Modeling and simulation of biogas-fueled power system

The main objective of this paper is to develop a complete model that fully simulate a biogas-fueled power plant which can be used to supply a rural farm with sufficient electricity. The reactor is fed with animal manure of the farm. The proposed model consists of three main parts; a biogas reactor, a microturbine (MT) coupled to a permanent magnet synchronous generator, and a storage system. The model describes the dynamics of an MT and it is suitable for both steady state and transient simulation and analysis. The volume of biogas output delivered from the Anaerobic Digester depends on the reactor volume, reactor temperature, and animal manure type. The storage system is used to store the excess value of biogas if any. It is composed of two parts: a comparator and a storage tank. The comparator compares the volume of biogas produced by the reactor with that needed to supply the load. An adaptive controller is developed to withstand the system against any transient condition such as suddenly load increase/decrease. The proposed model is implemented for chemical and physical behaviors of the biogas production process, as well as for different variables of MT-generator operations. The model is implemented in Matlab/Simulink environment and tested under different operating conditions in both steady state and transient status to study the impacts of different variables on the system output. The output results prove its applicability and effectiveness under different operating conditions.     

Comparative efficacy of certain plant extracts alone and combination with profenofos against Spodoptera littoralis (Boisd.) (Lepidoptera: Noctuidae)

Ethyl alcohol, acetone, and petroleum ether extracts of three plant species belonging to three different botanical families [Strychnos nux-vomica (Loganiaceae), Euphorbia lathyrus (Euphorbiaceae), and Datura stramonlum (Solanaceae)], a chemical insecticide; profenofos and their combinations were tested against second and fourth instars of Spodoptera littoralis under lab conditions. Results revealed that the ethanol extract of S. nux-vomica was the most effective among all plant extracts, where the corrected mortality% were 92, 81, 58, and 27% to 2nd instar and 89, 74, 34, and 11% to 4th instar at concentrations 0.5, 0.25, 0.125, and 0.0625%, respectively. Calculated LC₅₀'s were 0.11, 0.22, and 0.34% to 2nd instar and 0.17, 0.37, and 0.52% to 4th instar for ethanol, petroleum ether, and acetone extracts, respectively. Acetone extracts of all plants were of lower effect. The chemical insecticide profenofos displayed higher efficacy than plant extracts (LC₅₀ = 0.002 and 0.003% for S. littoralis 2nd and 4th larval instars, respectively). The co-toxicity factor reached 76 and 60 when mixing S. nux-vomica + profenofos and D. stramonlum + profenofos at ratio 1:1 against S. littoralis 2nd instar larvae, thus indicating a potentiating effect. While treatment of the 4th instar larvae by the same mixtures resulted in a co-toxicity factor below 20 at all mixing ratios indicating, only, an additive effect against this instar.     

Application of a Second-Order Kinetic Model to a Complex Melt Polymerization Reaction

A novel copolymer system has been synthesized using methyl hydroquinone diacetate (MHQDA), 1,4 naphthalene dicarboxylic acid (1,4 NDCA), and polybutylene terephthalate (PBT) using the melt polymerization technique. The optimum kinetic parameters pertinent to this system are reported in this study. A simple second-order reaction sequence summarizes catalyzed and uncatalyzed reactions between MHQDA, 1,4 NDCA, and PBT. The kinetic parameters for the copolymerization reaction were determined using a new second-order model. This technique was used to compute the moles of acetic acid generated in the polymerization process. The model was compared to that of the experimentally determined data. Close comparison (percentage error of less than 5%) was obtained between the experimental and theoretical data. The kinetic data support block copolyester formation. The thermal data also supports formation of block polymers.     

Materials,fuels, upgrading,economy, and life cycle assessment of the pyrolysis of algal and lignocellulosic biomass: a review

Climate change issues are calling for advanced methods to produce materials and fuels in a carbon–neutral and circular way. For instance, biomass pyrolysis has been intensely investigated during the last years. Here we review the pyrolysis of algal and lignocellulosic biomass with focus on pyrolysis products and mechanisms, oil upgrading, combining pyrolysis and anaerobic digestion, economy, and life cycle assessment. Products include oil, gas, and biochar. Upgrading techniques comprise hot vapor filtration, solvent addition, emulsification, esterification and transesterification, hydrotreatment, steam reforming, and the use of supercritical fluids. We examined the economic viability in terms of profitability, internal rate of return, return on investment, carbon removal service, product pricing, and net present value. We also reviewed 20 recent studies of life cycle assessment. We found that the pyrolysis method highly influenced product yield, ranging from 9.07 to 40.59% for oil, from 10.1 to 41.25% for biochar, and from 11.93 to 28.16% for syngas. Feedstock type, pyrolytic temperature, heating rate, and reaction retention time were the main factors controlling the distribution of pyrolysis products. Pyrolysis mechanisms include bond breaking, cracking, polymerization and re-polymerization, and fragmentation. Biochar from residual forestry could sequester 2.74 tons of carbon dioxide equivalent per ton biochar when applied to the soil and has thus the potential to remove 0.2–2.75 gigatons of atmospheric carbon dioxide annually. The generation of biochar and bio-oil from the pyrolysis process is estimated to be economically feasible.

     

Mobility of selected trace elements in Mediterranean red soil amended with phosphogypsum: experimental study

Soil amendment by phosphogypsum (PG) application becomes of increasing importance in agriculture. This may lead, however, to soil, plant, and groundwater contamination with trace elements (TEs) inherently present in PG. Monitoring of selected TEs (Pb, Zn, Cu, and Cd) distribution and mobility in a Mediterranean red soil profile has been performed in soil parcels applied with PG over a 16-month period. Concentrations were measured in soil and plant samples collected from various depth intervals at different points in time. TEs sequential extraction was performed on soil and PG samples. Results showed soil profile enrichment peaked 5 months after PG application for Cd, and 12 months for Pb, Zn, and Cu. Rainwater, pH, total organic carbon, and cationic exchange capacity were the main controlling factors in TEs accumulation in soils. Cd was transferred to a soil depth of about 20 cm. Zn exhibited mobility towards deeper layers. Pb and Cu were accumulated in around 20-55-cm-deep layers. PG increased the solubility of the studied TEs; PG-applied soils contained TEs bound to exchangeable and acid-soluble fractions in higher percentages than reference soil. Pb, Zn, and Cu were sorbed into mineral soil phases, while Cd was mainly found in the exchangeable (bio-available) form. The order of TEs decreasing mobility was Zn > Cd > Pb > Cu. Roots and leaves of existed plants, Cichorium intybus L., accumulated high concentrations of Cd (1-2.4 mg/kg), exceeding recommended tolerable levels, and thus signifying potential health threats through contaminated crops. It was therefore recommended that PG should be applied in carefully established, monitored, and controlled quantities to agricultural soils.     

Spongy Ni/Fe carbonate-fluorapatite catalyst for efficient conversion of cooking oil waste into biodiesel

Environmental Chemistry Letters - Biodiesel produced from animal and plant fat oils is sustainable, but there is a need for efficient heterogeneous catalysts for transesterification of crude oils...     

Cost,environmental impact,and resilience of renewable energy under a changing climate: a review

Energy derived from fossil fuels contributes significantly to global climate change, accounting for more than 75% of global greenhouse gas emissions and approximately 90% of all carbon dioxide emissions. Alternative energy from renewable sources must be utilized to decarbonize the energy sector. However, the adverse effects of climate change, such as increasing temperatures, extreme winds, rising sea levels, and decreased precipitation, may impact renewable energies. Here we review renewable energies with a focus on costs, the impact of climate on renewable energies, the impact of renewable energies on the environment, economy, and on decarbonization in different countries. We focus on solar, wind, biomass, hydropower, and geothermal energy. We observe that the price of solar photovoltaic energy has declined from $0.417 in 2010 to $0.048/kilowatt-hour in 2021. Similarly, prices have declined by 68% for onshore wind, 60% for offshore wind, 68% for concentrated solar power, and 14% for biomass energy. Wind energy and hydropower production could decrease by as much as 40% in some regions due to climate change, whereas solar energy appears the least impacted energy source. Climate change can also modify biomass productivity, growth, chemical composition, and soil microbial communities. Hydroelectric power plants are the most damaging to the environment; and solar photovoltaics must be carefully installed to reduce their impact. Wind turbines and biomass power plants have a minimal environmental impact; therefore, they should be implemented extensively. Renewable energy sources could decarbonize 90% of the electricity industry by 2050, drastically reducing carbon emissions, and contributing to climate change mitigation. By establishing the zero carbon emission decarbonization concept, the future of renewable energy is promising, with the potential to replace fossil fuel-derived energy and limit global temperature rise to 1.5 °C by 2050.

     

Detection and mapping of water pollution variation in the Nile Delta using multivariate clustering and GIS techniques

The limited water resources of Egypt lead to widespread water-stress. Consequently, the use of marginal water sources, such as agricultural drainage waters, provides one of the national feasible solutions to the problem. However, the marginal quality of the drainage waters may restrict their use.The objective of this research is to develop a tool for planning and managing the reuse of agricultural drainage water for irrigation in the Nile Delta. This is achieved by classifying the pollution levels of drainage water into several categories using a statistical clustering approach that may ensure simple but accurate information about the pollution levels and water characteristics at any point within the drainage system.The derived clusters are then visualized by using a Geographical Information System (GIS) to draw thematic maps based on the entire Nile Delta, thus making GIS as a decision support system. The obtained maps may assist the decision makers in managing and controlling pollution in the Nile Delta regions. The clustering process also provides an effective overview of those spots in the Nile Delta where intensified monitoring activities are required. Consequently, the obtained results make a major contribution to the assessment and redesign of the Egyptian national water quality monitoring network.     

Evaluation of dilute hydrochloric acid and acid ammonium oxalate as extractants for some heavy metals from Nile River sediments

The suitability of a 0.5 M HCl solution for extraction of Fe, Mn, Cd, Co, Cu, Pb, and Zn from Nile River sediments was evaluated by comparing its effectiveness with that of conventional acid ammonium oxalate (Tamm's solution) and aqua regia extraction solutions. The present study has shown that although the extraction data indicate that both 0.5 M HCl and acid ammonium oxalate solutions are able to extract heavy metals simultaneously from the adsorbed, organic, and precipitated phases of Nile sediments, the 0.5 M HCl solution is preferred. It provides a rapid, reliable, and inexpensive method of measuring environmentally mobile metal concentrations in the aquatic sediments. From an analytical chemistry point of view, the 0.5 M HCl extracts do not clog the atomizer of the spectrophotometer. Extraction with dilute HCl solution obviates the need to use chemicals, some of which are toxic or not available readily as a high-purity grade. A standard extraction method should be relatively simple, to conduct a routine analysis of large numbers of sediment samples, yet at the same time it should provide sufficient information for assessment of the environmental impact of particulate metals. Therefore, extraction with 0.5 M HCl solution is very suitable for heavy-metal pollution monitoring in the Nile River     

Assessment of metals in soil extracts and their uptake and movement within Tamarix nilotica at Lake Nasser banks,Egypt

This study aims to determine heavy-metal levels in soil from the banks of Lake Nasser, the ability of Tamarix nilotica to accumulate such metals from soil and hence its potential for phytoextraction. Soil and Tamarix samples were collected from the banks of four bights around Lake Nasser and analysed for Fe, Mn, Ca, Mg, Cr, Cu, Ni, Zn, Cd and Pb by atomic absorption spectrometry, whereas Na and K were measured by atomic emission spectrophotometry. Three different methods of extraction were used for the soil samples. Lead, copper and zinc were equally distributed between the exchangeable phase and Fe/Mn oxide-bound form, while other measured metals were mainly present in the Fe/Mn oxide fraction. With the exception of iron, all metals studied showed total concentrations within the geochemical background values. T. nilotica exhibited elevated concentrations of Na (36.2–48.5?mg?g^?1) and K (2.74–4.33?mg?g^?1) in stems, and relatively high concentrations of Pb, Cd and Co (0.39–1.03?µg?g^?1, 0.24–1.3?µg?g^?1 and 1.94–5.3?µg?g^?1, respectively) are found in plant leaves. Bioaccumulation factors of Na and K (9.3 and 12.63, respectively) were high in T. nilotica stems. While the bioaccumulation of Pb, Cd, Co and Ni (2870.1, 2035.4, 10.5 and 5313.2, respectively) was high in plant leaves, Fe, Mn, Ca and Mg were accumulated relatively equally in plant stems and leaves. T. nilotica was found to secrete high amounts of Na, Ca and K, in addition to small amounts of all accumulated metals except Cd and Cu. These secreted metals appeared as salt crystals (67.5% Na; 25.8% Ca; 5% Mg; 1.5% K and 0.16% trace and minor elements) on the plant surface. The concentrations of all the metals studied in T. nilotica were higher than in the salt crystals. Statistical analysis of the database suggests bioaccumulation of these metals from soil to T. nilotica. This reflects the importance of using T. nilotica as a model in the phytoremediation process as an established environmental clean-up technology.