钝化工艺对HEDP镀铜层耐蚀性的影响

采用盐水浸泡试验、硝酸点滴试验以及电化学测试方法,研究了苯并三氮唑、苯并三氮唑与Cr(Ⅲ)复配、苯并三氮唑与铈盐复配、Cr(Ⅵ)以及HAD无铬钝化工艺对HEDP镀铜层耐蚀性的影响。结果表明,经苯并三氮唑复配钝化液钝化处理后,钝化膜耐蚀性较单一的苯并三氮唑钝化稍有提高,但均不及Cr(Ⅵ)钝化处理,而经HAD无铬钝化处理后,钝化膜耐硝酸点滴时间最长,在3.5%Na Cl溶液中的Rct最大,icorr最小,耐蚀性明显优于Cr(Ⅵ)钝化处理。     

Determination of twisting angle of electrospun nanofiber bundle for continuous electrospinning system

Electrospinning continuously produced twisted nanofibers with a convergence coil and a rotating ring collector. The positively charged nozzle was used in the electrospinning process to deposit electrospun fibers of polyacrylonitrile onto a rotating ring collector. By withdrawing the electrospun fibers from the rotating ring collector, it was possible to spin the electrospun fibers yarn. In this study, theoretical approaches and numerical simulations were used to determine the twisting angle of the yarn. Using the equations developed in this study, we performed numerical simulations and compared the experimental results with the numerical simulation results. Mechanical properties of the fiber bundle were analyzed for twisting angle. It was confirmed the relationship among the winding drum, the ring collector, and flux of the fibers mass per time during electrospinning in the developed system. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45528.     

Agglomerate size evolution in modular twin‐screw extruder: Modeling and validation with CaCO3/LLDPE compounding experiments

The screw combination of twin‐screw extruder affects the filler size in inorganic filler‐reinforced polymeric compounds. This article tried to conveniently and precisely model the agglomerate size evolution in modular co‐rotating twin‐screw extruder. The break‐up process of agglomerate was analyzed to obtain the relationship between average deagglomerating energy (M) and agglomerate size, the result presented a mathematic relationship between M and agglomerate size. Numerical simulation study was conducted to consider the effect of kneading blocks (KB) or flight elements (FE) number on dispersion capacity of screw combination. The average deagglomerating energy, calculated based on POLYFLOW simulation, was introduced as major parameter to evaluate the dispersion capacity, which presented a proportional relationship to the KB or FE number. The model was developed by combining the agglomerate break‐up process and simulation results. In validation, CaCO₃/linear low‐density polyethylene (LLDPE) compounds were prepared by modular co‐rotating twin‐screw extruder with different screw combinations. The optical image analysis showed that CaCO₃ agglomerate size decreased with the KB or FE number rising, while it achieved minimum when the KB number was 4. The model was in accordance with the experimental results, and proved to be valid for KB and FE combinations in preparing CaCO₃/LLDPE compounds. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45535.     

Chemical Synthesis of K34‐Ubiquitylated H2B for Nucleosome Reconstitution and Single‐Particle Cryo‐Electron Microscopy Structural Analysis

Post‐translational modifications (e.g., ubiquitylation) of histones play important roles in dynamic regulation of chromatin. Histone ubiquitylation has been speculated to directly influence the structure and dynamics of nucleosomes. However, structural information for ubiquitylated nucleosomes is still lacking. Here we report an alternative strategy for total chemical synthesis of homogenous histone H2B‐K34‐ubiquitylation (H2B‐K34Ub) by using acid‐cleavable auxiliary‐mediated ligation of peptide hydrazides for site‐specific ubiquitylation. Synthetic H2B‐K34Ub was efficiently incorporated into nucleosomes and further used for single‐particle cryo‐electron microscopy (cryo‐EM) imaging. The cryo‐EM structure of the nucleosome containing H2B‐K34Ub suggests that two flexible ubiquitin domains protrude between the DNA chains of the nucleosomes. The DNA chains around the H2B‐K34 sites shift and provide more space for ubiquitin to protrude. These analyses indicated local and slight structural influences on the nucleosome with ubiquitylation at the H2B‐K34 site.     

Carbohydrate Analogue Microarrays for Identification of Lectin‐Selective Ligands

Fifty‐five mono‐ and disaccharide analogues were prepared and used for the construction of microarrays to uncover lectin‐selective ligands. The microarray study showed that two disaccharide analogues, 28′ and 44′ , selectively bind to Solanum tuberosum lectin (STL) and wheat germ agglutinin (WGA), respectively. Cell studies indicated that 28′ and 44′ selectively block the binding of STL and WGA to mammalian cells, unlike the natural ligand LacNAc, which suppresses binding of both STL and WGA to cells.     

Preparation and properties of novel pH‐sensitive core−shell microspheres for enhanced oil recovery

A novel pH‐sensitive core?shell microsphere was synthesized by growing sodium acrylate as a shell on crosslinked polyacrylamide particles as the core by surface‐initiated atom transfer radical polymerization. The structures and characteristics of the microspheres were confirmed by Fourier transform infrared spectroscopy, ¹H NMR spectroscopy, SEM, transmission electron microscopy and AFM. The viscosity and size of the microspheres in response to changes in pH value were also investigated. As a kind of potential profile control and flooding agent, the performances of permeability reduction and enhanced oil recovery were studied in designed experiments. © 2017 Society of Chemical Industry     

Triethanolamine–azodiisobutyronitrile mixture as a foaming agent for low‐density unsaturated polyester resin manufacturing at a low temperature

A triethanolamine (TEA)–azodiisobutyronitrile (AIBN) mixture was applied to the manufacturing of a low‐density unsaturated polyester resin (LDUPR) at a low temperature ranging from 53 to 66 °C. Hydrogen‐bonding activation in the TEA–AIBN mixture was put forward, and this agreed with the NMR and Fourier transform infrared (FTIR) spectroscopy results. A heat balance in the curing process of a vinyl ester unsaturated polyester resin (UPR) was examined and characterized by differential scanning calorimetry, FTIR spectroscopy, and scanning electron microscopy. The TEA–AIBN mixture decomposed easily because of the hydrogen‐bonding action between TEA and AIBN. The heat release of the activated AIBN decomposition led to the early endothermic polymerization of the vinyl ester UPR. Hydrogen‐bonding activation followed by the heat‐balance process enabled us to manufacture the LDUPR at low temperature. The optimal parameters of LDUPR manufacturing, including a ratio of TEA to AIBN of 0.4 and a dosage of TEA–AIBN mixture of 2.5 phr at a curing temperature of 60 ± 1 °C, were defined by the testing of the apparent density (ρ) and compressive strength of LDUPR. Under these conditions, ρ was 0.39 ± 0.01 g/cm³, and the specific compressive strength was 33.92 ± 1.31 MPa g^?1 cm^?3. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44797.     

A poly(ethylene terephthalate) nonwoven sandwiched electrospun polysulfonamide fibrous separator for rechargeable lithium ion batteries

A poly(ethylene terephthalate) nonwoven sandwiched electrospun polysulfonamide (PSA) fibrous separator was developed for application in lithium‐ion batteries (LIBs). The poly(ethylene terephthalate) nonwoven served as a mechanical support and the PSA layers provided the separators with nanoporous structures. This novel composite separator possessed better thermal stability and electrolyte wettability than commercial polypropylene separator and the sandwiched nonwoven endowed the separator with an improved mechanical strength (17.7 MPa) compared to the pure electrospun PSA separator. The cells assembled with this composite separator displayed excellent discharge capacity (122.0 mAh g^?1 after 100 cycles) and discharge C‐rate capacity. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44907.     

Hydrophobic mesoporous acidic resin for hydroxyalkylation/alkylation of 2‐methylfuran and ketone to high‐density biofuel

Hydroxyalkylation/alkylation of biomass‐derived 2‐methylfuran with cyclic ketones (cyclopentanone and cyclohexanone) has great potential in synthesizing high‐density biofuel. But the conversion and selectivity are still unsatisfactory because the in‐situ formed water decreases the acidity of catalyst and induces side reaction. Herein, hydrophobic mesoporous resins with sulfonic acid group (PS) and fluoride sulfonic acid group (PCS) were synthesized by a simple solvothermal reaction and ion exchange treatment, which have good mesoporous structure with surface area of 300–700 m²/g. Notably, PS and PCS have better hydrophobicity and oleophilicity as compared to widely used sulfonic acid functional amberlyst‐15 and fluoride sulfonic acid functional nafion‐212. In the hydroxyalkylation/alkylation reaction, PS shows higher activity and selectivity than amberlyst‐15 while PCS surpasses nafion‐212. Furthermore, both PS and PCS have good recycling stability in consecutive 5 runs. After hydrodeoxygenation, two high‐density biofuels with density of 0.819 and 0.825 g/mL were obtained. © 2016 American Institute of Chemical Engineers AIChE J, 63: 680–688, 2017     

Preparation and evaluation of chitosan/β‐cyclodextrin magnetic nanoparticles as a photodegradable and hydrophobic drug delivery carrier

In this study, novel tumor targeting nanocarriers comprised of chitosan (CS)/β‐cyclodextrin (β‐CD) magnetic nanoparticles were prepared to improve the photodegradable stability and bioavailability of hydrophobic drug. Resveratrol (Res) with photodegradable and hydrophobic properties was selected as a model drug. The photodegradation rate of Res in Fe₃O₄ nanoparticles solution was 7.8 times lower than that in the ethanol solution_. In addition, the value of the saturation magnetization of CS/β‐CD nanoparticles was found to be 19.56 emu/g with characteristic of superparamagnetism. Approximately 90% Res was entrapped into the CS/β‐CD magnetic nanoparticles with the size distribution ranging from 200 to 359 nm, and the nanoparticles were spherical in shape with high zeta potentials. Furthermore, the formation of CS/β‐CD nanoparticles showed a sustained release in vitro. These results indicated that the obtained CS/β‐CD magnetic nanoparticles were a promising magnetic targeting carrier for photodegradable and hydrophobic drugs. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45076.