Chemical Recycling of CFRP in an Environmentally Friendly Approach.

A novel and environmentally friendly recycling approach for carbon-fiber-reinforced plastics (CFRP) was studied using not only nitric acid (HNO3) but also our chosen alkaline, sodium hydrogen carbonate (NaHCO3). The CFRP specimen was first immersed into 8 M HNO3 at 80 °C for 8 h, and then into 0.1 M NaHCO3 at 80 °C for 15 min to obtain resin-free recycled carbon fiber (rCFs). Using this new recycling method, it was shown that the recycling time was reduced to 8.3 h, whereas it originally took 24 h, as reported previously. It was shown that immersing the CFRP specimen into NaHCO3 caused a transesterification reaction with the remaining resin residue on the CF surface, which led to dissolving the resin into the NaHCO3 aqueous solution all at once. Additionally, NaHCO3 produced carbon dioxide gas while reacting with the resin residue; the CO2 gas physically helped removing the resin from the CF's surface. Moreover, evaluating the physical properties of the rCFs demonstrated an improvement in fiber strength and adhesiveness to resin. Therefore, this recycling method was shown to be effective in recovering high-quality rCFs in a relatively short recycling period.

Hydrothermal Synthesis and Characterization of Zeolite A from Corn (Zea Mays) Stover Ash.

This study deals with the impact of calcination, alkalinity, and curing time parameters on the hydrothermal synthesis of zeolite A. The zeolite A sample, produced from corncob-stalk-and-leaves (corn stover) ash was characterized using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), thermo-gravimetric analysis (TGA), and scanning electron microscopy (SEM). The results showed that calcination, alkalinity, and curing time have significant effects on the crystallization and the morphology of zeolite A. In addition, these parameters also impacted the cation exchange capacity. Furthermore, the synthesized zeolite A was obtained using a calcination temperature of 500 °C within two hours of airflow, which is much lower than the temperatures previously reported in the literature for an agricultural waste and other waste materials. A fusion ratio of corn stover ash:NaOH of 1.0:1.5 and a curing time of nine hours were achieved. This is a major result as this curing time is much lower than those featured in other studies, which can reach up to twenty-four hours. In this paper, cubic crystal with rounded edge of zeolite A, having a cation exchange capacity of 2.439 meq Na+/g of synthesized anhydrous zeolite A, was obtained, which can be a good candidate for ion-exchange separation.

Technological review on thermochemical conversion of COVID-19-related medical wastes.

COVID-19 pandemic has brought tremendous environmental burden due to huge amount of medical wastes (about 54,000 t/d as of November 22, 2020), including face mask, gloves, clothes, goggles, and sanitizer/disinfectant containers. A proper waste management is urgently required to mitigate the spread of the disease, minimize the environmental impacts, and take their potential advantages for further utilization. This work provides a prospective review on the possible thermochemical treatments for those COVID-19 related medical wastes (CMW), as well as their possible conversion to fuels. The characteristics of each waste are initially analyzed and described, especially their potential as energy source. It is clear that most of CMWs are dominated by plastic polymers. Thermochemical processes, including incineration, torrefaction, pyrolysis, and gasification, are reviewed in terms of applicability for CMW. In addition, the mechanical treatment of CMW into sanitized refuse-derived fuel (SRDF) is also discussed as the preliminary stage before thermochemical conversion. In terms of material flexibility, incineration is practically applicable for all types of CMW, although it has the highest potential to emit the largest amount of CO2 and other harmful gasses. Furthermore, gasification and pyrolysis are considered promising in terms of energy conversion efficiency and environmental impacts. On the other hand, carbonization faces several technical problems following thermal degradation due to insufficient operating temperature.

Optimizing and Characterizing Geopolymers from Ternary Blend of Philippine Coal Fly Ash, Coal Bottom Ash and Rice Hull Ash.

Geopolymers are inorganic polymers formed from the alkaline activation of amorphous alumino-silicate materials resulting in a three-dimensional polymeric network. As a class of materials, it is seen to have the potential of replacing ordinary Portland cement (OPC), which for more than a hundred years has been the binder of choice for structural and building applications. Geopolymers have emerged as a sustainable option vis-à-vis OPC for three reasons: (1) their technical properties are comparable if not better; (2) they can be produced from industrial wastes; and (3) within reasonable constraints, their production requires less energy and emits significantly less CO2. In the Philippines, the use of coal ash, as the alumina- and silica- rich geopolymer precursor, is being considered as one of the options for sustainable management of coal ash generation from coal-fired power plants. However, most geopolymer mixes (and the prevalent blended OPC) use only coal fly ash. The coal bottom ash, having very few applications, remains relegated to dumpsites. Rice hull ash, from biomass-fired plants, is another silica-rich geopolymer precursor material from another significantly produced waste in the country with only minimal utilization. In this study, geopolymer samples were formed from the mixture of coal ash, using both coal fly ash (CFA) and coal bottom ash (CBA), and rice hull ash (RHA). The raw materials used for the geopolymerization process were characterized using X-ray fluorescence spectroscopy (XRF) for elemental and X-ray diffraction (XRD) for mineralogical composition. The raw materials' thermal stability and loss on ignition (LOI) were determined using thermogravimetric analysis (TGA) and reactivity via dissolution tests and inductively-coupled plasma mass spectrometry (ICP) analysis. The mechanical, thermal and microstructural properties of the geopolymers formed were analyzed using compression tests, Fourier transform infra-red spectroscopy (FTIR), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). Using a Scheffé-based mixture design, targeting applications with low thermal conductivity, light weight and moderate strength and allowing for a maximum of five percent by mass of rice hull ash in consideration of the waste utilization of all three components, it has been determined that an 85-10-5 by weight ratio of CFA-CBA-RHA activated with 80-20 by mass ratio of 12 M NaOH and sodium silicate (55% H2O, modulus = 3) produced geopolymers with a compressive strength of 18.5 MPa, a volumetric weight of 1660 kg/m³ and a thermal conductivity of 0.457 W/m-°C at 28-day curing when pre-cured at 80 °C for 24 h. For this study, the estimates of embodied energy and CO2 were all below 1.7 MJ/kg and 0.12 kg CO2/kg, respectively.