耐克在天猫哪家是正品:有会翻译化学的吗

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Transmission electron microscopy (TEM) was used to
identify and characterize carbon nanotubes. Specimens for
TEM observation were prepared by ultra-sonicating carbon
nanotubes in alcohol, then dipping a TEM sample grid into
the dispersion. Nitrogen adsorption isotherms of nanotube
samples were measured at 77.5 K by an ASAP 2010
volumetric sorption analyzer (Micromeritics) with addi-
tional options for the micropore analysis. The volume of
adsorbed nitrogen at 77.5 K was measured as a function of
25 the equilibrium pressure over a range from 10 Torr to
the saturation vapor pressure. Prior to adsorption measure-
ments, samples were outgassed under vacuum at 573 K for
3 h. The pore size distributions (PSD) of samples were
obtained by analyzing the isotherm with BJH equation. To
check any significant chemical modification, the raw and conpurified
sample was analyzed by X-ray photoelectron
spectroscopy (XPS), respectively. Photoelectron spectra of
samples were measured using a PHI5300 X-ray photoelec-
tron spectrometer (PE Corp.) with Al Ka source. The
spectra were recorded at room temperature under high
vacuum. All binding energies (BE) were corrected for
sample charging using the BE of C as an external 1s
standard (284.6 eV). All data were analyzed with the aid of
an Applle Series 3500. Thermo-gravimetric analysis
(TGA) was used to determine the content of the Fe catalyst
in the sample, and a CAHN2000 thermo-gravimetric
analyzer was used to characterize weight loss during
oxidation of the samples in air with heating to 11008C at a
rate of 108C/min.

carbon nanotubes碳纳米管
micropore analysis微孔分析.
adsorbed nitrogen吸附态氮
saturation vapor pressure饱和蒸汽压
pore size distributions孔径分布
X-ray photoelectron spectrometer X射线光电子能谱
binding energies结合能
Thermo-gravimetric analysis热解重量分析(TGA)
Fe catalyst铁催化剂
external standard外标
Micromeritics比表面积-微孔洞测定仪
容量吸附分析仪volumetric sorption analyzer
透射电子显微学Transmission Electron Microscopy

透射电子显微镜(TEM)用于鉴定和测量碳纳米管。透射电子显微镜观察的样品在乙醇中用超声碳纳米管来制备,然后浸入TEM样品滤网进行分散。纳米管样品在77.5 K时的氮吸附等温线用ASAP-2010型容量吸附分析仪(比表面积-微孔洞测定仪) 测定,还可以用来做微孔分析。77.5 K时吸附态氮的体积测定条件是从10 Torr到饱和蒸汽压的恒压下。吸附测定前,样品在573 K 温度下在真空中烘3小时。样品的孔径分布(PSD)用BJH方程分析其等温线得到。为了检查任何显著的化学变化,样品的粗品和纯化产品分别用用X射线光电子能谱仪(XPS)分析。样品的光电子能谱用PHI5300型带有铝-Ka源的X射线光电子能谱(PE公司)测定。能谱在室温下高真空中得以记录。所有样品的结合能(BE)用碳的结合能作为外标 (284.6 eV)进行矫正。所有数据用Applle Series 3500型热解重量分析仪(TGA)分析。热解重量分析仪用于确定样品中铁催化剂的含量,用CAHN2000型热解重量分析仪用来检测样品以108度/分钟的速率加热到11008度(属于程序升温的,我做过)在空气中氧化损失的重量。外标

传输电子显微镜术(TEM) 使用辨认和描绘碳nanotubes 。标本为TEM 观察由超声波处理的碳nanotubes 准备了在酒精里, 然后浸洗TEM 样品栅格入分散作用。氮气nanotube 样品吸附等温线被测量了在77.5 K 由一台尽快2010 容量吸著分析仪(Micromeritics) 以addi- tional 选择为micropore 分析。被吸附的氮气的容量在77.5 K 被测量了作为25 功能平衡压力在一个范围从10 乇对饱和蒸气压力。在吸附措施ments 之前, 样品是outgassed 在真空之下在573 K 为3 h 。毛孔大小分布(PSD) 样品由分析获得了等温线以BJH 等式。检查任一重大化工修改, 未加工和conpurified 样品被X-ray 光电子分光学分析了(XPS), 各自地。光电子范围样品被测量了使用PHI5300 X-射线photoelec- tron 分光仪(PE Corp 。) 以Al 钾来源。光谱被记录了在室温在高真空之下。所有结合能(是) 被改正了为样品充电使用C 是作为外部1s 标准(284.6 eV) 。所有资料在Applle 系列的帮助下被分析了3500 。热重分析法的分析(TGA) 使用确定Fe 催化剂的内容在样品, 和热重分析法的分析仪被使用描绘减重在样品氧化作用期间在空气里以加热对11008C 以率的108C/min 的CAHN2000 。