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The imprinted polymers were prepared to absorb dichlorophen (DCP) by using mesoporous silica with ordered pores and high specific surface area. Both scanning electron microscopy and transmission electron microscopy results suggested that the mesoporous silica nanosphere pores had a periodic distribution. The imprinted layer of polymers was thin and uniform. The adsorption experiments showed that the adsorption of imprinted polymers was obviously improved due to the presence of mesoporous structure. The maximum adsorption capacity of MSNs@MIPs at 318 K was 91.1 mg/g, and the adsorption process rapidly reached the equilibrium within 40 min. The adsorption isotherm was well fitted by the Freundlich isotherm model, indicating that multimolecular layer adsorption mechanism governs the adsorption of DCP by the polymers. The adsorption of MSNs@MIPs complied with pseudo-second-order kinetic model. Both selective and regenerative experiments demonstrated that MSNs@MIPs can be successfully applied for selective adsorption of DCP.

Flexible photonic devices based on soft polymers enable real-time sensing of environmental conditions in various industrial applications. A myriad of fabrication techniques have been established for producing optical devices, including photo and electron-beam lithography, nano/femtosecond laser writing, and surface imprinting or embossing. However, among these techniques, surface imprinting/embossing is simple, scalable, convenient to implement, can produce nanoscale resolutions, and is cost-effective. Herein, we utilize the surface imprinting method to replicate rigid micro/nanostructures onto a commonly available PDMS substrate, enabling the transfer of rigid nanostructures into flexible forms for sensing at a nanometric scale. The sensing nanopatterned sheets were mechanically extended, and the extension was remotely monitored via optical methods. Monochromatic light (450, 532, and 650 nm) was transmitted through the imprinted sensor under various force/stress levels. The optical response was recorded on an image screen and correlated with the strain created by the applied stress levels. The optical response was obtained in diffraction pattern form from the flexible grating-based sensor and in an optical-diffusion field form from the diffuser-based sensor. The calculated Young’s modulus in response to the applied stress, measured through the novel optical method, was found in a reasonable range compared to the reported range of PDMS (360–870 kPa) in the literature.

Surface imprinting used for protein recognition in functional cavities is highly effective in imprinting biomacromolecules to avoid template encapsulation during the formation of a molecularly imprinted polymer (MIP) matrix. Herein, we introduce a facile surface-imprinting method based on two-step spin-coating and photopolymerization to design highly efficient imprinted sites on polymeric films to detect trypsin (TRY). Well-distributed template imprinting is successfully achieved for maximized sensing responses by controlling the composition of functional monomers and crosslinkers in the precursor solution and the concentration of TRY in the imprinting solution. The MIP film exhibits higher sensitivity (−841 ± 65 Hz/(μg/mL)) with a coefficient of determination of 0.970 and a higher imprinting factor of 4.5 in a 0.24 µg/mL TRY solution compared to the nonimprinted polymer (NIP) film. Moreover, the limit of detection and limit of quantification are calculated to be 25.33 and 84.42 ng/mL, respectively. Finally, the selectivity coefficient is within the range of 3.90–6.78 for TRY against other proteins. These sensing properties are superior to those of the corresponding nonimprinted polymer matrix. Thus, the proposed facile surface-imprinting method is highly effective for protein imprinting with high sensitivity and selectivity.

Using diatom as a material carrier, silane coupling agent aminopropyltrimethoxysilane (APS) was selected as the functional monomer, As (Ⅴ) was used as the template ion, and epichlorohydrin (ECH) was used as the crosslinking agent, the imprinted composite material with natural mineral material as carrier was prepared by the condensation reflux method. The results of scanning electron microscopy, X-ray powder diffraction, Fourier transform infrared spectroscopy and transmission electron microscopy show that the functional monomer APS is grafted successfully on the surface of diatom, and a stable imprinted pore forms after cross-linking with ECH. There are obvious grafts in the pores and surroundings of the diatom, and the internal regularity of the pores is more obvious. The selectivity coefficient of As (Ⅴ) imprinted composites under different binary systems was obtained by selective experiments. The selection ability and utilization prospect of As (Ⅴ) were summarized and evaluated based on experimental data.

Inducing residual stress in metallic glasses (MGs) is recognized to be beneficial for plasticity but the mechanisms on how it affects shear band nucleation, propagation and multiplication remain poorly understood. With the aid of experimental and computational approaches, we address this issue by comparatively studying the deformation behavior of two types of MG samples, which were individually prepared by surface imprinting and photo-chemical etching but having similar surface patterns. Results showed that the imprinted MGs exhibit simultaneously enhanced plasticity and compressive strength, while the etched ones show limited plasticity improvement and reduced strength. The enhanced mechanical properties of the imprinted MGs are attributed to the compressive residual stresses generated near the surfaces, rather than the resultant geometrical pits. Finite element analysis revealed that the residual stress induces obvious stress gradient and inhomogeneous plastic deformation, which facilitate heterogeneous nucleation of multiple shear bands near the surfaces. Complementary atomistic simulations further revealed that the stress gradient resulting from the residual stress slows down the shear banding dynamics and causes deflection and branching, which consequently promotes shear band multiplication during propagation. This work uncovers the interactions between the residual stresses and shear bands, which are useful for processing MGs with desirable mechanical properties.

Investigation of the effect of the polymer synthesis method on physicochemical properties of sorbents is one of the topical problems in the chemistry of macromolecular compounds that has high scientific and practical interest. Determination of the optimal synthesis method will make it possible to create sorbents with physicochemical properties that led to the realization of effective sorption. In this work, we investigated the effect of synthesis methods (Pickering emulsion polymerization and precipitation polymerization in solution) of granular polymers based on 2-hydroxyethyl methacrylate and ethylene glycol dimethacrylate on physicochemical and sorption properties. The synthesis by Pickering emulsion polymerization led to improvement of the n-propyl alcohol diffusion into the polymer network and to the formation of more homogeneous and structurally stable polymer networks. Creating selective polymer networks by Pickering emulsion polymerization compared to precipitation polymerization in solution led to an increase in porosity, creation of more segregated surface of granules, improvement of binding sites availability at the temperature of 37 °C, and formation of the homogeneous sorption surface with high affinity to target molecules at 25 °C and 37 °C. Selective polymers synthesized by both polymerization methods had the largest values of available sorption surfaces areas for target molecules at 37 °C.

In this research, a novel, sulfamethazine, thermosensitive, molecularly-imprinted polymer (MIP) with an obvious core⁻shell structure for the enrichment of sulfamethazine (SMZ), which involved temperature sensitive monomer N-Isopropylacrylamide, functional monomer methacrylic acid and cross-linking agents ethyleneglycol dimethacrylate (EGDMA) and N,N′-methylenebisacrylamide, was successfully compounded using the surface polymerization method. To ensure the best experimental group, we designed and compared three groups of controlled experiments of MIPs with different crosslinking agents. When the adsorption temperature was almost the lower critical solution temperature (LCST) of Poly(N-Isopropylacrylamide), the preparative MIPs showed outstanding adsorption capacity and specific identification to sulfamethazine. Moreover, this allowed the MIPs to better facilitate by combining the template molecules, as well as optimizing the imprinting factor. In addition, after 80 min, the adsorption of the MIPs leveled off and remained constant, and the adsorption quantity reached (a maximum of) at 8.1 mg·g−1.

Molecular imprinting is the technology of creating artificial recognition sites in polymeric matrices which are complementary to the template in their size, shape and spatial arrangement of the functional groups. Molecularly imprinted polymers (MIPs) and their incorporation with various transducer platforms are among the most promising approaches for detection of several analytes. There are a variety of molecular imprinting techniques used for the preparation of biomimetic sensors including bulk imprinting, surface imprinting (soft lithography, template immobilization, grafting, emulsion polymerization) and epitope imprinting. This chapter presents an overview of all of these techniques with examples from particular publications.