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Published November 19, 2020 | Submitted
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Ethanol-Drying Regeneration of N95 Respirators

Abstract

A critical shortage of respirators, masks and other personal protective equipment (PPE) exists due to the COVID-19 pandemic. Of particular need are N95 respirators, which use meltblown microfibers of charged polypropylene. An intensive search is underway to find reliable methods to lengthen the useful life of these normally disposable units. Recent experiments on respirators cleaned with ethanol solutions found drastic post-treatment drops infiltration efficiency (>40%). This has been attributed to a mechanism whereby ethanol disrupts the charges in the microfibers, reducing their ability to trap particles. The CDC/NIOSH has issued guidance directing clinicians and researchers to pursue other methods of decontamination. In our experiments, we replicated the drop in efficiency after 70% ethanol treatment, but we found that the efficiency rose again after more effective drying, which we achieved with a vacuum chamber. After drying at pressures of < ~6 mbar (0.6 kPa), the measured filtering efficiency rose to within 2% of the pre-washing value, and we found that this was sustained for 5 cleaning-drying cycles in three models of N95 masks. We stress that our tests are not meant to certify that the respirators are safe for use, which would require further, standardized, testing under NIOSH protocols. The tests presented here are used to understand basic mechanisms by which treatments can decrease or increase filtration efficiency. The main mechanism underlying the loss and recovery of filter efficiency seems to be the deposition and removal of water molecules adsorbed on the fiber surfaces, a hypothesis which is supported by several observations: (A) the filtering efficiency increases non-linearly with the weight loss during drying. (B) filtration efficiency shows an abrupt recovery as the vacuum pressure drops from 13 to 6 mbar, the range physically attributable to the removal of adsorbed water. (C) Optical microscopy of the microfiber layer reveals surface wetting of the fibers, which is most resistant to drying in dense regions of the fiber network. These observations indicate that losses in filter efficiency may be caused by the wicking of water into the dense fiber networks, reducing the available surface area for filtration. Such a degradation mechanism has two implications: (A) Ethanol and other aqueous decontamination methods may be more viable than previously assumed. Investigations of such methods should specify drying methods in their protocols. We employ vacuum chambers in this study, but other methods of removing adsorbed water could be equivalent. (B) This mechanism presents the possibility that mask filtration performance may be subject to degradation by other sources of moisture, and that the mask would continue to be compromised even if it appears dry. Further research is needed to determine the conditions under which such risks apply, and whether drying should be a routine practice for respirators undergoing extended use. This study introduces a number of methods which could be developed and validated for use in resource-limited settings. As the pandemic continues to spread in rural areas and developing nations, these would allow for local efforts to decontaminate, restore, and test medical masks.

Additional Information

The copyright holder for this preprint is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license. This version posted July 3, 2020. Funding Statement: No external funding. Data Availability: All data are available upon request. The authors have declared no competing interest. Author Declarations: All relevant ethical guidelines have been followed; any necessary IRB and/or ethics committee approvals have been obtained and details of the IRB/oversight body are included in the manuscript. Yes. All necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived. Yes. I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance). Yes. I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable. Yes.

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Submitted - 2020.04.12.20059709v1.full.pdf

Submitted - 2020.04.12.20059709v2.full.pdf

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Additional details

Created:
August 19, 2023
Modified:
October 20, 2023