The Use of Kenaf Fibre as a Natural Anti-Degradant in Recycled High-Density Polyethylene and Natural Rubber-Based Thermoplastic Elastomers.

As most plastic materials disintegrate without being properly reused after they are discarded, this present study developed a novel thermoplastic elastomer (TPE) using recycled high-density polyethylene (rHDPE) and natural rubber (NR) with kenaf fibre as a sustainable filler. Apart from being used as filler, this present study aimed to examine the use of kenaf fibre as a natural anti-degradant as well. The results indicated that the tensile strength of the samples was found to have significantly decreased after 6 months of natural weathering and had decreased by a further 30% after 12 months due to the chain scission of the polymeric backbones and the degradation of the kenaf fibre. However, the composites that contained kenaf fibre significantly retained their properties post-natural weathering. In terms of tensile strength and elongation at the break, the addition of only 10 phr of kenaf increased the retention properties by 25% and 5%, respectively. This is noteworthy as kenaf fibre also contains a certain amount of natural anti-degradants. Therefore, as the kenaf fibre improves the weather resistance of composites, plastic manufacturers could use it as either a filler or a natural anti-degradant.

Degradation of Diazo Congo Red Dye by Using Synthesized Poly-Ferric-Silicate-Sulphate through Co-Polymerization Process.

The ability of poly-ferric-silicate-sulphate (PFSS) synthesized via a co-polymerization process has been applied for the removal of diazo Congo red dye. A novel degradation pathway of diazo Congo red dye by using PFSS is proposed based on LC-MS analysis. Diazo Congo red dye was successfully removed using synthesized PFSS at lower coagulant dosages and a wider pH range, i.e., 9 mg/L from pH 5 to 7, 11 mg/L at pH 9, and 50 mg/L at pH 11. The azo bond cleavage was verified by the UV-Vis spectra of diazo Congo red-loaded PFSS and FTIR spectra which showed disappearance of the peak at 1584 cm-1 for -N=N- stretching vibrations. The synchronized results of UV-Vis spectra, FTIR, and the LC-MS analysis in this study confirmed the significance of the Si and Fe bond in PFSS towards the degradation of diazo Congo red dye. The successfully synthesized PFSS coagulant was characterized by FTIR, SEM, TEM, and HRTEM analysis. From this analysis, it was proven that PFSS is a polycrystalline material which is favorable for the coagulation-flocculation process. Based on all these findings, it was established that synthesized PFSS can be employed as a highly efficient polymeric coagulant for the removal of dye from wastewater.

Sustainable Recycling of Waste from Nitrile Gloves: Prolonging the Life Span by Designing Proper Curing Systems.

A massive demand for rubber-based goods, particularly gloves, was sparked by the emergence of the COVID-19 epidemic worldwide. This resulted in thousands of tons of gloves being scrapped due to the constant demand for the items, endangering our environment in a grave way. In this work, we aimed to focus on the utilization of waste nitrile gloves (r-NBR) as a component blended with natural rubber (NR). The life span and other related properties of the blend can be improved by proper control of the chemical recipe. This study assessed three types of crosslinking systems, namely sulfur (S), peroxide (DCP), and mixed sulfur/peroxide (S/DCP) systems. The results indicate that choosing S/DCP strongly affected the tensile strength of the blend, especially at relatively high contents of r-NBR, improving the strength by 40-60% for cases with 25-35 phr of r-NBR. The improvement depended on the crosslink types induced in the blends. It is interesting to highlight that the thermal resistance of the blends was significantly improved by using the S/DCP system. This indicates that the life span of this blend can be prolonged by using a proper curing system. Overall, the S/DCP showed the best results, superior to those with S and DCP crosslinking systems.

Strategies towards Producing Non-Polar Dolomite Nanoparticles as Nanofiller for Copolymer Nanocomposite.

Poly (ethylene-co-vinyl acetate) (PEVAc) is a copolymer endowed with high elasticity and resilient properties, potentially utilized in various applications. However, the tensile strength of this copolymer is insufficient for use in certain applications that require enough strength to tolerate high external tension or stress. In this study, dolomite was proposed as a nanofiller to reinforce the PEVAc. Raw dolomite was physically and chemically modified in order to improve its mix ability and interfacial adhesion between the PEVAc and dolomite. Initially, the size of dolomite was reduced by combining the ball-milling and tip-sonication methods. SEM, TEM, and XRD were used to characterize the morphology/structure of the raw dolomite and the size-reduced dolomite. Then, a particle size analysis was performed to confirm the average particle size. Our results show that the particle size of dolomite was reduced from 150 µm to 441.4 nm by the physical modification process (size reduction). Based on the TEM analysis, the Feret diameter (df) of the dolomite particles was also reduced from ~112.78 µm to ~139.58 nm only. This physically modified dolomite is referred as dolomite nanoparticles (DNPs), since one or more of its dimensions is less than 100 nm (e.g., thickness and width). To further improve the dolomite and PEVAc matrix interactions, chemical modification of the DNPs were performed by treating the DNPs with stearic acid, forming non-polar dolomite nanoparticles (NP-DNPs). The presence of stearic acid in dolomite was confirmed through FTIR and contact angle analyses. A PEVAc nanocomposite film with NP-NPDs as a nanofiller appeared more homogeneous and exhibited the highest increment in tensile strength and elongation at break. These findings indicated that the combination of ball milling and tip sonication is an efficient method for producing very fine dolomite particles up to the nano-size range, whereas chemical surface modifications improved the compatibility between the dolomite and the copolymer. The combination of these physical and chemical modifications helped to develop a homogeneous copolymer nanocomposite system with improved tensile properties.

Potency of Urea-Treated Halloysite Nanotubes for the Simultaneous Boosting of Mechanical Properties and Crystallization of Epoxidized Natural Rubber Composites.

Halloysite nanotubes (HNTs) are naturally occurring tubular clay made of aluminosilicate sheets rolled several times. HNT has been used to reinforce many rubbers. However, the narrow diameter of this configuration causes HNT to have poor interfacial contact with the rubber matrix. Therefore, increasing the distance between layers could improve interfacial contact with the matrix. In this work, Epoxidized Natural Rubber (ENR)/HNT was the focus. The HNT layer distance was successfully increased by a urea-mechanochemical process. Attachment of urea onto HNT was verified by FTIR, where new peaks appeared around 3505 cm-1 and 3396 cm-1, corresponding to urea's functionalities. The intercalation of urea to the distance gallery of HNT was revealed by XRD. It was also found that the use of urea-treated HNT improved the modulus, tensile strength, and tear strength of the composites. This was clearly responsible for interactions between ENR and urea-treated HNT. It was further verified by observing the Payne effect. The value of the Payne effect was found to be reduced at 62.38% after using urea for treatment. As for the strain-induced crystallization (SIC) of the composites, the stress-strain curves correlated well with the results from synchrotron wide-angle X-ray scattering.

Effect of Sago Starch Modifications on Polystyrene/Thermoplastic Starch Blends.

The preparation of polystyrene/thermoplastic starch (PS/TPS) blends was divided into three stages. The first stage involved the preparation of TPS from sago starch. Then, for the second stage, PS was blended with TPS to produce a TPS/PS blend. The ratios of the TPS/PS blend were 20:80, 40:60, 60:40, and 80:20. The final stage was a modification of the composition of TPS/PS blends with succinic anhydride and ascorbic acid treatment. Both untreated and treated blends were characterized by their physical, thermal, and surface morphology properties. The obtained results indicate that modified blends have better tensile strength as the adhesion between TPS and PS was improved. This can be observed from SEM micrographs, as modified blends with succinic anhydride and ascorbic acid had smaller TPS dispersion in PS/TPS blends. The micrograph showed that there was no agglomeration and void formation in the TPS/PS blending process. Furthermore, modified blends show better thermal stability, as proved by thermogravimetric analysis. Water uptake into the TPS/PS blends also decreased after the modifications, and the structural analysis showed the formation of a new peak after the modification process.

Synergistic Effect of Maleated Natural Rubber and Modified Palm Stearin as Dual Compatibilizers in Composites based on Natural Rubber and Halloysite Nanotubes.

The performance of rubber composite relies on the compatibility between rubber and filler. This is specifically of concern when preparing composites with very different polarities of the rubber matrix and the filler. However, a suitable compatibilizer can mediate the interactions. In this study, composites of natural rubber (NR) with halloysite nanotubes (HNT) were prepared with maleated natural rubber (MNR) and modified palm stearin (MPS) as dual compatibilizers. The MPS dose ranged within 0.5-1.5 phr, while the MNR dose was fixed at 10 phr in all formulations. It was found that the mixed MNR/MPS significantly enhanced modulus, tensile strength, and tear strength of the composites. The improvements were mainly due to improved rubber-HNT interactions arising from hydrogen bonds formed in the presence of these two compatibilizers. This was clearly verified by observing the Payne effect. Apart from that, the MPS also acted as a plasticizer to provide improved dispersion of HNT. It was clearly demonstrated that MNR and MPS as dual compatibilizers improved rubber-HNT interactions and reduced filler-filler interactions, which then improved tensile and tear strengths, as well as dynamical properties. Therefore, the mix of MNR and MPS had a great potential to compatibilize non-polar rubber with HNT filler.

Preparation and Characterization of Low-Molecular-Weight Natural Rubber Latex via Photodegradation Catalyzed by Nano TiO2.

Natural rubber is one of the most important renewable biopolymers used in many applications due to its special properties that cannot be easily mimicked by synthetic polymers. To sustain the existence of natural rubber in industries, modifications have been made to its chemical structure from time to time in order to obtain new properties and to enable it to be employed in new applications. The chemical structure of natural rubber can be modified by exposure to ultraviolet light to reduce its molecular weight. Under controlled conditions, the natural rubber chains will be broken by photodegradation to yield low-molecular-weight natural rubber. The aim of this work was to obtain what is known as liquid natural rubber via photodegradation, with titanium dioxide nanocrystals as the catalyst. Titanium dioxide, which was firstly synthesized using the sol⁻gel method, was confirmed to be in the form of an anatase, with a size of about 10 nm. In this work, the photodegradation was carried out in latex state and yielded low-molecular-weight natural rubber latex of less than 10,000 g/mol. The presence of hydroxyl and carbonyl groups on the liquid natural rubber (LNR) chains was observed, resulting from the breaking of the chains. Scanning electron microscopy of the NR latex particles showed that titanium dioxide nanocrystals were embedded on the latex surface, but then detached during the degradation reaction.

Genotoxicity assessment of biphasic calcium phosphate of modified porosity on human dental pulp cells using Ames and Comet assays.

Biphasic Calcium Phosphate (BCP) with a ratio of 20/80 Hydroxyapatite (HA)/Beta-tricalcium phosphate (ß-TCP) promotes the differentiation of human dental pulp cells (HDPCs). In the current study, the genotoxicity of locally produced BCP of modified porosity (65%) with a mean pore size of 300micrometer (µm) was assessed using Comet and Ames assays. HDPCs were treated with BCP extract at three different inhibitory concentrations which were obtained based on cytotoxicity test conducted with concurrent negative and positive controls. The tail moment of HDPCs treated with BCP extract at all three concentrations showed no significant difference compared to negative control (p>0.05), indicating that BCP did not induce DNA damage to HDPCs. The BCP was evaluated using five tester strains of Salmonella typhimurium TA98, TA100, TA102, TA1537 and TA1538. Each strain was incubated with BCP extract with five different concentrations in the presence and absence of metabolic activation system (S9) mix. Concurrently, negative and positive controls were included. The average number of revertant colonies per plate treated with the BCP extract was less than double as compared to the number of revertant colonies in negative control plate and no dose-related increase was observed. Results from both assays suggested that the BCP of modified porosity did not exhibit any genotoxic effect under the present test conditions.

Effect of biphasic calcium phosphate scaffold porosities on odontogenic differentiation of human dental pulp cells.

Calcium phosphates (CaP) of different porosities have been widely and successfully used as scaffolds with osteoblast cells for bone tissue regeneration. However, the effects of scaffold porosities on cell viability and differentiation of human dental pulp cells for dentin tissue regeneration are not well known. In this study, biphasic calcium phosphate (BCP) scaffolds of 20/80 hydroxyapatite to beta tricalcium phosphate ratio with a mean pore size of 300 µm were prepared into BCP1, BCP2, BCP3, and BCP4 of 25%, 50%, 65%, and 75% of total porosities, respectively. The extracts of these scaffolds were assessed with regard to cell viability, proliferation, and differentiation of human dental pulp cells. The high alkalinity, and more calcium and phosphate ions release that were exhibited by BCP3 and BCP4 decreased the viability and proliferation of human dental pulp cells as compared to BCP1 and BCP2. BCP2 significantly increased both cell viability and cell proliferation. However, the cells cultured with BCP3 extract revealed high alkaline phosphatase (ALP) activity and high expression of odontoblast related genes, collagen type I alpha 1, dentin matrix protein-1, and dentin sialophosphoprotein as compared to that cultured with BCP1, BCP2, and BCP4 extracts. The results highlight the effect of different scaffold porosities on the cell microenvironment and demonstrate that BCP3 scaffold of 65% porosity can support human dental pulp cells differentiation for dentin tissue regeneration.

Effect of different calcium phosphate scaffold ratios on odontogenic differentiation of human dental pulp cells.

Calcium phosphate (CaP) scaffolds have been widely and successfully used with osteoblast cells for bone tissue regeneration. However, it is necessary to investigate the effects of these scaffolds on odontoblast cells' proliferation and differentiation for dentin tissue regeneration. In this study, three different hydroxyapatite (HA) to beta tricalcium phosphate (ß-TCP) ratios of biphasic calcium phosphate (BCP) scaffolds, BCP20, BCP50, and BCP80, with a mean pore size of 300µm and 65% porosity were prepared from phosphoric acid (H2PO4) and calcium carbonate (CaCO3) sintered at 1000°C for 2h. The extracts of these scaffolds were assessed with regard to cell viability and differentiation of odontoblasts. The high alkalinity, more calcium, and phosphate ions released that were exhibited by BCP20 decreased the viability of human dental pulp cells (HDPCs) as compared to BCP50 and BCP80. However, the cells cultured with BCP20 extract expressed high alkaline phosphatase activity and high expression level of bone sialoprotein (BSP), dental matrix protein-1 (DMP-1), and dentin sialophosphoprotein (DSPP) genes as compared to that cultured with BCP50 and BCP80 extracts. The results highlighted the effect of different scaffold ratios on the cell microenvironment and demonstrated that BCP20 scaffold can support HDPC differentiation for dentin tissue regeneration.

Synthesis of linear low-density polyethylene-g-poly (acrylic acid)-co-starch/organo-montmorillonite hydrogel composite as an adsorbent for removal of Pb(ΙΙ) from aqueous solutions.

The purpose of this work is to remove Pb(II) from the aqueous solution using a type of hydrogel composite. A hydrogel composite consisting of waste linear low density polyethylene, acrylic acid, starch, and organo-montmorillonite was prepared through emulsion polymerization method. Fourier transform infrared spectroscopy (FTIR), Solid carbon nuclear magnetic resonance spectroscopy (CNMR)), silicon(-29) nuclear magnetic resonance spectroscopy (Si NMR)), and X-ray diffraction spectroscope ((XRD) were applied to characterize the hydrogel composite. The hydrogel composite was then employed as an adsorbent for the removal of Pb(II) from the aqueous solution. The Pb(II)-loaded hydrogel composite was characterized using Fourier transform infrared spectroscopy (FTIR)), scanning electron microscopy (SEM)), and X-ray photoelectron spectroscopy ((XPS)). From XPS results, it was found that the carboxyl and hydroxyl groups of the hydrogel composite participated in the removal of Pb(II). Kinetic studies indicated that the adsorption of Pb(II) followed the pseudo-second-order equation. It was also found that the Langmuir model described the adsorption isotherm better than the Freundlich isotherm. The maximum removal capacity of the hydrogel composite for Pb(II) ions was 430mg/g. Thus, the waste linear low-density polyethylene-g-poly (acrylic acid)-co-starch/organo-montmorillonite hydrogel composite could be a promising Pb(II) adsorbent.