scholarly journals TEMPERATURE CHARACTERISTICS FOR THE METABOLISM OF CHLORELLA

1934 ◽  
Vol 18 (2) ◽  
pp. 209-213 ◽  
Author(s):  
C. S. French
Keyword(s):  
Hydrogen Peroxide ◽  
Low Temperatures ◽  
Temperature Characteristics ◽  
First Order

The decomposition of hydrogen peroxide by intact Chlorella cells follows a first order course at very low temperatures, but at higher temperatures gives falling first order constants. Between 0.6° and 20°C. the value of µ is 10,500 calories.

THE THERMAL DECOMPOSITION OF HYDROGEN PEROXIDE VAPOUR. II.

1947 ◽  
Vol 25b (2) ◽  
pp. 135-150 ◽  
Author(s):  
Paul A. Giguère
Keyword(s):  
Activation Energy ◽  
Hydrogen Peroxide ◽  
Thermal Decomposition ◽  
Low Temperatures ◽  
Hydrocyanic Acid ◽  
Quartz Surface ◽  
First Order ◽  
Acid Washing ◽  
Reaction Vessels ◽  
Low Pressures

The decomposition of hydrogen peroxide vapour has been investigated at low pressures (5 to 6 mm.) in the temperature range 50° to 420 °C., for the purpose of determining the effect of the nature and treatment of the active surfaces. The reaction was followed in an all-glass apparatus and, except in one case, with one-litre round flasks as reaction vessels. Soft glass, Pyrex, quartz, and metallized surfaces variously treated were used. In most cases the decomposition was found to be mainly of the first order but the rates varied markedly from one vessel to another, even with vessels made of the same type of glass. On a quartz surface the decomposition was preceded by an induction period at low temperatures. Fusing the glass vessels slowed the reaction considerably and increased its apparent activation energy; this effect was destroyed by acid washing. Attempts to poison the surface with hydrocyanic acid gave no noticeable result. The marked importance of surface effects at all temperatures is considered as an indication that the reaction was predominantly heterogeneous under the prevailing conditions. Values ranging from 8 to 20 kcal. were found for the apparent energy of activation. It is concluded that the decomposition of hydrogen peroxide vapour is not very specific as far as the nature of the catalyst is concerned.

Multifactorial optimization of the decolorisation parameters of wastewaters resulting from dyeing flowers

2009 ◽  
Vol 59 (7) ◽  
pp. 1361-1369 ◽  
Author(s):  
Edison Gil Pavas ◽  
Miguel Ángel Gómez-García
Keyword(s):  
Hydrogen Peroxide ◽  
Organic Matter ◽  
Experimental Design ◽  
Order Reaction ◽  
Pseudo First Order Reaction ◽  
First Order ◽  
Effluent Standards ◽  
Degradation Of Dyes ◽  
Pseudo First Order ◽  
Dyes Mixture

This work deals with the treatment of the wastewaters resulting from the process of dyeing flowers. In some local cases for growing flowers near to Medellín (Colombia), wastewater color was found to be one of the main problems in meeting local effluent standards. Wastewaters were treated by photodegradation process (which includes photocatalysis) to achieve the degradation of dyes mixture and organic matter in the wastewater. A multifactorial experimental design was proposed, including as experimental factors the following variables: pH, and the concentration of both catalyst (TiO2) and hydrogen peroxide (H2O2). According to the obtained results, at the optimized variables values, it is possible to reach a 99% reduction of dyes, a 76.9% of mineralization (TOC) and a final biodegradability of 0.834. Kinetic analysis allows proposing a pseudo first order reaction for the reduction, the mineralization, and the biodegradation processes.

Treatment of VX Hydrolysate with Ultraviolet Light and Hydrogen Peroxide

1997 ◽  
Vol 2 (3) ◽  
Author(s):  
Michael G. MacNaughton ◽  
James R. Scott
Keyword(s):  
Hydrogen Peroxide ◽  
Ultraviolet Light ◽  
Pilot Scale ◽  
Methylphosphonic Acid ◽  
Chemical Agent ◽  
Organosulfur Compounds ◽  
Two Phase ◽  
First Order ◽  
Engineering Study ◽  
Inorganic Sulfate

AbstractAn engineering study was performed to evaluate the use of ultraviolet light and hydrogen peroxide to destroy caustic-neutralized VX nerve agent in the U.S. chemical agent stockpile as an alternative to incineration. Whereas caustic neutralization completely destroys VX, (3-ethyl-S-2-(diisopropylamino)ethyl methylphosphonothiolate, the reaction leaves a complex two-phase mixture containing organic phosphates and organosulfur compounds which require treatment prior to ultimate disposal. Studies performed in laboratory-scale (320-mL), bench-scale (10-L) and pilot-scale (20-L) reactors demonstrated that the principal products of the caustic neutralization-ethyl methylphosphonic acid (EMPA), methylphosphonic acid (MPA), 2-(diisopropylamino)ethyl sulfide (RSR), disulfide (RSSR) and the other mixed sulfides-could be oxidized to inorganic sulfate, phosphate, ammonia and carbon dioxide. The reaction was zero order above 1000 mg/L and pseudo first order below. To mineralize 10,000 lb of VX per day to less than 10 mg/L organic carbon would require more than 1100 lamps of 30 kW each.

Photocatalysed Oxidation of Toxic Organics

1987 ◽  
Vol 19 (3-4) ◽  
pp. 381-390 ◽  
Author(s):  
M. Brett Borup ◽  
E. Joe Middlebrooks
Keyword(s):  
Hydrogen Peroxide ◽  
Ultraviolet Radiation ◽  
Organic Compounds ◽  
Hydroxyl Radicals ◽  
Reaction Rate ◽  
Oxidation Process ◽  
Dimethyl Phthalate ◽  
First Order ◽  
Toxic Organics ◽  
Catalyzed Oxidation

The feasibility of treating water contaminated by two toxic organic compounds with an ultraviolet light catalyzed oxidation process using hydrogen peroxide as an oxidant is investigated. In this process hydrogen peroxide is decomposed by ultraviolet radiation producing hydroxyl radicals. The hydroxyl radicals will then oxidize organic compounds via a complex chain of radical reactions. Tests showed that this photooxidation process could successfully remove isophorone and dimethyl phthalate from contaminated waters. A reaction rate expression which adequately describes the process was developed. The reaction rate was found to be first order with respect to hydrogen peroxide concentration, zero order with respect to organic concentration and a function of ultraviolet radiation intensity. The reaction did not exhibit autocatalytic characteristics.

Hydrogen Peroxide Decay in Waters with Suspended Soils: Evidence for Biologically Mediated Processes

1990 ◽  
Vol 47 (5) ◽  
pp. 888-893 ◽  
Author(s):  
William J. Cooper ◽  
Richard G. Zepp
Keyword(s):  
Hydrogen Peroxide ◽  
Natural Water ◽  
Water Samples ◽  
First Order ◽  
Natural Water Samples ◽  
Major Reaction Product ◽  
Major Reaction ◽  
Chemical Sterilization ◽  
Pseudo First Order ◽  
Catalyzed Oxidation

Hydrogen peroxide decay studies have been conducted in suspensions of several well-characterized soils and in natural water samples. Kinetic and product studies indicated that the decay was biologically-mediated, and could be described by pseudo first-order rate expressions. At an initial H2O2 concentration of 0.5 μM, the hydrogen peroxide half-life varied from 1 to 8 h. The decay was inhibited by thermal and chemical sterilization of the soils. Peroxidase activity was inferred in several natural water samples, where the suspended particles catalyzed the oxidation of p-anisidine by hydrogen peroxide. The mass spectrum of the major reaction product indicated that it was the dimer, possibly benzoquinone-4-methoxyanil, a product that also was observed from the horseradish peroxidase-catalyzed oxidation of p-anisidine by hydrogen peroxide.

scholarly journals A theoretical study of a possible model of paramagnetic alums at low temperatures

1940 ◽  
Vol 176 (965) ◽  
pp. 203-213 ◽  
Keyword(s):  
Magnetic Field ◽  
Low Temperatures ◽  
Theoretical Study ◽  
Spontaneous Magnetization ◽  
Critical Value ◽  
Transition Curve ◽  
Thin Specimen ◽  
First Order ◽  
Freely Suspended ◽  
Line Of Critical Points

An attempt is made to examine theoretically the properties of paramagnetic alums at low temperatures. The model taken is a lattice of freely suspended magnets, all interactions except purely magnetic being neglected. Even with this simplification it is impossible at present to make rigorous calculations of the partition function, either on classical or quantum lines. A simple model is proposed, which is really a generalization of the Bragg - Williams theory enabling one to take account of the effect of a magnetic field. The few configurations whose energies are known are used to fix arbitrary constants in the expression assumed for the energy. The theory predicts that the state of lowest energy is either a spontaneously magnetized, state for a long thin specimen, or a state in which alternate rows of magnets point in opposite directions for a sphere, spontaneous magnetization appearing in an ellipsoid with an eccentricity greater than a certain critical value. The transition curve bounding the region in which the antiparallel state is stable consists partly of a line of Curie points corresponding to transitions of the second, order, passing smoothly into a line of critical points corresponding to a transition of the first order. The effect of shape on the magnetic properties of the specimen seems to be experimentally verified, but the rough nature of the theory prevents it being more than qualitative.

Tacoma controls tastes and odours with ozone

2007 ◽  
Vol 55 (5) ◽  
pp. 137-144 ◽  
Author(s):  
M. Carlson ◽  
T. Chen ◽  
C. McMeen ◽  
I.H. Suffet ◽  
M. Zhang
Keyword(s):  
Hydrogen Peroxide ◽  
Analytical Methods ◽  
Contact Time ◽  
Solid Phase Microextraction ◽  
Solid Phase ◽  
First Order ◽  
Ozone Dose ◽  
Gorge Reservoir ◽  
Flavour Profile ◽  
As Solid Phase

The study is focussed on the conditions that would provide the best ozone oxidation to decrease the taste and odour of the water from Eagle Gorge Reservoir. This study incorporated advanced analytical methods, such as solid phase microextraction (SPME) and flavour profile analyses (FPA), to evaluate the best method for improving taste and odour. The study developed first-order relationships between ozone dose and the oxidation of several taste and odour compounds. The results focussed on the importance and interactions between ozone dose, pH, hydrogen peroxide and contact time.

On the Green-function theory of the spin- Heisenberg ferromagnet

1968 ◽  
Vol 46 (9) ◽  
pp. 1021-1028 ◽  
Author(s):  
S. T. Dembinski
Keyword(s):  
Green Function ◽  
Curie Temperature ◽  
Low Temperatures ◽  
Random Phase Approximation ◽  
Function Theory ◽  
Random Phase ◽  
Exact Result ◽  
Heisenberg Ferromagnet ◽  
First Order ◽  
The Green Function

A new first-order decoupling scheme for the Green function appearing in the theory of the spin-[Formula: see text] Heisenberg ferromagnet is introduced. At low temperatures the magnetization has no spurious term in T3 and the coefficient of the term in T4 is within a few percent of the Dyson exact result. The Curie temperature is equal to the random phase approximation Curie temperature.

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