Chitosan-rectorite nanospheres immobilized on polystyrene fibrous mats via alternate electrospinning/electrospraying techniques for copper ions adsorption
Creators
- 1. Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and Energy, Hubei Key Lab of Biomass Resource Chemistry and Environmental Biotechnology, School of Resource and Environmental Science, Wuhan University, Wuhan 430079 (China)
- 2. School of Chemistry and Chemical Engineering, Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, Guangxi University, Nanning 530004 (China)
- 3. College of Life Science, Yangtze University, Jingzhou 434025 (China)
Description
Highlights: • CS or CS-REC was electrosprayed to nanospheres to enlarge their surface area. • CS-REC immobilized on PS mats could improve the hydrophilicity. • The intercalation of CS chains with REC interlayers was helpful for adsorption. • Ca2+-REC with cation exchange could improve the adsorption capacity. • The composite mats kept high adsorption ability after three cycles. - Abstract: Chitosan (CS), as a kind of well characterized biopolymer, has been used for heavy metal adsorption due to its low cost and high efficacy. However, when used directly, chitosan particles had small surface area and weak mechanical strength which is unfavorable to metal adsorption and reused. Besides, it cannot be easily recycled that may cause a secondary pollution. In this paper, CS and layered silicate rectorite (REC) were fully mixed and the mixtures were subsequently electrosprayed nano-sized spheres, which were immobilized on the surface of electrospun polystyrene (PS) mats for metal adsorption. The morphology analysis taken from SEM confirmed that CS-REC nanospheres were loaded on the surface of PS fibrous mats. Small Angle X-ray diffraction patterns showed that the interlayer distance of REC in composite mats was enlarged by the intercalation of CS chains; such structure meant bigger surface area which was helpful for metal adsorption. The data of contact angle implied that PS mats coated with CS-REC nanospheres exhibited better hydrophilicity than PS mats, which was conductive to adsorption rate. Besides, the copper ions adsorption of composite mats was tested at different conditions including the adsorption time, the initial pH and the initial concentration of copper ion. The results demonstrated that PS mats coated with CS-REC nanospheres had the adsorption capacity up to 134 mg/g. In addition, the addition of REC containing Ca2+ could also improve the metal adsorption because of cation exchange. The desorption assay indicated that PS mats immobilized with CS and CS-REC still kept high adsorption ability which retained 74% and 78% after three adsorption-desorption cycles.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apsusc.2017.07.159Additional details
Identifiers
- DOI
- 10.1016/j.apsusc.2017.07.159;
- PII
- S0169-4332(17)32160-8;
Publishing Information
- Journal Title
- Applied Surface Science
- Journal Volume
- 426
- Journal Page Range
- p. 545-553
- ISSN
- 0169-4332
- CODEN
- ASUSEE
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49072864
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY; S36: MATERIALS SCIENCE;
- Descriptors DEI
- ADSORPTION; CALCIUM IONS; CATIONS; CLATHRATES; CONCENTRATION RATIO; COPPER IONS; DESORPTION; HEAVY METALS; ION EXCHANGE; MIXTURES; MORPHOLOGY; NANOSTRUCTURES; PH VALUE; POLYSTYRENE; SCANNING ELECTRON MICROSCOPY; SILICATES; SURFACE AREA; SURFACES; X-RAY DIFFRACTION
- Descriptors DEC
- CHARGED PARTICLES; COHERENT SCATTERING; DIFFRACTION; DIMENSIONLESS NUMBERS; DISPERSIONS; ELECTRON MICROSCOPY; ELEMENTS; IONS; MATERIALS; METALS; MICROSCOPY; ORGANIC COMPOUNDS; ORGANIC POLYMERS; OXYGEN COMPOUNDS; PETROCHEMICALS; PETROLEUM PRODUCTS; PLASTICS; POLYMERS; POLYOLEFINS; POLYVINYLS; SCATTERING; SILICON COMPOUNDS; SORPTION; SURFACE PROPERTIES; SYNTHETIC MATERIALS
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.