碘量法—原子吸收光度法测金的方法对比

总结了目前金矿矿山企业实际生产过程中金含量的测定方法的种类及简单的测定原理,并具有针对性的介绍了实际生产中常用的两种测定方法—活性炭富集碘量法和活性炭富集原子吸收法。因两种测定方式中前期的试样处理及富集过程较为相似,于是将两种测定方法的原理,操作过程,数据结果对比分析等方面做了较为详细的讨论。对两种方法在实际操作中存在的问题给予分析,具有较高的实际生产指导意义。     

在线萃取流动注射分光光度法测定水中阴离子表面活性剂

在国标法GB 7494—1987的基础上,将在线萃取、在线分离技术与分光光度法相结合,研究了自动测定水中阴离子表面活性剂的新方法,使国标法中的各个操作步骤完全实现自动化。结果表明,新的自动测定法在0.034~2.00 mg/L浓度范围内,线性相关系数为0.999 9,检出限为0.008 6 mg/L,相对标准偏差3.8%(n=6),实际样品加标回收率为88.3%~100.0%。测定全过程相对密闭,人体不接触三氯甲烷,保护了分析人员的自身安全,方法操作简便,测定时间也较短,单个样品测定时间7 min。     

UPLC法同时测定阿托伐他汀钙中15个杂质含量

目的建立超高效液相色谱法(UPLC)同时测定阿托伐他汀钙原料药中15个杂质含量的方法。方法采用岛津Shim-pack Velox PFPP(2.1 mm×100 mm,1.8μm)色谱柱,以3.9 g/L醋酸铵缓冲液(pH 5.0):乙腈:甲醇:四氢呋喃(无稳定剂)=67:21:6:6为流动相A,3.9 g/L醋酸铵缓冲液(pH 5.0):乙腈:甲醇:四氢呋喃(无稳定剂)=27:61:6:6为流动相B;梯度洗脱,流速0.43 ml/min,检测波长244 nm,柱温35℃,样品室温度10℃;进样量1.8μl。结果阿托伐他汀钙及各杂质峰间分离良好,在0.3~3μg/ml范围内15个杂质均呈良好的线性关系(r均>0.999,n=6),各杂质平均回收率分别为96.3%,99.1%,99.9%,102.4%,96.4%,99.8%,99.4%,104.9%,106.4%,105.4%,100.1%,98.9%,94.7%,94.4%,101.4%,且不同浓度间平行性良好。15个杂质重复性、进样精密度、中间精密度均良好,48 h内均较稳定。此法除对色谱柱要求较高外,耐用性良好。结论本方法简便、快速、分离度好、专属性强,经方法学验证可用于阿托伐他汀钙原料药杂质质量控制。     

基于RFID标签阵列的睡眠期间呼吸量连续监测系统

睡眠期间连续且准确的呼吸量监测有助于推断用户的睡眠阶段以及提供一些慢性疾病的线索。现有工作主要针对呼吸频率进行感知和监测,缺乏对呼吸量进行连续监测的手段。针对上述问题提出了一种基于商用无线射频识别(RFID)标签的无线感知用户睡眠期间呼吸量的系统——RF-SLEEP。RF-SLEEP通过阅读器连续收集附着在胸部表面的标签阵列返回的相位值及时间戳数据,计算出呼吸引起的胸部不同点的位移量,基于广义回归神经网络(GRNN)构建胸部不同点的位移量与呼吸量之间的关系模型,从而实现对用户睡眠期间呼吸量的评估。RF-SLEEP通过在用户肩膀处附着双参考标签,消除用户睡眠期间翻转身体对胸部位移计算造成的误差。实验结果表明,RFSLEEP对不同用户睡眠期间的呼吸量连续监测的平均精确度为92.49%。     

大口径光学元件装夹转运结构设计及分析

为了实现大口径光学元件的安全装夹、转运,通过光学元件开槽与不开槽两种装夹方式的分析,得出开槽夹紧转运方式将带来微裂纹、应力集中、成本高等缺陷,提出了利用摩擦力克服光学零件的重力和惯性力的低应力装夹转运方案。通过对光学元件低应力夹紧结构设计,并利用有限元分析方法,得到不开槽装夹方式下,光学元件的最大主应力为1.11 MPa,最大切应力为0.73 MPa,远低于光学元件破坏的强度极限,且受力均匀,无应力集中现象。     

Broad-Spectral-Range Sustainability and Controllable Excitation of Hyperbolic Phonon Polaritons in α-MoO3

Hyperbolic phonon polaritons (HPhPs) in orthorhombic-phase molybdenum trioxide (α-MoO₃) show in-plane hyperbolicity, great wavelength compression, and ultralong lifetime, therefore holding great potential in nanophotonic applications. However, its polaritonic response in the far-infrared (FIR) range remains unexplored due to challenges in experimental characterization. Here, monochromated electron energy loss spectroscopy (EELS) in a scanning transmission electron microscope (STEM) is used to probe HPhPs in α-MoO₃ in both mid-infrared (MIR) and FIR frequencies and correlate their behaviors with microstructures and orientations. It is found that low structural symmetry leads to various phonon modes and multiple Reststrahlen bands (RBs) over a broad spectral range (over 70 meV) and in different directions (55–63 meV and 119–125 meV along the b-axis, 68–106 meV along the c-axis, and 101–121 meV along the a-axis). These HPhPs can be selectively excited by controlling the direction of swift electrons. These findings provide new opportunities in nanophotonic and optoelectronic applications, such as directed light propagation, hyperlenses, and heat transfer.     

Precise Extraction of Charge Carrier Mobility for Organic Transistors

Unreliable mobility values, and particularly greatly overestimated values and severely distorted temperature dependences, have recently hampered the development of the organic transistor field. Given that organic field‐effect transistors (OFETs) have been routinely used to evaluate mobility, precise parameter extraction using the electrical properties of OFETs is thus of primary importance. This review examines the origins of the various mobilities that must be determined for OFET applications, the relevant extraction methods, and the data selection limitations, which help in avoiding conceptual errors during mobility extraction. For increased precision, the review also discusses device fabrication considerations, calibration of both the specific gate‐dielectric capacitance and the threshold voltage, the contact effects, and the bias and temperature dependences, which must actually be handled with great care but have mostly been overlooked to date. This review serves as a systematic overview of the OFET mobility extraction process to ensure high precision and will also aid in improving future research.     

高氯酸铵含量对高铝富燃料推进剂中重要组分高氯酸铵/铝 一次燃烧性能和铝粉团聚的影响

采用CO2激光点火装置联合高速摄影系统及扫描电子显微镜等凝聚相燃烧产物分析技术，研究了高氯酸铵(AP)含量对高Al富燃料推进剂中重要组分AP/Al一次燃烧过程中燃烧现象、引燃时间、燃烧扩散时间、燃尽时间、燃烧效率、颗粒团聚及凝聚相燃烧产物的表面形貌、粒径及其分布的影响。结果表明，各AP/Al混合粉体的燃烧过程均可分为表面引燃、燃烧扩散和火焰熄灭3个阶段，但各样品在不同燃烧阶段的燃烧现象存在明显差异。AP含量由10wt%增至30wt%，样品燃烧剧烈程度增强，燃烧过程中固相颗粒的溅射现象越加明显；在火焰熄灭阶段，各样品燃烧由以停留在样品燃面处的燃烧为主逐渐变为以溅射颗粒的燃烧为主，且随反应进行，燃面已燃固相颗粒最先熄灭，各样品表面引燃时间、燃烧扩散时间、燃烧持续时间均缩短，即燃烧反应速率逐渐加快。在AP/Al混合物中，铝粉的燃烧效率、凝聚相燃烧产物粒度及其团聚程度随AP含量增加而增加。