United States Environmental Protection Agency EPA/540/SR-94/512 May 1994 SUPERFUND INNOVATIVE TECHNOLOGY EVALUATION Emerging Technology Summary Cross-Flow Pervaporation for Removal of VOCs from Contaminated Wastewater Pervaporation is a membrane tech- nology using & dense, nonporous poly- meric film to separate contaminated water from a vacuum source. The mem- brane preferentially partitions the vola- tile organic compounds (VOC) organic phase used In this test This process has proven to be an alternative to con- ventional technologies because it re- moves VOCs without requiring any pre- or post-treatments and Is cost-effec- tive. This Summary was developed by EPA's Risk Reduction Engineering Laboratory, Cincinnati, OH, to announce key findings of the SITE Emerging Tech- nology program that are fully docu- mented In a separate report (see ordering Information at back). Background Water contaminated with VOCs is en- countered throughout industry and in many groundwater and site remediation situa- tions. VOCs are common contaminants found in groundwater, leachate, and waste- water. Approximately 50% of the U.S. En- vironmental Protection Agency's (EPA's) list of priority pollutants is composed of VOCs—compounds known to be toxic, or carcinogenic, or both. Conventional technologies such as air stripping and activated carbon treatment are the current methods used to remove low concentrations of organic contaminants from various water sources. Previous work has demonstrated that pervaporation is a potentially suitable remediation method for Wastewater applications. The primary ob- jectives of this project were to develop an improved membrane and module design to make pervaporation a more cost-effec- tive method for removing VOCs from con- taminated water and to compare the improved pervaporation module and mem- brane design with conventional remediation technologies as well as other pervaporation module and membrane designs: Technology Description Pervaporation is a membrane process for removing VOCs from wastewater, leachate, and contaminated groundwater (Figure 1). For water treatment applica- tions, the membrane is made of an organophilic polymer such as modified sili- cone rubber, which exhibits high selectiv- ity for organic compounds while allowing very little passage of water. Only the mi- nor component (organic compounds) of the feed goes through the membrane, which reduces the potential for membrane fouling. One side of the membrane is in Printed on Recycled Paper ------- Pervaporation module Treated effluent Aqueous waste Feedpump Permeate Vacuum pump Organic liquid FJgun 1. Schematic of pervaporation process for removing VOCs from wastewater. contact with the VOC-contaminated wa- ter; the other side is exposed to a vacuum. VOCs are absorbed in the membrane and diffuse through to the other side where they are drawn off by vacuum. The treated water is depleted of VOCs and exits the pervaporation system for collection or dis- charge. VOCs passing through the mem- brane, now called permeate, are condensed and flow to a permeate collec- tion tank where gravity separation of wa- ter and VOCs occurs. The VOC phase is pumped from the base of the collection tank to storage. Collected water is re- turned to the pervaporation system for further treatment. Project Accomplishments During the project, membranes and modules were developed, and several module cartridges were produced to evalu- ate their performance. Testing was car- ried out at bench scale with separate synthetic wastewaters containing trichlo- roethytene (TCE), toluene, or ethylene dfchforide. These components vary sig- nificantly in volatility (as defined by Henry's Law Constant) and other secondary prop- erties. To Identify key operating param- eters, these components were tested at various temperatures and vacuum pres- sures. Bench testing was followed with pilot testing. A 5-ft2 membrane area was used to treat water contaminated with tolu- ene. Testing whh the 5-ft2 module verified the results of the bench testing. A com- puter model, developed from the bench- test results, was used to predict and optimize pervaporation conditions for ef- fective removal of VOCs from wastewa- ter. Results To Date The results of this project have shown that pervaporation performance depended greatly on both the membrane and mod- ule design. The module, composed of hol- low fibers, was designed to allow liquid to flow orthogonal to the fiber direction. This high mass transfer allowed the membrane surface area requirements to be minimized. The effective combination of membrane and module allowed the waste VOC to be concentrated by 5,000 to 50,000 times as it was removed from the wastewater. The permeate always separated into an aque- ous and organic phase. In practice, this would offer the possibility of recovering the organic fraction for industrial applica- tions. Pervapbratibn performance for VOC re- moval depends on (1) VOC type, (2) mem- brane type, (3) liquid turbulence in the module, (4) operating temperature, and (5) vacuum pressure. Pervaporation per- formance is optimal for VOCs with a solu- bility of less than 1%. High solubility VOCs, such as ethyl acetate, methylene chloride, and ethylene dichloride can, however, be considered but require higher operating temperatures to enhance VOC removal. Higher operating temperatures marginally increase operating costs. Membranes should be organophilic to minimize water passage. In this study, a modified silicons rubber membrane was used, and the pervaporation module demonstrated mass transfer coefficients above 100 u,m/s. This represents a performance enhancement of 2 to 4 times ithat of previous work. Furthermore, this enhancement reduces the membrane area requirement by 2 to 4 times for any given application. Membrane thickness and type reduce the passage of water and, thereby, increase separation factors. This reduces operating costs sig- nificantly. Operating temperature and vacuum pressure are interrelated. Since the ultimate vacuum pressure depends on the condenser temperature (minimum 0°C) and the VOC present in the condenser, the operating temperature of the feed must be sufficient (typically greater than 60°C) to provide a vapor pressure gradient (chemical potential) from the membrane to the condenser, j Pervaporation also has the following advantages over: conventional technolo- gies: I • No chemicals or air is added to the wastewater,'therefore fouling and scaling problems are avoided. • Pervaporation does not require sorbents or chemicals. • Monitoring for breakthrough is not required. j • Recovered solvents may be reused in industrial applications. • Degree of VOC removal is independent of concentration and type of VOC. I A cost comparison of pervaporation with conventional technologies was conducted for a 44-gpm application with 10 ppm TCE to be reduced to 0.1 ppm TCE. Cost analy- sis indicates that peryaporatipn was more cost-effective than air stripping and acti- vated carbon. i ------- Field testing through the SITE program will be carried out through 1994 to verify these pervaporation results. The full report was submitted in fulfill- ment of cooperative agreement CR- 815788 by the Wastewater Technology Center and Zenon Environmental Inc. un- der the sponsorship of the U.S. Environ- mental Protection Agency. •ft-U.S. GOVERNMENT PRINTING OFFICE: 19*4 - S50-O67/80257 ------- The EPA Project Manager, John Martin, is with the Risk Reduction Engineer- ing Laboratory, Cincinnati, OH 45268 (see below). The complete report, entitled "Cross-Flow Pervaporation System for Removal of VOCs from Contaminated Wastewater,"(Order No. PB94-170230; Cost: $19.50, subject to change) will be available only from National Technical Information Service 5285 Port Royal Road Springfield, VA221'61 Telephone: 703-487-4650 The EPA Project Officer can be contacted at Risk Reduction Engineering Laboratory U.S. Environmental Protection Agency Cincinnati, OH 45268 United States Environmental Protection Agency Center for Environmental Research Information Cincinnati, OH 45268 Official Business Penalty for Private Use $300 EPA/540/SR-94/512 BIJILK RATE POSTAGE & FEES PAID | EPA PERMIT No. G-35 ------- |