Synthesis of nitrogen- and iron-containing carbon dots,and their application to colorimetric and fluorometric determination of dopamine

Nitrogen- and iron-containing carbon dots (N,Fe-CDs) are synthesized by hydrothermal treatment of branched polyethylenimine (BPEI) and hemin at 180 °C. The N,Fe-CDs are mainly doped with nitrogen and trace amounts of iron(III). The N,Fe-CDs also display intrinsic fluorescence with excitation/emission maxima at 365/452 nm and a quantum yield of 27 %. The nanodots are shown to act as peroxidase mimics by catalyzing the oxidation of tetramethylbenzidine (TMB) by hydrogen peroxide to form a blue product whose quantity can be determined by photometry at 652 nm. This was exploited to design colorimetric and fluorometric assays for dopamine (DA). The colorimetric assay is based on the oxidation of DA by H₂O₂ in presence of the N,Fe-CDs and TMB. It has an instrumental detection limit of 40 nM (at an S/N ratio of 3), and a visual detection limit of 0.4 μM. The fluorometric assay is based on an inner filter effect that is caused by the formation of oxidized TMB which overlaps (and absorbs) the emission of the N,Fe-CDs located at 452 nm. The fluorometric detection limit is as low as 20 nM (at an S/N ratio of 3).

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Graphical abstract Carbon dots containing nitrogen and iron (N,Fe-CDs) were synthesized by hydrothermal treatment of branched polyethylenimine and hemin. The N,Fe-CDs display excellent fluorescent properties, peroxidase-like activity and potential application in colorimetric and fluorometric detection of dopamine.

     

Chemical activity of silver nanoparticles in anion-exchange matrices with respect to molecular oxygen dissolved in water

New silver-containing nanocomposites different in their dispersity of metal were synthesized on the basis of strongly and weakly basic anion-exchange resins. The chemical activity of the nanocomposites with respect to oxygen dissolved in water was investigated. It was shown that silver nanoparticles in samples based on strongly basic anion exchangers and weakly basic anion exchangers in the NO ₃ ^? salt form are not oxidized by oxygen; for weakly basic matrices in the free amine form, this process occurs to only a small extent. The resistance to oxygen is explained by inhibition of processes of formation of silver oxides. Nanocomposites based on strongly basic anion-exchange resins are recommended for testing as to catalytic activity.     

Coulometric determination of dissolved oxygen in water

The oxygen content of air-saturated distilled water has been determined at between 10 and 40 degrees by using a controlled-potential coulometric method based on an earlier published method for the iodometric determination of nitrite. The maximum error for the determinations was +/- 0.3% over the whole range, and the time of analysis about 3 min. An equation is given for the solubility in the measured range, and some thermodynamic functions are calculated.     

Synthesis,characterization of V2O5 nanoparticles and determination of catalase mimetic activity by new colorimetric method

Journal of Thermal Analysis and Calorimetry - This paper deals with an advanced colorimetric method used to determine the catalase mimetic activity of V2O5 nanoparticles by measuring the decrease...     

Titrimetric determination of dissolved oxygen in waste water

Winkler's procedure for the determination of dissolved oxygen has been modified to cope with substantial amounts of oxidizing or reducing substances in the samples. The manganese(III) is treated with an excess of hydroquinone, the unconsumed part of which is then titrated with standard ceric sulphate solution. A blank determination is also carried out, in which the order of addition of reagents is reversed so that the solution is always acidic, to allow for the interfering substances present. Results obtained by using this modified procedure on clean samples are in good agreement with results obtained by the usual Winkler method.     

Nitrosation of lignosulfonic acids for their colorimetric determination

The kinetics of lignosulfonic acid nitrosation in the presence of acetic and nitric acids used for generation of nitrous acid in combination with sodium nitrite was studied as applied to colorimetric determination of lignosulfonic acids.     

Thin layer gas electrode and its application to measurement of dissolved oxygen

A novel thin layer cell equipped with thin layer gas electrode (TLGE) was studied as electrochemical gas sensor for the measurement of dissolved oxygen in water or aqueous solutions. The working electrode (TLGE) is a hydrophobic gas diffusing electrode placed between the cell electrolyte and the solution to be tested. The hydrophobic pores in TLGE serve as a gas chamber. After the sampling period, in which the partial pressure of dissolved oxygen in test solution becomes in equilibrium with that in the gas chamber, the TLGE is polarized with square wave or linear potential signal. Then the Faradaic charge (Q) consumed in depletion of the oxygen contained in pores of TLGE is measured. The main merits of this system are good linearity between the partial pressure of dissolved oxygen in test solution and Q, low zero-reading, negligible liquid-gas difference, convenient calibration and very low temperature coefficient (ca. 0.5%/°C). This technique can also be applied to the measurement of oxygen partial pressure in gas phases.     

二氧化铈纳米微粒过氧化物酶活性及其在葡萄糖检测中的应用

合成了一种稳定和水溶性的聚丙烯酸修饰CeO2 NPs,利用动态光散射(DLS)、傅里叶变换红外光谱(FT-IR)和X射线光电子能谱(XPS)进行表征.结果表明,CeO2 NPs能够催化H2O2氧化3,3′,5,5′-四甲基联苯胺(TMB)发生显色反应,表现出过氧化物模拟酶催化活性.利用Raman和顺磁共振(EPR)光谱技术研究了其催化机理.基于CeO2 NPs催化TMB变色反应对H2O2浓度的依赖性和葡萄糖氧化酶能够催化溶解氧氧化葡萄糖产生H2O2的原理,构建了一种简单、灵敏、选择性高的测定血清中葡萄糖的检测方法.在优化条件下,测定葡萄糖的线性范围为0.5~10 mmol/L,检出限(3σ)为0.1 mmol/L.对1.0 mmol/L葡萄糖进行11次平行测定,其相对标准偏差为2.4%.该方法已成功用于血清样品中葡萄糖的测定.     

Studies on the determination of dissolved oxygen in water

Studies on the decomposition rates of the Mn(III) complex of cyclohexanediaminetetra-acetate (DCTA) in light and in darkness have shown that this complex is more stable than the one derived from ethylenediaminetetra-acetate. The optimum pH range for the determination of dissolved oxygen by means of the Mn(III)-DCTA complex is found to be between 3 and 4. The absorbance of this complex is independent of the amount of DCTA used (in the range 0.2–1.0 g) with water samples containing a maximum of 3.2 ppm of dissolved oxygen. Significant interferences are caused by the presence of CO²⁻₃, HCO⁻₃, S₂O²⁻₃, PO³⁻₄, I⁻, NO⁻₂, SO²⁻₃, Ca²⁺, Fe²⁺ and Fe³⁺ at 500 times the oxygen concentration.     

Synthesis of magnetic nanoparticles and their application to bioassays

Magnetic nanoparticles have been attracting much interest as a labeling material in the fields of advanced biological and medical applications such as drug delivery, magnetic resonance imaging, and array-based assaying. In this review, synthesis of iron oxide magnetic nanoparticles via a reverse micelle system and modification of their surface by an organosilane agent are discussed. Furthermore, as a practical biological assay system, the magnetic detection of biomolecular interactions is demonstrated by using the combination of a patterned substrate modified with a self-assembled monolayer and the magnetic nanoparticles.     

Novel colorimetric assay of LSD1 activity using gold nanoparticles

We have developed a simple and sensitive strategy for colorimetric LSD1 enzyme activity assay using avidin modified gold nanoparticles. The strategy is based on the vivid color change of a gold nanoparticle solution from red to violet upon addition of a test solution of peptide-antibody treated with LSD1. Thus, the presence of LSD1 in a sample can be determined by simple visual inspection with the naked eye. In addition, a wide range of LSD1 concentrations (13 pM to 0.13 μM) were quantitatively determined by spectrophotometry, which shows the possibility of quantitative analysis of the over expression levels of LSD1 in cancer tissue samples.     

Nickel oxide nanoparticles prepared by gelatin and their application toward the oxygen evolution reaction

Green synthesis of pure nickel oxide nanoparticles (nano-NiO) in aqueous medium has been carried out using gelatin. The particles have been characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive X-ray (EDAX). Gelatin plays an important role in the formation of the nano-NiO. TEM image shows the formation of nano-NiO with average particle size 16 nm, which agrees well with the XRD data. Moreover, efficient and stable nano-NiO-based anodes were fabricated by casting of the nano-NiO and multi-walled carbon nanotube solution (NiO-MWNT) on glassy carbon (NiO-MWNT/GC), platine (NiO-MWNT/Pt), and carbon paste (NiO-MWNT/CP) electrodes. The electrocatalysis of oxygen evolution reaction (OER) at modified electrodes has been examined using linear scanning voltammetry (LSV). The OER is significantly enhanced upon modification of the electrodes with NiO-MWNT, as demonstrated by a negative shift in the LSV curves at the NiO-MWNT-modified electrodes compared to that obtained at the unmodified ones. The maximum electrocatalytic activity toward the OER was obtained in alkaline media. The values of energy saving of oxygen gas at a current density of 5 mA cm^?2 Pt, CP, and GC electrodes are 14.1, 16.0, and 21.6 kW h kg^?1, respectively. The low cost as well as the marked stability of the modified electrodes makes them promising candidates in industrial water electrolysis process.     

White-light emissive upconversion nanoparticles for visual and colorimetric determination of the pesticide thiram

Microchimica Acta - A chip-based array is described for magnetic solid-phase microextraction (MSPME) of the ions of Pt, Au and Bi. Magnetic porous organic polymers (MOPs) prepared from magnetite...     

Chitosan-wrapped gold nanoparticles for hydrogen-bonding recognition and colorimetric determination of the antibiotic kanamycin

Microchimica Acta - The authors describe a colorimetric assay for the quantitation of antibiotic kanamycin. It is based on hydrogen-bonding recognition capability of gold nanoparticles (AuNPs) in a...     

The colorimetric determination of nickel,chromium, and manganese in steel

With the aid of the Spckkei absorptiometer the colonmetnc delerminations, of nickel (with dimethylglyoxime), chromium (with diphenylcarbazide) and manganese (after oxidation with periodate) in steel were critically sinveyed The following factors were examined. wave length of the light, concentration of the reagents, stability of the coloured solution, temperature, influence of excess non, relation of extinetion coefficient and concentration of the coloured solution, influence of Mo, V, W, Ti, Al, Co, Cu, Ni, Cr, Mn, P and Si.For each determination a recommended procedure is given, with the results of control analyses. The recommended procedures are rapid. They can be used with steels of widely differing composition. The methods are accurate within 5% of the actual Value. 1. NickleAfter neutrahsing the solution 5 ml (01 more) of concentrared ammonia (0.95) must be added. The temperature of the solution must be kept below 30° C before adding the dimethylglyoxime.The extinction coefficient is determined with light of 520 m/gm 2. ChromiumThe chromium is oxidised with hydrogen peroxide in alkaline solution. The influence of iron is ehminated by the addition of phosphoric acid. The recommended acidity is o.2 n, the quantily of diphenylcarbazide is 2 ml of a 1%'s solution in aceton. The determinations are made with a mercury lamp and filter (546 m/gm) 3. ManganeseThe solution of the sampie is boiled with ammoniumpersulphate and then oxidised with 300–500 mg of potassium periodate.The recommended acidity is 2 n, using a mixture of equal parts of sulphuric and phosphoric acids. The determinations are made with light of 520 m/gm.     

Kinase-catalyzed modification of gold nanoparticles: a new approach to colorimetric kinase activity screening

Peptide-stabilized gold nanoparticles have been enzymatically biotinylated by a kinase-catalyzed reaction using biotin-ATP as a cosubstrate. Upon mixing with avidin-modified particles, solutions of biotinylated particles change color from red to blue, indicating aggregation of particles. On the basis of this reaction, we have developed a simple colorimetric test to monitor kinase inhibitor activity.     

Synthesis of chiral iridium complexes immobilized on amphiphilic polymers and their application to asymmetric catalysis

This article details the enantioselective catalytic performance of crosslinked, polymer immobilized, Ir‐based, chiral complexes for transfer hydrogenation of cyclic imines to chiral amines. Polymerization of the achiral vinyl monomer, divinylbenzene, and a polymerizable chiral 1,2‐diamine monosulfonamide ligand followed by complexation with [IrCl₂Cp*]₂ affords the crosslinked polymeric chiral complex, which can be successfully applied to asymmetric transfer hydrogenation of cyclic imines. Polymeric catalysts prepared from amphiphilic achiral monomers have high catalytic activity in the reaction and can be used both in organic solvents and water to give chiral cyclic amines with a high level of enantioselectivity (up to 98% ee). The asymmetric reaction allows for reuse of the heterogeneous catalyst without any loss in activity or enantioselectivity over several runs. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3037–3044     

Indirect determination of oxygen dissolved in water by atomic absorption spectrometry

Summary Indirect Determination of Oxygen Dissolved in Water by Atomic Absorption Spectrometry O₂ dissolved in aqueous medium reacts quantitatively with thallium metal according to O₂+4 Tl+2 H₂O 4 Tl⁺+4 OH^–. The reaction takes place in a glass column filled up with small pieces of sheet metal. The Tl⁺ formed is measured by atomic absorption spectrometry. We study the influence of several factors (pH, temperature, salinity of the water). The results obtained from a statistical sample were compared with those provided by the amperometric method for direct determination of dissolved O₂ and we found a high degree of consistency between them.     

A compleximetric method for the determination of dissolved oxygen in water

A new method is proposed for the determination of dissolved oxygen in water. The iron(III) formed from FES at pH 7.5 is titrated with EDTA solution in presence of salicylic acid indicator after adjustment of the pH to about 2.4 The method is slightly less precise than the Winkler method for pure waters but more accurate for polluted waters; it is simple and convenient for field use.     

Highly phosphorescence iridium complexes and their application in organic light-emitting devices

A new series of iridium(III) mixed ligand complexes TBA[Ir(ppy)(2)(CN)(2)] (1), TBA[Ir(ppy)(2)(NCS)(2)] (2), TBA[Ir(ppy)(2)(NCO)(2)] (3), and [Ir(ppy)(2)(acac)] (4) (ppy = 2-phenylpyridine; acac = acetoylacetonate, TBA = tetrabutylammonium cation) have been developed and fully characterized by UV-vis, emission, IR, NMR, and cyclic voltammetric studies. The lowest energy MLCT transitions are tuned from 463 to 494 nm by tuning the energy of the HOMO levels. These complexes show emission maxima in the blue, green, and yellow region of the visible spectrum and exhibit unprecedented phosphorescence quantum yields, 97 +/- 3% with an excited-state lifetimes of 1-3 micros in dichloromethane solution at 298 K. The near-unity quantum yields of these complexes are related to an increased energy gap between the triplet emitting state and the deactivating e(g) level that have been achieved by meticulous selection of ligands having strong ligand field strength. Organic light-emitting devices were fabricated using the complex 4 doped into a purified 4,4'-bis(carbazol-9-yl)biphenyl host exhibiting a maximum of the external quantum efficiencies of 13.2% and a power efficiency of 37 lm/W for the 9 mol % doped system.