Comparative Efficiency Of Three Systems (O3, O3/H2O2, and O3/TiO2) For The Oxidation Of Natural Organic Matter In Water

CATAZONE is a new process of heterogeneous catalytic ozonation in which water is ozonated in the presence of a solid catalyst composed of titanium dioxide. The efficiency of this O₃/TiO₂ system has been compared to the two well-known oxidant systems: ozone alone and ozone combined with hydrogen peroxide.

This comparison was undertaken on three models of natural organic compounds : an aquatic fulvic acid, a protein and a disaccharide. The first results showed the following order of relative efficiency: O₃/TiO₂ > O₃/H₂O₂ > O₃ as far as Total Organic Carbon (TOC) removal was concerned.     

Effects Of Ozone On Kraft Process Pulp Mill Effluent

Effluent from a kraft process pulp mill was studied in a batch reactor for ozone doses between 50 and 200 mg O₃/L to identify the relative suitability of ozone application locations in the treatment process and see the improvements in biotreatability of wastewaters from a kraft process pulp mill. Laboratory acclimatized seed were used for BOD tests for ozonated and unozonated samples. The inhibitory effects were minimized by using optimum dilutions. The studies were divided into three major sections: characterization of mill effluent; ozone system calibration, and reactor design; and ozonation of mill effluent. Seed for Biochemical Oxygen Demand tests were acclimatized in batch units for primary, bleach and secondary effluents separately. The inhibitory effects which were noted with unacclimatized seed, were reduced by using laboratory acclimatized seed and optimum dilution which were determined during the characterization phase.

The batch reactor designed for the studies consisted of a cylindrical section for holding effluent, and a top spherical section for ozone/oxygen mixture. The reactor proved to be effective for controlling ozone dose. The variation in the applied ozone dose was less than 5 mg/L.

Bleach and primary effluents were treated with 50 and 100 mg/L ozone doses. Duplicate experiments were conducted for these effluents. Secondary effluent was studied for 50,100,150 and 200 mg/L ozone doses. Six replicate experiments were conducted for 50 and 100 mg/L ozone doses, whereas two experiments were carried out for 150 mg/L and one experiment for 200 mg/L ozone dose.

The results were analyzed using 't' test for paired experiments and ANOVA table for statistical confirmation. Residuals were plotted to check the assumptions of constant variance and normal distribution. The results indicated that 50 and 100 mg O₃/L effectively removed color from bleach effluent and primary effluent, but did not significantly change the BOD. Ozone was found to be effective for secondary effluent, as BOD₅ was increased by 65% for 50 and 100% for 100 mg O₃/L doses. The corresponding reduction in color was 62% and 82%, respectively. K_e and L_o values for the BOD equation were calculated by using the non-linear least square method for the BOD equation, giving joint confidence regions for the calculated parameters. It was concluded that ozone is most effective for the removal of color and the increase of BOD in secondary effluent.     

Ozone for Removal of Acute Toxicity from Logyard Run-Off

Stormwater run-off from wood handling facilities is garnering increasing attention from environmental regulators. In an effort to develop treatment methods to deal with the problem of toxic run-off from logyard and dryland sorts, we are currently investigating the use of ozone.

Samples of logyard run-off were obtained from two British Columbia coastal sawmills. Ranges obtained for measured parameters of these samples were as follows: COD 2400-8700 mg/L, tannins and lignins 160-2500 mg/L, BOD 190-1900 mg/L, acute (Microtox) toxicity EC₅₀ 2%–27% v/v. Centrifuged samples were treated with ozone doses up to approximately 0.5 mg ozone/mg COD in a lab-scale reactor.

Ozonation was found to significantly reduce toxicity (80%-90%), tannin and lignin (TL) (90%-95%) and dehydroabietic acid (DHA) (95%-100%) levels. There were moderate reductions in COD (30-35%) and BOD (15%-25%). At slightly acidic to neutral pH, pH had no effect on the rate of COD oxidation; TL and toxicity removal were slightly improved in neutral solutions compared to acidic ones, while DHA removal significantly improved     

The Basic Clinical Applications of Ozone Therapy

Medical ozone is a mixture of ozone and oxygen, prepared via silent electrical discharge, within a concentration range of 0.05 volume % O₃ to max. 5.0 volume % O₃.

In order to exclude its toxic effect on the pulmonary epithelium, the medical ozone/oxygen mixture is administered so that exposure of the respiratory tract is avoided at all times, i.e., without the disturbing effects of its odor.     

Use Of Static Mixer For Oxidation And Disinfection By Ozone

Ozone is used in drinking water treatment as a biocide, as an oxidant and as a pretreatment in order to improve the performance of subsequent processes. Increasing concern over the quality of drinking water has led to a number of new stringent regulations in the control of chemical and microbiological contaminants. Disinfection deals with the concept of “CT”, which is the need to maintain a certain minimum concentration for a given time. Under ideal laboratory conditions, it is 0.4 mg O₃/L for 4 min. In practice, since the method for the CT determination has not been finalized by the EPA, “T” can be the minimum detention time of 90% of total flow, and “C” can be a measured ozone residual at the outlet of cells of the contactor. New standards for micropollutants in drinking water imply an optimization of the ozonation step, by improving the ozone transfer from gas to water, and the control of the detention time as well as ozone residual within the contactor.

All these considerations have led us to use static mixers to transfer ozone into water. This process enables us to control the ozone concentration in water and detention time. It is a very simple system, with very low maintenance requirements due to the lack of moving parts. Civil engineering is minimized. A pilot scale study is presented here. It took place at the Méry-sur-Oise water treatment plant, on a pilot plant working at 8-12 m³/h. It is composed of a static mixer for the transfer of ozone from gas to liquid, linked to an air lift to separate gas from liquid, providing ozonated water.

The optimization of transfer was achieved by studying the impact of water flow, gas flow and ozone concentration in the gas. It is possible to reach 90% of transfer in less than 15 s. Headloss (ΔP) across the mixer is a function of gas and water flows and remains economically very acceptable as 0.15 bar for 12 m³/h.

Atrazine removal was studied using a static mixer, an air lift and a contact pipe 80-m long, providing an optimum contact time phase, working as a plug flow reactor. Ozone and H₂O₂/O₃ treatments were compared. The maximum reduction of atrazine concentrations (e.g., for an infinite contact time) is a function of the amount of transferred ozone, but H₂O₂ influences the kinetics of the reaction. In the presence of H₂O₂ with a ratio of H₂O₂ to O₃ of 0.4 w/w, maximum elimination is reached in 2 min 30 s.

The effect of such treatments on environmental bacteria also was followed. A counting of total germs at 20°C showed a decrease of 1- to 3-logs 10 after 1 min 30 s of contact time for about 2 mg/L of transferred ozone. No significant difference between treatments with or without H₂O₂ was shown. The same conclusions were obtained from heterotrophic plate counts (37°C) and epifluorescence countings.     

Comparison of Ozone and Hydroxyl Radical-Induced Oxidation of Chlorinated Hydrocarbons in Water

The efficiency of ozonation and advanced oxidation processes such as ozone/UV, ozone/H₂O₂ and H₂O₂/UV was assessed for chlorinated hydrocarbons using a closed batch-type system. 1,1-Dichloropropene (DCPE), trichloroethylene (TCE), 1-chloropentane (CPA), and 1,2-dichloroethane (DCA) were used as model compounds.

The direct reaction between substrates and ozone predominated at lower pH, which resulted in the efficient oxidation of the olefin, DCPE. At higher pH, ozonation resulted in more efficient oxidation of the chlorinated alkanes, with a corresponding decrease in the efficiency of DCPE oxidation. Consistent results were observed for ozone/H₂O₂ and ozone/UV treatment. Due to slow UV-induced decomposition of H₂O₂, the process using H₂O₂/UV (254 nm) resulted in very slow oxidation of all four compounds.

The total ozone requirement to achieve a given degree of elimination (to 37% of the original concentration), δ0.37, was used to assess the combined effects of the direct and indirect reactions for different types of waters.     

The Photochemical Generation of Ozone : Present State–of–the–Art

This paper reflects an investigation of the feasibility of photochemical generation of ozone by irradiating gases containing oxygen with Hg lamps of the highest performance emitting the 185 nm line. Besides the expected photostationary equilibrium, determining factors for practical yields in ozone generation by the 185 nm wavelength are : the reactor and gas temperature, the reactor geometry, and the gas composition, as well as the pressure.

Further developments are expected in the field of lamp construction and also improvement of reactor geometry. A better knowledge of the aging of the lamps is required, as well as of the photochemical reactions of oxygen in the technologies applied.

Systems presently available are most promising for application on small scale or in areas of public water distribution which have no developed structure.

     

Hydroxyl Radical Oxidation Processes For The Removal Of Triazine From Natural Water

The purpose of this study was to point out processes that can provide triazine oxidation via hydroxyl radical production in a water treatment line. We focus our attention on:

- oxido-flocculation, using Fe²⁺, H₂O₂

- inter-oxidation, using O₃, H₂O₂ and eventually an heterogeneous catalyst.

- disinfection, using UV, O₃ and H₂O₂ combinations.

Results show that triazines can be removed by all these processes with different efficiencies. At full scale, the O₃/H₂O₂ process presents the best performances from an economical and technical point of view.     

Effects of Atmospheric Chemical and Climate Change on Tropospheric Ozone

Changes in atmospheric levels of certain pollutants (CH₄, CO, NO_X, nonmethane hydrocarbons) have the potential to affect tropospheric O₃ formation and the abundance of the free radical OH on a global scale. Perturbations to stratospheric O₃ and climate (temperature and moisture) also can influence tropospheric O3 and OH. We have used a tropospheric photochemical model with projections of CO, NO_X, and CH₄ to predict tropospheric ozone and OH changes from 1980-2030. The calculations simulate the background chemistry of various global regions and assume that increases in CH₄ and CO will continue at current rates. Predicted changes in tropospheric O₃ and OH are different in urban and nonurban areas, and in marine and continental regions.

Generally, increasing levels of CH₄ and CO at constant NO_X levels will increase O₃ and suppress OH. A rough estimate of possible global changes shows tropospheric O3 increasing ?10% from 1980 to 2030 and OH decreasing ?10% during that period. When calculations are performed assuming that stratospheric ozone depletion and climate warming occur at anticipated rates during the same period, tropospheric O₃ enhancement and OH loss in nonurban areas are both reduced relative to changes assuming that only CH₄ and CO emissions change.

Regional changes in surface-level O₃, OH and the water-soluble oxidant H₂O₂ are estimated for the year 2030. Increases in CO and CH₄ suppress OH and enhance O₃ and H₂O₂ in nonpolluted (low NO_X) areas. In urban environments (background NO_X > 1 ppbv), increases in CO and CH₄ add significantly to all three oxidants, O₃, OH and H₂O₂. Changes in and near urban areas may be of greatest magnitude, but the high levels of OH (and H₂O₂) found in the tropics indicate that perturbations in that region could dominate future global oxidant changes.     

Influence of Ozone Application Methods on Efficacy of Ozone Decolorization of Pulp Mill Effluents

This study statistically examined the impacts of ozone application methods on the two representative types of pulp mill effluents. To facilitate statistical evaluation, the experiments were designed as paired block experimental series, and the pooled experimental errors in each block were used for t-test and ANOVA analysis.

Two different ozone application modes were investigated using two specially designed ozone reactor systems. System I consisted of a two-phased reactor which introduced the total amount of ozone to the wastewater in single instance with proper mixing. System II provided ozone to wastewater at a desired rate by controlling the flow and concentration of the ozone/oxygen gas mixture in a once-through flow mode.     

The Oxidation of Manganese and Disinfection By Ozonation in Water Purification Processing

The surface water of a river has been used as the raw water by the Waterworks Bureau of Osaka City. At present, the manganese contained in the raw water is oxidized by breakpoint chlorination and all oxides are removed by coagulation, sedimentation followed by rapid sand filtration, with chlorine being used as the final disinfectant.

Prechlorination was not conducted in the ongoing pilotplant experiment of an advanced water purification process with ozone and granular activated carbon. It is necessary, therefore, to oxidize manganese by the oxidative effect of ozone instead of prechlorination.

It is important for the treatment of manganese to adjust the ozone dosage because manganese is oxidized up to the soluble septavalent state by the surplus ozone. Since ozone does not continue to exist for very long in water, though its disinfecting power is high, final disinfection by chlorine is required.     

Iron and Manganese Removal with Ozonation in the Presence of Humic Substances

The conditions for the removal of iron and manganese contained in slightly mineralized water, rich in humic substances, were determined in a case where an intermediate oxidation was provided in a conventional potabilization line comprising a coagulationflocculation stage with iron salts.

The experiments were conducted both on a synthetic water, with or without addition of humic substances, and on raw water from the Moulin-Papon dam. While iron was easily removed by simply increasing the pH measurement from 8.2 to 8.5 without intermediate oxidation, ozonation applied to water with a pH of nearly 8.4 did not enable the manganese to be removed with a low ozone dose (about 1 mg/L) unless a significant amount of bicarbonates (120 to 130 mg/L as CaCO₃) were injected prior to the ozonation-filtration stage.

As it removes the manganese from the water, intermediate ozonation also removes the abatement of organics on the filters, and lowers the THM buildup potential.     

Research Note: O3 or O2 and Ag: A New Catalyst Technology for Aqueous Phase Sanitation

Silver deposited on an inert surface with a very large area exhibits a strong catalytic interaction with oxygen which results in strong bactericidal activity. This catalytic process is fundamentally different from other known silver-based approaches which deliver low levels of silver ions into water.

Two factors appear to control the rate of this catalytic reaction process: (1) the size and dispersion of the silver crystals and surface area of the supporting bed; and (2) the volume of oxygen in solution. The source of the oxygen can be atmospheric oxygen dissolved in the water or, for a greatly enhanced reaction rate, dissolved ozone produced by an ozone generator. In this process, oxygen molecules absorbed onto the catalyst surface are subsequently transferred to other oxidizable substrates including bacteria and viruses.

These catalytic oxidizing reactions exhibit two properties of significance in the sanitation of water. First, because oxygen on the catalyst surface reacts with both living and nonliving substrates, bacteria or viruses which are in the water flowing over the catalyst-containing medium are killed or inactivated on contact by the oxidizing reactions (i.e., without requiring the release of metals into water). Second, oxygen also is transferred to oxidizable inorganics (such as bromide ion) to generate readily measurable and relatively stable “residual” oxidizers/disinfectants that continue to sanitize water downstream.

Results of this Author's experiments have been independently replicated by sources from the University of Arizona, and at Herbert V. Shuster, Inc. Laboratories in Massachusetts.     

Influence of Ozone on the Photocatalytic Oxidation of Organic Compounds

Heterogeneous photocatalytic oxidation processes using titanium oxide as a photocatalyst are widely discussed topics in research for water and waste water treatment. Oxygen fed into the systems is normally used as oxidizing agent. However few investigations exist concerning the use of ozone as an additional oxidant. In this work the influence of ozone on the photocatalytic degradation of organic compounds are described. The results are compared with those by using ozone, UV/O₃ and UV/TiO₂/O₂. The oxidation reactions were performed at pH 3 and 7.

In this research compounds of the different classes were used: glyoxal, pyrrole-2-carboxylic acid, p-toluenesulfonic acid and naphthalene-1,5-disulfonic acid. Depending on the classes of compounds in some cases the elimination rates of the initial compounds is enhanced by using UV/TiO₂/O₃ compared to UV/O₃ or O₃ alone. But in all cases greatest DOC elimination is achieved by using UV/TiO₂/O₃.     

Reactivity Studies In The Ozonolysis Of Pollutants Using A Perforated Spinning Disc Reactor To Enhance Mass Transfer

A perforated spinning disc ozone contactor is described with reference to its use as an absorber with simultaneous chemical reaction.

Greatly enhanced mass transfer coefficients k_L are measured whilst simultaneously maintaining low ozone loss. Comparisons of k_L and volumetric coefficient, k_L a values, are made with more conventional packed or bubble columns.

Acetic acid, 2-propanol and 4-nitrophenol, representing a wide reactivity range, are used to elucidate the applicability of rotating contactors in effluent treatment. It has been possible to study the effects of surface activity on mass transfer with subsequent reaction and to generate design data for the next generation of rotating contactors.     

New Pilot Plant Studies at the Budapest Waterworks

The quality of water provided by the Budapest Waterworks should comply with the standards prescribed by the European Community. According to these provisions, on one of the major water-producing regions (Csepel Island), rows of wells of 60,000 m³/day yield have been closed recently, and in the immediate future further plants would have been closed because of the high iron and manganese content of the water.

The raw water obtained from 100 different wells will be purified by a water treatment plant of 150,000 m³/day capacity. Considering the high iron content (0.05–0.15 mg/L) and manganese content (0.05–0.2 mg/L), the raw water fails to comply with the requirements of the potable water standard.

Since 1990, over a period of three years, we conducted water purification experiments in several stages. In these, three methods of oxidizing as well as single and double layer open rapid filters were applied to oxidize the manganese (and, to a lesser extent, the water) present in dissolved form, resp., to destroy various living organisms.

In the course of the experiments, it became clear that the chlorine and chlorine + air methods are efficient in case of a small quantity of iron to be oxidized and only 20–25% of the dissolved manganese content could be oxidized.

Neither of the two methods could ensure firm management of microbiological and bacteriological characteristics. The best results were obtained by ozone oxidation, in which case the chemical oxidizing process was almost fully completed and even the chlorine-resistant living organisms could be destroyed.

On the basis of the experiments carried out, the investment program of the water treatment plant was worked out and the conditions of an international tender were compiled whose winner will be commissioned to build up the water works in the time period 1993–1996. One of the main steps of the proposed technology is the ozone treatment.     

CHLORINATION KINETICS OF Nb2O5

The reaction of single sintered pellets of α-Nb₂O₅ with chlorine and carbon monoxide was studied in the temperature range from 773 K to 1073 K using a thermogravimetric apparatus. The rate controlling step of the reaction was determined from experiments carried out at variable gas flow rates, gas composition, surface geometry, pellet porosity and temperature. The vapor phase transport reaction can be written as:

Nb₂O₅(s) + 3Cl₂ (g) + 3CO(g) = 2NbOCl₃ (g) + 3CO₂(g).

Up to 60% conversion, the amount of volatilized product was found to be directly proportional to the time of reaction. The external surface area of the pellets remains unchanged up to this stage while the intergranular morphology changes.

These results were compared with reaction rates of commercial pyrochlore concentrate in order to establish the fundamental reaction stages of the process of extraction of Nb₂O₅ from pyrochlore.     

Oxidation of 1,3,5‐trichlorobenzene using advanced oxidation processes

The oxidation of 1,3,5‐trichlorobenzene (TCB) by ozone, ozone/UV, ozone/H₂O₂ and ozone/UV/H₂O₂ was studied. All studies were conducted in a continuously‐flowing completely mixed reactor (CFCMR), operated at steady‐state conditions using a hydraulic retention time of 10 minutes. The greatest removal of TCB using ozone/H₂O₂ treatment was achieved using a H₂O₂ concentration of 60 μM. At low pH values (approx. 2) ozone/UV performed significantly better than either ozone alone or ozone/H₂O₂. However, at circumneutral pH, the removal efficiencies of TCB by ozone/UV and ozone/H₂O₂ and ozone/UV/H₂O₂ were essentially equal (～ 97% for TCB). The removal efficiency of ozone alone was ～93% for TCB. At high pH (> 9) there was no advantage in supplementing ozone with either UV or H₂O₂ as the removal efficiencies for all processes studied were essentially equal.

The effect of humic acid and bicarbonate on the removal of TCB was studied. At 1.6 mg/L humic acid, 92–95% of the TCB was oxidized by the processes studied. The removal of TCB by ozone alone was significantly affected by the presence of bicarbonate ion. For the other processes at 10 mM bicarbonate, approximately 80% of the TCB was oxidized.     

First Year Operation Report of the Corona Discharge Ozone Swimming Pool Water Treatment Systems at the Peck Aquatic Facility,Milwaukee, Wisconsin

The two corona discharge ozone swimming pool water treatment systems installed in the Peck Aquatic Center in Milwaukee, WI now have been in continuous operation since September, 1987. The two pools are part of the Karl Jewish Campus Facility of the Harold and Judy Sampson Campus of the Milwaukee Jewish Community Center.

The operation of these water treatment systems has shown that safe and high quality pool water is obtained reliably and economically. One pool (Main Pool) is of Olympic size, the other (Learner pool) is designed especially for use by children. Both pools utilize a full corona discharge ozone water treatment system. They were the first ozone systems in the U.S. to be built for public pools using the process of ozonation, flocculation, filtration, ozone removal and residual chlorination.

An extensive testing program was initiated in cooperation with the Wisconsin Department of Health. The bacteriological water quality from these swimming pools was in compliance with Wisconsin State Health Regulations and the German DIN Standard 19,643.

The first year of operation of the Peck Aquatic Center has shown that the corona discharge ozone pool water treatment process can:

1) Operate reliably in a public swimming pool environment without the need for highly or special operator qualifications.

2) Produce continuously bacteria- and virus-free pool water without the harmful and unpleasant effects of chlorine.

3) Creates a user constituency group praising and promoting the use of “minimal chlorine swimming” in the community.     

Pilot-Scale Evaluation Of The Effects Of Mixing On Ozone Disinfection Of Escherichia Coli In A Semi-Batch,Stirred Tank Reactor

A research program was undertaken to examine the effects of mixing intensity and post-ozonation conditions on the survival of Escherichia coli ATCC 11775 in a high quality secondary wastewater effluent with a total organic carbon content of 8 mg/L and a chemical oxygen demand of 26 mg/L. The study was conducted using a pilot-scale, semi-batch stirred tank reactor with a 6-blade Rushton turbine. Two power conditions were investigated: 255 W/m³ and 870 W/m³. Two post-ozonation conditions also were investigated. In the first, a headspaceless sample was withdrawn and stored in the dark, in a quiescent condition. For the second, the gas flow to the reactor was stopped, but mixing was continued.

For equivalent contact times, it was found that two orders of magnitude more E. coli survived under the second post-ozonation condition when compared with the first condition. There was also a significant difference associated with the mixing intensity in the contactor, with the higher power input resulting in less efficient inactivation of E. coli.

The results confirm the importance of designing an ozone contactor to promote the maintenance of aqueous ozone in the contactor. In addition, optimum ozone mass-transfer may require different contacting conditions than those required for optimum disinfection performance. It was concluded that the design of ozone contactors should consider the use of at least two-stages: one optimized for ozone mass-transfer and one optimized for disinfection contacting.