This document provides information on air filter testing equipment from FEC. It describes testing systems that can test various types of air filters according to standards like EN 779 and ASHRAE 52.2. The systems can test parameters like flow rate, differential pressure, dust holding capacity, and efficiency. They include components like test ducts, centrifugal blowers, aerosol generators, and particle counters. FEC offers customizable filter testing solutions at various throughput capacities.
Validation Of System For Compressed Air Quality Imtiaz Rastgar
Food, Pharma and several other manufacturing industries need compressed air with precise control on oil-in-air, dust particles and moisture levels. Instruments and standards of compressed air quality are described by Imtiaz Rastgar, Chairman Rastgar Group and Ex CEO of Engineering Development Board, Ministry of Industries, Government of Pakistan, Islamabad.
Validation Of System For Compressed Air Quality Imtiaz Rastgar
Food, Pharma and several other manufacturing industries need compressed air with precise control on oil-in-air, dust particles and moisture levels. Instruments and standards of compressed air quality are described by Imtiaz Rastgar, Chairman Rastgar Group and Ex CEO of Engineering Development Board, Ministry of Industries, Government of Pakistan, Islamabad.
Heating, ventilation, and air conditioning is the technology of indoor and vehicular environmental comfort. Its goal is to provide thermal comfort and acceptable indoor air quality.
Control on Cleanroom Environmental Monitoring (Pharmaceutical)Srinath Sasidharan
A general consideration of Environmental Monitoring in Pharmaceutical manufacturing area. Cleanroom Monitoring Tools and Utilities: Author Sreenath Sasidharan (Geltec Healthcare FZE)
A Brief Overview on Active Air Sampling Procedure for Environment Monitoringijtsrd
In this paper, we are going to discuss the ‘Active Air Sampling procedure for EM'. EM stands for Environment Monitoring. Environment monitoring is performed in the pharmaceutical manufacturing plants to monitor the contamination of viable and non viable particle count. Viable particle count can be observed through the ‘Settle Plate method, Active Air Sampling, Surface Monitoring contact plate and swab test , and Personnel Monitoring method'. Non viable particles are dust particles and other non living particles. Active Air sampling is performed by microbiologist in the production and manufacturing area using the equipment known as ‘Air Sampler'. A media plate of SCDA Soybean Casein Digest Agar prepared under sterile condition by the microbiologist. The media plate is then allowed to adjust under the ‘Air Sampler hood' and then it is used for sampling purpose. Air sampler captures 1000L air as per validated time in a 1cubic meter of volume and therefore air sampling is thus performed in the middle of the surrounding area. The sampled plate is then incubated, and after then the required incubation is provided, and the plate is thus analyzed to determine whether our manufacturing area meets the level of expected counts or it crosses the required limit and, on this basis, the reporting is thus generated on regular basis. Juhi Rastogi | Faiz Hashmi ""A Brief Overview on Active Air Sampling Procedure for Environment Monitoring"" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-3 , April 2019, URL: https://www.ijtsrd.com/papers/ijtsrd22987.pdf
Paper URL: https://www.ijtsrd.com/pharmacy/pharmacy-practice/22987/a-brief-overview-on-active-air-sampling-procedure-for-environment-monitoring/juhi-rastogi
Pharmaceutical HVAC (Heating, ventilating, and air conditioning; also heating...Palash Das
This slide is represent the HVAC design,qualification and operational approach. As we know HVAC is important system for maintaining clean room. This presentation is made based on the requirement of Pharmaceutical Industry. All parameter are considered based on the current guidelines aspect.
FDA Compliance Programme Manual : Program 7356.002A is a manual which FDA investigators follow while inspection Sterile drug manufacturing operations This guidance for FDA Investigators covers the manufacture and testing of all sterile drug products, including Drugs that are sterilized by filtration or other means, aseptically processed, and drug products that are terminally sterilized.
The type of products covered by this program include
Sterile bulk drugs
Ophthalmic drugs
Otic dosage forms
Small volume parenteral (SVS)
Products for small molecule and licensed biological therapeutic drug products,
Large volume parenteral (LVP) products, and
Any other drug products required to be sterile or labeled as sterile.
Excluded under this Programme
Center for Biologics Evaluation and Research (CBER) regulated products
Veterinary drug product
At the end of this compliance guide 7356.002A questions have been given to help FDA investigators understand the manufacturing operations better and help in conduct of Inspections. Subsequent slides gives summary of these questions, which we feel, will help us prepare for an Inspection.
Heating, ventilation, and air conditioning is the technology of indoor and vehicular environmental comfort. Its goal is to provide thermal comfort and acceptable indoor air quality.
Control on Cleanroom Environmental Monitoring (Pharmaceutical)Srinath Sasidharan
A general consideration of Environmental Monitoring in Pharmaceutical manufacturing area. Cleanroom Monitoring Tools and Utilities: Author Sreenath Sasidharan (Geltec Healthcare FZE)
A Brief Overview on Active Air Sampling Procedure for Environment Monitoringijtsrd
In this paper, we are going to discuss the ‘Active Air Sampling procedure for EM'. EM stands for Environment Monitoring. Environment monitoring is performed in the pharmaceutical manufacturing plants to monitor the contamination of viable and non viable particle count. Viable particle count can be observed through the ‘Settle Plate method, Active Air Sampling, Surface Monitoring contact plate and swab test , and Personnel Monitoring method'. Non viable particles are dust particles and other non living particles. Active Air sampling is performed by microbiologist in the production and manufacturing area using the equipment known as ‘Air Sampler'. A media plate of SCDA Soybean Casein Digest Agar prepared under sterile condition by the microbiologist. The media plate is then allowed to adjust under the ‘Air Sampler hood' and then it is used for sampling purpose. Air sampler captures 1000L air as per validated time in a 1cubic meter of volume and therefore air sampling is thus performed in the middle of the surrounding area. The sampled plate is then incubated, and after then the required incubation is provided, and the plate is thus analyzed to determine whether our manufacturing area meets the level of expected counts or it crosses the required limit and, on this basis, the reporting is thus generated on regular basis. Juhi Rastogi | Faiz Hashmi ""A Brief Overview on Active Air Sampling Procedure for Environment Monitoring"" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-3 , April 2019, URL: https://www.ijtsrd.com/papers/ijtsrd22987.pdf
Paper URL: https://www.ijtsrd.com/pharmacy/pharmacy-practice/22987/a-brief-overview-on-active-air-sampling-procedure-for-environment-monitoring/juhi-rastogi
Pharmaceutical HVAC (Heating, ventilating, and air conditioning; also heating...Palash Das
This slide is represent the HVAC design,qualification and operational approach. As we know HVAC is important system for maintaining clean room. This presentation is made based on the requirement of Pharmaceutical Industry. All parameter are considered based on the current guidelines aspect.
FDA Compliance Programme Manual : Program 7356.002A is a manual which FDA investigators follow while inspection Sterile drug manufacturing operations This guidance for FDA Investigators covers the manufacture and testing of all sterile drug products, including Drugs that are sterilized by filtration or other means, aseptically processed, and drug products that are terminally sterilized.
The type of products covered by this program include
Sterile bulk drugs
Ophthalmic drugs
Otic dosage forms
Small volume parenteral (SVS)
Products for small molecule and licensed biological therapeutic drug products,
Large volume parenteral (LVP) products, and
Any other drug products required to be sterile or labeled as sterile.
Excluded under this Programme
Center for Biologics Evaluation and Research (CBER) regulated products
Veterinary drug product
At the end of this compliance guide 7356.002A questions have been given to help FDA investigators understand the manufacturing operations better and help in conduct of Inspections. Subsequent slides gives summary of these questions, which we feel, will help us prepare for an Inspection.
FEC Offer The Filter Mask Testing Equipment for R&D of Filter media, Mask Filter Media used in medical or Industrial application, quality control validation. As per International Standard.
Features :
Equipment is operating HMI Touch Screen Panel or Computerized operated with PLC Scada software based operating system, with (Optional) imported Germany particle counter direct reading on Computer screen Like Initial Pressure drop, Final Pressure Drop, Dust Holding Restriction capacity, Particle data (Optional) , Also can operate Run & Stop of Equipment, Flow Set, Dust Feed, data…
WRI’s brand new “Food Service Playbook for Promoting Sustainable Food Choices” gives food service operators the very latest strategies for creating dining environments that empower consumers to choose sustainable, plant-rich dishes. This research builds off our first guide for food service, now with industry experience and insights from nearly 350 academic trials.
Characterization and the Kinetics of drying at the drying oven and with micro...Open Access Research Paper
The objective of this work is to contribute to valorization de Nephelium lappaceum by the characterization of kinetics of drying of seeds of Nephelium lappaceum. The seeds were dehydrated until a constant mass respectively in a drying oven and a microwawe oven. The temperatures and the powers of drying are respectively: 50, 60 and 70°C and 140, 280 and 420 W. The results show that the curves of drying of seeds of Nephelium lappaceum do not present a phase of constant kinetics. The coefficients of diffusion vary between 2.09.10-8 to 2.98. 10-8m-2/s in the interval of 50°C at 70°C and between 4.83×10-07 at 9.04×10-07 m-8/s for the powers going of 140 W with 420 W the relation between Arrhenius and a value of energy of activation of 16.49 kJ. mol-1 expressed the effect of the temperature on effective diffusivity.
"Understanding the Carbon Cycle: Processes, Human Impacts, and Strategies for...MMariSelvam4
The carbon cycle is a critical component of Earth's environmental system, governing the movement and transformation of carbon through various reservoirs, including the atmosphere, oceans, soil, and living organisms. This complex cycle involves several key processes such as photosynthesis, respiration, decomposition, and carbon sequestration, each contributing to the regulation of carbon levels on the planet.
Human activities, particularly fossil fuel combustion and deforestation, have significantly altered the natural carbon cycle, leading to increased atmospheric carbon dioxide concentrations and driving climate change. Understanding the intricacies of the carbon cycle is essential for assessing the impacts of these changes and developing effective mitigation strategies.
By studying the carbon cycle, scientists can identify carbon sources and sinks, measure carbon fluxes, and predict future trends. This knowledge is crucial for crafting policies aimed at reducing carbon emissions, enhancing carbon storage, and promoting sustainable practices. The carbon cycle's interplay with climate systems, ecosystems, and human activities underscores its importance in maintaining a stable and healthy planet.
In-depth exploration of the carbon cycle reveals the delicate balance required to sustain life and the urgent need to address anthropogenic influences. Through research, education, and policy, we can work towards restoring equilibrium in the carbon cycle and ensuring a sustainable future for generations to come.
Artificial Reefs by Kuddle Life Foundation - May 2024punit537210
Situated in Pondicherry, India, Kuddle Life Foundation is a charitable, non-profit and non-governmental organization (NGO) dedicated to improving the living standards of coastal communities and simultaneously placing a strong emphasis on the protection of marine ecosystems.
One of the key areas we work in is Artificial Reefs. This presentation captures our journey so far and our learnings. We hope you get as excited about marine conservation and artificial reefs as we are.
Please visit our website: https://kuddlelife.org
Our Instagram channel:
@kuddlelifefoundation
Our Linkedin Page:
https://www.linkedin.com/company/kuddlelifefoundation/
and write to us if you have any questions:
info@kuddlelife.org
Willie Nelson Net Worth: A Journey Through Music, Movies, and Business Venturesgreendigital
Willie Nelson is a name that resonates within the world of music and entertainment. Known for his unique voice, and masterful guitar skills. and an extraordinary career spanning several decades. Nelson has become a legend in the country music scene. But, his influence extends far beyond the realm of music. with ventures in acting, writing, activism, and business. This comprehensive article delves into Willie Nelson net worth. exploring the various facets of his career that have contributed to his large fortune.
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Introduction
Willie Nelson net worth is a testament to his enduring influence and success in many fields. Born on April 29, 1933, in Abbott, Texas. Nelson's journey from a humble beginning to becoming one of the most iconic figures in American music is nothing short of inspirational. His net worth, which estimated to be around $25 million as of 2024. reflects a career that is as diverse as it is prolific.
Early Life and Musical Beginnings
Humble Origins
Willie Hugh Nelson was born during the Great Depression. a time of significant economic hardship in the United States. Raised by his grandparents. Nelson found solace and inspiration in music from an early age. His grandmother taught him to play the guitar. setting the stage for what would become an illustrious career.
First Steps in Music
Nelson's initial foray into the music industry was fraught with challenges. He moved to Nashville, Tennessee, to pursue his dreams, but success did not come . Working as a songwriter, Nelson penned hits for other artists. which helped him gain a foothold in the competitive music scene. His songwriting skills contributed to his early earnings. laying the foundation for his net worth.
Rise to Stardom
Breakthrough Albums
The 1970s marked a turning point in Willie Nelson's career. His albums "Shotgun Willie" (1973), "Red Headed Stranger" (1975). and "Stardust" (1978) received critical acclaim and commercial success. These albums not only solidified his position in the country music genre. but also introduced his music to a broader audience. The success of these albums played a crucial role in boosting Willie Nelson net worth.
Iconic Songs
Willie Nelson net worth is also attributed to his extensive catalog of hit songs. Tracks like "Blue Eyes Crying in the Rain," "On the Road Again," and "Always on My Mind" have become timeless classics. These songs have not only earned Nelson large royalties but have also ensured his continued relevance in the music industry.
Acting and Film Career
Hollywood Ventures
In addition to his music career, Willie Nelson has also made a mark in Hollywood. His distinctive personality and on-screen presence have landed him roles in several films and television shows. Notable appearances include roles in "The Electric Horseman" (1979), "Honeysuckle Rose" (1980), and "Barbarosa" (1982). These acting gigs have added a significant amount to Willie Nelson net worth.
Television Appearances
Nelson's char
Natural farming @ Dr. Siddhartha S. Jena.pptxsidjena70
A brief about organic farming/ Natural farming/ Zero budget natural farming/ Subash Palekar Natural farming which keeps us and environment safe and healthy. Next gen Agricultural practices of chemical free farming.
UNDERSTANDING WHAT GREEN WASHING IS!.pdfJulietMogola
Many companies today use green washing to lure the public into thinking they are conserving the environment but in real sense they are doing more harm. There have been such several cases from very big companies here in Kenya and also globally. This ranges from various sectors from manufacturing and goes to consumer products. Educating people on greenwashing will enable people to make better choices based on their analysis and not on what they see on marketing sites.
1. FEC
R
World Class Filter Testing Equipments
An ISO 9001 Certified co.
Hepa Filter Testing Equipments
2. 1 www.fecproduct.com
Latest Air Filter Testing System Without / With Dust Particle System. Test rig upgrade according to EN
779 and Asher 52.2. Schematic Diagram for air filter test system as per BS EN 779 S.S 304 Grade.
Flow rate : 600 to 6000
Differential Pressure : Digital
Test aerosol : Salt Type
Loading dust : Ashrae test dust, ISO12103-A2 and ISO 12103-A4
Filter samples : Pocket and cassette filters with max Dimensions 610x610mm (other filter also can be
test)
Flat sheet filter media : Also can be test as on per order request
Air supply : min. 5 bar
Dust feeder : Special designed for dispense the dust
FEC offer the air filter test rig as per international standard various type of capacity 6,000 cfm other higher
capacity is also available on customer demand we can test on this equipment life & efficiency test, dust holding
capacity, Pressure restriction test, Pressure drop, flow etc as per EN 779 Test Standard.
Test object•
Dust feed device•
Mixer orifice•
Perforated plate•
Final filter•
Measuring device for pressure loss•
Set up for determination of synthetic dust weight arrestance
Technical Spcification
Measuring device for volume flow•
Flow straightener•
Fan•
Timer•
Volume tester meter•
Temperature and relative humidity of test air•
3. 2www.fecproduct.com
Set up for determination of synthetic dust weight arrestance
Part 1
Part 2
Set up for determination of atmospheric dust spot efficiency
Test object•
Dust feed device•
Mixer orifice•
Perforated plate•
Final filter•
Measuring device for pressure loss•
Measuring device for volume flow•
Filter test Duct will be made from S.S Grade with high capacity centrifugal blower and 610mm x 610mm size
of test duct width housing for pre filter fine filter and test filter also attachment will be all type of filter for clean
room filters, flow and pressure difference, particle upstream particle downstream, will be digitally display due to
software through the control unit we some accessory recommended for pal as gemany.
Test duct S.S. Suitable for air filter as required capacity•
High capacity centrifugal blower with motor•
Aerosol generator with drying system salt type•
Features
Flow straightener•
Fan•
Probe (sampling tube)•
Timer•
Volume tester meter•
Vacuum pump•
Temperature and relative humidity of test air•
4. www.fecproduct.com
The teat rig suitable for test the air filter test according to standard EN 779 and ASHRE 52.2 below men-
tion parameters you can test
Flow rate V/S differential pressure•
Dust holding capacity•
Efficiency of filter and restriction pressure•
The filter samples can be easily installed into the rotatable and movable filter housing•
The test duct is divided info 6 duct sections and fabricated air proof.•
Suction part duct side and blower outside•
The pressure measuring facilities in duct section up stream and down stream digital sensor•
Butter fly valve for set the desired flow and pressure•
Flow measuring device imported digital sensor with digital will be attached in duct•
3
Flow rate V/S Diffrential pressure•
Over Pressure Aerosol DetectionDOP / PAO Test•
The filter samples can be easily installed into the movable filter housing.•
The test duct is divided into 4 duct sections and fabricated airproof.•
Suction part duct side and blower outside•
Imported Differential pressure measuring on operating panel duct section up stream and down stream digital•
sensor
Butter fly valve for set the desired flow and pressure•
Flow measuring device imported digital sensor with display will be attached in duct•
The Test Rig suitable for test the air filter test according to your mention List
5. www.fecproduct.com
Size : 355 x 255 x 230•
Weight Approx : 8.0 Kg•
Compressed air 5.5 to 11 cfm@ 20 PSI•
Capacity maximum 5 Ltr•
Testing range 50 to 5400 cfm Aerosol Generation 2 or 4 Laskin nozzele adjustable•
Aerosole O/P @ 540 cfm : 100 mg/m3 or microgel/l mg/m3 or microgel/l•
Features :
DOP/PAO Aerosol Generator
4
DOP/PAO testing is a very quick process that tests the integrity of the HEPA (High
Efficiency Particulate Air) filter using DOP or PAO solutions in their operational
conditions.These solutions gen- erate a gas type smoke and then generate gas
particles that will be greater than .03 microns. The test will certify the HEPA filter
is fully functioning and there is no leakage or damage.
Meaning of DOP
DOP (Dispersed Oil Particulate) is a dispersed aerosol used to test the integrity of HEPA filters.
Meaning of PAO
PAO (Poly Alpha Ole fin) is a non-carcinogen liquid which is a most common replacement for DOP.
DOP Test
Any equipment that has a HEPA filter should be tested every time the equipment is moved or going to be used on
a new project (every four weeks if on same project). For the best results testing should be done on-site to ensure
that the units have not been damaged due to transportation or daily activities at the work site.
Also rough handling of the equipment can cause the filter seals to become
loose from around the HEPA filter therefore causing leakage and making them
unsafe for workers who are counting on them while working in hazardous con-
ditions.
HEPA filters are composed of usually fiberglass fibers randomly arranged.
To qualify as HEPA the air filter must remove at least 99.97% of all airborne
particles greater than 0.3 micrometers in diameter from the air that passes
through it.
6. www.fecproduct.com5
Aerosol Photometer : Including scanning probe with LED and Vibrating alarm, audio able alarm, shoulder strap,
spare fuse, and Calibration certificate.
Standard Features : High resolution Graphical Display, Menu driven software function automatic Zero and
ranging proven LED Light source (Light Chamber) Reference setting for multiple testing reagent retains re-
frence setting when powered off display up-stream Ref. / Concentration setting stable at low concentration of
aerosol. Probe selectable audible visual, Vibrating Alrm plug and play suitable length USB Interface with light
weight heavy duty aluminum case accept world wide voltage.
Filter test Duct will be made from S.S Grade with suitable capacity centrifugal blower and duct size 610 mm ×
610 mm size of test duct with housing for Test Hepa filter also optional attachment will be all type of filter for
clean room filters, measuring parameters - Flow and pressure difference, particle upstream particle downstream
with three chanel hand held imported particle counter will be digitally display with computer software. With
operating panel
Square Test Duct S.S suitable for air filter as above mention required capacity•
High Capacity Centrifugal Blower with motor•
Aerosol Generator•
Imported hand held particle counter•
Photometer for hepa filter Integrity DOP / PAO test•
Aerosol Detection
7. www.fecproduct.com 6
The Handheld Particle Counter offers the most features and flexibility for customers interested in a low cost and
versatile handheld particle counter. The Model 9303 features a sturdy yet lightweight high-impact injection-mold-
ed plastic design for easy handling. The instrument is easy to configure using an intuitive keypad. The internal
memory can store up to 1,500 sample records of particle count data which can be conveniently viewed on screen
or download using a USB port to it Secure Software.
The instrument reports up to three particle size simultaneously. The middle channel is user selectable for 0.5,
1.0, 2.0, or 2.5 µm. The model 9303 complies with all the stringent requirements set forth in ISO 21501-4. It is
calibrated with NIST traceable PSL spheres using world-class Classifier and Condensation Particle Counters, the
recognized standard for particle measurements.
0.3 to 25 µm size range•
0.1 CFM (2.83 L/min) flow rate•
Up to three channels of simultaneous data•
ISO 21501-4 compliant•
USB serial output•
Compatible with Lite Secure•
1,500 sample record storage•
250 location labels•
Large 3.2-inch (8.1-cm) display•
On screen data review•
User selectable middle size channel•
Removable Li-ion battery•
Intuitive keypad menus•
High impact injection molded plastic•
Features and Benefits:
Handheld Particle Counter - Three Channel
8. The Handheld Particle Counter offers the most features and flexibility for customers interested in versatile hand-
held particle contamination monitoring. The features an ergonomic handle with thumb controls, for easy one-
hand operation. The 3.6 inch (9.1-cm) color touch screen interface makes it easy to configure and operate. The
Model 9306 can generate pass/fail reports for ISO 14644-1, EU GMP Annex 1, and FS209E. Particle count data
can be conveniently viewed on screen, downloading using Lite Secure Software, or printed directly to an optional
external printer.
Multiple particle counters configurations can be conveniently stored and uploaded as needed using the Lite Se-
cure data download and reporting software supplied as standard. The Model 9306 complies with all the stringent
requirements set forth in ISO 21501-4. These particle counters are calibrated with NIST traceable PSL spheres
using world-class Classifier and Condensation Particle Counters, the recognized standard for particle measure-
ments.
Features and Benefits:
Complies with all requirements of ISO 21501-4•
0.1 CFM (2.83 L/min) flow rate•
Measures up to six channels of simultaneous data•
Model 9306-V2 provides unique variable binning option•
Mass Concentration option (density parameter is user-configurable)•
Integrated handle for one hand operation•
Removable, rechargeable Li-ion battery•
Compatible with Lite Secure and FMS 5 software packages•
USB Cable, USB Storage Device and Ethernet data transfer•
Data Storage: 250 zones, 999 locations, and 10,000 samples•
Provides pass/fail reporting on ISO 14644-1, EU GMP, and FS209E•
External reporting of ISO 14644-1, EU GMP, and FS209E via Lite Secure•
Optional Temperature/ RH sensor available•
www.fecproduct.com7
Handheld Particle Counter - Six Channel
9. www.fecproduct.com 8
Leaking Tester For Hepa Filter
FEC is the high class heap filter leakage tester high-efficiency cleaning air filtration system. The manufacturer
must test each hepa filter before packaging and delivery. So far, the most popular test methods for hepa filter are
photometer scanning and counter scanning. These two methods are popular, but high labor-consuming and in-
efficient. Besides, filter in certain structure such as W-type can’t be tested. Under this condition, the market call
on an easy-operation, high-efficiency and reliable tester for leaking.
The machine is a new type leaking tester ,which is self developed and produced according to the theory that the
mist can be filtered by hepa filter in the basic of mist leaking test by Xinxiang North Filter Co.,Ltd, complying
with the demand of the market.
II. Technical Parameter
Rated voltage 220V/380V 50HZ
Rated power 3.56KW
Oil barrel capacity 2.5L
Weight of machine 350kg
Standard size of inside Chamber Max. 1000x1000x1000mm also as per customer requirement :
size of filter 1200x700x300mm
Min. size of filter 300x300mm
Max. wind pressure of leak testing 1210Pa
Max. mist output 210m3/min
10. www.fecproduct.com9
III. Performance Characteristics
Fuming particle diameter is between 0.3 ~ 0.5 um, particle arranged evenly, and in line with the dust particle•
size of the counting scanning method, able to meet the requirements of HEPA filters leaking test.
For a wide range of various types of HEPA filters with and without separators to detect.•
High detection efficiency, only two seconds for single filter detection, cut detection time short, and reduce the•
cost of production.
Meet environmental requirements, the device emitted mist without any harm to the operator. The detection•
process has no mist emission outwards, no impact on the surrounding environment.
Electrical control system , easy to operate with high reliability.•
Cheap raw material consumables, negligible testing cost. It is currently the most cost-effective HEPA filter•
tester in domestic.
IV. Operation Instruction
Check all the power supply and make sure all of them are comply with the instruction before starting up the•
machine and tidy up all the sundries on the platform.
Adding pure water in the water channel of the air leak tester, making the liquid level be about 2mm lower•
than the mist outlet. Adding tap water into the water tank, making sure the liquid level be in the range of the
mark.
Turn on the air switch inside of the electrical cabinet. When the “Power” sign lights up, it means the power is•
already on.
11. www.fecproduct.com 10
This tester is used for testing the compression strength testing for big size box up to
less then 1 mtr cube . With, it’s also available to test the column compress strength of
the corrugated box, plastic container, tin container etc . It is equipped with a precise
ball screw, which drives the compression platen steadily along the guide track to com-
press the specimen. A high accurate load cell detects the compression signal via the
analyses of test program to display the test results on the indicator.
Hepa Filter Box Compression Tester
FEC Shipper Carton Transport Testing – This is testing of one or two complete shipper
cartons of product that includes vibration (the item is put on a vibrating platform for a
length of time) and also drop testing (the car- ton is dropped from varying heights at vary-
ing angles). After the testing is complete the product and packaging inside the cartons is
inspected and damage recorded.
FEC Shipper Carton Conditioning Testing – This is testing of one or two complete
shipper cartons of product where the carton is exposed to high temperature, high tempera-
ture with high humidity, and low temperature, each extreme condition for 24 hours. After
all three days of testing the packaging and product inside is evaluated.
Hepa Filter Drop Test
FEC Carton Bursting Strength Testing – One key determinant of the strength of a carton is
the bursting strength. The bursting strength is a measure of how much pressure is needed
on one square inch of carton to cause a break in the material. The bursting strength of a
carton is generally reported in pounds per square inch. A high-quality shipper or master
carton should test at a minimum of 150lbs/sq inch. A high quality color box or inner box
should test at at least 90lbs/sq inch.
Hepa Filter Bursting Strength Testing
Carton Edge Crush Testing (ECT or ECR) – This is another common test performed on a
carton or color box to determine its strength. This test is used to determine the force that
will crush a standard size of board standing on an edge.
These five tests are not the end-all be-all for testing your packaging.
More to come in regard to testing other packaging materials besides
cartons and boxes, and also how to check these materials when you’re in
the factory.
Hepa Filter Unde transportation vibration Test
12. Some Our Valued Customers
Sales Office: 9A, Gurudwara Road, Hari Vihar (Kakraula), Opp. Metro Poll No. 816, New Delhi 110043 (INDIA)
Correspondence Address : Plot No. 35, K-1 Extn., Bank Wali Gali Gurudwara Road, Mohan Garden, Uttam Nager,
Delhi-110059
Cell - 9811478874, 9811938703, 9212912990
E-Mail : info@fecproduct.com / inquiry_fec@yahoo.com
Website : www.fecproduct.com