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Molecularly imprinted polymer hollow spheres (MIHSs) were produced by using hexanitrohexaazaisowurtzitane (HNIW or CL-20) as a template, silica nanospheres as a sacrificial matrix, acrylamide as a functional monomer, ethylene glycol dimethacrylate as a cross-linker and acetonitrile as a porogen at 4 °C under UV irradiation. This sorbent was applied to the selective solid-phase extraction (SPE) of several explosives simultaneously by using a newly-developed SPE procedure. For the first time, 2,4,6-trinitrotoluene (TNT), 1,3,5-trinitro-1,3,5-triazacyclohexane (RDX), 1,3,5,7-tetranitro-1,3,5,7-tetraazacyclooctane (HMX) and CL-20 were selectively extracted and determined simultaneously from simulated post-blast samples prepared from motor oil and vacuum pump oil. The matrix effects were successfully eliminated and accurate quantization was achieved. When the loading amounts of HMX, RDX, TNT and CL-20 were, respectively, below 10, 2, 5 and 20 nmol for 100 mg of MIHS, these explosives were almost retrieved completely (above 98%). For the MIHSs and non-imprinted polymer hollow spheres (NIHSs), in acetonitrile and methanol, the imprinting factors (IFs) of CL-20 and tetraacetyldibenzylhexaazaisowurtzitane (TADB, a structural analogue of CL-20) changed dramatically, from 7.75 to 1.57 and 0.88 to 2.39, respectively. It highlighted the significant effect of solvents on imprinted sites. [ABSTRACT FROM AUTHOR]

We developed a photonic crystal (PhC) sensor for the quantification of 2,4,6-trinitrotoluene (TNT) in solution. Monodisperse (210 nm in diameter) molecularly imprinted colloidal particles (MICs) for TNT were prepared by the emulsion polymerization of methyl methacrylate and acrylamide in the presence of TNT as a template. The MICs were then self-assembled into close-packed opal PhC films. The adsorption capacity of the MICs for TNT was 64 mg TNT/g. The diffraction from the PhC depended on the TNT concentration in a methanol/water (3/2, v/v) potassium dihydrogen phosphate buffer solution (pH = 7.0, 30 mM). The limit of detection (LOD) of the sensor was 1.03 μg. The color of the molecularly imprinted colloidal array (MICA) changed from green to red with an 84 nm diffraction red shift when the TNT concentration increased to 20 mM. The sensor response time was 3 min. The PhC sensor was selective for TNT compared to similar compounds such as 2,4,6-trinitrophenol, 2,4-dinitrotoluene, 2,6-dinitrotoluene, 2-nitromesitylene, 4-nitrotoluene, 2-nitrotoluene, 1,3-dinitrobenzene, methylbenzene, 4-nitrophenol, 2-nitroaniline, 3-aminophenol and 3-nitroaniline. The sensor showed high stability with little response change after three years storage. This sensor technology might be useful for the visual determination of TNT. [ABSTRACT FROM AUTHOR]

Ion mobility spectrometry (IMS) was explored in the selective detection of nitrobenzene compounds in industrial waste water and surface water, and the selectivity was theoretically elucidated with the transformation energy in the product ion formation reaction. A linear detection range of 0.5–50 ppm and a limit of detection (LOD) of 0.1 ppm were found for 2,4,6-trinitrotoluene (TNT). With the IMS as the detection system of molecularly imprinted polymer (MIP) separation technique, the MIP-IMS system was proved to be excellent method to detect trace amount of nitrobenzene compounds in surface water, in which more than 87% of nitrobenzene compounds could be adsorbed on MIPs with 90–105% of recovery. [ABSTRACT FROM AUTHOR]

As a typical antibiotic that is harmful to the health of human beings and widely used in animal husbandry, oxytetracycline (OTC) has a potential threat to the food safety. Therefore, the design of portable sensors for efficiently monitoring trace amounts of OTC in foods is vital to maintain safe food supply in our daily life. Herein, a two-dimensional (2D) molecularly imprinted photonic crystal hydrogel (MIPCH) sensor for the detection of OTC was fabricated by combining the photonic crystal (PC) method and molecular imprinting technique. In this regard, OTC was used as imprinted template to form the MIPCH sensor with specific binding sites during polymerization. After the removal of template, the obtained MIPCH possessed the specific nanocavities that were complementary to target compound, OTC. In addition, the response of the MIPCH to tetracyclines (TCs) in aqueous solution was monitored through a readable change of Debye diffraction ring, which is related to the particle spacing variation of MIPCH in response to the target molecules. As the concentration of OTC increased from 0 to 60 μM, the particle spacing of MIPCH sensor increased to about 94 nm and the structural color redshifted from blue to red. More importantly, the detection of OTC in milk sample by this portable, cost-effective MIPCH sensor has also been achieved at the same range of OTC. With the increasing concentration of OTC in milk sample, the particle spacing of MIPCH sensor increased about 92 nm and the structural color of MIPCH changed from blue through green to orange. Image 1 • A novel 2D molecularly imprinted PC was developed for the fast screening of trace level residues of OTC in milk. • The detection could be realized by naked eyes through observing the diffraction ring or structural color. • The sensor also showed advantages in easy preparation and specificity towards the targets. [ABSTRACT FROM AUTHOR]