水泥干法窑尾烟气中二氧化硫测试方法比对研究

针对水泥干法窑尾排放烟气的特点,采用非分散紫外吸收法、定电位电解法与在线CEMS系统常用的非分散红外吸收法对烟气中SO2进行现场比对测试。测试结果表明,非分散紫外吸收法能够较好地避免烟气中CO对SO2监测的干扰,其测定结果与非分散红外吸收法测定结果差异较小,而定电位电解方法与非分散红外吸收法测定结果差异较大。非分散紫外吸收法适用于水泥干法窑尾高CO浓度条件下低浓度SO2的测试。     

低温冷冻靶微管燃料充注流动冷凝特性

低温冷冻靶是惯性约束核聚变装置的关键部件之一。冷冻靶靶丸位于黑腔内部,需要利用微管完成燃料充注。针对燃料在微管内发生气液相变后流入靶丸这一关键过程,研究了微通道流体与常规流体流动传热的差异。基于微通道特性对流体流动传热方程进行修正,同时建立了气液相变模型,对微充气管内燃料充注过程进行了数值计算分析。得到重力和表面张力的影响,在微通道中,重力作用可以忽略,表面张力起重要作用。得到了微尺度效应包括速度滑移和温度跳跃对流动传热过程的影响。对多种充气管结构进行比较分析,为选型提供指导。通过选择不同进口条件和出口条件,对充注量控制和充注条件选择提供了指导方案,实际充注时需要同时提高进口温度和压力,保证连续可控充注。     

Multicomponent Solar Cells with High Fill Factors and Efficiencies Based on Non-Fullerene Acceptor Isomers

Multicomponent organic solar cells (OSCs), such as the ternary and quaternary OSCs, not only inherit the simplicity of binary OSCs but further promote light harvesting and power conversion efficiency (PCE). Here, we propose a new type of multicomponent solar cells with non-fullerene acceptor isomers. Specifically, we fabricate OSCs with the polymer donor J71 and a mixture of isomers, ITCF, as the acceptors. In comparison, the ternary OSC devices with J71 and two structurally similar (not isomeric) NFAs (IT-DM and IT-4F) are made as control. The morphology experiments reveal that the isomers-containing blend film demonstrates increased crystallinity, more ideal domain size, and a more favorable packing orientation compared with the IT-DM/IT-4F ternary blend. The favorable orientation is correlated with the balanced charge transport, increased exciton dissociation and decreased bimolecular recombination in the ITCF-isomer-based blend film, which contributes to the high fill factor (FF), and thus the high PCE. Additionally, to evaluate the generality of this method, we examine other acceptor isomers including IT-M, IXIC-2Cl and SY1, which show same trend as the ITCF isomers. These results demonstrate that using isomeric blends as the acceptor can be a promising approach to promote the performance of multicomponent non-fullerene OSCs.     

Fractionation of Raw and Parboiled Rice Husks with Deep Eutectic Solvents and Characterization of the Extracted Lignins towards a Circular Economy Perspective

In the present work, rice husks (RHs), which, worldwide, represent one of the most abundant agricultural wastes in terms of their quantity, have been treated and fractionated in order to allow for their complete valorization. RHs coming from the raw and parboiled rice production have been submitted at first to a hydrothermal pretreatment followed by a deep eutectic solvent fractionation, allowing for the separation of the different components by means of an environmentally friendly process. The lignins obtained from raw and parboiled RHs have been thoroughly characterized and showed similar physico-chemical characteristics, indicating that the parboiling process does not introduce obvious lignin alterations. In addition, a preliminary evaluation of the potentiality of such lignin fractions as precursors of cement water reducers has provided encouraging results. A fermentation-based optional preprocess has also been investigated. However, both raw and parboiled RHs demonstrated a poor performance as a microbiological growth substrate, even in submerged fermentation using cellulose-degrading fungi. The described methodology appears to be a promising strategy for the valorization of these important waste biomasses coming from the rice industry towards a circular economy perspective.     

无排放加注的主要影响因素分析

无排放加注作为一项节能环保的技术,可以满足环境、能源、空间、安全等多方面的要求,日益受到重视。在整理分析国内外对无排放加注已得出的研究成果和已给出的代表性观点的基础上,着重论述了影响无排放加注的主要因素方面的研究成果。通过分析各主要影响因素及其影响规律和控制方法,可以为无排放加注的成熟运用提供参考。     

Determining the local coordination of aluminium in cement using electron energy loss near-edge structure

The local site symmetry of aluminium in Al-substituted calcium silicate hydrate phases, similar to those found in hardened Portland cement pastes, has been determined by experimental measurement and theoretical modelling of the electron energy loss near-edge structure associated with the aluminium K-edge measured using parallel electron energy loss spectroscopy in the transmission electron microscope. Changes in the local aluminium environment were observed between different regions of the microstructure which are explained in terms of aluminium substitution into both tetrahedral silicon and octahedral magnesium sites. This spatially-resolved information is in excellent agreement with²⁷Al and²⁹Si magic angle spinning nuclear magnetic resonance data on bulk samples as well as the predictions based upon compositional trends derived from the results of energy dispersive X-ray and electron energy loss elemental microanalysis. In a wider context we wish to stress the complementarity of both spatially-resolved and bulk spectroscopic techniques, which possess differing degrees of sensitivity, in the analysis of materials science samples.     

Shear Bond Strength and Film Thickness of a Naturally Antimicrobial Modified Dental Luting Cement

Although several natural plants and mixtures have been known and used over the centuries for their antibacterial activity, few have been thoroughly explored in the field of dentistry. Thus, the aim of this study was to enhance the antimicrobial activity of a conventional glass ionomer cement (GIC) with natural plant extracts. The effect of this alteration on the bond strength and film thickness of glass ionomer cement was evaluated and related to an 0.5% chlorohexidine modified GIC. Olive leaves (Olea europaea), Fig tree (Ficus carica), and the leaves and roots of Miswak (Salvadora persica) were used to prepare an alcoholic extract mixture. The prepared extract mixture after the evaporation of the solvent was used to modify a freeze-dried glass ionomer cement at three different extracts: water mass ratios 1:2, 1:1, and 2:1. An 0.5% chlorhexidine diacetate powder was added to a conventional GIC for the preparation of a positive control group (CHX-GIC) for comparison. The bond strength to dentine was assessed using a material-testing machine at a cross head speed of 0.5 mm/min. Failure mode was analyzed using a stereomicroscope at 12× magnification. The cement film thickness was evaluated in accordance with ISO standard 9917-1. The minimum number of samples in each group was n = 10. Statistical analysis was performed using a Kruskal–Wallis test followed by Dunn’s post hoc test for pairwise comparison. There was a statistically insignificant difference between the median shear bond strength (p = 0.046) of the control group (M = 3.4 MPa), and each of the CHX-GIC (M = 1.7 MPa), and the three plant modified groups of 1:2, 1:1, 2:1 (M = 5.1, 3.2, and 4.3 MPa, respectively). The CHX-GIC group showed statistically significant lower median values compared to the three plant-modified groups. Mixed and cohesive failure modes were predominant among all the tested groups. All the tested groups (p < 0.001) met the ISO standard of having less than 25 µm film thickness, with the 2:1 group (M = 24 µm) being statistically the highest among all the other groups. The plant extracts did not alter either the shear bond strength or the film thickness of the GIC and thus might represent a promising additive to GICs.     

The Crystal Structures of two Anhydrous Magnesium Hydroxychloride Phases from in situ Synchrotron Powder Diffraction Data

The crystal structures of two members of the solid solution series Mg(OH)_xCl_y x+y = 2, Mg(OH)_1.7Cl_0.3 (P$\tilde {3}$ m1, a = 3.169(2) Å, c = 5.530(12), V = 48.1(1) ų at T = 365 °C) and MgOHCl (R$\tilde {3}$ m, a = 3.3877(4) Å, c = 17.534(4) Å, V = 174.27(6) ų at T = 625 °C) were determined from in situ synchrotron powder diffraction data at high temperature upon dehydration of 3Mg(OH)₂·MgCl₂·8H₂O (F3) and 5Mg(OH)₂·MgCl₂·8H₂O (F5) phases. The crystal structures of Mg(OH)_1.7Cl_0.3 (example of ss‐type‐OH) and MgOHCl (example of ss‐type‐Cl) can be related to the C19 (CdCl₂) and C6 (CdI₂) structure type, respectively, with the disordered chloride and hydroxide anions occupying the same crystallographic site in layers.     

First seconds in a building's life-in situ synchrotron X-ray diffraction study of cement hydration on the millisecond timescale

Setting cement: highly dynamic hydration processes that occur during the first seconds of cement hydration were studied by time-resolved synchrotron X-ray diffraction. Polycarboxylate ether additives were found to influence the formation of the initial crystalline hydration products on a molecular level.     

Optimisation of hardness and setting time of dental zinc phosphate cement using a design of experiments

The main objective of this study is to demonstrate the application of strategy of an experiment design to optimize the compressive strength and setting time of zinc phosphate cement used in the dental application. For this work, the extreme vertices design was chosen. Its factors are components of the mixture forming a ternary system: zinc oxide, aluminum phosphate and orthophosphoric acid (ZnO–AlPO₄–H₃PO₄). The local region of dental cement – in simplex space- explored and limited by upper and lower limits of the three components of the mixture. The optimization of each response and then all together by graphical methods allowed us to obtain the adequate cement.