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本文以SnCl4·5H2O和氧化石墨烯为先驱物, 乙醇水溶液为溶剂, 采用一种简单的水热法一步合成了具有可见光催化活性的SnO2量子点(约3–5 nm)与石墨烯复合结构, 利用透射电子显微镜(TEM), 高分辨透射电子显微镜(HRTEM), X射线衍射仪(XRD), 傅里叶变换红外光谱(FT-IR)等技术对其结构进行了表征, 利用紫外可见吸收光谱(UV-vis)分析了其光学性能, 罗丹明-B染料为目标降解物研究了SnO2量子点/石墨烯复合结构可见光催化性能. 结果表明: 与纯SnO2、纯石墨烯相比, 复合结构显示出了很高的可见光催化活性. 通过对其结构进行分析, 我们提出了SnO2量子点/石墨烯复合结构的形成机制及其可见光催化活性机理. 相似文献
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两亲性树枝状大分子作为药物缓释载体的研究 总被引:1,自引:0,他引:1
利用胆酸对1代聚酰胺-胺树枝状大分子进行修饰,得到两亲性树枝状大分子(PAMAM1-CA6)。采用1H-NMR和酸碱滴定法测得每个1代PAMAM分子上共价键连了6个胆酸分子。PAMAM1-CA6在水相中自组装成纳米粒子,粒径约为273nm。以抗癌药物氨甲喋呤为模型考察了此两亲性树枝状大分子对药物的缓释行为。在碱性条件下(pH=10),PAMAM1-CA6对氨甲喋呤的释放较为缓慢;随着溶液pH的降低,药物的释放速率明显加快。说明PAMAM1-CA6对氨甲喋呤的释放具有环境响应性。体外细胞实验的结果表明,PAMAM1-CA6能够显著地提高氨甲喋呤的疗效。因此,这类由低代树枝状大分子制得的材料有望成为新型的药物控释载体。 相似文献
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The thermal behavior, miscibility, crystallite conformation and thermal stability ofcrosslinked(CL-) PVA/PVP blends were studied by DSC and TG methods, respectively. DSCresults showed that in the blend, the crystallinity,T_m and T_c of PVA were obviously lower thanthose of pure PVA; the crystal growth changed from three dimensional to two dimensional andonly a single T_g was detected. These facts demonstrated that this crystalline and amorphousblend have good miscibility. TG curves showed that providing the quantity of K_2S_2O_8 added ismore than 3 wt%,in the blends PVA will form a stable CL-network, whose thermal degradationtemperature was near to that of PVP. But crosslinking reaction will not take place for PVP. Theprocesses of thermal degradation of CL-blends are based on combining both the thermaldegradation of PVP and that of PVA crosslinked with corresponding quantity of K_2S_2O_8 CL-agent, respectively. The UV measurements showed that 75 wt% of PVP may be remained in CL-blend hydrogelscrosslinked by adding (3--5 wt% )K_2S_2O_8. This is mainly due to the stable CL-network formed and the good compatibility and properentanglement between the composites in the CL-blends. 相似文献
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以碳纳米管(CNTs)和丙烯腈-丁二烯-苯乙烯(ABS)为原料,通过熔融共混法制备CNTs/ABS复合材料,利用旋转流变仪研究其流变行为、拉伸试验机研究其拉伸性能,并得出部分适宜的加工工艺以期为今后实际生产提供参考.结果 表明:复合材料的黏度随温度的上升而下降,且有明显的剪切变稀行为;CNTs的加入会提高复合材料的流动... 相似文献
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