首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到19条相似文献,搜索用时 109 毫秒
1.
以聚乙烯醇(PVA)作为络合剂与醋酸镁反应制得前驱体,采用静电纺丝法制得聚乙烯醇(PVA)/醋酸镁复合纤维,经焙烧后得到分布均匀、具有较高比表面积和多孔结构的。MgO纳米纤维.对所制得的纳米纤维的结晶度、纯度和表面形貌,分别采用X射线粉末衍射、差热一热重分析(TG-DTA)、红外光谱(IR)、扫描电镜(SEM)等分析测试手段进行了表征.结果表明,煅烧温度对纳米纤维的结晶度和形貌有很大影响.  相似文献   

2.
静电纺丝制备自修复功能纤维及其自愈合性能表征   总被引:1,自引:0,他引:1  
应用静电纺丝技术,以聚苯乙烯和愈合剂的共混溶液为纺丝液,制备了含有愈合剂的功能纤维,并以其制备了具有自修复性能的纤维/树脂复合材料.通过扫描电子显微镜(SEM)、红外光谱(FTIR)、荧光显微镜等对纤维的形貌和结构进行了表征,探讨了纺丝溶液的组成对纤维形貌和结构的影响.纤维中愈合剂的含量随纺丝液中愈合剂浓度的增加而增大,但可纺性随之变差.通过SEM观察了所制备的复合材料表面预制裂纹的修复,在一定温度下裂纹处纤维中的愈合剂(分别为环氧和其固化剂)释放并进一步反应,经过愈合复合材料的拉伸强度提高了2.81 MPa,力学性能明显改善.  相似文献   

3.
通过静电纺丝技术制备了磷钼酸/PMMA复合纤维,研究了PMMA的相对分子质量、磷钼酸的含量及混合溶剂中DMF与乙醇的体积比对复合纤维形貌及直径的影响。通过扫描电镜(SEM)对复合纤维的形貌进行了观察,并测试了不同条件纺丝溶液的电导率、黏度和表面张力。研究发现,PMMA的相对分子质量和DMF与乙醇的体积比对复合纤维的形貌影响较为明显,磷钼酸的含量对复合纤维的直径影响显著。较为理想的纺丝条件为:PMMA的重均分子量为60000,纺丝液中磷钼酸的含量为16mg/mL,DMF与乙醇的体积比为6∶4。  相似文献   

4.
李从举  黄丽  肖斌  冯苹 《化学学报》2010,68(6):571-575
首先合成了纳米磷酸钙(NCP),用扫描电镜(SEM)和X射线衍射(XRD)进行了表征.再利用静电纺丝法制备了PLA/NCP复合纳米纤维,对纤维进行了TEM,SEM,XRD以及单轴拉力测试的表征.TEM和XRD测试表明,NCP已成功掺杂到聚乳酸纤维中,获得的纤维为复合纤维.SEM测试表明,NCP在溶液中浓度较小时,复合纳米纤维的形貌变化不大;NCP浓度超过PLA质量的7%后,纤维表面出现粒状物;随着浓度继续增大,粒状物逐渐增多,最后很难成纤.拉伸实验结果表明,复合纤维拉伸强度先随着NCP浓度的增加而增大,但NCP浓度超过7%后拉伸强度随着浓度的增加反而减小.  相似文献   

5.
静电纺丝是一种简单有效的制备聚合物纳米纤维的技术,在组织工程、药物控释和传感器等方面具有广泛的应用。采用静电纺丝技术制备得到的纳米纤维膜具有比表面积大、孔隙率高和易于分离回收等优点,可以作为一种优良的酶固定化载体,目前在酶固定化领域受到了广泛的关注。本文综述了近年来静电纺丝纳米纤维膜固定化酶的研究进展,在阐述静电纺丝纳米纤维膜制备技术的基础上,详细介绍了纳米纤维膜表面担载法和包埋法固定化酶的原理和方法,分析了不同固定化方法的优缺点,并讨论了静电纺丝纳米纤维膜固定化酶的应用前景,对静电纺丝纳米纤维膜固定化酶的发展方向进行了展望。  相似文献   

6.
以聚乙烯醇溶液为络合剂与醋酸锌反应制得前驱体溶液,采用静电纺丝法制备PVA/Zn(Ac)2复合纳米纤维,经过高温煅烧得到直径为100 nm的ZnO纳米纤维,采用差热-热重分析、红外光谱分析、X射线粉末衍射分析及扫描电镜等手段对其进行了表征.光催化降解酸性品红溶液的实验结果表明,太阳光照65 min使质量浓度为45 mg/L酸性品红水溶液的脱色率达93%;另外,重复使用ZnO纳米纤维4次之后,其光催化降解率仍能达到70%以上.这充分说明ZnO纳米纤维具有良好的光催化性能.  相似文献   

7.
采用静电纺丝技术将导电聚苯胺(PANI)和铕/铽稀土配合物掺杂到高分子基质聚乙烯吡咯烷酮(PVP)中,制备出荧光导电复合纳米纤维。用扫描电镜(SEM)、荧光光谱仪(FL)、宽频介电松驰谱仪对荧光导电复合纳米纤维的性能进行分析,结果显示,在270nm紫外光激发下,铕系列与铽系列复合纳米纤维分别发出红光和绿光。同时,复合纳米纤维的电导率可以达到1.18×10~(-6) S/cm,两种复合纳米纤维同时具有优异的荧光性能及良好的导电功能。  相似文献   

8.
以辛酸亚锡为催化剂, 胆固醇(CHOL)为共引发剂引发D,L-丙交酯开环聚合, 制备了胆固醇-g-聚(D,L-乳酸)(CHOL-g-PDLLA)低聚物, 采用偏光显微镜(POM)和差示扫描量热(DSC)方法考察了其液晶特性. 通过静电纺丝技术制备了CHOL/PDLLA和CHOL-g-PDLLA /PDLLA复合纳米纤维膜, 对其形貌、界面相容性、孔隙率、拉伸性能和细胞相容性进行了研究. 结果表明, CHOL-g-PDLLA为一种热致胆甾型液晶, 液晶温度区间为21.8~74.5 ℃; CHOL-g-PDLLA/PDLLA复合纳米纤维膜的纤维形态良好, 表面均匀光滑, 孔隙率在70%~75%之间, 且其界面相容性优于相应的CHOL/PDLLA. 随着CHOL和CHOL-g-PDLLA含量的增加, 复合纳米纤维膜的拉伸强度逐渐下降, 但CHOL-g-PDLLA/PDLLA复合纳米纤维膜的拉伸强度显著大于CHOL/PDLLA. 体外骨髓间充质干细胞培养结果显示, CHOL-g-PDLLA/PDLLA复合纳米纤维膜具有良好的细胞相容性, 且优于相应的PDLLA和CHOL/PDLLA纳米纤维膜.  相似文献   

9.
采用高压静电纺丝技术, 在非对称异型电极上制备得到放射状聚酰亚胺(PI)纳米纤维膜. 采用环境扫描电子显微镜(ESEM)观察了PI膜的微观形貌以及纳米纤维的排列状态; 采用接触角测量仪研究了水滴浸润性的变化; 采用高敏感性力学微电力学天平测量了水滴的黏附力, 分析了微观形貌变化与水滴浸润性质和黏附性质的关系. 结果表明, 该PI纳米纤维膜沿着非对称异型电极三角电极至弧型电极方向纤维排列由密到疏, 呈放射状, 具有独特的微结构梯度; 整个纤维膜上的PI纳米纤维直径均一且具有光滑均匀表面, 纤维与纤维之间的距离约为几微米到几十微米. 由于PI纳米纤维膜所具有的独特的微结构梯度, 致使沿着微结构梯度方向水滴的接触角(从超疏水到疏水)和黏附力(从低黏附到高黏附)均表现出梯度变化的特征.  相似文献   

10.
静电纺丝法制备超细聚苯乙烯纳米纤维   总被引:1,自引:0,他引:1  
采用静电纺丝方法制备了超细聚苯乙烯纤维, 通过向溶液中添加有机胺盐并降低溶液浓度将纤维的平均直径降至100 nm, 并研究了盐的添加量对纤维直径的影响.  相似文献   

11.
林美娟  王文  章文贡 《应用化学》2004,21(12):1241-0
Eu(OPri)3/Tb(OPri)3共掺杂P(MMA-co-St);Eu(OPri)3/Tb(OPri)3;共掺杂;P(MMA-co-St);荧光性能  相似文献   

12.
Ferroelectric polymers, such as poly(vinylidene fluoride-trifluoroethylene)[P(VDF-TrFE) or PVTF] have attracted growing interest in developing flexible devices because of their excellent ferroelectricity and piezoelectricity. High coercive field(Ec) inherent to PVTF for switching its polarization, however, is not beneficial for practical memory or sensor device application. Different strategies, including irradiation and interface control, have been thus developed to reduce Ec. Despite many efforts, a facile approach to tailoring intrinsic Ec of PVTF has not been documented. In this work, an optically controlled Ec was reported, which is achieved for the first time by introducing photosensitive MAPbI3 nanocrystals into PVTF matrix. When exposed to the irradiation of 532 nm laser light, a decreased Ec of the composites can be achieved reversibly by increasing the light density. The decreased level of Ec increases as the MAPbI3 content enhanced, and a 10.7% reduction of Ec can be achieved in 15%(mass fraction) MAPbI3/PVTF samples. These results could be attributed to loading an internal stress on PVTF, which was generated by the photostriction of MAPbI3 nanocrystals. This explanation was further supported by in-situ XRD results under irradiation of 532 nm laser light. Our findings may offer the opportunity to optically modulate the ferroelectric properties of PVTF composites for optimized device performances.  相似文献   

13.
Preparation of Thick PZT Ceramic Film by an Interfacial Polymerization   总被引:1,自引:0,他引:1  
The formation of a PZT film of 10–20 m in thickness via an interfacial polymerization of metal-organic precursors has been studied. A commercially available PZT precursor solution developed for dip- or spin-coating was diluted with hexane containing acetylacetone as chelating agent. The solution was poured on water contained in a teflon reaction container of 88 mm inside diameter. A translucent gel film was formed at the interface of the two immiscible liquids. While floating on water it shrank as the evaporation of solvent proceeded until its diameter decreased to about 45% of its initial value. The dried gel film was almost pore free and its thickness was estimated to be about 10 m.  相似文献   

14.
Ferroelectric polymers are particularly attractive for applications in flexible electronic devices, and controlling its crystalline phase growth is crucial for obtaining optimized ferroelectric properties. Herein we report that a very low introduction (0.2% (w)) of single-domain ferroelectric PbTiO3 nanoplates can effectively mediate the nucleation and subsequent growth of a crystalline phase within P (VDF-TrFE) (denoted by PVTF), forming highly oriented films and significantly improving the ferroelectric properties due to an alignment of the polarization directions of the polymer and the nanoplates.  相似文献   

15.
In this paper a synthetic Poly(L-lactic-co-ϵ-caprolactone) [P(LLA-CL)] (75:25) copolymer has been fabricated into a nanofibrous structure by electrospinning. The polymer crystal structure has been investigated by DSC and x-ray diffraction method. During electrospinning at room temperature, a crystallization of LLA sequence in the P(LLA-CL) copolymer could not form, while a relatively regular arrangement of CL sequence was observed. In order to obtain a tubular scaffold, a rotating mandrel was designed to collect the fiber, so that the tubular scaffold can be retrieved from the mandrel with an inner diameter same as that of the outer diameter of the mandrel. An auxiliary electrode with a sharp edge and a negative charge was set under the mandrel to guide the fiber deposition on the mandrel. When the sharp edge bar was vertical to the rotating axle of the mandrel and just beneath the spinning nozzle, nanofibers with circumferential alignment were obtained. With this method it is possible to obtain a tubular scaffold with suitable fiber alignment for blood vessel tissue engineering.  相似文献   

16.
Summary: We have used the process of electrospinning to produce fibers of poly(dicyclopentadiene) with diameters on the submicron scale. The material, formed from a monomer‐catalyst solution, polymerized in flight during the electrospinning process. Fibers were collected over trenches etched in silicon and the Young's moduli were measured using an atomic force microscope to measure force‐displacement curves. The resulting values of Young's moduli are larger than typical values for bulk polymer material.

SEM image of suspended PDCPD fiber.  相似文献   


17.
PZT (PbZr0.53Ti0.47O3) films and powders have been prepared by a precursor mixture containing Pb(NO3)1.5EO3 (EO3=triethylene glycol) and Zr- and Ti-methoxy ethanolates. The gel films have been deposited on Si/Ti/Pt substrates and on glass substrates from which they can easily be removed. The PZT films on the Si/Ti/Pt substrates were prepared with thicknesses up to 200 nm per layer after heating to 700°C. The phase development on heat-treatment of loose gel films to yield PZT was investigated by Powder-XRD, FT-IR, SEM-EDS, TEM-EDS, thermo-mass spectroscopy and DSC and the PZT was found to form in the region 550–700°C. PZT powders of 50–5000 nm sizes were prepared by hydrolysis under basic conditions and washing with water followed by heat-treatment to 650°C.  相似文献   

18.
We present a hydrothermal method to deposit PZT films. It uses a single-step hydrothermal process and user-friendly precursors. Pb(Zr0.52,Ti0.48)O3 polycrystalline films, 5–10 μm thick, were produced in an aqueous basic solution (4M KOH) on a titanium substrate in a closed autoclave at 180 °C. A time-depending study to see the evolution of the films' formation is described. Some actuation testing is also presented.  相似文献   

19.
采用原位聚合法制备了乙烯基酯树脂(VER)/苯乙烯-乙烯-丙烯(SEPS)嵌段共聚物复合材料,并用SEM、DSC等对其结构进行了表征,研究了组分变化对VER/SEPS的结构及其力学性能的影响。结果表明:原位聚合法制得的VER/SEPS复合材料具有互穿网络(IPN)结构;随着体系中SEPS含量的增加,最大拉伸强度呈下降趋势,断裂伸长率和冲击强度呈现上升趋势;当wSEPS<0.175,wVER=0.15时杨氏模量可提高约800%。  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号