CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Guansheng Ma,Yuefeng Yan,Yuming Feng,Kaili Zhang,Boshi Gao,Jun Weng,Guangyu Qin,Seeram Ramakrishna,Xiaoxiao Huang
To cope with different environments of application, electromagnetic wave absorption (EWA) materials with multifunctionality have attracted a wide range of interests. And excessive heavy metal ions in aqueous solutions seriously affect people’s health and pose a major challenge to environmental safety. In this study, carbon microtube/carbon nanotube (CMT/CNT) composites were fabricated via carbonization and chemical vapor deposition (CVD) methods. The CNT wrapped with cobalt nanoparticles were grown in situ on the CMT which derived from kapok fiber. By varying the concentration of cobalt precursors, the EWA and Cu(II) adsorption performances of CMT/CNT can be efficiently tuned. Optimizing the cobalt content to 2 wt% resulted in a minimum reflection loss ( RL ) of −66.14 dB at a matching thickness of 1.91 mm, with an effective absorption bandwidth (EAB) of 5.35 GHz. The adsorption capacity of Cu(II) by the CMT/CNT composite can reach 102.01 mg/g when the initial Cu(II) concentration is 500 mg/L. This research not only shows great promise for applications in the field of EWA materials but also holds significant potential for heavy metal ion removal and as a catalyst carrier, among other areas.
✓ 已验证
DOI
高影响因子
PHYSICA C-SUPERCONDUCTIVITY AND ITS APPLICATIONS
·
2024
·
IF 1.3
Wenbin Jin,Nan Liu,Fang Cheng,Zongqing Ma,Yongchang Liu,Pingzhan Si,Hongliang Ge
We report the C substitution effects in MgB 2 bulks on the lattice parameters, FWHM, and critical current density ( J c ) as a function of doping level. It is shown that using carbon-coated boron powder can effectively control the grain growth of MgB 2 during the whole sintering process. Accompanied by the rapid cooling process, the final average grain size can be restrained within merely 50 nm, and the J c value of the sample can be significantly improved at high field. On top of that, adding Cu is also considered a key factor in improving the current carrying property of the graphene-doped sample throughout the whole field, which can be attributed to the formation of the MgCu 2 alloy phase.
✓ 已验证
DOI
高影响因子
JOURNAL OF ENVIRONMENTAL ENGINEERING
·
2024
·Vol. 150
·期 5
·04024016
·
IF 1.6
Chenglong Zou,Qun Wu,Kun Guan,Fahui Nie,Sulin Xiang
Biochar with abundant functional groups, porous structure, and high specific surface area has been widely used as an adsorbent for the removal of metal ions, and its low production costs make it economically suitable for large-scale application in various industries. Hydroxyapatite nanoparticles were used to functionalize magnetic rice husk biochar (MBC) to produce hydroxyapatite functionalized magnetic rice husk biochar (HAP@MBC) in this study. The functional groups, magnetism performance, surface morphology, and aperture structure of HAP@MBC were characterized to explore the feasibility of its application in the treatment of wastewater containing Cu(II) ions. It is found that the maximum adsorption removal rate reaches 96.02% at 35°C, pH=5.0, with an adsorbent dosage of 0.65 g/L and an initial Cu(II) ion concentration of 50 mg/L. Additionally, adsorption kinetics, isotherms, and thermodynamics were analyzed to probe into the adsorption mechanism of Cu(II) ions by HAP@MBC. The results show that the adsorption process is very close to the pseudo-second-order model, indicating that the adsorption process is mainly controlled by chemisorption. The adsorption of Cu(II) ions can also be fitted by the intraparticle diffusion model, revealing that the adsorption rate is limited by intraparticle diffusion as well as other factors. Moreover, the adsorption process is consistent with the Langmuir isotherm, and the saturated adsorption capacity is calculated to be 81.59 mg/g. Thermodynamic analysis shows that the value of adsorption enthalpy change is 48.35 kJ/mol, suggesting the adsorption process is chemisorption. More precisely, it is a spontaneous entropy-increasing reaction, and an increase in the temperature is conducive to the adsorption. To sum up, HAP@MBC exhibits perfect adsorption properties and has the potential to be a novel and promising adsorbent for the removal of Cu(II) ions.
✓ 已验证
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2023
·
IF 8.6
Lixian Wang,Lizhi Zhao,Didi Si,Zhixin Li,Huiqin An,Hui Ye,Qingping Xin,Hong Li,Yuzhong Zhang
Metalloporphyrin-based nanozymes are effective peroxidase-like catalysts for dye degradation; however, their reusability is a challenge due to the nanoscale dimensions. Membrane technology has the advantages of high efficiency, low energy consumption, and easy operation. Here, we integrate poly (vinylidene fluoride) (PVDF) membrane with nanozyme for effective decolorization of Congo Red (CR). A nanozyme (Cu@Cu-FeTCPP) is prepared by growth of copper hydroxide-copper oxide (Cu(OH) 2 -CuO) nanocomposites onto the metal organic framework (MOF) nanosheet consisting of tetrakis-(4-carboxyphenyl)-porphyrin iron ligands and cupric ion nodes. The functional membrane is achieved by loading Cu@Cu-FeTCPP nanozyme on the PVDF membrane surface (Cu@Cu-FeTCPP/PVDF). The as-prepared membrane shows catalytic activity for the degradation of CR. Under flow through conditions, the catalytic degradation in tangential flow plays a major role in overall decolorization of CR, far exceeding the contribution of adsorption. The membrane can rapidly catalyze the dye degradation even at different operating pressures (0.1–0.7 kPa) and feed solutions with higher CR concentrations (eg. 60 mg·L -1 ). Compared with the static batch catalysis and the free nanozyme catalysis, the membrane exhibits higher decolorization efficiency and outstanding reusability in the continuous flow process owing to the promoted mass transfer. After 40 min of continuous flow reaction in a feed solution containing CR (40 mg·L -1 ) and H 2 O 2 (50 mM), the decolorization efficiency approaches 90% and remains above 85% after five catalytic cycles. The membrane with enzyme-mimicking ability has application prospect in wastewater treatment.
✓ 已验证
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2021
·
IF 10.588
Qingming Song,Ya Liu,Lingen Zhang,Zhenming Xu
With a huge amount of waste liquid crystal displays (LCDs) generated annually, their proper recycling raises continuous concern to realize pollution control (heavy metal and liquid crystal) and resource recovery (indium). However, due to their multi-metal feature, traditional hydrometallurgy lacks of sufficient selectivity, which makes the recycling route lengthy, costly, and generate more waste. Electrodeposition acts as a promising technique for selective metal extraction from multi-metal system due to its high selectivity and electron as clean reagent. To fully develop its application in metal recovery, stepwise Cu/MoO 2 and In electrodeposition from In-Cu-Mo-Fe waste LCD leachate is explored in depth. Electrochemical behavior analysis shows Cu and MoO 2 can be first electrodeposited for their higher electroreduction potential. Cl - plays a key role in accelerating indium electroreduction kinetics, which largely shortens the extraction time without the sacrifice of current efficiency . This accelerating effect is attributed to the increased concentration of electroactive species or collision frequency . Under optimized condition, 99.41% of indium (> 99% purity) can be electrodeposited within 13 h with high current efficiency. This study provides a cleaner approach for waste LCDs recycling and gives implications for the potential application of electrochemical technique in e-waste recycling.
✓ 已验证
DOI
高影响因子
ORGANIC ELECTRONICS
·
2021
·
IF 3.721
Ting-Hong Huang,Cheng Luo,Dan Zheng
Cationic and neutral mononuclear Cu(I) complexes, [Cu(PPh 3 ) 2 (PmH)]BF 4 (1a), [Cu(DPEphos) (PmH)]BF 4 (2a), [Cu(Xantphos) (PmH)]BF 4 (3a), [Cu(PPh 3 ) 2 (Pm)] (1b), [Cu(DPEphos) (Pm)] (2b) and [Cu(Xantphos) (Pm)] (3b) (PPh 3 = triphenylphosphine , DPEphos = bis(2-diphenylphosphinophenyl)ether, Xantphos = 9, 9-dimethyl-bis(diphenylphosphino)xanthenes, PmH = 2-(pyridin-2-yl)benzimidazole, Pm=(2-(Pyridin-2-yl)benzimidazolate), have been prepared and characterized by IR, 1 H NMR, 13 C NMR, 31 P NMR, XRD, elemental analysis and X-ray crystal structure analysis. The structural analysis shows that each of Cu(I) complexes includes a tetrahedral [Cu(NN) (PP)] + moiety, and temperature variation from 99 K to 298 K leads to the change of bonds lengths, angles and weak interactions. Meanwhile, theoretical calculations indicate that the differences between cationic and neutral Cu(I) complexes affect the composition of HOMO and LUMO orbitals, and the effect of temperature on Mülliken atomic charges is limited. Furthermore, neutral Cu(I) complexes 1b–3b show better luminescence in comparison to cationic Cu(I) complexes 1a-3a at room temperature , and temperature variations from 99 K to 298 K result in changing photoluminescence to some extent, which partly agrees with the related calculation results. In these cationic and neutral Cu(I) complexes, the maximum phosphorescent lifetime and quantum yield reach respectively 137 μs and 42% at room temperature. Moreover, cationic and neutral Cu(I) complexes are utilized to fabricate the monochromatic LEDs, showing favorable electroluminescence with the maximum EQE of 7.10%.
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2015
·
IF 4.504
Xiaorong Gan,Huimin Zhao,Xie Quan,Yaobin Zhang
An ultrasensitive electrochemical sensor for Cu 2+ detection was first developed based on p-aminothiophenol (PATP) anchored on the surface of Au nanoparticle-decorated hydrogen-incorporated TiS 2 nanosheets (PATP/Au-H x TiS 2 ). In the synthesis process, the plane edges of H x TiS 2 nanosheets offered Au nanoparticles with incubation sites for the heterogeneous nucleation and growth. On the other hand, Au nanoparticles were not only served as an excellent electrical catalyst to facilitate electron transfer and as a substrate for loading PATP molecules by Au-S valent bonds, but also could effectively avoid the aggregation of H x TiS 2 nanosheets . Due to the synergetic effects from Au-H x TiS 2 for signal amplification, the as-formed electrochemical sensor exhibited highly sensitive and selective assaying of Cu 2+ with a detection limit of 90 pM (3σ) and a linear range from 0.2 nM to 5 μM, under optimal conditions. Its specificity was ascribed to the strong coordination interaction between Cu 2+ and N atoms of imine moieties in PATP after electrochemical oxidation .
✓ 已验证
DOI
高影响因子
ChemPhotoChem
·
2025
·
IF 3
Mengrong Zhang,Sha Ni,Zichao Yang,Min Zhang,Zhongjie Guan,Jianjun Yang
Graphical Cu-modified monoclinic TiO 2 nanoflowers with OVs (Cu 1 TB-1.5) promote the reactivity and selectivity of CO 2 reduction to CO under visible light. CO selectivity is 99.6%, and the cycling stability is excellent. The Cu 1 TB-1.5 facilitates the formation of the intermediate COOH* during the photocatalytic process, thus improving the yield and selectivity of CO. The photoreduction of CO 2 has attracted extensive attention as a promising solution to global warming. In this study, Cu-modified TiO 2 (B) (CuTB) nanoflowers with oxygen vacancies (OVs) are designed and synthesized via hydrothermal treatment and photodeposition to promote the reactivity and selectivity of CO 2 reduction to CO under visible light. The CO and CH 4 yields of sample Cu 1 TB-1.5 under visible light are 5.72 and 0.02 μmol g −1 h −1 , wherein the CO yield was 15.5 times that of sample TB; its selectivity is 99.6%, and the cycling stability is excellent. OVs can broaden the light absorption of TB to the visible light region, and Cu promotes photoinduced electron transfer from TB to the Cu species and act as an active center. The OVs and Cu can synergistically enhance charge separation, CO 2 adsorption, and CO 2 conversion. The Cu 1 TB-1.5 facilitates the formation of the intermediate COOH* during the photocatalytic process, thus improving the yield and selectivity of CO. This research provides a unique idea for the development of novel highly selective photocatalysts.
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Xingrui Li,Zihao Ma,Jiangmin Guo,Yu Zhang,Tianmeng Ye,Shaojun Liu,Peng Xing,Hao Song,Weihong Wu,Chenghang Zheng,Xiang Gao
Recycling Li, P and Fe from cathodes of spent LiFePO 4 batteries plays a significant role in mitigation of Li resources shortage, as well as environmental protection. In this study, black mass from spent LiFePO 4 batteries were subjected to roasting at 600 °C under a nitrogen atmosphere to inhibit the oxidation of Fe 2+ . Then, Li, Fe and P in the black mass were successfully leached into the solution under optimal conditions (2 mol/L H 2 SO 4 , liquid to solid ratio of 10:1, temperature of 35℃, 300r/min stirring for 120 min), that achieved the initial separation of these elements from graphite and part of Al. Subsequently, a two-stage precipitation process, consisting of a cementation reaction followed by pH value adjustment, was employed to sequentially remove Cu and Al from the leaching solution. The total separation efficiencies for Cu and Al achieved 99.93 % and 95.37 % (based on contents of black mass), respectively. After separation of Cu and Al, 96.03 % of Li and 83.69 % of P present in the black mass were successfully recovered in the forms of Li 2 CO 3 and FePO 4 , respectively. The strategy developed herein provides valuable guidance for the resource utilization of P, Fe and Li, demonstrating promising potential for industrial-scale applications.
✓ 已验证
DOI
高影响因子
Journal of Materials Chemistry B
·
2025
·
IF 5.7
Ying Hu,Mingjun Li,Xun Xu,Nan Ma,Jiahao Luo,Xiaoxuan Wu,Qixiang Ping,Xiao Lin,Tingbin Zhang,Chunyong Liang,Lei Yang
Prosthetic joint infection (PJI) remains a significant challenge in clinical applications. It not only impedes the recovery of bone tissue at the site of bone defect but also leads to multiple debridements, long-lasting antibiotic treatment and even secondary replacement. Titanium alloy Ti6Al4V (TC4) is widely used in orthopedic implants due to its excellent mechanical properties and biocompatibility; however, it lacks inherent antibacterial and osteoinductive functions. In this study, a composite coating based on polyvinyl alcohol (PVA) with tissue repair and antibacterial properties was applied on the surface of TC4. A PVA gel coating functionalized with terpyridine and catechol groups (PVA–TP–CA) was synthesized and subsequently complexed with copper (Cu) ions. The differential binding affinities of TP and CA groups to Cu enabled a sustained and controlled release of metal ions. Furthermore, a micro–nano surface structure was fabricated on TC4 using femtosecond laser technology to achieve a micro–nano structure interface and enhanced bonding strength. Biological evaluations demonstrated that the modified surface significantly improved the antibacterial, angiogenic, and osteogenic properties of TC4. These findings indicate that this multifunctional composite coating holds great promise for surface modification of orthopedic implants, offering an effective strategy for preventing PJI while promoting bone regeneration.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Water
·
2025
·Vol. 17
·期 14
·2161
·
IF 3
Qiliang Xiao,Jun Nan
This study presents the development of a novel Cu–Co–O-codoped graphitic carbon nitride (g-C3N4) catalyst for efficient peroxymonosulfate (PMS) activation to degrade sulfamethoxazole (SMX) in aqueous environments. The synthesized Cu–Co–O-g-C3N4catalyst demonstrated exceptional catalytic performance, achieving 90% SMX removal within 10 min—significantly outperforming pristine g-C3N4(14%) and O-doped g-C3N4(22%)—with a reaction rate constant of 0.63 min−1. The superior activity was attributed to the synergistic effects of Cu-Co bimetallic doping and oxygen incorporation, which enhanced the active sites, stabilized metal ions, and minimized leaching. Mechanistic studies revealed a dual-pathway degradation process: (1) a radical pathway dominated by sulfate radicals (SO4•−) and (2) a non-radical pathway driven by singlet oxygen (1O2), with the latter identified as the dominant species through quenching experiments. The catalyst exhibited broad pH adaptability and optimal performance at neutral to alkaline conditions. Characterization techniques (XRD, FTIR, XPS) confirmed successful doping and revealed that oxygen incorporation modified the electronic structure of g-C3N4, improving charge carrier separation. This work provides a sustainable strategy for antibiotic removal, addressing key challenges in advanced oxidation processes (AOPs), and highlights the potential of multi-heteroatom-doped carbon nitride catalysts for water purification.
✓ 已验证
产品关联
DOI
高影响因子
POLYMER
·
2025
·
IF 4.5
Ya-Qi Wang,Qing He,Zhi-Yang Zhang,Lei Zhang,Na-Juan Yuan,Yong Liu,Hai-Tao Ren,Xu Han
Although the low molecular weight poly(2,6-dimethyl-1,4-phenyl oxide) (LMW-PPO) has been extensively applied in the field of 5G communication, the complicated procedures involved in the synthesis of LMW-PPO and efficient recovery of the homogeneous catalysts are still challenging nowadays. In this study, five ionic liquids (ILs) have been successfully synthesized, and LWM-PPO is directly synthesized using different Cu(OAc) 2 -ILs complexes as catalysts. Among them, Cu(OAc) 2 - IL(a) not only exhibits the high yield of LWM-PPO (83.68%, M n =3.6✕10 3 ) with the low 3,3’,5,5’-tetramethyl-4,4’-diphenoquinone (DPQ) yield (0.12%) and polydispersity index (PDI, 1.39) in methanol, but also maintains high stability after being recycled for 5 times. In addition, with increasing H 2 O contents in the system from 1.0% to 5.0%, the M n values of PPO decrease from 2.9✕10 3 to 2.4✕10 3 with the narrow PDI values in the range of 1.22-1.45, indicating that trace H 2 O effectively promotes the formation of binuclear Cu(II) complex between Cu(OAc) 2 ·H 2 O and ILs, which then polymerizes 2,6-dimethylphenol (DMP) to LMW-PPO. The synthesized LMW-PPO exhibits high thermostability ( T d5% =427.07-430.52°C), low glass transition temperature ( T g =167.6-180.3°C), and low dielectric constant ( D k =2.14-2.64, 1 GHz) and dielectric loss ( D f =2.83✕10 -3 -4.91✕10 -3 , 1 GHZ), indicating that it is more appropriate to be used in the field of 5G communication. This study provides new insight on the importance of ILs in direct synthesis of LMW-PPO with high performances.
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）