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1.
The formation of the Tm(III) complex with 1-(2-pyridylazo)-2-naphthol (PAN or HL) in aqueous-methanol mixtures (50 and 75%v/v) was studied by a spectrophotometric method. The equilibrium constant for the complexing reaction and the stability constant of the complex TmL
2+ were calculated. The solvent extraction of Tm(III) byPAN in carbon tetrachloride from aqueous and aqueous-methanol phase was investigated. The extraction equilibrium constants and two-phase stability constants for the TmL
3 and the TmL
3(MeOH)3 complexes were evaluated. It was confirmed that the addition of methanol to the aqueous phase (above 25%v/v) causes a synergistic effect.
Extraktion von Ionen der Seltenerdmetalle mit 1-(2-Pyridylazo)-2-naphthol (PAN), 5. Mitt.: Komplexbildung und Gleichgewichtsverteilung von Thulium (III) mitPAN
Zusammenfassung Die Bildung des Komplexes von Tm(III) mit 1-(2-Pyridylazo)-2-naphthol (PAN oder HL) in Wasser-Methanol Mischungen (50 und 75%v/v) wurde mit einer spektrophotometrischen Methode untersucht. Die Gleichgewichtskonstante für die Reaktion der Komplexbildung und die Stabilitätskonstante des Komplexes TmL 2+ wurden berechnet. Die Extraktion von Tm(III) mittelsPAN in Kohlenstofftetrachlorid aus Wasser oder Wasser-Methanol wurde untersucht. Die Werte der Extraktionsgleichgewichtskonstante sowie der zweiphasigen Beständigkeitskonstante für die Komplexe TmL 3 und TmL 3(MeOH)3 wurden berechnet. Es wurde festgestellt, daß die Zugabe von Methanol zur wäßrigen Phase (25%v/v) einen synergistischen Effekt hat.相似文献
2.
A highly selective and sensitive anodic stripping differential pulse polarographic method has been developed for the determination of trace amount of bismuth in various samples after adsorption of its 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol complex on amberlite XAD-2 resin in the pH range of 2.0-3.0. The retained analyte on the resin recovered with 10.0 ml of 2 M hydrochloric acid and bismuth is determined by anodic stripping differential pulse polarography. In this case, 0.15 μg of bismuth can be concentrated in the column from 1100 ml of aqueous sample, where its concentration is as low as 0.14 ng ml−1 and the linearity is maintained in the concentration range 0.05-160 μg ml−1 in final solution with a correlation coefficient of 0.999 and relative standard deviation of ±1.2%. Various parameters such as the effect of pH, flow rate, and interference of number of metal ions on the determination of bismuth have been studied in detail to optimize the conditions for determination of bismuth in standard alloys: Nippon Keikinzoku Kogyo (NKK CRM No. 916 aluminum alloy); (NKK CRM No. 1021 Al, Si, Cu, Zn alloy); and (NKK CRM No. 920 aluminum alloy), biological samples: National Institute for Environmental Studies (NIES, No. 5 human hair; NIES, No. 7 tea leaves) and water samples: (spring water, river water; Kerman water; and Shiraz water). 相似文献
3.
《Journal of Coordination Chemistry》2012,65(8):1293-1301
Interaction of 1-(2-pyridylazo)-2-naphthol (PAN) with [Mo(CO)6] in air resulted in formation of the tricarbonyl oxo-complex [Mo(O)(CO)3(PAN)], 1. The dicarbonyl complex [Ru(CO)2(PAN)], 3, was obtained from the reaction of [Ru3(CO)12] with PAN. In presence of triphenyl phosphine (PPh3), the reaction of PAN with either Mo(CO)6 or Ru3(CO)12 gave [Mo(CO)3(PAN)(PPh3)], 2, and [Ru(CO)2(PAN)(PPh3)], 4. All the complexes were characterized by elemental analysis, mass spectrometry, IR, and NMR spectroscopy. The thermal properties of the complexes were also investigated by thermogravimetry. 相似文献
4.
A new polystyrene-divinylbenzene resin containing 1-(2-thiazolylazo)-2-naphthol (TAN) functional group was synthesized and its sorption behavior for 19 metal ions including Zr(IV), Hf(IV) and U(VI) was investigated by batch and column experiments. The chelating resin showed a high sorption affinity for Zr(IV) and Hf(IV) at pH 2. Some parameters affecting the sorption of the metal ions are detailed. The breakthrough and overall capacities were measured under optimized conditions. The overall capacities of Zr(IV) and Hf(IV) that were higher than those of the other metal ions were 0.92 and 0.87 mmol/g, respectively. The elution order of metal ions at pH 4 was evaluated as: Zr(IV)>Hf(IV)>Th(IV)>V(V)>Nb(V)>Cu(II)>U(VI)>Ta(V)>Mo(VI)>Cr(III)>Sn(IV)>W(VI). Quantitative recovery of most metal ions except Zr(IV) was achieved using 2 M HNO3. Desorption and recovery of Zr(IV) was successfully performed with 2 M HClO4 and 2 M HCl. 相似文献
5.
《Journal of Saudi Chemical Society》2014,18(5):674-680
The Amberlite XAD-7 resin modification was carried out by loading 2-(1-(4-chlorophenyl)-4,5-diphenyl-1H-imidazol-2yl)-4-nitrophenol (CPDPINP). Subsequently, this new sorbent was applied for the enrichment of metal ions such as Cu2+, Ni2+, Co2+ Zn2+ and Pb2+ ions. The effect of various parameters on their sorption and following recoveries was studied in column procedure. The preconcentrated ions were eluted by appropriate eluent and their contents were quantified by FAAS. This method has preconcentration factor of 150 and enrichment factor in the range of 20.8–29.1. At optimum values of all variables, the proposed method has linear calibration graphs in the range of 0.01 up to 0.29 μg mL−1 with detection limit (3SDb/m, n = 15) between 1.6 and 2.6 ng mL−1. This protocol is usable for successful analysis of Cu2+, Ni2+, Co2+ Zn2+ and Pb2+ ions in different matrices with reasonable recoveries (>93%) and acceptable relative standard deviation (<4.7%). 相似文献
6.
2-{[1-(3,4-Dihydroxyphenyl)methylidene]amino}benzoic acid (DMABA) was loaded on Amberlite XAD-16 (AXAD-16) via azo linker and the resulting resin AXAD-16-DMABA explored for enrichment of Zn(II), Mn(II), Ni(II), Pb(II), Cd(II), Cu(II), Fe(III) and Co(II). The optimum pH values for extraction are 6.5-7.0, 5.0-6.0, 5.5-7.5, 5.0-6.5, 6.5-8.0, 5.5-7.0, 4.0-5.0 and 6.0-7.0, respectively. The sorption capacity was found between 97 and 515 μmol g−1 and the preconcentration factors from 100 to 450. Tolerance limits for foreign species are reported. The kinetics of sorption is fast as t1/2 is ≤5 min. The chelating resin can be reused for 50 cycles of sorption-desorption without any significant change (<1.5%) in the sorption capacity. The limit of detection values (blank +3 s) are 1.12, 1.38, 1.76, 0.67, 0.77, 2.52, 5.92 and 1.08 μg L−1 for Zn(II), Mn(II), Ni(II), Pb(II), Cd(II), Cu(II), Fe(III) and Co(II), respectively. The enrichment on AXAD-16-DMABA coupled with monitoring by flame atomic absorption spectrometry (FAAS) is used to determine all the metal ion ions in river and synthetic water samples, Co in vitamin tablets and Zn in milk samples. 相似文献
7.
Chunnuan Ji Chunhua Wang Hou Chen Changmei Sun Qiang Xu Yanzhi Sun Chao Wei 《Talanta》2007,73(2):195-201
A new chelating resin containing bis[2-(2-benzothiazolylthioethyl)sulfoxide] was synthesized using chloromethylated polystyrene as material and characterized by elemental analysis and infrared spectra. The adsorption capacities of the newly formed resin for Hg2+, Ag+, Cu2+, Zn2+, Pb2+, Mn2+, Ni2+, Cd2+ and Fe3+ were investigated over the pH range 1.0-6.0. The resin exhibited no affinity for alkali or alkaline earth metal ions. The maximum adsorption capacities of the resin for Hg2+, Ag+, Cu2+, Zn2+, Pb2+, Mn2+, Ni2+, Cd2+ and Fe3+ were 1.49, 0.96, 0.58, 0.11, 0.37, 0, 0.24, 0.36 and 0.25 mmol g−1, respectively. In column operation it had been observed that Hg2+ and Ag+ in trace quantity could be separated from different binary mixtures and Hg2+ could be effectively removed from industrial wastewater and the natural water spiked with Hg2+ at usual pH. 相似文献
8.
A novel method that utilizes 1-(2-formamidoethyl)-3-phenylurea-modified activated carbon (AC-1-(2-formamidoethyl)-3-phenylurea) as a solid-phase extractant has been developed for simultaneous preconcentration of trace Cr(III), Cu(II), Fe(III) and Pb(II) prior to the measurement by inductively coupled plasma atomic emission spectrometry (ICP-AES). Experimental conditions for effective adsorption of trace levels of Cr(III), Cu(II), Fe(III) and Pb(II) were optimized using batch and column procedures in detail. The optimum pH value for the separation of metal ions simultaneously on the new sorbent was 4. And the adsorbed metal ions could be completely eluted by using 2.0 mL 2.0 mol L−1 HCl solution. Common coexisting ions did not interfere with the separation and determination of target metal ions. The maximum static adsorption capacity of the sorbent at optimum conditions was found to be 39.8, 39.9, 77.8 and 17.3 mg g−1 for Cr(III), Cu(II), Fe(III) and Pb(II), respectively. The detection limits of the method were found to be 0.15, 0.41, 0.27 and 0.36 ng mL−1 for Cr(III), Cu(II), Fe(III) and Pb(II), respectively. The relative standard deviation (RSD) of the method was lower than 4.0% (n = 8). The method was successfully applied for the preconcentration of trace Cr(III), Cu(II), Fe(III) and Pb(II) in natural and certified samples with satisfactory results. 相似文献
9.
Use of 1-(2-pyridylazo)-2-naphthol as the post column reagent for ion exchange chromatography of heavy metals in environmental samples 总被引:1,自引:0,他引:1
Supalax Srijaranai Wijitra Autsawaputtanakul Tipwan Khameng Richard L. Deming 《Microchemical Journal》2011,99(1):152-158
Ion exchange chromatography (IEC) using a bi-functional column (quaternary ammonium and sulfonate groups), followed by post-column reaction (PCR) with 1-(2-pyridylazo)-2-naphthol (PAN), was used to separate and quantitate Cu(II), Ni(II), Zn(II), Co(II), Cd(II), Mn(II) and Hg(II) at low concentration levels. IEC-PCR separation was achieved within 14 min using the mobile phase containing 3 mmol L− 1 2,6-pyridinedicarboxylic acid (PDCA) and 3 mmol L− 1 oxalate at pH 12.5. Effects of pH as well as PAN, detergent and chloride ion concentrations during post-column reaction on detector response were examined. Detection limits were less than 4.5 μg L− 1 for all metals except Hg(II) (19 μg L− 1) using spectrophotometric measurements at 550 nm. Analytical validations showed good linearity for detection up to 6.0 mg L− 1, with R2 higher than 0.99. Precisions based on retention time evaluation for intra-day and inter-day measurements with the relative standard deviation (RSD) were less than 2.9% and 3.6%, respectively. The method gave good accuracy with the recoveries ranged from 80.5 to 105% for all metal ions studied. The proposed method was applied to the analysis of metal ions in environmental samples (leachate, soil and sediment) in Northeastern Thailand. The results were in good agreement with atomic spectroscopic measurements on the same samples. 相似文献
10.
Syed Ashfaq Nabi Mu Naushad Amjad Mumtaz Khan 《Colloids and surfaces. A, Physicochemical and engineering aspects》2006,280(1-3):66-70
Anion exchange resin Amberlite IR-400 has been modified with napthol blue–black. Effect of concentration, time, pH and temperature on the sorption of dye has been studied. The uptake sequence of various metal ions in a number of solvents has been determined. On the basis of distribution coefficients (Kd) in a number of solvent systems, some important binary separations of metal ions of analytical interest have been exploited. The practical applicability of the modified material has been demonstrated in the analysis of synthetic and commercially available antacid and antioxidant formulations namely digene and I-Vit. 相似文献
11.
Safari Z Gholivand MB Hosseinzadeh L 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,78(5):1606-1610
The complexation reactions between Ni(2+), Co(2+) and Zn(2+) metal ions with PAN in methanol (MeOH), acetonitrile (AN) and dimethyl sulfoxide (DMSO) were studied using a spectrophotometric method. The stability constants of the resulting complexes were determined from computer fitting absorbance mole-ratio data. The results revealed that the stability constants of complexes are varying in order of Ni(2+)相似文献
12.
Mostafa Khajeh Esmael Sanchooli 《International journal of environmental analytical chemistry》2013,93(5):613-619
A simple procedure based on magnetic nanoparticles has been developed for analytical purposes. In this method, 1-(2-pyridylazo)-2-naphthol (PAN)-modified magnetic nanoparticles (MNPs) were used for separation and pre-concentration of manganese(II) ions from aqueous samples. This method combines the use of a solution solvent with separation of magnetic nanoparticles from sample solution using a magnet. The influence of different parameters, such as amount of extractant (PAN) loaded on the nanoparticles, pH of solution, adsorption time, amount of modified nanoparticle, type and amount of eluents for desorption of manganese from magnetic nanoparticles were evaluated. The effect of various cationic and anionic interferences on the percentage recovery of manganese was also studied. Manganese ions were adsorped from a solution at pH 9.5 and desorbed from nanoparticles with 10?mL of DMSO?:?HNO3 (1?:?1, v/v). The detection limit of the proposed method was found to be 0.11?µg?L?1. The method was employed to recover and determine the level of manganese in different water samples. 相似文献
13.
A membrane filtration procedure for the preconcentration and atomic absorption spectrometric determination of Pb(II), Co(II) and Fe(III) ions in natural water samples has been established. Cellulose nitrate membrane filters (0.45 μm and 47 mm diameter) were used in all experiments. The procedure is based on chelate formation of the analyte metals with 1‐(2‐pyridylazo) 2‐naphtol (PAN) and on retention of the chelates on cellulose nitrate membrane filter. The cellulose nitrate membrane and analyte ions were completely dissolved by 500 μL of nitric acid at 85 °C on a hood and then metal determinations were performed by flame atomic absorption spectrometry. The method was applied to natural water samples for the determination of analyte ions with satisfactory results, e.g., recoveries > 95%, RSD's < 10%. 相似文献
14.
1—间甲氧苯基—2—二甲胺甲基环己醇的合成与结构研究 总被引:3,自引:0,他引:3
通过间溴苯甲醚与2-二甲胺甲基环己酮反应制得1-间甲氧苯基-2-二胺甲基环己醇,对其分离得到相应的顺反异构体,对反应的立体化学进行了分析,并对^13C NMR谱确定了顺反异构体的构型。 相似文献
15.
Gopalan Venkatesh 《Talanta》2007,71(1):282-287
Amberlite XAD-16 was loaded with 4-{[(2-hydroxyphenyl)imino]methyl}-1,2-benzenediol (HIMB) via azo linker and the resulting resin AXAD-16-HIMB explored for enrichment of Zn(II), Mn(II), Ni(II), Pb(II), Cd(II), Cu(II), Fe(III) and Co(II) in the pH range 5.0-8.0. The sorption capacity was found between 56 and 415 μmol g−1 and the preconcentration factors from 150 to 300. Tolerance limits for foreign species are reported. The kinetics of sorption is not slow, as t1/2 is ≤15 min. The chelating resin can be reused for seventy cycles of sorption-desorption without any significant change (<2.0%) in the sorption capacity. The limit of detection values (blank + 3 s) are 1.72, 1.30, 2.56, 2.10, 0.44, 2.93, 2.45 and 3.23 μg l−1 for Zn, Mn, Ni, Pb, Cd, Cu, Fe and Co, respectively. The enrichment on AXAD-16-HIMB coupled with flame atomic absorption spectrometry (FAAS) monitoring is used to determine the metal ion ions in river and synthetic water samples, Co in vitamin tablets and Zn in powdered milk samples. 相似文献
16.
17.
The present work has focused on the modification of multiwalled carbon nanotube with a ligand,l-(2-pyridylazo)-2-naphthol, and its potential application for the development of a new,simple and selective modified glassy carbon electrode for stripping voltammetric determination of Cd(Ⅱ).The analytical curve for Cd(Ⅱ) ions covered the linear range varying from 0.8 up to 220.4μgL-1.The limit of detection was found to be 0.1μgL-1,while the relative standard deviation(RSD) at 50.0μgL-1 was 1.8%(n=5).This modified electrode was successfully applied for determination of Cd(Ⅱ) in some water samples. 相似文献
18.
Danuta M. Czakis-Sulikowska Anna Malinowska 《Monatshefte für Chemie / Chemical Monthly》1988,119(6-7):677-681
The formation ofPAN complexes in the systems:Ln(III)—PAN—alcohol—water [whereLn(III) = Pr, Nd, Sm, Eu, Gd, Tb, alcohol - ethanol andLn(III) = Eu, alcohol =n-propanol, isopropanol] was investigated by a spectrophotometric method. Equilibrium constants for the reactionLn
3++HLLnL
2++H+ (HL =PAN) and stability constants of complexesLnL
2+ are reported.
Komplexbildung einiger Seltenerdmetalle mit 1-(2-Pyridylazo)-2-naphthol (PAN) in alkoholisch-wäßrigen Lösungen
Zusammenfassung Die Bildung der Komplexe vonPAN in den SystemenLn(III)—PAN—Alkohol—Wasser [Ln(III) = Pr, Nd, Sm, Eu, Gd, Tb, Alkohol = Ethanol undLn(III) = Eu, Alkohol =n-Propanol, Isopropanol] wurde mit einer spektrophotometrischen Methode untersucht. Die Gleichgewichtskonstanten der ReaktionenLn 3++HLLnL 2++H+ (HL =PAN) und die Stabilitätskonstanten der KomplexeLnL 2+ wurden berechnet.相似文献
19.
Danuta M. Czakis-Sulikowska Anna Malinowska 《Monatshefte für Chemie / Chemical Monthly》1986,117(4):437-441
The formation ofPAN complexes in the systemsLn(III)—PAN—alcohol-water (where:Ln(III)=Ho, Lu and alcohol=ethanol,n-propanol,iso-propanol) was investigated by a spectrophotometric method. Equilibrium constants for the reactionLn
3+ + HLLnL
2+ + H+ (HL=PAN) and stability constants of complexesLnL
2+ were calculated.
Untersuchungen zur Komplexbildung von Ho(III) und Lu(III) mit 1-(2-Pyridylazo)-2-naphthol (PAN) in alkoholisch-;wä\rigen Lösungen
Zusammenfassung Die Bildung der Komplexe vonPAN in den SystemenLn(III)—PAN—Alkohol-Wasser (Ln(III)=Ho, Lu; Alkohol=Ethanol,n-Propanol,iso-Propanol) wurde mit einer spektrophotometrischen Methode untersucht. Die Gleichgewichtskonstanten der ReaktionenLn 3+ + HLLnL 2+ + H+ (HL==PAN) und die Stabilitätskonstanten der KomplexeLnL 2+ wurden berechnet.相似文献
20.
Sema Demirci Çekiç 《Analytica chimica acta》2004,505(1):15-24
XAD copolymer resins may be functionalized with heavy metal ion-selective ligands either by covalent linkage to the polymer backbone or by impregnation. These resins may be tailored to be specific for certain heavy metals by adjusting the adsorption and elution parameters, thereby enabling simple and cost-effective spectrophotometric and flame atomic absorption spectrometry (FAAS) determinations of these metals without requiring the more sophisticated coupled instrumental techniques. For the synthesis of o-aminobenzoic acid (ABA)-immobilized XAD-4 copolymer resin that is expected to preconcentrate a number of transition and heavy metals, the azo-linkage method was chosen. For this purpose the copolymer was nitrated, reduced to the corresponding amine, converted to the diazonium salt with nitrite, and reacted with o-aminobenzoic acid to produce the XAD-ABA sorbent. This sorbent was capable of preconcentrating Pb(II), Cd(II), Ni(II), Co(II) and Zn(II) from weakly acidic or neutral aqueous solution. The retained metals were eluted with 1.0 M HNO3 from the resin column, and were subsequently determinated with by flame atomic absorption spectrometry. The developed resin preconcentration and determination method was successfully applied to the analysis of a synthetic metal mixture solution, a certified reference material (CRM) of coal sample, and brackish lake water. 相似文献