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121.
含氰基侧基聚芳醚砜的合成与表征 总被引:1,自引:0,他引:1
汉2,6-二卤苯甲腈、4,4′-二氯二苯砜、4,4′-二羟基二苯砜、间苯二酚、对苯二酚、酚酞及双酚A为主要原料,合成了含不同结构单元和不同氰基含量的含氰基侧基的聚芳醚砜,并采用IR、^13CNMR等分析手段对其结构进行了表征,同时研究了结构单元和氰基含量对聚芳醚砜性能的影响。 相似文献
122.
微乳液介质—1—(2—吡啶偶氮)—2—萘酚光度法测定汽油中环烷酸铁的含量 总被引:8,自引:2,他引:8
本研究了微乳液为介质时,铁与1-(2-吡啶偶氮)-2-萘酚(PAN)的显色反应。选择730nm处为测定波长,ε为1.4×10^4L.mol^-^1.cm^-^1,铁量在0-50μg/25ml范围内符合比耳定律,该法适用于汽油中环烷酸铁的测定。 相似文献
123.
本文用微分脉冲极谱法研究了多酚氧化酶的活性测定和酶的反应动力学。应用于马铃薯等10余种植物样品的酶活力测定,结果良好。方法简便快速,重现性好。 相似文献
124.
Yan?Zhang Changchun?Wang Wuli?Yang Bin?Shi Shoukuan?FuEmail author 《Colloid and polymer science》2005,283(11):1246-1252
Biodegradable tri-component diblock copolymer was synthesized by bulk copolymerization of ε-caprolactone (CL) and D, L-lactide (LA) in the presence of methoxy poly(ethylene glycol) (MePEG), using stannous octoate as catalyst. Their chemical
structure and physical properties were investigated by GPC, NMR, DSC, TGAand XRD. The increase of CL/LA ratio in the diblock
copolymer leads to lower T
g, higher decomposition temperature and crystallinity. Nanoparticles formulated from MePEG–poly(CL-co-LA) (PCAE) possess spherical structure, which was characterized by dynamic light scattering (DLS) and transmission electron
microscopy (TEM). The DLS results indicate that the particle size increased with the increase of CL/LA ratio and the hydrophobic
fragment length in the copolymer. The drug encapsulation efficiency and the drug release behavior in vitro conditions of camptothecin
were measured by high performance liquid chromatography (HPLC). The encapsulation efficiency can be achieved as high as 84.4%
and the release behavior can be made well-controlled. MePEG–poly(CL-co-LA) nanoparticles might have a great potential as carriers for hydrophobic drugs. 相似文献
125.
A method has been developed for the speciation of trace dissolved Fe(II) and Fe(III) in water by coupling gallic acid (GA) modified nanometer-sized alumina micro-column separation with inductively coupled plasma mass spectrometry (ICP-MS). The separation of Fe(II) and Fe(III) was achieved based on the obvious difference in reaction kinetics between Fe(II) and Fe(III) with GA. Fe(III) was selectively retained on the micro-column at pH 5.5-6.5, while Fe(II) could not be retained by the micro-column at the whole tested pH range of 1.0-6.5, and passed through the micro-column. The Fe(II) can be determined by ICP-MS directly without preconcentration/separation procedure, while Fe(III) retained on the micro-column was then eluted with 1.0 mL of 1 mol L(-1) HCl and determined by ICP-MS. The parameters affecting the separation of Fe(II) and Fe(III) were investigated systematically and the optimum separation conditions were established. Under the optimized conditions, the detection limits of 0.48 microg L(-1) and 0.24 microg L(-1) with relative standard deviation of 5.6% and 4.3%(C= 5 microg L(-1), n= 7) for Fe(II) and Fe(III) were found, respectively. No obvious effect on the speciation of Fe(II) and Fe(III) was found with the change of the ratio of Fe(II) and Fe(III) from 0 ratio 10 to 10 ratio 0. The proposed method was applied for the determination of trace Fe(II) and Fe(III) in environmental water and the recoveries for spiked samples were found to be in the range of 97-105%. 相似文献
126.
采用示差脉冲伏安法,在乳酸脱氢酶(LDH)酶促体系“丙酮酸盐 + NADH +H+ (?) 乳酸盐 + NAD+”中,通过检测NAD+还原峰电流的变化,测定了不同条件下(不同酶用量、缓冲液pH值以及温度)LDH的活性、酶促体系的米氏常数KmNADH以及最大反应速率vmax。并且在最佳实验条件下,通过检测LDH活性的改变,实验考察了3种纳米物质(ZnS,TiO2(R)和TiO2(A))对乳酸脱氢酶酶促体系的影响。 相似文献
127.
In order to explore the transfer mechanism of chromium(III) in mammals, a novel complex [Cr(ASA)(en)2]Cl· 2H2O, bis(ethylenediamine‐ κ 2 N,N′)(4‐aminosalicylic acid‐ κ 2 O,O′) chromium(III) monochloride dihydrate was synthesized (4‐aminosalicylic acid=H2ASA, ethylenediamine=en). The crystal structure belongs to orthorhombic system with the space group P212121 by means of X‐ray diffraction. The characteristic for transfer of Cr3+ from the compound to the low‐molecular‐mass chelator EDTA and the iron‐binding protein apoovotransferrin (apoOTf) was followed by UV‐visible (UV‐Vis) and fluorescence spectra in 0.01 mol·L?1 Hepes at pH 7.4. The second order rate constants were calculated. Those spectra in conjunction were used to obtain more accurate information about the interaction of chromium complex with apoOTf. The experimental results indicate that Cr3+ can be transferred from the complex to apoOTf with the retention of the 4‐aminosalicylic acid acting as a synergistic anion. 相似文献
128.
Xiu Hui Lu Hai Bin Yu Wei Rong Wu Yue Hua Xu 《International journal of quantum chemistry》2007,107(2):451-457
Mechanisms of the cycloaddition reaction between singlet difluoromethylene carbene and acetone have been investigated with the second‐order Møller–Plesset (MP2)/6‐31G* method, including geometry optimization and vibrational analysis. Energies for the involved stationary points on the potential energy surface (PES) are corrected by zero‐point energy (ZPE) and CCSD(T)/6‐31G* single‐point calculations. From the PES obtained with the CCSD(T)//MP2/6‐31G* method for the cycloaddition reaction between singlet difluoromethylene carbene and acetone, it can be predicted that path B of reactions 2 and 3 should be two competitive leading channels of the cycloaddition reaction between difluoromethylene carbene and acetone. The former consists of two steps: (i) the two reactants first form a four‐membered ring intermediate, INT2, which is a barrier‐free exothermic reaction of 97.8 kJ/mol; (ii) the intermediate INT2 isomerizes to a four‐membered product P2b via a transition state TS2b with an energy barrier of 24.9 kJ/mol, which results from the methyl group transfer. The latter proceeds in three steps: (i) the two reactants first form an intermediate, INT1c, through a barrier‐free exothermic reaction of 199.4 kJ/mol; (ii) the intermediate INT1c further reacts with acetone to form a polycyclic intermediate, INT3, which is also a barrier‐free exothermic reaction of 27.4 kJ/mol; and (iii) INT3 isomerizes to a polycyclic product P3 via a transition state TS3 with an energy barrier of 25.8 kJ/mol. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2007 相似文献
129.
Muhammad Mufazzal Saeed 《Journal of Radioanalytical and Nuclear Chemistry》2006,267(2):427-433
Summary The sorption of microquantities of Tm(III) ions on washed polyurethane foam (PUF) from a mixture of aqueous solution and ethanol
containing PAN was examined. The maximum sorption of 3.18. 10-6M solution of Tm(III) ions was observed at pH 8 with 30-minute equilibration time. The optimum ratio of aqueous-ethanol phase
for the sorption of Tm(III) ions was found to be 3:1 v/v, respectively. The sorption rate of metal ions on PUF is followed a first order kinetics and obeyed the equation for an intra
particle diffusion process. The equilibrium concentration data of Tm(III) ions could be described satisfactorily by several
adsorption isotherms. The Freundlich adsorption isotherm constants 1/nand KFare 0.66±0.02 and (5.7±0.3). 10-3mol. g-1, respectively. The Langmuir isotherm constants for monolayer coverage (Q) and binding strength of sorption (b) are (2.5±0.7). 10-5mol. g-1and (1.6±0.1). 104l. mol-1, respectively. The sorption capacity derived from Dubinin-Radushkevich (D-R) isotherm is (1.7±0.2). 10-4mol. g-1and the sorption free energy (E) is 9.8±0.2 kJ. mol-1indicating chemisorption phenomena. The thermodynamic parameters indicate that the sorption of Tm(III) ions onto PUF is endothermic,
entropy driven and spontaneous in nature. 相似文献
130.
本文报道了一种新型三维亚磷酸锌[HO(CH2)2NH3]2•[Zn3(HPO3)4]的合成和晶体结构。在它的结构中,ZnO4和HPO3严格按照顶点连接的方式交替相连。骨架结构存在两个沿着不同方向无限延伸的由ZnO4和HPO3组成的四元环链,在[0 1 0]、[0 4 15]和[0 -4 15]三个方向形成了三个交叉8元环孔道,有机胺阳离子起着平衡电荷和稳定骨架的结构。它的晶体数据为:[HO(CH2)2NH3]2•[Zn3(HPO3)4],M=640.21, 正交晶系, Fdd2空间群, a=2.8528, b=0.8426, c=1.6159nm, Z=8, V=3.884nm3, R1=0.0219, wR2=0.0544。 相似文献