Grafting nanocellulose with diethylenetriaminepentaacetic acid and chitosan as additive for enhancing recycled OCC pulp fibres

This paper develops a novel paper additive for effectively recycling old corrugated container (OCC) by functionalizing nanocellulose (NC) with diethylenetriaminepentaacetic acid (DTPA) and chitosan (CS), and investigate the reinforcing mechanisms and effect of the developed additive on the physical properties of recycled OCC pulp handsheets. The tensile, tear and burst index, air permeability, tensile energy absorption (TEA), and drainage performance of the recycled OCC handsheets are examined. Fourier transform infrared FTIR) spectroscopy, thermal gravimetric analysis (TGA) and scanning electron microscopy (SEM) are used for the chemical and microstructure characterization of both NC based additives and paper from recycled OCC pulp. The results show that functional groups on the NC based additive, such as carboxyl, amino and hydroxyl groups, can bond with the hydroxyl groups on the recycled OCC fibres to generate a chemical bond. This leads to an increase in the crosslinks and bonding area between the fibres, which increases their tensile strength and improves their recycling rate. SEM shows that the paper with NC based additives had tighter inter-fibre bonds and smaller paper pore structure. Addition of 0.3% NC-DTPA-CS additive results in optimal properties of the recycled OCC paper with an increase by 31.64%, 22.28% and 36.6% of tensile index, tear index, burst index respectively, and the air permeability decreases by 36.92%. Graphical Abstract

The Effect of Sulfated Zirconia and Zirconium Phosphate Nanocomposite Membranes on Fuel-Cell Efficiency

To investigate the effect of acidic nanoparticles on proton conductivity, permeability, and fuel-cell performance, a commercial Nafion® 117 membrane was impregnated with zirconium phosphates (ZrP) and sulfated zirconium (S-ZrO2) nanoparticles. As they are more stable than other solid superacids, sulfated metal oxides have been the subject of intensive research. Meanwhile, hydrophilic, proton-conducting inorganic acids such as zirconium phosphate (ZrP) have been used to modify the Nafion® membrane due to their hydrophilic nature, proton-conducting material, very low toxicity, low cost, and stability in a hydrogen/oxygen atmosphere. A tensile test, water uptake, methanol crossover, Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), and scanning electron microscopy (SEM) were used to assess the capacity of nanocomposite membranes to function in a fuel cell. The modified Nafion® membrane had a higher water uptake and a lower water content angle than the commercial Nafion® 117 membrane, indicating that it has a greater impact on conductivity. Under strain rates of 40, 30, and 20 mm/min, the nanocomposite membranes demonstrated more stable thermal deterioration and higher mechanical strength, which offers tremendous promise for fuel-cell applications. When compared to 0.113 S/cm and 0.013 S/cm, respectively, of commercial Nafion® 117 and Nafion® ZrP membranes, the modified Nafion® membrane with ammonia sulphate acid had the highest proton conductivity of 7.891 S/cm. When tested using a direct single-cell methanol fuel cell, it also had the highest power density of 183 mW cm−2 which is better than commercial Nafion® 117 and Nafion® ZrP membranes.

Synthesis and Characterization of Zn–Organic Frameworks Containing Chitosan as a Low-Cost Inhibitor for Sulfuric-Acid-Induced Steel Corrosion: Practical and Computational Exploration

In this work, a Zn–benzenetricarboxylic acid (Zn@H3BTC) organic framework coated with a dispersed layer of chitosan (CH/Zn@H3BTC) was synthesized using a solvothermal approach. The synthesized CH/Zn@H3BTC was characterized by Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscope (FESEM), thermal gravimetric analysis (TGA), and Brunauer, Emmett, and Teller (BET) surface area. The microscopic observation and the analysis of the BET surface area of CH/Zn@H3BTC nanocomposites indicated that chitosan plays an important role in controlling the surface morphology and surface properties of the Zn@H3BTC. The obtained findings showed that the surface area and particle size diameter were in the range of 80 m2 g−1 and 800 nm, respectively. The corrosion protection characteristics of the CH/Zn@H3BTC composite in comparison to pristine chitosan on duplex steel in 2.0 M H2SO4 medium determined by electrochemical (E vs. time, PDP, and EIS) approaches exhibited that the entire charge transfer resistance of the chitosan- and CH/Zn@H3BTC-composite-protected films on the duplex steel substrate was comparatively large, at 252.4 and 364.8 Ω cm2 with protection capacities of 94.1% and 97.8%, respectively, in comparison to the unprotected metal surface (Rp = 20.6 Ω cm2), indicating the films efficiently protected the metal from corrosion. After dipping the uninhabited and protected systems, the surface topographies of the duplex steel were inspected by FESEM. We found the adsorption of the CH/Zn@H3BTC composite on the metal interface obeys the model of the Langmuir isotherm. The CH/Zn@H3BTC composite revealed outstanding adsorption on the metal interface as established by MD simulations and DFT calculations. Consequently, we found that the designed CH/Zn@H3BTC composite shows potential as an applicant inhibitor for steel protection.

Acoustic Properties of a New Composite Material Obtained from Feather Flour and Recycled Polypropylene

Sustainable materials made from recycled materials are an alternative to traditional materials (synthetic ones) and present a lower environmental impact. Due to the fact that natural fibers were successfully used to produce environmentally friendly sound adsorbing materials, biocomposites made from recycled polypropylene (PPR), feathers flour (FF) with / without compatibilizers (C) were obtained and characterized from the point of view of their acoustical behavior. Obtained materials were characterized also from the morphological and compositional point of view by scanning electron microscopy and thermal gravimetric analysis. All tested samples presented sound adsorption properties but the best results were obtained for the biocomposites with FF content of 10%-20%.

Application of radiation grafted waste polypropylene fabric for the effective removal of Cu (II) and Cr (III) ions

This study focuses on the adsorption of hazardous Cr (III) and Cu (II) ions from aqueous solution by applying modified waste polypropylene (PP) fabric as an adsorbent. Pre-irradiation technique was performed for grafting of sodium styrene sulfonate (SSS) and acrylic acid (AAc) onto the PP fabric. The monomer containing 8% SSS and 16% AAc in water was used. Graft yield at 30 kGy radiation dose was 390% when 4% NaCl was added as additive. The prepared adsorbent was characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), thermo-gravimetric analysis (TGA) and dynamic mechanical analyzer (DMA). The influences of different parameters including pH, contact time, temperature and initial metal ion concentration were also investigated. The equilibrium adsorption data were better fitted to the Langmuir isotherm model with maximum monolayer adsorption capacity 384.62 mg/g for Cr (III) and 188.68 mg/g for Cu (II) ions. The kinetic data were better explained by pseudo first-order kinetic model having good matching between the experimental and theoretical adsorption capacity. The adsorption process was spontaneous, endothermic and thermodynamically feasible. Furthermore, investigation of desorption of metal ions and reuse of the adsorbent suggesting that the adsorbent is an efficient and alternative material in the removal of Cr (III) and Cu (II) from aqueous media.

Microstructure and Thermal Property of Designed Alginate-Based Polymeric Composite Foam Materials Containing Biomimetic Decellularized Elastic Cartilage Microscaffolds

This study presents a designed alginate-based polymeric composite foam material containing decellularized elastic cartilage microscaffolds from porcine elastic cartilage by using supercritical fluid and papain treatment for medical scaffold biomaterials. The microstructure and thermal property of the designed alginate-based polymeric composite foam materials with various controlled ratios of alginate molecules and decellularized elastic cartilage microscaffolds were studied and characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and differential thermal gravimetric analysis (TGA/DTG). The microstructure and thermal property of the composite foam materials were affected by the introduction of decellularized elastic cartilage microscaffolds. The designed alginate-based polymeric composite foam materials containing decellularized elastic cartilage microscaffolds were ionically cross-linked with calcium ions by soaking the polymeric composite foam materials in a solution of calcium chloride. Additional calcium ions further improved the microstructure and thermal stability of the resulting ionic cross-linked alginate-based polymeric composite foam materials. Furthermore, the effect of crosslinking functionality on microstructures and thermal properties of the resulting polymeric composite foam materials were studied to build up useful information for 3D substrates for cultivating and growing cartilage cells and/or cartilage tissue engineering.

Osmium Recovery as Membrane Nanomaterials through 10–Undecenoic Acid Reduction Method

The recovery of osmium from residual osmium tetroxide (OsO4) is a necessity imposed by its high toxicity, but also by the technical-economic value of metallic osmium. An elegant and extremely useful method is the recovery of osmium as a membrane catalytic material, in the form of nanoparticles obtained on a polymeric support. The subject of the present study is the realization of a composite membrane in which the polymeric matrix is the polypropylene hollow fiber, and the active component consists of the osmium nanoparticles obtained by reducing an alcoholic solution of osmium tetroxides directly on the polymeric support. The method of reducing osmium tetroxide on the polymeric support is based on the use of 10-undecenoic acid (10–undecylenic acid) (UDA) as a reducing agent. The osmium tetroxide was solubilized in t–butanol and the reducing agent, 10–undecenoic acid (UDA), in i–propanol, t–butanol or n–decanol solution. The membranes containing osmium nanoparticles (Os–NP) were characterized morphologically by the following: scanning electron microscopy (SEM), high-resolution SEM (HR–SEM), structurally: energy-dispersive spectroscopy analysis (EDAX), Fourier transform infrared (FTIR) spectroscopy. In terms of process performance, thermal gravimetric analysis was performed by differential scanning calorimetry (TGA, DSC) and in a redox reaction of an organic marker, p–nitrophenol (PNP) to p–aminophenol (PAP). The catalytic reduction reaction with sodium tetraborate solution of PNP to PAP yielded a constant catalytic rate between 2.04 × 10−4 mmol s–1 and 8.05 × 10−4 mmol s−1.

Comparing the Physico-Chemical Characteristics of Formulated and Marketed Yashada Bhasma

The present study is aimed to observe the difference in the Physico-Chemical characteristics of the marketed and formulated bhasma samples through X-Ray Diffraction analysis (XRD), Dynamic Light Scattering (DLS), Zeta potential, Thermo-Gravimetric analysis (TGA), Scanning Electron Microscopy (SEM) and Energy Dispersive X-Ray analysis (EDAX), apart from organoleptic methods. Inductively Coupled Plasma Mass Spectroscopy (ICPMS) analysis was also done to observe the presence of trace and heavy metals so that the safety of all these samples could be ensured. XRD shows variation in oxide nature of zinc as well crystallite size in all bhasma samples. DLS and SEM results show difference in particle size of marketed bhasma samples as compared to formulated Yashada bhasma. EDAX and ICPMS also confirm the alteration in elemental composition of all these bhasma samples. Thus, it can be concluded that these ayurvedic medicines should be prepared strictly using the formulation methods as mentioned in the Ayurvedic texts. This will help the prepared products to adopt the inherent quality of the ancient system of medicine, which shall be useful and devoid of any side effects for human consumption.

The Effect of the Multi-doping Strategy on Stabilization of the Cubic δ-phase in the Bi2O3-based Solid Electrolyte Systems in Terms of the SOFC Applications

In this study, the effects of multi-doping strategy on phase stabilization and electrical conductivity for the doped Bi 2 O 3 system were investigated. All solid mixtures were created by solid state reactions according to a certain stoichiometric ratio in atmospheric conditions. The structural, electrical, thermal and surface characterizations of the created samples were performed by x-ray diffraction method (XRD), four point-probe technique (4-PPT), differential thermal analysis/thermo gravimetric analysis (DTA/TGA) and scanning electron microscope (SEM), respectively. From XRD results, it was seen that the fcc δ-phase could be stabilized by using only 1:1:1:2 or 2:2:2:1 dopant content ratio (in here, “1:” is corresponds to” 5%” mole). The other compounds prepared out of this ratios were mixed phase because of the containing both α-phase peaks and δ-phase peaks on their XRD pattern. When the all samples were compared in terms of electrical conductivity at 750 °C, it was observed that the fcc δ-phase stabilized samples exhibited higher conductivity than that of other compounds as expected. The highest electrical conductivity was for the sample, dopant content ratios of which are 1: 1: 1: 2, with 0.014 S.cm -1 at 750 °C and also it had the lowest activation energy (0.51 eV) among all samples. On the other hand, according to the thermal analysis results, it was concluded that phase transition occurred only on the DTA curve of the sample given with dopant content ratios 1:1:1:1 due to presence of endothermic peak on its DTA curve at 729°C during the heating process. Also, for this sample, it was clearly predicted from the electrical conductivity graphs depending on temperature that the phase transition occurred at just that temperature (729 °C) due to the sudden increase in conductivity by indicating phase transition from the α-phase to the cubic δ-phase. The SEM analysis pointed out that grain size decreased as total dopant ratio increased and also the grain boundary changed sharply with the increase in the total dopant ratio.

Activation of Blast Furnace Slag with CFB Fly Ash as a Supplementary Binder Material: Hydration Products and Effects of Sulfate Attack

Circulating Fluidized Bed (CFB) combustion is a clean technology for burning, with advantages of adapting to a large variety of fuel, high combustion efficiency, lower NOx emissions, and stable operation. The residue collected from the ash-hoppers of the electrostatic precipitator of the CFB boiler is called CFB fly ash. This paper presents the hydration development on the application of CFB fly ash to activating blast furnace slag (BFS) as a supplementary binder material (SBM) for replacement of Portland cement in making concrete. Investigation of the hydration products of cement pastes prepared with combinations of BFS and CFB fly ash were conducted by means of X-ray diffraction, thermal gravimetric analysis, and scanning electronic microscope. Test results show that the main hydration products of the CFB fly ash-BFS blended pastes were found to be hydrated calcium silicate (C-S-H), ettringite, gypsum, and some portlandite. Considering that CFB fly ash produced from the combustion of high-sulfur coke has high SO3 contents, the volume stability of mortar made from CFB fly ash-activated BFS was subjected to tests in accordance with ASTM C1012 and ASTM C1038 for evaluating the internal and external sulfate attack, respectively. The results indicate that, due to the high sulfur (SO3) content of CFB fly ash, the expansion caused by internal sulfate attack (ISA) increased with increasing proportion of CFB fly ash in the mixture. In contrast, no significant expansion was observed in the external sulfate attack (ESA) test, regardless of the proportion of CFB fly ash in the mixture. In order for the CFB fly ash to serve as a supplementary binder material and to maintain adequate volume stability, the amount of CFB fly ash used for the activation of BFS is recommended to be no more than 20% of the SBM.