Radially aligned hierarchical N-doped porous carbon beads derived from oil-sand asphaltene for long-life water filtration and wastewater treatment.

The application of waste-derived highly efficient adsorbent for organic pollutants removal from water and wastewater is presented. Highly porous carbon beads with radially aligned macrochannels were prepared from asphaltene. Well-ordered inwardly aligned macrovoids favored solute diffusion and maximized the liquid accommodation capacity. A further N-doping could modulate the sorbent hydrophilicity leading to an outstanding absorption performance for a range of organic solvents and oily chemicals. N-doped carbon beads were effective sorbents of lopinavir (LNV) and ritonavir (RNV) from water and wastewater. The process of sorption was fast, and the highest removal was noted for RNV than LPV. N-doping favored LNV and RNV adsorption due to the increased porous structure of N-doped asphaltene beads. The chemisorption of both LPV and RTV was a rate-limiting step. The presence of co-pollutants in treated wastewater enhanced LPV and RNV removal and an up to 470 % increase was noted. The presence of LPV or RTV in distilled water was not toxic to Aliivibrio fischeri or even can stimulate their growth. However, after the adsorption process, the solution of RTV reduced its toxicity significantly and the final solution was not toxic. The opposite effect was noted for LPV. Given the repeatability, high removal performance, and cost-effectiveness of the asphaltene-based carbon microtubes when compared to other well-known sorbents such as carbon nanotubes, they demonstrated great potential as a low-cost and effective agent for long-life water filtration and wastewater treatment.

Rational Design of Mussel-Inspired Hydrogels with Dynamic Catecholato-Metal Coordination Bonds.

Nature has often been the main source of inspiration for designing smart functional materials. As an example, mussels can attach to almost any wet surfaces, for example, wood, rocks, metal, etc., due to the presence of catechols containing amino acid 3,4-dihydroxyphenyl-l-alanine (DOPA). Fabrication of mussel-inspired hydrogels using dynamic catecholato-metal coordination bonds has recently been in the limelight because of the hydrogels' ease of gelation, interesting self-healing, self-recovery, adhesiveness, and pH-responsiveness, as well as shear-thinning and mechanical properties. Mussel inspired hydrogels take advantage of catechols, for example, DOPA in the blue mussel, to undergo catecholatometal gelation through coordination chemistry. This review explores the latest developments in the fabrication of such hydrogels using catecholato-metal coordination bonds, and discusses their potential applications in sensors, flexible electronics, tissue engineering, and wound dressing. Moreover, current challenges and prospects of such hydrogels are discussed. The main focus of this paper is on providing a deeper understanding of this growing field in terms of chemistry, physics, and associated properties.

The key structural features governing the free radicals and catalytic activity of graphite/graphene oxide.

The presence of unpaired electrons (radicals) due to structural defects is believed to contribute to the catalytic reactivity of carbon materials. Graphite oxide and graphene oxide (GO) consist of significant structural defects and hence are considered more reactive than graphite and graphene. However, the relationship between their radical content/reactivity and their physical and chemical structures remains unknown, which limits the fabrication of high efficiency carbon-based catalysts. In this work, we progressively oxidize graphite to achieve graphite oxide and GO with different levels of oxidation and different sizes. It is observed that a maximal radical content can be achieved on graphite oxide with a C/O ratio of ca. 3.0 and a thickness of around 50 nm. Such a graphite oxide contains about 45% of π bonds and 38% of oxygenated bonds, respectively. Thinner or thicker sheets have lower radical contents due to over or insufficient oxidation, respectively. Single GO sheets with high radical contents can only be produced through a combination of oxidation and reduction. The catalytic activity of the graphite/graphene oxide for phenol degradation was found to be linearly correlated to their radical contents. The observations are significant for the advancement of carbon-based metal-free catalysis.

Dynamic plant-derived polysaccharide-based hydrogels.

Plant-derived polysaccharides are widely used to fabricate hydrogels because of their ease of gelation and functionalization, plus exceptional biological properties. As an example, nanocellulose is a suitable candidate to fabricate hydrogels for tissue engineering applications due to its enhanced mechanical and biological properties. However, hydrogels are prone to permanent failure whilst under load without the ability to reform their networks once damaged. Recently, considerable efforts are being made to fabricate dynamic hydrogels via installation of reversible crosslinks within their networks. In this paper, we review the developments in the design of dynamic hydrogels from plant-derived polysaccharides, and discuss their applications in tissue engineering, sensors, bioelectronics devices, etc. The main goal of the paper is to elucidate how the network design of hydrogels can influence their dynamic properties: self-healing and self-recovery. Complementary to this, current challenges and prospects of dynamic plant-derived hydrogels are discussed.

Converting waste textiles into highly effective sorbent materials.

Activated carbon fibres with a tubular structure and exfoliated surface were produced utilizing cotton textile waste as the precursor. The synthesized carbon fibres were freeze dried resulting in a tubular structure and large pore size distribution. The absorption properties against various oils and organic solvents were accessed, these fibres showed some of the highest absorption capabilities reported for cellulose based carbons, in particular for olive oil, gasoline and chloroform.

Dynamic Hydrogels and Polymers as Inks for Three-Dimensional Printing.

Developing rationally designed dynamic hydrogels and polymers as inks for 3D printing is in the limelight today. They would enable us to precisely fabricate complex structures in high resolutions and modular platforms with smart functions (e.g., self-healing and self-recovery), as well as tunable mechanical, chemical, and biological properties. In this paper, we explore recent developments in dynamic hydrogels and polymers as inks for 3D printing and discuss their properties and applications in tissue engineering, biomedicine, soft robotics, and sensors. The main scope of the paper is to give a deeper understanding of the field in terms of chemistry, physics, and associated properties. Moreover, the challenges and prospects of hydrogel/polymer inks will be discussed. We envisage that 3D printed dynamic hydrogels and polymers will provide unprecedented opportunities in designing and fabricating smarter structures.

Surface nanogrooving of carbon microtubes.

Extrusion processing of carbon tubes can be problematic due to their poor interfacial interactions with polymeric matrices. Surface chemical modification of carbon tubes can be utilized to create bonding sites to form networks with polymer chains. However, chemical reactions resulting in intermolecular primary bonding limit processability of extrudate, since they cause unstable rheological behaviour, and thus decrease the stock holding time, which is determinative in extrusion. This study presents a method for the synthesis of carbon microtubes with physically modified surface area to improve the filler and matrix interfacial interactions. The key concept is the formation of a nanogrooved topography, through acoustic cavitation on the surface of processing fibres. The effect of nanogrooving on roughness parameters is described, along with the role of surface modified carbon tubes on rheological behaviour, homogeneity, and coherency of extrudate. The measurements showed that nanogrooving increases the surface area of carbon microtubes, as a result, die swelling of the extrudate is reduced. Furthermore, after solidification, the mechanical strength of composite is reinforced due to stronger interactions between nanogrooved carbon tubes and polymer matrix.

Effects of nanozeolite/starch thermoplastic hydrogels on wound healing.

BACKGROUND: Wound healing is a complex biological process. Some injuries lead to chronic nonhealing ulcers, and healing process is a challenge to both the patient and the medical team. We still look forward an appropriate wound dressing. MATERIALS AND METHODS: In this study, starch-based nanocomposite hydrogel scaffolds reinforced by zeolite nanoparticles (nZ) were prepared for wound dressing. In addition, a herbal drug (chamomile extract) was added into the matrix to accelerate healing process. To estimate the cytocompatibility of hydrogel dressings, fibroblast mouse cells (L929) were cultured on scaffolds. Then, 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium-bromide assay test and interaction of cells and scaffolds were evaluated. For evaluating healing process, 48 male rats were randomly divided into four groups of four animals each (16 rats at each step). The ulcers of the first group were treated with the same size of pure hydrogels. The second group received a bandage with the same size of hydrogel/extract/4 wt% nZ (hydrogel NZE). The third group was treated with chamomile extract, and the fourth group was considered as control without taking any medicament. Finally, the dressings were applied on the chronic refractory ulcers of five patients. RESULTS: After successful surface morphology and cytocompatibility tests, the animal study was carried out. There was a significant difference between starch/extract/4 wt% nZ and other groups on wound size decrement after day 7 (P < 0.05). At the clinical pilot study step, the refractory ulcers of all five patients were healed without any hypersensitivity reaction. CONCLUSION: Starch-based hydrogel/zeolite dressings may be safe and effective for chronic refractory ulcers.

Incorporation of mesoporous silica nanoparticles into random electrospun PLGA and PLGA/gelatin nanofibrous scaffolds enhances mechanical and cell proliferation properties.

Poly(lactic-co-glycolic acid) (PLGA) and PLGA/gelatin random nanofibrous scaffolds embedded with different amounts of mesoporous silica nanoparticles (MSNPs) were fabricated using electrospinning method. To evaluate the effects of nanoparticles on the scaffolds, physical, chemical, and mechanical properties as well as in vitro degradation behavior of scaffolds were investigated. The mean diameters of nanofibers were 974±68nm for the pure PLGA scaffolds vs 832±70, 764±80, and 486±64 for the PLGA/gelatin, PLGA/10wt% MSNPs, and the PLGA/gelatin/10wt% MSNPs scaffolds, respectively. The results suggested that the incorporation of gelatin and MSNPs into PLGA-based scaffolds enhances the hydrophilicity of scaffolds due to an increase of hydrophilic functional groups on the surface of nanofibers. With porosity examination, it was concluded that the incorporation of MSNPs and gelatin decrease the porosity of scaffolds. Nanoparticles also improved the tensile mechanical properties of scaffolds. Using in vitro degradation analysis, it was shown that the addition of nanoparticles to the nanofibers matrix increases the weight loss percentage of PLGA-based samples, whereas it decreases the weight loss percentage in the PLGA/gelatin composites. Cultivation of rat pheochromocytoma cell line (PC12), as precursor cells of dopaminergic neural cells, on the scaffolds demonstrated that the introduction of MSNPs into PLGA and PLGA/gelatin matrix leads to improved cell attachment and proliferation and enhances cellular processes.

Porous starch/cellulose nanofibers composite prepared by salt leaching technique for tissue engineering.

Starch/cellulose nanofibers composites with proper porosity pore size, mechanical strength, and biodegradability for cartilage tissue engineering have been reported in this study. The porous thermoplastic starch-based composites were prepared by combining film casting, salt leaching, and freeze drying methods. The diameter of 70% nanofibers was in the range of 40-90 nm. All samples had interconnected porous morphology; however an increase in pore interconnectivity was observed when the sodium chloride ratio was increased in the salt leaching. Scaffolds with the total porogen content of 70 wt% exhibited adequate mechanical properties for cartilage tissue engineering applications. The water uptake ratio of nanocomposites was remarkably enhanced by adding 10% cellulose nanofibers. The scaffolds were partially destroyed due to low in vitro degradation rate after more than 20 weeks. Cultivation of isolated rabbit chondrocytes on the fabricated scaffold proved that the incorporation of nanofibers in starch structure improves cell attachment and proliferation.