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HomeMy WebLinkAboutWI0600068_Other Correspondence_20101101APPENDIX 3: CASE STUDIES State Coalition for Remediati f Drycleaners (SCRD) - Single Profile lay Page 1 of 5 Site Profiles Publications State Federal Reference Links Comments Site Profiles - View General Information Site Name and Location: Description: Historical activity that resulted In contamination. Contaminants: Contaminants: Contaminants present and the highest amount detected in both soil and groundwater (please avoid giving ranges). Other Contaminants Present: Indicates what other contaminants were found on -site Deepest Significant Groundwater Contamination: Quick-N-Easy Wash-O-Mat and Artistic Cleaners Wichita, Kansas, United States Two former drycleaner facilities are sources within the large multi -source Gilbert -Mosley Site in Wichita, Kansas. The inactive facilities are within a commercial area that is surrounded by residential areas. Quick-N-Easy Wash-O-Mat was a coin - operated laundry with self-service drycleaning, while the Artistic Cleaners was a standard commercial drycleaner service. The Kansas Department of Health & Environment (KDHE) conducted site investigations in 1990 and distinguished the boundaries of the contaminant plumes resulting from the drycleaners separately from the rest of the Gilbert -Mosley Site. KDHE accepted the Quick-N-Easy and Artistic sites into the State of Kansas Drycleaning Facility Release Trust Fund in 1996. Contaminant Conc in GW cis-1,2-Dichloroethene 40 µg/L Tetrachloroethene 1,500µg/L 9,930 µ/kg (PCE) Trichloroethene (TCE) 190 µg/L 25 ft bgs Conc. in Soil http://www.drycleancoalition.org/profiles/display.cfin?id=36 11/1/2010 State Coalition for Remediati f Drycleaners (SCRD) - Single Profile lay Page 2 of 5 Plume Size: 2,000 ft x 400 ft wide x 25 ft Site Hydrology: Depth to Groundwater: Lithology and Subsurface Geology: Conductivity: Gradient: 15 ft bgs Silt and clay, 1-12 ft bgs (clays are tight) Silty sand grading to sand/gravel, 12-40 ft bgs Shale (bedrock), 40 ft bgs 1.68 ft/day ft/day 0.002 ft/ft Pathways and DNAPL Presence: Pathways: DNAPL Presence: Groundwater Soil Yes Remediation Scenario: Cleanup Goals: Reduce PCE and degradation compound groundwater contamination to below Alternate Cleanup Levels (ACL) which are risk -based levels established by the City of Wichita. The ACLs for groundwater in Wichita's Gilbert -Mosley Site are: PCE = 14 µg/L, TCE = 21 µg/L, cis 1,2-DCE = 70. Reduce soil contamination in accordance with KDHE Risk -Based Standards: PCE & TCE = 200 µg/kg, cis 1,2-DCE = 800 mg/kg. Technologies: Technologies Used: Other technologies used: Why the technology was selected: In Situ: Chemical Oxidation Soil Vapor Extraction SVE was chosen due to the presence of buildings and utilities affecting access to the source areas. SVE is normally not a good choice for tight clays, but in this case an inefficient system is better than none at all. Permanganate injection was a new innovative technology that showed good potential so this site was chosen for a pilot test. The property surrounding the buildings was readily accessible for injection rigs and KDHE has a hazardous material storage building in the area allowing proper storage of the permanganate material. http://www.drycleancoalition.org/profiles/display.cfm?id=36 11/1/2010 State Coalition for Remediat f Drycleaners (SCRD) - Single Profile play Page 3 of 5 Date implemented: Final remediation design: 1999 (and continue at present) The contractor installed a SVE system and completed two phases of sodium permanganate injections. The SVE wells targeted three "hot spots." The permanganate injection solution, known as Liquox, is a 40% liquid solution. In Phase I, the contractor diluted Liquox with water to 4%, and used direct push technology methods to inject approximately 757 gal of this solution. The contractor used three injection intervals within each of 33 probes, and injected a total of 25 gal of solution per probe. Injection time lasted 20 50 min depending on the formation intake of the solution. Sampling revealed that PCE concentrations decreased, degradation compound concentrations increased, and then PCE concentrations rebounded. KDHE concluded that the volume and concentration of permanganate was insufficient in Phase I. The contractor then diluted Liquox with water to 15% for Phase II, and injected a total of 1,472 gal. Phase II included six vertical injection intervals within each of 64 probes. The contractor injected approximately 23 gal of solution in each probe. Results and Next Steps: Results to The permanganate injections have not significantly date: reduced overall PCE concentrations, except for in the area of the sewer line release. PCE concentrations rebounded and even increased shortly after both injection phases. The residual DNAPL in the soil appears to inhibit the success of the injection solutions. The source has not been sufficiently removed and continues to serve as a source for groundwater contamination. KDHE has concluded that permanganate desorbed residual DNAPL PCE off of the soil particles and caused it to dissolve in the groundwater causing an initial increase in concentrations. Once the permanganate was completely used, the remaining PCE likely resorbed to the soil particles or remained mobile: Therefore, KDHE believes that insufficient quantities of Liquox may limit the success of the treatment. Natural factors, such as iron and microorganisms, also compete for the permanganate and decrease the quantity available to treat the contaminants. SVE appears to be effective, but relatively tight clays prevent a large radius of influence around the SVE wells. SVE has no impact on the permanganate http://www.drycleancoalition.org/profiles/display.cfin?id=36 11/1/2010 State Coalition for Remediat f Drycleaners (SCRD) - Single Profile lay Page 4 of 5 Next Steps: injections. KDHE has continued to evaluate sampling events, and will use these results to determine the next cleanup steps. The most recent sampling event revealed PCE concentrations up to 530 µg/L, TCE concentrations up to 85 µg/L, and cis-1,2-DCE concentrations up to 30 lam-• New larger diameter SVE wells (2 - 3 feet diameter) are proposed. THe wells will be installed using a cable -tool rig or bucket auger rig. Costs: Cost for $23,033 Assessment: Cost to $105,718 Design and Implement: Cost for $61,928 Operation and Maintenance: Total Costs for Cleanup: Lessons Learned: Lessons Learned: 1. It is absolutely essential to remove the source prior to permanganate treatment events. Once the permanganate solution was used up, the source continued to release PCE. The volume and concentration of Liquox, therefore, was insufficient to treat the contamination. Substantially increased volumes may cause the technology to be cost prohibitive with limited budgets. 2. The sodium permanganate injection pilot study provided enhanced groundwater monitoring, therefore the O&M costs with this site are higher than normal. 3. KDHE also identified difficulty associated with injection process. Although the contractors were able to use standard probe rod diameters, there was nothing to prevent upward movement along the sides of the rod. This posed occasional problems. KDHE has requested the contractor to provide better injection method to seal the annulus space around the probe rods. 4. Sodium, manganese, and chloride levels were elevated following the sodium permanganate injections. Some levels initially exceeded allowable http://www.drycleancoalition.org/profiles/display.cfm?id=36 11 / 1/2010 State Coalition for Remediati f Drycleaners (SCRD) - Single Profile lay Page 5 of 5 Contacts: Principal Point of Contact: levels, but quickly reduced to acceptable levels. 5. Standard auger -installed SVE wells may have smeared borehole walls which negatively influenced the SVE systems abilities. 6. 7. 8. Bob Jurgens KDHE Bureau of Environmental Remediation Curtis Bldg., 1000 SW Jackson, Suite 410 Topeka, KS 66612-1367 785-291-3250 bjurgens@kdhe.state.ks.us Contractors: Alan Rittgers, Project Manager Burns and McDonnell 9400 Ward Parkway Kansas City, MO 64114 816-822-3893 email:arittge@burnsmcd.com Todd Anderson, P.G., Project Geologist BE&K/Terranext 13202 West 98th Street Lenexa, KS 66215 913-894-4000 email: tanderson@bektnxt.com Site Specific References: Site Specific References: Images: Images of Site: http://www.drycleancoalition.org!profiles/display.cfm?id=36 Profile last updated on Apr 03, 2006 http://www.drycleancoalition.org/profiles/display.cfm?id=36 11/1/2010 APPENDIX B - Case Studies 1. Former Garden City Laundry and Cleaning Company, 7th Street Site, Garden City, KS Background The former Garden City Laundry and Cleaning Company was located at 410 North 8th Street in GadenCity,Kansas. This dry-cleaning establishment was in operation from 1952 to 1970, and was demolished in the mid-1970s. Releases of perchloroethylene (PCE) occurred through spills and generally poor operating procedures after the facility switched from petroleum -based (stoddard) solvents to PCE. The contamination was discovered by testing Garden City Public Water Supply (PWS) well 18 for volatile organic compounds (VOCs) in January, 1986, as part of a state-wide effort to test PWS wells for VOCs. Further sampling of PWS well 18 was done in 1993 as part of a preliminary assessment (PA) and screening site inspection (SSI). An expanded site investigation (ESI) involving additional sampling and collection of background information on site activities was conducted in 1995. This ESI identified the Garden City Laundry as the source of the; contamination inPWSwell 18. Levels of PCE in this well have remained relatively steady, below the 5 microgram p er liter (ug/L) maximum contaminant level (MCL). After the ESI was completed, the site was tiansfenedtothe State Dry-cleaning Trust fund in 1995. Further characterization of the groundwater plume was done by the Dry-cleaning Trust fund in 1997-1998 as a follow-up to the ESI. Site Hvdrogeoloav The surface geology around the site consists of sandy loam soils of the Las Animas association, undaainby as much as 56 feet of sand and gravel alluvial deposits which make up the upper aquifer beneath the site. The samples containing PCE were taken from this upper aquifer. This alluvium overlies a confining layer of silt approximately 30 to 60 feet thick, with a vertical conductivity of 0.01 to 0.0001 feet per day. Beneath the confining layer is a lower aquifer of stratified sands and gravel with some clay and silt. This lower aquifer is more than 100 feet thick and includes the Oglblaaquifer, which supplies most of the PWS wells in Garden City. The hydraulic conductivity of the lower aquifer has been calculated at 80 to 150 feet per day. Beneath the lower aquifer is bedrock of Cretaceous age consisting primarily of shales and limestones, although some sandstone lenses ampiesentin the bedrock and are tapped by a few wells. Bedrock is found 250-300 feet below ground surface (bgs). The Arkansas River is located approximately three-quarters of a mile south of the site. Groundwater flow direction in the shallow aquifer, in the vicinity of the site, appears to be towards oneofthePWS wells, apparently due to the well's cone of depression in the water table. The water table is found approximately 20 feet bgs. Groundwater flow direction in the deep aquifer is to the south. Receptors Impacted Most of the population of Garden City (27,036 persons as of 1995) receives water from 11 PWS wells.Noneof these wells provide more than 40% of the total water supply, so contamination from PWSwells 10 and 18 is substantially diluted before reaching any receptors. Numerous private and community wells exist within four miles of the site; water from these wells, if impacted by contaminants from the site, would not be treated or diluted prior to consumption by receptors. Remedial Objectives Investigation by KDHE defined the extent of the PCE plume migrating away from the site and its concentration gradient. Pumping ofPWS well 18 is drawing the plume towards the well, indicating that PCE concentrations in the well may increase over time. Therefore, the objective was to install B1 a treatment system across the central, high -concentration lobe of the plume to halt its advance and reduce concentrations in the distal portions of the plume. Selection of Teclmoloav and Desien Parameters This site was selected for implementation of innovative remedial technology, in the form of in situ chemical oxidation, because the contamination plume was relatively small and well-defined, and the subsurface geology was simple, well characterized, and suitable for the process. The high hydraulic conductivity of the contaminated aquifers simplifies the delivery of oxidants to the affected zones. The site's hydrogeology is relatively simple and well-defined, so very little untreated contaminant shouldmnain in impermeable zones, minimizing the potential for contaminant rebound after in situ treatment ceases. Ozone sparging, combined with soil vapor extraction, was chosen as the remedial technology to serve as a technology demonstration project. The equipment selected consists of a KV Associates C-Sparger control system with dual Spargepoint wells. These wells combine dual ozone sparging points, dual well screens, inflatable packer, and a recirculating pump. During operation, ozone is released fast from the lower spargep oint, then the upper. Following these two sparging intervals, the in-wellpump is activated to circulate ozonated water surrounding the well through the two screened intervals, increasing the well's radius of influence. This cycle is repeated for each well in series. Soil vapor extraction was implemented by connecting a suction line to the top of the four -inch C- sparge well to extract excess ozone and gaseous breakdown products of PCE bubbling out of the saturated zone. SVE control equipment, also supplied by KV Associates, consisted of a vacuum blowerexhausting all four wells in parallel, with a flowmeter and pressure gauge to monitor system p erformance. Implementation of Technology A linear array of four sparging/ SVE wells was placed across the path of the highest -concentration portion of the advancing plume, spaced at 60-foot intervals. The radius of influence of these wells were determined to overlap, based on SVE vacuum tests of one of the wells which created differential pressures in all other wells. Two nearby monitoring wells were installed to help charactaizetheeffectiveness of the remediation. The system was brought on-line in August of 1998. The ozone -air mixture was supplied to the sparging wells (one at atime) at approximately 2 cubic feet per minute, at pressures of 5-10 psi, with an ozone concentration of 1.5-2.5 ppm. Operational Performance and Problems The performance of this system cannot be adequately determined, due to numerous equipment failures that prevented the system from working for more than a few days or weeks at a time. Most ofthesefaiures were attributable to the C-Sparger control system. The control unit is very complex and installed in a relatively3small enclosure that led to overheating problems. In addition, the ozone compressor created substantial vibration, which caused failures of electronic components, electrical connections, and mechanical fittings. Follow-up sampling to evaluate reductions in PCE concentration have not yet been conducted. Costs Purchasing installing, and maintaining the components of the C-Sparger and SVE systems, as well as twornonitoring wells near the linear sparging/ SVE array, cost approximately $81,000. Costs can be broken down as follows: C-Sparger controller, SVE controller, and downhole components - $31,000 B2 Installation of four sparge wells and two monitoring wells - $25,000 Operation, maintenance, and repairs, August 1998-December 1999 - $25,000 Follow-up Activities After extensive consultation with KV Associates on the design of their C-Sparger controller, the manufacturer changed the design to better isolate the mechanical and electrical components from each other. The controller is now housed in two separate enclosures. The new controller was installed at the site in January 2000. Minor adjustments have been performed on the system, and it is currently operating. Follow-up sampling for preliminary evaluation of the system's ability to remediate the plume will be conducted in the near future. Point of Contact M. Saqib Khan Kansas Department of Health and Environment (785) 296-8025 2. 25th and Main Dry Cleaning Site, Hutchinson, KS Background The25°iandMainsite in Hutchinson encompasses three former facilities at two locations: the former IdealClonnas at 2500 N. Main, the former American Uniform at 2500 N. Main, and the former One HourMartinizing at 2522 N. Main. Public water supply (PWS) wells in Hutchinson were tested for volatileorgmic compounds (VOCs) in 1982 as part of a statewide effort, and PWS wells 2, 8, 9, and 12waefound to contain perchloroethylene (PCE). PWS wells 9 and 12 were removed from service in 1989 due to levels of PCE in excess of the federal maximum contaminant level (MCL). KDHE conducted a PA/SI on PWS well 12 in 1991 and PWS well 9 in 1992, which identified the dry -clew ingfaciilities at 25th and Main as one potential source of PCE contamination in groundwater. Ane anded site investigation (ESI) of these wells was completed in 1993 to better define the site hydrogeology and the extent of the contaminant plume. The site was transferred to the State Dry- cleaning Trust fund in 1995. In 1998, this site was chosen to implement a pilot test of KV Associates' C-Sp arge ozone sparging system. The objective of the initial test phase was to determine the efficiency of removal with this technology, its radius of influence around the spargingwell, and other parameters necessary to plan a full-scale installation. A four -inch ozone spargingwell was drilled to a depth of 35 feet, and five two-inch monitoring wells were drilled at different distances from the well and screened at progessively deeper depths, to determine the radius of influence of the C-Sparge well and its effect on the downgradient concentrations of PCE. System operation started June 10, 1998. Aflatlmz days of system operation, fine bubbles of air/ozone were observed in all wells within 40 feet, indicating the well created a substantial radius of influence. Sampling of the sparging well and monitoring wells occurred daily for the first five days of operation, and approximately biweekly thereafter, concluding on August 27, 1998. Data on PCE concentration and dissolved oxygen from thesesamp les indicated the system was remediating a portion of the plume. Estimates of the radius ofinfluence, based on the site hydrogeolog' and samp ling results, indicate that the well could treat an elliptical region 90 feet long (in the direction of flow), 80 feet wide, and 50 feet deep. Based on these results, a full-scale ozone sparging system was designed and installed. B3 GET Innovative EavironsnenaU 7irhnok's, Inc Project Summary Former Dry Cleaning Facility, TN A former dry cleaning facility in central Tennessee was targeted for chemical oxidation due to the high concentrations of tetrachloroethene (PCE) and trichloroethene (TCE). The remedial plan addressed the concentrations of all chlorinated compounds in the source area. The dosage calculations took into account both the sorbed and dissolved fractions within each targeted area as well as well as the naturally occurring oxidizer demand and longevity of the MnO4 species. IET recommended that two permanent, two inch, injection wells be installed, screened both into the bedrock solution cavities and the soil bedrock interface as shown below and that two of the existing wells be converted to injection points. The remedial design addressed contamination present from 60-70 feet bgs, a dark red moist, silty clay that was determined to be a source of contamination. Remediation Plan Four permanent injection points were utilized to emplace the chemical oxidant into the subsurface. IET chose to utilize a powdered, pharmaceutical grade, high purity KMnO4 suspended in a NaMnO4 solution for injections occurring in the saturated zone. As a result of the maximum 3% solubility of the KMnO4, the addition of KMnO4 to a solution of soluble NaMnO4 provides a long lasting source of oxidant due to the in -situ concentration present in the subsurface that is below the 3% solubility of the material. The granular KMnO4 serves as a longer -term MnO4 release agent in the injection areas thus allowing for prolonged substrate oxidation. IET delivered the oxidants as a colloidal suspension allowing for uniform and effective delivery of the dual oxidant slurry. Results from the injection event indicate that the remedial materials were successfully emplaced in the subsurface, with no surfacing. CVOC concentrations have decreased substantially from the pre -injection baseline sampling event. (9 : hepure. - te technologies inc innovative solutions for groundwater treatment MSDS: Sodium Permanganate (40%) DATE ISSUED- 12104 SECTION 1 - CHEMICAL, PR )J)UCT IDENT1FTgATTON PRODUCT NAME: •Sodium Permangin*te Solution DESCRIPTION: •40%minimum as NaMnO4 SKTION 2 - cOMEQSIT[QN /XNFORMA,TIQN QN INGEWET CI1EMICAL NAME 70 TIN, ' Sodium Permanganate 40-42 Zmg Mn per cubic • • rnettr of air SWTION 3 - HAZARDS IDE fEWCATION EMERGENCY OVERVIEW: • EFFECTS OF OVEREXPOSURE EYES: SKIN: INGESTION: INHALATION: EFFECTS OF OVEREXPOSURE CAS No, *10101-50 5 - ACUTE *Sodium Permanganate is damaging to eye tissue on contact. It may cause bums that result in damage to the eye. *Momentary contact of solution at room temp may be irritating to the skin. (caving brown stains. • I f swallowc4may case burns to mucous membranes of the mouth,throat,csophagus, and stomach "May cause irritation to the respiratory tract - CHRONIC • PRIMARY ROUTE OF ENTRY: • SECTION 4 - FIRST AIL) ISIDIASURES EYES: SKIN: INGESTION: INHALATION: 'PHYSICIANS NOTE: *Flush immediately wilt large amounts of water for at least t 5 minutes. Seek medical attention immed'arcly. *Wash contaminated u+tet with water. Sock medical attention if irritation persists. *If person is conscious, give large amounts of water or milk. Seek medical nttention. • Remove person from contaminated area to fresh air. Seek medical attention. *Decomposition products are alkaline, SECTION S - FIRE- FIGHTING MEASURES FI ASHPOINT: FLAMMABILITY: AUTOFLAMMASILITIY: EXPLOSION HAZARD: EXTINGUISHING MEDIA: "None •Nonflammable 'None EXPLOSIVE LIMITS: LOWER: n'a UPPER:n/a 'Explosive in contsct with sulfuric acid or pc oxides,or readily oxidizable substances Use large amounts ofwater. Duce to contain. EMERGENCY: Chemtrec - 1-800-424-9300 (6) hpdre9- technolo ies inc innovative solutions for groundwater treatment SPECIAL EXPOSURE HAZARDS IN FIRE: Keep containers cool by spraying with water if exposed to fin:. SPECIAL PROTECTIVE EQUIPMENT FOR A FIRE: Self-contained breathing apparatus should be worn. EGS14N 6 - ACCIDENTAL RELEASE MEASURES ENVIRONMENTAL PRECAUTIONS: *Contain spill by collecting the liquid in a pit or holding behind a dam. Dilute to approx 6% solution with water and then reduce with sodium thiosulfatc,a bisulfate or ferrous Nall solution. METHODS FOR CLEANUP: "Flush with abundant water into the sewer. if permitted by fcdcral.st❑te, and local authorities. IFnot,collccd and treat as above, SECTION 7 - HANDLJNG AND STOIUGZ HANDLING: `Wash hands thoroughly with soap and water after handling. STORAGE: 'Store in a cool, well -ventilated arch. Segregate from acids.peroxIdes, Formaldehyde,and all combustible..ortrnic or easily oxidized materials. SECT1ON $ - EXPOSURE. CONTROL / PER9NAL PROTi1r,Ci'ION ENGINEI?RiNG CONTROLS: General ventilation is recommended. Eyewash and safety shower stations must be located in the immediate area. EXPOSURE GUiDELTNES: not established PERSONAL PROTECTION EQUIPMENT: RESPIRATORY:NIOSH-approved self-contained breathing apparatus for exposure to levels above limits. HAND: Rubber gloves and boots. EYE: Chemical goggles which are splash and dust proof or face 5hicld. SKIN: if clothing is contaminated_ wash skin and launder cfothinG. NOTE: REFORE EATING, DRINKING OR SMOKING. WASH FACE AND HANDS l'HOROIJGHi..Y WITH SOAP AND WATER. SECTION 9 - i'HYSICAi. AND CHEMICALtROl'ERTIIES PHYSICAL STATE, COLOR AND ODOR: *Purple Solution PH as is: •5-7 BOIL.JNG POINT: *105 degrees C FLASH POINT: VAPOR PRESSURE: •760 rmn Ng @ 105 degrees C SPECIFIC GRAVITY: '1.36-1.39 SOLURELiTY iN WATER: 'Miscible in all proportions viSCOSITY: - EMERGENCY: Chemtrec - 1-800-424-9300 6 hptJre technolog ies inc SECTION 10 - STABILITY AND REACTIVITY innovative solutions for groundwater treatment HAZARDOUS POLYMERIZATION: "material is not known to polymerize CHEMICAL STABILITY: 'Stable under normal conditions CONDITIONS TO AVOID: `contact with incompatible materials or hcat(275• 1) MATFRIAI.S TO AVOID: •Acids,peroxides,formaldehyde.antifree7z,hydraulic fluids,and all combustible organic or readily oxidiznb[e materials HAZARDOUS DECOMPOSITION PRODUCTS: ''may form corrosive fumes in n the SECTION 11 - TOXICOU)GICAL INFORMATION ACUTE TOXICITY: IRRITANCY: SENSITIZATION: irritating to body tissue with which it comes into contact SUB -ACUTE., SUB -CHRONIC AND PROLONGED TOXICITY:No known cases of chronic poisoning due to permanganates have been reported. EMPIRICAL DATA ON EFFEC IS ON HUMANS: has not been classified as a carcinogen by OSHA.NTP.IARC SECTION 12 - ECOLOGICAL INFORMATION PERSISTENCE IN THE ENVIRONMENT:Permanganate has a low estimated lifetime in the envirornent BIOLOGICAL OXYGEN DEMAND:In non -reducing and non -acidic environments MnO2 is insoluble CHEMICAL OXYGEN DEMAND: AQUATIC TOXICITY: No data Daphnia mama Fathead minnow OTHER INFORMATION: ` Discharge of this product mutt be in accordance with all federal, state, kcal or other applicable laws and regulations. SECTOOI( 13 - DISeOSAJ CQNSWER, LTIOTVS DISPOSAL METHOD: *Ts considered a D001 hazardous (ignitable) waste.For disposal, see section 6 SECTION 14 - 'TRANSPORTATION INFORMATION DOT SHIPPING NAME: Pcrmanganates,rnorganic,aqucous solution.n.o.s. UN Number: UN3214 DOT HAZARD CLASS: Oxidizer 5. I PACKING GROUP; TI SECTION 15 REGULATORY INFORMATION TOXIC SUBSTANCES CONTROL ACT (TSCA): All components of this product are listed in the Toxic Substances Control Act inventory. COMPREHENS1VF ENVIRONMENTAL RESPONSE, COMPENSATION AND LIABILITY ACT (CERCLA): Not Listed SUPERPUND AMENDMENTS AND REAUTHORIZATION ACT (SARA'fide 111)- Section 311 Hazard Cntegodes:302/303 not listed 311/312 hanard Catagorios: Firc.acnte and chronic ERGENCY: Chemtrec - 1-800-424-9300 h4pure- 9 technolo ies inc innovative solutions for groundwater treatment toxicity Section 313 contains 20a/. manganese compounds as part of the chemical stnictnre and is subject to the reporting requirtMents section313 of title III Acute Health: Vex Chronic Health: Na Fitt: No Sudden Release of Pressure: No Reactive: No SUPERFUND AMENDMENTS AND REAUTHORIZATION ACT (SARA Title Ili) Section 3 11: Components of this product subject to reporting: none s1 c 1JON tb - 10N HMIS RATINGS HEALTH: 1 FLAMMABILITY: 0 REACTIVITY: 0 SPECIAL HAZARD: Oxidizer The inror'Rmtion and revornntendrttr0tt contained in ibis M.razs! Safety Data $hcxt rove boos complied From uwnxs believed !o be rehab} and to rcpaxent the hest opinion am the subject as of the date on rick skeet However. no minty, bataranMe of ropecsentvina, cxprefaod ar irnp!icd, i< enndo by 172 Int i .trios (.LC., ns io the eor:ocnteeax cv,trfTrtkney of ►hie information or to dre rC_culm !o be nhraiiaad from the use sh rct . EMERGENCY: Chemtrec - 1-800-424-9300 HAZARDOUS DECOMPOSITION PRODUCTS : HAZARDOUS POLYMERIZATION CONDITIONS TO AVOID : N/A = NOT APPLICABLE he�urem technologies inc TRADE NAME : CAS NUMBER : SYNONYMS: CHEMICAL FAMILY FORMULA : innovative solutions for groundwater treatment MSDS: Potassium Permanganate COMPONENT SECTION A - PRODUCT INFORMATION POTASSIUM PERMANGANATE, TECHNICAL GRADE REVISION DATE : JUNE 7, 2006 7722-64-7 PERMANGANATE OF POTASH; CHAMELEON MINERAL; PERMANGANIC ACID, POTASSIUM SALT OXIDIZERS KMn04 SECTION B - HAZARDOUS COMPONENTS CAS NO. POTASSIUM PERMANGANATE 7722-64-7 (AS INORGANIC MANGANESE COMPOUND CONTAINING 34-35% Mn) 98% MIN. PELJTLV 5 mg/m3 as Mn - OSHA CEILING LIMIT 0.2 mg�/m3 as Mn - ACGIH TWA 0.2 rrg/m as Mn Fume - ACGIH TWA SECTION C - PHYSICAL PROPERTIES BOILING POINT (°C) : MELTING POINT (°C) : VAPOR PRESSURE (mm Hg) : VAPOR DENSITY (AIR=1) SOLUBILITY IN WATER : ODOR THRESHOLD: APPEARANCE & ODOR : N/A DECOMPOSES AT < 240 NOT KNOWN! N/A SOLUBLE, 6.38 g/100cc @ 200°C N/A DARK PURPLE CRYSTALS WITH METALLIC LUSTER: ODORLESS SPECIFIC GRAVITY : FREEZING POINT (°) : PERCENT VOLATILE (BY WT.) : EVAPORATION RATE : pH ( % IN WATER) : SECTION D - FIRE & EXPLOSION DATA 2.7 N/A N/A N/A NOT KNOWN FLASH POINT (°) : N/A FLAMMABLE LIMITS : LEL : (N/A) UEL : (N/A) AUTO IGNITION TEMP (° F): (N/A) EXTINGUISHING MEDIA : WATER : (X) FOAM : () CO2: () DRY CHEMICAL: () SPECIAL FIRE FIGHTING PROCEDURES : PRODUCT IS NOT COMBUSTIBLE BUT IS A STRONG OXIDIZER. CONTACT WITH OXIDIZABLE SUBSTANCES, EITHER IN THE SOLID OR DRY STATE, CAN CAUSE EXPLOSIVE AND OR FLAMMABLE REACTIONS. EXTINGUISH FIRE WITH LARGE QUANTITIES OF WATER. DIKE TO CONTAIN RUNOFF. WATCH FOR RAPID BURNING AND BE PREPARED TO RETREAT TO A SAFE DISTANCE. POISONOUS GAS IS PRODUCED IN FIRE - WEAR A NIOSH APPROVED SELF-CONTAINED BREATHING APPARATUS OPERATED IN PRESSURE DEMAND OR POSITIVE PRESSURE MODE AND FULL PROTECTIVE GEAR. CONTAINERS MAY EXPLODE IN FIRE. COOL FIRE EXPOSED CONTAINERS WITH FLOODING QUANTITIES OF WATER SPRAY. UNUSUAL FIRE & EXPLOSION HAZARDS : STRONG OXIDIZERS MAY EXPLODE AND DECOMPOSE SPONTANEOUSLY IF EXPOSED TO INTENSE HEAT, CONCENTRATED ACIDS, HYDROGEN PEROXIDE, REDUCING AGENTS OR ORGANIC SUBSTANCES. VIOLENT REACTION MAY OCCUR WITH FINELY DIVIDED AND READILY OXIDIZABLE SUBSTANCE. INCREASES FLAMMABILITY OF COMBUSTIBLE MATERIALS. SECTION E - REACTIVITY DATA STABILITY : STABLE UNDER NORMAL CONDITIONS INCOMPATIBILITY : POTASSIUM PERMANGANATE IS A STRONG OXIDIZER, SPONTANEOUSLY EXPLOSIVE OR FLAMMABLE ON CONTACT WITH MANY INCOMPATIBLES. AVOID CONTACT WITH ALCOHOLS. ARSENITES, IODIDES, ACIDS, CHARCOAL, COMBUSTIBLE ORGANIC MATERIALS, FERROUS AND MERCUROUS SALTS, HYPOPHOSPHITES, HYPOSULFITES, SULFITES, PEROXIDES, OXALATES, INORGANIC OXIDIZABLE MATERIALS, METAL POWDERS, WOOD, GLYCERINE, POLYPROPYLENE, AND HEAT. CONTACT WITH HYDROCHLORIC ACID WILL LIBERATE CHLORINE GAS. DO NOT MIX WITH FORMALDEHYDE. TOXIC, CORROSIVE FUMES OF K10 AND/OR SMOKE MAY EVOLVE WHEN IN A FIRE WILL NOT OCCUR CONTACT WITH INCOMPATIBLE MATERIALS; EXCESSIVE HEAT (>150°C); PHYSICAL IMPACT OR FRICTION EMERGENCY: Chemtrec - 1-800-424-9300 hepure- tec9hnolo ies inc SECTION F - PERSONAL PROTECTIVE EQUIPMENT INFO RESPIRATORY EQUIPMENT : PROTECTIVE GLOVES : EYE PROTECTION : VENTILATION : OTHER PROTECTIVE EQUIPMENT : THRESHOLD LIMIT VALUE : PRIMARY ROUTES OF EXPOSURE : ORAL LD,0 : DERMAL IRRITATION -RABBIT : EYE IRRITATION -RABBIT : OSHA PEL : ACGIH TLV : EFFECTS OF OVEREXPOSURE : KNOWN EFFECTS ON OTHER ILLNESSES : LISTED CARCINOGEN : innovative solutions for groundwater treatment USE A NIOSH/MSHA DUST AND MIST RESPIRATOR OR AN AIR SUPPLIED RESPIRATOR WHERE THE POTENTIAL FOR OVEREXPOSURE EXISTS. RUBBER OR PLASTIC GLOVES CHEMICAL GOGGLES OR FACE SHIELD USE MECHANICAL OR LOCAL EXHAUST TO MAINTAIN EXPOSURE BELOW THE PERMISSIBLE EXPOSURE LIMIT OR THRESHOLD LIMIT VALUE (SEE SECTION B). PROTECTIVE WORK CLOTHING INCLUDING AN APRON; ACCESS TO EYE WASH FOUNTAIN AND SAFETY DRENCH SHOWER. SECTION G - HEALTH HAZARD DATA 0.2 mg/m3 as Mn (INORGANIC MANGANESE COMPOUND) and Mn FUME EYES & SKIN CONTACT, INHALATION, INGESTION 1090 mg/kg (RAT); 780 mg/kg MALE RAT; 525 mg/kg FEMALE RAT; ORAL -HUMAN LDLo: 143 mg/kg NOT TESTED NOT TESTED 5 mg/m3 AS Mn CEILING LIMIT 0.2 mg/m3 as Mn (INORGANIC MANGANESE COMPOUND) and Mn FUME SKIN CONTACT: CONTACT WITH DRY CRYSTALS OR CONCENTRATED SOLUTIONS WILL IRRITATE AND ACT AS A CORROSIVE, CAUSING BURNS TO SKIN AND BODY TISSUE ON CONTACT. CONTACT AREA WILL BE STAINED BROWN AND THE OUTER LAYER OF SKIN WILL POSSIBLY HARDEN. EYE CONTACT: CONTACT WITH EYES CAN CAUSE SEVERE BURNS RESULTING IN EYE DAMAGE. INHALATION: INHALATION OF DUST, MIST. OR SOLUTION SPRAY WILL IRRITATE NOSE, THROAT, AND RESPIRATORY TRACT CAUSING COUGHING, CHEST TIGHTNESS, AND POSSIBLE DAMAGE TO THE RESPIRATORY SYSTEM. HIGH INHALATION EXPOSURES CAN CAUSE A BUILDUP OF FLUID IN THE LUNGS (PULMONARY EDEMA) WHICH MAY RESULT IN DEATH. INGESTION: INGESTION CAN CAUSE SEVERE IRRITATION OR BURNS TO MOUTH, THROAT, ESOPHAGUS, AND STOMACH WITH DIFFICULTY IN BREATHING. NAUSEA, GASTROINTESTINAL EFFECTS, AND POSSIBLE KIDNEY DAMAGE. EXPERIMENTAL REPRODUCTIVE AND MUTATION DATA HAVE BEEN REPORTED IN LITERATURE. CHRONIC: REPEATED OR PROLONGED SKIN CONTACT MAY CAUSE DEFATTING AND DERMATITIS. LONG TERM INHALATION OF MANGANESE DUSTS (USUALLY IN FORM OF MANGANESE OXIDES) MAY LEAD TO A HIGH INCIDENCE OF UPPER RESPIRATORY INFECTIONS, LUNG IRRITATION, AND POSSIBLE CENTRAL NERVOUS SYSTEM DISORDERS WITH SYMPTOMS SIMULATING PARKINSON'S DISEASE. CAN AGGRAVATE PRE-EXISTING SKIN, RESPIRATORY, AND NERVOUS SYSTEM CONDITIONS. NONE (X) OSHA () NTP () IARC () OTHER () SECTION H - EMERGENCY & FIRST AID DATA SKIN : CAN CAUSE IRRITATION OR BURNS. WASH AREA IMMEDIATELY WITH LARGE AMOUNTS OF WATER WHILE QUICKLY REMOVING CONTAMINATED CLOTHING. SEEK MEDICAL ATTENTION. EYES : CAN CAUSE SEVERE BURNS RESULTING IN PERMANENT DAMAGE. FLUSH EYES WITH LARGE AMOUNTS OF WATER FOR AT LEAST 15 MINUTES, LIFTING UPPER AND LOWER LIDS. DO NOT USE A CHEMICAL ANTIDOTE. SEEK MEDICAL ATTENTION IMMEDIATELY. INHALATION : REMOVE THE PERSON FROM EXPOSURE. BEGIN RESCUE BREATHING IF BREATHING HAS STOPPED AND CPR IF HEART ACTION HAS STOPPED. SEEK MEDICAL ATTENTION IMMEDIATELY. MEDICAL OBSERVATION IS RECOMMENDED FOR 24 TO 48 HOURS AFTER BREATHING OVEREXPOSURE, AS PULMONARY EDEMA MAY BE DELAYED. INGESTION : CAN CAUSE BURNING OF THROAT, NAUSEA, VOMITING AND STOMACH PAIN. A TRACHEOTOMY MAY BE REQUIRED IF SWELLING IN THROAT BLOCKS AIR. IF CONSCIOUS AND NOT CONVULSING, GIVE LARGE QUANTITIES OF WATER. SEEK MEDICAL ATTENTION IMMEDIATELY. SECTION I - SPILL & DISPOSAL INFORMATION STEPS TO BE TAKEN IN CASE OF SPILL OR LEAK: WEAR FULL PROTECTIVE EQUIPMENT (SEE SECTION 8). RESTRICT ACCESS TO AREA OF SPILL / LEAK UNTIL CLEAN UP IS COMPLETE. REMOVE ALL COMBUSTIBLE MATERIALS FROM AREA. ABSORB SOLUTION SPILLS (LIQUIDS) IN VERMICULITE, DRY SAND, EARTH, OR A SIMILAR MATERIAL AND DEPOSIT IN SEALED CONTAINERS. SWEEP OR SHOVEL UP POWDERED/CRYSTALLINE MATERIAL. AVOID GENERATING DUST. TRANSFER TO CLEAN METAL DRUM FOR DISPOSAL AS RCRA HAZARDOUS WASTE. FLUSH SPILL AREA WITH ABUNDANT QUANTITIES OF WATER. KEEP RUNOFF FROM ENTERING SEWERS OR WATERWAYS TO PREVENT A POSSIBLE EXPLOSION HAZARD. CONTACT THE DEP AND EPA FOR SPECIFIC RECOMMENDATIONS ON DISPOSAL. WASTE DISPOSAL INFORMATION: DISPOSE OF AS HAZARDOUS WASTE IN ACCORDANCE WITH LOCAL, STATE (DEP) AND FEDERAL REGULATIONS (EPA). RCRA HAZARDOUS WASTE . NO () YES (X) RCRA N : (D001, D003) CHARACTERISTIC OF IGNITABILITY, REACTIVITY N/A = NOT APPLICABLE EMERGENCY: Chemtrec - 1-800-424-9300 hepure technologies inc CERCLA : NO () YES (X) RQ (100 LBS.) FOLLOW ALL LOCAL, STATE AND FEDERAL INFORMATION AND REGULATIONS SECTION J • OTHER REGULATORY INFORMATION innovative solutions for groundwater treatment TSCA: WE CERTIFY THAT ALL COMPONENTS OF THIS PRODUCT ARE REGISTERED UNDER THE REGULATIONS OF THE TOXIC SUBSTANCES CONTROL ACT. SARA TITLE 111, SECT. 313: LISTED (X) NOT LISTED () HMIS: HEALTH (3) FLAMMABILITY (0) REACTIVITY (3) DOT REGULATED: YES: (X) NO: () RQ: (100 LBS.) IF REGULATED, PROPER SHIPPING NAME: POTASSIUM PERMANGANATE HAZARD CLASS: (5.1) IDENTIFICATION NO: (UN1490) PACKING GROUP: (II) LABEL REQUIRED: (OXIDIZER) INLAND BIL: RQ, POTASSIUM PERMANGANATE, 5.1, UN1490, PACKING GROUP II, OXIDIZER EMERGENCY RESPONSE GUIDE NO.: (140) SECTION K • SPECIAL PRECAUTIONS FOR INDUSTRIAL USE ONLY HANDLING & STORAGE INFORMATION: PROTECT CONTAINERS FROM PHYSICAL SHOCK AND DAMAGE. MUST BE STORED TO AVOID CONTACT WITH STRONG ACIDS (SUCH AS HYDROCHLORIC, SULFURIC AND NITRIC); ANY ORGANIC MATERIAL; OR ANY OTHER COMBUSTIBLE OR OXIDIZABLE SOLID, LIQUID OR GAS SINCE VIOLENT REACTIONS OCCUR. AVOID STORAGE ON WOODEN FLOORS. ISOLATE FROM ALL HEAT AND IGNITION SOURCES. STORE IN TIGHTLY CLOSED CONTAINERS IN A COOL WELL -VENTILATED AREA. OTHER PRECAUTIONS : DO NOT EAT, SMOKE OR DRINK WHERE POTASSIUM PERMANGANATE IS HANDLED, PROCESSED, OR STORED. WASH THOROUGHLY BEFORE EATING OR SMOKING. DO NOT DRY SWEEP FOR CLEAN UP. USE A VACUUM OR A WET METHOD TO REDUCE DUST DURING CLEANUP. TREAT EMPTY CONTAINERS OF THIS PRODUCT AS HAZARDOUS SINCE THEY MAY STILL CONTAIN PRODUCT RESIDUES. IN ACCORDANCE WITH GOOD PRACTICES OF PERSONAL HYGIENE. HANDLE WITH DUE CARE AND AVOID ANY UNNECESSARY CONTACT WITH THIS PRODUCT THIS INFORMATION IS BEING SUPPLIED TO YOU UNDER OSHA "RIGHT TO KNOW' REGULATION 29 CFR 1910.1200 AND IS OFFERED IN GOOD FAITH AS TYPICAL VALUES AND NOT AS PRODUCT SPECIFICATION. THE INFORMATION IS BELIEVED TO BE TRUE AND ACCURATE. NO WARRANTY. EXPRESSED OR IMPLIED. REGARDING THE ACCURACY OF THIS DATA, THE HAZARD CONNECTED WITH USE OF THE MATERIAL, OR THE RESULTS TO BE OBTAINED FROM THE USE THEREOF. IS MADE UNITED MINERAL 8 CHEMICAL CORPORATION AND ITS SUPPLIERS ASSUME NO RESPONSIBILITY FOR DAMAGE OR INJURY FROM THE USE OF THE PRODUCT DESCRIBED HEREIN. UNITED MINERAL 8 CHEMICAL CORPORATION EMERGENCY: Chemtrec - 1-800-424-9300