The largest database of trusted experimental protocols

Model uv 1900

Manufactured by Shimadzu
Sourced in Japan

The Shimadzu UV 1900 is a UV-Vis spectrophotometer designed for precise and efficient absorption measurements. It features a wavelength range of 190 to 1100 nm and can perform single-beam and double-beam analyses. The UV 1900 offers high-speed scanning and data acquisition capabilities to support a variety of analytical applications.

Automatically generated - may contain errors

6 protocols using model uv 1900

1

Physicochemical Properties of Deep Eutectic Solvents

Check if the same lab product or an alternative is used in the 5 most similar protocols
The physicochemical properties determined in this study were density, polarity, and viscosity. Density measurement was carried out by weighing a known volume of DES dispensed from a micropipette previously calibrated using purified water. The Nile Red dye was added to each DES as a solvatochromic probe to determine λmax, the wavelength at which the maximum visible light absorption occurred [30 (link)]. A UV-vis spectrophotometer (Model UV-1900, Shimadzu, Kyoto, Japan) was used to scan the DES-dye mixtures in the 400–700 nm range and Equation (1) was used to calculate the Nile Red polar parameter ENR (in kcal/mol). Viscosity test was performed using a Brookfield viscometer at room temperature with LV spindle no. 1 at 6, 12, and 30 rpm.

+ Open protocol
+ Expand
2

Determination of Total Phenolic Content

Check if the same lab product or an alternative is used in the 5 most similar protocols
Using the Folin–Ciocalteu method and gallic acid as the reference, the total phenolic content of the aqueous leaf extract was determined [26 ]. To 1 mL of extract, 1 mL of Folin–Ciocalteu reagent and 2 mL of Na2CO3 (20% w/v) were added, and then distilled water was used to make up a volume of 10 mL. This mixture was then allowed to stand for 8 min and was finally centrifuged at 6000 rpm for 10 min. At 730 nm, using the UV-vis double beam spectrophotometer (Model UV 1900 Shimadzu), the absorbance of the supernatant solution was measured against a blank. Similarly, the blank was prepared but instead of extract, it contained respective solvent.
+ Open protocol
+ Expand
3

Characterization of Biosynthesized Silver Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
The UV-Vis absorption spectrum of AgNPs in the wavelength range of 350–550 nm was recorded using a UV-Vis double beam spectrophotometer (Model UV 1900, Shimadzu, Kyoto, Japan). Deionised water was used as control. The hydrodynamic size distributions, zeta potential, and polydispersity index (PDI) of nanoparticles were determined by using Particle Size Analyzer (PSA Microtracnanotrac wave II, Anton Paar, Graz, Austria) instrument. The surface morphology of biosynthesized AgNPs was analyzed with the help of Field emission scanning electron microscopy (FESEM, JSM-7610FPlus, JEOL Ltd., Akishima, Japan) operating at an accelerating voltage of 0.1 to 30 kV equipped with an energy dispersive X-ray spectroscopy (EDX) detector for elemental mapping. On a JEM/2100 PLUS running at 200 kV, High resolution transmission electron microscopy (HRTEM) was successfully performed. A drop of the biosynthesized AgNPs dispersed in ethanol was placed at 400 mesh copper grid coated with a holey carbon film for the HRTEM investigations. The chemical composition of plant extract and AgNPs were studied by using FTIR spectrophotometer (Perkin Elmer, Waltham, MA, USA) and spectra was taken in the 4000–650 cm−1 region.
+ Open protocol
+ Expand
4

ABTS Radical Scavenging Activity Assay

Check if the same lab product or an alternative is used in the 5 most similar protocols
ABTS radical scavenging activity was determined by ABTS assay, as described by Sinthusamran et al. (Sinthusamran and Benjakul, 2018 ) with some modifications. Briefly, the stock solutions included a 7.0 mM ABTS solution and a 140 mM potassium persulfate solution. The working solution was prepared by mixing the two stock solutions (5 mL+88 μL) and allowing them to react for 12 h at room temperature in the dark, and then diluting with absolute ethanol to the absorbance at 734 nm of 0.70 ± 0.020. The sample (10 μL) was mixed with 0.2 mL of freshly prepared ABTS assay solution. Then the mixture was left at room temperature for 20min in the dark. The absorbance at 734 nm was read using a double beam spectrophotometer (Model UV-1900, Shimadzu, Kyoto, Japan). The blank was prepared in the same manner, except that distilled water was used instead of the sample. The ABTS radical scavenging activity was calculated as follows: scavenging effect (%) = (1- As/A0) x 100%, where As is the absorbance of the sample, and A0 is the absorbance of the blank control.
+ Open protocol
+ Expand
5

Characterization of Biosynthesized Silver Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
The UV-vis absorption spectrum of AgNPs was measured using a UV-vis double beam spectrophotometer (Model UV 1900, Shimadzu) in the wavelength range of 350–550 nm. The hydrodynamic size distributions, zeta potential, and polydispersity index (PDI) of nanoparticles were calculated using the PSA Microtracnanotrac wave II equipment. The surface morphology of biosynthesized AgNPs was investigated using field emission scanning electron microscopy (JSM-7610FPlus) working at an accelerating voltage of 0.1 to 30 kV. On a JEM/2100 PLUS running at 200 kV, high-resolution transmission electron microscopy (HRTEM) was successfully completed. A drop of the biosynthesized AgNPs dissolved in ethanol was applied on a copper grid with a 400 mesh and a holey carbon film covering for the HRTEM experiments. A Perkin Elmer FT-IR spectrophotometer was used to analyze the chemical composition of the leaf extract and AgNPs.
+ Open protocol
+ Expand
6

Flavonoid Content Determination

Check if the same lab product or an alternative is used in the 5 most similar protocols
Using an aluminum chloride colorimetric assay and catechin as a standard, the total flavonoid count was determined [27 ]. To 1 mL of extract, 4 mL of distilled water, 0.3 mL of 5% NaNO2, and, after 5 min, 0.3 mL of 10% AlCl3 solution were added and mixed properly. Immediately, 2 mL of 1 M NaOH was added and, using distilled water, the volume was made up to 10 mL. After mixing the solution thoroughly, at 510 nm, the absorbance of the solution was measured against a blank using a UV-vis double beam spectrophotometer (Model UV 1900 Shimadzu). Similarly, the blank was prepared, but instead of extract, it contained the respective solvent.
+ 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!