Influence of Electrospinning Parameters on the Morphology of Electrospun Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) Fibrous Membranes and Their Application as Potential Air Filtration Materials.

A large number of non-degradable materials have severely damaged the ecological environment. Now, people are increasingly pursuing the use of environmentally friendly materials to replace traditional chemical materials. Polyhydroxyalkonates (PHAs) are receiving increasing attention because of the unique biodegradability and biocompatibility they offer. However, the applications of PHAs are still limited due to high production costs and insufficient study. This project examines the optimal electrospinning parameters for the production of PHA-based fibrous membranes for air filtration. A common biodegradable polyester, Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), was electrospun into a nanofibrous membrane with a well-controlled surface microstructure. In order to produce smooth, bead-free fibers with micron-scale diameters, the effect of the process parameters (applied electric field, solution flow rate, inner diameter of hollow needle, and polymer concentration) on the electrospun fiber microstructure was optimized. The well-defined fibrous structure was optimized at an applied electric field of 20 kV, flow rate of 0.5 mL/h, solution concentration of 12 wt.%, and needle inner diameter of 0.21 mm. The morphology of the electrospun PHBV fibrous membrane was observed by scanning electron microscopy (SEM). Fourier transform infrared (FTIR) and Raman spectroscopy were used to explore the chemical signatures and phases of the electrospun PHBV nanofiber. The ball burst strength (BBS) was measured to assess the mechanical strength of the membrane. The small pore size of the nanofiber membranes ensured they had good application prospects in the field of air filtration. The particle filtration efficiency (PFE) of the optimized electrospun PHBV fibrous membrane was above 98% at standard atmospheric pressure.

Reverse Micellar Dyeing of Cotton Fabric with Reactive Dye Using Biodegradable Non-Ionic Surfactant as Nanoscale Carrier: An Optimisation Study by One-Factor-at-One-Time Approach.

This study investigates the feasibility of using biodegradable secondary alcohol ethoxylate (SAE) non-ionic surfactant as a building block for the formation of reverse micelles, functioning as reactive dye carriers for the dyeing of cotton fabric in non-aqueous octane medium. Ten dyeing parameters were optimised, by a one-factor-at-a-time approach, namely: (i) effect of colour fixation agent; (ii) surfactant-to-water mole ratio; (iii) surfactant-to-co-surfactant mole ratio; (iv) volume of soda ash; (v) volume of dye; (vi) solvent-to-cotton ratio; (vii) dyeing temperature; (viii) dyeing time; (ix) fixation time; (x) soda-ash-to-cotton ratio. The colour properties, fastness properties and physical properties of SAE-dyed samples were experimentally compared with the conventional water-dyed samples. The optimised condition was found when SAE samples were dyed as follows: (a) 1:20 surfactant-to-water ratio; (b) 1:8 surfactant-to-co-surfactant ratio; (c) 10:1 solvent ratio; (d) 40 min dyeing time; (e) 60 min fixation time; and (f) 70 °C dyeing and fixation temperature. The results showed that SAE-dyed samples have better colour strength, lower reflectance percentage and comparable levelness, fastness and physical properties than that of water-dyed samples. SEM images revealed that the dyed cotton fibres had no severe surface damage caused by an SAE-based reverse micellar dyeing system. The TEM image depicts that the reverse micelle was of nanoscale, spherical-shaped and had a core-shell structure, validating the presence of reverse micelle as a reactive dye carrier and the potential of an SAE-based reverse micellar system for dyeing of cotton fabrics.

The onset of surface-enhanced Raman scattering for single-particle detection of submicroplastics.

Microplastics represent an emerging environmental problem worldwide, raising ecological and food safety concerns. Compared to microplastics, there is growing evidence of an even higher abundance of submicro- and nanoplastics in the environment, but a reliable monitoring method for detecting these smaller-sized plastics is lacking. Herein we presented the application of surface-enhanced Raman scattering (SERS) for this purpose. Particles of polystyrene (PS; 600 nm) were used as the probe analyte. Gold nanourchins (AuNU; 50 nm), i.e. urchin-shaped nanoparticles with irregular spikes around the core, were used as the SERS-active substrate. The effectiveness of SERS on PS was evaluated at a single-particle level with different numbers of AuNU in order to determine the minimum conditions required for the onset of the SERS effect. Our findings suggest that SERS of a single particle of PS can be induced by as few as 1-5 particles of AuNU, and that the use of excitation wavelength at 785 nm is appropriate to meet the red-shifted surface plasmon resonance of AuNU upon aggregation. These specifications provide additional information for the development of SERS-based tools for detecting plastic particles < 1 µm in food and environmental samples.

Effects of temperature and particle concentration on aggregation of nanoplastics in freshwater and seawater.

Microplastics have become a significant environmental problem worldwide. Compared with microplastics, nanoplastics are apparently more abundant and harmful but their environmental processes are less well understood. The fate and ecological impacts of nanoplastics in aquatic environments are largely determined by their aggregation properties, which were investigated here using pure water and artificial seawater prepared in the laboratory, as well as river water and coastal seawater collected from subtropical Hong Kong. The tests were carried out at an environmentally realistic temperature range (15-35 °C) with particle concentrations over four orders of magnitude (0.1-100 mg L-1). Under these experimental conditions, parameters of dynamic light scattering were used to determine the extent of aggregation and colloidal stability of polystyrene nanospheres (nPS), a common test model of nanoplastics. Our results showed that aggregation of nPS was minimal in pure water and river water, but became strong under the ionic strength of artificial seawater and coastal seawater, in which 70 nm nPS could aggregate to > 2000 nm, and this aggregation clearly increased with increase in temperature and particle concentration. The aggregates with increasing size and decreasing colloidal stability were deposited more quickly. Findings from this study imply an increased risk of nanoplastics to marine benthic organisms through the aggregation and deposition processes, particularly in warmer waters.

Nanobubble-assisted scaling inhibition in membrane distillation for the treatment of high-salinity brine.

In this study, we report the use of nanobubbles (NBs) as a simple and facile approach to effectively delay scaling in membrane distillation (MD) during the treatment of highly saline feed (100 g L-1). Unlike conventional gas bubbling in MD for improving the hydrodynamic flow conditions in the feed channel, here we generated air NBs with an average size of 128.81 nm in the feed stream and examined their impact on membrane scaling inhibition during MD operation. Due to their small size, neutral buoyancy, and negative surface charge, NBs remain in suspension for a longer time (14 days), providing homogenous mixing throughout the entire feed water. The MD performance results revealed that severe membrane scaling happened during the DCMD treatment of high salinity brine in the absence of nanobubbles, which dramatically reduced the distillate flux to zero after 13 h. A one-time addition of air NBs in the saline feed significantly reduced salt precipitation and crystal deposition on the PVDF membrane surface, delayed the occurrence of flux decline, prevented membrane wetting, thereby prolonging the effective MD operating time. With similar feed concentration and operating conditions, only 63% flux decline after 98 h operation was recorded in nanobubble-assisted MD. Two key explanations were suggested for the delayed membrane scaling upon addition of air NBs in the MD feed: (1) NB-induced turbulent flow in the feed channel that increases the surface shear forces at the membrane surface, alleviating both temperature and concentration polarization effect, (2) electrostatic attractions of the counterions to the negatively charged NBs, which reduces the availability of these ions in the bulk feed for scale formation.

In Vivo Biodistribution, Clearance, and Biocompatibility of Multiple Carbon Dots Containing Nanoparticles for Biomedical Application.

Current research on the use of carbon dots for various biological systems mainly focuses on the single carbon dots, while particles that contain multiple carbon dots have scarcely been investigated. Here, we assessed multiple carbon dots-crosslinked polyethyleneimine nanoparticles (CDs@PEI) for their in vivo biodistribution, clearance, biocompatibility, and cellular uptake. The in vivo studies demonstrate three unique features of the CDs@PEI nanoparticles: (1) the nanoparticles possess tumor-targeting ability with steady and prolonged retention time in the tumor region. (2) The nanoparticles show hepatobiliary excretion and are clear from the intestine in feces. (3) The nanoparticles have much better biocompatibility than the polyethyleneimine passivated single carbon dots (PEI-CD). We also found that pegylated CDs@PEI nanoparticles can be effectively taken up by the cells, which the confocal laser scanning microscope can image under different excitation wavelengths (at 405, 488, and 800 nm). These prior studies provide invaluable information and new opportunities for this new type of intrinsic photoluminescence nanoparticles in carbon dot-based biomedical applications.

Determination of microplastics in the edible green-lipped mussel Perna viridis using an automated mapping technique of Raman microspectroscopy.

Microplastics are prevalent in marine environments and seafood and thus can easily end up in human diets. This has raised serious concerns worldwide, particularly in Hong Kong where the seafood consumption per capita can be three times higher than the global average. This study focused on the green-lipped mussel Perna viridis, a popular seafood species which is subject to a high risk of contamination by microplastics due to its filter-feeding nature. P. viridis was collected from five mariculture sites in Hong Kong and assessed for its body load of microplastics using an automated Raman mapping approach. Microplastics were found in all sites, with an average of 1.60-14.7 particles per mussel per site, or 0.21-1.83 particles per g wet weight. Polypropylene, polyethylene, polystyrene and polyethylene terephthalate were detected among the microplastics, mainly as fragments or fibres in the size range of 40-1000 µm. It was estimated that through consumption of P. viridis, the population in Hong Kong could ingest up to 10,380 pieces of microplastics per person per year. These estimated rates were high compared to the values reported worldwide, suggesting the potential human health risk of microplastics in Hong Kong and adjacent areas.

Improved Raman spectroscopy-based approach to assess microplastics in seafood.

Microplastics represent an emerging environmental issue and have been found almost everywhere including seafood, raising a great concern about the ecological and human health risks they pose. This study addressed the common technical challenges in the assessment of microplastics in seafood by developing an improved protocol based on Raman spectroscopy and using the green-lipped mussel Perna viridis and the Japanese jack mackerel Trachurus japonicus as the test models. Our findings identified a type of stainless-steel filter membranes with minimal Raman interference, and a combination of chemicals that achieved 99-100% digestion efficiency for both organic and inorganic biomass. This combined chemical treatment reached 90-100% recovery rates for seven types of microplastics, on which the surface modification was considered negligible and did not affect the accuracy of polymer identification based on Raman spectra, which showed 94-99% similarity to corresponding untreated microplastics. The developed extraction method for microplastics was further combined with an automated Raman mapping approach, from which our results confirmed the presence of microplastics in P. viridis and T. japonicus collected from Hong Kong waters. Identified microplastics included polypropylene, polyethylene, polystyrene and poly(ethylene terephthalate), mainly in the form of fragments and fibres. Our protocol is applicable to other biological samples, and provides an improved alternative to streamline the workflow of microplastic analysis for routine monitoring purposes.

Graphene Oxide/Reduced Graphene Oxide Enhanced Noniridescent Structural Colors Based on Silica Photonic Spray Paints with Improved Mechanical Robustness.

In contrast to traditional pigment colors, structural colors have developed a great potential in practical applications, thanks to their unique nonfading and color tunable properties; especially amorphous photonic structures with noniridescent structural colors have attracted considerable attention and their applications have expanded to more fields. Herein, graphene oxide (GO) and reduced graphene oxide (RGO) enhanced noniridescent structural colors with excellent mechanical robustness were established by a time-saving approach named spray coating, which allows for rapid fabrication of angular independent structural colors by spraying different photonic spray paints (PSPs) to ensure color multiplicity that was adjusted by the silica nanoparticles (SiO2 NPs) sizes onto the substrates. The incorporation of poly(methyl methacrylate-butyl acrylate) (PMB) improved the adhesion existing among SiO2 inter-nanoparticles and between SiO2 NPs and the substrates, taking advantages of the low glass transition temperature (Tg) of butyl acrylate derivative polymer and made PMB embedded PSPs coated patterns being imparted with good mechanical robustness and abrasive resistance. The peculiar light adsorption of GO and RGO across visible light spectrum facilitate higher color saturation. The improvement in color saturation of GO and RGO doped PSPs is expected to boost the promising applications in structurally colored paintings, inks and other color-related optical fields.

Fabrication of Structural-Coloured Carbon Fabrics by Thermal Assisted Gravity Sedimentation Method.

Structural-coloured poly(styrene-methyl methacrylate-acrylic acid) (Poly(St-MMA-AA)) deposited carbon fabrics (Poly(St-MMA-AA)/PCFs) with fascinating colours (salmon, chartreuse, springgreen, skyblue, mediumpurple) changing with the (Poly(St-MMA-AA) nanoparticle sizes can be facilely fabricated by the thermal-assisted gravity sedimentation method that facilitates the self-assembly of Poly(St-MMA-AA) colloidal nanoparticles to generate photonic crystals. The particle sizes of Poly(St-MMA-AA) copolymer with core/shell structure varying from 308.3 nm to 213.1 nm were controlled by adjusting the amount of emulsifier during emulsion polymerisation. The presence of the intrinsic chemical information of Poly(St-MMA-AA) copolymer has been ascertained by Raman and Fourier Transform Infrared (FT-IR) Spectroscopy analysis. Colour variation of the as-prepared structural-coloured carbon fabrics (Poly(St-MMA-AA)/PCFs) before and after dipping treatment were captured while using an optical microscope. The structural colours of Poly(St-MMA-AA)/PCFs were assessed by calculating the diffraction bandgap according to Bragg's and Snell's laws. The Poly(St-MMA-AA) photonic crystal films altered the electrical properties of carbon fabrics with the resistivity growing by five orders of magnitude. The differential electrical resistivity between Poly(St-MMA-AA)/PCFs and wet Poly(St-MMA-AA)/PCFs combined with the corresponding tunable colours can be potentially applied in several promising areas, such as smart displays, especially signal warning displays for traffic safety.

Reverse Micellar Dyeing of Cotton Fiber with Reactive Dyes: A Study of the Effect of Water pH and Hardness.

Effects of hardness and the pH value of water in a water pool on PEG-based nonionic surfactant dyeing of cotton fiber with reactive dyes in a heptane reverse micelle system were investigated in terms of the color yield, reflectance, CIE L*a*b* value, and unlevelness. Results reveal that the effect of the water-pool pH value on the color yield and reflectance are more significant than the effect of hardness in the water pool. The dyed fabrics under an alkaline water-pool condition obtain a lower color yield and higher reflectance percentage than those under acidic and nearly neutral conditions. The increase of hardness in a water pool has higher influence on unlevelness of dyed samples than the increase or decrease of the pH value in a water pool. The changes in hardness and the pH value in a water pool did not result in a significant change in CIE L*a*b* values of dyed specimens, and no chromatic change was found in dyed fabrics. Excellent washing fastness results of the dyed fabrics, guaranteeing adequate removal of unfixed dyes, assure accuracy of the results in a spectrophotometric measurement.

A Computer Color-Matching Study of Reverse Micellar Dyeing of Wool with Reactive Dyes.

Computer color-matching (CCM) and the levelness of poly(ethylene glycol)-based reverse-micellar dyed wool fabrics in octane and nonane were investigated and compared with a conventional water-based dyeing system. Reflectance curves and calibration curves exhibited no chromatic change and maintained high linearity in both dyeing systems. The linearity of water-dyed calibration curves was slightly higher than that of the reverse-micellar dyed curves. The color yield, in term of K/Ssum values, of solvent-dyed samples was found to be generally higher than that of water-based dyed samples at various calibrated dye concentrations. The concentrations predicted by CCM were close to the theoretical concentrations for both dyeing methods. This indicates that octane- and nonane-assisted reverse-micellar dyeing of wool is able to generate color recipes comparable to the conventional water-based dyeing system. The solvent-dyed samples, measured by the relative unlevelness indices (RUI), exhibit good-to-excellent levelness, which is highly comparable with the water-dyed samples.

Aqueous Synthesis of Multi-Carbon Dot Cross-Linked Polyethyleneimine Particles with Enhanced Photoluminescent Properties.

Heavy-metal-free fluorescent nanoparticles with high photostability and low toxicity are highly desirable as imaging probes for biological applications. Here, a novel synthetic strategy to prepare ultrabright multi-carbon dot cross-linked PEI particles, namely CDs@PEI, through self-assembly of hydrophobically modified PEI and in situ generations of carbon dots within residual monomer-swollen micelles is reported. The resulting particles consist of numerous carbon dots, which are individually and homogeneously embedded within the PEI network, and have an average hydrodynamic diameter of approximately 100 nm with ζ-potential above +35 mV. The CDs@PEI particles possess the synergistic effect of photoluminescent carbon dot and crosslink-enhanced emission of PEI, giving the particles superior optical properties such as high fluorescence quantum yield (up to 66%) in the aqueous system, excitation-dependent emission phenomenon, stable fluorescence in a wide pH range, and resistance to photobleaching.

Dyeing Properties of Cotton with Reactive Dye in Nonane Nonaqueous Reverse Micelle System.

In this study, we explored the dyeing behavior of cotton with reactive dyes in poly(ethylene glycol)-based reverse micelle system in nonaqueous alkane medium of nonane (C9H20). Calibration of dyeing databases for both conventional aqueous-based dyeing method and nonaqueous nonane reverse micellar dyeing method was initially established, along with simulated dyeing of standard samples with known concentrations. Several color difference formulae were used to conduct computer color matching (CCM), by matching the color between batch samples and the standard samples, for both dyeing methods. Excellent color matching results were achieved as both dyeing methods showed that the CCM-predicted concentrations were nearly the same as the known concentrations. It indicates that utilizing nonane as a solvent to facilitate reverse micellar dyeing of cotton can achieve good color matching when compared with that of the conventional aqueous-based dyeing system. Relative unlevelness indices were used to evaluate the evenness of the dyed samples. Good to excellent levelness results were obtained, comparable to that of the conventional aqueous-based dyeing system. Color fastness to laundering of nonane reverse micellar dyed samples was found to be good for industrial applications. In addition, during the reverse micellar dyeing process, only very low level of volatile organic compound content was detected and 98% nonane could be recovered simply by fractional distillation. The results in this study explored the practical usage of nonane nonaqueous reverse micellar approach on the dyeing of cotton with the use of reactive dyes.

Effect of graphene oxide inclusion on the optical reflection of a silica photonic crystal film.

In this study, the inclusion of graphene oxide in silica photonic crystals was found to affect optical reflectance intensity and reflectance peak broadening. The quantitative relationship between weight percentage and the reflected light intensity and corresponding wavelength shift of light GO-decorated photonic crystals was studied, providing a useful parameter in the rational design of antireflection coatings for GO-based photonic crystal films. Comparison of the experimental results with a pure SiO2 particle film shows that a SiO2 particle surface layer incorporated with a fixed graphene oxide weight percentage results in broadening of the peak and a decrease in reflectance intensity. The percentage of the reduction in reflectance intensity is a function of particle size, as indicated by the structured color film surface, demonstrating the possibility of estimating the effect of different graphene oxide inclusion percentages on the antireflection properties of photonic crystal films.

Octane-Assisted Reverse Micellar Dyeing of Cotton with Reactive Dyes.

In this study, we investigated the computer colour matching (CCM) of cotton fabrics dyed with reactive dye using the octane-assisted reverse micellar approach. The aim of this study is to evaluate the colour quality and compare the accuracy between CCM forecasting and simulated dyeing produced by conventional water-based dyeing and octane-assisted reverse micellar dyeing. First, the calibration of dyeing databases for both dyeing methods was established. Standard samples were dyed with known dye concentrations. Computer colour matching was conducted by using the colour difference formula of International Commission on Illumination (CIE) L*a*b*. Experimental results revealed that the predicted concentrations were nearly the same as the expected known concentrations for both dyeing methods. This indicates that octane-assisted reverse micellar dyeing system can achieve colour matching as good as the conventional water-based dyeing system. In addition, when comparing the colour produced by the conventional water-based dyeing system and the octane-assisted reverse micellar dyeing system, the colour difference (ΔE) is ≤1, which indicates that the reverse micellar dyeing system could be applied for industrial dyeing with CCM.

Green Synthesis of Smart Metal/Polymer Nanocomposite Particles and Their Tuneable Catalytic Activities.

Herein we report a simple and green synthesis of smart Au and Ag@Au nanocomposite particles using poly(N-isopropylacrylamide)/polyethyleneimine (PNIPAm/PEI) core-shell microgels as dual reductant and templates in an aqueous system. The nanocomposite particles were synthesized through a spontaneous reduction of tetrachloroauric (III) acid to gold nanoparticles at room temperature, and in situ encapsulation and stabilization of the resultant gold nanoparticles (AuNPs) with amine-rich PEI shells. The preformed gold nanoparticles then acted as seed nanoparticles for further generation of Ag@Au bimetallic nanoparticles within the microgel templates at 60 °C. These nanocomposite particles were characterized by TEM, AFM, XPS, UV-vis spectroscopy, zeta-potential, and particle size analysis. The synergistic effects of the smart nanocomposite particles were studied via the reduction of p-nitrophenol to p-aminophenol. The catalytic performance of the bimetallic Ag@Au nanocomposite particles was 25-fold higher than that of the monometallic Au nanoparticles. Finally, the controllable catalytic activities of the Au@PNIPAm/PEI nanocomposite particles were demonstrated via tuning the solution pH and temperature.

Influence of temperature on the formation and encapsulation of gold nanoparticles using a temperature-sensitive template.

This data article describes the synthesis of temperature-sensitive and amine-rich microgel particle as a dual reductant and template to generate smart gold/polymer nanocomposite particle. TEM images illustrate the influence of reaction temperature on the formation and in-site encapsulation of gold nanoparticles using the temperature-sensitive microgel template. Thermal stability of the resultant gold/polymer composite particles was also examined.

Synthesis and characterization of solvent-invertible amphiphilic hollow particles.

Previous researches on solvent-dependent polymer systems mainly focus on amphiphilic invertible polymers (AIPs), which are capable of forming solvent-dependent micellar or inverse micellar assemblies. However, polymer particles that are invertible in response to solvent polarity are almost unexplored. In this paper, we report a new type of invertible hollow polymer (IHP) particle that is comprised of polyethylenimine-g-poly(methyl methacrylate) (PEI-g-PMMA) copolymer. The amphiphilic PEI-g-PMMA hollow particles were first prepared through synthesis of well-defined PEI/PMMA core-shell particles, followed by removal of PMMA homopolymer from the core. The resulting IHP particles can be stably dispersed in both nonpolar solvent and water. We have investigated the morphology and surface property of the particles in both dichloromethane (DCM) and water using transmission electron microscopy, water contact angle measurement, and X-ray photoelectron spectroscopy analysis to gain insight into this unique particle dispersibility. Sustainability of the solvent-invertible property was carefully studied through repeated treatment of the IHP particles in DCM or water for up to six cycles. Solvent-dependent property of the dry films formed by IHP particles was also investigated through water contact angle measurement. Increasing water content on the DCM-treated IHP particle film could reduce the water contact angle from 94° to 51°. Our results demonstrate that the amphiphilic hollow particles are a new type of polymer design for smart materials that are invertible in response to nonpolar and aqueous media in both dispersed and solid states.