Room-Temperature In-Situ Design and Use of Graphene Oxide-SBA-16 Composite for Water Remediation and Reusable Heterogeneous Catalysis

2017 ◽  
Vol 2 (5) ◽  
pp. 1835-1842 ◽  
Author(s):  
Haribandhu Chaudhuri ◽  
Subhajit Dash ◽  
Radha Gupta ◽  
Devendra Deo Pathak ◽  
Ashis Sarkar
Keyword(s):  
Graphene Oxide ◽  
Heterogeneous Catalysis ◽  
Room Temperature ◽  
Water Remediation

Facile Synthesis of Cu/Cu2O Nanoparticles–Graphene Composites for Efficient Detection of NO2 at Room Temperature

NANO ◽  
2016 ◽  
Vol 11 (09) ◽  
pp. 1650102 ◽  
Author(s):  
Xin Liu ◽  
Jianbo Sun
Keyword(s):  
Graphene Oxide ◽  
Reduced Graphene Oxide ◽  
Room Temperature ◽  
Fast Response ◽  
Efficient Detection ◽  
Reduced Graphene ◽  
Cu2o Nanoparticles ◽  
Oxide Composites ◽  
Facile Solvothermal Method

Cu/Cu2O nanoparticles-reduced graphene oxide composites (CuGCs) have been successfully prepared by a facile solvothermal method. The combined characterizations indicate the successful formation of CuGCs. The [Formula: see text] 3 nm Cu/Cu2O nanoparticles homogeneously in situ grow on reduced graphene oxide sheets. CuGCs-based gas sensors were investigated for detection of NO2 at room temperature. The CuGCs exhibited fast response behavior, relatively high response and could achieve a detection limit as low as 5[Formula: see text]ppm. Furthermore, sensing mechanism and the reason for enhancing sensing performance have also been discussed.

Enhanced NO2 sensing performance of reduced graphene oxide by in situ anchoring carbon dots

2017 ◽  
Vol 5 (27) ◽  
pp. 6862-6871 ◽  
Author(s):  
Jing Hu ◽  
Cheng Zou ◽  
Yanjie Su ◽  
Ming Li ◽  
Nantao Hu ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Reduced Graphene Oxide ◽  
Gas Sensor ◽  
Carbon Dots ◽  
Room Temperature ◽  
Low Cost ◽  
High Sensitivity ◽  
Reduced Graphene ◽  
Sensing Performance

A room-temperature NO2 gas sensor of high sensitivity, selectivity and stability based on a low-cost, all-carbon nanoscale heterostructure and eco-friendly 2D rGO–CD hybrids.

Otoconia perfect/imperfect crystals

1994 ◽  
Vol 52 ◽  
pp. 42-43
Author(s):  
César D. Fermin ◽  
Dale Martin
Keyword(s):  
Image Processing ◽  
Room Temperature ◽  
Phosphotungstic Acid ◽  
Gallus Domesticus ◽  
Crystal Matrix ◽  
Organic Templates ◽  
Image Processing Algorithms ◽  
Processing Algorithms ◽  
Diffraction Patterns

Otoconia of higher vertebrates are interesting biological crystals that display the diffraction patterns of perfect crystals (e.g., calcite for birds and mammal) when intact, but fail to produce a regular crystallographic pattern when fixed. Image processing of the fixed crystal matrix, which resembles the organic templates of teeth and bone, failed to clarify a paradox of biomineralization described by Mann. Recently, we suggested that inner ear otoconia crystals contain growth plates that run in different directions, and that the arrangement of the plates may contribute to the turning angles seen at the hexagonal faces of the crystals.Using image processing algorithms described earlier, and Fourier Transform function (2FFT) of BioScan Optimas®, we evaluated the patterns in the packing of the otoconia fibrils of newly hatched chicks (Gallus domesticus) inner ears. Animals were fixed in situ by perfusion of 1% phosphotungstic acid (PTA) at room temperature through the left ventricle, after intraperitoneal Nembutal (35mg/Kg) deep anesthesia. Negatives were made with a Hitachi H-7100 TEM at 50K-400K magnifications. The negatives were then placed on a light box, where images were filtered and transferred to a 35 mm camera as described.

In Situ Localization of PPAR Gamma and Uncoupling Protein in Mouse Embryo Sections Using Digoxigenin-Labeled Riboprobes

1996 ◽  
Vol 54 ◽  
pp. 32-33
Author(s):  
C. Jennermann ◽  
S. A. Kliewer ◽  
D. C. Morris
Keyword(s):  
Alkaline Phosphatase ◽  
Room Temperature ◽  
Uncoupling Protein ◽  
Ppar Gamma ◽  
Nuclear Hormone Receptor ◽  
Full Length ◽  
Northern Analysis ◽  
Peroxisome Proliferator

Peroxisome proliferator-activated receptor gamma (PPARg) is a member of the nuclear hormone receptor superfamily and has been shown in vitro to regulate genes involved in lipid metabolism and adipocyte differentiation. By Northern analysis, we and other researchers have shown that expression of this receptor predominates in adipose tissue in adult mice, and appears first in whole-embryo mRNA at 13.5 days postconception. In situ hybridization was used to find out in which developing tissues PPARg is specifically expressed.Digoxigenin-labeled riboprobes were generated using the Genius™ 4 RNA Labeling Kit from Boehringer Mannheim. Full length PPAR gamma, obtained by PCR from mouse liver cDNA, was inserted into pBluescript SK and used as template for the transcription reaction. Probes of average size 200 base pairs were made by partial alkaline hydrolysis of the full length transcripts. The in situ hybridization assays were performed as described previously with some modifications. Frozen sections (10 μm thick) of day 18 mouse embryos were cut, fixed with 4% paraformaldehyde and acetylated with 0.25% acetic anhydride in 1.0M triethanolamine buffer. The sections were incubated for 2 hours at room temperature in pre-hybridization buffer, and were then hybridized with a probe concentration of 200μg per ml at 70° C, overnight in a humidified chamber. Following stringent washes in SSC buffers, the immunological detection steps were performed at room temperature. The alkaline phosphatase labeled, anti-digoxigenin antibody and detection buffers were purchased from Boehringer Mannheim. The sections were treated with a blocking buffer for one hour and incubated with antibody solution at a 1:5000 dilution for 2 hours, both at room temperature. Colored precipitate was formed by exposure to the alkaline phosphatase substrate nitrobluetetrazoliumchloride/ bromo-chloroindlylphosphate.

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