American Journal of Environmental Science and Engineering

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Conversion of Carbon Dioxide from Air to Methanol, Formaldehyde, Formic Acid and Ammonium Pentaborate Tetrahydrate

Received: Jul. 22, 2019    Accepted: Aug. 14, 2019    Published: May 28, 2020
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Abstract

A process for sequestering CO2 from air by sparging air through an NH4OH solution and adding NaBH4 produces formic acid, formaldehyde, methanol and ammonium pentaborate tetrahydrate in appreciable yields. This sparging chemistry centers around the well-known phenomenon of carbonate in strong bases. The newly discovered chemistry is based on H- as a nucleophile that can attack a nucleofuge, the carbonyl in carbonate in strong base. NaHCO3 was used as a positive control for the sparging method giving nearly identical IR spectra for sparged NH4OH and, NaHCO3 added NH4OH. This novel chemistry can be shown to produce H- substitution products of sulfate and phosphate esters of carbohydrates. The H- nucleophile adds one, two and three H atoms to carbonate, for formic acid, formaldehyde and methanol, respectively, two H atoms to sulfate esters and one H atom to phosphate. In this way phosphate versus sulfate substitution can be discerned by mass spectrometry using this chemistry. The pH profile of the reaction mixture for the NaHCO3 dissolved in 1 N NH4OH first dropped below starting pH possibly because the reaction vessel was capped, allowing NH3(g) to evolve and possibly drive the reaction forward. But then the pH returned to a slight lower pH than the starting pH 11.4. This novel chemistry may allow a sustainable reduction in the green-house gas, CO2, worldwide, to relieve pressure on food uses for corn and thereby avert food shortages throughout the world.

DOI 10.11648/j.ajese.20200402.11
Published in American Journal of Environmental Science and Engineering ( Volume 4, Issue 2, June 2020 )
Page(s) 13-16
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Sequestration by Sparging Air, Conversion of CO2, Formic Acid, Methanol, Formaldehyde, Ammonium Pentaborate Tetrahydrate

References
[1] Finholt, A.; Jacobson, E.; The Reduction of Carbon Dioxide to Formic Acid with Lithium Aluminum Hydride J. Am. Chem. Soc. 74 (15) 3943-3944 (1952).
[2] Madson, M.; Manufacturing of MeOH, formaldehyde, formic acid and ammonium pentaborate tetrahydrate and references therein, patent, US 8, 685, 355 B2 (2014).
[3] Madson, M.; Method of discerning carbohydrate esters patent US 9, 726, 671 B2 (2017).
[4] Christus, J.; Madson, M.; Possible Mimics of Duffy Binding Protein-II for Plasmodium vivax Binding Endothelial Cells or Binding Plasmodium falciparum by Mimicking Epitope on Erythrocyte Binding Antigen-175 A World Journal of Food Science and Technology 2 (2) 44-54 (2018).
[5] Christus, J.; Madson, M.; Possible Treatment of Mycobacterium Lepramatous with Bovine Milk World Journal of Food Science and Technology 2 (3) 55-61 (2018).
[6] Christus, J.; Madson, M.; Preparation of 2,5-anhydro di-(hydrido) di-phosphate di-hydrate Mannitol (Glucitol) from Banana Fruit Yields a Possible Fructose 1,6 Bisphosphate Aldolase Inhibitor (s) accepted for publication World Journal of Food Science and Technology (2019).
[7] Christus, J.; Madson, M.; Preparation of Possible P Selectin Inhibitor from Bovine Thyroglobulin, (di-hydrido) Sulfo Hydrate 1,5 Anhydro L-fucitol accepted for publication World Journal of Food Science and Technology (2019).
[8] Madson, M.; Method of isolating and analyzing oligosaccharides in glycoproteins patent US 9, 625, 468 B1 (2017).
[9] Madson, M.; Method for isolating and identifying fruit oligosaccharides in banana fruit US patent 9, 557, 335 B2 (2017).
[10] Muetterties, E.; Ed. Boron Hydride Chemistry, Academic Press New York 1975.
[11] Wang Y.; Yu, Z-X. Rhodium-Catalyzed [5 + 2 + 1] Cycloaddition of Ene–Vinylcyclopropanes and CO: Reaction Design, Development, Application in Natural Product Synthesis, and Inspiration for Developing New Reactions for Synthesis of Eight-Membered Carbocycles Acc. Chem. Res. 20154882288-2296.
[12] A non-syn-gas catalytic route to methanol production Wu, C-T.; Yu, K.; Liao, F.; Young, N.; Nellist, P.; Dent, A.; Kroner, A.; et al and Tsang, S.; Nature Communications 3, Article number: 1050 (2012).
[13] Chmiekniak, T.; Sciazko, M. Co-gasification of biomass and coal for methanol synthesis Applied Energy 74 (3–4) 393-403 (2003).
[14] McKendry, P.; Energy production from biomass (part 2): conversion technologies Bioresource Technology 83, (1) 47-54 (2002).
[15] Lim, C-H.; Holder, A.; Hynes, J.; Musgrave, C.; Reduction of CO2 to Methanol Catalyzed by a Biomimetic Organo-Hydride Produced from Pyridine J. Am. Chem. Soc. 20141364516081.
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  • APA Style

    Jesus Christus, Michael Arden Madson. (2020). Conversion of Carbon Dioxide from Air to Methanol, Formaldehyde, Formic Acid and Ammonium Pentaborate Tetrahydrate. American Journal of Environmental Science and Engineering, 4(2), 13-16. https://doi.org/10.11648/j.ajese.20200402.11

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    ACS Style

    Jesus Christus; Michael Arden Madson. Conversion of Carbon Dioxide from Air to Methanol, Formaldehyde, Formic Acid and Ammonium Pentaborate Tetrahydrate. Am. J. Environ. Sci. Eng. 2020, 4(2), 13-16. doi: 10.11648/j.ajese.20200402.11

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    AMA Style

    Jesus Christus, Michael Arden Madson. Conversion of Carbon Dioxide from Air to Methanol, Formaldehyde, Formic Acid and Ammonium Pentaborate Tetrahydrate. Am J Environ Sci Eng. 2020;4(2):13-16. doi: 10.11648/j.ajese.20200402.11

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  • @article{10.11648/j.ajese.20200402.11,
      author = {Jesus Christus and Michael Arden Madson},
      title = {Conversion of Carbon Dioxide from Air to Methanol, Formaldehyde, Formic Acid and Ammonium Pentaborate Tetrahydrate},
      journal = {American Journal of Environmental Science and Engineering},
      volume = {4},
      number = {2},
      pages = {13-16},
      doi = {10.11648/j.ajese.20200402.11},
      url = {https://doi.org/10.11648/j.ajese.20200402.11},
      eprint = {https://download.sciencepg.com/pdf/10.11648.j.ajese.20200402.11},
      abstract = {A process for sequestering CO2 from air by sparging air through an NH4OH solution and adding NaBH4 produces formic acid, formaldehyde, methanol and ammonium pentaborate tetrahydrate in appreciable yields. This sparging chemistry centers around the well-known phenomenon of carbonate in strong bases. The newly discovered chemistry is based on H- as a nucleophile that can attack a nucleofuge, the carbonyl in carbonate in strong base. NaHCO3 was used as a positive control for the sparging method giving nearly identical IR spectra for sparged NH4OH and, NaHCO3 added NH4OH. This novel chemistry can be shown to produce H- substitution products of sulfate and phosphate esters of carbohydrates. The H- nucleophile adds one, two and three H atoms to carbonate, for formic acid, formaldehyde and methanol, respectively, two H atoms to sulfate esters and one H atom to phosphate. In this way phosphate versus sulfate substitution can be discerned by mass spectrometry using this chemistry. The pH profile of the reaction mixture for the NaHCO3 dissolved in 1 N NH4OH first dropped below starting pH possibly because the reaction vessel was capped, allowing NH3(g) to evolve and possibly drive the reaction forward. But then the pH returned to a slight lower pH than the starting pH 11.4. This novel chemistry may allow a sustainable reduction in the green-house gas, CO2, worldwide, to relieve pressure on food uses for corn and thereby avert food shortages throughout the world.},
     year = {2020}
    }
    

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    AB  - A process for sequestering CO2 from air by sparging air through an NH4OH solution and adding NaBH4 produces formic acid, formaldehyde, methanol and ammonium pentaborate tetrahydrate in appreciable yields. This sparging chemistry centers around the well-known phenomenon of carbonate in strong bases. The newly discovered chemistry is based on H- as a nucleophile that can attack a nucleofuge, the carbonyl in carbonate in strong base. NaHCO3 was used as a positive control for the sparging method giving nearly identical IR spectra for sparged NH4OH and, NaHCO3 added NH4OH. This novel chemistry can be shown to produce H- substitution products of sulfate and phosphate esters of carbohydrates. The H- nucleophile adds one, two and three H atoms to carbonate, for formic acid, formaldehyde and methanol, respectively, two H atoms to sulfate esters and one H atom to phosphate. In this way phosphate versus sulfate substitution can be discerned by mass spectrometry using this chemistry. The pH profile of the reaction mixture for the NaHCO3 dissolved in 1 N NH4OH first dropped below starting pH possibly because the reaction vessel was capped, allowing NH3(g) to evolve and possibly drive the reaction forward. But then the pH returned to a slight lower pH than the starting pH 11.4. This novel chemistry may allow a sustainable reduction in the green-house gas, CO2, worldwide, to relieve pressure on food uses for corn and thereby avert food shortages throughout the world.
    VL  - 4
    IS  - 2
    ER  - 

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Author Information
  • Research and Development, Bio Logistics Limited Liability Company, Ames, USA

  • Research and Development, Bio Logistics Limited Liability Company, Ames, USA

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