人骨骼中~(228)Th、~(230)Th和~(232)Th含量的同时测定

本文介绍了用α谱仪同时测定人骨骼中~(228)Th、~(230)Th和~(232)Th含量的方法。样品用浓 HNO_3和 H_2O_3湿灰化,草酸钙共沉淀载带、CL-5208萃淋树脂和743阳离子交换树脂联合分离后,电沉积制源,在低温半导体α谱仪上测量。该方法对~(234)Th的全程回收率为95.0±1.7%,对铀和镭的去污系数分别为6.3×10~4和1.5×10~3,对~(228)Th、~(230)Th、~(232)Th 的探测下限分别为0.432、0.135和0.108Bq/kg(鲜重)。     

A novel open-loop high-speed CMOS sample-and-hold

A new open-loop high-speed CMOS sample-and-hold is presented. Based on new method for further reduction of voltage-dependent charge injection, a new CMOS sample-and-hold was designed. Simulation results confirm the effectiveness of this method. Over 10 dB improvement in signal-to-noise ratio, compared to the signal-to-noise ratio of conventional bottom plate sampling S/Hs was achieved with this method. A comparison between newly designed S/H and the bottom-plate sampling S/H is presented.     

硅中硼离子注入校准样品的研制

本文主要介绍了硅中硼离子注入校准样品的制备与研究。分别用三台SIMS仪器对样品进行了深度剖析与比对,并对用作校准目的的样品主要参数进行了定值。     

挖掘机工作装置实验样本长度确定方法及程序系统

本文通过对某液压挖掘机工作装置实验样本长度的研究,详细讨论了样本长度的确定方法,重点分析了趋势曲线拟合法,提出了样本长度精度区间分析的方法,并在处理大量实验数据的基础上,从载荷分布及寿命估算的角度做了实际的验证.编制了应用程序,使样本长度确定至寿命估算整个过程程序化.     

高速宽带取样-滤波数字化系统中高斯滤波器的设计

本文基于频域逼近的方法提出了高斯滤波器的设计理论,得出了带宽归一化的各阶高斯滤波器的通用计算公式。并对高斯滤波器的数字化时间窗口、回复时间参数等进行了计算。     

企业材料耗用的统计分析与评价

本文利用回归分析导出材料耗用的回归方程 ,并对方程进行拟合优度检测和显著性检验 ,以及对材料耗用情况进行综合评价。     

How to study drying shrinkage microcracking in cement-based materials using optical and scanning electron microscopy?

Three different ‘destructive’ microscopy methods were tested on their ability to show drying shrinkage microcracks on a specimen cross-section. The first two were methods in which the microcracks were impregnated with a fluorescent epoxy and examined with fluorescence microscopy. In one method, the impregnation was applied before making the cross-section and in the other after making the cross-section. In the third method, the sample was kept wet constantly and examined in an environmental scanning electron microscope (ESEM). It was concluded that the method in which the dried specimen was impregnated before making the cross-section was the most reliable method to record drying shrinkage microcracks. With this method, it was possible to impregnate the complete drying shrinkage microcrack pattern in the studied cement-based materials from the surface, and there was no risk of recording microcracks introduced by sample preparation.     

C pm MPPAC for manufacturing quality control applied to the precision voltage reference process

The multiprocess performance analysis chart (MPPAC) based on the process capability index C_pm, called C_pm MPPAC, is developed for analysing the manufacturing quality of a group of processes in a multiple process environment. The C_pm MPPAC conveys critical information of multiple processes regarding the departure of the process and process variability from one single chart. Existing research works on MPPAC are restricted to obtaining quality information from one single sample of each process ignoring sampling errors. The information provided from existing MPPAC charts, therefore, is unreliable and misleading and results in incorrect decisions. In this paper, we consider the natural estimator of C_pm based on multiple samples. Based on the natural estimator of C_pm, we consider the sampling errors by providing an explicit formula with the Matlab program to obtain the estimation accuracy of the C_pm. We tabulate the sampling accuracy of C_pm for sample size determination so that the engineers/practitioners can use it for their in-plant applications. An example of multiple precision voltage reference (PVR) processes is presented to illustrate the applicability of C_pm MPPAC for manufacturing quality control.     

NPHMC: An R-package for estimating sample size of proportional hazards mixture cure model

Due to advances in medical research, more and more diseases can be cured nowadays, which largely increases the need for an easy-to-use software in calculating sample size of clinical trials with cure fractions. Current available sample size software, such as PROC POWER in SAS, Survival Analysis module in PASS, powerSurvEpi package in R are all based on the standard proportional hazards (PH) model which is not appropriate to design a clinical trial with cure fractions. Instead of the standard PH model, the PH mixture cure model is an important tool in handling the survival data with possible cure fractions. However, there are no tools available that can help design a trial with cure fractions. Therefore, we develop an R package NPHMC to determine the sample size needed for such study design.