Influence of Al-doped ZnO and Ga-doped ZnO substrates on third harmonic generation of gold nanoparticles

Principal role of substrate types on the nonlinear optical properties of Au NP was investigated. Third harmonic generation (THG) studies were carried out for Au NP deposited on the Al-doped ZnO (AuNP/AZO) and Ga-doped ZnO (AuNP/GZO) substrates at fundamental wavelength of 20 ns Er:glass laser (generating at 1540 nm wavelength) during photostimulation by the 532 nm 15 ns laser pulses. Sizes of Au NP were 5 nm, 10 nm, 20 nm, and 30 nm. The output signal was registered at 513 nm. The photoinduced power density was increased from 0 up to 800 MW/cm². So in our work we explore the role of the substrate on the optically stimulated non-linear optical properties during simultaneous photo stimulation near the inter-band transition. The results were studied depending on the type of substrate and the sizes of the deposited nanoparticles. The analysis was done within a framework of interaction between the photoinduced light and SPR wavelengths. Control of the photoinduced temperature was done.     

离子色谱法同时测定不同时段酸雨中17种离子

应用离子色谱法同时测定不同时段酸雨中17种离子的含量。样品经离心沉淀后,经0.45μm滤膜过滤,滤液供离子色谱分析。阴离子分离时用Shodex SI-52 4E阴离子色谱柱,并用3.6mmol·L-1碳酸钠-0.6 mmol·L-1碳酸氢钠缓冲溶液作为淋洗液;阳离子分离时用TSKGEL阳离子色谱柱,并用2mmol·L-1硝酸溶液作为淋洗液,采用电导检测器进行检测。17种离子均在一定的质量浓度范围内与其峰面积呈线性关系,方法的检出限(3S/N)在1.4~18.7μg·L-1之间。回收率在95.0%~105%之间,测定值的相对标准偏差(n=6)在1.7%~7.2%之间。     

离子色谱法测定合成气制烯烃产物中的C_1~C_6有机酸

采用离子色谱建立了合成气制烯烃(SGTO)水相产物和油相产物中C1~C6有机酸的测定方法。对分离条件进行了优化,使用标准样品测定了线性范围和工作曲线,考察了方法的精密度和准确度,确定了SGTO油相产物样品的碱洗条件,并对SGTO水相产物和油相产物样品进行了测定。结果表明:C1~C6有机酸的质量浓度在各自配制的质量浓度范围内呈现良好的线性关系,相关系数均大于0.99。标准溶液的回收率测定表明回收率在95.6%~104.3%之间,5次重复测定的相对标准偏差(RSD)在0.4%~3.6%之间,表明该方法具有良好的准确性和精密度。SGTO油相产物中的加标回收率在91.1%~96.8%之间,5次重复测定的RSD为0.7%~2.3%,准确性可以满足实际分析的需要。实际SGTO水相产物和油相产物中C1~C6有机酸的分析结果表明,SGTO水相产物中C2~C4有机酸含量较高,而SGTO油相产物中C4~C6有机酸含量较高。本研究对SGTO反应研究、催化剂制备、工艺优化以及设备材料的选择具有重要意义。     

Direct separation of the enantiomers of ramosetron on a chlorinated cellulose‐based chiral stationary phase in hydrophilic interaction liquid chromatography mode

Ramosetron is an enantiopure active pharmaceutical ingredient marketed in Japan since 1996 and later in a few Southeast Asian countries predominantly as an antiemetic for patients receiving chemotherapy. In this study, a simple and rapid high‐performance liquid chromoatography method for the separation of ramosetron and its related enantiomeric impurity by using hydrophilic interaction liquid chromatography mode is presented. Chiral resolution was performed on an analytical column (100 mm × 4.6 mm id) packed with 3 μm particles of cellulose‐based Chiralpak IC‐3 chiral stationary phase. Using a mobile phase containing acetonitrile–water–diethylamine (100:10:0.1, v/v/v) and setting the column temperature at 35°C, the resolution value was 7.35. At a flow rate of 1 mL/min, the enantioseparation was completed within 5 min. The proposed method was partially validated and it has proven to be sensitive with limit of detection and limit of quantitation of the (S)‐enantiomer impurity of 44.5 and 133.6 ng/mL.     

应用于802.11a的5.7GHz CMOS LNA设计

使用0.18μm CMOS工艺设计应用于802.11a WLAN的U-NII高频段5.7GHz的LNA.首先选取LNA结构,推导出噪声模型,然后选取在固定功率消耗下最小噪声系数对应的晶体管尺寸,再进行输入输出阻抗匹配和电路调整优化.在使用Bond Wire不加Pad时提供-22.014dB S11,-44.902dB S22,15.063dB S21,-39.44dB S12,2.453dB/2.592dB的噪声系数(NF),-4.1915dBm的三阶互调输入点(IIP3),-15.6dBm的功率1dB压缩点(P1dB)和10mW的功率消耗(Pd).完全考虑Bond Wire和Pad效应的性能参数也已经给出,但噪声系数恶化为3.21/3.23dB,S参数在电路调整优化之后变化不大,整体性能比较突出.     

一种高输入电压高PSRR的带隙基准电路设计

在高压宽输入范围的芯片中,高压电源一般不直接作为带隙基准电路的电源。传统方案采用齐纳二极管加源随器将高压输入转换为低压电源,为带隙基准供电,然而低压电源波动过大,降低了带隙基准的PSRR。电源由反馈环路产生,可以提供高PSRR性能。文章提出了一种输入电压范围为5～65 V,通过闭环负反馈产生低压电源和1.2 V基准电压的带隙基准电路,适用于宽输入电压芯片,如Buck、电机驱动或模拟ASIC芯片。该带隙基准电路的电源是将自身产生的电流流经PMOS,由PMOS的V_GS确定。因此低压电源不随输入电压变化,线性调整率极低。该电路由预处理电路、启动电路和带隙基准电路组成,采用负反馈稳压设计,不使用齐纳二极管,不引入额外的掩膜层,降低了电路成本。在CSMC 0.25μm BCD工艺下,基准电压线性调整率低至0.000 091%,输入电压在5～65 V范围内基准变化小于1μV,低频PSRR为-160 dB@100 Hz,温度系数为2.8×10^-5/℃。     

Speciation of Arsenic Compounds in the Urine of Rats Orally Exposed to Dimethylarsinic Acid Ion Chromatography with ICP–MS as an Element-Selective Detector

A combined ion chromatography (IC) with inductively coupled plasma mass spectrometry (ICP—MS) system as an element-selective detector has been used for the determination of arsenic compounds. Seven arsenic compounds were separated by cation-exchange chromatography. Subsequently, the separated arsenic compounds were directly introduced into the ICP—MS and were detected at m/z =75. Detection limits for the seven arsenic compounds ranged from 0.8 to 3.8 μg As/l. The IC–ICP–MS system was applied to the determination of arsenic compounds in the urine of dimethylarsinic acid (DMAA)-exposed rats. DMAA was the most abundant arsenic compound detected. Arsenous acid, monomethylarsonic acid and trimethylarsine oxide were also detected.     

Magnesium hydroperoxyacetate (MHPA) and magnesium dihydroperoxide (MDHP): New antibacterial agents for fibrous substrates

Water-dispersable products have been prepared from the reaction of magnesium acetate tetrahydrate with hydrogen peroxide at mole ratios of 1 : 2 to 1 : 40 to produce compositions with active oxygen or peroxide contents of 1–30%. The products are believed to be stoichiometric mixtures of HOO Mg OAc and HOO Mg OOH that vary in composition with the molar ratios used. These new compounds are hydrolytically stable at ambient temperatures for extended periods (at least 60 days) and thermally stable below 300°C. Pad-cure processes are described for applying the above reaction products as a dispersion in water or aqueous hydrogen peroxide or as a foam in aqueous hydrogen peroxide to impart antibacterial activity to celulosics, synthetic fibers and fiber blends. The textiles are treated with dispersions or foam containing 10–17% of the reaction products derived from mole ratios of 1 : 2 to 1 : 40 magnesium acetate tetrahydrate: hydrogen peroxide. On subsequent heating for 2–4 min at 120–150°C, washing and drying, the modified textiles contain durably bound active oxygen or peroxide (0.1–1.7%) that has activity against representative gram-positive and gramnegative bacteria for up to 50 launderings.     

基于RFID专用读写模块和IC卡的手机支付新方案的研究

本文首先研究了移动支付业务需求、业务模式、技术背景与实现方式,然后描述了将RFID技术与移动通信技术相结合实现移动支付业务的技术方案,最后针对国内移动支付的发展现状,详细介绍了基于RFID专用读写模块和IC卡的手机移动支付新方案.     

MIMO通信系统中一种新的自适应均衡方法

该文提出了时变频率选择性衰落环境下多输入多输出(MIMO)通信系统中一种新的基于递归最小二乘(RLS)的自适应干扰对消的判决反馈均衡方法(RLS-IC-DFE)。该方法将每个数据子流上的自适应判决反馈均衡器等效为一个加长的新的均衡器,并把已解出的子流数据作为新的输入参数,应用RLS算法自适应调整新的均衡器参数。仿真结果表明,该文提出的自适应干扰对消的判决反馈均衡器可以自适应跟踪信道变化,同时比已有的判决反馈均衡器(RLS-DFE)能提供更好的误符号率(SER)性能。