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This paper provided a new hybridization strategy for a poly(phenylacetylene)-based CSP. The HCSP exhibited a good solvent tolerability, and the introduction of CHCl3 into the eluent can improve the chiral resolution performance.

Aim and Objective: The similarities comparison of biological sequences is the important task in bioinformatics. The methods of the similarities comparison for biological sequences are divided into two classes: sequence alignment method and alignment-free method. The graphical representation of biological sequences is a kind of alignment-free methods, which constitutes a tool for analyzing and visualizing the biological sequences. In this article, a generalized iterative map of protein sequences was suggested to analyze the similarities of biological sequences. Materials and Methods: Based on the normalized physicochemical indexes of 20 amino acids, each amino acid can be mapped into a point in 5D space. A generalized iterative function system was introduced to outline a generalized iterative map of protein sequences, which can not only reflect various physicochemical properties of amino acids but also incorporate with different compression ratios of component of generalized iterative map. Several properties were proved to illustrate the advantage of generalized iterative map. The mathematical description of generalized iterative map was suggested to compare the similarities and dissimilarities of protein sequences. Based on this method, similarities/dissimilarities were compared among ND5 proteins sequences, as well as ND6 protein sequences of ten different species. Results: By correlation analysis, the ClustalW results were compared with our similarity/dissimilarity results and other graphical representation results to show the utility of our approach. The comparison results show that our approach has better correlations with ClustalW for all species than other approaches and illustrate the effectiveness of our approach. Conclusion: Two examples show that our method not only has good performances and effects in the similarity/dissimilarity analysis of protein sequences but also does not require complex computation.

OBJECTIVE To evaluate risk factors associated with the persistence of human papillomavirus (HPV) after cervical excision in patients with high-grade squamous intra-epithelial neoplasia (HSIL). METHODS A retrospective cohort study enrolled 550 patients who underwent cervical excision for HSIL between January 2015 and January 2018. The effects of various factors were assessed using univariate and multi-variate analyses. RESULTS The mean age of patients was 42.6 [standard deviation (SD) 8.7, range 22-64] years, and the mean duration of follow-up was 29.0 (SD 4.8, range 24-36) months. Persistent HPV infection after cone excision was detected in 78 (14.2%) patients. Univariate logistic regression analysis revealed that advanced age (>35 years), menopausal status, HPV type (HPV16/18), abnormal vaginal micro-ecological morphology, type of excision (loop electrosurgical excision procedure) and positive margin were closely associated with the persistence of HPV. Multi-variate analysis indicated that menopausal status [odds ratio (OR) 4.708, 95% confidence interval (CI) 2.770-8.001; p

As a part of China’s Chang’e-4 lunar far side mission, two lunar microsatellites for low frequency radio astronomy, amateur radio and education, Longjiang-1 and Longjiang-2, were launched as secondary payloads on 20 May 2018 together with the Queqiao L2 relay satellite. On 25 May 2018, Longjiang-2 successfully inserted itself into a lunar elliptical orbit of 357 km × 13,704 km, and became the smallest spacecraft which entered lunar orbit with its own propulsion system. The satellite carried the first amateur radio communication system operating in lunar orbit, which is a VHF/UHF software defined radio (SDR) designed for operation with small ground stations. This article describes and evaluates the design of the VHF/UHF radio and the waveforms used. Flight results of the VHF/UHF radio are also presented, including operation of the radio, performance analysis of downlink signals and the first lunar orbit UHF very-long-baseline interferometry (VLBI) experiment., Satellites with amateur radio communication capabilities have not been operated in lunar orbit before. Here, the authors present the design and performance of a VHF/UHF software-defined radio developed for and tested on lunar microsatellites.

The resistive random access memory (RRAM) devices based on polyvinylpyrrolidone (PVP) and PVP:PVP:zinc oxide nanoparticle (ZnO NP) active layers have bistable electrical switching behavior. Herein, via a series of storage performance tests, it was proved that the ITO/PVP:ZnO/Al device has a higher ON/OFF current ratio and better memory performance than the ITO/PVP/Al device. Moreover, at 13 wt% concentration of ZnO NPs, optimal storage performance was obtained, the switch state current ratio significantly increased, and the threshold voltage obviously decreased. The conduction mechanism of the devices was further discussed. The device having inorganic nanoparticles embedded in the polymer has excellent storage performance, which has potential application value in data storage.

A large number of natural aggregates are used in the field of construction materials, resulting in the exhaustion of natural aggregates. Therefore, looking for an alternative will slow down the consumption of natural aggregates. The sintering method not only consumes a lot of energy to prepare aggregates but also produces a lot of pollutants. In this study, silico-manganese (SM) slag was dried, ground into powder, and used as raw material. Solid and liquid alkaline activator methods were used to prepare SM slag non-burning aggregate (SMNA) by the cold bonding method. The effects of grinding time, amounts of solid and liquid alkaline activators, curing temperature, and the amount of added fly ash on aggregate properties were investigated. The aggregate microstructure was characterized by XRD, SEM, and FTIR methods, and the toxic leaching analysis of aggregate was performed. The results showed that with a fixed amount of liquid activator (16.2% wt.) and solid activator (15% wt.) and fly ash (20% wt.), respectively, and curing was performed at room temperature, the aggregate properties were optimal: the bulk density of 1236.6–1476.9 kg/m3 and the water absorption lower than 4.9–5.5%. The apparent density was 1973.1–2281.6 kg/m3, and the bulk crushing strength was 24.7–27.9 MPa. The XRD, SEM, and FTIR results indicated that amorphous gel could be formed from SM under an alkaline activator, improving the aggregate strength. The results of toxic leaching showed that the aggregate prepared from SM exhibited environmentally friendly characteristics. The SMNA was obtained via the simple and low-energy consumption production process, paving the new way toward large-scale utilization of SM.

Solvent response gels were synthesized by copolymerization of hydrophobic butyl methacrylate (BMA) and hydrophilic methacrylic acid (MAA) with cross-linker N,N′-methylenebis(acrylamide) (BIS) in a ...

In this study, poly(9,9-dioctylfluorene-2,7-diyl) (PFO) was synthesized through the Suzuki reaction, and it was characterized. A sandwich type memory device based on PFO and PFO:ZnO, was fabricated using rotary-coating technology. I–V characteristics of the device were studied, and the effects of ZnO nanoparticle (NP) doping content on the performances of the device were discussed. The best doping content of ZnO NPs was found by processing the experimental results (4.76 wt%). Also, the stability of the device was tested, and it was found that the device remained stable after a long testing period. Furthermore, the switching mechanism of the device was discussed.

Shape-memory hydrogels can be fixed to an arbitrary temporary shape and recover their permanent shape under appropriate stimulus conditions. Their shape-memory behavior and biocompatible mechanical and chemical properties impart them with many biomedical applications. However, like most hydrogels, traditional shape-memory hydrogels suffer from intrinsic brittleness due to the network inhomogeneity and high water content. In the past, the double network (DN) scheme has been proved a robust method to improve the mechanical performance of hydrogels. Although 3D printing of DN hydrogels has been realized before, 3D printable shape-memory DN hydrogels have not been achieved so far. In this work, we propose a one-pot method for printing a biocompatible shape-memory DN hydrogel via fused deposition method. The two networks incorporated to the hydrogel ink are polyacrylamide (PAAm) and gelatin. The PAAm network is covalently cross-linked and responsible for the permanent shape, while the gelatin network has thermoreversible cross-links and responsible for fixing the temporary shape. The DN hydrogel shows 3 to 7 times higher fracture toughness than a single network gelatin or PAAm hydrogel and can be fixed to 300% of its original length under tension and 10% of its original thickness under compression. The ink compositions are tuned for optimal printing quality and shape-memory performance. The robust mechanical integrity and dramatic shape transformation capability of the 3D-printed shape-memory DN hydrogel will open-up new potential applications in transformative medical robots and self-deployable devices.

Traditional shape-morphing hydrogels rely on structural implementation of inhomogeneity inside the material during fabrication to realize predetermined complex shape change upon activation. In recent years, several systems with reprogrammable shape-morphing capabilities have been developed. Among those, the photoresponsive hydrogels offer the best spatial and temporal control. However, for most photoresponsive hydrogels, upon light irradiation, they simultaneously deform, which requires the projection of the light pattern to be continuously adaptive to the deforming gel. It is impractical for complex 3D morphing. In this paper, by incorporating two photodissociable molecules that can form a reactive ion couple upon light activation into one hydrogel, the light irradiation process is decoupled with the morphing process, and the consumption of the reactive ion couple drives the reversible photochemical reaction forward. Consequently, the photochemical reaction efficiency is improved, and the photoresponsive molecules are locked in the activated state until a recovery stimulus is applied. Based on the proposed general scheme, a specific example is given by incorporating the triphenylmethane leucohydroxide and 2-nitrobenzaldehyde molecules into a polyacrylamide hydrogel. The swelling behavior is characterized, and the reprogrammable morphing with precisely controlled geometry is demonstrated.

Dopamine-containing hydrogels were synthesized by copolymerization of dopamine methacrylamide (DMA), N,N-dimethylacrylamide (DMAA), and an N,N'-methylenebisacrylamide (BIS) crosslinker in a mixed solvent of water and DMSO. The association of DMA was formed by simply immersing in water to facilely reinforce the hydrogel due to the introduction of the second physical crosslinking. The tensile strength of the hydrogels was increased greatly and regulated in a wide range from 200 kPa to over 2 MPa. The association of DMA was destroyed upon immersing in DMSO. This reversible formation and dissociation of the association structure endowed the hydrogel with shape memory and actuating capabilities. Rapid shape fixing in water and complete shape recovery in DMSO was realized within several minutes. Bioinspired functional soft actuators were designed based on the reversible association and metal ion coordination of DMA, including fast responsive hydrogel tentacles, programable multiple shape change, reversible and versatile painting and writing "hydrogel paper". The facile preparation and strength regulation provide a new way to design novel soft actuators through solvent exchange, and will inspire more complex applications upon combining the association with other properties of mussel inspired dopamine derivatives.

The dopamine containing hydrogels with rapid responsive shape memory capability were synthesized by a one-pot method. The temporary shape of hydrogel was fixed within 20 s in NaOH solution by the tris-complex crosslinking of metal-ligand complex between Fe3+ ions and catechol groups, while the permanent shape was recovered completely in HCl solution within 60 s upon the change from tris-complex to mono-complex. The hydrogel showed unique spontaneous actuation behavior. It could curl spontaneously without further external force deformation when immersed in NaOH solution again after the first shape recovery in HCl solution. This might be attributed to the competitive result of swelling and additional tris-complex crosslinking formation when immersed in NaOH solution. In addition, the hydrogels also had proper modulus, elongation ratio and tensile strength. Such hydrogel provides a new candidate material for designing soft actuators and robots modulated with spontaneous actuating.

Facile preparation, rapid actuating, and versatile actions are great challenges in exploring new kinds of hydrogel actuators. In this paper, we presented a facile sticking method to prepare Janus bilayer and multilayer hydrogel actuators that benefited from a special tough and adhesive PAA-clay hydrogel. Combining physical and chemical cross-linking reagents, we endowed the PAA gel with both toughness and adhesion. This PAA gel was reinforced by further cross-linking with Fe3+. These two hydrogels with different cross-linking densities exhibited different swelling capabilities and moduli in the media manipulated by pH and ionic strength, thus acting as promising candidates for soft actuators. On the basis of these gels, we designed hydrogel actuators of rapid response in several minutes and precisely controlled actuating direction by sticking two hydrogel layers together. Elaborate soft actuators such as bidirectional bending flytrap, gel hand with grasp, open, and gesturing actions as well as word-writin...

A conjugated alternating polymer based on fluorene and triphenylamine, namely poly[(9,9-dioctyl)-2,7-fluorene-co-triphenylamine] (PF–TPA), in which triphenylamine (TPA) as electron donor and hole transporting group was devised and synthesized on the basis of the Suzuki coupling method. The structural properties of the copolymer can be verified by Fourier transform infrared (FT-IR) spectroscopy, hydrogen and carbon nuclear magnetic resonance (1H-NMR, 13C-NMR). Nonvolatile memory devices with bistable electrical switching behavior were observed based on active layers of both fluorene–triphenylamine copolymer (PF–TPA) and PF–TPA:carbon nanotubes (CNTs) hybrid composite materials. Typical formed composite-based device with sandwich configuration, indium tin oxide (ITO)/PF–TPA:CNTs/Al, was demonstrated superior rewritable flash memory property compare to the ITO/PF–TPA/Al device with a greater ON/OFF state current ratio. In addition, the optimal storage characteristics occurs when the doping concentration of CNTs was at a certain value (CNTs = 0.3 mg mL−1), which leading to the ON/OFF state current ratio added up to 2 orders of magnitude and the switching threshold voltage reduced prominently. The conductance switching mechanism of devices was also further discussed. After testing, the devices have good stability and durability, which have a potential application value in data storage.

Organic electric memory devices have broad application prospects. In the present paper, a new kind of polyfluorene-based material containing methoxytriphenylamine groups was synthesized, which exhibited good Flash-type storage characteristics. The material was further doped with Ag NPs to improve storage performance. With appropriate amount of Ag NPs, the device presented an ON/OFF current ratio up to 1.1 × 104 with excellent stability. In addition, the switching characteristics of the device were discussed through data fitting and molecular orbital calculation.

Poly(9,9-dioctylfluorene-2,7-diyl) (PFO) was synthesized under a Suzuki coupling reaction, and its structure was proved by Fourier transform infrared (FT-IR) spectroscopy, and hydrogen and carbon nuclear magnetic resonance (1H-NMR and 13C-NMR). A nonvolatile organic memristor, based on active layers of PFO and PFO:GO composite, was prepared by spin-coating and the influence of GO concentration on the electrical characteristics of the memristor was investigated. The results showed that the device had two kinds of conductance behavior: electric bistable nonvolatile flash memory behavior and conductor behavior. With an increase in GO concentration, the device has an increased ON/OFF current ratio, increasing from 2.1 × 101 to 1.9 × 103, a lower threshold voltage (VSET), decreasing from −1.1 V to −0.7 V, and better stability. The current remained stable for 3 hours in both the ON state and OFF state, and the ON and OFF state current of the device did not change substantially after 9000 read cycles.

Rapid response and strong mechanical properties are desired for smart materials used in soft actuators. A bioinspired hybrid hydrogel actuator was designed and prepared by series combination of three trunks of tough polymer-clay hydrogels to accomplish the comprehensive actuation of "extension-grasp-retraction" like a fishing rod. The hydrogels with thermo-creep and thermo-shrinking features were successively irradiated by near-infrared (NIR) to execute extension and retraction, respectively. The GO in the hydrogels absorbed the NIR energy and transformed it into thermo-energy rapidly and effectively. The hydrogel with adhesion or magnetic force was adopted as the "hook" of the hybrid hydrogel actuator for grasping object. The hook of the hybrid hydrogel actuator was replaceable according to applications, even with functional materials other than hydrogels. This study provides an innovative concept to explore new soft actuators through combining response hydrogels and programming the same stimulus.

Dynamin-related proteins (DRPs) are large GTPases involved in a wide range of cellular membrane remodeling processes. In Arabidopsis thaliana, two paralogous land plant-specific type DRPs, DRP2A and DRP2B, are thought to participate in the regulation of post-Golgi trafficking. Here, we examined their molecular properties and functional relationships. qRT-PCR and GUS assays showed that DRP2A and DRP2B were expressed ubiquitously, although their expressions were strongest around root apical meristems and vascular bundles. Yeast two-hybrid, bi-molecular fluorescent complementation, and co-immunoprecipitation mass spectrometry analyses revealed that DRP2A and DRP2B interacted with each other. In observations with confocal laser scanning microscopy and variable incidence angle fluorescent microscopy, fluorescent fusions of DRP2A and DRP2B almost completely co-localized and were mainly localized to endocytic vesicle formation sites of the plasma membrane, clathrin-enriched trans-Golgi network and the cell plate in root epidermal cells. Treatments with wortmannin, an inhibitor of phosphatidylinositol 3-/4-kinases, latrunculin B, an inhibitor of actin polymerization, and oryzalin, an inhibitor of microtubule polymerization, increased the resident time of DRP2A and DRP2B on the plasma membrane. These results show that DRP2A and DRP2B function coordinately in multiple pathways of post-Golgi trafficking in phosphatidylinositol 3- or 4-kinase and cytoskeleton polymerization-dependent manners.

A novel multivalent cations-triggered shape memory hydrogels were synthesized in a one-pot method, and interpenetrating double network was formed by chemically cross-linked polyacrylamide (PAM) network and physically cross-linked sodium carboxymethyl cellulose network. The temporary shape was fixed by complexation between a native biopolymer, sodium carboxymethyl cellulose (CMC), and transition metal ions, specifically Fe3+, Ag+, Al3+, Cu2+, Ni2+, and Mg2+. In particular, CMC-Fe3+ hydrogel exhibits excellent shape fixity ratio (95%). Therefore, we chose PAM/CMC1.0-Fe3+ hydrogel as the model material and further investigated its shape recovery process. It was found that a wide range of molecules and anions could be applied to break off the temporary cross-links between CMC and Fe3+. The PAM/CMC composite hydrogels also exhibited excellent tunable mechanical properties. The mechanical properties of the composite hydrogel can be adjusted by changing the cross-linking densities. The presented strategy could enrich the construction as well as application of biopolymers based shape memory hydrogels.

Shape memory hydrogels containing over 76 wt % of water were synthesized in a one-pot method, and interpenetrating double network was formed by physically cross-linked gelatin network and chemically cross-linked polyacrylamide (PAM) network with graphene oxide (GO). The temporary shape was quickly fixed by cooling in ice water for 30 s after deformation at 80 °C for 10 s. Shape recovery started in 10 s under near-infrared (NIR) irradiation and almost completed within 60 s depending on the curling angle. A small amount of GO in the hydrogels (≤1.5 mg/mL) played a key role in NIR energy absorption and transformation into thermal energy. The hydrogel without GO showed no response to the NIR irradiation and cannot recover to its permanent shape by NIR irradiation. Temperature sweep was conducted in the cycle of 20 °C → 80 °C → 20 °C, and the structure change in the hydrogels with temperature was investigated according to the storage modulus G' and tangent of the loss angle tan δ as a function of the hydrogel composition. The shape-memory capability was confirmed as the contribution from the triple-helix cross-linking network of gelatin. High mechanical toughness (strength400 kPa and broken strain500%) was achieved by the double-network with the sacrificial gelatin network and GO bridging to dissipate deformation energy. The optimized composition of the hydrogel was found to be a key point to realize stable temporary shape and rapid recovery to the permanent shape controlled by NIR irradiation with reasonable strength. The facile preparation and noncontact gentle stimulus of the present hydrogel hold great potential to be used in soft actuator materials.

A multiple shape memory and self-healing poly(acrylic acid)-graphene oxide-Fe3+ (PAA-GO-Fe3+) hydrogel with supertough strength is synthesized containing dual physically cross-linked PAA network by GO and Fe3+. The first GO cross-linked hydrogel can be reversibly reinforced by immersing in FeCl3/HCl and pure water and softened by immersing in HCl. The tensile strength is 2.5 MPa with the break strain of 700%. Multiple shape memory capability is found depending on this unique feature, the hydrogel can be fixed in four temporary shapes by adjusting the immersing time in FeCl3/HCl and pure water, and recovered in sequence by immersing in HCl. This hydrogel also exhibits perfect self-healing behavior, the cut as-prepared hydrogel is almost completely healed by immersing in FeCl3/HCl. Besides, the hydrogel shows enhanced electrical conductivity with the presence of GO and Fe3+. This supertough hydrogel provides a new way to design soft actuators.