18-Env-B4 Site Assessment and Remediation · May 2014
Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)
National Exams — May 2014 — 04-Env-B4 / Site Assessment and Remediation. 3 hours duration; open-book exam (any non-communicating calculator permitted). The paper is split into Section A (five questions, candidates asked to answer three) and Section B (three questions, candidates asked to answer two), each question worth 20 marks. All eight questions are solved below for completeness.
Reference texts. Suthersan & Payne, Remediation Engineering: Design Concepts (CRC Press); Gavaskar, Gupta, Sass, Janosy & O'Sullivan, Design Guidance for Application of Permeable Reactive Barriers for Groundwater Remediation (Battelle/EPA, 2000); ASTM E1527 Standard Practice for Phase I Environmental Site Assessments and ASTM E1903 Standard Practice for Phase II ESA; Mercer & Cohen (1990), “A review of immiscible fluids in the subsurface,” Journal of Contaminant Hydrology; Freeze & Cherry, Groundwater; Davis & Cornwell, Introduction to Environmental Engineering (6th ed.); Ontario Reg. 153/04 under the Environmental Protection Act (Record of Site Condition regime); BC Environmental Management Act — Contaminated Sites Regulation.
Question text not reproduced: the examination questions are © Engineers and Geoscientists BC. Open the official past paper (linked at the top of this page) to read the question, then follow the worked solution below.
A zero-valent iron (Fe⁰) permeable reactive barrier (PRB) is installed as a wall of granular iron across the width and depth of the contaminant plume, oriented perpendicular to groundwater flow, so that the plume passes through it under its own natural gradient with no pumping (a purely passive, in-situ treatment train). PCE reacts abiotically at the iron surface: the iron corrodes ($\text{Fe}^0 \rightarrow \text{Fe}^{2+} + 2e^-$), and the released electrons reductively dechlorinate PCE, stripping chlorine atoms stepwise (or, more favourably, via beta-elimination that bypasses the more toxic intermediates) to non-chlorinated end products such as ethene and ethane. Because the reaction occurs at the iron surface, its rate is normalized to the surface area of iron presented to the water — the surface-area rate constant $k_{sa}$ supplied in this question — rather than to the iron's mass or the barrier's bulk volume directly.
Given. $C_0 = 95$ mg/L, $C_t = 5\ \mu\text{g/L} = 0.005$ mg/L, plume cross-section $A = 80$ m², groundwater (seepage) velocity $v = 0.12$ m/d, aquifer porosity $n = 0.35$, iron specific surface area $a_s = 1.0$ m²/g, $k_{sa} = 2.1\times10^{-3}$ L/(m²·h) with only 35% activity at the 10°C site temperature, safety factor SF = 3.
Find. The total mass of granular Fe⁰ (metric tons) required in the barrier.
Approach. Model the barrier as a plug-flow packed bed: water carrying PCE flows through a fixed mass of iron, and PCE degrades as a pseudo-first-order surface reaction. Integrating the mass balance along the flow path gives the classic packed-bed design equation $W = Q\ln(C_0/C_t)/(k_{sa}a_s)$ — the total iron mass needed depends only on the water flux, the required log-removal, and the rate parameters, not on the barrier's thickness (mass and thickness trade off against each other for a fixed iron packing density).
| Quantity | Value |
|---|---|
| $k_{sa}$ at 10°C | $7.35\times10^{-4}$ L/(m²·h) |
| Darcy flux through barrier | 0.042 m/d (Q = 3.36 m³/d) |
| Required log-removal, ln(C₀/Cᷯ) | 9.85 |
| Fe⁰ mass, no safety factor | 1.877 t |
| Fe⁰ mass, design (SF = 3) | 5.63 metric tons |