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This paper reports on the testing and evaluation of a passive autoranging (AR) method designed to dynamically extend the measurement range of a photonic current transducer (PCT) to pave the way toward a realization of a combined metering- and protection-class current sensor. The PCT utilizes a current transformer (CT), a piezoelectric transducer (PZT), and a fiber Bragg grating (FBG) to enable current measurement at multiple points in an electrical power network whereby multiple sensors are deployed and interrogated serially using a single optical fiber. The autoranging technique relies on incorporating static MOSFET switches to instantaneously short individual serially connected CT burdens in response to a measured current magnitude exceeding pre-set thresholds. The AR circuit switching events produce distinctive signal features that are used by the proposed switching algorithm to apply appropriate scaling factors to reconstruct the measured current from the optical signal. It is shown through laboratory experiments that the AR circuit correctly reacts to pre-set burden current thresholds of 130% of the nominal value and 22 times the nominal value, signifying its "metering" and "protection" range boundaries. The circuit reaction time is below 4 ms, rendering it suitable for standard power system protection purposes. Moreover, the operation of the AR circuit is demonstrated for burden currents of up to 100 A for over 1 s, satisfying a test procedure for the secondary CT circuit, as required by some power system operators. It is demonstrated that the proposed switching algorithm allows for a correct reconstruction of the burden currents from the optical signal acquired by the FBG interrogator, offering the potential to realize a dual-class optical current sensor.

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In this paper, we present a novel technique for passively autoranging a photonic current transducer (PCT) that incorporates a current transformer (CT), piezoelectric transducer (PZT) and fiber Bragg grating (FBG). Due to the usage of single-mode fiber and FBG, multiple PCTs can be interconnected and distributed over a long distance, for example along a power network, greatly reducing the cost of sensor deployment and offering other unique advantages. The autoranging technique relies on the usage of multiple, serially connected CT burden resistors and associated static MOSFET switches to realize instantaneous shortening of the resistors in response to increasing measured current. This functionality is realized passively, utilizing a modular, µW-power comparator circuit that powers itself from the electrical energy supplied by the CT within a small fraction of the 50/60 Hz cycle. The resultant instantaneous changes in sensor gain will be ultimately detected by the central FBG interrogator through real-time analysis of the optical signals and will be used to apply appropriate gain scaling for each sensor. The technique will facilitate the usage of a single PCT to cover an extended dynamic range of the measurement that is required to realize a combined metering- and protection-class current sensor. This paper is limited to the description of the design process, construction, and testing of a prototype passive autoranging circuitry for integration with the PCT. The two-stage circuitry that is based on two burden resistors, 1 Ω and 10 Ω, is used to prove the concept and demonstrate the practically achievable circuit characteristics. It is shown that the circuit correctly reacts to input current threshold breaches of approximately 2 A and 20 A within a 3 ms reaction time. The circuit produces distinct voltage dips across burden resistors that will be used for signal scaling by the FBG interrogator.

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A highly sensitive quantum dot (QD)-based western blot assay with extended dynamic range was developed. Bimodal size distribution QD (BQ) immunoprobes composed of small size single QD (7.3 nm) and big size QD nanobead (QB) (82.9 nm) were employed for fluorescent western blot immunoassay on a membrane. Small size QD immunoprobes contributed to wider dynamic range of assay, while big size QB immunoprobes provided higher detection sensitivity. This BQ-based western blot assay can achieve a wide dynamic range (from 7.8 to 4000 ng IgG) and is nearly as sensitive as commercial available ultrasensitive chemiluminescent methods, just using a simple gel imager with UV light (365 nm) excitation and red light filter (610 nm). The fluorescent signals of BQ western blot were stable for 10 min, while chemiluminescent signals faded after 1 min. Moreover, this BQ immunoprobe was utilized for the detection of housekeeping protein and specific target proteins in complex cell lysate samples. The limit of detection of housekeeping protein is 0.25 µg of cell lysate, and the signal intensities were proportional to loading protein amount in a wide range from 0.61 to 80 µg. We believe that this new strategy of bimodal size distribution nanoparticles can also be expanded for other functional nanoparticle-based biological assays to improve the sensitivity and extend the dynamic range. Graphical abstract.

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