The influence of relative humidity
(RH) on adhesion forces demands
clarification. Adhesion forces at silica/silica and silica/graphene
interfaces were measured on an atomic force microscope to investigate
the evolution behaviors with RH and the contact time dependence at
a certain RH. For the silica/silica interface, the adhesion force
at a location by decreasing RH is independent of RH, but increases
as a whole with RH both at a location and in the force volume mode
by increasing RH. However, for the silica/graphene interface at a
location, the adhesion force remains unchanged with RH as a whole
by reducing RH and tends to decrease as a whole by increasing RH.
In the force volume mode, the adhesion force at the silica/graphene
interface is independent of RH. For the silica/silica interface, the
adhesion force increases logarithmically with dwell time at a low
RH and remains unchanged at a high RH. However, for the silica/graphene
interface, the force is not dependent on RH at low and high RHs. The
results can serve to further understand the mechanisms and behaviors
of adhesion forces and promote the anti-adhesion design for small-scale
silicon-based structures.
A novel approach of periodate oxidation coupled with high-performance liquid chromatography (HPLC)-fluorescence detection (FLD) for the quantitative determination of 3-chloro-1,2-propanediol (3-MCPD) has been established. The essence of this approach lies in the production of chloroacetaldehyde by the oxidization cleavage of 3-MCPD with sodium periodate and the HPLC analysis of chloroacetaldehyde monitored by an FLD detector after fluorescence derivatization with adenine. The experimental parameters relating to the efficiency of the derivative reaction such as concentration of adenine, chloroacetaldehyde reaction temperature, and time were studied. Under the optimized conditions, the proposed method can provide high sensitivity, good linearity (r(2) = 0.999), and repeatability (percent relative standard deviations between 2.57% and 3.44%), the limits of detection and quantification were 0.36 and 1.20 ng/mL, respectively, and the recoveries obtained for water samples were in the range 93.39-97.39%. This method has been successfully applied to the analysis of real water samples. Also this method has been successfully used for the analysis of vegetable oil samples after pretreatment with liquid-liquid extraction; the recoveries obtained by a spiking experiment with soybean oil ranged from 96.27% to 102.42%. In comparison with gas chromatography or gas chromatography-mass spectrometry, the proposed method can provide the advantages of simple instrumental requirement, easy operation, low cost, and high efficiency, thus making this approach another good choice for the sensitive determination of 3-MCPD.
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