Disintegration Tester LDIT-T2012

Introduction

Disintegration Tester operates with a basket lifting frequency of 30 to 32 per minute providing accurate results. It has automatic control system for temperature, time, and frequency to ensure consistent performance. The tester includes alternative displays for preset and real-time data for effective monitoring. It features splash proof control buttons that protect against moisture, enhancing durability and safety. Our tester is ideal for evaluating the quality of tablets and capsules with accuracy. This pharmaceutical machinery is designed to meet the rigorous requirements of modern laboratory operations, ensuring high precision, reliability, and ease of use for various experimental applications.

Applications

Disintegration tester is widely used in chemical laboratories and pharmaceutical industries to evaluate the disintegration time and quality of tablets and capsules.

Specifications

Number of basket lifting set	3 sets
Lifting frequency of the basket	30 to 32/ min
Lifting distance of basket	55 ± 1 mm
Minimum spacing from screen to bottom of beaker	25 ± 2 mm
Mesh size	2 mm (as per standard configuration)
Automatic time range	5 to 120 min
Work noise	< 60 dB
Temperature prefabrication range	Room Temperature to 50℃, display resolution: 0.1℃
Temperature control accuracy	± 0.3℃
Time prefabrication range	1 to 900 min
Time control accuracy	0.5 min
Accuracy of temperature control	37 ± 0.5℃
Dimension (L × W × H)	540 × 320 × 440 mm
Power supply	220 V/50 Hz
Total power	600 W
Gross weight	25 kg

Features

3 baskets with 18 tubes

Microprocessor-controlled system

Even ℃ temperature maintenance

Transparent organic glass bath

Auto-diagnose and over-temperature alarm

FAQs

1. What are the key factors to consider when selecting this pharmaceutical machinery for laboratory use?

When selecting this pharmaceutical machinery, key factors include: 1) The instrument's precision and accuracy to meet experimental requirements; 2) Compatibility with the types of samples and applications you will be working with; 3) Ease of use and maintenance requirements; 4) Safety features to protect operators and samples; 5) Calibration and certification requirements; 6) Cost-effectiveness and long-term reliability; 7) Technical support and service availability from the supplier. Evaluating these factors ensures that the instrument meets your laboratory's specific needs.

2. How often should this pharmaceutical machinery be calibrated to ensure accurate results?

It is recommended to calibrate this pharmaceutical machinery at least once every 6-12 months under normal usage conditions. More frequent calibration (every 3-6 months) may be necessary if: 1) The instrument is used continuously for extended periods; 2) It is exposed to harsh environmental conditions (temperature fluctuations, humidity, dust); 3) It is used for critical applications requiring high precision; 4) The instrument has been moved or subjected to physical shock; 5) Calibration checks indicate significant deviations from standard values. Always follow the manufacturer's calibration guidelines.

3. What are the common maintenance procedures required for this pharmaceutical machinery?

Common maintenance procedures include: 1) Regular cleaning of the instrument's exterior and sample contact surfaces to prevent contamination and ensure proper operation; 2) Inspection of moving parts (if applicable) for wear and lubrication as recommended by the manufacturer; 3) Replacement of consumable parts (filters, bulbs, reagents) according to usage guidelines; 4) Verification of performance parameters (temperature, pressure, voltage) regularly; 5) Storage of the instrument in a clean, dry environment when not in use; 6) Keeping a maintenance log to track service activities and identify potential issues early; 7) Following the manufacturer's specific maintenance schedule for optimal performance and longevity.

4. Can this pharmaceutical machinery be used with different types of samples, and are there any compatibility considerations?

Yes, this pharmaceutical machinery can be used with a variety of sample types, but compatibility considerations are important: 1) Check if the instrument's materials are compatible with the chemical composition of your samples (avoid corrosive or reactive substances that may damage the instrument); 2) Ensure that the sample volume and concentration are within the instrument's recommended range; 3) For biological samples, consider sterility requirements and potential cross-contamination risks; 4) For volatile or hazardous samples, ensure proper ventilation and safety precautions are in place; 5) Consult the manufacturer's documentation for specific sample compatibility guidelines, and perform compatibility tests with new sample types before regular use.

5. What should be done if the pharmaceutical machinery malfunctions or produces inconsistent results?

If malfunctions or inconsistent results occur: 1) First, check the instrument's user manual for troubleshooting guidelines specific to the issue; 2) Verify that the instrument is properly calibrated and within its calibration period; 3) Inspect for obvious issues such as loose connections, damaged parts, or incorrect settings; 4) Clean the instrument thoroughly to remove any contamination that may affect results; 5) Repeat the experiment with a known standard sample to determine if the issue is with the instrument or the sample; 6) If the problem persists, discontinue use of the instrument to prevent further damage or inaccurate results; 7) Contact technical support or a qualified service technician for diagnosis and repair, providing details of the issue and any troubleshooting steps already performed.