12 research outputs found
Development of Ambient Nanogibbsite Synthesis and Incorporation of the Method To Embed Ultrafine Nano-Al(OH)<sub>3</sub> into Channels and Partial Alumination of MCM-41
An
ultrafine aluminum hydroxide nanoparticle suspension was prepared
via the controlled titration of [AlĀ(H<sub>2</sub>O)<sub>6</sub>]<sup>3+</sup> with l-arginine to pH 4.6. The prepared material,
predominantly 10ā30 nm in diameter, was purified by GPC and
subsequently identified as the gibbsite (or hydrargillite) polymorph
via FTIR, powder XRD, and elemental analysis. The materialās
chemical environment and morphology were probed using <sup>27</sup>Al/<sup>1</sup>H NMR, FTIR, ICP-OES, TEM-EDS, XPS, XRD, and N<sub>2</sub> adsorption experiments. Furthermore, by incorporating the
newly developed synthetic route, AlĀ(OH)<sub>3</sub> was partially
loaded inside the mesopores (2.7 nm) of MCM-41. EDS and NMR analysis
indicated that both tetrahedral and octahedral Al (O<sub>h</sub>/T<sub>d</sub> = 1.4) are incorporated at 11% w/w total Al and that the
Si/Al ratio is 2.9, indicating that part of the Al is embedded in
the Si framework. In addition, differences in elemental composition
between surface XPS and bulk EDS analysis provided insight into the
distribution of Al within the material. A higher Si/Al ratio was observed
on the external surface (3.6) of MCM-41 compared to that of the internal
(2.9) cavities. Estimated O/Al ratios suggest predominantly AlĀ(O)<sub>3</sub> and AlĀ(O)<sub>4</sub> motifs present near the core and external
surface, respectively. This novel methodology produces Al-MCM-41 with
relatively high Al content while preserving the ordered SiO<sub>2</sub> framework and can be used in lateral applications where incorporating
hydrated or anhydrous Al<sub>2</sub>O<sub>3</sub> is desired
Concentration series for four <i>Gingko biloba</i> secondary metabolites.
<p>Concentration series for four <i>Gingko biloba</i> secondary metabolites.</p
Repellent rate of medicament with <i>Gingko biloba</i> secondary metabolites to <i>Hyphantria cunea</i> larvae.
<p>EGB: extract of ginkgo biloba; GF: gingko flavonoids; GL: ginkgolide; BB: bilobalide; CG: control group.</p
Classification of tree health based on the extent of pest feeding and the degree of damage to Ginkgo biloba.
<p>Classification of tree health based on the extent of pest feeding and the degree of damage to Ginkgo biloba.</p
Antifeedant rate of leaf discs soaked by treated with <i>Gingko biloba</i> secondary materials.
<p>EGB: extract of ginkgo biloba; GF: gingko flavonoids; GL: ginkgolide; BB: bilobalide.</p
Instars of <i>Hyphantria cunea</i> larvae infesting branches treated with <i>Ginkgo biloba</i> secondary metabolites.
<p>Instars of <i>Hyphantria cunea</i> larvae infesting branches treated with <i>Ginkgo biloba</i> secondary metabolites.</p
Analysis of artificial diet choice by <i>Hyphantria cunea</i> larvae using diets containing different types of <i>Gingko biloba</i> secondary materials.
<p>A: 4% extract of ginkgo biloba; B: 8% extract of ginkgo biloba; C: 16% extract of ginkgo biloba; D: 2% gingko flavonoids; E: 0.4% ginkgolide; F: 0.2% bilobalide.</p
Analysis of the enzyme activities of four detoxifying enzymes of <i>Hyphantria cunea</i> larvae fed artificial diets with <i>Gingko biloba</i> secondary metabolites.
<p>(A)The enzymatic activity of GSTs were measured in different feeding time. (B)The enzymatic activity of GSTs were measured in different larvae instar. (C)The enzymatic activity of CarE were measured in different feeding time. (D)The enzymatic activity of CarE were measured in different larvae instar. (E)The enzymatic activity of AChE were measured in different feeding time. (F)The enzymatic activity of AChE were measured in different larvae instar. (G)The enzymatic activity of MFO were measured in different feeding time. (H)The enzymatic activity of MFO were measured in different larvae instar. EGB: extract of ginkgo biloba; GF: gingko flavonoids; GL: ginkgolide; BB: bilobalide; CG: contral group. Different letters above bars indicate significant differences (P<0.05).</p
A Water-Soluble Cationic Zinc Lysine Precursor for Coating ZnO on Biomaterial Surfaces
A novel water-soluble
cationic zinc lysine coordination compound, [ZnĀ[(C<sub>6</sub>H<sub>14</sub>N<sub>2</sub>O<sub>2</sub>)]<sub>2</sub>Cl]ĀClĀ·2H<sub>2</sub>O (<b>1</b>), has been designed and synthesized and
its crystal structure determined. The aqueous solution of this coordination
compound is not only transparent and stable at room temperature but
it is also nearly neutral
(pH ā¼ 7). It is worth noting that zinc oxide (ZnO) forms in
situ upon dilution of a solution of the compound. The bioactivity
of ZnO has been confirmed using an Alarma Blue assay. These unique
properties allow the coordination compound to gently grow ZnO coating
with excellent antibacterial benefits onto biomaterial surfaces in
a facile and safe manner
Solid-State <sup>27</sup>Al NMR Spectroscopy of the Ī³āAl<sub>13</sub> Keggin Containing Al Coordinated by a Terminal Hydroxyl Ligand
We
report solid-state <sup>27</sup>Al NMR spectroscopic results for the
sulfate salt of the Ī³-Al<sub>13</sub> Keggin cluster, Ī³-[AlO<sub>4</sub>Al<sub>12</sub>(OH)<sub>25</sub>(OH<sub>2</sub>)<sub>11</sub>]Ā[SO<sub>4</sub>]<sub>3</sub>Ā·[H<sub>2</sub>O]<sub>14</sub>,
that provide a spectroscopic signature for partial hydrolysis of this
Keggin-type cluster. In <sup>27</sup>Al multiple-quantum magic-angle
spinning NMR spectra, all 13 Al positions of the cluster are at least
partially resolved and assigned with the aid of density functional
theory (DFT) calculations of the <sup>27</sup>Al electric field gradients.
The isotropic chemical shift of the single tetrahedral site, 75.7
ppm, is nearly identical to that reported for solutions from which
the cluster crystallizes. Reflecting broadly similar coordination
environments, the octahedral Al show mostly small variations in isotropic
chemical shift (+7 to +11 ppm) and quadrupolar coupling constant (<i>C</i><sub>Q</sub>; 6ā7.5 MHz), except for one resonance
that exhibits a much smaller <i>C</i><sub>Q</sub> and another
site with a larger value. DFT calculations show that deprotonation
of a terminal water ligand, to form an Ī·-OH group, causes a
large reduction in the <sup>27</sup>Al <i>C</i><sub>Q</sub>, allowing assignment of a distinct, narrow peak for octahedral Al
to this hydroxyl-terminated site. This result suggests a relationship
between octahedral <sup>27</sup>Al NMR line width and hydrolysis for
solids prepared from Keggin-type clusters