Search

The synergistic effect of single-crystal structure and dual doping in Li-rich cobalt-free cathode materials was thoroughly investigated. Lithium-ion pouch cells employing Sb/Sn doped Li 1.2 Mn 0.6 Ni 0.2 O 2 and graphite exhibited a specific capacity of 191.01 mA h g -1 at 1C rate and exceptionally stable performance upon cycling, with capacity retention of 87.24% of their initial capacity after 250 cycles at 1C rate. The strategic combination of morphology manipulation and dual ion doping has markedly diminished cation mixing and expanded the Li interstitial sites within the cathode lattice. This work offers significant insights into the mechanisms responsible for the structural decline of Li-rich cobalt-free cathodes, emphasizing the importance of stabilizing the cathode lattice structure at high potential. These findings suggest promising potential for this material to meet the demanding energy density criteria for electric vehicles. Finally, this research provides practical strategies for effectively implementing high-voltage cobalt-free cathodes, offering valuable guidance for future applications.

In this work, bacterial cellulose (BC) derived from Nata de Coco is a polysaccharide material, and it is further processed into bacterial cellulose nanocrystal (BCNC) via acid hydrolysis. Then BCNC is doped with transition metals to enhance its amine/hydrogen sulfide response. Therefore, the aim of this study is to investigate the use of transition metals as indicators to detect amine and hydrogen sulfide gas for efficiently monitoring food spoilage. BCNCs were treated with various concentrations of silver nitrate (AgNO 3 ) and copper sulfate pentahydrate (CuSO 4 ·5H 2 O). Then the dropwise addition of ascorbic acid was applied to reduce Ag + and Cu 2+ to Ag 0 (silver nanoparticle) and Cu 0 (copper nanoparticle), which refer to red brown and red wine colors, respectively. The results indicated that BCNC/Ag nanoparticles were spherical, while BCNC/Cu nanoparticles exhibited a rod-like structure. XRD results also presented the incorporation of Ag and Cu nanoparticles, as confirmed by both crystallography structures. Furthermore, UV-Vis spectra showed the adsorption bands at 422-430 nm and 626-629 nm, belonging to Ag and Cu nanoparticles. After H 2 S and ammonia gas exposure, BH/Ag and BH/Cu films turned black from brown and red. In conclusion, transition metal-doped BCNCs exhibit potential for innovative food spoilage gas sensors., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

Lithium-sulfur batteries (LSBs) show promise for achieving a high energy density of 500 W h kg -1 , despite challenges such as poor cycle life and low energy efficiency due to sluggish redox kinetics of lithium polysulfides (LiPSs) and sulfur's electronic insulating nature. We present a novel 2D Ti 3 C 2 Mxene on a 2D graphitic carbon nitride (g-C 3 N 4 ) heterostructure designed to enhance LiPS conversion kinetics and adsorption capacity. In a pouch cell configuration with lean electrolyte conditions (∼5 μL mg -1 ), the g-C 3 N 4 -Mx/S cathode exhibited excellent rate performance, delivering ∼1061 mA h g -1 at C/8 and retaining ∼773 mA h g -1 after 190 cycles with a Coulombic efficiency (CE) of 92.7%. The battery maintained a discharge capacity of 680 mA h g -1 even at 1.25 C. It operated reliably at an elevated sulfur loading of 5.9 mg cm -2 , with an initial discharge capacity of ∼900 mA h g -1 and a sustained CE of over 83% throughout 190 cycles. Postmortem XPS and EIS analyses elucidated charge-discharge cycle-induced changes, highlighting the potential of this heterostructured cathode for commercial garnet LSB development.

A newly designed colorimetric sensing film has been developed to determine the spoilage gas from food deterioration. The fabrication of sensing film used for food labels based on bacterial cellulose and carboxymethyl cellulose composite film (BC/CMC) incorporated with Bis(imidazolium) tetrachlorocuprate, HIm 2 CuCl 4 was focused. The BC/CMC composite films were prepared by vacuum filtration and then dipped into the (5-20 % w/w) HIm 2 CuCl 4 solution. Subsequently, they were dried at 60 °C to obtain the BC/CMC-Cu film. For monitoring fish freshness, the TVB-N level was considered an indicator of determining fish spoilage. In addition, the color change was evaluated and expressed as Lab color values and total color difference (TCD). According to the sensing response, the TCD values of the sensing films had continuously changed, corresponding to the ammonia gas, which is one of the TVB-N gases. Based on the variations in Lab color values exposed to ammonia gas at room temperature, the film color shifted from the initial lime green color to the final blue color due to the substitution of metal-ligand bonding. Finally, this colorimetric sensing film can be employed as a potential food freshness indicator in intelligent packaging., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

An electrochemical lateral flow immunoassay (eLFIA) strip with high reproducibility was developed to rapidly and accurately detect Streptococcus suis serotype 2. This proposed strip was fabricated by integrating ratiometric electrochemical detection and LFIA (R-eLFIA). The R-eLFIA exhibited excellent reproducibility, which was improved by 3.8 times compared to a single electrode. A dual-working screen-printed graphene electrode (SPGE) was designed by tuning the working electrode with electroactive species in the biosensing system. Ferrocene carboxylic acid (Fc) was used as a signal probe, and sunset yellow (SY) at one working electrode was used as an internal reference signal to provide a built-in correction for reducing the effects of inherent background current. S. suis serotype 2-specific antibodies were immobilized on a nitrocellulose membrane of LFIA, which is located on the position of Fc-SPGE. In the presence of the analyte, an immunocomplex formed on the region of Fc-SPGE, causing a decrease in Fc current while SY current remained constant. The current ratio's decrease was proportional to S. suis serotype 2's concentration. Under optimization, this biosensor showed good linearity in the range of 10 2 -10 10  CFU/mL with a limit of detection of 10 CFU/mL and achieved a rapid detection time (15 min). Moreover, the R-eLFIA biosensor exhibited excellent reproducibility and high selectivity and was applied in human serum samples. Thus, this study successfully matched the advantages of the ratiometric strategy and LFIA and has great potential to be used as an effective tool for rapidly detecting S. suis serotype 2 in clinical samples., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Rehabilitative capabilities of any tissue engineered scaffold rely primarily on the triad of (i) biomechanical properties such as mechanical properties and architecture, (ii) chemical behavior such as regulation of cytokine expression, and (iii) cellular response modulation (including their recruitment and differentiation). The closer the implant can mimic the native tissue, the better it can rehabilitate the damage therein. Among the available fabrication techniques, only 3D bioprinting (3DBP) can satisfactorily replicate the inherent heterogeneity of the host tissue. However, 3DBP scaffolds typically suffer from poor mechanical properties, thereby, driving the increased research interest in development of load-bearing 3DBP orthopedic scaffolds in recent years. Typically, these scaffolds involve multi-material 3D printing, comprising of at-least one bioink and a load-bearing ink; such that mechanical and biological requirements of the biomaterials are decoupled. Ensuring high cellular survivability and good mechanical properties are of key concerns in all these studies. 3DBP of such scaffolds is in early developmental stages, and research data from only a handful of preliminary animal studies are available, owing to limitations in print-capabilities and restrictive materials library. This article presents a topically focused review of the state-of-the-art, while highlighting aspects like available 3DBP techniques; biomaterials' printability; mechanical and degradation behavior; and their overall bone-tissue rehabilitative efficacy. This collection amalgamates and critically analyses the research aimed at 3DBP of load-bearing scaffolds for fulfilling demands of personalized-medicine. We highlight the recent-advances in 3DBP techniques employing thermoplastics and phosphate-cements for load-bearing applications. Finally, we provide an outlook for possible future perspectives of 3DBP for load-bearing orthopedic applications. Overall, the article creates ample foundation for future research, as it gathers the latest and ongoing research that scientists could utilize., (Creative Commons Attribution license.)

Electrochemical DNA sensors can be operated in either static or flow-based detection schemes. In static schemes, manual washing steps are still necessary, resulting in a tedious and time-consuming process. In contrast, in flow-based electrochemical sensors, the current response is collected when the solution flows through the electrode continuously. However, the drawback of such a flow system is the low sensitivity due to the limited time for the interaction between the capturing element and the target. Herein, we propose a novel electrochemical capillary-driven microfluidic DNA sensor to combine the advantages of static and flow-based electrochemical detection systems into a single device by incorporating burst valve technology. The microfluidic device with a two-electrode configuration was applied for the simultaneous detection of two different DNA markers, human immunodeficiency virus-1 (HIV-1) and hepatitis C virus (HCV) cDNA, via the specific interaction between pyrrolidinyl peptide nucleic acids (PNA) probes and the DNA target. The integrated system, while requiring a small sample volume (7 μL for each sample loading port) and less analysis time, achieved good performance in terms of the limits of detection (LOD) (3SD blank /slope) and quantification (LOQ) (10SD blank /slope) at 1.45 nM and 4.79 nM for HIV and 1.20 nM and 3.96 nM for HCV, respectively. The simultaneous detection of HIV-1 and HCV cDNA prepared from human blood samples showed results that are in complete agreement with the RT‒PCR assay. The results qualify this platform as a promising alternative for the analysis of either HIV-1/HCV or coinfection that can be easily adapted for other clinically important nucleic acid-based markers., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Multiple functional-material-filled nitrile butadiene rubber/chloroprene rubber (NBR/CR) acoustic composites were extensively studied and prepared. According to the orthogonal test table L25 (5 6 ), 25 groups of samples were prepared by using a low-temperature one-time rubber mixing process. With tensile strength, average transmission loss, and damping peak as indexes, the influence degree of different factors and levels on the properties of acoustic composites was quantitatively discussed and analyzed. The matrix weight analysis was employed to optimize the material formula of rubber composites, and the corresponding influence weight was given. Results showed that the acoustic composite with blending ratio of 70/30 for NBR/CR matrix had preferable mechanical and acoustic properties; adding mica powder (MP) and montmorillonite (MMT) in matrix contributed to improve all above three indexes owing to their specific lamellar structures; hollow glass beads (HGB) had a positive influence on improving acoustic property due to its hollow microcavities, however, it had a negative impact on damping property because of the smooth spherical surfaces. Accordingly, the optimal formulation was found to be NBR/CR blending ratio of 70/30, MP of 10 phr (per hundred rubber), HGB of 4 phr, and MMT of 10 phr.

Operating the dry reforming reaction photocatalytically presents an opportunity to produce commodity chemicals from two greenhouse gases, carbon dioxide and methane, however, the top-performing photocatalysts presented in the academic literature invariably rely on the use of precious metals. In this work, we demonstrate enhanced photocatalytic dry reforming performance through surface basicity modulation of a Ni-CeO 2 photocatalyst by selectively phosphating the surface of the CeO 2 nanorod support. An optimum phosphate content is observed, which leads to little photoactivity loss and carbon deposition over a 50-hour reaction period. The enhanced activity is attributed to the Lewis basic properties of the PO 4 3- groups which improve CO 2 adsorption and facilitate the formation of small nickel metal clusters on the support surface, as well as the mechanical stability of CePO 4 . A hybrid photochemical-photothermal reaction mechanism is demonstrated by analyzing the wavelength-dependent photocatalytic activities. The activities, turnover numbers, quantum efficiencies, and energy efficiencies are shown to be on par with other dry-reforming photocatalysts that use noble metals, representing a step forward in understanding how to stabilize ignoble nickel-based dry reforming photocatalysts. The challenges associated with comparing the performance of photocatalysts reported in the academic literature are also commented on., (© 2023. The Author(s).)

Technical lignins, kraft, soda, lignoboost, and hydrolysis lignins were used for the production of carbon particles at different carbonization temperatures, 1000 °C and 1400 °C. The results showed that the lignin source and carbonization temperature significantly influenced the carbon quality and microstructure of the carbon particles. Soda lignin carbonized up to 1400 °C showed higher degree of graphitization and exhibited the highest electrical conductivity of 335 S·m -1 , which makes it suitable for applications, such as electromagnetic interference shielding and conductive composite based structural energy storage devices. The obtained carbon particles also showed high surface area and hierarchical pore structure. Kraft lignin carbonized up to 1400 °C gives the highest BET surface area of 646 m 2 g -1 , which makes it a good candidate for electrode materials in energy storage applications. The energy storage application has been validated in a three-electrode set up device, and a specific capacitance of 97.2 F g -1 was obtained at a current density of 0.1 A g -1 while an energy density of 1.1 Wh kg -1 was observed at a power density of 50 W kg -1 . These unique characteristics demonstrated the potential of kraft lignin-based carbon particles for electrochemical energy storage applications.

Regioselectively substituted nanocellulose was synthesized by protecting the primary hydroxyl group. Herein, we took advantage of the different reactivities of primary and secondary hydroxyl groups to graft large capping structures. This study mainly focuses on regioselective installation of trityl protecting groups on nanocellulose chains. The elemental analysis and nuclear magnetic resonance spectroscopy of regioselectively substituted nanofibrillated cellulose (NFC) suggested that the trityl group was successfully grafted in the primary hydroxyl group with a degree of substitution of nearly 1. Hansen solubility parameters were employed, and the binary system composed of an ionic liquid and pyridine as a base was revealed to be the optimum condition for regioselective functionalization of nanocellulose. Interestingly, the dissolution of NFC in the ionic liquid and the subsequent deprotection process of NFC substrates hardly affected the crystalline structure of NFC (3.6% decrease in crystallinity). This method may provide endless possibilities for the design of advanced engineered nanomaterials with multiple functionalities. We envisage that this protection/deprotection approach may lead to a bright future for the fabrication of multifunctional devices based on nanocellulose.

Food contamination leading to the spoilage and growth of undesirable bacteria, which can occur at any stage along the food chain, is a significant problem in the food industry. In the present work, biopolymer polybutylene succinate (PBS) and polybutylene succinate/tapioca starch (PBS/TPS) films incorporating Biomaster-silver (BM) and SANAFOR ® (SAN) were prepared and tested as food packaging to improve the lifespan of fresh chicken breast fillets when kept in a chiller for seven days. The incorporation of BM and SAN into both films demonstrated antimicrobial activity and could prolong the storability of chicken breast fillets until day 7. However, PBS + SAN 2%, PBS/TPS + SAN 1%, and PBS/TPS + SAN 2% films showed the lowest microbial log growth. In quality assessment, incorporation of BM and SAN into both film types enhanced the quality of the chicken breast fillets. However, PBS + SAN 1% film showed the most notable enhancement of chicken breast fillet quality, as it minimized color variation, slowed pH increment, decreased weight loss, and decelerated the hardening process of the chicken breast fillets. Therefore, we suggest that the PBS + SAN and PBS/TPS + SAN films produced in this work have potential use as antimicrobial packaging in the future.

In the present work, the ductile formation mechanism of a newly proposed torsion configuration has been investigated. One of the unique attributes of this paper is the first-time disclosure of the design and fabrication of a novel prototype screw with torsional flow character validating the orthogonal test model experimentally. The torsional spiral flow patterns that occurred in the torsion channel cause a ductile deformation of polymer in the form of a spiral, which in turn enhances the radial convection, achieving an effective mass transfer of material from the top region to the bottom region and vice versa. Furthermore, the characteristic parameters of torsion configuration have a significant influence on the plasticizing and melting capability of polymer. By range analysis and weight matrix analysis, the best factor and level combination was obtained. Results indicated that the aspect ratio of the torsion channel is almost equal to 1, and the plasticizing and melting capability of polymer is optimal. This novel design innovation offers a paradigm shift in the energy-efficient plasticization of polymer compounds.

Date palm fiber ( Phoenix dactylifera L.) is a natural biopolymer rich in lignocellulosic components. Its high cellulose content lends them to the extraction of tiny particles like microcrystalline cellulose (MCC) and nanocrystalline cellulose (NCC). These cellulose-derived small size particles can be used as an alternative biomaterial in wide fields of application due to their renewability and sustainability. In the present work, NCC (A) and NCC (B) were isolated from date palm MCC at 60 min and 90 min hydrolysis times, respectively. The isolated NCC product was subjected to characterization to study their properties differences. With the hydrolysis treatment, the yields of produced NCC could be attained at between 22% and 25%. The infrared-ray functional analysis also revealed the isolated NCC possessed a highly exposed cellulose compartment with minimized lignoresidues of lignin and hemicellulose. From morphology evaluation, the nanoparticles' size was decreased gradually from NCC (A) (7.51 nm width, 139.91 nm length) to NCC (B) (4.34 nm width, 111.51 nm length) as a result of fragmentation into cellulose fibrils. The crystallinity index was found increasing from NCC (A) to NCC (B). With 90 min hydrolysis time, NCC (B) showed the highest crystallinity index of 71% due to its great cellulose rigidity. For thermal analysis, NCC (B) also exhibited stable heat resistance, in associating with its highly crystalline cellulose structure. In conclusion, the NCC isolated from date palm MCC would be a promising biomaterial for various applications such as biomedical and food packaging applications.

Single-crystal solid-liquid dual-phase hybrid organic-inorganic ligand frameworks with reversible sensing response facilitated by external stimuli have received significant attention in recent years. This report presents a significant leap in designing electronic structures that display reversible dual-phase photoluminescence properties from single-crystal hybrid ligand frameworks. Three-dimensional Cu(C 3 N 2 H 4 ) 4 Cl 2 complex frameworks were formed through the intermolecular hydrogen bonding and π⋯π stacking supramolecular interactions. The absorption band peaks at 627 nm were assigned to d-d transition showing 10Dq = 15,949 cm -1 and crystal field stabilization energy (CFSE) = 0.6 × 10Dq = 114.4 kJmol -1 , while the ligand-to-metal charge transfer (LMCT) of complexes was displayed at 292 nm. The intense luminescence band results from LMCT present at 397 nm. Considering its structure, air stability, framework forming and stable luminescence in aqueous solution, the Cu(C 3 N 2 H 4 ) 4 Cl 2 complex shows potential for luminescence Cu-based sensors using emission intensity to detect heavy metal ion species.

The design and high-throughput manufacturing of thin renewable energy devices with high structural and atomic configurational stability are crucial for the fabrication of green electronics. Yet, this concept is still in its infancy. In this work, we report the extraordinary durability of thin molecular interlayered organic flexible energy devices based on chemically tuned cellulose nanofiber transparent films that outperform glass by decreasing the substrate weight by 50%. The nanofabricated flexible thin film has an exceptionally low thermal coefficient of expansion of 1.8 ppm/K and a stable atomic configuration under a harsh fabrication condition (over 190 °C for an extended period of 5 h). A flexible optoelectronic device using the same renewable cellulose nanofiber film substrate was found to be functionally operational over a life span of 5 years under an intermittent operating condition. The success of this device's stability opens up an entirely new frontier of applications of flexible electronics.

Photoresponsive functionalized nanofilms were prepared via radical polymerization of carbazole units on a nanofibrillated cellulose (NFC) backbone via one-pot procedure. Herein, NFC was functionalized with active carbazole units as pendant organic moieties. The nanofilms were characterized by UV-vis and fluorescence spectroscopy, Fourier transformed infrared (FTIR) and Raman spectroscopy, 13 C NMR and proton NMR spectra, contact angle analysis, mechanical testing, and scanning electron microscopy (SEM). The fabricated nanofilms exhibited large tensile strength (∼110 MPa), higher hydrophobicity and luminescence activity. The results indicated that the prepared optically active nanofilms present potential applications in the fields of flexible organic light emitting devices., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Various carbon materials have been developed for energy storage applications to address the increasing energy demand in the world. However, the environmentally friendly, renewable, and nontoxic bio-based carbon resources have not been extensively investigated towards high-performance energy storage materials. Here, we report an anisotropic, hetero-porous, high-surface area carbon aerogel prepared from renewable resources achieving an excellent electrical double-layer capacitance. Two different green, abundant, and carbon-rich lignins which can be extracted from various biomasses, have been selected as raw materials, i.e., kraft and soda lignins, resulting in clearly distinct physical, structural as well as electrochemical characteristics of the carbon aerogels after carbonization. The obtained green carbon aerogel based on kraft lignin not only demonstrates a competitive specific capacitance as high as 163 F g -1 and energy density of 5.67 Wh kg -1 at a power density of 50 W kg -1 when assembled as a two-electrode symmetric supercapacitor, but also shows outstanding compressive mechanical properties. This reveals the great potential of the carbon aerogels developed in this study for the next-generation energy storage applications requiring green and renewable resources, lightweight, robust storage ability, and reliable mechanical integrity.

Stable blue fluorescent nitrogen doped carbon dots (N-CDs) with a very high quantum yield up to 81% has been reported for the first time. Novel N-CDs were synthesized through an efficient and rapid one-step hydrothermal synthesis process from diethylenetriamine as nitrogen source and a novel carbon source trans-aconitic acid. The nanosized particles of N-CDs were in the range of 2-8 nm and uniformly distributed in molecular level. The N-CDs showed high selectivity toward Fe 3+ with low detection limit of 10.42 nmol L -1 (with corresponding linear range of 2-50 μmol L -1 ) enabling them for ion detection application and also exhibited high fluorescence stability in extreme pH conditions. Novel N-CDs also presented a green emission shift under acidic condition (pH~2) which makes them a potential sensing probe for security papers, food packaging and bio-medical detection sensors. A security paper sensor device has been fabricated and its operation function has been validated by making real time detection of color. The novel and facile to manufacture carbon dots has potential applications ranging from biological nano-sensors for security document to color-switch sensing and bio-imaging., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Steam generation through efficient utilization of solar energy is a promising technology in addressing the challenge of global freshwater shortage and water pollution. One of the biggest hurdles for traditional photothermal membranes to function continuously in a high temperature, high salt, and corrosive environment has been attributed to their rapid decline of mechanical properties. In this work, a highly efficient solar-driven interfacial water evaporation system has been developed via a polydopamine/carbon/silicon (PCS) composite membrane supported by a floating insulation foam substrate. A 3.1 fold increase in the water vaporization rate was recorded compared with the pure water system. The 2D-carbon nanolayer on the surface was successfully prepared by carbonizing low-cost linear polyethylene with a glass fiber (GF) membrane as the substrate, and then the carbon membrane was modified with dopamine to control water transport on the carbon coating and within the glass fiber. The PCS membrane has a high efficiency for solar steam generation owing to high optical absorption and has excellent solar thermal conversion capability. The evaporation rate and solar thermal conversion efficiency of the PCS membrane under simulated sunlight irradiation with 1 sun (1 kW·m -2 ) are 1.39 kg·m -2 ·h -1 and 80.4% respectively, which are significantly higher compared to GF membrane, carbon/silicon (CS) membrane, and pure water without a photothermal membrane. The water evaporation system retained high efficiency after 20 cycles under simulated sunlight irradiation of 1 sun. This study provides critical insight on the design and fabrication of a highly efficient and durable evaporation system.

Heterogeneous thermal catalytic processes are vital for industrial production of fuels, fertilizers, and other chemicals necessary for sustaining human life. However, these processes are highly energy-intensive, requiring a vast consumption of fossil fuels. An emerging class of heterogeneous catalysts that are thermally driven but also exhibit a photochemically enhanced rate can potentially reduce process energy intensity by partially substituting conventional heat (where fossil fuels are needed) with solar energy. Such catalyst systems have yet to be practically utilized. Here, we demonstrate a compact electrically heated photo- and thermal annular reactor module to reduce CO 2 to CO, via the reverse water gas shift reaction. A first-principles-based design approach was taken in developing a SiO 2 on an Al photo- and thermal catalyst system for the model photo- and thermal indium oxide hydroxide (In 2 O 3- x (OH) y ) catalysts. A 5-fold light enhancement in the CO production rate and over 70 h of stable CO production were achieved. This represents the highest light enhancement effect reported for this model photocatalyst to date. The reactor presented herein allows continuous operation and a significant reduction of 31% in heater power consumption when provided with an additional 2 suns of irradiation, demonstrating the strong photo- and thermal-harvesting performances of the catalyst system developed in this work.

This research work is the first to report thermal stability, heat deformation resistance, and crystallization behavior of a Polyethylene (PE)-based biphasic polyolefin system reinforced with Reduced Graphene Oxide (RGO), which was obtained through Graphene Oxide (GO) chemical reduction. Polypropylene (PP) represented the polymeric dispersed phase. A strategic PE/PP/RGO manufacturing procedure was employed to thermodynamically localize RGO at the PE/PP interface, as confirmed by Transmission Electron Microscopy (TEM), bringing a uniform micro phase dispersion into the macro phase. In addition, studies of PE non-isothermal crystallization kinetics indicated that the morphology tunable micro phase and the nanolayered RGO promoted a nucleation-controlled PE crystallization, which was supported by Polarized Light Optical Microscopy (PLOM). This, together with fine morphology, justified the remarkable enhancement registered for the ternary system's thermal stability and heat deformation resistance. Different filler loads were employed, with weight fractions of 2% and 4%. It was observed that the former, being better exfoliated and more homogeneously distributed at the PE/PP interface than the latter, led to a more improved PE crystallization, alongside a greater ternary system's thermal properties. Moreover, the thermal stability of PE/PP reinforced with 2% of RGO was even higher than that of virgin PP, while their heat deformation resistance values were found to be similar. Therefore, this unique outcome provides industries, such as the energy and automotive sectors, with the opportunity to substitute PP-rich products with those mostly comprised of a cheaper, more abundant, yet performant PE.

Novel and unique applications of nanocellulose are largely driven by the functional attributes governed by its structural and physicochemical features including excellent mechanical properties and biocompatibility. In recent years, thousands of groundbreaking works have helped in the development of targeted functional nanocellulose for conductive, optical, luminescent materials, and other applications. The growing demand for sustainable and renewable materials has led to the rapid development of greener methods for the design and fabrication of high-performance green nanomaterials with multiple features, and consequently new challenges and opportunities. The present review article discusses historical developments, various fabrication and functionalization methods, the current stage, and the prospects of flexible energy and hybrid electronics based on nanocellulose., (Copyright © 2020 Dias, Konar, Leão, Yang, Tjong and Sain.)

A novel torsion screw has been proposed to resolve the inadequate control of mass transfer and the thermal management of two component polymer blends and their carbon fiber composites. The novel torsional screw distinctly introduced radial flow in the torsion screw channel, which is a significant improvement over the flow pattern developed by the conventional screw. The heat transfer and mixing behavior of melt mixtures are enhanced by adapting screws with torsion elements compared with the traditional screw elements. Heat transfer efficacy in the polypropylene-polystyrene bi-phasic extrusion process improved with the increase in torsion element numbers. An increased number of newly designed torsional elements also improved the dispersion of minor phase in bi-phase polypropylene-polystyrene composition and their carbon fiber composites. The unique flow pattern induced by the torsion elements shows a synergistic effect on the melt-phase mass flow and the thermal flow field facilitating phase-to-phase thermal and molecular mobility and enhanced fiber orientation, crystallinity and mechanical properties of composite made from recycled carbon fiber/polypropylene. Microtomographs of recycled carbon fiber demonstrated the extraordinary ability of a torsion screw element to orient carbon fiber in both axial and radial directions.

Background: This paper provides a critical review of biopolymer-based substrates, especially the cellulose derivatives, for their application in buccal drug delivery. Drug delivery to the buccal mucous has the benefits of immobile muscle, abundant vascularization and rapid recovery, but not all the drugs can be administered through the buccal mucosa (e.g., macromolecular drugs), due to the low bioavailability caused by their large molecular size. This shortfall inspired the rapid development of drug-compounding technologies and the corresponding usage of biopolymer substrates., Methods: Cellulose derivatives have been extensively developed for drug manufacturing to facilitate its delivery. We engaged in structured research of cellulose-based drug compounding technologies. We summarized the characteristic cellulose derivatives which have been used as the biocompatible substrates in buccal delivery systems. The discussion of potential use of the rapidly-developed nanocellulose (NC) is also notable in this paper., Results: Seventy-eight papers were referenced in this perspective paper with the majority (sixty-five) published later than 2010. Forty-seven papers defined the buccal drug delivery systems and their substrates. Fifteen papers outlined the properties and applications of cellulose derivatives. Nanocellulose was introduced as a leading edge of nanomaterial with sixteen papers highlighted its adaptability in drug compounding for buccal delivery., Conclusion: The findings of this perspective paper proposed the potential use of cellulose derivatives, the typical kind of biopolymers, in the buccal drug delivery system for promoting the bioavailability of macromolecular drugs. Nanocellulose (NC) in particular was proposed as an innovative bio-binder/carrier for the controlled-release of drugs in buccal system., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)

The effect of unidirectional (UD) carbon fibre hybridisation on the tensile properties of flax fibre epoxy composite was investigated. Composites containing different fibre ply orientations were fabricated using vacuum infusion with a symmetrical ply structure of 0/+45/-45/90/90/-45/+45/0. Tensile tests were performed to characterise the tensile performance of plain flax/epoxy, carbon/flax/epoxy, and plain carbon/epoxy composite laminates. The experimental results showed that the carbon/flax fibre hybrid system exhibited significantly improved tensile properties over plain flax fibre composites, increasing the tensile strength from 68.12 MPa for plain flax/epoxy composite to 517.66 MPa (670% increase) and tensile modulus from 4.67 GPa for flax/epoxy to 18.91 GPa (305% increase) for carbon/flax hybrid composite. The failure mechanism was characterised by examining the fractured surfaces of tensile tested specimens using environmental scanning electron microscopy (E-SEM). It was evidenced that interactions between hybrid ply interfaces and strain to failure of the reinforcing fibres were the critical factors for governing tensile properties and failure modes of hybrid composites.

This review article discusses advancement in electro-stimulated gel, recent perspectives in materials selectivity in electro-simulated gels, the gel deformation mechanism, and their applications in various advanced fields. This paper also considered the challenges associated with chemistry, drying process and mechanics of electro-responsive gels and proposed future opportunities to further advance the science and technology of these gel-based devices. More specifically this review summarized novel materials capable of producing an elevated response to low energy stimuli that are being extensively studied globally in recent years. Subsequently, the electro-response gels formulated by reinforcing selective materials such as electro-active polymers, conductive polymers, and piezoelectric materials were discussed. These gels are stimulated by application of low dosage of an electrical field to enhance their inherent mechanical and responsive attributes. This article further reviewed the theoretical understanding of simulation of some exclusive response parameters and forces to describe the deformation mechanism of electro-response materials. The major findings of the study are better understanding of the nature of gels to be used for the wearable artificial muscles, sensors, actuators, robotics, lenses, biomedical and as soft materials, their dependence on the material type, device response behaviour in the electro-stimulated field and their stability under various end use conditions. The graphic art shown below depicts the main functions of the reviewed gels, their mechanism of function depending on the applications. It is anticipated that the development of the soft electro-simulated materials is going to grow in future due to expansion of the use of artificial intelligence in devices including robotics., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Industrial ecology, sustainable manufacturing, and green chemistry have been considered platform-based approaches to the reduction of the environmental footprint. Recently, nanofibrillated cellulose (NFC) has gained significant interest due to its mechanical properties, biodegradability, and availability. These outstanding properties of NFC have encouraged the development of a more sustainable substrate for electronics. In this context, the combination of NFC and conductive polymers may create a new class of biocomposites to be used in place of conventional electronics which are not optimally designed for use in flexible and mechanically robust devices. In this study, polythiophene was grafted onto nanocellulose surface at appropriate reaction times to obtain a strong, flexible, foldable films with capacity for electrical conductivity. Nanocomposites films were synthesized by a one-step reaction in which a 3-methyl thiophene monomer was oxidatively polymerized onto nanocellulose backbone. The nature of the fabricated NFC films changed from insulator to semiconductor material upon oxidative polymerization., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Over the span of the past decade, carbon dots (CDs) synthesized from renewable organic resources (organic CDs) have gathered a considerable amount of attention for their photoluminescent properties. This review will focus on organic CDs synthesized using clean chemistry and conventional synthetic chemistry from organic sources and their fluorescence mechanisms, such as quantum confinement effect and surface/edge defects, before outlining their performance in electronic applications, including organic photovoltaic devices, organic light-emitting devices, biosensors, supercapacitors, and batteries. The various organic resources and methods of organic CDs synthesis are briefly covered. Many challenges remain before the adoption of CDs can become widespread; their characterization, structure, functionality, and exact photoluminescent mechanism all require additional research. This review aims to summarize the current research outcomes and highlight the area where further research is needed to fully use these materials.

Bamboo-derived biocarbon (BA900) and wood-derived biocarbon (THOC700) have exhibited graphite-like characteristics through transmission electron microscopy, X-ray diffraction (XRD), and Attenuated Total Reflectance (ATR) spectroscopy analysis. Lightweight composites of biocarbons were manufactured by a mechanism of shear controlled melt-phase mixing, ensuring the preservation of biocarbon pore structures and simultaneously taking full advantage of low density polyolefin substrates. Effective tensile strength was improved by approximately 10% in the polypropylene-based bamboo carbon composite, whereas no appreciable improvement was observed in the tensile and impact strength of bamboo-derived biocarbon formulations compared to neat polymer. However, the tensile and flexural moduli and flexural strength of the THOC700-PP composites were significantly enhanced, by 56%, 67%, and 19%, respectively, compared to neat polymer. The most significant finding of the investigation was the retention of density in polyolefin polymer (ρ PP  = 0.91; ρ THOC  = 0.95; ρ BA900  = 0.99), with enhanced mechanical performance useful for lightweighting applications. Bamboo biocarbon provides a viable alternative to another abundantly available industrial carbon feedstock, reclaimed carbon fiber (RCF), in manufacturing thermoplastic composites. The origin of the carbon plays an important role in defining ultimate composite performance. A mechanism for retaining lightweight structural performance has been proposed in this original work, paving the way to develop next-generation lightweight thermoplastic structures for transportation and other industrial and consumer products., (Copyright © 2019. Published by Elsevier B.V.)

This work aims to provide an overview of producing value-added products affordably and sustainably from greenhouse gases (GHGs). Methanol (MeOH) is one such product, and is one of the most widely used chemicals, employed as a feedstock for ≈30% of industrial chemicals. The starting materials are analogous to those feeding natural processes: water, CO 2 , and light. Innovative technologies from this effort have global significance, as they allow GHG recycling, while providing society with a renewable carbon feedstock. Light, in the form of solar energy, assists the production process in some capacity. Various solar strategies of continually increasing technology readiness levels are compared to the commercial MeOH process, which uses a syngas feed derived from natural gas. These strategies include several key technologies, including solar-thermochemical, photochemical, and photovoltaic-electrochemical. Other solar-assisted technologies that are not yet commercial-ready are also discussed. The commercial-ready technologies are compared using a technoeconomic analysis, and the scalability of solar reactors is also discussed in the context of light-incorporating catalyst architectures and designs. Finally, how MeOH compares against other prospective products is briefly discussed, as well as the viability of the most promising solar MeOH strategy in an international context., Competing Interests: The authors declare no conflict of interest.

Cellulose nanofibers (CNF) were isolated from Curauá fibers (Ananas erectifolius L. B. Smith) through a mechanical grinder preceded by mild chemical treatment. Morphology and surface characteristics of the fibers were followed until it reaches the nanoscale as long and flexible nanofibers. In aqueous suspensions, SAXS techniques revealed that such nanofibers present a twisted ribbon structure while rheological measurements demonstrate its high viscosity and a thixotropic behavior. These characteristics suggests the potential application of CNF in biomedical field, which, in turn, stimulates the toxicological studies of such materials. The obtained materials do not show any sign of cytotoxicity by direct or indirect assays for cell viability and cell morphology using Vero cells. Moreover, during the adhesion test, the cells demonstrated higher affinity to the CNF surface. It can be related to its surface properties and its obtaining conditions, which did not use any hazardous chemicals., (Copyright © 2018. Published by Elsevier Ltd.)

Tea polyphenols have received much attention from the pharmaceutical and food industries owing to their extraordinary antioxidant and antibacterial characteristics. However, tea polyphenols are very unstable in processing and storage, since they are sensitive to the environmental factors like temperature, light and pH. Therefore, the effective application of tea polyphenols requires a protective mechanism to maintain its activity. The utilization of compounded tea polyphenols, instead of raw materials, can potentially help to improve their stability. This review focuses on the summarization of the compounding technologies for tea polyphenols, including physical technologies, chemical-interfacial technologies and nano-scale compounding technologies. Of which, the emerging nano cellulose bio-carrier, as a promising technology, is particularly proposed., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.)

Although there is a growing interest in utilizing nanocellulose fibres (NCFs) based composites for achieving a higher sustainability, mechanical performance of these composites is limited due to the poor compatibility between fibre reinforcement and polymer matrices. Here we developed a bio-nanocomposite with an enhanced fibre/resin interface using a hybrid-toughened epoxy. A strong reinforcing effect of NCFs was achieved, demonstrating an increase up to 88% in tensile strength and 298% in tensile modulus as compared to neat petro-based P-epoxy. The toughness of neat P-epoxy was improved by 84% with the addition of 10wt% bio-based E-epoxy monomers, which also mitigated the amount of usage of bisphenol A (BPA). The morphological analyses showed that the hybrid epoxy improved the resin penetration and fibre distribution significantly in the resulting composites. Thus, our findings demonstrated the promise of developing sustainable and high performance epoxy composites combing NCFs with a hybrid petro-based and bio-based epoxy resin system., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

The addition of short fibers has been experimentally observed to slow the stress relaxation of viscoelastic polymers, producing a change in the relaxation time constant. Our recent study attributed this effect of fibers on stress relaxation behavior to the interfacial shear stress transfer at the fiber-matrix interface. This model explained the effect of fiber addition on stress relaxation without the need to postulate structural changes at the interface. In our previous study, we developed an analytical model for the effect of fully aligned short fibers, and the model predictions were successfully compared to finite element simulations. However, in most industrial applications of short-fiber composites, fibers are not aligned, and hence it is necessary to examine the time dependence of viscoelastic polymers containing randomly oriented short fibers. In this study, we propose an analytical model to predict the stress relaxation behavior of short-fiber composites where the fibers are randomly oriented. The model predictions were compared to results obtained from Monte Carlo finite element simulations, and good agreement between the two was observed. The analytical model provides an excellent tool to accurately predict the stress relaxation behavior of randomly oriented short-fiber composites., Competing Interests: The authors declare no conflict of interest. The founding sponsors had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, and in the decision to publish the results.

Although it has been experimentally shown that the addition of short-fibers slows the stress relaxation process in composites, the underlying phenomenon is complex and not well understood. Previous studies have proposed that fibers slow the relaxation process by either hindering the movement of nearby polymeric chains or by creating additional covalent bonds at the fiber-matrix interface that must be broken before bulk relaxation can occur. In this study, we propose a simplified analytical model that explicitly accounts for the influence of polymer viscoelasticity on shear stress transfer to the fibers. This model adequately explains the effect of fiber addition on the relaxation behavior without the need to postulate structural changes at the fiber-matrix interface. The model predictions were compared to those from Monte Carlo finite-element simulations, and good agreement between the two was observed., Competing Interests: The authors declare no conflict of interest. The founding sponsors had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, and in the decision to publish the results.

Natural fibers can be attractive reinforcing materials in thermosetting polymers due to their low density and high specific mechanical properties. Although the research effort in this area has grown substantially over the last 20 years, manufacturing technologies to make use of short natural fibers in high volume fraction composites; are still limited. Natural fibers, after retting and preprocessing, are discontinuous and easily form entangled bundles. Dispersion and mixing these short fibers with resin to manufacture high quality, high volume fraction composites presents a significant challenge. In this paper, a novel pneumatic design for dispersion of natural fibers in their original discontinuous form is described. In this design, compressed air is used to create vacuum to feed and convey fibres while breaking down fibre clumps and dispersing them in an aerosolized resin stream. Model composite materials, made using proof-of-concept prototype equipment, were imaged with both optical and X-ray tomography to evaluate fibre and resin dispersion. The images indicated that the system was capable of providing an intimate mixture of resin and detangled fibres for two different resin viscosities. The new pneumatic process could serve as the basis of a system to produce well-dispersed high-volume fraction composites containing discontinuous natural fibres drawn directly from a loosely packed source.

Background: The ascomycete fungus Ophiostoma ulmi was responsible for the initial pandemic of the massively destructive Dutch elm disease in Europe and North America in early 1910. Dutch elm disease has ravaged the elm tree population globally and is a major threat to the remaining elm population. O. ulmi is also associated with valuable biomaterials applications. It was recently discovered that proteins from O. ulmi can be used for efficient transformation of amylose in the production of bioplastics., Results: We have sequenced the 31.5 Mb genome of O.ulmi using Illumina next generation sequencing. Applying both de novo and comparative genome annotation methods, we predict a total of 8639 gene models. The quality of the predicted genes was validated using a variety of data sources consisting of EST data, mRNA-seq data and orthologs from related fungal species. Sequence-based computational methods were used to identify candidate virulence-related genes. Metabolic pathways were reconstructed and highlight specific enzymes that may play a role in virulence., Conclusions: This genome sequence will be a useful resource for further research aimed at understanding the molecular mechanisms of pathogenicity by O. ulmi. It will also facilitate the identification of enzymes necessary for industrial biotransformation applications.

For proper treatment, recycling, or disposal of the pulp and paper mill secondary sludge qualitative and quantitative determination of its characteristics are necessary. Chemical extraction, quantitative characterization, and spectroscopic experiments have been performed to determine the molecular composition and chemical functionality of a pulp and paper mill secondary sludge. In order to extract the low-molecular-weight substances, soxhlet extraction with polar and non-polar solvents was performed where most of the target substances (17±1.3%.) were extracted after 2 hours. Over time, this extraction followed a first-order kinetics. Fiber analyses have shown 12±3% lignin, 28±3% cellulose, and 12±4% hemicelluloses content. The ash content was about 17±0.5%. In this work, 7 and 16% intra- and extracellular polymeric substances, respectively, were extracted from the secondary sludge. EPS and mixture of intra- and extracellular biopolymers have shown similar chemical functionalities. These analyses confirmed that the paper secondary sludge consisted mainly of wood fiber, i.e. lignocellulosic substances, along with proteins and polysaccharides originated from microorganisms.

Cellulose nanofibers were extracted from the agricultural residues, wheat straw and soy hulls, by a chemi-mechanical technique to examine their potential for use as reinforcement fibers in biocomposite applications. The structure of the cellulose nanofibers was investigated by transmission electron microscopy. The wheat straw nanofibers were determined to have diameters in the range of 10-80 nm and lengths of a few thousand nanometers. By comparison, the soy hull nanofibers had diameter 20-120 nm and shorter lengths than the wheat straw nanofibers. Chemical characterization of the wheat straw nanofibers confirmed that the cellulose content was increased from 43% to 84% by an applied alkali and acid treatment. FT-IR spectroscopic analysis of both fibers demonstrated that this chemical treatment also led to partial removal of hemicelluloses and lignin from the structure of the fibers. PXRD results revealed that this resulted in improved crystallinity of the fibers. After mechanical treatments of cryocrushing, disintegration and defibrillation, the thermal properties of the nanofibers were studied by the TGA technique and found to increase dramatically. The degradation temperature of both nanofiber types reached beyond 290 degrees C. This value is reasonably promising for the use of these nanofibers in reinforced-polymer manufacturing.

Oil-seed flax shive has been promoted as a raw material for low-end paper making because of its overall cost benefit over hardwood and groundwood pulp and increasing demand for low-cost pulp in rigid packaging applications. We have made refiner mechanical pulp from oil-seed shives by using a 300 mm Sprout-Bauer pilot refiner. The factors controlled during refining were: consistency, multi-pass refining, temperature, spacing between the plates and polyol-anhydride reactant concentration. Based on the results in this study it is apparent that unmodified shives develop low mechanical strength, shorter fibers and large amount of fines. Chemical modification of shives with a pre-reacted mixture of polyol-anhydride reduces refining energy consumption, improves strength performance but decreases scattering coefficient. From the results of investigation it is suggested that chemically modified refiner pulp from shives cannot be used for high-grade paper manufacture but it can be used as a low-cost filler for low-end applications in packaging or low-performance decorative papers.