Intelligent technologies powering clean incineration of municipal solid waste: A system review.

Cleanliness has been paramount for municipal solid waste incineration (MSWI) systems. In recent years, the rapid advancement of intelligent technologies has fostered unprecedented opportunities for enhancing the cleanliness of MSWI systems. This paper offers a review and analysis of cutting-edge intelligent technologies in MSWI, which include process monitoring, intelligent algorithms, combustion control, flue gas treatment, and particulate control. The objective is to summarize current applications of these techniques and to forecast future directions. Regarding process monitoring, intelligent image analysis has facilitated real-time tracking of combustion conditions. For intelligent algorithms, machine learning models have shown advantages in accurately forecasting key process parameters and pollutant concentrations. In terms of combustion control, intelligent systems have achieved consistent prediction and regulation of temperature, oxygen content, and other parameters. Intelligent monitoring and forecasting of carbon monoxide and dioxins for flue gas treatment have exhibited satisfactory performance. Concerning particulate control, multi-objective optimization facilitates the sustainable utilization of fly ash. Despite remarkable progress, challenges remain in improving process stability and monitoring instrumentation of intelligent MSWI technologies. By systematically summarizing current applications, this timely review offers valuable insights into the future upgrade of intelligent MSWI systems.

Comparative study by microwave pyrolysis and conventional pyrolysis of pharmaceutical sludge: Resourceful disposal and antibiotic adsorption.

Compared with conventional pyrolysis, microwave pyrolysis has superior heat transfer performance and promotes the decomposition of organic matter. The paper focuses on the harmless treatment and resource utilization of pharmaceutical sludge (PS) by microwave heating and conventional heating methods. The experimental results showed that the conventional pyrolysis gas is dominated by CO2, CO and H2. For microwave pyrolysis gas, the "microwave effect" promoted secondary cracking of volatile fractions and increases the content of CH4, CxHy, H2 and CO through condensation, aromatization, and dehydrogenation. Conventional pyrolysis oils contained the highest percentage of oxygenated compounds. However, high-temperature microwave radiation accelerated the cleavage of polar oxygenated molecular bonds and long-chain hydrocarbons, thereby increasing the aromatics content of pyrolysis oils. The solid residues obtained from microwave pyrolysis is highly graphitized and porous, with a surface area of 146.2 m2/g. Furthermore, the solid residue was rich in pyridine-N and pyrrole-N that could be utilized for adsorption and catalysis. The MA-600 removes up to 99% of tetracycline (TC) in 6 h. It was also found that the adsorption process of TC by the two pyrolysis residues was consistent with the proposed secondary and Freundlich models.

Direct determination of high-concentration As(III) by UV high-reference differential absorption spectroscopy for cleaner As(III) removal promotion via sulfurization.

The current methods for determining high-concentration As(III) in the high-acid matrix from the copper smelting industry are complex, time-consuming, and costly. This limits effective modulation of sulfurizing agent dosage for As(III) removal via sulfurization, aggravating hazardous waste generation. Herein, a simple, rapid, and nondestructive UV high-reference differential absorption spectroscopy was developed to directly determine high-concentration As(III) in simulated high-acid wastewater. Time-dependent density functional theory calculations indicated that the spectral curve redshift with As(III) concentration increasing was related to the decrease of electron transition energies and energy gaps. When using high-reference solutions, the least redshift in the maximum absorption wavelength and the highest upper limit of linear fitting concentration could be obtained. Therefore, the piecewise quantitative linear model of differential absorbance and concentration was established under high-reference. The quantitative range of the model within 0.06-20.00 g/L As(III) with a mean relative error of < 5.0 % and standard recovery rates within 98.0 %-104.0 % indicated high accuracy. Additionally, the relative standard deviations of < 1.5 % (n = 5) revealed good precision. All results indicated the high feasibility of the developed method in alleviating linear deviation caused by redshift and absorption saturation. Furthermore, it has potential significance in saving sulfurizing agent dosage and reducing hazardous waste generation from the source, thereby facilitating a cleaner process for removing As(III) via sulfurization.

Biochar-Assisted Catalytic Pyrolysis of Oily Sludge to Attain Harmless Disposal and Residue Utilization for Soil Reclamation.

Pyrolysis of oily sludge (OS) is a feasible technology to match the principle of reduction and recycling; however, it is difficult to confirm the feasible environmental destination and meet the corresponding requirements. Therefore, an integrated strategy of biochar-assisted catalytic pyrolysis (BCP) of OS and residue utilization for soil reclamation is investigated in this study. During the catalytic pyrolysis process, biochar as a catalyst intensifies the removal of recalcitrant petroleum hydrocarbons at the expense of liquid product yield. Concurrently, biochar as an adsorbent can inhibit the release of micromolecular gaseous pollutants (e.g. HCN, H2S, and HCl) and stabilize heavy metals. Due to the assistance of biochar, pyrolysis reactions of OS are more likely to occur and require a lower temperature to achieve the same situation. During the soil reclamation process, the obtained residue as a soil amendment can not only provide a carbon source and mineral nutrients but can also improve the abundance and diversity of microbial communities. Thus, it facilitates the plant germination and the secondary removal of petroleum hydrocarbons. The integrated strategy of BCP of OS and residue utilization for soil reclamation is a promising management strategy, which is expected to realize the coordinated and benign disposal of more than one waste.

Low-Temperature Catalytic Ozonation of Multitype VOCs over Zeolite-Supported Catalysts.

Volatile organic compounds (VOCs) are an important source of air pollution, harmful to human health and the environment, and important precursors of secondary organic aerosols, O3 and photochemical smog. This study focused on the low-temperature catalytic oxidation and degradation of benzene, dichloroethane, methanethiol, methanol and methylamine by ozone. Benzene was used as a model compound, and a molecular sieve was selected as a catalyst carrier to prepare a series of supported active metal catalysts by impregnation. The effects of ozone on the catalytic oxidation of VOCs and catalysts' activity were studied. Taking benzene as a model compound, low-temperature ozone catalytic oxidation was conducted to explore the influence of the catalyst carrier, the active metal and the precious metal Pt on the catalytic degradation of benzene. The optimal catalyst appeared to be 0.75%Pt-10%Fe/HZSM(200). The catalytic activity and formation of the by-products methylamine, methanethiol, methanol, dichloroethane and benzene over 0.75%Pt-10%Fe/HZSM(200) were investigated. The structure, oxygen vacancy, surface properties and surface acidity of the catalysts were investigated. XRD, TEM, XPS, H2-TPR, EPR, CO2-TPD, BET, C6H6-TPD and Py-IR were combined to establish the correlation between the surface properties of the catalysts and the degradation activity.

Catalytic ozonation of dichloromethane at low temperature and even room temperature on Mn-loaded catalysts.

Five Mn-loaded catalysts were synthesized on γ-Al2O3, TiO2, ZrO2, nano γ-Al2O3 and nanoZrO2 supports. The catalytic ozonation of DCM (dichloromethane) was evaluated under industrial conditions (i.e., temperature, O3 input, H2O and SO2 content). According to results, >90% DCM conversion without O3 residue was achieved for all samples at 120 °C and an O3/DCM ratio of 6. At 20-120 °C, the highest Mn3+ content, abundant surface oxygen species and more weak acid sites led to the best performance of Mn/nanoAl2O3 (M/A-II). At 20 °C and 120 °C, 80% and 95% DCM can be degraded respectively on M/A-II at 20 °C with matched surface oxygen species and acidity. An O3/DCM ratio of 6 was optimal for performance and economy. For the effects of complex exhaust, both H2O and SO2 deactivated M/A-II. The H2O-induced deactivation was recoverable and also removed surface-deposited chlorine-containing species, enhancing the HCl selectivity. Finally, the Cl equilibrium of the reaction was comprehensively analyzed.

Evaluation of the Flexibility for Catalytic Ozonation of Dichloromethane over Urchin-Like CuMnOx in Flue Gas with Complicated Components.

The evaluation of the poisoning effect of complex components in practical gas on DCM (dichloromethane) catalytic ozonation is of great significance for enhancing the technique's environmental flexibility. Herein, Ca, Pb, As, and NO/SO2 were selected as a typical alkaline-earth metal, heavy metal, metalloid, and acid gas, respectively, to evaluate their interferences on catalytic behaviors and surface properties of an optimized urchin-like CuMn catalyst. Ca/Pb loading weakens the formation of oxygen vacancies, oxygen mobility, and acidity due to the fusion of Mn-Ca/Pb-O, leading to their inferior catalytic performance with poor CO2 selectivity and mineralization rate. Noticeably, the presence of As induces excessively strong acidity, facilitating the inevitable formation of byproducts. Catalytic co-ozonation of NO/DCM is achieved with stoichiometric ozone addition. Unfortunately, SO2 introduction brings irreversible deactivation due to strong competition adsorption and the loss of active sites. Unexpectedly, Ca loading protects active sites from an attack by SO2. The formation of unstable sulfites and the released Mn-O structure offset the negative effect from SO2. Overall, the catalytic ozonation of DCM exhibits a distinctive priority in the antipoisoning of metals with the maintenance of DCM conversion. The construction of more stable acid sites should be the future direction of catalyst design; otherwise, catalytic ozonation should be arranged together with post heavy metal capture and a deacidification system.

Pollution Levels and Risk Assessment of Heavy Metals in the Soil of a Landfill Site: A Case Study in Lhasa, Tibet.

As an important ecological security barrier in China, the ecological environment of Tibet has aroused widespread concern domestically and overseas. Landfills are a major solid waste treatment approach in Tibet but also cause severe environmental pollution. To date, there are no studies related to the pollution risk of landfills in Tibetan areas. This study investigated the pollution levels, ecological risk, health risk, and possible pollution sources of eight heavy metals in the soils around a landfill site in Lhasa, Tibet. The results indicated that the concentrations of heavy metals in soil were relatively low, only cadmium (Cd), arsenic (As), copper (Cu), chromium (Cr), zinc (Zn), nickel (Ni), and lead (Pb) were 1-2 times higher than the corresponding background value. The values of the single pollution index and geo-accumulation index show that the study area is most seriously polluted by Cd and As. Based on the Nemerow pollution index and the pollution load index, over 83.3% and 8.33% of soil sampling sites had light and moderate contamination levels. According to the results of potential ecological risk evaluation, the potential ecological risk of heavy metals in soil was very low, and only one out of the 72 sampling sites exhibited considerable ecological risk. Cd, As, and mercury (Hg) served as the dominant ecological risk contributors and contributed over 45.0%, 14.1%, and 18% of the ecological risk. The results of the health risk evaluation showed that adults have a higher risk of cancer (1.73 × 10-5), while the non-carcinogenic risk for adults was low. Waste disposal activities and construction activities have a significant influence on soil heavy metal concentrations, causing a higher pollution level in the southeast part of the landfill site in Lhasa.

Catalytic ozonation of CH2Cl2 over hollow urchin-like MnO2 with regulation of active oxygen by catalyst modification and ozone promotion.

This paper firstly reported efficient catalytic ozonation of CH2Cl2 (dichloromethane, DCM) at low temperature over hollow urchin-like MnO2 with high chlorine resistance. Regulations on morphologies and Cu doping, as well as ozone promotion were conducted to optimize active oxygen of MnO2 catalysts, contributing to excellent catalytic behaviors. Cu doping MnO2 with hollow urchin-like morphology attained a stable 100% DCM conversion with O3/DCM molar ratio of 10 at 120 °C. The ozone utilization rate, final products, and byproducts distribution were discussed. Abundant crystal defects, low-valance Mn/Cu, Oads, and weak acidity, as well as better low temperature reducibility contributed to its superior performance. During DCM catalytic ozonation, DCM oxidation exhibited competitive effect on O3 decomposition due to the occupation of intermediates (CH2ClO3·, O-CH2Cl, and O-CH2 -O) over active sites that should belong to O3 originally. Nevertheless, O3 decomposition exhibited synergistic effects on DCM oxidation with promotion on active oxygen. Density functional theory (DFT) calculations confirmed the positive effect on oxygen vacancy formation and O3/DCM adsorption from Cu doping. The possible mechanism for DCM catalytic ozonation included four parts, including O3/DCM adsorption, O3 activation, DCM oxidation, and electron replenishment. This paper provides new insight for catalytic elimination of chlorinated alkanes at mild conditions.

Catalytic Decomposition of Residual Ozone over Cactus-like MnO2 Nanosphere: Synergistic Mechanism and SO2/H2O Interference.

Ground-level ozone is an irritant and is harmful to human respiratory and nervous systems. Thus, four manganese oxides with different crystals were hydrothermally synthesized to decompose residual ozone (deO3) in an ozone synergistic-oxidation system. Among them, a cactus-like MnO2-IV nanosphere exhibited the highest deO3 activity, with excellent tolerance to water vapor and SO2/H2O, which could maintain >88% deO3 efficiency in the high-humidity and sulfur-containing conditions. It benefits from the unique morphology, high specific surface area, superior redox properties, oxygen chemisorption capabilities, abundant surface-active hydroxyl species, and low valence Mn species. More importantly, the detailed interference mechanism of O2/O3/H2O/SO2 molecules on MnO2-IV was revealed utilizing in situ diffused reflectance infrared Fourier transform spectroscopy and X-ray photoelectron spectroscopy. H2O generally caused recoverable deactivation, but that caused by SO2 was irreversible. The synergistic effect of SO2/H2O promoted the formation of an unstable sulfate species, thereby deepening the deactivation but inhibiting the irreversible poisoning. Finally, nine specific steps to decompose ozone via surface-active hydroxyl/intermediates were established.

Pyrolysis Behaviors and Residue Properties of Iron-Rich Rolling Sludge from Steel Smelting.

Iron-rich rolling sludge (FeRS) represents a kind of typical solid waste produced in the iron and steel industry, containing a certain amount of oil and large amounts of iron-dominant minerals. Pyrolysis under anaerobic environment can effectively eliminate organics at high temperatures without oxidation of Fe. This paper firstly investigated comprehensively the pyrolysis characteristics of FeRS. The degradation of organics in FeRS mainly occurred before 400 °C. The activation energy for pyrolysis of FeRS was extremely low, ca. 5.44 kJ/mol. The effects of pyrolytic temperature, atmosphere, heating rate, and stirring on pyrolysis characteristics were conducted. Commonly, the yield of solid residues maintained around 85 wt.%, with approximately 13 wt.% oil and 2 wt.% gas. Due to the low yield of oil and gas, their further utilization remains difficult despite CO2 introduction which could upgrade their quality. The solid residues after pyrolysis exhibited porous properties with co-existence of micropores and mesopores. Combined with the high content of zero-valent iron, magnetic property, hydrophobic characteristic, and low density, the solid residues could be further utilized for water pollution control and soil remediation. Moreover, the solid residues were suitable for sintering to recover valuable iron resources. However, the solid residues also contained certain heavy metals, such as Cd, Cr, Cu, Ni, Pb, and Zn, which might cause secondary pollution during their utilization. In particular, the toxic Cr possessed high content, which should be treated with detoxification and removal. This paper provides fundamental information for pyrolysis of FeRS and utilization of solid residues.

Utilizing waste duckweed from phytoremediation to synthesize highly efficient FeNxC catalysts for oxygen reduction reaction electrocatalysis.

Duckweed is a universal aquatic plant to remove nitrogen source pollutants in the field of phytoremediation. Due to the naturally abundant nitrogen, synthesis of carbon materials from duckweed would be a high-value approach. In oxygen reduction reaction (ORR) of metal-air batteries and fuel cells, non-noble metals and heteroatoms co-doped electrocatalysts with excellent catalytic activity and remarkable stability are promising substitutes for Pt-based catalysts. The first-class ORR performance is determined by appropriate pore structure and active sites, which are strongly associated with the feasible synthesis methods. Herein, a facile one-step synthesis strategy for the transition metals- and nitrogen-codoped carbon (MNxC) based catalysts with hierarchically porous structure was developed. The MNxC (M = Fe, Co, Ni, and Mn) active sites were constructed and FeNxC (D-ZB-Fe) was the best electrocatalyst with excellent ORR performance. Results showed that D-ZB-Fe exhibited an obvious honeycomb porous structure with specific surface area of 1342.91 m2·g-1 and total pore volume of 1.085 cm3·g-1. It also possessed considerable active atoms and sites, where the proportion of pyridine N and graphite N was up to 72.9%. The above feature made for a superior ORR electrocatalytic activity. In specific, the onset and half-wave potential were 0.974 V and 0.857 V vs. RHE (Reversible Hydrogen Electrode), respectively. When compared with performances of commercial Pt/C, the four-electron pathway and relatively low peroxide yield, ca. 5%, were almost equivalent. Furthermore, D-ZB-Fe showed an excellent stability and remarkably methanol tolerance by the durability test. In conclusion, this research provides a new synthesis strategy of electrocatalysts with porous structures and active sites.

Products distribution and pollutants releasing characteristics during pyrolysis of waste tires under different thermal process.

Pyrolysis has been widely utilized to achieve resource recovery of waste tires by attaining oil and carbon black. However, due to the stacking effect of fixed bed, the heat and mass transfer is insufficient during the pyrolysis process of waste tires. Additionally, the harmful N/S/Cl pollutants and heavy metals are inevitable that has been ignored. This paper systematically studied the effect of promoting heat and mass transfer on the oil quality and pollutant releasing characteristics during the pyrolysis of waste tires. A fixed bed pyrolizer with multifunction was innovatively designed to conduct fast pyrolysis by equipping an intermittent feeder and slow pyrolysis by equipping an agitator. Fast pyrolysis with feeding step by step and slow pyrolysis with stirring could promote the heat and mass transfer, which was firstly researched in lab-scale reactor. The experimental results demonstrated that slow pyrolysis with stirring was recommended with the target of acquiring pyrolytic oil. Promoting heat and mass transfer could improve the quality of oil and increase the retaining proportion of S in char during both fast and slow pyrolysis. The combustion of pyrolysis oil and gas generated more dioxins (0.6 ng/gwt) than the total dioxins in pyrolytic gas and oil (0.06 ng/gwt).

Triple combination of natural microbial action, etching, and gas foaming to synthesize hierarchical porous carbon for efficient adsorption of VOCs.

Fungi residue, vinasse, and biogas residue differ from general biomass waste due to natural microbial action. Microbial fermentation helps create natural channels for the permeation of activators and produces proteins for natural nitrogen doping. Inspired by these advantages on porous carbon synthesis, this study adopted dual activators of KOH and KHCO3 to synthesize porous carbon with different pore ratios for efficient adsorption of volatile organic compounds (VOCs). The fungi residue possessed the least lignin due to the most severe microbial action, contributing to the best pore structures after activation. The etching effect from potassium compounds and gas foaming from the carbonate decomposition contributed to creating hierarchical porous carbon with ultra-high surface area, ca. 1536.8-2326.5 m2/g. However, KHCO3 addition also caused nitrogen erosion, such that lower adsorption capacity was attained even with a higher surface area when the mass ratio of KOH/KHCO3 decreased from 2.5:0.5 to 2:1. The maximum adsorption capacities of chlorobenzene (CB) and benzene (PhH) reached 594.0 and 394.3 mg/g, respectively. Pore structure variations after adsorption were evaluated by freeze treatment to discover the adsorption mechanism. The surface area after CB and PhH adsorption decreased 40.3% and 34.5%, respectively. Most of the mesopores might transform into micropores due to the mono/multilayer stacking of adsorbates. The VOC adsorption kinetics were simulated by the Pseudo-first- and -second-order models and Y-N model. This paper provides a new approach for high-value biomass waste utilization after microbial action to synthesize efficient adsorbents for VOCs.

Insoluble matrix proteins from shell waste for synthesis of visible-light response photocatalyst to mineralize indoor gaseous formaldehyde.

HCHO is the most concerned indoor air pollutant that photocatalytic degradation is a feasible approach. To achieve efficient and complete degradation of HCHO under visible light irradiation, heteroatoms are usually doped in TiO2. But using natural materials as a dopant instead of expensive and toxic chemicals to fertilize TiO2 remains challenging. This paper proposes a sustainable and green approach to synthesize an efficient N, Ca co-doped TiO2 photocatalyst (TIMP) by using the insoluble matrix proteins (IMPs) extracted from abalone shell. TIMP-0.8 achieves near completely degradation HCHO within 45 min under visible light at ambient temperature and exhibits superior stability after 7 cycles. TIMP-0.8 has monodispersity with smaller diameter, high porosity, abundant defects and high adsorption affinity for surface hydroxyls compared with pure TiO2. With the assistance of IMPs, the rate-determining step of HCHO degradation changes from -COOH oxidation to spontaneous decomposition of HCO3-, significantly facilitating the elimination and mineralization of HCHO. Overall, IMPs from abalone shell are natural surfactant, bio-templet, and dopant for TiO2 modification, contributing to desirable visible-light photocatalytic performance for HCHO degradation. This paper provides new insight for high-value utilization of waste shell and photocatalytic indoor purification.

Comparative Investigation on Chlorobenzene Oxidation by Oxygen and Ozone over a MnOx/Al2O3 Catalyst in the Presence of SO2.

Catalytic oxidation of volatile organic compounds (VOCs) usually encounters complicated components in flue gas causing severe deactivation that restrict its application in specific conditions. The Cl substitution in chlorobenzene further increases poisoning risks. Ozone assistance has unique superiority that can overcome these bottleneck problems. Herein, this study performs a comparative investigation of CB oxidation by oxygen and ozone over a simple Mn/Al2O3 catalyst. CB conversion suffered from slight deactivation in oxygen atmosphere (from 90 to 70%) and more severe deactivation in the presence of SO2 (from 90 to 45%) at 480 °C. Introduction of ozone successfully attained high CB conversion at low temperature (120 °C) with excellent stability and less byproducts. Especially, CB oxidation by ozone maintained its original conversion in the presence of SO2. The deactivation process was simulated by synthesizing several sulfated catalysts. Direct sulfation on Mn/Al2O3 attained more severe deactivation in CB conversion and CO2 formation than sulfation on the Al2O3 support. Ozone with a strong oxidation property promoted the CB oxidation cycle, facilitated desorption of carbonaceous intermediates, and protected MnOx species from severe erosion, thus exhibiting high and stable performance in CB oxidation.

A critical review on energy recovery and non-hazardous disposal of oily sludge from petroleum industry by pyrolysis.

This review systematically reports the pyrolysis of oily sludge (OS) from petroleum industry in regards to its dual features of the energy recovery potential and the environmental risks. The petroleum hydrocarbons are the nonbiodegradable fractions in OS that possess hazardous properties, i.e. ignitability and toxicity. Besides, complicated hazardous elements (i.e. N, S and Cl) and heavy metals inherently existing in OS further aggravate the environmental risks. However, the high oil content and heating value of OS contribute to its huge energy resource potential. Considering the energy demand and the environmental pressure, the ultimate purposes of the OS management are to enhance the oil recovery efficiency to minimize the oil content as well as to stabilize the hazardous elements and heavy metals into the solid residue. Among various OS management technologies, pyrolysis is the most suitable approach to reach both targets. In this review paper, the pyrolysis principle, the kinetics and the product distribution in three-phases are discussed firstly. Then the effects of operating parameters of the pyrolysis process on the quality and the application potential of the three-phase products, as well as the hazardous element distribution are discussed. To further solve the dominant concerns, such as the oil content in the solid residue, the pyrolytic oil quality and the migration of hazardous elements and heavy metals, the potentials of the catalytic pyrolysis and the co-pyrolysis with additives are also summarized. Also, the typical pyrolysis reactors are then presented. From the perspective of the energy efficiency and the non-hazardous disposal, the integrated technology combining the pyrolysis and the combustion for the OS management is recommended. Finally, the remaining challenges of OS pyrolysis encountered in the research and the industrial application are discussed and the related outlooks are itemized.

Hazardous elements flow during pyrolysis of oily sludge.

Oily sludge (OS) is a hazardous waste and pyrolysis is a promising technology to achieve energy recovery and non-hazardous disposal simultaneously. However, the distribution of hazardous elements, including N/S/Cl and heavy metals, in pyrolytic products possibly causes secondary pollution. This study conducted a systematic research on hazardous elements flow during OS pyrolysis under variant temperature. Results showed that N/S/Cl in OS were distributed 44.77-15.51 wt%, 83.29-80.22 wt%, and 78.59-73.41 wt% into the solid residues after pyrolysis, respectively. Elevating pyrolysis temperature facilitated more N/S/Cl flowing into pyrolytic oil and gas. The macromolecular N-/S-/Cl-containing compounds, including amides, amines, nitriles, sulfonates, chloroalkanes, etc., were widely distributed in pyrolytic oil and gas products. The micromolecular N-/S-/Cl-containing pollutants released between 200 and 400 °C included HCN, NH3, NOx, H2S, CH4S, CS2, SO2, and HCl, which originated from the decomposition of the amine N, organic sulfide and sulfone-S, and inorganic Cl, respectively. The main pollutants released at above 400 °C included NH3, HCN, NOx, CS2, and SO2, which were derived from the decomposition of heterocyclic N and inorganic pyritic-S and sulfate-S. Moreover, the solid residues intercepted more than 60.0 wt% of total heavy metals, which should be concerned in the future.

Effects of reaction conditions on products and elements distribution via hydrothermal liquefaction of duckweed for wastewater treatment.

Wastewater treatment by duckweed is a naturally sustainable technology. However, its development is limited due to the lack of a follow-up treatment of duckweed. The duckweed was proposed for the treatment of rural domestic wastewater and agricultural wastewater, and it was further processed to produce bio-oil via hydrothermal liquefaction at various temperatures (250 °C-370 °C) and residence times (15-60 min). The highest bio-oil yield of 35.6 wt% was obtained at 370 °C, 45 min. The higher heating value of bio-oil was 40.85 MJ/kg, and the H/C ratio (1.72-1.98) was similar to that of petroleum (1.84). The gas chromatography-mass spectrometry analysis results revealed that the bio-oil mainly consisted of N-heterocycles, cyclic ketones, esters, amides, long-chain hydrocarbons, phenols, and aromatic intermediates. Valuable compounds (3-pyridinol, 2-pyrrolidinone, and its analogues) of high concentration were identified in the water-soluble organic matter. Compared with other materials, this study produced higher-quality bio-oil and water-soluble organic matter.

The role of seashell wastes in TiO2/Seashell composites: Photocatalytic degradation of methylene blue dye under sunlight.

This paper proposes a sustainable and facile approach for the synthesis of photocatalysts in which shell waste is used as support material. The synthesized photocatalysts exhibited a significant performance in the mineralization of organic substances under solar irradiation or artificial lighting. Calcined abalone shell with a TiO2 loading of 23.4% led to a significant improvement in optical absorption: the degradation efficiencies of methylene blue (MB) after 140 min under UV light, vis light, UV-vis light, and natural sunlight were 93%, 96%, 100%, and 100%, respectively. Notably, the byproducts obtained after the degradation by commercial P25 TiO2 disappeared with the utilization of shell waste as support material. The Na, Sr, S present in the calcined abalone shell were doped into the substitutional sites of TiO2 and were indispensable to achieve the desired band-gap narrowing and photocatalytic performance; moreover, the Ti and Zn oxides in the calcined abalone shell acted as semiconductors and improved the charge separation efficiency of TiO2. Above all, this paper describes a green synthesis based on the use of waste seashell. This material acts as an excellent photocatalyst support for environmental pollution treatments, leading to the 'control of waste by waste' and opening up new possibilities for shell waste reutilization and sustainable chemistry.