화학공학소재연구정보센터
Polymer(Korea), Vol.40, No.5, 769-773, September, 2016
폴리다이아세틸렌-폴리다이메틸실록산 기반의 클로로포름 검출센서
Development of Polydiacetylene-Polydimethylsiloxane Based Chloroform Sensor
E-mail:
초록
본 연구에서는 용매변색성을 지니는 폴리다이아세틸렌(polydiacetylene, PDA)을 중합하여 이를 함유한 폴리다이메틸실록산(polydimethylsiloxane, PDMS) 기반의 필름센서를 개발하였으며 이를 이용하여 클로로포름에서의 용매변색을 확인하였다. 다이아세틸렌(diacetylene, DA) 단량체인 2-methoxyethyl pentacosa-10,12-diynoate(PCDA-EGME)를 합성하고 저온에서 254 nm UV를 조사하여 PDA를 광 중합한 후, 이를 PDMS에 내포시켜 필름 센서를 제조하였다. 필름형 센서는 적색(λmax=545 nm)을 띠고 있으며, 센서를 클로로포름에 노출시키면 황색(λmax=477 nm)으로 변하는 것을 관찰하였다. 총 19 종의 용매 중 클로로포름에서 선택적으로 변색이 발생하였으며 이를 이미지 분석을 통해 CMYK 중 yellow, magenta 값을 추출하여 차이 값을 분석하였다.
In this study, we have developed a solvatochromic polydiacetylene(PDA)-embedded polydimethylsiloxane (PDMS) film-type sensor for selective colorimetric detection of chloroform. PDA-PDMS film was readily fabricated by mixing PDA which was derived from 2-methoxyethyl pentacosa-10,12-diynoate (PCDA-EGME) and PDMS precursor. The PDA embedded PDMS film displayed a red (λmax=545 nm) to yellow (λmax=477 nm) colorimetric transition upon exposure to chloroform. The film-type sensor was found to be selective for chloroform among 19 common solvents.
  1. Yu G, Gao J, Hummelen JC, Wudl F, Heeger AJ, Science, 270, 5243 (1995)
  2. Janata J, Josowicz M, Nat. Mater., 2(1), 19 (2003)
  3. Jang H, Song K, Kim SH, Polym. Korea, 35(4), 370 (2011)
  4. Bousquet A, Awada H, Hiorns RC, Dagron-Lartigau C, Billon L, Prog. Polym. Sci, 39, 1847 (2014)
  5. McQuade DT, Pullen AE, Swager TM, Chem. Rev., 100(7), 2537 (2000)
  6. Park J, Son Y, Polym. Korea, 38(6), 809 (2014)
  7. Jang G, Seo S, Lee TS, Sens. Actuators B-Chem., 221, 1229 (2015)
  8. Mueller A, O'Brien DF, Chem. Rev., 102(3), 727 (2002)
  9. Ahn DJ, Kim JM, Acc. Chem. Res., 41, 805 (2008)
  10. Lee YH, Yim KH, Heo J, Choi JS, Polym. Korea, 38(1), 43 (2014)
  11. Pumtang S, Siripornnoppakhun W, Sukwattanasinitt M, Ajavakom A, J. Colloid Interface Sci., 364(2), 366 (2011)
  12. Eaidkong T, Mungkarndee R, Phollookin C, Tumcharern G, Sukwattanasinitt M, Wacharasindhu S, J. Mater. Chem., 22, 5970 (2012)
  13. Lee J, Chang HT, An H, Ahn S, Shim J, Kim JM, Nat. Commun., 4, 2461 (2013)
  14. Yang JE, Lee S, Bhak G, Lee M, Jeong DH, Jung S, Paik SR, Sens. Actuators B-Chem., 227, 313 (2016)
  15. Jackman RJ, Wilbur JL, Whitesides GM, Science, 269(5224), 664 (1995)
  16. Heckele M, Schomburg WK, J. Micromech. Microeng., 14, R1 (2004)
  17. Park IS, Heo E, Nam YS, Lee CW, Kim JM, J. Photochem. Photobiol. A-Chem., 238, 1 (2012)
  18. Nam YS, Yoo I, Yarimaga O, Park IS, Park DH, Song S, Kim JM, Lee CW, Chem. Commun., 50, 4251 (2014)
  19. Park DH, Hong J, Park IS, Lee CW, Kim JM, Adv. Funct. Mater., 24(33), 5186 (2014)
  20. Park IS, Park HJ, Kim JM, ACS Appl. Mater. Interfaces, 5, 8805 (2013)
  21. Park IS, Park HJ, Jeong W, Nam J, Kang Y, Shin K, Chung H, Kim JM, Macromolecules, 49(4), 1270 (2016)
  22. Lee JN, Park C, Whitesides GM, Anal. Chem., 75, 6544 (2003)