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1.
Synthesis of Nitrogen Doped Multilayered Graphene Flakes: Selective Non‐enzymatic Electrochemical Determination of Dopamine and Uric Acid in presence of Ascorbic Acid. 下载免费PDF全文
Sudip Biswas Rashmita Das Dipanjan Chakraborty Rajib Bandhyopadhyay Panchanan Pramanik 《Electroanalysis》2015,27(5):1253-1261
Nitrogen doped multilayered graphene (NDMLG) is synthesized by annealing the black fluffy mass obtained by decomposing the complex prepared from Zn(OAc)2, diethanolamine and triethanolamine. The NDMLG has been characterized by HRTEM, FESEM, XRD, XPS, Raman spectroscopy, BET which indicate formation of nitrogen doped multilayer graphene flakes with high surface area. NDMLG shows better electrochemical oxidation property towards Dopamine, Uric acid and Ascorbic acid. The linear response ranges for determination of DA, UA and AA are 0.5–150 µM, 3–60 µM and 80–2000 µM respectively and the detection limits (S/N=3) are 15 nM, 15 nM, 580 nM, respectively in the mixture. 相似文献
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提出了反相高效液相色谱法测定三羟乙基胺硬脂酸酯中单硬脂酸酯、双硬脂酸酯、三硬脂酸酯的含量。以C18硅胶键合柱(250 mm×4.6 mm,5μm)为分离柱,甲醇与氯仿混合溶液为流动相梯度淋洗,用电雾式检测器检测。三羟乙基胺单、双、三硬脂酸酯的线性范围分别为2.0~50.0,1.0~50.0,1.2~50.0 mg.L-1,方法的检出限(3S/N)分别为1.8,0.5,1.0 mg.L-1。 相似文献
3.
Li RenZhengguo Jin Weidong WangHui Liu Junyun LaiJingxia Yang Zhanglian Hong 《Applied Surface Science》2011,258(4):1353-1358
Stoichiometric, phase-controllable SnS nanocrystals (NCs) were prepared by a solution chemical synthesis using triethanolamine-assisted diethylene glycol solvent, tin(II) chloride and thioacetamide as precursors at injection temperature of 180-220 °C. The influences of triethanolamine adding amounts, injection temperature, refluxing time on crystal phase, growth morphology and optical property of the synthesized SnS NCs were investigated. The results showed that both orthorhombic (OR) and zinc-blende (ZB) phase of SnS NCs could be formed by altering triethanolamine amounts. 相似文献
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XU Mancai OU Zhize SHI Zuoqing XU Mingcheng LI Haitao YU Shanxin HE Binglin 《Chinese Journal of Reactive Polymers》2000,(1)
1. INTRODUCTIONReduction of organic compounds by NaBH, is often used in organic synthesis. The reactiollis only proceeded in the interface between the organic phase and water phase because of the lowsolubility of NaBH. in organic compounds, and this results in the slow reaction rate and lowyield. In order to increase the reaction rate and yield, NaBH, was converted totetraalkylammonium borohydrides II' 'l, and this made the operating process complex and greatamount of quaternary ammon… 相似文献
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在含有邻苯二胺和三乙醇胺(TEA)的酸性溶液中,用循环伏安法(CV)在铂电极上制备聚邻苯二胺(PoPD)薄膜.通过对该薄膜进行深入的电化学分析,并将结果与无三乙醇胺参与的聚邻苯二胺的性能进行比较,发现在三乙醇胺参与下得到的聚邻苯二胺薄膜在铂电极表现出更好的粘附性,同时在氢离子选择性电极方面表现出优良的性能.在pH 2~13范围内具有良好的Nernst响应,直线斜率为59.62 mV/pH,相关系数达0.99以上,碱性条件下响应时间可缩短至30 s左右.该电极对大多数普通干扰物具有较好的选择性,可用于实际样品的测试. 相似文献
6.
Facilitated transport of silver(I) ions in acidic medium, across a supported liquid membrane (SLM) by using triethanolamine (TEA) as carrier, dissolved in cyclohexanone, has been investigated. The parameters studied are HNO3 concentration variation in the feed, pH of the feed solution, carrier concentration in the membrane phase, silver(I) ions concentration in the feed phase and KCN concentration in the stripping phase. Increase in H+ concentration by increasing HNO3 concentration from 0.5 to 1 M results into an increase in silver ions flux but a decrease in flux has been found beyond 1 M HNO3 concentration in the feed, providing a maximum flux of 3.21 × 10−7 mol/m2 s at 1 M HNO3. Increase in TEA concentration inside the membrane enhances flux with its maximum value at 2.25 M TEA. Further increase in the concentration of TEA leads to a decreased rate of transport due to the increase in viscosity of membrane liquid. The optimum conditions for Ag(I) ions transport are 1 M HNO3 (feed), 2.25 M TEA (membrane) and 1.5 M KCN in the stripping phase. It has been observed that Ag(I) flux across the membrane tends to increase with increase in Ag(I) ions concentration in the feed phase. Applying the studied conditions to silver plating waste solutions, Ag ions have been removed up to 99% in a time interval of 5 h. 相似文献
7.
A novel thin-film composite (TFC) membrane for nanofiltration (NF) was developed by the interfacial polymerization of triethanolamine (TEOA) and trimesoyl chloride (TMC) on the polysulfone (PSf) supporting membrane. The active surface of the membrane was characterized by using FT-IR, XPS and SEM. The performance of TFC membrane was optimized by studying the preparation parameters, such as the reaction time of polymerization, pH of aqueous phase and the concentration of reactive monomers. It is found that the membrane performance is related to the changes of the monomer content in the aqueous phase rather than in the organic phase. Furthermore, the nanofiltration properties of the TFC membrane were tested by examining the separating performance of various salts at 0.6 MPa operating pressure. The rejection to different salt solutions decreased as per the order of Na2SO4 (82.2%), MgSO4 (76.5%), NaCl (42.2%) and MgCl2 (23%). Also, streaming potential tests indicated that isoelectric point of the TFC membrane is between pH 4 and 5. Moreover, the investigation of the flux for NaCl solution at different pH showed that the polyester NF composite membrane is also particularly suitable for treating acidic feeds: the flux increased from 8.4 to 11.5 L/m2 h when pH of the feed decreased from 9 to 3. Additionally, the TFC membrane exhibits good long-term stability. 相似文献
8.
C. Giachetti 《Chromatographia》1998,48(5-6):443-449
Summary Low amounts of triethanolamine, collected in ORBO 53 tubes during air sampling, required the development of a very sensitive
method for determination. After desorption and silylation reaction with trimethylsilyl imidazole/trimethyl chlorosilane, the
derivative was analyzed by gas chromatography-mass spectrometry on an Ultra 2 silica capillary column in single ion monitoring
mode (retention time: about 6 min). The method has a detection limit of 1–2 pg with a desorption efficiency of about 81%.
Linearity of response was ascertained in the ranges 10–100 ng and 100–1000 ng. Short-term method validation was carried out
by intra- and inter-day assays on three amounts for each reference calibration curve. All results satisfied the pre-defined
acceptance criteria. In general, the whole procedure was easily performed and was appropriate for our needs. Breakthrough
volume was appropriate for our needs. Breakthrough volume was determined on authentic samples and was about 40–60 L, using
a flow rate of 1 L·min−1. The amounts of triethanolamine found in the samples ranged from 150 to 250 ng (about 2.5–4.2 μg·m−3). 相似文献
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