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Recently, the generation of spatial gradient nanoparticle assemblies has attracted much attention. Such assemblies can be intriguing templates for building novel molecular architectures, and be employed as a combinatorial tool for quick determination of interaction selectivity for nanoparticles. In this communication, we report on convenient contact printing based techniques for generating lateral gradients containing nanoparticles with tunable geometry, scale and steepness. In the first method, octadecyltrichlorosilane (OTS) gradient surfaces were generated via the contact printing approach, and then spaces un-occupied by OTS molecules were back-filled with an amine-terminated silane, which allows the grafting of nanoparticles that were surface functionalized with carboxylic acid. By varying the size and geometry of the stamp, different geometrical gradients were generated. In addition, by changing the stamping procedures, either well-defined stepwise gradients or continuous gradients can be achieved. Furthermore, the contact printing based technique can be utilized in combination with diffusion of the aminosilane molecules to directly create its gradient, and consequently a nanoparticle density gradient.  相似文献   
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This paper presents a simple and low-cost method for patterning poly(dimethylsiloxane) (PDMS) barriers in porous support such as paper for the construction of flexible microfluidic paper-based analytical devices (μPADs). The fabrication method consisted of contact-printing a solution of PDMS and hexane (10:1.5 w/w) onto chromatographic paper using custom-designed rubber stamps containing the patterns of μPADs. After penetrating the paper (∼30 s), the PDMS is cured to form hydrophobic barriers. Under optimized conditions, hydrophobic barriers and hydrophilic channels with dimensions down to 949 ± 88 μm and 771 ± 90 μm (n = 5), respectively, were obtained. This resolution is well-suitable for most applications in analytical chemistry. Chemical compatibility studies revealed that the PDMS barriers were able to contain some organic solvents, including acetonitrile and methanol, and aqueous solutions of some surfactants. This find is particularly interesting given that acetonitrile and methanol are the most used solvents in chromatographic separations, non-aqueous capillary electrophoresis and electroanalysis, as well as aqueous solutions of surfactants are suitable mediums for cell lyses assays. The utility of the technique was evaluated in the fabrication of paper-based electrochemical devices (PEDs) with pencil-drawn electrodes for experiments in static cyclic voltammetry and flow injection analysis (FIA) with amperometric detection, in both aqueous and organic mediums.  相似文献   
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