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The integration of optimization techniques and deep learning models, which offer a promising avenue for improving the efficiency and sustainability of biodiesel production processes from baobab seed oil (BSO), is rare. This study utilized a multi-input-multioutput (MIMO) deep learning technique and the most recent central composite design (CCD) optimization tool to model and optimize the yield and properties of biodiesel produced from BSO. First, the baobab seed oil was extracted using a solvent extraction method. BSO was subsequently analyzed and converted to biodiesel by reacting CH3OH catalyzed by waste banana bunch stalk biochar activated by KOH. Multiobjective optimization and prediction of the biodiesel yield (Y) and several key fuel properties, including the cetane number (CN), kinematic viscosity (VS), and purity (P), were achieved. With better correlation coefficients of 0.9709, 0.9464, and 0.9714 for response training, response testing, and response validation, respectively, and a root-mean-square error of 0.00755, the MIMO model on the logsig transfer function accurately predicted the biodiesel yield and properties more than did the MISO and response surface methodology models. The optimum Y (96 wt %), CN (48), VS (3.3 mm2/s), and P (98.3%) were concurrently accomplished at a reaction temperature of 56 °C, a reaction time of 115 min, a CH3OH/BSO molar ratio of 15:1, a catalyst dosage of 6 wt %, and a stirring speed of 400 rpm with 98% optimal validation accuracy. CCD sensitivity analysis revealed that the CH3OH/BSO ratio was the most sensitive (50.9%) input predictor among the other input variables studied.
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Hydrothermal carbonization has gained attention in converting wet organic solid waste into hydrochar with many applications such as solid fuel, energy storage material precursor, fertilizer or soil conditioner. Recently, various catalysts such as organic and inorganic catalysts are employed to guide the properties of the hydrochar. This review presents a summarize and a critical discussion on types of catalysts, process parameters and catalytic mechanisms. The catalytic impact of carboxylic acids is related to their acidity level and the number of carboxylic groups. The catalysis level with strong mineral acids is likely related to the number of hydronium ions liberated from their hydrolysis. The impact of inorganic salts is determined by the Lewis acidity of the cation. The metallic ions in metallic salts may incorporate into the hydrochar and increase the ash of the hydrochar. The selection of catalysts for various applications of hydrochars and the environmental and the techno-economic aspects of the process are also presented. Although some catalysts might enhance the characteristics of hydrochar for various applications, these catalysts may also result in considerable carbon loss, particularly in the case of organic acid catalysts, which may potentially ruin the overall advantage of the process. Overall, depending on the expected application of the hydrochar, the type of catalyst and the amount of catalyst loading requires careful consideration. Some recommendations are made for future investigations to improve laboratory-scale process comprehension and understanding of pathways as well as to encourage widespread industrial adoption.
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In order to effectively utilize organic matter in sewage sludge (SS), a new porous carbon material was successfully prepared from SS with deep eutectic solvents (DES) (boric acid and urea), in which DES was firstly used to solvent to separate organic matter, also playing the role as a B and N donor as well as acid activator to form porous B, N-carbons. As-synthesized B, N-carbon electrode materials possessed a high specific capacitance of 251.4 F/g at a current density of 1 A/g. It retained 84.28% of the capacitance at an ultrahigh current density of 5 A/g. The energy density was 9.502 Wh/Kg at a power density of 245.4 W/kg in 6 M KOH in symmetric supercapacitor.
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Carbono , Esgotos , Capacitância Elétrica , Solventes , UreiaRESUMO
A Pyroprobe 5000 pyrolyzer connected to a gas chromatography-time-of-flight mass spectrometry (Py-GC-TOF-MS) was used to analyze the decomposition behavior of waste tire (WT). Effects of several typical parameters such as heating rate, atmosphere, reaction temperature, retention time, and zeolites on molecular composition and relative contents of the liquid products were investigated. Without added zeolite, the pyrolysis products mainly consisted of limonene, 1,4-pentadiene, and monocyclic aromatic hydrocarbons (MAHs) such as benzene, toluene, ethylbenzene, and xylene (BTEX). L-limonene was the dominant fraction (> 85%) of the limonene. Temperature and time presented the most significant effect on the liquid products' molecular composition and relative content, and increasing temperature and time reduced the contents of alkenes and increased the concentration of MAHs. With added zeolite, the molecular composition of the liquid products was greatly affected. All the liquid products produced with zeolite had higher MAHs and lower alkenes compared with those without added zeolite. Among the zeolites tested, Hß was the most beneficial catalyst to the production of aromatic hydrocarbons as the MAHs reached the highest value of 53.09%. The N, S-compound mainly consisted of benzothiazole and 2-methyl-benzothiazoles-important rubber accelerators. The O, S-compound mainly consisted of sulfones or sulfoxides.
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Alcadienos , Hidrocarbonetos Aromáticos , Zeolitas , Alcenos , Benzeno , Benzotiazóis , Catálise , Temperatura Alta , Limoneno , Borracha , Sulfonas , Sulfóxidos , Tolueno , Xilenos , Zeolitas/químicaRESUMO
The high content of nitrogen in hydrochar produced from hydrothermal carbonization (HTC) of sewage sludge (SS) leads to serious NOx pollution when the hydrochar is used as a solid fuel. Mg-Ga layered double hydroxides (LDHs), Mg-Al LDHs and their calcined samples (layered double oxides, LDO) were prepared. The LDHs and LDO all can notably promote the removal of nitrogen element, in which organic-N was transferred to NH4+-N to cause increasing pH value. Mg-Al LDO showed the highest efficiency for the removal of nitrogen among the catalysts. The thermal decomposition of the N-organic matter with acidic sites in catalyst was the key step to release NH3. The key role of basic sites in Mg-Al LDO was that it can effectively destroy the cell wall and extracellular polymeric substances structure. The lipid-like substance did not participate in the carbonization reaction, but they can be absorbed by the hydrochar. Partial SS floc directly transformed to hydrochar according to "solid-solid" reaction. The reaction pathways of remove nitrogen were proposed.
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Nitrogênio , Esgotos , Hidróxido de Alumínio , Carbono , Hidróxido de Magnésio , TemperaturaRESUMO
Shrimp processing and consumption generate large amounts of waste shrimp shell (WSS) rich in chitin and protein. Herein, we successfully synthesized WSS-based hydrochar (WSH) adsorbent through deproteinization and deacetylation followed by hydrothermal carbonization (HTC) and acid washing. For comparison, another hydrochar (CCH) adsorbent was synthesized from HTC of commercial chitosan under identical conditions. Specifically, WSH contained rich nitrogen-containing functional groups with a long aliphatic chains structure. Acid etching of calcium carbonate in WSS led to a higher specific surface area of WSH (12.65 m2/g) which was nearly 6 times higher than that of CCH (2.13 m2/g). The lower deacetylation degree of WSH was responsible for higher amide I and amino groups retained therein. Under an optimal initial solution pH of 4.0, WSH could rapidly achieve a superb adsorption capacity of 755.08 mg/g for methyl orange molecule. Moreover, the adsorption process followed a pseudo-second-order kinetics model and was well described by a monolayer adsorption pattern based on the Langmuir isotherm model with correlation coefficients higher than 0.9989. Prominent adsorption performance of WSH for methyl orange was mainly attributed to electrostatic interactions, while steric hindrance effect had a detrimental impact on the adsorption capacity of CCH. Superb adsorption capacity and excellent regeneration performance suggest WSH could be a promising and affordable adsorbent candidate for anionic dye removal.
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Exoesqueleto , Compostos Azo/isolamento & purificação , Poluentes Químicos da Água/isolamento & purificação , Purificação da Água/métodos , Adsorção , Animais , Crustáceos , Concentração de Íons de Hidrogênio , Cinética , ÁguaRESUMO
The characterization of products produced from hydrothermal liquefaction of algal biomass is helpful to better understand the effect of different kinds of raw materials on the properties of the product fractions. The data presented in this article are related to the research article entitled "Integration of hydrothermal liquefaction and supercritical water gasification for the improvement of energy recovery from algal biomass" (Duan et al., 2018) [1]. In this data article, the compositions of gaseous products produced from hydrothermal liquefaction of eight different algae feedstocks at 350⯰C for 60â¯min were analyzed by gas chromatography. The molecular and elemental compositions of the crude bio-oils produced from hydrothermal liquefaction of eight different algae feedstocks at 350⯰C for 60â¯min were analyzed by comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry and organic elemental analyzer. The color of aqueous phases before and after they were subjected to supercritical water gasification was recorded by a high-resolution camera.
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A comprehensive comparison of hydrothermal liquefaction (HTL) to the pyrolysis of duckweed was conducted to determine the yields and components of the crude bio-oils and their distillates. The upgrading behaviors of the distillates were thoroughly investigated with the use of used engine oil as a solvent. With all other variables fixed, HTL produced crude bio-oil with a lower H/C ratio (1.28⯱â¯0.03) than pyrolysis did (1.45⯱â¯0.04). However, its distillates had a higher H/C ratio (1.60⯱â¯0.05) and total yield (66.1⯱â¯2.0â¯wt%) than pyrolysis (1.46⯱â¯0.04 and 47.2⯱â¯1.4â¯wt%, respectively). Phenolics and nitrogenous heterocycles constituted relatively major proportions of the two crude bio-oils and most of their distillates. Obvious differences in molecular composition between the two crude bio-oils and their distillates were ascribed to the distinct impacts of HTL and pyrolysis and were affected by the distillate temperature. Co-hydrotreating with used engine oil (UEO) provided the upgraded bio-oils much higher H/C ratios (~1.78⯱â¯0.05) and higher heating values (~45.5⯱â¯1.4â¯MJ·kg-1), as well as much lower contents of N, O and S compared to their initial distillates. Aromatics and alkanes constituted a large proportion in most of upgraded bio-oils. N removal from the pyrolysis distillates was easier than from the HTL distillates. Distinct differences in yields and molecular compositions for the upgraded bio-oils were also attributed to the different influences associated with the two conversion routes.
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BACKGROUND: In this study, a two-step processing method (hydrothermal liquefaction followed by catalytic upgrading) was used to produce upgraded bio-oil. A comprehensive screening analysis of algal species, including four microalgae and four macroalgae, was conducted to bridge the gap between previous accounts of microalgae and macroalgae hydrothermal liquefaction and the upgrading process of the resulting crude bio-oils. RESULTS: Hydrothermal liquefaction using eight algal biomasses was performed at 350 °C for 1 h. The microalgae always produced a higher crude bio-oil yield than the macroalgae due to their high lipid content, among which Schizochytrium limacinum provided the maximum crude bio-oil yield of 54.42 wt%. For microalgae, higher amounts of N in the biomass resulted in higher amounts of N in the crude bio-oil; however, contrary results were observed for the macroalgae. The crude bio-oils generated from both the microalgae and macroalgae were characterized as having a high viscosity, total acid number, and heteroatom content, and they were influenced by the biochemical compositions of the feedstocks. Next, all eight-crude bio-oils were treated at 400 °C for 2 h with 10 wt% Ru/C using tetralin as the hydrogen donor. The hydrogen source was provided after tetralin was transformed to naphthalene. All the upgraded bio-oils had higher energy densities and significantly lower N, O, and S contents and viscosities than their corresponding crude bio-oils. However, the H/C molar ratio of the upgraded bio-oils decreased due to the absence of external hydrogen relative to the crude bio-oils. The S content of the upgraded bio-oil produced from upgrading the Schizochytrium limacinum crude bio-oil was even close to the 50 ppm requirement of China IV diesel. CONCLUSIONS: Microalgae are better feedstocks than macroalgae for liquid fuel production. Biochemical components have a significant impact on the yield and composition of crude bio-oil. Tetralin does not perform as well as external hydrogen for controlling coke formation. The S content of the upgraded bio-oil can be reduced to 76 ppm for the crude bio-oil produced from Schizochytrium limacinum. Upgraded bio-oils have similar properties to those of naphtha and jet fuel.
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Supercritical water gasification (SCWG) of the microalga Chlorella pyrenoidosa was examined with a catalyst mixture of Ru/C and Rh/C in a mass ratio of 1:1. The influences of temperature (380-600°C), water density (0-0.197g/cm3), and catalyst loading (0-20wt%) on the yields and composition of the gaseous products and the gasification efficiency were examined. The temperature and water density significantly affected the SCWG of the microalgae. The hydrogen gasification efficiency was more dependent on the temperature, while the carbon gasification efficiency was more dependent on the water density. The gaseous products mainly consisted of CH4, H2, CO, and CO2, with smaller amounts of C2-C3 hydrocarbons. CH4 made up half of the mole fraction of the gaseous products under most reaction conditions. A synergistic effect between Ru/C and Rh/C existed during the SCWG of the microalgae, and this effect favored the production of CH4. The role of the catalyst mixture became indistinct at higher temperatures. Hydrogen atoms from the water were transferred to the gaseous products during the SCWG, leading to hydrogen gasification efficiencies that exceeded 100%. The main components of the bio-oil were aromatics and nitrogen-containing compounds, and the main aromatics consisted of azulene and anthracene. The nitrogen-containing compounds are potential poisons to the catalyst mixture.
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Chlorella/fisiologia , Eliminação de Resíduos Líquidos/métodos , Poluentes da Água/metabolismo , Carbono , Catálise , Gases , Temperatura Alta , Hidrogênio , Esgotos , TemperaturaRESUMO
Two new lead rare-earth polyborates, PbTbB7O13 and PbEuB7O13, have been successfully synthesized via a high temperature molten salt method. Single crystal X-ray diffraction analysis reveals that they are isostructural and feature a 2D layer structure that contains alternating layers of [B7O13]∞ and [Tb]∞. The [B7O13]∞ layer is constructed of BO3 and BO4 groups with the fundamental building block of B7O17 (3Δ4â¡: <Δ2â¡>Δ<Δ2â¡>). Solid solutions of PbTb1-xEuxB7O13 (x = 0-1) were prepared via a solid state reaction and the photoluminescence properties were studied. The results show that under UV or near-UV excitation, the luminescence colour of samples of PbTb1-xEuxB7O13 (x = 0-1) can be tuned from green through yellow to red by simply adjusting the relative Eu3+ and Tb3+ concentrations, because of the Tb3+ â Eu3+ energy transfer mechanism.