Chen Shiliang, Teng Qiaoling
Qianjiang College, Hangzhou Normal University, Hangzhou 310012, China.
Materials (Basel). 2017 Jul 24;10(7):846. doi: 10.3390/ma10070846.
We report the fabrication of a tetra-amino cobalt (II) phthalocyanine (CoPc)-immobilized bacterial cellulose (BC) functional nanocomposite, CoPc@BC, by quantitative immobilization of CoPc onto a BC membrane. Lab-cultured BC was oxidized by NaIO₄ to generate aldehyde groups on BC for the subsequent CoPc immobilization, the processing conditions were optimized by monitoring both the generated aldehyde content and the resulting CoPc loading. X-ray photoelectron spectroscopy (XPS) was employed to characterize the change of the element bonding environment during the functionalization processes. The CoPc@BC functional nanocomposite was utilized for the treatment of reactive red X-3B dye wastewater. The CoPc molecules in the CoPc@BC nanocomposite can function as an "antenna" to adsorb the target anionic dye molecules, the adsorption takes place both on the surface and in the interior of CoPc@BC. A catalytic membrane reactor (CMR) was assembled with the CoPc@BC nanocomposite, the performance of CMR was evaluated based on the catalytic oxidation behavior of reactive red X-3B, with H₂O₂ as an oxidant. Highly-reactive hydroxyl radical (OH) was involved in the catalytic oxidation process, as detected by electron paramagnetic resonance (EPR). Under optimal operating conditions of a flow rate of 6 mL/min, a reaction temperature of 50 °C, and an H₂O₂ concentration of 10 mmol/L, the decoloration rate of CMR was as high as 50 μmol⋅min⋅g.
我们报道了一种通过将四氨基钴(II)酞菁(CoPc)定量固定在细菌纤维素(BC)膜上制备的CoPc固定化细菌纤维素(BC)功能纳米复合材料CoPc@BC。实验室培养的BC用NaIO₄氧化,在BC上生成醛基以用于后续的CoPc固定化,通过监测生成的醛含量和最终的CoPc负载量来优化加工条件。采用X射线光电子能谱(XPS)来表征功能化过程中元素键合环境的变化。CoPc@BC功能纳米复合材料用于处理活性红X-3B染料废水。CoPc@BC纳米复合材料中的CoPc分子可作为“天线”吸附目标阴离子染料分子,吸附发生在CoPc@BC的表面和内部。用CoPc@BC纳米复合材料组装了催化膜反应器(CMR),基于以H₂O₂为氧化剂的活性红X-3B的催化氧化行为评估了CMR的性能。通过电子顺磁共振(EPR)检测发现,高活性羟基自由基(OH)参与了催化氧化过程。在流速为6 mL/min、反应温度为50℃、H₂O₂浓度为10 mmol/L的最佳操作条件下,CMR的脱色率高达50 μmol⋅min⋅g。