中风化花岗岩中嵌岩桩承载性能原位试验与极限承载力预测

为深入探究中风化花岗岩中嵌岩桩的竖向抗压承载特性,对12根嵌岩桩进行了单桩竖向抗压静载原位试验与ABAQUS有限元数值模拟,通过多种方法对嵌岩单桩极限承载力进行评价,明确中风化花岗岩中嵌岩桩竖向抗压承载性状。研究表明:12根中风化花岗岩中嵌岩桩并非表现出完全端承桩,而是呈摩擦型桩或摩擦端承桩的性状;中风化花岗岩地基中的嵌岩桩竖向抗压极限承载力较高,桩顶沉降小,满足工程对基础的承载要求;有限元模拟荷载-沉降曲线与实测荷载-沉降曲线走势吻合度较高,桩顶沉降误差较小;本试验条件下,桩端阻力占桩顶荷载的56.9%,桩侧摩阻力占比为43.1%,桩侧摩阻力在荷载传递过程中发挥较充分;有限元模拟得到的单桩极限承载力与指数函数模型的预测结果较为吻合,可用于嵌岩桩单桩竖向抗压极限承载力的预测,以及嵌岩桩承载性状和荷载传递规律的分析。     

Characteristic strength and acoustic emission properties of weakly cemented sandstone at different depths under uniaxial compression

As coal mining is extended from shallow to deep areas along the western coalfield,it is of great significance to study weakly cemented sandstone at different de...     

Recent Advances in Porphyrin-Based Systems for Electrochemical Oxygen Evolution Reaction

Oxygen evolution reaction (OER) plays a pivotal role in the development of renewable energy methods, such as water-splitting devices and the use of Zn–air batteries. First-row transition metal complexes are promising catalyst candidates due to their excellent electrocatalytic performance, rich abundance, and cheap price. Metalloporphyrins are a class of representative high-efficiency complex catalysts owing to their structural and functional characteristics. However, OER based on porphyrin systems previously have been paid little attention in comparison to the well-described oxygen reduction reaction (ORR), hydrogen evolution reaction, and CO₂ reduction reaction. Recently, porphyrin-based systems, including both small molecules and porous polymers for electrochemical OER, are emerging. Accordingly, this review summarizes the recent advances of porphyrin-based systems for electrochemical OER. Firstly, the electrochemical OER for water oxidation is discussed, which shows various methodologies to achieve catalysis from homogeneous to heterogeneous processes. Subsequently, the porphyrin-based catalytic systems for bifunctional oxygen electrocatalysis including both OER and ORR are demonstrated. Finally, the future development of porphyrin-based catalytic systems for electrochemical OER is briefly prospected.     

Neurotoxicity of Chronic Co-Exposure of Lead and Ionic Liquid in Common Carp: Synergistic or Antagonistic?

Previous studies have indicated that the harmful heavy metal lead (Pb) contamination in aquatic systems has caused intelligence development disorders and nervous system function abnormalities in juveniles due to the increased permeability of the blood–brain barrier. Ionic liquids (ILs) are considered “green” organic solvents that can replace traditional organic solvents. Studies have found the presence of ILs in soil and water due to chemical applications or unintentional leakage. Therefore, what would happen if Pb interacted with ILs in a body of water? Could ILs enable Pb to more easily cross the blood–brain barrier? Therefore, we examined the combined exposure of Pb and ILs in common carp at low concentration (18.3 mg L⁻¹ of Pb(CH₃COO)₂•3 H₂O and 11 mg L⁻¹ of the IL 1-methyl-3-octylimidazolium chloride, 5% of their LC₅₀) for 28 days in the present study. The result of a neurobehavioral assay showed that chronic exposure of lead at lower concentrations significantly altered fish movement and neurobehaviors, indicating that lead exposure caused neurotoxicity in the carp. Increases in the neurotransmitter dopamine levels and injuries in the fish brain accounted for neurobehavioral abnormalities induced by lead exposure. Moreover, we also found that lead could easily cross the blood–brain barrier and caused significant bioaccumulation in the brain. Particularly, our study indicated that the ionic liquid could not synergistically promote blood–brain barrier permeability and hence failed to increase the absorption of lead in the fish brain, suggesting that the combined exposure of lead and ILs was not a synergistic effect but antagonism to the neurotoxicity. The results of this study suggested that ILs could recede the Pb induced neurotoxicity in fish.     

A Multifunctional and Fast-Response Lysosome-Targetable Fluorescent Probe for Monitoring pH and Isoxaflutole

A new chemosensor, namely N-(2-morpholinoethyl)acetamide-4-morpholine-1,8-naphthimide (MMN), was designed and synthesized through an amidation reaction. MMN was fabricated as a multifunctional fluorescent probe for monitoring pH and isoxaflutole. MMN exhibited excellent stability in MeCN/H₂O (v/v, 9/1), with an obvious “off–on” fluorescence response toward pH changes due to intramolecular charge transfer (ICT), where the linear response ranges of MMN in the weakly acidic system were from 4.2 to 5.0 and from 5.0 to 6.0 with apparent pK_a = 4.62 ± 0.02 and 5.43 ± 0.02. Based on morpholine as the lysosome targetable unit, MMN could selectively locate lysosomes in live cells. MMN also successfully detected the presence of H⁺ in test papers. Finally, MMN could specifically recognize isoxaflutole at a detection limit of 0.88 μM. A possible sensing mechanism was identified based on density function theory calculations. These results indicate that MMN could be a superior potential chemosensor for detecting pH and isoxaflutole selectively and sensitively and could be used in real sample detection.