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11.2D: Microscale Distillation

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    483295
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    There are a variety of methods used to distill small amounts of material \(\left( < 10 \: \text{mL} \right)\). The goal of all of these variations is to minimize the loss of material. A certain amount of sample is always necessary to fill the apparatus before distillation occurs, and this quantity (called the "holdup volume") normally condenses after cooling, often back into the original distilling flask. Therefore, minimizing the path length between distilling and receiving flasks can increase the recovery with distillation. Another approach to increase recovery on the microscale is to minimize the number of joints in the apparatus, which may not be perfectly airtight, and can contribute to leaking of material.

    Hickman Head

    A Hickman head can be used to distill \(1\)-\(3 \: \text{mL}\) of material. It is often connected to a conical vial or a round bottom flask and a reflux condenser is placed on the top (Figure 11.35a). The entire setup is then placed into a heating matel, controlled with a variac (green box) (Figure 11.35b). The solution boils, condenses on the sides of the flask and collects in the lip of the Hickman head. The distillate can be collected by opening the black top on the side of the Hickman head and using a pipet to retrieve the liquid (Figure 11.35c).

    Screenshot 2024-08-13 at 1.11.39 PM.png

    Figure 11.35: a) Microscale distillation using a Hickman head, b) Entire reaction setup with a Hickman head, c) Retrieval of the distillate by pipette

    \(^{10}\)Prices were found in the Chemglass catalog in March 2016.


    This page titled 11.2D: Microscale Distillation is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by Lisa Nichols via source content that was edited to the style and standards of the LibreTexts platform.