Contactless Conductivity Microfluidic Chip for Rapid Determination of Soil Nitrogen and Potassium Content

ObjectiveThe content of nitrogen (N) and potassium (K) in the soil directly affects crop yield, making it a crucial indicator in agricultural production processes. Insufficient levels of the two nutrients can impede crop growth and reduce yield, while excessive levels can result in environmental pollution. Rapidly quantifying the N and K content in soil is of great importance for agricultural production and environmental protection.MethodsA rapid and quantitative method was proposed for detecting N and K nutrient ions in soil based on polydimethylsiloxane (PDMS) microfluidic chip electrophoresis and capacitively coupled contactless conductivity detection (C4D). Microfluidic chip electrophoresis enables rapid separation of multiple ions in soil. The electrophoresis microfluidic chips have a cross-shaped channel layout and were fabricated using soft lithography technology. The sample was introduced into the microfluidic chip by applying the appropriate injection voltage at both ends of the injection channel. This simple and efficient procedure ensured an accurate sample introduction. Subsequently, an electrophoretic voltage was applied at both ends of the separation channel, creating a capillary zone electrophoresis that enables the rapid separation of different ions. This process offered high separation efficiency, required a short processing time, and had a small sample volume requirement. This enabled the rapid processing and analysis of many samples. C4D enabled precise measurement of changes in conductivity. The sensing electrodes were separated from the microfluidic chips and printed onto a printed circuit board (PCB) using an immersion gold process. The ions separated under the action of an electric field and sequentially reach the sensing electrodes. The detection circuit, connected to the sensing electrodes, received and regulated the conductivity signal to reflect the variance in conductivity between the sample and the buffer solution. The sensing electrodes were isolated from the sample solution to prevent interference from the high-voltage electric field used for electrophoresis.Results and DiscussionsThe voltage used for electrophoresis, as well as the operating frequency and excitation voltage of the excitation signal in the detection system, had a significant effect on separation and detection performance. Based on the response characteristics of the system output, the optimal operating frequency of 1 000 kHz, excitation voltage of 50 V, and electrophoresis voltage of 1.5 kV were determined. A peak overshoot was observed in the electrophoresis spectrum, which was associated with the operating frequency of the system. The total noise level of the system was approximately 0.091 mV. The detection limit (S/N = 3) for soil nutrient ions was determined by analyzing a series of standard sample solutions with varying concentrations. The detection limited for potassium (K+), ammonium (NH4+), and nitrate (NO3‒) standard solutions were 0.5, 0.1 and 0.4 mg/L, respectively. For the quantitative determination of soil nutrient ion concentration, the linear relationship between peak area and corresponding concentration was investigated under optimal experimental conditions. K+, NH4+, and NO3‒ exhibit a strong linear relationship in the range of 0.5~40 mg/L, with linear correlation coefficients (R2) of 0.994, 0.997, and 0.990, respectively, indicating that this method could accurately quantify N and K ions in soil. At the same time, to evaluate the repeatability of the system, peak height, peak area, and peak time were used as evaluation indicators in repeatability experiments. The relative standard deviation (RSD) was less than 4.4%, indicating that the method shows good repeatability. In addition, to assess the ability of the C4D microfluidic system to detect actual soil samples, four collected soil samples were tested using MES/His and PVP/PTAE as running buffers. K+, NH4+,Na+, Chloride (Cl‒), NO3‒, and sulfate (SO43‒) were separated sequentially within 1 min. The detection efficiency was significantly improved. To evaluate the accuracy of this method, spiked recovery experiments were performed on four soil samples. The recovery rates ranged from 81.74% to 127.76%, indicating the good accuracy of the method.ConclusionsThis study provides a simple and effective method for the rapid detection of N and K nutrient ions in soil. The method is highly accurate and reliable, and it can quickly and efficiently detect the contents of N and K nutrient ions in soil. This contactless measurement method reduced costs and improved economic efficiency while extending the service life of the sensing electrodes and reducing the frequency of maintenance and replacement. It provided strong support for long-term, continuous conductivity monitoring.