一种提高测试序列质量的方法

针对电路测试序列质量低而导致测试费用高的问题,提出了修改扫描选择子序列提高测试序列质量的方法．通过组合测试集转化生成测试序列,研究分析组合测试集与转化测试序列的质量．通过修改测试序列的扫描选择子序列,使其能在相同的测试时间内检测更多故障,减少测试所需时间,降低测试费用．基准电路实验结果表明,应用本文方法测试序列质量明显提高,相同故障覆盖率下,所需测试时间仅为典型方法的50％．     

数据集市技术浅析

数据集市是当前数据仓库建设的重要环节,本文通过对目前某电信的数据现状进行分析,给出了两种数据集市的建设方案,并分别对两种方案特点进行了描述。解决了电信所遇到的数据问题。     

一种新型瞬变电磁发射机去过冲系统设计

针对瞬变电磁发射机发射电流过冲造成探测盲区的问题,提出了一种新型瞬变电磁发射机去过冲系统设计方案。该方案在发射线圈两端并联一个优化的RLC二阶电路,在发射电流下降到接近零时接通该电路,让发射电流按指数衰减,从而有效去除电流过冲。仿真与实验结果表明,该方案能够去除发射电流的过冲振荡,减小探测盲区。     

副井提升系统安全回路及上位机优化改造

针对煤矿副井提升系统安全回路软硬件及上位机中存在的不足进行了优化改造,改进了过卷试验方式,将闸系统紧停信号引入安全回路,并将安全回路各节点状态信号引入RSView32人机界面,实时显示安全回路状态;根据现场检修需要,在上位机增加了复位显示功能及行程偏差大报警信号。实际应用表明,该优化改造可迅速定位故障节点,实现软硬件互查。     

一种新型瞬变电磁仪发射电路设计

为提高瞬变电磁仪测量的准确度,设计了基于FPGA的瞬变电磁仪发射电路。该电路采用EXB841模块设计驱动电路,实现对H桥路上下臂MOSFET的有效驱动;利用改进的H桥路设计及改变传统桥路的控制策略,实现对MOSFET的超短时间关断;采用RCD吸收保护电路降低尖峰电压干扰,改善发射电路输出波形。试验结果表明,该发射电路的发射信号过压仅为正常信号的1.33倍,振荡时间为500ns,下降沿时间为700ns,实现了发射电流的快速关断,且稳定性好。     

多路输出反激式开关电源的改进与实现

针对传统开关电源存在的控制芯片供电方式耗能较大、反馈电路光耦有效输入电流范围窄两个问题,对传统电源电路进行了改进,设计并实现了一款性能优良的48V转+5V、±15V,输出功率25W的三路输出反激式开关电源。样机输出电压精度为0.2%(+5V)、0.53%(+15V)、0.6%(-15V),输出电压纹波为20mV(+5V)、50mV(+15V)、60mV(-15V),电压精度和纹波率均满足小于1%的要求;测试表明:该电源性能优良,具有效率高,稳压精度高,负载调整率高等优点,有很高的生产应用价值。     

Synthesis and properties of poly(amide–imide)s based on N,N′‐bis(4‐carboxyphenyl)‐4,4′‐oxydiphthalimide,p‐aminobenzoic acid and various aromatic diamines

A new diimide–diacid monomer, N,N′‐bis(4‐carboxyphenyl)‐4,4′‐oxydiphthalimide (I), was prepared by azeotropic condensation of 4,4′‐oxydiphthalic anhydride (ODPA) and p‐aminobenzoic acid (p‐ABA) at a 1:2 molar ratio in a polar solvent mixed with toluene. A series of poly(amide–imide)s (PAI, III_a–m) was synthesized from the diimide–diacid I (or I′, diacid chloride of I) and various aromatic diamines by direct polycondensation (or low temperature polycondensation) using triphenyl phosphite and pyridine as condensing agents. It was found that only III_k–m having a meta‐structure at two terminals of the diamine could afford good quality, creasable films by solution‐casting; other PAIs III using diamine with para‐linkage at terminals were insoluble and crystalline; though III_g–i contained the soluble group of the diamine moieties, their solvent‐cast films were brittle. In order to improve their to solubility and film quality, copoly(amide–imide)s (Co‐PAIs) based on I and mixtures of p‐ABA and aromatic diamines were synthesized. When on equimolar of p‐ABA (m = 1) was mixed, most of Co‐PAIs IV had improved solubility and high inherent viscosities in the range 0.9–1.5 dl g^?1; however, their films were still brittle. With m = 3, series V was obtained, and all members exhibited high toughness. The solubility, film‐forming ability, crystallinity, and thermal properties of the resultant poly(amide–imide)s were investigated. © 2002 Society of Chemical Industry     

Well-defined polymer precursors synthesized by RAFT polymerization of N,N-dimethylacrylamide/N-acryloxysuccinimide: random and block copolymers

N,N-dimethylacrylamide (DMA) and N-acryloxysuccinimide (NAS) were copolymerized by the reversible addition–fragmentation chain transfer (RAFT) polymerization technique, to obtain random and block copolymer precursors onto which different side-groups may be statistically grafted via the reactive NAS units. These reactive copolymers have interesting applications in various fields such as coatings and paints, water purification and biology. Random poly(DMA-co-NAS) copolymer chains were synthesized with a 75/25 molar ratio, high conversion, an excellent molecular weight (MW) control from 5000 to 130 000 g mol⁻¹, and low polydispersity index (M_w/M_n<1.1). Poly(DMA-b-NAS) block copolymers were synthesized by a two step method, in which a poly(DMA) homopolymer was prepared first and then used as macro-chain transfer agent to polymerize NAS. For example, a poly(DMA-b-NAS) sample was obtained with an average molecular weight of 44 300/7400 g mol⁻¹ corresponding to 447 DMA and 44 NAS units. Such block copolymers had not yet been synthesized by any controlled polymerization technique. They can be used to prepare polymers with exactly the same backbone and an increasing number of different side groups (e.g. hydrophobic, ionic or fluorescent).     

Interphases in the Adhesive Bonding of Fluoropolymers

Strong and durable adhesive bonds may be made between polytetrafluoroethylene (PTFE) and either cyanoacrylate (CA) or epoxy adhesives, if the PTFE surface is modified by the use of a “primer” such as triphenylphosphine (TPP) or diaminodiphenylmethane (DDM). The primer mixes with the PTFE surface, and the modified surface is then capable of forming an interphase, tens to hundreds of nanometers thick, where interpenetration of the adhesive and adherend occurs. Using CA adhesives, PTFE/CA/PTFE block compression shear bond strength (ASTM D4501-85) of over 10 MPa can be achieved, with failure occurring cohesively. Initial work with epoxy adhesives indicates that the use of DDM primer gives adhesive bonds comparable in strength with those produced by modification of the fluoropolymer surface by sodium naphthalenide.     

Investigation of conductivity characteristics of nitrile butadiene rubber vulcanizates filled with semiconducting carbide ceramic

SiC‐ and B₄C‐filled NBR rubber composites were prepared with various volume fractions of filler by a conventional roll‐mill method. The morphological structures of the NBR–SiC and NBR–B₄C composites were analyzed by scanning electron microscopy. The dependence of room‐temperature volume resistivity (ρ_v) on the concentration of filler in the two systems was studied. In addition, variation in the number of current carriers (n), mobility carriers (μ), dielectric constant (ε), and dielectric loss factor (tan δ) on filler concentration in the two systems were investigated in detail. The applicability of composites as negative temperature coefficient (NTCR) linear thermistors was studied by the dependence of volume resistivity on temperature. The resistivity showed negative temperature dependence and changed linearly with temperature parallel. The conduction mechanism of the conductivity of the two composites was analyzed in terms of the computed activation energy and hopping energy. Change in volume resistivity as a function of frequency for the two systems was also investigated. Finally, the dependence of volume resistivity on applied pressure and possible real applications of these composites as transducers in pressure sensors were also studied. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2158–2165, 2007