Showing papers on "Thermogravimetry published in 2023"

Kinetic Study of Pyrolysis of Coniferous Bark Wood and Modified Fir Bark Wood

Abstract: We report on the kinetics of pyrolysis of bark wood of four coniferous tree species: fir (Abies sibirica), larch (Larix sibirica), spruce (Picea obovata), and cedar (Pinus sibirica) denoted as FB, LB, SB, and CB, respectively. Thermogravimetry (TG) and differential scanning calorimetry (DSC) methods were used to study the influence of KCl and K3PO4 compounds on the process of thermal decomposition of fir bark and determine the main thermal effects accompanying this process. As a result of the studies carried out, it was found that KCl additives practically do not affect the decomposition of hemicelluloses, but they shift the maximum decomposition of the cellulose peak in the direction of decreasing temperature to 340.9 °C compared to untreated bark (357.5 °C). K3PO4 promotes the simultaneous decomposition of hemicelluloses and cellulose in the temperature range with a maximum of 277.8 °C. In both cases, the additions of KCl and K3PO4 reduce the maximum rate of weight loss, which leads to a higher yield of carbon residues: the yield of char from the original fir bark is 28.2%, in the presence of K3PO4 and KCl it is 52.6 and 65.0%, respectively. Using the thermogravimetric analysis in the inert atmosphere, the reaction mechanism has been established within the Criado model. It is shown that the LB, SB, and CB thermal decomposition can be described by a two-dimensional diffusion reaction (D2) in a wide range (up to 0.5) of conversion values followed by the reactions with orders of three (R3). The thermal decomposition of the FB occurs somewhat differently. The diffusion mechanism (D2) of the FB thermal decomposition continues until a conversion value of 0.6. As the temperature increases, the degradation of the FB sample tends to R3. It has been found by the thermogravimetric analysis that the higher cellulose content prevents the degradation of wood. The bark wood pyrolysis activation energy has been calculated within the Coats–Redfern and Arrhenius models. The activation energies obtained within these models agree well and can be used to understand the complexity of biomass decomposition.

Effect of alkaline treatment on the thermal stability, degradation kinetics, and thermodynamic parameters of pineapple crown fibres

Abstract: Pineapple crown is generally discarded as waste but constitutes an important source of lignocellulosic fibres. In this work, the effect of alkaline treatment on the chemical composition, pyrolysis kinetics, and thermodynamic characteristics of pineapple crown fibres (PCF) were investigated by chemical composition, Fourier transform infrared spectroscopy (FTIR), scanning electronic microscopy (SEM), X-rays diffraction (XRD), and thermogravimetry. Chemical composition analysis indicated cellulose content increased from 18.93 to 57.00% after NaOH treatment. PCF fibre diameter was reduced from 6.1 to 4.3 μm after mercerization. The FTIR results confirmed the removal of non-cellulosic compounds. XRD analysis indicated fibre's crystallinity index rose from 53 to 62% in reason of NaOH treatment. Thermogravimetric results confirm that alkaline-treated PCF (ATPCF) presented higher thermal stability than non-treated PCF (NTPCF). The solid-state thermal degradation mechanism for NTPCF and ATPCF occurred by the diffusion process and random nucleation, respectively. The thermodynamic parameters of NTPCF indicated that a small amount of energy is required to obtain the reaction products and thus bioenergy production from NTPCF pyrolysis will be easier, while ATPCF required more energy to initiate a degradation reaction and could be used as filler in polymeric composites.

Thermal Decomposition Process Analysis of Jarosite Residue

Abstract: In this work, a mineralogical study and thermal decomposition analysis of jarosite residue sample from a zinc plant were carried out. The mineralogical analysis showed that the jarosite residue is mainly composed of four components, including jarosites, sulfates–hydroxides, sulfides and spinel. The distribution of relevant metallic elements in these components was characterized using a sequential extraction process. The X-ray diffraction results showed that AFe3(OH)6(SO4)2 and ZnFe2O4 are the main components of the jarosite residue sample. The thermal decomposition mechanisms of ammoniojarosite and sodium jarosite were studied by TG-DSC (Thermogravimetric analysis–differential scanning calorimetry). The thermal decomposition process and the corresponding mechanism of the jarosite residue were analyzed. The jarosite thermal decomposition process includes the removal of crystal water, dihydroxylation and deammoniation, desulfonation of component jarosite and desulfonation of component zinc sulfate.

Reactivation of hydrated cement powder by thermal treatment for partial replacement of ordinary portland cement

Abstract: Abstract Cement is the strength-forming component of concrete. It has been a major building material for more than a century. However, its production is accountable for a considerable percentage of global CO 2 emissions and is very energy-intensive. The Ordinary Portland Cement (OPC) production is a thermal process at around 1450 °C. This study shows that the reactivation of Hydrated Cement Powder (HCP) can be successful at a much lower temperature. Therefore, the possibility of using HCP to replace parts of OPC in concrete reduces the energy consumption and the CO 2 emissions associated with OPC production. HCP, which may ultimately stem from recycled concrete, needs treatment to produce new concrete of the required mechanical strength. Using reactivated HCP in concrete, an optimum strength is achieved by heating the HCP in the range of 400–800 °C. Among other factors, the type of cement used influences the optimum heating temperature and attainable strength. This paper shows that 600 °C is an optimum heating temperature using the OPC type CEM I 52.5R. The crystalline phase transitions resulting from the thermal treatment were analyzed by X-ray diffraction (XRD), differential scanning calorimetry (DSC), and thermogravimetry (TG). The heat released during hydration was investigated, and scanning electron microscopy (SEM) displays the microstructure evolution. OPC can be partially replaced by thermally treated HCP in mortar, attaining similar mechanical strength values.

Hydroxylation Studies on High-Solid Load Magnesia Aqueous Suspensions

Abstract: The magnesia (MgO) hydroxylation behavior in dilute suspensions (below 50% volumetric solid loads) has been extensively studied over the past decades due to its role in refractory castables. However, its equivalent effects on concentrated systems have not been analyzed in such a systemic way, although they are known to be as or more deleterious than those observed in dilute systems. This study focuses on the hydroxylation behavior of different sources of magnesia (sinter and caustic magnesia) in aqueous suspensions prepared at various solids concentrations (17-96 vol%) and shaped by distinct methods. They were analyzed by thermogravimetry, apparent volumetric expansion measurements, X-ray diffraction, scanning electron microscopy, and in situ temperature measurements during curing. The ratio between experimental and theoretical extents of the hydroxylation degree resulted in the reaction yield. A comparison between samples containing the same water amount revealed those with caustic magnesia showed a faster evolution of hydroxylation degree, apparent volumetric expansion, and higher maximum internal temperature during curing. In both systems, the yield levels of compositions of heavier solid loads were higher, despite the small quantity of hydroxylation products formed. Significant differences in the products’ microstructure were observed and related to the ions' mobility toward crystallization nuclei.

Thermocatalytic Decomposition of Sesame Waste Biomass over Ni-Co-Doped MCM-41: Kinetics and Physicochemical Properties of the Bio-Oil

Abstract: The increase in industrialization and development has tremendously diminished fossil fuel resources. Moreover, the excessive use of fossil fuels has resulted in the release of various toxic gases and an increase in global warming. Hence, necessitating the need to search for a renewable energy source. In this study, sesame waste biomass (SWB), which is abundantly available in Pakistan, has been used as feedstock for obtaining bio-oil using the pyrolysis technique. Pyrolysis was carried out using thermogravimetry and a pyrolysis chamber. Firstly, thermogravimetric analysis was performed on biomass with/without a laboratory synthesized catalyst Ni/Co/MCM-41 in nitrogen at different temperature programmed rates of 5, 10, 15, and 20 °C/min. A four-stage weight loss was observed that pointed toward the vaporization of water, and degradation of hemicelluloses, cellulose, and lignin. The kinetics parameters were determined using the Kissinger equation. The activation energy for the decomposition reaction of hemicelluloses, cellulose, and lignin, without catalyst, was observed as 133.02, 141.33, and 191.22 kJ/mol, respectively, however, with catalyst it was found as 91.45, 99.76, and 149.65 kJ/mol, respectively. In the catalyzed reaction the results showed the lowest activation energy, which is an indication of the fact that the catalyst is successful in reducing the activation energy to a sufficient level. As the TG/DTG showed active degradation between 200 and 400 °C, therefore, the waste sesame biomass over Ni-Co/MCM-41 was pyrolyzed within the same temperature range in the pyrolysis chamber. Temperature and time were optimized for maximum oil yield. A maximum oil yield of 38% was achieved at 330 °C and 20 min. The oil obtained was studied using GCMS. The physicochemical characteristics of the oil were assessed, and it was found that if the oil was upgraded properly, it could serve as a fuel for commercial use.

Physicochemical Properties and Application of Silica-Doped Biochar Composites as Efficient Sorbents of Copper from Tap Water

Abstract: This article concerns research on new sorption materials based on silica-doped activated carbon. A two-stage synthesis involved pyrolysis of plant material impregnated in a water glass solution, followed by hydrothermal activation of the pyrolysate in KOH solution. The resulting composite can be used as a sorbent in drinking water filters. The proposed method of synthesis enables the design of materials with a surface area of approximately 150 m2·g−1, whose chemical composition and structure were confirmed by scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS), X-ray diffraction (XRD), thermogravimetry/differential thermal analysis (TG/DTA) and Fourier-transform infrared spectroscopy (FTIR). The sorption properties of the obtained materials were determined relative to copper ions using the batch experiment method. The optimal operating parameters of the obtained materials relative to copper ions are T = 313.15 K, pH = 5, S:L ratio = 4 g·dm−3 and t = 120 min. The research shows that the sorption kinetics of copper ions can be described by a pseudo-second-order model. The plotted copper(II) sorption isotherm clearly indicates the Langmuir model. Under optimal conditions, the maximum sorption of copper ions was 37.74 mg·g−1, which is a satisfactory result and confirms the possibility of using the obtained material in drinking water filters.

Sponge-liked Silica Nanoporous Particles for Sustaining Release and Long-Term Antibacterial Activity of Natural Essential Oil

Abstract: To improve the sustained release and long-term antibacterial activity of Chimonanthus nitens Oliv. essential oil (CEO), novel sponge-liked nanoporous silica particles (SNP) were synthesized via the soft template method, which was employed as a biocompatible carrier to prepare spong-liked nanoporous silica particles loading with CEO (CEO-SNP) through physical adsorption. The structure and properties of the samples were characterized via N2 adsorption/desorption measurements, thermogravimetry (TGA), Fourier transform infrared, SEM and TEM. The result showed that the SNP exhibited an excellent loading capability of CEO up to 76.3%. The thermal stability and release behavior of the CEO were significantly improved via the physical adsorption of the SNP materials. The release profile of CEO was in accordance with the first-order kinetic model, which meant that the release mechanism was drug Fick’s diffusion. The antibacterial evaluation results demonstrated that the CEO-SNP exhibited strong antibacterial activity against S. aureus, E. coli and P. aeruginosa. The antibacterial results have shown that the CEO-SNP could destroy the cell structure of bacteria, and result in the generation of oxidative stress and the release of nucleic acid. After storage of 30 d at 25 °C, the CEO-SNP still had the stronger antibacterial activity towards S. aureus, E. coli and P. aeruginosa in comparison with CEO. Therefore, the sponge-like silica nanoporous particles seemed to be a promising carrier for long-term stability and antibacterial delivery of CEO.

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

Abstract: 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.

Luminescent Cd coordination polymer based on thiazole as a dual-responsive chemosensor for 4-nitroaniline and CrO42− in water

Abstract: A novel highly fluorescent cadmium metal-organic framework, [Cd (DPTTZ) (OBA)] (IUST-3), synthesized by using two linkers 2, 5-di (pyridine-4-yl) thiazolo [5, 4-d] thiazole (DPTTZ) and 4, 4'-oxybis (benzoic acid) (OBA) simultaneously, which exhibits a two-dimensional framework. The characteristics of this Cd-MOF were investigated by single-crystal X-ray diffraction, Fourier transform infrared spectroscopy, elemental analysis, powder X-ray diffraction, and thermogravimetry analysis. The IUST-3 exhibits excellent luminescence property and good stability in water. Luminescent experiments indicate that the IUST-3 has remarkable sensitivity and selectivity for the detection of 4-nitroaniline (4-NA), and CrO42- anion with KSV = 1.03 × 105 M-1 (4-NA) and KSV = 2.93 × 104 M-1 (CrO42-) and low limit of detection 0.52 µM (4-NA) and 1.37 µM (CrO42-). In addition, the possible fluorescence quenching mechanism was explored in this paper.