Skip to main content

grant · indexed from Simpler.Grants.gov API

Cooperative Agreement for affiliated Partner with Northern Great Plains Cooperative Ecosystem Studies Unit

Geological Survey

Data quality: Source-backedSeen at source 4h agoVerified source
Published
14 Oct 2026
Deadline
14 Nov 2026
Coverage
US

Robust and reliable quantitative method to correct for solution chemistry interferences in molecularly imprinted polymer – electrochemical sensor (MIP-ES) measurements of complex environmental water matricesThe goal of this research is to develop a robust and reliable quantitative method to correct for solution chemistry interferences in MIP-ES measurements of complex environmental water matrices. One of the challenges using MIP-ES to measure contaminants such as per- and polyfluoroalkyl substances (PFAS) in environmental samples is understanding how bulk solution chemistry contributes to the electrochemical background signal. The development of a ratiometric comparison approach with MIP-ES will involve bench scale proof of concept testing and then escalate to field deployed trials. Instrumentation required for MIP-ES fabrication and sensing includes multichannel potentiostats capable of differential pulse voltammetry and cyclic voltammetry. Differential pulse voltammetry will be used to collect current differences at 1-minute and 15-minute incubation time points in the sample matrices. These current values will be used to build the ratiometric comparison approach.The ratiometric approach will involve the comparison of normalized current difference ratios, outlined in Equation 1, between a matrix matched solution that contains all matrix constituents minus the analyte in question and an unknown solution that is composed of the sample matrix and may or may not contain the analyte.The use of a ratiometric comparison isolates current differences from the association of the analyte with the MIP-ES binding sites from any change in current from interferent effects due to the rest of the sample matrix constituents (i.e., humic acids, fulvic acids, ions, non-fluorinated counterparts, etc.). A ratio close to 1 indicates the absence of the analyte due to similar normalized current difference values in the ratio. A statistically different ratio from 1 indicates the presence of the analyte in question in the sample matrix.This project supports the administration's priority to protecting human health by generating data and tools that identify potential risks to drinking water quality. By enabling early detection and informed decision-making, this work helps safeguard communities from exposure to harmful contaminants and ensures access to safe, clean drinking water.

Robust and reliable quantitative method to correct for solution chemistry interferences in molecularly imprinted polymer – electrochemical sensor (MIP-ES) measurements of complex environmental water matricesThe goal of this research is to develop a robust and reliable quantitative method to correct for solution chemistry interferences in MIP-ES measurements of complex environmental water matrices. One of the challenges using MIP-ES to measure contaminants such as per- and polyfluoroalkyl substances (PFAS) in environmental samples is understanding how bulk solution chemistry contributes to the electrochemical background signal. The development of a ratiometric comparison approach with MIP-ES will involve bench scale proof of concept testing and then escalate to field deployed trials. Instrumentation required for MIP-ES fabrication and sensing includes multichannel potentiostats capable of differential pulse voltammetry and cyclic voltammetry. Differential pulse voltammetry will be used to collect current differences at 1-minute and 15-minute incubation time points in the sample matrices. These current values will be used to build the ratiometric comparison approach.The ratiometric approach will involve the comparison of normalized current difference ratios, outlined in Equation 1, between a matrix matched solution that contains all matrix constituents minus the analyte in question and an unknown solution that is composed of the sample matrix and may or may not contain the analyte.The use of a ratiometric comparison isolates current differences from the association of the analyte with the MIP-ES binding sites from any change in current from interferent effects due to the rest of the sample matrix constituents (i.e., humic acids, fulvic acids, ions, non-fluorinated counterparts, etc.). A ratio close to 1 indicates the absence of the analyte due to similar normalized current difference values in the ratio. A statistically different ratio from 1 indicates the presence of the analyte in question in the sample matrix.This project supports the administration's priority to protecting human health by generating data and tools that identify potential risks to drinking water quality. By enabling early detection and informed decision-making, this work helps safeguard communities from exposure to harmful contaminants and ensures access to safe, clean drinking water. This financial assistance opportunity is being issued under a Cooperative Ecosystem Studies Units (CESU) Program. CESU's are partnerships that provide research, technical assistance, and education. Eligible recipients must be a participating partner of the Northern Great Plains Cooperative Ecosystem Studies Unit. Katie Calderkatherine_calder@ios.doi.gov Electronically submitted applications must be submitted no later than 11:59 PM, ET, on the listed application due date

Provenance

Simpler.Grants.gov API(official channel)Data quality: Source-backed
Publisher
Simpler.Grants.gov API· US
Source system
Simpler.Grants.gov API — Official API or feed
Verification
Verified — the publisher's own channel
Published
— stated by the source
Last seen at source
Last re-verified
not yet re-verified
Indexed by GLODA
Last updated
Record version
6fc63db145e2
How GLODA knows this — Source-backed · 1 fieldData quality: Source-backed
How each field is known
FieldHow we knowStateConfidence
Publication dateOfficial API or feedData quality: Source-backed100
Source
Simpler.Grants.gov API · Official API or feed · official-docs
Retrieval
seen · indexed
Record
6fc63db145e2 · source id f55851f1-8d9e-4d76-ae21-3d7d6f25d467
Computed
provenance-v1

States describe GLODA's confidence in its own fields, never a judgement on the notice or its parties. Methodology

Open this grant in the GLODA terminal

The notice above is the public record. Signing in adds the analysis: saved views and alerts on searches like this one, workflow and pipeline, exports and full workspace tooling.