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DNA/表面活性剂吸附层的相转变。

Phase Transitions in DNA/Surfactant Adsorption Layers.

机构信息

National Taiwan University of Science and Technology , Chemical Engineering Department, 43 Keelung Road, Section 4, 106 Taipei, Taiwan.

Institute of Chemistry, St. Petersburg State University , Universitetsky pr. 26, 198504 St. Petersburg, Russia.

出版信息

Langmuir. 2016 Dec 20;32(50):13435-13445. doi: 10.1021/acs.langmuir.6b03396. Epub 2016 Dec 7.

Abstract

The adsorption layers of complexes between DNA and oppositely charged surfactants dodecyltrimethylammonium bromide (DTAB) and cetyltrimethylammonium bromide (CTAB) at the solution/air interface were studied with surface tensiometry, dilational surface rheology, atomic force microscopy, Brewster angle microscopy, infrared absorption-reflection spectroscopy, and ellipsometry. Measurements of the kinetic dependencies of the surface properties gave a possibility to discover the time intervals corresponding to the coexistence of two-dimensional phases. One can assume that the observed phase transition is of the first order, unlike the formation of microaggregates in the adsorption layers of mixed solutions of synthetic polyelectrolytes and surfactants. The multitechniques approach together with the calculations of the adsorption kinetics allowed the elucidation of the structure of coexisting surface phases and the distinguishing of four main steps of adsorption layer formation at the surface of DNA/surfactant solutions.

摘要

采用表面张力法、动态表面流变法、原子力显微镜、布鲁斯特角显微镜、红外吸收反射光谱法和椭圆偏振法研究了 DNA 与带相反电荷的表面活性剂十二烷基三甲基溴化铵(DTAB)和十六烷基三甲基溴化铵(CTAB)在溶液/空气界面的复合物的吸附层。对表面性质的动力学依赖性的测量使得有可能发现与二维相共存的时间间隔。可以假设,与混合溶液中合成聚电解质和表面活性剂的吸附层中微团簇的形成不同,所观察到的相转变是一级相变。多技术方法以及吸附动力学的计算允许阐明共存表面相的结构,并区分 DNA/表面活性剂溶液表面吸附层形成的四个主要步骤。

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