Electrochemical growth of flowerlike gold nanoparticles on polydopamine modified ITO glass for SERS application

A functional biopolymer - polydopamine (Pdop) layer was easily modified on the surface of indium tin oxide substrates by spontaneous oxidative polymerization in a dopamine solution. The Pdop layer functions as a novel and promising protector for electrochemical growth of flowerlike gold nanostructures (AuNFs). Electrochemical investigations and SEM results demonstrate that Pdop coating is favored to rapid gold nucleation. The application of AuNFs in surface-enhanced Raman scattering is investigated by using rhodamine 6G as probe molecule. Its detection limit reaches as low as 10⁻¹² M. Pdop coating as a functional platform to prepare AuNFs is promising for potential applications in sensitive optical chemical sensors.     

Response surface analysis to evaluate the influence of deposition parameters on the electrodeposition of Cu–Co alloys in citrate medium

Copper–cobalt alloy coatings were deposited on mild steel substrates using sodium citrate electrolytes at room temperature and under direct current. A set of cathodic polarization curves was plotted by varying the mechanical stirring speed of the solution (0–400 rpm), using a range of current densities during the electrodeposition experiments. Factorial design was used to verify the influence of these deposition parameters on the cathodic efficiency, the copper and cobalt content in the coating, the corrosion current density of the coating/substrate system, and the efficiency of the coating in protecting the substrate. The electroplating experiments showed that, with the studied bath composition, high stirring speed and low current density lead to greater cathodic current efficiency and copper-rich coatings. On the other hand, high current density and low stirring speed yields coatings with high cobalt content and a lower cathodic efficiency. Our results show that the studied parameters affect the corrosion current density and the coating efficiency of the coating/substrate system in opposite ways. The best results were obtained increasing the current density and decreasing the mechanical stirring speed. Additionally, three samples were produced in selected deposition conditions. The coatings morphologies were compact, and their grain sizes seemed to enlarge with increasing stirring speed and decreasing current density.     

Having it both ways: delicate hierarchical structure and robust mechanical stability on micro/nanomaterials with mesoporous silica coating

Mesoporous silica (meso-SiO₂) was coated on the micro/nanomaterials with hierarchical structure such as flowerlike Fe₂O₃, flowerlike MgO, SnO₂ nanospheres, Co₃O₄ nanosheets and nanowires from a simple solution method. The structure of the nanomaterials and the silica coating before and after stirring in solution were characterizated by SEM and TEM. The results show that meso-SiO₂ coating was an ideal method to enhance the structural stability of fragile nanomaterials. The catalysis stability of flowerlike MgO was also enhanced by the meso-SiO₂ coating.     

Optimization of coating solution viscosity of hollow fiber‐supported polydimethylsiloxane membrane for CO2/H2 separation

To optimize the CO₂ permeation and CO₂/H₂ separation performance of hollow fiber‐supported polydimethylsiloxane (PDMS) membranes, the effect of the viscosity of the PDMS coating solution on surface morphologies, thickness of PDMS layer, and solution intrusion into surface pores of hollow fiber supports was investigated. Increases in both stirring time and standing time could increase the viscosity of the PDMS solution. The PDMS layer thickness increased when the coating solution viscosity increased, whereas the surface roughness of the PDMS layer markedly decreased and then slightly changed. Moreover, when the stirring time of the PDMS coating solution was 9 min and the standing time was increased from 2 min to 25 min, the CO₂ permeance first decreased, then increased to ～2250 GPU probably due to the decreased intrusion depth, and finally decreased because of the substantially increased thickness of the PDMS layer. However, the CO₂/H₂ selectivity increased to 3.4 with an increase in coating solution viscosity. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45765.     

Oxidative chemical polymerization of 3, 4‐ethylenedioxythiophene and its applications in antistatic coatings

The oxidative chemical polymerization of 3, 4‐ethylenedioxythiophene (EDOT) was conducted at room temperature in the presence of poly(styrene sulfonate) (PSS) as the doping agent, sodium supersulphate (Na₂S₂O₈) and ferric sulphate(Fe₂(SO₄)₃) as the compound oxidant and deionized water as the solvent. In order to remove sodium ion (Na⁺), ferric ion (Fe³⁺), and sulfate ion (SO4^2?), certain amount of ion exchanger was added after 24 h, the dark blue poly(3, 4‐ethylenedioxythiophene) (PEDT)/PSS solution was obtained. The influence of different proportions of EDOT and PSS, different proportions of EDOT and the compound oxidant, different stirring rates on the morphology, and surface resistivity were discussed. The influence of pH value of the PEDT/PSS solution, the coating thickness, and soak time on the surface resistivity was investigated. Recipe and experimental conditions were optimized and the PEDT/PSS solution was obtained with excellent performance which has relatively low in surface resistance, good water tolerance, and light transmittance. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Fabrication and performances of preceramic polymer-based high-temperature High emissivity coating

High emissivity coatings on nickel-based superalloy, with good infrared radiating ability and good high temperature resistance, were prepared at room temperature, using preceramic polymer cured at room-temperature as coating former and CeO₂ and B₄C as passive high emissivity fillers. The influences of high temperature and wind channel test on the microstructure and thermal performance of the high emissivity coating were investigated in detail. The high emissivity coating has good thermal stability and no cracking and flaking after heating at 1100 K and the wind tunnel test. The emissivity of the coating reached 0.85−0.92 between room temperature and 1100 K. The high emissivity coating on the nickel-based alloy can make the back temperature of the nickel-based alloy decrease from 686 to 646 ℃.     

In situ growth of multilayered crystals in amorphous matrix: Thermal,dynamic mechanical,and morphological analysis of nylon‐6/epoxy composites

A new procedure for processing of epoxy/polyamide blend was explored via solution polymerization of ε‐caprolactam in N‐methylpyrollidone (NMP), which resulted in a suspension of nylon‐6 in solvent at room temperature. The suspension was blended with water based epoxy resin using mechanical stirring at room temperature. Several films were prepared from blend by varying the amount of nylon‐6 without curing agent. All films were fully characterized for thermal and dynamic mechanical properties using differential scanning calorimetry and dynamic mechanical analysis. The addition of nylon‐6 had a plasticizing effect on epoxy evident by decrease in glass transition temperature (T_g). The reaction between nylon‐6 and epoxy was studied using Fourier transform infrared spectroscopy by following the characteristic epoxy peak (914 cm^?1). The growth of nylon‐6 crystals in epoxy matrix lead to spherulitic multiphase morphology, which was observed under scanning electron microscope. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3319–3327, 2013     

三价铬镀液电镀铬的工艺研究

研究了一种环保型的三价铬电镀工艺。讨论了电镀时间、pH、温度、搅拌方式以及阴极电流密度对镀层的影响。结果表明:镀层厚度增长随着电镀时间的延长呈现先快后慢的趋势;pH=3.5时可以获得厚度适中、外观光亮的镀层;镀层的光亮程度随着温度的升高而增加,45℃时最佳;不搅拌;该工艺的可操作电流密度较宽,Jκ在4～6 A/dm2。     

Synthesis of π-conjugated organoboron polymers by haloboration-phenylboration polymerization of aromatic diynes

π-Conjugated organoboron polymers were prepared by haloboration-phenylboration polymerization beween diyne monomers and bromodiphenylborane. The polymerization was carried out by adding a slightly excess amount of bromodiphenylborane to a tetrachloroethane solution of diynes at room temperature under nitrogen and stirring the reaction mixture for 4 hours at 100°C. The obtained polymers were soluble in common organic solvents such as THF and chloroform. Their molecular weights were estimated to be several thousands by gel permeation chromatographic analysis. In UV-vis absorption spectra, bathochromic shift of λ_max and absorption edge in comparison with the corresponding monomers were observed, which indicates the π-conjugation via vacant p-orbital of boron atom.     

Oxidation protective MoSi2-SiC-Si coating for graphite materials prepared by slurry dipping and vapor silicon infiltration

A novel kind of dense MoSi₂-SiC-Si coating was prepared on the surface of graphite substrate by slurry dipping and vapor silicon infiltration process. Mo-SiC-C precoating was fabricated via slurry dipping method, and then MoSi₂-SiC-Si coating with dense structure consisting of Si, MoSi₂ and SiC was obtained by vapor silicon infiltration process. The isothermal oxidation tests at temperatures from 800 to 1600 °C and TGA test from room temperature to 1500 °C were used to evaluate the oxidation resistance ability of the MoSi₂-SiC-Si coating. The experimental results indicate that the prepared coating has good oxidation protection ability at a wide temperature range from room temperature to 1600 °C. Meanwhile, the oxidation of the coated samples is a weight gain process at temperatures from 800 to 1500 °C due to the formed SiO₂ layer on the surface of coating. After oxidation for 220 h at 1600 °C, the weight loss of the coated sample was only 0.96%, which is considered to be the excessive consumption of the outer coating and the appearance of defects in the coating. Two layers can be observed in the coating after oxidation, namely, SiO₂ layer and MoSi₂-SiC-Si layer.     

Boron removal by means of chemical precipitation with calcium hydroxide and calcium borate formation

Boron removal was investigated by chemical precipitation from aqueous solutions containing boron using calcium hydroxide. pH, initial boron concentration, amount of Ca(OH)₂, stirring speed and solution temperature were selected as operational parameters in a batch system. The highest boron removal efficiency was reached at pH 1.0. Increasing initial boron concentration and amount of calcium hydroxide raised to boron removal efficiency. Boron removal efficiency was highest at a stirring speed of 150 rpm. The most important parameter affecting boron removal efficiency was solution temperature. Increasing solution temperature increased importantly boron removal. XRD analysis showed that CaB₃O₃(OH)₅·4H₂O, which is a borate mineral called inyoite, occurred between Ca(OH)₂ and borate ions. As a result of the obtained experimental data, when the optimum operational conditions were selected, over 96% of boron removal efficiency was reached by this method.     

Transport and related properties of paint films. II. Dynamic mechanical properties and humidity effects

A systematic four-stage investigation of eight unpigmented coating formulations, including three vinyl, two polyurethanes, and three epoxy systems was done to provide baseline structural information upon which an improved understanding and an optimization of protective coatings can be founded. First, the results from dynamic mechanical measurements are provided and discussed for the base polymer component in each coating system. Second, the effects of humidity on the dynamic mechanical properties of these base polymers were determined at room temperature. The extent of property degradation was monitored by calculating the T_g depression with increased humidity, assuming a temperature–humidity superposition. The extent of degradation, as monitored by the T_g, was found to correlate directly with the level of hydrogen bonding in these coatings. Third, the influence of typical coating additives (a TCP plasticizer and a rosin hardener) on the properties of two of the vinyl coating systems was investigated. In the final stage, the synergistic effects of absorbed moisture and these additives on the coatings properties were investigated at room temperature. Increases in the concentration of these additives was found to magnify the degradation effect of increased humidity. This magnified degradation has been assigned to increased water absorption with increases in the concentration of either of these additives.     

Testing of starch-based carbohydrate polymer coatings for enhanced urea performance

In this study, starch–urea–borate adhesives were developed for coating the slow release urea. The physical properties of the developed adhesives were studied as a function of temperature, heating time, stirring rate, and pH. It was found that for certain specific adhesive composition, pH and stirring rate, the complete gelatinization time and corresponding adhesive viscosity do not remain constant with temperature. The suspension heated at 75°C reached its maximum viscosity after 21 min of heating, thereafter, remained constant over time. In contrast, the suspension heated at 80°C reached its peak viscosity after 12 min of heating. Further heating after 12 min caused a steady decrease in viscosity from its peak value of 450–339 cP. Once the adhesive physical properties were completely understood, a dripping solution technique was used to coat the urea granules with coating thickness ranging from 0.15 to 0.7 mm. It was noticed that the overall nutrients release time of the coated urea was three times higher than the uncoated urea. It was also concluded that the mechanical strength of coated urea strongly depends on the adhesive composition and coating thickness.     

Effect of MoS2 content on friction and wear properties of Mo and S co-doped CrN coatings at 25–600 °C

With increasingly harsh working environments for mechanical systems and the rapid development of various high-tech industries, requirements for the stable operation of mechanical systems are increasing in a wide temperature range. Mo and S co-doped CrN coatings with different MoS₂ contents were prepared via unbalanced magnetron sputtering to provide better friction properties to the coatings at high temperatures. Scanning electron microscopy and nanoindentation were adopted to analyze the microstructure and mechanical performance. The mechanical performance of the coatings was enhanced by increasing the MoS₂ content, however, excessive MoS₂ reduced the mechanical properties of the coatings. Besides, the adhesion of the coatings first increased and then decreased rapidly with the increase of the MoS₂ content. In addition, the residual stress of the coating first decreased and then increased upon increasing the MoS₂ content. The high-temperature tribological behavior of the coatings was measured from room temperature (25 °C) to 600 °C. The CrN/MoS₂-0.6A coating was found to exhibit low friction and wear coefficient at room temperature and relatively good comprehensive properties at high temperature. This study provides a feasible design for engineering applications and lays the foundations for the preparation of coatings with superior high-temperature friction properties.     

Effect of silicon/graphite ratio and temperature on oxidation protective properties of SiC/ZrB2–SiC coatings prepared by pack cementation

To investigate the silicon/graphite ratio and temperature on preparation and properties of ZrB₂–SiC coatings, ZrB₂, silicon, and graphite powders were used as pack powders to prepare ZrB₂–SiC coatings on SiC coated graphite samples at different temperatures by pack cementation method. The composition, microstructure, thermal shock, and oxidation resistance of these coatings were characterized and assessed. High silicon/graphite ratio (in this case, 2) did not guarantee higher coating density, instead could be harmful to coating formation and led to the lump of pack powders, especially at temperatures of 2100 and 2200 °C. But residual silicon in the coating is beneficial for high density and oxidation protection ability. The SiC/ZrB₂–SiC (ZS50-2) coating prepared at 2000 °C showed excellent oxidation protective ability, owing to the residual silicon in the coating and dense coating structure. The weight loss of ZS50-2 after 15 thermal shocks between 1500 °C and room temperature, and oxidation for 19 h at 1500 °C are 6.5% and 2.9%, respectively.     

钢铁常温环保型黑色转化膜的研究

实验研究了一种适用于钢铁的常温环保型黑色转化膜处理技术,通过考察溶液组分及工艺参数对膜层耐蚀性能的影响,获得了膜层制备的最佳条件,硫酸铜点滴法检验耐蚀时间可达174s,并探讨了成膜机理。     

A gradient composite coating to protect SiC-coated C/C composites against oxidation at mid and high temperature for long-life service

To improve the oxidation resistance of carbon/carbon (C/C) composites at mid and high temperature, a gradient composite coating was designed and prepared on SiC-coated C/C composites by in situ formed-SiO₂ densifying the porous SiC-ZrSi₂ pre-coating. SiO₂ gradient distribution was conducive to inhibiting the cracking of the coating. A dual-layer structure with the outer dense layer and the inner microporous layer was formed in the coating during densifying. The dense layer had excellent oxygen diffusion resistance and the microporous layer alleviated CTE mismatch between SiC inner coating and dense layer. Moreover, ZrSiO₄ particles inhibited crack propagation and stabilized SiO₂ glass. Therefore, the coating can protect the C/C composites from oxidation at 1473 K, 1573 K and 1773 K for 810 h, 815 h and 901 h, respectively. The coated samples underwent 30 thermal cycles between room temperature and 1773 K without mass loss, exhibiting good thermal shock resistance.     

Plasma electrolytic fluorination on Al alloys: Coating growth and plasma discharge behavior

The plasma electrolytic fluorination (PEF) process was conducted on 6061 Al alloy in the NH4F-EG non-aqueous electrolyte at room temperature. The microstructure and composition of the resultant coating were characterized by SEM, EDS, XRD and XPS. Also the coating growth and plasma discharge behavior were investigated by means of a well-designed jig, digital camera and OES, in order to understand the process characteristics. Results showed that the coating was dominantly composed of AlF₃, and characterized by a flake-like microstructure accompanying with some micro-pores and numerous micro-cracks. The internal of the coating was porous with a compact barrier layer near the substrate/coating interface. The fluorination of the substrate contributed the inward growth of the coating. PEF discharge sparks were characterized by tiny size and weak intensity during the whole process, of which the plasma electron temperature was about (3510 ± 110) K. Also, the discharge behavior and coating growth mechanism of the PEF process on Al alloy were discussed.     

Oxidation protection of carbon/carbon composites with SiC/indialite coating for intermediate temperatures

In order to improve the oxidation resistance of carbon/carbon composites at intermediate temperatures, a novel double-layer SiC/indialite coating was prepared by a simple and low-cost method. The internal SiC transition layer was prepared by pack cementation and the external indialite glass–ceramic coating was produced by in situ crystallization of ternary MgO–Al₂O₃–SiO₂ glass. The microstructures and morphologies of coating were determined by scanning electron microscopy (SEM), X-ray diffraction (XRD) and energy dispersive spectroscopy (EDS). Oxidation resistance of the as-coated C/C composites was evaluated in ambient air at temperature from 800 °C to 1200 °C. Nearly neglectable mass loss was measured after 100 h isothermal oxidation test, indicating that SiC/indialite coating possesses excellent oxidation protection ability. The as-coated samples have a good thermal shock resistance and no obvious damage was found in the coating even after suffered more than 11 thermal cycles between test temperature and room temperature. The oxidation protection mechanism of this coating was also discussed.     

Flue gas desulfurization by citrate process and optimization of working parameters

In this study, model flue gas was bubbled into 0.25 L tribasic sodium citrate (TSC) solution being in 0.5 L glass absorber to remove its SO₂ content. Size of gas bubbles, absorption temperature, gas flow rate, solution concentration and stirring rate were taken as working parameters to investigate their effect on SO₂ removal from flue gas. The Taguchi's experimental design method was used to obtain optimum values of working parameters for SO₂ saturation time of the TSC solution selected as a quality characteristic. The optimum levels of parameters to maximize the SO₂ saturation time of TSC solution were coarse bubbles for gas delivery, 35 °C for absorption temperature, 1.5 slm for gas flow rate, 0.5 M for TSC solution concentration and 500 rpm for stirring rate. Under these conditions, the SO₂ saturation time of the TSC solution was achieved as 511 min in average. The most effective parameters on the absorption of SO₂ in TSC solutions were ranked to the least as solution concentration, gas flow rate, size of gas bubbles, absorption temperature and stirring rate.