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Desalination and Water Treatment · 2024 · IF 1

Facile fabrication of multifunctional superoleophobic and antifouling metal mesh by dip-coating polyanion for efficient oil/water mixtures as well as emulsions separation

Chao Yang,Jun Yang,Ge Song,Limin Zang,Qifan Liu,Jianhui Qiu,Xue Yang,Chun Wang

Oil/water separation has recently attracted a great deal of attention for research due to the frequent occurrence of an oil spill as well as the increase of industrial and household oily wastewater. Therefore, the purpose of this study is to demonstrate underwater superoleophobic crosslinked phosphorylated poly(vinyl alcohol) hydrogel coated stainless steel mesh (CL-PPVA@SSM), which was fabricated using a simple dip-coating method and aldol reaction on the mesh substrate. The as-prepared CL-PPVA@SSM is capable of separating oil from a variety of different oil/water mixtures with high separation efficiency up to 99.2%, excellent recyclability and fast water permeate flux of 467.7 L m –2 h –1 , which makes it suitable for the separation of oil-water mixtures from oil-water emulsions. Also, in the oil-water separation process, the CL-PPVA@SSM is capable to remove organic dye from the water. The CL-PPVA@SSM exhibits stability under various harsh conditions such as mechanical abrasion. Importantly, the CL-PPVA@SSM shows a massive potential to separate kitchen waste oil/water mixtures due to the underwater superoleophobic property as required for the recycling of kitchen waste oil. Therefore, this method has been met with a promising application prospect of practical application.

研究领域: 材料科学 · 环境工程 · 高分子化学 · 表面工程 · 化学工程 · 纳米技术 · 水处理技术
✓ 已验证 DOI 高影响因子
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Arabian Journal of Geosciences · 2019 ·Vol. 12 ·期 7 ·256 · IF 1.141

A novel binary compound flooding system based on DPG particles for enhancing oil recovery

Li Weitao,Wei Falin,Xiong Chunming,Ouyang Jian,Zhao Guang,Shao Liming,Dai Mingli

Aiming at deep profile control in water flooding reservoirs, a heterogeneous combination flooding system, composed of dispersed particle gel (DPG) and a zwitterionic surfactant (THSB), was developed. The mean particle diameter was adjusted and then the DPG morphology and diameter were characterized using a laser scanning, confocal microscope, and dynamic light scattering. The effects of DPG concentration, temperature, pH, and salinity on THSB interfacial tension (IFT) were investigated. A method for determining DPG concentration was proposed, and the dynamic retention and migration mechanisms of the particles were evaluated, using cores with different permeabilities. Finally, the oil displacement mechanism of the combination flooding system was explored through visual simulation experiments and scanning electron microscopy. The results showed that the particle diameter was 2.5 μm, that compared with a surfactant system, the IFT of the combination flooding system was relatively low, and that the temperature, pH, and NaCl content of solutions had little effect on THSB IFT. Since specific matching relationships between DPG particles and reservoir pore throats existed, the retention amount and injection pressure were improved with the increased core permeability. Visual simulation experiments revealed the oil recovery mechanism of the combination flooding system. This combination flooding system can be used in reservoirs under varied conditions, as the particle diameter can be adjusted on a case-by-case basis, and the THSB surfactant proved to be high-temperature resistant and high-salinity tolerant. The combination flooding system can be applied to deep profile control and oil displacement, in oil fields.

研究领域: 石油工程 · 提高采收率 · 油田化学 · 渗流力学 · 油气田开发
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2020 ·Vol. 138 ·期 7 ·49856 · IF 2.52

Effect of pore orientation on shear viscoelasticity of cellulose nanocrystal/collagen hydrogels

Donglei Liu,Xufeng Dong,Huiying Liu,Yiping Zhao,Min Qi

Motivated by a need to replicate structural and viscoelastic properties of soft tissue, such as cartilage, the structural hydrogels with viscoelastic feature have been of interest in biomedical application. However, the effect of pore alignment on their viscoelastic properties has been largely underestimated. This work prepared cellulose nanocrystal (CNC)/collagen hydrogels with different pore orientations, including horizontally aligned pores, random pores and vertically aligned pores, and integrated them into a multilayered hydrogel with multi-structure which mimics cartilage construct. The stress relaxation rate (τ 1/2 ), creep rate (γ 1/2 ), storage modulus ( G′ ) and loss modulus ( G″ ) increased in the order of the vertical, random, multi-structural, and horizontal. G′ value of the horizontal increased up to 300% relative to the vertical in the strain amplitude and frequency sweep. Maxwell–Weichert and Variable Network Density models were used to explain phenomena, and the experimental curves fitted well with the theoretical models. These results reveal that the viscoelastic properties of hydrogel can be influenced by pore orientation except conventional component concentration.

研究领域: 生物材料 · 组织工程 · 生物力学 · 高分子科学 · 再生医学
✓ 已验证 DOI 高影响因子
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MATERIALS & DESIGN · 2016 · IF 3.997

Bio-inspired design and fabrication of an ultralight and strong nano-carbon gradient composite

Yanjie Wang,Min Li,Weibang Lu,Yizhuo Gu,Shaokai Wang,Rui Sun,Xuetong Zhang,Qingwen Li,Zuoguang Zhang

A nano-carbon composite, consisting of a graphene aerogel-carbon nanotube (CNT) film, is constructed by coating a strong and flexible CNT film onto the surface of a porous graphene aerogel core. The prepared gradient composite, ultralight and strong, can carry objects more than 15,000 times its own weight, exhibiting impressive compression resistance. Compared to the original graphene aerogel , the composite exhibits 8–9-fold increased values in its elastic modulus and compressive strength at a strain of 20% and an approximately 10-fold increase in electrical conductivities in the axial direction . In addition, the elastic recovery ability after compressive deformation and the ability to preserve liquid are also improved.

研究领域: 材料科学 · 纳米科技 · 复合材料工程 · 生物启发设计 · 力学性能研究 · 功能材料 · 电学性能
✓ 已验证 DOI 高影响因子
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PHYSICAL CHEMISTRY CHEMICAL PHYSICS · 2015 ·Vol. 17 ·期 38 ·25525-25535 · IF 4.493

Volume phase transition mechanism of poly[oligo(ethylene glycol)methacrylate] based thermo-responsive microgels with poly(ionic liquid) cross-linkers

Yuanyuan Zhou,Hui Tang,Peiyi Wu

Thermo-dynamic volume phase transition mechanisms of poly[oligo(ethylene glycol)methacrylate] (POEGMA) based microgels with poly(ionic liquid) (PIL) cross-linking moieties are investigated in detail on the basis of temperature-dependent Fourier transform infrared (FTIR) spectroscopy. The original FTIR data are further analysed by two-dimensional correlation spectroscopy (2Dcos) with the perturbation correlation moving window (PCMW) technique. It is observed that the content of hydrophilic PIL cross-linking structure strongly affects the temperature induced volume phase transition mechanism of microgels in which the less cross-linked microgel exhibits a sharp volume phase transition process while the highly cross-linked microgel presents a broad transition behavior. Peculiarly, the dehydration of C–H groups acts as the driving force for the whole phase transition process within the less cross-linked microgel network and cooperative response of chemical groups is identified. It is deduced that the hydrophilic PIL moieties develop polymer–water–polymer interactions with CO groups as CO⋯D2O–PIL hydrogen bonds emerge in the less cross-linked system. As regards the highly cross-linked microgel system, the phase transition process is driven by the disruption of hydrogen bonds between CO groups and water molecules while the response of C–H groups becomes insensitive. PIL moieties passively dehydrate following the dehydration of C–H groups on oligo(ethylene glycol) side chains and no hydrogen bond between CO group and IL–D2O association appears during the phase transition process.

研究领域: 高分子科学 · 软物质物理 · 生物材料 · 药物递送 · 智能响应材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY · 2022 · IF 6.76

Redeposition mechanism on silicon oxide layers during selective etching process in 3D NAND manufacture

Zihan Zhou,Yunwen Wu,Huiqin Ling,Jie Guo,Su Wang,Ming Li

3D NAND flash memory with vertically stacked cells has been developed to break through the limits of technology nodes. However, during the selective etching process, it is difficult to ensure the byproducts diffuse away from the trenches in the multistacked layers. Once saturated, the byproduct causes abnormal redeposition on the SiO 2 layers. This problem has restricted the development of high-density 3D NAND memory. To solve this problem, the composition and formation mechanism of the redeposited layer must be clarified. In this study, a ternary-wafer system comprising a Si 3 N 4 /SiO 2 /Si 3 N 4 stack was fabricated to study the redeposition mechanism, and the morphology, elastic properties , and chemical composition of the redeposited layer were clarified. The redeposited layer consists of spherical particles with elastic surfaces (average Young’s modulus of 24.17 GPa). The particles were confirmed to comprise colloidal silica gel covered by silanols . By considering the chemistry of silica , the redeposition mechanism was proposed as follows: colloidal silica gel is formed by the aggregation of silicic acids from Si 3 N 4 etching, which adsorb onto the SiO 2 layer through oxide bridges and hydrogen bonding . Our work will contribute to the development of high-density 3D NAND memory.

研究领域: 微电子学 · 半导体工艺 · 材料科学 · 表面化学 · 纳米材料 · 固态物理 · 集成电路制造
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Rational reconfiguration of a gradient redox mediator with in-situ fabricated gel electrolyte for Li–air batteries

Yinwei Fu,Xiaofeng Lei,Huiming Yin,Xizheng Liu

Flexible lithium–air batteries (LABs) with a redox mediator (RM) in the electrolyte demonstrate enhanced round-trip efficiency. However, their cycle performance is unsatisfactory due to severe corrosion of the Li metal anode. Herein, we propose a two step gelatinization strategy to fabricate a gradient RMs (including LiI, TMPD, and DMPZ) gel electrolyte, in which the bare electrolyte gelatinization on the Li surface and then the electrolyte contained RMs sequentially gelled on the formed gel. The RMs mainly distributed at the surface and anchored at the cathode side. By suppressing the shuttle of RMs in the electrolyte and alleviating the passivation of the Li anode, the mid-charging potentials can reach 3.44 and 4.08 V at the 15th cycle with and without the LiI mediator, respectively. The energy efficiency is 63% even at the 150th cycle, whereas the corresponding energy efficiency are only 47% and 51% for the LABs with liquid and normal gel electrolytes, respectively. Moreover, the cycle life of the battery containing the gradient gel electrolyte is three times longer than that with the liquid electrolyte. The gel electrolyte further offers the flexibility of the device, and the laminated cells thus fabricated can readily operate under harsh bending conditions.

研究领域: 电化学 · 能源材料 · 纳米材料 · 界面化学 · 储能技术 · 先进电池 · 功能高分子 · 柔性电子
✓ 已验证 DOI 高影响因子
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Advanced Healthcare Materials · 2024 ·Vol. 14 ·期 1 ·2402272 · IF 10

Genetically Engineered Bacteria as A Living Bioreactor for Monitoring and Elevating Hypoxia-Activated Prodrug Tumor Therapy

Hongwei Zhang,Linfu Chen,Qian Chen,Qiufang Chen,Jun Zhou

Tirapazamine (TPZ), an antitumor prodrug, can be activated in hypoxic environment. It specifically targets the hypoxic microenvironment of tumors and produces toxic free radicals. However, due to the tumor is not completely hypoxic, TPZ often fails to effectively treat the entire tumor tissue, resulting in suboptimal therapeutic outcomes. Herein, a low pathogenic Escherichia coli TOP10 is utilized to selectively colonize tumor tissues, disrupt blood vessels, and induce thrombus formation, leading to the expansion of hypoxic region and improving the therapeutic effect of TPZ. Additionally, a thermosensitive hydrogel is constructed by Pluronic F-127 (F127), which undergoes gelation in situ at the tumor site, resulting in sustained release of TPZ. To monitor the therapeutic process, it is genetically modified TOP10 by integrating the bioluminescent system luxCDABE (TOP10-Lux). The bioluminescent signal is associated with tumor hypoxia enhancement and thrombus formation, which is beneficial for therapeutic monitoring with bioluminescence imaging. In the murine colon cancer model, the TOP10-Lux combined with TPZ-loaded F127 hydrogel effectively suppressed tumor growth, and the treatment process is efficiently monitored. Together, this work employs genetically modified TOP10-Lux to enhance the therapeutic efficacy of TPZ and monitor the treatment process, providing an effective strategy for bacteria-based tumor-targeted chemotherapy and treatment monitoring.

研究领域: 肿瘤学 · 微生物治疗 · 分子影像学 · 药物递送 · 生物材料 · 转化医学 · 合成生物学
✓ 已验证 DOI 高影响因子
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JOURNAL OF THE CHINESE CHEMICAL SOCIETY · 2017 ·Vol. 64 ·期 2 ·231-238 · IF 0.935

Effect of Sodium Alginate on the Properties of Thermosensitive Hydrogels

Jie Wu,Zongmei Wu,Xuejiao Sun,Shichao Yuan,Ruling Zhang,Qingliang Lu,Yueqin Yu

Sodium alginate (SA) was combined with poly( N -isopropylacrylamide) (PNIPAAm) to prepare thermosensitive hydrogels through semi-interpenetrating polymer network (semi-IPN) and fully interpenetrating polymer network (full-IPN). The thermosensitive, swelling, mechanical, and thermal properties of pure PNIPAAm, SA/PNIPAAm semi-IPN, and Ca-alginate/PNIPAAm full-IPN hydrogels were investigated. The formation of semi-IPN and full-IPN significantly improved the hydrogels’ swelling capability and mechanical properties without altering their thermosensitivity. 5-Fluorouracil (5-Fu) was selected as a model drug to study the release behaviors of the hydrogels. It was found that in vitro controlled drug release from semi-IPN hydrogels showed an initial release burst, followed by a slower and sustained release, before reaching equilibrium. Full-IPN hydrogels showed slow and sustained release during the whole process. Temperature and pH were found to affect the rate of drug release. Ca-alginate/PNIPAAm full-IPN hydrogels have potential application as drug delivery matrices in controlled drug release.

研究领域: 生物材料 · 药剂学 · 高分子科学 · 组织工程 · 药物递送系统
✓ 已验证 DOI 高影响因子
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MACROMOLECULAR MATERIALS AND ENGINEERING · 2017 ·Vol. 303 ·期 2 ·1700396 · IF 2.863

A Dual-Crosslinked Strategy to Construct Physical Hydrogels with High Strength, Toughness, Good Mechanical Recoverability, and Shape-Memory Ability

Zhihui Qin,Rui Niu,Chenjue Tang,Jun Xia,Feng Ji,Dianyu Dong,Haitao Zhang,Shuo Zhang,Junjie Li,Fanglian Yao

A novel type of physical hydrogel based on dual-crosslinked strategy is successfully synthesized by micellar copolymerization of stearyl methacrylate, acrylamide, and acrylic acid, and subsequent introduction of Fe 3+ . Strong hydrophobic associations among poly(stearyl methacrylate) blocks form the first crosslinking point and ionic coordination bonds between carboxyl groups and Fe 3+ serve as the second crosslinking point. The mechanical properties of the hydrogel can be tuned in a wide range by controlling the densities of two crosslinks. The optimal hydrogel shows excellent mechanical properties (tensile strength of ≈6.8 MPa, elastic modulus of ≈8.0 MPa, elongation of ≈1000%, toughness of 53 MJ m −3 ) and good self-recovery property. Furthermore, owing to stimuli responsiveness of physical interaction, this hydrogel also shows a triple shape memory effect. The combination of two different physical interactions in a single network provides a general strategy for designing of high-strength hydrogels with functionalities.

研究领域: 高分子材料科学 · 生物医用材料 · 组织工程 · 智能响应材料 · 软物质物理
✓ 已验证 DOI 高影响因子
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JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS · 2018 ·Vol. 56 ·期 19 ·1281-1286 · IF 2.499

Hydrogen bond-reinforced double-network hydrogels with ultrahigh elastic modulus and shape memory property

Yan Jie Wang,Chen Yu Li,Zhi Jian Wang,Yiping Zhao,Li Chen,Zi Liang Wu,Qiang Zheng

Development of tough hydrogels has greatly expanded their applications as load-bearing materials. However, the elastic modulus of tough hydrogels is usually lower than 1 MPa. It remains a challenge to design tough hydrogels with high modulus. We report here a series of tough double-network (DN) hydrogels with ultrahigh elastic modulus (up to 200 MPa) by forming robust hydrogen bonds between the first poly(acrylic acid) network and the second poly( N -isopropyl acrylamide) network. The dense cooperative hydrogen bonds greatly reduce the segmental mobility and thus improve the rigidity of gel matrix. Owing to the dynamic nature of hydrogen bonds, the modulus of hydrogels is strongly influenced by temperature and pH, affording the gels shape memory property. The strategy by forming robust noncovalent bonds between interpenetrating networks should be applicable to other systems for designing tough and versatile hydrogels with diverse promising applications. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56 , 1281–1286

研究领域: 高分子物理 · 生物材料 · 软物质科学 · 智能响应材料 · 组织工程
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2015 ·Vol. 132 ·期 20 · IF 1.768

Synthesis of hyperbranched polymers by free radical addition-coupling polymerization with A3/B2 and A2A′/B2 approaches

Yaobin Liu,Zhiqiang Fan

Two tribromide compounds, 1,3-(propanoic acid, 2-bromo-)-2-(2-bromo-1-oxopropylamino)propyl ester (A 1 ) and trimethylolpropane tris(2-bromopropionate) (A 2 ), were synthesized. By Cu/ N,N,N′,N′,N″ -pentamethyldiethylenetriamine (PMDETA)-mediated radical addition-coupling polymerization (RACP) of 2-methyl-2-nitrosopropane (MNP) with the tribromide compounds, two types of hyperbranched polymers were synthesized under mild conditions, respectively. Polymerization degrees of the polymers increased with time gradually, which is in line with a step-growth polymerization mechanism. By tracing the polymerization process by gel permeation chromatography and NMR analysis, proper reaction conditions to get hyperbranched polymers was obtained. Based on the results of NMR analysis on the polymer chain structure, mechanism of forming hyperbranched polymer has been proposed, which includes formation of carbon radicals from the tribromo monomer through single electron transfer, their reaction with MNP to form nitroxide radicals, and cross-coupling reaction of the nitroxide radicals with other carbon radicals. The gelation point of the A 2 -MNP system is larger than that of the A 1 -MNP system, indicating that probability of intramolecular cyclization in A 2 -MNP RACP system is higher than the A 1 -MNP system. The reactivity of —NHCOCH(CH 3 )Br group of A 1 is lower than its two —OCOCH(CH 3 )Br groups, and this resulted in longer distance between two adjacent branch points in the hyperbranched polymer of A 1 -MNP than the A 2 -MNP system. It is possible to adjust the chain structure of RACP-based hyperbranched polymer by changing the reactivity of the functional groups in A 3 monomer. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41972.

研究领域: 高分子化学 · 聚合物合成 · 功能高分子 · 材料化学 · 有机合成方法学
✓ 已验证 DOI 高影响因子
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