Condition monitoring of a single-stage gearbox with artificially induced gear cracks utilizing on-line vibration and acoustic emission measurements

The condition monitoring of a lab-scale, single stage, gearbox using different non-destructive inspection methodologies and the processing of the acquired waveforms with advanced signal processing techniques is the aim of the present work. Acoustic emission (AE) and vibration measurements were utilized for this purpose. The experimental setup and the instrumentation of each monitoring methodology are presented in detail. Emphasis is given on the signal processing of the acquired vibration and acoustic emission signals in order to extract conventional as well as novel parameters-features of potential diagnostic value from the monitored waveforms. Innovative wavelet-based parameters-features are proposed utilizing the discrete wavelet transform. The evolution of selected parameters/features versus test time is provided, evaluated and the parameters with the most interesting diagnostic behaviour are highlighted. The differences in the parameters evolution of each NDT technique are discussed and the superiority of AE over vibration recordings for the early diagnosis of natural wear in gear systems is concluded.     

强电场电离放电产生羟基等离子体反应过程的研究

从强电场等离子体反应室结构、电介质材料及加工工艺等方面出发．研究了在建立强电场并把O2、H2O电离后在分子层次上加工成OH^ 、eaq^-(水合电子)等自由基的等离子体反应过程。用这种方法产生的自由基的浓度、产成量均能满足工程上的需要．达到绿色化学12条原则要求,从源头上解决了环境污染问题。着重研究了羟基治理烟气SO2的绿色资源化的新方法．在无吸收剂、催化剂条件下,仅在0．8s内就能把烟气中SO2、H2O和O2电离后在分子层次上加工成H2SO4。     

Advanced statistical evaluation of the complex formation constants from electrophoretic data II: Diastereomeric ion-pairs of (R,S)-N-(3,5-dinitrobenzoyl)leucine and tert-butylcarbamoylquinine

Intermolecular association and ion-pair formation, respectively, between a cationic chiral selector, viz. o-9-(tert-butylcarbamoyl) quinine (CQN), and the both enantiomers of anionic N-(3,5-dinitrobenzoyl)leucine, (R)-DNB-Leu and (S)-DNB-Leu, were investigated by affinity capillary electrophoresis (ACE). Thus, binding constants of the both diastereomeric ion-pairs, (R) and (S)-DNB-Leu/CQN associates, were determined by different experimental setups and correction of nonlinear effects. A reciprocal setup was employed for the high-affinity (S)-enantiomer, and the experimental mobility data obtained for CQN at variable (S)-DNB-Leu concentrations in the background electrolyte were linearized and evaluated by advanced statistical model. A binding constant of K_S=125.1 l mol⁻¹ was afforded. The constant for the (R)-enantiomer, which is outside the range suitable for direct affinity CE, was obtained from indirect affinity CE utilizing the separation of the DNB-Leu racemate at a single appropriate CQN concentration in the BGE (resolution method) taking advantage of the known constant for the (S)-enantiomer yielding a binding constant of K_R=2.51 l mol⁻¹. Thereby, the so-called “constant time method” was adopted for the required precise measurement of the effective mobilities of the both enantiomers. A combined approach of reciprocal affinity CE with racemic DNB-Leu as additive and the resolution method confirmed the results. The resulting constants evidence excellent enantioselectivity of the tert-butylcarbamoyl derivative of the cinchona alkaloid quinine as chiral selector for N-(3,5-dinitrobenzoyl) derivatives of amino acids.     

Topical Problems in Elemental Analysis of Advanced Ceramic Materials

Selected prominent problems in the analysis of advanced ceramic materials are surveyed. The importance of reliability of results is discussed in the field of elemental trace- and microanalysis in view of its interaction with economy, power of detection, local resolution and speciation selectivity. Particular problems in the analysis of major constituents, trace components and microlocal distributions are based on the striking propertics of ceramics; they are exemplified. Analytical assistance must start from the beginning of the production processing, in the preparation of the powdered base materials. Determination of the stoichiometry requires high accuracy and differentiation of chemical species in bulk and surface analysis of ceramic base powders. Element trace determination by direct instrumental methods requires standard reference materials for calibration; these are currently inavailable in a sufficient variety. For optimum reliability and power of detection, element traces must be prepared in isolated form in a small excitation volume for analysis. A review on the state-of-the-art of wet-chemical combined procedures is presented. Decomposition position procedures are emphasized, due to their risk of contributing severe systematic error. Combustion in elementary fluorine is presented for decomposition of refractory materials. The performance of some direct procedures is discussed. Very efficient methods are available for element trace determinations in ceramic materials, offering high detection power. Several approaches for high-resolution local microanalysis in non-conductive ceramic materials are identified as the most promising development in the analysis of sintered compact ceramic products and devices.     

中英化学教材“化学反应速率”内容比较研究

“化学反应速率”综合体现了微粒观、实验观及科学本质观等化学基本观念,是提高学生科学素养的重要载体。从内容选取、内容编排与内容呈现3个方面对英国索尔特高级化学课程教材与国内化学教材中“化学反应速率”相关内容的编写进行比较,并简要阐述几点对化学教材编写和化学教学的启示。     

中子成像技术在元素分析中的应用

中子成像作为一种快速、直观的无损检测技术,在核工业、航空航天、新能源、地质、考古、先进制造等多个领域得到广泛应用。中子成像利用中子不带电、穿透能力强、对轻元素敏感、可区分同位素和近邻元素等特性,非常适合开展含氢元素、近邻元素和同位素等材料的无损检测。本文概述了中子成像技术的基本原理及特点,并结合中国先进研究堆(CARR)中子成像装置上的应用案例, 重点介绍了国内外中子成像技术在储氢材料、燃料电池、岩石、核燃料元件、古代文物等领域的典型应用。随着中子成像技术的不断发展和广泛应用,有望为我国更多领域研究提供更强有力的技术支撑。     

Forced oscillation of second-order neutral equations

ＩｎｔｒｏｄｕｃｔｉｏｎＴｈｅｓｔｕｄｙｏｆｔｈｅｏｓｃｉｌｌａｔｏｒｙａｎｄａｓｙｍｐｔｏｔｉｃｂｅｈａｖｉｏｒｏｆｔｈｅｓｏｌｕｔｉｏｎｓｏｆｎｅｕｔｒａｌｄｅｌａｙｄｉｆｆｅｒｅｎｔｉａｌｅｑｕａｔｉｏｎｓ,ｂｅｓｉｄｅｓｉｔｓｔｈｅｏｒｅｔｉｃａｌｉｎｔｅｒｅｓｔ,ｉｓｉｍｐｏｒｔａｎｔｆｒｏｍｔｈｅｖｉｅｗｐｏｉｎｔｏｆａｐｐｌｉｃａｔｉｏｎｓ.Ｆｏｒｅｘａｍｐｌｅ,ｓｅｃｏｎｄ＿ｏｒｄｅｒｎｅｕｔｒａｌｄｉｆｆｅｒｅｎｔｉａｌｅｑｕａｔｉｏｎｓｈａｖｅａｐｐｌｉｃａｔｉｏｎｓｉｎｐｒｏｂ…