Kean Wang

Hollow Fiber Membrane Decorated with Ag/MWNTs: Toward Effective Water Disinfection and Biofouling Control

The currently applied disinfection methods during water treatment provide effective solutions to kill pathogens, but also generate harmful byproducts, which are required to be treated with additional efforts. In this work, an alternative and safer water disinfection system consisting of silver nanoparticle/multiwalled carbon nanotubes (Ag/MWNTs) coated on a polyacrylonitrile (PAN) hollow fiber membrane, Ag/MWNTs/PAN, has been developed. Silver nanoparticles of controlled sizes were coated on polyethylene glycol-grafted MWNTs. Ag/MWNTs were then covalently coated on the external surface of a chemically modified PAN hollow fiber membrane to act as a disinfection barrier. A continuous filtration test using E. coli containing feedwater was conducted for the pristine PAN and Ag/MWNTs/PAN composite membranes. The Ag/MWNT coating significantly enhanced the antimicrobial activities and antifouling properties of the membrane against E. coli. Under the continuous filtration mode using E. coli feedwater, the relative flux drop over Ag/MWNTs/PAN was 6%, which was significantly lower than that over the pristine PAN (55%) at 20 h of filtration. The presence of the Ag/MWNT disinfection layer effectively inhibited the growth of bacteria in the filtration module and prevented the formation of biofilm on the surface of the membrane. Such distinctive antimicrobial properties of the composite membrane is attributed to the proper dispersion of silver nanoparticles on the external surface of the membrane, leading to direct contact with bacterium cells.

Surface activated carbon nanospheres for fast adsorption of silver ions from aqueous solutions.

We report the synthesis and activation of colloidal carbon nanospheres (CNS) for adsorption of Ag(I) ions from aqueous solutions. CNS (400-500 nm in diameter) was synthesized via simple hydrothermal treatment of glucose solution. The surface of nonporous CNS after being activated by NaOH was enriched with -OH and -COO(-) functional groups. Despite the low surface area (<15m(2)/g), the activated CNS exhibited a high adsorption capacity of 152 mg silver/g. Under batch conditions, all Ag(I) ions can be completely adsorbed in less than 6 min with the initial Ag(I) concentrations lower than 2 ppm. This can be attributed to the minimum mass transfer resistance as Ag(I) ions were all deposited and reduced as Ag(0) nanoparticles on the external surface of CNS. The kinetic data can be well fitted to the pseudo-second-order kinetics model. The adsorbed silver can be easily recovered by dilute acid solutions and the CNS can be reactivated by the same treatment with NaOH solution. The excellent adsorption performance and reusability have also been demonstrated in a continuous mode. The NaOH activated CNS reported here could represent a new type of low-cost and efficient adsorbent nanomaterials for removal of trace Ag(I) ions for drinking water production.

Role of interface in dispersion and surface energetics of polymer nanocomposites containing hydrophilic POSS and layered silicates

Three different hydrophilic nanofillers--natural and synthetic layered silicate as well as octaammonium polyhedral oligomeric silsesquioxane (POSS)--were incorporated into polyamide-6 by a solution-mixing method. The surfaces of the resulting polymer nanocomposites were characterized by X-ray diffraction, polarized optical microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy and contact angle measurements. All polymer nanocomposites displayed enhancement in surface hydrophilicity as well as increase in surface free energy due to surface enrichment of the nanofillers. The degree of enhancement was found to depend on both nanofiller type and dispersion state. Interfacial interactions in the form of hydrogen bonding played an important role in affecting the dispersion state of the layered silicates. Exfoliated layered silicates caused a larger increase in hydrophilicity than aggregated layered silicate. On the other hand, aggregated POSS molecules were able to induce a large increase in hydrophilicity. Significant spreading of water was also observed on surfaces containing POSS molecules. Surface models have been proposed to explain these phenomena.

Chitosan-Carrageenan Polyelectrolyte Complex for the Delivery of Protein Drugs

A chitosan-carrageenan polyelectrolyte complex (PEC) was prepared by salt induced impeding of polyplex formation method and was encapsulated with bovine serum albumin (BSA) to study the potential to be tailored to the pH responsive oral delivery of protein drugs. The FTIR spectra showed the successful formation of the PEC under the experimental condition. The release kinetics of BSA from the PEC was studied in the simulated gastrointestinal fluids with and without digestive enzymes. The prepared PEC showed the nature of pH-sensitivity. A typical controlled release of BSA from the PEC (180 μg of BSA from 3 mg of PEC) was obtained in the simulated intestinal fluid (SIF, pH 7.5), which was due to the significant swelling and disintegration of PEC, but little amount of BSA was released (11 μg of BSA from 3 mg of PEC) in the simulated gastric fluid (SGF, pH 1.2), confirming acidic stability of the prepared PEC. The presence of digestive enzymes was found not to affect the response of PEC to ambient pH value, but to speed up the release of BSA from carriers.

Influence of hydroxyapatite crystallization temperature and concentration on stress transfer in wet-spun nanohydroxyapatite-chitosan composite fibres.

Hydroxyapatite possesses appropriate osteoconductivity and biocompatibility for hard-tissue replacement implants but suffers from brittleness. One approach to overcome this problem is to incorporate nanometre hydroxyapatite (nHA) into a polymer matrix, such as chitosan, to yield a hydroxyapatite-chitosan (HC) composite. Here, a novel HC composite was synthesized and its elastic properties were investigated by varying (1) nHA concentration and (2) crystallization temperature (T), where T is a parameter which influences the morphology of the crystals. Crystals of nHA were precipitated at T = 40 degrees C and 100 degrees C, blended in a chitosan matrix, and wet-spun to yield fibres of HC composites at 5, 15, 20 and 40% concentrations (mass fraction of nHA). Scanning electron microscopy and energy-dispersive x-ray spectroscopy revealed a uniform distribution of nanocrystallites within the fibre. Tensile testing revealed that HC fibres, which comprised nHA treated at T = 100 degrees C, possessed low tensile strength, sigma(0), and stiffness, E, at low nHA concentrations but high sigma(0) and E at higher concentrations, i.e. beyond a 15% mass fraction of nHA. However, with nHA treated at T = 40 degrees C, the fibres yielded high sigma(0) and E at low nHA concentrations but low sigma(0) and E at high concentrations. The results strongly implicate the underlying effect of crystallite morphology on stress transfer at different concentrations.

Elasticity, thermal stability and bioactivity of polyhedral oligomeric silsesquioxanes reinforced chitosan-based microfibres

In Fig. 4 of this article, a typographical error was made in reporting the mechanical parameters. The y-axis label of Fig. 4b should be ‘Stiffness, E [GPa]0; the y-axis label of Fig. 4d should be ‘Fracture strain energy density, u [MPa]0. This error does not affect the caption of Fig. 4 or the conclusion of the paper. The correct graph is shown below. The authors would like to apologize for any confusion the error may have caused.

Selection of a practical assay for the determination of the entire range of acetyl content in chitin and chitosan: UV spectrophotometry with phosphoric acid as solvent

The rapidly expanding use of chitomaterials in biomedical applications demands accurate and precise analytical methods to determine physico-chemical characteristics, especially the acetyl content of the sample. The analytical methods available for the determination of the acetyl content of the biomaterials are quite different in efficiency, accuracy and precision. Out of 22 analytical methods reviewed, XRD, DSC, FTIR (KBr pellet), solid state (13)C CP/MAS NMR, and acid hydrolysis-HPLC and the spectrophotometry assay using phosphoric acid as solvent (PUV) were selected in this study. The validity and applicability of these methods were investigated with a wide range of chitin and chitosan samples varying acetyl content, preparation methods, and sources. The XRD, DSC, and FTIR (KBr pellet) methods showed poor accuracy with the samples of diverse preparations and sources. The PUV method was modified and accuracy of the method was examined against absolute methods: solid state (13)C CP/MAS NMR and acid hydrolysis-HPLC methods. The correlations between these three methods were >0.9. Therefore, the PUV method was selected as the most generally acceptable method based on its accuracy, reliability, simplicity, and instrument availability.

A facile method for processing lignin reinforced chitosan biopolymer microfibres: optimising the fibre mechanical properties through lignin type and concentration

A chitosan biopolymer microfibre—reinforced by lignin—has been processed by a wet-spinning method. To optimise the fibre mechanical and structural properties two types of lignin, with molecular weights 28 000 g mol−1 and 60 000 g mol−1, were examined and the chitosan fibre was blended with the respective lignin type at 1, 3, 5, 7 and 8 wt% lignin concentrations. The main effects of lignin type and concentration, as well as the interaction between the two parameters, on the fibre tensile stiffness, extensibility, strength and toughness were evaluated using the two-factor analysis of variance. Significant variations in the respective mechanical properties were observed with varying lignin concentrations (P < 0.05). The magnitude of the respective mechanical properties is low at 1 wt% but peaks at 3 wt% before decreasing steadily with increasing lignin concentration. Except for extensibility, significant variations in the strength and toughness were observed with respect to lignin type (P < 0.05); variations in the stiffness were masked by interactions between lignin type and concentration. These results were related to the dispersion of lignin in the fibre and the nature of the bonds between lignin and chitosan, based on findings from scanning electron microscopy and Fourier transform infrared spectroscopy. This new method for the fabrication of chitosan biopolymer microfibre is inexpensive and versatile and could lend itself to the production of high performance biocomposite structures.

How Sensitive Is the Elasticity of Hydroxyapatite-Nanoparticle-Reinforced Chitosan Composite to Changes in Particle Concentration and Crystallization Temperature?

Hydroxyapatite (HA) nanoparticle-reinforced chitosan composites are biocompatible and biodegradable structural materials that are used as biomaterials in tissue engineering. However, in order for these materials to function effectively as intended, e.g., to provide adequate structural support for repairing damaged tissues, it is necessary to analyse and optimise the material processing parameters that affect the relevant mechanical properties. Here we are concerned with the strength, stiffness and toughness of wet-spun HA-reinforced chitosan fibres. Unlike previous studies which have addressed each of these parameters as singly applied treatments, we have carried out an experiment designed using a two-factor analysis of variance to study the main effects of two key material processing parameters, namely HA concentration and crystallization temperature, and their interactions on the respective mechanical properties of the composite fibres. The analysis reveals that significant interaction occurs between the crystallization temperature and HA concentration. Starting at a low HA concentration level, the magnitude of the respective mechanical properties decreases significantly with increasing HA concentration until a critical HA concentration is reached, at around 0.20–0.30 (HA mass fraction), beyond which the magnitude of the mechanical properties increases significantly with HA concentration. The sensitivity of the mechanical properties to crystallization temperature is masked by the interaction between the two parameters—further analysis reveals that the dependence on crystallization temperature is significant in at least some levels of HA concentration. The magnitude of the mechanical properties of the chitosan composite fibre corresponding to 40 °C is higher than that at 100 °C at low HA concentration; the reverse applies at high HA concentration. In conclusion, the elasticity of the HA nanoparticle-reinforced chitosan composite fibre is sensitive to HA concentration and crystallization temperature, and there exists a critical concentration level whereby the magnitude of the mechanical property is a minimum.

A Novel Time Lag Method to Measure the Permeation of Vapor-Gas Mixtures

A novel time lag method was proposed to study the permeation of gas mixtures or vapor-gas mixtures. This technology, which is based on the difference in the boiling points of the components, can simultaneously measure the mass transport properties of each component. The permeation of a binary mixture of H 2 O(v)/CO 2 was measured on a composite polymer membrane to demonstrate the feasibility of the technology. The method is low-cost and convenient for the future study of the permeation/separation of such gas mixtures as natural gas, flue gas, etc.