柠檬酸月桂醇酯的合成

介绍了柠檬酸月桂醇酯的合成方法,并经正交实验得出合成的最佳工艺条件:反应温度132℃,反应时间120min,月桂醇/柠檬酸=1:1(mol比),催化剂用量:0.2g。     

Action of chelators on solid iron in phosphate-containing aqueous solutions

To study the effect of strong iron-ligands on steel corrosion, mild steel electrodes were immersed in solutions containing 20 mM phosphate buffer (pH=7.2) and between 0.01 mM and 1 M of either the iron(II)-chelators 2,2^′-bipyridine or FerroZine, or the iron(III)-chelators citrate or acetylacetonate. Resulting surface reactions were investigated by quantifying the electrochemical potential (E), the electrochemical polarization resistance (R_p), the corrosion current (I_corr) and the release of iron into solution. The surface was further analyzed by scanning electron microscopy (SEM/SEM-EDAX) and atomic force microscopy. Concentrations of 0.1 mM of any of the chelators led to slight, temporary changes in E, I_corr and R_p. Concentrations of 10 mM resulted in characteristic changes of E, which were the same for all chelators and in the precipitation of FePO₄ in the case of citrate and acetylacetonate, or vivianite [Fe₃(PO₄)₂ · 8H₂O] in the case of bipyridine and FerroZine. Concentrations of 1 mM of both iron(III)-chelators led to a temporary drop of E similar to that found with 0.1 mM chelator. With iron(II)-chelators, E dropped to about −500 mV before oscillating for several days. The amplitudes of the oscillations were up to 200 mV with periods of 30 and 20-25 min for bipyridine and FerroZine, respectively.     

柠檬酸三丁酯、乙酰柠檬酸三丁酯合成工艺的研究

以柠檬酸、正丁醇为原料，采用直接酯化法合成了柠檬酸三丁酯。以柠檬酸三丁酯、乙酐和正丁醇为原料，采用共乙酰化-酯化法合成出乙酰柠檬酸三丁酯，并联产乙酸正丁酯。考察了催化剂用量、原料配比、反应温度、反应时间等因素对反应过程的影响，确定了较佳的操作条件，柠檬酸三丁酯收率≥98％，乙酰柠檬酸三丁酯收率≥98％。采用活性炭脱色技术对产品进行精制，明显改善了产品的色泽。     

~(99)Tc~m-MDP、~(99)Tc~m(V)-DMSA和~(99)Tc4~m-Citrate显像对骨组织良恶性疾病鉴别诊断的对比研究

为评价99Tcm(V)二巯基丁二酸钠(DMSA)显像和99Tcm枸缘酸(Citrate)显像在骨转移癌和骨及骨关节炎症诊断中的意义,对骨转移癌患者和骨及骨关节炎症患者各18例分别进行99Tcm亚甲基二膦酸(MDP)、99Tcm(V)DMSA和99TcmCitrate全身显像,并比较了它们的显像结果。18例经病理学、CT或MRI证实有骨转移癌的患者,99TcmMDP显像共检出64个病灶,99Tcm(V)DMSA显像显示在与99TcmMDP显像相同部位同检出49个病灶,而99TcmCitrate显像仅检出1个病灶。18例经细菌学、CT或MRI证实的骨及骨关节炎症患者,99TcmMDP显像共检出22个病灶,99Tcm(V)DMSA显像显示在与99Tcm MDP显像相同部位同检出17个病灶,99TcmCitrate显像检出16个病灶。本组病例99Tcm(V)DMSA显像诊断骨转移癌的灵敏度为76.56%,特异性为22.73%; 99TcmCitrate显像诊断骨转移癌的灵敏度仅为1.56%,特异性为27.27%。99Tcm(V)DMSA显像诊断骨及骨关节炎症的灵敏度为77.27%,特异性为23.44%;99TcmCitrate显像诊断骨及骨关节炎症的灵敏度为72.73%,特异性为98.44%。以上结果表明,99Tcm(V)DMSA显像在诊断骨转移癌和骨组织炎症时应该慎重,因为它不能区分骨组织的良恶性病变性质,其对骨组织的良恶性病变性质的鉴别诊断应排除外骨组织炎症、骨折等骨组织良性病变的干扰。而99TcmCitrate     

Structural,microstructural, and magnetic studies of Y3Fe5-xNixO12 garnet nanoparticles

This paper reports the structural and magnetic properties of a series of Y₃Fe_5-xNi_xO₁₂ (x = 0, 0.05, 0.1, and 0.2) nanopowders synthesized by the citrate combustion method. We have discussed the change in different properties with the variation in calcination temperatures as well as the Ni ion substitution in yttrium iron garnet. X-ray diffraction study confirmed the desired garnet phase formation in all the calcined powders, and the crystallinity improved with an increase in calcination temperature. The crystallite sizes were observed in the range 47–52 nm and 84–94 nm for the samples calcined at 800 and 1000 °C, respectively. Scanning electron micrographs confirmed that the grains were in the nanometre range (132–170 nm) at 800 °C and increased (351–363 nm) at 1000 °C. Larger grains at high calcination temperature resulted in the enhanced saturation magnetization and a decrease in coercivity. Curie temperature (T_c) was observed in the range 558–560 K for all the calcined Y₃Fe_5-xNi_xO₁₂ samples. Nickel substitution for iron sites in Y₃Fe_5-xNi_xO₁₂ decreased the saturation magnetization and enhanced the coercivity. This could be related to the substitution of Ni ions for tetrahedral iron sites, which changed the magnetic exchange interactions of different lattice sites. The magnetic anisotropy constant (K) increases with the enhancement of calcination temperature, whereas it decreases with nickel ion substitution in Y₃Fe_5-xNi_xO₁₂. This study suggests that the structural and magnetic properties can be tuned by Ni substitution for the Fe ions in Y₃Fe₅O₁₂ garnets at different calcination temperatures, which make them promising candidates for various technological applications.     

利用蛋壳生产柠檬酸钙的初步研究

为充分利用蛋壳中的CaCO3,采用中和法制备柠檬酸钙,使其中的无机钙转化为有机钙,进行了煅烧条件、原料配比、反应物浓度、温度、时间等因素对产物收率和纯度的影响实验研究。结果表明：最适宜工艺条件分别为：蛋壳在900℃煅烧分解1-2h,CaO收率为95％以上。中和反应条件：石灰乳浓度5％,柠檬酸浓度50％,反应温度60℃,反应时间1h,产品收率高、质量好、安全无毒。     

柠檬酸的应用与开发

本文介绍了柠檬酸的生产概况、用途和柠檬酸深加工产品的制法及用途。开发新的使用途径是柠檬酸生产行业的发展方向。     

HPAM／柠檬酸铝胶态分散凝胶形成条件研究

采用一种简化的实验程序测定胶态分散凝胶（ＣＤＧ）的转变压，用测得的转变压值作为评价参数，考察由ＨＰＡＭ、柠檬酸铝、硫脲、氯化钾组成的ＣＤＧ的形成条件及相对强度。所考察的形成条件包括ＨＰＡＭ的来源和浓度，柠檬酸铝和氯化钾的浓度，ｐＨ值，绝大部分实验工作在４０℃和ｐＨ＝７．０的条件下进行，用一组实验考察了温度的影响（７０℃和４０℃）。     

Synthesis and magnetic properties of nano-sized Cu0.5Ni0.5Fe2O4 via citrate and aloe vera: A comparative study

In this report, Cu_0.5Ni_0.5Fe₂O₄ nanoparticles were synthesized by solgel using eco-friendly aloe vera extract and citric acid separately and their properties were discussed. Structural, Functional, morphological, magnetic properties of the samples were characterized using X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Transmission electron microscopy (TEM), Vibrating sample magnetometer (VSM). XRD exhibited the samples have single phase cubic spinel with average size of 46.4?nm and 35.45?nm. Two characteristics bands of ferrite were confirmed by FTIR. TEM indicated different morphology of the samples with some regularity. VSM data showed that higher coercivity for the sample prepared by aloe vera extract.     

BiFeO3 films on steel substrate by the citrate method

We deposited BiFeO₃ films on stainless steel substrates using a simple low-temperature wet-chemical route. Bismuth and iron nitrates were used as metal source and citric acid as chelating agent to prepare a water solution and deposit the film by dipping the steel substrate in the viscous solution. We have investigated the composition, crystallinity and structure of the BiFeO₃ film on steel by X-ray diffraction, X-ray photoelectron spectroscopy, high resolution scanning electron microscopy, conventional and high resolution transmission electron microscopy, and energy dispersive spectroscopy techniques. The film deposited on the steel substrate has two sublayers: a very thin (about 100 nm) nanocrystalline layer, with crystallite size of few nanometers, and a thicker (below 1 μm) crystalline layer.