Renewable photo-/electrocatalytic coreduction of CO and nitrate to urea is a promising method for high-value utilization of CO . However, because of the low yields of the urea synthesis by photo-/electrocatalysis process, the accurate quantification of low concentration urea is challenging. The traditional diacetylmonoxime-thiosemicarbazide (DAMO-TSC) method for urea detection has a high limit of quantification and accuracy, but it is easily affected by NO in the solution, which limits its application scope. Thus, the DAMO-TSC method urgently requires a more rigorous design to eliminate the effects of NO and accurately quantify urea in nitrate systems. Herein, a modified DAMO-TSC method is reported, which consumes NO in solution through a nitrogen release reaction; hence, the remaining products do not affect the accuracy of urea detection. The results of detecting urea solutions with different NO concentrations (within 30 ppm) show that the improved method can effectively control the error of urea detection within 3%.
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http://dx.doi.org/10.1002/smtd.202300003 | DOI Listing |
Small Methods
September 2023
Beijing Key Laboratory of Membrane Materials and Engineering, Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.
Anal Biochem
October 2013
Center for Pharmaceutical Biotechnology, University of Illinois at Chicago, Chicago, IL 60607, USA.
Dihydroorotase (DHOase) is the third enzyme in the de novo pyrimidine biosynthesis pathway and is a potential new antibacterial drug target. No target-based high-throughput screening (HTS) assay for this enzyme has been reported to date. Here, we optimized two colorimetric-based enzymatic assays that detect the ureido moiety of the DHOase substrate, carbamyl-aspartate (Ca-asp).
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