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自动切换转换通道的A/D转换器AD7938及其应用 总被引:3,自引:1,他引:2
AD7938是AD公司推出的新型12位高速8输入通道模数转换器,片内自带顺序管理器,能智能切换转换通道,通道接入方式可设定为8路单端、4路差分、4路或7路准差分等4种方式,支持字和字节模式的并行接口,内置2.5V参考电压源,模拟、数字电源分开供电且可不同,软件设定输入电压范围和输出数据格式,功耗很低并具待机、停机模式,使用非常灵活方便。本文介绍了其功能特性和使用方法,并介绍了其与EZ-USB AN2131QC接口,应用于基于USB接口的数据采集卡中的方法。 相似文献
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Kyoung‐Hee Lee Jung‐Ki Park Whi‐Joong Kim 《Journal of Polymer Science.Polymer Physics》1999,37(3):247-252
The polymer electrolytes composed of poly(acrylonitrile‐co‐lithium methacrylate) [P(AN‐co‐LiMA)], ethylene carbonate (EC), and LiClO4 salts have been prepared. The ion groups in the P(AN‐co‐LiMA) were found to prevent EC from crystallization through their ion–dipole interactions with the polar groups in the EC. This suppression of the EC crystallization could lead to the enhancement of the ion conductivity at subambient temperature. The polymer electrolytes based on the PAN ionomer with 4 mol % ion content exhibited ion conductivities of 2.4 × 10−4 S/cm at −10°C and 1.9 × 10−3 S/cm at 25°C by simply using EC as a plasticizer. In the polymer electrolytes based on the PAN ionomer, ion motions seemed to be coupled with the segmental motions of the polymer chain due to the presence of the ion–dipole interaction between the ion groups in the ionomer and the polar groups in the EC, while the ion transport in the PAN‐based polymer electrolytes was similar to that of the liquid electrolytes. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 247–252, 1999 相似文献
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2006年7月1日,欧盟关于在电子电气设备中限制使用某种有害物质的指令(RoHS 指令)正式实施,对出口电子电气设备的检验和监管带来了一个新的挑战,本文就检验检疫部门新检验监管模式提出了一些思考和建议,面对当前各式各样的企业应对措施,在帮扶企业的同时,提出了一些现今企业忽视的而又较为重要的要素,为企业如何应对欧盟RoHS指令提出了指引. 相似文献
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本文介绍运用QC法,在提高LBS70—型声表面波窄带滤波器成品率方面所取得的明显效果。 相似文献
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MAN向B—ISDN过渡方法的研究 总被引:1,自引:0,他引:1
本文比较了利用窄带ISDN和帧中继技术与利用城域网(MetropolitanAreaNetwork-MAN)来实现过渡的两种方案,指出利用MAN过渡到B-ISDN具有更多的优越性,MAN是为适应局域网(LAN)互连和高速数据通信而发展起来的,网距离通常可达30~50km,由于它的信元格式和传输方式上与B-ISDN的兼容性,使得它成为从现有网络向B-ISDN过渡的最佳中介域网技术。 相似文献
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Viviane Van Hoof Hugo Cluckers Vera Verhaeghe Marleen Truyens An Hennebel 《Accreditation and quality assurance》2004,10(1-2):20-26
The automation of test validation procedures in a routine clinical laboratory by integrating artificial intelligence with the lab information system (LIS) is the focus of this study. Test validation consists of three layers: (1) acceptance of patient results based on technical criteria (technical validation), (2) acceptance of patient results based on internal quality control (QC) results (QC validation) and (3) medical validation of the patient protocol. The emphasis here is put on QC validation. General concepts regarding the setting of performance limits for internal QC results are briefly reviewed. As a practical example, we describe how the different layers of test validation were integrated with Molis, a LIS (Sysmex, Barchon, Belgium) used in a routine clinical biochemistry lab. PGP5 software (PGP, Brussels, Belgium) is used for technical validation and is installed on a Linx work-cell (Thermo Clinical Labsystems, Vantaa, Finland). The latter integrates four different Vitros instruments (OCD, Beerse, Belgium). QC validation and medical validation are performed with QC-Today (IL, Zaventem, Belgium) and VALAB (Erim, Toulouse, France), respectively. Both programs are bi-directionally coupled with the LIS. After 2 years of experience with this integrated system, it is clear that automation of validation rules and procedures has enhanced efficiency and overall quality of patient results.Presented at the Ninth Conference on Quality in the Spotlight, 18–19 March 2004, Antwerp, Belgium. 相似文献