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Municipal solid waste (MSW), a carbon-intensive waste stream, may create both instant and indirect impacts onto environmental and climate management. Despite multiple studies made for greenhouse gases (GHGs) emissions of municipal waste, this research aims to achieve a comprehensive assessment for the carbon cycle by exploring evolution of waste composition and temporal-spatial disparities in waste management. Carbon flows embodied in MSW have been estimated across 31 provinces in Mainland China in the period 2000-2018. This improved estimation could be 15-40% smaller than the conventional estimation employing a constant waste composition. Aggregately some 578 ± 117 megatonnes carbon (MtC) were contained in MSW, including 239 ± 60 Mt of fossil carbon and 339 ± 58 Mt of degradable organic carbon. After treatment, 299 ± 66 MtC were possibly deposited in landfills and dumps. 279 ± 51 MtC were released to the atmosphere, creating net GHGs emissions equivalent to1870 ± 334 megatonnes of CO2 (MtCO2e). MSW generation in China nearly doubled during the period, net GHGs emissions increased by 1.8×, whereas fossil carbon grew by a factor of 3.5, mainly propelled by an increasing content of waste plastic in MSW. More rapid growth was witnessed in provinces in southern China than in northern. Distinct spatial-temporal evolution of waste and carbon metabolism was driven by increment, composition, and management effects. In the long run, the increment and composition effects may drop off. Enhanced practices of waste management integrating the circular economy are needed to fully recycle carbon flows, minimize emissions, and manage carbon deposits in aging landfills and dumps.

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Industrial solid waste management and recycling are important to environmental sustainability. In this study, cobalt (Co) nanoparticles encapsulated in paint sludge-derived activated carbon (AC) were fabricated. The Co-AC possessed high conductivity, magnetic properties and abundant metal oxide impurities (TiAlSiOx), which was applied as multifunctional catalyst for peroxymonosulfate (PMS) activation. Compared to pure AC, the Co-AC exhibited significant enhanced performance for degradation of tetracycline hydrochloride (TCH) via PMS activation. Mechanism studies by in situ Raman spectroscopy, Fourier infrared spectroscopy, electrochemical analysis and electron paramagnetic resonance suggested that surface-bonded PMS (PMS*) and singlet oxygen (1O2) are the dominant reactive species for TCH oxidation. The non-radical species can efficiently oxidize electron-rich pollutants with high efficiency, which minimized the consumption of PMS and the catalyst. The removal percentages of TCH reached 97 % within 5 min and âˆ¼ 99 % within 15 min in the Co-AC/PMS system. The Co active sites facilitated PMS adsorption to form the PMS* and the TiAlSiOx impurities provided abundant oxygen vacancy for generation of the 1O2. In addition, the Co-AC/PMS system achieved high efficiency and stability for oxidation of the target pollutants over a long-term continuous operation. This work not only offers a cost-effective approach for recycling industrial waste but also provides new insights into the application of waste-derived catalyst for environmental remediation.

RESUMEN

Burning and dumping textile wastes have caused serious damage to the environment and are a huge waste of resources. In this work, cobalt nanoparticles embedded in active carbon fiber (Co/ACF) were prepared from bio-based fabric wastes, including cotton, flax and viscose. The obtained Co/ACF was applied as a catalyst for the heterogeneous activation of peroxymonosulfate (PMS) to remove bisphenol A (BPA) from an aqueous solution. The results showed that cotton-, flax- and viscose-derived Co/ACF all exhibited excellent performance for BPA degradation; over ~97.0% of BPA was removed within 8 min. The Co/ACF/PMS system exhibited a wide operating pH range, with a low consumption of the catalyst (0.1 g L-1) and PMS (0.14 g L-1). The high specific surface area (342 m2/g) and mesoporous structure of Co/ACF allowed the efficient adsorption of pollutants as well as provided more accessible active sites for PMS activation. This study provided an example of using textile wastes to produce a valuable and recyclable catalyst for environmental remediation.

RESUMEN

The simultaneous reduction of Cr(VI) and sequestration of the resulting Cr(III) in one process is highly desirable as a cost-effective and environmental-friendly approach for the decontamination of Cr(VI)-polluted wastewater. However, most of the existing adsorptive materials are only effective in low pH environments (pH = 1-3), severely restricting the adsorption efficiency and cost effectiveness. Herein, we proposed a chitosan-based magnetic porous microsphere (PPy@PMCS) for simultaneous Cr(VI) reduction and Cr(III) sequestration in a wide pH range. Benefiting from its abundant interaction sites, Cr(VI) was effectively adsorbed on the surface and then immediately reduced to Cr(III) with much lower toxicity. Most importantly, the resulting Cr(III) was in-situ sequestrated by the complexation of chitosan matrix. As a result, PPy@PMCS exhibited a maximum Cr(VI) adsorption capacity of 330.42 mg/g at pH 2.0 and an adsorption capacity of 167.82 mg/g even at near neutral pH (6.0), which is superior to most reported adsorbents. Furthermore, the exhausted PPy@PMCS can be rapidly separated from solutions under an external magnetic field and facilely regenerated. The proposed novel biopolymer-based material shows great application potentials in wastewater treatment.

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RESUMEN

Heterogeneous activation of peroxymonosulfate (PMS) is one of the most promising techniques for wastewater treatment. Herein, an ingenious system by coupling of photocatalysis and PMS activation was developed, using hollow-structured amorphous prussian blue (A-PB) decorated on graphitic carbon nitride (g-C3N4) as the catalyst. Degradation of bisphenol A (BPA) via the A-PB-g-C3N4 mediated PMS activation under visible light (Vis) was systematically investigated. Astonishingly, it was found that ~ 82.0%, 92.6%, 98.2% and 99.3% of BPA (40 mg/L) were removed within 2, 4, 6 and 7 min, respectively, suggesting the extremely strong oxidizing capacity of the A-PB-g-C3N4/PMS/Vis system. Synergistic effect between the decorated A-PB and the g-C3N4 substrate promoted the Fe(III)/Fe(II) redox cycling and facilitated the charge transfer at the A-PB/g-C3N4 heterojunction interface. As a result, both photocatalysis and heterogeneous activation of PMS were boosted in the A-PB-g-C3N4/PMS/Vis system, leading to the production of large amount of reactive oxygen species (ROS). The various ROS (SO4•-, HO•, •O2- and 1O2) was responsible for the ultrafast degradation of BPA. Moreover, the A-PB-g-C3N4 catalyst also exhibited outstanding reusability and stability, retaining 98.9% of the removal percentage for BPA after five consecutive reaction cycles. This study suggests that the A-PB-g-C3N4 can be an all-rounder to bridge photocatalysis and PMS activation, and shed a new light on the application of multiple ROS for the ultrafast elimination of micropollutants from wastewater.

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In this work, nitrogen-rich graphene-like carbon sheets (N-GLCS) with high specific surface area (488.4m2/g), narrow pore distribution and high N-doping (18.4 at%) were prepared and applied as both adsorbent and catalyst for the removal of bisphenols. Adsorption experiments demonstrated the high adsorption capacities of the N-GLCS toward bisphenol F (BPF) (222.9mg/g), bisphenol A (BPA) (317.8mg/g), and bisphenol C (BPC) (540.4mg/g). Results showed that about 98.6% of BPA (70mg/L) was removed at pH 7.0 within 80min after the adsorption-catalytic degradation process. The N-GLCS also showed a superb reusability for the catalytic oxidative degradation of BPA (70mg/L) with the removal percentage maintains over 83% after 5 cycles. With the synergistic combination of the excellent adsorption and catalytic properties of the N-GLCS, trace amount of pollutants can be preconcentrated and immobilized at the surface of N-GLCs, at the same time, active radicals were also produced at the surface of the N-GLCS by the activation of peroxydisulfate (PS), and finally the pollutants can be degraded in-situ by the active radicals. These findings provide a new avenue towards the efficient removal of trace-level EDCs from water solution by using the coupled adsorption-advanced oxidation processes.