Despite these concerns, the results of the current field applications with respect to contaminant reduction are promising, and no major adverse impacts on the environment have been reported so far. It is thus expected that these trials will contribute to promoting the technology in Europe.
Heterogeneous catalysis is one of the fastest developing branches of chemistry. Moreover, it is strongly connected to popular environment-related applications. Owing to the very fast changes in this field, for example, numerous discoveries in nanoscience and nanotechnologies, it is believed that an update of the literature on heterogeneous catalysis could be beneficial. This review not only covers the new developments of heterogeneous catalysis in environmental sciences but also touches its historical aspects. A short introduction to the mechanism of heterogeneous catalysis with a small section on advances in this field has also been elaborated. In the first part, recent innovations in the field of catalytic air, water, wastewater and soil treatment are presented, whereas in the second part, innovations in the use of heterogeneous catalysis for obtaining sustainable energy and chemicals are discussed. Catalytic processes are ubiquitous in all branches of chemistry and there are still many unsolved issues concerning them.
Nanoscale zerovalent iron (nZVI) is commonly used in advanced groundwater remediation processes. Here, we present a combined experimental and computational approach to elucidate the mechanism and kinetics of the reaction of nZVI with water under anaerobic conditions, which represents the basic reaction controlling the stability of nZVI in groundwater. The reaction kinetics was monitored at temperatures of 25 and 80 °C by 57 Fe Mossbauer spectroscopy on frozen dispersion samples. The experimentally determined rate constant for reaction of nZVI with water at 25 °C was 1.14 × 10 −3 h −1 ; the activation barrier measured for 60 nm sized nanoparticles (ΔG ⧧ 298K (aq) = 26.3 kcal/mol) fits the range delineated by two limiting theoretical models from advanced quantum chemical calculations: rate-limiting activation barriers of 31.6 and 18.0 kcal/mol depending on the computational model, i.e., an iron atom and an infinite iron surface, respectively. The computations indicated a two-step reaction mechanism involving two one-electron transfer processes: the first can be described by the reaction Fe + H 2 O → HFeOH, which represents the rate-limiting step, and the second by HFeOH + H 2 O → Fe(OH) 2 + H 2 . At 25 °C, the reaction product was identified experimentally as Fe(OH) 2 , which forms flat layered sheets extensively overgrowing nZVI particles. At 80 °C, ferrous hydroxide undergoes secondary anaerobic transformation to magnetite (Fe 3 O 4 ).
Contamination by chloroethenes has a severe negative effect on both the environment and human health. This has prompted intensive remediation activity in recent years, along with research into the efficacy of natural microbial communities for degrading toxic chloroethenes into less harmful compounds. Microbial degradation of chloroethenes can take place either through anaerobic organohalide respiration, where chloroethenes serve as electron acceptors; anaerobic and aerobic metabolic degradation, where chloroethenes are used as electron donors; or anaerobic and aerobic co-metabolic degradation, with chloroethene degradation occurring as a by-product during microbial metabolism of other growth substrates, without energy or carbon benefit. Recent research has focused on optimising these natural processes to serve as effective bioremediation technologies, with particular emphasis on (a) the diversity and role of bacterial groups involved in dechlorination microbial processes, and (b) detection of bacterial enzymes and genes connected with dehalogenation activity. In this review, we summarise the different mechanisms of chloroethene bacterial degradation suitable for bioremediation and provide a list of dechlorinating bacteria. We also provide an up-to-date summary of primers available for detecting functional genes in anaerobic and aerobic bacteria degrading chloroethenes metabolically or co-metabolically.
The prospective uses of tree gum polysaccharides and their nanostructures in various aspects of food, water, energy, biotechnology, environment and medicine industries, have garnered a great deal of attention recently. In addition to extensive applications of tree gums in food, there are substantial non-food applications of these commercial gums, which have gained widespread attention due to their availability, structural diversity and remarkable properties as 'green' bio-based renewable materials. Tree gums are obtainable as natural polysaccharides from various tree genera possessing exceptional properties, including their renewable, biocompatible, biodegradable, and non-toxic nature and their ability to undergo easy chemical modifications. This review focuses on non-food applications of several important commercially available gums (arabic, karaya, tragacanth, ghatti and kondagogu) for the greener synthesis and stabilization of metal/metal oxide NPs, production of electrospun fibers, environmental bioremediation, bio-catalysis, biosensors, coordination complexes of metal-hydrogels, and for antimicrobial and biomedical applications. Furthermore, polysaccharides acquired from botanical, seaweed, animal, and microbial origins are briefly compared with the characteristics of tree gum exudates.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.