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1.
采用磷酸溶液对芳纶纤维(Kevlar)进行了表面改性,通过考察其表面化学结构、元素组成、表面形貌及表面粗糙度的变化研究了磷酸对Kevlar纤维表面改性的效果.结果发现,改性后的纤维表面引入了含氧基团,并产生了明显的刻蚀作用.利用溶液预浸渍工艺和高温模压成型技术制备了Kevlar增强双马来酰亚胺树脂(BMI)复合材料,通...  相似文献   

2.
超高相对分子质量聚乙烯纤维的表面改性研究   总被引:1,自引:0,他引:1  
选择乙烯-醋酸乙烯酯共聚物作为表面改性剂,将其溶解在二甲苯中制成复合萃取液,对超高相对分子质量聚乙烯(UHMWPE)冻胶纤维进行萃取,经干燥和超倍拉伸制得表面改性UHMWPE纤维。对改性前后纤维的表面化学结构、结晶性能、表面粘接性能和力学性能进行了比较。结果表明:加入表面改性剂后,纤维表面引入了极性基团,结晶形态不变,纤维与树脂的抗界面剪切强度大大增加,纤维的力学性能变化不大。  相似文献   

3.
以乙烯-醋酸乙烯酯共聚物(EVA)作为共混改性剂,将其溶解在超高相对分子质量聚乙烯(UHMWPE)纺丝溶液中,制得共混改性UHMWPE冻胶纤维;对改性UHMWPE冻胶纤维进行萃取,干燥和热拉伸制得改性UHMWPE纤维;研究了改性前后纤维的结构与性能.结果表明:共混改性后UHMWPE纤维表面引入了极性基团,纤维与树脂基体...  相似文献   

4.
研究了自制芳纶表面改性剂A和胶粘剂类型对芳纶布/天然橡胶复合材料界面粘合性能的影响,并利用SEM分析了芳纶纤维改性前后的表面形貌和复合材料剥离界面形貌。结果表明,使用改性剂A处理的芳纶布、开姆洛克胶粘剂和天然橡胶制成的复合材料粘合强度达到了13.9kN/m,与未处理芳纶布相比提高了162%,较间苯二酚/甲醛/胶乳胶粘剂(RFL)的提高了61%;复合材料剥离界面微观形貌为橡胶撕裂和芳纶纤维劈裂共存;改性剂A对芳纶表面浸润良好,二者有一定程度的化学反应。  相似文献   

5.
选用硅烷偶联剂KH-550,KH-560和钛酸酯偶联剂NDZ-201作为表面改性剂,对超高相对分子质量聚乙烯(UHMWPE)冻胶纤维在萃取阶段进行表面处理,经干燥、超拉伸制得表面改性UHMWPE纤维。采用红外光谱仪、接触角测量仪测定了纤维的表面化学结构和表面润湿性能,采用单纤维树脂包埋-拔出法测定了纤维与树脂基体的界面剪切强度,比较了改性前后纤维的力学性能变化。结果表明:改性后纤维表面引入了极性基团,硅烷偶联剂KH-550对UHMWPE纤维的表面改性效果最好。采用质量分数为1%的硅烷偶联剂KH-550溶液处理后,纤维与环氧树脂间的界面剪切强度提高了87.8%,纤维的断裂强度和模量分别提高了6.9%和32.6%。  相似文献   

6.
Technora纤维的表面改性研究   总被引:2,自引:0,他引:2  
采用不同浓度的2,4-甲苯二异氰酸酯(TDI)溶液对Technora纤维(芳纶)进行表面改性,对处理前后的样品进行了扫描电镜、单丝抗拉强度、界面抗剪切强度、红外和表面浸润性测试。结果表明该方法能在对纤维力学性能无损伤的情况下,有效的改善界面性能和表面浸润性。  相似文献   

7.
由于芳纶纤维表面光滑且呈现化学惰性,与环氧树脂等基体材料结合后界面性能较差。为此,采用多巴胺在不同时间下对改进型芳纶Ⅲ纤维表面进行改性处理,并研究了对环氧树脂/多巴胺改性芳纶纤维界面性能的影响。对扫描电子显微镜对纤维改性前后表面形貌进行表征,发现纤维改性后表面粗糙度提高,利于与环氧树脂间界面结合。利用傅里叶变换红外光谱、X射线光电子能谱对纤维改性前后基团和表面元素含量进行表征,改性后纤维表面活性基团增加,极性增强。通过热重分析表明聚多巴胺成功吸附在纤维表面。测量纤维表面接触角,改性后的接触角更小,有利于环氧树脂润湿纤维。采用横向丝束复合材料的拉伸强度表征环氧树脂/芳纶纤维的界面性能。最终确定了多巴胺浓度为2 g/L,在多巴胺溶液中处理4 h为最佳条件,在该条件拉伸强度比为改性前提高了28.06%,拉伸弹性模量提高了14.68%。  相似文献   

8.
选择乙烯-醋酸乙烯酯共聚物作表面改性剂,将其溶解在二甲苯中,对超高相对分子质量聚乙烯(UHMWPE)冻胶纤维进行萃取,然后经过多级热拉伸制得改性UHMWPE纤维。对冻胶纤维的萃取动力学、改性前后纤维的表面化学结构、表面粘结性能和力学性能进行了比较。结果表明:加入表面改性剂后,冻胶纤维的萃取除油速率变慢;纤维与树脂基体的粘结强度大大提高;纤维的力学性能略有下降。  相似文献   

9.
研究了甲苯-2,4-二异氰酸酯(TDI)分子结构中的异氰酸酯基团(─NCO)与蒙脱土(MMT)表面羟基的修饰反应,以反应程度P(TDI)为指标,考察了反应时间、反应温度、TDI的用量以及蒙脱土活化条件对改性反应程度的影响。结果表明,TDI改性蒙脱土的最佳条件为:反应时间80 min,反应温度80℃,MMT与TDI质量比为1∶0.3,蒙脱土活化条件为250℃、反应2 h,反应程度可达到34.28%。IR,XRD测试改性物TDI/MMT,结果表明,TDI与蒙脱土片层表面的羟基发生反应,引入了─NCO基团,改性后的蒙脱土的层间距较原土有所增大,从而实现了蒙脱土的有机化改性。  相似文献   

10.
植物纤维和树脂的界面相容性差一直制约着天然纤维复合材料的发展和应用。分别对剑麻纤维(SF)进行了碱-偶联协同处理和碱-接枝协同处理,并利用双螺杆挤出机制备了SF/高密度聚乙烯(HDPE)复合材料。观察了剑麻纤维表面以及复合材料断面的微观形貌,表征了改性前后纤维基团的变化,研究了协同改性处理对剑麻纤维及其复合材料力学性能的影响。结果表明,碱-偶联协同处理的改性效果更好,剑麻纤维与HDPE的相容性得到明显改善,复合材料最大拉伸强度和弯曲强度相对于未改性纤维复合材料分别提高18.64%和20.25%。  相似文献   

11.
The thermomechanical behavior of fluorinated and oxyfluorinated Kevlar fiber‐reinforced ethylene propylene (EP) composites has been studied. The composites have been prepared using brabender mixer and are cured using compression molding technique. FTIR study has been performed to understand the chemical reaction occurred due to modification of composites. Thermal behavior and crystallinity have been studied by DSC, TGA, DMTA, and XRD. These studies show that thermal stability, storage modulus, as well as crystallinity of the treated Kevlar fiber‐reinforced EP increases in comparison to the untreated derivative because the surface‐modified Kevlar fiber results in good adhesion between the fiber surface and EP matrix. Tensile strength increases in case of treated Kevlar fiber‐reinforced EP in comparison to the untreated one. SEM study supports all the above results. AFM results show that surface roughness increases because of the surface modification resulting from the incorporation of functional group‐induced Kevlar fiber. Polym. Compos. 27:205–212, 2006. © 2006 Society of Plastics Engineers  相似文献   

12.
In this study, we present a new approach to modify the surface of Kevlar‐29 fiber by the complexation. The surface of Kevlar‐29 fiber was treated by calcium chloride (CaCl2) ethanol solution. The structure and morphology of the modified Kevlar‐29 fiber were characterized by Fourier transform infrared spectroscopy, X‐ray photoelectron spectroscopy, X‐ray diffraction instrument, atomic force microscopy, and scanning electron microscopy. The results showed that CaCl2 treatment's method can cause changes of the chemical groups of Kevlar‐29 fiber. The amino‐groups of Kevlar‐29 fiber were freed and the contents of ‐C‐N‐ increased. The changes can improve the surface roughness of Kevlar‐29 fibers. This can increase the adhesive of Kevlar fiber/epoxy composites. From the ILSS and mechanical properties values, it can be concluded that treatment with 5 wt % CaCl2 for 5 h is the optimum complexation condition. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41358.  相似文献   

13.
先后利用Fenton试剂和缩水甘油氧丙基硅烷偶联剂(KH560)对碳纳米管(CNTs)进行表面修饰,制备了不同种类的环氧树脂(EP)/CNTs复合材料并对其性能进行了研究。结果表明:CNTs经过Fenton试剂处理后,其表面成功引入羟基,进一步用KH560修饰后成功地引入了环氧基官能团。Fenton试剂的组成可以有效控制羟基基团的数目,并进一步决定环氧基官能团的数目。单独采用Fenton试剂处理或Fenton试剂和KH560共同处理都可以改善CNTs的分散性能,提高EP/CNTs复合材料的玻璃化温度(Tg)和热稳定性能,但后者的处理效果更好。  相似文献   

14.
This research applied the methodology of metalation and grafting alkoxysilane to modify the surface of Kevlar‐29 fiber. The surface properties of the modified Kevlar fiber were characterized by scanning electron microscopy, X‐ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, atomic force microscopy, and Brunauer‐Emmett‐Teller isothermal adsorption analysis. The relationship between surface characteristics of Kevlar fiber and its interfacial adhesion of Kevlar fiber‐reinforced epoxy resin composites was also discussed. Compared with the untreated fiber, the surface of the modified Kevlar fiber was much rougher, its oxygen content increased by about 12%, the surface area enlarged about 10 times, and the wetting behavior improved. Due to the modification of the fiber, the adhesion between the fiber and the resin matrix was markedly improved and the Interlaminar Shear Strength of its epoxy composites increased by about 57%. POLYM. COMPOS. 28:412–416, 2007. © 2007 Society of Plastics Engineers.  相似文献   

15.
为改善Kevlar纤维在三元乙丙橡胶中的使用性能,用化学方法对Kevlar纤维进行键合C=C的表面处理.通过傅里叶变换红外光谱、扫描电镜和X射线光电子能谱对表面改性进行鉴定,并进行纤维处理前后纤维抗拉伸强度和绝热层配方试验.实验结果表明,纤维经过表面改性,拉伸强度下降15%,其与三元乙丙橡胶制得的绝热层力学性能有显著提...  相似文献   

16.
A novel and efficient method was developed for surface‐modification of Kevlar fibers by multi‐wall carbon nanotubes (MWCNTs). Kevlar fibers were immersed in a solution mixed with Hexamethylene diisocyanate, 1,4‐diazabi‐cyclo [2,2,2] octane (DABCO), and toluene to introduce pendant amine groups before the COCl‐functionalized carbon nanotubes were chemically grafted onto the surface of modified fibers under ultrasonic condition. The characterization of resulting fiber involved in SEM, infrared spectroscopy, and tensile measurement. Results indicated over 20% of the fiber surface were coated by MWCNTs even after washing, which indicated a good adhesion. Furthermore, the mean value of tensile strength of Kevlar fiber was improved by 12% compared with original one. And the interlaminar shear strength (ILSS) of the fiber‐reinforced bismaleimides composite was increased by 30%. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012  相似文献   

17.
The influence of sizing agent on interfacial shear strength (IFSS) of carbon fiber/epoxy (CF/EP) and carbon fiber/bismaleimide (CF/BMI) was investigated. Since sizing agent can alter physicochemical properties of CF surface, possible affecting factors, including sizing reactivity, chemical reactions between sizing and resin, wettability of fiber with resin, fiber surface roughness, and chemical composition of fiber surface, were discussed. It is found that contact angle of fiber with resin and sufficient chemical reactions between sizing and resin reveal strong correlation with the interfacial adhesion of CF/EP and CF/BMI, while the effect of surface roughness and the amount of oxygen on the fiber surface are relatively weak. Due to EP type of the composition, the sizing agent tends to improve the wettability of CF with EP, while goes against for the fiber with BMI. POLYM. COMPOS., 254–261, 2016. © 2014 Society of Plastics Engineers  相似文献   

18.
Summary Horseradish peroxidase catalyzed grafting of acrylamide (AM) onto Kevlar fibers in mixed solvents of dioxane and water was studied. The factors affecting the grafting reaction, such as solvents composition, reaction time, temperature, pH of reaction media, concentration of acrylamide and hydrogen peroxide were examined. The modified fiber was characterized with IR, scanning electron microscopy (SEM), elemental analysis, XPS, contact angle measurement and the grafting yield. The O/C ratio and N/C ratio on the surface increased after treatment and the surface of the Kevlar fiber became rougher. The contact angle decreased from 80 to 45 after grafting, indicating the wettability of the fiber increased after modification. All the results suggested that AM have been grafted onto the Kevlar surface through HRP-mediated radical initiated grafting reaction. And the probably mechanism of HRP catalyzed grafting of AM onto Kevlar surface was proposed.  相似文献   

19.
借助傅立叶变换红外光谱仪、扫描电子显微镜、X射线光电子能谱仪和强力拉伸仪分析研究了Kevlar 49和芳纶Ⅲ的化学结构、表面特征及力学性能。结果表明:芳纶Ⅲ的红外谱图上多出了苯并咪唑环的吸收峰;芳纶Ⅲ的表面较粗糙,Kevlar 49表面较光滑,芳纶Ⅲ和Kevlar 49纤维表面的碳、氧元素均比化学式计算值有所增加,但氮元素含量下降;芳纶Ⅲ表面的极性基团种类比Kevlar 49多。芳纶Ⅲ的单纤维拉伸强度是Kevlar 49的1.5倍,断裂伸长率比Kevlar49提高了45%~65%;2种纤维的断裂方式均为劈裂断裂,具有皮芯结构,但芳纶Ⅲ分子间的作用力比Kevlar49纤维强。  相似文献   

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