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They feature a factor of ten increase in speed over general purpose devices without sacrificing DC performance. The LM series has internal unity gain frequency compensation.
This considerably simplifies its application since no external components are necessary for operation. However, unlike most internally compensated amplifiers, external frequency compensation may be added for optimum performance. Overcompensation can be used with the amplifier for greater stability when maximum bandwidth is not needed. Further, a single capacitor can be added to reduce the 0. These devices are easy to apply and offer an order of magnitude better AC performance than industry standards such as the LM C temperature range.
The LM is specified from 0? C Lead Temperature Soldering, 10 sec. Small Outline Package Vapor Phase 60 sec. Infrared 15 sec. C ? C, the LM is ? C, and the LM is ? For operating at elevated temperatures, devices in the H08 package must be derated based on a thermal resistance of ?
The thermal resistance of the dual-in-line package is ? Note 3: The inputs are shunted with back-to-back diodes for overvoltage protection.
Therefore, excessive current will flow if a differential input voltage in excess of 1V is applied between the inputs unless some limiting resistance is used. C LM ,? C LM , and 0? C LM Also, power supplies must be bypassed with 0. F disc capacitors. The LM is in a unity-gain non-inverting configuration.
VIN is stepped from? The slew rates between? Note 8: Human body model, 1. Fast Summing Amplifier Differential Amplifier www.
Output zero. Full scale adjust. As used herein: 1. Life support devices or systems are devices or systems which, a are intended for surgical implant into the body, or b support or sustain life, and whose failure to perform when properly used in accordance with instructions for use provided in the labeling, can be reasonably expected to result in a significant injury to the user. A critical component is any component of a life support device or system whose failure to perform can be reasonably expected to cause the failure of the life support device or system, or to affect its safety or effectiveness.
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