Energy regulations in power supply

The extreme power supply has become a staple part of system design for the electronics engineer. It provides a convenient means by which to add an AC front-end to a product which already meets international safety approvals. It also provides a faster time to market, with the option to use a connector which suits the application and reduces the risk of a generic power supply being plugged in and causing damage. By supplying a lower DC voltage to the equipment, it becomes easier to design a compact product that complies with all the necessary safety standards a key consideration in applications in the consumer, industrial and medical marketsstontronics2

It’s based on the International Efficiency Mark (IEM) scheme developed by the US Environmental Protection Agency as part of the Energy Star program. The IEM scheme calls for manufacturers to test the efficiency of the power supply under different load conditions: not just no-load but also intermediate loads through to 100%. An average of the four active load conditions provides an overall efficiency rating for the supply. The no-load measurement is treated separately.

There are differences in the legislation which covers efficiency for external power supplies used for IT equipment, the global trade environment encourages manufacturers to adopt designs that can be sold in as many territories as possible. A Level VI-rated power supply delivers that ability. Suppliers can use the improved specifications in territories that have less stringent regulation as a means of competitive differentiation.

There are exceptions to the US regulations for external power supplies. One is for products intended for medical use and which require approval from an agency such as the US Federal Food and Drug Administration. The medical environment has, for reasons of safety, a number of stringent requirements. For Canada, Europe, and the US, the power supply manufacturer needs to provide a full risk assessment and accompanying documentation that follows the procedures laid out in the third edition of the IEC 60601. Other countries follow an older procedure laid out in the second edition of IEC 60601, but changes in legislation in the near future will likely make the fourth edition of the standard the one to follow.stontronics-adaptor2

In addition to a risk-analysis procedure intended to ensure there is no risk of harm to patient or operator, the fourth edition reflects the higher complexity of the electronic environment around medical systems. Electromagnetic compatibility is now such an important issue that it forms part of the fourth edition standard.

The focus on safety in medical power supplies does not detract from the overall thrust of development in this area to be one of energy efficiency. Although there is no requirement for the same level of efficiency from medical supplies as that in supplies for generic IT equipment in the European or US regulations, the market demands designs that have a similar performance to Level V. The availability of Level VI power adaptors with approvals to US and European standards provides manufacturers with the confidence that they can design them into their final systems and be assured of the ability to serve customers worldwide.

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Author: mhblogweb

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