In this study, the performances of H2S, NH3, and HCl sensors for real-time monitoring in small emission facilities (4, 5 grades in Korea) were evaluated at high concentration conditions of those gases. And the proper approach for the collection of reliable measurement data by sensors was suggested through finding out the effect on sensor performances according to changes in temperature and humidity (relative humidity, RH) settings. In addition, an assessment on sensor data correction considering the effects produced by environmental settings was conducted. The effects were tested in four different conditions of temperature and humidity. The sensor performances (reproducibility, precision, lower detection limit (LDL), and linearity) were good for all three sensors. The intercept (ADC0) values for all three sensors were good for the changes of temperature and humidity conditions. The variation in the slope value of the NH3 sensor showed the highest value, and this was followed by the HCl, H2S sensors. The results of this study can be helpful for data collection by enabling the more reliable and precise measurements of concentrations measured by sensors.

The electrochemical type gas sensor has the advantage of being easy to use due its small size, and it is also relatively inexpensive. However, its output can easily vary depending on temperature and humidity conditions. Therefore, it is important to ascertain the exact output characteristics of a sensor according to the measuring environment in order to improve measurement accuracy for any set of given conditions. The purpose of this study is to obtain basic information about the output characteristics of a sensor that is used both indoor and outdoor according to the variation in temperature and humidity conditions in order to improve the accuracy of the sensor. To achieve this result, a calibration curve was made using ammonia standard gas and the calibration factor was calculated using the calibration curve and the measuring accuracy was confirmed with regard to the ammonia sensor. Based on the test results, the variation of the sensor output value was large in relation to temperature and humidity variation. It was found that the output value from the sensor at higher temperature and humidity conditions was also higher. However, the measuring accuracy of the sensor could be improved by more than 10% by applying the calibration factor and an average accuracy of more than 97% could be achieved. It is anticipated that the result of this study can be used as basic data to obtain more accurate results using electrochemical sensors for a given set of temperature and humidity conditions, and therefore, it can also be considered that the reliability and applicability of electrochemical sensors can be improved.

산업이 발달함에 따라 이산화탄소, 휘발성 유기 화합물, 일산화탄소 등과 같은 독성 가스의 감지 및 모니터링이 중요시되고 있다. 새롭게 합성된 0 차원의 비납계 무기 페로브스카이트 소재는 광학적 방법과 전기적 방법을 융합하여 사용할 수 있는 가스 센서 특성을 가진다. 친환경 가스 센서는 결정의 상변이를 기반으로, 광학 및 전기적 특성 변화를 가져 하이드록실기 감지가 가능하며, 하이드록실기 극성과의 상관관계를 통해 차세대 센서 소자로의 응용 가능성이 기대된다.

Four types of metal oxide semiconductor gas sensor arrays were used to observe the aroma and spoilage odor emitted during the ripening process of plum & banana fruits. All gas sensors showed a high correlation (R=0.82~0.90) with the olfactory. The TGS 2603 sensor showed a high correlation of 0.90 between the odor generated and sensory perception of smell in the process of ripening and decaying fruits. In addition, it showed a very high correlation of 0.91 with the decay rate of the plum sample, and the significance probability through one-way ANOVA was also less than 0.05, which confirmed it as an optimal gas sensor (TGS 2603). Principal component analysis was performed using all the data. The cumulative variability was 99.54%, which could be explained only by two principal components, and the first principal component was 95.11%, which was related to the freshness of the fruit. It was analyzed as fresh fruit in the negative(-) direction and decayed fruit in the positive(+) direction.

We used three gas sensors to monitor hydrogen sulfide, ammonia, and volatile organic compounds (VOCs), which were frequently emitted from environmental facilities, such as municipal wastewater treatment, livestock manure treatment, and food waste composting facilities. Two electrochemical (EC) sensors for detecting hydrogen sulfide and ammonia, and a photoionization detector (PID) sensor for detecting VOCs were characterized in this study. The performance of their linearity by concentration levels, lower detection limit (LDL), repeatability, reproducibility, precision, and response time were tested under the laboratory condition. The linearity according to concentration levels were favorable for all three sensors with high correlation coefficients (R2 > 0.98). The ammonia sensor showed the highest LDL (18.6 ppb) and the hydrogen sulfide and VOC sensors showed 22.3 ppb and 26.7 ppb of LDL, respectively. The reproducibility and precision were favorable for all three sensors, indicating a lower relative standard deviation (RSD) than 0.9% in the reproducibility test and 7.2% in the precision test. The response times to reach target concentration were varied from 1 to 12 minutes. The ammonia sensor needed 12 minutes of response time at 1 ppm target the NH3 concentration and the hydrogen sulfide and VOC sensors needed less than 2 minutes of response time.

The gas sensor is essential to monitoring dangerous gases in our environment. Metal oxide (MO) gas sensors are primarily utilized for flammable, toxic and organic gases and O3 because of their high sensitivity, high response and high stability. Tungsten oxides (WO3) have versatile applications, particularly for gas sensor applications because of the wide bandgap and stability of WO3. Nanosize WO3 are synthesized using the hydrothermal method. Asprepared WO3 nanopowders are in the form of nanorods and nanorulers. The crystal structure is hexagonal tungsten bronze (MxWO3, x =< 0.33), characterized as a tunnel structure that accommodates alkali ions and the phase stabilizer. A gas detection test reveals that WO3 can detect acetone, butanol, ethanol, and gasoline. This is the first study to report this capability of WO3.

Nickel oxide(NiO) thin films, nanorods, and carbon nanotube(CNT)/NiO core-shell nanorod structures are fabricated by sputtering Nickel at different deposition time on alumina substrates or single wall carbon nanotube templates followed by oxidation treatments at different temperatures, 400 and 700 oC. Structural analyses are carried out by scanning electron microscopy and x-ray diffraction. NiO thinfilm, nanorod and CNT/NiO core-shell nanorod structurals of the gas sensor structures are tested for detection of H2S gas. The NiO structures exhibit the highest response at 200 oC and high selectivity to H2S among other gases of NO, NH3, H2, CO, etc. The nanorod structures have a higher sensing performance than the thin films and carbon nanotube/NiO core-shell structures. The gold catalyst deposited on NiO nanorods further improve the sensing performance, particularly the recovery kinetics.

In2O3 doped WO3 powders were prepared by a polymer solution route and their NO2 gas sensing properties were analyzed. The synthesized powders showed nano-sized particles with specific surface areas of 6.01~21.5 m2/g and the particle size and shape changed according to the content of In2O3. The gas sensors fabricated with the synthesized powders were tested at operating temperatures of 400~500 oC and 100~500 ppm concentrations of NO2 atmosphere. The particle size and In2O3 content affected on the initial sensor resistance in an air atmosphere. The highest sensitivity (8.57 at 500 oC), which was 1.77 higher than the sensor consisting of the pure WO3 sample, was measured in the 0.5 mol% In2O3 doping sample. In addition, the response time and recovery time were improved by the addition of In2O3.

Urchin-structured zinc oxide(ZnO) nanorod(NR) gas sensors were successfully demonstrated on a polyimide(PI) substrate, using single wall carbon nanotubes(SWCNTs) as the electrode. The ZnO NRs were grown with ZnO shells arranged at regular intervals to form a network structure with maximized surface area. The high surface area and numerous junctions of the NR network structure was the key to excellent gas sensing performance. Moreover, the SWCNTs formed a junction barrier with the ZnO which further improved sensor characteristics. The fabricated urchin-structured ZnO NR gas sensors exhibited superior performance upon NO2 exposure with a stable response of 110, fast rise and decay times of 38 and 24 sec, respectively. Comparative analyses revealed that the high performance of the sensors was due to a combination of high surface area, numerous active junction points, and the use of the SWCNTs electrode. Furthermore, the urchin-structured ZnO NR gas sensors showed sustainable mechanical stability. Although degradation of the devices progressed during repeated flexibility tests, the sensors were still operational even after 10000 cycles of a bending test with a radius of curvature of 5 mm.

The changes in the aroma and spoilage odor emitted from eleven ‘Hongro’ apples during ten weeks’ storage were investigated using six types of metal oxide semiconductor gas sensor arrays. The gas sensors used in the evaluation were sensitive to apple-emitted aroma or spoilage odor, and a high reproducibility of 5% relative standard deviation or less was confirmed. Significantly, the change in apple-emitted aroma or spoilage odor was easily distinguished by the optimal gas sensor and a significant correlation (r=0.992) between decay rate and sensitivity change was observed. The results of a principal component analysis of the signal patterns obtained by data standardization using the optimal gas sensor showed a clear classification between decayed sampler groups and undecayed sampler groups.

This study was designed to assess the odor characteristics of paprika with metal oxide gas sensors. Non-decayed paprika and decayed paprika were assessed by sensor array system comprising 10 kinds of sensors. Three representative sensors were selected from among the 10. Selection was based on a correlation analysis between sensors from the results of the sensor array assessment on non-decayed paprika. It was found that the odor variation characteristics of paprika can be assessed by metal oxide gas sensors and that the odor variation characteristics of paprika are different depending on the type of gas sensors. The odor characteristics of paprika were different according to the color, the presence or absence of decay, the location of decay, the type of sensor, and the passage of time. Regardless of decay, the sensor response value of orange paprika was the highest, with the 2611 sensor yielding the highest response value. The SB-AQ1 sensor could not identify the difference in odor characteristics depending on the location of decay, while detection was possible by both SB-41 and 2611 sensors.

The gas sensor sensitivity value of three methods (simple application method, vaporization method, and chamber method) were compared in order to establish a method for the measurement of liquid odor substances. In order to select the representative sensors from among the 16 sensors constituting the gas sensor array, cluster analysis, regression analysis, and correlation analysis were performed. Sensors with excellent correlation in terms of reactivity were selected as representative sensors of each measurement method. As a result, it was shown that the reactivity and the correlation increased in the order of simple application method < vaporization method < chamber method. Through a variance analysis using the sensitivity values of selected representative sensors, it was shown that the simple application method had statistical significance at the level of 99.9% (p<0.001) in three of the representative sensors in four clustering groups. The vaporization method and the chamber method showed statistical significance at a level of 99.9% (p<0.001) for all representative sensors in each clustering group. If the reactivity were improved by controlling the sensitivity of the sensor, the simple application method and vaporization method could also be used as a method of measuring the liquid material with gas sensor array.

SnO2:CNT thick films for gas sensors were fabricated by screen printing method on alumina substrates and were annealed at 300 oC in air. The nano SnO2 powders were prepared by solution reduction method using tin chloride (SnCl2.2H2O), hydrazine (N2H4) and NaOH. Nano SnO2:CNT sensing materials were prepared by ball-milling for 24h. The weight range of CNT addition on the SnO2 surface was from 0 to 10 %. The structural and morphological properties of these sensing material were investigated using X-ray diffraction and scanning electron microscopy and transmission electron microscope. The structural properties of the SnO2:CNT sensing materials showed a tetragonal phase with (110), (101), and (211) dominant orientations. No XRD peaks corresponding to CNT were observed in the SnO2:CNT powders. The particle size of the SnO2:CNT sensing materials was about 5~10 nm. The sensing characteristics of the SnO2:CNT thick films for 5 ppm H2S gas were investigated by comparing the electrical resistance in air with that in the target gases of each sensor in a test box. The results showed that the maximum sensitivity of the SnO2:CNT gas sensors at room temperature was observed when the CNT concentration was 8wt%.

Fabrication of iron oxide/carbon nanotube composite structures for detection of ammonia gas at room temperature is reported. The iron oxide/carbon nanotube composite structures are fabricated by in situ co-arc-discharge method using a graphite source with varying numbers of iron wires inserted. The composite structures reveal higher response signals at room temperature than at high temperatures. As the number of iron wires inserted increased, the volume of carbon nanotubes and iron nanoparticles produced increased. The oxidation condition of the composite structures varied the carbon nanotube/iron oxide ratio in the structure and, consequently, the resistance of the structures and, finally, the ammonia gas sensing performance. The highest sensor performance was realized with 500 oC/2 h oxidation heat-treatment condition, in which most of the carbon nanotubes were removed from the composite and iron oxide played the main role of ammonia sensing. The response signal level was 62% at room temperature. We also found that UV irradiation enhances the sensing response with reduced recovery time.

Impedancemetric NOx (NO and NO2) gas sensors were designed with a stacked-layer structure and fabricated using LaCrxCo1-xO3 (x = 0, 0.2, 0.5, 0.8 and 1) as the receptor material and Li1.3Al0.3Ti1.7(PO4)3 plates as the solid-electrolyte transducer material. The LaCrxCo1-xO3 layers were prepared with a polymeric precursor method that used ethylene glycol as the solvent, acetyl acetone as the chelating agent, and polyvinylpyrrolidone as the polymer additive. The effects of the Co concentration on the structural, morphological, and NOx sensing properties of the LaCrxCo1-xO3 powders were investigated with powder Xray diffraction, field emission scanning electron microscopy, and its response to 20~250 ppm of NOx at 400 oC (for 1 kHz and 0.5 V), respectively. When the as-prepared precursors were calcined at 700 oC, only a single phase was detected, which corresponded to a perovskite-type structure. The XRD results showed that as the Co concentration of the LaCrxCo1-xO3 powders increased, the crystal structure was transformed from an orthorhombic phase to a rhombohedral phase. Moreover, the LaCrxCo1-xO3 powders with 0 ≤ x < 0.8 had a rhombohedral symmetry. The size of the particles in the LaCrxCo1-xO3 powders increased from 0.1 to 0.5 μm as the Co concentration increased. The sensing performance of the stack-structured LaCrxCo1-xO3/Li1.3Al0.3Ti1.7(PO4)3 sensors was found to divide the impedance component between the resistance and capacitance. The response of these sensors to NO gas was more sensitive than that to NO2 gas. Compared to other impedancemetric sensors, the LaCr0.8Co0.2O3/Li1.3Al0.3Ti1.7(PO4)3 sensor exhibited good reversibility and reliable sensingresponse properties for NOx gases.

Nanorod ZnO and spherical nano ZnO for gas sensors were prepared by hydrothermal reaction method and hydrazine method, respectively. The nano-ZnO gas sensors were fabricated by a screen printing method on alumina substrates. The gas sensing properties were investigated for hydrocarbon gas. The effects of Co concentration on the structural and morphological properties of the nano ZnO:Co were investigated by X-ray diffraction and scanning electron microscope (SEM), respectively. XRD patterns revealed that nanorod and spherical ZnO:Co with a wurtzite structure were grown with (1 0 0), (0 0 2), (1 0 1) peaks. The sensitivity of nanorod and spherical ZnO:Co sensors was measured for 5 ppm CH4 and CH3CH2CH3 gas at room temperature by comparing the resistance in air with that in target gases. The highest sensitivity to the CH4 and CH3CH2CH3 gas of spherical nano ZnO:Co sensors was observed at Co 6 wt%. The spherical nano ZnO:Co sensor exhibited a higher sensitivity to hydrocarbon gas than nanorod ZnO.