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The product was filtered and dried under vacuum at 70 °C up to a constant weight and was stored in a desiccator to avoid moisture.
The samples were brought to room temperature in a desiccator to avoid condensation of humidity.
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The crucible with ash was put in a desiccator to cool.
Subsequently, the catalyst was removed from the furnace and kept in a desiccator to prevent contact with air.
Excess water was wicked away using a small piece of absorbent paper and the sample was placed in a desiccator to dry.
The manifold, still holding the microelectrodes, was then placed in a desiccator to cool.
The purified SDS was kept under a dried atmosphere and reduced pressure in a desiccator to prevent its hydrolysis.
Cells were mounted on an aluminum stub and placed in a desiccator to dry overnight or until needed.
The dried ionic liquids were stored at room temperature in a desiccator to the exclusion of light.
Following printing, the arrays were left in a desiccator to dry for 48 hours, and then UV cross-linked (800 mJ/cm2).
The petioles of the leaves were wrapped with parafilm and set in the groove of a modified vacuum desiccator to create a seal and to avoid damage to leaves.
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