Articles via Databases
Articles via Journals
Online Catalog
E-books
Research & Information Literacy
Interlibrary loan
Theses & Dissertations
Collections
Policies
Services
About / Contact Us
Administration
Littman Architecture Library
This site will be removed in January 2019, please change your bookmarks.
This page will redirect to https://digitalcommons.njit.edu/theses/1333 in 5 seconds

The New Jersey Institute of Technology's
Electronic Theses & Dissertations Project

Title: The oxidation of methylene chloride over manganese dioxide catalyst
Author: Du, Jun
View Online: njit-etd1990-011
([xviv], 76 pages ~ 2.9 MB pdf)
Department: Department of Chemical Engineering, Chemistry and Environmental Science
Degree: Master of Science
Program: Environmental Science
Document Type: Thesis
Advisory Committee: Shaw, Henry (Committee chair)
Bozzelli, Joseph W. (Committee member)
Farrauto, Robert J. (Committee member)
Date: 1990
Keywords: Transition metal oxidation catalyst
Oxidative effectiveness
Corrosive exposure to chlorine and HCI
Availability: Unrestricted
Abstract:

This research presents results from a study with the goal of using a transition metal oxidation catalyst, manganese dioxide (MnO2) I to convert low concentrations of methylene chloride (CH2Cl2) in air and in a methane/air stream into CO2, H2O and HCl. Our objectives were to determine the oxidative effectiveness of the catalyst and its durability under the corrosive exposure to chlorine, HCl and other likely stack gas contaminants.

Experiments were carried out in a tubular packed bed integral reactor using gas chromatographic (FID and TCD) analysis for chlorocarbons and non-dispersive infrared analysis for CO and CO2. The results indicate:

  1. The light-off temperature for oxidation of the CH2Cl2/air mixture over MnO2 is on the order of 500 K for space velocities from 1.67 to 6.67 v/v/sec.

  2. There are two regions where rate is controlling: (i) in the range of 513-625 K, rate is controlled by kinetics, where higher temperatures increase conversion of CH2CL2 and selectivity to CHCl3 and CCl4, and (ii) above 675 K, the rate is controlled by bulk mass transfer, where the reaction rate is an insensitive function of temperature.

  3. A typical material balance at 708 K shows that 100 ppm CH2CL2 are converted to 8.4 ppm CO2, 32.7 ppm CHCl3 9.2 ppm CCl4, 3.7 ppm HU (determined by titration) , and 34.4 ppm CH2CL2 come through unreacted.

  4. The overall rate constant is: k = 9,600 (±600) Exp[-12.7(±0.2)/RT] in 1/sec where, activation energy is 12.7 kcal/mol and gas constant 1.987 cal/(mol K).

  5. Increased residence time changes selectivity from CHCl3 to CCl4.

  6. Oxychlorination (the catalytic conversion of HCl to Cl2 in the presence of O2) apparently effectiveness of MnO2 to produce CHCl3 and CCl4.

  7. Since MnO2 converts CH2Cl2 to higher chlorinated products rather than just CO2 and HCl, it is not suitable as an incinerator catalyst.


If you have any questions please contact the ETD Team, libetd@njit.edu.

 
ETD Information
Digital Commons @ NJIT
Theses and DIssertations
ETD Policies & Procedures
ETD FAQ's
ETD home

Request a Scan
NDLTD

NJIT's ETD project was given an ACRL/NJ Technology Innovation Honorable Mention Award in spring 2003