Review of renewable energy-based hydrogen production processes for sustainable energy innovation

In this review,we primarily analyze the hydrogen production technologies based on water and biomass,including the economic,technological,and environmental impacts of different types of hydrogen production technologies based on these materials,and comprehensively compare them.Our analyses indicate that all renewable energy-based approaches for hydrogen production are more environmentally friendly than fossil-based hydrogen generation approaches.However,the technical ease and economic efficiency of hydrogen production from renewable sources of energy needs to be further improved in order to be applied on a large scale.Compared with other renewable energy-based methods,hydrogen production via biomass electrolysis has several advantages,including the ease of directly using raw biomass.Furthermore,its environmental impact is smaller than other approaches.Moreover,using a noble metal,catalyst-free anode for this approach can ensure a considerably low power consumption,which makes it a promising candidate for clean and efficient hydrogen production in the future.

Strategies for CO2 capture from different CO2 emission sources by vacuum swing adsorption technology

Different VSA(Vacuum Swing Adsorption) cycles and process schemes have been evaluated to find suitable process configurations for effectively separating CO2 from flue gases from different industrial sectors. The cycles were studied using an adsorption simulator developed in our research group, which has been successfully used to predict experimental results over several years. Commercial zeolite APGIII and granular activated carbon were used as the adsorbents. Three-bed VSA cycles with- and without-product purge and 2-stage VSA systems have been investigated. It was found that for a feed gas containing 15% CO2(representing flue gas from power plants), high CO2 purities and recoveries could be obtained using a three-bed zeolite APGIII VSA unit for one stage capture, but with more stringent conditions such as deeper vacuum pressures of 1–3 k Pa. 2-stage VSA process operated in series allowed us to use simple process steps and operate at more realistic vacuum pressures. With a vacuum pressure of 10 k Pa, final CO2 purity of 95.3% with a recovery of 98.2% were obtained at specific power consumption of 0.55 MJ·(kg CO2)-1from feed gas containing15% CO2. These numbers compare very well with those obtained from a single stage process operating at1 k Pa vacuum pressure. The feed CO2 concentration was very influential in determining the desorption pressure necessary to achieve high separation efficiency. For feed gases containing N 30% CO2, a singlestage VSA capture process operating at moderate vacuum pressure and without a product purge, can achieve very high product purities and recoveries.

Research Progress for the Development of Li-Air Batteries: Addressing Parasitic Reactions Arising from Air Composition

Li-air batteries are an extremely attractive technology for electrical energy storage,especially in long-range electric vehicles,owing to their high theoretical specific energy.However,many issues still exist before their practical realization.Herein,the sole complexity of electrode reaction in Li-air batteries is presented.And the critical components that influence the electrochemical performance of aprotic Li-air batteries operating in ambient air are discussed.These include the mechanisms and pathways of CO_(2)/Li_(2)CO_(3) and H_(2)O/LiOH,catalysts of CO_(2) reduction/evolution reactions,and reactions between the Li anode and air constituents.If these challenges can be solved,Li-air batteries will soon be realized for practical application.Some hot topics in field of Li-air batteries should be focused,such as the fundamental mechanism research referring to interfacial reactions of atmosphere components on porous electrode and Li metal anode,high-efficiency solid catalyst design,and discovery of suitable soluble redox mediators.

Hollow ZSM-5 encapsulated with single Ga-atoms for the catalytic fast pyrolysis of biomass waste

The development of efficient metal-zeolite bifunctional catalysts for catalytic fast pyrolysis(CFP) of biomass waste is highly desirable for bioenergy and renewable biofuel production.However,conventional metal-loaded zeolites often suffer from metal sintering during pyrolysis and are thus inactivated.In this study,single-site Ga-functionalized hollow ZSM-5(GaO_x@HS-Z5) was synthesized via an impregnationdissolution-recrystallization strategy without H_(2) reduction.The Ga atom was coordinated to four oxygen atoms in HS-Z5 frameworks.Benefitting from the highly dispersed single-Ga atoms and hollow zeolite framework,3GaO_x@HS-Z5 performed the best in producing hydrocarbon-rich bio-oil compared to impregnated 3GaO_x/HS-Z5 and H_(2)-reduced 3Ga@HS-Z5 in the maize straw CFP.In particular,3GaO_x@HS-Z5 delivered the highest bio-oil yield(23.6 wt%) and hydrocarbon selectivity(49.4 area%).3GaO_x@HS-Z5 also retained its structural integrity and catalytic activity after five pyrolysis-regeneration cycles,demonstrating its advantage in practical biomass CFP.The elimination of H_(2) reduction during the synthesis of catalyst provides an additional advantage for simplifying the CFP process and reducing operating costs.The retained Ga micro-environment and anti-sintering properties were unique for 3GaO_x@HS-Z5,as severe metal sintering occurred during pyrolysis for other metals(e.g.,NiO_x,ZnO_x,FeO_x,and CoO_x) that encapsulated HS-Z5.

Accurate design of spatially separated double active site in Bi_(4)NbO_(8)Cl single crystal to promote Z-Scheme photocatalytic overall water splitting

The efficiency of photocatalytic overall water splitting was mainly limited by the slow reaction kinetics of water oxidation.How to design effective surface active site to overcome the slow water oxidation reaction was a major challenge.Here,we propose a strategy to accelerate surface water oxidation through the fabrication spatially separated double active sites.FeCoPi/Bi_(4)NbO_(8)Cl-OVs photocatalyst with spatially separated double active site was prepared by hydrogen reduction photoanode deposition method.Due to the high matching of the spatial loading positions of FeCoPi and OVs with the photogenerated charge distribution of Bi_(4)NbO_(8)Cl and corresponding reaction mechanisms of substrate,the FeCoPi and OVs on the(001)and(010)crystal planes of Bi_(4)NbO_(8)Cl photocatalyst provided surface active site for water oxidation reaction and electron shuttle reaction(Fe^(3+)/Fe^(2+)),respectively.Under visible light irradiation,the evolution O_(2)rate of FeCoPi/Bi_(4)NbO_(8)Cl OVs was 16.8μmol h^(-1),as 32.9 times as Bi_(4)NbO_(8)Cl.Furthermore,a hydrogen evolution co-catalyst PtRu@Cr_(2)O_(3)was prepared by sequential photodeposition method.Due to the introduction of Ru,the Schottky barrier between PbTiO_(3)and Pt was effectively reduced,which promoted the transfer of photogenerated electrons to PtRu@Cr_(2)O_(3)thermodynamically,the evolution H_(2)rate on PtRu@Cr_(2)O_(3)/PbTiO_(3)increased to 664.8 times.On based of the synchronous enhancement of the water oxidation performance on FeCoPi/Bi_(4)NbO_(8)Cl-OVs and water reduction performance on PtRu@Cr_(2)O_(3)/PbTiO_(3),a novel Z-Scheme photocatalytic overall water splitting system(FeCoPi/Bi_(4)NbO_(8)Cl-OVs)mediated by Fe^(3+)/Fe^(2+)had successfully constructed.Under visible light irradiation,the evolution rates of H_(2)and O_(2)were 2.5 and 1.3μmol h^(-1),respectively.This work can provide some reference for the design of active site and the controllable synthesis of OVs spatial position.On the other hand,the hydrogen evolution co catalyst(PtRu@Cr_(2)O_(3))and the co catalyst FeCoPi for oxygen evolution contributed to the construction of an overall water splitting system.

CO_(2)-capture research and Clean Energy Technologies Research Institute(CETRI)of University of Regina,Canada:history,current status and future development

Clean Energy Technologies Research Institute(CETRI)was formerly known as the International Test Centre for CO_(2)Capture in the early 2000s.The original focus of the centre was to help lower the carbon intensity of the current energy sources to low-carbon ones in Canada.Currently,CETRI’s mandates have expanded and now include most of the low-carbon and near-carbon-free clean-energy research activities.Areas of research focus include carbon(CO_(2))capture,utilization and storage(CCUS),near-zero-emission hydrogen(H_(2))technologies,and waste-to-renewable fuels and chemicals.CETRI also brings together one of the most dynamic teams of researchers,industry leaders,innovators and educators in the clean and low-carbon energy fields.

动力锂离子电池Li3V2(PO4)3正极材料的研究进展

阐述了Li3V2(PO4)3研究的重要意义,综述了动力锂离子电池Li3V2(PO4)3正极材料的研究现状,重点对Li3V2(PO4)3材料的结构特点、电化学性能、充放电机制、合成方法以及掺杂改性进行了总结和探讨。展望了Li3V2(PO4)3材料的发展趋势,并认为采用Li3V2(PO4)3作为正极材料,是今后高性能动力锂离子电池的发展趋势。

Status and challenges facing representative anode materials for rechargeable lithium batteries

Rechargeable lithium batteries have been widely regarded as a revolutionary technology to store renewable energy sources and extensively researched in the recent several decades.As an indispensable part of lithium batteries,the evolution of anode materials has significantly promoted the development of lithium batteries.However,since conventional lithium batteries with graphite anodes cannot meet the ever-increasing demands in different application scenarios(such as electric vehicles and large-scale power supplies)which require high energy/power density and long cycle life,various improvement strategies and alternative anode materials have been exploited for better electrochemical performance.In this review,we detailedly introduced the characteristics and challenges of four representative anode materials for rechargeable lithium batteries,including graphite,Li_(4)Ti_(5)O_(12),silicon,and lithium metal.And some of the latest advances are summarized,which mainly contain the modification strategies of anode materials and partially involve the optimization of electrode/electrolyte interface.Finally,we make the conclusive comments and perspectives,and draw a development timeline on the four anode materials.This review aims to offer a good primer for newcomers in the lithium battery field and benefit the structure and material design of anodes for advanced rechargeable lithium batteries in the future.

Modification of CaO-based sorbents prepared from calcium acetate for CO_2 capture at high temperature

CaO-based sorbent is considered to be a promising candidate for capturing CO_2 at high temperature. However,the adsorption capacity of CaO decreases sharply with the increase of the carbonation/calcination cycles. In this study, CaO was derived from calcium acetate(CaAc_2), which was doped with different elements(Mg, Al,Ce, Zr and La) to improve the cyclic stability. The carbonation conversion and cyclic stability of sorbents were tested by thermogravimetric analyzer(TGA). The sorbents were characterized by N_2 isothermal adsorption measurements, scanning electron microscopy(SEM) and X-ray diffraction(XRD). The results showed that the cyclic stabilities of all modified sorbents were improved by doping elements, while the carbonation conversions of sorbents in the 1st cycle were not increased by doping different elements. After 22 cycles, the cyclic stabilities of CaO–Al, CaO–Ce and CaO–La were above 96.2%. After 110 cycles, the cyclic stability of CaO–Al was still as high as 87.1%. Furthermore, the carbonation conversion was closely related to the critical time and specific surface area.

Quantitative Analysis of Carbon Content in Bituminous Coal by Laser-Induced Breakdown Spectroscopy Using UV Laser Radiation

The carbon content of bituminous coal samples was analyzed by laser-induced breakdown spectroscopy. The 266 nm laser radiation was utilized for laser ablation and plasma generation in air. The partial least square method and the dominant factor bused PLS method were used to improve the measurement accuracy of the carbon content of coal. The results showed that the PLS model could achieve good measurement accuracy, and the dominant factor based PLS model could further improve the measurement accuracy. The coefficient of determination and the root-mean-square error of prediction of the PLS model were 0.97 and 2.19%, respectively; and those values for the dominant factor based PLS model were 0.99 and 1.51%, respectively. The results demonstrated that the 266 nm wavelength could accurately measure the carbon content of bituminous coal.

Accuracy improvement of quantitative analysis of calorific value of coal by combining support vector machine and partial least square methods in laser-induced breakdown spectroscopy

Laser-induced breakdown spectroscopy(LIBS) is a potential technology for online coal property analysis,but successful quantitative measurement of calorific value using LIBS suffers from relatively low accuracy caused by the matrix effect.To solve this problem,the support vector machine(SVM) and the partial least square(PLS) were combined to increase the measurement accuracy of calorific value in this study.The combination model utilized SVM to classify coal samples into two groups according to their volatile matter contents to reduce the matrix effect,and then applied PLS to establish calibration models for each sample group respectively.The proposed model was applied to the measurement of calorific values of 53 coal samples,showing that the proposed model could greatly increase accuracy of the measurement of calorific values.Compared with the traditional PLS method,the coefficient of determination(R2) was improved from 0.93 to 0.97,the root-mean-square error of prediction was reduced from 1.68 MJ kg-1 to1.08 MJ kg-1,and the average relative error was decreased from 6.7% to 3.93%,showing an overall improvement.

A 150000 t·a^(-1) Post-Combustion Carbon Capture and Storage Demonstration Project for Coal-Fired Power Plants

1.Introduction Climate change is one of the most severe challenges facing the world today.At present,China produces total annual carbon dioxide(CO_(2))emissions of over 10 billion tonnes,topping the world in this regard.Although coal empowers China’s economic development,its use presents a great challenge to the nation’s desired goals of peaking carbon emissions and achieving carbon neutrality.In this context,the low-carbon utilization of coal is an inevitable trend for future development.Exploring new ways to reduce CO_(2) emissions on a large scale in the utilization of coal—especially during coal-fired power generation—is essential in order for China to achieve carbon neutrality.

The synthesis and application of zeolitic material from fly ash by one-pot method at low temperature

A new route to prepare zeolitic material was introduced in this work. Compared with traditional methods, the new route showed lower energy consume. The effect of pre-treatment conditions on structure and crystalline phase was investigated, revealing that the mullite crystalline phase in fly ash could be converted to amorphous phase by alkali at low temperature. The removal performance of heavy metal ions on designed material was also investigated, and we found that the intermediate product showed higher adsorption capacity on Ni^(2+) than zeolite A.

Effect of pre-calcination for modified CaO-based sorbents on multiple carbonation/calcination cycles

In the present work,the effect of pre-calcination on carbonation conversion and cyclic stability of modi fied CaObased sorbent was investigated by thermogravimetric analyzer(TGA).The modi fied CaO-based sorbents with CaAc_2 as precursor were respectively doped with different elements(Mg,Al,Ce,Zr and La).The speci fic surface area,pore volume and pore size distribution were tested by N_2 isothermal adsorption measurements.The phase compositions of sorbents were characterized by X-ray diffraction(XRD).The results showed that the cyclic stabilities of the sorbents were improved by pre-calcination.The pre-calcination was conducted at 900°C for 5 h in air by the muf fle furnace.With pre-calcination,the cyclic stabilities of sorbents could be as high as 96% after 22 cycles,such as CaO-Al,CaO-Ce and CaO-La.After contact with air,the carbonation conversions of spent sorbents with pre-calcination suddenly increased by about one-sixth due to the change of channel structure by hydration.Both the cyclic stability of sorbent and the durability of reactivation were related to the structural stability of sample,especially the stability of mesopores between 2 nm and 5.5 nm.The present work also provided an easy and low-cost method for reactivating the spent CaO-based sorbents.

Hybrid polymer electrolyte for Li–O_2 batteries

Li–O_2 batteries have attracted much attention because of their high specific energy. However, safety problem generated mainly from the flammable organic liquid electrolytes have hindered the commercial use of Li–O_2 batteries. One of the competitive alternatives is polymer electrolytes due to their flexibility and non-flammable property. Moreover, the hybrid polymer electrolyte with enhanced electrochemical properties would be achieved by incorporating inorganic filler, liquid plasticizer and redox mediator into the polymer. While most researches of the hybrid polymer electrolyte focused on Li-ion batteries, few of them took account into its application in Li–O_2 batteries. In this review, we mainly discuss hybrid polymer electrolytes for Li–O_2 batteries with different composition. The critical issues including conductivity and stability of electrolytes are also discussed in detail. Our review provides some insights of hybrid polymer electrolytes for Li–O_2 batteries and offers necessary guidelines for designing the suitable hybrid polymer electrolyte for Li–O_2 batteries as well.

Synergistic effect of polyoxometalate solution and TiO_2 under UV irradiation to catalyze formic acid degradation and their application in the fuel cell and hydrogen evolution

The synergistic effect of H_3PMo_(12)O_(40) or H_3PW_(12)O_(40) polyoxometalate solution(POM) and TiO_2 to catalyze formic acid oxidation was investigated. Under UV irradiation, hole and electron were photogenerated by TiO_2. Formic acid was oxided by the photogenerated hole and photogenerated electron was transferred to reduce polyoxometalate. With this design, formic acid can be converted into electricity in the fuel cell and hydrogen can be generated in the electrolysis cell without noble metal catalyst. Unlike other noble metal catalysts applied in the fuel cells and electrolysis cell, POM and TiO_2 are stable and low cost. The maximum output power density of liquid formic acid fuel cell after 12 h UV irradiation is 5.21 mW/cm^2 for phosphmolybdic acid and 22.81 m W/cm^2 for phosphotungstic acid respectively. The applied potential for the hydrogen evolution is as low as 0.8 V for phosphmolybdic acid and 0.6 V for phosphotungstic acid.

以F200和Sorbead WS为保护层真空变压吸附捕集CO_2(英文)

In order to solve the water issues when 13X zeolite was applied to capture CO 2 from wet flue gas by vacuum swing adsorption process, multi-layered adsorption system was considered regarding activated alumina F200 and silica gel based Sorbead WS as pre-layer materials. LBET (extended Largmuir-BET) model and extended CMMS (cooperative multimolecular sorption) equation were simulated respectively to describe water loading on F200 and Sorbead WS. The two equations can be well added into our in-house simulator to simulate double-layered CO 2 -VSA (vacuum swing adsorption) process. Results indicated that water can be successfully stopped in pre-layers with a good CO 2 capture performance.

Heterogeneous numerical modelling for the auto thermal reforming of crude glycerol in a fixed bed reactor

A mathematical model for the catalytic autothermal reforming(ATR)reaction of synthetic crude glycerol to hydrogen in a fixed bed tubular reactor(FBTR)and over an in-house developed metal oxide catalyst is presented in this work.The heterogeneous model equations account for a two-phase system of solid catalyst and bulk feed gas.Also,the ATR of crude glycerol reaction scheme and intrinsic kinetic rate model over an active,selective,and stable nickel-based catalyst were integrated in the developed model.Also,the model was validated using experimental data generated in our labs for the ATR of synthetic crude glycerol.The modelling results adequately described the detailed gas product composition and distribution,temperature profiles,and conversion propagation in the axial direction of the fixed bed reactor over a wide range of reaction temperature(773–923 K)and mass-time(12.71–158.23 g cat·min·(mol C)^(-1)).The crude glycerol conversion predicted with the model showing a close resemblance to those obtained experimentally with an average absolute deviation(AAD)of less than 8%.The maximum crude glycerol conversion and hydrogen yield were found to be 92%and 3 mol hydrogen/mol crude glycerol,respectively.Also,the gas product concentration profile in the reactor was adequately described(90%)accuracy with a hydrogen concentration of 39%(volume).

(2+1)-dimensional dissipation nonlinear Schrdinger equatio for envelope Rossby solitary waves and chirp effect

In the past few decades, the （1 ＋ 1）-dimensional nonlinear Schr6dinger （NLS） equation had been derived for envelope Rossby solitary waves in a line by employing the perturbation expansion method. But, with the development of theory, we note that the （1＋1）-dimensional model cannot reflect the evolution of envelope Rossby solitary waves in a plane. In this paper, by constructing a new （2＋1）-dimensional multiscale transform, we derive the （2＋1）-dimensional dissipation nonlinear Schrodinger equation （DNLS） to describe envelope Rossby solitary waves under the influence of dissipation which propagate in a plane. Especially, the previous researches about envelope Rossby solitary waves were established in the zonal area and could not be applied directly to the spherical earth, while we adopt the plane polar coordinate and overcome the problem. By theoretical analyses, the conservation laws of （2＋ 1）-dimensional envelope Rossby solitary waves as well as their variation under the influence of dissipation are studied. Finally, the one-soliton and two-soliton solutions of the （2＋ 1）-dimensional NLS equation are obtained with the Hirota method. Based on these solutions, by virtue of the chirp concept from fiber soliton communication, the chirp effect of envelope Rossby solitary waves is discussed, and the related impact factors of the chirp effect are given.

Optimal Allocation of Public Transport Hub Based on Load Loss Value and the Economy of Distribution Network

The rapid development of electric buses has brought a surge in the number of bus hubs and their charging and discharging capacities.Therefore,the location and construction scale of bus hubs will greatly affect the operation costs and benefits of an urban distribution network in the future.Through the scientific and reasonable planning of public transport hubs on the premise of meeting the needs of basic public transport services,it can reduce the negative impact of electric bus charging loads upon the power grids.Furthermore,it can use its flexible operation characteristics to provide flexible support for the distribution network.In this paper,taking the impact of public transport hub on the reliability of distribution network as the starting point,a three-level programming optimization model based on the value and economy of distribution network load loss is proposed.Through the upper model,several planning schemes can be generated,which provides boundary conditions for the expansion of middle-level optimization.The normal operation dispatching scheme of public transport hub obtained from the middle-level optimization results provides boundary conditions for the development of lower level optimization.Through the lower level optimization,the expected load loss of the whole distribution system including bus hub under the planning scheme given by the upper level can be obtained.The effectiveness of the model is verified by an IEEE-33 bus example.