首页 | 本学科首页   官方微博 | 高级检索  
     


Adsorption of RDX and HMX in Rapid Small-Scale Column Tests: Implications for Full-Scale Adsorbers
Authors:Matthew C. Morley  Jennifer L. Henke  Gerald E. Speitel   Jr.
Affiliation:1Assistant Professor, Dept. of Civil Engineering, Univ. of Nebraska Lincoln, W348 Nebraska Hall, Lincoln, NE 68588-0531.
2Environmental Engineer, CH2M-Hill, 12377 Merit Dr., Suite 1000, Dallas, TX 75251.
3John J. McKetta Professor in Engineering and Chairman, Dept. of Civil Engineering, The Univ. of Texas at Austin, 1 University Station Stop C1700, Austin, TX 78712-0273.
Abstract:The high explosive (HE) compounds royal demolition explosive or hexahydro-1,3,5-trinitro-1,3,5-triazocine (RDX) and high melting explosive or octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) have been detected as groundwater contaminants at many military facilities. This research evaluated adsorption of RDX and HMX with granular activated carbon (GAC) to provide guidance for the design and operation of GAC adsorbers for treatment of HE-contaminated groundwater. Five GACs were screened using rapid small-scale column tests (RSSCTs), after which additional tests were performed with the two GACs that most effectively treated mixtures of RDX and HMX (Calgon F400 and Northwestern LB-830). GAC service life as a function of empty-bed contact time (EBCT) was determined using RSSCTs for a range of simulated full scale EBCTs with influent concentrations of 2,200 μg RDX/L and 350 μg HMX/L. Increasing the influent concentration of either contaminant significantly reduced the predicted service life, as did preloading GAC with groundwater natural organic matter. In batch isotherm tests, RDX was less adsorbable than HMX under all conditions studied. Concurrent loading of natural organic matter reduced the Freundlich K for RDX, whereas adsorption of HMX was not affected. Of the GACs tested, Calgon F400 most effectively removed RDX and HMX.
Keywords:Adsorption  Activated carbon  Ground-water pollution  Explosives  Isotherms  
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号