n -丁基黄药和二丁基黄药在金属载体和金红石上吸附特性的原位原子力光谱比较研究

IF 0.5 Q4 CHEMISTRY, MULTIDISCIPLINARY Journal of Siberian Federal University. Chemistry Pub Date : 2019-09-01 DOI:10.17516/1998-2836-0131
A. Karacharov, M. Likhatski
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引用次数: 1

摘要

研究了丁基黄药钾和二丁基黄药与金属Ti、不锈钢和α-TiO2表面的相互作用。用固滴法测量接触角结果表明,用丁基黄药钾水溶液或二丁基黄药乳状液处理初始底物表面,使底物具有更强的疏水性。利用原位原子力光谱,表面活性物质的吸附被证明会增加粘附力的大小和其范围内的作用在接近悬臂尖到疏水和亲水样品的表面。当悬臂顶端从样品表面缩回时,其粘附力和粘附范围均达到最大,最大可达150nm。力曲线更陡峭,这与研究样品表面纳米气泡的形成引起毛细源的远程疏水力有关。二丁基二氧原表现出高活性的试剂性质,在疏水表面和在较小程度上的亲水表面上都能形成纳米级气体结构
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A Comparative Study of Features of Sorption of N-Buthylxanthate and Dibuthyldixanthogen Onto Metallic Supports and Rutile Using in situ Atomic Force Spectroscopy
An interaction of potassium buthylxanthate and of dibuthyldixanthogen with metallic Ti, stainless steel and α-TiO2 surfaces was studied. Contact angle measurements by sessile drop technique showed that the treatment of initial substrate surfaces with potassium buthylxanthate aqueous solution or with dibuthyldixanthogen emulsion render them more hydrophobic. Using in situ atomic force spectroscopy, the sorption of surface active substances was shown to give rise to an increase in both adhesive force magnitude and the range within it acts at the approach of cantilever tip to the surface of both hydrophobic and hydrophilic samples. The maximum of both adhesive force and their range, up to 150 nm, took place in case of retract of cantilever tip from sample surface. Force curves are steeper, which related with the formation of nanobubbles on the surfaces of samples under study arising the longrange hydrophobic force of capillary origin. Dibuthyldixanthogen exhibited highly-active reagent properties inducing the formation of nanoscale gas structures on both hydrophobic and, in less extent, hydrophilic surfaces
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发文量
13
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