Electrospun nanofiber membranes are frequently used in adsorption processes thanks to their high specific surface area, tailored surface functionality, and fiber uniformity. However, they are still facing challenges such as low mechanical stability and unfavorable mass transport properties. In this study, an ultra-light and robust 3D nanofiber aerogel (NFA) or nanofiber sponge with tunable porosity and flexibility was synthesized from short pullulan/polyvinyl alcohol/polyacrylic acid nanofibers using a freeze casting process followed by thermal crosslinking. We demonstrate time the application of such NFAs in batch and continuous adsorption systems and compare their performance with flat nanofiber membranes (NFM). The NFAs proved to be promising adsorbents for cationic dyes due to their high adsorption capacity (383 mg/g) and their reusability. Langmuir isotherm was a suitable model for describing the adsorption process. The endothermic system followed a pseudo second order kinetic model and intra-fiber adsorption is found to be involved in the adsorption process. Dye adsorption by 3D NFAs was four times faster than for the respective flat NFMs and when used in a continuous process as a deep-bed filter, the pressure drop through the NFA was reduced by a factor of 40 while maintaining equal adsorption performance as for the NFM.
A biofilm fluidized sand bed column reactor (14 L) has been operated in the three-phase mode on a soluble glucose-yeast hydrolysate substrate in which the biofilm-sand phase (1-2.5 L) was suspended by direct aeration of the bed. Within two weeks a tight biofilm was formed whose activity resulted in a 90% reduction, with loads of 10.7 kg TC/m(3)day. The residence time was 1 h. The biofilm remained intact during operation with high residence times (up to 23 h) over three weeks. Oxygen transfer coefficients varied with aeration rate and sand quantity between 0.02 and 0.04 s(-1) during non growth conditions; they decreased with increasing amounts of clean sand and were higher and relatively independent of the sand fraction with biofilm-covered sand. Aeration rates used in the 14 L reactor were 23-40 L/min (2.4-4.1 cm/s) and were sufficient to suspend 78-92% f the biofilm-covered sand. Clean sand was 50-75% suspended. Oxygen uptake rates varied between 15.4 and 23.1 mol/m(3) h.
The objective of this study was to determine the influence of viscosity on micromixing in turbulent flow. It was first necessary to find a suitable viscosity-raising additive. HEC (hydroxyethyl cellulose) proved to be better than previously studied additives [sorbitol and carboxymethylcellulose (CMC)]. In concentrations up to 1 wt-'70, HEC solutions are almost Newtonian with viscosities independent of pH over the range 2 to 10. HEC had no effect on the reaction rate constants and the spectrophotometric analysis of the fast, competing reactions used -the diazo coupling between 1 -naphthol and diazotized sulphanilic acid. The viscosity can then be raised by around an order of magnitude by adding less than 1 wt-'70 HEC to this reaction system. Diazo couplings were conducted in a 20 1 semi-batch tank reactor stirred by a Rushton turbine at two viscosity levels (0.9 and 6.2 mPa s). Long feed times ensured that micromixing was controlling. More bisazo dye was formed in the more viscous solution, all other conditions being unchanged, indicating more intense segregation and slower micromixing.This was also shown by visualising the extent of neutralisation zones, with more spreading and slower micromixing being observed in viscous solution. Higher turbine speeds reduced this spreading. One feed point near and one far from the turbine were employed: the strong inhomogeneity of the turbulence led to smaller amounts of bisazo dye when the feed was added to the turbine suction, irrespective of the viscosity. All results agreed with the trends predicted by the engulfment model of micromixing. Its simplest form assigns an average energy dissipation rate to the reaction zone: the values obtained are of similar magnitude to those measured by physical techniques and were related to the spreading of the reaction zone.
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