In order to pursue criminals as quickly and efficiently as possible, forensic analysts
must glean a wealth of information from a limited set of evidence in a short
amount of time. This research aims to expand the information acquired from
a crime scene by increasing understanding of blood drying behavior. Blood
is a mixture of biological colloids and proteins, the drying of which has been
examined for some time. These experiments overwhelmingly use anticoagulants
such as EDTA and tri-sodium citrate to extend the lifetime and transportability
of the blood by preventing coagulation, making it easier to perform laboratory
experiments. While experiments using anticoagulated blood produce useful
information for personalised medicine, they may be of limited relevance for the
typical crime scene. To extend the usefulness of blood droplet research to reallife
crime scenes where coagulation naturally occurs, fresh blood coagulation and
a coagulation-like process utilised by the medical community for clotting assays
were introduced to small whole blood droplets. Gravimetrics, optical coherence
tomography, and image analysis of drying time-lapses for various geometries were
used to examine three major areas: evaporation dynamics, cracking patterns, and
substrate adhesion. Experiments found important differences in the delamination,
internal dynamics, and final morphology of the droplets which may impact
forensic conclusions, though the drying time and evaporation rate were found
to be identical across all treatments
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