共查询到20条相似文献,搜索用时 31 毫秒
1.
Behavior of hydrogen peroxide in alkaline medium has been studied by direct current (DC) polarography with dropping mercury electrode (DME) aiming to apply it in antioxidant (AO) activity determination. Development of a peroxide anodic current having form of a peak, instead of common polarographic wave, has been investigated. As a base for this investigation the interaction of H2O2 with anodically dissolved mercury was followed. Formation of mercury complex [Hg(O2H)(OH)] has been confirmed. The relevant experimental conditions, such as temperature, concentration and pH dependence, as well as time stability of hydrogen peroxide anodic current, have been assessed. Development of an AO assay based on decrease of anodic current of hydrogen peroxide in the presence of antioxidants (AOs) has been described. Under optimized working conditions, a series of benzoic acids along with corresponding cinnamate analogues have been tested for hydrogen peroxide scavenging activity. In addition, the assay versatility has been confirmed on various complex samples. 相似文献
2.
Degradation of Acid Orange 7 by Gliding Arc Discharge Plasma in Combination with Advanced Fenton Catalysis 总被引:1,自引:0,他引:1
ChangMing Du LuLu Zhang Jing Wang ChuangRong Zhang HongXia Li Ya Xiong 《Plasma Chemistry and Plasma Processing》2010,30(6):855-871
A new plasma–catalysis process of gliding arc discharge (GAD) plasma with zero–valent iron (ZVI) was examined. Because GAD
plasma creates an acidic environment, solid iron releases ferrous ions which act as a catalyst for the decomposition of the
hydrogen peroxide. A comparative study of the catalytic effects between Fe2+ and Fe0 in GAD plasma was investigated. The decolorization reactions of Acid Orange 7 (AO7) followed pseudo–first–order kinetics.
And the rate constants for the process of GAD with ZVI was increased by 30% and by 19%, respectively, compared with the process
of GAD alone and the process of GAD with ferrous. The investigations of solution pH and hydrogen peroxide both demonstrated
that the GAD plasma induced conditions are much suitable for advanced Fenton reactions. The corrosion of ZVI in GAD plasma
can give continuous ferrous ions to sustain Fenton reaction. Also, ZVI was demonstrated to have favorable reusable feature. 相似文献
3.
Mayer I Pittner F Hermann M Missbichler A 《Applied biochemistry and biotechnology》2007,143(2):164-175
A highly sensitive method for measuring the activity of the enzyme diamine oxidase (DAO) independent of the type of substrate
is described. The principle of the assay is to determine the amount hydrogen peroxide generated as a reaction product during
oxidation of diamines by DAO. PSatto™, a highly sensitive luminescence reagent, was used to generate a signal depending on
the hydrogen peroxide concentration based on the action of horseradish peroxidase. DAO is specifically captured from a sample
by an antibody immobilized to microwell plates, and the substrate is added to the bound enzyme. Various diamines were used
as substrates; the peroxide produced is directly proportional to the amount of DAO bound to the specific antibodies. With
this very sensitive method, it is possible to detect pmol amounts of generated hydrogen peroxide in plasma matrix corresponding
to the biological activity of DAO. 相似文献
4.
Joshua Franclemont Selma Mededovic Thagard 《Plasma Chemistry and Plasma Processing》2014,34(4):705-719
The objective of this research effort is to develop a more comprehensive understanding of how molecules get degraded in plasma during an electrical discharge in water. The study correlates the intensity of hydroxyl (OH) radicals in the plasma and physicochemical properties of aqueous solutions of methanol, ethanol, acetonitrile, acetone, dimethyl sulfoxide (DMSO), dimethyl formamide (DMF), phenol, hydroquinone, caffeine, and bisphenol A (BPA). To determine the tendency of the used compounds to penetrate the plasma, their vapor pressures, Henry’s constants, aqueous solubilities, reaction rate constants with OH radicals, and octanol–water partition coefficients are compared and correlated with plasma spectroscopic and hydrogen peroxide (H2O2) measurements. OH radicals are precursors to the formation of hydrogen peroxide and any compound that diffuses into the plasma will react with and lower the intensity of OH radicals and therefore the concentration of hydrogen peroxide in the bulk liquid. Optical emission spectroscopy (OES) reveals that all the used compounds diffuse inside the plasma channel regardless of their vapor pressure where they get oxidized (primarily by OH radicals) and thermally degraded. Results also indicate that hydrophobicity (i.e., octanol–water partition coefficient) is the most important property that determines a compound’s tendency to diffuse inside the plasma channel; hydrophobic compounds readily penetrate the plasma whereas hydrophilic compounds tend to stay in the bulk liquid. The rate of formation of hydrogen peroxide is independent of the type of the compound present in the bulk liquid which confirms that this molecule is formed at the plasma interface. 相似文献
5.
Min Fang Lei Wang Peng Wang Yinzhu Shang Rong Zhang Xiaoting Qiao Liang Liu ZhiYong Gong 《Journal of the Iranian Chemical Society》2016,13(10):1937-1944
A simple and selective colorimetric biosensor was presented based on high catalysis of hemin–graphene hybrid nanosheets coupled with enzyme inhibitions. Alcohol oxidase (AO) can catalyze the oxidations of methanol to produce hydrogen peroxide (H2O2). Subsequently, the resulting H2O2 could be catalyzed to oxidize 3,3,5,5-tetramethylbenzidine (TMB) and then produce a blue color reactions by using hemin–graphene hybrid nanosheets with intrinsic peroxidase-like activity. The activity of AO could be selectively inhibited by the copper ions, and therefore, the oxidase-catalyzed reactions of TMB was decreased. Fortunately, other metal ions even at 10 or 100 times copper ions concentrations showed no intensive inhibitions to the AO activity. Based on this functional materials-enzyme inhibitions system, a simple, selective and sensitive colorimetric biosensor was established to determine copper ions in soft drinks. The linear relationship was obtained from 5 nM to 1 μM, and the detections limit was 1.4 nM. The results were in good agreement with those obtained by the classic ICP-MS. It was demonstrated that the proposed method had an excellent practical perspective on the determinations of copper ions in foodstuff samples. 相似文献
6.
Degradation of Methylene Blue by RF Plasma in Water 总被引:1,自引:0,他引:1
T. Maehara I. Miyamoto K. Kurokawa Y. Hashimoto A. Iwamae M. Kuramoto H. Yamashita S. Mukasa H. Toyota S. Nomura A. Kawashima 《Plasma Chemistry and Plasma Processing》2008,28(4):467-482
Radio frequency (RF) plasma in water was used for the degradation of methylene blue. The fraction of decomposition of methylene blue and the intensity of the spectral line from OH radical increased with RF power. RF plasma in water also produced hydrogen peroxide. The density of hydrogen peroxide increased with RF power and exposure time. When pure water (300 mL) is exposed to plasma at 310 W for 15 min, density of hydrogen peroxide reaches to 120 mg/L. Methylene blue after exposed to plasma degraded gradually for three weeks. This degradation may be due to chemical processes via hydrogen peroxide and tungsten. The comparison between the experimental and calculated spectral lines of OH radical (A–X) shows that the temperature of the radical is around 3,500 K. Electron density is evaluated to be ?3.5 × 1020 m?3 from the stark broadening of the Hβ line. 相似文献
7.
Crude extract of kohlrabi (Brassica oleracea gongylodes) was prepared by a simple procedure and its enzymatic activity and total protein concentration were determined. It was found that this crude extract is a rich source of peroxidase (POx) and has high specific activity. Cross-linked polyvinylpyrrolidone was used as a stabilizer in the preparation of the crude extract. The POx activity of kohlrabi crude extract did not vary for at least 2 months when deoxygenated and stored at 4 degrees C. This extract was applied for the spectrofluorometric determination of hydrogen peroxide using homovanillic acid as a fluorogenic substrate. POx catalyzes the hydrogen peroxide oxidation of homovanillic acid to produce a dimer which shows strong fluorescence at 420 nm with excitation at 312 nm. In the optimum conditions, the calibration graph for hydrogen peroxide was linear up to 190 ng mL(-1), with a detection limit of 4.4 ng mL(-1). The relative standard deviation (RSD) was 1.48% for 50 ng mL(-1) hydrogen peroxide. The proposed method was successfully applied to the determination of hydrogen peroxide in honey. The concentration-time profile of H2O2 produced upon dilution of honey was studied and H2O2 contents of some different honeys from various areas of Iran were determined. 相似文献
8.
Zhidkova TV Proskurnina EV Parfenov EA Vladimirov YA 《Analytical and bioanalytical chemistry》2011,401(1):381-386
The bright chemiluminescence has been observed in the system: Co2+/hydrogen peroxide/lucigenin. The chemiluminescence intensity was directly proportional to either cobalt, hydrogen peroxide,
or lucigenin concentrations. A procedure of determination of superoxide dismutase (SOD) activity by the chemiluminescence
method in the cobalt–hydrogen peroxide–lucigenin system at pH 8.5 is suggested. A linear dependence was established between
a relative chemiluminescence intensity and SOD concentration in the range of SOD concentrations between 0 and 4.5 nM, c
1/2 = 0.8 nM. The determination of SOD activity was performed in several tissue samples (rat plasma, erythrocyte hemolysate,
and liver mitochondria). A technique of tissue sample preparation with the use of thermal inactivation of interfering proteins
at 60 °C was used. The method was successfully applied for comparison of the efficiency of SOD mimetics. 相似文献
9.
Nobumasa Hojo Hirofusa Shirai Yoshiki Chujo Sadao Hayashi 《Journal of polymer science. Part A, Polymer chemistry》1978,16(2):447-455
Decomposition of hydrogen peroxide was examined was examined by using Cu(II)–poly(vinyl alcohol) (PVA) as catalyst. The rates of decomposition were measured. Electronic spectra and infrared spectra of Cu(II)–PVA complex systems were determined at various stages of decomposition. Effect of addition of various amines to the Cu(II)–PVA system on catalytic action was considered. The relation between the initial rate and the initial concentration of hydrogen peroxide varied in accordance with the rate expression of Michaelis-Menten type. Cu(II)–PVA complex was found to have a large catalytic activity, while the polymeric PVA ligand and copper(II) ion exhibited less activity than Cu(II)–PVA complex. For hydrogen peroxide decomposition, Cu(II)–PVA complex showed catalytic activity when a stable complex of planar structure formed, while many other polymer complexes reported by other authors showed the catalytic activity when they were in unstable complex forms. An amine substituent has a critical influence on the rate of hydrogen peroxide decomposition. The mechanism in the first step of reaction for hydrogen peroxide decomposition is discussed. 相似文献
10.
Bacteria were isolated from wastewater containing highly concentrated hydrogen peroxide that had been used to clean the pure water delivery system in a semiconductor plant. One bacterium was selected for its high hydrogen peroxide degradation activity. In the presence of 1 % hydrogen peroxide, it degraded 72.5 % in 5 min. It showed 100 % viability after 6 h at 1 % hydrogen peroxide. Even at 3 % hydrogen peroxide, it survived for more than 6 h. This bacterium was named as Bacillus nitroreducens PLC9 since its 16S rRNA showed 100 % similarity with the recently reported new species B. nitroreducens. Purified catalase from B. nitroreducens PLC9 was characterized as a thermo-alkali-stable hydroperoxidase type II catalase, and it is suggested as a new type of catalase based on following: (1) it is stable over a broad pH range (pH?4–11); (2) it is consisted of homodimers with a molecular weight of 66 kDa (total molecular weight, 134 kDa); (3) its activity was not inhibited by 3-amino-1,2,4-triazole; and (4) its N-terminal sequence has never been reported before. Both B. nitroreducens PLC9 and the isolated catalase can be used for efficient degradation of hydrogen peroxide at high concentrations. 相似文献
11.
12.
Degradation of acridine orange (AO) in aqueous solution by Fenton's reagent (Fe2+ and H2O2) was investigated. The effects of different reaction parameters such as initial AO concentration, pH value of solution, ferrous concentration, hydrogen peroxide concentration, and the presence of chloride ion on the oxidative degradation of AO were investigated. Under optimum conditions, 2 mM H2O2, 0.4 mM Fe2+ and pH 3.0, the initial 0.2 mM AO solution was reduced by 95.8% within 10 min. The primary intermediates of the degradation reaction of AO were identified. The analytical results indicated that the N‐de‐methylation degradation of AO dye took place in a stepwise manner to yield mono‐, di‐, tri‐, and tetra‐N‐de‐methylated AO species generated during the Fenton process. The probable degradation pathways were proposed and discussed. 相似文献
13.
Lane BS Vogt M DeRose VJ Burgess K 《Journal of the American Chemical Society》2002,124(40):11946-11954
This paper describes a method, discovered and refined by parallel screening, for the epoxidation of alkenes. It uses hydrogen peroxide as the terminal oxidant, is promoted by catalytic amounts (1.0-0.1 mol %) of manganese(2+) salts, and must be performed using at least catalytic amounts of bicarbonate buffer. Peroxymonocarbonate, HCO(4)(-), forms in the reaction, but without manganese, minimal epoxidation activity is observed in the solvents used for this research, that is, DMF and (t)BuOH. More than 30 d-block and f-block transition metal salts were screened for epoxidation activity under similar conditions, but the best catalyst found was MnSO(4). EPR studies show that Mn(2+) is initially consumed in the catalytic reaction but is regenerated toward the end of the process when presumably the hydrogen peroxide is spent. A variety of aryl-substituted, cyclic, and trialkyl-substituted alkenes were epoxidized under these conditions using 10 equiv of hydrogen peroxide, but monoalkyl-alkenes were not. To improve the substrate scope, and to increase the efficiency of hydrogen peroxide consumption, 68 diverse compounds were screened to find additives that would enhance the rate of the epoxidation reaction relative to a competing disproportionation of hydrogen peroxide. Successful additives were 6 mol % sodium acetate in the (t)BuOH system and 4 mol % salicylic acid in the DMF system. These additives enhanced the rate of the desired epoxidation reaction by 2-3 times. Reactions performed in the presence of these additives require less hydrogen peroxide and shorter reaction times, and they enhance the yields obtained from less reactive alkene substrates. Possible mechanisms for the reaction are discussed. 相似文献
14.
《Electroanalysis》2018,30(1):27-30
For the first time Co2SnO4 (CTO)/Carbon nanotubes (CNT) composites were prepared and used to modify glassy carbon electrodes for the amperometric determination of hydrogen peroxide. The catalytic activity of composites towards the oxidation of hydrogen peroxide was dependent on the quantity of CNT present in the composite and to the pH of the medium. The pure cobalt stannate phase with a ratio of 3 : 1 (CTO:CNT) exhibited the best catalytic activity towards hydrogen peroxide oxidation at low potentials (0.200 and 0.500 V). A linear relationship between current and hydrogen peroxide concentration was obtained with a sensitivity of 95 and 258 μA mM−1 and a detection limit of 0.130 and 0.08 μM respectively. 相似文献
15.
16.
A selective and sensitive assay of substrates (hypoxanthine, xanthine and allopurinol) of xanthine oxidase by reversed-phase liquid chromatography coupled with the use of immobilized enzyme reactors is described. These compounds were oxidized by immobilized xanthine oxidase and produced hydrogen peroxide, which was determined fluorometrically using immobilized peroxidase and p-hydroxyphenylacetic acid. The detection limits of hypoxanthine, xanthine and allopurinol were approximately 50, 120 and 130 pg per injection, respectively. Immobilized xanthine oxidase inhibited by oxipurinol during the assay was reactivated by 2,6-dichlorophenolindophenol and could be used for a long period without a significant activity loss. These methods were applied to plasma and urine samples. 相似文献
17.
The interaction between fullerene C60 and catalase enzyme was studied with a fullerene C60‐coated piezoelectric (PZ) quartz crystal sensor. The partially irreversible response of the C60‐coated PZ crystal sensor for catalase was observed by the desorption study, which implied that C60 could chemically react with catalase. Thus, immobilized fullerene C60‐catalase enzyme was synthesized and applied in determining hydrogen peroxide in aqueous solutions. An oxygen electrode detector with the immobilized C60‐catalase was also employed to detect oxygen, a product of the hydrolysis of hydrogen peroxide which was catalyzed by the C60‐catalase. The oxygen electrode/C60‐catalase detection system exhibited linear responses to the concentration of hydrogen peroxide and amount of immobilized C60‐catalase enzyme that was used. The effects of pH and temperature on the activity of the immobilized C60‐catalase enzyme were also investigated. Optimum pH at 7.0 and optimum temperature at 25 °C for activity of the insoluble immobilized C60‐catalase enzyme were found. The immobilized C60‐catalase enzyme could be reused with good repeatability of the activity. The lifetime of the immobilized C60‐catalase enzyme was long enough with an activity of 93% after 95 days. The immobilized C60‐catalase enzyme was also applied in determining glucose which was oxidized with glucose oxidase resulting in producing hydrogen peroxide, followed by detecting hydrogen peroxide with the oxygen electrode/C60‐catalase detection system. 相似文献
18.
19.
Zhi-heng Shu Cai-lian Fan Hong-yan Wei Zi-ting Li Hisayoshi Norimoto Xi-yang Tang Zhi-hong Yao Xin-sheng Yao Yi Dai 《Journal of separation science》2023,46(17):2300331
An efficient strategy for the identification of potential nephroprotective substances in Zhu-Ling decoction has been established with the integration of absorbed components characterization, pharmacokinetics, and activity evaluation. A qualitative method was developed to characterize the chemical constituents absorbed components in vivo of Zhu-Ling decoction by using ultra-performance liquid chromatography-quadrupole-time-of-flight mass spectrometry. A quantitative method was established and validated for the simultaneous determination of eight compounds in rat plasma by using ultra-performance liquid chromatography-triple quadruple tandem mass spectrometry. Finally, the nephroprotective activities of absorbed components with high exposure were assessed by cell survival rate, superoxide dismutase, and malondialdehyde activities in hydrogen peroxide–induced Vero cells. As a result, 111 compounds in Zhu-Ling decoction and 36 absorbed components were identified in rat plasma and urine, and poricoic acid A, poricoic acid B, alisol A, 16-oxo-alisol A, and dehydro-tumulosic acid had high exposure levels in rat plasma. Finally, poricoic acid B, poricoic acid A, 16-oxo-alisol A, and dehydro-tumulosic acid showed remarkable nephroprotective activity against Vero cells damage induced by hydrogen peroxide. Besides, superoxide dismutase and malondialdehyde activities were obviously regulated in hydrogen peroxide–induced Vero cells by treatment with the four compounds mentioned above. Therefore, these four compounds were considered to be effective substances of Zhu-Ling decoction due to their relatively high exposure in vivo and biological activity. This study provided a chemical basis for the action mechanism of Zhu-Ling decoction in the treatment of chronic kidney diseases. 相似文献
20.
Masaki Mifune Katsuyoshi Sugimoto Akimasa Iwado Hiromichi Akizawa Noriko Motohashi Yutaka Saito 《Analytical sciences》2003,19(4):569-573
A flow injection analysis system of hydrogen peroxide was developed. The present system is based on measuring of the absorbance of a quinoid dye formed by the following reaction catalyzed by peroxidase: Phenol + 4-Aminoantipyrine + 2H2O2 --> Peroxidase --> Quinoid dye + 4H2O. A column packed with aminopropyl-glass beads modified with amanganese(III)-tetra(4-carboxyphenyl)porphine derivative (Mn-TCPP(G) column), which has peroxidase-like activity, was used in place of an immobilized peroxidase column in the above reaction. The linear range of the calibration curve was 0.4-80 microg/ml hydrogen peroxide. The relative standard deviation of this system was 2.97% (n = 100, 10 microg/ml hydrogen peroxide 20 microl injection). The Mn-TCPP(G) column has sufficiently stability for the continuous injection of hydrogen peroxide untill 100 times. The advantageous feature of the Mn-TCPP(G) column was a less-electrostatic interaction between the mother glass beads and the anionic chromogen or quinoid dye formed and the stability in terms of the storage, temperature and moisture. The determination of serum glucose was achieved by attaching an immobilized glucose oxidase column to this system without deproteinization. 相似文献