Tetraphenylethylene-conjugated polycation covered iron oxide nanoparticles for magnetic resonance/optical dual-mode imaging

Magnetic resonance (MR)/optical dual-mode imaging with high sensitivity and high tissue resolution have attracted many attentions in biomedical applications. To avert aggregation-caused quenching of conventional fluorescence chromophores, an aggregation-induced emission molecule tetraphenylethylene (TPE)-conjugated amphiphilic polyethylenimine (PEI) covered superparamagnetic iron oxide (Alkyl-PEI-LAC-TPE/SPIO nanocomposites) was prepared as an MR/optical dual-mode probe. Alkyl-PEI-LAC-TPE/SPIO nanocomposites exhibited good fluorescence property and presented higher T2 relaxivity (352 Fe mM−1s−1) than a commercial contrast agent Feridex (120 Fe mM−1s−1) at 1.5 T. The alkylation degree of Alkyl-PEI-LAC-TPE effects the restriction of intramolecular rotation process of TPE. Reducing alkane chain grafting ratio aggravated the stack of TPE, increasing the fluorescence lifetime of Alkyl-PEI-LAC-TPE/SPIO nanocomposites. Alkyl-PEI-LAC-TPE/SPIO nanocomposites can effectively labelled HeLa cells and resulted in high fluorescence intensity and excellent MR imaging sensitivity. As an MR/optical imaging probe, Alkyl-PEI-LAC-TPE/SPIO nanocomposites may be used in biomedical imaging for certain applications.

Adsorption Properties of Soft Hydrophobically Functionalized PSS/MA Polyelectrolytes

We investigated the adsorption properties of the newly synthesized, hydrophobically functionalized polyelectrolyte (HF-PE), poly(4-styrenesulfonic-co-maleic acid) copolymer (PSS/MA). The hydrophobic alkyl side chains (C12 or C16) were incorporated into the polyelectrolyte backbone via the labile amid linker to obtain the soft HF-PE product with the assumed amount of 15% and 40% degree of grafting for every length of the alkyl chain, i.e., PSS/MA-g-C12NH2 (15% or 40%) as well as PSS/MA-g-C16NH2 (15% or 40%). In the present contribution, we determined both the effect of grafting density and the length of alkyl chain on adsorption at water/air and water/decane interfaces, as well as on top of the polyelectrolyte multilayer (PEM) deposited on a solid surface. The dependence of the interfacial tension on copolymer concentration was investigated by the pendant drop method, while the adsorption at solid surface coated by poly(diallyldimethylammonium chloride)/poly(styrene sulphonate) PEM by the quartz crystal microbalance with dissipation (QCM-D), attenuated total reflection Fourier transform infrared spectroscopy (FTIR-ATR) and contact angle analysis. We found that surface activity of the hydrophobized copolymer was practically independent of the grafting ratio for C16 side chains, whereas, for C12, the copolymer with a lower grafting ratio seemed to be more surface active. The results of QCM-D and FTIR-ATR experiments confirmed the adsorption of hydrophobized copolymer at PEM along with the modification of water structure at the interface. Finally, it can be concluded that the hydrophobically modified PSS/MA can be successfully applied either as the efficacious emulsifier for the formation of (nano)emulsions for further active substances encapsulation using the sequential adsorption method or as one of the convenient building blocks for the surface modification materials.

Preparation of PP-g-(AA-MAH) Fibers Using Suspension Grafting and Melt-Blown Spinning and its Adsorption for Aniline

This paper uses polypropylene (PP) as the matrix and acrylic acid (AA) and maleic anhydride (MAH) as functional monomers to prepare PP-g-(AA-MAH) fibers by suspension grafting and melt-blown spinning technology that are easy to industrially scale-up. The fibers can be used to adsorb aniline. Results showed that the grafting ratio reached the maximum of 12.47%. The corresponding optimal conditions were grafting time of 3 h, AA: MAH = 0.75, total monomer content of 55%, benzoyl peroxide 1.4%, xylene concentration of 6 mL/g PP, and deionized water content of 8 mL/g PP. Owing to its good fluidity and thermal stability, the product of suspension grafting can be used for melt-blown spinning. Infrared spectroscopic and nuclear magnetic resonance spectroscopic analyses indicated that AA and MAH were successfully grafted onto PP fibers. After grafting, the hydrophilicity of PP-g-(AA-MAH) fiber increased. Therefore, it had higher absorptivity for aniline and the adsorption capacity could reach 42.2 mg/g at 45 min and pH = 7. Moreover, the PP-g-(AA-MAH) fibers showed good regeneration performance.

Synthesis of carboxymethyl starch grafted polyvinyl imidazole (CMS-g-PVIs) and their role as an absorbent for the removal of phenol

Cigarette industry plays an important role in the economy of the advanced countries. But the cigarette smoke contains toxic chemicals such as phenol which causes various kind of diseases and affect human life. In this paper, we synthesized carboxymethyl starch grafted poly vinyl imidazole (CMS-g-PVIs) by reacting carboxymehtyl starch (CMS) with vinyl imidazole (VI). The structures of the CMS-g-PVIs were investigated by ¹H NMR and FT-IR. The crystalline properties of the CMS and CMS-g-PVIs were checked by XRD. The thermal properties of the original CMS and CMS-g-PVIs were investigated by TGA analysis. It was found that the modified starches had high thermal stability due to aromatic imidazole ring. The modified starches also showed more rough and distorted morphology as compared to native CMS. The CMS-g-PVIs were subjected for phenol adsorption and showed adsorption efficiencies of 0.170 g/g, 0.190 g/g, 0.192 g/g and 0.199 g/g for CMS, CMS-g-PVI 1, CMS-g-PVI 2 and CMS-g-PVI 3, respectively. Due to higher grafting ratio, CMS-g-PVI 3 showed good adsorption efficiency of 0.199 g/g for phenol. The obtained results showed that the grafting of vinyl imidazole on CMS can increase the adsorption efficiency of native CMS towards phenol.

Preparation of PP-g-(AA-MAH) Fibers Using Suspension Grafting and Melt-blown Spinning and Its Adsorption for Aniline in Wastewater

This paper uses polypropylene (PP) as the matrix and acrylic acid (AA) and maleic anhydride (MAH) as functional monomers to prepare PP-g-(AA-MAH) fibers by suspension grafting and melt-blown spinning technology that are easy to industrially scale-up. The fibers can be used to adsorb aniline from wastewaters. Results showed that the grafting ratio reached the maximum of 12.47%. The corresponding optimal conditions were grafting time of 3h, AA : MAH = 0.75, total monomer content of 55%, benzoyl peroxide 1.4%, xylene concentration of 6 mL/g PP, and deionized water content of 8 mL/g PP. Owing to its good fluidity and thermal stability, the product of suspension grafting can be used for melt-blown spinning. Infrared spectroscopic and nuclear magnetic resonance spectroscopic analyses indicated that AA and MAH were successfully grafted onto PP fibers. After grafting, the hydrophilicity of PP-g-(AA-MAH) fiber increased. Therefore, it had higher adsorptivity for aniline and the adsorption capacity could reach 42.2 mg/g at 45 min. Moreover, the PP-g-(AA-MAH) fibers showed good regeneration performance.

l-Arginine Grafted Poly(Glycerol Sebacate) Materials: An Antimicrobial Material for Wound Dressing

This study focuses on the development and evaluation of a novel wound dressing material. l-arginine grafted poly(glycerol sebacate) materials (PGS-g-Arg) are developed by chemical conjugation of l-arginine on poly(glycerol sebacate) chains and the mechanical property, water vapor transmission rate, antimicrobial functions and biocompatibility are investigated. At various l-arginine grafting ratio, the mechanical properties are tunable. It was found that between 7–13% l-arginine grafting ratios, the tensile strengths of PGS-g-Arg were similar to that of natural skin. These materials are shown with a low water vapor transmission rate, 6.1 to 10.3 g/m2/h, which may form a barrier and assist in the closure of wounds. Inhibition in the growth of Pseudomonas aeruginosa and Staphylococcus aureus was observed on PGS-g-Arg, and a series of experiments were conducted to confirm its biocompatibility. In summary, l -arginine grafted poly(glycerol sebacate) may offer a novel option for wound dressing.

Preparation and application of a xylan-based antibacterial papermaking additive to protect against Escherichia coli bacteria

A xylan-based antimicrobial additive agent was prepared and studied for use in paper products against Escherichia coli bacteria. The derived cationic-xylan-grafted-guanidine polymer (CX-g-PHGH) was successfully synthesized by graft copolymerization of cationic-xylan with polyhexa-methylene guanidine hydrochloride (PHGH) using ceric ammonium nitrate as an initiator. The obtained CX-g-PHGH had a maximum PHGH grafting ratio of 18.4% and efficiency of 58.4% and showed good viscosity and thermal stability. Furthermore, the paper samples prepared in this work were reinforced noticeably with the addition of CX-g-PHGH, after which exhibited improved mechanical properties. Compared to the reference paper without any of the xylan derivatives, the index of tensile, tear, burst, and folding endurance of the paper were increased by up to 20.1%, 25.3%, 30.2%, and 77.8%, respectively. Moreover, the prepared CX-g-PHGH paper exhibited efficient antimicrobial barrier properties against E. coli bacteria, by which many applications based on the new xylan derived additive agent obtained in this work could be found, especially in field of antimicrobial paper products against E. coli bacteria from contaminated food.

Synthesis of Grafted Cationic Starch with DMDAAC Using Ammonium Persulfate/Carbamide Initiation System

Using ammonium persulfate (APS)/carbamide initiation system, cationic grafted starch was prepared by the graft copolymerization of starch with diallydimethylammonium chloride (DMDAAC). The synthesized polymer was confirmed by FTIR, NMR, and XRD. And the morphology was characterized by SEM. The optimum conditions of graft copolymerization were determined and the flocculation properties of the cationic grafted starch were investigated using diatomite suspension. The obtained results showed that grafting ratio (G) and grafting efficiency (GE) have an increased trend along with the increase of mass ratio of starch to monomer. G, GE and cationic degree (DC) increased with the rise of mole ratio of AM to DMDAAC. When the total concentration of the monomers in the system is fixed, increasing APS concentration up to 0.33×10-3 M caused a rise for the G, GE and DC. The optimum temperature and the time were 40 °C and 5 h, respectively. The result also showed that the cationic grafted starch has excellent flocculation performance whether in acid, alkaline or neutral conditions.

Preparation and Application of a Xylan-Based Antibacterial Additive Agent against Escherichia Coli Bacteria

In this work, a xylan-based antimicrobial additive agent was prepared and aimed for uses in paper products against Escherichia coli bacteria. The derived Cationic-Xylan-grafted-PHGH (CX-g-PHGH) was successfully synthesized by graft copolymerization of cationic-xylan with guanidine polymer (PHGH) using ceric ammonium nitrate as initiator. The obtained CX-g-PHGH had maximum PHGH grafting ratio of 18.45% and efficiency of 58.45%, and showed good viscosity and thermal stability. Furthermore, the paper samples prepared in this work were reinforced obviously with the addition of CX-g-PHGH by improved mechanical properties. Compared to the reference paper without any of the xylan-derivatives, the index of tensile, tear, burst and folding endurance of the paper had increases up to 20.07%, 25.31%, 30.20% and 77.78%, respectively. Moreover, the prepared CX-g-PHGH paper exhibited an efficient antimicrobial activity against E. coli bacterial, by which a lot of applications based on the new xylan-derived additive agent obtained in this work could be found, especially in field of antimicrobial paper products against E. Coli bacteria from contaminated food.