Skip to main content

Novel Liquid Diffusion Tube Determines Electrolytes’ Relative Free Diffusion Velocities, Hydration Numbers and Overwhelmingly Revalidates Electrolytic Diffusion Law

  • Chapter
  • First Online:
Chemistry for Sustainable Development

Abstract

A novel liquid diffusion tube closed and cylindrical termed Diffusimeter was fabricated from glass tube and straight bore stopcocks to measure relative velocities of electrolytes in free diffusion. Solutions of two electrolytes known to give characteristic reaction were put one above each of two stopcocks and then released concurrently to diffuse head on through water in the diffusion path and finally to produce a precipitate or color as indicator at the encounter. Experimental objective required entry of time elapsed for the reaction mark to appear and the distances traveled by the electrolytes. The velocity ratio termed distance traveled ratio (DTR) was found to match with the Molar Mass Ratio Square Root (MMRSR) of the electrolyte pair taken in order. A direct proportionality between the velocity and the square root of molar mass was thus revalidated. The heavier electrolyte moved faster contrary to the gaseous diffusion. The results hinted hydration numbers of the diffusing electrolytes. Diffusion velocities of 30 salts were determined using this novel, innovative Diffusimetric Method named DTR model. Surprisingly NH4Cl and NH4SCN showed similar velocities. HCl and LiCl showed low diffusion rates due to their cations’ high charge to size ratio. Apparently MgCl2, CaCl2, and SrCl2 diffused with one H2O each but BaCl2, AgNO3, and FeIII alum with none. NaCl showed relatively high rate which traces its fitness as antibacterial agent and biosalt in human. Na2SO4 and K2SO4 showed identical velocities which together with metatheses hypothesize sylvite mineral formation mechanism over geological periods. Close diffusion rates of ZnCl2 and CdCl2 traces reasons for cadmium’s presence in zinc ores. Diffusion controlled effects are shown in FeIII salts’ reactions with NH4SCN; the DTR reveals reactant pair’s encounter nature at their conjunction. Manipulating electrolytes’ concentrations crystalline precipitates were obtained.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Similar content being viewed by others

References

  1. Graham TH (1883) Philos Mag J Sci 175–191; 269–276; 351–358

    Google Scholar 

  2. Fick A (1855) Philos Mag 10:30

    Google Scholar 

  3. Narasimhan TN (2004) Fick’s insights on liquid diffusion. EOS Trans Am Geophys Union 85(499):501

    Google Scholar 

  4. Shaw DJ (1992) Introduction to colloid and surface chemistry, 4th edn. Butterworth and Heinemann Ltd., London, 26

    Google Scholar 

  5. Jacobs MH (1967) Diffusion processes. McGraw-Hill, New York, pp 13–74

    Google Scholar 

  6. Khair A, Golzar Hossain GM, Saiful Alam M, Zakir Hossain Shaheen M (2010) Bangladesh Patent, Int. Cl5 G01N 13/00, 1004924

    Google Scholar 

  7. Emsley J (1991) The elements, 2nd edn. Oxford University Press, New York, pp 88–106

    Google Scholar 

  8. Shriver DF, Atkins PW, Langford CH (1991) Inorganic chemistry. Oxford University Press, Oxford, p 608

    Google Scholar 

  9. Cotton FA, Wilkinson G, Gaus L (1987) Basic inorganic chemistry, 2nd edn. Wiley, New York, p 271

    Google Scholar 

  10. Cotton FA, Wilkinson G (1972) Advanced inorganic chemistry, 3rd edn. Interscience, New York, p 217

    Google Scholar 

  11. Matwiyoff NA, Taube H (1968) J Am Chem Soc 90:2796

    Article  CAS  Google Scholar 

  12. Nakamura S, Meiboom S (1967) J Am Chem Soc 89:1765

    Article  CAS  Google Scholar 

  13. Hatashi H, Sarkari M, Zeinali M, Zare Aliabadi H (2010) Austr J Basic Appl Sci 4:4766–4771

    Google Scholar 

  14. Lewis RJ Sr (1993) Hawley’s condensed chemical dictionary, 12th edn. Van Nostrand Reinhold, New York, p 1110

    Google Scholar 

  15. Cotton FA, Wilkinson G, Murillo CA, Bochmann M (1999) Advanced inorganic chemistry, 6th edn. Wiley Interscience, New York, p 605

    Google Scholar 

  16. King EL (1964) How chemical reactions occur. W. A Benjamin, New York, p 65

    Google Scholar 

  17. Partington JR (1965) A textbook of inorganic chemistry, 6th edn. ELBS and Macmillan & Co Ltd., London, p 784

    Google Scholar 

  18. Katakis D, Gordorn G (1987) Mechanisms of inorganic reactions. Wiley, New York, p 72

    Google Scholar 

  19. Wells AF (1993) Structural inorganic chemistry, 5th edn. Oxford Science, New York, p 444

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Abul Khair .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2012 Springer Science+Business Media B.V.

About this chapter

Cite this chapter

Khair, A. et al. (2012). Novel Liquid Diffusion Tube Determines Electrolytes’ Relative Free Diffusion Velocities, Hydration Numbers and Overwhelmingly Revalidates Electrolytic Diffusion Law. In: Gupta Bhowon, M., Jhaumeer-Laulloo, S., Li Kam Wah, H., Ramasami, P. (eds) Chemistry for Sustainable Development. Springer, Dordrecht. https://doi.org/10.1007/978-90-481-8650-1_12

Download citation

Publish with us

Policies and ethics