Effect of fiber treatment on the mechanical properties of LDPE-henequen cellulosic fiber composites

The degree of mechanical reinforcement that could be obtained by the introduction of henequen cellulosic fibers in a low-density polyethylene, LDPE, matrix was assessed experimentally. Composite materials of LDPE-henequen cellulosic fibers were prepared by mechanical mixing. The concentration of randomly oriented fibers in the composite ranged between 0 and 30% by volume. The tensile strength of these composite materials increased up to 50% compared to that of LDPE. There is also a noticeable increase in Young's modulus for the composite materials that compares favorably with that of LDPE. As expected, the addition of the fibers decreases the ultimate strain values for the composite materials. The thermal behavior of the LDPE-henequen cellulosic fibers materials, studied by differential scanning calorimetry, DSC, showed that the presence of the fibers does not affect the thermal behavior of the LDPE matrix; thus, the interaction between fiber and matrix is probably not very intimate. Preimpregnation of the cellulosic fibers in a LDPE-xylene solution and the use of a silane coupling agent results in a small increment in the mechanical properties of the composites, which is attributed to an improvement in the interface between the fibers and the matrix. The shear properties of the composites also increased with increasing fiber content and fiber surface treatment. It was also noted that the fiber surface treatment improves fiber dispersion in the matrix. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 65: 197–207, 1997     

Preparation of Rayon Fiber-Reinforced Polypropylene Composites by Extrusion Techniques

Hybrid composites from rayon fibers (～2–5 cm size) and polypropylene (PP) were fabricated by using an extruder. Fibre content of the composite was varied from 5–30% by weight and physico-mechanical properties of the composites were measured. Surface morphology as observed by SEM showed good interface adhesion between rayon and PP matrix. Furthermore inclusion of rayon (up to 15% fiber inclusion) in the composite increased tensile, bending and hardness properties. As the fiber content in the composite increased more than 15%, physico-mechanical properties decreased due to the decrease of fiber matrix adhesion. The change of tensile properties due to environmental aging was carried out by keeping the composite under soil for 1 month and tensile properties were measured periodically. The aging result suggests that composites retained about 75% of its original tensile and bending strength even after 1 month soil burial. The modified fibers were also used for the study. As such the fibers were treated with vinyl-trimethyoxysilane and methanol solution and irradiated under UV before being used with PP in extruder. The results showed retardation of the physico-mechanical properties for composites obtained from irradiated rayon fibers than the composites fabricated from non irradiated rayon fibers.     

Modification of Low-surface Energy Fibers used as Reinforcement in Cementitious Composites: A Review

This paper provides a review on the surface modification of low-surface energy fibers (polypropylene, polyethylene, and nylon) and discusses on the effects of these treatments toward the physical/mechanical properties of cement-based composite materials. These properties include the tensile, flexural, compressive strength and toughness, stress–strain behavior, modulus of elasticity, and workability. The effects of these treatments on the changes in the fiber/cement matrix interfacial properties are also presented. Studies have shown that various surface treatments have been used to improve the efficiency of the low-surface energy synthetic fibers in the cementitious composites. The modifications are on the basis of physical, chemical, and mechanical methods. The main achievements found have been the development of fibers with modified surface to optimize fiber–matrix adhesion. Moreover, the recently developed surface modifications will allow obtaining high-performance cementitious materials reinforced with the synthetic fibers.     

Precursors for Carbon and Graphlte Fibers

Abstract

Commercial production of carbon and graphite fiber products has been dominated by technology based on the thermal conversion of rayon and polyacrylonitrile fibers. In fact, a wide range of potentially useful and low-cost precursors exist. Most recently, pitch-based fibers have materialized as strong contenders for carbon fiber production. This study is a comprehensive analysis of carbon fiber precursors. It presents a data base for the development of a generalized theory for the prediction of formation of carbon fibers with high mechanical properties.     

大豆蛋白/粘胶共混纤维的结构与性能

采用湿法纺丝制备大豆蛋白/粘胶共混纤维,分析测试了共混纤维的结构形态与物理机械性能的关系,并与其他类型的蛋白质改性纤维进行了比较。实验结果表明共混纤维的力学性能与蛋白质比例有关,随着蛋白质质量分数的增加,纤维的强度降低;共混纤维的截面形状和黏胶纤维相似,但表面沟槽更为明显。     

Studies of the effect of fiber surface and matrix rheological properties on nonwoven reinforced elastomer composites

The influence of fiber type and fiber-surface properties on matrix flow behavior was investigated using structural reaction injection-molding (SRIM). The influence of fiber type, fiber-surface properties, and matrix type on strength properties in elastomeric composites reinforced with nonwoven fibrous structures was investigated using tensile tests on elastomer composite samples from SRIM and latex coagulation (LC) fabrication methods and the microbond strength method on individual fibers. The fibers used were PET, LLDPE, and p-aramid. Fibers were treated with epoxy, styrene, and isocyanate derivatives, which make the surface chemically reactive. Treatments were also made with NaOH and a copolymer of polyester and polyol ether, causing a change in the fiber surface energy. The matrix types were polyurethane elastomer and natural rubber. The results show that the surface treatments which produced a change in the surface energy influenced the flow rate of the matrix polymer during the composite fabrication process. The treatments resulted in chemically reactive fiber surfaces which improved the fiber-matrix bond strength without affecting the Young's modulus of the composite material. Good correlation was found between bond strength and surface energy including the dispersive component of surface energy in the case of polyurethane elastomer and surface-modified PET fibers. The age of the polyurethane matrix has a marked influence on the bond strength. The fiber volume fraction in composites has a strong influence on the Young's modulus of the elastomer composite. © 1995 John Wiley & Sons, Inc.     

Surface Characterization of Differently Pretreated Flax Fibers and Their Application in Fiber-Reinforced Composites

Strong natural bast fibers, especially flax fibers, can be used to replace glass fibers in reinforced composites. The properties of natural fibers depend largely on maturity, retting and processing. Two chemical treatments were applied to retted and semiretted flax fibers to create better fiber to resin bonding and to show the effect of retting degree and successive purification processes on the mechanical properties of natural composite materials. Retted and semiretted flax fibers have been scoured and bleached with the objective of removing surface impurities and developing finer structure. To investigate the effect of adhesion promoter on the mechanical properties of natural fiber composite, a composite sample was prepared from bleached retted flax pretreated with adhesion promoter Isostearoyltitanate (ISTT).

After treatments the fibers got cleaner and the measurements showed that the fiber fineness as well as the surface free energy increased. The treatments were accompanied by decrease in the fiber tenacity but it has been found not to be reflected to the final mechanical properties of the composite. No improvement was remarked by using Isostearoyltitanate for surface modification.     

Influence of interfacial interactions on the properties of PVC/cellulosic fiber composites

The surface properties at the interface between thermoplastic and cellulosic fibers strongly influence the mechanical properties of plastic/cellulosic fiber composites. This paper examines the role of surface acid-base properties of plasticized PVC and cellulosic fibers on the mechanical properties of the composites. The acid-base surface characteristics of cellulosic fibers were modified by treating the fibers with γ-aminopropyltriethoxysilane (A-1100), dichlorodiethylsilane, phthalic anhydride, and maleated polypropylene. The empirical acid (K_A) and base (K_D) characteristics (i.e., electron donor/acceptor abilities) of untreated and treated fibers, as well as plasticized PVC, were determined using inverse gas chromatography (IGC) technique. These parameters were used to yield information on the acid-base pair interactions that were correlated with the tensile and notched Izod impact properties of the composites. Acid-base pair interactions have been found to be a valuable parameter in the design of surface modification strategies intended to optimize the tensile strength of the composites. By tailoring the acid-base characteristics of cellulosic fibers and plasticized PVC, a composite with equal tensile strength and greater modulus than unfilled PVC was developed. However, the acid-base factors did not correlate with tensile modulus, the elongation at break, and the notched Izod impact property of PVC/newsprint fiber composites. Aminosilane has been observed to be a suitable adhesion promoter for PVC/wood composites improving significantly the tensile strength of the composites. Other treatments (dichlorodiethylsilane, phtalic anhydride, and maleated polypropylene) were found to be ineffective, giving similar strength compared to the composites with untreated cellulosic fibers. FTIR spectroscopy results suggested that aminosilane was effective because treated cellulosic fibers can react with PVC to form chemical bonds. The resulting bond between PVC and cellulosic fibers accounts for the effectiveness of aminosilane, when compared with other coupling agents.     

Wood fiber surface treatment level effects on selected mechanical properties of wood fiber-cement composites

The objective of this study was to determine the effects of sodium (N) silicate, potassium (K) silicate, and silane (Si) treatment levels on newspaper and unbleached kraft fibers for enhancing selected mechanical properties of wood fiber-cement composites compared to untreated wood fiber-cement composites. Both wood fiber types were treated with selected aqueous solution strengths, air dried, and mixed with water and cement. The bending and compression properties of the specimens were determined after 28 days of hydration. Results of this study indicated that the aqueous chemical treatments of the wood fibers enhanced some of the mechanical properties of wood fiber-cement composites compared to the untreated wood fiber-cement composites. The enhancement depended on chemical treatment and wood fiber type. All three chemical treatments of newspaper fiber enhanced the normalized toughness values compared to the untreated newspaper fiber-cement composites. In addition, higher treatment levels using N silicate with newspaper fiber improved the compressive strength and bending modulus of the composites compared to the untreated newspaper fiber-cement composites. Kraft fiber treated with all three chemicals enhanced the compressive strength, bending modulus and bending strength compared to the untreated kraft fiber-cement composites. However, only silane-treated kraft fiber improved the normalized toughness values compared to the untreated kraft fiber-cement composites. The results of the study indicated that certain chemical treatments react better with different wood fiber types resulting in selected mechanical property enhancements.     

Influence of the fiber surface properties on the mechanical strength of unidirectional fiber composites

The influence of the thermodynamic adhesion between fibers and matrix on the mechanical properties of a continuous fiber reinforced composite is studied for two systems: carbon fiber reinforced poly(ether ether ketone) and glass fiber reinforced poly(ether imide). The fibers are modified chemically and characterized by measuring the contact angle formed by molten resin on the fibers. Various fiber treatments yield a wide range of contact angles, which are determined optically. Unidirectional fiber reinforced laminates are manufactured and transverse flexural strength is measured with the values reported as a function of the specific work of adhesion. It is shown that adhesion at the fiber-resin interface correlates with both the composite strength and the void morphology within the laminate after consolidation.     

Influence of pulp bleaching and compatibilizer selection on performance of pulp fiber reinforced PLA biocomposites

This article focuses on the effect of pulp bleaching and emerging commercial compatibilizers on physical performance of pulp fiber reinforced poly(lactic acid) (PLA) biocomposites. Industrially bleached and unbleached hardwood kraft pulp fibers are treated with several additive types, and compounded with PLA to fiber content of 30 wt %. After injection molding, the produced biocomposites are evaluated by their mechanical performance and fiber–matrix adhesion. For selected materials, fiber surface and fiber properties are reflected to composite performance by analyzing the compositions, dimensions, and lignin coverage of original fibers, as well as fiber dispersion and dimensions after melt processing. As a conclusion, unbleached kraft pulp fibers provide significant improvement in physical properties of PLA/pulp fiber composites. Of the screened compatibilizers, epoxidated linseed oil has a clear positive effect on performance when bleached kraft pulp fibers are used. The improvements correspond to enhanced fiber–matrix adhesion and differences in remaining fiber length distributions. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47955.     

Curing characteristics and mechanical properties of alkali‐treated grass‐fiber‐filled natural rubber composites and effects of bonding agent

To improve adhesion between fiber and matrix, natural rubber was reinforced with a special type of alkali‐treated grass fiber (Cyperus Tegetum Rox b). The cure characteristics and mechanical properties of grass‐fiber‐filled natural rubber composites with different mesh sizes were studied with various fiber loadings. Increasing the amount of fibers resulted in the composites having reduced tensile strength but increased modulus. The better mechanical properties of the 400‐mesh grass‐fiber‐filled natural rubber composite showed that the rubber/fiber interface was improved by the addition of resorcinol formaldehyde latex (RFL) as bonding agent for this particular formulation. The optimum cure time decreased with increases in fiber loading, but there was no appreciable change in scorch time. Although the optimum cure time of vulcanizates having RFL‐treated fibers was higher than that of the other vulcanizates, it decreased with fiber loading in the presence of RFL as the bonding agent. But this value was lower than that of the rubber composite without RFL. Investigation of equilibrium swelling in a hydrocarbon solvent was also carried out. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3151–3160, 2006     

Elastomers based on cellulose fibers. II. Ethyl acrylate grafting onto disulfide-crosslinked cellulose

Partially disulfide-crosslinked viscose rayon fibers (? S? S? 2.3 mole/10⁴ g. cellulose) were prepared by means of mercaptoethylation and successive oxidation and then grafted to the extent of 200–1200% graft-on of ethyl acrylate with or without preswelling by zinc chloride, by using the ceric ion method. The tensile strength, breaking elongation, initial modulus, elastic recovery, and extension energy loss of the modified fibers were measured. In the disulfide-crosslinked, about 1000% ethyl acrylate-grafted fibers with preswelling, typical rubber elasticity was found. The disulfide crosslinkage in the grafted fibers was found generally to be capable of cleaving and re-forming by the reduction and successive oxidation treatments, and the properties were also well reversible. Therefrom, it was confirmed that intermolecular crosslinking between cellulose molecules plays an important role for developing of elastomeric properties, as was found for the methylene-crosslinked and grafted fiber reported previously. Most of elastomeric properties in our grafted fibers seem to be essentially attributable to the random conformation of the decrystallized, disoriented, and weakly crosslinked cellulose chains which are embedded in a matrix of flexible graft polymers.     

Processability and mechanical properties of ternary composites PP/EPDM/GF

The enhancement of the mechanical properties of neat PP is achieved by the addition of glass fibers and EPDM rubber. The Young's modulus and notched Charpy impact strength of the composites obtained are improved with respect to the original polymer, leading to a new composite material with a very good balance of toughness and rigidity properties. The tensile behavior of these multiphase systems is successfully compared with theoretical predictions using the Halpin‐Tsai/Nielsen theory for uniaxially short fiber composites, which considers the matrix as a blend with spherical particles and can predict the tensile modulus considering an average fiber orientation angle. An accurate morphological study performed by scanning electron microscopy (SEM) shows a very good dispersion of the rubbery phase into the neat matrix. No special affinity between the rubber and the fibers is reported. The good dispersion and the small particle diameter indicate the good processability of the ternary systems studied.     

Inverse gas chromatography for the determination of the dispersive surface free energy and acid–base interactions of a sheet molding compound. I. Matrix material and glass

Sheet molding compound is a material composed of a polyester thermosetting matrix with a thermoplastic, an inorganic filler, a metal oxide, reinforcement fibers, and material performance enhancers embedded in the crosslinked matrix. To achieve the optimum mechanical properties required for the composite material, the surface free energy of the polyester composite needs to be understood. In this study, the composite matrix and glass reinforcement fibers are compared with respect to their surface free energy and acid–base characteristics on the basis of inverse gas chromatography measurements. The inverse gas chromatography results for the matrix and glass are compared to previous results found for sized and unsized cellulosic fibers. The inverse gas chromatography data are used to assess chemical modifications performed on the biobased fibers to predict improvements in the fiber/matrix interaction, and this provides inferences on the overall composite cohesion. Our results show first that any fiber reinforcement system for the polyester composite material has to be acidic to promote good adhesion as the matrix system is very basic and second that the individual dispersive surface energies of the components of the matrix interact in a weighted average to determine the overall surface energy of the composite. Also, a commercial glass reinforcement sized for polyester has been found to have a lower interaction parameter than literature values for cellulosic fibers. This finding suggests that cellulosic fibers might have an advantage in competing with a conventional glass‐fiber reinforcement system in fiber/matrix bonding for sheet molding compound composites. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

废弃天然纤维增强高密度聚乙烯复合材料性能研究

选用纺织工业废弃苎麻落麻纤维和造纸工业废弃的竹屑纤维为增强体,采用双螺杆熔融共混挤出工艺,制备天然纤维增强高密度聚乙烯（PE-HD）复合材料。考察纤维种类、含量变化对天然纤维增强复合材料熔体流动速率、微观断面形貌、拉伸性能、弯曲性能的影响。结果表明,2种废弃纤维都能有效提高PE-HD的拉伸性能和弯曲性能,其中苎麻落麻纤维的增强效果优于竹屑纤维,加入20% 苎麻落纤维复合材料拉伸强度比纯PE-HD提高21%,弯曲强度提高了41.9%。     

Microstructure and properties of CNTs reinforced CVI-pyrocarbon matrix

Pyrocarbon (PyC) matrices were prepared in two kinds of quartz fiber preforms by chemical vapor infiltration (CVI), and then the fibers were leached by HF. Effects of CNTs on the microstructures and mechanical properties of the quartz fiber reinforced carbon composites and PyC matrices, as well as the interface behaviors of the fiber reinforced composites, were discussed. Randomly oriented CNTs reinforced PyC micro-composites account for the pseudo ISO structure and contribute to the mechanical properties of the PyC matrix. Relative strength between reinforcement and matrix and interface bonding significantly affect the mechanical behaviors of the quartz fiber reinforced pyrocarbon composites: Quartz fiber with low strength and strong interface bonding result in limited strengthening effect on flexural strength of the fiber reinforced composite; low strength unidirectional quartz fiber and weak interface bonding in a much stronger matrix result in limited strengthening effect on tensile strength of the composite.     

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.     

Effect of Plasma Treatment of Polyethylene Fibers on Interface and ementitious Composite Properties

It is well known that interfaces in composites play an important role in determining composite properties. In this paper, preliminary results of the improvement in tensile properties of a fiber-reinforced cementitious composite due to plasma treatment of the discontinuous polyethylene fibers are reported. Specific focus is placed on the pseudo strain-hardening composite properties induced by fiber reinforcements and associated load transfer from crackbridging fibers to matrix. Single fiber pullout tests support that the composite property improvement is indeed derived from interfacial property enhancement of the plasma treatment process.     

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.