Bamboo cellulose was prepared by chemical process involving dewaxing, delignification, and mercerization process. Four samples namely, green bamboo fiber (GBF), dewaxed bamboo fiber (DBF), delignified bamboo fiber (DLBF), and cellulose fiber (CF) had been analysed. FTIR and TGA analysis confirmed the removal of hemicellulose and lignin at the end stage of the process. FTIR results reveal that the D-cellulose OH group occurred at 1639 cm−1region. SEM micrograph showed that mercerization leads to fibrillation and breakage of the fiber into smaller pieces which promote the effective surface area available for contact. Barrer, Joiyner, and Halenda (BJH) method confirmed that the effective surface area of CF is two times larger compared to GBF. CF showed the highest activation energy compared to GBF. It indicates that CF was thermally stable.

The tensile properties of chemically treated jute fiber reinforced polyethylene/clay nanocomposites were investigated. Nanocomposites were prepared using hot press moulding technique by varying jute fiber loading (5, 10, 15 and 20 wt%) for both treated and untreated fibers. Raw jute fibers were chemically treated with benzene diazonium salt to increase their compatibility with the polyethylene matrix. Physical and mechanical properties were subsequently characterized. Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) analysis was utilized to study physical properties. Tensile test was conducted for mechanical characterization. FTIR and SEM study showed interfacial interaction among jute fiber, polyethylene and nanoclay. It was observed that at optimum fiber content (15 wt%), treated composites exhibited improvements in tensile strength and modulus by approximately 20 % and 37 % respectively over the raw ones. On the other hand, this composite exhibited improvements in tensile strength and modulus by approximately 8 % and 15 % respectively over the composites without nanoclay. However, treated jute fiber reinforced composites showed better tensile properties compared with untreated ones and also nanoclay incorporated composites enhanced higher tensile properties compared without nanoclay ones.

a b s t r a c tNanoclay is considered potential nanofiller for the manufacturing of natural fiber nanocomposites. The hydrophilic nature of natural fibers affects negatively its adhesion to hydrophobic polymer matrix. In the present study, propionic anhydride (PA) treated jute were used for the manufacturing of jute/ polyethylene/nanoclay nanocomposites. Different amount (wt%) of montmorillonite (MMT) were used as nanofiller in order to optimize the nanoclay in the composite system. Finally, the nanocomposites were prepared using hot press machine at 5, 10, 15, and 20 wt% fiber loadings. Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), tensile tests, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and chemical resistance test were used to evaluate the morphological, thermo-mechanical and chemical resistance properties of the composites.

Hybrid composites were fabricated by hexamethylene diisocyanate (HDI) treated jute–bamboo fiber, nanoclay, tin(IV) oxide nanopowder, and low‐density polyethylene. The composites were characterized by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis, and differential scanning calorimetry. Surface morphology, tensile testing, and water absorption test were also reported. FTIR results revealed that treated fiber had covalence bonding with polymer matrix which enhanced mechanical properties. All HDI‐treated hybrid composites showed significant improvement in activation energy, lower crystallinity index, significant high tensile strength, and Young's modulus compared to untreated hybrid composites. All treated hybrid composites also showed extreme low water absorption. The addition of nanoclay or tin(IV) oxide into treated hybrid composites had a negative impact on thermal‐mechanical properties. Surface morphological results revealed the bonding condition among hybrid composites. J. VINYL ADDIT. TECHNOL., 24:358–366, 2018. © 2017 Society of Plastics Engineers

In the present study, batai wood (Paraserianthes moluccana) was impregnated with a combination of styrene, methyl methacrylate, and nanoclay in order to improve compression strength, thermal stability, and surface morphology. Styrene (ST) and methyl methacrylate (MMA) cross-linker introduced a co-polymerization reaction with cellulose in the wood cell wall and produced wood polymer composites (WPCs), as confirmed by Fourier Transform Infrared (FT-IR) Spectroscopy. The mechanical properties of the WPCs were significantly increased compared to the raw wood. Thermal properties of both raw wood and WPCs were evaluated by thermogravimetric analysis (TGA). WPCs exhibited higher thermal stability relative to the raw wood due to the copolymerization reaction. The surface morphologies of the fracture surface for both the raw wood and WPCs were recorded using scanning electron microscopy (SEM). The SEM micrographs reveal that after polymerization, WPCs show smoother texture and adhesion compared to that of raw wood.

Polyvinyl alcohol (PVA)/fumed silica/clay nanocomposites are prepared via solution intercalation by exploiting phase separation based on the bridging of particles by polymer chains. PVA/fumed silica/clay nanocomposites are characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy, and thermogravimetric analysis. Mechanical properties are determined by universal testing machine. From FTIR results, it indicates that IR spectrum for PVA/fumed silica/clay nanocomposites, especially PVA/fumed silica/clay (1.30E) nanocomposites, is much broader than pure PVA and other clay nanocomposites. The better interfacial bonding between PVA/fumed silica/clay (1.30E) nanocomposites are reflected in the improvement of the mechanical properties as well as thermal stability. The surface area analysis result proves that the PVA/fumed silica/clay (1.30E) nanocomposites have higher surface area and pore volume with less pore size. With the addition of 1.30E clay to the composite system, the tensile strength and modulus had shown the highest values as well as higher activation energy for thermal decomposition. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41843.

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In this study, the physical, morphological, mechanical and thermal properties of furfuryl alcohol/2-ethylhexyl methacrylate/halloysite nanoclay wood polymer nanocomposites (FA-co-EHMA-HNC WPNCs) were investigated. FA-co-EHMA-HNC WPNCs were prepared via an impregnation method and the properties of the nanocomposites were characterized through the weight percent gain, Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), three-point flexural test, dynamic mechanical thermal analysis (DMTA), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) analysis and moisture absorption test. The weight percent gain in the 50:50 FA-co-EHMA-HNC WPNC was the highest compared with the raw wood (RW) and other WPNCs. The FT-IR results confirmed that polymerization took place in the nanocomposites, especially 50:50 FA-co-EHMA-HNC WPNC, which had a reduced amount of hydroxyl groups. The SEM results revealed that the 50:50 FA-co-EHMA-HNC WPNC had the smoothest and most uniform surface among all of the nanocomposites. The 50:50 FA-co-EHMA-HNC WPNC showed the highest flexural strength and modulus of elasticity. The results revealed that the storage modulus and loss modulus of the FA-co-EHMA-HNC WPNCs were higher and the tan δ of FA-co-EHMA-HNC WNPCs was lower compared with the RW. The FA-co-EHMA-HNC WPNCs exhibited the higher thermal stability in the TGA and DSC analysis. The 50:50 FA-co-EHMA-HNC WPNC exhibited remarkably lower moisture absorption compared with the RW. Overall, this study proved that the ratio 50:50 FA-co-EHMA ratio was the most suitable for introduction in the in the RW.