Kunlin Song

Porous Carbon Nanofibers from Electrospun Biomass Tar/Polyacrylonitrile/Silver Hybrids as Antimicrobial Materials

A novel route to fabricate low-cost porous carbon nanofibers (CNFs) using biomass tar, polyacrylonitrile (PAN), and silver nanoparticles has been demonstrated through electrospinning and subsequent stabilization and carbonization processes. The continuous electrospun nanofibers had average diameters ranging from 392 to 903 nm. The addition of biomass tar resulted in increased fiber diameters, reduced thermal stabilities, and slowed cyclization reactions of PAN in the as-spun nanofibers. After stabilization and carbonization, the resultant CNFs showed more uniformly sized and reduced average diameters (226-507 nm) compared to as-spun nanofibers. The CNFs exhibited high specific surface area (>400 m(2)/g) and microporosity, attributed to the combined effects of phase separations of the tar and PAN and thermal decompositions of tar components. These pore characteristics increased the exposures and contacts of silver nanoparticles to the bacteria including Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli, leading to excellent antimicrobial performances of as-spun nanofibers and CNFs. A new strategy is thus provided for utilizing biomass tar as a low-cost precursor to prepare functional CNFs and reduce environmental pollutions associated with direct disposal of tar as an industrial waste.

Morphological influence of cellulose nanoparticles (CNs) from cottonseed hulls on rheological properties of polyvinyl alcohol/CN suspensions

The present work describes the isolation of cellulose nanoparticles (CNs) with different morphologies and their influence on rheological properties of CN and CN-poly (vinyl alcohol) (PVA) suspensions. Cottonseed hulls were used for the first time to extract three types of CNs, including fibrous cellulose nanofibers, rod-like cellulose nanocrystals and spherical cellulose nanoparticles through mechanical and chemical methods. Rheology results showed that the rheological behavior of the CN suspensions was strongly dependent on CN concentration and particle morphology. For PVA/CN systems, concentration of PVA/CN suspension, morphology of CNs, and weight ratio of CN to PVA were three main factors that influenced their rheology behaviors. This research reveals the importance of CN morphology and composition concentration on the rheological properties of PVA/CN, providing new insight in preparing high performance hydrogels, fibers and films base on PVA/CN suspension systems.

Soy Protein Isolate As Fluid Loss Additive in Bentonite-Water-Based Drilling Fluids.

Wellbore instability and formation collapse caused by lost circulation are vital issues during well excavation in the oil industry. This study reports the novel utilization of soy protein isolate (SPI) as fluid loss additive in bentonite-water based drilling fluids (BT-WDFs) and describes how its particle size and concentration influence on the filtration property of SPI/BT-WDFs. It was found that high pressure homogenization (HPH)-treated SPI had superior filtration property over that of native SPI due to the improved ability for the plugging pore throat. HPH treatment also caused a significant change in the surface characteristic of SPI, leading to a considerable surface interaction with BT in aqueous solution. The concentration of SPI had a significant impact on the dispersion state of SPI/BT mixtures in aquesous solution. At low SPI concentrations, strong aggregations were created, resulting in the formation of thick, loose, high-porosity and high-permeability filter cakes and high fluid loss. At high SPI concentrations, intercatlated/exfoliated structures were generated, resulting in the formation of thin, compact, low-porosity and low-permeability filter cakes and low fluid loss. The SPI/BT-WDFs exhibited superior filtration property than pure BT-WDFs at the same solid concentraion, demonstrating the potential utilization of SPI as an effective, renewable, and biodegradable fluid loss reducer in well excavation applications.

Effect of compression combined with steam treatment on the porosity, chemical compositon and cellulose crystalline structure of wood cell walls.

The changes of porosity, chemical composition and cellulose crystalline structure of Spruce (Picea abies Karst.) wood cell walls due to compression combined with steam treatment (CS-treatment) were investigated by nitrogen adsorption, confocal Raman microscopy (CRM) and X-ray diffraction (XRD), respectively. A number of slit-shaped mesopores with a diameter of 3.7nm was formed for the CS-treated wood, and more mesopores were found in the steam-treated wood. CRM results revealed cellulose structure was affected by treatment and β-aryl-ether links associated to guaiacyl units of lignin was depolymerized followed by re-condensation reactions. The crystallinity index (CrI) and crystallite thickness (D200) of cellulose for CS-treated wood were largely increased due to crystallization in the semicrystalline region. Higher degree of increase in both CrI and D200 was observed in both the earlywood and latewood of steam-treated wood, ascribing to the greater amount of mesopores in steam-treated wood than CS-treated wood.

On the stability and chemorheology of a urea choline chloride deep-eutectic solvent as an internal phase in acrylic high internal phase emulsions

High internal phase emulsions are an interesting emulsion subset attainable by surpassing the critical volume of uniform spherical arrangement resulting in a new metastable polyhedral motif. By profiting from their stability time frame and through the introduction of a polymerizable phase, these unique structures can be “locked” in place, affording interconnected hierarchically porous polymers. Rheological exploration has establishing several emulsion stability key parameters including surfactant concentration, internal phase volume fraction (ϕ), interfacial tension (σ), phase polarity, and temperature. Because the majority of HIPEs studied are aqueous, additional parameters such as internal phase viscosity have not been studied in detail. Deep-eutectic solvents (DES) are a new generation of green solvents sharing several ionic liquid properties. DES provide an ideal opportunity to study nonaqueous polar internal phases of increased viscosity while expanding on the conditions for polymerization to potential scale up applications. This study presents the first detailed investigation on the DES-non ionic surfactant HIPE systems. Shear stability of non-aqueous HIPEs was evaluated taking into account continuous phase viscosity as well as monomer and surfactant molecular nature (i.e. chain length and functionality). HIPE polymerization was evaluated through isothermal oscillatory time-sweep experiments. Longer tail methacrylic monomers presented preferential stability over acrylic or short tail monomers. Furthermore, emulsions showed improved stability and elasticity compared to aqueous HIPEs due to their high internal phase viscosity. Internal phase viscosity mediated by hydrogen bonding increased activation energy as estimated by complex viscosity plots.

Non-Isothermal Crystallization of Poly (vinylidene fluoride)/Poly (methyl methacrylate)/Cellulose Nanocrystal Nanocomposites

Poly (vinylidiene fluoride) (PVDF)/poly (methyl methacrylate) (PMMA)/cellulose nanocrystal (CNC) nanocomposites were prepared by solution blending. Non-isothermal crystallization of PVDF/PMMA (70/30) blend and its composites was investigated using differential scanning calorimetry. It was found that the addition of CNCs played a positive role in both the crystallization rate and crystallization percentage. The addition of CNCs increased the initial crystallization temperature, peak crystallization temperature, and crystalline enthalpy. The Avrami index indicated that CNCs did not change the crystallization mechanism; while other parameters derived from Jeziorny theory and Mos method, including Z c , F(t), and α, further verified the positive role played by CNCs.

Electrospun Nanofibers Made of Silver Nanoparticles, Cellulose Nanocrystals, and Polyacrylonitrile as Substrates for Surface-Enhanced Raman Scattering

Nanofibers with excellent activities in surface-enhanced Raman scattering (SERS) were developed through electrospinning precursor suspensions consisting of polyacrylonitrile (PAN), silver nanoparticles (AgNPs), silicon nanoparticles (SiNPs), and cellulose nanocrystals (CNCs). Rheology of the precursor suspensions, and morphology, thermal properties, chemical structures, and SERS sensitivity of the nanofibers were investigated. The electrospun nanofibers showed uniform diameters with a smooth surface. Hydrofluoric (HF) acid treatment of the PAN/CNC/Ag composite nanofibers (defined as p-PAN/CNC/Ag) led to rougher fiber surfaces with certain pores and increased mean fiber diameters. X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) results confirmed the existence of AgNPs that were formed during heat and HF acid treatment processes. In addition, thermal stability of the electrospun nanofibers increased due to the incorporation of CNCs and AgNPs. The p-PAN/CNC/Ag nanofibers were used as a SERS substrate to detect p-aminothiophenol (p-ATP) probe molecule. The results show that this substrate exhibited high sensitivity for the p-ATP probe detection.