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碳点触发的醋酸纤维素光催化降解。

Carbon Dot-Triggered Photocatalytic Degradation of Cellulose Acetate.

机构信息

Department of Fibre and Polymer Technology, KTH Royal Institute of Technology, Teknikringen 56, Stockholm 100 44, Sweden.

Wallenberg Wood Science Center (WWSC), KTH Royal Institute of Technology, Teknikringen 56, Stockholm 100 44, Sweden.

出版信息

Biomacromolecules. 2021 May 10;22(5):2211-2223. doi: 10.1021/acs.biomac.1c00273. Epub 2021 Apr 27.

Abstract

Chemical modification of biopolymers, before use in thermoplastic applications, can reduce the susceptibility to open environment degradation. We demonstrate carbon dots (CDs) as green photocatalytic triggers that can render the common cellulose derivative, cellulose acetate (CA), degradable under open environment relevant conditions. CD-modified cellulose acetate (CA + CD) films were subjected to UV-A irradiation in air and simulated sea water, and the degradation process was mapped by multiple spectroscopic, chromatographic, and microscopy techniques. The addition of CDs effectively catalyzed the deacetylation reaction, the bottleneck preventing biodegradation of CA. The photocatalytically activated degradation process led to significant weight loss, release of small molecules, and regeneration of cellulose fibers. The weight loss of CA + CD after 30 days of UV-A irradiation in air or simulated sea water was 53 and 43%, respectively, while the corresponding values for plain CA films were 12 and 4%. At the same time the weight average molar mass of CA + CD decreased from 62,000 to 11,000 g/mol and 15,000 g/mol during UV-A irradiation in air and simulated sea water, respectively, and the degree of substitution (DS) decreased from 2.2 to 1.6 both in air and in water. The aging in water alone did not affect the weight average molar mass, but the DS was decreased to 1.9. Control experiments confirmed the generation of hydrogen peroxide when aqueous CD dispersion was subjected to UV-A irradiation, indicating a free radical mechanism. These results are promising for the development of products, such as mulching films, with photocatalytically triggered environmental degradation processes.

摘要

在将生物聚合物用于热塑性应用之前,对其进行化学修饰可以降低其对开放环境降解的敏感性。我们证明了碳点(CDs)是绿色光催化触发剂,可以使常见的纤维素衍生物醋酸纤维素(CA)在开放环境相关条件下可降解。将 CD 修饰的醋酸纤维素(CA + CD)薄膜在空气中和模拟海水中进行 UV-A 照射,并通过多种光谱、色谱和显微镜技术来绘制降解过程。添加 CDs 可有效催化脱乙酰反应,该反应是阻止 CA 生物降解的瓶颈。光催化激活的降解过程导致显著的重量损失、小分子的释放和纤维素纤维的再生。在空气中或模拟海水中经 30 天 UV-A 照射后,CA + CD 的失重率分别为 53%和 43%,而普通 CA 薄膜的相应值分别为 12%和 4%。同时,CA + CD 的重均摩尔质量在空气中和模拟海水中经 UV-A 照射分别从 62,000 降至 11,000 g/mol 和 15,000 g/mol,取代度(DS)分别从 2.2 降至 1.6,无论是在空气中还是在水中。单独水老化不会影响重均摩尔质量,但 DS 降低至 1.9。对照实验证实,当水相 CDs 分散体受到 UV-A 照射时会产生过氧化氢,表明存在自由基机制。这些结果有望开发具有光催化触发环境降解过程的产品,例如覆盖膜。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbcc/8382246/dea639c15e9f/bm1c00273_0002.jpg

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