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<br />t 19. The analyses presented in Appendix F indicates that the material was <br />ground to -10 mesh and thoroughly blended. The textural analyses of <br />the tailing material presented in Appendix D indicated that <br />approximately 81Y of the whole tailing were smaller than 200 mesh. The <br />tailing analyses conducted to determine resulting water quality may <br />therefore not be representative of the final tailing due to the <br />variation in particle size. Please address. <br />Response: The tailings materials used in the tests were actual tailings <br />' generated from small scale mill processing in Battle Mountain <br />Gold Company`s Battle Mountain, Nevada laboratory. All materials <br />for the acidification neutralization potential tests were run <br />' through either a 10 mesh or 100 mesh sieve to ensure consistency <br />in test results. The tailings materials were run through the 10 <br />mesh sieve and, as could be expected, all material passed through <br />the sieve. <br />Exhibit D, Section D.6.2 revised to discuss sample origin 4/20/89. <br />20. Was the tailing material processed through the flotation and or the <br />carbon-in-leach circuit prior to analysis? If so, please describe the <br />processing methods, chemicals utilized, duration and rinsing methods. <br />If not, the simulation should be made, with actual expected ore size <br />' represented, to predict the disposed tailing effluent water Quality. <br />Response: The sample was representative of the actual material expected on <br />site after processing through the flotation and carbon-in-leach <br />circuit. The original sample tested and presented in the permit <br />application was not dewatered prior to testing since at that time <br />BMR was planning a traditional tailings impoundment. When BMR <br />decided to dewater the tailings/concentrates prior to disposal <br />a new sample which included the dewatering was tested. Test <br />results for the dewatered sample are now included in Appendix F. <br />Both samples tested were processed through the same circuit as <br />described below. The sample was ground to 80% passing 250 microns <br />in the presence of 0.15 pounds of potassium a;ayl xanthate per ton <br />of ore. The ground sample was floated for approximately five <br />minutes using 0.05 pounds of glycol per ton of ore to maintain <br />a stable froth bed. The flotation tails were filtered. The <br />flotation concentrate was ground to 80% passing 75 microns. The <br />concentrate slurry was adjusted to pH 11 with type 3 Portland <br />cement. Sodium cyanide was added at the rate of 8 pounds oer ton <br />1 of concentrate. The concentrate was leached fur fo~•ty eight hours <br />at ambient temperature. The concentrate slurry was filtered and <br />the filtrate was recovered for analysis. The filter cake was <br />rinsed with 250 grams of fresh water per 1000 grams of solids. <br />The washed concentrate solids were recombined with the flotation <br />tails and packaged for shipment to the SRK laboratory. <br />Exhibit D Section D.6.2 revised to discuss sample origin 4/20/89. <br />21. Please discuss what effect the dilute sulfuric acid used in the batch <br />' tests have on the sulfate concentrations reported in the tailings <br /> <br />