Biosorption of nickel and cadmium using Pachira aquatica Aubl. peel biochar.

This study aimed to assess the value of Pachira aquatica Aubl. fruit peels by exploring their applicability in the biosorption process for the removal of Ni(II) and Cd(II) metal ions. The Pachira aquatica Aubl. fruit peel biochar (PAB) was extensively characterized through various techniques, including proximate analysis, helium pycnometer, XRD, SEM, point of zero charge determination, zeta potential measurement, and Boehm titration. Subsequently, kinetic, isotherm, and thermodynamic batch biosorption studies were conducted, followed by column biosorption tests. The characteristics of PAB, including low moisture content, a neutral point of zero charge, porosity, an irregular and heterogeneous structure, a negatively charged surface, and the presence of functional groups, indicate its remarkable capacity for efficiently binding with heavy metals. Biosorption equilibrium time was achieved at 300 min for both ions, fitting well with a pseudo second-order kinetic model and Langmuir isotherm model. These data suggest that the biosorption process occurred chemically in monolayer. The column C presented an exhaust volume of 1200 mL for Ni(II) and 1080 for Cd(II) and removal of 98% and 99% of removal for Ni(II) and Cd(II), respectively. In summary, PAB demonstrates substantial potential as a biosorbent for effectively removing heavy metals, making a valuable contribution to the valorization of this co-product and the mitigation of environmental pollution.

Advancements and Prospects in Perovskite Solar Cells: From Hybrid to All-Inorganic Materials.

Hybrid perovskites, materials composed of metals and organic substances in their structure, have emerged as potential materials for the new generation of photovoltaic cells due to a unique combination of optical, excitonic and electrical properties. Inspired by sensitization techniques on TiO2 substrates (DSSC), CH3NH3PbBr3 and CH3NH3PbI3 perovskites were studied as a light-absorbing layer as well as an electron-hole pair generator. Photovoltaic cells based on per-ovskites have electron and hole transport layers (ETL and HTL, respectively), separated by an ac-tive layer composed of perovskite itself. Major advances subsequently came in the preparation methods of these devices and the development of different architectures, which resulted in an efficiency exceeding 23% in less than 10 years. Problems with stability are the main barrier to the large-scale production of hybrid perovskites. Partially or fully inorganic perovskites appear promising to circumvent the instability problem, among which the black perovskite phase CsPbI3 (α-CsPbI3) can be highlighted. In more advanced studies, a partial or total substitution of Pb by Ge, Sn, Sb, Bi, Cu or Ti is proposed to mitigate potential toxicity problems and maintain device efficiency.

Hydrothermal Synthesis and Properties of Nanostructured Silica Containing Lanthanide Type Ln-SiO2 (Ln = La, Ce, Pr, Nd, Eu, Gd, Dy, Yb, Lu).

The nanostructured lanthanide-silica materials of the Ln-SiO2 type (Ln = La, Ce, Pr, Nd, Eu, Gd, Dy, Yb, Lu) were synthesized by the hydrothermal method at 100 °C, using cetyltrimethylammonium as a structural template, silica gel and sodium silicate as a source of silicon, and lanthanide oxides, with Si/Ln molar ratio = 50. The resulting materials were calcined at 500 °C using nitrogen and air, and characterized by X-ray diffraction (XRD), Fourier-Transform infrared absorption spectroscopy, scanning electron microscopy, thermogravimetry (TG), surface area by the BET method and acidity measurements by n-butylamine adsorption. The XRD and chemical analysis indicated that the SiO2 presented a hexagonal structure and the incorporation of lanthanides in the structure changes the properties of the Ln-SiO2 materials. The heavier the lanthanide element, the higher the Si/Ln ratio. The TG curves showed that the decomposition of the structural template occurs in the materials at temperatures below 500 °C. The samples showed variations in specific surface area, mean pore diameter and silica wall thickness, depending on the nature of the lanthanide. The incorporation of different lanthanides in the silica generated acid sites of varied strength. The hydrothermal stability of the Ln-SiO2 materials evaluated at high temperatures, evidenced that the properties can be controlled for application in adsorption and catalysis processes.

Renewable aromatics through catalytic flash pyrolysis of pineapple crown leaves using HZSM-5 synthesized with RHA and diatomite.

The influence of reactor temperature of 300  and 600 °C and the acidity of the ZSM-5 and HZSM-5 catalysts on the pyrolysis product yields of the pineapple crown leaves have been investigated in a fixed bed reactor Py-GC/MS. The ZSM-5 catalyst was hydrothermally synthesized with a Si/Al ratio 50, using residual diatomite and rice husk ash as alternative sources of Al and Si for catalyst cost reduction. For the HZSM-5 synthesis, calcined ZSM-5 was activated by ion exchange between Na+ and H+. The catalysts structure was confirmed by the XRD and Rietveld treatment, SEM, FTIR, FRX, TGA and BET results. Analytical pyrolysis of the biomass was carried out at 500 °C in a Py-5200 HP-R pyrolyzer connected to the GC/MS and the pyrolysis vapors were transported to a catalytic bed at 300 and 600 °C. The results showed that the increase in the catalytic bed temperature promoted increased the aromatic content. The main pyrolysis products of the PCL were oxygenated compounds that were converted at 600 °C using the HZSM-5 catalyst into high value renewable aromatic compounds for the chemical industry, such as benzene, toluene, xylene, etilbenzene, thereby confirming the deoxygenation activity of synthesized catalyst to produce renewable aromatics compounds which are important platform chemicals and precursors for jet fuels, gases, polymers and solvents.

Ex situ catalytic biomass pyrolysis using mesoporous Ti-MCM-41.

Biomass has attracted considerable attention as energy, economic, and environmental asset, as result of its abundance and range of properties. The use of mesoporous catalysts during fast pyrolysis has been a highly important route to improve efficiency as well adding value to biomass. The addition of titanium to molecular sieves increases the efficiency of the pyrolysis reaction by improving production and selectivity of products of interest. This study aims at analyzing the catalytic pyrolysis products of elephant grass using titanium catalysts prepared at different Si/Ti molar ratios, i.e., 25 and 50. The material was supported on MCM-41 for the catalytic pyrolysis of biomass. The biomass pyrolysis reactions were performed in a micropyrolyzer coupled to a GC/MS analyzer. The Ti-MCM-41 samples were characterized by XRD, BET-specific area, and UV-visible. The distribution of pyrolysis products depended on process parameters such as temperature and catalyst type. The highest yield for hydrocarbon production, such as styrene, benzene, methylbenzene, and naphthalene, was observed at 600 °C using Si/Ti equal to 50.

Characterization and pyrolysis of Chlorella vulgaris and Arthrospira platensis: potential of bio-oil and chemical production by Py-GC/MS analysis.

Biofuels have been seen as potential sources to meet future energy demand as a renewable and sustainable energy source. Despite the fact that the production technology of first-generation biofuels is consolidated, these biofuels are produced from foods crops such as grains, sugar cane, and vegetable oils competing with food for crop use and agricultural land. In recent years, it was found that microalgae have the potential to provide a viable alternative to fossil fuels as source of biofuels without compromising food supplies or arable land. On this scenario, this paper aims to demonstrate the energetic potential to produce bio-oil and chemicals from microalgae Chlorella vulgaris and Arthrospira platensis. The potential of these biomasses was evaluated in terms of physical-chemical characterization, thermogravimetric analysis, and analytical pyrolysis interfaced with gas chromatograph (Py-GC/MS). The results show that C. vulgaris and A. platensis are biomasses with a high heating value (24.60 and 22.43 MJ/kg) and low ash content, showing a high percentage of volatile matter (72.49 and 79.42%). These characteristics confirm their energetic potential for conversion process through pyrolysis, whereby some important aromatic compounds such as toluene, styrene, and phenol were identified as pyrolysis products, which could turn these microalgae a potential for biofuels and bioproduct production through the pyrolysis.

Effect of the order and disorder of BaMoO4 powders in photoluminescent properties.

The study of the photoluminescent properties affected by order and disorder of the BaMoO(4) powders is the principal objective in this work. BaMoO(4) compounds were prepared using soft chemical process called Complex Polymerization Method. In this work, different deagglomeration types and different heating rates were used to promote different disorder degrees. Scheelite type phase (BaMoO(4)) was determined by X-ray Diffraction (XRD), Fourier Transformed Infra-Red (FTIR) and Raman spectroscopy after heat treating the sample at 400 degrees C. The room temperature luminescence spectra revealed an intense single-emission band in the visible region. Based on XRD and Raman data it was observed that the transition between the completely disordered structure to completely ordered structure is a good condition for photoluminescence (PL) emission. The best PL emission is obtained when the material possesses short range disorder, i.e., is periodically ordered (XRD), but some disorder as measured by Raman spectroscopy. The excellent optical properties observed for disordered BaMoO(4) suggested that this material is a highly promising candidate for optical applications.

Synthesis, characterization and photophysical properties of Eu3+ doped in BaMoO4.

In this work Ba(0.99)Eu(0.01)MoO(4) (BEMO) powders were prepared by the first time by the Complex Polymerization Method. The structural and optical properties of the BEMO powders were characterized by Fourier Transform Infra-Red (FTIR), X-ray Diffraction (XRD), Raman Spectra, High-Resolution Scanning Electron Microscopy (HR-SEM) and Photoluminescent Measurements. XRD show a crystalline scheelite-type phase after the heat treatment at temperatures greater than 400 degrees C. The ionic radius of Eu(3+) (0.109 nm) is lower than the Ba(2+) (0.149 nm) one. This difference is responsible for the decrease in the lattice parameters of the BEMO compared to the pure BaMoO(4) matrix. This little difference in the lattice parameters show that Eu(3+) is expected to occupy the Ba(2+) site at different temperatures, stayed the tetragonal (S(4)) symmetry characteristic of scheelite-type crystalline structures of BaMoO(4). The emission spectra of the samples, when excited at 394 nm, presented the (5)D(1)-->(7)F(0, 1 and 2) and (5)D(0)-->(7)F(0, 1, 2, 3 and 4) Eu(3+) transitions at 523, 533, 554, 578, 589, 614, 652 and 699 nm, respectively. The emission spectra of the powders heat-treated at 800 and 900 degrees C showed a marked increase in its intensities compared to the materials heat-treated from 400 to 700 degrees C. The decay times for the sample were evaluated and all of them presented the average value of 0.61 ms. Eu(3+) luminescence decay time follows one exponential curve indicating the presence of only one type of Eu(3+) symmetry site.