Efficient removal of As(V) from simulated arsenic-contaminated wastewater via a novel metal–organic framework material: Synthesis,structure, and response surface methodology

A novel metal–organic framework material {[N(C₂H₅)₃][Zn₂(ptmda)₂(μ₂-H₂O)]·(H₂O)_0.5}_n { GUT-3 ; H₂ptmda is 4,4′-([p-tolylazanediyl]bis [methylene])dibenzoic acid} was successfully synthesized using the hydrothermal method and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. GUT-3 has a two-dimensional network based on dinuclear [Zn₂(ptmda)₂(μ₂-H₂O)]⁻ building units which formed an eightfold interpenetration network in GUT-3 molecules. Hirshfeld surface analysis revealed that H–H, C–H, and O–H bonds accounted for the majority of intermolecular interactions. Moreover, the interactions between GUT-3 and As(V) – the form of As(V) is AsO₄³⁻ – were analyzed in aqueous solutions in a batch system to study the effect of pH, concentration, adsorbent dose, adsorption time, adsorption temperature, and shaking speed. The kinetic and isotherm data of arsenic adsorption on GUT-3 were accurately modeled by pseudo-second-order, Langmuir (q_m = 33.91 mg/g), and Freundlich models. The Box–Behnken response surface method was used to optimize the adsorption conditions of As(V) from the simulated arsenic-contaminated wastewater. The effect of various experimental parameters and optimal experimental conditions was ascertained using the quadratic model.     

Insights into the Control of Optoelectronic Properties in Mixed-Stacking Charge-Transfer Complexes

Although cocrystallization has provided a promising platform to develop new organic optoelectronic materials, it is still a big challenge to purposely design and achieve specific optoelectronic properties. Herein, a series of mixed-stacking cocrystals (TMFA, TMCA, and TMTQ) were designed and synthesized, and the regulatory effects of the acceptors on the co-assembly behavior, charge-transfer nature, energy-level structures, and optoelectronic characteristics were systematically investigated. The results demonstrate that it is feasible to achieve effective charge-transport tuning and photoresponse switching by carefully regulating the intermolecular charge transfer and energy orbitals. The inherent mechanisms underlying the change in these optoelectronic behaviors were analyzed in depth and elucidated to provide clear guidelines for future development of new optoelectronic materials. In addition, due to the excellent photoresponsive characteristics of TMCA, TMCA-based phototransistors were investigated with varying light wavelength and optical power, and TMCA shows the best performance among all reported cocrystals under UV illumination.     

Co-hydrolysis and Seed-Induced Synthesis of Basic Mesoporous ZSM-5 Zeolites with Enhanced Catalytic Performance

For zeolite catalysts, the regulation of active site and pore structure plays an important role in the enhancement of their catalytic performance. In this work, a one-pot and organic template-free co-regulation route is proposed to straightforwardly synthesize basic mesoporous ZSM-5 zeolites with adjustable alkaline-earth metal species. The synthesis pathway combines two decisive strategies: 1) the seed-induced interface assembly growth method and 2) the acidic co-hydrolysis/condensation of aluminosilicate species and alkaline-earth metal (e.g., Mg, Ca, Sr, or Ba) sources. It is interesting that the mesoporous structure was self-evolved through particle-attached seed-interfacial crystallization without the assistance of any template. Meanwhile, the incorporation of alkaline-earth metals species is homogeneous and highly dispersed in the solid products during the whole crystallization process, and finally generate the superior basicity. Catalysis tests of the as-synthesized samples displayed their novel performance in the typical base reaction of Knoevenagel condensation, even for bulky substrates owing to the enhanced diffusion arising from the meso/microporous network. This finding opens new possibilities for facile, cost-effective, and environmentally friendly synthesis of mesoporous high-silica zeolites with tunable acid/base properties, and deepens our understanding of the particle-attached crystallization.     

A Robust Mixed-Lanthanide PolyMOF Membrane for Ratiometric Temperature Sensing

Temperature sensors play a significant role in biology, chemistry, and engineering, especially those that can work accurately in a noninvasive manner. We adopted a photoinduced post-synthetic copolymerization strategy to realize a membranous ratiometric luminescent thermometer based on the emissions of two lanthanide ions. This novel mixed-lanthanide polyMOF membrane exhibits not only the integrity and temperature sensing behaviour of the Ln-MOF powder but also excellent mechanical properties, such as flexibility, elasticity, and processability. Moreover, the polyMOF membrane shows remarkable stability under harsh conditions, including high humidity, strong acid and alkali (pH 0–14), which allowed the mapping of temperature distributions in extreme circumstances. This work highlights a simple strategy for polyMOF membrane formation and pushes forward the further practical application of Ln-MOF-based luminescent thermometers in various fields and conditions.     

A five-component one-pot synthesis of phosphatidylinositol pentamannoside (PIM5)

A practical and efficient synthesis of phosphatidylinositol pentam annoside (PIM₅) was achieved based on a five-component one-pot sequential glycosylation protocol with exclusive regio- and stereo-selectivity.     

Superhydrophobic surfaces fabricated by microstructuring of stainless steel using a femtosecond laser

Fabrication of superhydrophobic surfaces induced by femtosecond laser is a research hotspot of superhydrophobic surface studies nowadays. We present a simple and easily-controlled method for fabricating stainless steel-based superhydrophobic surfaces. The method consists of microstructuring stainless steel surfaces by irradiating samples with femtosecond laser pulses and silanizing the surfaces. By low laser fluence, we fabricated typical laser-induced periodic surface structures (LIPSS) on the submicron level. The apparent contact angle (CA) on the surface is 150.3°. With laser fluence increasing, we fabricated periodic ripples and periodic cone-shaped spikes on the micron scale, both covered with LIPSS. The stainless steel-based surfaces with micro- and submicron double-scale structure have higher apparent CAs. On the surface of double-scale structure, the maximal apparent CA is 166.3° and at the same time, the sliding angle (SA) is 4.2°.     

强激光加载铝材料动态损伤特性及其微介观结构观测

在神光-Ⅱ装置上利用强激光加载铝材料进行高应变率（高于106 s-1）层裂实验,研究不同初始温度下高纯铝材料的动态损伤特性。采用任意反射面速度干涉仪测量样品自由面速度剖面,由自由面速度剖面计算纯铝样品层裂强度与屈服应力。结果表明:随着温度升高,材料层裂强度减小,屈服应力增大。对激光加载前后样品进行金相分析,观察不同初始温度下纯铝材料的微介观结构变化及其损伤特性。结果表明：随着温度升高,样品晶粒尺度缓慢增大,但在873 K（近熔点）时晶粒尺度急剧增加;层裂面附近小孔洞数目较多,孔洞尺寸也较大,而远离层裂面处,孔洞数目相对较少,且尺寸也较小;材料的断裂方式随温度升高由沿晶断裂为主逐渐变为穿晶断裂为主。     

Pivoting in Extended Rings for Computing Approximate Gr?bner Bases

It is well known that in the computation of Gr?bner bases arbitrarily small perturbations in the coefficients of polynomials may lead to a completely different staircase, even if the solutions of the polynomial system change continuously. This phenomenon is called artificial discontinuity in Kondratyev’s Ph.D. thesis. We show how such phenomenon may be detected and even “repaired” by using a new variable to rename the leading term each time we detect a “problem”. We call such strategy the TSV (Term Substitutions with Variables) strategy. For a zero-dimensional polynomial ideal, any monomial basis (containing 1) of the quotient ring can be found with the TSV strategy. Hence we can use TSV strategy to relax term order while keeping the framework of Gr?bner basis method so that we can use existing efficient algorithms (for instance the F ₅ algorithm) to compute an approximate Gr?bner basis. Our main algorithms, named TSVn and TSVh, can be used to repair artificial e{\epsilon}-discontinuities. Experiments show that these algorithms are effective for some nontrivial problems.