A bibliometric description of lignin applicability for the removal of chemical pollutants in effluents

Several industrial sectors produce tons of effluents daily containing a high amount of hazardous chemical pollutants that pose a major threat to the environment and human health. Current wastewater treatment methods, such as flocculation and activated carbon adsorption, have drawbacks linked to high material cost and too much energy consumption. Thus, the search for renewable, biodegradable, and efficient materials has been the object of research aimed at replacing the conventional materials used to cheapen processes and reduce environmental impacts. Lignin stands out in this context as it has low cost and high availability. Therefore, several scientific researches were developed to harness the potential of lignin, especially as adsorbent, for the removal of chemical agents from effluents. This paper presents a bibliometric review performed on the Scopus database, showing the evolution of studies related to the applicability of lignin in the removal of chemical pollutants in waters over the last five years. Data regarding annual publications, languages, journals, countries, institutions, keywords, and subjects were analyzed. The realized screening selected 130 articles that met the previously defined criteria. Results indicated a strong collaboration between countries and China's substantial contribution to the documents. The analysis also has shown that lignin is mainly used as adsorbent material, sorbent, flocculant agent, and hydrogel and presents important results and information for future researchers on this topic.The authors acknowledge financial assistance from the Brazilian research funding agencies such as CAPES (Coordination for the Improvement of Higher Education Personnel) under Finance Code 001, a Brazilian foundation within the Ministry of Education (MEC), CNPq (National Council for Scientific and Technological Development), a Brazilian foundation associated to the Ministry of Science and Technology (MCT), and FAPITEC/SE (the Foundation of Support to Research and Technological Innovation of the State of Sergipe).info:eu-repo/semantics/publishedVersio

Combining Electrocatalysts and Biobased Adsorbents for Sustainable Denitrification

Efficient treatment of domestic and industrial wastewater is one of the major challenges of the 21st century. Among the inorganic pollutants, nitrogen species are significant contaminants and the management of the nitrogen cycle is one the most crucial part of wastewater purification. Herein, we report an integrated method that minimizes the amount of used chemicals, can be empowered by renewable energy, uses renewables materials for ammonia recovery and is scalable. Complete denitrification of wastewater was achieved by combining electrochemical and adsorption treatment for real wastewater samples from the Stockholm water pilot plant. 98% of nitrate was selectively converted to ammonia over abundant copper electrocatalysts in Na2SO4 supporting electrolyte at –0.6 V vs. RHE within three hours. The valorized nitrate in form of ammonia could be recovered by means of cheap Kraft Lignin-SiO2 sorbents to achieve a total denitrification. The presented method is economically feasible, scalable and contributes to sustainable recycling within a circular economy.</div

Exploring the Origins of Improved Photocurrent by Acidic Treatment for Quaternary Tantalum-Based Oxynitride Photoanodes on the Example of CaTaO2N

Quaternary tantalum-based oxynitrides ATa(O,N)3, with electronic band gaps between 1.8 and 2.4 eV, are promising materials for photochemical water-splitting. The tailoring of their surface properties is a critical aspect to obtain efficient hole extraction. We report on the origin of improved photoelectrochemical (PEC) water oxidation by means of acidic treatment for this class of compounds on the example of cubic CaTaO2N particles. We address the effect of acidic treatment by using complementary physical characterization techniques, such as X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS), 1H and 14N solid-state nuclear magnetic resonance (NMR) spectroscopy, electron microscopy and electronic band structure calculations at the density functional theory (DFT) level. In combination with photoelectrochemical measurements, solid-state NMR indicates that the restructured surface displays a meaningfully higher concentration of terminating OH groups. Subsequent deposition of a nickel borate (NiBi) catalyst on the acid-treated surface yields a higher percentual upsurge of photocurrent in comparison to pristine CaTaO2N. Our results highlight the application of solid-state NMR spectroscopy for understanding of the semiconductor-catalyst interface in photochemical devices