• Skip to main content
  • Skip to after header navigation
  • Skip to site footer
ERN: Emerging Researchers National Conference in STEM

ERN: Emerging Researchers National Conference in STEM

  • About
    • About AAAS
    • About the NSF
    • About the Conference
    • Partners/Supporters
    • Project Team
  • Conference
  • Abstracts
    • Undergraduate Abstract Locator
    • Graduate Abstract Locator
    • Abstract Submission Process
    • Presentation Schedules
    • Abstract Submission Guidelines
    • Presentation Guidelines
  • Travel Awards
  • Resources
    • Award Winners
    • Code of Conduct-AAAS Meetings
    • Code of Conduct-ERN Conference
    • Conference Agenda
    • Conference Materials
    • Conference Program Books
    • ERN Photo Galleries
    • Events | Opportunities
    • Exhibitor Info
    • HBCU-UP/CREST PI/PD Meeting
    • In the News
    • NSF Harassment Policy
    • Plenary Session Videos
    • Professional Development
    • Science Careers Handbook
    • Additional Resources
    • Archives
  • Engage
    • Webinars
    • ERN 10-Year Anniversary Videos
    • Plenary Session Videos
  • Contact Us
  • Login

A co-oxidation model for the reductive detoxification of hexavalent chromium in ground water: Kinetic screening of renewable substrates for reduction of hexavalent chromium in co-oxidation reactions of ethanol.

Undergraduate #97
Discipline: Chemistry and Chemical Sciences
Subcategory: Chemistry (not Biochemistry)
Session: 1
Room: Exhibit Hall

Iiana Robinson - Regis University
Co-Author(s): Reina Sandoval, Regis University, Denver, CO; Surendra Mahapatro, Regis University, Denver, CO



Hexavalent chromium is a known carcinogen. The EPA has a drinking water standard of 0.1 milligrams per liter (mg/l) or 100 parts per billion (ppb) for total chromium.   Interestingly, chromium(III) is part of glucose tolerance factor (GTF) and Cr(III)-picolinate is a dietary supplement.  The source of chromium(VI) drinking water is mainly from industrial use (chrome plating and leather tanning), and due to the complex geochemistry involving rocks containing chromite and solid manganese dioxide (MnO2. nH2O; Birnessite, a common manganese mineral).  The express purpose of our study is to screen several renewable organic substrates that could potentially reduce hexavalent chromium to Cr(III) individually or in co-oxidation reactions with ethanol.  This list includes oxalic, lactic, citric, malic, tartaric, gallic and tannic acid.   We will report half-lives (t1/2) of first-order reactions under pseudo first-order conditions and discuss the transition state for the ter-molecular complex involving Cr(VI), ethanol and the hydroxy-acid.  Reductive detoxification of hexavalent chromium requires reliable methods for the quantitative estimation of Cr(VI). We will examine the relative merits of all available methods including chromate (CrO42-, shows a λmax a 372 nm (4.8 x 103 M-1 cm-1), EPA protocol method 7196A involving 1,5-diphenylcarbazide and the green radical cation ABTS●. 1.Genesis of hexavalent chromium from natural sources in soil and groundwater Christopher Oze, Dennis K. Bird, and Scott Fendorf, PNAS, 2007 104 (16), 6544-6549.    2.Reduction behavior of chromium(VI) with oxalic acid in aqueous solution Hao Peng &  Jing Guo ; Nature Scientific Reports volume 10, Article number: 17732 (2020)

Funder Acknowledgement(s): This research is supported by the Western Alliance to Expand Student Opportunities (WAESO)   Louis Stokes Alliance for Minority Participation (LSAMP) National Science Foundation (NSF) Cooperative Agreement No. HRD-1619524.

Faculty Advisor: Surendra Mahapatro, smahapat@regis.edu

Role: I researched background information and methods to detect hexavalent chromium in water. I also set up and conducted the tests with the different mixtures and on the machines.

Sidebar

Abstract Locators

  • Undergraduate Abstract Locator
  • Graduate Abstract Locator

This material is based upon work supported by the National Science Foundation (NSF) under Grant No. DUE-1930047. Any opinions, findings, interpretations, conclusions or recommendations expressed in this material are those of its authors and do not represent the views of the AAAS Board of Directors, the Council of AAAS, AAAS’ membership or the National Science Foundation.

AAAS

1200 New York Ave, NW
Washington,DC 20005
202-326-6400
Contact Us
About Us

  • LinkedIn
  • Facebook
  • Instagram
  • Twitter
  • YouTube

The World’s Largest General Scientific Society

Useful Links

  • Membership
  • Careers at AAAS
  • Privacy Policy
  • Terms of Use

Focus Areas

  • Science Education
  • Science Diplomacy
  • Public Engagement
  • Careers in STEM

Focus Areas

  • Shaping Science Policy
  • Advocacy for Evidence
  • R&D Budget Analysis
  • Human Rights, Ethics & Law

© 2023 American Association for the Advancement of Science