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Search for "nylon" in Full Text gives 33 result(s) in Beilstein Journal of Nanotechnology.
Facile synthesis of water-soluble carbon nano-onions under alkaline conditions
Beilstein J. Nanotechnol. 2016, 7, 758–766, doi:10.3762/bjnano.7.67
- and cleaned crucibles. In order to prepare C-dots, the homogenized sample was carbonized in a muffle furnace directly at 240 °C in atmospheric oxygen for 2 h. The residue was then dissolved in about 25 mL Milli-Q water, filtered through 0.45 μm nylon filter and the solution was purified by dialysis
- by nylon filters (0.45 μm). The filtered solution was then purified through dialyzer tube (MWCO, 3.5 kDa) for 3 days. Each purified solution was divided into two aliquots, the first one was dried completely for characterization analysis (dark-brown solid), while the second was used for the analysis
Comparative kinematical analyses of Venus flytrap (Dionaea muscipula) snap traps
Beilstein J. Nanotechnol. 2016, 7, 664–674, doi:10.3762/bjnano.7.59
- Freiburg. General cinematographic analyses For filming fast closure motions, traps were stimulated with a nylon thread on the trigger hairs of one lobe and recorded with a high-speed camera (Motion Scope Y4, Redlake, USA, recording speed 100 fps) in combination with a macro objective lens (Zeiss Makro
Gold nanoparticles covalently assembled onto vesicle structures as possible biosensing platform
Beilstein J. Nanotechnol. 2016, 7, 655–663, doi:10.3762/bjnano.7.58
- temperature of 20.0 ± 0.1 °C. The measurements were made by diluting the samples in a cuvette with distilled water. The water was filtered three times by using an Acrodisc with 0.45 µm Nylon membrane (Agilen) to remove dust or particles. To obtain valid results from DLS measurements, the knowledge of the
Organic and inorganic–organic thin film structures by molecular layer deposition: A review
Beilstein J. Nanotechnol. 2014, 5, 1104–1136, doi:10.3762/bjnano.5.123
- to make nylon 66 [8][50]. In the earlier work done by Shao et al. [8] the films were grown through polycondensation. The in situ FTIR studies by Du et al. [50] indicate that the deposition of nylon 66 displays characteristic ALD-type growth, i.e., linearity and self-limiting growth with the different
- precursor exposure lengths, although some ammonium chloride salt formation was observed. The highest GPC values for nylon 66 were 13.1 Å per cycle when deposited at 60 °C on pretreated Si(100) [8] and up to 19 Å per cycle on KBr substrates at the deposition temperature of 83 °C [50]. The latter value is
- somewhat higher than what the predicted unit-chain length, 17.4 Å, would suggest: This higher than predicted growth rate was attributed to a CVD-type growth. Kubono et al. [6] deposited nylon 79 from heptane-1,7-diamine and nonanedioyl dichloride at room temperature. The GPC value achieved, 18 Å per cycle
Measuring air layer volumes retained by submerged floating-ferns Salvinia and biomimetic superhydrophobic surfaces
Beilstein J. Nanotechnol. 2014, 5, 812–821, doi:10.3762/bjnano.5.93
- hanging them into a bend close to the tip of the needle with nylon strings, thereby ensuring a fixed lever arm between the applied weight and the strain gauge (Figure 5a). The change in resistance generated through the bending of the beam by buoyancy forces of the attached specimen was measured by means
- rectangular plastic straps using a polyvinylsiloxane (President Light Body, ISO 4823, Coltene Whaledent, Hamburg, Germany). Wafer replicas showed negative buoyancy without further modification. Wafers and mounted leaves were attached to two slings of nylon string (0.1 mm diameter), with which they were then
- measurement setup. a) Schematic drawing of the measurement setup. A bent metal needle is glued to a silicon strain gauge sensor and submerged under water. Specimens with air layer were hung onto the needle by nylon strings. b) Calibration curve of the force transducer using nine weights in the range between 1
Porous polymer coatings as substrates for the formation of high-fidelity micropatterns by quill-like pens
Beilstein J. Nanotechnol. 2013, 4, 377–384, doi:10.3762/bjnano.4.44
- 10.3762/bjnano.4.44 Abstract We explored the potentials of microarray printing using quill-like microcantilevers onto solid supports that are typically used in microspot printing, including paper, polymeric nitrocellulose and nylon membranes. We compared these membranes with a novel porous poly(2
- cell analysis) and medical applications in diagnostics such as the detection of pathogens or antibodies. Nitrocellulose films and nylon membranes are widely used as carriers for microarrays, usually with spot sizes in the range of 100 to 500 µm, easily accessible for current inkjet and spotting
- minute. However, technically the writing speed can be increased by the use of cantilever arrays, with the added option of intrinsic multiplexing [10]. Comparison of substrates First, we compared four different substrate systems (i.e., plain paper, nylon membrane, nitrocellulose, and a HEMA porous polymer
Synthesis and catalytic applications of combined zeolitic/mesoporous materials
Beilstein J. Nanotechnol. 2011, 2, 785–801, doi:10.3762/bjnano.2.87
- with the aid of TS-1 as catalyst. Ammoximation of cyclohexanone: This reaction is of major interest as cyclohexanone oxime is the intermediate in the manufacturing of caprolactam, the monomer for nylon 6. Conversion and selectivity of cyclohexanone to oxime is over 99% and the yield based on H2O2 is
Detection of interaction between biomineralising proteins and calcium carbonate microcrystals
Beilstein J. Nanotechnol. 2011, 2, 222–227, doi:10.3762/bjnano.2.26
- % sodium dodecyl sulfate (SDS), 10 mM dithiothreitol (DTT), and 10 mM Tris-HCl (pH 8.0). 2.5 mL of the supernatant liquid (protein solution, P) was filtered (NALGENE syringe filters with nylon membranes, pore size: 0.2 μm) and divided into 12 parts (first one 1.0 mL, the others 0.5 mL) with a PD-10 gel
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