Calculation of equilibrium distributions of chemical species in aqueous solutions by means of monotone sequences

1975 ◽  
Vol 7 (2) ◽  
pp. 99-115 ◽  
Author(s):  
Thomas J. Wolery ◽  
Lester J. Walters
Keyword(s):  
Aqueous Solutions ◽  
Chemical Species ◽  
Monotone Sequences ◽  
Equilibrium Distributions

JESS, a Joint Expert Speciation System – VI: thermodynamically-consistent standard Gibbs energies of reaction for aqueous solutions

2018 ◽  
Vol 42 (10) ◽  
pp. 7617-7629 ◽  
Author(s):  
Peter M. May ◽  
Darren Rowland
Keyword(s):  
Open Access ◽  
Aqueous Solutions ◽  
Chemical Species ◽  
Gibbs Energies ◽  
Metal Ligand

A large, open-access, sustainable database of relative Gibbs energies is developed for over 50 000 aqueous chemical species, including many metal–ligand complexes.

Complexation of Zr(IV) Precursors in Aqueous Solutions

1992 ◽  
Vol 271 ◽  
Author(s):  
J. Livage ◽  
M. Chatry ◽  
M. Henry ◽  
F. Taulelle
Keyword(s):  
Aqueous Solutions ◽  
Sol Gel ◽  
Chemical Species ◽  
Ionic Species ◽  
Whole Process ◽  
Charge Model ◽  
Partial Charge Model ◽  
Sol Gel Synthesis ◽  
Inorganic Precursors

ABSTRACTThe sol-gel synthesis of metal oxides can be performed via the hydroxylation and condensation of metal cations in aqueous solutions. The complexation of these ionic species by anions leads to the chemical modification of inorganic precursors at a molecular level. The whole process of hydrolysis and condensation can then be modified allowing a chemical control of the morphology, the structure and even the chemical composition of the resulting powder.The role of anions during the formation of condensed phases from inorganic precursors in aqueous solutions has to be taken into account. The complexing ability of these anions is described in the frame of the Partial Charge Model as a function of pH and the mean electronegativity of anionie and cationic chemical species. Experimental evidence for the complexation of zirconyl species in aqueous solutions will be given using multinuclear NMR of anions.

scholarly journals Chemical Species Produced from Some Diazaazulene Derivatives in Aqueous Solutions of Various Acidities

1970 ◽  
Vol 43 (8) ◽  
pp. 2283-2290 ◽  
Author(s):  
Yoshie Tanizaki ◽  
Hiroshi Hiratsuka ◽  
Toshihiko Hoshi
Keyword(s):  
Aqueous Solutions ◽  
Chemical Species

Ultrathin frozen sections of yeast without aldehyde prefixation

1978 ◽  
Vol 36 (2) ◽  
pp. 58-59
Author(s):  
K. J. Böhm ◽  
a. E. Unger
Keyword(s):  
Aqueous Solutions ◽  
Biological Material ◽  
Yeast Cells ◽  
Frozen Sections ◽  
Good Preservation ◽  
Ultrathin Frozen Sections

During the last years it was shown that also by means of cryo-ultra-microtomy a good preservation of substructural details of biological material was possible. However the specimen generally was prefixed in these cases with aldehydes.Preparing ultrathin frozen sections of chemically non-prefixed material commonly was linked up to considerable technical and manual expense and the results were not always satisfying. Furthermore, it seems to be impossible to carry out cytochemical investigations by means of treating sections of unfixed biological material with aqueous solutions.We therefore tried to overcome these difficulties by preparing yeast cells (S. cerevisiae) in the following manner:

Chemical Species Identification in an SEM by Changes in Emitted X-Ray Energies

1974 ◽  
Vol 32 ◽  
pp. 570-571
Author(s):  
R. H. Duff
Keyword(s):  
Species Identification ◽  
Valence Electron ◽  
Chemical Species ◽  
X Rays ◽  
Chemical Bonds ◽  
Small Shift ◽  
X Ray ◽  
Electron Transitions ◽  
Peak Energy ◽  
Chemical Combination

A material irradiated with electrons emits x-rays having energies characteristic of the elements present. Chemical combination between elements results in a small shift of the peak energies of these characteristic x-rays because chemical bonds between different elements have different energies. The energy differences of the characteristic x-rays resulting from valence electron transitions can be used to identify the chemical species present and to obtain information about the chemical bond itself. Although these peak-energy shifts have been well known for a number of years, their use for chemical-species identification in small volumes of material was not realized until the development of the electron microprobe.

Confocal Raman mapping

1992 ◽  
Vol 50 (2) ◽  
pp. 1514-1515
Author(s):  
J. Barbillat ◽  
M. Delhaye ◽  
P. Dhamelincourt
Keyword(s):  
Chemical Species ◽  
Diffraction Limit ◽  
Microscopic Level ◽  
Raman Mapping ◽  
Complete Spectrum ◽  
Laser Illumination ◽  
Ccd Detector ◽  
Raman Microprobe ◽  
Photodiode Array ◽  
Raman Image

Raman mapping, with a spatial resolution close to the diffraction limit, can help to reveal the distribution of chemical species at the surface of an heterogeneous sample.As early as 1975,three methods of sample laser illumination and detector configuration have been proposed to perform Raman mapping at the microscopic level (Fig. 1),:- Point illumination:The basic design of the instrument is a classical Raman microprobe equipped with a PM tube or either a linear photodiode array or a two-dimensional CCD detector. A laser beam is focused on a very small area ,close to the diffraction limit.In order to explore the whole surface of the sample,the specimen is moved sequentially beneath the microscope by means of a motorized XY stage. For each point analyzed, a complete spectrum is obtained from which spectral information of interest is extracted for Raman image reconstruction.- Line illuminationA narrow laser line is focused onto the sample either by a cylindrical lens or by a scanning device and is optically conjugated with the entrance slit of the stigmatic spectrograph.

Imaging polymers, proteins and dna in aqueous solutions with the atomic force microscope

1989 ◽  
Vol 47 ◽  
pp. 32-33
Author(s):  
S.A.C. Gould ◽  
B. Drake ◽  
C.B. Prater ◽  
A.L. Weisenhorn ◽  
S.M. Lindsay ◽  
...  
Keyword(s):  
Amino Acids ◽  
Dna Sequencing ◽  
Aqueous Solutions ◽  
Atomic Force Microscope ◽  
Piezoelectric Crystal ◽  
Atomic Force ◽  
Structure Of Molecules ◽  
Optical Lever

The atomic force microscope (AFM) is an instrument that can be used to image many samples of interest in biology and medicine. Images of polymerized amino acids, polyalanine and polyphenylalanine demonstrate the potential of the AFM for revealing the structure of molecules. Images of the protein fibrinogen which agree with TEM images demonstrate that the AFM can provide topographical data on larger molecules. Finally, images of DNA suggest the AFM may soon provide an easier and faster technique for DNA sequencing.The AFM consists of a microfabricated SiO2 triangular shaped cantilever with a diamond tip affixed at the elbow to act as a probe. The sample is mounted on a electronically driven piezoelectric crystal. It is then placed in contact with the tip and scanned. The topography of the surface causes minute deflections in the 100 μm long cantilever which are detected using an optical lever.

Supersonic jet spectrometry of chemical species resulting from thermal decomposition of polystyrene and polycarbonate

1992 ◽  
Vol 64 (19) ◽  
pp. 931A-940A ◽  
Author(s):  
Totaro Imasaka ◽  
Masami Hozumi ◽  
Nobuhiko Ishibashi
Keyword(s):  
Thermal Decomposition ◽  
Supersonic Jet ◽  
Chemical Species
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