IPI Spring 2021

Page 86

Manufacturing

The Effects of Heat from Electro-mechanical Components in Critical Instrumentation Heat in electronic and fluidic control systems such as those seen in analytical, scientific and medical instruments will in many cases be an unwanted byproduct of the excessive power required to initially operate electro-magnetic devices such as solenoid valves and electro-mechanical devices. Although the initial power is unavoidable, the need to maintain full power when the device has been energised becomes excess to requirement in many instances. In the majority of cases, it is possible to reduce the power to a level that maintains the required function but reduces the excessive currents being drawn, and in doing so there is less heat and a lower overall power requirement that can be considerable, depending on the number of devices present. Reducing power consumption is both cost-effective and desirable in this day and age of carbon-footprint awareness. Solenoid valves in particular are a source of localised heat which, if unchecked, can transfer to the media passing through them and in doing so can elevate the temperature beyond the desired limits, and can be a particular problem if the media is a physiological fluid or is heat-sensitive. However, any electro-magnetic device can emit heat and draw higher than necessary current if not intelligently controlled. Such devices can be as simple as electromagnetic clamps, locks and sorting devices.

Figure 1. Typical solenoid valve

Figure 2. Sample electro-magnet

One of the many laws of physics states that energy is the quantitative property that must be transferred to an object in order to perform work on, or to heat, the object. Energy is a conserved quantity; the law of conservation of energy states that energy can be converted in form, but not created or destroyed.

Simplistically speaking, that is all there is to it; however, each time there is a transfer from one form of power/energy to another, there will be some losses that are inherent in the device. The most wasteful phase is after the mechanical movement has been achieved and the magnetic circuit has been completed, the power to hold the device in position is considerably reduced. Assuming that the instrument’s design allows the same power to flow through the device, the excess power is liberated as heat and it is this heat build-up that should be addressed.

In the real world, we are more likely to think of the concept of power rather than pure energy as it is more relative to the tasks we need to perform. For electro-magnetic devices, the subject of this editorial, the principle is simple: Electricity In = Electro-Magnetic Field = Magnetic Attraction = Mechanical Movement.

Wasting power may not appear to be a major consideration for mains-powered

Figure 4. Sample power savings

equipment, but what if there is need for a battery-operated instrument with a long field life? Even mains-operated instruments can benefit from power reduction, savings on the cost of electronic power supplies and reduction in physical size and weight of the final instrument.

Figure 3. Temperature traces for a high-pressure solenoid valve 84 INTERNATIONAL PHARMACEUTICAL INDUSTRY

Electro-mechanical devices are designated to have specific duty ratings which will greatly affect their potential to generate excessive heat, and particular care needs to be taken when selecting such devices to match the application in hand. A 100% Spring 2021 Volume 13 Issue 1


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Articles inside

Cold Chain in 2021: COVID-19’s Continued Influence

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pages 102-103

Deploying AI in the War on Counterfeit Drugs

11min
pages 98-101

Granulation in Pharmaceutical Technology

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pages 94-97

Are Plant-based Softgels the New Gold Standard for Pharma?

9min
pages 90-93

The Effects of Heat from Electro-mechanical Components in Critical Instrumentation

8min
pages 86-89

Whitepaper: Together Beyond COVID-19 A Look at the Future

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pages 72-75

Next-generation Aseptic Tech Needed to Cut Contamination Risk

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Adopting Connected Drug Delivery Devices Top Tips for Pharmaceutical Companies

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pages 82-85

Redefining Healthcare: Digital Trends in 2021

6min
pages 76-77

Beta Glucans and Endotoxin Testing

7min
pages 70-71

How Approaches to Clinical Research Are Set to Change in the ‘New Normal’

10min
pages 66-69

Pharmacokinetic and Statistical Considerations in First-in-human Clinical Trials

12min
pages 62-65

Digital Medication Adherence in Clinical Trials

7min
pages 60-61

A Greener Future for the Inhalation Industry A Critical Year for Our Climate

9min
pages 52-55

The Danish Approaches for Personalised Medicine

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Key Considerations when Repositioning a Known Drug for Inhalation Therapy

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pages 48-51

Connectivity, Cybersecurity and Medical Devices What are the Threats?

12min
pages 56-59

Innovate UK-funded Project Results in Next-generation AI Drug Discovery Technology

16min
pages 38-43

The COVID-19 Catalyst – Accelerating the Move to Patient powered Medicine

11min
pages 34-37

Comparison of Regulatory Process of COVID-19 Vaccines Between Emerging Markets, EU

11min
pages 30-33

Respiratory Drug Development – Perspective from Spray and Aerosol Characterisation Expert

9min
pages 14-17

Managing Competition, Price and Access The changing paradigm for the pharmaceutical sector

9min
pages 26-29

EU MDR Changes are Only the Beginning – Ensure IFU Compliance Now and be Prepared for More to Come

7min
pages 20-21

Nemera: The Holistic Partner for Your Combination Product Development

14min
pages 10-13

Editor’s Letter

5min
pages 8-9

Marketing Medical Cannabis in Europe

5min
pages 18-19

Can the UK Solve its ‘Money Laundering’ Problem with the Proceeds of Medicinal Cannabis?

11min
pages 22-25
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