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Scintillators that exhibit X-ray-excited luminescence have great potential in radiation detection, X-ray imaging, radiotherapy, and non-destructive testing. However, most reported scintillators are limited to inorganic or organic crystal materials, which have some obstacles in repeatability and processability. Here we present a facile strategy to achieve the X-ray-excited organic phosphorescent scintillation from amorphous copolymers through the copolymerization of the bromine-substituted chromophores and acrylic acid. These polymeric scintillators exhibit efficient X-ray responsibility and decent phosphorescent quantum yield up to 51.4% under ambient conditions. The universality of the design principle was further confirmed by a series of copolymers with multi-color radioluminescence ranging from green to orange-red. Moreover, we demonstrated their potential application in X-ray radiography. This finding not only outlines a feasible principle to develop X-ray responsive phosphorescent polymers, but also expands the potential applications of polymer materials with phosphorescence features. The authors achieved the X-ray-excited organic phosphorescent scintillation from copolymers through copolymerization of bromine-substituted chromophores and acrylic acid and demonstrated their potential application in X-ray radiography.

A low-angle-dependent photonic crystal hydrogel (LAD-PCH) material was developed to simultaneously detect and remove uranyl ions (UO.sub.2.sup.2+). Different from traditional SiO.sub.2 photonic crystal hydrogel with the problem of angle dependency, the LAD-PCH material overcomes the restriction of observation direction. The LAD-PCH is a composite material with the photonic crystal array of 180-nm monodisperse CdS@SiO.sub.2 particles embedded into the functional hydrogel. As one UO.sub.2.sup.2+ can bind to multiple carboxyl groups and amide groups, the functional hydrogel fabricated by acrylic acid and acrylamide will shrink after chelating. These changes in the hydrogel volume alter the array spacing and trigger a blue shift of diffraction wavelength and naked-eye visual color changes of LAD-PCH. The color can vary from orange-red to orange, yellow, green, and cyan, corresponding to the determination range of 100 pM-100 [mu]M. The LAD-PCH material detects UO.sub.2.sup.2+ sensitively as the lowest detectable concentration is about 100 pM, and removes UO.sub.2.sup.2+ high-efficiently as the maximum adsorption capacity of U(VI) is about 1010 mg g.sup.-1 at 298 K. This LAD-PCH material is convenient and has potential to simultaneously monitor and remove UO.sub.2.sup.2+ from uranium-polluted water.

Haemonchus contortus is a blood-feeding gastrointestinal parasite that impacts grazing sheep, causing economic losses in animal production. Due to its anthelmintic resistance, alternative antiparasitic treatments like plant-based anthelmintics are necessary to explore. Artemisia cina (Asteraceae) is a plant whose n-hexane extract and ethyl acetate extract exhibit anthelmintic activity against H. contortus, the n-hexane more active. To discover additional bioactive metabolites, a chemical analysis was performed on ethyl acetate extract, which presented an LC.sub.90 of 3.30 mg/mL and allowed the isolation of 11-[(1R,5S,7R,8R,10S,)-1,8-dihydroxy-5,10-dimethyl-4-oxodecahydroazulen-7-yl] acrylic acid. This new sesquiterpene was identified through one and two-dimensional NMR. The compound was named cinic acid and displayed an LC.sub.50 of 0.13 (0.11-0.14) mg/mL and LC.sub.90 of 0.40 (0.37-0.44) mg/mL, which, compared with ethyl acetate extract larvicidal activity, was 256-fold more active at LC.sub.50 and 15.71-fold at LC.sub.90 . In this study, a new sesquiterpene with larvicidal activity against H. contortus L.sub.3 infective larvae was isolated from the ethyl acetate extract of Artemisia cina.

The design of novel binder systems is required for the high capacity silicon (Si) anodes which usually undergo huge volume change during the charge/discharge cycling. Here, we introduce a poly (acrylic acid sodium)-grafted-carboxymethyl cellulose (NaPAA- g -CMC) copolymer as an excellent binder for Si anode in lithium ion batteries (LIBs). The NaPAA- g -CMC copolymer was prepared via a free radical graft polymerization method by using CMC and acrylic acid as precursors. Unlike the linear, one-dimensional binders, the NaPAA- g -CMC copolymer binder is expected to present multi-point interaction with Si surface, resulting in enhanced binding ability with Si particles as well as with the copper (Cu) current collectors and building a stable solid electrolyte interface (SEI) layer on the Si surface. The NaPAA- g -CMC based Si anode shows much better cycle stability and higher coulombic efficiency than those made with the well-known linear polymeric binders such as CMC and NaPPA.

To prepare superabsorbent hydrogels, starch-graft-poly(acrylic acid) reinforced by cellulose nanofibers (CNF), was synthesized through free radical graft polymerization. The results of its biocompatibility tests exhibited that by increasing incubation time from 1 to 5 days, the numbers of living cells were increased on both reinforced and unreinforced hydrogels. However, the fraction of cells on the surfaces of the reinforced hydrogel is comparable to unreinforced samples. The swelling amounts in NaCl, CaCl2, and AlCl3 solutions were 193 ± 9, 110 ± 8, and 99 ± 7 (gwater/gabsorbent) for 5 wt% CNF-reinforced hydrogels and 109 ± 8, 62 ± 7, and 56 ± 6 (gwater/gabsorbent) for unreinforced hydrogels, respectively. Compressive strength and Young’s modulus of 5 wt% CNF-assisted hydrogels were also 63.3 and 31.6 kPa corresponding to 69% and 140% improvements compared with unreinforced one. The graft polymerization of acrylic acid monomer was controlled by monomer content and cross-linking percentage, in order to achieve the highest swelling capacity for hydrogels. Hydrogel swelling in water was 312 gwater/gabsorbent for unreinforced hydrogel and 523 gwater/gabsorbent for 5 wt% CNF-reinforced sample and water absorption kinetics results was in agreement with the pseudo-second-order model. The prepared CNF-reinforced starch-graft-poly(acrylic acid) hydrogels can be used in a wide range of medical application due to the enhanced hydrophilicity, mechanical strength, and biocompatibility.Graphic abstract

A composite polymer, hydroxyapatite/poly(acrylamide-acrylic acid), was synthesized by gamma-induced polymerization. The factors affecting the sorption process were evaluated. The removal increased with time and achieved equilibrium after 1 h for all initial concentration ranges (10–50 mg/L). The highest removal of Sr(II) was achieved using 50 mg/L at pH 6. The sorption process was found to follow a pseudo-first-order mechanism. The equilibrium data are best described by the Langmuir model, with a monolayer capacity of 53.59 mg/g. The values of thermodynamic parameters indicate that the sorption process is endothermic ( ΔH > 0), increases randomness ( ΔS > 0) and is spontaneous ( ΔG < 0). The results imply that the composite could be used as a promising low-cost material for the removal of radionuclides from radioactive waste.

This work aims to enhance the polarity of natural rubber by grafting copolymers onto deproteinized natural rubber (DPNR) to improve its compatibility with silica. Poly(acrylic acid-co-acrylamide)-grafted DPNR ((PAA-co-PAM)-DPNR) was successfully prepared by graft copolymerization with acrylic acid and acrylamide in the latex stage, as confirmed by FTIR. The optimum conditions to obtain the highest conversion, grafting efficiency, and grafting percentage were a reaction time of 360 min, a reaction temperature of 50 °C, and an initiator concentration of 1.0 phr. The monomer conversion, grafting efficiency, and grafting percentage were 91.9–94.1, 20.8–38.9, and 2.1–9.9%, respectively, depending on the monomer content. It was shown that the polarity of the natural rubber increased after grafting. The (PAA-co-PAM)-DPNR was then mixed with silica to prepare DPNR/silica composites. The presence of the (PAA-co-PAM)-DPNR and silica in the composites was found to improve the mechanical properties of the DPNR. The incorporation of 10 phr of silica into the (PAA-co-PAM)-DPNR with 10 phr monomer increased its tensile strength by 1.55 times when compared to 10 phr of silica loaded into the DPNR. The silica-filled (PAA-co-PAM)-DPNR provided s higher storage modulus, higher Tg, and a lower tan δ peak, indicating stronger modified DPNR/silica interactions and greater thermal stability when compared to silica-filled DPNR.