Graham T. T. Gibson

NANOELECTROSPRAY EMITTERS: TRENDS AND PERSPECTIVE

The benefits of electrospray ionization are many, including sensitivity, robustness, simplicity and the ability to couple continuous flow methods with mass spectrometry. The technique has seen further improvement by lowering flow rates to the nanoelectrospray regime (<1,000 nL/min), where sample consumption is minimized and sensitivity increases. The move to nanoelectrospray has required a shift in the design of the electrospray source which has mostly involved the emitter itself. The emitter has seen an evolution in architecture as the shape and geometry of the device have proved pivotal in the formation of sufficiently small droplets for sensitive MS detection at these flow rates. There is a clear movement toward the development of emitters that produce multiple Taylor cones. Such multielectrospray emitters have been shown to provide enhanced sensitivity and sample utilization. This article reviews the development of nanoelectrospray emitters, including factors such as geometry and the manner of applying voltage. Designs for emitters that take advantage of multielectrospray are emphasized.

Competitive adsorption of phosphate and carboxylate with natural organic matter on hydrous iron oxides as investigated by chemical force microscopy

Abstract The behaviour of phosphate and natural organic matter (NOM) in soils and aqueous media is strongly influenced by their association with surfaces of colloidal mineral oxide and oxyhydroxide particles of iron. Here we investigate the interaction of atomic force microscope (AFM) tips terminated with bis(11-thioundecanoic)phosphate and 16-thiohexadecanoic acid as a function of pH in the context of competitive phosphate–organic matter adsorption interactions at the surface of hydrous iron oxide colloids. Experiments were carried out on unmodified colloids as well as colloids coated with gallic acid, tannic acid or peat-derived humic material. The colloids were also examined by infrared spectroscopy (IR) and zeta potentiometry. Force titrations on a gallic acid control surface revealed that the main mode of interaction of this compound with the tips was hydrogen bonding. A strong interaction in the pH range 4–8 observed for the PO2H probe on the unmodified iron (hydroxy)oxide was attributed to a specific adsorption reaction with an A-type FeOH surface site. The CO2H tip displayed a strong but less specific interaction that extended over the pH range 4–10. Force titrations of probes against colloids post-precipitated with gallic acid, tannic acid or peat-derived humic material were significantly different than for the unmodified surfaces. Surface-bound organic molecules reduced the specific mid pH range interactions and gave rise to two new force titration features with maxima about pH 4 and 8, which were assigned to H-bonding between the probes and benzoic and phenolic groups of surface-bound organic acids, respectively.

Microstructured Photonic Fibers as Multichannel Electrospray Emitters

Novel multichannel electrospray emitters are presented that use silica-based microstructured fibers (MSFs) to split the flow allowing efficient desolvation during electrospray. The MSFs investigated in this study possess 30-168 individual fluidic channels (each channel being 5 microm in diameter) that form a 2D emitting array. Multiple flow paths afford stable electrospray at flow rates ranging from the microspray (e.g., 1000 nL/min) to the nanoelectrospray (e.g., 10 nL/min) regime with moderate to negligible flow-induced backpressures. The electrospray stability of highly aqueous solutions (up to 99.9% water with 0.1% acetic acid) is enhanced through modification of the emitting surface with a hydrophobic silylation reagent (chlorotrimethylsilane). Furthermore, by successfully spraying highly concentrated salt solutions, this study demonstrates that multichannel MSF emitters provide enhanced robustness to clogging, leading to increased operational throughput.

Potentiometric titration of metal ions in methanol

The potentiometric titrations of Zn2+, Cu2+ and 12 Ln3+ metal ions were obtained in ethanol to determine the titration constants (defined as the at which the [-OEt]/[Mx+]t ratios are 0.5, 1.5, and 2.5) and in two cases (La3+ and Zn2+) a complete speciation diagram. Several simple monobasic acids and aminium ions were also titrated to test the validity of experimental titration measurements and to establish new constants in this medium that will be useful for the preparation of buffers and standard solutions. The dependence of the titration constants on the concentration and type of metal ion and specific counterion effects is discussed. In selected cases, the titration profiles were analyzed using a commercially available fitting program to obtain information about the species present in solution, including La3+ for which a dimer model is proposed. The fitting provides the microscopic values for deprotonation of one to four metal-bound ethanol molecules. Kinetics for the La3+-catalyzed ethanolysis of paraoxon as a function of are presented and analyzed in terms of La3+ speciation as determined by the analysis of potentiometric titration curves. The stability constants for the formation of Zn2+ and Cu2+ complexes with 1,5,9-triazacyclododecane as determined by potentiometric titration are presented.

Fast preparation of photopolymerized poly(benzyl methacrylate-co-bisphenol A dimethacrylate) monoliths for capillary electrochromatography.

A novel porous polymer monolith was prepared in situ in a fused-silica capillary using photoinitiated polymerization. Bisphenol A dimethacrylate (BPADMA) was selected as a crosslinker, copolymerized with benzyl methacrylate (BMA) in the presence of a binary porogenic solvent consisting of cyclohexanol and 1-decanol in < or =10 min. The resulting poly(BMA-co-BPADMA) monoliths exhibited good permeability and mechanical stability. Mixtures of alkylbenzenes, polycyclic aromatic hydrocarbons (PAHs) or phenolic compounds were successfully separated by CEC. A similar monolith was also prepared with ethylene dimethacrylate (EDMA) as the crosslinker instead of BPADMA to compare the separation ability of the resulting monoliths. The results indicated that poly(BMA-co-BPADMA) monoliths have better selectivity for aromatic analytes and greater chromatographic stability in higher aqueous mobile phase.

Entrapment of functionalized silica microspheres with photo-initiated acrylate-based polymers.

The entrapment of silica-based microspheres, commonly used as stationary phases in chromatography, with an organic porous polymer based on poly(butyl acrylate-co-1,3-butanediol diacrylate) was explored. The spheres were immobilized by photopolymerization leading to entrapped beds within 75 microm i.d. fused silica capillaries, and were mechanically stable, resisting pressure drops of over 5600 psi (38.6 MPa) for only 1 cm of material. The morphology of the polymer formation around the spheres was investigated by SEM and corroborated with back pressure measurements, which indicated that the spheres were held together by encapsulating polymer. The entrapped material was extruded from the capillary in some cases to facilitate imaging. The entrapment conditions were explored, varying the polarity of the sphere surface, the solvent, and the monomers, revealing that polymer formation is based on partitioning of the monomers between the surface and solvent. The resulting polymer morphology is discussed with respect to the effects of confinement, supported by experiments with varying microsphere diameters. The columns described here have favourable properties for use in capillary chromatography and supported catalysis among other applications, and is suitable for lab-on-a-chip devices.

Bundled capillary electrophoresis using microstructured fibres.

Joule heating, arising from the electric current passing through the capillary, causes many undesired effects in CE that ultimately result in band broadening. The use of narrow‐bore capillaries helps to solve this problem as smaller cross‐sectional area results in decreased Joule heating and the rate of heat dissipation is increased by the larger surface‐to‐volume ratio. Issues arising from such small capillaries, such as poor detection sensitivity, low loading capacity and high flow‐induced backpressure (complicating capillary loading) can be avoided by using a bundle of small capillaries operating simultaneously that share buffer reservoirs. Microstructured fibres, originally designed as waveguides in the telecommunication industry, are essentially a bundle of parallel ∼5 μm id channels that extend the length of a fibre having otherwise similar dimensions to conventional CE capillaries. This work presents the use of microstructured fibres for CZE, taking advantage of their relatively high surface‐to‐volume ratio and the small individual size of each channel to effect highly efficient separations, particularly for dye‐labelled peptides.

Polymer microstructures with high aspect ratio and low polydispersity using photonic fibres as templates

Small-scale, one-dimensional structures are of great interest for their applicability in fields as diverse as medicine, catalysis, microelectronics and chemical analysis. Such structures include tubes, fibres/wires, and other extended linear forms. One popular approach to fabricating 1D structures is to form them inside a template and then remove the template, typically by selective chemical etching. In this work, microstructured fibres (MSFs) were used as a template to generate tubes, wires and porous monoliths from poly(divinylbenzene) or poly(butyl acrylate-co-butanediol diacrylate). MSFs are designed and marketed as photonic waveguides, and consist of an array of parallel channels fashioned in silica. The MSF manufacturing process typically involves stacking a number of tubes and rods in a preformed array followed by heating and drawing to a thin fibre. This process allows tight control over the channel size and shape, and as such these parameters are highly consistent between channels and between MSFs. Consequently, the 1D structures formed from these template channels share their low polydispersity, as well as their other characteristics such as ultrahigh aspect ratio and axial alignment.

Multiple electrosprays generated from a single polycarbonate microstructured fibre

Electrospray ionization (ESI) has been invaluable to the mass spectrometric detection of biomolecules, due largely to the sensitivity afforded by the ionization technique. Lower flow rates, e.g. in the nanoelectrospray regime, result in smaller initial electrosprayed droplets, leading to higher ionization efficiency and greater signal. One approach to improving sensitivity without lowering flow rate is to generate multiple electrosprays (MESs) from the same sample, essentially splitting one larger flow into smaller flows in the nanoESI regime. Presented here is a series of novel MES emitters in the form of polycarbonate fibres. Based on microstructured fibre (MSF) technology whereby a set of homogeneous parallel channels are formed in a heat-drawn fibre intended to conduct light, a custom design was fabricated in which 3, 6, 9 and 12 holes were arranged in a radial pattern to prevent inhomogeneities in the electric field. The MSFs have dimensions that are compatible with current standards in nanoESI equipment, and the tip is more compatible with standard MS orifices than other larger multielectrospray emitters. By measuring the spray current provided by the various emitters under the same solvent/voltage/total flow rate conditions, a plot was obtained clearly demonstrating the expected dependence on the square root of the number of holes, i.e. the number of independent electrosprays. With this firm proof of principle using this design/format, further effort is justified in developing similar emitters in alternative materials that better prevent surface wetting and allow greater hole density, ultimately leading to greater signal enhancement.

Fabrication of Patterned Superhydrophobic/Hydrophilic Substrates by Laser Micromachining for Small Volume Deposition and Droplet-Based Fluorescence

The deposition of nanoliter and subnanoliter volumes is important in chemical and biochemical droplet-based microfluidic systems. There are several techniques that have been established for the deposition/generation of small volumes including the use of surfaces with patterned differences in wettability. Many such methods require complex and time-consuming lithographic techniques. Here, we present a facile method for the fabrication of superhydrophobic surfaces with patterned hydrophilic regions by laser micromachining. A comprehensive study of fabrication parameters (laser machining speed, laser power, and patch size) on the material, patch wettability, and droplet volume is presented. Patch sizes as small as 100 μm diameter and as large as 1500 μm diameter were investigated, and volumes as low as 400 pL were observed. As an example application of such patterned materials and the deposition of small volumes, halide salts were preconcentrated on the hydrophilic patches, and their fluorescence quenching constants were rapidly calculated using a 3D-printed device coupled to a fluorescence spectrometer.