Sampling systems are one of the most complicated systems in a plan. They feature a variety of procedures and elements, all of which must work well together to create a process stream states’ analytical reading. This reading must be precise and timely since the critical outcome will be utilized to obtain control goals of a plant. below in this article, we will cover the 3 Common Challenges for Process Analyzer Accuracy.
Nevertheless, professionals in the plant, including technicians and engineers, realize the fact that a sampling sample can be quite fussy. Each system’s component has the potential to affect the accuracy of the process analyzer. This article highlights three common accuracy challenges encountered in a process analyzer to help your company enhance the analyzer’s readability.
1: Inappropriate tap locations
Selecting a tap location is a critical task. One of the objectives of choosing the right tap location is to prevent time delay. If the tap is placed on a process pipe’s section with a low-flow, it will take much longer for any transformation in the processed chemicals to demonstrate in the analytical outcome.
Combining volumes, such as tank or tower bottom, may also lead to postponement. Hence, the system designers should pick a place where the sample can be blended well, such as downstream of instigated turbulence from a flow orifice.
2: Misusage of the probe
When utilizing a probe to obtain a sample, ideally, it should be long enough to reach the process pipe’s middle third so that the operator can pull a representative sample. The operators can also obtain a more timely outcome near the process pipe’s centre due to the flow, which is faster around the area. Nevertheless, they should also consider the maximum allowable length to make sure that the probe will not encounter any resonant vibration.
Sometimes, it is enough to obtain only 15% of insertion into the diameter of the pipe. Moreover, the probe should not be unnecessarily broader since massive volume may result in time delay. On the other hand, if the operator uses a nozzle without a probe, the system is likely to receive a greater volume, possibly leading to a significant postponement.
3: Inappropriate sample conditioning
The operators should eliminate liquids from a gas sample in a sampling condition system. This action helps prevent damaging the process analyzer and compromise the result. They can eradicate big droplets in a gas sample via gravity (through a fallback tube) or inertia (through a cyclone). However, ultra-fine droplets which are suspended as aerosols need a coalescer.
Nevertheless, operators need to understand that the coalescers cannot filter out big droplets. Moreover, if the rate of flow is too high, smaller droplets might be pushed through the components of coalescer and do not drip out as they should. Additionally, if the sample vacates the coalescer, it will get saturated almost to dew point and near to condensing again.Â
Therefore, it is essential to leave the dew point by either increasing the temperature or reducing the pressure. Operators can generate a pressure drop with the use of a needle valve.
There are various components with the potentials to impact the accuracy of the process analyzer. You need to know and identify the common challenges to boost your analyzer’s efficiency. Some of the common accuracy challenges of process analyzer include an improper selection of tap locations, misusing the probe, and improper sample conditioning.
