Abstract: Provided is a method for reducing the amounts of fungal spores and small airborne particles in an enclosure, where the enclosure has or is in communication with an air handling system. The method comprises the steps of applying vacuum suction to the air handling system and contacting the air handling system with a first antimicrobial agent; applying a cleansing agent to the carpets and upholstery in the enclosure; fogging the enclosure with a second antimicrobial agent; releasing ozone within the enclosure for a period of time and terminating the release of ozone to allow the ozone concentration to return to normal levels; placing a reservoir containing tea tree oil into the air handling system, and initiating operation of an air purifier air in the enclosure, wherein for a period of at least 90 days, the airborne particles in the enclosure are fewer than 1.0 million airborne particles per cubic meter of air; the airborne fungal spores in the enclosure an amount at least 1.

Abstract: Provided is a method for reducing the amounts of fungal spores and small airborne particles in an enclosure, where the enclosure has or is in communication with an air handling system. The method comprises the steps of applying vacuum suction to the air handling system and contacting the air handling system with a first antimicrobial agent; applying a cleansing agent to the carpets and upholstery in the enclosure; fogging the enclosure with a second antimicrobial agent; releasing ozone within the enclosure for a period of time and terminating the release of ozone to allow the ozone concentration to return to normal levels; placing a reservoir containing tea tree oil into the air handling system, and initiating operation of an air purifier air in the enclosure, wherein for a period of at least 90 days, the airborne particles in the enclosure are fewer than 1.0 million airborne particles per cubic meter of air; the airborne fungal spores in the enclosure an amount at least 1.

Abstract: A method is disclosed for the dealkylation of alkylaryl ethers by reaction with aluminum triodide under reflux. The reaction is carried out in the presence of a catalytic amount of a quaternary ammonium iodide in a substantially non-aqueous organic solvent. The reaction product is then hydrolyzed with water. The quaternary ammonium iodide can be of the formula R.sub.4 N.sup.+ I.sup.-, wherein R is alkyl, and the solvent is preferably benzene or cyclohexane.