Production of combustible fuels and carbon nanotubes from plastic wastes using an in-situ catalytic microwave pyrolysis process.

This study performed in-situ microwave pyrolysis of plastic waste into hydrogen, liquid fuel and carbon nanotubes in the presence of Zeolite Socony Mobil ZSM-5 catalyst. In the presented microwave pyrolysis of plastics, activated carbon was used as a heat susceptor. The microwave power of 1 kW was employed to decompose high-density polyethylene (HDPE) and polypropylene (PP) wastes at moderate temperatures of 400-450 °C. The effect of plastic composition, catalyst loading and plastic type on liquid, gas and solid carbon products was quantified. This in-situ CMP reaction resulted in heavy hydrocarbons, hydrogen gas and carbon nanotubes as a solid residue. A relatively better hydrogen yield of 129.6 mmol/g as a green fuel was possible in this process. FTIR and gas chromatography analysis revealed that liquid product consisted of C13+ fraction hydrocarbons, such as alkanes, alkanes, and aromatics. TEM micrographs showed tubular-like structural morphology of the solid residue, which was identified as carbon nanotubes (CNTs) during X-ray diffraction analysis. The outer diameter of CNTs ranged from 30 to 93 nm from HDPE, 25-93 nm from PP and 30-54 nm for HDPE-PP mixure. The presented CMP process took just 2-4 min to completely pyrolyze the plastic feedstock into valuable products, leaving no polymeric residue.

Testing of Sr-Doped ZnO/CNT Photocatalysts for Hydrogen Evolution from Water Splitting under Atmospheric Dielectric Barrier Plasma Exposure.

Nonthermal plasma is a well-recognized environmentally advantageous method for producing green fuels. This work used different photocatalysts, including PZO, SxZO, and SxZCx for hydrogen production using an atmospheric argon coaxial dielectric barrier discharge (DBD)-based light source. The photocatalysts were produced using a sol-gel route. The DBD discharge column was filled with water, methanol, and the catalyst to run the reaction under argon plasma. The DBD reactor was operated with a 10 kV AC source to sustain plasma for water splitting. The light absorption study of the tested catalysts revealed a decrease in the band gap with an increase in the concentration of Sr and carbon nanotubes (CNTs) in the Sr/ZnO/CNTs series. The photocatalyst S25ZC2 demonstrated the lowest photoluminescence (PL) intensity, implying the most quenched recombination of charge carriers. The highest H2 evolution rate of 2760 µmol h-1 g-1 was possible with the S25ZC2 catalyst, and the lowest evolution rate of 56 µmol h-1 g-1 was observed with the PZO catalyst. The photocatalytic activity of S25ZC2 was initially high, which decreased slightly over time due to the deactivation of the photocatalyst. The photocatalytic activity decreased from 2760 to 1670 µmol h-1 g-1 at the end of the process.

Response Surface Methodology for the Synthesis and Characterization of Bio-Oil Extracted from Biomass Waste and Upgradation Using the Rice Husk Ash Catalyst.

Rice husk ash (RHA), a low-cost biomaterial, was utilized to form bio-oil from pyrolysis in a batch-stirred reactor, followed by its upgradation using the RHA catalyst. In the present study, the effect of temperature (ranging from 400 to 480 °C) on bio-oil production produced from RHA was studied to obtain the maximum bio-oil yield. Response surface methodology (RSM) was applied to investigate the effect of operational parameters (temperature, heating rate, and particle size) on the bio-oil yield. The results showed that a maximum bio-oil output of 20.33% was obtained at 480 °C temperature, 80 °C/min heating rate, and 200 µm particle size. Temperature and heating rate positively impact the bio-oil yield, while particle size has little effect. The overall R2 value of 0.9614 for the proposed model proved in good agreement with the experimental data. The physical properties of raw bio-oil were determined, and 1030 kg/m3 density, 12 MJ/kg calorific value, 1.40 cSt viscosity, 3 pH, and 72 mg KOH/g acid value were obtained, respectively. To enhance the characteristics of the bio-oil, upgradation was performed using the RHA catalyst through the esterification process. The upgraded bio-oil stemmed from a density of 0.98 g/cm3, an acid value of 58 mg of KOH/g, a calorific value of 16 MJ/kg, and a viscosity 10.5 cSt, respectively. The physical properties, GC-MS and FTIR, showed an improvement in the bio-oil characterization. The findings of this study indicate that RHA can be used as an alternative source for bio-oil production to create a more sustainable and cleaner environment.

Sensitivity Analysis of Thermal Degradation of Plastic Waste Using Statistically Assumed Exponential Factors and Activation Energies.

The rise in the production of plastic waste has prompted the exploration of various recovery options instead of landfilling, burning, and other unethical ways of decomposing. The experimentally generated rate constants for the thermal processing of plastic waste do not yield enough liquid fuels and gases for commercial-scale usage. It is imperative to predict kinetic rate constants statistically using an appropriate combination of activation energies (E a) and frequency factors (A o) for the optimized thermal valorization of plastic waste. This approach also assists in controlling the selectivity and quantity of the pyrolysis products. A statistical kinetic model was tested to find the best combination of rate constants from different combinations of E a and A o to pyrolyze the high-density polyethylene. Two series of E a and A o were first assumed using R software. These series were then used to predict kinetic rate constants and analyze their sensitivity independently using MATLAB. The rate constants were varied from their originally predicted values during the sensitivity analysis. It was found that the rate constant k(7) dominated the other predicted rate constants where high oil and gas yields were concerned. The gas yield increased from lower to higher extreme positions in the range of 60%-74% with the first series and from 65% to 81% with the second series. The maximum oil content was found around 74% and 65% with the first series and second series, respectively.

Kinetics and Adsorption Isotherms of Amine-Functionalized Magnesium Ferrite Produced Using Sol-Gel Method for Treatment of Heavy Metals in Wastewater.

This study is focused on the kinetics and adsorption isotherms of amine-functionalized magnesium ferrite (MgFe2O4) for treating the heavy metals in wastewater. A sol-gel route was adopted to produce MgFe2O4 nanoparticles. The surfaces of the MgFe2O4 nanoparticles were functionalized using primary amine (ethanolamine). The surface morphology, phase formation, and functionality of the MgFe2O4 nano-adsorbents were studied using the SEM, UV-visible, FTIR, and TGA techniques. The characterized nanoparticles were tested on their ability to adsorb the Pb2+, Cu2+, and Zn2+ ions from the wastewater. The kinetic parameters and adsorption isotherms for the adsorption of the metal ions by the amine-functionalized MgFe2O4 were obtained using the pseudo-first-order, pseudo-second-order, Langmuir, and Freundlich models. The pseudo-second order and Langmuir models best described the adsorption kinetics and isotherms, implying strong chemisorption via the formation of coordinative bonds between the amine groups and metal ions. The Langmuir equation revealed the highest adsorption capacity of 0.7 mmol/g for the amine-functionalized MgFe2O4 nano-adsorbents. The adsorption capacity of the nanoadsorbent also changed with the calcination temperature. The MgFe2O4 sample, calcined at 500 °C, removed the most of the Pb2+ (73%), Cu2+ (59%), and Zn2+ (62%) ions from the water.

Gold Nanorods for Doxorubicin Delivery: Numerical Analysis of Electric Field Enhancement, Optical Properties and Drug Loading/Releasing Efficiency.

The optical properties and electric field enhancement of gold nanorods for different cases were investigated in this study. The numerical analysis was carried out to understand the functionality and working of gold nanorods, while the experimental portion of the work was focused on the efficiency of gold nanorods for targeted drug delivery. COMSOL Multiphysics was used for numerical analysis. The theoretical results suggest the use of gold nanorods (AuNRs) for anticancer applications. The resonance peaks for gold nanorods of 10 nm diameter were observed at 560 nm. The resonance peaks shifted towards longer wavelengths with an increase in nanorod size. The resonance peaks showed a shift of 140 nm with a change in nanorod length from 25 to 45 nm. On the experimental side, 22 nm, 35 nm and 47 nm long gold nanorods were produced using the seed-mediated growth method. The surface morphology of the nanorods, as well as their optical characteristics, were characterized. Later, gold nanorods were applied to the targeted delivery of the doxorubicin drug. Gold nanorods showed better efficiency for doxorubicin drug loading time, release time, loading temperature, and release temperature. These results reveal that AuNRs@DA possess good ability to load and deliver the drug directly to the tumorous cells since these cells show high temperature and acidity.

Synthesis and Characterization of Manganese-Modified Black TiO2 Nanoparticles and Their Performance Evaluation for the Photodegradation of Phenolic Compounds from Wastewater.

The release of phenolic-contaminated treated palm oil mill effluent (TPOME) poses a severe threat to human and environmental health. In this work, manganese-modified black TiO2 (Mn-B-TiO2) was produced for the photodegradation of high concentrations of total phenolic compounds from TPOME. A modified glycerol-assisted technique was used to synthesize visible-light-sensitive black TiO2 nanoparticles (NPs), which were then calcined at 300 °C for 60 min for conversion to anatase crystalline phase. The black TiO2 was further modified with manganese by utilizing a wet impregnation technique. Visible light absorption, charge carrier separation, and electron-hole pair recombination suppression were all improved when the band structure of TiO2 was tuned by producing Ti3+ defect states. As a result of the enhanced optical and electrical characteristics of black TiO2 NPs, phenolic compounds were removed from TPOME at a rate of 48.17%, which is 2.6 times higher than P25 (18%). When Mn was added to black TiO2 NPs, the Ti ion in the TiO2 lattice was replaced by Mn, causing a large redshift of the optical absorption edges and enhanced photodegradation of phenolic compounds from TPOME. The photodegradation efficiency of phenolic compounds by Mn-B-TiO2 improved to 60.12% from 48.17% at 0.3 wt% Mn doping concentration. The removal efficiency of phenolic compounds from TPOME diminished when Mn doping exceeded the optimum threshold (0.3 wt%). According to the findings, Mn-modified black TiO2 NPs are the most effective, as they combine the advantages of both black TiO2 and Mn doping.