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  • Author or Editor: H. Du x
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Abstract  

An improved accurate coincidence correction formula has been deduced on the basis of Cox's theory considering the complex situations of differences in pulse shaping width as well as a relative delay existing between the two channels. The correctness has been examined by experiments.

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Abstract  

By substututing99Mo for the Mo in the reconstituted MoFe protein, the nuclear quadrupole interactions (NQI) of99Mo have been measured using the perturbed angular correlations (PAC). Two well-defined electric quadrupole interaction parameters have been observed. The configuration of the M-Center of the MoFe protein is identified by the quadrupole couplign constant Q1(412(9)MHz) and the asymmetry parameter 1(0.49(5)). Other parameters, VQ2(1939(13)MHz) and 1(0.90(1)), may correspond to a deformation M—Center of MoFe protein.

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Abstract  

This paper introduces a new type of extractant, sym-dibenzo-16-crown-5-oxyhydroxamic acid (HL). The extraction of UO 2 2+ , Na+, K+, Sr2+, Ba2+ and Br were studied with HL in chloroform. The results obtained show that UO 2 2+ can be quantitatively extracted at pH above 5, whereas the extractions of K+, Na+, Ba2+ and Br are negligible in the pH range of 2–7. The dependence of the distribution ratio of U(VI) on both the concentration of the HL and pH are linear, and they have the same slope of 2. This suggests that U(VI) appears to form a 12 complex with ligand.Uranium (VI) can be selectively separated and concentrated from interfering elements such Na, K, Sr and Br by solvent extraction with HL under specific conditions. The recovery of uranium is nearly 100% and the radionuclear purity of uranium is greater than 99.99%. Therefore, it has greatly improved the sensitivity and accuracy for the detection of trace uranium from seawater by neutron activation analysis.

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Abstract  

The free-radical bulk polymerization of 2,2-dinitro-1-butyl-acrylate (DNBA) in the presence of 2,2′-azobisisobutyronitrile (AIBN) as the initiator was investigated by DSC in the non-isothermal mode. Kissinger and Ozawa methods were applied to determine the activation energy (E a) and the reaction order of free-radical polymerization. The results showed that the temperature of exothermic polymerization peaks increased with increasing the heating rate. The reaction order of non-isothermal polymerization of DNBA in the presence of AIBN is approximately 1. The average activation energy (92.91±1.88 kJ mol −1) obtained was smaller slightly than the value of E a=96.82 kJ mol−1 found with the Barrett method.

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Abstract  

57Co was produced with high pure nature iron irradiated by 8.5MeV deuterons. TBP-benzene extraction method and anion-exchange method were used to separate and purify it. The purified57Co was prepared into standard solution of about 30 to 50 g Co2+/ml carrier concentration and about 0.1 mol/l HCl. The specific activity of the standard solution was measured with 4 (ppc)- coincidence counting method. The final result was 476.82(1±0.42%)Bq/mg.

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Abstract  

The behavior of153Sm-EDTMP in vitro and vivo is analyzed by the size exclusion HPLC. The experimental results show that EDTMP amounts have an obvious effect on the stability in vitro and uptake of153Sm-EDTMP in the liver. HPLC analysis of urine sample indicates that153Sm-EDTMP es excreted in the original form. The behavior in vivo of153Sm-EDTMP containing 4 μg is similar to that of153Sm-EDTMP containing 50 μg EDTMP at 1 h post-injection.

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Abstract  

DTPA-Octreotide(Pentetreotide), a somatostatin analogue which can bind specifically and with high affinity to somatostatin receptor in vitro and vivo, labeled with99mTc by tin reduction in acetate buffer, has been characterized by Reverse-phase High performance Liquid Chromatography. The effect of different solvents, mobile phase pH, linear gradient and the injected volume on the separation efficiency was evaluated. The results show that the separation efficiency is best using μBondapak-C18 (300×3.9 mm2), linear gradient of 40% to 80% methanol (1.0 ml/min) in 0.05M acetate buffer (pH 5.5) over a 30 min period and maintaining for another 10 min. The labeled product is a mixture which mainly consists of five components (a, b, c, d, e) successfully proved by HPLC. Paper chromatography is also evaluated in this paper. It may be used to determine the radiochemical purity of the labeling product, but is not a good choice for the verification each components.

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Abstract  

The preparation of a cold kit was introduced in the paper, and the effective quantities of the components (Vc, HEDP and SnCl2·2H2O) in the kit were determined. At the sametime, the effects of labelling kit on the reaction time, reaction temperature and animal distribution were studied in detail. The initial animal experiment showed the high uptake in the skeletal tissue, the clearance in the blood was quick.

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Abstract  

The stability constants for tracer concentrations of Co(II) complexes with the red earth fulvic acid were determined at pH 3.8–6.8 and ionic strength 0.0010–1.0 mol/l by using the cation exchange equilibrium method and the radiotracer60Co. The effects of ionic strength and pH on the stability constants of 1∶1 Co(II) complexes were investigated, and it was found that the stability constants of complexes of humic substances do not vary with ionic strength and pH in a manner similar to that of simple complexes.

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Abstract  

The stability constants for tracer concentrations of Co(II) complexes with both the red earth humic and fulvic acids were determined at pH 5.9 and ionic strength 0.010 mol/l by using theArdakani-Stevenson cation exchange equilibrium method and the radiotracer60Co. It was found that the 1:1 complexes of Co(II) with the red earth humic and fulvic acids were formed and that the average values of logβ (stability constant) of humic and fulvic acid complexes were 5.76±0.19 and 4.42±0.03, respectively.

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