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1.
本文报道用径向分布函数法对含氟的锌离聚体微现结构进行分析。从所测得的干涉函数、双体相关函数及径向分布函数等结构参量可知,锌离聚体的离子微区是由四配位锌氧四面体结构单元构成,配位数为4,Zn~(2+)-O键长2.24A,离子微区尺寸约为10.47A,其可能结构模式如图6所示。  相似文献   

2.
离聚体的结构表征:Ⅳ.径向分面函数法测定...   总被引:4,自引:0,他引:4  
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3.
离聚体的结构表征:Ⅱ.含氟离聚体的FT—IR研究   总被引:9,自引:1,他引:9  
本文报导了以甲基丙烯酸氟醇酯-丙烯酸共聚物为基础的羧酸型钙、钠离聚体在不同温度及时间下的FT-IR图谱的变化规律。探讨了在离聚体聚集态中钙、钠离子的局部配位形式及结构。  相似文献   

4.
离聚体的结构表征:V.含氟离聚体中离子...   总被引:7,自引:1,他引:7  
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5.
本文用DSC方法研究了羟酸型含氟离聚体中不同金属离子种类、可离子化基团含量、配位结构单元构型及离子微区大小对离聚体中离子微区稳定性的影响。实验表明:离聚体中金属离子配位能力愈强,羟酸含量愈高,离子微区尺寸愈大,则相应离聚体中离子微区稳定性愈大。铅高聚体>锌离聚体>钙离聚体>钠离聚体。  相似文献   

6.
由摩尔比分别为1:2和1:8的NiCl2·6H2O和Na2B4O7·10H2O作为反应物, 合成两种非晶态镍硼酸盐, 同时通过水热法合成β-Ni(OH)2. 化学分析和热重-微商热重法(TG-DTG)分析结果确定两种非晶态镍硼酸盐的分子组成分别为NiO·0.8B2O3·4.5H2O和NiO·B2O3·3H2O. 激光拉曼(Raman)实验结果表明镍硼酸盐样品中主要存在的硼氧阴离子为B3O3(OH)52-和B2O(OH)62-. 同步辐射扩展X射线吸收精细结构(EXAFS)方法对样品进行结构解析, 通过数据拟合给出样品中Ni 原子周围近邻配位原子种类、配位数以及原子间距离. 用不同晶体结构作为标准对两种非晶态镍硼酸盐进行拟合的结果表明, 样品中Ni 原子周围局域结构与Ni3B2O6晶体(ICSD No.31387)中的吻合较好. Ni 原子周围配位原子为O、B和Ni, 对于NiO·0.8B2O3·4.5H2O, 配位数分别为5.7、3.8和3.8, 配位距离分别为0.208、0.263 和0.311 nm; 对于NiO·B2O3·3H2O, 配位数分别为6.0、4.0 和4.0, 配位距离分别为0.207、0.262和0.310 nm.  相似文献   

7.
通过氯磺化共聚物的水解合成了乙烯-丙烯共聚物磺酸钠离聚物,对离聚物的结晶度和其中硫、氯、钠元素的含量进行了表征.当离子含量达到5—7 mol%时,离聚物的LAXD曲线出现离子峰;DSC指出Tg急剧升高,而低于此离子浓度的离聚物均不出现这些现象.反映出此离子浓度下的离聚物,离子基因可能聚集形成离子簇结构.  相似文献   

8.
含氟离聚体的多相结构及大分子链运动的NMR研究   总被引:1,自引:0,他引:1  
本文用13C自旋-自旋弛豫时间T2表征了以丙烯酸-1,1,5-三氢全氟戊酯-丙烯酸共聚物为基础的离聚体体系的多相结构和大分子链段运动特性,结果表明:离子微区和聚合物基体之间存在界面层,聚合物主链的运动活性与离聚体的共聚物组成、金属离子特性、离子化程度、离子微区的稳定性和离子微区内的精细结构均有密切关系.  相似文献   

9.
本文用~(13)C自旋-自旋弛豫时间T_2表征了以丙烯酸-1,1,5-三氢全氟戊酯-丙烯酸共聚物为基础的离聚体体系的多相结构和大分子链段运动特性,结果表明:离子微区和聚合物基体之间存在界面层,聚合物主链的运动活性与离聚体的共聚物组成、金属离子特性、离子化程度、离子微区的稳定性和离子微区内的精细结构均有密切关系.  相似文献   

10.
由摩尔比分别为1:2和1:8的NiCl2·6H2O和Na2B4O7·10H2O作为反应物,合成两种非晶态镍硼酸盐,同时通过水热法合成β-Ni(OH)2.化学分析和热重-微商热重法(TG-DTG)分析结果确定两种非晶态镍硼酸盐的分子组成分别为NiO·0.8B2O3·4.5H2O和NiO·B2O3·3H2O.激光拉曼(Raman)实验结果表明镍硼酸盐样品中主要存在的硼氧阴离子为B3O3(OH)52-和B2O(OH)62-.同步辐射扩展X射线吸收精细结构(EXAFS)方法对样品进行结构解析,通过数据拟合给出样品中Ni原子周围近邻配位原子种类、配位数以及原子间距离.用不同晶体结构作为标准对两种非晶态镍硼酸盐进行拟合的结果表明,样品中Ni原子周围局域结构与Ni3B2O6晶体(ICSD No.31387)中的吻合较好.Ni原子周围配位原子为O、B和Ni,对于NiO·0.8B2O3·4.5H2O,配位数分别为5.7、3.8和3.8,配位距离分别为0.208、0.263和0.311 nm;对于NiO·B2O3·3H2O,配位数分别为6.0、4.0和4.0,配位距离分别为0.207、0.262和0.310 nm.  相似文献   

11.
Core-shell and multilayered nanoparticles based on magnetite core with different metallic spacing and over-layers are prepared in one pot synthesis and characterized. The spacer layers were made from Au, Cu or Ag precursors. The nanoparticles were fabricated by a modified chemical seed based method. The obtained nanoparticles were examined by X-ray diffraction, Energy-dispersive X-ray spectroscopy, Transmission Electron Microscopy, Differential Scanning Calorimetry and Infrared spectroscopy. Magnetic properties of the nanoparticles were tested by Mössbauer spectroscopy and Magnetometry. Magnetization and Mössbauer measurements show that the presence of the metallic layers influences the magnetic state of the particles. XRD and EDX confirm layered structures of nanoparticles. Proposed synthesis allows for fabrication of layered particles with controlled morphology and register properties changes which are related to the nature of each subsequent layer.  相似文献   

12.
几种寡聚古罗糖醛酸的制备和结构表征   总被引:5,自引:1,他引:4  
以多聚古罗糖醛酸为原料,在稀酸加压条件下进行酸水解得到寡聚古罗糖醛酸混合物,用低压凝胶渗透色谱(LPGPC)和高效液相色谱(HPLC)进行分离纯化,并用荧光基团辅助碳水化合物电泳(FACE)检测纯度.运用IR,ESI/MS/MS,1D,2DNMR等方法对古罗糖醛酸二糖至五糖的化学结构进行了表征.  相似文献   

13.
二烃基锡双(O,O-二硫代磷酸酯)的合成和波谱研究   总被引:1,自引:0,他引:1  
合成了15个二烃基双(O,O-二硫代磷酸酯)化合物。利用IR、(1H、13C、119Sn)NMR表征了化合物的结构。这是一类六配位变形八面体结构的二烃基锡化合物。对化合物的质谱裂解机制进行了讨论。  相似文献   

14.
    
A homopolysaccharide fraction (PEP-1A) with desired immunomodulatory activity was isolated from culture broth of Parabacteroides distasonis. Structural characterization uncovered that PEP-1A had a molecular weight of 3.40 × 106 Da and possessed mannose merely. Comprehensive analysis of FT-IR, GC–MS and 1D/2D NMR confirmed that the structure of PEP-1A was expected as follows:
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Finally, the activity assays on RAW 264.7 macrophages showed that PEP-1A could promote proliferation, increase the production of reactive oxygen species (ROS), enhance the phagocytosis, and promote the secretion of nitric oxide (NO) and inflammatory cytokines including IL-1β, IL-6 and TNF-α. Furthermore, PEP-1A could give play to immunoregulation effect through NF-κB, MAPK and Akt signaling pathways. Collectively, the study of PEP-1A offers a molecular underpinning for the future application of PEP-1A as a potential immunostimulant.  相似文献   

15.
STRUCTURALCHARACTERIZATIONOFPd-SnO_2/D3520 CATALYSTSHuWeibing(HubeiInstituteforNationalities,Enshi,445000)ZhouZhongxin;ZhangM?..  相似文献   

16.
A zinc-nicotinate complex has been prepared by direct reaction of zinc acetate and nicotinic acid in the presence of template tetramethylethylenediamine and is characterized by elemental analysis, FTIR, and TGA/DTA. The Zn complex was a precursor for the synthesis of ZnO nanoparticles. A correlation of the thermal and spectral properties of the precursor complex with its structure has been discussed. Thermolysis under air was studied by thermogravimetry, and the resulting ZnO product was characterized by XRD and TEM, showing compact particles with a diameter of about 17–50?nm.  相似文献   

17.
STRUCTURALCHARACTERIZATIONOFPd-SnO_2/D_(3520)CATALYSTSHuWeibing(HubeiinstituteforNationalities,Enshi,445000)ZhouZhongxin;Zhang...  相似文献   

18.
La1-xCexFe1-y-nCoyRunO3三效催化剂的结构表征及催化性能   总被引:3,自引:0,他引:3  
用溶胶-凝胶法合成了La1-xCexFe1-y-nCoyRunO3(x,y=0.1~0.5,n=0.01~0.1)系列催化剂,XRD对晶体结构的表征发现,掺入Ru后基本结构未改变,但2θ值减小,晶胞参数变大.红外光谱分析表明,Ru改性的催化剂对应的特征峰位和峰形基本相似,但随着Ru掺杂量的增加,600cm-1附近的谱带向高波数方向移动,n=0.01的样品,ν1和ν2向低波数方向移动,n=0.05样品的ν1带出现最大吸收峰.XPS研究表明,掺杂Ru后Fe的外层电荷密度增大,并以多种价态存在;随着掺杂量的增加,表层中的Ce由与氧结合转变为与多羟基结合,其它氧种含量增加,催化活性增强.O2-TPD结果表明,掺杂Ru使催化剂表面的吸附氧和晶格氧脱附温度降低,A离子空位增加.H2-TPR研究表明,掺杂Ru使A离子空位增加,晶格氧活动性增强,催化活性提高;La0.8Ce0.2Fe0.7Co0.2Ru0.1O3的催化性能最佳.  相似文献   

19.
Na2Ti3O7 and Na2Ti6O13 were synthesized by sol-gel method in order to obtain pure phases. Different heat-treatments were applied on powders and pellets of these materials. The effects were studied by XRD, dilatometry, TGA-DTA, SEM and electrochemical impedance spectroscopy. Pure Na2Ti3O7 was obtained at 973 K. Sintering at 1373 K caused a partial decomposition into Na2Ti6O13. The Na2Ti3O7 powder sintered at 1273 K showed polygonal microstructure. Na2Ti3O7 pellets sintered at 1323 K for 10 h exhibited large structures. This latter microstructure decreased the electrical conductivity of Na2Ti3O7. Pure Na2Ti6O13 was obtained at 873 K. Sintering at 1073 K caused a partial decomposition into TiO2 (rutile). Na2Ti6O13 pellets sintered at 1323 K for 10 h exhibited common shrinkage behavior. This shrinkage process increased the electrical conductivity of this material. The presence of TiO2 resulted in a oxygen partial pressure dependence of the electrical conductivity.  相似文献   

20.
A structural and electrical characterization of the system NiNb2−xTaxO6 (0≤x≤2) is presented. For x≤0.25 materials with the columbite-type structure typical of NiNb2O6 have been obtained whereas for x≥1 tri-rutile-like oxides were obtained. The electrical properties are similar in both cases; they are semiconducting with very low electrical conductivity and very high activation energy, though slight differences were found as a function of Ta content. Improvement of conductivity by reducing the stoichiometric materials could not be achieved due to decomposition. In this connection, partial substitution of Nb or Ta by Ti has been carried out in order to create oxygen vacancies. Tantalum was partially replaced by Ti to a significant extent in the tri-rutile structure inducing a slight increasing of conductivity. However, for the columbite case neither Nb nor Ta could be partially replaced. This behavior is quite different from that reported for other similar columbites such as MnNb2O6−δ, which exhibits high electrical conductivity upon substitution of niobium by titanium.  相似文献   

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