Synthesis of highly luminescent carbon dots from postconsumer waste silk cloth and investigation of its electron transfer dynamics with methyl viologen dichloride

Synthesis of luminescent carbon dots (CDs) from biological waste materials is gaining more attention in the present-day scenario. We have synthesized highly luminescent (luminescence quantum yield, φ ​= ​19.1%), water-soluble CDs from a postconsumer waste silk cloth via a facile hydrothermal synthetic method. The resulting CDs are characterized and their photophysical properties are studied in detail. The electron transfer dynamics of CDs in presence of methyl viologen dichloride hydrate (MV²⁺) is systematically investigated in this work. Knowledge of the electron transfer dynamics of CDs is essential in the structural elucidation of CDs, prediction of sensing mechanisms and utilizing the CDs in energy storage devices.     

Quantification of the bisphosphonate alendronate using capillary electrophoresis mass spectrometry with dynamic pH barrage junction focusing

A quantitative method was developed for the direct identity confirmation and quantification of alendronate using CE-MS combined with a pH-assisted focusing technique, dynamic pH barrage junction focusing. A pH-induced variation in electrophoretic mobility led to online focusing of alendronate at the sample/pH barrage boundary, significantly improving the detection sensitivity. In addition, the use of a flow-through microvial CE electrospray interface and the multiple reaction monitoring mode of MS further improved the specificity and quantification capability of this technology. This quantitative method presented a wide linear dynamic range over 8–2000 ng/mL and an LOD of 2 ng/mL. A 460-fold improvement in sensitivity was obtained when pH barrage junction focusing was applied during the CE process, in comparison to when normal CE was conducted without online sample stacking. The superior detection sensitivity over previously reported methods enables direct analysis of bisphosphonate compounds, eliminating tedious pre-column sample enrichment and derivatization. Validation of alendronate content in a commercial drug tablet further proved the reliability and power of this method. This simple method with no sample derivatization, superior sensitivity, and short run time (<8 min) is a promising alternative for accurate quantification of alendronate and other types of bisphosphonate compounds in both drug formulations and plasma samples.     

Differentiating bulk nanobubbles from nanodroplets and nanoparticles

History has shown that it is not as easy as one might think to differentiate between bulk nanobubbles and nanodroplets or nanoparticles. It is generally easy to detect colloids (i.e. something that looks different, e.g. scatters light differently than its surrounding solvent), but less easy to determine the nature of these colloids. This has led to misinterpretations in the literature, where nanodroplets or nanoparticles have mistakenly been assumed to be nanobubbles. In this paper, we review a multitude of experimental methods and approaches to prove the existence of bulk nanobubbles. We conclude that combinations of optical detection with physical perturbations such as pressure or ultrasound, or phase-sensitive holographic methods are the most promising and convenient approaches.     

“Solid-Liquid” Vitrimers Based on Dynamic Boronic Ester Networks

The "solid-liquid" behavior of vitrimers have not been systematically investigated. Herein, a series of "solid-liquid" vitrimers bearing varying contents of dynamic boronic ester bonds were synthesized via thiol-ene click reactions. These vitrimers allow for flexibile modulation of their network structures and thus show a range of intriguing properties including high stretchability, flexible transition from elasticity to plasticity, strong strain rate dependence, and solid-liquid performance. The dynamic association rate of boronic ester bonds within these vitrimers could be apparently accelerated via increasing the content of boronic ester, which could be used to shape-program the flat vitrimer films into various complex 3 D structures just with external force. Materials with such versatile dynamic behavior may open up a range of new applications.     

Chronological protein synthesis in regenerating rat liver

Liver regeneration has been studied for decades; however, its regulation remains unclear. In this study, we report a dynamic tracing of protein synthesis in rat regenerating liver with a new proteomic technique, ³⁵S in vivo labeling analysis for dynamic proteomics (SiLAD). Conventional proteomic techniques typically measure protein alteration in accumulated amounts. The SiLAD technique specifically detects protein synthesis velocity instead of accumulated amounts of protein through ³⁵S pulse labeling of newly synthesized proteins, providing a direct way for analyzing protein synthesis variations. Consequently, protein synthesis within short as 30 min was visualized and protein regulations in the first 8 h of regenerating liver were dynamically traced. Further, the 3.5–5 h post partial hepatectomy (PHx) was shown to be an important regulatory turning point by acute regulation of many proteins in the initiation of liver regeneration.     

Cure monitoring of CFRP composites by dynamic mechanical analyser

The cure characteristics of carbon/MTM44-1 epoxy composite prepreg and neat MTM44-1 epoxy resin are monitored using a dynamic mechanical analyser (DMA). This study also assesses whether the simple containment device recommended by the DMA manufacturer for powder and gel is suitable for prepregs. The device is a disposable 0.1-mm thick stainless steel pocket. The cure behaviour of the packaged materials is compared with that of the unpackaged prepreg. All the samples are cured following the manufacturer's 180°C-isothermal schedule with heating rates of 2 °C/min and 5 °C/min. The tests highlight that: (i) the cure of composite prepregs and resin can be monitored using a DMA; (ii) the stainless steel pocket does not influence the cure of the prepreg and resin; and (iii) the softening and melting of the uncured resin, the resin low viscosity state and the subsequent gelation-vitrification-solidification of the resin are detected with this method.     

利用基于Gouy-Chapman模型的离子有效电荷定量表征离子特异性效应

离子特异性效应在固-液界面反应中是普遍存在的. 近期研究指出, 在较低电解质浓度的某些体系中, 离子特异性效应可能并非来源于色散力、经典诱导力、离子半径或水合半径的大小等, 而是界面附近强电场中的离子极化作用. 这种作用可使界面附近的吸附态反号离子被强烈极化(高达经典极化的10⁴倍). 强烈极化的结果将导致离子在界面附近受到的库仑力远远超过离子电荷所能产生的库仑力, 这体现在离子的有效电荷将远大于离子的实际电荷. 因此胶体体系中基于这种强极化的离子有效电荷可以用来定量表征离子特异性效应的强度. 本研究在蒙脱石-胡敏酸混合悬液凝聚过程中发现了Na⁺、K⁺、Ca²⁺、Cu²⁺四种离子的离子特异性效应, 提出了基于激光散射技术测定离子有效电荷的方法, 并成功获得了被强烈极化后的离子有效电荷数值. 实验测得的Na⁺、K⁺、Ca²⁺、Cu²⁺四种离子的有效电荷值分别为: Z_{Na(effective)}=1.46, Z_K(effective)=1.86, Z_{Ca(effective)}=3.92, Z_{Cu(effective)}=6.48.该结果表明: (1) 离子在强电场中的极化将大大提高离子的有效电荷, 从而极大地增强离子所受的库仑作用力;(2) 离子的电子层数越多, 离子极化越强烈, 离子的有效电荷增加越多.     

静态法和动态法测量乙醇饱和蒸气压的比较

物质的蒸气压是化学、化工、冶金、医药等领域的重要基础数据。测量饱和蒸气压是大学物理化学实验教学中的一个基础实验,测量方法主要有静态法和动态法,但两种方法的比较尚未见报道。本文通过比较,得出了两种方法的优缺点以及注意事项。     

Dynamic compressive strength properties of aluminium foams. Part I—experimental data and observations

This study of the dynamic compressive strength properties of metal foams is in two parts. Part I presents data from an extensive experimental study of closed-cell Hydro/Cymat aluminium foam, which elucidates a number of key issues and phenomena. Part II focuses on modelling issues.The dynamic compressive response of the foam was investigated using a direct-impact technique for a range of velocities from 10 to . Elastic wave dispersion and attenuation in the pressure bar was corrected using a deconvolution technique.A new method of locating the point of densification in the nominal stress-strain curves of the foam is proposed, which provides a consistent framework for the definition of the plateau stress and the densification strain, both essential parameters of the ‘shock’ model in Part II. Data for the uniaxial, plastic collapse and plateau stresses are presented for two different average cell sizes of approximately 4 and 14 mm. They show that the plastic collapse strength of the foam changes significantly with compression rate. This phenomenon is discussed, and the distinctive roles of microinertia and ‘shock’ formation are described. The effects of compression rates on the initiation, development and distribution of cell crushing are also examined. Tests were carried out to examine the effects of density gradient and specimen gauge length at different rates of compression and the results are discussed. The origin of the conflicting conclusions in the literature on the correlation between nominal strain rate (ratio of the impact velocity V_i to the initial gauge length l_o of the specimen) and the dynamic strength of aluminium alloy foams is identified and explained.     

具有弹性支座杆件的动力稳定性研究

研究了杆件具有弹性支座时直杆的动力稳定性问题，推导出了杆件的临界频率和动力不稳定边界，分析了弹簧刚度和阻尼对杆件动力稳定性的影响，研究表明杆件的侧向刚度愈大其结构的动力稳定性愈好，阻尼对杆的振动起有利作用，并提出了在实际工程中减小杆件振动的一些措施．