Can pyrolysis handle biomedical wastes?: Assessing the potential of various biomedical waste treatment technologies in tackling pandemics.

Globally, COVID-19 has not only caused tremendous negative health, social and economic impacts, but it has also led to environmental issues such as a massive increase in biomedical waste. The biomedical waste (BMW) was generated from centralized (hospitals, clinics, and research facilities) and extended (quarantine camps, COVID-19 test camps, and quarantined homes) healthcare facilities. Many effects, such as the possibility of infection spread, unlawful dumping/disposal, and an increase in toxic emissions by common BMW treatment facilities, are conjectured because of the rise in waste generation. However, it is also an opportunity to critically analyze the current BMW treatment scenario and implement changes to make the system more economical and environmentally sustainable. In this review, the waste disposal guidelines of the BMW management infrastructure are critically analyzed for many functional parameters to bring out possible applications and limitations of individual interventions. In addition, an investigation was made to select appropriate technology based on the environmental setting.

Can e-waste recycling provide a solution to the scarcity of rare earth metals? An overview of e-waste recycling methods.

Recycling e-waste is seen as a sustainable alternative to compensate for the limited natural rare earth elements (REEs) resources and the difficulty of accessing these resources. Recycling facilitates the recovery of valuable products and minimizes emissions during their transportation. Numerous studies have been reported on e-waste recycling using various techniques, including thermo-, hydro- and biometallurgical approaches. However, each approach still has technical, economic, social, or environmental limitations. This review highlights the potential of recycling e-waste, including outlining the current unutilized potential of REE recycling from different e-waste components. An in-depth analysis of e-waste generation on a global scale and Australian scenario, along with various hazardous impacts on ecosystem and human health, is reported. In addition, a comprehensive summary of various metal recovery processes and their merits and demerits is also presented. Lifecycle analysis for recovering REEs from e-waste indicate a positive environmental impact when compared to REEs produced from virgin sources. In addition, recovering REEs form secondary sources eliminated ca. 1.5 times radioactive waste, as seen in production from primary sources scenario. The review outcome demonstrates the increasing potential of REE recycling to overcome critical challenges, including issues over supply security and localized dependency.

Waste to energy: Trending key challenges and current technologies in waste plastic management.

Due to the 'forever' degrading nature of plastic waste, plastic waste management is often complicated. The applications of plastic are ubiquitous and inevitable in many scenarios. Current global waste plastics production is ca. 3.5 MMT per year, and with the current trend, plastic waste production will reach 25,000 MMT by 2040. However, the rapid growth in plastic manufacture and the material's inherent nature resulted in the accumulation of a vast amount of plastic garbage. The current recycling rate is <10 %, while the large volumes of discarded plastic waste cause environmental and ecological problems. Recycling rates for plastic vary widely by region and type of plastic. In some developed countries, the recycling rate for plastics is around 20-30 %, while in many developing nations, it is much lower. These statistics highlight the magnitude of the plastic waste problem and the urgent need for comprehensive strategies to manage plastic waste more effectively and reduce its impact on the environment. This review critically analyses past studies on the essential and efficient techniques for turning plastic trash into treasure. Additionally, an attempt has been made to provide a comprehensive understanding of the plastic upcycling process, the 3Rs policy, and the life-cycle assessment (LCA) of plastic conversion. The review advocates pyrolysis as one of the most promising methods of turning plastic trash into valuable chemicals. In addition, plastic waste management can be severely impacted due to uncontrollable events, such as Covid 19 pandemic. Recycling and chemical upcycling can certainly bring value to the end-of-life plastic. However, the LCA analysis indicated there is still a huge scope for innovation in chemical upcycling area compared to mechanical recycling. The formulation of policies and heightened public participation could play a pivotal role in reducing the environmental repercussions of plastic waste and facilitating a shift towards a more sustainable future.

Bio-oil and biochar from the pyrolytic conversion of biomass: A current and future perspective on the trade-off between economic, environmental, and technical indicators.

Over the years, the transformation of biomass into a plethora of renewable value-added products has been identified as a promising strategy to fulfil high energy demands, lower greenhouse gas emissions, and exploit under-utilized resources. Techno-economic analysis (TEA) and life-cycle assessment (LCA) are essential to scale up this process while lowering the conversion cost. In this study, trade-offs are made between economic, environmental, and technical indicators produced from these methodologies to better evaluate the commercialization potential of biomass pyrolysis. This research emphasizes the necessity of combining LCA and TEA variables to assess the performance of the early-stage technology and associated constraints. The important findings based on the LCA analysis imply that most of the studies reported in literature focussed on the global warming potentials (GWP) under environmental category by considering greenhouse gases (GHGs) as evaluation parameter, neglecting many other important environmental indices. In addition, the upstream and downstream processes play an important role in understanding the life cycle impacts of a biomass based biorefinery. Under upstream conditions, the use of a specific type of feedstock may influence the LCA conclusions and technical priority. Under downstream conditions, the product utilization as fuels in different energy backgrounds is crucial to the overall impact potentials of the pyrolysis systems. In view of the TEA analysis, investigations towards maximizing the yield of valuable co-products would play an important role in the commercialization of pyrolysis process. However, comprehensive research to compare the conventional, advanced, and emerging approaches of biomass pyrolysis from the economic perspective is currently not available in the literature.

Biomass pyrolysis: A review on recent advancements and green hydrogen production.

Biomass pyrolysis has recently gained increasing attention as a thermochemical conversion process for obtaining value-added products, thanks to the development of cutting-edge, innovative and cost-effective pyrolysis processes. Over time, new and novel pyrolysis techniques have emerged, and these processes can be tuned to maximize the production of high-quality hydrogen. This review examines recent advancements in biomass pyrolysis by classifying them into conventional, advanced and emerging approaches. A comprehensive overview on the recent advancements in biomass pyrolysis, highlighting the current status for industrial applications is presented. Further, the impact of each technique under different approaches on conversion of biomass for hydrogen production is evaluated. Techniques, such as inline catalytic pyrolysis, microwave pyrolysis, etc., can be employed for the sustainable production of hydrogen. Finally, the techno-economic analysis is presented to understand the viability of pyrolysis at large scale. The outlook highlights discernments into future directions, aimed to overcome the current shortcomings.

Probing the effect of Cu-SrO loading on catalyst supports (ZSM-5, Y-zeolite, activated carbon, Al2O3, and ZrO2) for aromatics production during catalytic co-pyrolysis of biomass and waste cooking oil.

In this work, Cu-SrO bimetallic catalyst was synthesised and examined for catalytic co-pyrolysis of ironbark (IB) and waste cooking oil (WCO) using Py-GC/MS. The effect of catalyst supports (ZSM-5, Y-zeolite, activated carbon, Al2O3, and ZrO2) on aromatic hydrocarbons yield was studied. The effect of catalyst support on the selectivity of gasoline (C8-C14), diesel (C15-C17), and heavy oil (>C20) components of bio-oil were studied. Non-catalytic co-pyrolysis of IB and WCO produced a heavy oil component of 58.7% (>C20). SrO initiated a ketonization reaction that converted carboxylic acids into new C-C bonds. The addition of Cu effectively promoted secondary cracking and aromatization reactions enhancing the hydrocarbon yield. Cu-SrO/ZSM-5 and Cu-SrO/Y-zeolite produced low acid content of 4.43% and 12.5%, respectively. Overall, the bimetallic catalyst Cu-SrO/ZSM-5 significantly increased the amount of C8-C14 compounds to 87.28% and reduced compounds over C20 to 1.19%.

Bioconversion of food and lignocellulosic wastes employing sugar platform: A review of enzymatic hydrolysis and kinetics.

Bioenergy and biochemicals can be sustainably produced through fermentation and anaerobic digestion (AD). However, this bioconversion processes could be more economical if the hydrolysis rates of substrates in bioreactors can be accelerated. In this review, the feasibilities of including enzymatic hydrolysis (EH) in various bioconversion systems were studied to facilitate the biological synergy. The reaction kinetics of EH in bioconversion systems comparing pretreated lignocellulosic biomass (LCB) and food waste (FW) substrates were reviewed. Possible strategies to improve the hydrolysis efficiency were explored, including co-cultivation during enzyme production and replacement of pure enzyme with on-site produced fungal mash during EH. Key insights into improvement of current AD and fermentation technologies were summarized and further formed into suggestions of future directions in techno-economic feasibility of biorefinery using mixture of the first-generation food crop feedstock with FW; and/or co-digestion of FW with LCB.

Thermal plasma gasification of organic waste stream coupled with CO2-sorption enhanced reforming employing different sorbents for enhanced hydrogen production.

In the past few years, rising concerns vis-à-vis global climate change and clean energy demand have brought worldwide attention to developing the 'biomass/organic waste-to-energy' concept as a zero-emission, environment-friendly and sustainable pathway to simultaneously quench the global energy thirst and process diverse biomass/organic waste streams. Bioenergy with carbon capture and storage (BECCS) can be an influential technological route to curb climate change to a significant extent by preventing CO2 discharge. One of the pathways to realize BECCS is via in situ CO2-sorption coupled with a thermal plasma gasification process. In this study, an equilibrium model is developed using RDF as a model compound for plasma assisted CO2-sorption enhanced gasification to evaluate the viability of the proposed process in producing H2 rich syngas. Three different classes of sorbents are investigated namely, a high temperature sorbent (CaO), an intermediate temperature sorbent (Li4SiO4) and a low temperature sorbent (MgO). The distribution of gas species, H2 yield, dry gas yield and LHV are deduced with the varying gasification temperature, reforming temperature, steam-to-feedstock ratio and sorbent-to-feedstock for all three sorbents. Moreover, optimal values of different process variables are predicted. Maximum H2 is noted to be produced at 550 °C for CaO (79 vol%), 500 °C for MgO (29 vol%) and 700 °C (55 vol%) for Li4SiO4 whereas the optimal SOR/F ratios are found to be 1.5 for CaO, 1.0 for MgO and 2.5 for Li4SiO4. The results obtained in the study are promising to employ plasma assisted CO2-sorption enhanced gasification as an efficacious pathway to produce clean energy and thus achieve carbon neutrality.

Pyrolysis of anaerobic digested residues in the presence of catalyst-sorbent bifunctional material: Pyrolysis characteristics, kinetics and evolved gas analysis.

We investigated the potential application of anaerobically digested residues for generating bioenergy in the presence of alkali bifunctional material, sodium zirconate (Na2ZrO3, NZ) using a thermogravimetric analyzer connected to a mass spectrometer. Isoconversional kinetic models, compensation effect and master-plots method were used on data obtained under multiple heating rates (10, 15 and 20 °C min-1) to calculate the activation energy (Eα) and pre-exponential value (A) and reaction mechanism. The average Eα for blend samples C-DSW (NZ mixed with digested municipal solid waste (DSW)), and C-DSM (NZ mixed with digested swine manure (DSM)) were 172.24 and 171.63 kJ mol-1, which were much lower when compared to plain samples, DSW (202.51 kJ mol-1) and DSM (215.22 kJ mol-1). The total gas yields increased by 19.5 and 17.1% for NZ blended samples C-DSW and C-DSM, respectively. In addition, the hydrogen yields also increased by 79 and 44% for C-DSW and C-DSM, respectively.

Progress in the development and use of refrigerants and unintended environmental consequences.

The world has entered into the "fourth-generation" of refrigerants, and it is an undeniable fact that we will continue to encounter several issues in identifying a suitable refrigerant that suits the purpose and poses no harm to the environment. The ever-changing regulations on the use of refrigerants have often posed great challenges to the refrigeration industry and there is a pressing need to develop new refrigerants and develop better equipment to use them. Theoretically, an ideal refrigerant should possess characteristics such as low-global warming potential (GWP), non-toxic, non-flammable, and zero-ozone depletion potential (ODP). In addition, the refrigerants are also expected to have excellent thermodynamic and thermophysical properties. Many new synthetic refrigerants have been reported as alternative refrigerants and have very low atmospheric life as well as low GWP and zero-ODP. However, it is irrefutable that most of the studies that reported the so-called new refrigerants are actually not new. From the invention of R-12 (Dichlorodifluoromethane) in 1930s to the invention of R-1234yf in 2000s, these substances are available for decades even before being recognized as refrigerants. This review attempts to provide chronicles on different aspects of refrigerants such as their progress since their invention in the early 1800s, classification and properties. In addition, concepts such as issues associated with the long-term use of refrigerants, barriers for the inclusion of low-GWP refrigerants, various protocols and accords that have occurred since the inception of refrigerants are also critically discussed.

Thermo-catalytic co-pyrolysis of ironbark sawdust and plastic waste over strontium loaded hierarchical Y-zeolite.

The objective of this research is to synthesize hierarchical strontium loaded Y-zeolite and study its application for ironbark (IB) and plastic waste (PW) co-pyrolysis. Commercial parent Y-zeolite (Si/Al = 2.48) was modified via sequential dealumination-desilication using citric acid and NaOH. Further, strontium (8 wt %) was loaded into the modified Y-zeolite via wet and dry impregnation methods. The prepared catalyst was characterized by N2 adsorption-desorption isothermal, field emission scanning electron microscopy (FESEM) combined with energy dispersive x-ray spectroscopy (EDS), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and Thermogravimetric analyzer (TGA). After dealumination (treatment using 0.1 M of citric acid), the external surface area and Si/Al ratio increased from 53.5 to 147.4 m2/g and 2.48 to 5.36, respectively. However, the sequential desilication treatment reduced Si/Al ratio from 5.36 to 2.57. In addition, Y-zeolite enhanced the total aromatic percentage and reduced the acidic group in co-pyrolysis oil.

Thermogravimetric and kinetic analysis to discern synergy during the co-pyrolysis of microalgae and swine manure digestate.

BACKGROUND: Co-pyrolysis of wastes with other feedstock can synergistically improve the rate of biomass decomposition and also help to resolve the issues related to limited availability feedstock. In this regards, synergistic interaction between feedstock during co-pyrolysis is an important aspect of research. As the constituents of aquatic and lignocellulosic biomass are different, and the decomposition pattern of aquatic biomass is dissimilar when compared to lignocellulosic biomass, it is important to understand whether these two biomasses interact during co-pyrolysis. RESULTS: Synergism in the co-pyrolysis of microalgae (MA), swine manure digestate (SWD), and their blends (MA/SWD) (w/w %), 2.5/7.5 (MD-1), 5/5 (MD-2), and 7.5/2.5 (MD-3), was evaluated based on decomposition behavior, gas yields, extent of thermal degradation, and kinetics. Extractives and volatiles in biomass enhanced the reaction kinetics and products yields, as indicated by the reduction in apparent activation energy of the blends, accompanied by an increase in H2, total gas yield, and extent in degradation. Thermogravimetric data, via isoconversional methods, were interpreted to achieve the apparent activation energies for the thermal degradation of the MA, SWD, and their blends. The best fit reaction models were identified using compensation effect and generalized master plots methods. Semi-quantitative method was used to quantify the evolved gas species. H2, CO, and CO2 were noted to be the dominant gases, implying that tar cracking and reforming reactions were predominant. CONCLUSIONS: Overall, synergy was noticed with respect to the pyrolysis of SWD biomass to gas products in the presence of MA biomass, whereas synergy was witnessed up to 50 w/w % MA in view of kinetic parameters as evaluation criteria.

Sustainability Analysis of Microalgae Production Systems: A Review on Resource with Unexploited High-Value Reserves.

Sustainability, at present, is a prominent component in the development of production systems that aim to provide the future energy and material resources. Microalgae are a promising feedstock; however, the sustainability of algae-based production systems is still under debate. Commercial market volumes of algae-derived products are still narrow. The extraction and conversion of primary metabolites to biofuels requires cultivation at large scales; cost-effective methods are therefore highly desirable. This work presents a complete and up to date review on sustainability analysis of various microalgae production scenarios, including techno-economic, environmental, and social impacts, both in large-scale plants for bioenergy production and in medium-scale cultivars intended for the production of high added-value chemicals. The results show that further efforts in algal-based research should be directed to improving the productivity, the development of multi product scenarios, a better valorization of coproducts, the integration with current industrial facilities to provide sustainable nutrient resources from waste streams, and the integration of renewable technologies such as wind energy in algae cultivars.

Impact of Flue Gas Compounds on Microalgae and Mechanisms for Carbon Assimilation and Utilization.

To shift the world to a more sustainable future, it is necessary to phase out the use of fossil fuels and focus on the development of low-carbon alternatives. However, this transition has been slow, so there is still a large dependence on fossil-derived power, and therefore, carbon dioxide is released continuously. Owing to the potential for assimilating and utilizing carbon dioxide to generate carbon-neutral products, such as biodiesel, the application of microalgae technology to capture CO2 from flue gases has gained significant attention over the past decade. Microalgae offer a more sustainable source of biomass, which can be converted into energy, over conventional fuel crops because they grow more quickly and do not adversely affect the food supply. This review focuses on the technical feasibility of combined carbon fixation and microalgae cultivation for carbon reuse. A range of different carbon metabolisms and the impact of flue gas compounds on microalgae are appraised. Fixation of flue gas carbon dioxide is dependent on the selected microalgae strain and on flue gas compounds/concentrations. Additionally, current pilot-scale demonstrations of microalgae technology for carbon dioxide capture are assessed and its future prospects are discussed. Practical implementation of this technology at an industrial scale still requires significant research, which necessitates multidisciplinary research and development to demonstrate its viability for carbon dioxide capture from flue gases at the commercial level.

Alkali Metal CO2 Sorbents and the Resulting Metal Carbonates: Potential for Process Intensification of Sorption-Enhanced Steam Reforming.

Sorption-enhanced steam reforming (SESR) is an energy and cost efficient approach to produce hydrogen with high purity. SESR makes it economically feasible to use a wide range of feedstocks for hydrogen production such as methane, ethanol, and biomass. Selection of catalysts and sorbents plays a vital role in SESR. This article reviews the recent research aimed at process intensification by the integration of catalysis and chemisorption functions into a single material. Alkali metal ceramic powders, including Li2ZrO3, Li4SiO4 and Na2ZrO3 display characteristics suitable for capturing CO2 at low concentrations (<15% CO2) and high temperatures (>500 °C), and thus are applicable to precombustion technologies such as SESR, as well as postcombustion capture of CO2 from flue gases. This paper reviews the progress made in improving the operational performance of alkali metal ceramics under conditions that simulate power plant and SESR operation, by adopting new methods of sorbent synthesis and doping with additional elements. The paper also discusses the role of carbonates formed after in situ CO2 chemisorption during a steam reforming process in respect of catalysts for tar cracking.