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In-situ monitoring techniques of reverse osmosis (RO) desalination systems, particularly those with chemical sensing capabilities, can provide the means for better understanding important scaling mechanisms as well as early scaling detection. In this work, both calcium sulfate and calcium carbonate scaling on RO membranes were detected concurrently in real time using Raman spectroscopy to provide a unique chemical fingerprint. Two different sampling methodologies (manual and automated) were employed, and their performance was evaluated by comparing the Raman detection times to concurrent values of flux decline. The manual sampling strategy resulted in the detection of calcium sulfate and calcium carbonate at mean permeate flux declines of 13 ± 10 % and 22 ± 3 %, respectively. The automated sampling strategy provided better performance, with detection of calcium sulfate and calcium carbonate at mean flux declines of 8 ± 5 % and 4 ± 3 %, respectively. The increasedsensitivity and decreased variability of the automated sampling strategy provided valuable preliminary insights for the selection of optimized sampling strategies. The ability to identify the chemical composition of different scaling crystals including their polymorphs is an important step toward better understanding of the crystallization pathways of multi-component feed streams used in seawater and brackish water RO desalination. 

In this work we present a two-dimensional micro-scale array of individually addressable, focal length tunable, electrowetting lenses fabricated using standard microfabrication techniques. The compact, transmissive nature of these arrays opens the possibility for integration into miniature optical systems involving wavefront shaping and beam steering. 

We have demonstrated an electronically controlled laser, generating 50 nJ picosecond pulses at 760 nm. The gain-switched pulses at 1032 nm are amplified in Yb-fiber and frequency converted in photonic crystal fiber using four-wave mixing. 

Optical sectioning structured illumination microscopy (OS-SIM) provides optical sectioning capability in wide-field microscopy. The required illumination patterns have traditionally been generated using spatial light modulators (SLM), laser interference patterns, or digital micromirror devices (DMDs) which are too complex to implement in miniscope systems. MicroLEDs have emerged as an alternative light source for patterned illumination due to their extreme brightness capability and small emitter sizes. This paper presents a directly addressable striped microLED microdisplay with 100 rows on a flexible cable (70 cm long) for use as an OS-SIM light source in a benchtop setup. The overall design of the microdisplay is described in detail with luminance-current-voltage characterization. OS-SIM implementation with a benchtop setup shows the optical sectioning capability of the system by imaging within a 500 µm thick fixed brain slice from a transgenic mouse where oligodendrocytes are labeled with a green fluorescent protein (GFP). Results show improved contrast in reconstructed optically sectioned images of 86.92% (OS-SIM) compared with 44.31% (pseudo-widefield). MicroLED based OS-SIM therefore offers a new capability for deep tissue widefield imaging. 

Direct monitoring techniques of fouling in membrane-based filtration processes can be implemented as part of an effort to reduce the negative effects of membrane fouling. In particular, monitoring techniques with chemical characterization capability are crucial for the formulation of effective fouling prevention and mitigation strategies. In the present work, Raman spectroscopy was applied as an in-situ monitoring technique for calcium carbonate scaling on commercial reverse osmosis membranes. The bench-scale Raman monitoring system allowed for a qualitative chemical assay of the scaled membrane surface at sequential downstream and upstream axial positions. The time evolution of the downstream and upstream calcium carbonate Raman signal was evaluated with respect to computed values of local concentration at the membrane surface, revealing a statistically significant dependence (p < 0.001). The real-time Raman data were bolstered by results of post-mortem analysis (scanning electron microscopy, gravimetric measurements, and laser interferometry). The employed technique was capable of detecting crystals with characteristic lengths <50 μm. Preliminary evidence of polymorph detection was also presented with recommendations for improvements in the technique. 

Imaging sub-diffraction dynamics of neural nanostructures involved in behaviors such as learning and memory in a freely moving animal is not possible with existing techniques. Here, we present a solution in the form of a two-photon (2P), fiber-coupled, stimulated emission depletion microscope and demonstrate its capabilities by acquiring super-resolution imaging of mammalian cells. A polarization-maintaining fiber is used to transport both the 2P excitation light (915 nm) and the donut-shaped depletion beam (592 nm), which is constructed by adding two temporally incoherent and orthogonally polarized Hermite–Gaussian fiber modes. The fiber output is insensitive to bending or temperature changes and is the first demonstration toward deep tissue super-resolution imaging in awake behaving animals. 

We demonstrate a two photon (2P) fiber STED microscope in which the excitation and STED light are delivered to the sample in polarization maintaining (PM) fiber.