

Double-Beam Scanning UV-Vis Spectrophotometer
双光束扫描紫外可见分光光度计
- SKU SPE-0003
- Spectrophotometers
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Wavelength range | 190–1100 nm |
|---|---|
| Spectral bandwidth | 0.1, 0.2, 0.5, 1, 2, 5 nm (selectable) |
| Wavelength accuracy | ±0.3 nm |
| Wavelength repeatability | ≤0.1 nm |
| Photometric range | −4 to 4 A |
| Photometric accuracy | ±0.002 A at 0–0.5 A |
By Lab Manufacturers China Technical TeamLast reviewed Standards: USP <857>, Ph. Eur. 2.2.25, ASTM E275
What is the Double-Beam Scanning UV-Vis Spectrophotometer?
A double-beam scanning UV-Vis spectrophotometer splits the light into reference and sample paths measured simultaneously, cancelling lamp drift. It offers lower stray light, higher photometric range and better stability for method validation, long scans and regulated quality control.
What is the Double-Beam Scanning UV-Vis Spectrophotometer?
A double-beam scanning UV-Vis spectrophotometer splits the light into reference and sample paths measured simultaneously, cancelling lamp drift. It offers lower stray light, higher photometric range and better stability for method validation, long scans and regulated quality control.
Overview
In a double-beam instrument a beam splitter or rotating chopper divides the monochromatic light into a sample beam and a reference beam. The detector compares the two signals almost simultaneously, so lamp intensity changes, detector drift and warm-up effects are largely cancelled. High-quality models use a double monochromator or a high-grade holographic grating to reach stray light below 0.01 %T and photometric range to 4 A or more. Variable bandwidth from 0.1 to 5 nm allows measurement of narrow peaks, and scan speeds of up to several thousand nm/min make full-spectrum work fast. Baseline correction and autozero compensate for cell mismatch. The design suits pharmacopoeial tests that specify resolution power, absorbance accuracy and stray light, and it is the usual basis for regulated QC laboratories. Accessories include Peltier cell holders, integrating spheres and multi-cell changers.
How does it work?
A spectrophotometer passes light from a lamp through a monochromator, which selects a narrow wavelength band using a diffraction grating or filter. The band then crosses a sample held in a cuvette, and a detector such as a silicon photodiode or photomultiplier tube records the transmitted intensity. Absorbance is calculated as the negative logarithm of transmittance, and the Beer–Lambert law relates it linearly to analyte concentration within a limited range. Light sources are typically a tungsten-halogen lamp for the visible range and a deuterium lamp for the ultraviolet. Single-beam designs measure reference and sample sequentially, while double-beam designs split the beam to compensate for lamp drift. Reflectance instruments replace the cuvette with an integrating sphere or a fixed 45/0 geometry to capture color data.
What are the key features?
- Simultaneous sample and reference measurement cancels lamp and detector drift.
- Variable bandwidth of 0.1–5 nm supports both narrow peaks and high-energy measurements.
- Stray light below 0.01 %T extends the usable absorbance range beyond 3 A.
- Built-in pharmacopoeia test routines check resolution, noise and accuracy.
- Accessories include Peltier holders, integrating spheres and six-position cell changers.
- Software supports audit trails and electronic signatures for regulated laboratories.
What are the technical specifications?
A typical double-beam scanning uv-vis spectrophotometer configuration offers wavelength range of 190–1100 nm, spectral bandwidth of 0.1, 0.2, 0.5, 1, 2, 5 nm (selectable), wavelength accuracy of ±0.3 nm, wavelength repeatability of ≤0.1 nm, photometric range of −4 to 4 A and photometric accuracy of ±0.002 A at 0–0.5 A. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Double-Beam Scanning UV-Vis Spectrophotometer is used in pharmacopoeial testing, method validation, materials and optical-filter characterization and kinetic and thermostatted studies. Across the wider Spectrophotometers class, laboratories also deploy it for nucleic acid and protein quantification, water and environmental colorimetric analysis and pharmaceutical and chemical QC.
Which standards and certifications apply?
Relevant standards and methods include USP <857>, Ph. Eur. 2.2.25, ASTM E275, ASTM E308, JJG 178 and IEC 61010-1. Certification candidates for this model are CE and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Place the instrument on a vibration-free bench away from direct sunlight and strong air currents, and allow 15–30 minutes of warm-up for lamp stabilization. Verify wavelength accuracy, photometric accuracy, stray light and baseline noise at defined intervals using certified reference filters or solutions. Keep cuvettes clean, matched and free of scratches, and use quartz cells below 340 nm. Deuterium and tungsten lamps have finite lifetimes, so record lamp hours and schedule replacement. Keep the sample compartment dry and protected from spills. In regulated environments, apply installation, operational and performance qualification and maintain calibration records.
How do I select the right Double-Beam Scanning UV-Vis Spectrophotometer?
Select a double-beam model when long scans, low drift, high absorbance range or regulated compliance are priorities. It costs more than single-beam designs and is unnecessary for simple fixed-wavelength assays. In an RFQ, specify stray-light limit, bandwidth options, photometric range, scan speed, required accessories and audit-trail or 21 CFR Part 11 software features.
How does it compare with other Spectrophotometers variants?
Start with the wavelength range: visible-only instruments cover roughly 320–1100 nm and suit colorimetric assays, while UV-capable models extend to 190 nm for nucleic acids, proteins and organic compounds. Next consider photometric stability and stray light, which determine the usable absorbance range; double-beam optics give lower drift for long kinetic runs and method validation. Spectral bandwidth matters for sharp absorption peaks, with 1–2 nm adequate for most quantitative work. Sample volume and format separate standard cuvette models from microvolume and portable designs. Regulated laboratories should check for software audit trails, electronic records support and verification routines. Finally, consider throughput, accessories such as Peltier cell holders or autosamplers, and whether the instrument must operate outside the laboratory.
Full specifications
| Wavelength range | 190–1100 nm |
|---|---|
| Spectral bandwidth | 0.1, 0.2, 0.5, 1, 2, 5 nm (selectable) |
| Wavelength accuracy | ±0.3 nm |
| Wavelength repeatability | ≤0.1 nm |
| Photometric range | −4 to 4 A |
| Photometric accuracy | ±0.002 A at 0–0.5 A |
| Stray light | ≤0.01 %T at 220 nm and 340 nm |
| Baseline flatness | ±0.001 A |
| Noise | ≤0.0003 A RMS at 500 nm |
| Scan speed | Up to 4000 nm/min |
| Light source | Deuterium and tungsten-halogen lamps |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Pharmacopoeial testing
- Method validation
- Materials and optical-filter characterization
- Kinetic and thermostatted studies
Key features
- Simultaneous sample and reference measurement cancels lamp and detector drift.
- Variable bandwidth of 0.1–5 nm supports both narrow peaks and high-energy measurements.
- Stray light below 0.01 %T extends the usable absorbance range beyond 3 A.
- Built-in pharmacopoeia test routines check resolution, noise and accuracy.
- Accessories include Peltier holders, integrating spheres and six-position cell changers.
- Software supports audit trails and electronic signatures for regulated laboratories.
Frequently asked questions about Double-Beam Scanning UV-Vis Spectrophotometer
It measures the sample and reference beams almost simultaneously, so changes in lamp output or detector sensitivity affect both equally and cancel in the ratio. This removes the need to re-zero frequently and stabilizes long scans and kinetic runs.
For reliable measurements above about 2 A, stray light should be 0.01 %T or lower at the test wavelength. Verify with cutoff solutions such as sodium iodide at 220 nm and sodium nitrite at 340 nm as described in pharmacopoeial chapters.
Matched cuvettes are recommended for the most accurate work because the reference and sample paths use separate cells. The instrument can store a baseline with both cells filled with blank, which corrects small differences in cell transmittance.
A spectrophotometer measures the intensity of light after it passes through or reflects from a sample at specific wavelengths. From this it reports transmittance, absorbance or reflectance, which can be converted to concentration using a calibration curve or to color coordinates such as CIE L*a*b*.
A colorimeter uses fixed filters or LEDs at a few wavelengths, while a spectrophotometer uses a monochromator to scan a continuous range. Spectrophotometers therefore offer higher spectral resolution, full spectra and greater flexibility, whereas colorimeters are simpler and suited to dedicated assays.
Ordinary glass and most plastics absorb strongly below about 340 nm, which would mask the sample signal. Fused quartz transmits down to roughly 190 nm, so it is required for nucleic acid measurements at 260 nm and for UV absorption of organic compounds.
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