65 research outputs found
Designed polyelectrolyte shell on magnetite nanocore for dilution-resistant biocompatible magnetic fluids.
Magnetite nanoparticles (MNPs) coated with poly(acrylic acid-co-maleic acid) polyelectrolyte (PAM) have been prepared with the aim of improving colloidal stability of core-shell nanoparticles for biomedical applications and enhancing the durability of the coating shells. FTIR-ATR measurements reveal two types of interaction of PAM with MNPs: hydrogen bonding and inner-sphere metal-carboxylate complex formation. The mechanism of the latter is ligand exchange between uncharged -OH groups of the surface and -COO(-) anionic moieties of the polyelectrolyte as revealed by adsorption and electrokinetic experiments. The aqueous dispersion of PAM@MNP particles (magnetic fluids - MFs) tolerates physiological salt concentration at composition corresponding to the plateau of the high-affinity adsorption isotherm. The plateau is reached at small amount of added PAM and at low concentration of nonadsorbed PAM, making PAM highly efficient for coating MNPs. The adsorbed PAM layer is not desorbed during dilution. The performance of the PAM shell is superior to that of poly(acrylic acid) (PAA), often used in biocompatible MFs. This is explained by the different adsorption mechanisms; metal-carboxylate cannot form in the case of PAA. Molecular-level understanding of the protective shell formation on MNPs presented here improves fundamentally the colloidal techniques used in core-shell nanoparticle production for nanotechnology applications
Development of scalable and versatile nanomaterial libraries for nanosafety studies: polyvinylpyrrolidone (PVP) capped metal oxide nanoparticles
The potential long-term environmental impact of manufactured nanomaterials (NMs) remains poorly understood, and the need to better predict NM fate and transformations and chronic effects is particularly urgent. Compared to their bulk counterparts, manufactured NMs can have distinct physical and chemical characteristics, which influence their behaviour, stability and toxicity. It is therefore essential to develop standard and reference NM libraries for environmental nanoscience and nano(eco)toxicology, and to facilitate a move towards computational prediction of NM fate, through quantitative structure–activity relationships for example. The aim of this work was to develop and fully characterise one such library, which included comparable NMs with a range of core chemistries, but the same capping agent and size range, for use in future studies to test the hypothesis that the core chemistry is a primary factor in controlling toxicity. The library contained the following NMs: 10k, 40k and 360k PVP capped ceria, zinc oxide and copper oxide (9 NMs in total). The work presented here upholds the underpinning hypothesis that the mechanism of NM formation is the same in all cases, suggesting that the protocol is very robust and has the potential to generate a wide range of comparable metal oxide NMs and potentially expand the library further with doped metal oxide and metal NMs. Characterisation by means of DLS (both size and zeta measurements), UV/Vis, XPS, FT-IR, TEM, STEM, EDX and EELS confirms that the tested synthesis protocol can easily and successfully be used to create stable PVP capped metal oxide NMs of reproducible sizes
Enhanced recovery in the management of mild gallstone pancreatitis: a prospective cohort study
Biomarcadores inflamatórios e de estresse oxidativo em cadelas submetidas à ovário-histerectomia videoassistida ou convencional
Designed Polyelectrolyte Shell on Magnetite Nanocore for Dilution-Resistant Biocompatible Magnetic Fluids
Crystal violet dye sorption over acrylamide/graphene oxide bonded sodium alginate nanocomposite hydrogel
The synthesis of acrylamide bonded sodium alginate (AM-SA) hydrogel and acrylamide/graphene oxide bonded sodium alginate (AM-GO-SA) nanocomposite hydrogel was successfully performed using the free radical method. The AM-SA and AM-GO-SA hydrogels were applied as composited adsorbents in crystal violet (CV) dye removal. The adsorption process experiments were performed discontinuously and the acquired data showed that the efficiency is more dependent on pH than other factors. The C–O, C[dbnd]O, and C[dbnd]C groups were detected in the produced hydrogels. The amount of surface area was computed to be 44.689 m2/g, 0.0392 m2/g, and 6.983 m2/g for GO, AM-SA, and AM-GO-SA nanocomposite hydrogel, respectively. The results showed that the experimental data follow the Redlich-Peterson isotherm model. Also, the maximum adsorption capacity of monolayer for CV dye adsorption was determined using AM-SA hydrogel and AM-GO-SA nanocomposite hydrogel 62.07 mg/g and 100.30 mg/g, respectively. In addition, the parameters RL, n, and E showed that the processes of adsorption of CV dye using both types of adsorbents are physical and desirable. Thermodynamically, the CV elimination was exothermic and spontaneous. Besides, thermodynamic results showed that the adsorption process is better proceeding at low temperatures. The experimental data followed a pseudo- second- order (PSO) kinetic model. Also, the Elovich model showed that AM-GO-SA nanocomposite hydrogel has more ability to absorb CV dye. Therefore, according to the obtained results, it can be stated that the produced hydrogels are efficient and viable composited adsorbent in removing CV dye from aqueous solution
Outstanding supercapacitor performance of nd-mn co-doped perovskite lafeo3@nitrogen-doped graphene oxide nanocomposites
Perovskites have been significantly considered as promising materials for electrochemical energy storage in the recent years. Co-doping of Mn and Nd with hydrothermally synthesized LaFeO3 (LF) perovskite resulted in La0.8Nd0.2Fe0.8Mn0.2O3 (LNFM) with significantly higher specific capacitance of 158 F/g at 50 mV/s compared to non-doped and single doped LF samples. Subsequently, LNFM/nitrogen-doped graphene oxide (NGO) nanocomposite was prepared and investigated. It was found out that the introducing of NGO substantially enhances the specific capacitance of the nanocomposite up to 1060 F/g at 50 mV/s. Besides, the composite revealed outstanding capacity retention as 92.4% after 10000 continuous cycle (85.37% for the LNFM sample). In overall, the electrochemical behavior of the composite with 1:1 ratio of LNFM/NGO confirms its high potential as supercapacitor for energy storage applications
Numerical solution of differential equations arising in fluid dynamics using Legendre wavelet collocation method
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