In this review, the roles of room temperature ionic liquids (RTILs) and RTIL based solvent systems as proposed alternatives for conventional organic electrolyte solutions are described. Ionic liquids are introduced as well as the relevant properties for their use in electrochemistry (reduction of ohmic losses), such as diffusive molecular motion and ionic conductivity. We have restricted ourselves to provide a survey on the latest, most representative developments and progress made in the use of ionic liquids as electrolytes, in particular achieved by the cyclic voltammetry technique. Thus, the present review comprises literature from 2015 onward covering the different aspects of RTILs, from the knowledge of these media to the use of their properties for electrochemical processes. Out of the scope of this review are heat transfer applications, medical or biological applications, and multiphasic reactions.

For the past two decades, with the increase in plastic consumption came a rise in plastic waste, with the bulk of it ending up in landfills, incinerated, recycled or leaking into the environment, especially in aquatic ecosystems. Plastic waste poses a significant environmental threat and a wealth issue due to its non-biodegradability and recalcitrant nature. Polyethylene (PE) remains one of the major utilized polymers in different applications amid all the other types because of its low production costs, simplistic nature prone to be modified and historically predominant researched material. Since the common methods for plastic disposal are troubled by limitations, there is a growing need for more appropriate and environment friendly methods alternatives. This study highlights several ways that can be used to assist PE (bio)degradation and mitigate its waste impact. Biodegradation (microbiological activity driven) and photodegradation (radiation driven) are the most promising for PE waste control. The shape of the material (powder, film, particles, etc.), the composition of medium, additives and pH, temperature and incubation or exposure times contribute to plastic degradation efficiency. Moreover, radiation pretreatment can enhance the biodegradability of PE, providing a promising approach to fighting plastic pollution. This paper relates the most significant results regarding PE degradation studies followed by weight loss analysis, surface morphology changes, oxidation degree (for photodegradation) and mechanical properties assessment. All combined strategies are very promising to minimize the polyethylene impact. However, there is still a long way to go through. The degradation kinetics is still low for the currently available biotic or abiotic processes, and complete mineralization is thoroughly unseen.

The novel Ag(I) and Cu(II) coordination polymers [Ag(μ₃-1κO;2:3κO′;4κN-HL)]_n∙n/2H₂O (1) and [Cu(en)₂(μ-1κO;2κN-L)]_n∙nH₂O (2) [HL⁻ = 2-(2-(1-cyano-2-oxopropylidene)hydrazinyl)benzene sulfonate] were synthesized and characterized by IR and ESI-MS spectroscopies, elemental and single crystal X-ray diffraction analyses. Compounds 1 and 2 as well as the already known complex salt [Cu(H₂O)₂(en)₂](HL)₂ (3) have been tested as homogenous catalysts for the cyanosilylation reaction of different aldehydes with trimethylsilyl cyanide, to provide cyanohydrin trimethylsilyl ethers. Coordination polymer 2 was found to be the most efficient one, with yields ranging from 76 to 88% in methanol, which increases up to 99% by addition of the ionic liquid [DHTMG][L-Lactate].

The copper(II) complexes [CuL(H₂O)₂]∙H₂O (1) and [CuL(dea)] (2) [L = 2-(2-(1,3-dioxo-1H-inden-2(3H)-ylidene)hydrazinyl)benzenesulfonate, dea = diethanolamine] were applied as catalysts in the peroxidative (with tert-butyl-hydroperoxide or hydrogen peroxide) conversion of cyclohexane to cyclohexanol and cyclohexanone, either in acetonitrile or in any of the ionic liquids [bmim][NTf₂] and [hmim][NTf₂] [bmim = 1-butyl-3-methylimidazolium, hmim = 1-hexyl-3-methylimidazolium, NTf₂ = bis(trifluoromethanesulfonyl) imide]. Tert-butyl-hydroperoxide led to better product yields, as compared to H₂O₂, with a selectivity directed towards cyclohexanone. The ILs showed a better performance than the conventional solvent for the copper complex 1. No catalytic activity was observed for 2 in the presence of an IL.