Measurements of Primary Sulfates with an Acid Condensation System

Abstract

Two techniques were used to measure primary sulfuric acid and sulfate emissions from two small package boilers burning nominal 0.3% sulfur fuels, one with 11 ppm vanadium and one with 4.3 ppm vanadium. Several of the particulate fractions from both sampling methods were analyzed for sulfuric acid using a selective solvent determination (SSD) procedure. The sulfuric acid present on the filters accounted for a minimum of 11% of the particulate emission rates. The observed conversion of sulfur dioxide to primary sulfate or primary sulfuric acid is reduced considerably when sulfate ion detected in an isopropanol impinger is attributed to sulfur dioxide conversion in the solution rather than to primary sulfuric acid. An additional reduction occurs when the method of calculating the conversion is based solely on sulfur weight. This study gives a fourfold reduction in percent conversion when compared to a similar study conducted earlier. Suggestions are offered for improvements in measurement methods and for a consistent technique for calculating sulfur conversion.