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分光光度法与火焰原子吸收光谱法测定钢中硼的比较 总被引:2,自引:0,他引:2
提出了萃取-分光光度法和火焰原子吸收光谱法测定钢中硼的两种方法,比较了两者的线性范围、检出限、样品测定结果等.试验发现:分光光度法和火焰原子吸收光谱法在硼含量分别为0.11~3.2 mg·L-1和0.05~3.24 mg·L-1范围内时,吸光度与其质量浓度呈线性关系,检出限(3S/N)分别为0.033,0.036 mg·L-1.经检验,两种方法的测定结果之间无显著性差异. 相似文献
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分光光度法测定工业水中的酚酞碱度 总被引:1,自引:0,他引:1
建立了分光光度法测定工业及锅炉用水中酚酞碱度的分析方法。以间硝基苯酚为显色剂,采用分光光度法,测定了吸光度与酚酞碱度之间的线性关系。对测定波长、显色剂用量、显色时间等条件进行优化选择,考察了该方法的准确度和精密度。方法检出限为0.004 5 mmol/L,测定结果的相对标准偏差为0.20%~0.70%(n=9),加标回收率为97.0%~99.0%。该方法检出限低,精密度高,受样品颜色,浑浊度等的影响小,适合工业及锅炉用水酚酞碱度的测定,尤其适用于低酚酞碱度水样。 相似文献
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建立了使用紫外分光光度法测定硫酸中氮氧化物的方法。利用高锰酸钾将试样中的亚硝酸根氧化成硝酸根,然后在硫酸(30%)介质中,于210nm波长处定量测定试样中氮氧化物的含量。方法检出限为0.0000075%,线性相关系数(r)为0.999 0,平均加标回收率为97.2%~102.8%,平均相对标准偏差(RSD,n=6)为2.9%~3.1%。方法灵敏度高、检出限低,操作简便、成本低,可应用于蓄电池电解液中氮氧化合物的检测。 相似文献
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在H2SO4介质中,痕量铁(Ⅲ)对KBrO3氧化乙基橙褪色反应有很强的阻抑作用,利用光度法检测阻抑反应过程中乙基橙浓度的变化,建立了铁(Ⅲ)-溴酸钾-乙基橙体系阻抑动力学光度法测定痕量铁(Ⅲ)的方法。在选定条件下,方法的线性范围为0.006~0.32μg/mL,检出限(3s/k)为0.0031μg/mL。 相似文献
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半胱胺修饰的CdS纳米粒子荧光猝灭法测定锰离子 总被引:1,自引:1,他引:0
常温下在水溶液中制备了半胱胺修饰的CdS纳米溶胶,并用原子力和扫描电子显微镜、傅立叶变换红外、紫外-可见分光光度法、荧光分光光度法测试技术对其进行了表征. 以修饰的纳米粒子为荧光探针,建立了荧光猝灭定量检测锰离子的新方法. 考察了不同缓冲体系、缓冲液浓度及缓冲液pH值、反应时间、纳米粒子浓度等多种因素的影响. 在最佳实验条件下,测定锰离子的线性区间为0.053 40~77.62 mg/L,检出限为0.016 78 mg/L. 方法经济、简单、快速、灵敏度高、检出限比较低、检测范围宽. 相似文献
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《Analytical letters》2012,45(13):2653-2675
ABSTRACT An electrochemical method was compared with a spectrophotometric method using a horseradish peroxidase (HRP)-based indirect enzyme-linked immunosorbent assay (ELISA) with direct antigen coating (DAC) technique for the determination of tobacco mosaic virus (TMV). In substrates for a spectrophotometric HRP-based ELISA method, was selected as the substrate for the electrochemical method as well as the spectrophotometric method. 2, 3-Diaminophenazine is the product of the oxidation of OPD with H2O2 catalyzed by HRP in the selected conditions. It is electroactive and has a sensitive voltammetric response at -0.93 V (vs. Ag/AgCl) in alkaline solution. The detection limit of free HRP, by second-order derivative linear-sweep voltammetry, is 1.1 mU/L. This method can be further used to detect TMV antigen. The peak current is linear with TMV concentration in the range of 0.25-5.0 ng/mL. The detection limit for TMV is 0.25 ng/mL and the highest dilution ratio detected for the infected leaf sap is 1:102400. Compared with the classical OPD ELISA spectrophotometric method, the detection limits of the electrochemical method for the clarified TMV and the infected leaf sap detection are about ten and four times lower, respectively. 相似文献
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A. A. Zhirkov A. A. Buchinskaya D. B. Petrenko M. A. Proskurnin Yu. M. Dedkov B. K. Zuev 《Journal of Analytical Chemistry》2010,65(6):596-601
The conditions of the spectrophotometric and thermal lens determination of aluminum with sulfo-5-nitro-4′-diethylamino-2,2′-dihydroxyazobenzene
have been compared. The limit of spectrophotometric detection of aluminum in aqueous solutions has been found to be 8 ng/mL.
On the basis of the conditions of spectrophotometric determination, the conditions for thermal lens determination have been
proposed (532.0 nm, exciting radiation power of 42 mW); they provide a decrease of the detection limit down to 0.6 ng/mL and
an increase of the sensitivity coefficient by an order of magnitude. It has been shown that, in the case of the thermal lens
determination of aluminum in water-organic mixtures (50 vol % of dimethyl sulfoxide or 30 vol % acetonitrile), the sensitivity
coefficient is respectively 9.1 and 6.3-fold higher as compared with the thermal lens determination in water. As a result,
the detection limits are reduced 2.5 and 10-fold, respectively. Aluminum has been determined by thermal lens spectrophotometry
in Moscow’s tap water using the standard addition method, its concentration being 0.79 ± 0.07 mg/L, which is above the threshold
limit value of the aluminum content of drinking water. 相似文献
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Yûetsu Danzaki Kunio Takada Kazuaki Wagatsuma 《Analytical and bioanalytical chemistry》1998,362(4):421-423
For the determination of Ta (> 0.0005 mass %) in iron and low-alloy steel spectrophotometric methods, e.g., after the extraction of the Ta-Victoria Blue B complex by benzene, are generally used. To avoid the application of poisonous benzene as extracting solvent and to improve the detection power, an ICP-AES method after the separation of Ta by coprecipitation with cupferron has been developed. The detection limit (3σ) of 0.6 μgTa/g is lower in comparison with spectrophotometric methods. Therefore, the method also allows the determination of Ta-concentrations in the μg/g-range in high-purity iron. 相似文献
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An indirect near-infrared spectrophotometric method for the determination of silicate, based on the absorbance of an equivalent amount of molybdenum-2-amino-4-chlorobenzenethiol complex in chloroform solution, has been developed. The green chloroform solution has an absorbance maximum at 715 nm. The development of the spectrophotometric method for the determination of silicate included a study of a buffer system for the purpose of maintaining the pH within a narrow optimum pH range, complex stability, effect of diverse ions, and conformity to Beer's law. The limit of detection is 0.034 mug of silicon per ml of aqueous heteropoly acid solution. 相似文献
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Hadad GM El-Gindy A Mahmoud WM 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2008,70(3):655-663
High-performance liquid chromatography (HPLC) and multivariate spectrophotometric methods are described for the simultaneous determination of ambroxol hydrochloride (AM) and doxycycline (DX) in combined pharmaceutical capsules. The chromatographic separation was achieved on reversed-phase C(18) analytical column with a mobile phase consisting of a mixture of 20mM potassium dihydrogen phosphate, pH 6-acetonitrile in ratio of (1:1, v/v) and UV detection at 245 nm. Also, the resolution has been accomplished by using numerical spectrophotometric methods as classical least squares (CLS), principal component regression (PCR) and partial least squares (PLS-1) applied to the UV spectra of the mixture and graphical spectrophotometric method as first derivative of the ratio spectra ((1)DD) method. Analytical figures of merit (FOM), such as sensitivity, selectivity, analytical sensitivity, limit of quantitation and limit of detection were determined for CLS, PLS-1 and PCR methods. The proposed methods were validated and successfully applied for the analysis of pharmaceutical formulation and laboratory-prepared mixtures containing the two component combination. 相似文献
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A spectrophotometric method for the determination of sulphathiazole (ST) has been developed, based on solid-phase spectrophotometry. The influence of experimental variables on fixation on Sephadex SP C-25 is discussed. The applicable concentration range is 0.10-10.00 mg/l., with a relative standard deviation of 0.62% and a detection limit of 0.02 mg/l. The accuracy and precision of the method are reported. The proposed method has been satisfactorily applied to the determination of sulphathiazole in pharmaceuticals. 相似文献
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N. A. Puretskii M. A. Proskurnin A. V. Pirogov 《Moscow University Chemistry Bulletin》2009,64(2):93-98
The conditions for the spectrophotometric and thermal-lens determination of diacetyl with creatine and 2-naphthol are proposed. The obtained value of the detection limit for spectrophotometry (at 527 nm), which amounts to 10 ng/mL, is fivefold lower than the existing values of the spectrophotometric determination of diacetyl. The conditions for the thermal-lens determination of diacetyl (λ = 514.5 nm, strength of the inducing radiation: 40 mW) based on the unmodified procedure of spectrophotometric determination were proposed. Along with a fivefold (down to 2 ng/mL) decrease in the detection limit, which is comparable with that for the determination of diacetyl by means of gas chromatography with mass spectrometric detection (detection limit of 0.7 ng/mL), thermal-lens determination is characterized by the enhancement of other performance parameters of the determination. It was shown that, contrary to the case when gas chromatography is used, ethanol does not interfere with both the spectrophotometric and the thermal-lens determination of acetyl. 相似文献
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A spectrophotometric method for the determination of trace water in organic solvents using a near infrared absorbing dye has been developed. This method is based on the effect that a minor change in polarity of the solvent caused by trace water content determines the extent of aggregation of a near-infrared dye monomer. This change can be detected spectrophotometrically. The calibration curves for methanol, ethanol, and isopropanol were determined. This method has the highest sensitivity (em = 16.73 unit) for water in isopropanol and the lowest sensitivity (em = 2.806 unit) for water in methanol. The correlation coefficient (R)(2) values for the regression lines ranges from 0.990-0.998. The linear range of the method for ethanol is 0.001-0.5%, for isopropanol is 0.001-0.1%, and for methanol is 0.001-1.0%. The limit of detection for ethanol, isopropanol, and methanol are 0.0001, 0.0001, and 0.005% water, respectively. The developed method is sensitive, simple and easy to operate, and the cost of analysis is low. 相似文献