amount of undiluted AEA solution added to obtain a 15-minute endpoint signified by 15-second metastable foam. Results were compared from several foam index test time trials that used different initial test concentrations to reach termination at selected times. Based on the coefficient of variation (CV), a 15-minute endpoint, with limits of 12 to 18 minutes was chosen. Various initial test concentrations were used to accomplish consistent contact times and concentration gradients for the 15-minute test endpoint for the fly ash samples. A set of four standard concentrations for the absolute foam index test were defined by regression analyses and a procedure simplifying the test process. The set of standard concentrations for the absolute foam index test was determined by analyzing experimental results of 80 tests on coal fly ashes with loss on ignition (LOI) values ranging from 0.39 to 23.3 wt.%. A regression analysis informed selection of four concentrations (2, 6, 10, and 15 vol.% AEA) that are expected to accommodate fly ashes with 0.39 to 23.3 wt.% LOI, depending on the AEA type. Higher concentrations should be used for high-LOI fly ash when necessary. A procedure developed using these standard concentrations is expected to require only 1-3 trials to meet specified endpoint criteria for most fly ashes. The AEA solution concentration that achieved the metastable foam in the foam index test was compared to the AEA equilibrium concentration obtained from the direct adsorption isotherm test with the same fly ash. The results showed that the AEA concentration that satisfied the absolute foam index test was much less than the equilibrium concentration. This indicated that the absolute foam index test was not at or near equilibrium. Rather, it was a dynamic test where the time of the test played an important role in the results. Even though the absolute foam index was not an equilibrium condition, a correlation was made between the absolute foam index and adsorption isotherms. Equilibrium isotherm equations obtained from direct isotherm tests were used to calculate the equilibrium concentrations and capacities of fly ash from 0.17 to 10.5% LOI. The results showed that the calculated fly ash capacity was much less than capacities obtained from isotherm tests that were conducted with higher initial concentrations. This indicated that the absolute foam index was not equilibrium. Rather, the test is dynamic where the time of the test played an important role in the results. Even though the absolute foam index was not an equilibrium condition, a correlation was made between the absolute foam index and adsorption isotherms for fly ash of 0.17 to 10.5% LOI. Several batches of mortars were mixed for the same fly ash type increasing only the AEA concentration (dosage) in each subsequent batch. Mortar air test results for each batch showed for each increase in AEA concentration, air contents increased until a point where the next increase in AEA concentration resulted in no increase in air content. This was maximum air content that could be achieved by the particular mortar system; the system reached its air capacity at the saturation limit. This concentration of AEA was compared to the critical micelle concentration (CMC) for the AEA and the absolute foam index.