Selected Phase Separation Renders High Strength and Toughness to Polyacrylamide/Alginate Hydrogels with Large-Scale Cross-Linking Zones.

High water content usually contradicts the mechanics for hydrogels, and achieving both characteristics is extremely challenging. Herein, a novel confined-chain-aggregation (CCA) strategy is developed to fabricate ultrastrong and tough hydrogels without sacrificing their inherent water capacity. Based on the popular polyacrylamide/alginate (PAAm/Alg) system with a double network (DN), a poor solvent exchange is induced once PAAm is fully cross-linked but prior to ionic cross-linking of alginate. In this case, the alginate chains are restricted by the chemical PAAm network and undergo a confined-chain aggregation, which guarantees an interpenetrating network of both polymers and simultaneously generates micron-scale aggregates. In addition, after the subsequent water uptake, the accompanying formation of hydrogen bonds and metal-ligand coordination stabilizes the newly formed alginate aggregates, serving as large-scale cross-linking zones. However, the PAAm chains are anchored by the preformed cross-linking points and convert back to the uniformly distributed, high-water-content state, achieving a selected phase separation in a DN system. The combined CCA and hybrid cation cross-linking method gives mechanical strength and toughness to the PAAm/Alg hydrogels to reach approximately 30 and 5 times the traditional methods, respectively. This investigation provides a general strategy for the development of a new generation of double-network hydrogels, which will expand their application as structural materials for cartilage and soft robotics.

Electrospinning Highly Concentrated Sodium Alginate Nanofibres without Surfactants by Adding Fluorescent Carbon Dots.

In this study, sodium alginate (SA) nanofibres were obtained by electrospinning via the assistance of traditional poly(ethyl oxide) (PEO) and dimethyl sulfoxide (DMSO) with a high SA/PEO ratio of up to 94:6. However, surfactants with more or less toxicities were replaced by nontoxic and fluorescent carbon dots (CDs) to improve spinnability. Experimental details were conducted by fixing the ratio of SA/PEO to 90:10. Then, the electrospinning products of solutions with different compositions were observed with scanning electron microscopy. Properties such as conductivity, surface tension and rheology of the solutions were investigated to determine the key influencing factors. Moreover, since CDs have excellent fluorescence properties, the fluorescent properties of the nanofibre membrane that was blended with CDs were then collected. In addition, in vitro cytotoxicity assessment of the nanofibres were conducted to evaluate the toxicities and biocompatibility.

Study on the Methods of Separation and Detection of Chelates.

The separation and purification techniques of chelates can improve the accuracy of detecting results of the chelation rate. As a quantitative indicator of metal ion chelates, the chelation rate can not only reflect the completion of chelation but also determine the amount of metal ions in different forms. The determination of chelation rate can help to determine the suitable chelating reaction conditions, make theoretical basis for the fertilizer efficiency, analyze the stability of chelating fertilizers and study the action mechanism of trace elements. In our study, the methods of separation free metal ions from mixture were reviewed first, including gel filtration chromatography, organic solvent precipitation, ion exchange chromatography, membrane separation and high performance liquid chromatography. Then, the qualitative analysis methods of chelates were introduced briefly, including chemical identification, infrared spectroscopy, ultraviolet spectroscopy. A detailed overview of the quantitative determination methods of chelates were also shown, such as ethylenediaminetetraacetic acid titration, chemical titration, atomic absorption spectrometry, inductively coupled plasma atomic emission spectrometry, inductively coupled plasma mass spectrometry, spectrophotometric, chemical modified electrode. In addition, the merits and demerits of chelated rate determination methods of various determination methods were analyzed, and summarized the applicability of various methods, which provided a theoretical basis for optimizing chelating process, characterizing the structure of chelates and analyzing the mechanism of chelating fertilizer. The current methods of measuring chelation rate were also summarized and prospected.

Preparation of Ion-Exchanged TEMPO-Oxidized Celluloses as Flame Retardant Products.

Cellulose, as one of the most abundant natural biopolymers, has been widely used in textile industry. However, owing to its drawbacks of flammability and ignitability, the large-scale commercial application of neat cellulose is limited. This study investigated some TEMPO-oxidized cellulose (TOC) which was prepared by selective TEMPO-mediated oxidation and ion exchange. The prepared TOC was characterized by Fourier transform infrared (FT-IR) spectroscopy and solid-state 13C-nuclear magnetic resonance (13C-NMR) spectroscopy. The thermal stability and combustion performance of TOC were investigated by thermogravimetry analysis (TG), microscale combustion calorimetry (MCC) and limiting oxygen index (LOI). The results demonstrated that the thermal stability of TOC was less than that of the pristine material cellulose, but the peak of heat release rate (pHHR) and the total heat release (THR) of all TOC were significantly reduced. Additionally, the LOI values of all TOC products were much higher 25%. In summary, the above results indicated that the modified cellulose with carboxyl groups and metal ions by selective oxidation and ion exchange endows efficient flame retardancy.

Preparation of CdTe/Alginate Textile Fibres with Controllable Fluorescence Emission through a Wet-Spinning Process and Application in the Trace Detection of Hg2+ Ions.

Fluorescent textile fibres (FTFs) are widely used in many industrial fields. However, in addition to fibres with good fluorescence, fibres with excellent colour controllability, structural stability and appropriate mechanical strength still need to be developed. In this work, CdTe/alginate composite FTFs are prepared by taking advantage of the interactions between CdTe nanocrystals (NCs) and alginate macromolecules via a wet-spinning machine with a CaCl2 aqueous solution as the coagulation bath. CdTe NCs were chemically fixed in the fibre due to the interactions among surface ligands, macromolecules and coagulators (calcium ions), which ensured the excellent dispersity and good stability of the fibres. Förster resonance energy transfer (FRET) between NCs in the fibre was found to be restricted, which means that the emission colour of the fibres was totally controllable and could be predicted. Other properties of alginate fibres, such as flame retardance and mechanical strength, were also well preserved in the fluorescent fibres. Finally, FTFs showed good selectivity toward trace Hg2+ ions over other metallic ions, and the detection could be identified by the naked eye.

Study on the preparation and flame retardant properties of an eco-friendly potassium-calcium carrageenan fiber.

Potassium-calcium carrageenan fibers were prepared in an eco-friendly fashion by wet spinning method. The forming process and flame retardant properties of this fiber compared with the traditional barium carrageenan fibers were studied in this paper. The results showed that the potassium ions were combined with the sulfate group in the carrageenan by ion bonding that made the potassium-calcium carrageenan fibers form a gel structure, which was a relative loose spatial network, while barium ions reacted with the sulfate groups of carrageenan to induce barium carrageenan fibers form a precipitated structure, which was a relative close spatial network. The limiting oxygen index, cone calorimeter, thermogravimetric analysis and pyrolysis-gas chromatography-mass spectrometry tests implied that K+-Ca2+ affected the pyrolysis behavior of potassium-calcium carrageenan fibers and catalyzed it to produce different pyrolysis products from Ba2+ in barium carrageenan fibers. In addition, the pyrolysis mechanism of potassium-calcium carrageenan fibers was elucidated in this paper.

Polychlorinated biphenyls, polychlorinated dibenzo-p-dioxins and dibenzofurans in marine and lacustrine sediments from the Shandong Peninsula, China.

Concentrations of polychlorinated biphenyls (PCBs), polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in sediments from Bohai Sea and Yellow Sea coastal waters and lakes in Shandong Peninsula were determined. The total PCB concentrations of the measured 50 congeners (Sigma50PCBs) in the sediments ranged from 273.7 to 644.5 pg g(-1) dw (dry weight). The PCB congener profiles in the lacustrine sediments were different from those in the marine sediments. TriCBs and TetraCBs were the dominant homologues in marine sediments, whereas in the sediments from the Nansi Lakes, contributions of PCB homologues were similar. The total concentrations of 2,3,7,8-PCDD/Fs ranged from 6.2 to 27.4 pg g(-1) dw. The congener profiles of 2,3,7,8-substituted PCDD/Fs for the sediments were generally similar for both the lakes and the coastal sea areas in Shandong Peninsula. They were characterized by high OCDD, followed by 1,2,3,4,6,7,8-HpCDD and OCDF. The congener profiles of PCDD/Fs in the sediments were consistent with the profiles of main dominant PCDD/Fs in pentachlorophenol and sodium pentachlorophenate products in China. PCDD/F-TEQ ranged from 0.11 to 0.80 pg TEQg(-1) dw. The dioxin-like PCB-TEQ had concentrations ranging from 0.03 to 0.08 pg TEQ g(-1) dw, mainly from PCB126. PCBs and PCDD/Fs concentrations found in the sediments were from background to low polluted levels.