Characterization of coffee residues pellets and their performance in a residential combustor

Spent coffee grounds (SCG) and coffee husks (CH) were evaluated as biofuels, after densification, for energy production. CH represent a specific problem for the coffee industry due to a low calorific value, high ash content, and a very low bulk density. Hence, the energetic potential of SCG (95 wt%)/CH (5 wt%) blend and pure SCG (100%) were examined. The blend of SCG and CH was limited to 5 wt% of CH because of the low bulk density of CH. Therefore, physicochemical and energetic characterizations of the produced pellets were performed. Thermogravimetric analyses were performed under nitrogen and air atmospheres to evaluate the CH behavior in the blend. Characterization study shows that both produced pellets could reach the French Agropellets standard (AQI). Thermal degradation showed that the mean reactivity of the SCG/HC pellets was higher than pure SCG. Then, combustion experiments were performed in a domestic combustor, after modification of the boiler power in order to improve its energetic performances. The presence of CH led to a rise of CO, NOx, VOC’s, and particle emissions. Nevertheless, the performances of the biofuels are almost in agreement the NF EN 12809 standard.     

Biosorption of copper from aqueous solutions by date stones and palm-trees waste

The removal of toxic metals from wastewaters by biosorption, based on the metal-binding capacities of various biological materials, has received much interest. However, the success of this approach depends on economic feasibility, which can be obtained by optimization of the environmental conditions. This paper evaluates, for the first time, the use of low-cost biosorbent (date stones (DS) and palm-tree waste (PTW)) to eliminate Cu(II) from aqueous solutions. The effect of some parameters on copper biosorption has been studied using date stones and palm-tree waste as solid sorbents. Results show that the highest percentage of copper adsorption was obtained for the smallest size of the sorbent particles. The biosorption process was found to occur rapidly, i.e. the maximum sorption capacity was reached within 20 min. The process involved pseudo-second-order kinetics with an activation energy value within the normal range considered for processes, where a physical interaction between the sorbate and the sorbent solid predominated. The thermodynamic parameters of the copper ions uptake onto the solid sorbents indicated that, the process was endothermic and proceeds spontaneously from the date stones. However, the thermodynamic studies of the adsorption of copper on palm-tree waste indicated that the process was exothermic and proceeds spontaneously.     

Thermal degradation kinetics and mechanisms of Posidonia Oceanica under inert and oxidative atmospheres

The thermal degradation characteristics of Posidonia Oceanica (PO), a marine biomass abundantly available on the coastal zone of the Mediterranean Basin, were investigated using thermogravimetric analysis under inert and oxidative atmospheres. The kinetic parameters of the both thermal degradations conditions were determined using n-reaction order model. Coats–Redfern and Phadnis–Deshpande methods were used to discuss the probable degradation mechanisms. Results showed that PO is an attractive alternative for energy production owing to its elevated heating value. Moreover, PO thermal degradation follows the usual shape of biomass decomposition. Hence, under inert atmosphere, its thermal degradation had two different stages after moisture release. The first stage corresponded to the volatiles release while the second stage corresponded to the char formation. The solid-state decomposition mechanisms followed by the devolatilization step of PO were two or three dimensional diffusion controlled reaction. However, the decomposition mechanism during PO char formation corresponded to a nucleation and growth mechanism. Under oxidative atmosphere, two stages were also observed corresponding to volatiles release and char combustion, respectively. The solid-state mechanism of volatiles release followed three dimensional diffusion controlled reaction while the char combustion mechanism corresponded to a contracting area phase boundary controlled reaction.