The cost of treating water purification plant water treatment residuals is high, with a low recovery rate and unstable effluent water quality, particularly in plants using lake and reservoir water sources in severe cold regions. Maximizing water resource utilization requires integrating water treatment residuals concentration and treatment effectively. Here, ceramic membrane technology was employed to separate supernatant and substrate after pretreatment. Optimal settling was achieved using 75 μm magnetic powder at 200 and 4 mg/L of nonionic polyacrylamide co-injection. Approximately 65% of the separated supernatant was processed by 0.1–0.2 μm Al2O3 ceramic membranes, yielding a membrane flux of 50 L/m2h and a water recovery rate of 99.8%. This resulted in removal rates of 99.3% for turbidity, 98.2% for color, and 87.7% for color and permanganate index (chemical oxygen demand, COD). Furthermore, 35% of the separated substrate underwent treatment with 0.1–0.2 μm mixed ceramic membranes of Al2O3 and SiC, achieving a membrane flux of 40 L/m2h and a water recovery rate of 73.8%. The removal rates for turbidity, color, and COD were 99.9%, 99.9%, and 82%, respectively. Overall, this process enables comprehensive concentration and treatment integration, achieving a water recovery rate of 90.7% with safe and stable effluent water quality.

Graphitic nitrogen-doped carbon film/nanoparticle composite, in which the films were wrapped and separated by the nanoparticles, was prepared through a simple co-calcination route. Due to its unique porous structure and improved nitrogen content, the as-prepared electrode material could exhibit high specific capacitances of 317.5 F g− 1 at 0.5 A g− 1 and 200.0 F g− 1 at 20 A g− 1, and stable cycling behavior with no capacitance decline after 10,000 cycles in three-electrode system. When assembled in two-electrode capacitor, its specific capacitance could be well kept at 265.5 F g− 1 at 0.5 A g− 1, and thus the supercapacitor with a high energy density of 9.22 Wh kg− 1 was obtained. The superior energy storage properties of the as-prepared material indicate its promising application as high-performance carbon-based electrode for supercapacitors.

We successfully synthesized a porous carbon material with abundant hexagonal boron nitride (h-BN) dispersed on a carbon matrix (p-BN-C) as efficient electrocatalysts for two-electron oxygen reduction reaction ( 2e− ORR) to produce hydrogen peroxide ( H2O2). This catalyst was fabricated via ball-milling-assisted h-BN exfoliation and subsequent growth of carbon structure. In alkaline solutions, the h-BN/carbon heterostructure exhibited superior electrocatalytic activity for H2O2 generation measured by a rotating ring-disk electrode (RRDE), with a remarkable selectivity of up to 90–97% in the potential range of 0.3–0.6 V vs reversible hydrogen electrode (RHE), superior to most of the reported carbon-based electrocatalysts. Density functional theory (DFT) simulations indicated that the B atoms at the h-BN heterostructure interface were crucial active sites. These results underscore the remarkable catalytic activity of heterostructure and provide a novel approach for tailoring carbon-based catalysts, enhancing the selectivity and activity in the production of H2O2 through heterostructure engineering.

In this paper, iron ore tailings (IOT) were separated from the tailings field and used to prepare cement stabilized macadam (CSM) with porous basalt aggregate. First, the basic properties of the raw materials were studied. Porous basalt was replaced by IOT at ratios of 0, 20 %, 40 %, 60 %, 80 %, and 100 % as fine aggregate to prepare CSM, and the effects of different cement dosage (4 %, 5 %, 6 %) on CSM performance were also investigated. CSM’s durability and mechanical performance with ages of 7 d, 28 d, and 90 d were studied with the unconfined compression strength test, splitting tensile strength test, compressive modulus test and freeze-thaw test, respectively. The changes in Ca2+ content in CSM of different ages and different IOT ratios were analyzed by the ethylene diamine tetraacetic acid (EDTA) titration method, and the micro-morphology of CSM with different ages and different IOT replaced ratio were observed by scanning electron microscopy (SEM). It was found that with the same cement dosage, the strengths of the IOT-replaced CSM were weaker than that of the porous basalt aggregate at early stage, and the strength was highest at the replaced ratio of 60 %. With a cement dosage of 4 %, the unconfined compressive strength of CSM without IOT was increased by 6.78 % at ages from 28 d to 90 d, while the splitting tensile strength increased by 7.89 %. However, once the IOT replaced ratio reached 100 %, the values increased by about 76.24 % and 17.78 %, which was better than 0 % IOT. The CSM-IOT performed better than the porous basalt CSM at 90 d age. This means IOT can replace porous basalt fine aggregate as a pavement base.

CO2 photocatalytic reduction is a carbon–neutral renewable energy technology. However, this technology is restricted by the low utilization of photocatalytic electrons. Therefore, to improve the separation efficiency of photogenerated carriers and enhance the performance of CO2 photocatalytic reduction. In this paper, g-C3N4/Pd composite with Schottky junction was synthesized by using g-C3N4, a two-dimensional material with unique interfacial effect, as the substrate material in combination with the co-catalyst Pd. The composite of Pd and g-C3N4 was tested to have a strong localized surface plasmon resonance effect (LSPR), which decreased the reaction barriers and improved the electron utilization. The combination of reduced graphene oxide (rGO) created a π–π conjugation effect at the g-C3N4 interface, which shortened the electron migration path and further improved the thermal electron transfer and utilization efficiency. The results show that the g-C3N4/ rGO/Pd (CRP) exhibits the best performance for photocatalytic reduction of CO2, with the yields of 13.57 μmol g− 1 and 2.73 μmol g− 1 for CO and CH4, respectively. Using the in situ infrared test to elucidate the intermediates and the mechanism of g-C3N4/rGO/Pd (CRP) photocatalytic CO2 reduction. This paper provides a new insight into the interface design of photocatalytic materials and the application of co-catalysts.

For the regeneration of diesel particulate filters (DPF) using non-thermal plasma (NTP), both cost-effectiveness and regeneration efficiency should be raised. This study compared and contrasted the physicochemical characteristics of carbon black and engine particulate matter (PM). After carbon black was put into the DPF, an experimental setup for the oxidation of PM using NTP was created. The findings showed that carbon black and PM samples had comparable oxidation traits, micronanostructures, and C/O elemental ratios. O3, the main active species in NTP, was susceptible to heat breakdown, and the rate of decomposition of O3 increases with increasing temperature. The removal effectiveness of carbon black first improved and subsequently declined with an increase in the NTP injection flow rate during offline DPF regeneration using NTP at room temperature. A relatively high carbon black removal efficiency of 85.1% was achieved at an NTP injection flow rate of 30 L/min.

중국 국가 통계국에서 발표한 데이터에 따르면, 2022년 60세 이상 인구는 전체의 19.6%이며, 2035년에는 4억을 초과하여 고령화 사회의 단계에 접어들 것이라고 한다. 질병의 발병률이 매우 높은 고령층은 의약품의 복용 과정에서 주의해야 할 점이 많은 반면, 이에 대한 이해가 부족하여 의약품의 복용에 따른 잠재적인 위험에 항상 노출되어 있다. 이에 따라 의약품 포장에 대한 고령층의 요구를 수용하고, 의약품 복용의 정확성과 편의성을 향상시키는 문제는 당면의 과제가 되고 있다. 본 연구는 디지털 휴먼 기술을 도입하여 의약품 포장의 혁신적인 디자인을 강구하고, 이를 통해 고령층의 의약품 관련 문제에 대한 해결을 목표로 한다. 의약품 포장 디자인에 디지털 휴먼 기술을 적용하는 것은 최근 디지털 발전의 추세에 부합하며, 고령층을 대상으로 하는 의약품 포장 디자인에 새로운 사로를 제공할 수 있다. 따라서 본 연구는 문헌 분석법 및 사례 분석법 등을 통해 고령층을 대상으로 하는 의약품 포장 디자인의 발전 현황을 파악하여, 기존 제한적인 정보만을 제공하던 단일 시각 형태의 전통적인 의약품 포장 디자인의 한계를 극복하고, 새로운 디자인 방안을 제시하여 고령층이 더 다양한 방식으로 의약품 포장을 통해 필요한 정보를 인식할 수 있도록 만들고자 하였다. 기존 의약품 포장 디자인에 대한 분석을 바탕으로 본 연구는 디지털 휴먼 기술과 의약품 포장의 결합에 대한 타당성을 도출했고, 실례를 통해 디지털 휴먼 기술이 의약품 포장에 있어 상당한 응용 가치와 잠재력을 가지고 있다는 사실을 검증하였다.

In this work, the trend in the performance of carbon fiber (CF) and its composite during self-polymerization of polydopamine (PDA) at carbon fiber surface was investigated by varying the self-polymerization time of dopamine in an aqueous solution. Research has shown that the PDA coating elevated the surface roughness and polarity of the inert fiber. The tensile strength of single carbon fiber was significantly improved, especially after 9 h of polydopamine self-polymerization, increasing by 18.64% compared with that of desized carbon fiber. Moreover, the interlaminar shear strength (ILSS) of CF-PDA9-based composites was 35.06% higher than that of desized CF-based composites. This research will provide a deep insight into the thickness and activated ingredients of dopamine oxidation and self-polymerization on interfacial compatibility of carbon fiber/epoxy resin composites.

Oxygen-rich porous carbon is of great interest for energy storage applications due to its improved local electronic structures compared with unmodified porous carbon. However, a tunable method for the preparation of oxygen-rich porous carbon with a special microstructure is still worth developing. Herein, a novel modification of porous carbon with different microstructures is facilely prepared via low-temperature solvothermal and KOH activation methods that employ the coal tar and eight substances, such as cellulose as carbon source and modifier, respectively. By testing the yield, surface group structure, lattice structures, morphology, thermal weight loss, and specific capacitance of carbonaceous mesophase, cellulose–hydrochloric acid is identified as the additive for the preparation of oxygen-rich coal tar-based porous carbon. The obtained porous carbon displays a specific surface area of up to 859.49 m2 g− 1 and an average pore diameter of 2.39 nm. More importantly, the material delivers a high capacity of 275.95 F g− 1 at 0.3 A g− 1 and maintains a high capacitance of 220 F g− 1 even at 10 A g− 1. When in a neutral electrolyte, it can still retain a reversible capacity of 236.72 F g− 1 at 0.3 A g− 1 and 136.79 F g− 1 at 10 A g− 1. This work may provide insight into the design of carbon anode materials with high specific capacity.

Seawater evaporation and purification powered by solar energy are considered as a promising approach to alleviate the global freshwater crisis, and the development of photothermal materials with high efficiency is imminent. In this study, cellulose nanofiber (CNF)/MXene/Ni chain (CMN) aerogels were successfully synthesized by electrostatic force and hydrogen bond interaction force. CMN10 achieved a favorable evaporation rate as high as 1.85 kg m− 2 h− 1 in pure water, and the corresponding evaporation efficiency could be up to 96.04%. Even if it is applied to seawater with multiple interference factors, its evaporation rate can still be 1.81 kg m− 2 h− 1. The superior seawater evaporation activity origins from the promoted separation of photoexcited charges and photothermal conversion by the synergy of Ni chain and MXene, as well as the water transport channel supported by the 3D structure frame of CNF. Most importantly, CMN aerogel can maintain water vapor evaporation rates above 1.73 kg m− 2 h− 1 under extreme conditions such as acidic (pH 2) and alkaline (pH 12) conditions. In addition, various major ions, heavy metals and organic pollutants in seawater can be rejected by CMN10 during desalination, and the rejection rates can reach more than 99.69%, ensuring the purity of water resources after treatment. This work shows the great potential of CMN aerogel as a high-efficiency solar evaporator and low-cost photothermal conversion material. Cellulose nanofiber (CNF)/MXene/Ni chain (CMN) aerogels demonstrated high evaporation of water from sea water.

The costs associated with law enforcement have seen a sharp increase, driven by rising personnel costs and the growing demand for policing services (Gascón, 2010; Urban Institute, 2020). Considerable discussion has arisen about how science can potentially help law enforcement “do more with less”, and some scholars have suggested introducing new crime control technologies to address this problem (e.g., Roach, 2022; Weisburd & Neyroud, 2011). With the onset of the COVID-19 pandemic, police departments around the world had additional demand, as they were made responsible for overseeing and ensuring compliance with COVID protocols. As a response, some countries (e.g., Singapore and China; Barrett, 2021) resorted to employing service robots either alongside or in place of police officers to assist with COVID-related compliance tasks.

Rechargeable zinc-based batteries (RZBs) with the advantages of high safety, low cost, abundant resources and environmental friendliness, are considered as advanced secondary battery systems that can be applied to large-scale energy storage. As an important cathode material for RZBs, NASICON-type Na3V2( PO4)3 (NVP) possesses three-dimensional and large-scale ion channels that facilitate the rapid diffusion of Zn2+, and has a higher average operating voltage compared with other vanadiumbased compounds, thus exhibiting the possibility of realizing RZBs with high energy density. However, NVP still has some problems, such as poor electronic conductivity and spontaneous dissolution in aqueous solution. The sluggish kinetics of Zn2+ (de)intercalation in NVP and dendritic growth on the Zn anode also contribute to the poor rate performance and short cycle life of the batteries. In this review, optimization strategies for the electrochemical performance of RZBs with NVP as cathode are systematically elaborated, including modification of NVP cathode and optimization of electrolyte. Several mainstream energy storage mechanisms and analysis methods in this battery system are sorted out and summarized. On this basis, the development direction of NVP–RZB system is further prospected.

Ship collision accidents not only endanger the safety of ships and personnel, but also may cause serious marine environmental pollution. To solve this problem, advanced technologies have been developed and applied in the field of intelligent ships in recent years. In this paper, a novel path planning algorithm is proposed based on particle swarm optimization (PSO) to construct a decision-making system for ship's autonomous collision avoidance using the process analysis which combines with the ship encounter situation and the decision-making method based on ship collision avoidance responsibility. This algorithm is designed to avoid both static and dynamic obstacles by judging the collision risk considering bad weather conditions by using BP neural network. When the two ships enter a certain distance, the optimal collision avoidance course and speed of the ship are obtained through the improved collision avoidance decision-making method. Finally, through MATLAB and Visual C++ platform simulations, the results show that the ship collision avoidance decision-making scheme can obtain reasonable optimal collision avoidance speed and course, which can ensure the safety of ship path planning and reduce energy consumption.

During nuclear waste vitrification, loss of sodium (Na) and boron (B) occurs, as these elements are highly volatile at high temperatures, which causes fluctuations in composition and consequently affects the properties of the glass products. In this study, we investigated the volatilization behaviors of Na and B from a simulated high-level waste glass as functions of heating temperature and dwelling duration. Based on the data obtained regarding the composition of Na and B and the structure of the glass, a hypothetical model was proposed to explain the volatilization behaviors of Na and B from a structural viewpoint. As the loss of Na and B during vitrification, the crystallization of the glass occurred. Thus, the crystallization behavior of the simulated waste glass upon composition deviation was studied.

Transition-metal phosphides (TMPs), a promising anode material for lithium-ion batteries (LIBs), are limited in application because of its serious volume effect in the cycle. In this work, a simple electrospinning strategy was proposed to restrict the grain size of CoP nanocrystals by nano-confined effect of carbon nanofibers with ligands. The addition of ligands not only could realize the uniform dispersion of CoP nanocrystals, but also strengthen the bond between the metals and carbon nanofibers. As a result, the CoP/CNF composite exhibits excellent lithium storage performance, and its reversible specific capacity could reach 1016.4 mAh g− 1 after 200 cycles at a current density of 200 mA g− 1. The research is anticipated to provide a new idea for the preparation of anode materials for lithium ion batteries.

High-temperature friction performances of graphite blocks (GBs) and zinc phosphate impregnated graphite blocks (IGBs) were evaluated under various friction temperatures. The surface of IGB exhibited extremely lower average friction coefficient values, that was 0.007 at 400 °C and 0.008 at 450 °C, in comparison to that of GB (0.13 at 400 °C and 0.16 at 450 °C, respectively). The worn surface of IGB in the high-temperature friction test was smoother and more complete than that of GB. The wear under high temperature and load caused the transformation of zinc pyrophosphate to zinc metaphosphate and the formation of a continuous large-area boundary lubrication layer combined with graphite and metallic element on the wear surface. The superior tribology property of IGB could be attributed to the digestion of iron oxides by tribo-chemical reactions and passivation of the exposed dangling covalent bonds. Specifically, the layered structure generated on the IGB wear interface effectively decreased the adhesive forces and prevented the surface from serious damage.

Coal-based graphite has become the main material of emerging industries. The microstructure of coal-based graphite plays an important role in its applications in many fields. In this paper, the effect of carbon disulfide/N-methyl-2-pyrrolidone solvent mixture extraction on the microstructure of bituminous coal-based graphite was systematically studied through preliminary extraction coupled with high-temperature graphitization. The graphitization degree g (75.65%) of the coal residue-based graphite was significantly higher than that of the raw coal-based graphite. The crystallite size La of the coal residue-based graphite was reduced by 47.06% compared with the raw coal-based graphite. The ID/ IG value of the coal residue-based graphite is smaller than that of the raw coal-based graphite. The specific surface area (16.72 m2/ g) and total pore volume (0.0567 m3/ g) of the coal residue-based graphite are increased in varying degrees compared with the raw coal-based graphite. This study found a carbon source that can be used to prepare coal-based graphite with high graphitization degree. The results are expected to provide a theoretical basis for further clean and efficient utilization of the coal residue resources.

The reduced graphene oxide (rGO) has attracted more and more attention in recent years. How to choose a suitable reduction method to prepare rGO is a critical problem in the preparation of graphene composites. In this work, the differences of rGO reduced by thermal, microwave, Ultraviolet (UV) and reducing agent were studied. The reduction degree and functional groups of rGO were compared by SEM, XPS, Raman, FTIR and TGA. Thermal can remove most of the oxygen-containing groups of graphene oxide (GO) and the thermal reduction is the most effective reduction method. UV light can directly act on the unstable oxygen-containing groups, and its reduction efficiency is second only to thermal reduction. The efficiency of chemical reduction is not as good as that of UV reduction, because the reducing agent only act on the surface of GO. Microwave reduction is a mild thermal reduction with the lowest efficiency, but the residual oxygen-containing groups increase the hydrophilicity of rGO. To sum up, this work studies that rGO prepared by different reduction methods has different characteristics, which provides a reference for selecting appropriate reduction methods to prepare graphene composites with better properties.

Bangladesh enjoys an advantageous geographical position. It has been a transit station for businessmen from South Asia, Southeast Asia, Central Asia and even Europe since ancient times. It is located at the intersection of China Economic Circle, South Asia Economic Circle and ASEAN Economic Circle, and is an important country along the belt and road initiative. The “Belt and Road” initiative was supported by Bangladeshi Prime Minister Sheikh Hasina. Since the “Belt and Road” initiative was put forward, China and Bangladesh have achieved remarkable results in policy communication, facility connectivity, smooth trade, capital financing and people-to-people communication. However, China and Bangladesh still face challenges in the political, security, economic and social fields to jointly build the “Belt and Road” initiative. In the new period, China and Bangladesh should strengthen political communication, promote the docking of China-Bangladesh development strategies, strengthen facility connectivity and industrial cooperation, promote cultural exchanges, promote the upgrading of cooperation between the two countries, and jointly build a high-quality “Belt and Road” initiative.