uv photodegradation
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Chemosphere ◽  
2022 ◽  
pp. 133573
Author(s):  
Ivan P. Pozdnyakov ◽  
Olga A. Snytnikova ◽  
Vadim V. Yanshole ◽  
Roman G. Fedunov ◽  
Vyacheslav P. Grivin ◽  
...  

2021 ◽  
Vol 232 (9) ◽  
Author(s):  
Diana Quispe-Arpasi ◽  
Beatriz E. Bueno ◽  
Evaldo L. G. Espíndola ◽  
Rogers Ribeiro ◽  
Giovana Tommaso

Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 1968 ◽  
Author(s):  
Jie-Mao Wang ◽  
Hao Wang ◽  
Erh-Chiang Chen ◽  
Yun-Ju Chen ◽  
Tzong-Ming Wu

The enhancement of the ultraviolet (UV) photodegradation resistance of biodegradable polymers can improve their application efficacy in a natural environment. In this study, the hexadecylamine modified layered zinc phenylphosphonate (m-PPZn) was used as a UV protection additive for poly(butylene adipate-co-terephthalate) (PBAT) via solution mixing. The results from the Fourier transform infrared spectroscopy (FTIR) and wide-angle X-ray diffraction analysis of the m-PPZn indicated the occurrence of hexadecylamine intercalation. FTIR and gel permeation chromatography were used to characterize the evolution of the PBAT/m-PPZn composites after being artificially irradiated via a light source. The various functional groups produced via photodegradation were analyzed to illustrate the enhanced UV protection ability of m-PPZn in the composite materials. From the appearance, the yellowness index of the PBAT/m-PPZn composite materials was significantly lower than that of the pure PBAT matrix due to photodegradation. These results were confirmed by the molecular weight reduction in PBAT with increasing m-PPZn content, possibly due to the UV photon energy reflection by the m-PPZn. This study presents a novel approach of improving the UV photodegradation of a biodegradable polymer using an organically modified layered zinc phenylphosphonate composite.


Author(s):  
Fenghua Jiang ◽  
Linqing Xie ◽  
Chengjun Sun ◽  
Yu Zhang ◽  
Jingxi Li ◽  
...  

2020 ◽  
Vol 6 (5) ◽  
pp. 1412-1420
Author(s):  
Moshan Chen ◽  
Ernest R. Blatchley

A UV treatment process with prechlorination promotes the direct UV photodegradation of anatoxin-a by forming an N–Cl bond on the amine group.


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