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Preconcentration of trace elements by adsorption onto a niobium wire for electrothermal atomization atomic

Satoshi KANECO, Hiroaki KITANAGA, Hideyuki KATSUMATA, Tohru SUZUKI

《化学科学与工程前沿（英文）》 2012年 第6卷 第4期   页码 432-435 doi: 10.1007/s11705-012-1219-z

摘要： In the present work, a new preconcentration method of trace elements by adsorption onto a niobium wire has been developed for electrothermal atomization atomic absorption spectrometry (ETAAS) with a tungsten tube atomizer. Detection limits (pg·mL ) by this method combined with ETAAS were 45 for bismuth, 7.0 for cadmium, 20 for copper, 1.3 for gold, 36 for lead, 65 for manganese, 9.5 for rhodium and 19 for silver.

关键词： preconcentration     adsorption onto niobium wire     electrothermal atomization atomic absorption spectrometry     tungsten tube atomizer     trace elements    

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Adsorption of herring sperm DNA onto pine sawdust biochar: Thermodynamics and site energy distribution

《环境科学与工程前沿（英文）》 2022年 第16卷 第11期 doi: 10.1007/s11783-022-1579-7

摘要：

● Adsorption of environmental deoxyribonucleic acid on biochar was studied.

关键词： Environmental deoxyribonucleic acid     Antibiotic resistance genes     Biochar     Adsorption thermodynamics    

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Adsorption property of direct fast black onto acid-thermal modified sepiolite and optimization of adsorption

Chengyuan SU, Weiguang LI, Yong WANG

《环境科学与工程前沿（英文）》 2013年 第7卷 第4期   页码 503-511 doi: 10.1007/s11783-012-0477-9

摘要： The adsorption of direct fast black onto acid-thermal modified sepiolite was investigated. Batch adsorption experiments were performed to evaluate the influences of experimental parameters such as initial dye concentration, initial solution pH and adsorbent dosage on the adsorption process. The three-factor and three-level Box-Behnken response surface methodology (RSM) was utilized for modeling and optimization of the adsorption conditions for direct fast black onto the acid-thermal modified sepiolite. The raw sepiolite was converted to acid-thermal modified sepiolite, and changes in the fourier transform infrared spectrum (FTIR) adsorption bands of the sample were noted at 3435 cm and 1427 cm . The zeolitic water disappeared and the purity of sepiolite was improved by acid-thermal modification. The decolorization rate of direct fast black adsorbed increased from 68.2% to 98.9% on acid-thermal modified sepiolite as the initial solution pH decreased from 10 to 2. When the adsorbent dosage reached to 2.5 g·L , 2.0 g·L , 1.5 g·L and 1.0 g·L , the decolorization rate was 90.3%, 86.7%, 61.0% and 29.8%, respectively. When initial dye concentration increased from 25 to 200 mg·L , the decolorization rate decreased from 91.9% to 60.0%. The RSM results showed that the interaction between adsorbent dosage and pH to be a significant factor. The optimum conditions were as follows: the adsorbent dosage 1.99 g·L , pH 4.22, and reaction time 5.2 h. Under these conditions, the decolorization rate was 95.1%. The three dimensional fluorescence spectra of direct fast black before and after treatment showed that the direct fast black was almost all adsorbed by the acid-thermal modified sepiolite.

关键词： direct fast black     acid-thermal modified sepiolite     adsorption     response surface methodology    

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Adsorption characteristics of ciprofloxacin onto g-MoS2<

Zhenyu Yang, Rong Xing, Wenjun Zhou, Lizhong Zhu

《环境科学与工程前沿（英文）》 2020年 第14卷 第3期 doi: 10.1007/s11783-019-1218-0

摘要： The g-MoS2 coated composites (g-MoS2-BC) were synthesized. The coated g-MoS2 greatly increased the adsorption ability of biochar. The synergistic effect was observed for CIP adsorption on g-MoS2-RC700. The adsorption mechanisms of CIP on g-MoS2-BC were proposed. The g-MoS2 coated biochar (g-MoS2-BC) composites were synthesized by coating original biochar with g-MoS2 nanosheets at 300°C(BC300)/700°C (BC700). The adsorption properties of the g-MoS2-BC composites for ciprofloxacin (CIP) were investigated with an aim to exploit its high efficiency toward soil amendment. The specific surface area and the pore structures of biochar coated g-MoS2 nanosheets were significantly increased. The g-MoS2-BC composites provided more π electrons, which was favorable in enhancing the π-π electron donor-acceptor (EDA) interactions between CIP and biochar. As a result, the g-MoS2-BC composites showed faster adsorption rate and greater adsorption capacity for CIP than the original biochar. The coated g-MoS2 nanosheets contributed more to CIP adsorption on the g-MoS2-BC composites due to their greater CIP adsorption capacity than the original biochar. Moreover, the synergistic effect was observed for CIP adsorption on g-MoS2-BC700, and suppression effect on g-MoS2-BC300. In addition, the adsorption of CIP onto g-MoS2-BC composites also exhibited strong dependence on the solution pH, since it can affect both the adsorbent surface charge and the speciation of contaminants. It was reasonably suggested that the mechanisms of CIP adsorption on g-MoS2-BC composites involved pore-filling effects, π-π EDA interaction, electrostatic interaction, and ion exchange interaction. These results are useful for the modification of biochar in exploiting the novel amendment for contaminated soils.

关键词： Adsorption     Ciprofloxacin     g-MoS2 nanosheets     Biochar     Soil remediation    

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Comparing the adsorption behaviors of Cd, Cu and Pb from water onto Fe-Mn binary oxide, MnO

Wei XU,Huachun LAN,Hongjie WANG,Hongming LIU,Jiuhui QU

《环境科学与工程前沿（英文）》 2015年 第9卷 第3期   页码 385-393 doi: 10.1007/s11783-014-0648-y

摘要： The adsorption potential of FMBO, FeOOH, MnO for the removal of Cd , Cu and Pb in aqueous systems was investigated in this study. Comparing to FMBO and FeOOH, MnO offered a much higher removal capacity towards the three metal ions. The maximal adsorption capacity of MnO for Cd , Cu and Pb were 1.23, 2.25 and 2.60 mmol·g , respectively. And that for FMBO were 0.37, 1.13, and 1.18 mmol·g and for FeOOH were 0.11, 0.86 and 0.48 mmol·g , respectively. The adsorption behaviors of the three metal ions on the three adsorbents were all significantly affected by pH values and heavy metal removal efficiency increased with pH increased. The Langmuir and Freundlich adsorption models were used to describe the adsorption equilibrium of the three metal ions onto the three adsorbents. Results showed that the adsorption equilibrium data fitted well to Langmuir isotherm and this indicated that adsorption of metal ions occurred on the three metal oxides adsorbents limited to the formation of a monolayer. More negative charged of MnO surface than that of FMBO and FeOOH could be ascribed by lower pH of MnO than that of FMBO and FeOOH and this could contribute to more binding sites on MnO surface than that of FMBO and FeOOH. The higher metal ions uptake by MnO than FMBO and FeOOH could be well explained by the surface charge mechanism.

关键词： heavy metals     Fe-Mn binary oxide     manganese dioxide     ferric hydroxide     adsorption    

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A ternary mechanism for the facilitated transfer of metal ions onto metal–organic frameworks: implications

《化学科学与工程前沿（英文）》   页码 1632-1642 doi: 10.1007/s11705-022-2187-6

摘要： Although metal–organic frameworks offer a new platform for developing versatile sorption materials, yet coordinating the functionality, structure and component of these materials remains a great challenge. It depends on a comprehensive knowledge of a “real sorption mechanism”. Herein, a ternary mechanism for U(VI) uptake in metal–organic frameworks was reported. Analogous MIL-100s (Al, Fe, Cr) were prepared and studied for their ability to sequestrate U(VI) from aqueous solutions. As a result, MIL-100(Al) performed the best among the tested materials, and MIL-100(Cr) performed the worst. The nuclear magnetic resonance technique combined with energy-dispersive X-ray spectroscopy and zeta potential measurement reveal that U(VI) uptake in the three metal–organic frameworks involves different mechanisms. Specifically, hydrated uranyl ions form outer-sphere complexes in the surface of MIL-100s (Al, Fe) by exchanging with hydrogen ions of terminal hydroxyl groups (Al-OH2, Fe-OH2), and/or, hydrated uranyl ions are bound directly to Al(III) center in MIL-100(Al) through a strong inner-sphere coordination. For MIL-100(Cr), however, the U(VI) uptake is attributed to electrostatic attraction. Besides, the sorption mechanism is also pH and ionic strength dependent. The present study suggests that changing metal center of metal–organic frameworks and sorption conditions alters sorption mechanism, which helps to construct effective metal–organic frameworks-based sorbents for water purification.

关键词： U(VI)     metal–organic frameworks     adsorption mechanism     metal node    

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Effect of co-existing organic compounds on adsorption of perfluorinated compounds onto carbon nanotubes

Shubo DENG,Yue BEI,Xinyu LU,Ziwen DU,Bin WANG,Yujue WANG,Jun HUANG,Gang YU

《环境科学与工程前沿（英文）》 2015年 第9卷 第5期   页码 784-792 doi: 10.1007/s11783-015-0790-1

摘要： Co-existing organic compounds may affect the adsorption of perfluorinated compounds (PFCs) and carbon nanotubes in aquatic environments. Adsorption of perfluorooctane sulfonate (PFOS), perfluorooctane acid (PFOA), perfluorobutane sulfonate (PFBS), and perfluorohexane sulfonate (PFH S) on the pristine multi-walled carbon nanotubes (MWCNTs-Pri), carboxyl functionalized MWCNTs (MWCTNs-COOH), and hydroxyl functionalized MWCNTs (MWCNTs-OH) in the presence of humic acid, 1-naphthol, phenol, and benzoic acid was studied. Adsorption kinetics of PFOS was described well by the pseudo-second-order model and the sorption equilibrium was almost reached within 24 h. The effect of co-existing organic compounds on PFOS adsorption followed the decreasing order of humic acid>1-naphthol>benzoic acid>phenol. Adsorbed amounts of PFOS decreased significantly in the presence of co-existing or preloaded humic acid, and both adsorption energy and effective adsorption sites on the three MWCNTs decreased, resulting in the decrease of PFOS adsorption. With increasing pH, PFOS removal by three MWCNTs decreased in the presence of humic acid and phenol. The adsorbed amounts of different PFCs on the MWCNTs increased in the order of PFBS

关键词： perfluorinated compounds     carbon nanotubes     competitive adsorption     humic acid     perfluorooctane sulfonate (PFOS)    

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Effects of phosphorus concentration on Cr(VI) sorption onto phosphorus-rich sludge biochar

DING Wenchuan,PENG Wenlong,ZENG Xiaolan,TIAN Xiumei

《环境科学与工程前沿（英文）》 2014年 第8卷 第3期   页码 379-385 doi: 10.1007/s11783-013-0606-0

摘要： To investigate effects of phosphorus content on Cr(VI) sorption onto phosphorus-rich biochar, sewage sludge of different phosphorus concentrations from 4 to 60 mg·g by dry weight were prepared and carbonized to make biochar for batch sorption experiments. Test results revealed that different phosphorous concentration of raw sludge had respective impacts on surface area, pore surface area, average pore diameter and pH value of derived biochar. The adsorption kinetics of phosphorus-rich biochar could be described by the pseudo-second-order model. The sorption isotherm data followed Langmiur model better than Freundlich model. Biochar produced from sludge with phosphorus concentration of 20 mg·g gave the largest chromium sorption capacity, which could be attributed to its largest surface area and pores surface area comparing with those of biochars from sludge with other phosphorus concentrations. The chromium loaded biochar was analyzed using Fourier Transform Infrared Spectroscopy and X-ray Diffraction measurement. The results indicated that chemical functional groups hydroxyl and methyl on surface of biochar were involved in Cr(VI) binding and its reducing to Cr(III). Then, a portion of Cr(III) in form of various phosphate precipitates was bound onto biochar surface and the rest was released into the solution. The experimental results suggested that phosphorus played an important role in pore and surface area development of sludge biochar during pyrolytic process. It also could react with Cr(III) on the biochar surface that impacted on capacity of Cr(VI) removal from solution by sludge biochar. Therefore, phosphorus concentration in sludge should be considered when sludge pyrolytic residue would be reused for heavy metals sorbing.

关键词： phosphorus     biochar     sewage sludge     hexavalent chromium     adsorption    

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Adsorption selectivity of salicylic acid and 5-sulfosalicylic acid onto hypercrosslinked polymeric adsorbents

LIU Fuqiang, CHEN Jinlong, LI Aimin, XIA Mingfang, FEI Zhenghao

《环境科学与工程前沿（英文）》 2007年 第1卷 第1期   页码 73-78 doi: 10.1007/s11783-007-0014-4

摘要： Both bottle-point and column-feeding experiments involving different solutes and sorbents were carried out to investigate the adsorption selectivity and separation performance of salicylic acid and 5-sulfosalicylic acid. Their adsorption isotherms onto such hypercrosslinked polymeric adsorbents as NDA-100 and NDA-99 could be well described by the Freundlich equations whose characteristics describe extrathermic and favorable adsorption processes. The adsorption towards NDA-100 mainly depended on the π-π interaction, while that towards NDA-99 was extremely influenced by the static-electric interaction. Additionally, the adsorptive capacity of salicylic acid on NDA-99 decreased while it increased on NDA-100 with the presence of 5-sulfosalicylic acid in the adsorptive environment as the competitive component. Comparatively, the adsorption capacity of 5-sulfosalicylic acid decreased on both resins with salicylic acid as the competitive component. In fact, the difference in the interaction between adsorbent and adsorbate resulted in the straight antagonism on the effective adsorption sites on the adsorbent. In conclusion, the adsorption selectivity of salicylic acid onto NDA-100 was obviously larger than that onto NDA-99 with the existence of 5-sulfosalicylic acid in the adsorptive environment. A satisfactory separation and recovery of tested solutes in aqueous phase could be foreseeably achieved by the sequencing adsorption technique involving NDA-100 as well as NDA-99.

关键词： 5-sulfosalicylic     bottle-point     hypercrosslinked polymeric     satisfactory separation     NDA-100    

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Evaluation of global niobium flow modeling and its market forecasting

《能源前沿（英文）》 2023年 第17卷 第2期   页码 286-293 doi: 10.1007/s11708-022-0823-y

摘要： Metal, as the indispensable material, is functioning the society from technology to the environment. Niobium (Nb) is considered a unique earth metal as it is related to many emerging technologies. The increasing economic growth exerts an increasing pressure on supply, which leads to its significance in the economic sector. However, few papers have addressed Nb sustainability, which forms the scope of this paper in order to start the process of Nb market forecasting based on some previous data and some assumptions. Therefore, this paper will discuss different thoughts in material substitution and the substance flow of Nb throughout a static flow using Nb global data to have a better understanding of the process of Nb from production to end of life. This shall lead to the identification of the market needs to determine its growth which is around 2.5% to 3.0%. Moreover, due to China’s huge Nb consumption which comes from the continuous development that is happening over the years, it will also briefly mention the Nb situation as well as its growth which according to statistics will grow steadily till 2030 by a rate of 4.0% to 6.0%. The results show that there should be some enhancement to Nb recycling potentials out of steel scrap. In addition, there should be more involvement of Nb in different industries as this would lead to less-used materials which can be translated to less environmental impact.

关键词： niobium (Nb)     sustainability     substance flow analysis     recycling     industrial ecology    

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Elevated temperature creep model of parallel wire strands

《结构与土木工程前沿（英文）》   页码 1060-1071 doi: 10.1007/s11709-023-0981-y

摘要： Parallel wire strands (PWSs), which are widely used in prestressed steel structures, are typically in high-stress states. Under fire conditions, significant creep effects occur, reducing the prestress and influencing the mechanical behavior of PWSs. As there is no existing approach to analyze their creep behavior, this study experimentally investigated the elevated temperature creep model of PWSs. A charge-coupled camera system was incorporated to accurately obtain the deformation of the specimen during the elevated temperature creep test. It was concluded that the temperature level had a more significant effect on the creep strain than the stress level, and 450 °C was the key segment point where the creep rate varied significantly. By comparing the elevated temperature creep test results for PWSs and steel strands, it was found that the creep strain of PWSs was lower than that of steel strands at the same temperature and stress levels. The parameters in the general empirical formula, the Bailey–Norton model, and the composite time-hardening model were fitted based on the experimental results. By evaluating the accuracy and form of the models, the composite time-hardening model, which can simultaneously consider temperature, stress, and time, is recommended for use in the fire-resistance design of pre-tensioned structures with PWSs.

关键词： parallel wire strands     experimental study     elevated temperature creep model    

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中国钽铌工业的进步与展望

何季麟

《中国工程科学》 2003年 第5卷 第5期   页码 40-46

摘要：

文章简要地回顾了九○五厂钽铌工业发展历程，并与世界钽铌工业作了对比分析。以详实的资料和基础数据，清晰地描述了我国钽铌工业发展现状和技术发展历程及其在世界钽铌工业发展中所处的地位和竞争能力；充分阐明了我国稀有金属钽铌资源及其在冶炼、加工技术领域中所存在的问题和面临的形势。从国家安全角度及行业整体发展的高度，提出了对国内稀有金属钽铌行业进行重组整合和积极开发国外资源的可持续发展的战略构想。

关键词： 钽铌工业     技术     可持续发展     市场    

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Numerical studies of dynamic behavior of liquid film on single-layer wire mesh with different wettabilities

《化学科学与工程前沿（英文）》   页码 1672-1680 doi: 10.1007/s11705-022-2205-8

摘要： Droplet impacting on the stainless steel wire mesh is very common in chemical devices, like a rotating packed bed. Surface wettability of wire mesh significantly affects the liquid flow pattern and liquid dispersion performance. However, the effect of surface wettability on the impaction phenomena at microscale such as liquid film is still unknown. In this work, the dynamic behavior of liquid film on the surface of wire mesh was analyzed by computational fluid dynamics simulation. The dynamic behavior of liquid film on the surface of wire mesh can be divided into the following three steps: (1) spreading step; (2) shrinkage process; (3) stabilizing or disappearing step. Effects of surface wettability, as well as operating conditions, on wetting area and liquid film thickness were studied. Compared to the hydrophilic wire mesh, the final wetting area of hydrophobic wire mesh is zero in most cases. The average liquid film thickness on the surface of hydrophilic wire mesh is 30.02–77.29 μm, and that of hydrophobic wire mesh is 41.76–237.37 μm. This work provided a basic understanding of liquid film flow at microscale on the surface with various surface wettabilities, which can be guiding the packing optimization and design.

关键词： stainless steel wire mesh     computational fluid dynamics     surface wettability     liquid film     impacting    

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Grafting of PEG400 onto the surface of LLDPE/SMA film

CHEN Gufeng, ZHANG Yi, XU Jiarui, ZHU Yafei

《化学科学与工程前沿（英文）》 2007年 第1卷 第2期   页码 128-131 doi: 10.1007/s11705-007-0024-6

摘要： Linear low-density polyethylene (LLDPE) was melt and blended with styrene-maleic anhydride copolymer (SMA). The blending films were then immersed in poly(ethylene glycol)400 (PEG400) at room temperature. The surface composition of the blend films was determined by Fourier transform infra-red spectroscopy coupled with a variable incidence angle attenuated total reflection accessory (ATR-FTIR). Results show that PEG400 can be grafted onto the surface of the films via esterification with SMA. The immersion of PEG promotes the enrichment of SMA onto the surface of the films. The water contact angle data show that grafting of PEG400 onto PE can greatly improve the hydrophilicity of the PE surface. These experiments show that surface functionalization of polyethylene films by blending SMA and then surface grafting of PEG is feasible, which suggest an effective and simple route for PE surface modification via blending and grafting.

关键词： hydrophilicity     temperature     effective     immersion     reflection accessory    

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Experimental study on wire breakage detection by acoustic emission

Limin SUN, Ji QIAN

《结构与土木工程前沿（英文）》 2011年 第5卷 第4期   页码 503-509 doi: 10.1007/s11709-011-0132-8

摘要： This paper experimentally investigated wire breakage detection in a steel cable by acoustic emission (AE) waveform. In the experiments, the attenuation laws of waveform amplitudes were discussed based on stress wave propagation in the wire, which was generated by kNocking and wire breakage. Then the wave velocity was calculated based on the reach time of the stress wave from each sensor. Finally, based on the waveform attenuation laws and the linear position method, the amplitude and energy of the source were confirmed through the measured waveform to identify the source category. The experimental results illustrated that the stress wave from different sources has a different frequency spectrum, and the amplitude attenuation factor varied with the stress wave frequency; high frequency waves had a greater attenuation factor. Compared with the other source, the wire breakage source contained a much higher energy, and thus, the wire breakage signal can be distinguished from the other source by comparing the non-attenuation energy at the source position.

关键词： acoustic emission (AE)     waveform     wire breakage     attenuation factor     wave velocity    

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标题 作者 时间 类型 操作

Preconcentration of trace elements by adsorption onto a niobium wire for electrothermal atomization atomic

Satoshi KANECO, Hiroaki KITANAGA, Hideyuki KATSUMATA, Tohru SUZUKI

期刊论文

Adsorption of herring sperm DNA onto pine sawdust biochar: Thermodynamics and site energy distribution

期刊论文

Adsorption property of direct fast black onto acid-thermal modified sepiolite and optimization of adsorption

Chengyuan SU, Weiguang LI, Yong WANG

期刊论文

Adsorption characteristics of ciprofloxacin onto g-MoS2<

Zhenyu Yang, Rong Xing, Wenjun Zhou, Lizhong Zhu

期刊论文

Comparing the adsorption behaviors of Cd, Cu and Pb from water onto Fe-Mn binary oxide, MnO

Wei XU,Huachun LAN,Hongjie WANG,Hongming LIU,Jiuhui QU

期刊论文

A ternary mechanism for the facilitated transfer of metal ions onto metal–organic frameworks: implications

期刊论文

Effect of co-existing organic compounds on adsorption of perfluorinated compounds onto carbon nanotubes

Shubo DENG,Yue BEI,Xinyu LU,Ziwen DU,Bin WANG,Yujue WANG,Jun HUANG,Gang YU

期刊论文

Effects of phosphorus concentration on Cr(VI) sorption onto phosphorus-rich sludge biochar

DING Wenchuan,PENG Wenlong,ZENG Xiaolan,TIAN Xiumei

期刊论文

Adsorption selectivity of salicylic acid and 5-sulfosalicylic acid onto hypercrosslinked polymeric adsorbents

LIU Fuqiang, CHEN Jinlong, LI Aimin, XIA Mingfang, FEI Zhenghao

期刊论文

Evaluation of global niobium flow modeling and its market forecasting

期刊论文

Elevated temperature creep model of parallel wire strands

期刊论文

中国钽铌工业的进步与展望

何季麟

期刊论文

Numerical studies of dynamic behavior of liquid film on single-layer wire mesh with different wettabilities

期刊论文

Grafting of PEG400 onto the surface of LLDPE/SMA film

CHEN Gufeng, ZHANG Yi, XU Jiarui, ZHU Yafei

期刊论文

Experimental study on wire breakage detection by acoustic emission

Limin SUN, Ji QIAN

期刊论文