1. Field of the Invention
The present invention relates to water treatment. More specifically, the present invention relates to a DC power driven ozone generator suitable for performing in-situ disinfection and detoxification of potable water to render it safe to drink.
2. Background of the Related Art
Water is the most likely source of sickness for people living in the areas with poor or lack of sanitation, such as, wild lands, mountains, lakes, and particularly places hit by natural disasters, for example, earthquake, hurricane, flood or tsunami. Protozoan parasites including Giaradia muris cysts, or Cryptosporidium oocysts, or both can be found in 97% of the surface water in the US. The former microorganism may cause chronicle beaver fever, while the latter may lead to serious cholera-like gastroenteritis in people who drink the infested water. On the other hand, pathogens like Eecherichia Coli, Shigella and hepatitis A virus can easily be found in waters contaminated by animal fecal wastes and domestic wastewaters.
By far, chlorine is the most widely used disinfectant for killing the water-borne microorganisms in public water supplies around the world. In addition to the distinctive odor and the ineffectiveness of handling the protozoan, the chlorine treatment may generate carcinogens from the reaction of the chlorine with the organics present in the water. In December 2005, the US Environment Protection Agency (EPA) had issued a Purifier Protocol and Standard that prohibits “residues from the disinfectant used for sterilizing drinking water”. Under this guideline, ultraviolet (UV) and ozone (O3) meet such standard as they are chemical-free disinfectants for purifying water. As a matter of fact, in Nice, France, ozone has been used to sterilize/disinfect the public water supply, since as early as 1906. Today, the UV irradiation process is included as one of the standard manufacturing processes in bottled-water and desalination plants. Ozone is listed as “Generally Recognized As Safe” (GRAS) for both potable and bottled water by the US Food and Drug Administration (FDA).
Electrolytic sterilization is a technique that uses an electric current to generate a disinfecting agent in water to serve as bactericide, virucide and or cyst inactivator. Among all chemicals, sodium chloride (NaCl) is the most popular precursor for making sodium hypochlorite (NaOCl) as the disinfectant as disclosed in the U.S. Pat. Nos. 3,622,479; 4,512,865 and 4,761,208. In the electrolytic detoxification, NaOCl is formed in electrochemical cells for removing ammonia (NH3) from water as disclosed in U.S. Pat. Nos. 5,935,392 and 6,348,143. In all of the foregoing reactions, OCl− ion is the oxidant adapted for sterilization or denitrification. Some of the ionic agents may survive the reactions and then become contaminants resulting in an increase of the TDS (Total Dissolved Solids) of the waters treated by OCl−. Many electrolytes specifically prepared to serve as the precursors for various agents formed electrolytically have been disclosed in numerous patents, for example, U.S. Pat. Nos. 5,531,883 and 5,997,702, just to name few. All in all, the chemicals added in the processes of electrolytic sterilization or electrolytic detoxification will become contaminants themselves, therefore leaving the treated water far from clean or safe.
Without adding any chemicals to the water to be treated, the sterilization of water is conducted through a direct electrolysis on sandwiched porous graphite electrodes as disclosed in U.S. Pat. No. 5,744,028, wherein the reaction current is too low to be effective. In U.S. Pat. No. 4,936,979, two alloy electrodes comprised of 88% copper (Cu), 10% tin (Sn) and 2% lead (Pb) are utilized electrolytic sterilization. The electrodes are consumed to provide 1 ppm (parts per million) Cu2+ for killing algae, as well as 0.5 ppt (parts per thousand) Sn2+ and 0.5 ppm Pb2+ for killing bacteria. The foregoing treatment may work for swimming pools, but it is incapable of eliminating the cyst contamination. Although ozone is a much more potent oxidant than OCl−, and applications of the gas are as versatile as from drinking-water sterilization, cleansing of semiconductor wafers as disclosed in U.S. Pat. No. 7,004,181, to medical treatments as disclosed in U.S. Pat. Nos. 5,834,030 and 6,902,670, nevertheless, the oxidizing gas is overwhelmingly generated by corona discharge. The silent discharge method has many problems, for example, a high working voltage, oxygen provision, gas leakage and ozone dissolution. Not only are the foregoing disadvantages absent from the electrolytic generation of ozone, but unique advantages are also present in the in-situ method as elaborated in U.S. Pat. No. 6,984,295. Without chemicals or electricity, ozone is produced via the absorption of 185 nm UV by oxygen as disclosed in U.S. Pat. No. 4,230,571. Recently, UV sterilizers have been fabricated into a hand-held device size for onsite sterilization of potable water. Compared to the aforementioned bulky electrolytic cells, the mini-size UV sterilizer is user-friendly, but the UV lamp is vulnerable to damage under external force.
Accordingly, the present invention provides a robust, chemical-free and compact ozone generator capable of being battery operated suitable for sterilizing/disinfecting and detoxifying potable waters.
The present invention is directed to a pocket-size ozone generator that can be immersed in water for in-situ sterilization/disinfection of water. The pocket size ozone generator may be driven by DC power, and is capable of generating ozone from within water at any point of use. In order to prolong the service life of the ozone generator, a durable and foul-free electrode is used for generating ozone.
An alkaline battery or rechargeable battery may serve as the main power source for driving the ozone generator to perform electrolysis on water to generate ozone. To minimize the size of the ozone generator, only a few batteries are required. Since the batteries can only deliver a small current, a supercapacitor is adapted to supplement the power deficiency of the battery. In addition, the supercapacitor can also extend the use-time of battery through the “load leveling” effect. Furthermore, two identical groups of supercapacitors are arranged to discharge and re-charge alternatively through a charging-discharging swing, or CD swing approach, so that the power delivered to the electrolysis reaction can be continuous and consistent.
Among the electrode materials available for ozone generation, platinum (Pt) or conducting diamond film (boron-doped diamond, BDD) may be selected for the sake of safety and hygiene. The decay of the foregoing electrode materials does not generate hazardous ingredients into the treated potable water. A plastic screen is disposed between the anode and cathode, which are symmetrical in shape and identical in composition, of the ozone generator to prevent an electrical short. The two electrodes and the plastic screen are fastened together. The electrode is easy to clean and maintain, and can be easily replaced. The ozone generator can also be used as a stirrer during treatment to ensure that all of the water is sterilized or detoxified. No air is required to be injected into the water during the treatment process, ozone is formed due to ionization of the water.
The surface area of the electrodes, the discharge rate of the battery, the capacitance of the supercapacitor, as well as the conductivity of the water to be treated collectively determine the concentration of ozone produced. Generally, the amount of ozone generated is sufficient for sterilization/disinfection of the water but safe for the users to drink. The sterilization time usually ranges around 30-60 seconds, and can kill most of the microbes contained in the water. The ozone generator may be equipped with a switch that can be used to operate the ozone generator for any desired preset time.
The present invention is best understood by reference to the embodiments described in the subsequent sections accompanied with the following drawings.
The preferred embodiments of the pocket-size ozone generator of the present invention are presented as follows.
In order to produce a sufficient and safe amount of ozone, the maximum operating power for the ozone generator to perform in-situ and rapid sterilization of water is designed at 6 W. Considering the variation of water conductivity from miscellaneous water sources, the operating voltage of the ozone generator is set at 6V. Accordingly, the operating current should be 1 A to deliver the required 6 W power. The targeted current is beyond the allowable or optimal discharge rate of primary batteries and secondary batteries alike. Conventionally, a step-up circuit using DC/DC converter is used for producing high currents from low-current inputs of batteries. Such a converter is often bulky and costly, and therefore not suitable for the pocket size ozone generator shown in
Supercapacitor 500a: (+) pole of 200→404a→404→406→406a→(−) pole of 200
Supercapacitor 500b: (+) pole of 200→408a→408→410→410a→(−) pole of 200
Initially, the terminals of the supercapacitors 500a and 500b carry no polarity before charging. As the supercapacitors 500a and 500b are charged, their terminals will have the same polarity as that of the battery 200. That is, terminals 404 and 406 will serve as the positive and negative electrodes of the supercapacitor 500a, and the terminals 408 and 410 serve as the positive and negative electrodes of the supercapacitor 500b, respectively. The CD swing is initiated by depressing the latch button (not shown), an audible clicking sound is indicative of the switching of the relays 402a and 402b between “closed” and “open” states leading to the switching of the supercapacitors 500a and 500b between charging and discharging states. The operation procedure of the CD swing may be described as follows. The operation procedure of the CD swing includes at least a first cycle, a second cycle and a third cycle.
The First Cycle.
The relay 402a is switched “on” (“open” state) and the relay 402b remains at “closed” state (i.e. “off” state). Meanwhile, the relay 402a changes the contact points of two terminals 404 and 406 of the supercapacitor 500a from 406a/404a to 406b/404b. Thus, the (+) terminal 404 of the supercapacitor 500a is in electrical contact with the two electrodes 600, whereas the supercapacitor 500b remains in parallel with the battery 200. Since the supercapacitor 500b is charged, the battery 200 is prevented from charging the supercapacitor 500b. However, the supercapacitor 500b is also connected in series with the supercapacitor 500a (408→408a→406b→406), the supercapacitors 500a and 500b deliver at the combining voltages of the supercapacitors 500a and 500b, or two times voltage of 200, to the electrodes 600 through (+) pole 404 of the supercapacitor 500a. If the super capacitor 500b releases some of its stored energy, it will be promptly replenished by the battery 200 so that the supercapacitor 500b remains charged ready for assuming the role of discharge.
The Second Cycle.
The relay 402a is “off” (“closed” state) and the relay 402b is “on” (i.e. “open” state). The supercapacitor 500a is connected in parallel with the battery 200 for recharging the energy released in the prior discharging cycle. The contact points of terminals 408 and 410 of the supercapacitor 500b are switched from terminals 408a/410a to 408b/410b. Hence, the supercapacitor 500b will deliver an electric power to the electrodes 600 in conjunction with the supercapacitor 500a. Meanwhile, the supercapacitor 500a is replenished by the battery 200 via their parallel connection.
The Third Cycle and Beyond.
The third cycle includes flow of the first cycle and the second cycle being alternately repeated for every odd-cycle and every even-cycle of CD swing respectively to provide a consistent power supply to the electrodes 600 until the preset sterilization time period has reached (until latch button is turned off) to complete the sterilization.
In the CD swing technique as described above, two identical sets of supercapacitor are employed to reciprocally switch between charging and discharging for continuously supplying consistent power to the electrodes 600 to rapidly generate ozone that is several folds more effective than many other widely used disinfecting chemicals, such as chlorine, chlorine oxide or chloroamines. According to Jensen in “Ozone: The Alternative for Clean Dialysis Water” (DIALYSIS & TRANSPLANTATION, Volume 27, Number 11, pp 708-712, November 1998), the concentration-time value ranges (expressed as mg/L-min) for 99% inactivation of various organisms by O3 at 5° C. is about 0.006-2.0 ppm-min. Thus, an operating voltage of 6V is sufficient to drive ozone generator of the present invention to generate the sufficient amount of O3. For example, about 1 A of operating current and about 0.5 F capacitance for each of the supercapacitors 500a and 500b are required for the compact ozone generator to produce sufficient amount of ozone in about 30-60 seconds. Nevertheless, with the 5V driving-voltage threshold of the relays 402a and 402b, 4 pieces of alkaline batteries are required. Other power sources, for example, rechargeable batteries, fuel cells or solar cells, can also be used for driving the ozone generator of the present invention. Different power sources deliver different voltage outputs, and accordingly the design of the power compartment of the ozone generator should be varied. Regardless of the power source, the power can be amplified by the supercapacitors 500a and 500b and the relay-operated circuit. The relays 402a and 402b have a low-frequency, about 6 cycles per second (6 Hz), mechanically switching devices, and the low frequency will lead to a large fluctuation of output voltage for the power sources using the CD swing. Other disadvantages of the CD swing technique using a relay mat include mechanical wearing due to numerous times of switching, and a fusion of the relay contacts from an excessive current flow through the relay. However, since the ozone generator of the present invention consume significantly less power and has a low-switching operation, the relays can work well for rapid in-situ sterilization of potable waters.
Before the initiation of charging-discharging process, the MOS-FETs L2 and L3 of the supercapacitor 500b are in the “closed” state, the MOS-FETs L1 and L4 of the supercapacitor 500a are in the “open” state, and the MOS-FETs R2 and R3 of the supercapacitor 500a are in the “closed” state and the MOS-FETs R1 and R4 are in the “open” state. Therefore, the supercapacitors 500a and 500b are connected in parallel with battery B, and the supercapacitors CL and CR are charged simultaneously to the same voltage and polarity of 200. Once the CD swing is initiated, the process will be conducted as follows:
The First Cycle
The supercapacitor 500a is in parallel with the battery 200, MOS-FETs L1 and L4 are in the “closed” state and MOS-FETs L2 and L3 of the supercapacitor 500b are in the “open” state. As a result, the supercapacitor 500b and the battery 200 are connected in series, thus, they discharge collectively to the load 718, or the electrodes of the ozone generator. The current delivered to load 718 is monitored by the current sensor 716 so that the power supplied to the ozone generator can be set at a desired level.
The Second Cycle.
The supercapacitor 500b is switched to the parallel configuration with the battery 200 (i.e. the MOS-FETs L2 and L3 are in the “closed” state, and the MOS-FETs L1 and L4 are in the “open” state), thus, the partially discharged supercapacitor 500b is replenished by the battery 200. Meanwhile, the supercapacitor 500a is switched into series connection with the battery 200 (i.e. MOS-FETs R1 and R4 are in the “closed” state, and MOS-FETs R2 and R3 are in the “open” state), thus, the supercapacitor 500a and the battery 200 discharge collectively to load 718 to generate ozone.
The Third Cycle and Beyond.
The third cycle, the first cycle and the second cycle, described above, that are repeated alternatively for every odd-cycle and every even-cycle furthering a CD swing technique, respectively, to provide a consistent power to the electrodes of the ozone generator of the present invention until the preset sterilization period has reached (i.e. until the latch button is depressed off) to complete the sterilization of the potable waters.
Batteries 200 with higher discharge rate than the alkaline batteries, for example, lithium ion battery, are employed with the electrodes shown in
A prototype ozone generator as shown in
During the sterilization treatment, the water was stirred by the ozone generator. Water from roadside ditch was more contaminated than that from the faucet, therefore, the former consumed more energy to accomplish sterilization. In both cases, as can be inferred from the table above, the waters were effectively sterilized and disinfected.
As it can clearly be seen from the above example and other in-house tests, the compact pocket sized ozone generator provided by the present invention can effectively perform in-situ sterilization of waters, and can easily be carried by the tourists traveling to places without adequate sanitation facilities. A tune of 99% inactivation of microbial and hazardous contaminants present in the potable waters can be achieved in just 30-60 seconds of treatment. The hand-held pocket size ozone generator can be operated by batteries, human power and renewable energies, and it requires no addition of chemicals to the water to be treated. After treatment, the ozone will be converted to oxygen without forming any residues in the treated waters. The amount of ozone is sufficient for sterilization and at a level that is harmless to the users. Thus, no chemicals are required to generate ozone, and the ozone generator only requires the replacement of spent batteries, while the electrodes and human-powered generator may be used a long-period of time.