Effect of plasma-activated water and buffer solution combined with ultrasound on fungicide degradation and quality of cherry tomato during storage

The purpose of this study was to examine plasma-activated buffer solution (PABS) and plasma-activated water (PAW) combined with ultrasonication (U) treatment on the reduction of chlorothalonil fungicide and the quality of tomato fruits during storage. To obtain PAW and PABS, an atmospheric air plasma jet was used to treat buffer solution and deionized water at different treatment times (5 and 10 min). For combined treatments, fruits were submerged in PAW and PABS, then sonicated for 15 min, and individual treatment without sonication. As per the results, the maximum chlorothalonil reduction of 89.29% was detected in PAW-U₁₀, followed by 85.43% in PABS. At the end of the storage period, the maximum reduction of 97.25% was recorded in PAW-U₁₀, followed by 93.14% in PABS-U₁₀. PAW, PABS, and both combined with ultrasound did not significantly affect the overall tomato fruit quality in the storage period. Our results revealed that PAW combined with sonication had a significant impact on post-harvest agrochemical degradation and retention of tomato quality than PABS. Conclusively, the integrated hurdle technologies effectively reduce agrochemical residues, which helps to lower health hazards and foodborne illnesses.     

DYNAMIC SIMULATION ANALYSIS OF CAPTURE AND BUFFER SYSTEM BASED ON CLAW-TYPE DOCKING MECHANISM

现有在轨服务的对接机构由于其尺寸大、结构复杂、对接目标单一等局限性因素,无法很好地为后续我国探月工程任务提供有力支撑,且受限于运载能力,对接机构的轻量化也是必不可少的一项环节.为研究可服务于未来月球空间站以及载人登月等高轨道任务的对接机构,设计了一种新型抱爪式对接机构,其采用异体同构周边式构型,可以实现主/被动飞行器之间的互换.利用 V 型槽与爪钩等结构部件实现飞行器对接过程中的捕获以 及能量消耗功能,从而实现两飞行器之间的稳固联接.该对接机构具备尺寸小、重量轻、结构简单、功能易实现等优势. 对其捕获缓冲系统进行了动力学分析,计算了缓冲元器件的参数对其捕获性能的影响,在 ADAMS 完成了数字虚拟样机的建立,结合实际两种典型的对接初始条件工况进行了仿真研究.研究结果表明,两种工况下的对接过程能量消耗满足设计要求,能够以较小的 V 型槽的碰撞力完成捕获,结果证明了捕获缓冲系统的可行性以及该构型对接机构具备较好实现任务的能力.     

高g值冲击下存储测试电路模块缓冲保护研究

为了采用弹载存储测试技术记录弹体高速侵彻硬目标过程中的加速度—时间曲线,必须对存储测试电路模块进行缓冲保护。本文利用非线性缓冲理论、技术,选择较理想的缓冲材料,设计出缓冲器件-泡沫铝试件,进行了静态压缩,得到应力-应变曲线,采用LS-DYNA模拟了空气炮冲击实验中泡沫铝试件的缓冲效果,并对应用于某型号弹侵彻混凝土靶的存储测试电路模块进行了缓冲保护,提高了数据的捕获率和电路模块的重复使用次数。通过试验证明了所设计缓冲器件对电路模块具有保护效果。     

Interactions of DNA with graphene and sensing applications of graphene field-effect transistor devices: A review

Graphene field-effect transistors (GFET) have emerged as powerful detection platforms enabled by the advent of chemical vapor deposition (CVD) production of the unique atomically thin 2D material on a large scale. DNA aptamers, short target-specific oligonucleotides, are excellent sensor moieties for GFETs due to their strong affinity to graphene, relatively short chain-length, selectivity, and a high degree of analyte variability. However, the interaction between DNA and graphene is not fully understood, leading to questions about the structure of surface-bound DNA, including the morphology of DNA nanostructures and the nature of the electronic response seen from analyte binding. This review critically evaluates recent insights into the nature of the DNA graphene interaction and its affect on sensor viability for DNA, small molecules, and proteins with respect to previously established sensing methods. We first discuss the sorption of DNA to graphene to introduce the interactions and forces acting in DNA based GFET devices and how these forces can potentially affect the performance of increasingly popular DNA aptamers and even future DNA nanostructures as sensor substrates. Next, we discuss the novel use of GFETs to detect DNA and the underlying electronic phenomena that are typically used as benchmarks for characterizing the analyte response of these devices. Finally, we address the use of DNA aptamers to increase the selectivity of GFET sensors for small molecules and proteins and compare them with other, state of the art, detection methods.     

Caffeine and glucosamine mobility shifts by adduction with 2‐butanol depended on interaction energy,charge delocalization,and steric hindrance in ion mobility spectrometry

Ion mobility spectrometry (IMS) is an analytical technique that separates gas‐phase ions drifting under an electric field according to their size to charge ratio. We used electrospray ionization‐drift tube IMS coupled to quadrupole mass spectrometry to measure the mobilities of glucosamine (GH⁺) and caffeine (CH⁺) ions in pure nitrogen or when the shift reagent (SR) 2‐butanol was introduced in the drift gas at 6.9 mmol m⁻³. Binding energies of 2‐butanol‐ion adducts were calculated using Gaussian 09 at the CAMB3LYP/6‐311++G(d,p) level of theory. The mobility shifts with the introduction of 2‐butanol in the drift gas were −2.4% (GH⁺) and −1.7% (CH⁺) and were due to clustering of GH⁺ and CH⁺ with 2‐butanol. The formation of GBH⁺ was favored over that of CBH⁺ because GBH⁺ formed more stable hydrogen bonds (83.3 kJ/mol) than CBH⁺ (81.7 kJ/mol) for the reason that the positive charge on CH⁺ is less sterically available than on GH⁺ and the charge is stabilized by resonance in CH⁺. These results are a confirmation of the arguments used to explain the drift behavior of these ions when ethyl lactate SR was used (Bull Kor Chem Soc 2014, 1023–1028). This study is a step forward to predict IMS separations of overlapping peaks in IMS spectra, simplifying a procedure that is trial and error by now.     

仪器车减震台的设计优化

本文介绍一种以塑性变形减震概念设计的用于地下爆炸地表层裂区内的仪器车减震台。文中叙述了设计的原理和计算方法。通过同普通的由弹簧和阻尼器构成的减震台的计算对比,说明这种以塑性变形减震概念设计的减震台具有许多优点。对减震台做了吊高达1.5m的落地冲击实验,其结果同计算一致。     

基于CPCI总线的雷达数据采集与控制系统显控软件设计

CPCI总线作为PCI总线的加固版本,目前已成为计算机上流行的高速外设接口总线。在工业自动化领域,进行数据采集和控制基本上也都是通过这一成熟技术来实现的。本文简要介绍该测量雷达和数据采集与控制系统的基本结构,以及CPCI总线标准,重点分析显控软件的功能需求,采用自顶向下的设计,并在VC环境下基于MFC架构利用多线程和双缓存技术以及多种ActiveX控件进行显控软件设计。实现了对测量雷达的控制以及对雷达回波的原始数据的实时存取和绘制。     

Absolute quantification of superoxide dismutase in cytosol and mitochondria of mice hepatic cells exposed to mercury by a novel metallomic approach

In the last years, the development of new methods for analyzing accurate and precise individual metalloproteins is of increasing importance, since numerous metalloproteins are excellent biomarkers of oxidative stress and diseases. In that way, methods based on the use of post column isotopic dilution analysis (IDA) or enriched protein standards are required to obtain a sufficient degree of accuracy, precision and high limits of detection. This paper reports the identification and absolute quantification of Cu,Zn-superoxide dismutase (Cu,Zn-SOD) in cytosol and mitochondria from mice hepatic cells using a innovative column switching analytical approach. The method consisted of orthogonal chromatographic systems coupled to inductively coupling plasma-mass spectrometry equipped with a octopole reaction systems (ICP-ORS-MS) and UV detectors: size exclusion fractionation (SEC) of the cytosolic and mitochondrial extracts followed by online anion exchange chromatographic (AEC) separation of Cu/Zn containing species. After purification, Cu,Zn-SOD was identified after tryptic digestion by molecular mass spectrometry (MS). The MS/MS spectrum of a doubly charged peptide was used to obtain the sequence of the protein using the MASCOT searching engine. This optimized methodology reduces the time of analysis and avoids the use of sample preconcentration and clean-up procedures, such as cut-off centrifuged filters, solid phase extraction (SPE), precipitation procedures, off-line fractions insolates, etc. In this sense, the method is robust, reliable and fast with typical chromatographic run time less than 20 min. Precision in terms of relative standard deviation (n = 5) is of 3–5% and detection limits is 0.21 ng Cu g⁻¹.     

Analysis of oligonucleotides by hydrophilic interaction liquid chromatography coupled to negative ion electrospray ionization mass spectrometry

Hydrophilic interaction liquid chromatography (HILIC) is here successfully coupled to negative-ion electrospray ionization time-of-flight mass spectrometry (ESI-TOFMS) for the analysis of synthetic and chemically modified oligonucleotides. Separation was performed on a 2.1 mm × 100 mm PEEK ZIC^® HILIC column packed with hydrophilic stationary phase with a permanent zwitterionic functional group and a particle size of 3.5 μm with an average pore diameter of 200 Å. A method was developed to separate homogeneous and heterogeneous oligonucleotides as well as methylated oligonucleotides using a quaternary pumping system containing ammonium acetate and water with an acetonitrile gradient. Analyses of oligonucleotides were performed by LC/MS with a detection limit of 2.5 picomole (20 mer) with signal to noise ratio (S/N) of 4.12. The influence of the eluent composition, type of buffer and its concentration, and organic modifier were also evaluated. The HILIC LC/MS method presented in this paper used common, ‘MS friendly’, mobile phases achieving sensitive and selective oligonucleotide analysis.