The largest database of trusted experimental protocols

4 protocols using uv 550 spectrophotometer

1

Characterization of Nanoscale Metal Oxides

Check if the same lab product or an alternative is used in the 5 most similar protocols
Experimental band gaps of MONs were obtained by collection from literature3,19–50 (link) and by experimental determination.
To control variables that influence band gaps of MONs as much as possible and to ensure the consistency of collected band gaps, a qualified data point from literature must meet the following demands: size of material is in the nanometer scale; particles must be spherical or approximate a spherical shape; particles have a single chemical makeup without any chemical modification on the surface; characterizations including X-ray diffraction, which verifies the crystalline structure of MONs, and UV-vis spectroscopic analysis are required.
Seven kinds of MONs (5 nm anatase-TiO2, 25 nm anatase-TiO2, 40 nm anatase-TiO2, 100 nm anatase-TiO2, 40 nm rutile-TiO2, 100 nm rutile-TiO2 and 50 nm ZnO) bought from Aladdin (http://www.aladdin-e.com/) were prepared for UV-vis spectroscopic analysis using UV-550 spectrophotometer produced by JASCO Corporation. To minimize possible errors, each determination for each material was repeated three times and the eventual outcome is the arithmetic mean of parallel experiments. The raw data of UV-vis spectroscopic analysis were transformed according to the Kubelka–Munk equation.51 The total data set of band gaps of MONs was split randomly into a training set and a validation set with a ratio of 3 : 1 (30 : 10).
+ Open protocol
+ Expand
2

Spectroscopy and Microscopy Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
A JASCO UV-550 spectrophotometer was used
for the measurements of UV–vis spectra. 1H NMR spectra
(1H-400 MHz) were recorded on a Bruker DPX 400 spectrometer.
Elemental analyses were carried out with an Elementary Vario El. IR
spectra were recorded using a Bruker Tensor 37 spectrometer. The TEM
measurements were achieved by using a JEOL TEM-2010 electron microscope
(Japan) equipped with a charge-coupled device camera, operated at
200 kV. SEM images were obtained using a JEOL JEM-6510A scanning electron
microscope at 10 kV. The AFM images were recorded from a Bruker Multimode
8 system with a silicon cantilever by using tapping mode. XRD was
measured on a Rigaku TTRIII X-ray diffractometer (Japan) with Cu Kα
radiation (λ = 1.54 Å), which was operated at 45 kV, 100
mA. F-4500 FL spectrophotometer and JASCO J-815 CD spectropolarimeter
were used for fluorescence spectral measurements and CD spectral measurements,
respectively. For photodegradation measurements, a 500 W xenon arc
lamp (CEL-LAX-500 W, Beijing Aulighttech Co. Ltd, China) served as
the light source. In addition, the photodegradation experiment was
performed on a photocatalytic reactor which came from Beijing Aulighttech
Co. Ltd, China.
+ Open protocol
+ Expand
3

Spectroscopic Analysis of Natural Compounds

Check if the same lab product or an alternative is used in the 5 most similar protocols
Optical rotations were measured on a JASCO DIP-1000 polarimeter. UV spectra were recorded on a JASCO UV-550 spectrophotometer. ECD spectra were obtained on a JASCO J-715 spectrometer, and IR spectra were measured on a JASCO FT-IR 4100 spectrometer (JASCO, Tokyo, Japan). NMR spectra were recorded on a Bruker AVANCE 700 MHz spectrometer (Bruker, MA, USA) using DMSO-d6 as solvent. ESI–MS and HRESI–TOF–MS were obtained with LCQ Fleet (Thermo Fisher Scientific, San Jose, CA, USA) and maXis 4G mass spectrometers (Bruker, Bremen, Germany), respectively. Column chromatography was performed on silica gel (70–230 mesh, Merck, Darmstadt, Germany) and Lichroprep RP-18 (40–63 μm, Merck, Darmstadt, Germany). MPLC was performed on a Biotage Isolera Prime chromatography system (Biotage, Uppsala, Sweden). Preparative HPLC was performed using Waters HPLC system equipped with two Waters 515 pumps with a 2996 photodiode-array detector (Waters Corporation, Milford, MA, USA) using an YMC J’sphere ODS-H80 column (4 μm, 150 × 20 mm, i.d., Kyoto, Japan, flow rate 6 mL/min). TLC was performed using precoated silica gel 60 F254 (0.25 mm, Merck, Darmstadt, Germany) plates, and spots were detected by a 10% vanillin-H2SO4 in water spray reagent.
+ Open protocol
+ Expand
4

Synthesis and Purification of GRAP Peptide

Check if the same lab product or an alternative is used in the 5 most similar protocols
The GRAP peptide of sequence LSKGQLEEFLEDNLAY was synthesized and partially purified by GenScript Corp (Piscataway, NJ). Purification was completed by HPLC (Rainin Dynamax, NY) using a reverse phase C18 semi-preparative column (Vydac) equilibrated in 0.05% aqueous TFA. Fractions containing > 98.0% pure peptide were pooled and lyophilized. The molecular mass of GRAP (MW theoretical value: 1869 Da) was checked after HPLC by MALDI-MS. As a control sample, we prepared TRXP peptide of sequence LSKGQLKEFLDANLAY (MW theoretical value: 1810 Da), corresponding to the amphipathic C-terminal α-helix of EcTRX. A C-terminal Tyr tag was added to each peptide sequence to allow concentration. Peptide concentration was calculated by measuring absorbance in the near-UV region using a JASCO UV-550 spectrophotometer. The extinction coefficient was ε 280nm = 1490 M -1 cm -1 for both peptides. Mass spectra were acquired with a 4800 MALDI TOF/TOF plus spectrometer. Iron concentration was determined using the method of 1,10-phenanthroline 52 .
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!