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| Overvoltage test performed on Telecom equipment in accordance with UL 60950 |
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| Collection of more than 2000 UL Standards |
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IAEI
News>Issue Listing>May/June 2002 >What Electrical Inspectors Don't See
| What Electrical Inspectors Don't See |
"Beauty is only skin deep," could not be truer than with electrical equipment. Under that pretty cover or inside that box could be a dangerous condition waiting to explode. |
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"Beauty is only
skin deep," could not be truer than with electrical
equipment. Under that pretty cover or inside that box could be
a dangerous condition waiting to explode.
Even after the cover
is opened a potential problem may not be easily revealed. That
first view may reveal the existence of some problems; however,
only after a detailed investigation and some sophisticated
tests could any reasonable determination be made that there is
no danger.
Investigation is
necessary to assure that a product complies with the
applicable product safety standard. The standard is developed
by people who have had experience with that category of
products and are familiar with the National Electrical
Code. Conditions of misuse and abuse are usually major
considerations in the required items covered by the
investigation. Compliance with the standard is the best
assurance that an inspector could receive that the product is
safe. In order to provide this compliance, a test lab must use
a lot of expertise and test equipment to make the
determination.
The Standard
Identifying the standard is by itself not always easy.
Some products may have to be investigated to two and in some
cases multiple standards. For example, a computer connected to
and made part of a piece of machinery or medical equipment
must be investigated to both the machinery or medical standard
and the computer standard. Also, the location where the
equipment is used may bring into use another standard. Then,
there is equipment that is not completely covered in the scope
of any standard. With new technology equipment surfacing every
day, the lab must make important subjective judgments in
selecting a standard and/or applicable sections of a standard.
To properly investigate all potential hazards, locating and
applying the correct standard is of paramount importance.
The Physical
Inspection
After the standard has been identified, the product is
physically disassembled and inspected. All components are
investigated to assure they are recognized and that they are
correctly applied in the product. Just because a component is
recognized does not automatically make it suitable in the
product. The conditions of acceptability must be considered.
For example, many components have a temperature limitation. If
the application in the product would cause the component to
operate near this temperature, then the component must also be
rated for the temperature or it is unacceptable. Recognition
alone is not sufficient. Recognition of a component assures
that the component manufacturer will continue to manufacture
the product in accordance with the component standard.
However, only the lab can assure that the component is correct
in its application and meets the requirements in the end
product standard.
Other physical inspections include
measuring clearances and creepage distances between live
parts. This is a physical measurement and the distances
permitted are listed in the standard. At normal voltages the
distances are usually sufficient; however, the clearance
distances are intended to allow the circuit to safely handle
surges and transients that appear on power systems. This is a
crucial measurement because surge voltage tests are not always
part of the testing. Physical inspections also include an
evaluation of mounting, bracing, overall strength and
generally requires a high level of expertise to assure
compliance with the safety standard.
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Testing
Testing is performed on the product in accordance with
the requirements in the standard. Besides testing to verify
that a product operates under normal conditions, tests are
conducted to simulate abnormal conditions. Temperature tests
are performed by blocking air passages, disabling fans or
other similar situations to create excessive temperatures.
These temperatures may only appear during an extreme condition
or a malfunction within the unit however, depending on
requirements in the standard. Other tests may include surges
or overvoltages, or environmental tests including: vibration,
temperature, and humidity tests, depending on the product and
the standard. These are only a few examples of the tests, but
it is important to show that the tests are intended to produce
conditions that may easily occur during the product’s use.
The items uncovered by these tests cannot be detected by any
physical inspection. Only after the testing is completed can
there be any confidence that the product meets the standard.
Initial Factory
Inspection
It can be reasonably assured that the manufacturer can
make one good product that can pass the laboratory tests, but
can the manufacturer continue to produce and ship products
that meet all of the requirements? In other words, will each
subsequent product be exactly equal to the product that was
approved in the laboratory? This requires the manufacturer to
have in place some type of responsible quality control system.
He needs a final inspection procedure, which may include final
testing. Not until an inspection at the factory is
satisfactorily completed is the authorization to label and
sell the product obtained. It is also necessary to determine
that the manufacturer has the ability to continually make the
same product as was originally approved.
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Factory Follow-Up
Inspections
An electrical inspector or any user of electrical
equipment must be confident that the product meets the
requirements of the standard. The only way the lab can
continue to allow the use of its label is to obtain further
assurances that the product continues to comply with the
standard. This can only be done after the lab does all of the
items listed above and performs periodic visits to the
factory. It is necessary for the lab to know that all
requirements are continually met. Often there are some changes
that are necessary during the manufacturing. If a component
manufacturer can no longer continue to supply the component
that was originally approved, the manufacturer must let the
lab know of the change and get specific approval for the
substitution. The periodic inspection verifies that only
approved changes have been made. In addition there are some
requirements for testing at final inspection. The lab has to
be sure that the equipment and the procedure used by the
manufacturer are correct.
The only way the inspector can be sure the
product meets United States requirements and enforces the National
Electrical Code is to see that all of the above procedures
were followed. These include selecting the correct standard,
performing a thorough investigation, conducting initial
factory inspections and required periodic follow-up
inspections. In the world systems, U.S. laboratories are the
only laboratories that follow all of these procedures. In
Europe, CE marking does not include many of the U. S.
requirements. The standards are European and the tests may be
done by the manufacturer or anyone else. There is no
requirement for a qualified testing laboratory. There is no
follow-up inspection.
So in short, what the electrical inspector
should always see is a label from a U.S. accredited qualified
electrical testing laboratory. The NRTL program is an
accreditation program that sets down the requirements listed,
monitors and audits the laboratory on a regular basis to
provide the inspector confidence that the label can be relied
upon. The NRTL program is administered by the Occupational
Safety and Health Administration (OSHA). The program is to
assure safe products in the workplace, where OSHA has
jurisdiction. However, the value it has for authorities having
jurisdiction is to eliminate the need for each jurisdiction to
establish its own accreditation mechanism. Some jurisdictions
still choose to maintain control and approve the laboratories
they accept, that is good; however, it can add to the expense
and workload of the jurisdiction. Whatever means the authority
uses to accept the laboratory that allows his label to be
applied to a product saves the inspector the impossible task
of trying, on his own, to see if an electrical product is safe
and should be allowed to be part of an approved electrical
system.
Len Frier is a registered
professional electrical engineer in the state of
Maryland. He founded MET Laboratories in 1959. He
initiated the Nationally Recognized Testing Laboratory
Program at OSHA in 1988, and is charter member of the
National Electrical Testing Association (NETA). He is
former chairman of the ANSI Z34 committee on "Third
Party Certification," chairman of the American
Council on Electrical Safety (ACES), member of the ANSI
Accreditation Committee, and the American Council of
Independent Laboratories (ACIL). Presently, he is
director at MET Laboratories, Inc. and is active in
government affairs relating to US Certifications of
electrical products.
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