Preparation of Cu (II)/PEI–QPEI/SiO2 nanopowder as antibacterial material

The silica nanoparticles were prepared by the sol–gel process, and then twice modified and grafted by polyethylenimine (PEI) on their surface. After quaternary ammonium reaction and chelated copper reaction, the PEI/SiO₂, QPEI/SiO₂, PEI–QPEI/SiO₂ and Cu (II)/PEI–QPEI/SiO₂ nanopowders were obtained in turn. The morphology and structure of the products were characterized through SEM, EDX, HRTEM, FTIR and element analysis. At the same time, the antibacterial activity of the products to E. coli and Candida were evaluated through quantification and qualitative ways, e.g. microcalorimetric method and culture dish method. The results suggested that the Cu (II)/PEI–QPEI/SiO₂, a novel three-component functional nanopowder, presented the best antibacterial activity to both E. coli and Candida duo to the synergistic sterilization capability of the ammonium salt and copper ions, compared with other products. It indicated that the Cu (II)/PEI–QPEI/SiO₂ nanopowder could be a novel antibacterial nanomaterial to widely application in preventing and minimizing bacteria of the organism and environment in future.     

Melt crystallization of CuFe2S3 in the Cu–Fe–S system

The possibility of melt crystallization of the compound with CuFe₂S₃ composition was established by carrying out quasiequilibrium directional crystallization. The initial liquid had the following composition: Fe 33.3, Cu 16.7, and S 50.0 at.%. The produced sample consisted of three zones with different chemical compositions. The volume fraction of the first zone was 6 %, the second zone was 77 % and the third zone was 17 %. The composition of the first zone corresponded to pyrrhotite solid solution (poss). The second zone had the constant composition CuFe₂S₃. The third zone had variable composition. In the article this zone is not described. We constructed the curves describing the variations in the composition of solid ingot and melt during poss and CuFe₂S₃ crystallization, calculated the distribution coefficients of components, and determined the equation of phase reaction while transferring from the first to the second zone. A polythermal cross-section of phase diagram of the Cu–Fe–S system was built using the directional crystallization and thermal analysis of specially synthesized samples along the crystallization path. It is shown that stoichiometric CuFe₂S₃ compound crystallized from melt and the cross-section of phase diagram along the crystallization path is quasibinary. Thus, liquidus surface of the Fe–Cu–S system contains the region of primary crystallization of CuFe₂S₃, which is located between the crystallization fields of poss and intermediate solid solution.     

Z-scheme CuFe2O4–TiO2 nanocomposite microspheres for the photodegradation of methylene blue

Research on Chemical Intermediates - The design and synthesis of effective photocatalysts for photodegradation of persistent organic pollutants is of significant importance. Novel CuFe2O4...     

Sol–gel synthesis of Mn2O3/Al2O3/SiO2 hybrid nanocomposite and application for removal of organic dye

Journal of Sol-Gel Science and Technology - Nanocomposite of Mn2O3/Al2O3/SiO2 was prepared through an in situ sol–gel process, in which Mn2O3 nanocrystals were dispersed in the silica-alumina...     

On synthesis of Fe2SiO4/SiO2 and Fe2O3/SiO2 composites through sol–gel and solid-state reactions

Major processing factors in forming Fe₂SiO₄/SiO₂ and Fe₂O₃/SiO₂ powders via sol–gel synthesis followed by solid-state reactions are investigated. The results clearly indicate that the chemical compositions of the precursors, the ratio of the precursors, the nature of the catalyst used, and the gas atmosphere during solid-state reactions can all affect the outcome of the reaction product(s). The formation of Fe₂SiO₄/SiO₂ is enhanced by using the precursor iron(III) acetylacetonate as the Fe source with the precursor ratio of iron(III) acetylacetonate to tetraethyl orthosilicate being 1:1 and the addition of formic acid. Otherwise, crystalline Fe and Fe₃C are formed in place of Fe₂SiO₄. By altering the gas atmosphere during solid-state reactions from argon to oxygen, the reaction products change from Fe₂SiO₄/SiO₂ to Fe₂O₃/SiO₂. All of the observed phenomena can be rationalized via the degree of mixing of the Fe–O and Si–O domains at the molecular level in the gel network during sol–gel reactions and the presence of a reducing or oxidizing atmosphere during the solid-state reaction.     

Preparation of graphene/BaFe12O19–Ni0.8Zn0.2Fe2O4 nanocomposite and its microwave absorbing properties

BaFe₁₂O₁₉–Ni_0.8Zn_0.2Fe₂O₄/graphene nanocomposites were prepared by a deoxidation technique. The structure, morphology and electromagnetic properties of the samples were detected by means of X-ray diffraction, scanning electron microscope, transmission electron microscopy, Raman, thermogravimetric analysis. Results show that the BaFe₁₂O₁₉–Ni_0.8Zn_0.2Fe₂O₄ nanoparticles dispersed on the graphene sheets. The magnetic properties of the composites decreased with the increasing of graphene contents, However, the electrical conductivity is in the contrary. Measurement of electromagnetic parameters shows that when the mass ratio of BaFe₁₂O₁₉–Ni_0.8Zn_0.2Fe₂O₄ to graphene is 5:1, it can be matched well. The microwave absorption property of it is below ?10 dB at 6.8–8.2 GHz and the minimum loss value is ?19.63 dB at 7.2 GHz. The introduction of graphene can increase the dielectric loss and has an important effect on the microwave absorption properties.     

Synthesis of carboxymethyl β-cyclodextrin bonded Fe3O4@SiO2–NH2 core-shell magnetic nanocomposite adsorbent for effective removal of Pb(II) from wastewater

Journal of Sol-Gel Science and Technology - In this work, a novel functionalized magnetic Fe3O4@SiO2 core-shell nanoparticles grafted with carboxymethyl β-cyclodextrin (CM-β-CD) is...     

Thermal stability of ZrO2–SiO2 aerogel modified by Fe(III) ion

ZrO₂–SiO₂ aerogel modified by Fe(III) ion was prepared and the stability of the samples under high temperature was investigated. The structure and properties of modified aerogels were characterized by N₂ adsorption–desorption, FT-IR, XRD and TEM. The samples still contain a specific surface area about 228 m²/g after 1,000 °C 0.5 h calcinations. The inhibition of ZrO₂ particle growth is attributed to the Fe(III) ion modified aerogel surface, which strongly retards the ZrO₂ tetragonal phase transformation as well.     

A structural and Mössbauer study of complexes with Fe(2)(micro-O(H))(2) cores: stepwise oxidation from Fe(II)(micro-OH)(2)Fe(II) through Fe(II)(micro-OH)(2)Fe(III) to Fe(III)(micro-O)(micro-OH)Fe(III)

Dinuclear non-heme iron clusters containing oxo, hydroxo, or carboxylato bridges are found in a number of enzymes involved in O(2) metabolism such as methane monooxygenase, ribonucleotide reductase, and fatty acid desaturases. Efforts to model structural and/or functional features of the protein-bound clusters have prompted the preparation and study of complexes that contain Fe(micro-O(H))(2)Fe cores. Here we report the structures and spectroscopic properties of a family of diiron complexes with the same tetradentate N4 ligand in one ligand topology, namely [(alpha-BPMCN)(2)Fe(II)(2)(micro-OH)(2)](CF(3)SO(3))(2) (1), [(alpha-BPMCN)(2)Fe(II)Fe(III)(micro-OH)(2)](CF(3)SO(3))(3) (2), and [(alpha-BPMCN)(2)Fe(III)(2)(micro-O)(micro-OH)](CF(3)SO(3))(3) (3) (BPMCN = N,N'-dimethyl-N,N'-bis(2-pyridylmethyl)-trans-1,2-diaminocyclohexane). Stepwise one-electron oxidations of 1 to 2 and then to 3 demonstrate the versatility of the Fe(micro-O(H))(2)Fe diamond core to support a number of oxidation states with little structural rearrangement. Insight into the electronic structure of 1, 2', and 3 has been obtained from a detailed M?ssbauer investigation (2' differs from 2 in having a different complement of counterions). Mixed-valence complex 2' is ferromagnetically coupled, with J = -15 +/- 5 cm(-)(1) (H = JS(1).S(2)). For the S = (9)/(2) ground multiplet we have determined the zero-field splitting parameter, D(9/2) = -1.5 +/- 0.1 cm(-)(1), and the hyperfine parameters of the ferric and ferrous sites. For T < 12 K, the S = (9)/(2) multiplet has uncommon relaxation behavior. Thus, M(S) = -(9)/(2) <--> M(S) = +(9)/(2) ground state transition is slow while deltaM(S) = +/-1 transitions between equally signed M(S) levels are fast on the time scale of M?ssbauer spectroscopy. Below 100 K, complex 2' is trapped in the Fe(1)(III)Fe(2)(II) ground state; above this temperature, it exhibits thermally assisted electron hopping into the state Fe(1)(II)Fe(2)(III). The temperature dependence of the isomer shifts was corrected for second-order Doppler shift, obtained from the study of diferrous 1. The resultant true shifts were analyzed in a two-state hopping model. The diferric complex 3 is antiferromagnetically coupled with J = 90 +/- 15 cm(-)(1), estimated from a variable-temperature M?ssbauer analysis.     

Development of polybenzoxazine–silica–titania (PBZ–SiO2–TiO2) hybrid nanomaterials with high surface free energy

In the present work, silica and titania reinforced polybenzoxazine (PBZ–SiO₂–TiO₂) hybrid nanomaterial possessing high surface free energy have been developed using dimethylol-functional benzoxazine monomer (4HBA-BZ), tetraethoxysilane (TEOS), 3-(isocyanatopropyl)triethoxysilane (ICPTS), titaniumisopropoxide (TIPO) through an in situ sol–gel process. Data obtained from the contact angle measurement indicate that the hybrid materials are hydrophilic in nature and possess a high surface free energy. For example, hybrid PBZ obtained from 1:1:0.6:0.4 (m:m:w:w) ratio of 4HBA-BZ:ICPTS:TEOS:TIPO (PBST₄) exhibit a high surface free energy of 38.2 mJm^?2 which is higher than that of neat polybenzoxazine (29.5 mJm^?2). Further data resulted from thermal studies indicate that the hybrid PBZ possess higher values of T_g, thermal stability and char yield than those of neat PBZ.     

Magnetohydrodynamic flow of Cu–Fe3O4/H2O hybrid nanofluid with effect of viscous dissipation: dual similarity solutions

Journal of Thermal Analysis and Calorimetry - This study shows multiple solutions, heat transfer characteristics, and stability analysis of the magnetohydrodynamic (MHD) flow of hybrid nanofluid...     

Preparation of CdS–TiO2/Fe3O4 photocatalyst and its photocatalytic properties

The CdS modified TiO₂/Fe₃O₄ photocatalysts were prepared by sol–gel and immersion methods. The morphological, structural and optical properties of as-prepared samples were characterized by X-ray diffraction (XRD), UV–Vis absorption spectra, X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). The TEM observation showed that the surface of magnetite particles (Fe₃O₄) were coated by CdS–TiO₂ layer as loose clusters, and average diameter of composites particles was about 250 nm. UV–Vis absorption spectra indicated that CdS–TiO₂/Fe₃O₄ composites had pronounced red-shift compared with that of TiO₂/Fe₃O₄. The CdS–TiO₂/Fe₃O₄ composites exhibit higher photocatalytic activity than pure TiO₂ and TiO₂/Fe₃O₄ for the degradation of Reactive Brilliant Red X-3B dye (X-3B) aqueous solution under simulated sunlight, and the optimum content of CdS is 1.0 % (mol ratio of CdS to TiO₂). In addition, a gradual loss of photocatalytic activity can be observed in reusability test of CdS–TiO₂/Fe₃O₄ composites, and degradation of X-3B reached still to 78.9 % after five runs.     

Synthesis,crystal structure,thermal decomposition,and XPS studies of homo and heterotrinuclear Cu(II)–Cu(II)–Cu(II) and Cu(II)–Ni(II)–Cu(II) complexes obtained from salpn type ligands

In this study, a mononuclear CuL complex was prepared by the use of bis-N,N′-(salicylidene)-1, 3-propanediamine (LH₂) and Cu²⁺ ion. NiCl₂ and NiBr₂ salt were treated with this complex in dioxanewater medium and two new complexes [(CuL)₂NiCl₂(H₂O)₂] and [(CuL)₂NiBr₂(H₂O)₂)] with Cu(II)–Ni(II)–Cu(II) nucleus structure were obtained. In addition to this bis-N,N′-(2-hydroxybenzyl)-1,3-diaminopropane (L^HH₂) was prepared by the reduction of LH₂ with NaBH₄ in MeOH medium. The treatment of this reduced complex with Cu²⁺ ion resulted a complex [(CuL^H)₂CuCl₂] with a structure of Cu(II)–Cu(II)–Cu(II). The complexes prepared were characterized by the use of elemental analysis, IR spectroscopy, thermogravimetric and X-ray diffraction methods. The crystal structures of [(CuL)₂NiBr₂(H₂O)₂] (СIF file CCDC 1448402) and [(CuL^H)₂CuCl₂] (СIF file CCDC 1448401) complexes were elucidated. It was found that halogen ions are coordinated to terminal Cu²⁺ ions which are in a distorted square pyramid coordination sphere. It was determined that the central Cu(II), which joins terminal square pyramidal Cu(II), was coordinated only by the phenolic oxygens of the ligand while the central Ni(II) was coordinated by two phenolic oxygens of the organic ligand and two water molecules. These complexes were investigated by XPS and it was found that the terminal and central Cu²⁺ ions were different in Cu(II)–Cu(II)–Cu(II) complex. Also, the thermal degradation of the CuLH complex unit was observed to exothermic in contrast to the expectations.

     

Preparation and characterization of SO4 2−/Fe2O3–TiO2–Nd2O3 catalyst

This paper reports on the preparation of SO₄ ^2?/Fe₂O₃–TiO₂–Nd₂O₃ (SFTN) by combustion method. The effect of Nd content on catalytic activity was investigated. The prepared materials doped and undoped by Nd were compared by means of TG-DTG, XRD, FT-IR, NH₃-TPD and TEM techniques. Results indicated that the introduction of Nd improved the catalytic activities of the catalysts. Catalytic activity of SFTN was the highest with 98.3 % menthol conversion when Nd content was at 2 wt%. The introduction of Nd stabilized the coordination bond between the sulfate irons and the metallic oxides, helping in the formation of solid acid sites, enhancing the dispersion of catalyst particles, and inhibiting the growth of catalyst particles under heating.     

Fe(II)LSCo(III)LS]2 ⇔ [Fe(III)LSCo(II)HS]2 photoinduced conversion in a cyanide-bridged heterobimetallic molecular square

The self-assembly of [Fe(III){B(pz)(4)}(CN)(3)](-) and [Co(II)(bik)(2)(S)(2)](2+) affords the diamagnetic cyanide-bridged [Fe(II)(LS)Co(III)(LS)](2) molecular square which is converted into the corresponding magnetic [Fe(III)(LS)Co(II)(HS)](2) species under light irradiation at relatively low temperatures.     

Preparation and Characterization of Reduced Graphene Oxide–Fe3O4 Nanocomposites in Polyacrylamide

Russian Journal of Physical Chemistry A - A hydrogel nanocomposite composed of reduced graphene oxide (RGO), iron oxide (Fe3O4) nanoparticles, and polyacrylamide (PAM) was prepared using radical...     

Magnetic and spectral properties of Fe(II), Fe(III), Co(II), Ni(II), Cu(II) and Pd(II) chelates of 2′-hydroxy-3′-bromo-4-methoxy-5′-methylchalkone oxime (HBMMCO)

A number of chelates of the transition metal ions Fe²⁺, Fe³⁺, Co²⁺, Ni²⁺, Cu²⁺ and Pd²⁺ with 2′-hydroxy - 3′ - bromo - 4 - methoxy - 5′ - methylchalkone oxime (HBMMCO) have been synthesised. Attempts have been made to assign their probable structures on the basis of elemental analysis, molar conductance, thermal analysis, absorption and reflectance spectra, IR spectra and magnetic data. The magnetic susceptibility of the Co(II) chelate follows the Curie-Weiss law and the observed temperature dependance is in favour of an octahedral configuration. The Ni(II) chelate exhibits a 6-coordinate octahedral structure, whilst distorted octahedral geometry is suggested for the Cu(II) chelate. The Fe(II) and Fe(III) chelates have high spin octahedral configurations and the dimagnetic behaviour of the Pd(II) complex indicates a square planer configuration.     

Preparation,structure and magnetic study of a new linear 1-D Cu(II)–Gd(III) coordination polymer

A carboxylate-bridged Cu(II)–Gd(III) complex, [GdCu(CH₂CH(CH₃COO)₄(H₂O)₄] _n (NO₃) _n , was prepared and characterized. Single crystal X-ray analysis reveals the complex as a carboxylate-bridged 1-D Cu(II)–Gd(III) coordination polymer. The magnetic measurement showed this complex exhibiting weak ferromagnetic behavior.