Modified ferron assay for speciation characterization of hydrolyzed Al(III): a precise k value based judgment

2009 ◽  
Vol 59 (4) ◽  
pp. 823-832 ◽  
Author(s):  
Ye Changqing ◽  
Wang Dongsheng ◽  
Wu Xiaohong ◽  
Qu Jiuhui ◽  
John Gregory
Keyword(s):  
Kinetic Constant ◽  
Nonlinear Least Squares ◽  
Precise Determination ◽  
K Value ◽  
First Order ◽  
First Order Kinetics ◽  
Parallel Reactions

The speciation of Al-OH complexes in terms of Ala, Alb and Alc could be achieved by traditional ferron assay and Alb is generally considered as Al13, however, the inherent correlation between them remains an enigma. This paper presents a modified ferron assay to get precise determination of Al13 using nonlinear least squares analysis, and to clarify the correlation between Alb and Al13. Two parallel reactions conforming to pseudo-first-order kinetics can simulate the complicate reactions between polynuclear complexes and ferron successfully. Four types of experimental kinetic constant (k value) of Al-OH complexes can be observed by this method when investigating three typical aluminium solutions. Comparing with the results of 27Al NMR, the species with moderate kinetics around 0.001 s−1 can be confirmed to resemble to Al13 polycation. The other types of kinetics are also well-regulated in partially neutralized aluminium solutions with various OH/Al ratios (b values) in the range 0 ∼ 2.5. It would provide potential means to trace the in-situ formation of Al13 in dilute solutions such as coagulation with Al-based coagulants

scholarly journals An Electrochemical Process Comparison of As(III) in Simulated Groundwater at Low Voltage in Mixed and Divided Electrolytic Cells

Water ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 1126 ◽  
Author(s):  
Yanyan Qin ◽  
Yanping Cui ◽  
Lidan Lei ◽  
Ya Gao ◽  
Zhengwei Zhou ◽  
...  
Keyword(s):  
Low Voltage ◽  
Electrochemical Process ◽  
First Order ◽  
Electrolytic Cells ◽  
Process Comparison ◽  
First Order Kinetics ◽  
Simulated Groundwater ◽  
High Arsenic ◽  
High Arsenic Groundwater

A relatively low voltage can be favor of e- transfer and peroxide generation from dominant 2e--reduction of O2 on carbon materials as cathode, with low energy loss. In this study the conversion of As(III) in simulated high arsenic groundwater at low voltage was compared in a mixed and a anode–cathode separated electrolytic system. With applied voltages (the potential difference between cathode and anode) from 0.1 V to 0.8 V, As(III) was found to be efficiently converted to As(V) in the mixed electrolytic cells and in separated anodic cells. The complete oxidation of As(III) to As(V) at 0.1–0.8 V was also achieved on graphite in divided cathodic cells which could be long-running. The As(III) conversion process in mixed electrolytic cells, anodic cells and cathodic cells all conformed to the pseudo first-order kinetics equation. The energy consumed by As(III) conversion was decreased as the applied voltage declined. Low voltage electrolysis is of great significance for saving energy consumption and improving the current efficiency and can be applied to in-situ electrochemical pre-oxidation for As(III) in high arsenic groundwater.

scholarly journals Microfluidic characterization of macromolecular liquid–liquid phase separation

Lab on a Chip ◽  
2020 ◽  
Vol 20 (22) ◽  
pp. 4225-4234
Author(s):  
Anne Bremer ◽  
Tanja Mittag ◽  
Michael Heymann
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Precise Determination ◽  
Phase Morphology ◽  
Liquid Phase Separation ◽  
Dense Phase ◽  
Liquid Liquid Phase Separation

The microfluidic phase chip allows precise determination of the saturation concentrations of biomolecules that undergo liquid–liquid phase separation while also monitoring the dense-phase morphology.

In situ structure and force characterization of 2D nano-colloids at the air/water interface

Soft Matter ◽  
2019 ◽  
Vol 15 (42) ◽  
pp. 8475-8482
Author(s):  
Giovanni Li-Destri ◽  
Roberta Ruffino ◽  
Nunzio Tuccitto ◽  
Giovanni Marletta
Keyword(s):  
Quantitative Determination ◽  
Experimental Method ◽  
Water Interface ◽  
Liquid Interfaces ◽  
Interaction Forces ◽  
Air Water Interface

We have developed a novel experimental method, which enables quantitative determination of interaction forces between interfacial nanoparticles as a function of the inter-particle distance at liquid interfaces.

Effect of thiol oxidation and thiol export from erythrocytes on determination of redox status of homocysteine and other thiols in plasma from healthy subjects and patients with cerebral infarction

1995 ◽  
Vol 41 (3) ◽  
pp. 361-366 ◽  
Author(s):  
A Andersson ◽  
A Lindgren ◽  
B Hultberg
Keyword(s):  
Cerebral Infarction ◽  
Healthy Subjects ◽  
Redox Status ◽  
Reduced Form ◽  
Temperature Dependent ◽  
First Order ◽  
First Order Kinetics ◽  
Before And After ◽  
Reduced Forms

Abstract Changes in concentration of reduced and oxidized low-M(r) thiols were measured in blood and plasma before and after the separation of blood cells. If centrifugation of blood was postponed, the reduced form of homocysteine in plasma increased with time at 22 degrees C; in contrast, the concentrations of other reduced thiols (cysteine, glutathione, and cysteinylglycine) decreased. In plasma the reduced forms of all thiols disappeared at a rate that followed first-order kinetics. The rates of disappearance ("half-lives") were temperature-dependent; they were about the same for glutathione and homocysteine (11.7 and 14.3 min, respectively, at 22 degrees C) and somewhat higher for cysteinylglycine and cysteine. After establishing proper sampling conditions for reduced thiols, we measured this thiol fraction as well as free (non-protein-bound) and total thiols in 10 reference subjects and 19 patients with cerebral infarction. Mild but significant hyperhomocysteinemia involving total and free homocysteine (but not reduced homocysteine) was found in the patients.

In situ calibration and [H+] sensitivity of the fluorescent Na+indicator SBFI

2001 ◽  
Vol 280 (6) ◽  
pp. C1623-C1633 ◽  
Author(s):  
Abdoullah Diarra ◽  
Claire Sheldon ◽  
John Church
Keyword(s):  
Ph Dependence ◽  
Apparent Dissociation Constant ◽  
Simple Method ◽  
Standard Equation ◽  
In Situ Calibration ◽  
Apparent Decrease ◽  
Calibration Techniques

Despite the popularity of Na+-binding benzofuran isophthalate (SBFI) to measure intracellular free Na+ concentrations ([Na+]i), the in situ calibration techniques described to date do not favor the straightforward determination of all of the constants required by the standard equation (Grynkiewicz G, Poenie M, and Tsien RY. J Biol Chem 260: 3440–3450, 1985) to convert the ratiometric signal into [Na+]. We describe a simple method in which SBFI ratio values obtained during a “full” in situ calibration are fit by a three-parameter hyperbolic equation; the apparent dissociation constant ( K d) of SBFI for Na+ can then be resolved by means of a three-parameter hyperbolic decay equation. We also developed and tested a “one-point” technique for calibrating SBFI ratios in which the ratio value obtained in a neuron at the end of an experiment during exposure to gramicidin D and 10 mM Na+is used as a normalization factor for ratios obtained during the experiment; each normalized ratio is converted to [Na+]i using a modification of the standard equation and parameters obtained from a full calibration. Finally, we extended the characterization of the pH dependence of SBFI in situ. Although the K d of SBFI for Na+ was relatively insensitive to changes in pH in the range 6.8–7.8, acidification resulted in an apparent decrease, and alkalinization in an apparent increase, in [Na+]i values. The magnitudes of the apparent changes in [Na+]ivaried with absolute [Na+]i, and a method was developed for correcting [Na+]i values measured with SBFI for changes in intracellular pH.

POSITRON FACILITIES TESTS OF THE X-RAYS PRODUCED BY CRYSTALLINE UNDULATORS

2005 ◽  
Vol 19 (03) ◽  
pp. 85-98 ◽  
Author(s):  
S. BELLUCCI
Keyword(s):  
Positron Beam ◽  
Precise Determination ◽  
X Rays ◽  
Experimental Conditions ◽  
X Ray ◽  
Accelerated Particles

One of the main involvements of the INFN-Laboratori Nazionali di Frascati group in channeling researches is described, i.e. the crystal undulator R & D, with the characterization of the crystal undulator prototypes with SEM and the positron beam. We consider a precise determination of the optimal experimental conditions for channeling of this kind of accelerated particles through such microstructured crystals, as promising candidates for producing X-ray beams.

Precise Determination of Percent Cure of Epoxide Polymers and Composites via Fiber-Optic Raman Spectroscopy and Multivariate Analysis

1997 ◽  
Vol 51 (2) ◽  
pp. 247-252 ◽  
Author(s):  
Jeffrey F. Aust ◽  
Karl S. Booksh ◽  
Christopher M. Stellman ◽  
Richard S. Parnas ◽  
Michael L. Myrick
Keyword(s):  
Raman Spectroscopy ◽  
Multivariate Analysis ◽  
Real Time ◽  
Fiber Optic ◽  
Precise Determination ◽  
Probe Design ◽  
Epoxide Polymers ◽  
Time Determination

A method for real-time determination of the percent cure of epoxies via in situ fiber-optic Raman spectroscopy has been developed. This method utilizes a probe design developed for real-time monitoring of polymer curing and multivariate analysis to interpret the data and determine percent cure. This method was demonstrated to be reliable to ±0.54% of cure in laboratory samples over a 50–99% cure range. A preliminary study measuring cure percentage in an industrial, glass-reinforced composite has been shown to be reliable to ±0.82% in the 40–90% cure range.

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