Ming Gao, Yu Liu, Su Ma, Sai Ma, Xuedong Wang and Yanyan Li
{"title":"季铵聚合物离子液体基气泡增强分散固相萃取法测定再生水中5种磺胺类抗生素及其相互作用机理","authors":"Ming Gao, Yu Liu, Su Ma, Sai Ma, Xuedong Wang and Yanyan Li","doi":"10.1039/D5NJ01486G","DOIUrl":null,"url":null,"abstract":"<p >Herein, two kinds of quaternary ammonium polymeric ionic liquids (PILs) were prepared and rigorously characterized based on SEM, FT-IR, and <small><sup>1</sup></small>H NMR data. The PIL-based effervescence-enhanced dispersive solid-phase extraction (PILE-d-SPE) method was developed based on effervescent tablets containing PILs as extractants, tartaric acid as the acid source, NaHCO<small><sub>3</sub></small> as the alkaline source, and water-soluble starch as the filler. The positive charges on the surface of PILs and the negative charges on the surface of sulfonamide antibiotics (SAs) exhibited significant electrostatic attraction, thereby enhancing interactions between two PILs and SAs. P[VBTHEA]Cl exhibited higher extraction efficiency for five SAs than P[VBTEA]Cl, possibly because the structure of P[VBTHEA]Cl contained more –OH functional groups compared to that of P[VBTEA]Cl. Before and after extraction, the FT-IR spectra of the two PILs were significantly different from the O–H and C–H stretching–vibration absorption bands. DFT calculations show that the strong hydrogen bonds formed between P[VBTHEA]Cl and SDM resulted in the highest binding energy and, consequently, the highest SDM extraction recovery rate. Overall, the H-bonding induction effect was inferred to be the main reason for the superiority of P[VBTHEA]Cl over P[VBTEA]Cl in extraction efficiency. Using the one-factor-at-a-time approach, several important variables were optimized for determining SAs in reclaimed waters as follows: 200-mg PILs as extractants, 400-μL acetone as elution solvent, and 5-min elution. By integration with HPLC-DAD detection, this approach provided satisfactory analytical performance: a low detection limit (0.19–0.32 μg L<small><sup>−1</sup></small>) and appropriately fortified recovery (78.4–99.7%) for five SAs. Consequently, the P[VBTHEA]Cl-based E-d-SPE method is environmentally friendly, time-saving, easy to operate, and exhibits excellent analytical performance.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 26","pages":" 11095-11106"},"PeriodicalIF":2.5000,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Quaternary ammonium polymeric ionic liquid-based effervescence-enhanced dispersive solid-phase extraction for determining five sulfonamide antibiotics in reclaimed waters and their underlying interaction mechanisms†\",\"authors\":\"Ming Gao, Yu Liu, Su Ma, Sai Ma, Xuedong Wang and Yanyan Li\",\"doi\":\"10.1039/D5NJ01486G\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Herein, two kinds of quaternary ammonium polymeric ionic liquids (PILs) were prepared and rigorously characterized based on SEM, FT-IR, and <small><sup>1</sup></small>H NMR data. The PIL-based effervescence-enhanced dispersive solid-phase extraction (PILE-d-SPE) method was developed based on effervescent tablets containing PILs as extractants, tartaric acid as the acid source, NaHCO<small><sub>3</sub></small> as the alkaline source, and water-soluble starch as the filler. The positive charges on the surface of PILs and the negative charges on the surface of sulfonamide antibiotics (SAs) exhibited significant electrostatic attraction, thereby enhancing interactions between two PILs and SAs. P[VBTHEA]Cl exhibited higher extraction efficiency for five SAs than P[VBTEA]Cl, possibly because the structure of P[VBTHEA]Cl contained more –OH functional groups compared to that of P[VBTEA]Cl. Before and after extraction, the FT-IR spectra of the two PILs were significantly different from the O–H and C–H stretching–vibration absorption bands. DFT calculations show that the strong hydrogen bonds formed between P[VBTHEA]Cl and SDM resulted in the highest binding energy and, consequently, the highest SDM extraction recovery rate. Overall, the H-bonding induction effect was inferred to be the main reason for the superiority of P[VBTHEA]Cl over P[VBTEA]Cl in extraction efficiency. Using the one-factor-at-a-time approach, several important variables were optimized for determining SAs in reclaimed waters as follows: 200-mg PILs as extractants, 400-μL acetone as elution solvent, and 5-min elution. By integration with HPLC-DAD detection, this approach provided satisfactory analytical performance: a low detection limit (0.19–0.32 μg L<small><sup>−1</sup></small>) and appropriately fortified recovery (78.4–99.7%) for five SAs. Consequently, the P[VBTHEA]Cl-based E-d-SPE method is environmentally friendly, time-saving, easy to operate, and exhibits excellent analytical performance.</p>\",\"PeriodicalId\":95,\"journal\":{\"name\":\"New Journal of Chemistry\",\"volume\":\" 26\",\"pages\":\" 11095-11106\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-05-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d5nj01486g\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d5nj01486g","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Quaternary ammonium polymeric ionic liquid-based effervescence-enhanced dispersive solid-phase extraction for determining five sulfonamide antibiotics in reclaimed waters and their underlying interaction mechanisms†
Herein, two kinds of quaternary ammonium polymeric ionic liquids (PILs) were prepared and rigorously characterized based on SEM, FT-IR, and 1H NMR data. The PIL-based effervescence-enhanced dispersive solid-phase extraction (PILE-d-SPE) method was developed based on effervescent tablets containing PILs as extractants, tartaric acid as the acid source, NaHCO3 as the alkaline source, and water-soluble starch as the filler. The positive charges on the surface of PILs and the negative charges on the surface of sulfonamide antibiotics (SAs) exhibited significant electrostatic attraction, thereby enhancing interactions between two PILs and SAs. P[VBTHEA]Cl exhibited higher extraction efficiency for five SAs than P[VBTEA]Cl, possibly because the structure of P[VBTHEA]Cl contained more –OH functional groups compared to that of P[VBTEA]Cl. Before and after extraction, the FT-IR spectra of the two PILs were significantly different from the O–H and C–H stretching–vibration absorption bands. DFT calculations show that the strong hydrogen bonds formed between P[VBTHEA]Cl and SDM resulted in the highest binding energy and, consequently, the highest SDM extraction recovery rate. Overall, the H-bonding induction effect was inferred to be the main reason for the superiority of P[VBTHEA]Cl over P[VBTEA]Cl in extraction efficiency. Using the one-factor-at-a-time approach, several important variables were optimized for determining SAs in reclaimed waters as follows: 200-mg PILs as extractants, 400-μL acetone as elution solvent, and 5-min elution. By integration with HPLC-DAD detection, this approach provided satisfactory analytical performance: a low detection limit (0.19–0.32 μg L−1) and appropriately fortified recovery (78.4–99.7%) for five SAs. Consequently, the P[VBTHEA]Cl-based E-d-SPE method is environmentally friendly, time-saving, easy to operate, and exhibits excellent analytical performance.