Radical Singlet
激进单线态

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radical singlet oxygen
自由基单线态氧

Electron paramagnetic resonance (EPR) and quenching tests indicated that non-radical singlet oxygen (1O2) is the dominant contributor for HA degradation.

电子顺磁共振 (EPR) 和淬火测试表明非自由基单线态氧 (1O2) 是 HA 降解的主要贡献者。

Enhanced humic acid degradation by Fe3O4/ultrasound-activated peroxymonosulfate : Synergy index, non-radical effect and mechanism

radical singlet oxygen
自由基单线态氧

The active species capture experimental data and electron spin resonance (ESR) determinations revealed that both active radicals (like •SO4-, •OH, •O2-, h+) and nonradical singlet oxygen (1O2) participated in the CQ decomposition.

活性物质捕获实验数据和电子自旋共振 (ESR) 测定表明，活性自由基（如•SO4-、•OH、•O2-、h+）和非自由基单线态氧 (1O2) 都参与了 CQ 分解。

Photocatalysis-activated SR-AOP over PDINH/MIL-88A(Fe) composites for boosted chloroquine phosphate degradation: Performance, mechanism, pathway and DFT calculations

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10.1016/J.SEPPUR.2021.118466

Electron paramagnetic resonance (EPR) and quenching tests indicated that non-radical singlet oxygen (1O2) is the dominant contributor for HA degradation.

电子顺磁共振 (EPR) 和淬火测试表明非自由基单线态氧 (1O2) 是 HA 降解的主要贡献者。

Enhanced humic acid degradation by Fe3O4/ultrasound-activated peroxymonosulfate : Synergy index, non-radical effect and mechanism

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10.1016/J.APCATB.2021.120229

The active species capture experimental data and electron spin resonance (ESR) determinations revealed that both active radicals (like •SO4-, •OH, •O2-, h+) and nonradical singlet oxygen (1O2) participated in the CQ decomposition.

活性物质捕获实验数据和电子自旋共振 (ESR) 测定表明，活性自由基（如•SO4-、•OH、•O2-、h+）和非自由基单线态氧 (1O2) 都参与了 CQ 分解。

Photocatalysis-activated SR-AOP over PDINH/MIL-88A(Fe) composites for boosted chloroquine phosphate degradation: Performance, mechanism, pathway and DFT calculations

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10.1007/s10971-021-05574-2

The scavenging experiments and electron paramagnetic resonance technologies revealed that non-radical singlet oxygen (1O2), sulfate radicals(SO4•−) were associated as active species in the SrCoO2.

清除实验和电子顺磁共振技术表明，非自由基单线态氧(1O2)、硫酸根(SO4•-)与SrCoO2中的活性物质有关。

Singlet oxygen produced SrCoO2.5 in environmental protection: extraordinary electronic properties and promoted catalytic performance

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10.1016/j.jcis.2019.07.002

Quenching experiments and electron paramagnetic resonance demonstrated that non-radical singlet oxygen (1O2) was the dominant species for the oxidation of organic pollutants via electron transfer in the g-C3N4@COF/PMS system.

淬火实验和电子顺磁共振表明，非自由基单线态氧（1O2）是g-C3N4@COF/PMS系统中通过电子转移氧化有机污染物的主要物种。

Metal-free catalysts of graphitic carbon nitride-covalent organic frameworks for efficient pollutant destruction in water.

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Radical Singlet 激进单线态
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Radical Singlet(激进单线态)研究综述

Radical Singlet 激进单线态 - Electron paramagnetic resonance (EPR) and quenching tests indicated that non-radical singlet oxygen (1O2) is the dominant contributor for HA degradation. [1] The active species capture experimental data and electron spin resonance (ESR) determinations revealed that both active radicals (like •SO4-, •OH, •O2-, h+) and nonradical singlet oxygen (1O2) participated in the CQ decomposition. [2] The scavenging experiments and electron paramagnetic resonance technologies revealed that non-radical singlet oxygen (1O2), sulfate radicals(SO4•−) were associated as active species in the SrCoO2. [3] Quenching experiments and electron paramagnetic resonance demonstrated that non-radical singlet oxygen (1O2) was the dominant species for the oxidation of organic pollutants via electron transfer in the g-C3N4@COF/PMS system. [4]
电子顺磁共振 (EPR) 和淬火测试表明非自由基单线态氧 (1O2) 是 HA 降解的主要贡献者。 [1] 活性物质捕获实验数据和电子自旋共振 (ESR) 测定表明，活性自由基（如•SO4-、•OH、•O2-、h+）和非自由基单线态氧 (1O2) 都参与了 CQ 分解。 [2] 清除实验和电子顺磁共振技术表明，非自由基单线态氧(1O2)、硫酸根(SO4•-)与SrCoO2中的活性物质有关。 [3] 淬火实验和电子顺磁共振表明，非自由基单线态氧（1O2）是g-C3N4@COF/PMS系统中通过电子转移氧化有机污染物的主要物种。 [4]

radical singlet oxygen 自由基单线态氧

Electron paramagnetic resonance (EPR) and quenching tests indicated that non-radical singlet oxygen (1O2) is the dominant contributor for HA degradation. [1] The active species capture experimental data and electron spin resonance (ESR) determinations revealed that both active radicals (like •SO4-, •OH, •O2-, h+) and nonradical singlet oxygen (1O2) participated in the CQ decomposition. [2] The scavenging experiments and electron paramagnetic resonance technologies revealed that non-radical singlet oxygen (1O2), sulfate radicals(SO4•−) were associated as active species in the SrCoO2. [3] Quenching experiments and electron paramagnetic resonance demonstrated that non-radical singlet oxygen (1O2) was the dominant species for the oxidation of organic pollutants via electron transfer in the g-C3N4@COF/PMS system. [4]
电子顺磁共振 (EPR) 和淬火测试表明非自由基单线态氧 (1O2) 是 HA 降解的主要贡献者。 [1] 活性物质捕获实验数据和电子自旋共振 (ESR) 测定表明，活性自由基（如•SO4-、•OH、•O2-、h+）和非自由基单线态氧 (1O2) 都参与了 CQ 分解。 [2] 清除实验和电子顺磁共振技术表明，非自由基单线态氧(1O2)、硫酸根(SO4•-)与SrCoO2中的活性物质有关。 [3] 淬火实验和电子顺磁共振表明，非自由基单线态氧（1O2）是g-C3N4@COF/PMS系统中通过电子转移氧化有机污染物的主要物种。 [4]