Thermal behavior of vinyl ester resin matrix composites reinforced with alkali‐treated jute fibers

The thermal behavior of vinyl ester resin matrix composites reinforced with jute fibers treated for 2, 4, 6, and 8 h with 5% NaOH was studied with Thermo‐gravimetric analysis and differential scanning calorimetry. The moisture desorption peak shifted to a higher temperature, from 37 to 58.3°C, for all the treated‐fiber composites because of improved wetting of the fibers by the resin and stronger bonding at the interface. The degradation temperature of the vinyl ester resin in the composites was lowered to 410.3°C from that of the neat resin, 418.8°C. The X‐ray diffraction studies showed increased crystallinity of the treated fibers, which affected the enthalpy of the α‐cellulose and hemicellulose degradation. The hemicellulose degradation temperature remained the same (299.7°C) in all the treated‐fiber composites, but the enthalpy associated with the hemicellulose degradation showed an increasing trend in the treated composites with a small increase in the weight loss. This could be attributed to the increased hydrogen bonding between the more accessible ? OH groups of the hemicellulose in the noncrystalline region of the jute fiber and the resin. The degradation temperature of α‐cellulose was lowered from 364.2 to 356.8°C in the treated composites. The enthalpy of α‐cellulose degradation showed a decreasing trend with a lowering of the weight loss. The crystalline regions of the fiber, consisting of closely packed α‐cellulose chains, were bonded with the resin mainly on the surface through hydrogen bonds and became more resistant to thermal degradation; this reduced the weight loss. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 123–129, 2004     

Structural characterization and tensile properties of Borassus fruit fibers

The chemical and instrumental analysis of alkali‐treated Borassus fibers is carried out to explore the possibility of their use as reinforcement in green composites. The chemical analysis shows presence of α‐cellulose, hemicellulose, and lignin. This is further confirmed by FTIR and high‐resolution solid‐state ¹³C NMR spectroscopy. The influence of alkali treatment on morphology and mechanical properties is attempted by SEM and UTM techniques, respectively. The wide‐angle X‐ray diffraction analysis of the native and treated fibers shows that alkali treatment influences the crystallinity of the fibers. The efficacy of the Borassus fibers (native and treated) as a component of green composites is discussed. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Properties of ligno‐cellulose fiber Hildegardia

Studies on some properties such as the density, the degradation temperatures, the morphology and the spectral features of the ligno‐cellulose fiber Hildegardia were carried out in both untreated and alkali treated form. The fibers are found to have good morphology and moderate initial and final degradation temperatures. On alkali treatment, the lignin was found to be eliminated. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2216–2221, 2002     

Fracture behavior of vinylester resin matrix composites reinforced with alkali‐treated jute fibers

Jute fibers were treated with 5% NaOH solution for 4 and 8 h, respectively, to study the mechanical and impact fatigue properties of jute‐reinforced vinylester resin matrix composites. Mechanical properties were enhanced in case of fiber composites treated for 4 h, where improved interfacial bonding (as evident from scanning electron microscopy [SEM]) and increased fiber strength properties contributed effectively in load transfer from the matrix to the fiber; but their superior mechanical property was not retained with fatigue, as they showed poor impact fatigue behavior. The fracture surfaces produced under a three‐point bend test and repeated impact loading were examined under SEM to study the nature of failure in the composites. In case of untreated fiber composites, interfacial debonding and extensive fiber pullout were observed, which lowered the mechanical property of the composites but improved their impact fatigue behavior. In composites treated for 4 h under repeated impact loading, interfacial debonding occurred, followed by fiber breakage, producing a sawlike structure at the fracture surface, which lowered the fatigue resistance property of the composites. The composites with fibers treated with alkali for 8 h showed maximum impact fatigue resistance. Here, interfacial debonding was at a minimum, and the fibers, being much stronger and stiffer owing to their increased crystallinity, suffered catastrophic fracture along with some microfibrillar pullout (as evident from the SEM micrographs), absorbing a lot of energy in the process, which increased the fatigue resistance property of the composites. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 2588–2593, 2002     

Properties of lignocellulose tamarind fruit fibers

Untreated and alkali‐treated fibers from tamarind fruits were analyzed with Fourier transform infrared, chemical, X‐ray, and thermogravimetric methods. The morphology of the fibers before and after the alkali treatment was studied with scanning electron microscopy. The tensile properties of these fibers before and after the alkali treatment were also studied. The Fourier transform infrared and chemical analyses indicated lowering of the hemicellulose content by the alkali treatment of the fibers. The tensile modulus increased with the alkali treatment. X‐ray diffraction revealed an increase in the crystallinity of the fibers with the alkali treatment. The thermal stability of the fibers increased slightly with the alkali treatment. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Thermal characteristics of ethylene‐co‐vinyl acetate/cellulose microfibers composites

Cellulose microfibers were obtained from Hibiscus sabadariffa by steam explosion technique. Structural and surface analysis of the microfibers showed a reduction in diameter and changes in surface morphology from that of raw fibers. The chemical composition of fibers showed increase in α‐cellulose content and decrease in lignin and hemicelluloses for the microfibers. These factors were further confirmed by XRD, SEM, and FTIR results. The CMF were introduced to EVA at different loading by melt extrusion. The composites were analyzed for their thermal stability and phase transition using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). TGA analysis of the composites showed increased onset temperatures for composites compared with pure EVA indicating the superior thermal stability of the composites with fiber loading. DSC analysis shows increase in melting enthalpy and percentage crystallinity with fiber loading increases. Kinetic parameter for the degradation of the composites was obtained using Broido, Coats–Redfern, and Horowitz‐Metzger methods. POLYM. COMPOS., 2013. © 2013 Society of Plastics Engineers     

Influence of alkali treatment on the fine structure and morphology of bamboo fibers

Bamboo fibers in the form of strips and dust were treated with NaOH solution of varying concentration (10, 15, and 20%). These treated and untreated samples were then subjected to FTIR and morphological studies. Again XRD study was carried out on those treated and untreated bamboo samples in both strip and dust form. It was found that during alkali treatment a lattice transformation from cellulose‐I to cellulose‐II took place. It is observed from IR index value that the conversion is maximum in between 15 and 20% of alkali treatment. Swelling in NaOH introduces considerable changes in crystallinity, orientation angle, etc. Degree of crystallinity and crystallinity index for bamboo strips increases with increasing treatment concentration of alkali and falls off after 15% alkali concentration. This is also supported by d‐spacing value. Orientation factor f_x was calculated from the FWHM and it was found that f_x value has been increased from 0.9879 to 0.9915 for 15% alkali treated and again lowered to 0.8522 for 50% alkali treated samples. Same observation of X‐ray study was obtained for dust samples but at an earlier concentration. Morphological study of bamboo dust with scanning electron microscope indicates fibrillation at higher alkali concentration. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5050–5056, 2006     

Influence of alkali treatment on the structure of newcell fibers

Alkali treatment can change the structures and properties of cellulosic fibers. The aim of this work was to study the mechanism of structural changes of Newcell fibers treated with different alkali concentrations and two treatment methods. Raman spectra showed that the molecular conformation of Newcell fibers remained unchanged. X‐ray diffraction indicated that the crystal structure of Newcell cellulose II, treated with different alkali concentrations and different methods, did not change. With the increase of alkali concentration the crystallinty and crystallinity orientation index of Newcell fibers in their original length decreased slightly, whereas those of fibers in relaxed condition substantially decreased, and the crystallite size of 101¯ and 002 increased in both methods. The quasi‐crystallite disassociation and recrystallization in the quasi‐crystalline phase, during the process of alkali treatment, led to changes of crystallinity and orientation index of Newcell fibers. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1731–1735, 2004     

Effects of sunshine UV irradiation on the tensile properties and structure of ultrahigh molecular weight polyethylene fiber

This study investigated sunlight‐simulated ultraviolet (UV) beam irradiation on the tensile properties and structure of ultrahigh molecular weight polyethylene (UHMWPE) fibers. The tensile results showed that after 300 h sunlight UV irradiation, the tensile properties of the UHMWPE fibers were obviously degraded. Investigation of morphology revealed that the crystallinity was slightly increased, whereas the overall orientation and molecular weight of the fibers were decreased. SEM observations indicated that the degradation process was nonuniform throughout the fiber and a change from a ductile to a brittle fracture mechanism was found after UV irradiation. DMA results showed two β‐relaxations and one α‐relaxation in the original single filament, and UV irradiation led to the increased intensity of the high‐temperature β‐relaxation and the lowered position of the low‐temperature β‐relaxation. This indicated that irradiation‐induced molecular scission and branching were located primarily in the amorphous and the interface areas of the fiber. Changes in the thermal behavior were also examined by DSC. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2757–2763, 2003     

基于显微红外成像技术的碱处理丝瓜络纤维的研究

为了更好地研究碱处理浓度对丝瓜络成分的影响,采用显微红外成像技术对不同浓度碱处理后的丝瓜络进行表征。研究结果表明,碱处理可有效去除丝瓜络中的半纤维素,从而使纤维素含量增加。碱处理2 h条件下,5%的碱溶液即可去除丝瓜络中绝大部分的半纤维素,对于木质素去除也有一定效果;继续提高碱处理浓度并不会进一步降低半纤维素含量,且对木质素去除也没有明显效果,木质素相对含量反而有所上升。与传统的红外光谱法相比,采用显微红外成像技术可研究不同碱处理后丝瓜络中的半纤维素、木质素和纤维素在各扫描微区的组分分布情况,使丝瓜络纤维在碱处理前后形貌及其含量分析表达更加直观,具有图谱合一、可视性、高灵敏度等优点。     

Chemical modification of hemp,sisal, jute,and kapok fibers by alkalization

Plant fibers are rich in cellulose and they are a cheap, easily renewable source of fibers with the potential for polymer reinforcement. The presence of surface impurities and the large amount of hydroxyl groups make plant fibers less attractive for reinforcement of polymeric materials. Hemp, sisal, jute, and kapok fibers were subjected to alkalization by using sodium hydroxide. The thermal characteristics, crystallinity index, reactivity, and surface morphology of untreated and chemically modified fibers have been studied using differential scanning calorimetry (DSC), X‐ray diffraction (WAXRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM), respectively. Following alkalization the DSC showed a rapid degradation of the cellulose between 0.8 and 8% NaOH, beyond which degradation was found to be marginal. There was a marginal drop in the crystallinity index of hemp fiber while sisal, jute, and kapok fibers showed a slight increase in crystallinity at caustic soda concentration of 0.8–30%. FTIR showed that kapok fiber was found to be the most reactive followed by jute, sisal, and then hemp fiber. SEM showed a relatively smooth surface for all the untreated fibers; however, after alkalization, all the fibers showed uneven surfaces. These results show that alkalization modifies plant fibers promoting the development of fiber–resin adhesion, which then will result in increased interfacial energy and, hence, improvement in the mechanical and thermal stability of the composites. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2222–2234, 2002     

Characterization of alkali‐treated jute fibers for physical and mechanical properties

Changes occurring in jute fibers when treated with a 5% concentration of a NaOH solution for 0, 2, 4, 6, and 8 h were characterized by weight loss, linear density, tenacity, modulus, FTIR, and X‐ray measurements. A 9.63% weight loss was measured during 2 h of treatment with a drop of hemicellulose content from 22 to 12.90%. The linear density value showed no change until 2 h of treatment followed by a decrease from 33.0 to 14.5 denier by 56% after 6 h of treatment. The tenacity and modulus of the fibers improved by 45 and 79%, respectively, and the percent breaking strain was reduced by 23% after 8 h of treatment. X‐ray diffractograms showed increase in crystallinity of the fibers only after 6 h of treatment, while FTIR measurements showed much of the changes occurring by 2 h of treatment with an increased amount of OH groups. By measuring the rate of change of the modulus, tenacity, and percent breaking strain with the time of treatment, a clear transition was apparent at 4 h of treatment with the dissolution of hemicellulose, causing a weight loss and drop in the linear density before and development of crystallinity with an improvement in the properties after the transition time. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1013–1020, 2001     

Extraction and characterization of rice straw cellulose nanofibers by an optimized chemomechanical method

In this study, a chemomechanical method was performed to extract nanofibers from rice straw. This procedure included swelling, acid hydrolysis, alkali treatment, bleaching, and sonication. X‐ray diffractometer was employed to investigate the effect of acid hydrolysis conditions and other chemical treatments on the chemical structure of the extracted cellulose fibers. It was concluded that by increasing the acid concentration and hydrolysis time, the crystallinity of the extracted fibers was increased. The optimum acid hydrolysis conditions were found to be 2M and 2 h for the acid concentration and hydrolysis time, respectively. The chemical compositions of fibers including cellulose, hemicelluloses, lignin, and silica were determined by different examinations. It was noticed that almost all the silica content of fibers was solubilized in the swelling step. Moreover, the achieved results showed that the cellulose content of the alkali treated fibers was increased around 71% compared to the raw materials. ATR‐FTIR was applied out to compare the chemical structure of untreated and bleached fibers. The dimensions and morphology of the chemically and mechanically extracted nanofibers were investigated by scanning electron microscopy, field emission scanning electron microscopy, and transmission electron microscopy. The results of the image analyzer showed that almost 50% of fibers have a diameter within a range of 70–90 nm and length of several micrometers. The thermal gravimetric analyses were performed on the untreated and bleached fibers. It was demonstrated that the degradation temperature was increased around 19% for the purified fibers compared to raw materials. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40063.     

Comparison of the structures and properties of Lyocell fibers from high hemicellulose pulp and high α‐cellulose pulp

Lyocell fibers were produced from a cheap pulp with a high hemicellulose content and from a conventional pulp with a high α‐cellulose content. The mechanical properties, supermolecular structure, fibrillation resistance, and dyeing properties as well as the fibril aggregation size of the high hemicellulose Lyocell fiber and high α‐cellulose Lyocell fiber were compared. The results showed that the high hemicellulose spinning solution could be processed at a higher concentration, which improved the mechanical properties and the efficiency of the fiber process. Compared with the high α‐cellulose Lyocell fiber, the high hemicellulose Lyocell fiber had better fibrillation resistance and dyeing properties. Therefore, it is feasible that this cheap pulp with a high hemicellulose content can be used as a raw material for producing Lyocell fibers. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Effect of chemical modifications on the thermal stability and degradation of banana fiber and banana fiber‐reinforced phenol formaldehyde composites

Banana fiber has been modified by treatments with sodium hydroxide, silanes, cyanoethylation, heat treatment, and latex treatment and the thermal degradation behavior of the fiber was analyzed by thermogravimetry and derivative thermogravimetry analysis. Both treated and untreated fibers showed two‐stage decomposition. All the treatments were found to increase the thermal stability of the fiber due to the physical and chemical changes induced by the treatments. The thermal degradation of treated and untreated banana fiber‐reinforced phenol formaldehyde composites has also been analyzed. It was found that the thermal stability of the composites was much higher than that of fibers but they are less stable compared to neat PF resin matrix. Composite samples were found to have four‐stage degradation. The NaOH treated fiber‐reinforced composites have very good fiber/matrix adhesion and hence improvement in thermal stability is observed. Though both silane treatments increased the thermal stability of the composite the vinyl silane is found to be more effective. Heat treatment improves the crystallinity of the fiber and decreases the moisture content, hence an improved thermal stability. The latex treatment and cyanoethylation make the fiber surface hydrophobic, here also the composite is thermally more stable than untreated one. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

Scanning electron microscopy study of raw and chemically modified sisal fibers

Mercerization and acetylation treatments were applied to sisal fibers to enhance adhesion with polymer matrices in composites. The structures of the untreated and treated fibers were assessed with scanning electron microscopy. The waste from sisal‐fiber decortication consisted of mechanical, ribbon, and xylem fibers, and their ultimate cells varied considerably in size and shape. After mercerization and acetylation, the fibers and conductive‐vessel surfaces were successfully changed. The parenchyma cells were partially removed, and the fibrils started to split, because of the alkali action. This increased the effective surface area available for contact with the matrix. The mercerized and acetylated fibers were coated with cellulose acetate by the grafting of the acetyl group in the fibrils. The treatment used to remove lignin and hemicellulose caused changes in the fiber surface but did not damage the fiber structure because the fibrils remained joined in a bundle. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2333–2340, 2004     

Isolation and characterization of betel nut leaf fiber: Its potential application in making composites

Betel nut leaf fiber (BNLF) is a new finding as cellulosic filler for polymer composites. Its main constituents are 75% α‐cellulose, 12% hemicelluloses, 10% lignin, and 3% others matter, viscosity average molecular weight 132,000 and degree of crystallinity 70%. In the present work, BNLF reinforced polypropylene (PP) composites were prepared using heat press molding method. 5–20 wt% short length fiber is taken for getting benefits of easy manufacturing and the fiber was chemically treated with NaOH, dicumyl peroxide (DCP), and maleic anhydride‐modified PP (MAPP) to promote the interfacial bond with PP. The extent of modification of fiber was assessed on the basis of morphology, bulk density, moisture absorption, thermal, and mechanical properties of untreated fiber, treated fiber, and their reinforcing PP composites. The tensile and flexural strength of composites increase with the increase of fiber loading up to 10 and 20 wt%, respectively. It was also observed that Young's modulus and flexural modulus increase with fiber loading. The thermal degradation behavior of resulting composites was investigated. Among the various treated fibers, MAPP‐treated fiber composite showed best interfacial interactions as well as mechanical and thermal properties. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Properties of regenerated cellulose films plasticized with α‐monoglycerides

Regenerated cellulose (RC) films were plasticized with glycerol, glycerin α‐monobutyrate, glycerin α‐monocaproate, glycerin α‐monocaprylate, and glycerin α‐monocaprate. The structure and properties of the films were investigated by using Fourier transform IR, wide‐angle X‐ray diffraction, differential scanning calorimetry, scanning electron microscopy, and tensile tests. The experimental results showed that the addition of plasticizer enhanced the elongation at break, thermal stability, and crystallinity and lowered the tensile strength of the films. The formation of hydrogen bonds between the cellulose and plasticizers weakened the inter‐ and intra‐hydrogen bonds among cellulose molecules, leading to reduced tensile strength. These α‐monoglycerides have relatively good plasticizing effects. Compared with glycerol, the resistance against water washing of the synthesized compounds was significantly enhanced. With the increase of the carbochain length of the α‐monoglycerides, the plasticizing effect decreased but the resistance against water washing was enhanced. When the RC films were immersed in a 10% glycerin α‐monocaproate solution, the elongation at break increased to 15% and stayed at 14.8% after water washing. Glycerin α‐monocaproate might be better for plasticizing RC films than others. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3500–3505, 2003     

Effect of surface treatments on the thermal behavior and tensile strength of piassava (Attalea funifera) fibers

Piassava (Attalea funifera) fibers subjected to several surface chemical treatments and as‐received raw fibers were compared with respect to their thermal and tensile behaviors. The thermal degradation of the raw fibers was characterized by three main stages that corresponded to water release at low temperatures, decomposition of hemicellulose, and decomposition of α cellulose. Mercerization acted mainly on hemicellulose removal, and there was no change in the hydrophilic behavior of the fibers. The removal of hemicellulose split the fibers into microfibrils and favored the thermal decomposition of α cellulose. The same behavior was observed when the fibers were subjected to mercerization and acetylation. The fibers subjected to only acetylation showed thermal behavior similar to that of the raw fibers. With the acetylation treatment, a minor decrease in the hydrophilic character of the fibers was noted. Despite some differences in the thermal behavior, the tensile strengths of the raw and treated fibers were statistically equal. Complementary Fourier transform infrared and scanning electron microscopy analysis corroborated the thermogravimetric analysis/differential thermogravimetry results. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effect of alkali treatment on properties of the lignocellulose fabric Hildegardia

The uniaxial natural fabric from the tree Hildegardia populifolia was treated with 5% aqueous NaOH solution for 0, 2, 4, 6, and 8 h, and the resulting changes were analyzed by density, Fourier infrared spectroscopic, X‐ray, polarized microscopic, and scanning electron microscopic techniques. On alkali treatment, absorption of water and elimination of hemicellulose in the fabric were observed. In each case, the tensile strength, modulus, and percent elongation at break were determined. The tensile strength, modulus, and density were found to be maximum at 4 h of alkali treatment. Hemicellulose was found on the surface of the untreated fabric. After 6 and 8 h of alkali treatment, some microcracks developed in the fabric. The area of the void region in the fabric increased with the duration of alkali treatment. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1604–1608, 2003