Introduction to Nanoscience and Nanotechnology. Chris BinnsЧитать онлайн книгу.
Rosetta spacecraft was launched and 12 years later was installed in orbit around the comet 67P/Churyumov‐Gerasimenko, from where spectacular images of the 4 km wide nucleus like the one in Figure 2.14a were obtained. The orbiter collected pieces of dust from the plumes emerging from the comet on sticky targets and it was the first space mission that had an atomic force microscope (see Chapter 5, Section 5.4.4) onboard that could image the grains with nanometre resolution [23]. Typical dust grains had sizes of a few μm but closer inspection showed that these particles were compact agglomerates of smaller grains as shown in Figure 2.14b. The image displays a single dust grain about 1 μm across but it is composed of at least seven smaller particles smaller than 500 nm across and there is evidence that these are composed of yet smaller particles. This is consistent with current models of protoplanetary growth where the dust is composed of a hierarchy of aggregates with the smallest units being nanoparticles.
Figure 2.14 Rosetta mission to comet 67P/Churyumov‐Gerasimenko. (a) Photo of the 4 km wide comet nucleus taken by the Navcam aboard the ESA Rosetta mission to comet 67P/Churyumov‐Gerasimenko from a distance of 28.6 km.
Source: ESA/Rosetta/NAVCAM/CC BY‐SA IGO 3.0. Reproduced under Creative Commons CC BY‐SA 3.0 license.
(b) Atomic force microscope (AFM) image of a single ~1 μm dust particle from the comet showing that it is composed of smaller particles.
Source: Reproduced with the permission of the Nature Publishing Group from [23].
2.7 Environmental Applications of Nanoparticles
The chapter so far has focused on naturally occurring nanoparticles or those produced as a by‐product of human activity. In this final section, the use of nanoparticle technologies to address environmental issues will be described with reference to two examples, that is, removing toxins from water and recycling of plastics.
2.7.1 Water Remediation Using Magnetic Nanoparticles
Figure 2.15 shows some examples of how anthropogenic activities can pollute the soil beneath the water table including urban run‐off, farming, industry and waste disposal. Sulfur‐containing emissions can also enter clouds and be rained back in the form of acid rain while the mobile water beneath the surface enters rivers and the evaporated material enters clouds so that the pollution is redistributed over the land. Plants take up the contaminants, which can then enter the food chain or the pollution can accumulate in fish, which are subsequently eaten by humans as in the notorious case of mercury poisoning in Japan in 1956 with over 2000 victims [24]. The most common pollutants are heavy metals and organic compounds and even very low contamination levels in the ng/l range can lead to cancers, respiratory infections, and skin diseases.
Soil and groundwater remediation to reduce toxins to safe levels is thus an important activity and traditionally, water is cleaned using filter beds. For severe or toxic contamination, the use of nanoporous filters, which present a very large active surface to remove contaminants per unit volume of filter, is more effective. An issue with these, however, is the slow volume flow rate through them and more recently there has been great interest in an alternative approach, which is to present the large surface area as a dispersal of nanoparticles within the contaminated water.
Figure 2.15 Pollution of soil and groundwater by anthropogenic activities. Releases by factories, urban run‐off, farming and waste disposal all introduce contaminants into the soil. In addition, sulfur compounds released into the air enter clouds and are re‐deposited as acid rain. The flow of groundwater in the water table aquifer introduces the contaminants into waterways, which become a source of redistribution.
The most popular type of magnetic nanoparticle is so‐called nano zero‐valent iron (nZVI), which can be produced chemically on a large scale with a relatively simple reaction [25]. The zero‐valent label is used to denote unoxidized or pure metallic iron but the metal is so reactive that the formation of an oxide shell during synthesis is unavoidable. This, however, is beneficial to some processes and it protects the core from rapid oxidation, though the oxide will, over time, eat into the core. Under certain applications, the magnetic nanoparticles can be separated from the water using an applied magnetic field.
The nZVI removes contaminants by forming compounds with them and bonding them to the surface of the nanoparticles, which is greatly facilitated by the large surface area presented. This is typically 25 m2/g for commercially available nZVI powders but can reach 100 m2/g (see Problem 1, Chapter 1). The freshly synthesized nZVI particles have a thin porous oxide shell that allows contaminants to get very close to the iron/oxygen interface where the reactions take place. As they work, the nanoparticles get coated by a shell of the reaction products and eventually become inactive. The first demonstration of the method was in 1997 where it was used to remove chlorinated organic toxins [26] but since then it has been shown to clear a range of contaminants from groundwater including antibiotics, dyes, solvents, pesticides, metals, and radioactive isotopes. For a comprehensive list of contaminants removed see [27].
A common method of application is illustrated in Figure 2.16 for the case of mobile groundwater requiring a static filter. After assessing the geological conditions at the site to decide on the density of nanoparticles required, boreholes are drilled to the required depth and the nVZI powder mixed with water is introduced as a slurry under pressure. This permeates the aquifer (the layer of water‐bearing permeable rock) and forms a static filter through which the groundwater flows. In some applications, it may be more appropriate to inject mobile nanoparticles into the water flow where they are carried to the source of pollution.
The discussion has focused entirely on the chemical properties of iron without considering its magnetism, which, in principle, provides a simple mechanism to separate the contaminant‐holding particles from the water. In the presence of a magnetic field gradient, dB/dz, a magnetic particle with a magnetic moment, μ (see Chapter 1, Section 1.2), experiences a force, F, in the direction of the field gradient given by:
Figure 2.16 Application of nZVI particles to groundwater remediation. In the case of mobile groundwater.
Figure 2.17 Magnetic separation of Pb contamination from water. (a) Suspension of grapheme‐coated nVZI (G‐nVZI) nanoparticles at a density of 1 mg/mi. (b) Separation of the G‐nVZI with a bar magnet.
(2.6)
So