| Literature DB >> 29915874 |
Rasel Das1, Bey Fen Leo2,3, Finbarr Murphy4.
Abstract
Without nanosafety guidelines, the long-term sustainability of carbon nanotubes (CNTs) for water purifications is questionable. Current risk measurements of CNTs are overshadowed by uncertainties. New risks associated with CNTs are evolving through different waste water purification routes, and there are knowledge gaps in the risk assessment of CNTs based on their physical properties. Although scientific efforts to design risk estimates are evolving, there remains a paucity of knowledge on the unknown health risks of CNTs. The absence of universal CNT safety guidelines is a specific hindrance. In this paper, we close these gaps and suggested several new risk analysis roots and framework extrapolations from CNT-based water purification technologies. We propose a CNT safety clock that will help assess risk appraisal and management. We suggest that this could form the basis of an acceptable CNT safety guideline. We pay particular emphasis on measuring risks based on CNT physico-chemical properties such as diameter, length, aspect ratio, type, charge, hydrophobicity, functionalities and so on which determine CNT behaviour in waste water treatment plants and subsequent release into the environment.Entities:
Keywords: Carbon nanotube; Nanosafety; Physicochemical properties; Risk assessment; Water purifications
Year: 2018 PMID: 29915874 PMCID: PMC6005998 DOI: 10.1186/s11671-018-2589-z
Source DB: PubMed Journal: Nanoscale Res Lett ISSN: 1556-276X Impact factor: 4.703
Fig. 1Nanosafety clock. Clockwise rotation pertains to major CNT risk measurements in water purification. These major risks are detailed in subsequent sections of this paper
The toxicity profiles of different types of CNTs in comparison with asbestos (in vivo studies)
| Types of CNTs | Diameter/length | Cells types | Result | References |
|---|---|---|---|---|
| Asbestos | Diameter (0.394 μm ± 1.83 μm) | Mesothelioma (mice) | Development of extensive inflammatory and proliferative changes. The carcinogenic activity occurred. | [ |
| MWCNT (mixture with graphite nanofibres) | Length (5–25 μm) | Lungs (mice) | No significant lung inflammation or tissue damage but caused systemic immune function alterations. | [ |
| MWCNT | Length (0.5–6.1 μm) | Lungs (rat) | Release of pro-inflammatory and pro-fibrotic mediators which could lead to lung fibrosing diseases. | [ |
| MWCNT (Nanocyl NC 7000) | Length (5–15 nm) | Lungs (Wistar rat) | Increase in BALF total cell count, pronounced multifocal granulomatous inflammation and lung fibrotic were the negative effects. | [ |
| SWCNT | Length (0.7 μm) | Intratracheal instillation (Wistar rat) | There was no increase in total cell or neutrophil count in BALF. Well-dispersed SWCNT did not induce neutrophil inflammation in the lung. | [ |
| SWCNT | Length (0.1–1 μm) | Lung (mice) | Leads to lung fibrosis effect and acute inflammatory phase reaction were also observed. | [ |
| Rigid MWCNT | Length (5.29 μm) | Mesotheliomas (rat) | Mesothelial injury by thin and thick MWCNTs is responsible for the extent of inflammogenicity and carcinogenicity. | [ |
| Long MWCNT | Diameter (> 20 nm) | Mesothelial lining of the chest cavity (mice) | Fibroblast formation proliferation which can lead to pulmonary fibrosis. Formation of lesions known as granulomas and inflammation occurrence were included | [ |
Fig. 2CNT lifecycle. The life cycle of CNT related to risk assessment studies [18, 61]