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Benefit distribution of hybrid renewable energy system is related to the sustainability of its operation, and the distribution method of adjusting the share of power generation may affect its low-carbon effect. In order to investigate the method of benefit distribution that does not hinder renewable energy consumption, a two-stage dispatching model for hybrid wind-photovoltaic-thermal power system is established, and the ancillary service market is introduced to coordinate optimization. The first stage model aims at the equilibrium of power generation profits of power producers. Then in the second stage, the equilibrium profits are transformed into constraint, and the day-ahead dispatching model is constructed with the objective of minimizing comprehensive power purchase costs and maximizing renewable energy utilization after considering the balance of economy and social responsibility. The case study results are proved that the ancillary service market combined with profits guarantee constraint can optimize the benefit distribution of power producers without affecting the consumption of renewable energy as much as possible. The proposed strategy is more suitable for the areas where the power supply structure is still dominated by thermal power. Changes in dispatching results under different ancillary service prices are discussed, and management recommendations are put forward in the end. [ABSTRACT FROM AUTHOR]

Abstract: Range image analysis is one of the most important subjects in the fields of computer vision and pattern recognition, and range image segmentation is the key of the analysis. This paper presents a novel range image segmentation algorithm based on RHT (randomized Hough transform). The algorithm finds planar regions by utilizing RHT and has the advantage of insensitivity to noise. The proposed algorithm has been tested on a popular range image database (ABW image database) with comparisons to four other typical range image segmentation algorithms. The experiment results show that the proposed algorithm has a strong anti-noise ability and is well-performing in range image segmentation. [Copyright &y& Elsevier]

The existing literature demonstrates that the multi-energy combined power-dispatching system is crucial for resolving the mismatch between the installed capacity and the power generation through renewable energy. However, our knowledge of the impact mechanism of climate policies on this system is still limited. To address this gap, cost-accounting models that consider price fluctuation based on carbon emissions trading and renewable portfolio standards in China are proposed and applied to the integrated wind–photovoltaic–thermal power-dispatching system in Xinjiang. The scenarios analysis showed that in terms of reducing emissions, carbon emissions trading is more effective in cases with a high installed proportion of renewable power, whereas renewable portfolio standards are the opposite, as they are better in two cases in terms of energy saving. The sensitivity analysis indicates that the effect of renewable portfolio standards on the penetration rate of renewable power is constant. There is some potential for the design optimization of these two policies in China, and the characteristics of the power structure should be considered. These results can help the dispatching department in evaluating the impact of carbon emissions trading and renewable portfolio standards to optimize the dispatching strategy and provide directions for policy makers to improve the design. • Explore the interaction of carbon emissions trading and renewable portfolio standards. • Build costs accounting models for climate policies based on fluctuating price. • Analyze the dual effect of the policies in different hybrid power dispatching systems. • Propose policy recommendations to promote the application of policies in China. [ABSTRACT FROM AUTHOR]

• Establishing a dispatch model for integrated wind-photovoltaic-thermal power system. • Dynamic carbon emissions trading system applications in power market is considered. • Comprehensive benefits of five dispatch modes are compared. • Optimal mode was investigated using case study transmission project (China). To transmit renewable energy on-grid over a large-scale power transmission system, an optimal dispatch model for a multi-energy power generation system is essential. This paper proposed a multi-energy hybrid power dispatch model for an integrated wind-photovoltaic-thermal power system. We consider five different dispatch modes and a dynamic carbon emissions trading system. Design of the modes was based on dispatch objectives. Power dispatch was based on interactive planning of power units and carbon emissions trading. To compare the modes, a comprehensive benefit evaluation index for dispatching is established. The proposed model was applied to supporting power supply system of the Tianzhong ultra-high voltage direct-current transmission project in Xinjiang, China. The results confirmed that high-efficiency mode is an optimal dispatch mode for the power transmission system, and has the most significant benefits. The impact on the optimal mode of the renewable energy penetration rate and carbon emissions trading system, as the two main factors, were further investigated. It was found that high-efficiency mode could maximize existing renewable energy generation and reduce coal consumption and carbon emission used for power generation and has a positive effect on carbon reduction. However, initial quotas need to be controlled more strictly than prices. [ABSTRACT FROM AUTHOR]

[Display omitted] • Atomic layer deposition (ALD) used to fabricate metal–organic framework (MOF) materials is reviewed. • Seven combined methods using ALD technology and MOF synthesis are discussed. • Applications of MOF materials related to ALD technology are summarized. • New directions and perspectives for ALD-related MOF materials are provided. Atomic layer deposition (ALD) technology is an effective nanofabrication method used for various nanomaterials and thin films at the atomic level. Metal-organic framework (MOF) materials have a high porosity and specific surface area, and have been widely used in the fields of adsorption, separation, catalysis, sensors and devices. When ALD meets MOFs, some new combination methods can appear. In this review, the advances in MOFs synthesis related to ALD are summarized. These new synthetic methods of MOFs can be divided into seven categories: MOF gas-phase growth via ALD/MLD, MOF solvothermal growth on ALD metal oxide, MOF solvothermal growth and assembled on ALD metal oxide, MOF liquid-phase epitaxy growth on ALD metal oxide, MOF conversion from ALD metal oxide, MOF conversion via hydroxyl double salt from ALD metal oxide and MOF modification via ALD. Meanwhile, the upscaling applications of these ALD-related MOFs, such as in adsorption, separation, catalysis and energy, have further been reviewed. The perspectives of ALD based MOFs have also been provided. Such efforts are expected to provide guidance for developing new synthetic methods of MOFs related to ALD technology and thereby lead to new applications of ALD-related MOFs. [ABSTRACT FROM AUTHOR]

The coordination and electron configuration of radialene complexes CpM(C 2n H 2n ) (n = 3, 4) are investigated. For M = Sc, Ti, Fe, Co, Ni, the ground states of CpM(C 2n H 2n ) are low-spin states (singlet or doublet), while for M = V, Cr, Mn, the ground states are high-spin states (triplet or quartet). For M = Sc, Ti, V, Cr, Mn, Fe, Co, Ni, [3]radialene in the ground states of CpM(C 6 H 6 ) are ŋ 6 -, ŋ 6 -, ŋ 6 -, ŋ 4 -, ŋ 4 -, ŋ 4 -, ŋ 4 -, and ŋ 2 -coordinated; and [4]radialene in the ground states of CpM(C 8 H 8 ) are ŋ 8 -, ŋ 8 -, ŋ 6 -, ŋ 4 -, ŋ 4 -, ŋ 4 -, ŋ 4 -, and ŋ 2 -coordinated, respectively. Between metal atom and radialene in CpM(C 2n H 2n ), the metal-alkene interactions, which are caused by the exocyclic C C π-bonds that donate the lone pair electrons to the empty d-orbitals of metal atom, are dominant and fundamental. Besides, the special π-backbonding metal-aromatic interactions, which is overlapped by the lone pair on metal atom and the empty 2π-aromatic orbital on the cyclic C 3 or C 4 ring of [n]radialenes, may also exist in some ground states of CpM(C 2n H 2n ) complexes. [ABSTRACT FROM AUTHOR]

[Display omitted] • Reactions of bis(cyclopentadienyl) ruthenium (ruthenocene, RuCp 2) and cyclopentadienyl pyrrolyl ruthenium (RuCpPy) on the hydroxylated surface were explored by density functional theory calculations. • Ru precursors, such as bis(pyrrolyl) ruthenium (RuPy 2), were designed for H 2 O-based atomic layer deposition of RuO 2 · x H 2 O. • New cascade mechanism of H 2 O-based atomic layer deposition of RuO 2 · x H 2 O was proposed. As the unique nanofabrication technique, atomic layer deposition (ALD) can be used to deposit high-quality, uniform, and conformal nanoparticle coatings. Ru and its oxides (RuO x) are important materials in the fields of microelectronics and catalysis. In this work, the reaction of Ru precursors with different ligands on the hydroxylated surfaces were explored. The elimination of the pyrrolyl (Py) ligand is easier than that of the cyclopentadienyl (Py) ligand on the hydroxylated surface. The reaction involved in RuO 2 · x H 2 O ALD using RuPy 2 and H 2 O as precursors was further investigated. During the RuPy 2 reaction, the pyrrolyl ligand is eliminated by the substitution reaction with a surface hydroxyl group. However, the desorption of the pyrrole molecule is difficult due to the strong adsorption between the pyrrole molecule and Ru surface. During the H 2 O reaction, the H 2 O molecules further help the elimination of pyrrolyl ligands from the surface and the dissociative desorption of pyrrole molecules This unique reaction mechanism involved in the ALD of RuO 2 with the assistance of H 2 O can be termed new cascade mechanism. These findings provide theoretical guidance for precursor design and ALD growth of metal oxides. [ABSTRACT FROM AUTHOR]

• A novel binary metal sulfide Ni 3 Bi 2 S 2 is predicted to be synthesized from Bi 2 S 3 and Ni powder using DFT calculation. • Ni 3 Bi 2 S 2 proved a high-capacity, high-reversible, and easy-synthesized anode for sodium-ion batteries first. • Heterojunction-like Ni 3 Bi 2 S 2 /NiS-G composites surpassing most of the recently-reported same-type of sodium-ion batteries. In the context of scalable electrode production via ball-milling, achieving high cycling stability and electrochemical performance in bifunctional anodes for sodium ion batteries (SIBs) is crucial yet remains a significant challenge. To address these objectives, we have developed a unique hybrid anode nanocomposite characterized by its local multiphase nature. This composite involves the incorporation of novel ternary-Ni-Bi-S/binary-Ni-S nanomaterials onto exfoliated graphite nanosheets (Ni 3 Bi 2 S 2 /NiS-G) through a facile ball-milling process. Our combined experimental and theoretical investigations suggest that the interactions between graphite nanosheets and the layered structure of Ni 3 Bi 2 S 2 /NiS, along with the discharge products of Na 2 S, play pivotal roles in enhancing the Na+ diffusion rate and stability of the hierarchical configuration anode. Upon testing, the novel Ni 3 Bi 2 S 2 /NiS-G shows overwhelmingly higher electrochemical performance compared to the Ni 3 Bi 2 S 2 /NiS counterpart, the Ni 3 Bi 2 S 2 /NiS-G delivered a reversible capacity of 489.9 mAh/g at 0.2 A/g after 400 cycles, and displayed a high capacity of 387.3 and 339.6 mAh/g after 500 cycles at 1 A/g and 2 A/g, respectively, yielding a high capacity retention ratio of 84.8 % and 82.8 % of the 1st cycle. This work provided a novel approach for developing new bifunctional anode electrodes with high capacity and rate performance as well as superior cycling stability. [ABSTRACT FROM AUTHOR]

Substituting renewable energy for coal power under the carbon neutrality goal is an inevitable path for power system transformation, while the high share of renewable energy leads to a rapid rise in system flexibility demand. Currently, coal-fired power is still one of the most economical and reliable large-scale flexible resources in China. Therefore, the issue of how to mitigate the conflict between cleanliness and flexibility for coal-fired power is urgent to be solved. Accordingly, this paper established an optimization framework for the retirement and technology adoption of coal-fired power units with high spatial-temporal resolution, and the regional carbon emission budget is estimated from a top-down perspective. Secondly, a dynamic carbon quota allocation method considering technological innovation and adoption is proposed. The carbon trading cost of the units is evaluated from a bottom-up perspective, to realize the interaction between the obligatory policy constraints of the top-level target and the flexible incentives of the market mechanism. Finally, the empirical analysis was conducted in the Beijing-Tianjin-Hebei region of China. The optimal solution achieved by proposed method results in a substantial 27% reduction in total costs while keeping the increase in carbon emissions below 3%. By analyzing the dynamic evolution path of coal and the scale of diffusion of multi-type technologies, the differences in the roles coal power assuming at various stages of decarbonization are discussed. The robustness of the model and the validity of the proposed method were verified by comparing the dynamic/static carbon quota allocation. Overall, this study provides an effective optimization model for investigating the low-carbon technology adoption timing for coal power in Beijing-Tianjin-Hebei region, and offers valuable insights for other coal-dominated emerging economies seeking for power system transformation roadmap in the forthcoming net-zero carbon age. • A decision-making optimization model of CCPs low-carbon technology is proposed. • A dynamic CET system with upper-lower layer interaction is introduced. • The proposed dynamic CET system results in 27% reduction in total costs. • The high-resolution data of coal power in Beijing-Tianjin-Hebei region are used. • The strategy to solve the conflict between cleanliness and flexibility is given. [ABSTRACT FROM AUTHOR]

Abstract: Realizing the Semantic Web involves creating ontologies, a tedious and costly challenge. Reuse can reduce the cost of ontology engineering. Semantic Web ontologies can provide useful input for ontology reuse. However, the automated reuse of such ontologies remains underexplored. This paper presents a generic architecture for automated ontology reuse. With our implementation of this architecture, we show the practicality of automating ontology generation through ontology reuse. We experimented with a large generic ontology as a basis for automatically generating domain ontologies that fit the scope of sample natural language web pages. The results were encouraging, resulting in five lessons pertinent to future automated ontology reuse study. [Copyright &y& Elsevier]

At present, vigorously developing wind power, photovoltaic and other renewable energy has become one of the effective ways to deal with carbon dioxide emissions and energy supply and demand gap. Bringing renewable energy into the optimal configuration of power supply structure and reducing carbon emissions at the root will help promote the construction of clean, low-carbon, safe and efficient modern energy system. Therefore, starting from the theory of low-carbon economy, based on the traditional power planning model, this paper considers various uncertainties, introduces social welfare theory, and proposes the optimization scheme of thermal-solar-wind power system. The model is then applied to Southern Xinjiang supporting power project to study the investment behavior of low-carbon power, and the optimal low-carbon power decision-making behavior considering social benefits based on welfare is obtained. The results show that the proposed optimal configuration scheme of hybrid power can achieve the equilibrium between economic and social benefits, improve energy utilization efficiency and provide decision-making reference for policy makers. • A multi-objective power planning optimization model considering social benefits and economic cost was proposed. • Multi-uncertainty and interactions among multiple random variables were examined. • Solutions of various scenarios and different credibility levels were analyzed. • The optimization model can achieve better economic benefits while improving energy efficiency. [ABSTRACT FROM AUTHOR]

The LiNi 0.8 Co 0.1 Mn 0.1 O 2 cathode is susceptible to degradation due to the presence of trace amounts of HF generated from H 2 O interacting with the electrolyte salt LiPF 6. In this work, Al 2 O 3 -decorated carbon nanotubes was introduced as a conductive additive to safeguard the LiNi 0.8 Co 0.1 Mn 0.1 O 2 cathode, resulting in a significant enhancement of its reversible capacity and cycling stability. The electrode incorporated of Al 2 O 3 /CNTs delivered an initial discharge capacity of 184.1 mAh g−1 at 200 mA g−1 under 1.0 C, and retained 65.6 % of its capacity at 100th cycle, outperforming traditional electrodes. The synthesis of Al 2 O 3 /CNTs involves only two straightforward steps: precipitation and heat treatment. Additionally, the amount of this additive occupies a mere 2.0 wt% of the overall electrode material, making it suitable for large-scale applications. • Al 2 O 3 /CNTs was ultilized to elimiate the side reactions of the LiNi 0.8 Co 0.1 Mn 0.1 O 2 cathode. • The preparation processes of Al 2 O 3 /CNTs is very simple. • The material process is suitable for industrial applications. [ABSTRACT FROM AUTHOR]

[Display omitted] • Multifunctional Co atoms are doped on the twin Mn 0.3 Cd 0.7 S homojunction surface. • Co atoms regulate S electron property and build a fast H-migration channel at S sites. • H migration endows sufficient H to sustain HER and reduces the H 2 evolution barrier. • Co atoms on the cubic phase act as OER active sites to enhance oxidation activity. • The Z-scheme interfacial charge-transfer mechanism is achieved. Low kinetics of water dissociation, unfavorable hydrogen adsorption, and high water-oxidation barriers restrict the photocatalytic overall water splitting (OWS) efficiency over sulfides. Herein, multifunctional Co atoms are doped on the twin Mn 0.3 Cd 0.7 S homojunction surface for efficient photocatalytic hydrogen (H 2) and oxygen (O 2) evolution. An ultrafast hydrogen atom (H*) migration channel bridging the water dissociation/H 2 evolution step is established between cubic-S and hexagonal-S sites by introducing Co atoms, facilitating the HER kinetics. Specifically, Co atoms regulate the electron properties of neighboring S atoms and weaken their charge accumulation, which promotes cubic-S sites to capture sufficient H* from the water dissociation zone and accelerates hexagonal-S sites to release H 2 through the H* migration channel. Meanwhile, unsaturated Co atoms on the cubic phase as oxygen evolution reaction (OER) sites promote water deprotonation and optimize the kinetics of the rate-determining step to form OOH* intermediate, enhancing water oxidation activity. Co atoms strengthen the internal electric field of the homojunction and local polarized electric field by increasing the work function difference between the two phases and introducing the high spin polarization, inhibiting the bulk and surface recombination of photogenerated carriers. The Co 0.01 Mn 0.29 Cd 0.7 S exhibits visible-light-driven H 2 and O 2 evolution rates of 443.12 and 219.67 μmol g−1 h−1, about 50 times that of the Mn 0.3 Cd 0.7 S. This work provides some guidance for the design of homojunction photocatalysts with efficient OWS performance. [ABSTRACT FROM AUTHOR]

The objective of the traditional dispatching optimization model is to find the most economical scheduling mode, while ignoring the efficient use of renewable energy. To properly arrange thermal power generation and renewable energy power generation, this paper constructs an optimization model of the combined wind–photovoltaic (PV)–thermal dispatching system under a carbon emissions trading (CET) mechanism. The contribution of this paper is twofold. First, a dispatching optimization model is proposed, which not only considers the total cost but also takes into account the impact of the renewable energy spillage rate on the dispatching system. As a factor affecting renewable energy consumption, a carbon emissions trading mechanism has also been introduced into the dispatching system. The second contribution is to develop a model for predicting the output of renewable energy generation. Then, the optimization model is applied to the auxiliary power dispatching system of the Tianzhong ±800 kV UHV DC transmission channel in Xinjiang. The results indicate that under a carbon emissions trading mechanism, thermal power generation will be limited by the carbon emissions cost, thereby reducing the total cost of the system. Optimizing the spillage rate increases the share of renewable energy in the dispatching system, resulting in a 3.5% reduction in the actual spillage rate. The proposed model alleviates the serious problem of electricity being abandoned in the existing scheduling mode and helps to realize economical low-carbon dispatching of the power system. [ABSTRACT FROM AUTHOR]

Abstract Despite their high theoretical capacity, the practical commercialization of lithium-sulfur batteries have continued to face obstacles of low cycle stability and low efficiency, which stem from the dissolution and diffusion of lithium polysulfides intermediates in the electrolyte. Here, by means of comprehensive density functional theory computations, we exploited the potentials of the experimentally available metal-nitrogen/graphene as the anchoring material for high-performance Li-S batteries. Our results revealed that Cr-, Mn-, Fe-, Co-, and Cu-nitrogen/graphenes exhibit optimal interaction with soluble lithium polysulfides due to the synergistic effects between the metal and N atoms, which not only effectively traps the soluble lithium polysulfides to suppress the shuttle effects, but also well keeps their cyclic structures intact. Especially, the electronic properties of metal-nitrogen/graphenes are well preserved, and the computed voltages of discharge processes are larger than those of the well-established nitrogen-doped graphenes. Thus, the metal-nitrogen/graphene could present a kind of quite promising anchoring material for lithium sulfur battery cathodes to suppress the lithium polysulfides shuttle effect. Graphical abstract Unlabelled Image Highlights • Metal-N 4 /graphene restrains the shuttle effect via remarkable (but not strong) binding strength with Li 2 S n species. • The intactness of Li 2 S n species is well preserved after adsorption on metal-N 4 /graphene. • The conductance of metal-N 4 /graphene is nearly unchanged after adsorption of Li 2 S n species. • The computed voltages of discharge processes are larger than those of well-established N-doped graphenes. [ABSTRACT FROM AUTHOR]

[Display omitted] • Aluminum precursors bearing alkyl, hydrogen, halide, alkoxy and amino ligands were designed and investigated for Al 2 S 3 atomic layer deposition (ALD). • Amino ligands of aluminum precursors have the self-catalytic role and accelerate the reaction of Al 2 S 3 ALD. • Unlike the concerted elimination of the first amino ligand of aluminum precursors, the elimination of the second amino ligands on the surface is a stepwise process. As a unique nanotechnology, atomic layer deposition (ALD) has been extensively used for the preparation of various nanomaterials. An effective precursor is a prerequisite to ALD success. Herein, we designed and introduced alkyl, hydrogen, halide, alkoxy and amino ligands to aluminum precursors and investigated reaction mechanisms of Al 2 S 3 ALD through density functional calculations. The results show that aluminum precursors with alkyl, hydrogen and halide ligands are kinetically disadvantageous and with alkoxy groups are thermodynamically unfavorable and Al precursors bearing amino groups are thermodynamically and kinetically favorable for Al 2 S 3 ALD. The activity of trimethylaluminum (TMA) on the sulfydrylated surface is lower than that on the hydroxylated surface. The reaction barriers of the aluminum precursors bearing amino ligands on the sulfydrylated surface are obviously lower than that of TMA. Similarly, the barrier of the H 2 S reaction on the aminated surface is much lower than that on the methylated surface. All of the amino groups have a self-catalytic role and accelerate the reaction of Al 2 S 3 ALD. These insights into aluminum precursors bearing amino ligands for Al 2 S 3 ALD can provide theoretical guidance for the discovery of new precursors and the ALD preparation of other aluminum and sulfur compounds. [ABSTRACT FROM AUTHOR]

A series of liquid hydrocarbons (alkylbenzenes, alkanes, and alkenes) were obtained by a synergetic deoxy reforming (SDR) process of cellulose and linoleic acid methyl ester (LAME) at 350 °C and 4–6 MPa in a closed system without external source of hydrogen. The liquid product was obtained with a yield of 15 wt% at a LAME/cellulose ratio of 0.2. In contrast, the direct deoxy reforming of cellulose produces oil that contains plenty of phenols and oxygen-containing compounds. Due to the insufficiency of water employed (30 wt%), a radical reaction pathway was proposed. Quantum chemical calculations indicate that the radicals from LAME interfere with the reactions of the intermediate products from cellulose, being responsible for the removal of phenols and the formation of hydrocarbons. The SDR process offers an embryonic insight in an alternative technique for preparation of hydrocarbon fuels. [ABSTRACT FROM AUTHOR]

NiFe-based nanostructures have been attracting attentions as a promising non-noble metal electrocatalysts for oxygen evolution reaction in alkaline. In this paper, a bionic sunflower-like NiFe-polydopamine film was prepared via self-polymerization of dopamine-Ni2+/Fe3+ followed by partial pyrolysis process. In the films, NiO quantum dots are embedded in Fe-coupled polydopamine due to the space-confined effect of PDA. The self-activation process effect led to in-situ reconstruction of the generation of NiOOH and the migration of Fe sites to NiOOH surface. Abundant Fe sites on the NiOOH surface facilitated formation of stable O* intermediate. Moreover, the coordination-confined effect of PDA for Fe ions in the PDA network gave the PDANF catalyst excellent durability. The NiFe-polydopamine film exhibited excellent intrinsic OER activity with a low overpotential of 254.1 mV for 10 mA cm−2 and an unprecedentedly low Tafel slope of 23.3 mV dec−1. [Display omitted] • The bionic sunflower-like structure of metal-organic OER catalyst have been prepared. • The space-limiting effect of polydopamine leaded to the ultra-small size of NiO. • In situ reconstitution of the catalyst was induced by electrochemical activation. • Enrichment of Fe on the surface of NiOOH QDs provides abundant high-activity sites. • The catalyst exhibited high intrinsic activity and durability for OER reaction. [ABSTRACT FROM AUTHOR]

Abstract: The detection of lead ion is very important both in environment and in biological systems because of its toxicity. A fluoroionophore sensor, N-[4(1-pyrene)-butyroyl]-l-tryptophan (PLT), distinguishing Pb2+ from other 12 metal ions and exhibiting a very high sensitivity (0.15μM) in aqueous solution, has been reported. The present study describes the spectroscopic clarification of the intrinsic differences of the binding model between PLT with Pb2+ and with other ions. The fluorescent property of solid metal carboxylates reflects a character of the metal complex in solution, which results in a facility to solve problems by using solid sample of complex and vibrational spectroscopy. Both FT-infrared and Raman spectroscopy are employed to clarify the binding model between lead ion and its high sensitive and selective fluoroionophore sensor PLT, and essentially to explain why the metal ions other than Pb2+ cannot response to PLT. The IR spectral data clearly show that a bridging bidentate coordination occurs when PLT is coordinated with Cu2+ and Zn2+; while a chelating bidentate coordination between the carboxyl anion and Pb2+ exists in PLT–Pb, which is a new information beyond the NMR results in previous report. Meanwhile, the present study also indicates a characteristic interaction of lead ion and indole ring as well as the hydrogen bonding between amide groups. Furthermore, the quantum chemical calculations at the DFT level confirm the spectral and structural information of PLT–Pb2+ proposed by experiments. Thus, the type of coordination, the interaction of the indole ring with the metal ion, and the hydrogen bonding between amide groups in PLT–Pb are likely responsible for the high selectivity of PLT to the lead(II) ion. [Copyright &y& Elsevier]

Microaeration (dosing small quantities of air or oxygen) is an effective approach to facilitate anaerobic digestion (AD) process and has gained increased attention in recent years. The underlying mechanisms of the facilitation effect of microaeration on AD process were reviewed in terms of accelerating hydrolysis, scavenging hydrogen sulfide, and affecting microbial diversity. Process parameters and control strategies were summarized to reveal considerable factors in implementing microaeration-based AD process. In addition, current applications, including lab-, pilot- and full-scale level cases, were summarized to provide guidance for further improvement in large-scale applications. The challenges and future perspectives were also highlighted to promote the development of AD process associated with microaeration. Unlabelled Image • Microaeration in AD system facilitates processing efficiency and system stability. • The presence of oxygen leads to a high yield of facultative acidogens and excreted enzymes. • Microaeration rate is the foremost parameter connected to the AD performance. • The combination of aeration and AD has been applied in full-scale implementation successfully. [ABSTRACT FROM AUTHOR]