Authors:Xiao-Ling Xing, Feng-Qi Zhao, Shun-Nian Ma, Si-Yu Xu, Li-Bai Xiao, Hong-Xu Gao and Rong-Zu Hu
The thermal decomposition behavior of composite modified double-base propellant containing hexanitrohexaazaisowurtzitane (CL-20/CMDB propellant) was studied by microcalorimetry. The kinetic and thermodynamic parameters were obtained from the analysis of the heat flow curves. The effect of different proportion of CL-20 to the thermal decomposition behavior, kinetics, and thermal hazard was investigated at the same time. The critical temperature of thermal explosion (Tb), the self acceleration decomposition temperature (TSADT), and the adiabatic decomposition temperature rise (ΔTad) were calculated to evaluate the thermal hazard of the CL-20/CMDB propellant. It shows that the CMDB propellant with 38% CL-20 has relative lower values of E and lgA, and with 18% CL-20 has the highest potential hazard.
Authors:J. Zhi, W. Tian-Fang, L. Shu-Fen, Z. Feng-Qi, L. Zi-Ru, Y. Cui-Mei, L. Yang, L. Shang-Wen and Z. Gang-Zhui
The effects of aluminum (Al) and nickel (Ni) powders
of various grain sizes on the thermal decomposition of ammonium perchlorate
(AP) were investigated by TG and DSC in a dynamic nitrogen atmosphere. The
TG results show that Al powders have no effect on the thermal decomposition
of AP at conventional grain size, while the nanometer-sized Ni powders (n-Ni)
have a great influence on the thermal decomposition of AP with conventional
and superfine grain size. The results obtained by DSC and an in situ FTIR
analysis of the solid residues confirmed the promoting effects of n-Ni. The
effects of n-Ni have been ascribed to its enhancement on the gas phase reactions
during the second step decomposition of conventional grain size AP.
Authors:Yong He, Rui Ding, Hang Liu, Xiao Wang, Jing-Li Xu, Man Feng, Yu-Rong Chen, Chuan-Min Qi, Cheng Peng, Zhao-Hui Zhu, Yong-Hong Dang, Ming Wang and Yun-Chuan Ma
As degradation product of Antineoplaston A10 in vivo, phenylacetyl glutamine showed antitumor activities. According to literatures,
we designed and radiosynthesized a phenylacetyl glutamine derivative, which was achieved under a mild reaction condition.
Evaluations in vitro and in vivo were performed on tumor bearing mice. Excitingly, the radiochemical purity of (S)-2-((S)-2-(4-(3-fluoropropyl)benzamido)-3-phenylpropanamido)pentanedioic
acid ([18F]FBPPA) was 98%, and besides the best radiochemical yield was up to 46%. T/Bl (Tumor/Blood) and T/M (Tumor/Muscle) ratios
of [18F]FBPPA at 60 min post injection were 2.33 and 3.51. Meanwhile, it showed satisfied stability in vitro and in vivo, compared
with 2-[18F]fluorodeoxyglucose ([18F]FDG). Although [18F]FBPPA deserved further studies to make optimizations on its structure, the results revealed it might become a potential
PET imaging agent for detecting tumors.
Authors:Chuan-Min Qi, Yong He, Xiao Wang, Man Feng, Jing-Li Xu, Rui Ding, Hang Liu, Yu-Rong Chen, Fang Li, Zhao-Hui Zhu, Yong-Hong Dang, Shu-Ting Zhang and Ying Xie
d-glucosamine at concentration of certain range could kill tumor cells without influencing normal cells. There are also some
reports on the antitumor activity of d-glucosamine and its derivatives in murine models. It was therefore postulated that d-glucosamine might have the potential to invade tumor cells. We designed and radiosynthesized a glucosamine derivative, N-(2-[18F]fluoro-4-nitrobenzoyl)glucosamine ([18F]FNBG([18F]7)). Evaluations in vitro and in vivo were performed on tumor bearing mice. Excitingly, the radiochemical purity of [18F]FNBG([18F]7) was 99%, and besides the best radiochemical yield was up to 35%. The best T/Bl (Tumor/Blood) and T/M (Tumor/Muscle) ratios
of [18F]FNBG([18F]7) were 4.40 and 4.84. Although [18F]FNBG([18F]7) deserved further studies, the results revealed it might become a potential PET imaging agent for detecting tumors.