Quantification of amine functional groups on silica nanoparticles: a multi-method approach.

Ying Sun, Filip Kunc, Vinod Balhara, Brian Coleman, Oltion Kodra, Mohammad Raza, Maohui Chen, Andreas Brinkmann, Gregory P Lopinski, Linda J Johnston
Author Information
  1. Ying Sun: National Research Council Canada Ottawa ON Canada K1A 0R6 Linda.Johnston@nrc-cnrc.gc.ca.
  2. Filip Kunc: National Research Council Canada Ottawa ON Canada K1A 0R6 Linda.Johnston@nrc-cnrc.gc.ca.
  3. Vinod Balhara: National Research Council Canada Ottawa ON Canada K1A 0R6 Linda.Johnston@nrc-cnrc.gc.ca.
  4. Brian Coleman: National Research Council Canada Ottawa ON Canada K1A 0R6 Linda.Johnston@nrc-cnrc.gc.ca.
  5. Oltion Kodra: National Research Council Canada Ottawa ON Canada K1A 0R6 Linda.Johnston@nrc-cnrc.gc.ca.
  6. Mohammad Raza: National Research Council Canada Ottawa ON Canada K1A 0R6 Linda.Johnston@nrc-cnrc.gc.ca.
  7. Maohui Chen: National Research Council Canada Ottawa ON Canada K1A 0R6 Linda.Johnston@nrc-cnrc.gc.ca.
  8. Andreas Brinkmann: National Research Council Canada Ottawa ON Canada K1A 0R6 Linda.Johnston@nrc-cnrc.gc.ca. ORCID
  9. Gregory P Lopinski: National Research Council Canada Ottawa ON Canada K1A 0R6 Linda.Johnston@nrc-cnrc.gc.ca. ORCID
  10. Linda J Johnston: National Research Council Canada Ottawa ON Canada K1A 0R6 Linda.Johnston@nrc-cnrc.gc.ca. ORCID

Abstract

Surface chemistry is an important factor for quality control during production of nanomaterials and for controlling their behavior in applications and when released into the environment. Here we report a comparison of four methods for quantifying amine functional groups on silica nanoparticles (NPs). Two colorimetric assays are examined, ninhydrin and 4-nitrobenzaldehyde, which are convenient for routine analysis and report on reagent accessible amines. Results from the study of a range of commercial NPs with different sizes and surface loadings show that the assays account for 50-100% of the total amine content, as determined by dissolution of NPs under basic conditions and quantification by solution-state H NMR. To validate the surface quantification by the colorimetric assays, the NPs are modified with a trifluoromethylated benzaldehyde probe to enhance sensitivity for quantitative F solid state NMR and X-ray photoelectron spectroscopy (XPS). Good agreement between the assays and the determination from solid-state NMR is reinforced by elemental ratios from XPS, which indicate that in most cases the difference between total and accessible amine content reflects amines that are outside the depth probed by XPS. Overall the combined results serve to validate the relatively simple colorimetric assays and indicate that the reactions are efficient at quantifying surface amines, by contrast to some other covalent modifications that have been employed for functional group quantification.

References

  1. Org Biomol Chem. 2012 Feb 7;10(5):1025-31 [PMID: 22159282]
  2. Langmuir. 2013 Dec 10;29(49):15386-93 [PMID: 24199945]
  3. Anal Biochem. 1981 Oct;117(1):147-57 [PMID: 7316187]
  4. Anal Chem. 2015 Sep 15;87(18):9451-8 [PMID: 26280598]
  5. Langmuir. 2015 Jan 20;31(2):824-32 [PMID: 25514625]
  6. J Colloid Interface Sci. 2014 Apr 15;420:182-8 [PMID: 24559717]
  7. ACS Appl Mater Interfaces. 2017 Mar 8;9(9):8344-8353 [PMID: 28195455]
  8. Langmuir. 2012 Apr 3;28(13):5562-9 [PMID: 22428537]
  9. J Colloid Interface Sci. 2000 Dec 15;232(2):400-407 [PMID: 11097776]
  10. Langmuir. 2016 Apr 5;32(13):3253-61 [PMID: 26914738]
  11. Anal Chem. 1999 Jul 1;71(13):2554-7 [PMID: 21662801]
  12. J Agric Food Chem. 2004 Feb 11;52(3):385-406 [PMID: 14759124]
  13. Analyst. 2015 Mar 21;140(6):1804-8 [PMID: 25652135]
  14. Data Brief. 2016 Apr 07;7:1296-301 [PMID: 27141527]
  15. Anal Chem. 2015 Oct 6;87(19):10117-24 [PMID: 26334589]
  16. Anal Chem. 2017 Jan 3;89(1):681-687 [PMID: 28105822]
  17. ACS Appl Mater Interfaces. 2015 Oct 7;7(39):21682-9 [PMID: 26371804]
  18. Beilstein J Org Chem. 2014 Nov 20;10:2729-37 [PMID: 25550737]
  19. Anal Bioanal Chem. 2011 Mar;399(7):2503-9 [PMID: 21243340]
  20. J Am Chem Soc. 2014 Oct 1;136(39):13781-8 [PMID: 25153717]
  21. J Am Chem Soc. 2012 May 16;134(19):8268-76 [PMID: 22524503]
  22. Solid State Nucl Magn Reson. 2014 Feb-Apr;57-58:22-8 [PMID: 24300107]
  23. Langmuir. 2012 Jan 10;28(1):416-23 [PMID: 22128807]
  24. Anal Chem. 2018 May 1;90(9):5887-5895 [PMID: 29633836]
  25. Anal Chem. 2015 Mar 3;87(5):2685-92 [PMID: 25621905]
  26. Phys Chem Chem Phys. 2017 Jan 18;19(3):1781-1789 [PMID: 28058422]
  27. Sci Rep. 2015 Dec 01;5:17040 [PMID: 26621190]
  28. Anal Chem. 2015 Sep 15;87(18):9376-83 [PMID: 26284998]
  29. Anal Bioanal Chem. 2010 Feb;396(3):983-1002 [PMID: 20052578]
  30. Anal Chem. 2012 Apr 17;84(8):3654-61 [PMID: 22404690]
  31. Anal Chem. 2018 Nov 20;90(22):13322-13330 [PMID: 30372033]
  32. J Vac Sci Technol A. 2013 Sep;31(5):50820 [PMID: 24482557]

Word Cloud

Created with Highcharts 10.0.0assaysamineNPsfunctionalcolorimetricaminessurfacequantificationNMRXPSreportquantifyinggroupssilicaaccessibletotalcontentvalidateindicateSurfacechemistryimportantfactorqualitycontrolproductionnanomaterialscontrollingbehaviorapplicationsreleasedenvironmentcomparisonfourmethodsnanoparticlesTwoexaminedninhydrin4-nitrobenzaldehydeconvenientroutineanalysisreagentResultsstudyrangecommercialdifferentsizesloadingsshowaccount50-100%determineddissolutionbasicconditionssolution-stateHmodifiedtrifluoromethylatedbenzaldehydeprobeenhancesensitivityquantitativeFsolidstateX-rayphotoelectronspectroscopyGoodagreementdeterminationsolid-statereinforcedelementalratioscasesdifferencereflectsoutsidedepthprobedOverallcombinedresultsserverelativelysimplereactionsefficientcontrastcovalentmodificationsemployedgroupQuantificationnanoparticles:multi-methodapproach

Similar Articles

Cited By