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In this study, selective green synthesis of gold nanoparticles (nAu) with the use of Tarragon extract (Artemisia dracunculus) was investigated. Characterization of the synthetized nAu was carried out using several techniques including: UV-Vis, SEM, zeta potential analysis, DLS, and ATR-FTIR. Based on measurements of Tarragon extract by HPLC-MS, significant chemical substances participating as reducing and stabilizing agents were identified. FTIR confirmed typical functional groups that could be found in these acids on the nAu surface, such as O-H, C=O and C-O. The effects of various parameters (concentration of Tarragon extract, Au precursor, and initial pH of the synthesis) on the shape and size of the nanoparticles have been investigated. UV-Vis and SEM confirmed the formation of nAu at various concentrations of the extract and Au precursor and showed correlation between the added extract concentration and shift in maximal absorbance towards higher frequencies, indicating the formation of smaller nanoplates. Zeta potential determined at various pH levels revealed that its value decreased with pH, but for all experiments in the pH range of 2.8 to 5.0, the value is below - 30 mV, an absolute value high enough for long-term nAu stability. In order to evaluate nAu catalytic activity, the reduction of 4-nitrophenol to 4-aminophenol by sodium borohydride was used as a model system. The reaction takes place 1.5 times faster on Au-triangles than on Au-spherical NPs.

The production and use of chlorophenolic compounds in industry has led to the introduction of many xenobiotics, among them chlorophenols (CPs), into the environment. Five CPs are listed in the priority pollutant list of the U.S. EPA, with pentachlorophenol (PCP) even being proposed for listing under the Stockholm Convention as a persistent organic pollutant (POP). A green procedure for degrading such pollutants is greatly needed. The use of ferrate could be such a process. This paper studies the degradation of CPs (with an emphasis on PCP) in the presence of ferrate both in a spiked demineralized water system as well as in real contaminated groundwater. Results proved that ferrate was able to completely remove PCP from both water systems. Investigation of the effect of ferrate purity showed that even less pure and thus much cheaper ferrate was applicable. However, with decreasing ferrate purity, the degradability of CPs may be lower.

Hexachlorocyclohexane (HCH) isomers represent a family of formerly widely utilized pesticides that are persistent, capable of undergoing long-range transport and tend to bioaccumulate in human and animal tissue. Their widespread global utilization coupled with a propensity to adversely impact human health and the environment translates into an urgent need to develop feasible methodologies by which to treat HCH-impacted groundwater and soil. The present study was conducted to evaluate the efficacy of two persulfate-based oxidants: peroxydisulfate (S2O8 (2-), PDS) and peroxymonosulfate (HSO5 (-), PMS) activated by electrochemical processes (EC) to treat HCH-impacted environmental media. This research demonstrated that the optimal experimental conditions (oxidant dose and electrical current) were 2 mM PDS and 20 mA for an aqueous solution of 4 μM of summed HCHs (ΣHCH). GC/MS full scan analysis revealed the presence of 2,4,6-trichlorophenol as the only detectable intermediate formed during electro-activated PDS treatment of ΣHCH. The investigated method was tested on leachate from a known HCHs-impacted site in Hajek, Czech Republic which contained 106 μg/l of ΣHCH and 129 μg/l of chlorobenzenes. Results from batch treatment showed positive results for electro-activated PDS but only negligible effectiveness for electro-activated PMS. In addition to explaining the efficacy of the electro-activated PDS, this research also explored the basis for the differing reactivities of these two persulfates.

Purpose: Nanoscale zero valent iron (NZVI) is emerging as a new option for the treatment of contaminated soil and groundwater targeting mainly chlorinated organic contaminants (e.g., solvents, pesticides) and inorganic anions or metals. The purpose of this article is to give a short overview of the practical experience with NZVI applications in Europe and to present a comparison to the situation in the USA. Furthermore, the reasons for the difference in technology use are discussed. Method: The results in this article are based on an extensive literature review and structured discussions in an expert workshop with experts from Europe and the USA. The evaluation of the experiences was based on a SWOT (strength, weakness, opportunity, threat) analysis. Result: There are significant differences in the extent and type of technology used between NZVI applications in Europe and the USA. In Europe, only three full-scale remediations with NZVI have been carried out so far, while NZVI is an established treatment method in the USA. Bimetallic particles and emulsified NZVI, which are extensively used in the USA, have not yet been applied in Europe. Economic constraints and the precautionary attitude in Europe raise questions regarding whether NZVI is a cost-effective method for aquifer remediation. Challenges to the commercialization of NZVI include mainly non-technical aspects such as the possibility of a public backlash, the fact that the technology is largely unknown to consultants, governments and site owners as well as the lack of long-term experiences. Conclusion: 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