Kinetics of the Ammonium Acetate-Catalyzed Condensation of Vanillin and Nitromethane1

1951 ◽  
Vol 73 (5) ◽  
pp. 2268-2270 ◽  
Author(s):  
Thomas I. Crowell ◽  
Fausto A. Ramirez
Keyword(s):  
Ammonium Acetate ◽  
Kinetics Of

scholarly journals Investigation of the use of ammonium acetate as an alternative lixiviant in the leaching of malachite ore

2013 ◽  
Vol 19 (1) ◽  
pp. 25-34 ◽  
Author(s):  
Asım Künkül ◽  
Abdulvahap Gülezgin ◽  
Nizamettin Demirkiran
Keyword(s):  
Ammonium Acetate ◽  
Solution Concentration ◽  
Copper Extraction ◽  
Leaching Rate ◽  
Selective Leaching ◽  
Liquid Ratio ◽  
Copper Ore ◽  
Experimental Parameters ◽  
Leaching Reaction ◽  
Kinetics Of

The solutions containing ammonia allow for selective leaching of the copper from a copper ore. In this study, the leaching and kinetics of malachite ore were examined using ammonium acetate solutions as an alternative lixiviant. The effects of some experimental parameters on the leaching of malachite ore were investigated. A kinetic model to represent the effects of these parameters on the leaching rate was developed. It was determined that the leaching rate increased with increasing solution concentration, temperature and stirring speed, and decreasing particle size and solid-to-liquid ratio. It was found that the leaching reaction followed the mixed kinetic control model. The activation energy of this leaching process was determined to be 59.6 kJmol-1. Consequently, it was determined that ammonium acetate solutions could be used as an effective leaching agent for the copper extraction form malachite ore.

Kinetics of the Oxidation of Galena In Ammonium Acetate Solutions Under Oxygen Pressure

JOM ◽  
1956 ◽  
Vol 8 (8) ◽  
pp. 1096-1099
Author(s):  
D. P. Seraphim ◽  
C. S. Samis
Keyword(s):  
Oxygen Pressure ◽  
Ammonium Acetate ◽  
Kinetics Of

THE KINETICS OF METABOLISM OF GIBBERELLA FUJIKUROI IN STIRRED CULTURE

1964 ◽  
Vol 10 (3) ◽  
pp. 407-444 ◽  
Author(s):  
A. Borrow ◽  
Sheila Brown ◽  
E. G. Jefferys ◽  
R. H. J. Kessell ◽  
Eithne C. Lloyd ◽  
...  
Keyword(s):  
Growth Rate ◽  
Specific Growth Rate ◽  
Nitrogen Uptake ◽  
Exponential Growth ◽  
Ammonium Acetate ◽  
Specific Growth ◽  
Dry Weight ◽  
Gibberella Fujikuroi ◽  
Ammonium Tartrate ◽  
Kinetics Of

Some aspects are described of the kinetics of the growth of Gibberella fujikuroi in nitrogen-limited media containing either ammonium nitrate, ammonium acetate, ammonium tartrate, urea, or glycine. Also varied were inoculum size, agitation rate, pH, and initial concentrations of glucose and nitrogen source. The significance of kinetic parameters used in this, and published studies, is discussed.A lag phase was only found on ammonium acetate media or when high concentrations of glucose were present. Early growth was exponential on all nitrogen sources. On ammonium acetate the specific growth rate decreased at a dry weight of ca. 1 mg/g WS (Whole unfiltered Sample). On ammonium nitrate, early exponential growth utilized more NH3-nitrogen than NO3-nitrogen with a concomitant decrease in pH. In the range pH 3.0–2.8 NH3-nitrogen uptake and dry weight increase ceased, but NO3-nitrogen uptake continued, and the pH increased until growth and NH3-nitrogen uptake restarted. This pattern could be repeated. Finally, exponential growth was resumed at a low specific growth rate. On glycine, urea, and ammonium tartrate media, exponential growth continued to a dry weight of about 7 mg/g WS. During this period the uptakes relative to dry weight (contributions) of glucose, nitrogen, phosphate, and magnesium remained constant and were unaffected by the rate of agitation, as also was the specific growth rate, but the latter decreased with increasing glucose concentration.A period of linear growth could follow the exponential period. The contribution of glucose was greater, and that of phosphate and magnesium less, than during exponential growth. The dry weight at which exponential growth changed to linear growth was greater the higher the rate of agitation, and this change may be a response to oxygen restriction.After nitrogen exhaustion, fat and carbohydrate accumulation in the cells largely accounted for the increase in dry weight. The specific rates of dry weight increase and glucose uptake remained constant over the lower range of initial nitrogen concentrations. Both rates decreased with increasing nitrogen over the higher range.Gibberellic acid production began at, or soon after, nitrogen exhaustion. The amount present increased linearly with time. The productivity decreased with increasing glucose concentration, and first increased and then decreased with increasing initial nitrogen. The maximum amount produced was proportional to the initial nitrogen provided. Some published results are discussed in the light of these relations.

Direct observations of radiation-enhanced transformations in glass

1983 ◽  
Vol 41 ◽  
pp. 354-355
Author(s):  
J. F. DeNatale ◽  
D. G. Howitt
Keyword(s):  
Glass Matrix ◽  
Diffusion Mechanism ◽  
Bubble Formation ◽  
Silicate Glasses ◽  
Phase Decomposition ◽  
Direct Observations ◽  
Thin Foils ◽  
Oxygen Bubble ◽  
Electron Energy Loss ◽  
Kinetics Of

The electron irradiation of silicate glasses containing metal cations produces various types of phase separation and decomposition which includes oxygen bubble formation at intermediate temperatures figure I. The kinetics of bubble formation are too rapid to be accounted for by oxygen diffusion but the behavior is consistent with a cation diffusion mechanism if the amount of oxygen in the bubble is not significantly different from that in the same volume of silicate glass. The formation of oxygen bubbles is often accompanied by precipitation of crystalline phases and/or amorphous phase decomposition in the regions between the bubbles and the detection of differences in oxygen concentration between the bubble and matrix by electron energy loss spectroscopy cannot be discerned (figure 2) even when the bubble occupies the majority of the foil depth.The oxygen bubbles are stable, even in the thin foils, months after irradiation and if van der Waals behavior of the interior gas is assumed an oxygen pressure of about 4000 atmospheres must be sustained for a 100 bubble if the surface tension with the glass matrix is to balance against it at intermediate temperatures.

Irradiation behavior of pyrolytic silicon carbide

1983 ◽  
Vol 41 ◽  
pp. 72-73
Author(s):  
R. J. Lauf
Keyword(s):  
Silicon Carbide ◽  
Fission Products ◽  
Thermodynamics And Kinetics ◽  
Neutron Fluences ◽  
Fuel Particles ◽  
Sic Coatings ◽  
Irradiation Behavior ◽  
Kinetics Of ◽  
Htgr Fuel

Fuel particles for the High-Temperature Gas-Cooled Reactor (HTGR) contain a layer of pyrolytic silicon carbide to act as a miniature pressure vessel and primary fission product barrier. Optimization of the SiC with respect to fuel performance involves four areas of study: (a) characterization of as-deposited SiC coatings; (b) thermodynamics and kinetics of chemical reactions between SiC and fission products; (c) irradiation behavior of SiC in the absence of fission products; and (d) combined effects of irradiation and fission products. This paper reports the behavior of SiC deposited on inert microspheres and irradiated to fast neutron fluences typical of HTGR fuel at end-of-life.

The Ordered Phase Formation in Ti-Al-Ga Alloys

1970 ◽  
Vol 28 ◽  
pp. 440-441
Author(s):  
Shiro Fujishiro ◽  
Harold L. Gegel
Keyword(s):  
Thermal Stability ◽  
High Temperature ◽  
Titanium Alloys ◽  
Growth Kinetics ◽  
Stoichiometric Composition ◽  
Good Potential ◽  
Alpha Titanium ◽  
Cold Rolled ◽  
Kinetics Of ◽  
Thermal Stability Of

Ordered-alpha titanium alloys having a DO19 type structure have good potential for high temperature (600°C) applications, due to the thermal stability of the ordered phase and the inherent resistance to recrystallization of these alloys. Five different Ti-Al-Ga alloys consisting of equal atomic percents of aluminum and gallium solute additions up to the stoichiometric composition, Ti3(Al, Ga), were used to study the growth kinetics of the ordered phase and the nature of its interface.The alloys were homogenized in the beta region in a vacuum of about 5×10-7 torr, furnace cooled; reheated in air to 50°C below the alpha transus for hot working. The alloys were subsequently acid cleaned, annealed in vacuo, and cold rolled to about. 050 inch prior to additional homogenization

The structure of pre-mRNA and mRNA from erythroid cells

1978 ◽  
Vol 36 (2) ◽  
pp. 234-235
Author(s):  
A.-M. Ladhoff ◽  
B.J. Thiele ◽  
Ch. Coutelle ◽  
S. Rosenthal
Keyword(s):  
Bone Marrow ◽  
Structural Transformation ◽  
Electron Micrographs ◽  
Ammonium Acetate ◽  
Bone Marrow Cells ◽  
Erythroid Cells ◽  
Globin Mrna ◽  
Ordered Structures ◽  
Rabbit Bone ◽  
Rabbit Reticulocytes

The suggested precursor-product relationship between the nuclear pre-mRNA and the cytoplasmic mRNA has created increased interest also in the structure of these RNA species. Previously we have been published electron micrographs of individual pre-mRNA molecules from erythroid cells. An intersting observation was the appearance of a contour, probably corresponding to higher ordered structures, on one end of 10 % of the pre-mRNA molecules from erythroid rabbit bone marrow cells (Fig. 1A). A virtual similar contour was observed in molecules of 9S globin mRNA from rabbit reticulocytes (Fig. 1B). A structural transformation in a linear contour occurs if the RNA is heated for 10 min to 90°C in the presence of 80 % formamide. This structural transformation is reversible when the denatured RNA is precipitated and redissolved in 0.2 M ammonium acetate.

Ion Beam Induced Interfacial Reactions in Molybdenum Thin Films on Silicon

1981 ◽  
Vol 39 ◽  
pp. 162-163
Author(s):  
L. J. Chen ◽  
L. S. Hung ◽  
J. W. Mayer
Keyword(s):  
Ion Beam ◽  
Chemical Vapor ◽  
Interfacial Reactions ◽  
Practical Applications ◽  
Microelectronic Devices ◽  
Recent Emergence ◽  
Chemical Vapor Deposited ◽  
Atomic Mixing ◽  
Silicon Interface ◽  
Kinetics Of

When an energetic ion penetrates through an interface between a thin film (of species A) and a substrate (of species B), ion induced atomic mixing may result in an intermixed region (which contains A and B) near the interface. Most ion beam mixing experiments have been directed toward metal-silicon systems, silicide phases are generally obtained, and they are the same as those formed by thermal treatment.Recent emergence of silicide compound as contact material in silicon microelectronic devices is mainly due to the superiority of the silicide-silicon interface in terms of uniformity and thermal stability. It is of great interest to understand the kinetics of the interfacial reactions to provide insights into the nature of ion beam-solid interactions as well as to explore its practical applications in device technology.About 500 Å thick molybdenum was chemical vapor deposited in hydrogen ambient on (001) n-type silicon wafer with substrate temperature maintained at 650-700°C. Samples were supplied by D. M. Brown of General Electric Research & Development Laboratory, Schenectady, NY.

Electron Microscopy of the Nucleic Acid of Mouse Mammary Tumor Virus

1968 ◽  
Vol 26 ◽  
pp. 22-23
Author(s):  
N. H. Sarkar ◽  
Dan H. Moore
Keyword(s):  
Mammary Tumor ◽  
Mouse Mammary Tumor Virus ◽  
Ammonium Acetate ◽  
Dry Weight ◽  
Mouse Tumor ◽  
Mammary Tumor Virus ◽  
Rna Molecules ◽  
Mouse Mammary Tumor ◽  
Tumor Virus ◽  
The Subject

Mouse mammary tumor virus (MTV) is believed to contain about 0.8% single stranded ribonucleic acid (RNA). This value of RNA content was estimated on a dry weight basis. The subject of this report is an attempt to visualize the RNA molecules of MTV particles.MTV particles were isolated from RIII mouse (tumor incidence approximately 80%) milk according to the method described by Lyons and Moore. Purified virions from 5 ml of milk were finally suspended in 0.2 ml of PBS, pH 7.4 and was mixed with an equal volume of pronase (5 mg/ml). This mixture was incubated at 37°C for an hour. RNA was extracted three times using freshly prepared cold phenol. It was then treated three times with cold ethyl ether to remove any trace of phenol. The RNA thus extracted was divided into two parts. One part was diluted four fold with 8M urea to avoid aggregation of the molecules. The other part was left untreated. Both samples were then mixed with an equal volume of 1M ammonium acetate, adjusted to pH 8.0 with NH3 containing chymotrypsin at a concentration of 0.01%.

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