journal article·2007-12-01

Optical Carbon Dioxide Sensors Based on Silicone-Encapsulated Room-Temperature Ionic Liquids

Sergey M. Borisov, Magdalena Ch. Waldhier, Ingo Klimant, Otto S. Wolfbeis

Chemistry of Materials· Volume 19· Issue 25
Publisher page

Abstract

Novel optical carbon dioxide sensors are based on emulsion of room-temperature ionic liquids (RTILs)–1-butyl-3-methylimidazolium salts in a silicone matrix. Semiquantitative determination of CO 2 is achieved by dissolving an absorption-based pH indicator (thymol blue, TB, or bromthymol blue, BTB) in the RTIL. A quantitative fluorimetric sensor makes use of 8-hydroxypyrene-1,3,6-trisulfonate (HPTS). The response of the fluorimetric sensors to CO 2 can easily be linearized which makes (re)calibration of the sensor very simple. It is demonstrated that a reference inert fluorescent dye (4-dicyanomethylene-2-methyl-6-(4-(dimethylamino)styryl)-4 H -pyrane) can be added for ratiometric measurements. It is also shown that stable inorganic salts such as sodium phosphate can be used instead of quaternary ammonium hydroxides. Sensitivity of the material can be tuned by varying the p K a of an indicator. The sensors can find application in biotechnology, environmental monitoring, and food-packaging technology.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Ionic liquids properties and applications · Analytical Chemistry and Sensors · Advanced Chemical Sensor Technologies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Institute of Analytical Chemistry and Radiochemistry, University of Technology of Graz, Stremayrgasse 16, 8010 Graz, Austria, and Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, D-93040 Regensburg, Germany

References (46)

Show source-provided references
1. Wolfbeis O. S. · Microchim. Acta · 1998 · 129 · 18110.1007/BF01244739 ↗
2. Meruva R. K. · Biosens. Bioelectron. · 1998 · 13 · 20110.1016/S0956-5663(97)00097-3 ↗
3. Cooney C. G. · Sens. Actuators B · 2000 · 69 · 18310.1016/S0925-4005(00)00544-X ↗
4. Tabacco M. B. · Anal. Chem. · 1999 · 71 · 15410.1021/ac980513c ↗
5. Neurauter G. · Fresenius J. Anal. Chem. · 2000 · 366 · 48110.1007/s002160050097 ↗
6. Montegut C. G. · Deep-Sea Res., Part II · 2002 · 49 · 204910.1016/S0967-0645(02)00027-9 ↗
7. Mills A. · Sens. Actuators B · 1997 · 38 · 41910.1016/S0925-4005(96)02116-8 ↗
8. Ferguson J. A. · Anal. Chim. Acta · 1997 · 340 · 12310.1016/S0003-2670(96)00510-7 ↗
9. Ge X. · Biotechnol. Bioeng. · 2005 · 89 · 32910.1002/bit.20337 ↗
10. Church N. · Trends Food Sci. Technol. · 1994 · 5 · 34510.1016/0924-2244(94)90211-9 ↗
11. Mills A. · Analyst · 1993 · 118 · 83910.1039/an9931800839 ↗
12. Mills A. · Anal. Chem. · 1992 · 64 · 138310.1021/ac00037a015 ↗
13. Nivens D. A. · Talanta · 2002 · 58 · 54310.1016/S0039-9140(02)00323-5 ↗
14. Mills A. · Sens. Actuators B · 1994 · 21 · 8310.1016/0925-4005(94)80008-1 ↗
15. Mills A. · Anal. Chim. Acta · 1994 · 285 · 11310.1016/0003-2670(94)85015-1 ↗
16. von Bultzingslowen C. · Anal. Chim. Acta · 2003 · 480 · 27510.1016/S0003-2670(02)01653-7 ↗
17. von Bultzingslowen C. · Analyst · 2002 · 127 · 147810.1039/B207438A ↗
18. Borisov S. M. · Adv. Funct. Mater. · 2006 · 11 · 153610.1002/adfm.200500778 ↗
19. Severinghaus J. W. · J. Appl. Physiol. · 1958 · 13 · 51510.1152/jappl.1958.13.3.515 ↗
20. Zhujun Z. · Anal. Chim. Acta · 1984 · 160 · 30510.1016/S0003-2670(00)84536-5 ↗
21. He X. · Anal. Chem. · 1995 · 67 · 226410.1021/ac00109a054 ↗
22. Raemer, D. B.; Walt, D. R.; Munkholm, C.US Patent 5.005.572,1991.
23. Weigl B. H. · Sens. Actuators B · 1995 · 28 · 15110.1016/0925-4005(95)80041-7 ↗
24. Nakamura N. · Sens. Actuators B · 2003 · 92 · 9810.1016/S0925-4005(03)00098-4 ↗
25. von Bültzingslöwen C. · Anal. Chim. Acta · 2003 · 480 · 27510.1016/S0003-2670(02)01653-7 ↗
26. Borisov S. M. · Adv. Mater. · 2006 · 18 · 151110.1002/adma.200600120 ↗
27. Wolfbeis O. S. · Anal. Chim. Acta · 1986 · 185 · 32110.1016/0003-2670(86)80060-5 ↗
28. Hui, H. K.; Bankert, C. S.Eur. Pat. Appl. EP 1990-308694.0,1990.
29. Parker J. W. · Anal. Chem. · 1993 · 65 · 232910.1021/ac00065a027 ↗
30. Scovazzo P. · Ind. Eng. Chem. Res. · 2004 · 13 · 685510.1021/ie049601f ↗
31. Camper D. · Ind. Eng. Chem. Res. · 2004 · 43 · 304910.1021/ie034097k ↗
32. Lee B. C. · Chem. Eng. Data · 2006 · 51 · 89210.1021/je050357o ↗
33. Jacquemin J. · J. Chem. Thermodyn. · 2006 · 38 · 49010.1016/j.jct.2005.07.002 ↗
34. Oter O. · Sens. Actuators B · 2006 · 117 · 29510.1016/j.snb.2005.11.040 ↗
35. Oter O. · Anal. Bioanal. Chem. · 2006 · 386 · 122510.1007/s00216-006-0659-z ↗
36. Weigl B. H. · Sens. Actuators · 1995 · 28 · 15110.1016/0925-4005(95)80041-7 ↗
37. Werner T. · Analyst · 1995 · 120 · 162710.1039/an9952001627 ↗
38. Mohr G. J. · Adv. Mater. · 1997 · 9 · 110810.1002/adma.19970091410 ↗
39. Brandrup J. · 1999
40. Kermis H. R. · Biotechnol. Prog. · 2002 · 18 · 104710.1021/bp0255560 ↗
41. Klimant, I.; Huber, Ch.; Liebsch, G.; Neurauter, G.; Stangelmayer, A.; Wolfbeis, O. S.InSpringer Series in Fluorescence Spectroscopy;Valeur, B.; Brochon; J. C., Eds.Springer:Berlin,2001; Vol.1, p257.10.1007/978-3-642-56853-4_13 ↗
42. Huber Ch. · Anal. Chem. · 2001 · 73 · 209710.1021/ac9914364 ↗
43. Neurauter G. · Anal. Chim. Acta · 1999 · 382 · 6710.1016/S0003-2670(98)00748-X ↗
44. Borisov S. M. · Appl. Spectrosc. · 2006 · 60 · 116710.1366/000370206778664590 ↗
45. Mills A. · Analyst · 1999 · 124 · 68510.1039/a900531e ↗
46. Bishop E. · 1972