Identification of transformation products from fluorinated lithium-ion battery additives TPFPB and TPFPP: forever chemicals of tomorrow? DOI Creative Commons

Juliane Scholl,

Jan Lisec, Hajo Haase

и другие.

Analytical and Bioanalytical Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Сен. 13, 2024

Abstract Fluorinated organic compounds (FOCs) represent a class of synthetic chemicals distinguished by their resilient carbon–fluorine bonds, which demonstrate an ability to withstand environmental degradation over extended period. The integration FOCs into cutting-edge applications, including lithium-ion batteries (LiBs), presents considerable potential for harm that has not yet been sufficiently addressed. This study focuses on the fate two fluorinated aromatics, tris(pentafluorophenyl)borane (TPFP B ) and tris(pentafluorophenyl)phosphine P ), given important role in improving performance LiBs. To achieve this, laboratory simulation methods total oxidizable precursor assay, electrochemistry (EC), Fenton reaction, UV-C irradiation, hydrolysis were employed. Liquid chromatography gas coupled with high-resolution mass spectrometry used identification transformation products (TPs) prediction molecular formulae. Despite structural similarity between TPFP , distinct differences electrochemical behavior pathways observed. readily underwent hydroxylation hydrolysis, resulting wide range 49 TPs. A 28 TPs newly identified, oligomers highly toxic dioxins. In contrast, degraded exclusively under harsh conditions, requiring development innovative conditioning protocols EC. total, experiments yielded nine structurally different compounds, seven previously undescribed, partially defluorinated highlights risks associated use LiBs provides insight complex FOCs. Graphical

Язык: Английский

A critical review of Allura red removal from water: advancements in adsorption and photocatalytic degradation technologies, and future perspectives DOI
Noureddine El Messaoudi, Youssef Miyah, Neha Singh

и другие.

Journal of environmental chemical engineering, Год журнала: 2024, Номер 12(6), С. 114843 - 114843

Опубликована: Ноя. 17, 2024

Язык: Английский

Процитировано

26

Throwing Light on Synthetic Molecular Photoelectrocatalysis (Part II): selected recent transformations of organic compounds and a future perspective in organic synthesis DOI Creative Commons
Erick Steven Patiño-Alonzo, José Manuel Ramos-Villaseñor, Julio Romero‐Ibañez

и другие.

Current Opinion in Electrochemistry, Год журнала: 2025, Номер unknown, С. 101674 - 101674

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

Advances in p- and d-block nanocatalysts for efficient photocatalytic degradation of reactive blue dye: an environmental perspective DOI

Anam Shahzadi,

Adnan Majeed,

Shaimaa Hassan Mallah

и другие.

Environmental Technology Reviews, Год журнала: 2025, Номер 14(1), С. 517 - 539

Опубликована: Май 26, 2025

Язык: Английский

Процитировано

0

Base-driven dehydrohalogenation coupled with catalytic hydrodehalogenation as a novel strategy for rapid dehalogenation of halogenated organic compounds containing aliphatic C-X bonds DOI

Shuting Qin,

Chen Wu,

Xuanxuan Ma

и другие.

Journal of environmental chemical engineering, Год журнала: 2024, Номер 12(6), С. 114983 - 114983

Опубликована: Ноя. 29, 2024

Язык: Английский

Процитировано

0

Identification of transformation products from fluorinated lithium-ion battery additives TPFPB and TPFPP: forever chemicals of tomorrow? DOI Creative Commons

Juliane Scholl,

Jan Lisec, Hajo Haase

и другие.

Analytical and Bioanalytical Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Сен. 13, 2024

Abstract Fluorinated organic compounds (FOCs) represent a class of synthetic chemicals distinguished by their resilient carbon–fluorine bonds, which demonstrate an ability to withstand environmental degradation over extended period. The integration FOCs into cutting-edge applications, including lithium-ion batteries (LiBs), presents considerable potential for harm that has not yet been sufficiently addressed. This study focuses on the fate two fluorinated aromatics, tris(pentafluorophenyl)borane (TPFP B ) and tris(pentafluorophenyl)phosphine P ), given important role in improving performance LiBs. To achieve this, laboratory simulation methods total oxidizable precursor assay, electrochemistry (EC), Fenton reaction, UV-C irradiation, hydrolysis were employed. Liquid chromatography gas coupled with high-resolution mass spectrometry used identification transformation products (TPs) prediction molecular formulae. Despite structural similarity between TPFP , distinct differences electrochemical behavior pathways observed. readily underwent hydroxylation hydrolysis, resulting wide range 49 TPs. A 28 TPs newly identified, oligomers highly toxic dioxins. In contrast, degraded exclusively under harsh conditions, requiring development innovative conditioning protocols EC. total, experiments yielded nine structurally different compounds, seven previously undescribed, partially defluorinated highlights risks associated use LiBs provides insight complex FOCs. Graphical

Язык: Английский

Процитировано

0