Synthesis and characterization of composite based on cellulose acetate and hydroxyapatite application to the absorption of harmful substances
Introduction
Recently, composite materials based on calcium phosphate have attracted much attention (Azzaoui et al., 2013a, Azzaoui et al., 2013b, Needham et al., 2007). Hydroxyapatite is often used as a bone implant material; however, it is used to develop many composites for advanced technologies. Many studies that use bio monitoring used data on food contamination bisphenol A and the environment (Angerer et al., 2007, Boogaard, 2007, Calafat et al., 2006, Needham et al., 2007, Pirkle et al., 2005, Yang et al., 2006). This information served as the basis for estimating indirect human exposure to bisphenol A and its potential toxicity. Cellulose acetate is considered one of the essential esters of cellulose. According to the methods used, it can be widely used in different kinds of purposes; such as film formation and membranes. The toxicity of bisphenol A has been extensively studied covering a large range of doses; the study showed adverse effects at doses of 50 mg/kg body weight/day (EU, 2003, Goodman et al., 2006, Gray et al., 2004).
The technology employed for the extraction of BPA from aqueous samples includes solid phase micro-extraction (SPME) (Kasuga et al., 2003), liquid–liquid extraction (LLE) (Deng, Hao, & Wang, 2001) and solid-phase extraction (SPE) (Shafer & Simonian, 2002).
In this work, a novel analytical method based on enrichment and pretreatment of analytes in the water sample CA/HAp sorptive extraction and gas chromatography–mass spectrometry SIM mode have been developed for the rapid analysis of BPA in water. The obtained results demonstrated that CA/HAp/PEG 1000 combined with GC–MS is a simple, rapid and solvent-free method for the analysis of BPA in water.
The aim of this work was then to choose the best stationary phase (TFME) and best chromatographic method for the quantification of BPA in samples of baby food matrices, which could be used for routine controls.
Section snippets
Materials
Hydroxyapatite (HAp) was synthesized in our laboratory. The cellulose Acetate (CA) (99%), Calcium Nitrate Ca(NO3)2·4H2O (99%), Ammonium Hydrogen Phosphate (NH4)2·HPO4 (99%), DMF (Dimethylformamide) and Acetone were purchased from Aldrich. High purity distilled water was used throughout the whole experiment.
Synthesis of thin film; CA/HAp/PEG1000
The starting substances used in the production of hydroxyapatite were calcium nitrate tetra hydrate and di-ammonium hydrogen phosphate. HAp was produced by following a modified wet chemical
FTIR analysis
The FTIR spectra of the washed HAp, CA and CA/HAp/PEG 1000 composite as shown in Fig. 2. The bands at 3572 and 632 cm−1 belong to the vibration of hydroxyl (OH) group, the bands at 1089, 1045 and 962 cm−1 are the characterization of phosphate stretching vibration and the bands observed at 601, 570 cm−1 are owing to the phosphate being in vibration. It is clear from the IR analysis that, the precipitated powders are evidenced to be hydroxyapatite in nature. The presence of polyethylene glycol in
Conclusion
Synthesis of CA/HAp/PEG 1000 membranes was successfully achieved through dispersion of HAp particles homogeneously in the composite. The composite was characterized by IR and TGA/DTA study, swelling and weight loss shows an interaction between the organic matrix and the HAP matrix by the mean of hydrogen bonding. Morphology showed that the composite has good compatibility between the organic matrix and inorganic matrix (HAp and PLA), the method allows the production of very fine particles size
Acknowledgment
The authors extend their appreciation to the Deanship of Scientific Research at king Saud University for funding the work through the research group project no. RGP-089.
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