scholarly journals Self-Assembly Fabrication of Hollow Mesoporous Silica@Co–Al Layered Double Hydroxide@Graphene and Application in Toxic Effluents Elimination

2015 ◽  
Vol 7 (16) ◽  
pp. 8506-8514 ◽  
Author(s):  
Shu-Dong Jiang ◽  
Lei Song ◽  
Wen-Ru Zeng ◽  
Zheng-Qi Huang ◽  
Jing Zhan ◽  
...  
2020 ◽  
Vol 49 (9) ◽  
pp. 1078-1080
Author(s):  
Yue Shi ◽  
Junzheng Wang ◽  
Eisuke Yamamoto ◽  
Minoru Osada

2020 ◽  
Vol 6 ◽  
pp. 248-254
Author(s):  
Seong Hyun Kim ◽  
Yoo Sei Park ◽  
Chiho Kim ◽  
Il Yeong Kwon ◽  
Jooyoung Lee ◽  
...  

2017 ◽  
Vol 5 (12) ◽  
pp. 2245-2253 ◽  
Author(s):  
Yi-Xuan Chen ◽  
Rong Zhu ◽  
Zheng-liang Xu ◽  
Qin-Fei Ke ◽  
Chang-Qing Zhang ◽  
...  

The self-assembly of pifithrin-α-loaded layered double hydroxide/chitosan nanohybrid composites as a drug delivery system was demonstrated for the first time to improve the cytocompatibility and enhance the osteoinductivity for the treatment of bone defects.


2006 ◽  
Vol 12 (4) ◽  
pp. 225-230
Author(s):  
Botomei Anca ◽  
Emil Dumitriu ◽  
Hulea Vasile ◽  
Nastro Alfonso

An organo-mineral nanohybrid material in which the organic moiety is interleaved inside the inorganic lamella was prepared by using phenoxyacetate anions as a guest in the Mg-Al-layered double hydroxide lamella (as an inorganic host) by the self-assembly technique, anion exchange and the reconstruction methods. The powder XRD patterns of the resulted materials show that the basal spacing of the Mg-AI-layered double hydroxide with carbonate as the counter anions expanded from 7.7 ? to around 16.6 ? in the nanohybrid materials. IR studies show that the absorption bands of the resulting materials correspond to the characteristic functional groups of the host and the guest structures. When the two results are taken together, the expansion can be attributed to the intercalation of the phenoxyacetic acid in the inorganic interlamella for the formation of the nanohybrid material. The intercalation of phenoxyacetate anions was also confirmed by thermogravimetric analysis (TG).


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