Raju Kumar Gupta

Review: Raw Natural Fiber–Based Polymer Composites

The effective utilization of raw natural fibers as indispensable component in polymers for developing novel low-cost eco-friendly composites with properties such as acceptable specific strength, low density, high toughness, good thermal properties, and biodegradability is one of the most rapidly emerging fields of research in polymer engineering and science. In fact, raw natural fiber–reinforced composites are the subject of numerous scientific and research projects, as well as many commercial programs. Keeping in mind the immense advantages of raw natural fibers, in the present article we concisely review raw natural fiber/polymer matrix composites with particular focus on their mechanical properties.

Recent Progress on Ferroelectric Polymer-Based Nanocomposites for High Energy Density Capacitors: Synthesis, Dielectric Properties, and Future Aspects.

Dielectric polymer nanocomposites are rapidly emerging as novel materials for a number of advanced engineering applications. In this Review, we present a comprehensive review of the use of ferroelectric polymers, especially PVDF and PVDF-based copolymers/blends as potential components in dielectric nanocomposite materials for high energy density capacitor applications. Various parameters like dielectric constant, dielectric loss, breakdown strength, energy density, and flexibility of the polymer nanocomposites have been thoroughly investigated. Fillers with different shapes have been found to cause significant variation in the physical and electrical properties. Generally, one-dimensional and two-dimensional nanofillers with large aspect ratios provide enhanced flexibility versus zero-dimensional fillers. Surface modification of nanomaterials as well as polymers adds flavor to the dielectric properties of the resulting nanocomposites. Nowadays, three-phase nanocomposites with either combination of fillers or polymer matrix help in further improving the dielectric properties as compared to two-phase nanocomposites. Recent research has been focused on altering the dielectric properties of different materials while also maintaining their superior flexibility. Flexible polymer nanocomposites are the best candidates for application in various fields. However, certain challenges still present, which can be solved only by extensive research in this field.

Rapid synthesis of graft copolymers from natural cellulose fibers

Cellulose is the most abundant natural polysaccharide polymer, which is used as such or its derivatives in a number of advanced applications, such as in paper, packaging, biosorption, and biomedical. In present communication, in an effort to develop a proficient way to rapidly synthesize poly(methyl acrylate)-graft-cellulose (PMA-g-cellulose) copolymers, rapid graft copolymerization synthesis was carried out under microwave conditions using ferrous ammonium sulfate-potassium per sulfate (FAS-KPS) as redox initiator. Different reaction parameters such as microwave radiation power, ratio of monomer, solvent and initiator concentrations were optimized to get the highest percentage of grafting. Grafting percentage was found to increase with increase in microwave power up to 70%, and maximum 36.73% grafting was obtained after optimization of all parameters. Fourier transforms infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA/DTA/DTG) analysis were used to confirm the graft copolymerization of poly(methyl acrylate) (PMA) onto the mercerized cellulose. The grafted cellulosic polymers were subsequently subjected to the evaluation of different physico-chemical properties in order to access their application in everyday life, in a direction toward green environment. The grafted copolymers demonstrated increased chemical resistance, and higher thermal stability.

Graft copolymers of natural fibers for green composites.

In the present study, free radical induced graft-copolymerization of natural cellulosic polymers (Grewia optiva) has been carried out to develop the novel materials meant for green composites and many other applications. During the graft copolymer synthesis diverse reaction parameters that significantly affect the percentage of grafting were optimized. The structural, thermal and physico-chemical changes in the natural cellulosic polymers based graft copolymers have been ascertained with scanning electron micrography, Fourier transform infrared spectroscopy, thermogravimetric analysis (TGA) and swelling studies. The swelling studies of the grafted cellulosic polymers have been carried out in different solvents to assess the possible applicability of these natural polymers. Green composites were also prepared using raw/grafted cellulosic polymers. It has been found that grafted polymers (Grewia optiva) based green composites gives better tensile properties than the parent natural cellulosic polymers based composites.

Graft copolymers from cellulose: synthesis, characterization and evaluation.

Cellulose, a linear polysaccharide polymer with numerous glucose monosaccharide units is of enormous interest because of its applications in biosorption, biomedical, packaging, biofiltration and biocomposites. In this study, cellulose-graft-poly(butyl acrylate) copolymers were synthesized under microwave conditions. Effects of microwave radiation doses and different reaction parameters were optimized to get the optimum percentage of grafting. The dependence of optimum conditions for better physico-chemical properties of the cellulosic polymers was also determined. Fourier transform infrared spectroscopy (FT-IR) analysis was used to authenticate the chemical reaction taking place between cellulosic polymers and monomer. The thermogravimetric behavior of the raw and grafted cellulosic polymers was characterized by thermogravimetric analysis (TGA). The surface structure of the raw and grafted cellulosic polymers was analyzed through scanning electron microscopy (SEM). The graft copolymers have been found to be more moisture resistant and also showed better chemical and thermal resistance.

Surface modification of cellulose using silane coupling agent

Recently there has been a growing interest in substituting traditional synthetic polymers with natural polymers for different applications. However, natural polymers such as cellulose suffer from few drawbacks. To become viable potential alternatives of synthetic polymers, cellulosic polymers must have comparable physico-chemical properties to that of synthetic polymers. So in the present work, cellulose polymer has been modified by a series of mercerization and silane functionalization to optimize the reaction conditions. Structural, thermal and morphological characterization of the cellulose has been done using FTIR, TGA and SEM, techniques. Surface modified cellulose polymers were further subjected to evaluation of their properties like swelling and chemical resistance behavior.

Development of functionalized cellulosic biopolymers by graft copolymerization.

Natural lignocellulosic polymers are one of the most promising biodegradable, non-toxic and eco-friendly polymeric materials which have been used to develop various products for number of applications especially in green composites. However, these cellulosic materials have certain drawbacks, like sensitivity to water and moisture, and need to be modified. So in this article, a treatment of lignocellulose biopolymers with suitable acrylate monomer was investigated. The influence of different reaction parameters on efficiency (grafting) was investigated. SEM, TGA and Fourier transform infrared spectroscopy (FT-IR) were used to study the graft copolymerization between the monomer and hydroxyl groups of lignocellulosic biopolymers. This article also discusses swelling, and chemical resistance properties of the both the grafted/ungrafted cellulosic biopolymer and their potential candidature for green composite applications.

Gold-Nanoparticle-Functionalized In2O3 Nanowires as CO Gas Sensors with a Significant Enhancement in Response

We present the room-temperature sensing of gold nanoparticle (AuNP)-functionalized In(2)O(3) nanowire field-effect transistor (NW-FET) for low-concentration CO gas. AuNPs were functionalized onto In(2)O(3) nanowires via a self-assembled monolayer of p-aminophenyltrimethoxysilane (APhS-SAM). The nanowires were mounted onto the Au electrodes with both ends in Schottky contacts. High sensor response toward low concentration of CO gas (200 ppb-5 ppm) at room temperature is achieved. The presence of AuNPs on the surface of In(2)O(3) nanowire serves to enhance the CO oxidation due to a higher oxygen ion-chemisorption on the conductive AuNP surfaces. Detailed studies showed that the sensing capabilities were greatly enhanced in comparison to those of bare nanowires or low coverage of Au NP-decorated nanowires. When the sensor is exposed to CO, the CO molecules interact with the preadsorbed oxygen ions on the AuNP surface. The CO oxidation on the AuNPs leads to the transfer of electrons into the semiconducting In(2)O(3) nanowires and this is reflected as the change in conductance of the NW-FET sensor. This work provides a promising approach for fabricating nanowire devices with excellent sensing capabilities at room temperature.

Synthesis of lignocellulosic polymer with improved chemical resistance through free radical polymerization

Rising environmental awareness has resulted in a renewed interest in biological macromolecules obtained from renewable resources. So in view of technological significance of natural lignocellulosic polymers in numerous applications, the present study is an attempt to synthesize lignocellulosic polymers based graft copolymers using free radical polymerization. Different reaction conditions have been studied to synthesize the lignocellulosic graft copolymers. The graft copolymers have been characterized with scanning electron micrography (SEM), Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). The grafted samples have also been screened against different physico-chemical conditions to assess their applicability in different applications.

Graft Copolymers from Natural Polymers Using Free Radical Polymerization

The present research work deals with the surface modification of natural cellulosic polymers to develop novel materials for different applications. Natural cellulose-graft-poly (methyl acrylate) copolymers were prepared using the free radical induced graft copolymerization technique. Different reaction parameters were optimized to achieve the highest percentage of grafting of natural cellulose-graft-poly (methyl acrylate) copolymers. The natural cellulose graft copolymers were characterized by FT-IR, SEM, TGA, and physicochemical studies. For the evaluation of swelling and the physicochemical mechanism, swelling and chemical resistance studies were carried out in different solvents as well as chemicals.