Extraction and characterization of new cellulosic fibers from Indian mallow stem: An exploratory investigation

Natural fibers are one of the good alternative sources for replacing synthetic fiber and reinforcing polymer matrices because of their eco-friendly nature. This investigation deals with the extraction and characterization of new natural fiber from Indian mallow plant stem. The physico-chemical, thermal, and mechanical properties of Indian mallow fibers (IMFs) were reported and compared with other natural fibers for the first time. Cellulose (78.22%), wax (0.47%), density (1.33 g/cm³), and tensile strength (979.83 MPa) were recognized in IMFs. Fourier transform-infrared spectroscopy, X-ray diffraction, and thermo-gravimetric analysis confirmed that IMFs are rich in cellulose content and thermally stable with a crystallinity index of 72%.     

Characterization of new cellulosic fiber from the stem of Sida rhombifolia

Natural fibers play a vital role in the field of composites mainly due to their environmental friendliness, the nature of their disposal, and low energy requirement for processing. Recently, research ideas have focused on exploration of promising natural fibers with superior mechanical properties. Sida rhombifolia is one such perennial shrub from which high stiffness natural fibers can be extracted. The physico-chemical properties of Sida rhombifolia fibers (SRFs), crystallinity index (56.6%), higher cellulose (75.09 wt.%) content, and lower density (1320.7 kg/m³) were revealed and compared to those properties of other natural fibers.     

Extraction and characterization of alkali-treated red coconut empty fruit bunch fiber

This article discusses the extraction and characterization of new natural fiber extracted from red coconut empty fruit bunch. The physicochemical, mechanical, and thermal properties of alkali-treated red coconut empty fruit bunch fibers (ARCEFBFs) were reported and compared with other natural fibers for the first time. Cellulose content (65.02 wt%), wax (0.32 wt%), density (1.421 g/cc), and tensile strength (1299.49 MPa) were identified in ARCEFBFs. Fourier transform infrared spectroscopy and X-ray diffraction analysis confirmed that ARCEFBFs are rich in cellulose content with crystallinity index of 53.6%. Thermogravimetric analysis revealed that these fibers are thermally stable until 270.48°C.     

Extraction and characterization of new natural lignocellulosic fiber Cyperus pangorei

This research is focused on the study of the physical, chemical, mechanical, and thermal properties of a newly identified natural stem fiber, Cyperus pangorei. The chemical composition of Cyperus pangorei fibers (CPF) such as cellulose, lignin, ash, moisture, and wax contents was evaluated. Besides these, the fiber density was determined and the apparent diameter was measured using an optical microscope. Further, tensile, thermal, XRD, and FT-IR studies were performed to evaluate the suitability of the fiber as a reinforcement. The surface topography of CPF was analyzed using scanning electron microscopy (SEM). Encouraging properties such as increased stiffness, fiber texture, and higher thermal stability suggest the suitability of CPF as reinforcement in polymer matrices.     

Characterization of new natural cellulosic fiber from the Ipomoea staphylina plant

Natural fibers extracted from plants play a major role as reinforcement in polymer composite materials due to their superior properties. This work aims to comprehensively characterize the physical and chemical properties of Ipomoea staphylina fibers (ISFs), which are extracted from the stem of the Ipomoea staphylina plant. The ISFs show cellulose content (72.76 wt%), hemicelluloses content (13.6 wt%), density (1401 kg cm^?3), and tensile strength of 173–658 MPa with a strain rate of 2.03–6.63%. The thermal stability of ISFs illustrate that the fibers are stable up to a temperature of 311°C with kinetic activation energy of 99.82 kJ mol^?1.     

Characterization of new natural cellulosic fiber from the Perotis indica plant

This investigation summarizes the characteristics of biofiber extracted from the Perotis indica plant. Cellulose content (68.4 wt%), density (785 kg m^?3), crystallinity index (48.3%), tensile strength (317–1,608 MPa), and Young’s modulus (8.41–69.61 GPa) properties were identified in the P. indica fibers (PIFs), and thermal stability was studied using thermal gravimetric analysis and derivative thermogravimetric analysis, which revealed its cellulose degradation at a temperature of 339.1°C. Further, the properties of PIFs ensured that it can play an imperative role as new reinforcement as green composites in the manufacturing industries.     

Physico-chemical properties of new cellulosic fibers from the bark of Acacia planifrons

Identification of new natural fibers is growing due to their superior properties and the impetus for researchers to develop high-performance composites. This investigation was aimed at understanding the physico-chemical properties of Acacia planifrons fibers (APFs). The crystalline structure of APFs was analyzed by X-ray diffraction, and the crystallinity index (65.38%) was calculated. The chemical functional group of APFs was confirmed by Fourier transform-infrared spectroscopy, the thermal stability measured by thermogravimetric analysis, and surface characterization established by atomic force microscopy. Taken together, all the properties of APFs can play a vital role in establishing APFs as new reinforcement in polymer composites.     

A new study on effect of various chemical treatments on Agave Americana fiber for composite reinforcement: Physico-chemical,thermal, mechanical and morphological properties

This research is focused to fundamentally understand the benefits of using Agave Americana C. plant as potential reinforcement in polymeric composites. The fibers were extracted from the external part of the bark of the plant, which grows worldwide in pastures, grasslands, open woodlands, coastal and riparian zones. In order to use the natural fiber as reinforcement it is paramount important to probe their chemical composition, microstructural behavior and mechanical properties. Hence, firstly the extracted fibers were chemically treated with NaOH, stearic acid, benzoyl peroxide and potassium permanganate. The chemical composition in terms of cellulose, hemicellulose, lignin and other waxy substances were determined using a standard TAPPI method. FT-IR technique was used to understand the character of molecular bonds, crystallinity and their correlations with various bonds in fiber structure. The thermal stability was investigated through thermogravimetric and differential scanning calorimetric analysis, and the mechanical characterization was performed by applying standard tensile test. The surface morphology of fibers was examined through scanning electron microscopy (SEM) and finally reliability scrutiny of all the analysis was carried out. The results of chemical modification techniques applied on the surfaces of natural fibers allows to produce superior fibers used to form the novel composite materials for light-weight application.     

Physicochemical properties of new cellulosic Artisdita hystrix leaf fiber

The characterization of new natural fiber is increasing due to its excellent properties. This drives investigators to create high performance composites. The present investigation was designed to study the physicochemical properties of fibers obtained from the leaf of the Artistida hystrix. The Artistida hystrix fibers (AHFs) had crystallinity index (44.85%), cellulose (59.54 wt%), hemicellulose (11.35 wt%), lignin (8.42 wt%), and density (540 kg m^?3). The tensile strength of AHFs was 440 ± 13.4 MPa with an average strain rate of 1.57 ± 0.04%. The calculated microfibril angle of AHFs was 12.64 ± 0.45°, which influenced the mechanical properties.     

Extraction,modification, and characterization of natural ligno-cellulosic fiber strands from napier grass

Napier grass is a high-productivity perennial grass that is a very important forage for animals in the tropics. In this research work, fiber strands from Napier grass were extracted and the effect of acetic acid treatment on their chemical composition, morphological and structural changes, and tensile and thermal properties was studied. The acid treatment was carried out using glacial acetic acid solution at three different concentrations (5, 10, and 15%) for 2 h. Chemical analysis indicated lowering of amorphous hemicellulose content on acid treatment. FT-IR spectroscopic studies revealed variation of functional groups on acid treatment. Scanning electron micrographs indicated roughening of the surface of the fiber strands due to the removal of the hemicellulose layer on acid treatment. X-ray diffraction analysis indicated an increase in crystallinity of the fiber strands on acid treatment. The thermal stability and tensile properties of the fiber strands increased on acid treatment. This fiber has competitive advantages when evaluated with other natural fibers and can be developed further as a potential reinforcement in polymer matrix composites.     

The effect of grass fiber filler on curing characteristics and mechanical properties of natural rubber

Natural rubber is reinforced with a novel type of grass fiber (Cyperus Tegetum Rox b). The effects of fiber loading of different mesh sizes on curing characteristics and mechanical properties of grass fiber filled natural rubber composite are studied. Since 400 mesh grass fiber loaded natural rubber composite shows superior mechanical properties, therefore the effect of silane coupling agent was studied for this particular composite. Here composites were prepared by using water leached grass fiber. Optimum cure time increases with the increase in fiber loading but the change in scorch time is less. The same trend of increase in optimum cure time is observed in the presence of Si69. But the value is higher compared to that of rubber composite without Si69. With increase in the fiber loading, modulus and hardness of the composite increases but tensile strength decreases. The mechanical properties of the composite, namely moduli at 200 and 300% elongation and hardness increase in the presence of Si69 but tensile strength is less compared to that of the composite without Si69. Elongation at break is not much affected due to the presence of Si69. Copyright © 2004 John Wiley & Sons, Ltd.     

Extraction and characterization of natural cellulosic fiber from Passiflora foetida stem

This article presents a comprehensive characterization study of natural cellulosic fiber extracted from Passiflora foetida vine stem. The chemical composition of the obtained P. foetida fibers (PFFs) comprised high cellulose (77.9 wt%) and low lignin (10.47 wt%) content and had distinctly higher crystallinity (67.36%) of cellulose, which was determined by an X-ray diffractometer. The PFFs exhibited good tensile strength of 248?942 MPa associated with elongation (1.38?4.67%) during tensile testing. Thermogravimetric analysis revealed that the PFFs are thermally stable up to 320°C with kinetic activation energy of 85.46 kJ mol^?1; hence they ensure their suitability as a reinforcing phase in composites for potential applications.     

Physicochemical and tensile properties of alkaline-treated new natural cellulosic Gossypium arboreum fiber

This article describes the characterization of novel natural lignocellulosic bark fibers extracted from the stem of the Gossypium arboreum (cotton) plant. The G. arboreum stem fibers were treated with 5% (w/v) aqueous NaOH solution for different soaking times, and the Fourier transform infrared spectroscopy analysis was conducted to examine the chemical compounds of the raw and treated fibers. The cellulose content improved from 70.06 to 83.91% after the treatment. The X-ray diffraction results indicate that the crystalline index and size were enhanced. Thermogravimetric analysis was performed to study the thermal properties and found that the thermal stability was higher for the treated fibers. The tensile strength and modulus were increased for the alkaline-treated fibers compared to the untreated fibers.     

Physicochemical properties of alkali-treated new cellulosic fiber from cotton shell

The aim of this present investigation was to identify a new natural fiber from one of the cotton plant’s byproducts, which is chemically modified by alkaline treatment. Its characteristics were examined for the preparation of natural fiber–reinforced polymer composites. The cotton shell fibers (CSFs) were extracted from the cotton shell and its degree of crystallinity, crystallite size, chemical constituents group, and thermal stability were determined by X-ray diffraction, Fourier transform infrared (FTIR) spectroscopy and thermogravimetric analysis. The alkali treatment of CSFs is optimized at 5% (w/v) NaOH aqueous solution with 45 min soaking time.     

Characterization and Studies on Grafting of Methyl Methacrylate onto PAN Fibers

The graft copolymerization of methyl methacrylate (MMA) onto commercial acrylic fibers (PAN) has been studied using Azobis(isobutyro)nitrile (AIBN) as an initiator. MMA grafting initiated by radicals formed from thermal decomposition of AIBN. In this study, the effects of monomer and initiator concentration, time and temperature reaction on the grafting yield have been investigated.

The optimum conditions for this grafting reaction were obtained with an MMA concentration of 0.7 M, an AIBN concentration of 0.0073 M, a reaction temperature of T=85°C and with a 60 min reaction time.

The fiber structure has been investigated by different experimental techniques of characterization such as Fourier transform infrared spectroscopy (FT‐IR), calorimetric analysis (DSC), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), water absorption and the physical and mechanical properties has also been investigated in this study. The thermal analysis data showed that by increasing grafting yield, little changes have occurred in fibers samples up to 13.5% of grafting yield and the thermal transitions of grafted fibers have approximately the same behavior compared with the raw fibers sample. Grafting also slightly affected the fiber morphology. The experimental data of mechanical properties clearly show that by increasing grafting yield, max extension will decrease but this change up to 13.5% grafting yield is barely noticeable. Grafting of poly MMA improved water absorption.     

Structural modifications of swift heavy ion irradiated PEN probed by optical and thermal measurements

The effects of swift heavy ion irradiation on the structural characteristics of Polyethylene naphthalate (PEN) were studied. Samples were irradiated in vacuum at room temperature by lithium (50 MeV), carbon (85 MeV), nickel (120 MeV) and silver (120 MeV) ions with the fluence in the range of 1×10¹¹–3×10¹²  ions cm⁻². Ion induced changes were analyzed using X-ray diffraction (XRD), Fourier transform infra red (FT-IR), UV–visible spectroscopy, thermo-gravimetric analysis (TGA) and differential scanning calorimetry (DSC) techniques. Cross-linking was observed at lower doses resulting in modification of structural properties, however higher doses lead to the degradation of the investigated polymeric samples.     

Evaluation of physico-chemical properties of electron beam-irradiated polycarbonate film

In this work, polycarbonate (PC) film samples were irradiated with 10 MeV electrons at different doses ranging from 25 to 250 kGy. Characterization techniques viz. thermogravimetric analysis (TGA), Fourier transform infra-red spectroscopy (FTIR), X-ray diffraction analysis (XRD) and electron paramagnetic resonance (EPR) were exploited to understand the induced changes in the physico-chemical properties of the polymer. An increase in the decomposition temperature with increasing dose was observed, while the crystallinity remained unchanged as a result of the formation of cross-link bond. EPR technique characterized the stability of the free radicals in the irradiated PC. The result showed that cross-linking process occurs at low absorbed doses, whereas polymer degradation happens at higher doses.     

Investigation of structural,rheological and thermal properties of PMMA/ONi-Al LDH nanocomposites synthesized <Emphasis Type="Italic">via</Emphasis> solvent blending method: Effect of LDH loading

This article addresses the synthesis of organically tailored Ni-Al layered double hydroxide (ONi-Al LDH) and its use in the fabrication of exfoliated poly(methyl methacrylate) (PMMA) nanocomposites. The pristine Ni-Al LDH was initially synthesized by co-precipitation method and subsequently modified using sodium dodecyl sulfate to obtain ONi-Al LDH. Nanocomposites of PMMA containing various amounts of modified Ni-Al LDH (3 wt%-7 wt%) were synthesized via solvent blending method to investigate the influence of LDH content on the properties of PMMA matrix. Several characterization methods such as X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), rheological analysis, differential scanning calorimetry (DSC) and thermo gravimetric analysis (TGA), were employed to examine the structural, viscoelastic and thermal properties of PMMA/OLDH nanocomposites. The results of XRD and TEM examination confirm the formation of partially exfoliated PMMA/OLDH nanocomposites. The FTIR results elucidate that the characteristic bands for both pure PMMA and modified LDH are present in the spectra of PMMA/OLDH nanocomposites. Rheological analyses were carried out to examine the adhesion between polymer matrix and fillers present in the nanocomposite sample. The TGA data indicate that the PMMA nanocomposites exhibit higher thermal stability when compared to pure PMMA. The thermal decomposition temperature of PMMA/OLDH nanocomposites increases by 28 K compared to that of pure PMMA at 15% weight loss as a point of reference. In comparison with pure PMMA, the PMMA nanocomposite containing 7 wt% LDH demonstrates improved glass transition temperature (T _g) of around 3 K. The activation energy (E _a), reaction orders (n) and reaction mechanism of thermal degradation of PMMA/OLDH nanocomposites were evaluated using different kinetic models. Water uptake capacity of the PMMA/OLDH nanocomposites is less than that of the pure PMMA.     

Pyrolysis-FTIR and TGA techniques as tools in the characterization of blends of natural rubber and SBR

The employment of used tyres as a new source of raw materials for different applications can be a partial solution to the great environmental problems generated by these products concerning their disposal at waste depots. In this study, high-resolution thermogravimetric analysis (Hi-Res TGA) is used to quantify the elastomer composition of SBR/NR in tyre formulations. This technique provides the ability to generate TGA derivative profiles (DTGA), which can be used to distinguish different formulations from appropriate calibration curves. Infrared spectroscopy (FTIR) is also employed for composition quantification of used tyres and the results are compared to those obtained by Hi-Res TGA. Both analysis methods give satisfactory results when applied to elastomer mixtures of known composition and to tyre rubbers of unknown composition. The study confirms the accuracy of high-resolution TGA-DTGA technique for rapid quantitative determination of elastomer blends in used tyres.     

Adsorption and inactivation behavior of horseradish peroxidase on cellulosic fiber surfaces

The physical immobilization behavior of horseradish peroxidase (HRP) on cellulosic fiber surfaces was characterized using adsorption and inactivation isotherms measured by the depletion method followed by fitting of Langmuir’s and Freundlich’s models to the experimental data. The adsorption and inactivation behavior of simpler and relatively non-porous high and low crystalline cellulosic substrates (microcrystalline cellulose and regenerated cellulose) as well as more complex and porous cellulosic pulp fibers (bleached kraft softwood fibers) were investigated. The effect of the sorbent surface energy on HRP adsorption was demonstrated by increasing the hydrophobicity of the cellulosic fibers using an internal sizing agent. The influence of the fiber surface charge density on HRP adsorption was studied via modification of the cellulosic fibers using TEMPO (2,2,6,6-tetramethyl-1-piperidiniloxy radical)-mediated oxidation methods. Results showed that hydrophobic interactions had a much larger effect on HRP adsorption than electrostatic interactions. More hydrophobic fiber surfaces (lower polar surface energy) result in larger enzyme-fiber binding affinity constants and higher binding heterogeneity. It was also found that oxidation of the cellulosic fiber substrate reduces enzyme adsorption affinity but significantly increases the loading capacity per unit weight of the surface.