聚氨酯/碳纳米管复合材料的制备与表征

采用预聚体法制备了聚氨酯/碳纳米管(PU/CNTs)复合材料,考察了该复合材料中CNTs含量对复合材料电性能、力学性能和热性能的影响及复合材料的微观结构。结果表明,碳纳米管在聚氨酯体系中能够较好地分散;扩链/交联剂对PU/CNTs复合材料的导电性能影响较大,TMP比MOCA交联的PU/CNTs复合材料导电性能好;用TMP作交联剂制备的PU/CNTs复合材料的力学性能明显低于以MOCA为扩链剂的PU/CNTs复合材料的力学性能;随着CNTs的加入,PU/CNTs复合材料储能模量和耗能模量明显增加,复合材料的阻尼性能大幅度提高。     

碳纳米管聚氨酯复合材料的制备及其性能研究

将多壁碳纳米管超声分散后,利用直接共混法将分散液与水性聚氨酯混合,使其在平板上流延并烘干成膜,通过扫描电子显微镜(SEM)和X-射线衍射仪(XRD)对该材料的结构和性能进行表征,测定其透光率及抗张强度等,对该材料的性能进行了系统的研究.研究结果表明碳纳米管能够在聚氨酯中分散开,且碳纳米管能够很好的实现对聚氨酯的增强和增韧.     

聚氨酯/碳纳米管复合材料的制备及其性能研究

通过强碱球磨方法对多壁碳纳米管(MWCNTs)进行了改性处理,并对其化学结构和微观形态进行了分析.采用溶液共混法制备了聚氨酯(PUR)/MWCNTs复合材料.利用扫描电子显微镜、傅立叶变换红外光谱仪对其进行了表征.探讨了MWCNTs对PUR/MWCNTs复合材料力学性能、热稳定性以及电导率的影响.结果表明,MWCNTs...     

碳纳米管/聚氨酯复合材料的粘接性能

利用超声分散、酸处理以及表面活性剂分散的方法将碳纳米管分散到蓖麻油中,制备了蓖麻油型聚氨酯/碳纳米管(PUR/CNTs)复合材料,观察了该复合材料的微观结构,探讨了CNTs用量、酸处理时间以及表面活性剂的用量对复合材料粘接性能的影响。结果表明,随着蓖麻油中CNTs用量的增加,该复合材料的粘接强度不断提高,当增加到2%时,粘接强度提高84.4%;硝酸处理3 h的聚氨酯/碳纳米管复合材料的粘接强度最大,比未酸处理的复合材料增加15%;表面活性剂分散的聚氨酯/碳纳米管复合材料的粘接强度能得到进一步的提高。     

丙烯酸酯类聚氨酯/碳纳米管复合材料的制备和性能研究

以异佛尔酮-二异氰酸酯、聚乙二醇和甲基丙烯酸-β-羟乙酯合成的丙烯酸酯类聚氨酯预聚体为基体,添加改性碳纳米管,制备聚氨酯/碳纳米管复合材料。研究了碳纳米管的含量对复合材料的力学性能、热学性能和导电性能的影响。结果表明,当碳纳米管质量分数为0.4%时,复合材料的断裂伸长率提高了13%,冲击强度提高了20%,体积电阻率下降了5个数量级,而对热学性能基本没有影响。     

聚氨酯/碳纳米管功能复合材料的电学性能研究

采用溶液共混法制备了聚氨酯(PUR)/碳纳米管(CNTs)功能复合材料,并分别利用磁力分散和超声分散方法对CNTs进行分散,探讨了CNTs含量对PUR/CNTs复合材料电学性能的影响。结果表明,利用超声分散方法比磁力分散方法获得的CNTs在基体中的分散效果更好,并且随着超声分散时间的延长,分散效果越好;当分散时间为2 h、CNTs的质量分数为5%时,PUR/CNTs复合材料的体积电阻率趋于稳定,可以降到50 MΩ.cm,比纯PUR的体积电阻率下降了6个数量级。     

聚氨酯/碳纳米管复合材料的研究进展

综述了溶剂型聚氨酯/碳纳米管复合材料的制备方法,以及物理机械性能、电磁性能、生物相容性、耐热性和耐磨性等性能,简要介绍了水性聚氨酯/碳纳米管复合材料的制备及其性能,并提出了聚氨酯/碳纳米管复合材料的研究方向。     

喷雾干燥法制备聚氨酯/碳纳米管复合材料的结构与性能

通过喷雾干燥法制备了聚氨酯/碳纳米管复合材料。扫描电子显微镜和透射电子显微镜观察结果表明,碳纳米管在聚氨酯基体中分散较好。X-射线衍射测试表明,碳纳米管对复合材料的微相结构影响较小。随着碳纳米管用量的增加,动态力学性能测试表明复合材料的耐热性有了显著的改善。另外,该复合材料还表现出多功能特性,如高导电性和导热性。随着碳纳米管体积分数的增加,聚氨酯/碳纳米管复合材料的电导率逐渐提高,填充碳纳米管的聚氨酯复合材料的导电逾渗值约为5%。     

聚氨酯／碳纳米管复合材料的研究进展

近年来,利用碳纳米管制备聚氨酯复合材料引起人们的高度重视。本文对聚氨酯/碳纳米管复合材料的研究进展状况进行综述。概述了聚氨酯和碳纳米管的性质以及碳纳米管的改性处理方法;介绍了聚氨酯/碳纳米管复合材料的制备方法,包括物理共混法和原位聚合法;讨论了碳纳米管对复合材料力学性能、电学性能、光学性能以及其他性能的影响。结果表明,碳纳米管的加入使得复合材料在上述性能方面都有不同程度的改善。最后探讨了该研究领域存在的问题及今后可能的发展方向。     

碳纳米管改性聚氨酯复合材料

用原位聚合法制备两组聚氨酯(PUR)/碳纳米管(CNTs)复合材料.一组是在超声波作用下将CNTs直接和PUR复合;另一组是将硅烷偶联剂处理的CNTs在超声波作用下与PUR原位聚合制备PUR/CNTs复合材料.探讨了CNTs含量对复合材料电性能的影响,在w(CNTs)为1.0%时可用作抗静电材料.经硅烷偶联剂处理的CN...     

改性碳纳米管增强热塑性聚氨酯复合材料的性能研究

以碳纳米管（CNTs）和热塑性聚氨酯（TPU）为原料,通过硫酸（H₂SO₄）/硝酸（HNO₃）混合溶液处理碳纳米管颗粒表面以达到改性的效果,使用改性过后的碳纳米管熔融共混制备出TPU/CNTs复合材料。研究了不同含量的CNTs对TPU基体的流变、力学、耐磨性以及热性能的影响。结果表明, 改性过后的CNTs在TPU基体中形成了良好的分散性和相容性;TPU/CNTs复合材料在高频剪切下保留了复合材料的加工流动性,并且复合材料的拉伸强度以及耐磨性相较于TPU有明显的增强,其中在改性碳纳米管含量较低时,复合材料的力学性能改善较为明显;改性CNTs的加入提高了TPU基体的熔融温度和结晶度;改性CNTs的加入提高了复合材料的热降解温度,提高了TPU基体的热稳定性。     

PVC/碳纳米管复合材料的制备

采用原子转移自由基聚合(ATRP)在多壁碳纳米管(MWNTs)表面接枝聚丙烯酸丁酯(PBA)得到MWNTs-PBA,并以此对聚氯乙烯(PVC)改性,采用熔融共混法制备了PVC/MWNTs-PBA复合材料。傅里叶变换红外光谱分析及透射电子显微镜观察结果表明:采用ATRP法成功地将PBA接枝到MWNTs的表面。接枝了聚合物的碳纳米管可以提高复合材料的结晶温度(5 oC左右)、耐热温度(20 oC左右);复合材料的流变性能、导电性能也同时得以提高。     

Mechanical and surface properties of polyurethane/fluorinated multi‐walled carbon nanotubes composites

To improve the mechanical and surface properties of poly(etherurethane) (PEU), multi‐walled carbon nanotubes (MWCNTs) were surface grafted by 3,3,4,4, 5,5,6,6,7,7,8,8,8‐tridecafluoro‐1‐octanol (TDFOL) (MWCNT‐TDFOL) and used as reinforcing agent for PEU. Fourier‐transform infrared spectroscopy revealed the successful grafting of MWCNTs. PEU filled with MWCNT‐TDFOL could be well dispersed in tetrahydrofuran solution, and tensile stress–strain results and dynamic mechanical analysis showed a remarkable increase in mechanical properties of PEU by adding a small amount of MWCNT‐TDFOL. Contact angle testing displayed a limited improvement (just 9°) in the hydrophobicity of PEU surface by solution blending with MWCNT‐TDFOL. However, a large improvement of surface hydrophobicity was observed by directly depositing MWCNT‐TDFOL powder on PEU surface, and the water contact angle was increased from 80° to 138°. Our work demonstrated a new way for the modification of carbon nanotubes and for the property improvement of PEU. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Melt mixing of carbon fibers and carbon nanotubes incorporated polyurethanes

Polyurethane composites filled with carbon fibers (CF) and carbon nanotubes (CNT) were prepared by mixing and injection molding, and its mechanical as well as their thermal properties were investigated. Dynamic mechanical analysis (DMA), thermogravimetry analysis (TGA), and thermal conductivity tests were done, and the properties were evaluated as a function of the filler concentration. The storage modulus of the composites increased with fillers concentration, which also mean the increase of the stiffness, suggest a good adhesion between the polyurethane matrix and the fillers. Addition of more CF and CNT to the composites broadened and lowered the peak of tan δ specifies that the polyurethane composite became more elastic because there is a good adhesion between the fillers and the matrix. The addition of carbon fillers improves the thermal stability of the polyurethane. The inclusions of CNT show a better thermal stability when compared with CF. The addition of carbon fillers also increased the thermal conductivity of the polyurethane composites. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

磁性石墨烯/聚氨酯柔性复合材料的制备及自修复效能

为了提高复合材料的导电、导热及自修复性能,在传统共混法的基础上采用化学沉积法将四氧化三铁（Fe₃O₄）修饰到石墨烯上,得到磁性石墨烯,并将其与聚氨酯、碳纳米管共混后经磁场干预控制石墨烯片层的排列得到磁性石墨烯/聚氨酯柔性复合材料。采用SEM、Raman、FTIR对柔性复合材料的微观形貌、分子结构进行表征,并通过激光导热仪、四探针电阻率测定仪和万能试验机分析磁场调控对复合材料电、热、力学以及修复性能的影响。结果表明：磁场下柔性复合材料中的石墨烯片层排列规则,且层次分明,轮廓清晰可见;其热扩散系数相比于未加磁场提高了10 %~12 %,且在高温下具有稳定性,缺陷修复时间减少了50 %;对比出现缺陷前及修复后的复合材料发现,表面电阻率和抗拉强度分别相差0.006Ω·cm和2.4MPa,而无磁场环境下的变化量是其 3～4倍。     

Enhanced mechanical and thermal properties of rigid polyurethane foam composites containing graphene nanosheets and carbon nanotubes

The comparative study of rigid polyurethane foam (RPUF) nanocomposites based on graphene nanosheets (GNSs) and carbon nanotubes (CNTs) has been reported. A GNS content of 0.3 wt% in polyol turns to be optimal for its foamability with the isocyanate component, as verified by rheology measurements. Scanning electron microscopy and transmission electron microscopy observations reveal a homogeneous dispersion of GNSs and CNTs in the RPUF nanocomposites. Only 0.3 wt% loading of GNSs and CNTs led to 36% and 25% improvement respectively in the compressive modulus of the RPUF nanocomposites. Meanwhile, 16 °C and 14 °C improvements in the glass transition temperature confirm the important role of both the nanofillers in the heat resistance of RPUF nanocomposites. These results additionally indicate that GNSs work more effectively than CNTs in mechanical property and heat resistance enhancement of the RPUF nanocomposites. The superiority of GNSs over CNTs can be attributed to their wrinkled surface structure, unique two‐dimensional geometrical morphology and higher specific surface area, which results in stronger interaction and restriction of segmental motion at the interface between the GNSs and the RPUF matrix. In addition, changes in the thermal conductivity of the nanocomposites are negligible, indicating that incorporation of GNSs and CNTs will not hinder the application of RPUF nanocomposites as thermal insulators. On the contrary, the enhancement in mechanical properties and heat resistance will undoubtedly expand the application range of polyurethane foam materials. Copyright © 2012 Society of Chemical Industry     

碳纳米管/丙烯酸酯橡胶复合材料的制备及性能研究

采用自制的大分子表面改性剂对多壁碳纳米管(MWNTs)进行表面改性,制备改性MWNTs/丙烯酸酯橡胶(ACM)复合材料,研究改性MWNTs用量对复合材料性能的影响,并与炭黑补强的ACM性能进行对比.结果表明:用MWNTs填充ACM制备的材料,其性能远优于炭黑补强的ACM橡胶的性能;随着改性MWNTs用量的增大,复合材料...     

Preparation and properties of plasticized starch/multiwalled carbon nanotubes composites

In this work we have studied the utilization of multiwalled carbon nanotubes (MWCNTs) as filler‐reinforcement to improve the performance of plasticized starch (PS). The PS/MWCNTs nanocomposites were successfully prepared by a simple method of solution casting and evaporation. The morphology, thermal behavior, and mechanical properties of the films were investigated by means of scanning electron microscopy, wide‐angle X‐ray diffraction, differential scanning calorimetry, and tensile testing. The results indicated that the MWCNTs dispersed homogeneously in the PS matrix and formed strong hydrogen bonding with PS molecules. Compared with the pure PS, the tensile strength and Young's modulus of the nanocomposites were enhanced significantly from 2.85 to 4.73 MPa and from 20.74 to 39.18 MPa with an increase in MWCNTs content from 0 to 3.0 wt %, respectively. The value of elongation at break of the nanocomposites was higher than that of PS and reached a maximum value as the MWCNTs content was at 1.0 wt %. Besides the improvement of mechanical properties, the incorporation of MWCNTs into the PS matrix also led to a decrease of water sensitivity of the PS‐based materials. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Novel polyurethane elastomer continuous carbon fiber composites: Preparation and characterization

Preparation and characterization of novel polyurethane (PUR)–carbon fiber (CF) composites are reported. The reinforcement of PUR elastomers was achieved using unidirectional continuous CFs with different coatings (uncoated and epoxy and polyester resin coatings) by applying molding for the preparation of PUR‐CF composites. Considerable reinforcement of PUR was attained even at relatively low CF content, e.g., maximum stress and Young's modulus of PUR‐CF composite at CF content 3% (m/m) were found to be 3–5 and 4–10 times higher than those of the PUR‐matrix, respectively. In addition, a linear relationship between the Young's modulus and the CF content was found as well as linear variation of maximum stress with the CF content was also observed. The adhesion of CF to the PUR‐matrix was strong in each case as concluded from the strain–stress and the scanning electron microscopy (SEM) investigations. However, the extent of reinforcement of PUR at a given CF content was found to depend greatly on the coatings of CF, and increased in the following order: epoxy resin < polyester resin < uncoated. The effect of the coating of CF on the reinforcement of PUR is also discussed. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 287–292, 2007