Generally, the phase of the cold-atom interferometer is extracted from the atomic interference fringe, which can be obtained by scanning the chirp rate of the Raman lasers at a given interrogation time T. If mapping t...Generally, the phase of the cold-atom interferometer is extracted from the atomic interference fringe, which can be obtained by scanning the chirp rate of the Raman lasers at a given interrogation time T. If mapping the phase shift for each T with a series of measurements, the extraction time is limited by the protocol of each T measurement, and therefore increases dramatically when doing fine mapping with a small step of T. Here we present a new method for rapid extraction of the phase shift via phase demodulation. By using this method, the systematic shifts can be mapped though the whole interference area. This method enables quick diagnostics of the potential cause of the phase shift in specific time. We demonstrate experimentally that this method is effective for the evaluation of the systematic errors of the cold atomic gravimeter. The systematic phase error induced by the quadratic Zeeman effect in the free-falling region is extracted by this method. The measured results correspond well with the theoretic prediction and also agree with the results obtained by the fringe fitting method for each T.展开更多
A procedure for the preconcentration of copper was described in this paper using multi-walled carbon nanotubes (MWCNTs) oxidized by potassium permanganate as the adsorbent for the enrichment of trace copper in water s...A procedure for the preconcentration of copper was described in this paper using multi-walled carbon nanotubes (MWCNTs) oxidized by potassium permanganate as the adsorbent for the enrichment of trace copper in water samples. Important parameters, such as the sample pH, the concentration and volume of eluent, sample flow rate and volume, and interference of coexisting ions, were investigated. The obtained results indicated that proposed method possessed an excellent analytical performance. The linear range, the detection limit, and precison (RSD) were 1–100 ng/mL (R(2) = 0.9993), 0.32 ng/mL and 2.88%, respectively. The results showed that copper could be adsorbed quantitatively on the pretreated MWCNTs with potassium permanganate, and proposed method was very useful in the monitoring of copper in the environment.展开更多
Recently, the rapid progress of quantum sensing research reveals that Rydberg atoms have great potential in becoming high-precision centimeter-scale antennas for low-frequency fields. In order to facilitate efficient ...Recently, the rapid progress of quantum sensing research reveals that Rydberg atoms have great potential in becoming high-precision centimeter-scale antennas for low-frequency fields. In order to facilitate efficient and reliable detection of low-frequency fields via Rydberg atoms, we designed and implemented a heterodyne method based on the linear response to external signals under the condition of Rydberg electromagnetically induced transparency(EIT). Instead of relying on observing changes in the absorption of light by Rydberg atoms, our method focuses on the phase modulation effect on the probe laser induced by low-frequency fields via the Rydberg EIT mechanism and utilizes a special demodulation process to accurately retrieve signals including both amplitude and phase. The general principles of our method apply to both electric and magnetic fields, and it is even possible to realize a combination of both functionalities in the same apparatus. In particular, we experimentally demonstrate the full cycle of operations with respect to both cases. In measuring low-frequency electric fields,we discover that the Rydberg dipole–dipole interaction among atoms induces a linear superposition of Rydberg states with different angular momentum, generating a first-order response corresponding to the signature of the linear Stark effect. As Rydberg atoms have excellent coupling strengths with electric fields, our results indicate that our method can hopefully achieve high-precision performance for practical tasks in the future.展开更多
A new method for analysis of trace mercury in water samples was developed, based on the combination of preconcentration/separation using dithizone-modified nanometer titanium dioxide （TiO2） as a solid phase extracta...A new method for analysis of trace mercury in water samples was developed, based on the combination of preconcentration/separation using dithizone-modified nanometer titanium dioxide （TiO2） as a solid phase extractant and determination by cold vapor atomic adsorption spectrometry （CVAAS）. Dithizone was dissolved with alcohol and loaded on the surface of nano-sized TiO2 powders by stirring. The static adsorption behavior of Hg^2＋on the dithizone-modified nanoparficles was investigated in detail. It was found that excellent adsorption ratio for Hg^2＋ could be obtained in the pH range of 7-8 with an oscillation time of 15 rain, and a 5 mL of 3.5 mol·L^-1 HCI solution could quantitatively elute Hg^2＋ from nanometer TiO2 powder. Common coexisting ions caused no obvious influence on the determination of mercury. The mechanisms for the adsorption and desorption were discussed. The detection limit （30） for Hg^2＋ was calculated to be 5 ng·L^-1. The proposed method was applied to the determination of Hg^2＋ in a mineral water sample and a Zhujiang River water sample. By the standard addition method, the average recoveries were found to be 94.4%-108.3% with RSD （n = 5） of 2.9%-3.5%.展开更多
A simple and sensitive solid phase extraction utilizing C18 filled cartridges incorporated with dithizone for preconcentration of lead and its subsequent determination by flame atomic absorption spectrometry (FAAS) wa...A simple and sensitive solid phase extraction utilizing C18 filled cartridges incorporated with dithizone for preconcentration of lead and its subsequent determination by flame atomic absorption spectrometry (FAAS) was developed. Several parameters such as type, concentration and volume of eluent, pH of the sample solution, flow rate of extraction and volume of the sample were evaluated. The effect of a variety of ions on preconcentration and recovery was also investigated. At pH = 7.4 and 1.0 mol?L–1 HCl eluting them, lead ions were recovered quantitatively. The limit of detection (LOD) defined as 3Sbl was determined to be 8.1 μg L–1 for 500 mL of sample solution and eluted with 5 mL of 1.0 mol?L–1 HCl under optimum conditions. The accuracy and precision (RSD %) of the method were >90% and <10%, respectively. In the end, the proposed method was applied to a number of real sugar samples and the amount of lead was determined by spiking a known concentration of lead into the solution.展开更多
A simple and reproducible method for the rapid extraction and determination of trace amounts of copper（Ⅱ） ions using octadecyl-bonded silica membrane disks modified by N,N′-disalicylideneethylenediamine （DESDA） ...A simple and reproducible method for the rapid extraction and determination of trace amounts of copper（Ⅱ） ions using octadecyl-bonded silica membrane disks modified by N,N′-disalicylideneethylenediamine （DESDA） and atomic absorption spectrometry was presented. The method is based on complex formation on the surface of the ENVI-18 DISK^TM disks followed by stripping of the retained species by minimum amounts of appropriate organic solvents. The elution is efficient and quantitative. The effects of potential interfering ions, pH, ligand amount, stripping solvent, and sample flow rate were also investigated. Under the optimal experimental conditions, the break-through volume was found to about be 1000 mL providing a preconcentration factor of 500. The maximum capacity of the disks was found to be （389±4） μg for Cu^2＋. The limit of detection of the proposed method is 5 ng per liter. The method was applied to the extraction and recovery of copper in different water samples.展开更多
Fabry-Perot(F-P)-based phase demodulation of heterodyne light-induced thermoelastic spectroscopy(H-LITES)was demonstrated for the first time in this study.The vibration of a quartz tuning fork(QTF)was detected using t...Fabry-Perot(F-P)-based phase demodulation of heterodyne light-induced thermoelastic spectroscopy(H-LITES)was demonstrated for the first time in this study.The vibration of a quartz tuning fork(QTF)was detected using the F-P interference principle instead of an electrical signal through the piezoelectric effect of the QTF in traditional LITES to avoid thermal noise.Given that an Fabry-Perot interferometer(FPI)is vulnerable to disturbances,a phase demodulation method that has been demonstrated theoretically and experimentally to be an effective solution for instability was used in H-LITES.The sensitivity of the F-P phase demodulation method based on the H-LITES sensor was not associated with the wavelength or power of the probe laser.Thus,stabilising the quadrature working point(Q-point)was no longer necessary.This new method of phase demodulation is structurally simple and was found to be resistant to interference from light sources and the surroundings using the LITES technique.展开更多
In the present work, an easy solid phase extraction method using alumina modified with polyethylenimine as a new adsorbent was applied to the simultaneous extraction of copper, silver, and palladium ions prior to thei...In the present work, an easy solid phase extraction method using alumina modified with polyethylenimine as a new adsorbent was applied to the simultaneous extraction of copper, silver, and palladium ions prior to their determination with electrothermal atomic absorption spectrometry. The analytical procedure involved the complex formation of these cations with polyethylenimine as a chelating agent in buffer media of pH 7.0. Under the optimum conditions, a preconcentration factor of 200, 150, and 200, precision of ~5.4%, ＋4.7%, and ＋5.2% and linear calibration ranges of 15.0-140, 4.0-93, and 7.5-125 ng/L （in original solution） for Cu, Ag, and Pd were obtained, respectively. Also detection limits of 3.9,1.1, and 2.0 ng/L were obtained for Cu, Ag, and Pd, respectively. The proposed method was applied to the determination of copper, silver, and palladium in some real samples with satisfactory results.展开更多
A new method based on the cloud point extraction（CPE） for separation and preconcentration of nickel（Ⅱ） and its subsequent determination by graphite furnace atomic absorption spectrometry（GFAAS） was proposed, 8-...A new method based on the cloud point extraction（CPE） for separation and preconcentration of nickel（Ⅱ） and its subsequent determination by graphite furnace atomic absorption spectrometry（GFAAS） was proposed, 8-hydroxyquinoline and Triton X-100 were used as the ligand and surfactant respectively. Nickel（Ⅱ） can form a hy-drophobic complex with 8-hydroxyquinoline, the complex can be extracted into the small volume surfactant rich phase at the cloud point temperature（CPT） for GFAAS determination. The factors affecting the cloud point extraction, such as pH, ligand concentration, surfactant concentration, and the incubation time were optimized. Under the optimal conditions, a detection limit of 12 ng/L and a relative standard deviation（RSD） of 2.9% were obtained for Ni（Ⅱ） determination. The enrichment factor was found to be 25. The proposed method was successfully applied to the determination of nickel（Ⅱ） in certified reference material and different types of water samples and the recovery was in a range of 95%―103%.展开更多
We present the experimental demonstration of nondestructive detection of ^(171)Yb atoms in a magneto-optical trap(MOT) based on phase shift measurement induced by the atoms on a weak off-resonant laser beam. After loa...We present the experimental demonstration of nondestructive detection of ^(171)Yb atoms in a magneto-optical trap(MOT) based on phase shift measurement induced by the atoms on a weak off-resonant laser beam. After loading a green MOT of ^(171)Yb atoms, the phase shift is obtained with a two-color Mach–Zehnder interferometer by means of ±45 MHz detuning with respect to the ^(1)S_(0)–^(1)P_(1) transition. We measured a phase shift of about 100 mrad corresponding to an atom count of around 5 × 10^(5). This demonstrates that it is possible to obtain the number of atoms without direct destructive measurement compared with the absorption imaging method. This scheme could be an important approach towards a high-precision lattice clock for clock operation through suppression of the impact of the Dick effect.展开更多
本研究旨在建立一种高效、快速、选择性测定食品中痕量汞的方法。通过溶剂热法及后续的巯基化修饰,成功制备了一种新型巯基功能化磁性介孔二氧化硅(Thiol-functionalized Magnetic Mesoporous Silica,记为mSS@Fe_(3)O_(4))吸附剂。将该...本研究旨在建立一种高效、快速、选择性测定食品中痕量汞的方法。通过溶剂热法及后续的巯基化修饰,成功制备了一种新型巯基功能化磁性介孔二氧化硅(Thiol-functionalized Magnetic Mesoporous Silica,记为mSS@Fe_(3)O_(4))吸附剂。将该吸附剂用于磁性固相萃取(MSPE),结合原子荧光光谱法(AFS),构建了一种分析食品中痕量汞的新方法。通过X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)等手段对材料进行了表征,证实了巯基已成功接枝到磁性介孔二氧化硅表面。系统优化了萃取过程中的关键参数,包括样品pH值、吸附时间、吸附剂用量、洗脱液组成和上样体积。结果表明,归因于材料的介孔结构和高比表面积,吸附平衡在1 min内即可达到,实现了对Hg^(2+)的快速富集。在最优条件下,该吸附剂对Hg^(2+)的理论最大吸附容量(qm)为67.89 mg/g;在回收率保持>90%时,最大上样体积为200 mL,预浓缩因子可达200。该方法具有较宽的pH值(1~13)适用范围和优异的抗基质干扰能力。方法线性范围为0.10~4.0μg/L(相关系数r=0.9996),方法检出限(MDL)为0.012μg/kg,对空白样品进行7次平行测定的相对标准偏差(RSD)为2.4%(n=7)。通过对国家标准物质和多种实际样品(草鱼、大米等)的加标回收实验,验证了方法的准确性和可靠性,回收率在94.0%~106%。该方法集快速、高效、高选择性与高灵敏度于一体,为食品中痕量汞的常规监测提供了有力的技术支持。展开更多
The adsorption behavior of multiwalled carbon nanotubes （MWNTs） toward heavy elements has been investigated systemically, and a new method has been developed for the determination of trace elements in water samples ...The adsorption behavior of multiwalled carbon nanotubes （MWNTs） toward heavy elements has been investigated systemically, and a new method has been developed for the determination of trace elements in water samples based on preconcentration with mini-column packed with MWNTs prior to its determination by flame atomic absorption spectrometry （FAAS） The recommended parameters of proposed method influencing the preconcentration of the analytes, such as pH of the sample, sample flow rate and volume, elute solution and interfering ions, have been used. Under the optimized conditions, the calibration graphs were linear with the correlation coefficient range 0.9981-0.9995. According to the results, the metals were found 0.019-0.051, 0.011-0.031, 0.00-0.081, 0.00-0.0002, 0.007-0.0925, 0.00-0.0104 μg/L in water samples for Pb, Mn, Zn, Cd, Fe, Cu respectively. The percentage relative standard deviation （%RSD） for five replicate samples were 〈 5% in all cases. The method has been successfully applied to the determination of trace elements in some environmental samples with satisfactory results.展开更多
A sensitive and simple solid phase extraction method for the simultaneous determination of trace and toxic metals in environmental samples has been reported. The method is based on the adsorption of Zinc, Iron and Cop...A sensitive and simple solid phase extraction method for the simultaneous determination of trace and toxic metals in environmental samples has been reported. The method is based on the adsorption of Zinc, Iron and Copper on SDS-coated alumina nanoparticles, which is also modified with 3-mercapto-D-valine. The retained analyte ions on modified solid phase were eluted using 5 mL of 4 mol·L﹣1 HNO3. The analyte determination was carried out by flame atomic absorption spectrometry. The influences of some metal ion and anions on the recoveries of understudy analyte ion were investigated. The influences of the analytical parameters including pH, ligand and SDS amount, eluting solution (type and concentrations) and sample volume on metal ions recoveries were investigated. The extraction efficiency was > 98% with relative standard deviation lower than 3% the method has been successfully applied for the extraction and determination of these ions content in some real samples. Prepared adsorbent was characterized by SEM and FT-IR measurements.展开更多
In this study we investigated the enrichment ability of oxidized multiwalled carbon nanotubes （MWCNTs） and established a new method for the determination of trace cadmium in environment with flame atomic absorption ...In this study we investigated the enrichment ability of oxidized multiwalled carbon nanotubes （MWCNTs） and established a new method for the determination of trace cadmium in environment with flame atomic absorption spectrometry. The MWCNTs were oxidized by potassium permanganate under appropriate conditions before use as preconcentration packing. Parameters influencing the recoveries of target analytes were optimized. Under optimal conditions, the target analyte exhibited a good linearity （R^2=0.9992） over the concentration range 0.5-50 ng/ml. The detection limit and precision of the proposed method were 0.15 ng/ml and 2.06%, respectively. The proposed method was applied to the determination of cadmium in real-world environmental samples and the recoveries were in the range of 91.3%-108.0%. All these experimental results indicated that this new procedure could be applied to the determination of trace cadmium in environmental waters.展开更多
基金supported by the National Natural Science Foundation of China(Grant Nos.11174249 and 61475139)the Ministry of Science and Technology of China(Grant No.2011AA060504)+1 种基金the National Basic Research Program of China(Grant No.2013CB329501)the Fundamental Research Funds for the Central Universities,China(Grant No.2015FZA3002)
文摘Generally, the phase of the cold-atom interferometer is extracted from the atomic interference fringe, which can be obtained by scanning the chirp rate of the Raman lasers at a given interrogation time T. If mapping the phase shift for each T with a series of measurements, the extraction time is limited by the protocol of each T measurement, and therefore increases dramatically when doing fine mapping with a small step of T. Here we present a new method for rapid extraction of the phase shift via phase demodulation. By using this method, the systematic shifts can be mapped though the whole interference area. This method enables quick diagnostics of the potential cause of the phase shift in specific time. We demonstrate experimentally that this method is effective for the evaluation of the systematic errors of the cold atomic gravimeter. The systematic phase error induced by the quadratic Zeeman effect in the free-falling region is extracted by this method. The measured results correspond well with the theoretic prediction and also agree with the results obtained by the fringe fitting method for each T.
文摘A procedure for the preconcentration of copper was described in this paper using multi-walled carbon nanotubes (MWCNTs) oxidized by potassium permanganate as the adsorbent for the enrichment of trace copper in water samples. Important parameters, such as the sample pH, the concentration and volume of eluent, sample flow rate and volume, and interference of coexisting ions, were investigated. The obtained results indicated that proposed method possessed an excellent analytical performance. The linear range, the detection limit, and precison (RSD) were 1–100 ng/mL (R(2) = 0.9993), 0.32 ng/mL and 2.88%, respectively. The results showed that copper could be adsorbed quantitatively on the pretreated MWCNTs with potassium permanganate, and proposed method was very useful in the monitoring of copper in the environment.
基金supported by the Science and Technology Commission of Shanghai Municipality (Grant No.24DP2600202)the National Key R&D Program of China (Grant No.2024YFB4504002)+2 种基金Industrial Technology Development Research Program of Shanghai Institute of Optics and Fine Mechanicsthe National Natural Science Foundation of China (Grant No.92165107)the China Postdoctoral Science Foundation (Grant Nos.2024M753359 for S.J.and2022M723270 for X.W.)。
文摘Recently, the rapid progress of quantum sensing research reveals that Rydberg atoms have great potential in becoming high-precision centimeter-scale antennas for low-frequency fields. In order to facilitate efficient and reliable detection of low-frequency fields via Rydberg atoms, we designed and implemented a heterodyne method based on the linear response to external signals under the condition of Rydberg electromagnetically induced transparency(EIT). Instead of relying on observing changes in the absorption of light by Rydberg atoms, our method focuses on the phase modulation effect on the probe laser induced by low-frequency fields via the Rydberg EIT mechanism and utilizes a special demodulation process to accurately retrieve signals including both amplitude and phase. The general principles of our method apply to both electric and magnetic fields, and it is even possible to realize a combination of both functionalities in the same apparatus. In particular, we experimentally demonstrate the full cycle of operations with respect to both cases. In measuring low-frequency electric fields,we discover that the Rydberg dipole–dipole interaction among atoms induces a linear superposition of Rydberg states with different angular momentum, generating a first-order response corresponding to the signature of the linear Stark effect. As Rydberg atoms have excellent coupling strengths with electric fields, our results indicate that our method can hopefully achieve high-precision performance for practical tasks in the future.
基金the Natural Science Foundation of the Department of Education, Guangdong Province, China (No. 02025).
文摘A new method for analysis of trace mercury in water samples was developed, based on the combination of preconcentration/separation using dithizone-modified nanometer titanium dioxide （TiO2） as a solid phase extractant and determination by cold vapor atomic adsorption spectrometry （CVAAS）. Dithizone was dissolved with alcohol and loaded on the surface of nano-sized TiO2 powders by stirring. The static adsorption behavior of Hg^2＋on the dithizone-modified nanoparficles was investigated in detail. It was found that excellent adsorption ratio for Hg^2＋ could be obtained in the pH range of 7-8 with an oscillation time of 15 rain, and a 5 mL of 3.5 mol·L^-1 HCI solution could quantitatively elute Hg^2＋ from nanometer TiO2 powder. Common coexisting ions caused no obvious influence on the determination of mercury. The mechanisms for the adsorption and desorption were discussed. The detection limit （30） for Hg^2＋ was calculated to be 5 ng·L^-1. The proposed method was applied to the determination of Hg^2＋ in a mineral water sample and a Zhujiang River water sample. By the standard addition method, the average recoveries were found to be 94.4%-108.3% with RSD （n = 5） of 2.9%-3.5%.
文摘A simple and sensitive solid phase extraction utilizing C18 filled cartridges incorporated with dithizone for preconcentration of lead and its subsequent determination by flame atomic absorption spectrometry (FAAS) was developed. Several parameters such as type, concentration and volume of eluent, pH of the sample solution, flow rate of extraction and volume of the sample were evaluated. The effect of a variety of ions on preconcentration and recovery was also investigated. At pH = 7.4 and 1.0 mol?L–1 HCl eluting them, lead ions were recovered quantitatively. The limit of detection (LOD) defined as 3Sbl was determined to be 8.1 μg L–1 for 500 mL of sample solution and eluted with 5 mL of 1.0 mol?L–1 HCl under optimum conditions. The accuracy and precision (RSD %) of the method were >90% and <10%, respectively. In the end, the proposed method was applied to a number of real sugar samples and the amount of lead was determined by spiking a known concentration of lead into the solution.
文摘A simple and reproducible method for the rapid extraction and determination of trace amounts of copper（Ⅱ） ions using octadecyl-bonded silica membrane disks modified by N,N′-disalicylideneethylenediamine （DESDA） and atomic absorption spectrometry was presented. The method is based on complex formation on the surface of the ENVI-18 DISK^TM disks followed by stripping of the retained species by minimum amounts of appropriate organic solvents. The elution is efficient and quantitative. The effects of potential interfering ions, pH, ligand amount, stripping solvent, and sample flow rate were also investigated. Under the optimal experimental conditions, the break-through volume was found to about be 1000 mL providing a preconcentration factor of 500. The maximum capacity of the disks was found to be （389±4） μg for Cu^2＋. The limit of detection of the proposed method is 5 ng per liter. The method was applied to the extraction and recovery of copper in different water samples.
基金support from the National Natural Science Foundation of China(Grant Nos.62022032,62275065,61875047,61505041)the Key Laboratory of Opto-Electronic Information Acquisition and Manipulation(Anhui University)+1 种基金the Ministry of Education(Grant No.OEIAM202202)the Fundamental Research Funds for Central Universities.
文摘Fabry-Perot(F-P)-based phase demodulation of heterodyne light-induced thermoelastic spectroscopy(H-LITES)was demonstrated for the first time in this study.The vibration of a quartz tuning fork(QTF)was detected using the F-P interference principle instead of an electrical signal through the piezoelectric effect of the QTF in traditional LITES to avoid thermal noise.Given that an Fabry-Perot interferometer(FPI)is vulnerable to disturbances,a phase demodulation method that has been demonstrated theoretically and experimentally to be an effective solution for instability was used in H-LITES.The sensitivity of the F-P phase demodulation method based on the H-LITES sensor was not associated with the wavelength or power of the probe laser.Thus,stabilising the quadrature working point(Q-point)was no longer necessary.This new method of phase demodulation is structurally simple and was found to be resistant to interference from light sources and the surroundings using the LITES technique.
文摘In the present work, an easy solid phase extraction method using alumina modified with polyethylenimine as a new adsorbent was applied to the simultaneous extraction of copper, silver, and palladium ions prior to their determination with electrothermal atomic absorption spectrometry. The analytical procedure involved the complex formation of these cations with polyethylenimine as a chelating agent in buffer media of pH 7.0. Under the optimum conditions, a preconcentration factor of 200, 150, and 200, precision of ~5.4%, ＋4.7%, and ＋5.2% and linear calibration ranges of 15.0-140, 4.0-93, and 7.5-125 ng/L （in original solution） for Cu, Ag, and Pd were obtained, respectively. Also detection limits of 3.9,1.1, and 2.0 ng/L were obtained for Cu, Ag, and Pd, respectively. The proposed method was applied to the determination of copper, silver, and palladium in some real samples with satisfactory results.
基金Supported by the National Natural Science Foundation of China(No.20075009)
文摘A new method based on the cloud point extraction（CPE） for separation and preconcentration of nickel（Ⅱ） and its subsequent determination by graphite furnace atomic absorption spectrometry（GFAAS） was proposed, 8-hydroxyquinoline and Triton X-100 were used as the ligand and surfactant respectively. Nickel（Ⅱ） can form a hy-drophobic complex with 8-hydroxyquinoline, the complex can be extracted into the small volume surfactant rich phase at the cloud point temperature（CPT） for GFAAS determination. The factors affecting the cloud point extraction, such as pH, ligand concentration, surfactant concentration, and the incubation time were optimized. Under the optimal conditions, a detection limit of 12 ng/L and a relative standard deviation（RSD） of 2.9% were obtained for Ni（Ⅱ） determination. The enrichment factor was found to be 25. The proposed method was successfully applied to the determination of nickel（Ⅱ） in certified reference material and different types of water samples and the recovery was in a range of 95%―103%.
基金Project supported by the National Natural Science Foundation of China (Grant Nos. U20A2075,11803072,and 12374467)the Innovation Program for Quantum Science and Technology (Grant No. 2021ZD0300902)the Hubei Provincial Science and Technology Major Project (Grant No. ZDZX2022000004)。
文摘We present the experimental demonstration of nondestructive detection of ^(171)Yb atoms in a magneto-optical trap(MOT) based on phase shift measurement induced by the atoms on a weak off-resonant laser beam. After loading a green MOT of ^(171)Yb atoms, the phase shift is obtained with a two-color Mach–Zehnder interferometer by means of ±45 MHz detuning with respect to the ^(1)S_(0)–^(1)P_(1) transition. We measured a phase shift of about 100 mrad corresponding to an atom count of around 5 × 10^(5). This demonstrates that it is possible to obtain the number of atoms without direct destructive measurement compared with the absorption imaging method. This scheme could be an important approach towards a high-precision lattice clock for clock operation through suppression of the impact of the Dick effect.
文摘The adsorption behavior of multiwalled carbon nanotubes （MWNTs） toward heavy elements has been investigated systemically, and a new method has been developed for the determination of trace elements in water samples based on preconcentration with mini-column packed with MWNTs prior to its determination by flame atomic absorption spectrometry （FAAS） The recommended parameters of proposed method influencing the preconcentration of the analytes, such as pH of the sample, sample flow rate and volume, elute solution and interfering ions, have been used. Under the optimized conditions, the calibration graphs were linear with the correlation coefficient range 0.9981-0.9995. According to the results, the metals were found 0.019-0.051, 0.011-0.031, 0.00-0.081, 0.00-0.0002, 0.007-0.0925, 0.00-0.0104 μg/L in water samples for Pb, Mn, Zn, Cd, Fe, Cu respectively. The percentage relative standard deviation （%RSD） for five replicate samples were 〈 5% in all cases. The method has been successfully applied to the determination of trace elements in some environmental samples with satisfactory results.
文摘A sensitive and simple solid phase extraction method for the simultaneous determination of trace and toxic metals in environmental samples has been reported. The method is based on the adsorption of Zinc, Iron and Copper on SDS-coated alumina nanoparticles, which is also modified with 3-mercapto-D-valine. The retained analyte ions on modified solid phase were eluted using 5 mL of 4 mol·L﹣1 HNO3. The analyte determination was carried out by flame atomic absorption spectrometry. The influences of some metal ion and anions on the recoveries of understudy analyte ion were investigated. The influences of the analytical parameters including pH, ligand and SDS amount, eluting solution (type and concentrations) and sample volume on metal ions recoveries were investigated. The extraction efficiency was > 98% with relative standard deviation lower than 3% the method has been successfully applied for the extraction and determination of these ions content in some real samples. Prepared adsorbent was characterized by SEM and FT-IR measurements.
基金Project supported by the Hi-Tech Research and Development Program (863) of China (No.2006AA06Z424)Personal Innovation Foundation of Universities in Henan Province (No.[2005]-126)+1 种基金Youth Science Foundation of Henan Normal University (No.2004005)Natural Science Foundation of Henan Province (No.072300460010).
文摘In this study we investigated the enrichment ability of oxidized multiwalled carbon nanotubes （MWCNTs） and established a new method for the determination of trace cadmium in environment with flame atomic absorption spectrometry. The MWCNTs were oxidized by potassium permanganate under appropriate conditions before use as preconcentration packing. Parameters influencing the recoveries of target analytes were optimized. Under optimal conditions, the target analyte exhibited a good linearity （R^2=0.9992） over the concentration range 0.5-50 ng/ml. The detection limit and precision of the proposed method were 0.15 ng/ml and 2.06%, respectively. The proposed method was applied to the determination of cadmium in real-world environmental samples and the recoveries were in the range of 91.3%-108.0%. All these experimental results indicated that this new procedure could be applied to the determination of trace cadmium in environmental waters.
