Influence of complexing treatment and epoxy resin coating on the properties of aramid fiber reinforced natural rubber

In this work, natural rubber/aramid fiber (NR/AF) composites were prepared with master batch method. AF was modified by using epoxy resin (EP) and accelerator 2‐ethyl‐4‐methylimidazole (2E4MZ) through surface coating on the basis of the complexing treatment with CaCl₂ solution. Hydroxyl‐terminated liquid isoprene rubber (LIR) was regarded as a compatibilizer between EP and NR. It is found that the crystallinity on AF surface is decreased by complexing reaction with CaCl₂ solution. Swelling and mechanical properties of the vulcanized composites, such as swelling degree, tensile and tear strength, tensile modulus at 300% elongation, are measured, and the tensile fracture morphology and dynamic mechanical analysis of the composites are investigated. The results show that the mechanical properties of composites with modified fibers are improved obviously and interfacial adhesion between matrix and the fiber is enhanced, especially for the AF coated with EP and imidazole. The best comprehensive mechanical properties of the composites are obtained with using CaCl₂‐EP/2E4MZ system when the ratio of m(EP)/m(AF) is 3%. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42122.     

长玻璃纤维增强聚丙烯复合材料的力学性能研究

采用熔体浸渍技术制备了长玻璃纤维母料(LGF/PP-g-MAH/PP)增强聚丙烯(PP)复合材料(LGF/PP)。通过双螺杆挤出机制备了同等配比的短玻纤增强聚丙烯(SGF/PP)复合材料。研究了LGF含量、环氧树脂(EP)和固化剂(2E4MZ)对LGF/PP复合材料的力学性能影响。结果表明:当LGF质量分数为35%～40%时,LGF/PP的综合力学性能最好,且明显优于同样组成的SGF/PP复合材料。EP和含固化剂(2E4MZ)的EP对LGF/PP复合材料的力学性能提高有一定的作用。SEM照片分析表明:EP的加入能改善玻纤与聚丙烯基体的界面粘接。     

Effects of fiber surface chemistry and roughness on interfacial structures of electrospun fiber reinforced epoxy composite films

This work reported the effect of surface chemistry and roughness of electrospun fibers on fiber/matrix interfacial structures and the resultant macroscopical properties of composite films. Three types of fibrous mats composed of ultrafine fibers, that is, cellulose acetate (CANM), polyurethane (PUNM), and cellulose acetate/polyurethane composite (CAPUNM) were fabricated through electrospinning. CA fiber surfaces were rough with many hydroxyl groups; PU fiber surfaces were smooth, whereas CAPU composite fibers exhibited cocontiuous structure with rough surfaces. The fiber‐reinforced epoxy composite films were prepared by the solution impregnation method. The fractured surfaces of the composites were analyzed by scanning electron microscopy. Severe interfacial debonding and fiber pullouts were observed for PUNM/epoxy composites, while strong interfacial adhesion was formed for CANM/epoxy and CAPUNM/epoxy composites. The interfacial structure played important roles in the visible light transmittance of the composite films. For example, CANM/epoxy films showed the best optical property, whereas PUNM/epoxy films displayed the poorest light transmitting property and were translucent. The interfacial structure also affected the mechanical properties of the composites. The mechanical strength of fibrous mats followed an increasing order of CANM < CAPUNM < PUNM, but the mechanical strength of the composite films was in a reverse order, that is, CANM/epoxy > CAPUNM/epoxy > PUNM/epoxy. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Interfacial adhesion in sisal fiber/SBR composites: an investigation by the restricted equilibrium swelling technique

Short sisal fiber-reinforced styrene butadiene rubber (SBR) composites were prepared and characterized by the restricted solvent swelling technique. The solvent swelling characteristics of SBR composites containing untreated and bonding agent-added mixes were investigated in a series of aromatic solvents, such as benzene, toluene, and xylene. The diffusion experiments were conducted by the sorption gravimetric method. The adhesion between the rubber and short sisal fibers was evaluated from the restricted equilibrium swelling measurements. The anisotropy of swelling of the composite was confirmed by this study. The effect of fiber orientation in controlling the anisotropy of restricted swelling was also demonstrated. As the fiber content increased, the solvent uptake decreased, due to the increased hindrance and good fiber-rubber interactions. Bonding agent-added mixes showed enhanced restriction to swelling, due to the strong interfacial adhesion. The bonding system containing hexa-resorcinol in the mix produces an in-situ resin, which binds the fiber and the rubber matrix firmly. In addition, as the penetrant size increases from benzene to xylene, the uptake decreases. The swelling index values of the composites support this observation. Due to the improved adhesion between the short sisal fiber and SBR, the ratio of the volume fraction of rubber in the dry composite sample to the swollen sample (V _T) decreases. The extent of fiber orientation of the composites was also analysed from the restricted swelling method. SEM studies of the composite revealed the orientation of short fibers. The sorption data support the Fickian diffusion trend, which is typical in the case of cross-linked rubbers.     

Effect of functionalized elastomer addition on mechanical and interfacial properties of poly (butylene terephthalate)/glass fiber composites

In this study the effect of incorporation of ethylene‐co‐glycidylmethacrylate (GMA)‐co‐n‐butyl acrylate (nBA) terpolymer with an epoxy functional group, on the mechanical performance of short glass fiber (SGF)/Poly (butylene terephthalate) (PBT) composites has been investigated. Tensile test showed that incorporation of rubber phase in PBT/SGF composites results in loss of strength. However impact measurement exhibited an increase in impact strength with an increase in rubber content. Tensile and impact properties are discussed in terms of interfacial shear strength and morphology of composites. Morphological observation by SEM revealed a thin layer of polymer adhering to the surface of glass fibers indicating that epoxy functional group in the modifier reacts with fiber surface and PBT matrix. This reactivity of epoxy functional group is also supported by FTIR observations. The composites are also analyzed for % crystallinity using DSC and a strong correlation is found to exist between interfacial shear strength and % crystallinity. POLYM. COMPOS., 2012. © 2011 Society of Plastics Engineers     

Effects of the single layer CVD SiC interphases on the mechanical properties of the SiCf/SiC composites fabricated by PIP process

Owing to the degradation of the mechanical properties of the SiC fiber reinforced SiC matrix (SiCf/SiC) composites with the pyrocarbon (PyC) and BN interphases under oxidation environment and neutron irradiation, single layer SiC interphases prepared by chemical vapor deposition (CVD) process were employed to substitute for them. Effects of the CVD SiC interphases on the mechanical properties and interfacial characteristics of the SiCf/SiC composites fabricated by precursor infiltration and pyrolysis (PIP) process were investigated. Compared with the as-received SiCf/SiC composites, the SiCf/SiC composites with the single layer CVD SiC interphases exhibit an obvious toughened fracture behavior, the flexural strength of which is about 4 times that of the as-received SiCf/SiC composites. From the microstructural analysis, it can be confirmed that the SiC interphases play a key part in protecting the fibers from damage during composite preparation and weakening interfacial bonding, which can provide high in situ fiber strength and appropriate interfacial bonding strength for the SiCf/SiC composites.     

DMC/MVQ绝缘复合材料的制备及性能表征

针对硅橡胶力学性能差的特点,本工作以硅橡胶（MVQ）为基相,以团状模塑料（DMC）为增强相,以丁苯橡胶（SBR）为相容剂来制备DMC/MVQ绝缘复合材料,研究了SBR的用量对MVQ性能的影响。结果表明：SBR和MVQ共混制得的并用胶性能要比纯MVQ的性能好,其最佳配比为DMC 60phr,SBR 25phr,MVQ 75phr;制备的复合材料体积电阻率都在4.9×1012Ω.m以上,复合材料的绝缘性能良好;通过扫描电镜分析（SEM）和动态热机械分析（DMA）,研究了复合材料的相容性,SBR的加入改善了DMC/MVQ绝缘复合材料的相容性,增加了界面相互作用,提高了DMC/MVQ绝缘复合材料的性能。     

某高导热纤维及其复合材料性能研究

研究了某高导热纤维/环氧树脂单向层复合材料的导热系数和力学性能,发现某高导热纤维/环氧树脂单向层复合材料导热性能提高的同时其个别复合材料性能降低;分析认为某高导热纤维与环氧树脂的界面性能是影响复合材料力学性能的重要因素,同时研究了某高导热纤维的表面微观形貌和表面化学特性、结晶度及某高导热纤维/环氧树脂浸胶丝束的力学性能...     

Deformation mechanisms and mechanical properties of modified polypropylene/wood fiber composites

Mechanical properties and deformation mechanisms of polypropylene (PP)/wood fiber (WFb) composites modified with maleated polypropylene as compatibilizer and styrene-butadiene rubber (SBR) as impact modifier have been studied. The addition of maleated polypropylene to the unmodified polypropylene/wood fiber composite enhances the tensile modulus and yield stress as well as the Charpy impact strength. SBR does not cause a drop in the tensile modulus and yield strength because of the interplay between decreasing stiffness and strength by rubber modification and increasing stiffness and strength by good interfacial adhesion between the matrix and fibers. The addition of both maleated polypropylene and rubber to the polypropylene/wood fiber composite does not result in an improvement of effects based on maleated polypropylene and rubber, which includes possible synergism. The deformation mechanisms in unmodified polypropylene/wood fiber composite are matrix brittle fracture, fiber debonding and pullout. A polymeric layer around the fibers created from maleated polypropylene may undergo debonding, initiating local plasticity. Rubber particle cavitation, fiber pullout and debonding were the basic failure mechanisms of rubber-toughened polypropylene/wood fiber composite. When maleated polypropylene was added to this composite, fiber breakage and matrix plastic deformation took place. Polym. Compos. 25:521–526, 2004. © 2004 Society of Plastics Engineers.     

The role of interlayer grafting on the mechanical properties of magadiite/styrene‐butadiene rubber composites

This work examines the mechanisms by which magadiite (MGD), a synthetic layered silicate, acts as an active filler to provide high levels of mechanical reinforcement in styrene‐butadiene rubber (SBR) composites. Cetyltrimethylammonium (CTA⁺) expands the MGD layer spacing and promotes intercalation of SBR and silane coupling agent (Si69); the resulting CMGD/SBR composites have greater tensile moduli than comparable silica/SBR composites. CMGD was reacted in solution with Si69 (or MPTES) to prepare “pre‐grafted” MGD with varying levels of interlayer silane functionalization (SMGD). If the silane graft density is relatively low, the resulting SMGD/SBR composite has mechanical properties comparable to CMGD composites prepared with Si69 added during batch mixing. However, SMGD with high silane graft density does not permit SBR intercalation and produces composites with inferior mechanical properties, demonstrating the necessity of silane‐mediated interlayer grafting. Omitting Si69 from the formulation dramatically reduces the level of mechanical reinforcement as measured by DMA and tensile testing. Adding extra bulk sulfur (to replace sulfur omitted with Si69) does not produce composites with mechanical properties comparable to CMGD/SBR or SMGD/SBR prepared with Si69. This work demonstrates that silane‐mediated SBR‐MGD grafts within the MGD interlayer space are essential for achieving high levels of mechanical reinforcement in MGD/SBR composites. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45025.     

基于NOL环的高性能纤维与环氧树脂的匹配性研究

纤维与树脂的界面对复合材料的整体力学性能有着显著的影响。基于NOL环的宏观力学测试一般被用来反映复合材料的界面粘结性能,因此适用于评价纤维与树脂之间的宏观力学性能匹配性。为了探究高性能碳纤维T700SC、T800HB及高强玻璃纤维与环氧树脂的宏观力学性能匹配性,本研究首先根据GB/T 1458—2008国家标准制备NOL环试样,再借助NOL环的拉伸和层间剪切强度测试分析了高性能纤维与环氧树脂不同匹配组合宏观力学性能差异的原因,并寻找出最佳匹配组合。结果表明:玻璃纤维与环氧树脂的界面存在最佳的粘结强度,而且不同粘结强度导致拉伸强度和破坏机理不同,而碳纤维复合材料界面性能较差,容易分层破坏;T800HB与环氧树脂的宏观力学匹配性优于T700SC,环氧树脂力学性能、碳纤维的表面微观结构与性质以及环氧树脂与碳纤维之间的相互作用关系是影响界面粘结性能的根本原因。该研究在高性能纤维单向复合材料的材料选择与设计方面具有现实意义。     

Influences of liquid elastomer additive on the behavior of short glass fiber reinforced epoxy

In this study, improvements in mechanical and thermal behavior of short glass fiber (GF) reinforced diglycidyl ether of bisphenol-A (DGEBA) based epoxy with hydroxyl terminated polybutadiene (HTPB) modification have been studied. A silane coupling agent (SCA) with a rubber reactive group was also used to improve the interfacial adhesion between glass fibers and an epoxy matrix. 10, 20, and 30 wt% GF reinforced composite specimens were prepared with and without silane coupling agent treatment of fibers and also HTPB modification of epoxy mixture. In the ruber modified specimens, hardener and HTPB were premixed and left at room temperature for 1 hr before epoxy addition. In order to observe the effects of short glass fiber reinforcement of epoxy matrix, silane treatment of fiber surfaces, and also rubber modification of epoxy on the mechanical behavior of specimens, tension and impact tests were performed. The fracture surfaces and thermal behavior of all specimens were examined by scanning electron microscope (SEM), and dynamic mechanical analysis (DMA), respectively. It can be concluded that increasing the short GF content increased the tensile and impact strengths of the specimens. Moreover, the surface treatment of GFs with SCA and HTPB modification of epoxy improved the mechanical properties because of the strong interaction between fibers, epoxy, and rubber. SEM studies showed that use of SCA improved interfacial bonding between the glass fibers and the epoxy matrix. Moreover, it was found that HTPB domains having relatively round shapes formed in the matrix. These rubber domains led to improved strength and toughness, due mainly to the “rubber toughening” effect in the brittle epoxy matrix.     

Study on the effect of woven sisal fiber mat on mechanical and viscoelastic properties of petroleum based epoxy and bioresin modified toughened epoxy network

Sisal fiber reinforced biocomposites are developed using both unmodified petrol based epoxy and bioresin modified epoxy as base matrix. Two bioresins, epoxidized soybean oil and epoxy methyl soyate (EMS) are used to modify the epoxy matrix for effective toughening and subsequently two layers of sisal fiber mat are incorporated to improve the mechanical and thermomechanical properties. Higher strength and modulus of the EMS modified epoxy composites reveals good interfacial bonding of matrix with the fibers. Fracture toughness parameters K_IC and G_IC are determined and found to be enhanced significantly. Notched impact strength is found to be higher for unmodified epoxy composite, whereas elongation at break is found to be much higher for modified epoxy blend. Dynamic mechanical analysis shows an improvement in the storage modulus for bioresin toughened composites on the account stiffness imparted by fibers. Loss modulus is found to be higher for EMS modified epoxy composite because of strong fiber–matrix interfacial bonding. Loss tangent curves show a strong influence of bioresin on damping behavior of epoxy composite. Strong fiber–matrix interface is found in modified epoxy composite by scanning electron microscopic analysis. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42699.     

热解炭微观结构对炭/炭复合材料力学性能的影响

以PAN基针刺纤维毡为基体,采用等温化学气相渗透技术,在温度1000℃、压力5.0~20.0 kPa条件下制备了2种具有不同微观结构热解炭的炭/炭复合材料,研究了其力学性能与热解炭微观结构的关系. 结果表明,压力8.0 kPa下得到的具有单一低织构热解炭的炭/炭复合材料的断裂强度较高,为86±3 MPa,热解炭与炭纤维间界面结合紧密,加载过程中二者同时断裂,呈现明显的脆性断裂行为;压力10.0~20.0 kPa下得到的具有中织构-高织构-中织构热解炭的炭/炭复合材料的断裂强度稍低,为82±4 MPa,加载过程中材料内部不同织构热解炭间多层次界面通过改变裂纹扩展路径而延缓其扩展速度,断口形貌呈现锯齿状,表现出假塑性断裂特征.     

Relationship Between Interfacial Water Layer Adhesion Loss of Silicon/Glass Fiber-Epoxy Systems: A Quantitative Study

Water at the polymer/substrate interface is often the major cause of adhesion loss in coatings, adhesives, and fiber-reinforced polymer composites. This study critically assesses the relationship between the interfacial water layer and the adhesion loss in epoxy/siliceous substrate systems. Both untreated and silane-treated Si substrates and untreated and silane-treated E-glass fibers were used. Thickness of the interfacial water layer was measured on epoxy/Si systems by Fourier transform infrared-multiple total internal reflection (FTIR-MTIR) spectroscopy. Adhesion loss of epoxy/Si systems and epoxy/E-glass fiber composites was measured by peel adhesion and short-beam shear tests, respectively. Little water accumulation at the epoxy/Si substrate interface was observed for silane-treated Si substrates, but about 10 monolayers of water accumulated at the interface between the epoxy and the untreated Si substrate following 100 h of exposure at 24 °C. More than 70% of the initial epoxy/untreated Si system peel strength was lost within 75 h of exposure, compared with 20% loss after 600 h for the silane-treated Si samples. Shear strength loss in composites made with untreated E-glass fiber was nearly twice that of composites fabricated with silane-treated fiber after 6 months of immersion in 60 °C water. Further, the silane-treated composites remained transparent, but the untreated fiber composites became opaque after water exposure. Evidence from FTIR-MTIR spectroscopy, adhesion loss, and visual observation strongly indicated that a water layer at the polymer/substrate interface is mostly responsible for the adhesion loss of epoxy/untreated siliceous substrate systems and epoxy/untreated glass fiber composites and that FTIR-MTIR is a viable technique to reliably and conveniently assess the adhesion loss attributable to water sorption at the interface.     

Influence of epoxy sizing of carbon‐fiber on the properties of carbon fiber/cyanate ester composites

The high modulus carbon fiber (M40J) sized by epoxy resin E51 and E20 reinforced bisphenol A dicyanate (2,2′‐bis(4‐cyanatophenyl) isopropylidene resin composite was prepared in order to investigate the influence of epoxy sizing of the fiber on the properties of the composite. Differential scanning calorimetry (DSC) and fourier transforms infrared (FTIR) analysis showed that epoxy resin have catalytic effect on cure reaction of cyanate ester. Mechanical properties of the composite revealed that M40J fiber sized by epoxy resin could improve the flexural strength and interlaminar shear strength of M40J/bisphenol A dicyanate composites. The micro‐morphology of the composite fractures was studied by means of scanning electron microscopy (SEM). Reduced flaws were observed in the M40J‐bisphenol A dicyanate interface when the sized fiber was used. Water absorption of the composites was also investigated. It was found that the water absorption descended at the initial boiling stage (12 h). POLYM. COMPOS, 27: 591–598, 2006. © 2006 Society of Plastics Engineers     

Influence of starch on the properties of carbon‐black‐filled styrene–butadiene rubber composites

The influence of starch on the properties of carbon‐black‐filled styrene–butadiene rubber (SBR) composites was investigated. When the starch particles were directly melt‐mixed into rubber, the stress at 300% elongation and abrasion resistance decreased evidently with increasing starch amount from 5 to 20 phr. Scanning electron microscopy observations of the abrasion surface showed that some apparent craters of starch particles were left on the surface of the composite, which strongly suggested that the starch particles were large and that interfacial adhesion between the starch and rubber was relatively weak. To improve the dispersion of the starch in the rubber matrix, starch/SBR master batches were prepared by a latex compounding method. Compared with the direct mixing of the starch particles into rubber, the incorporation of starch/SBR master batches improved the abrasion resistance of the starch/carbon black/SBR composites. With starch/SBR master batches, no holes of starch particles were left on the surface; this suggested that the interfacial strength was improved because of the fine dispersion of starch. Dynamic mechanical thermal analysis showed that the loss factor at both 0 and 60°C increased with increasing amount of starch at a small tensile deformation of 0.1%, whereas at a large tensile strain of 5%, the loss factor at 60°C decreased when the starch amount was varied from 5 to 20 phr. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

The effect of fiber-matrix stress transfer on the strength of fiber-reinforced composite materials

A model for the mechanism of tensile failure in oriented fiber composites based on random fragmentation of the reinforcing fibers biased by stress concentrations at fracture sites has been developed. Single-fiber composites and composite strands of 34 to 36 volume percent fiber were prepared from an epoxy resin reinforced with Hercules AS4, HMS4, and IM6G carbon fibers. Fiber strength distributions and single-fiber composite fragmentation data were used to calculate theoretical composite tensile strengths, which were then compared with experimental values. The fractures in single-fiber composites were observed in situ under cross-polarized light, and the mechanisms of interfacial failure were discussed.     

丁苯橡胶/纳米硅铝管复合材料的制备工艺与性能

分别采用直接共混法、填料预处理法、原位改性分散法、乳液法制备了丁苯橡胶/纳米硅铝管（SBR/SANT）复合材料,并对其结构和性能进行了表征。结果表明：采用原位改性分散的方法能够有效改善填料与橡胶间的界面强度,制备得到力学性能优异的SBR/SANT复合材料。采用乳液法制得复合材料的填料分散较好,扫描电子显微镜观察到SANT基本以单管分散,其导热性能明显优于干法混合。随着纳米硅铝管用量增大,SBR/SANT复合材料的硬度、定伸应力、拉伸强度、撕裂强度和导热系数提高,拉断伸长率下降。     

Effect of deposited carbon nanotubes on interlaminar properties of carbon fiber‐reinforced epoxy composites using a developed spraying processing

Carbon fiber‐reinforced epoxy composites, with incorporated carboxylic multiwall carbon nanotubes (CNTs), were prepared using vacuum‐assisted resin infusion (VARI) molding, and the in‐plane and out‐of‐plane properties, including mode‐I (G_Ic) and mode‐II (G_IIc) interlaminar fracture toughness, interlaminar shear strength (ILSS), tensile, and flexural properties were measured. A novel spraying technique, which sprays a kind of epoxy resin E20 with high viscosity after spraying the CNTs, was adopted to deposit the CNTs on the surface of carbon fiber fabric. The E20 was used to anchor CNTs on the fabric surface, avoiding that the deposited CNTs were removed by the infusing resin during VARI process. The spraying processing, including spraying amount and spraying sequence, was optimized based on the distribution of CNTs on the fibers. After that, three composite specimen groups were fabricated using different carbon fiber fabrics, including as‐received, CNT‐deposited with E20, and CNT‐deposited without E20. The effects of CNTs on the processing quality and mechanical properties of carbon fiber‐reinforced polymer composites were studied. The experimental results show that all studied laminates have uniform thickness with designed values and no obvious defects form inside the laminates. Compared with the composite without CNTs, depositing CNTs with E20 increases by 24% in the average propagation G_Ic, by 11% in the propagation G_IIc and by 12% in the ILSS, while it preserves the in‐plane mechanical properties, However, depositing CNTs without E20 reduces interlaminar fracture toughness. These phenomena are attributed to the differences in the distribution of CNTs and the fiber/matrix interfacial bonding for different spraying processing. POLYM. COMPOS., 2013. © 2012 Society of Plastics Engineers