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Plastic waste can exist naturally for hundreds of thousands of years and harm humans, animals, and the environment. In this study, the energy and exergy performances (absorbed energy, energy efficiency, absorbed exergy, and exergy efficiency) of LDPE (low-density polyethylene) plastic particles assisted by microwave heating based on the experimental data as affected by microwave power, feeding load, and chamber volume were evaluated and analyzed. The results showed that as the microwave power raised from 500 to 900 W, the feeding load changed from 10 to 30 g, and the chamber volume decreased from 200 to 100 ml, (a) the absorbed energy at the heating time of 60 min increased from 19.73 kJ, 5.84 kJ, and 22.71 kJ to 37.69 kJ; (b) the energy efficiency for the whole heating process increased from 1.10%, 0.32%, and 1.26% to 2.09%; (c) the absorbed exergy at the heating time of 60 min increased from 0.308, 0.091, and 0.091 to 0.724 kJ; and (d) the exergy efficiency for the whole heating process increased from 0.017, 0.005, and 0.023 to 0.040%, respectively.
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The amount of biomass production each year is huge, and microwave-assisted pyrolysis of biomass to obtain biogas, bio-oil, and biochar is a promising method. In this study, silicon carbide (SiC) was selected as the microwave absorber, and the effects of microwave power (400, 450, 500, 550 and 600 W), reactor chamber volume (100, 150, 200, 250, and 300 W), and the mass ratio of SiC and corn straw (0, 0.25, 0.5, 0.75, and 1) on the heating performances of corn straw particles were investigated and presented in this study. When the microwave power increased from 400 to 600 W, the average heating rate of corn straw particles increased from 23.06 â /min to 101.46 â /min, and that of mixture particles of corn straw and SiC increased from 87.00 â /min to 236.88 â/min. When the reactor chamber volume increased from 100 to 300 mL, the average heating rate of corn straw particles decreased from 38.21 â/min to 22.54 â/min, and that of mixture particles of corn straw and SiC decreased from 98.84 â/min to 76.01 â/min. When the mass ratio of SiC and corn straw increased from 0 to 1, the average heating rate of mixture particles of corn straw and SiC increased from 101.46 â/min to 236.88 â/min. Some formulae with R2 values ranged from 0.971 to 0.998 were proposed to determine the transient temperatures of corn straw particles and mixture particles of corn straw and SiC.
RESUMO
Microwave-assisted heating is an effective heating method for thermochemical conversion of biomass. In this study, experimental syngas production from microwave-assisted air gasification of biomass in a fluidized bed reactor at different gasification temperatures, equivalence ratios and silicon carbide loads, was studied and reported. The results showed that the highest syngas yield (78.2 wt%), higher heating value (6.3 MJ/Nm3) and cold gas efficiency (81.8 %) were obtained at gasification temperature of 900 °C, equivalence ratio of 0.35 and silicon carbide load of 30 g, and the gasification temperature had significant influence on the syngas production. Microwave-assisted heating showed positive effect on tar reduction, i.e., the tar content at 900 °C (2.1 wt%) in this study was even lower than the tar content (3.2 wt%) from catalytic electrical air gasification of rice husk at 950 °C. Generally, the introduction of microwave-assisted heating showed positive effect on biomass gasification.
Assuntos
Gases , Micro-Ondas , Gases/química , Biomassa , TemperaturaRESUMO
In view of the problem that removing abnormal plants in breeding rape requires a large amount of labor and is inefficient, combined with the planting requirements of breeding rape, a shovel-tooth end-effector was designed, and a shovel-tooth removal test bench was built. A simulation model based on MBD (Multibody Dynamics)-DEM (Discrete Element Method) coupling was constructed. Then we conducted a Box-Behnken test with four factors and three levels. Taking the angle of soil penetration, speed of soil penetration, depth of soil penetration and speed of shovel-tooth gathering as the test factors, the soil penetration force and shovel-tooth gathering force as the test indicators. The mathematical regression model between test indicators and test factor was established. After optimizing the parameters of the model, the best combination of parameters with low soil penetration force and low shovel-tooth gathering force was obtained: angle of soil penetration of 84°, speed of soil penetration of 9 cm/s, depth of soil penetration of 8cm, and speed of shovel-tooth gathering of 6 cm/s. The simulation model was validated by field experiments. The average soil penetration force and average shovel-tooth gathering force of the three groups of pull-out tests were 34.8 N and 763.0 N, respectively. The removal rates were 96%, 92%, and 94%, all greater than 90%, indicating that the removal effect of the shovel-tooth end-effector was good, and the parameters were reasonably designed. The results can serve as reference for the design of rape abnormal plants removal device and the operation of MBD-DEM coupling simulation end-effector.
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Easy-to-manufacture Li2S-P2S5 glass ceramics are the key to large-scale all-solid-state lithium batteries from an industrial point of view, while their commercialization is greatly hampered by the low room temperature Li+ conductivity, especially due to the lack of solutions. Herein, we propose a nanocrystallization strategy to fabricate super Li+-conductive glass ceramics. Through regulating the nucleation energy, the crystallites within glass ceramics can self-organize into hetero-nanodomains during the solid-state reaction. Cryogenic transmission electron microscope and electron holography directly demonstrate the numerous closely spaced grain boundaries with enriched charge carriers, which actuate superior Li+-conduction as confirmed by variable-temperature solid-state nuclear magnetic resonance. Glass ceramics with a record Li+ conductivity of 13.2 mS cm-1 are prepared. The high Li+ conductivity ensures stable operation of a 220 µm thick LiNi0.6Mn0.2Co0.2O2 composite cathode (8 mAh cm-2), with which the all-solid-state lithium battery reaches a high energy density of 420 Wh kg-1 by cell mass and 834 Wh L-1 by cell volume at room temperature. These findings bring about powerful new degrees of freedom for engineering super ionic conductors.
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All-solid-state lithium-metal batteries (ASLMBs) are considered to be remarkably promising energy storage devices owing to their high safety and energy density. However, the limitations of current solid electrolytes in oxidation stability and ion transport properties have emerged as fundamental barriers in practical applications. Herein, a novel solid electrolyte is presented by in situ polymerization of salt-concentrated poly(ethylene glycol) diglycidyl ether (PEGDE) implanted with a three-dimensional porous L10 GeP2 S12 skeleton to mitigate these issues. The poly(PEGDE) endows more oxygen atoms to coordinate with Li+ , significantly lowering its highest occupied molecular orbital level. As a consequence, the electro-oxidation resistance of poly(PEGDE) exceeds 4.7 V versus Li+ /Li. Simultaneously, the three-dimensonal porous L10 GeP2 S12 skeleton provides a percolated pathway for rapid Li+ migration, ensuring a sufficient ionic conductivity of 7.7 × 10-4 S cm-1 at room temperature. As the bottlenecks are well solved, 4.5 V LiNi0.8 Mn0.1 Co0.1 O2 -based ASLMBs present fantastic cycle performance over 200 cycles with an average Coulombic efficiency exceeding 99.6% at room temperature.
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Solid-state lithium battery promises highly safe electrochemical energy storage. Conductivity of solid electrolyte and compatibility of electrolyte/electrode interface are two keys to dominate the electrochemical performance of all solid-state battery. By in situ polymerizing poly(ethylene glycol) methyl ether acrylate within self-supported three-dimensional porous Li1.3Al0.3Ti1.7(PO4)3 framework, the as-assembled solid-state battery employing 4.5 V LiNi0.8Mn0.1Co0.1O2 cathode and Li metal anode demonstrates a high Coulombic efficiency exceeding 99% at room temperature. Solid-state nuclear magnetic resonance results reveal that Li+ migrates fast along the continuous Li1.3Al0.3Ti1.7(PO4)3 phase and Li1.3Al0.3Ti1.7(PO4)3/polymer interfacial phase to generate a fantastic conductivity of 2.0 × 10-4 S cm-1 at room temperature, which is 56 times higher than that of pristine poly(ethylene glycol) methyl ether acrylate. Meanwhile, the in situ polymerized poly(ethylene glycol) methyl ether acrylate can not only integrate the loose interfacial contact but also protect Li1.3Al0.3Ti1.7(PO4)3 from being reduced by lithium metal. As a consequence of the compatible solid-solid contact, the interfacial resistance decreases significantly by a factor of 40 times, resolving the notorious interfacial issue effectively. The integrated strategy proposed by this work can thereby guide both the preparation of highly conductive solid electrolyte and compatible interface design to boost practical high energy density all solid-state lithium metal battery.
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Solid-state lithium batteries have drawn wide attention to address the safety issues of power batteries. However, the development of solid-state lithium batteries is substantially limited by the poor electrochemical performances originating from the rigid interface between solid electrodes and solid-state electrolytes. In this work, a composite of poly(vinyl carbonate) and Li10SnP2S12 solid-state electrolyte is fabricated successfully via in situ polymerization to improve the rigid interface issues. The composite electrolyte presents a considerable room temperature conductivity of 0.2 mS cm-1, an electrochemical window exceeding 4.5 V, and a Li+ transport number of 0.6. It is demonstrated that solid-state lithium metal battery of LiFe0.2Mn0.8PO4 (LFMP)/composite electrolyte/Li can deliver a high capacity of 130 mA h g-1 with considerable capacity retention of 88% and Coulombic efficiency of exceeding 99% after 140 cycles at the rate of 0.5 C at room temperature. The superior electrochemical performance can be ascribed to the good compatibility of the composite electrolyte with Li metal and the integrated compatible interface between solid electrodes and the composite electrolyte engineered by in situ polymerization, which leads to a significant interfacial impedance decrease from 1292 to 213 Ω cm2 in solid-state Li-Li symmetrical cells. This work provides vital reference for improving the interface compatibility for room temperature solid-state lithium batteries.
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A highly selective ligand exchange reaction is realized in the self-assembled monolayer (SAM) of a triruthenium cluster on a gold electrode surface under precise electrochemical potential control. CO as well as NO molecules, which are known to play key roles in many chemical, biological, and environmental systems, can be efficiently introduced into the SAM by electrochemically tuning the electronic state of the Ru site. These unique surface reactions are more convenient and efficient than conventional ligand exchange reactions in solution and could be used for the elucidation of the electron-transfer mechanism in a biological system as well as in the development of molecular sensors and devices.