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110 Second Avenue South,4D7,Pacheco,CA 94553 <br /> McCAMPBELL ANALYTICAL INC. Telephone:510-798-1620 Fax:510-798-1622 <br /> http://www.mccampbell.com E-mail:main@mccampbell.com <br /> EXPERIMENTAL DETAILS <br /> The experiment started on April 06 at 8 p.m. with 10 glass vessels each 1 L in size. A diagram is enclosed. <br /> Five vessels contained the sample, MS, MB, LCS, LCSD and the remaining 5 vessels contained 500ml DI for flow <br /> control purpose. <br /> The sample & MS vessels each contained 500g of soil and 500m1 of aquifer water that were gently shaken for 30 <br /> minutes prior to purging. <br /> The MS was treated like the sample except that it was spiked with 100mg of K2Cr�O7 which is equal 71 ppm of Cr 16 <br /> The MB is just 500m1 DI. LCS/LCSD contains 500ml DI and spiked with 100mg of K2Cr2O7 which is equal 71 ppm of <br /> Cr+6 <br /> Oxygen flow was initially set at 10 psi at the main regulator. Oxygen gas flowed to the ozone generator whose channel <br /> A and channel B were both set at 5 psi. The ozone flow from the ozone generator was directed to a glass splitter via <br /> Teflon tubing and then split into each vessel. The ozone gas exited from each vessel into an ozone scrubber that <br /> catalytically (no reactive chemicals) decomposed the 03. Purging continued for 5 days. All tubing& connections were <br /> Teflon or glass from the ozone generator to this point.The purge flow was monitored at the end of the scrubb tlet& <br /> tubing was restricted here to control the flow. See the following table for Ozone generating parameters. s reaction <br /> time progressed oxygen feed pressure nearly doubled but flows dropped two fold or more indicating that the system <br /> became "more restricted". This is easy to understand for the vessels that contained soil, but there is no definite <br /> explanation for those that contained only water. It is possible that condensed water in the ozone scrubbers is <br /> responsible. Comparison of this data with the ozone determinations shows that dissolved ozone concentration actually <br /> increases with lower flow rates, perhaps indicating that "self-purging" is significant. Dissolved ozone concentrations <br /> ranged from 0.029-0.066 mg/L&are tabulated in the results section. <br /> "Medial" sampling (during the 5 days of ozonation) was accomplished via a sipper tube that was immersed below the <br /> upper level of the aqueous phase&was accessed by disconnecting the reaction vessel outlet tubing& withdrawing 20- <br /> 30 ml of sample via a luer tipped syringe. Ozone flow was stopped during sampling. Generally 20ml of water was <br /> removed each time resulting in a 60/500 or 12%decrease in fluid volume. This factor has not been taken into account in <br /> the analytical data. <br /> Experimental Measurements of Oxygen Head Pressure&Ozone Flow <br /> Head Ozone Flow Measured at Scrubber Outlet(ml/min) <br /> Time of Measurement Pressure <br /> (psi) Sample MS MB LCS LCSD <br /> Initial: 8 pm,4/6/05 10 60 60 56 54 58 <br /> Day 1: 5 pm,4/7/5 13 43 48 58 56 59 <br /> Day 2: 5 pm,4/8/5 15 42 45 50 48 50 <br /> Day 5: 6 pm,4/11/5 18 13 13 24 26 26 <br /> At the end of Day 5 ozonation the ozone flow was permanently stopped & Final Water & Final soil samples were <br /> withdrawn. The Final soil was found contain 1 /0.8 = 125%more water than the Initial soil. This correction factor was `. <br /> significant for TTLC trace metals & this correction factor was applied to TTLC Final soil metals values i�s noted on <br /> their results page. <br /> A significant volume of water was removed for the Final water tests & —200ml DI was added to the sample for decay <br /> studies. Ozone & hexachrome were measured for another 8 days. Approximately 20-30m1 sample aliquots were <br /> withdrawn between 3-5 pm on each day from 04/12 —04/19. A syringe aliquot was withdrawn in the same way as for <br /> the medial samples except that the MB,LCS&LCSD were sub-sampled by pouring rather than by syringe withdrawal. <br />