Nonlinear transforms of ECG signals for digital QRS detection: aquantitative analysis

A class of algorithms has been developed which detects QRS complexes in the electrocardiogram (ECG). The algorithms employ nonlinear transforms derived from multiplication of backward differences (MOBD). The algorithms are evaluated with the American Heart Association ECG database, and comparisons are made with the algorithms reported by Okada (1979) and by Hamilton and Tompkins (1986). The MOBD algorithms provide a good performance tradeoff between accuracy and response time, making this type of algorithm desirable for real-time microprocessor-based implementation     

托卡马克能量约束及自举电流效应的初步考虑

基于Lee等人的离子温度梯度模导致的反常热能输运系数,本文研究了辅助加热托卡马克等离子体的能量约束行为,并对自举电流的效应作了初步考虑。结果表明,计算得到的能量约束时间随等离子体电流I_p和托卡马克大半径R增大而增长,随注入功率P_t、环向场B_t以及等离子体小半径α的增大而缩短。这些结果与Kaye-Goldston的经验约束定标具有相同的趋势。自举电流的存在总是导致能量约束时间的增加,当自举电流与总电流的比值γ较小时,能量约束时间的增加率约为γ/2。此外,自举电流将造成锯齿反转半径的减小。     

非磁杂质对高Tc超导电性的影响

本文证明了在氧化物高T_c超导体的Anderson晶格模型中,由于序参量是能量的函数,非磁掺杂也具有拆对效应,在稀掺杂情况下,求出了T_c随杂质浓度增加而线性下降的规律,与实验结果相符,文中还计算了掺杂对超导态密度中能隙的影响,结果表明,当非磁掺杂浓度增加时,零温能隙的减小比T_c的下降慢得多,从而在转变为正常态之前可能不出现类似通常BCS超导体磁性掺杂的无能隙区。 关键词：     

PECVD法制备低介电常数含氟碳膜研究

采用PECVD法制备了低介电常数薄膜a-C：F，研究了薄膜沉积速率与温度及射频功率的关系，测量了不同沉积条件下薄膜的介电常数，并用FTIR分析了薄膜的化学结构及成分，发现薄膜沉积速率与沉积条件密切相关，其介电性与其化学结构以及沉积条件密切相关。     

中子辐照对Pd80Si20与Pd77.5Cu6Si16.5非晶态合金结构的影响

本工作用X射线衍射技术示差扫描量热法(DSC)和内耗测量等手段研究金属-类金属非晶态合金Pd₈₀Si₂₀和Pd_77.5Cu₆Si_16.5中子辐照前后的微观结构变化。结果表明,辐照在两种样品的对关联函数g(r)以及径向分布函数RDF(r)上都引起明显的变化;辐照后样品的晶化温度和晶化热有所提高,结构变得更加无序,Pd₈₀Si₂₀非晶态合金的内耗在T关键词：     

上市公司高管薪酬和企业业绩关系研究

本运用我国生物医药上市公司的经验数据考察高管薪酬与企业业绩的关系问题。研究的结果表明高管薪酬水平与企业业绩显正相关，高管团队内的薪酬差距也与企业业绩显正相关，而高管持股则与企业业绩负相关，在统计上不显。因此章建议企业应该考虑股权激励的成本和效果，改善股权激励制度。研究还表明企业追求的目标是规模最大化而不是股东净资产收益率最大化。     

电路板故障诊断中神经网络信息融合技术的应用

将信息融合技术应用到导弹电子设备的电路板故障诊断之中．提出了一种基于红外热成像实验的温度故障隶属度函数构造形式以及改进的BP神经网络算法。进行了BP神经网络信息融合故障诊断的实验研究．从结果看信息融合能较好地解决电路板元件故障诊断的不确定性问题。     

2‐Cyanoprop‐2‐yl dithiobenzoate mediated reversible addition–fragmentation chain transfer polymerization of acrylonitrile targeting a polymer with a higher molecular weight

The reversible addition–fragmentation chain transfer (RAFT) polymerization of acrylonitrile (AN) mediated by 2‐cyanoprop‐2‐yl dithiobenzoate was first applied to synthesize polyacrylonitrile (PAN) with a high molecular weight up to 32,800 and a polydispersity index as low as 1.29. The key to success was ascribed to the optimization of the experimental conditions to increase the fragmentation reaction efficiency of the intermediate radical. In accordance with the atom transfer radical polymerization of AN, ethylene carbonate was also a better solvent candidate for providing higher controlled/living RAFT polymerization behaviors than dimethylformamide and dimethyl sulfoxide. The various experimental parameters, including the temperature, the molar ratio of dithiobenzoate to the initiator, the molar ratio of the monomer to dithiobenzoate, the monomer concentration, and the addition of the comonomer, were varied to improve the control of the molecular weight and polydispersity index. The molecular weights of PANs were validated by gel permeation chromatography along with a universal calibration procedure and intrinsic viscosity measurements. ¹H NMR analysis confirmed the high chain‐end functionality of the resultant polymers. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1272–1281, 2007