A polymer lab chip sensor with microfabricated planar silver electrode for continuous and on-site heavy metal measurement

This paper presents a reusable polymer lab chip sensor for continuous and on-site heavy metal monitoring in nature. In particular, detection of lead (Pb(II)), which is the most common heavy metal pollutant, has been performed using the proposed lab chip sensor. The miniaturized lab chip sensor consists of a microfabricated silver working electrode that replaces the conventional mercury and bismuth electrodes, an integrated silver counter and quasi-reference electrode, and microfluidic channels. The proposed sensor targets on-site environmental monitoring in a continuous fashion without disturbing or contaminating the sensing environment when it is reused. The reusability of the miniaturized lab chip sensor was characterized through forty-three consecutive measurements in non-deoxygenating standard solutions inside the microchannels using square-wave anodic stripping voltammetry (SWASV). With only 13.5 μL of sample volume the sensor chip showed a correlation coefficient of 0.998 for the Pb(II) concentration range of 1-1000 ppb with the limit of detection of 0.55 ppb at 300 s deposition time. The peak potentials during the forty-three consecutive SWASV measurements showed a relative standard deviation of 1.0%, with a standard deviation of 0.005 V. The high repeatability and linearity of the sensor over the large, three orders of magnitude, dynamic range of 1-1000 ppb showed that the developed sensor chip can be reused for a variety of on-site measurements such as for soil pore water or groundwater, using only micro-volumes.     

Micro-hotplates for high-throughput thin film processing and in situ phase transformation characterization

This paper presents the use of micro-hotplates (MHPs) as thermal processing and in situ characterization platforms for phase transformations in thin films. MHPs are fabricated by microsystem technology processes and consist of a SiO₂/Si₃N₄ membrane (app. 1 μm) supported by a bulk Si frame. Several embedded Pt thin films serve as heater and electrical measurement electrodes. It is shown that the MHPs have unique properties for the controlled annealing of thin film materials (up to 1270 K), as the annealing temperature and heating/cooling rates can be precisely controlled by in situ measurements. These rates can be extremely high (up to 10⁴ K/s), due to the low thermal mass of MHPs. The high cooling rates are especially useful for the fabrication of metastable phases (e.g. Fe₇₀Pd₃₀) by quenching. By measuring the resistivity of a thin film under test in situ as a function of the MHP temperature, microstructural changes (e.g. phase transformations) can be detected during heating and cooling cycles. In this paper, examples are presented for the determination of phase transitions in thin films using MHPs: the solid–liquid–gas phase transition (Al), the ferromagnetic–paramagnetic phase transition (Fe–Pt) and martensitic transformations (Ni–Ti–Cu, Fe–Pd). Furthermore, it is demonstrated that crystallization processes from amorphous to crystalline (Ni–Ti–Cu) can be detected with this method. Finally the application of MHPs in thin film combinatorial materials science and high-throughput experimentation is described.     

Simultaneous measurement of Pb, Cd and Zn using differential pulse anodic stripping voltammetry at a bismuth/poly(p-aminobenzene sulfonic acid) film electrode

A novel sensor was developed for simultaneous detection of Pb, Cd and Zn, based on the differential pulse anodic stripping response at a bismuth/poly(p-aminobenzene sulfonic acid) (Bi/poly(p-ABSA)) film electrode. This electrode was generated in situ by depositing simultaneously bismuth and the metals by reduction at −1.40 V on the poly(p-ABSA) modified electrode. Compared with the bismuth film electrode, the Bi/poly(p-ABSA) film electrode can yield a larger stripping signal for Pb, Cd and Zn. Under the optimum conditions, a linear response was observed for Cd and Zn in the range from 1.00 to 110.00 μg L⁻¹ and for Pb in the range from 1.00 to 130.00 μg L⁻¹. The detection limits of Pb(II), Cd(II) and Zn(II) were 0.80, 0.63 and 0.62 μg L⁻¹, respectively. Finally this sensor had been applied to the simultaneous determination of Pb(II), Cd(II) and Zn(II) in river water samples and the results were quite corresponding to the value obtained by atomic absorption spectrometry.     

In situ modification of lipid-loaded MCM-41 channels with bovine serum albumin at a planar lipid bilayer for biosensing

An in situ method for modifying a receptor site on mesoporous silica MCM-41 channels in planar lipid bilayers is described, in which bovine serum albumin (BSA) is covalently linked to the MCM-41 channels via head groups of lipids loaded in the nanopores. Prior to receptor modification, lipid-loaded MCM-41 channels were incorporated with lipid bilayers formed at an aperture of a Teflon film. The in situ coupling of BSA to lipid-loaded MCM-41 channels at the lipid bilayer interface was achieved by the sulfhydryl coupling method. The lipid bilayers containing BSA-modified MCM-41 exhibited channel-like currents, which were augmented in a concentration-dependent manner by the addition of anti-BSA at fM level. The in situ modification of lipid-loaded MCM-41 channels with BSA by the amine coupling technique was also investigated. The potential of the present approach for the development of channel-type biosensors is discussed in terms of modifying bilayer interfaces with bioreceptors.