Modeling and investigation of swelling kinetics of sodium carboxymethyl cellulose/starch/citric acid superabsorbent polymer.

Crosslinked hydrophilic polymers with high water absorption rates are known as superabsorbent polymers (SAPs). Most commercial superabsorbent polymers are made with acrylic acid, which is difficult to biodegrade. So, in this investigation, carboxymethyl cellulose (CMC) was utilized as a significant component in the synthesis of polysaccharide-based SAPs. Citric acid (CA) and starch were chosen as crosslinking agents because they are more eco-friendly, non-toxic, and biodegradable than traditional crosslinking agents. FTIR analysis revealed that the superabsorbent polymer product contains a crosslinked structure of CMC and starch with side chains that carry carboxylate functional groups. Superabsorbent weight loss and grafting data were satisfactorily studied using the TGA approach. Under optimum circumstances, the SAP2 water absorbency capacity in distilled water was 287.37 g.g-1 and SAP1 absorbency capacity in a solution containing 0.9 wt% NaCl was 52.18 g.g-1. Moreover, Schott's pseudo-second-order model was used to determine the kinetic swelling of the superabsorbent. The initial swelling rate of SAPs can be calculated using the Q∞ data acquired in the following order: SAP2 > SAP1 > SAP3 > SAP4 in distilled water and SAP1 > SAP2 > SAP3 > SAP4 in 0.9 wt% NaCl solution, respectively. The findings suggested that a small amount of citric acid introduced into the SAPs matrix could enhance the swelling rate of SAPs. The results of the cytotoxicity tests show that the extraction liquid of composite hydrogel fibers is less cytotoxic than the positive control. As well, SAP underwent in silico docking investigations on the DNA Gyrase enzyme. As the ligand is a monomer of SAP, it was a long chain of carbohydrate molecules with alcoholic groups, esters groups, and keto groups forms a strong binding interaction with DNA gyrase.

A Comparative Study of Gamma-Ray Irradiation-Induced Oxidation: Polyethylene, Poly (Vinylidene Fluoride), and Polytetrafluoroethylene.

Radiation techniques are used to modify the physical, chemical and biological properties of polymers. This induces crosslinking and degradation reactions of polymers by utilizing radicals generated through ionizing radiation. However, oxidation products (such as carbonyl) can be formed because oxidation occurs by chain scission in the presence of oxygen. Herein, we demonstrate the gamma-ray irradiation-induced oxidation with and without fluorine using polyethylene, polyvinylidene fluoride and polytetrafluoroethylene under the same conditions. In this study, changes in element-content and chemical-bond structures were analyzed before and after gamma-ray irradiation under air atmosphere. As a result, polytetrafluo-roethylene showed less oxidation and excellent thermal properties after the absorbed dose of 500 kGy. This can be attributed to the generation of stable perfluoroalkylperoxy radicals after gamma ray irradiation in the PTFE structure containing only CF2 groups, thereby hindering the oxidation reaction.

Integrating the Essence of a Metal-Organic Framework with Electrospinning: A New Approach for Making a Metal Nanoparticle Confined N-Doped Carbon Nanotubes/Porous Carbon Nanofibrous Membrane for Energy Storage and Conversion.

The fabrication of an economic and efficient multifunctional advanced nanomaterial with a rational composition and configuration by a facile methodology is a crucial challenge. Herein, we are the first to report the growth of Co nanoparticle-integrated nitrogen-doped carbon nanotubes (N-CNTs) on porous carbon nanofibers by simply heating in the situ-developed metal-organic framework (MOF)-based electrospun nanofibrous membrane with no need for an external supply of any additional precursors and reducing gases. The long and entangled N-CNTs originating from highly porous and graphitic carbon nanofibers offer good flexibility, large surface area, high porosity, high conductivity, the homogeneous incorporation of heteroatoms and metallic constituents, and an abundant exposure of active nanocatalytic sites. The as-developed nanoassembly demonstrates attractive characteristics for electrocatalytic hydrogen and oxygen evolution reactions and electrochemical energy storage. This strategy of integrating the essence of an MOF with electrospinning offers a new, direct, and cost-effective approach for making N-doped CNT-based multifunctional membranes.

Photothermal Fabrics for Efficient Oil-Spill Remediation via Solar-Driven Evaporation Combined with Adsorption.

Oil spill rapidly destroys aquatic system and threatens humans, requiring fast and efficient remedy for removal of oil. The conventional remedy employs water-floating oil adsorbents whose volume should be large enough to accommodate all oil ingredients. Here, we suggest a new concept for efficient oil-spill remediation, which combines solar-driven evaporation of light oil components and simultaneous adsorption of heavy oil components, namely, solar-driven evaporation of oil combined with adsorption (SEOA). To design photothermal oil absorbents for the efficient SEOA, we designed carbonaceous fabrics with high photothermal heating performance and oil-adsorption capacity by carbonizing nonwoven cotton fabrics. For three model organic solvents of octane, decane, and dodecane floating on water, the fabrics, respectively, accelerated the evaporation in factors of 2.0, 4.4, and 2.3 through photothermal heating under simulated sunlight condition. For the 1.18 mm thick crude oil floating on water, 70 and 77 wt % of crude oil were evaporated within 2 and 16 h, respectively, with the photothermal fabrics, whereas only 22 and 34 wt % was evaporated in the absence of the fabrics, indicating the dramatic enhancement of oil removal by solar-driven evaporation. The remaining heavy oil components were accommodated in the pores of the fabrics, removal of which showed an additional 18 wt % reduction; that is, a total 95 wt % of the crude oil was removed. The oil-treatment capacity is as high as 110 g g-1, which has never been achieved with conventional oil adsorbents to the best of our knowledge. We believe that our combinatorial SEOA approach potentially contributes to minimizing the environmental disaster through a fast and efficient oil-spill remediation.

Phytic acid controlled in situ synthesis of amorphous cobalt phosphate/carbon composite as anode materials with a high mass loading for symmetrical supercapacitor: amorphization of the electrode to boost the energy density.

Transition metal phosphate (TMPi)-based composites as anode electrode materials in supercapacitor applications are less reported. Herein, we report a phytic acid (PA)-assisted in situ-formed amorphous cobalt phosphate/carbon (CoPi/C) composite grown on a flexible woven carbon cloth (CC) via a simple one-step carbonization approach. The tunable synthesis of amorphous and crystalline composites is shown by simply controlling the concentration of the cobalt salts. The strategy for high mass loading to 12 mg cm-2 is also shown in this report. Importantly, the resulting amorphous electrode materials exhibit electric double-layer capacitance (EDLC) behavior that works over a wide potential range from -1.4 to +0.5 V in an aqueous solution of potassium hydroxide (2 M KOH) and from -1.5 to +1.5 V in sodium sulfate (1 M Na2SO4). The amorphous electrode as an anode is capable of delivering an areal capacitance up to 2.15 F cm-2 at a current density of 4 mA cm-2 (gravimetric capacitance up to 606.1 F g-1 at 1 Ag-1) and has a retention of 94.2% at 10 000 cycles. The flexible solid-state symmetric device fabricated shows an energy density of approximately 620.0 µW h cm-2 at a power density of 4.7 mW cm-2 (31.1 W h kg-1 at 476.0 W kg-1). This study offers a novel route for the generation of metal phosphate-based anode materials with high capacitance for symmetrical supercapacitor device with high energy density.

Improved pretreatment process using an electron beam for optimization of glucose yield with high selectivity.

In this study, electron beam irradiation (EBI) assisted by a dilute acid pretreatment process was investigated to improve the glucose yield and show high selectivity in the enzymatic hydrolysis of rice straw. In the first step, EBI of rice straw was performed at various doses ranging from 50 to 500 kGy. The electron beam-irradiated rice straw was then autoclaved with 3 % dilute acid at 120 °C for 1 h. The pretreated rice straw was finally subjected to enzymatic hydrolysis at 50 °C for 24, 48, and 72 h by 70 filter paper units (FPU)/mL cellulase and 40 cellobiose units (CbU)/mL glucosidase. Glucose was obtained with a very high selectivity of 92.7 % and a total sugar yield of 80 % from pretreated rice straw after 72 h of enzymatic hydrolysis.

Patterning of polymer nanocomposite resists containing metal nanoparticles by electron beam lithography.

Poly(vinyl pyrrolidone) (PVP)-stabilized silver nanoparticles (NPs) were used as a new nanocomposite resist for electron beam lithography. A nanocomposite resist prepared by reducing silver nitrate in an alcoholic PVP solution was patterned by using a scanning electron microscope equipped with a nanometer pattern generation system. Well-defined negative tone patterns with a good sensitivity of 200 microC/cm2 and a contrast of 2.83 were obtained using the prepared nanocomposite resist. In addition, the changes in the morphology and structure of the resist patterns with a thermal treatment temperature were investigated by a FE-SEM with an EDX. The results revealed that the patterns of Ag NPs were formed through sintering the formed resist patterns at above 300 degrees C.

Micropatterning of polymer-embedded metal nanoparticles by an ion beam contact lithography.

A convenient and effective method to pattern polymer-embedded metal nanoparticles by ion irradiation has been developed. The thin Pluronic films containing silver nitrate as a precursor of silver nanoparticles were irradiated through a pattern mask with accelerated proton (H+) ions. It was found from the UV-Vis measurement that the formation of silver nanoparticles in the Pluronic matrix was dependant on the amount of silver nitrate. The 50 microm line (pitch 150 microm) patterns of the Pluronic containing silver nanoparticles were obtained with the thin film irradiated to 1 x 10(16) ions/cm2. The heat treatment effect on the morphology of the patterns was investigated by using a scanning electron microscope with an energy dispersive X-ray spectrometer. The results confirmed that the silver nanoparticles were successfully embedded in the Pluronic patterns and the patterns were changed into large silver particles by a heat treatment above 350 degrees C.

Micropatterning of poly(vinyl pyrrolidone)/silver nanoparticle thin films by ion irradiation.

This study describes a new patterning method of poly(vinyl pyrrolidone) (PVP) containing silver nanoparticles by using ion irradiation. The thin films prepared from PVP/silver nanoparticle solutions were irradiated through a mask with accelerated H+ ions. Well-defined 50 microm line (pitch 150 microm) patterns were generated from the film irradiated at 1 x 10(16) ions/cm2. The heat treatment effect on the morphology of the patterns was investigated by using a scanning electron microscope with an energy dispersive X-ray spectrometer. The results confirmed that the silver nanoparticles were successfully immobilized in the PVP patterns and the patterns were changed into silver particles by heat treatment above 300 degrees C.