skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: A Monolithic 3D Printed Axisymmetric Co-Flow Single and Compound Emulsion Generator
We report a microfluidic droplet generator which can produce single and compound droplets using a 3D axisymmetric co-flow structure. The design considered for the fabrication of the device integrated a user-friendly and cost-effective 3D printing process. To verify the performance of the device, single and compound emulsions of deionized water and mineral oil were generated and their features such as size, generation frequency, and emulsion structures were successfully characterized. In addition, the generation of bio emulsions such as alginate and collagen aqueous droplets in mineral oil was demonstrated in this study. Overall, the monolithic 3D printed axisymmetric droplet generator could offer any user an accessible and easy-to-utilize device for the generation of single and compound emulsions.  more » « less
Award ID(s):
1711801
PAR ID:
10374329
Author(s) / Creator(s):
; ; ; ; ; ; ; ; ; ;
Date Published:
Journal Name:
Micromachines
Volume:
13
Issue:
2
ISSN:
2072-666X
Page Range / eLocation ID:
188
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract Double emulsions with core‐shell structures are versatile materials used in applications such as cell culture, drug delivery, and materials synthesis. A droplet library with precisely controlled dimensions and properties would streamline screening and optimization for specific applications. While microfluidic droplet generation offers high precision, it is typically labor‐intensive and sensitive to disturbances, requiring continuous operator intervention. To address these limitations, we present an artificial intelligence (AI)‐empowered automated double emulsion droplet library generator. This system integrates a convolutional neural network (CNN)‐based object detection model, decision‐making, and feedback control algorithms to automate droplet generation and collection. The system monitors droplet generation every 171 ms—faster than a Formula 1 driver's reaction time—ensuring rapid response to disturbances and consistent production of single‐core double emulsions. It autonomously generates libraries of 25 distinct monodisperse droplets with user‐defined properties. This automation reduces labor and waste, enhances precision, and supports rapid and reliable droplet library generation. We anticipate that this platform will accelerate discovery and optimization in biomedical, biological, and materials research. 
    more » « less
  2. Abstract Droplet microfluidics enables kHz screening of picoliter samples at a fraction of the cost of other high-throughput approaches. However, generating stable droplets with desired characteristics typically requires labor-intensive empirical optimization of device designs and flow conditions that limit adoption to specialist labs. Here, we compile a comprehensive droplet dataset and use it to train machine learning models capable of accurately predicting device geometries and flow conditions required to generate stable aqueous-in-oil and oil-in-aqueous single and double emulsions from 15 to 250 μm at rates up to 12000 Hz for different fluids commonly used in life sciences. Blind predictions by our models for as-yet-unseen fluids, geometries, and device materials yield accurate results, establishing their generalizability. Finally, we generate an easy-to-use design automation tool that yield droplets within 3 μm (<8%) of the desired diameter, facilitating tailored droplet-based platforms and accelerating their utility in life sciences. 
    more » « less
  3. The role of surface wetting properties and their impact on the performance of 3D printed microfluidic droplet generation devices for serial femtosecond crystallography (SFX) are reported. SFX is a novel crystallography method enabling structure determination of proteins at room temperature with atomic resolution using X-ray free-electron lasers (XFELs). In SFX, protein crystals in their mother liquor are delivered and intersected with a pulsed X-ray beam using a liquid jet injector. Owing to the pulsed nature of the X-ray beam, liquid jets tend to waste the vast majority of injected crystals, which this work aims to overcome with the delivery of aqueous protein crystal suspension droplets segmented by an oil phase. For this purpose, 3D printed droplet generators that can be easily customized for a variety of XFEL measurements have been developed. The surface properties, in particular the wetting properties of the resist materials compatible with the employed two-photon printing technology, have so far not been characterized extensively, but are crucial for stable droplet generation. This work investigates experimentally the effectiveness and the long-term stability of three different surface treatments on photoresist films and glass as models for our 3D printed droplet generator and the fused silica capillaries employed in the other fluidic components of an SFX experiment. Finally, the droplet generation performance of an assembly consisting of the 3D printed device and fused silica capillaries is examined. Stable and reproducible droplet generation was achieved with a fluorinated surface coating which also allowed for robust downstream droplet delivery. Experimental XFEL diffraction data of crystals formed from the large membrane protein complex photosystem I demonstrate the full compatibility of the new injection method with very fragile membrane protein crystals and show that successful droplet generation of crystal-laden aqueous droplets intersected by an oil phase correlates with increased crystal hit rates. 
    more » « less
  4. We study the formation of oil droplets from an initially trapped large oil ganglion under surfactant flooding, using a microfluidic device consisting of a two-dimensional array of regularly spaced square posts. We observe that above a critical capillary number for oil mobilization, breakage of the ganglion results in the formation of either trapped patches spanning multiple pores or numerous mobile droplets that exit the device at a velocity comparable to the average flooding fluid velocity. These mobile droplets, however, are only observed when above a secondary capillary number threshold. The formation of these droplets is found to involve the simultaneous occurrence of three different passive droplet generation mechanisms where a droplet is formed as it is pulled by perpendicular fluid flow, as it is pulled by co-axial fluid flow, and or as it splits due to collision with a post. Our results show that oil breakthroughs only occur when the oil is in the form of mobile drop- lets, suggesting that droplet formation can be an important condition for the mobility of residual oil in porous media. Additionally, this post-array microfluidic device can be used for the production of monodisperse droplets whose size can be controlled by the spacing of the posts. 
    more » « less
  5. Abstract Nonionic surfactants are increasingly being applied in oil recovery processes due to their stability and low adsorption onto mineral surfaces. However, these surfactants lead to the production of emulsified oil that is extremely stable and difficult to separate by conventional methods. This research characterizes the stability of crude oil mixed with a nonionic surfactant, L24–22, in a brine solution. When subjected to gravity separation, a middle oil‐rich and bottom water‐rich emulsion are generated for various water–oil ratios. Thermal treatments can effectively break oil‐rich emulsions, but the bottom water layer remains contaminated with micron‐sized crude oil droplets. A magnetic nanoparticle treatment is shown to demulsify the crude oil emulsions, dropping the total organic carbon (TOC) in the water layer from 1470 to 30 ppm. 
    more » « less