Incorporation of silver nanomaterial into polymer matrix can further accomplished their potential usage in real life
applications. In our previous study, silver nanoparticles (AgNPs) and silver-graphene oxide nanocomposites (AgGO)
were prepared via a rapid microwave-assisted method. Hereby, the as-synthesized AgNPs or AgGO was dispersed in a
chitosan solution. Subsequently, the resultant mixture solution was further coagulated in a coagulation bath containing
sodium hydroxide via a neutralization process. This resulted in the formation of spherical-shaped chitosan beads.
The structure of the beads showed that the chitosan beads embedded with AgGO exhibited a more porous structure as
compared to the plain chitosan beads. Furthermore, the chitosan beads containing AgNPs or AgGO were tested for
their antibacterial activity against Escherichia coli and Staphylococcus aureus. The antibacterial results indicated that
the silver nanomaterial contained chitosan beads could effectively inhibit the growth of both E. coli and S. aureus as
compared to the bare chitosan beads. The produced chitosan nanocomposite envisioned that can be potentially employed
for water disinfection purpose.
In this study, magnetic cellulose membranes (MCM) have been prepared by using cotton linter as cellulose source and NaOH/urea as cellulose solvent at different magnetite content. Cellulose was dissolved in pre-cooled NaOH/urea solvent at -13°C to form cellulose solution. The cellulose solution then was mix with magnetite (Fe3O4) nanoparticles synthesized via co-precipitation method of Fe2+ and Fe3+ in the presence of sodium hydroxide (NaOH) to form MCM. The MCMs formed at different percentage of Fe3O4 i.e., 10, 20 and 30%. Analysis from vibrating sample magnetometer (VSM) shows that the saturation magnetization of the MCM increase as the percentages of Fe3O4 nanoparticles increased. However, the addition of Fe3O4 nanoparticles in the regenerated cellulose membrane has decreased the crystallinity index of MCM. The surface morphology of the MCM showed that the Fe3O4 nanoparticles were dispersed in the pore of the membrane. Tensile test showed decreasing in the tensile strength of the cellulose membrane with the addition of Fe3O4 nanoparticle.
Recent developments have found the viability of chitosan as a new alternative additive in the pulp and paper technology.
This study was carried out to investigate the effect of chitosan as a paper coating which were prepared by dissolution in
acetic acid solution. The mechanical properties of coated paper were improved significantly compared with non-coated
paper. The FT-IR spectra showed peak evolution at 1558 cm-1 for coated paper due to the existence of amine group. Since
FT-IR spectra for the coated paper was almost identical to the chitosan spectrum, it is assumed that there is an obvious
physical interaction rather than the chemical interaction. The SEM micrographs showed that some of the chitosan has
occupied the pores and some of them adhered only on the surface. This may be due to the chemical similarities between
cellulose and chitosan which enhanced the strength of fiber matrixes via hydrogen bonding. The antibacterial property
of coated paper showed that chitosan in dried form has no significant effect but effective when applied as wet solution.
Membran selulosa terjana semula (MS) daripada pulpa teras kenaf telah berjaya dihasilkan menggunakan kaedah pra penyejukan dan digumpal menggunakan larutan asid sulfurik. MS disediakan daripada pelarutan selulosa kenaf dalam larutan akues NaOH/urea dan larutan selulosa seterusnya digumpal dengan H2SO4 pada kepekatan 5-12 peratus berat (% bt.) selama 1-10 min. Pengaruh kepekatan penggumpal H2SO4 dan masa penggumpalan ke atas struktur, saiz liang, sifat mekanik dan ketelusan cahaya MS telah dikaji menggunakan pembelauan sinar-X (XRD), imbasan mikroskop elektron tekanan boleh ubah (VPSEM), penguji regangan dan spektrofotometer ultra-violet sinar tampak (UV-vis). Keputusan VPSEM menunjukkan perubahan saiz liang membran bergantung kepada kepekatan larutan penggumpal H2SO4, manakala masa penggumpalan tidak mempengaruhi saiz liang membran. Membran yang direndam dengan larutan penggumpal pada kepekatan 10 % bt. dan masa pembekuan yang sederhana iaitu 5 min menunjukkan sifat mekanik yang lebih baik dengan nilai kekuatan regangan masing-masing 41.9 dan 43.5 MPa. Oleh itu, kajian ini dapat memberikan maklumat mengenai penyediaan MS dengan pelbagai saiz liang dan sifat mekanik dengan pengubahsuaian kepekatan dan masa penggumpalan.
Bio-novolac fibre made from phenol-formaldehyde derived oil palm empty fruit bunch (EFB) was produced using electrospinning method. The bio-novolac phenol-formaldehyde was prepared via liquefaction and resinification at two different molar ratios of formaldehyde to liquefied EFB (LEFB) (F:LEFB = 0.5:1 and 0.8:1). Electrospinning was applied to the bio-novolac phenol-formaldehyde (BPF) in order to form smooth and thin as-spun fibre. The BPF was electrospun at 15 kV and 15 cm distance between needle and collector at a flow rate of 0.5 mL/h. At lower molecular weight of BPF resin, beads formation was observed. The addition of poly(vinyl) butyral (Mw = 175,000 - 250,000) has improved the fibre formation with lesser beads hence produced more fibre. Polymer solution with higher molecular weight produced better quality fibre.
The physico-mechanical and chemical properties of enzyme retting kenaf and shredded empty fruit bunch of oil palm
fibres (EFB) were analyzed by chemical extraction, microscopic, spectroscopic, thermal and X-ray diffraction method.
Polypropylene (PP), a petroleum based fibre, was also included to compare the properties of synthetic fibre with natural
fibres. Chemical extraction analysis showed that cellulose was the major component in both kenaf and EFB fibres which
are 54% and 41.34%, respectively. Silica content of EFB was 5.29% higher than kenaf that was 2.21%. The result of
thermogravimetric analysis showed that kenaf has higher thermal decomposition rate compared to EFB fibre. However,
the residue for EFB fibre was higher than kenaf due to higher content in inorganic materials. The residual content of PP
fibre was only 1.13% which was lower than the natural fibre. The diameter of EFB fibre bundle was 341.7 µm that was
three times higher than kenaf. Microscopy study demonstrated that EFB surface was rough, porous and embedded with
silica while kenaf showed smooth surface with small pith. Higher porosity in EFB was due to the lower fibre density that
was 1.5 kg/cm3 compared to kenaf that was 1.62 kg/cm3. Kenaf has illustrated significant higher tensile strength (426.4
MPa) than EFB (150 MPa) and this result is in parallel to the pattern of the crystalline value for both fibres, 65% and
50.58%, respectively.
Absorption is one of the effective, simple and economical methods to remove oil from oily wastewater. The most widely
used approach is to utilize lignocellulosic biomass as oil absorbent. However, the hygroscopic of cellulose have limited
the oil-water separation capability of lignocellulosic fibers. In this study, the surface functionality of oil palm empty
fruit bunch (EFB) fibers was slightly altered by grafting reduced graphene oxide (rGO). The modified EFB fibers show
a distinct morphological and chemical characteristics changes as the surface of fibers has been coated with rGO. This
was supported by FTIR analysis with the diminishing peak of hydroxyl group region of EFB fibers. While the surface
modification on EFB fibers shows a diminution of a hydrophilic characteristic of 131.6% water absorption in comparison
with 268.9% of untreated EFB fibers. Moreover, modified fibers demonstrated an oil-water separation increment as well,
as it shows 89% of oil uptake and improved ~17 times of oil selectivity in oil-water emulsion than untreated EFB fibers.
The factors responsible for the low solubility percentage of oil palm empty fruit bunch (OPEFB) cellulose pulp compared
to kenaf when dissolved in aqueous NaOH/urea solvent system was reported. Physical and chemical properties of both
cellulose pulp were studied and compared in terms of the lignin content, viscosity average molecular weight (Mη),
crystallinity index (CrI), cellulose pulp structure and their zero span tensile strength. The structure of both OPEFB and
kenaf cellulose pulp were characterized using high powered microscope and field emission scanning electron microscopy
(FESEM) assisted by ImageJ® software. The results show that the most significant factor that affected the OPEFB and
kenaf cellulose dissolution in NaOH/-urea solvent was the Mη with OPEFB having a higher Mη of 1.68×105 compared to
5.53 × 104 for kenaf. Overall, kenaf cellulose appeared to be produced in higher quantities presumably due to its lower
molecular weight with superior tensile strength and permeability in comparison to OPEFB.