Carbon Recovery Research Articles

The influence of ball collision charging on carbon recovery of fly ash triboelectrostatic separation

ABSTRACT The recovery of unburned carbon particles from fly ash by triboelectrostatic separation can realize energy conservation and solid waste recycling. Collision charging by metal ball has been proposed to enhance the particle charging and improve the unburned carbon recovery efficiency. It can increase the particle contact area, shorten the contact time, and improve the charge–mass ratio of particles. The charging model of ball collision was established. The collision charging process between particles and ball was simulated by CFD-DEM coupling method. The influence of ball material and gas velocity on the charge–mass ratio was studied, and that of gas velocity and voltage on separation was evaluated by experiments. The results showed that the collision charge between particles and metal ball was greater than that between particles. With the gas velocity of 30 m/s, Cu ball collisions obtained a relative maximum charge–mass ratio of 0.393nC/g and 0.275nC/g for carbon and ash particles, respectively. The reasonable experimental conditions were gas velocity of 20 m/s and voltage of 15kV. The loss on ignition of 14.3% and carbon recovery of 90.36% were obtained. Compared with the no-ball system, the ball collision improved the carbon recovery rate by 55.20%.

Potential of enriched phototrophic purple bacteria for H2 bioconversion into single cell protein

Single cell protein (SCP) has emerged as an alternative protein source, potentially based on the recovery of carbon and nutrients from waste-derived resources as part of the circular economy. From those resources, gaseous substrates have the advantage of an easy sterilization, allowing the production of pathogen-free SCP. Sterile gaseous substrates allow producing pathogen-free SCP. This study evaluated the use of an enriched phototrophic purple bacteria (PPB) consortium for SCP production using H2 and CO2 as electron and C sources. The influence of pH (6.0–8.5), temperature (15–50 °C) and light intensity (0–50 W·m−2) on the growth kinetics and biomass yields was investigated using batch tests. Optimal conditions were found at pH 7, 25 °C and light intensities over 30 W·m−2. High biomass and protein yields were achieved (~ 1 g CODbiomass·g CODH2consumed−1 and 3.9–4.4 g protein·g H2−1) regardless of the environmental conditions, being amongst the highest values reported from gaseous streams. These high yields were obtained thanks to the use of light as a sole energy source by the PPB consortium, allowing a total utilization of H2 for growth. Hydrogen uptake rates varied considerably, with values up to 61 ± 5 mg COD·d−1 for the overall H2 consumption rates and 2.00 ± 0.14 g COD·g COD−1·d−1 for the maximum specific uptake rates under optimal growth conditions. The latter value was estimated using a mechanistic model able to represent PPB growth on H2. The biomass exhibited high protein contents (>50 % w/w) and adequate amino acid profiles, showing its suitability as SCP for feed. PPB were the dominant bacteria during the experiments (relative abundance over 80 % in most tests), with a stable population dominated by Rhodobacter sp. and Rhodopseudomonas sp. This study demonstrates the potential of enriched PPB cultures for H2 bioconversion into SCP.

Targeted synergy of cation exchange-driven extracellular carbon release and lysozyme-catalyzed intracellular carbon release for maximizing carbon source recovery from waste activated sludge

Short-chain fatty acids as superior carbon recovery from waste activated sludge have received rising attentions. This study quantified contributions of cation exchange (CE) and lysozyme on the targeted carbon source migration. The innovative targeted pattern for extracellular and intracellular carbon source release was proposed. The 1-day synergetic treatment at optimal CE resin dosage of 1.75 g/g SS and lysozyme dosage of 10 % drove considerable carbon source release and particulate carbon source solubilization, which occupied 35.31 % of total sludge solid carbon sources. The CE dominantly contributed to extracellular polymeric substances disruption and extracellular carbon source release, with the percentage of 39.47–48.13 %. In this case, The Lyso was the strongest contributor to microbial cell lysis and intracellular carbon source release, with the proportions of 49.53–75.76 %. Subsequently, approximately 56.54–58.49 % of the originally dissolved carbon sources (mostly proteins and carbohydrates) were bio-degraded into micromolecular carbon sources with high bioavailability in a short-term anaerobic fermentation (2 days). Correspondingly, satisfactory carbon recovery rate of 23.06 % was obtained, which was 7.30 times higher than the control. The synergy of CE and lysozyme greatly improved kinetic speeds and performances of endogenous carbon source migration and recovery. Such synergetic treatment of CE and lysozyme not only provided novel insights into carbon fate in anaerobic fermentation, but also achieved remarkable carbon source release and recovery benefits with economic incomes of 190.8–283.4 CNY/ton sludge.

Determination of carbon-14 in marine biota using oxidation combustion and gel suspension liquid scintillation counting

In this study, we report a new analytical method for determination of 14C in marine biota utilizing oxidation combustion separation combined with CaCO3 suspension of precipitates for liquid scintillation counting (LSC). The main factors affecting the oxidation combustion efficiency of tube combustion furnace and the counting efficiency of the LSC were systematically investigated and optimized. Under the optimal combustion conditions, the combustion recovery of carbon ranged from 85.6 % to 92.4 % for five marine samples. And the method achieved a detection limit of 0.13 Bq/g for 14C and repeatability of 3.9–9.1 %. The analytical turnover time was 6 h, and up to six samples could be processed simultaneously. Assessment of uncertainty components showed that the uncertainty in counting was the largest contributor, followed by combustion recovery and counting efficiency. The developed method enables reliable measurement of 14C in marine biota, providing valuable analytical tool for risk assessment purposes.

Using Multisource High-Resolution Remote Sensing Data (2 m) with a Habitat–Tide–Semantic Segmentation Approach for Mangrove Mapping

Mangrove wetlands are hotspots of global biodiversity and blue carbon reserves in coastal wetlands, with unique ecological functions and significant socioeconomic value. Annual fine-scale monitoring of mangroves is crucial for evaluating national conservation programs and implementing sustainable mangrove management strategies. However, annual fine-scale mapping of mangroves over large areas using remote sensing remains a challenge due to spectral similarities with coastal vegetation, tidal periodic fluctuations, and the need for consistent and dependable samples across different years. In previous research, there has been a lack of strategies that simultaneously consider spatial, temporal, and methodological aspects of mangrove extraction. Therefore, based on an approach that considers mangrove habitat, tides, and a semantic segmentation approach, we propose a method for fine-scale mangrove mapping suitable for long time-series data. This is an optimized hybrid model that integrates spatial, temporal, and methodological considerations. The model uses five sensors (GF-1, GF-2, GF-6, ZY-301, ZY-302) to combine deep learning U-Net models with mangrove habitat information and algorithms during low-tide periods. This method produces a mangrove map with a spatial resolution of 2 m. We applied this algorithm to three typical mangrove regions in the Beibu Gulf of Guangxi Province. The results showed the following: (1) The model scored above 0.9 in terms of its F1-score in all three study areas at the time of training, with an average accuracy of 92.54% for mangrove extraction. (2) The average overall accuracy (OA) for the extraction of mangrove distribution in three typical areas in the Beibu Gulf was 93.29%. When comparing the validation of different regions and years, the overall OA accuracy exceeded 89.84% and the Kappa coefficient exceeded 0.74. (3) The model results are reliable for extracting sparse and slow-growing young mangroves and narrow mangrove belts along roadsides. In some areas where tidal flooding occurs, the existing dataset underestimates mangrove extraction to a certain extent. The fine-scale mangrove extraction method provides a foundation for the implementation of fine-scale management of mangrove ecosystems, support for species diversity conservation, blue carbon recovery, and sustainable development goals related to coastal development.

New insight into Fe(VI)-driven carbon migration and recovery in short-term anaerobic fermentation of waste activated sludge

The short-chain fatty acids produced from waste activated sludge were deemed as the preferred carbon sources, however the specific carbon migration and recovery patterns have been rarely reported. This study demonstrated that Fe(VI) was capable of driving interphase carbon release and biotransformation towards carbon recovery in short-term anaerobic fermentation (48 h). Interestingly, the Fe(VI)-derived alkaline condition played the foremost and continuous driving force in interphase carbon migration with the proportions of 50.53–70.52 %, while the advanced oxidization provided the second most contributions of 25.46–45.82 % in short-acting role. Correspondingly, numerous extracellular and intracellular carbon sources of 136.66 mg C/g VSS were released in 4-h Fe(VI) treatment by structural protein molecule loosening, which were mainly composed of proteins (tryptophan and tyrosine), polysaccharides and humic acids. Meanwhile, 48.73 % of the dissolved carbon sources were bio-transformed for improving sludge acidification, contributing to the overall carbon recovery of 63.68 mg C/g VSS. The effective carbon source extraction was implemented by solid–liquid separation. The high C/N in fermentative liquid was achievable, suggesting considerable bio-availability of the recovered carbon sources. This indeed created economic benefits and carbon-emission reduction depending on alternative carbon source utilization and residual sludge solid reduction.

Organic binding iron formation and its mitigation in cation exchange resin assisted anaerobic digestion of chemically enhanced primary sedimentation sludge

Fe based chemically enhanced primary sedimentation (CEPS) is an effective method of capturing the colloidal particles and inorganic phosphorous (P) from wastewater but also produces Fe-CEPS sludge. Anaerobic digestion is recommended to treat the sludge for energy and phosphorus recovery. However, the aggregated sludge flocs caused by the coagulation limited sludge hydrolysis and P release during anaerobic digestion process. In this study, cation exchange resin (CER) was employed during anaerobic digestion of Fe-CEPS sludge with aims of prompting P release and carbon recovery. CER addition effectively dispersed the sludge flocs. However, the greater dispersion of sludge flocs could not translate to higher sludge hydrolysis. The maximum hydrolysis and acidification achieved at lower CER dosage of 0.5 g CER/g TS. It was observed that the extents of sludge hydrolysis and acidification had a strongly negative correlation with the organic binding iron (OBI) concentration. The presence of CER during anaerobic digestion favored Fe(III) reduction to Fe(II), and then further induced iron phase transformation, leading to the OBI formation from the released organic matters. Meanwhile, higher CER dosage resulted in higher P release efficiency and the maximum efficiency at 4 g CER/g TS was four times than that of the control. The reduction of BD-P, NaOH-P and HCl-P in solid phase contributed most P release into the supernatant. A new two-stage treatment process was further developed to immigrate the OBI formation and improve the carbon recovery efficiency. Through this process, approximately 45% of P was released, and 63% of carbon was recovered as methane from Fe-CEPS sludge via CER pretreatment.

Membrane crystallization for recovery of lithium carbonate crystals: Study on process parameters and salts effect for Li2CO3-NaCl-KCl-LiCl solutions

In this work, membrane crystallization (MCr) process was employed for recovery of lithium carbonate (Li2CO3) crystals from synthetic brine solutions. First, the effect of the main operating conditions in MCr, including feed temperature (40, 50, and 60 °C) and flowrate (0.81, 1, and 1.3 L/min) was investigated on the crystallization of Li2CO3 in a binary solution. Next, the effect of main inorganic salts in the brine solutions (i.e., NaCl, KCl, and LiCl) and the mixture of them on the MCr performance and crystallization of Li2CO3 were investigated. In-line microscope, light microscope, scanning electron microscope, and X-ray diffraction test were used to observe the crystallization and characterize the obtained crystals. The obtained results revealed that feed temperature is the main parameter to dominate the nucleation and crystal formation and growth. Thus, the higher the feed temperature, the faster the crystal formation and the larger the crystals. The average crystal size increased from 9.59 to 30.51 μm, when the feed temperature increased from 40 to 60 °C, respectively. However, smaller crystals were observed with adding NaCl and KCl to the solution. Moreover, none of the operating parameters nor the salts additives did affect the crystals shape and the obtained Li2CO3 crystals possess needle-like shape.

Biorefinery integration of a green protein platform for maximum resource utilization

Biorefineries are often proposed to reduce environmental impact, enhance energy independence, and minimize waste generation while generating multiple valuable products. In this work, an integrated biorefinery approach is proposed to improve the overall process performance of a system combining a green biorefinery (GB), hydrothermal liquefaction (HTL), and anaerobic digestion (AD) to produce a leaf protein concentrate, bio-crude, and biogas. Festulolium and ryegrass, two varieties of forage grasses, were employed as feedstock. Two different maceration technologies were evaluated for protein recovery, more severe maceration led to a 75 % increase in protein content in the leaf protein concentrate (LPC) when compared to a standard maceration. The fiber residues produced by the grass processing were converted to biocrude using HTL. This step was not affected by the maceration step and the use of brown juice as HTL media proved to be beneficial. The bio-crude yield of the grass fiber residues was similar for both biomasses and maceration steps, ranging from 25.7 to 32.1 %. Finally, the HTL process water and the brown juice were subjected to anaerobic digestion to produce biogas. The brown juice from ryegrass resulted in higher methane production compared to HTL water but adding brown juice to HTL water did not reduce the lag times observed for pure HTL water. The integration of GB, HTL, and AD is shown to be effective in increasing the overall carbon and nitrogen recovery of the starting biomass.

Recovery of carbon from spent carbon cathode by alkaline and acid leaching and thermal treatment and exploration of its application in lithium-ion batteries.

The spent carbon cathode (SCC) is a hazardous solid waste from aluminum production. It has an abundant carbon source and a unique graphitic carbon layer structure, making it a valuable waste for recycling. This paper uses alkaline and acid leaching methods to report a straightforward way of extracting recovered carbon (RC) from SCC as anode material for lithium-ion batteries (LIBs). The results show that alkaline and acid leaching conditions at 70 °C with 1 M NaOH and HCl solution individually in 6 h and a liquid-solid ratio of 20:1 can result in RC with up to 94.63% carbon content than 49.38% in SCC, exhibiting a typical graphite structure. SCC and RC materials are obtained after calcination at 400 °C in an inert atmosphere and used as anode materials (SCC-400 and RC-400). In this paper, The initial charging specific capacities are 490.0 mA h g-1, 195.4 mA h g-1, and 423.2 mA h g-1and initial coulombic efficiencies (ICE) are 67.8%, 78.9%, and 72.0% of RC-400, SCC, and SCC-400. RC-400 also shows excellent capacity retention and impedance values. This exciting finding provides a viable, non-hazardous, and resourceful method for treating and disposing of SCC from aluminum electrolysis.

Recovery of residual carbon from coal gasification fine slag by a combined gravity separation-flotation process

Recovering inner residual carbon is important for fully utilizing coal gasification fine slag (CGFS) resources. In this study, we adopted a combined gravity-separation and flotation process to efficiently recover residual carbon by considering the characteristics of the CGFS and optimizing the operating factors of the process. CGFS is principally a mixture of residual carbon and ash, with low-density particles containing more of the former. Accordingly, residual carbon is preliminarily enriched by gravity separation, in which gas velocity (vg) and water velocity (vw) significantly impact separation efficiency, followed by feed volume (m). The residual carbon in the initial concentrate was preliminarily enriched (i.e., loss on ignition (LOI): 55.90%; combustible recovery (Ro): 72.36%) under appropriate operating conditions (i.e., vw = 0.04 m/s, vg = 3 m/s, m = 150 g). Moreover, the quality of the flotation concentrate was most influenced by collector dosage (mc), followed by aeration rate (η), frother dosage (mf), stirring speed (w), and grinding time (t) during flotation of the primary concentrate. The flotation concentrate exhibited LOI and Ro values of 90.95% and 50.34%, respectively, under the optimal flotation conditions (i.e., mc = 20 kg/t, mf = 15 kg/t, w = 2600 rad/min, η = 200 L/h, t = 360 s); it has a high residual carbon content and is an ideal raw material for preparing fuels or carbon materials.

White-rot fungus Phlebia floridensis ITM 12: Laccase production, oxidoreductase profile, and hydrogen-peroxide independent activity.

Phlebia genus is a relevant group of fungi with a crucial role in numerous ecosystems. In tropical and subtropical areas this genus allows the efficient degradation of lignin and carbon recovery; however, the majority of these fungal species remain undiscovered. The main purpose of this work was to determine the enzymatic activity of extracellular proteins of a novel Phlebia floridensis strain isolated in Yucatan Peninsula, Mexico. The results that are reported here demonstrate that the soluble protein extract of P. floridensis can degrade a broad spectrum of recalcitrant compounds. This induced protein extract is able to modify not only phenolic and nonphenolic compounds, but also anthroquinone dyes, even without the addition of exogenous hydrogen peroxide. Using liquid chromatography-mass spectrometry (LC-MS), we were able to identify a novel chloroperoxidase in enzymatic extract. As far as we know, this is the first report about the presence of this type of enzyme in the Phlebia genus.

Separation and recovery of zinc from blast furnace dust via coordination leaching of Cl− and hydrolysis of NH4+

Blast furnace dust (BFD) is a by-product of iron-making process, a typical hazardous waste containing abundant recyclable components. In this study, a NH4Cl cooperative coordination leaching method was proposed for the selective separation and recovery of zinc from BFD. The thermodynamic analysis results revealed that ZnO and ZnSO4 from BFD can be converted to zinc-chlorine coordination compounds (ZnCli2−i, i = 1,2,3,4) in the cooperative actions of NH4+ and Cl− ions. The experimental results showed that the leaching efficiency of zinc reached 85.64% while iron and carbon was enriched from 46.76% to 57.96% under the optimal experimental conditions. The leaching residue with a total content 2.53% of Zn, Cl, K and Na can be returned to sintering for the recovery of iron and carbon. Moreover, the XRD, SEM-EDS and chemical phase analysis results of BFD and residue demonstrated that a small amount ZnO, ZnS and ZnFe2O4 were not leached and remained in the leaching residue. Additionally, a novel method of low-temperature crystallization was adopted to recover zinc from filtrate. The crystallization efficiency of zinc reached 80.96% and the obtained crystal was confirmed to be special Zn(NH3)2Cl2. Thus, this work not only achieved the separation and recovery of zinc from BFD, but also solved the disposal problem of leaching residue and crystallization solution, providing a guidance for the resource utilization of hazardous BFD.

An investigation of nanobubble enhanced flotation for fly ash decarbonization

Froth flotation is often employed to remove unburned carbon in the fly ash produced as a coal combustion by-product before it can be utilized in the cement or similar industries. However, with the deterioration of coal quality and environmental regulations getting stricter, fly ash has become increasingly more difficult to be purified by the flotation process and the limitations of traditional flotation techniques have become more obvious for ultrafine particles such as fly ash. Nanobubbles have proven effective in enhancing the flotation performance with fine and ultrafine particles. In this study the effect of nanobubbles on fly ash flotation decarbonization and underlying mechanisms have been investigated with a flotation column under various experimental conditions using a Chinese fly ash sample. The results have demonstrated that nanobubbles are able to significantly improve the efficiency of decarbonization of fly ash flotation. Typically the use of nanobubbles increased the recovery of unburnt carbon by 3–15 % and reduced the fly ash LOI by 0.2 %–3.5 %. It has also been shown that nanobubble flotation reduced the required dosages of frother and collector by approximately one half. New mechanisms of nanobubbles improving fly ash decarbonization flotation performance were explored from the perspectives of bubble-particle interactions and solution surface tensions.

Higher burn severity stimulates postfire vegetation and carbon recovery in California

As the climate continues to warm, the severity of wildfires is increasing. However, the potential impact of higher burn severity on ecosystem resilience and regional carbon balance is still not clear. There are ongoing debates regarding whether increased burn severity stimulates or delays postfire vegetation and carbon recovery. In this study, we utilized remote sensing data to analyze burn severity and vegetation observations, as well as model simulations to assess wildfire carbon emissions and ecosystem carbon fluxes. Our focus was on examining the dynamics of vegetation and carbon flux following wildfires spanning up to 16 years in California, a region that has experienced significant intensification in burn severity over the past two decades. Our findings revealed that more severe burns resulted in greater vegetation damage and carbon releases. However, they also facilitated faster postfire vegetation and carbon recovery. In comparison to the average burn severity, the most severe burns caused an additional 62–128 % loss of vegetation, 21–80 % higher instant wildfire carbon emissions, and 45–110 % more postfire carbon sources. Nonetheless, high-severity burns exhibited accelerated postfire recoveries in both vegetation growth and ecosystem carbon sink. Carbon sinks, which persisted for up to 15 years after high-severity burns, partially offset a significant proportion of the extra postfire carbon sources, ranging from 84 to 107 % (excluding instant emissions). However, this offset effect was insufficient to fully compensate for the combined impact of postfire carbon sources and instant wildfire carbon emissions. Consequently, on the decadal time scale relevant to regional climate policies, the increasing severity of fires poses a threat to the objective of maintaining California's natural and working lands as a net carbon sink. Moreover, it exacerbates climate warming by enhancing carbon releases from ecosystems.

Exploring the mechanism and negentropy of photogranules for efficient carbon, nitrogen and phosphorus recovery from wastewater

Entropy is a fundamental concept in thermodynamics that characterizes the level of disorder or chaos within a system. Negative entropy is the process of fixing unavailable disordered energy into available ordered energy, which can serve as a valuable indicator of the sustainability and efficiency of wastewater treatment process. This study explored the utilization of photogranules (light-driven aerobic granular sludge) as a wastewater treatment process with minimal energy dissipation and effective resource recovery. This study focuses on the carbon, nitrogen, and phosphorus cycling pathways of photogranules, including treatment performance, resource recovery, neg-entropy evaluation (NEE), and their corresponding metabolic mechanisms. Photogranules showed 94.1 % COD, 96.1 % ammonium and 88.9 % phosphorus removal ratios, respectively. Moreover, the successful recovery of proteins 337.61 mg/g, polysaccharides 87.67 mg/g, lipid 206.6 mg/g, which achieved negentropy. Notably, the microorganisms Scenedesmus, responsible for carbon fixation, and Allorhizobium, responsible for nitrogen fixation, play pivotal roles in driving the negentropy process. During carbon fixation, light energy is converted into chemical energy through the process of photosynthesis, The dark reaction phase of photosynthesis involves the production of glucose, and it has been found to have a thermodynamic value of −14134.8 J/(mol·K), indicating a decrease in entropy. Thermodynamic modeling further supports the concept that photogranules achieve negentropy. They accomplish this by effectively sequestering and converting non-renewable light resources into a state of low entropy. In summary, NEE provides a novel insight into not only the sustainability of photogranules but also other wastewater treatment process.

Meta-analysis of carbon stocks and biodiversity outcomes across Brazilian restored biomes

Ecosystem restoration strategies vary widely in the techniques applied and ecological contexts. We conducted a meta-analysis to evaluate how restoration success varies across socio-ecological contexts, taxonomic groups and biomes. Restoration success is quantified as the percentage of each ecological metric value attained in the restoration site compared to the reference systems. We show that restoration success is different for plants, animals, and soils and across ecological indicators. Abundance of individuals is easier to restore than carbon stocks, which are easier than species diversity. However, abundance may be a poor indicator of ecosystem recovery because there is no unidirectional trend over time, and abundance often fails to distinguish restored from degraded areas. We also found that carbon stocks in the soil and in the vegetation are restored at analogous paces, but the recovery of soil carbon stocks is less variable than plant stocks across sites. Our results demonstrate that different restoration techniques are effective in recovering diversity and carbon stocks, but assisted natural regeneration showed a slightly higher success compared to other strategies. However, there is a considerable difficulty in restoring converted and degraded areas to achieve conditions similar to the original ecosystems. It is critical and timely to investigate benefits and effectiveness of ecosystem restoration techniques to biodiversity and carbon recovery different ecosystem types to improve the restoration effectiveness.

Comparative Analysis of Pigeonpea Stalk Biochar Characteristics and Energy Use under Different Biochar Production Methods

The disposal of crop residues from agricultural fields is often seen as a burden due to the difficulties involved. However, this study aims to turn pigeonpea stalks into biochar, which can serve as a fuel substitute and soil amendment to sequester carbon. Different pyrolysis methods were employed to investigate the variations in yield, physicochemical characteristics, and higher heating value (HHV) of biochar produced from pigeonpea stalks. The biochar produced using a muffle furnace exhibited higher fixed carbon and ash content. These characteristics make it beneficial for restoring degraded agricultural soils by enhancing carbon sequestration. In addition, the muffle furnace biochar demonstrated a total potential carbon ranging from 262.8 to 264.3 g of carbon per kilogram of biochar, along with a CO2 reduction potential ranging from 77.17 to 79.68 CO2 eq per kg. Both the European Biochar Certificate and the International Biochar Initiative confirmed the agronomic abilities of the biochar and its compliance with the highest quality standards for soil carbon sequestration, with 0.11 H/C and 0.7 O/C ratios. Furthermore, biochar produced by muffle furnace from pigeonpea stalks exhibited superior fixed carbon recovery efficiency (181.66 to 184.62%), densification (5.86 to 6.83%), energy density (1.77 to 2.06%), energy retention efficiency (54.80 to 56.64%), fuel ratio (18.95 to 22.38%), and HHV (30.66 to 32.56 MJ kg−1). Additionally, it had lower H/C and O/C ratios, suggesting its potential as an alternative solid fuel. The results of the characterization of biochar with scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) revealed that the biochar samples prepared with both the methods had carbonyl (C=O), C=C, and aromatic C-H functional groups; however, the biochar prepared in the muffle furnace had more porosity. In summary, this study highlights the potential of using pigeonpea stalks to produce biochar, which can be utilized as a renewable fuel substitute and soil amendment to sequester carbon. The biochar derived from the muffle furnace exhibited desirable physicochemical characteristics, high carbon content, and excellent energy properties, making it a promising option for various applications.

Characteristics of vegetation carbon sink carrying capacity and restoration potential of China in recent 40 years

Improving vegetation carbon sink is a key measure for China to achieve the goal of carbon neutrality. However, the gradual saturation of vegetation carbon fixation under the constraints of climate change and human activities has limited the long-term and sustainable growth of vegetation carbon sinks, resulting in significant uncertainty in understanding future carbon sink capacity and recovery potential. In this study, NPP has been selected as a carbon sink indicator to quantitatively evaluated the carbon sink carrying capacity (CSCC) and the carbon sink resilience (CSR) of China. Results demonstrated that (1) the NPP of vegetation cover areas in China exhibited an increasing trend from 1981 to 2018, with an average growth rate of 1.66 g C m−2 yr.−1 and a total net NPP increase of 0.32 P g C. (2) The average CSCC in China was 658.59 g C m−2 yr.−1, with a total amount of 4.13 Pg C yr.−1. The NPP exceeded 60% of CSCC in various years, and the total NPP in 2018 was 3.26 Pg C yr.−1, which reached 78.74% of CSCC. In the future, carbon sink that can be increased is 0.88 Pg C yr.−1, with an increase proportion of 21.26%. (3) From 2000 to 2018, the NPP of vegetation-covered area (VCA) in China had generally maintained a positive succession trend with the stronger CSR. Only four provinces (HUN, CQ, AH, and JS) in China showed the extremely strong levels of CSR. The study has revealed the huge and sustainable CSCC and restoration potential in China over the past 40 years, and has provided spatial positioning and theoretical guidance for future ecological carbon sink restoration and benefit assessment.

A double-edged sword: Constructed wetland-microbial fuel cells promote organics removal via entrapment

Recently, constructed wetland-microbial fuel cells (CW-MFCs) are found to enhance the organics removal via the connection of the external circuit. Yet, it is unclear why the energy output is unmatched with the enhancement of the organics removal. This study compared the dynamic changes of the organics in a CW-MFC microcosm operated under the close circuit and open circuit. As a result, the close circuit facilitated the organics removal by 9 % before the proportional discharge of carbon metabolites. This suggested that organics entrapment should account for the huge loss of carbon recovery; and closing the external circuit could further promote the organics entrapment. Besides, polyhydroxybutyrate was found accumulated in the MFC culture experiment, evidencing that the fed-batch mode of operation could result in a feast-famine pattern of microbial metabolism. Despite the fast organics entrapment during the first hours, prolonging the operation time would lead to continuous carbon gas emission, along with the substantially elevated coulombic efficiency. Together, these results explained the substantial COD removal enhancement with low electricity yield, and cautioned the safe use of the MFC integration to spare the system from overaccumulation of organics.