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Determination of boron concentration in uranium fuel samples by ICP-OES following a separation step by cation exchange resin 被引量:2
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作者 Yan Luo Hai-Xia Cong +3 位作者 rong-rong cui Chang-Qing Cao Wei Zhou Zhong-Qi Zhao 《Nuclear Science and Techniques》 SCIE CAS CSCD 2018年第3期165-171,共7页
The boron content of uranium fuel samples with boron concentrations in the range of 0.05–10 μg/g was determined using inductively coupled plasma optical emission spectrometry(ICP-OES) after the uranium was separated... The boron content of uranium fuel samples with boron concentrations in the range of 0.05–10 μg/g was determined using inductively coupled plasma optical emission spectrometry(ICP-OES) after the uranium was separated by cation exchange. The samples were dissolved in 3 M HNO_3 on a hot plate at 150℃ and evaporated to near dryness. The residues were redissolved in 0.2 M HNO-_3 and passed through a column loaded with Dowex 50WX8-400 resin. Uranium was adsorbed on the resin,while boron was easily eluted with 0.2 M HNO_3. The boron content of the effluent was determined using ICPOES. Several strategies were employed to improve the reliability of the experimentally determined boron content.The addition of mannitol and proper control of the evaporation process were shown to be effective in preventing boron loss during sample dissolution and evaporation. The memory effect was eliminated by flushing the system with 1.5% ammonia for 30 s between successive sample runs,and the matrix match method was used to eliminate the matrix effect arising from mannitol during the ICP-OES analysis. The accuracy of the results of the analysis was determined by addition recovery tests and by comparison with the results of three Chinese certified reference materials(GBW04242, GBW04243, and GBW04232). Using the method we developed, the limit of detection for boron was as low as 0.05 μg/g in uranium fuel samples, and the relative standard deviations for 0.1–0.5 g uranium samples with 0.05–2 μg/g of boron were within 9%. 展开更多
关键词 BORON DETERMINATION ICP-OES BORON evaporation Memory effect Matrix MATCH method Resin SEPARATION
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Influence of Molecular Stacking Pattern on Excited State Dynamics of Copper Phthalocyanine Films
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作者 Meng Li Wen-hui Li +8 位作者 Yu-jie Hu Jing Leng Wen-ming Tian Chun-yi Zhao Jun-xue Liu rong-rong cui Sheng-ye Jin Chuan-hui Cheng Shu-lin Cong 《Chinese Journal of Chemical Physics》 SCIE EI CAS CSCD 2022年第6期900-906,I0073,共8页
Photophysical processes occurring within organic semiconductors is important for designing and fabricating organic solar cells.Copper phthalocyanine(CuPc)is a typical electron acceptor.In this work,the triplet exciton... Photophysical processes occurring within organic semiconductors is important for designing and fabricating organic solar cells.Copper phthalocyanine(CuPc)is a typical electron acceptor.In this work,the triplet exciton lifetime is prolonged by altering the molecular stacking pattern of the CuPc film.For CuPc thin films,the excited state decays are mainly determined by the triplet-triplet annihilation process.The ultrafast transient absorption measurements indicate that the primary annihilation mechanism is one-dimensional exciton diffusion collision destruction.The decay kinetics show a clearly time-dependent annihilation rate constant withγ∝t^(-1/2).Annihilation rate constants are determined to beγ0=(2.87±0.02)×10^(-20)cm^(3)·s^(-1/2)and(1.42±0.02)×10^(-20)cm^(3)·s^(-1/2)for upright and lyingdown configurations,respectively.Compared to the CuPc thin film with an upright configuration,the thin film with a lying-down configuration shows longer exciton lifetime and higher absorbance,which are beneficial to organic solar cells.The results in this work have important implications on the design and mechanistic understanding of organic optoelectronic devices. 展开更多
关键词 CUPC PHOTOPHYSICS Excited state Triplet-triplet annihilation Organic solar cell
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02(1△) Yield Measurement by Raman Spectroscopy With Elimination of Chlorine Fluorescence Interference
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作者 rong-rong cui Wen-bo Shi +3 位作者 Lie-zheng Deng He-ping Yang Guo-he Sha Cun-hao Zhang 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2012年第2期142-146,I0003,共6页
Deleterious chlorine fluorescence was found to occur at the same frequency as the Raman scattering of 02 (1 A) and 02 (3 E), seriously affecting the 02 (1 A) yield measurement in the reaction of chlorine with ba... Deleterious chlorine fluorescence was found to occur at the same frequency as the Raman scattering of 02 (1 A) and 02 (3 E), seriously affecting the 02 (1 A) yield measurement in the reaction of chlorine with basic hydrogen peroxide by use of the Raman spectroscopy technique. To solve this problem we have taken advantage of the fact that Raman radiation is always strongly polarized while fluorescence is essentially non-polarized in a gaseous medium. When chlorine utilization of a singlet oxygen generator is 88%, 02(1A) yield reaches (42.4±7.4)% with the effect of chlorine fluorescence completely eliminated. 展开更多
关键词 Chemical oxygen iodine laser Singlet oxygen yield Spontaneous Raman spec-troscopy Chlorine fluorescence
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