Journal of Applied Spectroscopy
·
2014
·Vol. 81
·期 5
·807-811
·
IF 0.514
Liu Y.,Fan J.,Ma W.,Fu Ch.
An aqueous two-phase system of acetone and (NH 4 ) 2 SO 4 mixture has been developed for the extractive separation of copper (Cu). The complex formed by Cu(II) and Nuclear Fast Red was found to be extracted into the acetone-rich upper phase, and the absorbance of the complex was determined at 465 nm. Beer’s law was obeyed over the concentration range of ~0.6–3.2 mg/l for Cu(II) with a good linearity. The proposed method has been applied to the separation and determination of Cu(II) in seafood samples with a coefficient of variation less than 2.8%. The recovery obtained was ~96.3–101.7%.
研究领域:
分析化学
·
环境化学
·
食品安全检测
✓ 已验证
DOI
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2014
·
IF 2.129
Jiao Zhao,Yunhui Lu,Chongyang Fan,Jun Wang,Yaling Yang
A novel and simple method for the sensitive determination of trace amounts of nitrite in human urine and blood has been developed by combination of cloud point extraction (CPE) and microplate assay. The method is based on the Griess reaction and the reaction product is extracted into nonionic surfactant Triton-X114 using CPE technique. In this study, decolorization treatment of urine and blood was applied to overcome the interference of matrix and enhance the sensitivity of nitrite detection. Multi-sample can be simultaneously detected thanks to a 96-well microplate technique. The effects of different operating parameters such as type of decolorizing agent, concentration of surfactant (Triton X-114), addition of (NH 4 ) 2 SO 4, extraction temperature and time, interfering elements were studied and optimum conditions were obtained. Under the optimum conditions, a linear calibration graph was obtained in the range of 10–400 ng mL −1 of nitrite with limit of detection (LOD) of 2.5 ng mL −1 . The relative standard deviation (RSD) for determination of 100 ng mL −1 of nitrite was 2.80%. The proposed method was successfully applied for the determination of nitrite in the urine and blood samples with recoveries of 92.6–101.2%.
研究领域:
分析化学
·
医学检验
✓ 已验证
产品关联
DOI
PubMed
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2022
·
IF 4.831
Ling Wu,Feng Li,Haidong Yu,Luping Shen,Mingxi Wang
Spectrophotometry is an economic and rapid method for detecting oxalic acid (OA), while the reported methods have some drawbacks, such as narrow linear range, long response time, delicate operation and required expensive reagents. Herein, we found that the as-synthesized Fe(III)-sulfosalicylate (FeSSA) could be used as an efficient colorimetric chemosensor to detect OA, and the established FeSSA-based fading spectrophotometry showed prominent advantages over the existing ones in detecting OA. The as-established method has wider linear range of 0.80–160 mg/L with regression coefficient ≥ 0.999, while the widest linear range is just 2.7–54 mg/L among the reported ones. Moreover, the method has low limit of detection (0.74 mg/L), extremely fast response (several seconds), satisfactory selectivity, high accuracy and precision. Most importantly, its reliability was further verified by employing it to determine OA concentration during the degradation process of organic pollutants. The measured OA concentration at any time interval was perfectly consistent with those determined by the well-recognized high performance liquid chromatography (HPLC). These confirmed that the FeSSA-based fading spectrophotometry is an efficient, simple, fast, accurate and economic method to determine OA in a wide concentration range.
研究领域:
分析化学
·
环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
·
2020
·Vol. 20
·期 7
·4015-4022
·
IF 1.134
Wang Baomin,Deng Shuang,Zhao Lu
Graphene nanoplates (GNPs) are carbon nanomaterials with two-dimensional structure which is easy to reunite and their dispersion is necessary before using. The existing methods for dispersion characterization mainly include UV spectrophotometry, scanning electron microscope (SEM), transmission
electron microscopy (TEM) and Atomic Force Microscopy (AFM). In this research study, sodium dodecyl benzene sulfonate (SDBS), polyoxyethylene (40) nonylphenyl ether, branched (CO890), polyvinyl pyrrolidone (PVP) and cetyltrimethyl ammonium bromide (CTAB) were used as dispersants, and ultrasonic
treatment was employed as dispersion method. Ultraviolet spectrum for GNPs showed that some errors were attained, resulting from dispersant at 274 nm characteristic wavelength of GNPs dispersions with deionized water as controlled sample. The errors could be eliminated if dispersant solution
was used as controlled sample. The microstructures of dispersed GNPs observed by SEM, TEM and AFM suggested that the GNPs were dispersed uniformly with 2.5 g/L SDBS, which showed the best dispersion effect. Raman spectrum indicated that more chaotic distribution and edge structures were achieved
after dispersion.
研究领域:
材料科学
·
纳米技术
✓ 已验证
DOI
PubMed
高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2019
·Vol. 26
·期 26
·27063-27072
·
IF 2.914
Wang Mengyun,Wang Daiyao,Qiu Shiyi,Xiao Junyang,Cai Huahua,Zou Jing
In this study, a sensitive and low-cost multi-wavelength spectrophotometric method for the determination of hydrogen peroxide (H 2 O 2 ) in water was established. The method was based on the oxidative coloration of 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) via Fenton reaction, which resulted in the formation of green radical (ABTS •+ ) with absorbance at four different wavelengths (i.e., 415 nm, 650 nm, 732 nm, and 820 nm). Under the optimized conditions ( C ABTS = 2.0 mM, C Fe 2+ = 1.0 mM, pH = 2.60 ± 0.02, and reaction time ( t ) = 1 min), the absorbance of the generated ABTS •+ at 415 nm, 650 nm, 732 nm, and 820 nm were well linear with H 2 O 2 concentrations in the range of 0–40 μM ( R 2 > 0.999) and the sensitivities of the proposed Fenton-ABTS method were calculated as 4.19 × 10 4 M –1 cm –1 ,1.73 × 10 4 M –1 cm –1 , 2.18 × 10 4 M –1 cm –1 , and 1.96 × 10 4 M –1 cm –1 , respectively. Meanwhile, the detection limits of the Fenton-ABTS method at 415 nm, 650 nm, 732 nm, and 820 nm were respectively calculated to be 0.18 μM, 0.12 μM, 0.10 μM, and 0.11 μM. The absorbance of the generated ABTS •+ in ultrapure water, underground water, and reservoir water was quite stable within 30 min. Moreover, the proposed Fenton-ABTS method could be used for monitoring the variations of H 2 O 2 concentration during the oxidative decolorization of RhB in alkali-activated H 2 O 2 system.
研究领域:
分析化学
·
环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ANALYTICAL LETTERS
·
2024
·
IF 1.6
Yanli Yu,Guangming Zhou,Ziyi Huang
A novel method has been developed for accurately quantifying arsenic species, including As(III), As(V), and total inorganic arsenic, in drinking water. The technique combines ultraviolet-visible spectrophotometry with cloud point extraction (UV/CPE), ensuring high sensitivity and selectivity. The methodology relies on complex formation between As(III) and Pyronin B in the presence of tartaric acid. The resulting complex is efficiently extracted into the surfactant-rich phase consisting of 5.0% (v/v) Triton X-114. Under optimized conditions, a linear calibration relationship from 3 to 500 µg/L is obtained. The method offers low detection and quantification limits of 1.04 and 3.48 µg/L, respectively, with a corresponding relative standard deviation below 5% for 11 replicates. Furthermore, spiked samples demonstrated excellent recovery values from 95.1% to 102.3%. The accuracy was verified by the analysis of the standard reference material SRM 1643e (trace elements in water), revealing no significant differences at the 95% confidence level. The approach was successfully utilized for the quantification of As(III), As(V), and total inorganic arsenic in commercial and domestic drinking water.
研究领域:
分析化学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
RSC Advances
·
2016
·Vol. 6
·期 57
·52255-52263
·
IF 3.289
Yusheng Yuan,Yalan Wang,Shaopu Liu,Yuanfang Li,Ruilin Duan,Hui Zhang,Xiaoli Hu
It is of great significance to develop an eco-friendly and sensitive platform for the detection of 6-mercaptopurine (6-MP) because of its side effects and variable activity. Herein, fluorescence quenching and spectrophotometric methods for the detection of 6-mercaptopurine (6-MP) using carbon dots (CDs) as a fluorescence probe are established. 6-MP not only serves to shelter the CDs effectively from being quenched, but also to reverse the quenching and restore the fluorescence due to its ability to remove Hg2+ from the surface of CDs. After the experimental conditions are optimized, the linear range for the detection of 6-MP is 0.04 to 12 μmol L−1, and the detection limit is 0.01 μmol L−1. When it refers to the spectrophotometric method, the linear range is 0.08 to 12 μmol L−1 and the detection limit is 0.02 μmol L−1. The CDs with 6-MP are systematically characterized with transmission electron microscopy (TEM), ultraviolet-visible (UV-vis) absorption and so on. Furthermore, the proposed methods are not only expected to become a potential tool for the fast response of 6-MP but also possess the potential for practical application to be applied in the determination of 6-MP in human serum samples with satisfactory results.
研究领域:
分析化学
·
药物分析
·
生物医学
✓ 已验证
产品关联
DOI
高影响因子
MICROCHEMICAL JOURNAL
·
2024
·
IF 4.9
Xuefei Zhang,Fanfei Min,Lingyun Liu
Ca 2+ is an important cation in coagulants used in the treatment of mine wastewater such as coal slime water, and its concentration directly affects the settling and flotation of coal slime water. The rapid determination of Ca 2+ concentration is of great significance to guiding industrial production. Herein, the complexation color development—visible spectrophotometry (CCDVS) method was proposed to obtain the concentration information of Ca 2+ , wherein 1-(1-Hydroxy-4-methyl-2-phenylazo)-2-naphthol-4-sulfonic acid (Calmagite) was used as an indicator and the mechanism of complexation between the indicator and Ca 2+ was explored. The strong correlation between spectral data and Ca 2+ concentration (R 2 = 0.997) indicated that this method could be used for Ca 2+ detection, thereby a quantitative model was proposed to predict Ca 2+ concentration by using the complexation color development—visible light absorption data. The chemical element and bonding analysis confirmed that Ca 2+ was complexed with the sulfonic acid group on the indicator skeleton in the form of Ca(OH) + intermediate in an alkaline environment. The generated complexation product (-S-O-Ca(OH) + ) could stably absorb 620 nm light energy, and its absorption performance remained 99.8% after standing for 60 min. The relative standard deviation of the detection results of Ca 2+ in different calcium source solutions was as low as 1.24%, which confirmed the strong calcium source compatibility of the proposed method. More importantly, the successful application of this method in the determination of Ca 2+ concentration at different points in industrial coal slime water system proved its advantages of high accuracy (relative error is as low as 5.01%), low cost and simple operation. The LOD of this method is 0.038 mg/L. Therefore, the complexation color development—visible spectrophotometry method can maximize the potential for cost reduction and efficiency improvement in mine wastewater treatment.
研究领域:
环境科学
·
分析化学
✓ 已验证
产品关联
DOI
高影响因子
Analytical Methods
·
2012
·Vol. 5
·期 4
·1046-1051
·
IF 1.547
Juan-Juan Ye,Wei Feng,Miao-Miao Tian,Jun-Ling Zhang,Wei-Hong Zhou,Qiong Jia
A novel magnetic adsorbent, magnetic microsphere functionalized with Cyanex272, has been successfully synthesized via a chemical bonding alkylation method. A flow injection on-line preconcentration, with a micro-column packed with the as-synthesized magnetic adsorbent, coupled with UV-Vis spectrophotometric method was developed for the determination of phenol at a wavelength of 270 nm. Various experimental parameters were optimized as follows: eluent (methanol), sample flow rate (1.4 mL min−1), sample volume (1.4 mL), sample pH (5.0), and eluent flow rate (2.2 mL min−1). Under the optimum conditions, the intra-day and inter-day relative standard deviations were 1.37% and 2.69% (n = 5), respectively. The proposed method has been successfully applied to the determination of phenol in phenol ear drops, compound borax solution, and phenol ointment samples and the accuracy was assessed through recovery experiments.
研究领域:
分析化学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
ANALYTICAL BIOCHEMISTRY
·
2022
·
IF 3.191
Guozeng Wang,Zhihao Jiang,Qing Xiao,Chang Jiang,Xian'ai Shi
Omega-transaminases (ω-TAs) have attracted considerable interest for their use in asymmetric synthesis of chiral amines with a high degree of optical purity and yield. The rapid evaluation of the characteristics of newly identified or engineered ω-TAs is important for industrial applications. In this study, a visible spectrophotometric assay was developed for rapid quantitative determination of ω-TA activities based on the transamination of 2-(4-nitrophenyl)ethan-1-amine to generate a red product ( E )- N -(4-nitrophenethyl)-2-(4-nitrophenyl)ethen-1-amine. After various co-solvents were evaluated, dimethyl sulfoxide (DMSO) was considered optimal because the red product exhibits good solubility and retains its original color. The red product dissolved in DMSO has its highest absorbance at 465 nm, and its concentration has a good linear relationship with the absorbance. A spectrophotometric assay was established and validated using conventional HPLC analysis (<10% divergence). This method was then used to characterize an ω-TA from thermophilic Geobacillus thermoleovorans and an ω-TA obtained from the metagenome of a soda lake. The results demonstrated that ω-transaminase enzymatic properties could be characterized simply, rapidly, and at low cost, using this newly established visible spectrophotometric assay method.
研究领域:
生物化学
·
工业酶学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Journal of Chemistry
·
2019
·
IF 1.727
Fei Chang,Zhong Bing He,Quan Zhou
Four kinds of Al-TiO2 solid samples with different Ti/Al ratios of 1 : 0.1, 1 : 0.09, 1 : 0.07, and 1 : 0.05 were synthesized via a solid-phase synthesis method and characterized by XRD, SEM, EDS, BET, and other techniques. The prepared solids were used for separation of the bioderived product danshensu, the content of which was determined by UV spectrophotometry. Moreover, the effects of extract concentration, PH value, adsorption time, and ethanol elution volume were investigated. The results showed that these Al-TiO2 samples had good adsorption and desorption ability. Especially, the solid Al-TiO2 with a Ti/Al ratio of 1 : 0.05 is more suitable for the separation of danshensu, exhibiting a higher adsorption (77.70%) under 2 h adsorption time and pH = 3; meanwhile, the high desorption rate (70.29%）was received under 80% ethanol and the sample concentration of 3.0 mg/mL.
研究领域:
材料科学
·
分析化学
·
药学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY
·
2017
·Vol. 28
·期 8
·1475-1482
·
IF 1.198
Xu Zhiqun,Wu Qiao,Duan Yunjian,Yang Meixia,Ou Minrui,Xu Xiaoping
Bisphenol A (BPA) is an industrial material which can lead to endocrine disorders. In this work, a simple and sensitive spectrophotometric method for determination of BPA using diazotization-coupling reaction was presented. To achieve the best performance of the developed method, the experimental parameters were optimized in terms of reagent concentration, reaction time, pH, and temperature. Under the optimal conditions, the absorbance increased linearly with the increasing concentration of BPA in the range of 0.16-10.4 µg mL-1 with the correlation coefficient of 0.9991 and the detection limit of 0.05 µg mL-1. Results achieved with the spectrophotometric method were compared with those obtained using high performance liquid chromatography (HPLC) method. The proposed method was successfully applied to determine BPA in milk and water bottle samples and satisfactory results were obtained, which make it very suitable for routine analysis of BPA in quality control laboratories.
研究领域:
分析化学
·
环境科学
·
食品安全
✓ 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）