添加剂对聚吡咯/氧化石墨纳米复合材料结构和性能的影响

采用单体原位聚合法制备了三种聚吡咯/氧化石墨纳米复合材料。通过XRD、FT-IR和TEM对产物进行结构表征,探讨了未加添加剂及分别以N aOH和十二烷基苯磺酸钠为添加剂制得的聚吡咯/氧化石墨纳米复合材料的结构与性能的差别。结果表明,未加添加剂和以N aOH为添加剂时产物为非晶态的剥离型聚吡咯/氧化石墨纳米复合材料;而以十二烷基苯磺酸钠为添加剂时可得到具有层状有序结构的插层型聚吡咯/氧化石墨纳米复合材料。插层型聚吡咯/氧化石墨纳米复合材料的导电和电化学性能优于剥离型聚吡咯/氧化石墨纳米复合材料,它们的提高归因于聚吡咯分子链共轭程度的增加。     

聚苯胺/氧化石墨的合成及其在DNA识别上的应用

采用层离/吸附和原位聚合相结合的方法合成了聚苯胺/氧化石墨复合材料（PAn/GO）.利用TEM、AFM、XRD、FTIR等方法对PAn/GO的结构和电化学性能进行了研究.以PAn/GO修饰炭糊电极为工作电极,采用方波伏安法（SWV）检测了单链小牛胸腺DNA（CTssDNA）和双链小牛胸腺DNA（CTdsDNA）.研究结果表明：PAn/GO为当量直径约60 nm～70 nm的扁球状纳米颗粒,这些纳米颗粒呈链状聚集,并具有电化学活性;聚苯胺（PAn）以双层平行排列的方式嵌入氧化石墨层间和包覆在氧化石墨表面两种形式与氧化石墨结合;PAn/GO修饰炭糊电极识别单链小牛胸腺DNA（CTssDNA）和双链小牛胸腺DNA（CTdsDNA）时的峰电位分别为90.99 mV和18.00 mV.     

聚苯乙烯/氧化石墨纳米复合材料的制备与性能

利用十六烷基三甲基溴化铵对氧化石墨进行插层改性。以原住插层聚合的方式合成了聚苯乙烯／氧化石墨（PS／GO）纳米复合材料。用XRD和TEM进行的形态研究表明,氧化石墨被剥离成10nm-30nm厚的层片而分散在聚合物基体中。热重分析证明PS／GO复合材料比PS材料和普通石墨粉填充的PS材料表现出更好的热稳定性。     

聚合物／石墨纳米复合材料的研究进展

简介了石墨的结构特征；阐述了聚合物／石墨纳米复合材料的研究意义；综合评述了聚合物／石墨纳米复合材料的制备方法，其中，特别详细叙述了插层复合技术；介绍了若干知名学者在聚合物／无机粒子／石墨纳米复合材料方面所做的工作，并指出，作者在上述成果的基础上研发出的“反胶束模板—原位聚合纳米复合技术”，能使独特的结构特征和优异的综合性能完美地结合起来，使材料刚柔并济，并将其性能提高到空前的高度。最后，作者展望了本研究领域的发展前景。     

溶液聚合制聚丙烯酰胺/蒙脱土纳米复合材料

利用溶液聚合法制备了聚丙烯酰胺／蒙脱土插层复合材料。XRD、IR等表明，聚丙烯酰胺已进入蒙脱土层间，并使之剥离。DSC表明，剥离型纳米复合材料的热稳定性提高，这是由于蒙脱土纳米片层与基体大分子链相互作用的结果。研究结果表明，复合材料调湿性能优于基体材料。     

聚吡咯/氧化石墨复合材料的制备及其电容性能

以氧化石墨为载体,采用木质素磺酸钠作为掺杂剂,氯化铁作为氧化剂,引发吡咯单体在氧化石墨层发生化学原位聚合反应,制备了聚吡咯(PPy)/氧化石墨复合材料。通过XRD、FTIR和SEM分析分别对复合材料的物相组成、结构和微观形貌进行了表征,通过TGA分析研究了复合材料的热稳定性,采用恒电流充放电、循环伏安和电化学阻抗谱等方法测试分析其电化学性能。研究表明:采用化学原位聚合的方法合成的PPy/氧化石墨复合材料具有"层-球"状的"三明治"型微观结构,以便形成良好的导电网络,其结晶度高、排列规整、缺陷少,复合材料中吡咯单体通过N-H键与氧化石墨的含氧官能团发生键合。PPy/氧化石墨复合材料新颖的微观结构和良好的化学键合状态使其表现出优异的电容性能。在电流密度分别为0.5、1.0、2.0和5.0 A/g时的比电容分别为500、460、427和396 F/g;经过1000次恒电流(2.0 A/g)充放电循环后, PPy/氧化石墨复合材料的比电容保持率为97.2%。      

原位聚合制备不饱和聚酯树脂/高岭土纳米复合材料及性能表征

利用超声法制备了高岭土-DMSO插层复合物前驱体,采取二步取代,原位聚合制备了不饱和聚酯树脂/高岭土纳米复合材料,并用XRD、FT-IR等手段对材料结构进行了表征,研究了纳米复合材料的阻燃性能。结果表明:当DMSO分子插入到高岭土层间时,d(001)值由0.717 nm增大到1.12 nm,插层率为91%,而不饱和聚酯树脂取代DMSO进入高岭土层间后,表征层状结构的d(001)特征衍射峰完全消失,高岭土内表面羟基吸收特征峰(3651 cm-1)和DMSO两个甲基的对称和反对称伸缩振动的吸收特征峰消失。燃烧实验表明这种材料相比纯树脂具有更好的阻燃性能。     

石墨烯补强乳液聚合橡胶研究进展

石墨烯具有优异的力学和电学性能,是制备橡胶纳米复合材料的重要填料。介绍了石墨烯与氧化石墨烯的结构、性质和表征;重点阐述了石墨烯与氧化石墨烯补强乳聚丁苯和丁腈橡胶的原理、方法以及橡胶纳米复合材料的性能;主要通过非官能化和官能化石墨烯、石墨烯混合填料对乳聚丁苯丁腈橡胶进行补强;补强方法包括原位聚合法、溶液混合法、熔融混合法和胶乳共凝聚法;改善了橡胶的机械性能、导电导热性和气体阻隔性等性能。并对石墨烯作为橡胶补强剂的发展作了展望。     

新型抗凝血纳米复合材料的制备及其性能研究

利用溶液插层法合成了新型的硅橡胶/氧化石墨-十六烷基三甲基溴化铵-肝素抗凝血纳米复合材料.通过FT-IR、XRD、SEM和机械性能测试了解改性氧化石墨微观纳米结构对材料宏观性能的影响;溶血试验和血小板粘附试验测定表明硅橡胶/改性氧化石墨抗凝血纳米复合材料的血液相容性得到极大的改善;这种新型的、兼具优良血液相容性和良好力学性能的复合材料可望在生物医学工程方面得到应用.     

一步法制备聚苯乙烯/MoS2插层复合材料及结构与氧化行为研究

用阴离子聚合法原住一步合成了PS／MoS2插层复合材料，通过XRD、FT-IR及SEM对复合材料的结构进行了表征，结果表明，MoS2经聚苯乙烯插层后，层间距扩大了0．672nm，形成的是插层型复合材料。通过XPS对一步法和两步法(剥层重堆法)制备的插层复合材料的氧化行为进行了研究，结果表明，一步法和两步法合成的PS／MoS2插层复合材料的氧化行为不同，前者主要是MoS2中的Mo^4 氧化为Mo^6 ，后者主要是MoS2中的S^2-氧化为S^6 。     

Enhancement of electroconductivity of polyaniline/graphene oxide nanocomposites through in situ emulsion polymerization

The present study introduces a systematic approach to disperse graphene oxide (GO) during emulsion polymerization (EP) of Polyaniline (PANI) to form nanocomposites with improved electrical conductivities. PANI/GO samples were fabricated by loading different weight percents (wt%) of GO through modified in situ EP of the aniline monomer. The polymerization process was carried out in the presence of a functionalized protonic acid such as dodecyl benzene sulfonic acid, which acts both as an emulsifier and protonating agent. The microstructure of the PANI/GO nanocomposites was studied by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, UV–Vis spectrometry, Fourier transform infrared, differential thermal, and thermogravimetric analyses. The formed nanocomposites exhibited superior morphology and thermal stability. Meanwhile, the electrical conductivities of the nanocomposite pellets pressed at different applied pressures were determined using the four-probe analyzer. It was observed that the addition of GO was an essential component to improving the thermal stability and electrical conductivities of the PANI/GO nanocomposites. The electrical conductivities of the nanocomposites were considerably enhanced as compared to those of the individual PANI samples pressed at the same pressures. An enhanced conductivity of 474 S/m was observed at 5 wt% GO loading and an applied pressure of 6 t. Therefore, PANI/GO composites with desirable properties for various semiconductor applications can be obtained by in situ addition of GO during the polymerization process.     

Structural analysis of graphene oxide/silver nanocomposites: optical properties,electrochemical sensing and photocatalytic activity

In the present study, graphene oxide/silver (GO/Ag) nanocomposites were synthesized via a facile simple one pot chemical reduction method using ethylene glycol/sodium borohydrate (EG/NaBH₄) as solvent and reducing agent. GO was selected as a substrate and stabilizer to prepare GO/Ag nanocomposites. The synthesized GO/Ag nanocomposites were characterized by a series of techniques. Highly monodispersed stable crystalline silver nanoparticles having a face-centered cubic (fcc) phase were confirmed by X-ray powder diffraction (XRD) on GO signature. Scanning electron microscopy images showed that Ag nanoparticles are deposited on the GO sheet with a narrow size distribution. Transmission electron microscopy observations revealed that large numbers of Ag nanoparticles were uniformly distributed on GO sheet and well separated with an average size of 18 nm. Ultraviolet–visible (UV–Vis) spectroscopic results showed the peak of GO and surface plasmon resonance (SPR) of Ag nanoparticles. The SPR property of GO/Ag nanocomposites showed that there was an interaction between Ag nanoparticles and GO sheet. The intensities of the Raman signal of GO/Ag nanocomposites are gradually increased with attachment of Ag nanoparticles i.e. there is surface-enhanced Raman scattering activity. Electrochemical investigations indicated that the nanocomposites possessed an excellent performance for detecting towards 4-nitrophenol. An application of the obtained GO/Ag nanocomposites as a catalyst in the reduction of 4-nitrophenol to 4-aminophenol by NaBH₄ was demonstrated. The GO/Ag nanocomposites exhibited high activity and stability for the catalytic reduction of 4-nitrophenol. The prepared GO/Ag nanocomposites act as photo-catalysts.     

An efficientfficient,controllable and facile two-step synthesis strategy: Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>@RGO composites with various Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> nanoparticles and their supercapacitance properties

An efficient,controllable,and facile two-step synthetic strategy to prepare graphene-based nanocomposites is proposed.A series of Fe3O4-decorated reduced graphene oxide (Fe3O4@RGO) nanocomposites incorporating Fe3O4 nanocrystals of various sizes were prepared by an ethanothermal method using graphene oxide (GO) and monodisperse Fe3O4 nanocrystals with diameters ranging from 4 to 10 nm.The morphologies and microstructures of the as-prepared composites were characterized by X-ray diffraction,Raman spectroscopy,nitrogen adsorption measurements,and transmission electron microscopy.The results show that GO can be reduced to graphene during the ethanothermal process,and that the Fe3O4 nanocrystals are well dispersed on the graphene sheets generated in the process.The analysis of the electrochemical properties of the Fe3O4@RGO materials shows that nanocomposites prepared with Fe3O4 nanocrystals of different sizes exhibit different electrochemical performances.Among all samples,Fe3O4@RGO prepared with Fe3O4 nanocrystals of 6 nm diameter possessed the highest specific capacitance of 481 F/g at 1 A/g,highlighting the excellent capability of this material.This work illustrates a promising route to develop graphene-based nanocomposite materials with a wide range of potential applications.     

One step synthesis of β-FeOOH nanowire bundles/graphene oxide nanocomposites

A nanocomposite of graphene oxide (GO) and β-ferric oxyhydroxide (β-FeOOH) nanowire bundles is synthesized by in situ hydrolysis of the precursor ferric chloride and GO nanosheets. Characterization by X-ray diffraction, transmission electron microscopy, and thermogravimetric analysis established the composite structure of the synthesized sample. The results revealed that the surface of GO nanosheets was uniformly assembled by numerous nanowire bundles with diameters in the range of 30–50 nm and lengths of 100–150 nm. Furthermore, β-FeOOH/GO nanocomposites showed a very high adsorption capacity of Congo red and thus these nanocomposites can be used as good adsorbents and can be used for the removal of organic dye from the waste water system.     

Synthesis and properties of polystyrene/Fe-montmorillonite nanocomposites using synthetic Fe-montmorillonite by bulk polymerization

Fe-montmorillonite (Fe-MMT) was hydrothermally synthesized. It was modified by cetyl trimethylammonium bromide (CTAB) and successfully synthesized polystyrene/Fe-montmorillonite (PS/Fe-MMT) nanocomposites via bulk polymerization for the first time. The resulting nanocomposites were characterized by X-ray diffraction (XRD) spectra, transmission electron microscopy (TEM), high resolution electronic microscopy (HREM), thermal gravimetric analysis (TGA) and cone calorimeter. XRD, TEM and HREM indicated that both intercalated and exfoliated-intercalated structures were observed. In comparison with pure PS, the thermal stability was notably improved in the presence of clay. From cone calorimetry it was found that the peak of heat release rate (HRR) was significantly reduced by the formation of the nanocomposites. Also intercalated nanocomposites were more effective than exfoliated-intercalated nanocomposites in fire retardancy.     

Superparamagnetic magnetite nanocrystals-graphene oxide nanocomposites: facile synthesis and their enhanced electric double-layer capacitor performance

Superparamagnetic magnetite nanocrystals-graphene oxide (FGO) nanocomposites were successfully synthesized through a simple yet versatile one-step solution-processed approach at ambient conditions. Magnetite (Fe3O4) nanocrystals (NCs) with a size of 10-50 nm were uniformly deposited on the surfaces of graphene oxide (GO) sheets, which were confirmed by transmission electron microscopy (TEM) and high-angle annular dark field scanning transmission election microscopy (HAADF-STEM) studies. FGO with different Fe3O4 loadings could be controlled by simply manipulating the initial weight ratio of the precursors. The M-H measurements suggested that the as-prepared FGO nanocomposites have a large saturation magnetizations that made them can move regularly under an external magnetic field. Significantly, FGO nanocomposites also exhibit enhanced electric double-layer capacitor (EDLC) activity compared with pure Fe3O4 NCs and GO in terms of specific capacitance and high-rate charge-discharge.     

热处理条件对氧化石墨结构和导电性能的影响

氧化石墨是石墨的氧化产物．由于它的碳层表面引入了很多极性功能团，使得很多分子都能够嵌入其层间形成纳米复合物，但也正是这些功能团使得它散失了石墨良好的导电性。为了考察氧化石墨受热处理后还原的可能性，通过X-射线衍射、扫描电镜、红外光谱分析以及元素分析等手段研究了氧化石墨在不同热处理条件下的结构变化。研究发现热处理时的升温速度对氧化石墨的结构影响很大，快速升温时，氧化石墨迅速分解，发生膨胀形成类似于膨胀石墨的含有丰富的50nm至5μm左右孔洞的一种结构；而当缓慢升温时，氧化石墨随着热处理温度的升高，逐渐恢复成类似于石墨的结构，同时电导率也随热处理温度的升高而提高，当热处理温度高于180℃时，电导率大于1S／cm。这些结果表明利用氧化石墨作为前驱体，通过先制备聚合物／氧化石墨纳米复合物后经热处理来得到导电性的聚合物／碳纳米复合材料是可行的。     

纳米金磁颗粒的组装法制备及其核酸分离性能

以丙烯酰胺为单体,采用原位聚合法制备了Fe3O4/聚丙烯酰胺纳米磁粒(Fe3O4/PAM);利用胺基与金的相互作用,借助自组装法在Fe3O4/PAM表面组装金胶体制备了草莓型纳米金磁颗粒(Fe3O4/PAM/Au);用TEM、VSM、UV-vis对其进行了表征,并考察了表面修饰核酸探针的金磁颗粒对核酸靶分子的分离能力。结果表明,Fe3O4/PAM/Au粒子的粒径为36～56nm,具有超顺磁性,饱和磁化强度为31.2emu/g,分散在磷酸盐缓冲液中的Fe3O4/PAM/Au完全磁分离的时间为6min。修饰核酸探针的Fe3O4/PAM/Au粒子可以借助核酸杂交作用分离核酸靶分子,分离能力为118pmol/mg。