Analysis of the Shrinkage Effect on Mass Transfer During Convective Drying of Sawdust/Sludge Mixtures

Convective drying of wastewater sludges and sawdust/sludge mixtures was studied. The first part of this work was an experimental study performed in a cross-flow convective dryer using 500 g of wet material extruded through a disk with circular dies of 12 mm. The results showed that the sawdust addition has a positive impact on the drying process from a mass ratio of 2/8, on a dry basis, with observed drying rates higher than the original sludge. The second part of this work consisted of developing a drying model in order to identify the internal diffusion coefficient and convective mass transfer coefficient from the experimental data. A comparison was made between fitted drying curves, well represented by the Newton's model, and the analytical solutions of the diffusion equation applied to a finite cylinder. Variations of dimensional characteristics, such as the volume and exchange surface of the sample bed, were obtained by X-ray tomography. This technique allowed us to confirm that shrinkage, which is an important phenomenon occurring during sludge and sawdust/sludge mixture drying, must be taken into account. The results showed that both the internal diffusion coefficient and convective mass transfer coefficient were affected by mixing and sawdust addition. The internal diffusion coefficient changed from 7.77 × 10^?9 m²/s for the original sludge to 7.01 × 10^?9 m²/s for the mixed sludge and then increased to 8.35 × 10^?9 m²/s for the mixture of a mass ratio of 4/6. The convective mass transfer coefficient changed from 9.70 × 10^?8 m/s for the original sludge to 8.67 × 10^?8 m/s for the mixed sludge and then increased to 12.09 × 10^?8 m/s for the mixture of a mass ratio of 4/6. These results confirmed that sawdust addition was beneficial to the sludge drying process as the mass transfer efficiency between the air and material increased. Reinforcing the texture of sludge by adding sawdust can increase the drying rate and decrease the drying time, and then the heat energy supply will be reduced significantly. The study also showed that neglecting shrinkage phenomenon resulted in an overestimation for the internal diffusion coefficient for the convective drying of sludges and sawdust/sludge mixtures.     

Rayleigh-like instability in the ion-shaping of Au-Ag alloy nanoparticles embedded within a silica matrix

We have studied how spherical 23 ± 3 nm Au(45)Ag(55) nanoparticles embedded within a silica matrix transform into prolate nanorods and nanowires by irradiating them with swift heavy ions. Samples were irradiated at room temperature and normal incidence with 74 MeV Kr and 36 MeV S ions for fluences up to 1.0 × 10(15) cm(-2). We demonstrate the existence of two regimes: (i) below a critical fluence, ～ 2.0 × 10(14) cm(-2), the transformation of the spherical nanoparticle into a nanorod is an individual process, i.e. each nanoparticle transforms into a single nanorod; (ii) for larger fluences the transformation from nanorod to nanowire becomes a collective process, i.e. the break up and dissolution of unstable nanorods contribute to the growth of long nanowires. The passage from the first to the second regime can be interpreted in terms of a Rayleigh-like instability under irradiation. The latter becomes active when the diameter of the nanowire approaches its saturation width under irradiation. Furthermore, we show that the composition of the alloy is only slightly modified during the ion-shaping process. Finally, the energy and the fluence thresholds for deformation and the deformation strain-rate are estimated.     

Treatment of arsenic-containing solutions using chitosan derivatives: uptake mechanism and sorption performances

Modified chitosan gel beads, which had been prepared by the molybdate adsorption and coagulation (in the presence of molybdate) methods, were tested for As(III) and As(V) removal from dilute solutions (in the range 5-20 mg As L-1). The sorbent is very efficient at removing As(V) from acid solutions (optimum pH close to pH 2-3), whereas the sorption capacities are significantly lower for As(III) uptake (230 mg As(V) g-1 Mo, 70 mg As(III) g-1 Mo, respectively). Since the sorption proceeds in acidic solutions with a partial release of molybdate and with residual concentrations (ca. 500 micrograms As L-1) above the regulations for drinking water, the process appears to be directed to the treatment of industrial effluents or as a pre-concentration process. The mechanism of As(V) sorption is related to the ability of molybdate ions to complex As(V) ions in acid solutions. The uptake mechanism was confirmed by XPS analysis and desorption studies. In the case of As(III) sorption the mechanism of uptake is not identified since no complex has been cited in the literature regarding As(III) binding to Mo (VI), which was also identified by XPS analysis as the sorption site. As(V) sorption is not influenced by the presence of co-ions, with the exception of phosphate anions at low concentration, and silicate at high relative concentration. Arsenic desorption can be performed using phosphoric acid solutions.     

Syntheses of poly[N-(2,2 dimethoxyethyl)-N-methyl acrylamide] for the immobilization of oligonucleotides

Radical-initiated polymerization of N-(2,2 dimethoxyethyl)-N-methylacrylamide has been carried out either in chloroform or methanol using 2,2′-azobisisobutyronitrile as an initiator, allowing us to prepare acetal containing water-soluble polymers. A kinetic study in both solvents showed that this monomer fairly homopolymerized (k_p · k_t^−1/2 = 1 mol^−1/2 L^1/2 s^−1/2). Static light scattering was used to characterize the molecular weight of these polymers. In addition, the Mark–Houwink–Sakurada relationship was established based on viscosity measurements performed at 25°C in water. Recovery of the aldehyde moieties on the polymer was achieved under mild conditions using a diluted inorganic solution. The analysis of the formation of aldehyde groups was performed by ¹H- and ¹³C-NMR. The covalent binding of oligodeoxyribonucleotides was carried out in water/acetonitrile mixtures with subsequent NaBH₄ reduction of the imine bonds so as to stabilize the polymer/oligodeoxynucleotide conjugates. © 1996 John Wiley & Sons, Inc.     

Weighted least squares estimation of background in EELS imaging

In quantitative Electron Energy Loss Spectrometry, a weighted least squares estimation should theoretically be used to estimate the background law below core edge energy, since the variances of the data vary. However, it is found that proper weighting makes the above edge signal-to-noise ratio decrease rather than increase. This result is discussed, and the influence of the bias introduced by the logarithmic transformation of the data is quantified.     

Transferring the calibration of direct solar irradiance to diffuse-sky radiance measurements for CIMEL Sun-sky radiometers

Two types of sunphotometric measurement are considered in this study: direct-Sun irradiance and diffuse-sky radiance. Based on CIMEL CE318 Sun-sky radiometer characteristics, we introduce a gain-corrected solid angle that allows interconverting calibration coefficients of these two types of measurement, thus realizing a "vicarious" radiance calibration. The accuracy of the gain-corrected solid angle depends on the number of available historical calibration records. The method is easy to use, provided that at least one laboratory calibration has been made previously. Examples coming from three distinct CE318 versions belonging to the AERONET/PHOTONS network are presented to provide details on the vicarious calibration method and protocols. From the error propagation analysis and the comparison with laboratory results, the uncertainty of the vicarious radiance calibration is shown to be comparable with the laboratory one, e.g., 3%-5%.