利用8098单片机的热电偶参比端温度的全补偿方法

本文介绍在采用微机来进行热电偶测温处理时,通过查表的方法实现参比端温度的完全补偿,并完成热电势到温度的处理。     

有源结构声辐射自适应控制系统的一种新算法

提出了一种适用于有源结构声辐射自适应控制系统的新算法,它直接利用传感器拾取的干扰信号和误差信号实时地建立系统模型和误差通道模型,通过解Ｄｉｏｐｈａｎｔｉｎｅ方程得到自适应控制模型,仿真表明新算法较传统的Ｆｉｌｔｅ－ＸＬＭＳ等算法具有更好的收敛性。     

Active site of praseodymium orthovanadate catalyst in oxidative dehydrogenation of propane

The pure phase of praseodymium orthovanadate (PrVO₄) has been prepared by the citrate method. The active site of Pr-VO₄ was studied by ESR, NO-TPD, O₂-TPD and¹⁸O₂-isotope exchange methods. The results of ESR and NO-TPD confirmed the presence of V⁴⁺ in the catalyst.¹⁸O₂-isotope exchange was through a single exchange procedure. From the result of O₂ + TPD and the kinetic study of¹⁸O₂-isotope exchange, one can reach a conclusion that the V⁴⁺ species associated with oxygen vacancies are the site for O₂ activation. The adsorbed O₂ or O⁻ are the active oxygen species in propane oxidative dehydrogenation.     

Kinetic model for the smectite to illite transformation in active geothermal systems

The smectite to illite transformation in active geothermal systems of New Zealand can be simulated by a first-order reaction kinetic model, which provides direct estimates about the minumum ages of active geothermal systems themselves. The derived kinetic values show that the smectite to illite transformation is sensitive to both temperature and time.     

高柔土建结构振动主动控制的研究进展

阐述了高耸柔性结构振动主动控制的必要性、基本概念及其关键技术,综述了其研究现状及存在的问题,并指出高耸柔性结构机敏化／智能化是确保结构安全性与耐久性的重要途径。     

Enantioselective synthesis of hydroxy-substituted α-methyl-α-amino acids using Al and Mn derivatives of cyclo-(L-Ala-L-AIa) bis-Iactim ethers

Aluminum and manganese derivatives of lithiated bis-lactim ethers of cyclo-(L-Ala-L-Ala) were used for the enantioselective synthesis of -hydroxy and polyhydroxy -amino acids of the 2-methyIserine series. A new variant of the synthesis of these acids via 3-acyl-2, 5-dialkoxy-3, 6-dimethyl-3, 6-dihydropyrazines is proposed.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 590–595, March, 1993.     

Resistance to Surfactant and Protein Fouling Effects at Conducting Diamond Electrodes

Boron‐doped diamond thin‐film electrodes display negligible fouling effects in the presence of high levels of surface‐active materials, including proteins. Dramatic improvements in the stability of the analyte response (compared to common glassy carbon and carbon paste electrodes) are illustrated using bovine serum albumin (BSA), gelatin, and Triton X‐100 in connection with repetitive square‐wave voltammetric (SWV) measurements. The voltammetric response of ascorbic acid at the diamond electrode exhibits negligible shifts in peak potentials and minimal depressions of current signals over a wide range of surfactant concentrations (0–750 ppm). For example, the diamond electrode exhibited 70, 50 and 60 mV potential shifts for 10 repetitive voltammetric scans in the presence of 100 ppm BSA, gelatin and Triton X‐100, respectively, compared to 120, 190, and 280 mV shifts observed at the glassy carbon electrode. Furthermore, only 4.3 and 6.2% of the initial current decays were observed in the presence of 100 ppm Triton X‐100 and gelatin, respectively (compared to 45.2 and 34.4% diminutions at the glassy carbon electrode). Such improved performance was also confirmed from the SWV measurements of uric acid, dihydroxyphenylacetic acid, and catechol. The greatly improved resistance to surfactant interference reflects the fact that the as‐grown diamond thin film, composed of oxide‐free and hydrogen‐terminated surface, has a relatively lower surface energy and minimal electrostatic attributes, either specific or general, so that little adsorption of surface‐active agents occurs. The topographic AFM images of the diamond electrode surface confirm a negligible BSA fouling effect after repetitive SWV measurements. Such enhanced antifouling features make diamond electrodes very attractive for numerous real‐life electroanalytical applications.     

固体炭对一氧化氮低温催化解离还原反应的影响——Ⅱ.复合催化剂中铁在载体炭上化学形态的研究

用~(57)Fe穆斯堡尔谱研究了炭载型复合催化剂中铁化学形态随温度的变化,及各活性组分、助剂对铁化学形态的影响;并通过ESR谱考察了复合催化剂中不同活性组分对铁在载体炭表面电子特性的影响。研究结果表明,复合催化剂中各活性组分、助剂和载体炭与铁之间存在着强相互作用。在350～650℃,载体炭可将铁从Fe_2O_3还原到Fe_3O_4、FeO、α-Fe和生成炭化铁。活性组分Cu和助剂K可改变催化剂中铁周围的电子密度,促进铁在载体炭上从高价态向低价态还原。同时还发现催化剂中Na和Cr对铁有很强的助分散作用。     

对硝基氯苄与活性亚甲基化合物的反应

对硝基苄基衍生物可以与许多阴离子起单电子转移的亲核取代反应。Kornblum等以对硝基氯苄为底物,2-乙氧羰基香豆满-3-酮的钠盐为阴离子,作了深入的研究,得出对硝基氯苄与2-乙氧羰基香豆满-3-酮钠盐的C-烷化反应机理为自由基链式亲核取代反应。同时,Russell等提出对硝基氯苄与2-