429 research outputs found

    Technology Survey and Development Tendency Investigation on ITO Films

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    综述了铟锡氧化物(ITO)薄膜的生产技术概况及其发展趋势。介绍了ITO薄膜的主要制备技术的制备原理,包括磁控溅射法、溶胶-凝胶法、化学气相沉淀法、喷雾热分解法及真空蒸发法等5种制膜工艺,并对其优缺点进行了分析。指出ITO薄膜生产技术的发展趋势为:1)大力开发溶胶-凝胶工艺;2)进一步深入研究其合成机理与性能;3)拓宽应用领域;4)开发先进的薄膜制备工艺技术。The technology survey and development tendency of ITO films were reviewed.The preparation principles of the main production processes of ITO films were introduced,including DCMS,CVD,Sol-gel process,chemical vapor deposition,spray-pyrolysis and vacuum evaporation,and their merits and demerits were analyzed.Based on the analysis results,the development tendency of production technology of ITO thin film are investigated as follows:(1) Developing the sol-gel process strongly;(2) Further studying their synthesis mechanism and properties;(3) Exploiting their application area;(4) Developing advanced preparation technology of thin film.国家自然科学基金资助项目(20306031

    基于FBG传感技术的复合材料加筋板低速冲击损伤监测

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    针对碳纤维增强树脂基复合材料低速冲击损伤的实时监测,本文设计将布拉格光纤光栅(FBG)传感器埋植在复合材料加筋板结构的三角填充区,在线监测复合材料T型加筋板冲击损伤过程。分别将FBG传感器埋植于复合材料层合板内部和复合材料T型加筋板的三角填充区,对比FBG传感器的埋入对复合材料层合板与复合材料T型加筋板对力学性能的影响,结果表明内埋FBG传感器的复合材料层合板试样的拉伸强度比未埋植传感器的层合板试样降低了约5%,但在FBG传感器的破坏应变范围内,FBG传感器可以准确、实时地监测复合材料的应变信号。将FBG传感器埋入复合材料T型加筋板的三角填充区,内埋FBG传感器的加筋板样件压缩破坏载荷与未埋植的样件基本一致。通过对比加筋板蒙皮上冲击位置、冲击能量对FBG传感器测得的冲击过程持续时间和最大应变值的影响,表明冲击过程持续时间随着冲击能量增加而延长,最大应变值随着冲击距离的增加呈下降趋势,而最大应变值随着冲击能量的增加呈上升趋势。利用FBG传感器测得的应变信号可初步实现对复合材料T型加筋板蒙皮冲击损伤位置及冲击能量的实时监测。国家重点研发计划(2016YFD0700603);;航空科学基金(2016ZF68011);;江苏省重点研发计划(BE2015007);;福建省科技创新平台建设计划(2014H2006

    茶多糖TGC的结构表征

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    采用气相色谱-质谱联用技术(GC-MS)分析均一茶多糖TGC的单糖组成,并与NMR,圆二色谱、紫外扫描等其他分析方法结合,对茶多糖TGC的一级结构及其在溶液中的构象加以探讨.结果表明:茶多糖TGC是由鼠李糖、阿拉伯糖、木糖、葡萄糖、甘露糖和半乳糖等6种单糖组成,它在水溶液中应以有序的螺旋构象存在,其一级结构为:主链的骨架结构由鼠李糖、葡萄糖和半乳糖构成,这3种单糖都有可能连接支链,不接支链时其连接方式为b1→3,支链主要由阿拉伯糖构成,其连接方式可为b1→2,b1→3,b2→3三种,木糖以b1→存在于主链和支链的末端.教育部高等学校骨干教师资助计划项目;; 江西省主要学科学术和技术带头人培养计划项目资

    H_2在K~0-MWCNTs上储存和吸附/脱附特性研究

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    利用高压容积法辅以卸压升温脱附排水法,测定金属K修饰多壁碳纳米管对H2的吸附储存容量.结果表明,在室温(25℃),7.25MPa实验条件下,x%K0-MWCNTs(x%=30%~35%,质量百分数)对H2的吸附储存容量可达3.80wt%(质量百分数),是相同条件下单纯MWCNTs氢吸附储量的2.5倍;室温下卸至常压的脱附氢量为3.36wt%(占总吸附氢量的~88%),后续升温至673K的脱附氢量为0.41wt%(占总吸附氢量的~11%).利用LRS和H2-TPD-GC/MS等谱学方法对H2/K0-MWCNTs吸附体系的表征研究表明,H2在K0-MWCNTs上吸附存在非解离(即分子态)和解离(即原子态)两种吸附态;在≤723K温度下,H2/K0-MWCNTs体系的脱附产物几乎全为H2气;723K以上高温脱附产物不仅含H2,也含有CH4,C2H4和C2H2等C1/C2-烃

    Plasmid DNA Delivery into the Skin via Electroporation with a Depot-Type Electrode

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    Objectives: Non-viral mediated plasmid DNA transfection by electroporation (EP) is an established method for gene transfection. In this study, the usefulness of direct EP at an intradermal (i.d.) site (DEP) with implanted electrodes to achieve a high protein expression level was investigated. In addition, DEP application with various intervals with a low application voltage was also evaluated to confirm its effect on protein expression. Methods: Green fluorescent protein (GFP)- and luciferase-encoding DNA were administrated, and GFP and luciferase were evaluated. Results: A higher protein expression level was observed after green fluorescent protein (GFP)- and luciferase-encoding DNA were delivered by i.d. injection followed by DEP application. When luciferase expression was observed with an in vivo imaging system, continuous expression was confirmed over 21 days after i.d. injection followed by DEP at 100 V. This approach provided increased gene expression levels compared with conventional EP methods via the stratum corneum layer. In addition, the effect of application voltage on luciferase expression was investigated; two-time applications (repeated DEP) at 20 V with 5 min intervals showed similar luciferase expression level to single DEP application with 100 V. Histological observations showed the skin became thicker after a single DEP at 100 V, whereas no apparent thickness changes were confirmed after repeated DEP at 20 V with 5 min intervals. Conclusions: This study revealed that direct i.d. voltage application achieved high protein expression levels even at low voltages. Skin is a promising administration site for DNA vaccines, so this approach may be effective for DNA vaccine delivery into skin tissue.Article number: 1219, This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/)

    山梨県丹波山村旧役場文書の学術的意義に関する検討序説

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    Simultaneous determination of 7 nucleosides in Asterias rollestoni using reversed-phase high performance liquid chromatography

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    建立了罗氏海盘车中7种核苷化合物的反相高效液相色谱分析测定方法。采用超声波辅助提取,选用两根不同的C18色谱柱串联,以甲醇和0.2%(体积分数)乙酸/水溶液为流动相梯度洗脱分离。优化的色谱条件为:柱温为室温,检测波长为260nM,流速为0.8Ml/MIn,进样量为20μl。结果表明,7种核苷化合物在一定的浓度范围内线性关系良好,次黄嘌呤和胸苷的线性范围为0.65~40Mg/l,尿苷、黄嘌呤和肌苷的线性范围为0.80~40Mg/l,胸腺嘧啶的线性范围为1.15~40Mg/l,鸟苷的线性范围为0.50~40Mg/l。样品中7种核苷化合物的加标回收率为90.00%~105.00%,相对标准偏差为0.72%~3.23%。该方法操作简便、灵敏度高、重复性好,回收率高,适用于罗氏海盘车中7种核苷类成分的同时分析,也可用于罗氏海盘车的质量控制和综合评价。A method for the simultaneous determination of 7 nucleosides in Asterias rollestoni was devel-oped using reversed-phase high performance liquid chromatography ( RP-HPLC) .Analytes were extracted by ultrasonic-assisted extraction and separated on two different C18 columns,which were connected in se-ries,under the gradient elution with the mobile phases of methanol and 0.2% ( v/v) acetic acid/water at room temperature.The chromatographic conditions were as follows: flow rate,0.8 mL/min; detection wavelength,260 nm; injection volume,20 μL.Under the optimized conditions,good linear relationships between the values of mass concentrations and the peak areas of hypoxanthine,uridine,xanthine,thy-mine,inosine,guanosine and thymidine were observed in the ranges of 0.65-40,0.80-40,0.80-40,1.15-40,0.80-40,0.50-40,and 0.65-40 mg/L,respectively.The relative standard devia-tions were around 0.72%-3.23% and the recoveries were around 90.00%-105.00%.The results showed that the developed method is sensitive,accurate and reproducible.It is suitable for the analysis of nucleosides in Asterias rollestoni with high recoveries and it is expected to be used for the quality control and evaluation of Asterias rollestoni.国家自然科学基金项目(20905017);海洋公益性行业科研专项(200705011;200805039);海洋局青年基金项目(2010140);海洋一所基本科研业务专项(GY-022008T32;2010G25);中国科学院实验海洋生物学重点实验室开放基金课
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