Search citation statements
Paper Sections
Citation Types
Year Published
Publication Types
Relationship
Authors
Journals
A new method using fluorescence was developed to detect Hg2+ ions in water. This method relied on the reaction between NH2‐MIL‐53(Al) and 5‐bromo‐2‐hydroxyacetophenone. The method was carefully fine‐tuned for optimal reaction conditions and analytical parameters like pH levels, nanosensor quantity, and detection limits. It showed great linearity in detecting Hg2+ ions in the range of 0.0–3.0 ppm (0.0–1.50 × 10−5 M), with a very low detection limit of 1.65 × 10−2 ppm (8.23 × 10−8 M). We tested how well the method can distinguish between different substances by investigating whether other common substances in water samples would interfere. The results were positive, as the presence of these substances did not significantly affect the accuracy of detecting Hg2+ ions, confirming the method's reliability. In order to confirm its dependability, we conducted a quantitative test to detect Hg2+ ions in water samples. The recovery rates obtained ranged from 97.16% to 103.2%, demonstrating the method's precision and accuracy. A comparison with inductively coupled plasma optical emission spectrometry (ICP‐OES), a well‐known method for analyzing trace metals, produced similar results, further instilling confidence in the 5Br2HA = N‐Al‐MOF nanosensor that was developed. In general, this research emphasizes the exciting potential of the new nanosensor in detecting Hg2+ ions in various water and cosmetic samples. It provides a strong and dependable alternative to traditional detection methods.
A new method using fluorescence was developed to detect Hg2+ ions in water. This method relied on the reaction between NH2‐MIL‐53(Al) and 5‐bromo‐2‐hydroxyacetophenone. The method was carefully fine‐tuned for optimal reaction conditions and analytical parameters like pH levels, nanosensor quantity, and detection limits. It showed great linearity in detecting Hg2+ ions in the range of 0.0–3.0 ppm (0.0–1.50 × 10−5 M), with a very low detection limit of 1.65 × 10−2 ppm (8.23 × 10−8 M). We tested how well the method can distinguish between different substances by investigating whether other common substances in water samples would interfere. The results were positive, as the presence of these substances did not significantly affect the accuracy of detecting Hg2+ ions, confirming the method's reliability. In order to confirm its dependability, we conducted a quantitative test to detect Hg2+ ions in water samples. The recovery rates obtained ranged from 97.16% to 103.2%, demonstrating the method's precision and accuracy. A comparison with inductively coupled plasma optical emission spectrometry (ICP‐OES), a well‐known method for analyzing trace metals, produced similar results, further instilling confidence in the 5Br2HA = N‐Al‐MOF nanosensor that was developed. In general, this research emphasizes the exciting potential of the new nanosensor in detecting Hg2+ ions in various water and cosmetic samples. It provides a strong and dependable alternative to traditional detection methods.
Recurring environmental challenges and the global energy crisis have led to intensified research on alternative energy sources. Hydrogen has emerged as a promising solution, produced through electrochemical, thermochemical, and biological methods. This study presents the advantages and disadvantages of these technologies. It also provides pertinent data on hydrogen production, identifying world‐leading countries in hydrogen production, such as the USA, Japan, and China, and the government policies that they have adopted. It reports market trends such as hydrogen synthesis by water electrolysis, the high cost of the electrolyzers used, and incentives for the carbon market to become competitive with other alternative energy sources. It also highlights startups from around the world that are developing innovative methodologies for producing hydrogen. The study concludes that integrating hydrogen production concepts with social, environmental, and industry interests is essential.
This study describes the development of a multifunction chromoionophoric probe‐based nano‐conjugate material for the colorimetric determination, recovery, and removal of palladium and cobalt ions (Pd(II) and Co(II)) ions from electronic wastes and electroplating wastewater. The chromoionophoric probe‐based nano‐conjugate material was prepared using a building‐block approach by anchoring the 4‐[(E)‐(2‐hydroxyphenyl)diazenyl]‐1‐nitrosonaphthalen‐2‐ol (HDN) organic chromoionophoric probe onto nano‐spherical silica material carrier. The prepared materials were characterized using different techniques, such as TEM, SEM XRD, and BET. The HDN chromoionophoric probe‐based nano‐conjugate material was evaluated for its effectiveness in detecting and removing Pd(II) and Co(II) ions from electronic wastes and electroplating wastewater by testing various parameters such as pH, sensing system temperature, reaction kinetic, nano‐conjugate material amount, stability of the chromoionophoric probe‐based nano‐conjugate material and the existence of other coexisting metal ions. The HDN chromoionophoric probe‐based nano‐conjugate material demonstrated high selectivity and sensitivity for the colorimetric ion‐sensing of Pd(II) and Co(II) ions, with a detection limit of 7.18 and 208 nM, respectively. The method displayed optimal sensing at pH levels of 6.0 and 8.0 for Pd(II) and Co(II) ions, respectively, and the presence of other metal ions did not meaningfully influence the performance of the ion‐detection due to the powerful ability of the chromoionophoric probe‐based nano‐conjugate material. The adsorption capacity of the chromoionophoric probe‐based nano‐conjugate material towards Pd(II) and Co(II) ions was investigated and the outcomes were 163.40 and 128.57 mg/g, respectively. The chromoionophoric probe‐based nano‐conjugate material could be regenerated by eluting the adsorbed Pd(II) and Co(II) ions with 0.15 M HCl solution. In addition, the material could be reused multiple times, with almost no decrease in its initial performance after regeneration. Based on the findings, the chromoionophoric probe‐based nano‐conjugate material shows potential for environmental recovery, removal, and detection of Pd(II) and Co(II) ions from electronic wastes and electroplating wastewater, indicating its potential as a multi‐function solution for environmental concerns and issue and could be even commercialized and used at a larger scale.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.