Cellulose whiskers were isolated from kenaf (Hibiscus cannabinus L.) bast fibers via sulfuric acid and hydrochloric acid hydrolysis. Raw kenaf bast, NaOH treated, bleached fibers, sulfuric acid whiskers (SAW) and hydrochloric acid whiskers (HClW) morphology, functional groups, crystallinity, and thermal stability were characterized. The TEM im ages showed that the sulfuric acid and HCl whiskers have average diameters and length range of 3 nm and 100 - 500 nm, respectively. The FTIR study indicated that during the conversion process, most of the hemicellulose and almost all the lignin were removed by the NaOH and subsequent bleaching treatments. The crystallinity of HCl whiskers was found to be higher (84%) than that of sulfuric acid whiskers (72%). Thermogravimetric analysis indicated that HCl whiskers had better thermal stability than the sulfuric acid ones. In addition, a two-stage decomposition behavior was revealed by TGA in the sulfuric acid whiskers because of incorporation of the sulfate group with the cellulose crystals.
Cellulose is the most abundant biorenewable material on earth. It is an infinite source of raw material for environmentally-friendly and biocompatible products [
The crystalline region of microfibrils, called cellulose whiskers, is almost defect-free, with the consequence of axial physical properties of cellulose biogenesis approaching those of perfect crystals [
The advancement in nanotechnology has brought about a trend in isolating whiskers from various cellulose sources such as ramie [
Acid hydrolysis can be used to isolate cellulose whiskers. It is a simple process which can be carried out using different type of acid and combinations of concentration, time and temperature [8,13,14]. The amorphous part of cellulose more susceptible undergoes acidic hydrolysis compared to crystalline part. Nevertheless, the crystalline part can be smoothly hydrolyzed by concentrated acids such as concentrated sulfuric acid and supersaturated hydrochloric acid [
Previously studies highlighted a potential for kenaf fiber to act as filler or reinforcement agent in biocomposites [17-19]. Kenaf (Hibiscus cannabinus L.) consists of two separate parts known as bast and core. The bast is the outer section of the plant stem while the core is its inner part [
As stated above, numerous studies have investigated the isolation and properties of cellulose whiskers. Based on our knowledge very little information has been reported on characterization of cellulose whiskers from kenaf bast. Therefore, the main objective of this work was to isolate cellulose whiskers from kenaf bast fibers by acid hydrolysis and to characterize their properties. The influence of different solvents on the morphology, crystallinity, and thermal stability of the resulting whiskers were also evaluated.
Four-month old kenaf stems of variety 36 were obtained from the experimental plot of the National Kenaf and Tobacco (NKTB) Company, Malaysia. Sulfuric acid (95%), chloroform, and HCl (37%) were purchased from Aldrich while sodium chlorite and sodium hydroxide were supplied by RND I-Tech Sdn., Malaysia. The harvested kenaf stems were peeled to separate the outer part (bast) from the inner part (core). The bast was then dried in an industrial oven to a moisture content of 9.8%.
The whiskers were isolated from kenaf bast fibers following the method of Siquera et al. [
Kenaf bast was ground to 0.25 mm size by FRITSCH universal cutting mill pulverisette and treated with 4% (w/w) NaOH solution at 80˚C for 2 hours. This treatment was repeated 3 times. After each treatment, fibers were filtered and washed with distilled water until the alkali was completely removed. A subsequent bleaching treatment of the fibers using the same amount of acetate buffer, aqueous chlorite (1.7% w/w), and distilled water was applied in order to bleach the fibers. The bleaching treatment was carried out four times at 80˚C for 2 hours (each treatment) under mechanical stirring. Acid hydrolysis was performed by subjecting 4% - 6% (w/w) bleached kenaf bast pulp into pre-heated 65% (v/v) sulfuric acid at a temperature of 50˚C for 60 min. The suspension was constantly mixed using magnetic stirrer. Then, the hydrolyzed pulp was centrifuged at 4000 rpm for 30 min and dialyzed in distillated water. Subsequently, the whiskers suspension was homogenized by using an Ultra Turax T25 homogenizer for 5 min. Some drops of chloroform were added as protectant to the whiskers suspension which was stored at 4˚C.
The second hydrolysis treatment was conducted using HCl as described by Braun et al. [
Scanning electron microscopy (SEM) analysis was performed using a Jeol JSM 7600F Scanning Electron Microscope. Glimmer plates were fixed with conducting carbon on a specimen holder and then a drop of diluted fibril (raw kenaf bast, NaOH treated, or bleached fibers)/ water suspension (1:20 w/v) was put onto it. The samples were air-dried and the remaining fibrils were sputtered with a platinum layer about 5 nm thick. The images were taken with an accelerating voltage of 2 kV and 100 fibers diameter was measured.
The size and shape of whiskers were studied using a transmission electron microscope Hitachi model H-7100. A drop of diluted kenaf whiskers suspension was deposited on the carbon-coated grids and allowed to dry at room temperature. The grid was stained with a 0.5% solution of uranyl acetate and dried at room temperature. Measurement of 150 fibers diameter were carried out using an image analyzer program, XL Docu.
A Fourier transform infrared spectroscopy (FTIR) study was done using Perkin-Elmer spectrometer 100. Prior to this analysis, all fibers were ground to a diameter of about 100 µm and then mixed with KBr to prepare homogeneous suspensions and afterwards pressed into transparent pellets and analyzed in transmittance mode within the range of 4000 - 500 cm−1.
Structural and phase analyses of the samples were implemented using an X-ray diffractometer (Philips P W 3040/60 X’pert Pro) with CuKα radiation (wavelength of 1.5405 Å) and step-scan mode (2θ range: 5˚ - 60˚). The crystalline index of cellulose, CIr, was calculated using the following equation [
where I002 is the intensity of lattice peak diffraction and Iam is the peak intensity of the amorphous fraction. A diffraction angle of around 2θ = 22.5˚ was peak for plane (002) and the lowest intensity at a diffraction angle of around 2θ = 18.0˚ was measured as the amorphous part.
Thermal stability data was obtained using the TGA/ SDTA 851 (Mettler Toledo) thermogravimetric analyzer under linear temperature conditions. The samples were heated in platinum crucibles within the temperature range 35˚C - 600˚C at a rate of 10˚C/min in a nitrogen atmosphere.
The isolation of whiskers from kenaf bast is a multistep process which involves chemical treatments. Firstly, the fibers should be separated from their cell walls in order to be able to study the properties of this nanomaterial. Proper chemical treatment to obtain the whiskers without damaging the fibers is needed.
chemical treatments on the morphology of kenaf bast fibers.