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排序方式: 共有62条查询结果,搜索用时 390 毫秒
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Summary High pressure liquid chromatographic methods for the determination of diphenylmethane-4,4-diisocyanate (MDI) and toluene diisocyanate (TDI) in chemical products are described. The MDI- and TDI monomers were determined as their urea derivative formed by the reaction with 9-(methyl aminomethyl)-anthracene. Using these methods MDI- and TDI monomer concentrations have been determined in 55 chemical products: sealing waxes, insulating- and adhesive foam, hardener, primer, adhesives and surface coatings. The recovery of both MDI and TDI monomers from various types of chemical product was found to be 92–97%, and the relative standard deviations of the methods was <5% for all types of products. 相似文献
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A cylindrical chemosorptive denuder in series with a glass fibre filter has been evaluated for sampling toluene diisocyanate (TDI) aerosols. The sampler is designed for measuring personal exposure to diisocyanates. Several denuder coatings and derivatising reagents were investigated. Dimethylpolysiloxane (SE-30) and 5% phenyl dimethylpolysiloxane (SE-54) with either dibutylamine (DBA) or dipentylamine (DPeA) as derivatising reagents yielded the lowest vapour breakthrough (the amount (%) of the vapour that passes through the denuder), close to values predicted by theory. Immobilisation of the SE-30 denuder coating by in-situ cross-linking yielded comparable results. With an SE-30/DBA-coated denuder operating within an airflow range of 100–500 mL min–1, the phase separation was shown to be consistent with theoretical predictions derived by use of the Gormley–Kennedy equation. This provides a means of calculating the vapour breakthrough and correcting experimentally obtained values with regard to vapour–particulate phase distribution, suggesting that the denuder can provide accurate phase-distribution measurements. The SE-30/DBA denuder can be used over a concentration range spanning nearly six orders of magnitude. Its capacity is sufficient to perform 15-min exposure measurements of a TDI aerosol with air concentrations as high as 1,700 g m–3, 40 times higher than the Swedish occupational exposure limit (OEL). At the other end of the range, the estimated limit of detection (LOD) was less than 2 ng m–3 for both the vapour and the aerosol phases when LC–ESI–MS–MS was used for chemical analysis.Electronic Supplementary Material Supplementary material for this article is available at 相似文献
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时间延迟积分型面阵CMOS图像传感器MTF速度失配模型研究 总被引:3,自引:2,他引:1
研究了时间延迟积分型面阵互补金属氧化物半导体(CMOS)图像传感器调制传递函数(MTF)速度失配特性,在分析累加级数、像素尺寸、镜头放大倍数、行周期及电机运动速度失配等影响因素的基础上,建立了MTF速度失配模型。基于现场可编程门阵列(FPGA)开发板,搭建面阵CMOS图像传感器实现线阵时间延时积分(TDI)的CMOS测试系统。实验结果表明,在光强为3lx,速度失配M(ΔV/V)<2,8级时间延迟积分与面阵成像相比,MTF值提高50%;当累加级数为8级,速度失配满足M(ΔV/V)=2的速度失配容限时,奈奎斯特频率处的MTF值下降10%,当速度失配达到M(ΔV/V)=10时,MTF值下降35%。 相似文献
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利用TDI CCD成像数值仿真模型,研究了TDI CCD测量系统的测角精度随扫描镜速度稳定度的变化规律。首先根据TDI CCD推扫成像的物理过程,建立了数值仿真模型,设计了从光学像和扫描镜稳定度到数字图像的仿真链路;然后利用图像重心计算方法求取图像中心坐标并得到目标点的角位置坐标;通过蒙特卡诺法进行海量打靶试验,对结果进行统计得到扫描镜各稳定度水平上的测量精度值;最后将某工程样机的扫描镜速度稳定度带入仿真模型,仿真结果表明:测试误差增大5.67 μrad,达到了像元角分辨率的1/4。在光学测量系统的系统设计时,需要考虑像元分辨率及扫描镜稳定度的综合影响,选用合适的扫描镜稳定度要求,使测量角分辨率满足用户需求。 相似文献
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针对时间延时积分电荷耦合器件积分级数对成像质量的影响,提出了一种航天遥感相机中时间延时积分电荷耦合器件积分级数的最优选择方法.构造了典型成像系统的信噪比与积分级数关系模型和调制传递函数与卫星姿态角和积分级数的函数模型;以信噪比和调制传递函数的容许值为约束条件,推导出了任意条件下时间延时积分电荷耦合器件的可选积分级数区间并给出了最优的积分级数解,给出了对应的增益设置指导函数.运用仿真实验对该方法进行验证,并与传统方法进行比较,结果表明:该方法能够选取最优的积分级数,从而获得满足信噪比和调制传递函数指标的最佳成像质量;若该值不存在,依然能获取相对最佳的折中值和视觉效果;同时,本文成像效果优于传统方法. 相似文献
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《Analytical letters》2012,45(10):1193-1207
Abstract Measurements of airborne concentrations of (monomeric) 2,4- and 2,6-toluene diisocyanate (2,4- and 2,6- TDI), 4,4′ - diisocyanato diphenylmethane (MDI) and phthalic anhydride have been performed at 17 Danish manufactories using these compounds in the production of polyurethane foams, insulating materials, elastomers, coatings, lacquers and glues. Diisocyanate vapours at workplaces were collected in impingers, containing a solution of 9-(N-methylaminomethyl)-anthracene (1 × 10?4 M) in toluene. By reaction with this amine compound the diisocyanates are converted to stable urea derivatives. Phthalic anhydride particles were collected on glass fiber filters. For separation and detection of the diisocyanate derivatives and the phthalic acid formed upon hydrolysis of its anhydride, reversed phase high performance liquid chromatography on a bonded octadecylsilyl phase using isocratic elution with acetonitrile/water and UV-monitoring at Λ = 254 nm were used. The results obtained for each manufactory are presented. 相似文献