Title of Invention	A PROCESS TO MANUFACTURE STABILIZED ALKALI OF ALKALINE EARTH METAL HYPROBROMITE AND USES THEREOF IN WATER TREATMENT TO CONTROL MICROBIAL FOULING
Abstract	A method for preparing a stabilized aqueous alkali or alkaline earth metal hypobromite solution comprising the steps of: mixing an aqueous solution of alkali or alkaline earth metal hypochlorite having from about 5 percent to about 70 percent by weight available halogen as chlorine with a water soluble bromide ion source; allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0.5 to 70 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite; adding to the unstabilized solution of alkali or alkaline earth metal hypobromite a stabilizer selected from the group consisting of carbonic acids, hydrogen cyanide, carboxylic acids, amino acids, sulfuric acids, phosphoric acids and boric acids; and recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution,

Title of Invention

A PROCESS TO MANUFACTURE STABILIZED ALKALI OF ALKALINE EARTH METAL HYPROBROMITE AND USES THEREOF IN WATER TREATMENT TO CONTROL MICROBIAL FOULING

Abstract

A method for preparing a stabilized aqueous alkali or alkaline earth metal hypobromite solution comprising the steps of: mixing an aqueous solution of alkali or alkaline earth metal hypochlorite having from about 5 percent to about 70 percent by weight available halogen as chlorine with a water soluble bromide ion source; allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0.5 to 70 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite; adding to the unstabilized solution of alkali or alkaline earth metal hypobromite a stabilizer selected from the group consisting of carbonic acids, hydrogen cyanide, carboxylic acids, amino acids, sulfuric acids, phosphoric acids and boric acids; and recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution,

Full Text	The present invention relates to a method of preparing a stabilized alkali or alkaline earth metal hypobromite to control microbiofouling, more specifically, a stabilized sodium hypobromite solution the characteristics of which include non- volatility, high free halogen residual, lower bromate formation, reduced generation of absorbable organic halogen in process waters, as well as improved performance against biofouling. 3. Background of the Invention Aqueous solutions of sodium hypochlorite are widely used in cooling water towers; bleaching processes; treatment of recreational waters including swimming pool water, water slide and other water game equipment, spas, and whirlpools; disinfectants; laundry detergents; and, industrial biocides including applications in the petroleum industry. However, a major disadvantage of NaOCl is its instability. As is well known in the art. several methods are used to stabilize NaOCl. The Self et al. reference (U.S. Pat. No. 3,328.294) described a continuous process to stabilize hypochlorite with an equal molar ratio of sulfamic acid. This process was improved upon by Rutkiewic reference (U.S. Pat. No. 3,767,586) who added a buffer which aided in pH control increasing the stability of concentrated solutions. Bromine has various advantages over chlorine for water treatment such as better performance in high pH or amine environments and a lower volatility. However, sodium hypobromite, the bromine analog to chlorine bleach, is not stable under typical storage conditions, and as such, is not commercially available. Instead, bromine is typically delivered to water treatment systems by various inefficient or inconvenient methods. The art described by either Self et al. or Rutkiewic does not mention a method to stabilize the well known precarious sodium hypobromite molecule as disclosed within this invention. Also, this disclosure shall improve upon the art of Rutkiewic by formulating a more stable, concentrated NaOBr solution in the absence of a buffer. In one such bromine delivery method, NaBr is oxidized in situ by introducing gaseous chlorine or NaOCl into the process water stream. Another technique uses a stable perbromide (Br,-) solution containing 30 - 40 percent bromine. The perbromide solution releases bromide and bromine when injected into water systems. The formed bromine hydrolyzes instantly to hypobromous and hydrobromic acids. Alternatively, bromine chloride may be added to aqueous process streams wherein it hydrolyzes to hypobromous and hydrochloric acids. All of these bromine delivery systems have inherit disadvantages. Gaseous chlorine, perbromide, and bromine chloride have high halogen vapor pressures which present safety concerns in handling and storage. Also, these concentrated halogen solutions are corrosive to many metal surfaces found in process equipment either by their high vapor pressures or by the release of one mole of hydrohalic acids in water systems yielding localized low pH environments. As such, none of these methods provide a stable bromine product that can be safely and easily handled while meeting environmental requirements (more fully discussed below), such as low bromate and absorbable organic halogen generation, and having a high free halogen residual and a low volatility (resulting in a greatly reduced odor and vapor-phase corrosion). In addition, a portion of the expensive bromine compound is wasted through an ineffective by-product in some delivery schemes. Thus, the need for a safe, convenient, economical, stable bromine water treatment product remains and is significant. The Goodenough et al. reference (U.S. Pat. No. 3,558,503), teaches stabilization of bromine using any compound which reacted reversibly with bromine. The disclosed compounds include: (a) water-soluble primary and secondary amines or amides; and, (b) sulfamic acid and its water-soluble salts. However, the bromine solutions prepared according to the Goodenough et al. reference teachings are not stable enough for practical use in commercial cooling water, oil field and other industrial applications. Sulfamic acid, according to the Goodenough et al. reference, is employed as a free acid or as one of its water-soluble salts such as the sodium, potassium or ammonium salt. However, the manner in which the bromine solutions are prepared provide relatively low stabilities and low available halogen concentrations compared with the discoveries claimed within this invention disclosure. The Goodenough et al. reference charges elemental bromine into aqueous solution prior to stabilization. Because elemental bromine is used in the process disclosed in the Goodenough et al. reference, this process is difficult to complete as well as potentially hazardous since elemental bromine is a fuming, corrosive, toxic liquid. The Goodenough et al. reference mentions that the available bromine concentration immediately following preparation was about 1 percent by weight. The low bromine concentration achieved by this method was due in part to bromine being soluble at just 4 percent in cold water. Additionally, bromine is wasted in the process disclosed in the Goodenough et al. reference. The reaction according to this process is as follows: Because the produced HBr does not function as a biocide, one half of the bromine adds nothing to the strength of the biocidal species, HOBr. This invention disclosure improves on the Goodenough et al. reference by means of a safer, easier, and more economical process. Much higher levels of available halogen for disinfection were attained using the invention disclosed in this application, as shown in Table I below, by stabilizing the sodium salt (NaOBr) generated during manufacture. As previously mentioned, sodium hypobromite is unstable and therefore not commercially available. If a stabilized form of NaOBr is proposed, the stabilization process must occur quickly after NaOBr is made. The method described in the Goodenough et al. reference could not achieve these increased bromine levels as the order of reagent addition described in the reference was deemed not critical to the operability of the method. Since NaOBr is synthesized by the following reaction, NaOCl + NaBr NaOBr + NaCl, addition of the stabilizer prior to bromide oxidation would not permit the formation of NaOBr. When water is treated with many halogenated biocides, undesirable halogenated organics can be generated as by-products. These compounds are causing increased environmental and health concerns. It is generally known that low molecular weight halogenated organics are more easily biologically degraded than higher molecular weight species. However, the low molecular weight forms may be more toxic to aquatic and mammalian organisms. Differentiation of these halogenated organics is costly, time consuming and requires the use of gas chromatography, high performance liquid chromatography or gel permeation chromatography. Absorbable Organic Halogen, "AOX", was chosen as a method of measuring the sum of halogenated organic compounds without speciation. AOX is used as an effluent monitoring parameter of water or wastewater in Europe and North America. In the United States, the Environmental Protection Agency ("EPA") is looking closely at AOX discharge in the pulp and paper industry. An object of the present invention is to provide a stable NaOBr solution that can be used to control microbial fouling with minimal AOX generation. The problems associated with controlling AOX levels, being a more recent developing environmental concern, have not been previously resolved in the industry. The United States EPA extrapolates some animal carcinogenesis with the presence of low bromate levels found in drinking water. Bromate may appear from the ozonation of bromide-containing water raising some concerns in the drinking water industry. Bromate may also be formed by the disproportionation of hypobromite. This reaction occurs at a greater rate in alkaline environments. Hence, if bleach is added to a NaBr solution, the high pH environment could lead to the undesirable production of bromate. One use of the present invention, which was previously unknown and is surprising, is to greatly minimize bromate formation by stabilizing hypobromite when conditions are favorable for bromate production. The petroleum industry experiences biological problems, including microbiologically influenced corrosion, both localized and general, in oil field waters. In addition, bacteria can plug the wellbore surface in waterflood injection wells. The bacteria form slime plugs, reducing injectivity. Treatment with stable bromine water is a convenient method of dealing with these and similar problems. It is an object of the present invention to provide a process whereby aqueous solutions of sodium hypobromite can be produced which are relatively resistant to degradation and/or decomposition and which are relatively non-corrosive and non- volatile, yet which retain an improved capacity for oxidation and bactericidal activity. Another object of the present invention is to provide a stable sodium hypobromite solution in which the formation of AOX is minimized while providing improved microbial fouling control. Other objects and advantages of the present invention will become obvious from the following description thereof. Summary of the Invention The invention, according to one embodiment is a method for preparing a stabilized aqueous alkali or alkaline earth metal hypobromite solution. The method comprises the steps of: a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite having from about 5 percent to about 70 percent available halogen as chlorine with a water soluble bromide ion source; b. Allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0.5 to 70 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite; c. Adding to the unstabilized solution of alkali or alkaline earth metal hypobromite an aqueous solution of an alkali metal sulfamate in a quantity to provide a molar ratio of alkali metal sulfamate to alkali or alkaline earth metal hypobromite is from about 0.5 to about 7; and, d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution. Description of the Preferred Embodiments One embodiment of the invention is a method for preparing a stabilized aqueous alkali or alkaline earth metal hypobromite solution. The method comprises the steps of: a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite having from about 5 percent to about 70 percent available halogen as chlorine with a water soluble bromide ion source; b. Allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0.5 to 70 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite; c. Adding to the unstabilized solution of alkali or alkaline earth metal hypobromite an aqueous solution of an alkali metal sulfamate in a quantity to provide a molar ratio of alkali metal sulfamate to alkali or alkaline earth metal hypobromite is from about 0.5 to about 7; and, d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution. The alkali or alkaline earth metal hypochlorite is selected from the group consisting of sodium hypochlorite, potassium hypochlorite, magnesium hypochlorite, lithium hypochlorite, and calcium hypochlorite. The amount of hypochlorite used will vary depending upon which hypochlorite salt is used. The bromide ion source is selected from the group consisting of sodium bromide, potassium bromide, lithium bromide, and hydrobromic acid. As shown in the examples, in a more preferred embodiment, the alkali or alkaline earth metal hypochlorite is sodium hypochlorite, the bromide ion source is sodium bromide, and the alkali or alkaline earth metal hypobromite is sodium hypobromite. The aqueous solution of unstabilized alkali or alkaline earth metal hypobromite may contain from about 0.5 to about 70 percent by weight alkali or alkaline earth metal hypobromite, more preferrably from about 1 to about 30 percent by weight alkali or alkaline earth metal hypobromite, and most preferrably from about 4 to about 15 percent by weight alkali or alkaline earth metal hypobromite. The pH of the stabilized aqueous alkali or alkaline earth metal hypobromite solution is from about 8 to about 14 and more preferrably from about 11 to about 14. The the molar ratio of the alkali metal sulfamate to the sodium hypobromite is preferrably from about 0.5 to about 7, more preferrably from about 0.5 to about 4, and most preferrably from about 0.5 to about 2. Another embodiment of the invention is a stabilized aqueous solution of an alkali or alkaline earth metal hypobromite which is prepared by the steps of: a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite having from about 5 percent to about 70 percent available halogen as chlorine with a water soluble bromide ion source; b. Allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0.5 to 30 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite; c. Adding to the unstabilized solution of alkali or alkaline earth metal hypobromite an aqueous solution of an alkali metal sulfamate in a quantity to provide a molar ratio of alkali metal sulfamate to alkali or alkaline earth metal hypobromite is from about 0.5 to about 7; and, d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution. The alkali or alkaline earth metal hypochlorite is selected from the group consisting of sodium hypochlorite, potassium hypochlorite, magnesium hypochlorite, lithium hypochlorite, and calcium hypochlorite. The amount of hypochlorite used will vary depending upon which hypochlorite salt is used. The bromide ion source is selected from the group consisting of sodium bromide, potassium bromide, lithium bromide, and hydrobromic acid. As shown in the examples, in a more preferred embodiment, the alkali or alkaline earth metal hypochlorite is sodium hypochlorite, the bromide ion source is sodium bromide, and the alkali or alkaline earth metal hypobromite is sodium hypobromite. The aqueous solution of unstabilized alkali or alkaline earth metal hypobromite may contain from about 0.5 to about 70 percent by weight alkali or alkaline earth metal hypobromite, more preferrably from about 1 to about 30 percent by weight alkali or alkaline earth metal hypobromite, and most preferrably from about 4 to about 15 percent by weight alkali or alkaline earth metal hypobromite. The pH of the stabilized aqueous alkali or alkaline earth metal hypobromite solution is from about 8 to about 14 and more preferrably from about 11 to about 14. The the molar ratio of the alkali metal sulfamate to the sodium hypobromite is preferrably from about 0.5 to about 7, more preferrably from about 0.5 to about 4, and most preferrably from about 0.5 to about 2. The invention can be used in an industrial water system. Such water systems would contain from about 0.05 to about 1000 ppm, more preferably from about 0.05 to about 10 ppm, and most preferably from about 0.1 to about 5 ppm of the stabilized aqueous solution of an alkali or alkaline earth metal hypobromite. The invention can be used in the laundering of soiled garments where the soiled garments are washed in an aqueous media, such as water, containing a detergent and a bleaching agent. The stabilized aqueous solution of an alkali or alkaline earth metal hypobromite can be used as the bleaching agent. The invention can also be used in the manufacture of cellulosic materials in which cellulosic fibers are bleached with an oxidizing agent. The stabilized aqueous solution of an alkali or alkaline earth metal hypobromite can be used as the oxidizing agent. The invention can be used in the control of microbiofouling in a recreational water system in which an oxidizing agent is added to control microbiofouling. The stabilized aqueous solution of an alkali or alkaline earth metal hypobromite can be used as the oxidizing agent. The invention can be used in the control of microbiofouling occurring on the surfaces of equipment in contact with produced oil field waters. An anti-microbiofouling effective amount of stabilized aqueous solution of an alkali or alkaline earth metal hypobromite can be added to the produced oil field waters. The invention can also be used in the control of microbiofouling in aqueous systems. An effective anti-microbiofouling amount of stablized aqueous solution of an alkali or alkaline earth metal hypobromite can be added to aqueous systems. In another embodiment, the invention is a method of preventing microbiofouling on the surfaces of equipment in contact with in an industrial water system. The method comprises adding to the aqueous system an anti-microbiologically effective amount of a stabilized sodium hypobromite solution. The stabilized sodium hypobromite solution is prepared by the steps of: a. Mixing an aqueous solution of sodium hypochlorite having from about 5 percent to about 30 percent available halogen (as chlorine) with sodium bromide; b. Allowing the sodium bromide and the sodium hypochlorite to react to form a 0.5 to 30 percent by weight aqueous solution of unstabilized sodium hypobromite; c. Adding to the unstabilized solution of sodium hypobromite an aqueous solution of an alkali metal sulfamate in a quantity to provide a molar ratio of alkali metal sulfamate to sodium hypobromite of from about 0.5 to about 7; and, d. Recovering a stabilized aqueous sodium hypobromite solution. The industrial water systems include cooling water systems, cooling ponds, reservoirs, sweetwater applications, decorative fountains, pasteurizers, evaporative condensors, hydrostatic sterilizers and retorts, gas scrubber systems, and air washer systems. Another embodiment of the invention is a method for preparing a stabilized aqueous alkali or alkaline earth metal hypobromite solution when the level of available halogen as chlorine is below about 5 percent. The method comprises the steps of: a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite [wherein the percent of available halogen (as chlorine) is less than about 5] with a water soluble bromide ion source; b. Allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0.5 to 5 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite; c. Adding to the unstabilized solution of alkali or alkaline earth metal hypobromite an aqueous solution of an alkali metal sulfamate having a temperature of at least 50 °C in a quantity to provide a molar ratio of alkali metal sulfamate to alkali or alkaline earth metal hypobromite is from about 0.5 to about 7; and, d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution. When the level of available halogen as chlorine is below about 5 percent, the amount of water in which the stabilizer, the alkali metal sulfamate, is dissolved into must be decreased. At this point, the amount of water is low enough that the alkali metal sulfamate is only sparingly soluble in the water. Therefore, the temperature of the aqueous alkali metal sulfamate solution must be maintained above 50 °C to keep the alkali metal sulfamate in solution until the solution is added to the aqueous solution of unstablized sodium hypobromite. Once mixed with the sodium hypobromite solution, solubility is no longer a concern, and the resulting stabilized sodium hypobromite solution solution does not need to be maintained above 50 °C. The alkali or alkaline earth metal hypochlorite is selected from the group consisting of sodium hypochlorite, potassium hypochlorite, magnesium hypochlorite, lithium hypochlorite, and calcium hypochlorite. The amount of hypochlorite used will vary depending upon which of the hypochlorite is used. The bromide ion source is selected from the group consisting of sodium bromide, potassium bromide, lithium bromide, and hydrobromic acid. As shown in the examples, in a more preferred embodiment, the alkali or alkaline earth metal hypochlorite is sodium hypochlorite, the bromide ion source is sodium bromide, and the alkali or alkaline earth metal hypobromite is sodium hypobromite. The aqueous solution of unstabilized alkali or alkaline earth metal hypobromite may contain from about 0.5 to about 70 percent by weight alkali or alkaline earth metal hypobromite, more preferrably from about 1 to about 30 percent by weight alkali or alkaline earth metal hypobromite. and most preferrably from about 4 to about 15 percent by weight alkali or alkaline earth metal hypobromite. The pH of the stabilized aqueous alkali or alkaline earth metal hypobromite solution is from about 8 to about 14 and more preferrably from about 11 to about 14. The the molar ratio of the alkali metal sulfamate to the sodium hypobromite is preferrably from about 0.5 to about 7, more preferrably from about 0.5 to about 4, and most preferrably from about 0.5 to about 2. Another embodiment of the invention is a stabilized aqueous solution of an alkali or alkaline earth metal hypobromite which is prepared by the steps of: a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite [wherein the percent of available halogen (as chlorine) is less than about 5] with a water soluble bromide ion source; b. Allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0.5 to 5 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite; c. Adding to the unstabilized solution of alkali or alkaline earth metal hypobromite an aqueous solution of an alkali metal sulfamate having a temperature of at least 50 °C in a quantity to provide a molar ratio of alkali metal sulfamate to alkali or alkaline earth metal hypobromite is from about 0.5 to about 7; and, d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution. As discussed above, when the level of available halogen as chlorine is below about 5 percent, the amount of water in which the stabilizer, the alkali metal sulfamate, is dissolved into must be decreased. At this point, the amount of water is low that the alkali metal sulfamate is only sparingly soluble in the water. Therefore, the temperature of the aqueous alkali metal sulfamate solution must be maintained above 50 °C to keep the alkali metal sulfamate in solution until the solution is added to the aqueous solution of unstablized sodium hypobromite. Once mixed with the sodium hypobromite solution, solubility is no longer a concern, and the resulting stabilized sodium hypobromite solution solution does not need to be maintained above 50 °C. The alkali or alkaline earth metal hypochlorite is selected from the group consisting of sodium hypochlorite, potassium hypochlorite, magnesium hypochlorite, lithium hypochlorite, and calcium hypochlorite. The amount of hypochlorite used will vary depending upon which of the hypochlorite is used. The bromide ion source is selected from the group consisting of sodium bromide, potassium bromide, lithium bromide, and hydrobromic acid. As shown in the examples, in a more preferred embodiment, the alkali or alkaline earth metal hypochlorite is sodium hypochlorite, the bromide ion source is sodium bromide, and the alkali or alkaline earth metal hypobromite is sodium hypobromite. The aqueous solution of unstabilized alkali or alkaline earth metal hypobromite may contain from about 0.5 to about 70 percent by weight alkali or alkaline earth metal hypobromite, more preferrably from about 1 to about 30 percent by weight alkali or alkaline earth metal hypobromite, and most preferrably from about 4 to about 15 percent by weight alkali or alkaline earth metal hypobromite. The pH of the stabilized aqueous alkali or alkaline earth metal hypobromite solution is from about 8 to about 14 and more preferrably from about 11 to about 14. The the molar ratio of the alkali metal sulfamate to the sodium hypobromite is preferrably from about 0.5 to about 7, more preferrably from about 0.5 to about 4, and most preferrably from about 0.5 to about 2. In another embodiment, the invention is a method of preventing microbiofoisling on the surfaces of equipment in contact with in an industrial water system. The method comprises adding to the aqueous system an anti-microbiologically effective amount of a stabilized sodium hypobromite solution. The stabilized sodium hypobromite solution is prepared by the steps of: a. Mixing an aqueous solution of sodium hypochlorite [wherein the percent of available halogen (as chlorine) is less than about 5] with sodium bromide; b. Allowing the sodium bromide and the sodium hypochlorite to react to form a 0.5 to 5 percent by weight aqueous solution of unstabilized sodium hypobromite; c. Adding to the unstabilized solution of sodium hypobromite an aqueous solution of an alkali metal sulfamate having a temperature of at least 50 °C in a quantity to provide a molar ratio of alkali metal sulfamate to sodium hypobromite of from about 0.5 to about 7; and, d. Recovering a stabilized aqueous sodium hypobromite solution. As discussed above, when the level of available halogen as chlorine is below about 5 percent, the amount of water in which the stabilizer, the alkali metal sulfamate, is dissolved into must be decreased. At this point, the.amount of water is low that the alkali metal sulfamate is only sparingly soluble in the water. Therefore, the temperature of the aqueous alkali metal sulfamate solution must be maintained at at least 50 °C to keep the alkali metal sulfamate in solution until the solution is added to the aqueous solution of unstablized sodium hypobromite. Once mixed with the sodium hypobromite solution, solubility is no longer a concern, and the resulting stabilized sodium hypobromite solution solution does not need to be maintained at at least 50 °C. Yet another embodiment of the application provides for the use of an alternative stabilizer to the aqueous alkali metal sulfamate. The contemplated stabilizer may be selected from the group consisting of acid amide derivatives of: carbonic acids, hydrogen cyanide, carboxylic acids, amino acids, sulfuric acids, phosphoric acids and boric acids. More specifically, the preferred stabilizers are selected from the group consisting of urea, thiourea, creatinine, cyanuric acids, alkyl hydantoins, mono or di ethanolamine, organic sulfonamides, biuret, sulfamic acid, organic sulfamates and melamine. All of the stabilizers are compounds having an N-H or NH2 group adjacent to an electron withdrawing functional group such as C=0, S=0, P=0, or B=0. This invention provides several differences over the known art, including a specific order of addition in the manufacturing process whereby a stabilized sodium hypobromite solution is produced having improved stability, non-volatility, reduced bromate and AOX formation, improved microbiofouling control, and an increased free halogen residual in cooling water. The stability of the stabilized hypobromite solution, as compared to the stabilized bromine disclosed in the Goodenough et al. reference and unstabilized sodium hypobromite in Table I, is greatly increased. Based on the surprising increased stability of the stabilized sodium hypobromite of this invention, it is apparent that the order of addition in the process of manufacture is critical. The chemical mechanism for halogen biocide stabilization by sulfamic acid has been proposed as follows: When X is CI, the reaction applies to stabilized chlorine. When X is Br, the reaction applies to stabilized bromine. The degree of stabilization is expressed as the concentration ratio of Xstable to Xfree. The Xfree concentration of the stabilized bromine was detectable while the concentration of the Xfree for stabilized chlorine was not. It was concluded that the chlorine in the stabilized chlorine was completely stabilized while the bromine in the stabilized bromine exists in both free and stabilized forms. This contributes in part to the increased antimicrobial properties of stabilized NaOBr over stabilized NaOCl which will be described in more detail in Example 3. Absorbable organic halogen (AOX) is an important environmental parameter particularly in Europe. AOX can form from the reaction of some halogenated compounds with organics. The minimization of AOX by stabilizing NaOBr is a surprising benefit described in this disclosure. Pathway A: AOX formation by HOX Where R-H can be the organic contaminants in cooling water or biomacromolecules and X-R is measured as AOX. Pathway B: This stabilized halogen reaction generates no X-R (AOX) as in Pathway A. When free chlorine (HOC1) or free bromine (HOBr) is used, AOX will be formed in accordance with the mechanism described by Pathway A. When stabilized chlorine is used as a biocide, only Pathway B is possible because no free HOC1 exists in the system. Thus, no or very low AOX will be formed using this product (see Table II below). When stabilized bromine is used, both free and stabilized bromine forms coexist. Thus, both pathways A and B proceed and result in some AOX formation. However, the amount of AOX will be far less than when all of the halogen is in the form of free bromine (HOBr). Apparently, the proposed mechanism explains the cause of AOX reduction due to the use of stabilized halogen biocides. The mechanism should be applicable to other stabilized halogen products when ammonia, amines or amides are used as the stabilizing agents. In order to reduce the AOX formation by a stabilized halogen biocide, it is preferable to select strong stabilizing agents so that Pathway B can dominate. However, the drawback to a very stable halogenated compound is the generally decreased oxidation power that, in most cases, is directly correlated to its biocidal efficacy. Testing has shown that stabilized bromine is much more effective as a biocide than stabilized chlorine. Therefore, to reduce the AOX formation and at the same time maintain the compound's biocidal efficacy requires a well balanced selection of the stabilizing agent. The following examples are presented to describe preferred embodiments and utilities of the invention and are not meant to limit the invention unless otherwise stated in the claims appended hereto. Example 1: Preparation of Stabilized Sodium Hvpobromite with a Critical Order of Addition In order to demonstrate the constancy of stabilized NaOBr, solutions of sodium hypochlorite and sodium bromide were mixed forming NaOBr then stabilized with sodium sulfamate as described below. Sodium hypochlorite solution was diluted in demand-free water. This diluted solution was titrated by the DPD-FAS method. The available chlorine level present in the original solution was determined to be 15 percent. 42.4 grams of the neat NaOCl solution were added to 20.5 grams of a 45 percent NaBr solution. This reaction forms unstabilized NaOBr. The stabilization solution was formulated with 9.6 grams of sulfamic acid, 14 grams of water, and 13.2 grams of 50 percent sodium hydroxide. The stabilization solution is then added with stirring to the NaOBr. The order of addition is critical in this process which differs from the Goodenough et al. reference. For instance, if the stabilizer was added to NaOCl prior to NaBr introduction, the bromide would not be oxidized to hypobromite. Also, bromine solutions prepared in the manner referenced above gave more stable oxidizing species than the prior art. Bromine solutions stabilized as explained in the Goodenough et al. reference exhibited a decrease in halogen activity from an initial concentration of 1 percent to 0.77 percent after fourteen days representing an active ingredient loss of 23 percent. The stabilization procedure described here improved on the prior art as the decline of active ingredient was only 1 percent after 84 days (see Table I above). An unstabilized NaOBr solution prepared in an similar process by replacing sulfamic acid with distilled water lost 94 percent available halogen during the same period. Example 2: Less AOX is Formed in Stabilized Halogen Solutions AOX is a generic class of compounds which includes all organic molecules containing halogen. Limits for AOX discharge from cooling water systems have already been established in some European countries. To simulate AOX formation during stabilized and unstabilized sodium hypobromite action in cooling water, a mixed bacterial culture typically found in cooling water was cultivated in L-broth overnight and the cells harvested by centrifugation. The cell pellet was washed with synthetic cooling water (90 ppm calcium, 50 ppm magnesium, 110 ppm "M" alkalinity, pH 8.0 -8.2) twice to remove the remaining organic medium. Cells were then resuspended into an equal volume of cooling water. A capped dark bottle served as the reactor. Synthetic cooling water was added to the bottle followed by the washed bacterial stock yielding approximately 107 cells/ml. Stabilized NaOBr or unstabilized NaOBr was dosed into this bacterial suspension at a final concentration of 1, 2, 3, or 4 ppm total halogen (as chlorine). Headspace in the bottle was minimized to avoid the evaporative loss of halogenated orizanics and the solution stirred for 24 hours to simulate a typical cooling system. Immediately before AOX analysis, the sample was acidified to pH 2.0 with concentrated nitric acid. A Mitsubishi TOX-10 Analyzer was used according to US EPA Method 9020 to measure the AOX concentration in the samples. Ultrapure water was used for the preparation of all reagents and standard solutions to prevent any contamination. The amounts of AOX formed in each such treatment is shown in Table II below. Cooling water with stabilized NaOBr formed less AOX than treatments using unstabilized NaOBr at equivalent halogen concentrations. Linear regressions were performed on both sets of data to obtain linear-fit equations shown below for both stabilized and unstabilized NaOBr: Stabilized NaOBr: AOX (ppb) = 23.3 X Dose (ppm) Unstaibilized NaOBr: AOX (ppb) = 53.9 X Dose (ppm) Testing also showed that stabilization of NaOCl reduced AOX generation in cooling water dosed with two ppm total residual (see Table II). Example 3: Antibacterial Activity of Stabilized Sodium Hvpobromite Freshly prepared solutions of stabilized and unstabilized sodium hypobromite were diluted then added to cooling water in order to achieve a one ppm free halogen residual (as chlorine). Sodium hypochlorite was stabilized in the same fashion as described for NaOBr in Example One with the exception that NaBr was directly replaced with distilled water. Stabilized and unstabilized sodium hypochlorite were diluted then added to cooling water at a final concentration of one ppm free halogen residual (as chlorine). The volumes of all solutions needed to achieve a one ppm free halogen residual (as chlorine) was recorded. Following 6 and 21 days of dark storage, identical dilmions of stabilized and unstabilized sodium hypohalite solutions were prepared and the volume originally required for a one ppm free halogen residual (as chlorine) was added to cooling water containing approximately 10 Pseudomonas aeruginosa cells / mL. Aliquots were extracted at 10 and 30 minutes into cooling water dilution blanks containing a halogen neutralizer (0.05 percent Na2S203) then enumerated on tryptone glucose extract agar. Stabilized NaOBr retained its antibacterial activity after storage while the unstabilized form lost its efficacy against Pseudomonas aeruginosa (see Table III below). The results were even more dramatic as the storage period increased. This effect was likely due to the disproportionation of the unstable hypobromite ion into the non-biocidal species bromide and bromate. Surprisingly, NaOCl stabilized in the same manner as NaOBr was comparatively ineffective under the conditions tested (Table III). Example 4: Depression of Bromate Formation Following Stabilization of Sodium Hypobromite Hypohalite ions are known to disproportionate into halate and halide under alkaline condilions. Halate ions are undesirable degradants being suspect carcinogens and are under consideration for governmental regulation. The reaction of NaBr with NaOCl can yield significant amounts of bromate in elevated pH environments. Surprisingly, the stabilization of NaOBr with sodium sulfamate greatly minimized bromate formation (see Table IV below). Stabilized and unstabilized sodium hypobromite solutions were prepared as described in Example One. These solutions were stored in the dark at room temperature during the course of the study. Eight month old samples of stabilized and unstabilized NaOBr, both maintained at pH 14, a condition suitable for bromate formation, were assayed for bromate. A Dionex 4000 series gradient ion chromatography system equipped with AG9-SC/AS9-SC columns and a conductivity detector was used to measure the bromate concentration in the samples. The chromatograph was operated according to a method currently under investigation by the EPA for the analysis of bromate in ozonated drinking water. Purified water from an Interlake Water Systems deionization system was used for the preparation of all reagents and standard solutions to prevent contamination. As noted above, the pH of these solutions was high which favors bromate formation. However, NaOCl, which contains significant amounts of NaOH, is typically diluted with system water prior to the introduction of the bromide species in most industrial applications. The pH of this diluted system would be lower than the neat NaOCl / NaBr formulation described above theoretically minimizing bromate formation. The available chlorine in a NaOCl sample diluted (1:100) with distilled water was titrated by the DPD-FAS method. A solution of 45 percent sodium bromide was added to the dilute NaOCl at a molar ratio of 1 CU : 1 Br" forming NaOBr. This reaction proceeded for thirty minutes. Then, appropriate volumes of this dilute NaOBr solution were added to cooling water (pH 8.3) giving total available halogen levels of 1, 2, 3, and 4 ppm (as Cl2) as determined by the DPD-FAS method. Similarly, a dilution of stabilized sodium hypobromite (1:100) was made in distilled water. Dilute stabilized NaOBr was added to cooling water (pH 8.3) giving total available halogen levels of I, 2, 3, and 4 ppm (as Cl2) as determined by the DPD-FAS method. Bromate analysis then proceeded in the manner described above. Bromate was not detected in any of the cooling water samples dosed with either stabilized or unstabilized dilute NaOBr at typical use concentrations. These results signify the safety factor for bromate built into the stabilized sodium hypobromite formulation as well as the industrial in situ oxidation of NaBr with dilute NaOCl. Example 5: Use of Stabilized NaOBr Increased the Percentage of Free Residual in a Recirculating Cooling Water System Compared to Other Stabilized Halogen Compounds A major drawback to some commercial stabilized chlorine products for industrial water treatment is the low percentage of free chlorine residual delivered to the water system. This effect is due to the strength of the chemical bond between the stabilizer, usually a nitrogenous compound, and chlorine. Chloramines, ie. combined chlorine, are weaker microbicides than free chlorine. However, bromamines are considered to be nearly as effective against microorganisms as free bromine. Thus, it is essential to have a high percentage of the total available halogen in the free form when chlorine products are employed. Conversely, this phenomenon is not as crucial when employing stabilized NaOBr. A commercial heating, ventilation and air conditioning ("HVAC") cooling system was sequentially treated with stabilized NaOCl, a bromochloroalkylhydantoin, and finally stabilized NaOBr. There was a low percentage of free chlorine relative to total available halogen present in the stabilized NaOCl treated system (see Table V below). A lower percentage of free halogen was measured when a different stabilization system, an alkylhydantoin, was employed with bromine and chlorine (see Table V below). However, when stabilized NaOBr was fed into this system, the percentage of free available halogen relative to the total residual measured quickly increased (see Table V below). These phenomena imply that less stabilized NaOBr is required to obtain a free available halogen residual than the equivalent amount of stabilized NaOCl. Example Six: Stabilization of Sodium Hvpobromite Reduces Volatility If a biocide is highly volatile, its performance may be adversely affected. For example, the biocide may flash off in the highly aerated conditions of a cooling tower or an air washer. This would lower the biocide concentration in the cooling water wasting the product. Halogen volatility also leads to vapor-phase corrosion of susceptible equipment surfaces. In addition, halogen volatility may cause worker discomfort due to the "swimming pool" aroma. Thus, the need for an efficacious oxidizing biocide with low volatility is evident. Concentrated solutions of either NaOCl, NaOBr, or stabilized NaOBr were added to a beaker. Halogen vapors were detected from the NaOCl and NaOBr solutions. No odors were noticed from the stabilized NaOBr. This is an improvement over existing products by minimizing halogen odors in product storage areas. Bleach, NaOCl, is not commonly used in air washer systems due to some of the reasons listed above. Once an effective microbial control dose is achieved, the halogen odor may be so overwhelming that workers would not be able to comfortably operate in the treated areas. The low volatilization of stabilized NaOBr overcomes this drawback. Stabilized sodium hypobromite was added at elevated use concentrations to two textile mill air washers in order to investigate its volatility. Then the air was monitored throughout the mill. A Sensidyne air monitoring device outfitted with halogen detection tubes was used to instantaneously detect halogen in the air. The lower detection limit was 50 ppb which is below the Threshold Limit Value-Short Term Exposure Limit for bromine as established by OSHA. In addition, halogen badges were placed throughout textile mills in order to detect halogen vapors over extended periods of time. Neither monitoring system detected any halogen present in the air following the elevated stabilized NaOBr dose. No halogen odors were encountered in either the air washer unit or the return air. The microbial population was enumerated before and after stabilized NaOBr addition. The microbial population following dosing was reduced by greater than one order of magnitude. This example demonstrates the utility of stabilized sodium hypobromite in controlling the bacterial population while adding no halogen odor to the system area. Changes can be made in the composition, operation and arrangement of the method of the present invention described herein without departing from the concept and scope of the invention as defined in the following claims: We Claim: 1. A method for preparing a stabilized aqueous alkali or alkaline earth metal hypobromite solution comprising the steps of: a) mixing an aqueous solution of alkali or alkaline earth metal hypochlorite having from about 5 percent to about 70 percent by weight available halogen as chlorine with a water soluble bromide ion source; b) allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0,5 to 70 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite; c) adding to the unstabilized solution of alkali or alkaline earth metal hypobromite a stabilizer selected from the group consisting of carbonic acids, hydrogen cyanide, carboxylic acids, amino acids, sulfuric acids, phosphoric acids and boric acids; and d) recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution. 2. The method as claimed in claim 1. wherein the alkali or alkaline earth metal hypochlorite is selected from the group consisting of sodium hypochlorite, potassium hypochlorite, lithium hypochlorite, magnesium hypochlorite, and calcium hypochlorite. The method as claimed in claim 1, wherein the bromide ion source is selected from the group consisting of sodium bromide potassium bromide, lithium bromide, and hydrobromic acid. The method as claimed in claim 1, wherein the alkali or alkaline earth metal hypochlorite is sodium hypochlorite, the bromide ion source is sodium bromide, and the alkali or alkaline earth metal hypobromite is sodium hypobromite. The method as claimed in claim ls wherein the aqueous solution of unstabilized alkali or alkaline earth metal hypobromite contains from about 1 to about 30 percent by weight alkali or alkaline earth metal hypobromite. The method as claimed in claim 1, wherein the aqueous solution of unstabilized alkali or alkaline earth metal hypobromite contains from about 4 to about 15 percent by weight alkali or alkaline earth metal hypobromite. The method as claimed in claim 4, wherein the aqueous solution of unstabilized sodium hypobromite contains from about 1 to about 30 percent by weight sodium hypobromite. The method as claimed in claim 4, wherein the aqueous solution of unstabilized sodium hypobromite contains from about 4 to about 15 percent by weight sodium hypobromite. The method as claimed in claim 7, wherein the pH of the stabilized aqueous sodium hypobromite solution is from about 8 to about 14. The method as claimed in claim 8, wherein the pH of the stabilized aqueous sodium hypobromite solution is from about 1 to about 14, The method as claimed in claim 9, wherein the molar ratio of the stabilizer to the sodium hypobromite is from about 0.5 to about 4. The method as claimed in claim 10, wherein the molar ratio of the stabilizer to the sodium hypobromite is from about 0.5 to about 2. A stabilizer aqueous solution of an alkali or alkaline earth metal hypobromite which is prepared by the steps of: a) mixing an aqueous solution of alkali or alkaline earth metal hypochlorite having from about 5 percent to about 70 by weight percent available halogen as chlorine with a water soluble bromide ion source; b) allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0,5 to 70 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite; c) adding to the unstabilized solution of alkali or alkaline earth metal hypobromite a stabilizer selected from the group consisting of carbonic acids, hydrogen cyanide, carboxylic acids, amino acids, sulfuric acids, phosphoric acids and boric acids; and, d) recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution. An industrial water system containing from about 0.05 to about 1000 ppm of the solution as claimed in claim 13, The stabilized aqueous solution as claimed in claim 13. wherein the stabilizer is selected from the group consisting of urea, thiourea, creatinine, cyanuric acids, alkyl hydantoins, mono or di ethanolamine, organic sulfonamides, biuret, sulfamic acid, organic sulfamales and in elam ine. The method as claimed in claim i, wherein the stabilizer is selected from the group consisting of urea, thiourea, creatinine, cyanuric acids, alkyl hydantoins, mono or di ethanolamine, organic sulfonamides, biuret, sulfamic acid, organic sulfamates and melamine. A method for preparing a stabilized aqueous alkali or alkaline earth metal hypobromite solution comprising the steps of: mixing an aqueous solution of alkali or alkaline earth metal hypochlorite having from about 5 percent to about 70 percent by weight available halogen as chlorine with a water soluble bromide ion source; allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0.5 to 70 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite; adding to the unstabilized solution of alkali or alkaline earth metal hypobromite a stabilizer selected from the group consisting of carbonic acids, hydrogen cyanide, carboxylic acids, amino acids, sulfuric acids, phosphoric acids and boric acids; and recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution,

Full Text

The present invention relates to a method of preparing a stabilized alkali or
alkaline earth metal hypobromite to control microbiofouling, more specifically, a
stabilized sodium hypobromite solution the characteristics of which include non-
volatility, high free halogen residual, lower bromate formation, reduced generation of
absorbable organic halogen in process waters, as well as improved performance against
biofouling.
3. Background of the Invention
Aqueous solutions of sodium hypochlorite are widely used in cooling water
towers; bleaching processes; treatment of recreational waters including swimming pool
water, water slide and other water game equipment, spas, and whirlpools; disinfectants;
laundry detergents; and, industrial biocides including applications in the petroleum
industry. However, a major disadvantage of NaOCl is its instability. As is well known in
the art. several methods are used to stabilize NaOCl. The Self et al. reference (U.S. Pat.
No. 3,328.294) described a continuous process to stabilize hypochlorite with an equal

molar ratio of sulfamic acid. This process was improved upon by Rutkiewic reference
(U.S. Pat. No. 3,767,586) who added a buffer which aided in pH control increasing the
stability of concentrated solutions.
Bromine has various advantages over chlorine for water treatment such as better
performance in high pH or amine environments and a lower volatility. However, sodium
hypobromite, the bromine analog to chlorine bleach, is not stable under typical storage
conditions, and as such, is not commercially available. Instead, bromine is typically
delivered to water treatment systems by various inefficient or inconvenient methods. The
art described by either Self et al. or Rutkiewic does not mention a method to stabilize the
well known precarious sodium hypobromite molecule as disclosed within this invention.
Also, this disclosure shall improve upon the art of Rutkiewic by formulating a more
stable, concentrated NaOBr solution in the absence of a buffer.
In one such bromine delivery method, NaBr is oxidized in situ by introducing
gaseous chlorine or NaOCl into the process water stream. Another technique uses a
stable perbromide (Br,-) solution containing 30 - 40 percent bromine. The perbromide
solution releases bromide and bromine when injected into water systems. The formed
bromine hydrolyzes instantly to hypobromous and hydrobromic acids. Alternatively,
bromine chloride may be added to aqueous process streams wherein it hydrolyzes to
hypobromous and hydrochloric acids.
All of these bromine delivery systems have inherit disadvantages. Gaseous
chlorine, perbromide, and bromine chloride have high halogen vapor pressures which
present safety concerns in handling and storage. Also, these concentrated halogen
solutions are corrosive to many metal surfaces found in process equipment either by their

high vapor pressures or by the release of one mole of hydrohalic acids in water systems
yielding localized low pH environments. As such, none of these methods provide a
stable bromine product that can be safely and easily handled while meeting
environmental requirements (more fully discussed below), such as low bromate and
absorbable organic halogen generation, and having a high free halogen residual and a low
volatility (resulting in a greatly reduced odor and vapor-phase corrosion). In addition, a
portion of the expensive bromine compound is wasted through an ineffective by-product
in some delivery schemes. Thus, the need for a safe, convenient, economical, stable
bromine water treatment product remains and is significant.
The Goodenough et al. reference (U.S. Pat. No. 3,558,503), teaches stabilization
of bromine using any compound which reacted reversibly with bromine. The disclosed
compounds include:
(a) water-soluble primary and secondary amines or amides; and,
(b) sulfamic acid and its water-soluble salts.
However, the bromine solutions prepared according to the Goodenough et al. reference
teachings are not stable enough for practical use in commercial cooling water, oil field
and other industrial applications.
Sulfamic acid, according to the Goodenough et al. reference, is employed as a free
acid or as one of its water-soluble salts such as the sodium, potassium or ammonium salt.
However, the manner in which the bromine solutions are prepared provide relatively low
stabilities and low available halogen concentrations compared with the discoveries
claimed within this invention disclosure. The Goodenough et al. reference charges
elemental bromine into aqueous solution prior to stabilization. Because elemental

bromine is used in the process disclosed in the Goodenough et al. reference, this process
is difficult to complete as well as potentially hazardous since elemental bromine is a
fuming, corrosive, toxic liquid.
The Goodenough et al. reference mentions that the available bromine
concentration immediately following preparation was about 1 percent by weight. The
low bromine concentration achieved by this method was due in part to bromine being
soluble at just 4 percent in cold water. Additionally, bromine is wasted in the process
disclosed in the Goodenough et al. reference. The reaction according to this process is as
follows:

Because the produced HBr does not function as a biocide, one half of the bromine adds
nothing to the strength of the biocidal species, HOBr. This invention disclosure improves
on the Goodenough et al. reference by means of a safer, easier, and more economical
process.
Much higher levels of available halogen for disinfection were attained using the
invention disclosed in this application, as shown in Table I below, by stabilizing the
sodium salt (NaOBr) generated during manufacture. As previously mentioned, sodium
hypobromite is unstable and therefore not commercially available. If a stabilized form of
NaOBr is proposed, the stabilization process must occur quickly after NaOBr is made.
The method described in the Goodenough et al. reference could not achieve these
increased bromine levels as the order of reagent addition described in the reference was
deemed not critical to the operability of the method. Since NaOBr is synthesized by the

following reaction, NaOCl + NaBr NaOBr + NaCl, addition of the stabilizer prior to
bromide oxidation would not permit the formation of NaOBr.
When water is treated with many halogenated biocides, undesirable halogenated
organics can be generated as by-products. These compounds are causing increased
environmental and health concerns. It is generally known that low molecular weight
halogenated organics are more easily biologically degraded than higher molecular weight
species. However, the low molecular weight forms may be more toxic to aquatic and
mammalian organisms. Differentiation of these halogenated organics is costly, time
consuming and requires the use of gas chromatography, high performance liquid
chromatography or gel permeation chromatography. Absorbable Organic Halogen,
"AOX", was chosen as a method of measuring the sum of halogenated organic
compounds without speciation. AOX is used as an effluent monitoring parameter of
water or wastewater in Europe and North America. In the United States, the
Environmental Protection Agency ("EPA") is looking closely at AOX discharge in the
pulp and paper industry. An object of the present invention is to provide a stable NaOBr
solution that can be used to control microbial fouling with minimal AOX generation. The
problems associated with controlling AOX levels, being a more recent developing
environmental concern, have not been previously resolved in the industry.
The United States EPA extrapolates some animal carcinogenesis with the
presence of low bromate levels found in drinking water. Bromate may appear from the
ozonation of bromide-containing water raising some concerns in the drinking water
industry. Bromate may also be formed by the disproportionation of hypobromite. This
reaction occurs at a greater rate in alkaline environments. Hence, if bleach is added to a

NaBr solution, the high pH environment could lead to the undesirable production of
bromate. One use of the present invention, which was previously unknown and is
surprising, is to greatly minimize bromate formation by stabilizing hypobromite when
conditions are favorable for bromate production.
The petroleum industry experiences biological problems, including
microbiologically influenced corrosion, both localized and general, in oil field waters. In
addition, bacteria can plug the wellbore surface in waterflood injection wells. The
bacteria form slime plugs, reducing injectivity. Treatment with stable bromine water is a
convenient method of dealing with these and similar problems.
It is an object of the present invention to provide a process whereby aqueous
solutions of sodium hypobromite can be produced which are relatively resistant to
degradation and/or decomposition and which are relatively non-corrosive and non-
volatile, yet which retain an improved capacity for oxidation and bactericidal activity.
Another object of the present invention is to provide a stable sodium hypobromite
solution in which the formation of AOX is minimized while providing improved
microbial fouling control. Other objects and advantages of the present invention will
become obvious from the following description thereof.
Summary of the Invention
The invention, according to one embodiment is a method for preparing a
stabilized aqueous alkali or alkaline earth metal hypobromite solution. The method
comprises the steps of:

a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite
having from about 5 percent to about 70 percent available halogen as chlorine with a
water soluble bromide ion source;
b. Allowing the bromide ion source and the alkali or alkaline earth metal
hypochlorite to react to form a 0.5 to 70 percent by weight aqueous solution of
unstabilized alkali or alkaline earth metal hypobromite;
c. Adding to the unstabilized solution of alkali or alkaline earth metal
hypobromite an aqueous solution of an alkali metal sulfamate in a quantity to provide a
molar ratio of alkali metal sulfamate to alkali or alkaline earth metal hypobromite is from
about 0.5 to about 7; and,
d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite
solution.
Description of the Preferred Embodiments
One embodiment of the invention is a method for preparing a stabilized aqueous
alkali or alkaline earth metal hypobromite solution. The method comprises the steps of:
a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite
having from about 5 percent to about 70 percent available halogen as chlorine with a
water soluble bromide ion source;
b. Allowing the bromide ion source and the alkali or alkaline earth metal
hypochlorite to react to form a 0.5 to 70 percent by weight aqueous solution of
unstabilized alkali or alkaline earth metal hypobromite;

c. Adding to the unstabilized solution of alkali or alkaline earth metal
hypobromite an aqueous solution of an alkali metal sulfamate in a quantity to provide a
molar ratio of alkali metal sulfamate to alkali or alkaline earth metal hypobromite is from
about 0.5 to about 7; and,
d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite
solution.
The alkali or alkaline earth metal hypochlorite is selected from the group
consisting of sodium hypochlorite, potassium hypochlorite, magnesium hypochlorite,
lithium hypochlorite, and calcium hypochlorite. The amount of hypochlorite used will
vary depending upon which hypochlorite salt is used.
The bromide ion source is selected from the group consisting of sodium bromide,
potassium bromide, lithium bromide, and hydrobromic acid. As shown in the examples,
in a more preferred embodiment, the alkali or alkaline earth metal hypochlorite is sodium
hypochlorite, the bromide ion source is sodium bromide, and the alkali or alkaline earth
metal hypobromite is sodium hypobromite.
The aqueous solution of unstabilized alkali or alkaline earth metal hypobromite
may contain from about 0.5 to about 70 percent by weight alkali or alkaline earth metal
hypobromite, more preferrably from about 1 to about 30 percent by weight alkali or
alkaline earth metal hypobromite, and most preferrably from about 4 to about 15 percent
by weight alkali or alkaline earth metal hypobromite.
The pH of the stabilized aqueous alkali or alkaline earth metal hypobromite
solution is from about 8 to about 14 and more preferrably from about 11 to about 14. The
the molar ratio of the alkali metal sulfamate to the sodium hypobromite is preferrably

from about 0.5 to about 7, more preferrably from about 0.5 to about 4, and most
preferrably from about 0.5 to about 2.
Another embodiment of the invention is a stabilized aqueous solution of an alkali
or alkaline earth metal hypobromite which is prepared by the steps of:
a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite
having from about 5 percent to about 70 percent available halogen as chlorine with a
water soluble bromide ion source;
b. Allowing the bromide ion source and the alkali or alkaline earth metal
hypochlorite to react to form a 0.5 to 30 percent by weight aqueous solution of
unstabilized alkali or alkaline earth metal hypobromite;
c. Adding to the unstabilized solution of alkali or alkaline earth metal
hypobromite an aqueous solution of an alkali metal sulfamate in a quantity to provide a
molar ratio of alkali metal sulfamate to alkali or alkaline earth metal hypobromite is from
about 0.5 to about 7; and,
d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite
solution.
The alkali or alkaline earth metal hypochlorite is selected from the group
consisting of sodium hypochlorite, potassium hypochlorite, magnesium hypochlorite,
lithium hypochlorite, and calcium hypochlorite. The amount of hypochlorite used will
vary depending upon which hypochlorite salt is used.
The bromide ion source is selected from the group consisting of sodium bromide,
potassium bromide, lithium bromide, and hydrobromic acid. As shown in the examples,
in a more preferred embodiment, the alkali or alkaline earth metal hypochlorite is sodium

hypochlorite, the bromide ion source is sodium bromide, and the alkali or alkaline earth
metal hypobromite is sodium hypobromite.
The aqueous solution of unstabilized alkali or alkaline earth metal hypobromite
may contain from about 0.5 to about 70 percent by weight alkali or alkaline earth metal
hypobromite, more preferrably from about 1 to about 30 percent by weight alkali or
alkaline earth metal hypobromite, and most preferrably from about 4 to about 15 percent
by weight alkali or alkaline earth metal hypobromite.
The pH of the stabilized aqueous alkali or alkaline earth metal hypobromite
solution is from about 8 to about 14 and more preferrably from about 11 to about 14. The
the molar ratio of the alkali metal sulfamate to the sodium hypobromite is preferrably
from about 0.5 to about 7, more preferrably from about 0.5 to about 4, and most
preferrably from about 0.5 to about 2.
The invention can be used in an industrial water system. Such water systems
would contain from about 0.05 to about 1000 ppm, more preferably from about 0.05 to
about 10 ppm, and most preferably from about 0.1 to about 5 ppm of the stabilized
aqueous solution of an alkali or alkaline earth metal hypobromite.
The invention can be used in the laundering of soiled garments where the soiled
garments are washed in an aqueous media, such as water, containing a detergent and a
bleaching agent. The stabilized aqueous solution of an alkali or alkaline earth metal
hypobromite can be used as the bleaching agent.
The invention can also be used in the manufacture of cellulosic materials in which
cellulosic fibers are bleached with an oxidizing agent. The stabilized aqueous solution of
an alkali or alkaline earth metal hypobromite can be used as the oxidizing agent.

The invention can be used in the control of microbiofouling in a recreational
water system in which an oxidizing agent is added to control microbiofouling. The
stabilized aqueous solution of an alkali or alkaline earth metal hypobromite can be used
as the oxidizing agent.
The invention can be used in the control of microbiofouling occurring on the
surfaces of equipment in contact with produced oil field waters. An anti-microbiofouling
effective amount of stabilized aqueous solution of an alkali or alkaline earth metal
hypobromite can be added to the produced oil field waters.
The invention can also be used in the control of microbiofouling in aqueous
systems. An effective anti-microbiofouling amount of stablized aqueous solution of an
alkali or alkaline earth metal hypobromite can be added to aqueous systems.
In another embodiment, the invention is a method of preventing microbiofouling
on the surfaces of equipment in contact with in an industrial water system. The method
comprises adding to the aqueous system an anti-microbiologically effective amount of a
stabilized sodium hypobromite solution. The stabilized sodium hypobromite solution is
prepared by the steps of:
a. Mixing an aqueous solution of sodium hypochlorite having from about 5
percent to about 30 percent available halogen (as chlorine) with sodium bromide;
b. Allowing the sodium bromide and the sodium hypochlorite to react to
form a 0.5 to 30 percent by weight aqueous solution of unstabilized sodium hypobromite;
c. Adding to the unstabilized solution of sodium hypobromite an aqueous
solution of an alkali metal sulfamate in a quantity to provide a molar ratio of alkali metal
sulfamate to sodium hypobromite of from about 0.5 to about 7; and,

d. Recovering a stabilized aqueous sodium hypobromite solution.
The industrial water systems include cooling water systems, cooling ponds,
reservoirs, sweetwater applications, decorative fountains, pasteurizers, evaporative
condensors, hydrostatic sterilizers and retorts, gas scrubber systems, and air washer
systems.
Another embodiment of the invention is a method for preparing a stabilized
aqueous alkali or alkaline earth metal hypobromite solution when the level of available
halogen as chlorine is below about 5 percent. The method comprises the steps of:
a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite
[wherein the percent of available halogen (as chlorine) is less than about 5] with a water
soluble bromide ion source;
b. Allowing the bromide ion source and the alkali or alkaline earth metal
hypochlorite to react to form a 0.5 to 5 percent by weight aqueous solution of
unstabilized alkali or alkaline earth metal hypobromite;
c. Adding to the unstabilized solution of alkali or alkaline earth metal
hypobromite an aqueous solution of an alkali metal sulfamate having a temperature of at
least 50 °C in a quantity to provide a molar ratio of alkali metal sulfamate to alkali or
alkaline earth metal hypobromite is from about 0.5 to about 7; and,
d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite
solution.
When the level of available halogen as chlorine is below about 5 percent, the
amount of water in which the stabilizer, the alkali metal sulfamate, is dissolved into must
be decreased. At this point, the amount of water is low enough that the alkali metal

sulfamate is only sparingly soluble in the water. Therefore, the temperature of the
aqueous alkali metal sulfamate solution must be maintained above 50 °C to keep the
alkali metal sulfamate in solution until the solution is added to the aqueous solution of
unstablized sodium hypobromite. Once mixed with the sodium hypobromite solution,
solubility is no longer a concern, and the resulting stabilized sodium hypobromite
solution solution does not need to be maintained above 50 °C.
The alkali or alkaline earth metal hypochlorite is selected from the group
consisting of sodium hypochlorite, potassium hypochlorite, magnesium hypochlorite,
lithium hypochlorite, and calcium hypochlorite. The amount of hypochlorite used will
vary depending upon which of the hypochlorite is used.
The bromide ion source is selected from the group consisting of sodium bromide,
potassium bromide, lithium bromide, and hydrobromic acid. As shown in the examples,
in a more preferred embodiment, the alkali or alkaline earth metal hypochlorite is sodium
hypochlorite, the bromide ion source is sodium bromide, and the alkali or alkaline earth
metal hypobromite is sodium hypobromite.
The aqueous solution of unstabilized alkali or alkaline earth metal hypobromite
may contain from about 0.5 to about 70 percent by weight alkali or alkaline earth metal
hypobromite, more preferrably from about 1 to about 30 percent by weight alkali or
alkaline earth metal hypobromite. and most preferrably from about 4 to about 15 percent
by weight alkali or alkaline earth metal hypobromite.
The pH of the stabilized aqueous alkali or alkaline earth metal hypobromite
solution is from about 8 to about 14 and more preferrably from about 11 to about 14. The
the molar ratio of the alkali metal sulfamate to the sodium hypobromite is preferrably

from about 0.5 to about 7, more preferrably from about 0.5 to about 4, and most
preferrably from about 0.5 to about 2.
Another embodiment of the invention is a stabilized aqueous solution of an alkali
or alkaline earth metal hypobromite which is prepared by the steps of:
a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite
[wherein the percent of available halogen (as chlorine) is less than about 5] with a water
soluble bromide ion source;
b. Allowing the bromide ion source and the alkali or alkaline earth metal
hypochlorite to react to form a 0.5 to 5 percent by weight aqueous solution of
unstabilized alkali or alkaline earth metal hypobromite;
c. Adding to the unstabilized solution of alkali or alkaline earth metal
hypobromite an aqueous solution of an alkali metal sulfamate having a temperature of at
least 50 °C in a quantity to provide a molar ratio of alkali metal sulfamate to alkali or
alkaline earth metal hypobromite is from about 0.5 to about 7; and,
d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite
solution.
As discussed above, when the level of available halogen as chlorine is below
about 5 percent, the amount of water in which the stabilizer, the alkali metal sulfamate, is
dissolved into must be decreased. At this point, the amount of water is low that the alkali
metal sulfamate is only sparingly soluble in the water. Therefore, the temperature of the
aqueous alkali metal sulfamate solution must be maintained above 50 °C to keep the
alkali metal sulfamate in solution until the solution is added to the aqueous solution of
unstablized sodium hypobromite. Once mixed with the sodium hypobromite solution,

solubility is no longer a concern, and the resulting stabilized sodium hypobromite
solution solution does not need to be maintained above 50 °C.
The alkali or alkaline earth metal hypochlorite is selected from the group
consisting of sodium hypochlorite, potassium hypochlorite, magnesium hypochlorite,
lithium hypochlorite, and calcium hypochlorite. The amount of hypochlorite used will
vary depending upon which of the hypochlorite is used.
The bromide ion source is selected from the group consisting of sodium bromide,
potassium bromide, lithium bromide, and hydrobromic acid. As shown in the examples,
in a more preferred embodiment, the alkali or alkaline earth metal hypochlorite is sodium
hypochlorite, the bromide ion source is sodium bromide, and the alkali or alkaline earth
metal hypobromite is sodium hypobromite.
The aqueous solution of unstabilized alkali or alkaline earth metal hypobromite
may contain from about 0.5 to about 70 percent by weight alkali or alkaline earth metal
hypobromite, more preferrably from about 1 to about 30 percent by weight alkali or
alkaline earth metal hypobromite, and most preferrably from about 4 to about 15 percent
by weight alkali or alkaline earth metal hypobromite.
The pH of the stabilized aqueous alkali or alkaline earth metal hypobromite
solution is from about 8 to about 14 and more preferrably from about 11 to about 14. The
the molar ratio of the alkali metal sulfamate to the sodium hypobromite is preferrably
from about 0.5 to about 7, more preferrably from about 0.5 to about 4, and most
preferrably from about 0.5 to about 2.
In another embodiment, the invention is a method of preventing microbiofoisling
on the surfaces of equipment in contact with in an industrial water system. The method

comprises adding to the aqueous system an anti-microbiologically effective amount of a
stabilized sodium hypobromite solution. The stabilized sodium hypobromite solution is
prepared by the steps of:
a. Mixing an aqueous solution of sodium hypochlorite [wherein the percent
of available halogen (as chlorine) is less than about 5] with sodium bromide;
b. Allowing the sodium bromide and the sodium hypochlorite to react to
form a 0.5 to 5 percent by weight aqueous solution of unstabilized sodium hypobromite;
c. Adding to the unstabilized solution of sodium hypobromite an aqueous
solution of an alkali metal sulfamate having a temperature of at least 50 °C in a quantity
to provide a molar ratio of alkali metal sulfamate to sodium hypobromite of from about
0.5 to about 7; and,
d. Recovering a stabilized aqueous sodium hypobromite solution.
As discussed above, when the level of available halogen as chlorine is below
about 5 percent, the amount of water in which the stabilizer, the alkali metal sulfamate, is
dissolved into must be decreased. At this point, the.amount of water is low that the alkali
metal sulfamate is only sparingly soluble in the water. Therefore, the temperature of the
aqueous alkali metal sulfamate solution must be maintained at at least 50 °C to keep the
alkali metal sulfamate in solution until the solution is added to the aqueous solution of
unstablized sodium hypobromite. Once mixed with the sodium hypobromite solution,
solubility is no longer a concern, and the resulting stabilized sodium hypobromite
solution solution does not need to be maintained at at least 50 °C.
Yet another embodiment of the application provides for the use of an alternative
stabilizer to the aqueous alkali metal sulfamate. The contemplated stabilizer may be

selected from the group consisting of acid amide derivatives of: carbonic acids, hydrogen
cyanide, carboxylic acids, amino acids, sulfuric acids, phosphoric acids and boric acids.
More specifically, the preferred stabilizers are selected from the group consisting of urea,
thiourea, creatinine, cyanuric acids, alkyl hydantoins, mono or di ethanolamine, organic
sulfonamides, biuret, sulfamic acid, organic sulfamates and melamine. All of the
stabilizers are compounds having an N-H or NH2 group adjacent to an electron
withdrawing functional group such as C=0, S=0, P=0, or B=0.
This invention provides several differences over the known art, including a
specific order of addition in the manufacturing process whereby a stabilized sodium
hypobromite solution is produced having improved stability, non-volatility, reduced
bromate and AOX formation, improved microbiofouling control, and an increased free
halogen residual in cooling water.
The stability of the stabilized hypobromite solution, as compared to the stabilized
bromine disclosed in the Goodenough et al. reference and unstabilized sodium
hypobromite in Table I, is greatly increased. Based on the surprising increased stability
of the stabilized sodium hypobromite of this invention, it is apparent that the order of
addition in the process of manufacture is critical.

The chemical mechanism for halogen biocide stabilization by sulfamic acid has
been proposed as follows:

When X is CI, the reaction applies to stabilized chlorine.
When X is Br, the reaction applies to stabilized bromine.
The degree of stabilization is expressed as the concentration ratio of Xstable to Xfree.
The Xfree concentration of the stabilized bromine was detectable while the concentration
of the Xfree for stabilized chlorine was not. It was concluded that the chlorine in the
stabilized chlorine was completely stabilized while the bromine in the stabilized bromine
exists in both free and stabilized forms. This contributes in part to the increased
antimicrobial properties of stabilized NaOBr over stabilized NaOCl which will be
described in more detail in Example 3.
Absorbable organic halogen (AOX) is an important environmental parameter
particularly in Europe. AOX can form from the reaction of some halogenated compounds
with organics. The minimization of AOX by stabilizing NaOBr is a surprising benefit
described in this disclosure.
Pathway A: AOX formation by HOX

Where R-H can be the organic contaminants in cooling water or biomacromolecules and
X-R is measured as AOX.
Pathway B:

This stabilized halogen reaction generates no X-R (AOX) as in Pathway A. When free
chlorine (HOC1) or free bromine (HOBr) is used, AOX will be formed in accordance with
the mechanism described by Pathway A.
When stabilized chlorine is used as a biocide, only Pathway B is possible because
no free HOC1 exists in the system. Thus, no or very low AOX will be formed using this
product (see Table II below).
When stabilized bromine is used, both free and stabilized bromine forms coexist.
Thus, both pathways A and B proceed and result in some AOX formation. However, the
amount of AOX will be far less than when all of the halogen is in the form of free
bromine (HOBr).
Apparently, the proposed mechanism explains the cause of AOX reduction due to
the use of stabilized halogen biocides. The mechanism should be applicable to other
stabilized halogen products when ammonia, amines or amides are used as the stabilizing
agents.
In order to reduce the AOX formation by a stabilized halogen biocide, it is
preferable to select strong stabilizing agents so that Pathway B can dominate. However,
the drawback to a very stable halogenated compound is the generally decreased oxidation
power that, in most cases, is directly correlated to its biocidal efficacy. Testing has
shown that stabilized bromine is much more effective as a biocide than stabilized
chlorine. Therefore, to reduce the AOX formation and at the same time maintain the
compound's biocidal efficacy requires a well balanced selection of the stabilizing agent.

The following examples are presented to describe preferred embodiments and
utilities of the invention and are not meant to limit the invention unless otherwise stated
in the claims appended hereto.
Example 1:
Preparation of Stabilized Sodium Hvpobromite with a Critical Order of Addition
In order to demonstrate the constancy of stabilized NaOBr, solutions of sodium
hypochlorite and sodium bromide were mixed forming NaOBr then stabilized with
sodium sulfamate as described below. Sodium hypochlorite solution was diluted in
demand-free water. This diluted solution was titrated by the DPD-FAS method. The
available chlorine level present in the original solution was determined to be 15 percent.
42.4 grams of the neat NaOCl solution were added to 20.5 grams of a 45 percent NaBr
solution. This reaction forms unstabilized NaOBr. The stabilization solution was
formulated with 9.6 grams of sulfamic acid, 14 grams of water, and 13.2 grams of 50
percent sodium hydroxide. The stabilization solution is then added with stirring to the
NaOBr. The order of addition is critical in this process which differs from the
Goodenough et al. reference. For instance, if the stabilizer was added to NaOCl prior to
NaBr introduction, the bromide would not be oxidized to hypobromite. Also, bromine
solutions prepared in the manner referenced above gave more stable oxidizing species
than the prior art. Bromine solutions stabilized as explained in the Goodenough et al.
reference exhibited a decrease in halogen activity from an initial concentration of 1
percent to 0.77 percent after fourteen days representing an active ingredient loss of 23
percent. The stabilization procedure described here improved on the prior art as the
decline of active ingredient was only 1 percent after 84 days (see Table I above). An

unstabilized NaOBr solution prepared in an similar process by replacing sulfamic acid
with distilled water lost 94 percent available halogen during the same period.
Example 2:
Less AOX is Formed in Stabilized Halogen Solutions
AOX is a generic class of compounds which includes all organic molecules
containing halogen. Limits for AOX discharge from cooling water systems have already
been established in some European countries. To simulate AOX formation during
stabilized and unstabilized sodium hypobromite action in cooling water, a mixed bacterial
culture typically found in cooling water was cultivated in L-broth overnight and the cells
harvested by centrifugation. The cell pellet was washed with synthetic cooling water (90
ppm calcium, 50 ppm magnesium, 110 ppm "M" alkalinity, pH 8.0 -8.2) twice to remove
the remaining organic medium. Cells were then resuspended into an equal volume of
cooling water. A capped dark bottle served as the reactor. Synthetic cooling water was
added to the bottle followed by the washed bacterial stock yielding approximately 107
cells/ml. Stabilized NaOBr or unstabilized NaOBr was dosed into this bacterial
suspension at a final concentration of 1, 2, 3, or 4 ppm total halogen (as chlorine).
Headspace in the bottle was minimized to avoid the evaporative loss of halogenated
orizanics and the solution stirred for 24 hours to simulate a typical cooling system.
Immediately before AOX analysis, the sample was acidified to pH 2.0 with concentrated
nitric acid. A Mitsubishi TOX-10 Analyzer was used according to US EPA Method 9020
to measure the AOX concentration in the samples. Ultrapure water was used for the
preparation of all reagents and standard solutions to prevent any contamination. The

amounts of AOX formed in each such treatment is shown in Table II below. Cooling
water with stabilized NaOBr formed less AOX than treatments using unstabilized NaOBr
at equivalent halogen concentrations. Linear regressions were performed on both sets of
data to obtain linear-fit equations shown below for both stabilized and unstabilized
NaOBr:
Stabilized NaOBr: AOX (ppb) = 23.3 X Dose (ppm)
Unstaibilized NaOBr: AOX (ppb) = 53.9 X Dose (ppm)
Testing also showed that stabilization of NaOCl reduced AOX generation in
cooling water dosed with two ppm total residual (see Table II).

Example 3:
Antibacterial Activity of Stabilized Sodium Hvpobromite
Freshly prepared solutions of stabilized and unstabilized sodium hypobromite
were diluted then added to cooling water in order to achieve a one ppm free halogen
residual (as chlorine). Sodium hypochlorite was stabilized in the same fashion as
described for NaOBr in Example One with the exception that NaBr was directly replaced
with distilled water. Stabilized and unstabilized sodium hypochlorite were diluted then
added to cooling water at a final concentration of one ppm free halogen residual (as
chlorine). The volumes of all solutions needed to achieve a one ppm free halogen
residual (as chlorine) was recorded. Following 6 and 21 days of dark storage, identical
dilmions of stabilized and unstabilized sodium hypohalite solutions were prepared and
the volume originally required for a one ppm free halogen residual (as chlorine) was
added to cooling water containing approximately 10 Pseudomonas aeruginosa cells /
mL. Aliquots were extracted at 10 and 30 minutes into cooling water dilution blanks
containing a halogen neutralizer (0.05 percent Na2S203) then enumerated on tryptone
glucose extract agar. Stabilized NaOBr retained its antibacterial activity after storage

while the unstabilized form lost its efficacy against Pseudomonas aeruginosa (see Table
III below). The results were even more dramatic as the storage period increased. This
effect was likely due to the disproportionation of the unstable hypobromite ion into the
non-biocidal species bromide and bromate. Surprisingly, NaOCl stabilized in the same
manner as NaOBr was comparatively ineffective under the conditions tested (Table III).

Example 4:
Depression of Bromate Formation Following Stabilization of Sodium Hypobromite
Hypohalite ions are known to disproportionate into halate and halide under
alkaline condilions. Halate ions are undesirable degradants being suspect carcinogens
and are under consideration for governmental regulation. The reaction of NaBr with
NaOCl can yield significant amounts of bromate in elevated pH environments.
Surprisingly, the stabilization of NaOBr with sodium sulfamate greatly minimized
bromate formation (see Table IV below). Stabilized and unstabilized sodium
hypobromite solutions were prepared as described in Example One. These solutions were

stored in the dark at room temperature during the course of the study. Eight month old
samples of stabilized and unstabilized NaOBr, both maintained at pH 14, a condition
suitable for bromate formation, were assayed for bromate. A Dionex 4000 series gradient
ion chromatography system equipped with AG9-SC/AS9-SC columns and a conductivity
detector was used to measure the bromate concentration in the samples. The
chromatograph was operated according to a method currently under investigation by the
EPA for the analysis of bromate in ozonated drinking water. Purified water from an
Interlake Water Systems deionization system was used for the preparation of all reagents
and standard solutions to prevent contamination.

As noted above, the pH of these solutions was high which favors bromate
formation. However, NaOCl, which contains significant amounts of NaOH, is typically
diluted with system water prior to the introduction of the bromide species in most
industrial applications. The pH of this diluted system would be lower than the neat
NaOCl / NaBr formulation described above theoretically minimizing bromate formation.
The available chlorine in a NaOCl sample diluted (1:100) with distilled water was titrated
by the DPD-FAS method. A solution of 45 percent sodium bromide was added to the
dilute NaOCl at a molar ratio of 1 CU : 1 Br" forming NaOBr. This reaction proceeded
for thirty minutes. Then, appropriate volumes of this dilute NaOBr solution were added

to cooling water (pH 8.3) giving total available halogen levels of 1, 2, 3, and 4 ppm (as
Cl2) as determined by the DPD-FAS method. Similarly, a dilution of stabilized sodium
hypobromite (1:100) was made in distilled water. Dilute stabilized NaOBr was added to
cooling water (pH 8.3) giving total available halogen levels of I, 2, 3, and 4 ppm (as Cl2)
as determined by the DPD-FAS method. Bromate analysis then proceeded in the manner
described above. Bromate was not detected in any of the cooling water samples dosed
with either stabilized or unstabilized dilute NaOBr at typical use concentrations. These
results signify the safety factor for bromate built into the stabilized sodium hypobromite
formulation as well as the industrial in situ oxidation of NaBr with dilute NaOCl.
Example 5:
Use of Stabilized NaOBr Increased the Percentage of Free Residual in a Recirculating
Cooling Water System Compared to Other Stabilized Halogen Compounds
A major drawback to some commercial stabilized chlorine products for industrial
water treatment is the low percentage of free chlorine residual delivered to the water
system. This effect is due to the strength of the chemical bond between the stabilizer,
usually a nitrogenous compound, and chlorine. Chloramines, ie. combined chlorine, are
weaker microbicides than free chlorine. However, bromamines are considered to be
nearly as effective against microorganisms as free bromine. Thus, it is essential to have a
high percentage of the total available halogen in the free form when chlorine products are
employed. Conversely, this phenomenon is not as crucial when employing stabilized
NaOBr. A commercial heating, ventilation and air conditioning ("HVAC") cooling
system was sequentially treated with stabilized NaOCl, a bromochloroalkylhydantoin,

and finally stabilized NaOBr. There was a low percentage of free chlorine relative to
total available halogen present in the stabilized NaOCl treated system (see Table V
below). A lower percentage of free halogen was measured when a different stabilization
system, an alkylhydantoin, was employed with bromine and chlorine (see Table V
below). However, when stabilized NaOBr was fed into this system, the percentage of
free available halogen relative to the total residual measured quickly increased (see Table
V below). These phenomena imply that less stabilized NaOBr is required to obtain a free
available halogen residual than the equivalent amount of stabilized NaOCl.

Example Six:
Stabilization of Sodium Hvpobromite Reduces Volatility
If a biocide is highly volatile, its performance may be adversely affected. For
example, the biocide may flash off in the highly aerated conditions of a cooling tower or
an air washer. This would lower the biocide concentration in the cooling water wasting
the product. Halogen volatility also leads to vapor-phase corrosion of susceptible
equipment surfaces. In addition, halogen volatility may cause worker discomfort due to
the "swimming pool" aroma. Thus, the need for an efficacious oxidizing biocide with
low volatility is evident.

Concentrated solutions of either NaOCl, NaOBr, or stabilized NaOBr were added
to a beaker. Halogen vapors were detected from the NaOCl and NaOBr solutions. No
odors were noticed from the stabilized NaOBr. This is an improvement over existing
products by minimizing halogen odors in product storage areas.
Bleach, NaOCl, is not commonly used in air washer systems due to some of the
reasons listed above. Once an effective microbial control dose is achieved, the halogen
odor may be so overwhelming that workers would not be able to comfortably operate in
the treated areas. The low volatilization of stabilized NaOBr overcomes this drawback.
Stabilized sodium hypobromite was added at elevated use concentrations to two textile
mill air washers in order to investigate its volatility. Then the air was monitored
throughout the mill. A Sensidyne air monitoring device outfitted with halogen detection
tubes was used to instantaneously detect halogen in the air. The lower detection limit
was 50 ppb which is below the Threshold Limit Value-Short Term Exposure Limit for
bromine as established by OSHA. In addition, halogen badges were placed throughout
textile mills in order to detect halogen vapors over extended periods of time. Neither
monitoring system detected any halogen present in the air following the elevated
stabilized NaOBr dose. No halogen odors were encountered in either the air washer unit
or the return air. The microbial population was enumerated before and after stabilized
NaOBr addition. The microbial population following dosing was reduced by greater than
one order of magnitude. This example demonstrates the utility of stabilized sodium
hypobromite in controlling the bacterial population while adding no halogen odor to the
system area.

Changes can be made in the composition, operation and arrangement of the
method of the present invention described herein without departing from the concept and
scope of the invention as defined in the following claims:

We Claim:
1. A method for preparing a stabilized aqueous alkali or alkaline earth
metal hypobromite solution comprising the steps of:
a) mixing an aqueous solution of alkali or alkaline earth metal
hypochlorite having from about 5 percent to about 70 percent
by weight available halogen as chlorine with a water soluble
bromide ion source;
b) allowing the bromide ion source and the alkali or alkaline earth
metal hypochlorite to react to form a 0,5 to 70 percent by
weight aqueous solution of unstabilized alkali or alkaline earth
metal hypobromite;
c) adding to the unstabilized solution of alkali or alkaline earth
metal hypobromite a stabilizer selected from the group
consisting of carbonic acids, hydrogen cyanide, carboxylic
acids, amino acids, sulfuric acids, phosphoric acids and boric
acids; and
d) recovering a stabilized aqueous alkali or alkaline earth metal
hypobromite solution.
2. The method as claimed in claim 1. wherein the alkali or alkaline
earth metal hypochlorite is selected from the group consisting of
sodium hypochlorite, potassium hypochlorite, lithium
hypochlorite, magnesium hypochlorite, and calcium hypochlorite.

The method as claimed in claim 1, wherein the bromide ion source
is selected from the group consisting of sodium bromide potassium
bromide, lithium bromide, and hydrobromic acid.
The method as claimed in claim 1, wherein the alkali or alkaline
earth metal hypochlorite is sodium hypochlorite, the bromide ion
source is sodium bromide, and the alkali or alkaline earth metal
hypobromite is sodium hypobromite.
The method as claimed in claim ls wherein the aqueous solution of
unstabilized alkali or alkaline earth metal hypobromite contains
from about 1 to about 30 percent by weight alkali or alkaline earth
metal hypobromite.
The method as claimed in claim 1, wherein the aqueous solution of
unstabilized alkali or alkaline earth metal hypobromite contains
from about 4 to about 15 percent by weight alkali or alkaline earth
metal hypobromite.
The method as claimed in claim 4, wherein the aqueous solution
of unstabilized sodium hypobromite contains from about 1 to about
30 percent by weight sodium hypobromite.

The method as claimed in claim 4, wherein the aqueous solution of
unstabilized sodium hypobromite contains from about 4 to about
15 percent by weight sodium hypobromite.
The method as claimed in claim 7, wherein the pH of the stabilized
aqueous sodium hypobromite solution is from about 8 to about 14.
The method as claimed in claim 8, wherein the pH of the stabilized
aqueous sodium hypobromite solution is from about 1 to about 14,
The method as claimed in claim 9, wherein the molar ratio of the
stabilizer to the sodium hypobromite is from about 0.5 to about 4.
The method as claimed in claim 10, wherein the molar ratio of the
stabilizer to the sodium hypobromite is from about 0.5 to about 2.
A stabilizer aqueous solution of an alkali or alkaline earth metal
hypobromite which is prepared by the steps of:
a) mixing an aqueous solution of alkali or alkaline earth metal
hypochlorite having from about 5 percent to about 70 by weight
percent available halogen as chlorine with a water soluble
bromide ion source;

b) allowing the bromide ion source and the alkali or alkaline earth
metal hypochlorite to react to form a 0,5 to 70 percent by
weight aqueous solution of unstabilized alkali or alkaline earth
metal hypobromite;
c) adding to the unstabilized solution of alkali or alkaline earth
metal hypobromite a stabilizer selected from the group
consisting of carbonic acids, hydrogen cyanide, carboxylic
acids, amino acids, sulfuric acids, phosphoric acids and boric
acids; and,
d) recovering a stabilized aqueous alkali or alkaline earth metal
hypobromite solution.
An industrial water system containing from about 0.05 to about
1000 ppm of the solution as claimed in claim 13,
The stabilized aqueous solution as claimed in claim 13. wherein
the stabilizer is selected from the group consisting of urea,
thiourea, creatinine, cyanuric acids, alkyl hydantoins, mono or di
ethanolamine, organic sulfonamides, biuret, sulfamic acid, organic
sulfamales and in elam ine.

The method as claimed in claim i, wherein the stabilizer is
selected from the group consisting of urea, thiourea, creatinine,
cyanuric acids, alkyl hydantoins, mono or di ethanolamine, organic
sulfonamides, biuret, sulfamic acid, organic sulfamates and
melamine.

A method for preparing a stabilized aqueous alkali or alkaline earth metal
hypobromite solution comprising the steps of: mixing an aqueous solution of
alkali or alkaline earth metal hypochlorite having from about 5 percent to
about 70 percent by weight available halogen as chlorine with a water
soluble bromide ion source; allowing the bromide ion source and the alkali
or alkaline earth metal hypochlorite to react to form a 0.5 to 70 percent by
weight aqueous solution of unstabilized alkali or alkaline earth metal
hypobromite; adding to the unstabilized solution of alkali or alkaline earth
metal hypobromite a stabilizer selected from the group consisting of
carbonic acids, hydrogen cyanide, carboxylic acids, amino acids, sulfuric
acids, phosphoric acids and boric acids; and recovering a stabilized aqueous
alkali or alkaline earth metal hypobromite solution,

Documents:

1304-CAL-1998-FORM-27.pdf

1304-cal-1998-granted-abstract.pdf

1304-cal-1998-granted-assignment.pdf

1304-cal-1998-granted-claims.pdf

1304-cal-1998-granted-correspondence.pdf

1304-cal-1998-granted-description (complete).pdf

1304-cal-1998-granted-examination report.pdf

1304-cal-1998-granted-form 1.pdf

1304-cal-1998-granted-form 18.pdf

1304-cal-1998-granted-form 2.pdf

1304-cal-1998-granted-form 5.pdf

1304-cal-1998-granted-pa.pdf

1304-cal-1998-granted-reply to examination report.pdf

1304-cal-1998-granted-specification.pdf

1304-cal-1998-granted-translated copy of priority document.pdf

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Patent Number

230351

Indian Patent Application Number

1304/CAL/1998

PG Journal Number

09/2009

Publication Date

27-Feb-2009

Grant Date

25-Feb-2009

Date of Filing

27-Jul-1998

Name of Patentee

NALCO CHEMICAL COMPANY

Applicant Address

ONE NALCO CENTER, NAPERVILLE, ILLINOIS

Inventors:

#	Inventor's Name	Inventor's Address
1	ANTHONY W. DALLMIER	1683 KAUTZ ROAD, AURORA, ILLINOIS 60504
2	WILLIAM F. MCCOY	735 THORNAPPLE DRIVE, NAPERVILLE, ILLINOIS 60540

PCT International Classification Number

A6IK 33/14 CO2F 1/50

PCT International Application Number

N/A

PCT International Filing date

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	08/904,375	1997-08-01	U.S.A.