RSC Advances

Liu, Yupeng; Xu, Peidi; Liang, Zhe; Xie, Ruoxiao; Ding, Mingyu; Liu, Hongxia; Liang, Qionglin

doi: 10.1039/c8ra04192jpmid: 35540297

Fiber-based materials with microchannels have drawn considerable attention in recent years owing to their ability to mimic intrinsic morphologies of living tissues. Folded morphologies, which are common in vivo, such as in skeletal muscle capillaries and intestine luminal endoderm, play important roles in the achievement of tissue functions. Here, microfibers with folded hollow channels are fabricated. Channel morphologies, such as straight-folded, double-folded and double-helical channels, can be regulated by adjusting flow conditions in the microfluidic devices. To further demonstrate the potential to be used in tissue engineering, intestine and skeletal muscle constructs are fabricated using these microfibers as building blocks. Furthermore, the properties of perfusability, permeability, cytocompatibility and weavability of the microfibers are evaluated. The asymmetric molecular distributions in the microfibers provide promising platforms for the study of nutrient exchange and energy supplement between normal and tortuous tissues. The new features of biofibers and proof-of-concept of tissue constructs with folded morphologies may contribute to the development of regenerative medicine and drug screening in the future.

Ryu, Ian Seungwan; Liu, Xiaohui; Jin, Ying; Sun, Jirun; Lee, Young Jong

doi: 10.1039/c8ra02919apmid: 30386590

We quantitatively analyze multiple hydrogen bonds in mixtures of two monomers: urethane dimethacrylate (UDMA) and triethylene glycol-divinylbenzyl ether (TEG-DVBE). The carbonyl stretching band in infrared (IR) absorption spectra is deconvoluted into free and hydrogen-bonded carbonyl groups. The amounts of the sub-components are determined for 21 mixture compositions and initially analyzed using a simple stoichiometric model (based on one dominant hydrogen acceptor group per monomer species) for the equilibrium state of hydrogen bond formation. However, our in-depth stoichiometric analysis suggests that at least two UDMA acceptor groups (carbonyl and alkoxy oxygens) and one TEG-DVBE acceptor group (ether oxygen) contribute to intermolecular hydrogen bonding interactions. This finding is further supported by a quantitative analysis of the hydrogen bonding effect on the N–H stretching band. Moreover, the equilibrium constants of these hydrogen bond formations confirm that the inter-association between UDMA and TEG-DVBE is non-negligible in comparison to the UDMA self-associations. Such quantitative information on intermolecular interactions provides insight into the effect of hydrogen bonding on the copolymerization kinetics of these monomer mixtures.

Sajid, Muhammad Munir; Khan, Sadaf Bashir; Shad, Naveed Akthar; Amin, Nasir; Zhang, Zhengjun

doi: 10.1039/c8ra03890bpmid: 35540250

A BiVO4/FeVO4 nanocomposite photocatalyst was successfully synthesized via a hydrothermal method. The prepared heterojunction photocatalyst was characterized physically and chemically using XRD, SEM, EDX, XPS, BET, FT-IR, Raman, UV-vis DRS, EPR and photoluminescence techniques. BiVO4/FeVO4 was explored for its photocatalytic activity by the decomposition of crystal violet (CV) organic dye under visible radiation. This experiment showed that BiVO4/FeVO4 at a ratio of 2 : 1 completely degrades CV within 60 min. In addition, BiVO4/FeVO4 was investigated for the electrochemical detection of the useful analyte ascorbic acid using electrochemical impedance spectroscopy (EIS) and cyclic voltammetry techniques. This work reveals the potential of the BiVO4/FeVO4 nanocomposite for applications in environmental disciplines as well as in biosensing.

Roshani, Ramin; Ardeshiri, Fatemeh; Peyravi, Majid; Jahanshahi, Mohsen

doi: 10.1039/c8ra02908cpmid: 35540253

In order to enhance the flux and wetting resistance of PVDF membranes for MD applications, we have developed a novel PVDF blend nanocomposite membrane using a polystyrene/ZnO (PS/ZnO) hybrid nanocomposite. The PS/ZnO nanocomposite was synthesized by free radical polymerization of styrene in the presence of vinyltrimethoxysilane (VTMS) grafted on the surface of ZnO nanoparticles. The blend nanocomposite membrane is fabricated via the phase inversion method and we examined the effects of the PS/ZnO nanocomposite on porosity, mechanical properties, hydrophobicity, LEPw, morphology, surface roughness and MD performance. It was found that the addition of the PS/ZnO hybrid nanocomposite (0.25, 0.5 and 0.75%) resulted in an increase in porosity (>70%), which is attributed to increased pore size and reduction of the spongy layer thickness. Furthermore, the addition of the nanocomposite also improved the surface roughness and contact angle. Comparison between the neat and modified membrane shows that with incorporation of the PS/ZnO nanocomposite, the desalination flux of 30 g L−1 saline aqueous solution significantly increased and rejection reached 99.99%. Meanwhile, during 100 hours continuous desalination process, the membranes composed of 0.75% PS/ZnO hybrid nanocomposite exhibited high performance stability (15.79 kg m−2 h−1) compared with the neat PVDF membrane.

Lu, Yun; Zhou, Jiawei; Hu, Tianyuan; Zhang, Yifeng; Su, Ping; Wang, Jiadian; Gao, Wei; Huang, Luqi

doi: 10.1039/c8ra03468kpmid: 35540266

Tripterygium regelii is a rich source of triterpenoids, containing many types of triterpenes with high chemical diversity and interesting pharmacological properties. The cDNA of the multifunctional oxidosqualene cyclase (TrOSC, GenBank accession number: MH161182), consisting of a 2289 bp open reading frame and coding for 762 amino acids, was cloned from the stems and roots of Tripterygium regelii. Phylogenetic analysis using OSC genes from other plants suggested that TrOSC might be a mixed-amyrin synthase. The coding sequence was cloned into the expression vector pYES2 and transformed into the yeast Saccharomyces cerevisiae. The resulting products were analysed by GC-MS. Surprisingly, although it showed 76% sequence identity to lupeol synthase from Ricinus communis, TrOSC was found to be a multifunctional triterpene synthase producing both α- and β-amyrin, the precursors of ursane and oleanane type triterpenes, respectively. qRT-PCR analysis revealed that the transcript of TrOSC accumulated mainly in roots and stems. Taken together, our findings contribute to the knowledge of key genes in the pentacyclic triterpene biosynthesis pathway.

Li, Zhipeng; Wang, Zhong Lin; Wang, Zhiwei

doi: 10.1039/c8ra02447bpmid: 35540301

The sculpting of crystalline materials from amorphous films by electron beam irradiation in transmission electron microscopy (TEM) offers an effective way for fabrication of nanostructure and devices. However, the synthesis of multifunctional complex oxide and related composites for possible device application is difficult to achieve. Here, we show that the crystallization pathways of amorphous bismuth ferrite films could be tuned by controlled electron beam irradiation and in situ heating in TEM. The results show that Bi segregates from amorphous films and then aggregates into crystalline nanoparticles (the particle size can be tuned by electron dose rates) under electron beam irradiation below 100 °C, while Bi2Fe4O9 nanocrystals are observed at boundary areas between quasi-liquid Bi nanoparticles at 300 °C due to the cooperative effect of electron beam irradiation and thermal heating. Moreover, the Bi/Bi2Fe4O9 metal/semiconductor solid state heterostructure with nearly atomically sharp interfaces emerges when cooling down to room temperature. This finding expands the variety of nanostructures synthesized by electron bombardment and offers a new way to fabricate complex architectures and possible functional devices at the nanometer scale with direct in situ TEM observation and monitoring.

Wu, Xiren; Shen, Xin; Fan, Shuran; Trivedi, Manoj; Li, Boahong; Kumar, Abhinav; Liu, Jianqiang

doi: 10.1039/c8ra04145hpmid: 35540252

A new Pb(ii)-based 2D MOF comprising π-conjugated ligand 4′-(1H-tetrazol-5-yl)-[1,1′-biphenyl]-3,5-dicarboxylic acid (TZBPDC) and having the formula {[PbNa(TZBPDC)](H2O)(DMF)2}n (1) has been synthesized. Structural characterization of 1 indicates that the MOF has a 4-connected (4,4) motif. The photoluminescent investigation indicates that 1 can behave as potential luminescent sensor for the detection of nitroaromatic compounds (NACs), especially 2,4-dinitrophenol (2,4-DNP) and ferric ions, through the decrease in its luminescence intensity. Additionally, 1 also displays excellent capacity for the photodegradation of methylene orange (MO), which is a constituent of wastewater discharge. The most plausible mechanisms for the decrease in the luminescent intensity of 1 in the presence of different NACs have been explored though theoretical calculations, and the photocatalysis of 1 for organic dyes has been addressed using density of states (DOS) and partial DOS calculations.

Douk, Abdollatif Shafaei; Farsadrooh, Majid; Damanigol, Farzane; Moghaddam, Alireza Ansari; Saravani, Hamideh; Noroozifar, Meissam

doi: 10.1039/c8ra03718cpmid: 35540256

New self-assembled architectures have received great interest in nanotechnology, and are a highly desired target in recent studies. Among self-assembled architectures, noble metal aerogels are an important class owing to their collective characters as well as widespread applications. The synthesis of noble metal aerogels still faces several obstacles such as long hydrogel creation time and complicated multistep strategies. In this paper, we propose an efficient and useful approach to create the three-dimensional network of a Pd–Cu aerogel. This way offers a number of advantages including one-pot synthesis, simplicity, and short time to prepare the hydrogel. The Pd–Cu aerogel was prepared by the reduction of H2PdCl4 and CuCl2 in the presence of sodium carbonate by using glyoxylic acid monohydrate as a reducing agent followed by supercritical CO2 drying. The Pd–Cu aerogel was applied as an anode catalyst for electrooxidation process of formic acid, and depicts much higher electrocatalytic activity and durability compared to the Pd/C. We believe that the exceptional three-dimensional nanostructures fabricated by this route are powerful and promising catalysts for application in direct formic acid fuel cells (DFAFCs), which may open great opportunities for widespread applications such as catalysis, sensors, optoelectronics, electrochemical energy systems, etc.

Xiao, Wen-Jing; Wang, Jiandong; Li, Hong-Jiao; Liang, Long; Xiang, Xuan; Chen, Xue-Qiang; Li, Jingjing; Lu, Zhengquan; Li, Wei-Shi

doi: 10.1039/c8ra04405hpmid: 35540294

The formation of high quality homogeneous active component films is essential to the fabrication of many organic optoelectronic devices, especially those having a large area module. However, most small molecule (SM) semiconductors are unable to achieve such a goal via solution processing because their large and rigid π-conjugated structures generally drive them to aggregate or crystallize into inhomogeneous domains in the process. In this work, a SM semiconductor (SM-DPP6T) based on a diketopyrrolopyrrole (DPP) center with three thiophene units on both sides encounters the same problem. However, when its molecules are interconnected with soft alkyl linkers and change into a poly(rod-coil) polymer, PRC-DPP6T, the problem is solved. Compared with SM-DPP6T, PRC-DPP6T can form a high quality homogeneous film with much better uniformity and coverage on silicon wafers by spin-coating. Moreover, the so-prepared PRC-DPP6T field-effect transistors displayed a much narrower performance distribution and comparable mobility when compared with those based on SM-DPP6T (0.17 vs. 0.15 cm2 V−1 s−1). These results demonstrate that the interconnection of SM semiconductor molecules with soft non-conjugated linkers is a promising way to improve film formation quality while keeping mobility intact.

Hussein, Mahmoud A.; Abu-Zied, Bahaa M.; Asiri, Abdullah M.

doi: 10.1039/c8ra03109fpmid: 35540285

The present study is aimed to fabricate composite materials containing epoxy resin (EPYR) reinforced by mixed carbon-based nano-fillers in the form of graphene nano-platelet (GNP) and multi-walled carbon nanotube (MWCNT) using the dissolution casting technique with the help of ultrasonic assistance. The pure epoxy resin was reinforced by variable loading of mixed GNP/MWCNT in situ, and the epoxy resin is denoted as EPYR/GNP/MWCNT2–30. The numbers 2–30 corresponded to the final mass ratio of the nano-fillers. The designed products were reinforced by variable percentages of GNP/MWCNTs. XRD, FT-IR, thermal analyses, FE-SEM, TEM and electrical conductivity were utilized as identification techniques to confirm the structures of these composite materials. An excellent evidence for the composite formation was given by XRD diffraction patterns and FT-IR spectroscopy. The introduced amounts of mixed nano-fillers showed significant effects on the thermal, conducting and coating behaviors of pure EPYR. Pure EPYR and EPYR/GNP/MWCNT20,30 showed higher thermal stabilities than other materials in the range of 400–410 °C. EPYR/GNP/MWCNT20 also showed remarkable increase in the thermal stability compared to other materials. T10 represents the temperatures at which 10% weight losses are examined. Pure EPYR and its related EPYR/GNP/MWCNT2–30 displayed similar thermal stabilities at T10 temperature (330 ± 4 °C). The morphological features were examined by SEM and TEM; these features showed that the nanocomposite components were extremely compatible. The in situ electrical conductivity values showed noticeable enhancement for the formulations of EPYR/GNP/MWCNT2–10. Moreover, the coating performance of EPYR was tested by water uptake experiments and electrochemical impedance; both tests proved that the mixed GNP/MWCNT nano-fillers remarkably improved the pure EPYR coating due to the ionic charge transfer resistance and elevated barrier behaviour. The coating resistance variations values (CRv) of EPYR/GNP/MWCNT10 were the highest among the measured composition values, closely followed by those of EPYR/GNP/MWCNT20 and EPYR/GNP/MWCNT30.