Valuable metals recovery from spent ternary lithium-ion battery:A review

Ternary lithium-ion batteries(LIBs),widely used in new energy vehicles and electronic products,are known for their high en-ergy density,wide operating temperature range,and excellent cycling performance.With the rapid development of the battery industry,the recycling of spent ternary LIBs has become a hot topic because of their economic value and environmental concerns.To date,a con-siderable amount of literature has reported on the recycling of spent ternary LIBs designed to provide an efficient,economical,and envir-onmentally friendly method for battery recycling.This article examines the latest developments in various technologies for recycling spent ternary LIBs in both research and practical production,including pretreatment,pyrometallurgy,hydrometallurgy,pyro-hydrometallurgy,and direct regeneration.Suggestions for addressing challenges based on the benefits and disadvantages of each method are made.Finally,through a comparison of the feasibility and economic benefits of various technologies,the challenges faced during battery recycling are summarized,and future development directions are proposed.

Template-free synthesis of core-shell Fe_(3)O_(4)@MoS_(2)@mesoporous TiO_(2) magnetic photocatalyst for wastewater treatment

TiO_(2)is the dominant and most widely researched photocatalyst for environmental remediation,however,the drawbacks,such as only responding to UV light(<5%of sunlight),low charge separation efficiency,and difficulties in recycling,have severely hindered its practical application.Herein,we synthesized magnetically separable Fe_(3)O_(4)@MoS_(2)@mesoporous TiO_(2)(FMmT)photocatalysts via a simple,green,and template-free solvothermal method combined with ultrasonic hydrolysis.It is found that FMmT possesses a high specific surface area(55.09 m2·g−1),enhanced visible-light responsiveness(~521 nm),and remarkable photogenerated charge separation efficiency.In addition,the photocatalytic degradation efficiencies of FMmT for methylene blue(MB),rhodamine B(RhB),and tetracycline(TC)are 99.4%,98.5%,and 89.3%within 300 min,respectively.The corresponding degradation rates are 4.5,4.3,and 3.1 times higher than those of pure TiO_(2)separately.Owing to the high saturation magnetization(43.1 A·m^(2)·kg^(−1)),FMmT can achieve effective recycling with an applied magnetic field.The improved photocatalytic activity is closely related to the effective transport of photogenerated electrons by the active interlayer MoS_(2) and the electron–hole separation caused by the MoS_(2)@TiO_(2)heterojunction.Meanwhile,the excellent light-harvesting ability and abundant reactive sites of the mesoporous TiO_(2)shell further boost the photocatalytic efficiency of FMmT.This work provides a new approach and some experimental basis for the design and performance improvement of magnetic photocatalysts by innovatively incorporating MoS2 as the active interlayer and integrating it with a mesoporous shell.

Effect of samarium on the N_(2) selectivity of Sm_(x)Mn_(0.3-x)Ti catalysts during selective catalytic reduction of NO_(x) with NH_(3)

This work aims to study the improvement effect of Sm on Mn-based catalysts for selective catalytic reduction (SCR) of NO with NH3.A series of Sm_(x)Mn_(0.3-x)-xTi catalysts (x=0,0.1,0.15,0.2,and 0.3) were prepared by co-precipitation.Activity tests indicated that the Sm_(0.15)Mn_(0.15)Ti catalyst showed superior performances,with a NO conversion of 100%and N_(2)selectivity above 87%at 180–300℃.The characterizations showed that Sm doping suppressed the crystallization of TiO_(2)and Mn2O3phases and increased the specific surface area and acidity.In particular,the surface area increased from 152.2 m^(2)·g^(-1)for Mn0.3Ti to 241.7 m^(2)·g^(-1)for Sm_(0.15)Mn_(0.15)Ti.These effects contributed to the high catalytic activity.The X-ray photoelectron spectroscopy (XPS) results indicated that the relative atomic ratios of Sm^(3+)/Sm and Oβ/O of Sm_(0.15)Mn_(0.15)Ti were 76.77at%and 44.11at%,respectively.The presence of Sm contributed to an increase in surface-absorbed oxygen (Oβ) and a decrease in Mn^(4+)surface concentration,which improved the catalytic activity.In the results of hydrogen temperature-programmed reduction(H_(2)-TPR),the presence of Sm induced a higher reduction temperature and lower H_(2)consumption (0.3 mmol·g^(-1)) for the Sm_(0.15)Mn_(0.15)Ti catalyst compared to the Mn0.3Ti catalyst.The decrease in Mn^(4+)weakened the redox property of the catalysts and increased the N_(2)selectivity by suppressing N_(2)O formation from NH3oxidation and the nonselective catalytic reduction reaction.The in situ diffuse reflectance infrared Fourier transform spectra (DRIFTs) revealed that NH3-SCR of NO over the Sm_(0.15)Mn_(0.15)Ti catalyst mainly followed the Eley–Rideal mechanism.Sm doping increased surface-absorbed oxygen and weakened the redox property to improve the NO conversion and N_(2)selectivity of the Sm_(0.15)Mn_(0.15)Ti catalyst.

Phase evolution and properties of glass ceramic foams prepared by bottom ash,fly ash and pickling sludge

Municipal solid waste incineration products of bottom ash(BA),fly ash(FA),and pickling sludge(PS),causing severe environ-mental pollution,were transformed into glass ceramic foams with the aid of CaCO3 as a pore-foaming agent during sintering.The effect of the BA/FA mass ratio on the phase composition,pore morphology,pore size distribution,physical properties,and glass structure was investigated,with results showing that with the increase in the BA/FA ratio,the content of the glass phase,Si-O-Si,and Q3Si units decrease gradually.The glass transmission temperature of the mixture was also reduced.When combined,the glass viscosity decreases,causing bubble coalescence and uneven pore distribution.Glass ceramic foams with uniform spherical pores are fabricated.When the content of BA,FA,and PS are 35wt%,45wt%,and 20wt%,respectively,contributing to high performance glass ceramic foams with a bulk density of 1.76 g/cm3,porosity of 56.01%,and compressive strength exceeding 16.23 MPa.This versatile and low-cost approach provides new insight into synergistically recycling solid wastes.

Preparation and hydration of industrial solid waste-cement blends:A review

Industrial solid waste(ISW)-cement blends have the advantages of low carbon,low energy consumption,and low pollution,but their clinker replacement level in low carbon cement is generally low.To address this challenge,this study considers the latest progress and development trends in the ISW-cement blend research,focusing on the activation of ISWs,the formation of ISW-cement blends,and their associated hydration mechanisms.After the mechanical activation of ISWs,the D50(average size)typically drops below 10μm,and the specific surface area increases above 350 m2/kg.Thermal activation can increase the glassy-phase content and reactivity of ISWs,where the coal gangue activation temperature is usually set at 400-1000°C.Furthermore,the roles of ISWs in the hydration of ISW-cement blends are divided into physical and chemical roles.The physical action of ISWs usually acts in the early stage of the hydration of ISW-cement blends.Subsequently,ISWs participate in the hydration reaction of ISW-cement blends to generate products,such as C-(A)-S-H gels.Moreover,alkali activation affects the hydration kinetics of ISW-cement blends and modifies the proportion of gels.Environmental impacts and costs of ISW-cement blends have also been discussed to guide stakeholders in selecting sustainable ISWs.

Study of Inverse Lithography Approaches based on Deep Learning

Computational lithography(CL)has become an indispensable technology to improve imaging resolution and fidelity of deep sub-wavelength lithography.The state-of-the-art CL approaches are capable of optimizing pixel-based mask patterns to effectively improve the degrees of optimization freedom.However,as the growth of data volume of photomask layouts,computational complexity has become a challenging problem that prohibits the applications of advanced CL algorithms.In the past,a number of innovative methods have been developed to improve the computational efficiency of CL algorithms,such as machine learning and deep learning methods.Based on the brief introduction of optical lithography,this paper reviews some recent advances of fast CL approaches based on deep learning.At the end,this paper briefly discusses some potential developments in future work.

Promotion effect of niobium on ceria catalyst for selective catalytic reduction of NO with NH3

The CeO_(2),Ce-Nb-O_(x) and Nb_(2)O_(5) catalysts were synthesized by citric acid method and the promotion effect of Nb on ceria for selective catalytic reduction(SCR)of NO with NH_(3) was investigated.The catalytic activity measurements indicate that the mixed oxide Ce-Nb-O_(x) presents a higher SCR activity than the single oxide CeO_(2) or Nb_(2)O_(5) catalyst.In addition,the Ce-Nb-O_(x) catalyst shows high resistance towards H_(2)O and SO_(2) at 280℃.The Raman,X-ray photoelectron spectra and temperature programmed reduction with H_(2) results indicate that the incorporation of Nb provides abundant oxygen vacancies for capturing more surface adsorbed oxygen,which provides a superior redox capability and accelerates the renewal of active sites.Furthermore,the Fourier transform infrared spectra and temperature programmed desorption of NH_(3) results suggest that niobium pentoxide shows high surface acidity,which is partly retained in the Ce-Nb-O_(x) catalyst possessing a high content of Lewis and Br?nsted acid sites.Therefore,the incorporation of Nb improves both the redox and acidic capacities of Ce-Nb-O_(x) catalyst for the SCR reaction.Here,the redox behavior is primarily taken on Ce and the acidity is well improved by Nb,so the synergistic effect should exist between Ce and Nb.In terms of the reaction mechanism,in situ DRIFT experiments suggest that both NH_(3) on Lewis acid sites and NH_(4)^(+) on Bronsted acid sites can react with NO species,and adsorbed NO and NO_(2) species can both be reduced by NH_(3).In the SCR process,O_(2) primarily acts as the accelerant to improve the redox and acid cycles and plays an important role.This work proves that the combination of redox and acidic properties of different constituents can be feasible for catalyst design to obtain a superior SCR performance.