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1. Effects of residual disinfectants on the redox speciation of lead( ii )/( iv ) minerals in drinking water distribution systems

   https://doi.org/10.1039/d0ew00706d  

   Avasarala, Sumant ; Orta, John ; Schaefer, Michael ; Abernathy, Macon ; Ying, Samantha ; Liu, Haizhou ( February 2021 , Environmental Science: Water Research & Technology)

   null (Ed.)

   This study investigated the reaction kinetics on the oxidative transformation of lead( ii ) minerals by free chlorine (HOCl) and free bromine (HOBr) in drinking water distribution systems. According to chemical equilibrium predictions, lead( ii ) carbonate minerals, cerussite PbCO 3(s) and hydrocerussite Pb 3 (CO 3 ) 2 (OH) 2(s) , and lead( ii ) phosphate mineral, chloropyromorphite Pb 5 (PO 4 ) 3 Cl (s) are formed in drinking water distribution systems in the absence and presence of phosphate, respectively. X-ray absorption near edge spectroscopy (XANES) data showed that at pH 7 and a 10 mM alkalinity, the majority of cerussite and hydrocerussite was oxidized to lead( iv ) mineral PbO 2(s) within 120 minutes of reaction with chlorine (3 : 1 Cl 2  : Pb( ii ) molar ratio). In contrast, very little oxidation of chloropyromorphite occurred. Under similar conditions, oxidation of lead( ii ) carbonate and phosphate minerals by HOBr exhibited a reaction kinetics that was orders of magnitude faster than by HOCl. Their end oxidation products were identified as mainly plattnerite β-PbO 2(s) and trace amounts of scrutinyite α-PbO 2(s) based on X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS) spectroscopic analysis. A kinetic model was established based on the solid-phase experimental data. The model predicted that in real drinking water distribution systems, it takes 0.6–1.2 years to completely oxidize Pb( ii ) minerals in the surface layer of corrosion scales to PbO 2(s) by HOCl without phosphate, but only 0.1–0.2 years in the presence of bromide (Br − ) due the catalytic effects of HOBr generation. The model also predicts that the addition of phosphate will significantly inhibit Pb( ii ) mineral oxidation by HOCl, but only be modestly effective in the presence of Br − . This study provides insightful understanding on the effect of residual disinfectant on the oxidation of lead corrosion scales and strategies to prevent lead release from drinking water distribution systems. 

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2. Impact of iron‐rich scale in service lines on lead release to water

   https://doi.org/10.1002/aws2.1188  

   Bae, Yeunook ; Pasteris, Jill D. ; Giammar, Daniel E. ( August 2020 , AWWA Water Science)

   Total iron and total lead concentrations were correlated in water that had stagnated in laboratory‐scale experiments with sections of 10 harvested lead service lines (LSLs) from Providence, Rhode Island. One of these sections had much greater lead release and pH decrease during stagnation, and the inner surface of this service line had a thick coating of iron oxide scale. The iron‐rich scale was composed of coarse‐grained iron oxides (lepidocrocite and magnetite) covered with a thin lead‐bearing layer (hydrocerussite). Complementary batch experiments with pure iron oxides found that their surfaces accelerated the oxidation of Pb(II) from hydrocerussite, which produced PbO_2(s)and decreased the pH. While the findings presented are for LSLs from Providence, the co‐occurrence of iron oxides and lead corrosion products is widespread. The results highlight the importance of considering iron corrosion when evaluating processes that control lead concentrations in tap water.

    

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3. Photolytic reaction of dissolved organic matter and bromide ions promote the formation of manganese oxides

   Gao, Zhenwei ; Liu, Jing ; Skurie, Charlie ; Zhu, Yaguang ; Jun, Young-Shin ( March 2022 , American Chemical Society National Meeting)

   Manganese (Mn) oxide solids widely exist in nature, serving as both electron donors and acceptors for a variety of redox reactions. Previous studies have highlighted the adsorption of dissolved organic matter (DOM) on Mn oxides, as well as the reduction of Mn oxides by DOM. Here, we show the underappreciated roles of photolytic reactions of DOM in Mn2+(aq) oxidation and its consequential formation of Mn oxide solids. During the photolysis of DOM, reactive intermediates including excited triplet state DOM (3DOM*), hydroxyl radical (•OH), superoxide radical (O2•−), hydrogen peroxide (H2O2), and singlet oxygen (1O2) can be generated. Among them, we found that O2•− was responsible for Mn oxidation. In addition, in the presence of bromide ions (Br−), the photolytic reactions between DOM and Br− formed reactive bromide radicals and facilitated the oxidation of Mn2+(aq) to Mn oxide solids. Moreover, the composition of DOM affected its oxidative capability. When DOM contained more aromatic functional groups, we observed more oxidation of Mn2+ to Mn oxides. These new findings advance our knowledge of natural Mn2+ oxidation and Mn(III/IV) oxide formation, as well as the hitherto overlooked oxidative role of DOM in the oxidation of metal ions in surface water under sunlight illumination. 

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4. Palladium( ii )-assisted activation of thioglycosides

   https://doi.org/10.1039/D1OB00004G  

   Escopy, Samira ; Singh, Yashapal ; Demchenko, Alexei V. ( March 2021 , Organic & Biomolecular Chemistry)

   null (Ed.)

   Described herein is the first example of glycosidation of thioglycosides in the presence of palladium( ii ) bromide. While the activation with PdBr 2 alone was proven feasible, higher yields and cleaner reactions were achieved when these glycosylations were performed in the presence of propargyl bromide as an additive. Preliminary mechanistic studies suggest that propargyl bromide assists the reaction by creating an ionizing complex, which accelerates the leaving group departure. A variety of thioglycoside donors in reactions with different glycosyl acceptors were investigated to determine the initial scope of this new reaction. Selective and chemoselective activation of thioglycosides over other leaving groups has also been explored. 

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5. Photochemically-assisted Formation of Manganese Oxide Solids in the Presence of Dissolved Organic Matter and Bromide Ions

   Gao, Zhenwei ; Liu, Jing ; Skurie, Charlie ; Zhu, Yaguang ; Jun, Young-Shin ( June 2022 , the 2022 Association of Environmental Engineering and Science Professors (AEESP) Research and Education Conference)

   Dissolved natural organic matter (DOM) is a complex matrix of organic matter that is ubiquitous in natural aquatic environments. So far, substantial research has been conducted on the DOM adsorption on Mn oxides as well as the reduction processes of Mn oxides by DOM. However, little is known about the oxidative roles of DOM in oxidizing Mn2+(aq) to Mn(III/IV) oxide solids. Sunlight-driven processes can initiate the degradation of DOM accompanied by the formation of photochemically produced reactive intermediates, including excited triplet state DOM (3DOM*), hydroxyl radical (•OH), superoxide radical (O2•−), hydrogen peroxide (H2O2), and singlet oxygen (1O2). Further, in the presence of halide ions, reactive halogen species can be generated by reactions between 3DOM* and halide ions, and by reactions between •OH and halide ions. In this study, we found that the solution pH controlled the oxidation of Mn2+(aq) to Mn oxide solids during photolysis of DOM. Among the reactive oxygen species, Mn2+(aq) was found to be oxidized to Mn oxide solids mainly by O2•−. The DOM with different quantities of aromatic functional groups affected its oxidative capability. With the addition of bromide ions (Br−), Mn2+(aq) oxidation was promoted further by formation Br radicals, which can also oxidize Mn2+(aq) to Mn oxide solids. These findings can help us better understand the oxidative role of DOM in the formation of Mn oxide solids in organic-rich surface water. In addition, this study assists in comprehending the impacts of the photolytic reactions between DOM and halide ions and their resulting reactive oxygen and halogen species on the oxidation and reduction processes of other transition metal oxides in the environment. 

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