超音速火焰喷涂含铝或锌中间层的YSZ热障涂层

在镁合金基底表面直接制备热障涂层,涂层的耐蚀性较差。采用超音速火焰喷涂法在镁合金基底和热障涂层之间分别制备了Al涂层和Zn涂层。通过XRD,SEM和EDS对涂层进行物相、微观结构和点扫描元素分析,采用电化学工作站对Al涂层试样和Zn涂层试样进行耐腐蚀性分析,同时研究了含Al中间层和含Zn中间层的热障涂层的抗热震性能。结果表明:Al涂层表面粗糙度(10.237±0.527μm)大于Zn涂层表面粗糙度(7.171±0.488μm),且喷涂过程中仅有轻微氧化。Al涂层试样的耐腐蚀性优于Zn涂层试样。含Zn中间层的热障涂层具有更好的抗热震性能。     

选择性固相微萃取涂层的研究进展

固相微萃取装置的核心部分是它的涂层,涂层的种类和厚度是影响分析灵敏度和选择性的最重要因素。具选择性的涂层可增强固相微萃取的分离能力,扩展它的应用范围。本文介绍了固相微萃取的类型,综述了近年来选择性固相微萃取涂层的研究进展,包括溶胶-凝胶涂层、限进介质涂层、分子印迹涂层等涂层的研制及应用。     

Nd_2O_3在宽带激光制备稀土活性梯度陶瓷涂层中的作用研究

采用宽带激光熔覆技术,通过在涂层中加入稀土氧化物Nd_2O_3来改善涂层显微组织、表面形貌和提高涂层生物活性、细胞相容性的方法,制备了一种梯度生物活性陶瓷涂层。利用金相分析、SEM分析手段对涂层显微组织、形貌进行了研究;通过模拟体液(SBF)浸泡实验考察了涂层活性;采用人成骨细胞与涂层材料共培养的方式,验证了细胞在涂层表面的粘附生长和定向分化能力。结果表明:涂层中添加Nd_2O_3时,涂层显微组织和表面形貌优于没有加入Nd_2O_3的涂层;加入Nd_2O_3的涂层表面生成的HA+β-TCP相多于没有添加Nd_2O_3的涂层,生物活性更好;添加Nd_2O_3的涂层具有更好的细胞相容性和细胞活性。     

金属氧化物涂层钛阳极的研究*

金属氧化物涂层钛阳极是指在以钛为阳极的基体表面涂上金属氧化物的电极,简称DSA。本文综述了钛基金属氧化物涂层电极的研究进展,包括钛基钌系涂层电极、钛基锡系涂层电极、钛基铅系涂层电极,以及其它氧化物涂层电极。评述了多元化钛基涂层的性能、各种涂层制备方法的优势与不足,阐明了掺杂稀土以及添加中间层对钛阳极的影响,同时展望了钛基金属氧化物涂层电极的发展方向。     

固相微萃取涂层及其形貌特征研究

采用物理涂渍、溶胶-凝胶技术(sol-gel)制备了固相微萃取(SPME)固相涂层：),γ-Al2O3涂层、聚丙烯酸树脂涂层、聚酰亚胺-二氧化硅溶胶凝胶涂层、聚酰亚胺-二氧化钛涂层。通过扫描电镜显示涂层表面形貌,并比较了萃取容量与涂层形貌间的关系.证明涂层的微观形态结构对涂层性能具有一定的影响,可以通过微观形态分析,了解不同微观结构对宏观性质的影响。     

梯度层不同配比对等离子喷涂Mo/8YSZ功能梯度热障涂层残余应力的影响规律研究

传统的金属/陶瓷双层热障涂层因不同涂层热物性参数的差异,易在涂层内部产生过大的残余应力,影响涂层质量及可靠性,而采用梯度结构的热障涂层,可实现涂层厚度方向热物性参数的连续平滑过渡,从而减小涂层间的残余应力,提升涂层的可靠性。梯度层配比不同,将使得涂层残余应力的分布情况及数值大小不同,为了研究不同梯度层配比对Mo/8YSZ功能梯度热障涂层残余应力的影响规律,利用ANSYS有限元分析软件建立了等离子喷涂Mo/8YSZ双层热障涂层及功能梯度热障涂层的数值模型,并在模型中考虑了材料热物性参数随温度变化,对比传统双层热障涂层,分析了不同梯度层配比对喷涂构件残余应力数值大小及分布区域的影响规律。结果表明:在喷涂参数相同的情况下,功能梯度热障涂层系统相比于双层热障涂层系统,径向最大残余拉应力与压应力均增大,轴向最大残余应力减小;伴随着过渡层第一层Mo比例的增加,喷涂构件的最大轴向残余拉应力增大,喷涂构件的最大轴向残余压应力减小;伴随着过渡层第一层Mo含量的增大,基体与涂层界面拉应力的分布区域增大,压应力的分布区域减小;采用功能梯度热障涂层结构,由于缓和了不同种类涂层间热物性参数的差异,可显著改善喷涂构件轴向的应力突变情况。     

抗结冰涂层: 从表面化学到功能化表面

在交通运输、航空航天、电力通信等诸多领域,结冰给人类和社会带来很大危害和安全隐患。现有的抗结冰方法如机械除冰、加热除冰以及喷洒化学试剂等虽然有效,但是存在耗能大和环境污染等问题。在基体表面涂装具有抗结冰性能的功能涂层被认为是一种必要的切实有效的方法,近年来备受关注。本文在介绍了涂层抗结冰原理及基体表面结冰影响因素的基础上,详细综述了近年来各类抗结冰涂层取得的研究成果,主要包括牺牲性涂层、疏冰涂层和超疏水涂层。重点介绍了制备抗结冰涂层所用的材料及方法,并分析了各种抗结冰涂层的优缺点,指出了抗结冰涂层目前存在的问题,最后对抗结冰涂层的发展趋势进行了分析和展望。     

固相微萃取法的纤维涂层的研究进展

对近十年中固相微萃取法的纤维涂层研究进展作了评述。内容涉及涂层的作用及性质,涂层萃取的原理,选择涂层的原则,纤维涂层制备技术的进展,应用现状及其优缺点等主题。对溶胶法的技术及原理作了重点介绍。还对固相微萃取法的纤维涂层的未来发展提出了展望（引述文献46篇）。     

SiO2纳米粒子对溶胶凝胶涂层性能的影响

在高强钢表面制备了防护性溶胶凝胶涂层,并研究了不同浓度二氧化硅纳米粒子的加入对于涂层形貌、耐蚀性和硬度的影响。采用扫描电子显微镜(SEM)和电子能谱(EDS)观察了涂层的微观结构和成分;采用显微硬度计测试了涂层的硬度;采用电化学方法研究了二氧化硅纳米粒子的浓度对于涂层耐蚀性能的影响;采用傅里叶红外光谱研究涂层的化学结构,进而探讨了二氧化硅纳米粒子对于涂层的强化机理。结果显示涂层加入二氧化硅纳米粒子的最佳浓度为500 mg.L-1,此条件下的涂层表面均匀致密,有较高的硬度并且在3.5%NaCl溶液中体现出较好的耐蚀作用。纳米粒子在溶胶中反应形成活性羟基基团并与硅烷发生反应生成空间网状结构,从而强化涂层。     

CeO_2添加剂对等离子ZrO_2涂层抗热震性的影响

在ZrO2陶瓷涂层中加入适量的CeO2,使陶瓷涂层的抗热震性能得到提高,这主要是由于CeO2的加入,涂层的微小孔隙增加、涂层产生细微的网状裂纹,增加了微裂纹密度,从而降低了涂层的弹性模量,释放了涂层中的应力,提高了涂层的裂纹失稳扩展时的临界温差ΔTc,并可阻止裂纹沿单方向的快速扩展,使涂层的抗热震起裂性能和抗热震失效能力得到提高。其中,CeO2加入量为9%效果最佳,过量加入CeO2,会过早地促进裂纹的扩展、断裂,不利于提高涂层的抗热震性能。     

Streaming current measurements in zirconia-coated capillaries

The electroosmotic flow created in zirconia-modified capillaries has been previously investigated. In this paper, we compared the electroosmotic data set with streaming current measurements and we related all these data through zeta-potential. Streaming current measurements give an excellent indication on the direction and the value of the electroosmotic mobility of an electrolyte/capillary system for a large set of experimental conditions: 2 < pH < 12, 0 < ACN < 80 %, 10(-4) M < [SO(2- )4 ] < 4 x 10(-2) M. A good correlation between zeta-potential from streaming current measurements and zeta-potential from electroosmotic mobility measurements was observed (r2 = 0.95). However, the values obtained from streaming current were always slightly lower than the one calculated from electroosmotic mobility (slope = 0.86, sigma = 0.06). In zirconia-coated capillaries the zeta-potential can be tuned from -50 to +100 mV depending on the composition of the electrolyte.     

On the pH hysteresis of electroosmotic mobility with capillary zone electrophoresis in silica capillary

Summary A porous gel model of silica-solution interface was proposed to explain the pH hysteresis effect on the electroosmotic mobility with capillary zone electrophoresis in silica capillaries. It is speculated that, under acidic preconditionings of the capillaries, a porous gel layer is formed at the silica-solution interface, and the magnitudes of potential and electroosmotic mobility are then reduced due to the penetration of electrolyte counterions to the gel layer. On the other hand, under basic preconditionings, a fresh silica surfaces is created by dissolution of silica in alkaline conditions, and this would result in higher values of potential and electroosmotic mobility. The Guoy-Chapman-Stern-Grahame model was employed to simulate the pH-dependence of electroosmotic mobility for the silica capillaries with a gelling surface and with a fresh surface. The predicted data were compared with the experimental results and shown to support the explanation.     

Thermoplastic microchannel fabrication using carbon dioxide laser ablation

We report the procedures of machining microchannels on Vivak co-polyester thermoplastic substrates using a simple industrial CO(2) laser marker. To avoid overheating the substrates, we develop low-power marking techniques in nearly anaerobic environment. These procedures are able to machine microchannels at various aspect ratios. Either straight or serpent channel can be easily marked. Like the wire-embossed channel walls, the ablated channel surfaces become charged after alkaline hydrolysis treatment. Stable electroosmotic flow in the charged conduit is observed to be of the same order of magnitude as that in fused silica capillary. Typical dynamic coating protocols to alter the conduit surface properties are transferable to the ablated channels. The effects of buffer acidity on electroosmotic mobility in both bare and coated channels are similar to those in fused silica capillaries. Using video microscopy we also demonstrate that this device is useful in distinguishing the electrophoretic mobility of bare and latex particles from that of functionalized ones.     

Quaternary ammonium substituted agarose as surface coating for capillary electrophoresis

A novel positively charged polymer of quaternary ammonium substituted agarose (Q-agarose) has been synthesized and explored for use as a coating in capillary electrophoresis. The fast and simple coating procedure is based on a multi-site electrostatic interaction between the polycationic agarose polymer and the negatively charged fused-silica surface. By simply flushing fused-silica capillaries with hot polymer solution a positively charged, hydrophilic deactivation layer is achieved. The polymer surface provides an intermediate electroosmotic flow of reversed direction, over a range of pH 2-11, compared to unmodified fused-silica. The coating procedure was highly reproducible with an RSD of 4%, evaluated as the electroosmotic flow mobility for 30 capillaries prepared at 10 different occasions. The application of Q-agarose coated capillaries in separation science was investigated using a set of basic drugs and model proteins and peptides. Due to the intermediate electroosmotic flow generated, the resolution of basic drugs could be increased, compared to using bare fused-silica capillaries. Moreover, the coating enabled separation of proteins and peptides with efficiencies up to 300.000 plates m(-1).     

ITP in dynamically double-coated fused-silica capillaries

Bidirectional ITP in fused-silica capillaries double-coated with Polybrene and poly-(vinylsulfonate) is a robust approach for analysis of low-molecular-mass compounds. EOF towards the cathode is strong (mobility >4.0 x 10(-8) m(2)/Vs) within the entire pH range investigated (2.40-8.08), dependent on ionic strength and buffer used and, at constant ionic strength, higher at alkaline pH. Electrokinetic separations and transport in such coated capillaries can be described with a dynamic computer model which permits the combined simulation of electrophoresis and electroosmosis in which the EOF is predicted either with a constant (i.e. pH- and ionic strength-independent) or a pH- and ionic strength-dependent electroosmotic mobility. Detector profiles predicted by computer simulation agree qualitatively well with bidirectional isotachopherograms that are monitored with a setup comprising two axial contactless conductivity detectors and a UV absorbance detector. The varying EOF predicted with a pH- and ionic strength-dependent electroosmotic mobility can be regarded as being realistic.     

Measurement of electroosmotic flow in plastic imprinted microfluid devices and the effect of protein adsorption on flow rate.

Several commercially available plastic materials were used as substrates in the fabrication of microfluid channels for biochemical analysis. Protocols for fabrication using the wire-imprinting method are reported for polystyrene, polymethylmethacrylate and a copolyester material. Channel sealing was accomplished by low-temperature bonding of a substrate of similar material; therefore, each channel was composed of a single material on all sides. The electroosmotic flow in 25-microm imprinted channels was evaluated for each substrate material. The copolyester material exhibited the highest electroosmotic flow mobility of 4.3 x 10(-4) cm2 V(-1) s(-1) which is similar to that previously reported for fused-silica capillaries. Polystyrene exhibited the lowest electroosmotic flow mobility of 1.8 x 10(-4) cm2 V(-1) s(-1). Plots of linear velocity versus applied electric field strength were linear from 100 V cm(-1) to 500 V cm(-1) indicating that heat dissipation is effective for all substrates in this range. Electroosmotic flow was reevaluated in the plastic channels following incubation in antibody solution to access the non-specific binding characteristics of a common biochemical reagent onto the substrate materials. All materials tested showed a high degree of non-specific adsorption of IgG as indicated by a decrease in the electroosmotic flow mobility in post-incubation testing.     

Evaluation of migration behaviour of therapeutic peptide hormones in capillary electrophoresis using polybrene-coated capillaries

Modelling electrophoretic mobility as a function of pH can be simultaneously used for determination of ionization constants and for rapid selection of the optimum pH for separation of mixtures of the modelled compounds. In this work, equations describing the effect of pH on electrophoretic behaviour were used to investigate migration of a series of polyprotic amphoteric peptide hormones between pH 2 and 12 in polybrene-coated capillaries. Polybrene (hexadimethrin bromide) is a polymer composed of quaternary amines that is strongly adsorbed by the fused-silica inner surface, preventing undesired interactions between the peptides and the inner capillary wall. In polybrene-coated capillaries the separation voltage must be reversed, because of the anodic electroosmotic flow promoted by the polycationic polymer attached to the inner capillary wall. The possibility of using polybrene-coated capillaries for determination of accurate ionization constants has been evaluated and the optimum pH for separation of a mixture of the peptide hormones studied has been selected. Advantages and disadvantages of using bare fused-silica and polybrene-coated capillaries for these purposes are discussed.     

Investigation of the stability of polyelectrolyte multilayer coatings in open-tubular capillary electrochromatography using laser scanning confocal microscopy

A simple polyelectrolyte multilayer (PEM) coating procedure was used for the development of stable modified capillaries. PEM coatings were constructed in fused-silica capillaries using alternating rinses of cationic and anionic polyelectrolytes. The multilayer coatings investigated in this study consisted of two and twenty layer pairs, or bilayers. A bilayer is one layer of a cationic polymer and one layer of an anionic polymer. Poly(diallyldimethylammonium chloride) was used as the cationic polymer, and the polymeric surfactant poly(sodium N-undecanoyl-L-leucylvalinate) was used as the anionic polymer. Previous studies for both chiral and achiral separations have shown that PEM-coated capillaries have excellent reproducibilities, remarkable endurance, and strong stabilities against extreme pH values when used in open-tubular capillary electrochromatography (OT-CEC). In this study, the stability of the coatings was further investigated after exposure to 0.1 M and 1.0 M NaOH. Structural changes of these coatings were monitored using laser scanning confocal microscopy (LSCM) after flushing the capillaries with NaOH. This technique allowed observation of the degradation of the coatings. Observations are discussed in terms of separations using OT-CEC. Electropherograms obtained from the chiral separation of 1,1'-binaphthyl-2,2'-dihydrogenphosphate in OT-CEC showed a decrease in selectivity and an increase in electroosmotic mobility after long exposure to NaOH. The ability to recover the capillaries by exposure to NaOH was also demonstrated. Measurements of electroosmotic mobility and selectivity showed that 2-bilayer and 20-bilayer PEM coatings could be completely removed from the capillary surface after approximately 3.5 and 9.5 h, respectively, of continuous exposure to 1 M NaOH.     

Polypyrrole-Coated and Polysulfate-Modified CE Capillaries

Fused-silica capillaries covalently coated with polypyrrole offer some interesting properties for capillary electrophoresis. The polymeric, surface-bonded coating is chemically stable and reduces the adsorptive properties of the silica surface. At the same time, the weak positive surface charges offer the possibility of creating a strongly anionic surface when poly-sulfates are used as counter-ions. This affords an electroosmotic flow which is largely independent of pH. With sodium dodecyl sulfate in the background electrolyte, this effect is further enhanced. The potential of the approach is demonstrated with the separation of herbicides by micellar electrokinetic chromatography. Repeatability of electroosmotic mobility of less than 1% RSD is achieved.     

Open-tubular capillary electrochromatography of small polar molecules using etched, chemically modified capillaries

The migration characteristics of small polar molecules are evaluated on etched, chemically modified capillaries with four different moieties (C5, C18, diol and cholesterol) bonded onto a silica hydride surface. The effects of pH on migration are used to determine the possible contributions of eletrophoretic mobility, electroosmotic flow (EOF) and analyte/bonded phase interactions. The EOF on etched capillaries is more complicated than on ordinary fused capillaries because it changes from anodic to cathodic as the pH is raised. A mixture of neurotransmitters and related compounds is used to further evaluate the effects of the bonded moiety on the separation properties of this particular electrophoretic format.