Catalytic wet air oxidation of high BPA concentration over iron-based catalyst supported on orthophosphate.

The catalytic performance of Fe supported on nickel phosphate (NiP) was evaluated for the removal of bisphenol A (BPA) by catalytic wet air oxidation (CWAO) at 140 °C and 25 bar of pure oxygen pressure. The prepared NiP and Fe/NiP materials were fully characterized by XRD, N2-physisorption, H2-TPR, TEM, and ICP analysis. Iron (Fe/NiP) impregnation of NiP support enhanced the BPA removal efficiency from 37.0 to 99.6% when CWAO was performed. This catalyst was highly stable given the operating conditions of acidic medium, high temperature, and high pressure. The Fe/NiP catalyst showed an outstanding catalytic activity for oxidation of BPA, achieving almost complete removal of BPA in 180 min at a concentration of 300 mg/L, using 4 g/L of Fe/NiP. No iron leaching was detected after the CWAO of BPA. The stability of Fe/NiP was performed over three consecutive cycles, noting that BPA conversion was not affected and iron leaching was negligible. Therefore, this catalyst (Fe/NiP) could be considered as an innocuous and effective long-lasting catalyst for the oxidation of harmful organic molecules.

Investigation of (co)-combustion kinetics of biomass, coal and municipal solid wastes.

Investigation of thermal behaviors of biomass waste, biochar, coal, municipal solid waste (MSW) and their mixtures were aimed in the present study using both thermogravimetric analysis and differential scanning calorimeter techniques. In fact, this paper intends to interpret the influence of mixtures on activation energy. In this purpose, Coats and Redfern were used. Then, the relative error Δmerror was calculated to quantify the synergism degree. Precisely, it was about 5.34% for biomass/coal, 5.52% for biomass/cardboard, 5.67% for biomass/biochar, 5.93% for biomass/synthetic rubber and 6.05% for biomass/plastic mixtures. This phenomenon was justified by the interaction between C-C bond of biochar, coal and MSW radicals with C-H and C-O bonds of biomass.

Municipal solid waste higher heating value prediction from ultimate analysis using multiple regression and genetic programming techniques.

Municipal solid waste (MSW) management presents an important challenge for all countries. In order to exploit them as a source of energy, a knowledge of their calorific value is essential. In fact, it can be experimentally measured by an oxygen bomb calorimeter. This process is, however, expensive. In this light, the purpose of this paper was to develop empirical models for the prediction of MSW higher heating value (HHV) from ultimate analysis. Two methods were used: multiple regression analysis and genetic programming formalism. Both techniques gave good results. Genetic programming, however, provides more accuracy compared to published works in terms of a great correlation coefficient (CC) and a low root mean square error (RMSE).

Steam activation of waste biomass: highly microporous carbon, optimization of bisphenol A, and diuron adsorption by response surface methodology.

Highly microporous carbons were prepared from argan nut shell (ANS) using steam activation method. The carbons prepared (ANS@H2O-30, ANS@H2O-90, and ANS@H2O-120) were characterized using X-ray diffraction, scanning electron microscopy, Fourier-transform infrared, nitrogen adsorption, total X-ray fluorescence, and temperature-programmed desorption (TPD). The ANS@H2O-120 was found to have a high surface area of 2853 m2/g. The adsorption of bisphenol A and diuron on ANS@H2O-120 was investigated. The isotherm data were fitted using Langmuir and Freundlich models. Langmuir isotherm model presented the best fit to the experimental data suggesting micropore filling of ANS@H2O-120. The ANS@H2O-120 adsorbent demonstrated high monolayer adsorption capacity of 1408 and 1087 mg/g for bisphenol A and diuron, respectively. The efficiency of the adsorption was linked to the porous structure and to the availability of the surface adsorption sites on ANS@H2O-120. Response surface method was used to optimize the removal efficiency of bisphenol A and diuron on ANS@H2O-120 from aqueous solution. Graphical abstract ᅟ.

Toward new benchmark adsorbents: preparation and characterization of activated carbon from argan nut shell for bisphenol A removal.

The use of argan nut shell as a precursor for producing activated carbon was investigated in this work. Two activated carbons AC-HP and AC-Na were prepared from argan nut shell by chemical activation method using phosphoric acid (H3PO4) and sodium hydroxide (NaOH), respectively. Textural, morphological, and surface chemistry characteristics were studied by nitrogen physisorption, TGA, SEM, TXRF, FTIR, XRD, and by determining the pHPZC of the AC-HP. The adsorption experiments revealed that AC-HP was more efficient in adsorption of BPA due to high specific surface area (1372 m2/g) compared to AC-Na (798 m2/g). The obtained adsorption data of BPA on AC-HP correlated well with the pseudo-second-order model and the Langmuir isotherm (Qmax = 1250 mg/g at 293 K). The thermodynamic parameters (ΔG° < 0, ΔH° < 0, and ΔS° < 0) indicate that adsorption of BPA on AC-HP was spontaneous and exothermic in nature. The regeneration of AC-HP showed excellent results after 5 cycles (95-93%). This work does not only provide a potential way to use argan nut shell but also represents a sustainable approach to synthesize AC-HP, which might be an ideal material for various applications (energy storage, catalysis, and environmental remediation).

Effect of materials mixture on the higher heating value: Case of biomass, biochar and municipal solid waste.

The heating value describes the energy content of any fuel. In this study, this parameter was evaluated for different abundant materials in Morocco (two types of biochar, plastic, synthetic rubber, and cardboard as municipal solid waste (MSW), and various types of biomass). Before the evaluation of their higher heating value (HHV) by a calorimeter device, the thermal behavior of these materials was investigated using thermogravimetric (TGA) and Differential scanning calorimetry (DSC) analyses. The focus of this work is to evaluate the calorific value of each material alone in a first time, then to compare the experimental and theoretical HHV of their mixtures in a second time. The heating value of lignocellulosic materials was between 12.16 and 20.53MJ/kg, 27.39 for biochar 1, 32.60MJ/kg for biochar 2, 37.81 and 38.00MJ/kg for plastic and synthetic rubber respectively and 13.81MJ/kg for cardboard. A significant difference was observed between the measured and estimated HHVs of mixtures. Experimentally, results for a large variety of mixture between biomass/biochar and biomass/MSW have shown that the interaction between biomass and other compounds expressed a synergy of 2.37% for biochar 1 and 6.11% for biochar 2, 1.09% for cardboard, 5.09% for plastic and 5.01% for synthetic rubber.