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EVALUATION OF PHOSPHATE ION-SELECTIVE MEMBRANES AND COBALT-BASED ELECTRODES FOR SOIL NUTRIENT SENSING

机译:磷酸盐离子选择性膜和钴基电极对土壤养分的评估

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A real-time soil nutrient sensor would allow efficient collection of data with a fine spatial resolution to accurately characterize within-field variability for site-specific nutrient application. Ion-selective electrodes are promising candidates because they have rapid response, directly measure the analyte, and are small and portable. Our goal was to investigate the ability of three different phosphate ion-selective electrodes (two fabricated with organotin compound-based PVC membranes, and one fabricated from a cobalt rod) used in conjunction with Kelowna soil extractant to determine phosphorus over the typical range of soil concentrations. Electrodes using organotin compound-based PVC membranes containing bis(p-chlorobenzyl)tin dichloride as an ionophore exhibited sensitive responses to (HPO{sub}4){sup}(2-) over a range of 10{sup}(-4) to 10{sup}(-1) mol/L in Tris buffer at pH 7. They were nearly insensitive to phosphate when using Kelowna soil extractant as the base solution, perhaps because of the high concentration of fluoride (0.015 mol/L) in the Kelowna solution. In addition, the life of the membranes was less than 14 days. Electrodes using another tin-compound-based PVC membrane containing tributyltin chloride as an ionophore also provided unsatisfactory results, showing much less sensitivity to (H{sub}2PO{sub}4){sup}- than previously reported. The cobalt rod-based electrodes exhibited sensitive responses to (H{sub}2PO{sub}4){sup}- over a range from 10{sup}(-5) to 10{sup}(-1) mol/L total phosphate concentration with a detection limit of 10{sup}(-5) mol/L in the Kelowna solution. This detection range would encompass the typical range of soil phosphorus concentrations measured in agricultural fields. The selectivity of the cobalt electrodes was satisfactory for measuring phosphates in the presence of each of six interfering ions, i.e., (HCO{sub}3){sup}-, Cl{sup}-, Br{sup}-, (NO{sub}3){sup}-, Ac{sup}-, and F{sup}-, with the electrodes being 47 to 1072 times more responsive to phosphate than to the tested interfering ions.
机译:实时土壤养分传感器可以有效收集具有精细空间分辨率的数据,以准确表征特定地点养分施用的田间变异性。离子选择电极是有希望的候选物,因为它们具有快速响应,直接测量分析物,体积小且便于携带的优点。我们的目标是研究将三种不同的磷酸根离子选择电极(两根用有机锡化合物基PVC膜制成,另一根由钴棒制成)与基洛纳土壤萃取剂结合使用的能力,以测定典型土壤范围内的磷浓度。使用含有二氯化双(对氯苄基)锡作为离子载体的有机锡化合物基PVC膜的电极在10 {sup}(-4)范围内表现出对(HPO {sub} 4){sup}(2-)的敏感响应pH值为7的Tris缓冲液中的浓度达到10 {sup}(-1)mol / L。当使用基洛纳土壤萃取剂作为基础溶液时,它们对磷酸盐几乎不敏感,这也许是因为氟中的高浓度(0.015 mol / L)基洛纳解决方案。另外,膜的寿命少于14天。使用另一种包含三丁基氯化锡作为离子载体的锡化合物基PVC膜的电极也不能令人满意,结果显示对(H {sub} 2PO {sub} 4){sup}-的敏感性比以前报道的要低得多。钴棒基电极对(H {sub} 2PO {sub} 4){sup}-的敏感响应范围为10 {sup}(-5)至10 {sup}(-1)mol / L基洛纳溶液中磷酸盐的检出限为10 {sup}(-5)mol / L。该检测范围将包括在农业领域中测得的土壤磷浓度的典型范围。钴电极的选择性对于在六个干扰离子(即(HCO {sub} 3){sup}-,Cl {sup}-,Br {sup}-,(NO { sub} 3){sup}-,Ac {sup}-和F {sup}-,电极对磷酸盐的响应性比被测干扰离子高47至1072倍。

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