Dual Beam UV-VIS 2002 XE Spectrophotometer

Labindia Analytical Dual Beam UV-VIS 2002 XE Spectrophotometer with Xenon Lamp provides the best wavelength coverage across the working range of the spectrometer for consistently high performance. The high-energy Xenon flash lamp is active only when spectrum is being acquired and provides years of worry-free operation and low cost of ownership. The major benefit afforded by fluorescence detection is the inherent high sensitivity of the technique coupled with outstanding specificity. Labindia UV-VIS 2002XE is designed to meet high requirement for precision measurement in the research and production of organic chemistry, biochemistry, medical testing, food testing, environmental protection, water testing industry, etc. The latest system and long optical system ensure high accuracy and good stability of the instrument. It is the best choice of high quality spectrophotometer.

At Labindia, we manufacture state-of-the-art Spectrophotometers ranging from fully automatic ones to UV-VIS Spectrophotometers. The spectrometer is a highly flexible, versatile and high-quality instrument that is carefully crafted for the modern laboratory.

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Dual Beam UV-VIS 2002XE Spectrophotometer
Standard Features of Dual Beam UV-VIS 2002XE Spectrophotometer (XENON LAMP)
  • Photometry Measurement
    Measure absorbance and transmission at any defined wavelength.
  • Multi – Wavelength Measurement
    Measure absorbance and transmission at multiple wavelength and analyze the results by built-in methods
  • Time Scanning
    Determine absorbance at any time interval and defined wavelength.
  • Kinetics
    Determine absorbance at any time interval and defined wavelength. It can be used to monitor real time enzyme reaction and calculate enzyme activity according to the results. The reaction rates of samples can be calculated by setting the interval time.
  • Quantitation
    By measuring reference samples and establish standard curve, to determine unknown samples. Support built-in and customized formulation to establish standard curve.
  • DNA/Protein Determination
    According to the sample type, chose suitable method to determine DNA, RNA and Protein concentration.
  • Wavelength Scanning
    Determine full wave length absorbance and transmission at defined wave length interval, generate and analyze the graph by built-in methods.
  • Customized Methods
    Users can adjust the calculation methods upon own requirement and use it in corresponding determining module.
Typical Specification

 

Spectrum

UV-Visible

Spectrum Range

190-1100nm

Type

Dual Beam

Bandwidth

2nm

Lamp

XENON

Detector

Dual Silicon photodiode

User Interface

5-inch colour touchscreen

Output

USB, Serial port, Bluetooth (Optional)

Wavelength range

190-1100

Wavelength Accuracy

+-0.3 nm

Wavelength repeatability

+_0.2 nm

Wavelength resolution

0.1 nm

Photometric range

-0.3 to 3 A

Photometric accuracy

0.5 A_ 0.002A, for 1 A_ 0.004A

Photometric repeatability

0.5 A_ 0.001A, for 1 A_ 0.002A

Stray light

220 nm < 0>

Baseline Flatness

 +- 0.002A

Scan speed

3000 nm/min

Slew speed

7500 nm/min

Monochromator Type

Re_exive, holographic, Czerney-turner,

Scanning Monochromator

Capacity

Single Cell and Multi-cell up to 4 (Standard)

Power

100 ~ 240 V AC, 50/60 Hz, 100 W

Dimension

456*360*185 mm

Weight

10.5 kg

Optional Accessory

Specular Reflection Accessory, Integrating Sphere 60mm / 100mm Automatic 8 Cell Changer, long path cell holder, Peltier Solid Sample holder etc.

FAQs

1. What does a UV spectrophotometer measure?

UV-Vis Spectroscopy (or Spectrophotometry) is a quantitative technique used to measure how much a chemical substance absorbs light. This is done by measuring the intensity of light that passes through optical components with respect to the intensity of light through a reference sample or blank.

2. What are the main components of a UV VIS spectrophotometer?

There are four basic components to a simple single beam UV/Vis spectrophotometer; a light source, a monochromator, a sample, and a detector.

3. What is the difference between UV and visible spectrophotometry?

Molecules having non-bonding electrons can absorb the energy in the form of UV or visible light to excite these electrons to higher molecular orbitals. ... Ultraviolet-Visible Spectroscopy is absorption spectroscopy in the UV and visible portion of the electromagnetic spectrum.

4. Is infrared radiation dangerous?

In general, no -- at least from naturally occurring physical processes. Any form of radiation -- including visible light or radio waves -- could potentially be dangerous if highly concentrated into a narrow beam (that is the principle of lasers) of very high power.

5. What is the function of UV spectrophotometer?

UV / Vis spectrophotometer measures the absorbance of a light when it passes through a sample. The light absorbed is proportional to the quantity of a chemical in the sample.

Spectrophotometers