Photodegradation of Dyes From Cual Batik Waste Using TiO2 Photocatalyst From Ilmenite Bangka

Cual batik is one of the local products of the Bangka Belitung Islands. The expansion of cual batik in Bangka Belitung continues to increase, resulting in an increase in the production of cual batik cloth. Cual batik contains remasol dyes which are carcinogenic so that waste handling is appropriate and safe for the surrounding environment. One of them is using the TiO2 photocatalytic method from ilmenite Bangka. The results of XRF characterization showed that the TiO2 content after magnetic separator and HCl washing reached 69,975% and 77,260%. The results of XRD characterization showed that the optimal temperature of calcination was at 700ºC with the peak diffraction intensity of anatase TiO2 crystals at 2θ 48.9º, 53.53º and 53.92º. In FTIR characterization, there is a functional group spectrum of titanium dioxide (TiO2) at the absorption wave number 795 cm-1 showing Ti-O-Ti stretching vibrations, at wavenumber 2326 cm-1 showing Ti-O stretching vibrations. The results of photodegradation of cual batik waste showed a decrease in the dye content of remazol briliant blue when exposed to UV lamps and sunlight at contact times of 30, 60, and 90 minutes 85.21%, 82,75%, and 86,72% (UV light); 70,75%, 78,92%, and 93.51% (sunlight).

Collinearity of alpha-helices or beta strands in membrane proteins causes a characteristic peak centred on 4.9 Å resolution in diffraction intensity profiles, inducing higher diffraction anisotropy

Diffraction anisotropy is a phenomenon that impacts more specifically membrane proteins, compared to soluble ones, but the reasons for this discrepancy remained unclear. Often, it is referred to a difference in resolution limits between highest and lowest diffraction limits as a signature for anisotropy. We show in this article that there is no simple correlation between anisotropy and difference in resolution limits, with notably a substantial number of structures displaying various anisotropy with no difference in resolution limits. We further investigated diffraction intensity profiles, and observed a peak centred on 4.9Å resolution more predominant in membrane proteins. Since this peak is in the region corresponding to secondary structures, we investigated the influence of secondary structure ratio. We showed that secondary structure content has little influence on this profile, while secondary structure collinearity in membrane proteins correlate with a stronger peak. Finally, we could further show that the presence of this peak is linked to higher diffraction anisotropy.SynopsisMembrane protein diffraction anisotropy originates from a peak at 4.9 Å resolution in intensity profiles, due to secondary structure collinearity.

Facile Molecular Weight Determination of Polymer Brushes Grafted from One-Dimensional Diffraction Grating by SI-ATRP Using Reflective Laser System

Gelatin was immobilized selectively on the amide groups-modified bottom of a trench array of a photoresist template with 2 μm resolution by the ethyl(dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide reaction. The gelatin-immobilized line array was brominated to generate a macroinitiator for atom transfer radical polymerization. Poly(methacrylic acid) (PMAA) brushes were grafted from the macroinitiator layer as line arrays of one-dimensional diffraction gratings (DGs) for various grafting polymerization times. A laser beam system was employed to analyze the optical feature with a characteristic diffraction effect of the PMAA DGs at a 45° incident angle along the transverse magnetic and transverse electric polarization. The growth of the PMAA brush lines increased both their heights and widths, leading to a change in the reflective diffraction intensity. The PMAA brushes under various grafting polymerization times were cleaved from the substrate by digestion of gelatin with trypsin, and their molecular weights were obtained by gel permeation chromatography. The change degree of the diffraction intensity varied linearly with the molecular weight of the PMAA brushes over a wide range, from 135 to 1475 kDa, with high correlation coefficients. Molecular weight determination of polymer brushes using the reflective diffraction intensity provides a simple method to monitor their growth in real time without polymer brush cleavage.

Sodium rare earth metal amides Na3 RE(NH2)6 (RE = La–Nd, Er, Yb) from ammonothermal synthesis

The amides Na3 RE(NH2)6 have been obtained from the metals in supercritical ammonia under ammonobasic conditions at 573 K and 70 MPa for RE = La–Nd, and at 473 K and 40 MPa for RE = Er, Yb. All compounds are formed in the hot zone within a temperature gradient, indicating a retrograde solubility under the applied process conditions. These amides represent soluble intermediates in ammonothermal binary rare earth metal nitride synthesis. All compounds were obtained as microcrystalline powders, while single crystals of those amides containing the heavier rare earth metals could be isolated. The crystal structures were solved and refined from single-crystal and powder X-ray diffraction intensity data. The results of vibrational spectroscopy are reported. Thermal analysis measurements under inert gas atmosphere demonstrated a decomposition to the respective black binary rare earth metal nitrides REN1−δ .

One-Dimensional Diffraction Grating of Poly(Methacrylic Acid) Brushes For The Rapid Label-Free Detection of Yersinia Pestis With a Reflective Laser System

Background: Because of the low sensitivity of commercial products, development of a facile method to rapidly identify plague on-site remains highly attractive. Line arrays of poly(methacrylic acid) (PMAA) brushes were grafted using a photoresist template to fabricate one-dimensional diffraction gratings (DGs). The as-prepared samples first bound protein G to immobilize and orient the tails of the antibody of Yersinia pestis (abY). A laser beam was employed to analyze the 2D and 3D reflective signals of DGs at an incident angle of 45°. The abY-tailed PMAA DG possessed an optical feature with a characteristic diffraction effect along the SII, in which the projection of the laser beam on the plane of the DG chip was parallel to the strips, and ST configurations, in which they were perpendicular. A fluidic diffraction chip based on the abY-tailed PMMA DG was fabricated to examine the ability to detect Yersinia pestis along the ST configuration. Results: Upon flowing through the chip, Yersinia pestis was attached to the abY-tailed PMMA DG, which changed the diffraction intensity. The degree of the diffraction intensity exhibited a linear response to Yersinia pestis at concentrations from 102 to 107 CFU mL−1, and the limit of detection was 75 CFU mL−1, 1000 times lower than a commercial product (Alexter Bio-Detect Test). The diffractive sensor could selectively detect Yersinia pestis in spiked serum samples, with excellent standard deviation and recovery. Conclusion: Our platform provides a simple, label-free method for on-site plague diagnosis to prevent the highly rapid transmission of plague.

Indium Ammoniates from Ammonothermal Synthesis: InAlF6(NH3)2, [In(NH3)6][AlF6], and [In2F(NH3)10]2[SiF6]5 ∙ 2 NH3

The ammonothermal synthesis of three ammoniates of indium, namely InAlF6(NH3)2, [In(NH3)6][AlF6], and [In2F(NH3)10]2[SiF6]5 ∙ 2 NH3 was successful from near-ammononeutral conditions in the presence of fluoride ions. Initially, all these compounds were obtained upon corrosion of the applied liner and crucible material Si3N4, which also contains small amounts of aluminum. The syntheses were performed in supercritical ammonia (T = 753 K, p up to 307 MPa). The crystal structures were solved and refined from single crystal X-ray diffraction intensity data. InAlF6(NH3)2 crystallizes as a typical layer-type structure with corner-sharing [InF4(NH3)2]– and [AlF6]3− octahedra. [In(NH3)6][AlF6] features isolated [In(NH3)6]3+ and [AlF6]3− octahedra. The crystal structure of [In2F(NH3)10]2[SiF6]5 ∙ 2 NH3 contains [(NH3)5In–F–In(NH3)5]5+ octahedra doubles next to [SiF6]2− octahedra and ammonia molecules. All intermediates have strong hydrogen bonding systems. The results from vibrational spectroscopy are reported.

Turning parameter optimization for diffraction effect suppression of diamond-turned surface combining surface micro-topography model and scattering theory

The diamond-turning process is a mean optical surface generation technique with high figure accuracy and surface finish. The diamond-turned surface has a significant diffraction effect introduced by the tool marks remaining on the surface, which heavily degrade the optical performance in the visible wavelength spectrum. The traditional approach that was used to eliminate this effect was polishing. In this paper, we present a method to find turning parameters that can generate an optical surface without diffraction effect directly by coupling a surface micro-topography model of a turned surface via the scattering theory The surface micro-topography model of the turned surface reveals the relationship between tool marks and the diamond-turning parameters (DTPs). The scattering theory reveals the relationship between diffraction intensity distributions (DIDs) and surface micro-topography of the turned surface. Therefore, we obtained the relationship between DIDs and DTPs. The diffraction effect is considered to be eliminated when the first-order diffraction intensity is less than 0.01% of incidence intensity. The criterion of turning parameters for diffraction elimination is then obtained. Finally, turning experiments are performed to confirm the effectiveness of this method, and the diffraction-free surface finish is achieved.