WC/MMT纳米复合材料制备及其对PNP的电催化活性

以剥离后的蒙脱石(MMT)为载体,将浸渍法与原位还原技术相结合制备了碳化钨/蒙脱石(WC/MMT)纳米复合材料。采用X射线衍射、扫描电子显微镜和透射电子显微镜等手段对样品进行了表征。结果表明,剥离后蒙脱石的片层厚度为10～15 nm,层间距增大,边缘发生卷曲;复合材料由碳化钨(WC)、碳化二钨(W₂C)和蒙脱石组成,碳化钨颗粒均匀地分布于蒙脱石外表面。采用循环伏安法测试了样品对对硝基苯酚(PNP)的电化学还原性能,结果表明,WC/MMT纳米复合材料对对硝基苯酚具有良好的电催化活性,且具有较好的稳定性。蒙脱石是碳化钨基复合电催化材料良好的载体。     

蒙脱石的湿法机械球磨剥离

以内蒙古钙基蒙脱石为原料,通过湿法改型、改性制备了钠基蒙脱石和有机蒙脱石.分别以钙基蒙脱石、钠基蒙脱石和有机蒙脱石为对象,在乙醇中湿法机械球磨、超声处理蒙脱石,利用XRD、TEM、AFM等手段研究了机械球磨法对不同层间离子的蒙脱石剥离效果.结果表明,内蒙古钙基蒙脱石湿法钠化及有机化效果良好,机械球磨法剥离钠基蒙脱石效果最佳,剥离型蒙脱石片层尺寸小于200 nm,其平均厚度约为15 nm;有机蒙脱石层间有机物具有稳定蒙脱石片层的作用,有机改性不能促进机械球磨法对蒙脱石片层的剥离.     

聚丙烯/蒙脱土纳米复合材料的结构及物理性能研究

采用化学反应法制备了Ziegler-Natta/有机改性蒙脱土复合催化剂,并通过丙烯单体原位插层聚合法制备出聚丙烯/蒙脱土(PP/MMT)纳米复合材料,研究了复合材料的微观结构、热性能以及加工稳定性等。结果表明,原位聚合法制备的复合材料为剥离型纳米复合材料,其中MMT片层以纳米尺寸均匀分散在PP基体中,MMT平均厚度小于10nm;随MMT含量的提高,复合材料的热稳定性提高;原位聚合制备的PP/MMT纳米复合材料在长时间剪切过程中部分MMT会发生自聚集,控制剪切时间可以有效防止MMT的自聚集;原位聚合制备的PP/MMT复合材料(粉料)中,PP以α晶型为主,纳米MMT的引入并不会诱导生成聚丙烯β晶型,复合材料中β晶型的出现与退火条件有关。     

蒙脱石有机化对PVA/蒙脱石复合薄膜的性能影响

以精制钠基蒙脱石(Na-MMT)、有机化蒙脱石(OMMT)和聚乙烯醇(PVA)为原料,通过水溶液插层-流延成膜法制备纳米复合薄膜。通过X射线衍射(XRD)、扫描电子显微镜(SEM)和热重分析(TGA)对复合材料的结构和性能进行表征,重点探讨蒙脱石有机化对PVA/MMT复合薄膜性能的影响。结果表明Na-MMT和OMMT纳米颗粒在PVA基体中均得到了良好分散;有机改性剂的存在促使PVA/MMT复合薄膜的MMT片层间距扩撑更大,但由于其与PVA相容性较差,导致有效插入MMT片层间的PVA分子较少,PVA/MMT复合薄膜的热稳定性改善效果不明显。     

不同蒙脱石的有机插层及聚合剥离

以成因、类型、性质不同的6种蒙脱石为原料,制备了有机插层和聚酰胺6／蒙脱石纳米复合材料。研究了蒙脱石矿物类型、成分及阳离子交换容量对其有机插层及聚合剥离的影响。结果表明：有机插层蒙脱石层间距随插层剂用量及阳离子交换容量的增加而增加,低阳离子交换容量及高钠含量蒙脱石更有利于插层剥离。钠化对蒙脱石有机插层影响不明显。     

固相法与液相法合成Al/Mg-LDH处理模拟含氟废水的比较

层状双金属氢氧化物(LDH)因其特殊的层状结构、层间距的可调性,以及层板内阴离子数量与种类的多样性,制备无机或无机/有机复合功能材料,可广泛地应用于催化、医药、吸附等领域。Mg/Al-LDH因结构特性在吸附领域受到关注。因此,制备Mg/Al-LDH已成为国内外该领域的研究热点。但是,Mg/Al-LDH作为吸附材料对含氟废水进行研究的文献很少见。本文根据文献报道用不同方法合成Mg/Al-LDH。用氟化钠作为原料配制模拟污水,用不同法合成的LDH做吸附剂进行吸附试验,对两种不同的LDH的吸附性能做了比较。     

剥离型葡萄糖酸蒙脱石的制备及其表征

利用葡萄糖酸改性碱性钙基膨润土制备了一种与水溶性高分子材料亲合性较强的剥离型葡萄糖酸蒙脱石.通过单因素实验,分析了葡萄糖酸用量、反应温度、分散剂浓度等因素对葡萄糖酸蒙脱石剥离的影响,认为蒙脱石剥离可能是由于层间发生激烈的中和反应造成的.电子显微镜扫描表明这种剥离型蒙脱石为片状结构,纳米片的厚度为75～100 nm; DSC测定表明该葡萄糖酸蒙脱石的失水温度与葡萄糖酸钙相同,葡萄糖酸基团分布在纳米片的表面上;IR 扫描表明葡萄糖酸与蒙脱石的结合方式为化学键;XRD表征说明该葡萄糖酸蒙脱石仍为层状结构,为多层蒙脱石晶片组成.将该葡萄糖酸蒙脱石添加到木薯淀粉糊中,能使淀粉糊的黏性增加一倍.     

聚乙烯醇/蒙脱石纳米复合材料的结构与性能

通过溶液插层 流延成膜法,以聚乙烯醇和钠质蒙脱石为原料,制备出了不同蒙脱石含量的聚乙烯醇/蒙脱石纳米复合材料薄膜。用X射线衍射(XRD)、扫描电子显微镜(SEM)、热重分析(TGA)和力学性能测试对复合材料的结构和性能进行了表征。结果表明,聚乙烯醇分子成功进入蒙脱石的层间,实现了在纳米尺度上的复合;蒙脱石含量高于7 5wt%形成插层型的纳米复合材料,低于7 5wt%形成剥离型的纳米复合材料;在SEM图片上还观察到了纳米复合材料的微观结构。纳米复合材料的热稳定性、拉伸强度和直角撕裂强度均比纯聚乙烯醇有很大提高。     

剥离型聚苯胺/蒙脱石介孔材料制备与结构表征

采用插层聚合法制备剥离型聚苯胺/蒙脱石介孔材料,着重研究了过硫酸铵的加入量、pH值和反应时间对吸附材料结构与性能的影响,利用XRD、FT-IR和BET比表面积测试法等手段对吸附材料的结构特性进行了表征.结果表明:过硫酸铵剂的加入量为4 g、pH值为3.0、聚合反应时间为1.5h时,制备出孔径为35.66 nm、比表面积为22.51 m2/g的剥离型聚苯胺/蒙脱石介孔材料.     

有机蒙脱石改性PA6/ABS合金材料的制备和性能

利用环氧化合物(EP)表面处理蒙脱石(MMT),制备的有机蒙脱石(OMMT)层片间距增加到5.13 nm,热降解温度高达380.3℃。研究了苯乙烯与马来酸酐(MAH)的共聚物(SMA)对PA6/ABS合金的增容效果,当增容剂用量为4%,合金的综合性能最好。制备了PA6/ABS/OMMT复合材料,随着SMA含量的增加,PA6/ABS/OMMT复合材料力学性能和耐热温度都有较大幅度的提高。     

Morphology and thermal stabilization mechanism of LLDPE/MMT and LLDPE/LDH nanocomposites

The morphology and thermal stabilization mechanism of polymeric nanocomposites prepared by solution intercalation of linear low density polyethylene (LLDPE) with montmorillonite (MMT), MgAl layered double hydroxide (LDH), and ZnAl LDH have been studied by X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic Fourier transform infrared (FTIR) spectroscopy, and thermogravimetric analysis (TGA). Both LLDPE/MMT and LLDPE/MgAl LDH nanocomposites exhibit mixed intercalated-exfoliated structures, whereas the LLDPE/ZnAl LDH nanocomposites exhibit completely exfoliated structures because the ZnAl LDH layers can be easily broken during the refluxing process. All nanocomposites show significantly enhanced thermal stability compared with virgin LLDPE due to the increases of the effective activation energy (E_α) during degradation process. However, LDHs nanocomposites show much higher thermal degradation temperatures than MMT nanocomposites with the same filler content because they have much higher E_α than MMT nanocomposites at the early degradation stage. The data of real time FTIR spectroscopy and morphological evolution reveal a catalytic dehydrogenation effect presents in MMT nanocomposites, which may decrease the E_α of degradation and thermal stability of MMT nanocomposites.     

Ethylene vinyl acetate/Mg‐Al LDH nanocomposites by solution blending

Partially exfoliated ethylene vinyl acetate (EVA‐40, 40% vinyl acetate content)/layered double hydroxide (LDH) nanocomposites using organically modified layered double hydroxide (DS‐LDH) have been synthesized by solution intercalation method. X‐ray diffraction (XRD) and transmission electron microscopy (TEM) studies of nanocomposites shows the formation of exfoliated LDH nanolayers in EVA‐40 matrix at lower DS‐LDH contents and partially intercalated/exfoliated EVA‐40/MgAl LDH nanocomposites at higher DS‐LDH contents. These EVA‐40/MgAl LDH nanocomposites demonstrate a significant improvement in tensile strength and elongation at break for 3 wt% of DS‐LDH filler loading compare to neat EVA‐40 matrix. Thermogravimetric analysis also shows that the thermal stability of the nanocomposites increases with DS‐LDH content in EVA‐40. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Effect of the incorporation of montmorillonite-layered double hydroxide nanoclays on the corrosion protection of epoxy coatings

A series of layered double hydroxide (LDH)/montmorillonite (MMT) nanocomposite coating, LDH nanocomposite coating, and MMT nanocomposite coating were successfully prepared. The nanocomposite materials were characterized by X-ray diffraction and scanning electron microscopy (SEM). To understand the effect of MMT and LDH on the corrosion inhibition performance of epoxy resin coatings immersed in 3.5 wt% saline solution at 90°C, electrochemical impedance spectroscopy and an autoclave test were performed on epoxy resin; epoxy resin blended with LDH, MMT, and LDH + MMT (LM) coatings painted on Q345 steel. The metal/coating interfaces were observed by SEM and energy-dispersive spectroscopy. Results showed that addition of LDH and MMT improved the protection properties of the epoxy resin coatings. The corrosion protection of the LM nanocomposite coating was superior to that of the other coatings. This finding can be attributed to the ionic selectivity and barrier effect of MMT and LDH nanoclay platelets dispersed within the composite coatings.     

Layer double hydroxide and sodium montmorillonite multilayer coatings for the flammability reduction of flexible polyurethane foams

Flexible polyurethane foam (PUF) is coated by layer‐by‐layer (LbL) assembly using branched polyethyleneimine (BPEI), poly(acrylic acid) (PAA), and two different charged nanoparticles, such as sodium montmorillonite (Na‐MMT) and layered double hydroxide (LDH). Three different deposition strategies, that is, bilayer, trilayer, and quadlayer, exhibit different coating growth, morphology, and flammability properties. Changing the nanosheet from LDH to MMT dramatically alter the coating mass for the same number of layers. A five bilayer PAA/BPEI+LDH coating reduced the peak heat release rate by 40% and the average heat release rate by 70%, which is two times more effective than commercial fire retardants (FRs) and other LbL‐FR coatings for PUF. MMT and LDH mixed multilayers resulted in effective flame‐retardant coatings with less coating mass by manipulating the deposition strategy. This study manifests the flexibility of LbL to fine‐tune flammability reduction by switching the coating weight gains, which is significant to accelerate the development of other LbL coating regardless of the intended applications. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41767.     

聚合物/层状硅酸盐纳米复合材料的制备研究

本文以聚丙烯和有机蒙脱土为原料，采用插层复合法制备聚合物／层状硅酸盐纳米复合材料，用透射电镜对复合材料的结构进行表征，测定了复合材料的力学性能，结果表明，用马来酸酐化聚丙烯作界面相容剂，聚丙烯大分子链分子插层进入到有机改性蒙脱土的硅酸盐片层中间，并且聚丙烯／蒙脱土纳米复合材料的力学性能有一定的提高。     

Natural rubber/cis‐1,4‐polybutadiene nanocomposites: Vulcanization behavior,mechanical properties,and thermal stability

Natural rubber/cis‐1,4‐polybutadiene (NR/BR) blends with two types of layered nanofillers, montmorillonite (MMT) and layered double hydroxide (LDH), both in pristine and organically modified forms are produced and investigated. Faster curing is found for all the NR/BR blends, except for the one containing the unmodified MMT. This effect can be attributed to the groups placed in the interlayer regions of the clays; more precisely to ammonium groups for the organo‐MMTs and to ? OH groups for LDHs. Mechanical properties and thermal stability of rubber compounds are investigated. It has been demonstrated that the performance of the final nanocomposite is significantly affected by the kind of clay. Particularly, the organo‐MMTs provoke an improvement of the mechanical properties and increase the thermal stability of about 4–5° C in respect to the pure NR/BR matrix. On the contrary, the poor compatibility of unmodified MMT and of LDH clays with the rubber blend is evident and no enhancement on the composite performance has been observed. POLYM. ENG. SCI., 2013. © Society of Plastics Engineers     

Synthesis and characterization of ethylene vinyl acetate/Mg–Al layered double hydroxide nanocomposites

Mg–Al layered double hydroxide (LDH)/Ethylene vinyl acetate (EVA‐28) nanocomposites were prepared through solution intercalation method using organically modified layered double hydroxide (DS‐LDH). DS‐LDH was made by the intercalation of sodium dodecyl sulfate (SDS) ion. The structure of DS‐LDH and its nanocomposites with EVA‐28 was determined by X‐ray diffraction (XRD) and transmission electron microscope (TEM) analysis. XRD analysis shows that the original peak of DS‐LDH shifted to lower 2θ range and supports the formation of intercalated nanocomposites while, TEM micrograph shows the presence of partially exfoliated LDH nanolayers in addition to orderly stacked LDH crystallites in the polymer matrix. The presence of LDH in the nanocomposites has been confirmed by Fourier transform infrared (FTIR) analysis. The mechanical properties show significant improvement for the nanocomposite with respect to neat EVA‐28. Thermogravimetric (TGA) analysis shows that thermal stability of the nanocomposites is higher than that of EVA‐28. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1845–1851, 2007     

Preparation and characterization of exfoliated layered double hydroxide/silicone rubber nanocomposites

Silicone rubber (SR)/Mg–Al layered double hydroxide (LDH) nanocomposites were prepared by the solution intercalation of SR crosslinked by a platinum‐catalyzed hydrosilylation reaction into the galleries of dodecyl sulfate intercalated layered double hydroxide (DS–LDH). X‐ray diffraction and transmission electron microscopy analysis showed the formation of exfoliated structures of organomodified LDH layers in the SR matrix. The tensile strength and elongation at break of SR/DS–LDH (5 wt %) were maximally improved by 53 and 38%, respectively, in comparison with those of the neat polymer. Thermogravimetric analysis indicated that the thermal degradation temperature of the exfoliated SR/DS–LDH (1 wt %) nanocomposites at 50% weight loss was 20°C higher than that of pure SR. Differential scanning calorimetry analysis data confirmed that the melting temperature of the nanocomposites increased at lower filler loadings (1, 3, and 5 wt %), whereas it decreased at a higher filler loading (8 wt %). The relative improvements in the solvent‐uptake resistance behavior of the SR/DS–LDH nanocomposites were also observed. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

LDH@MMT/MZBMSO的制备及其在皮革中的阻燃性能

采用水热法在蒙脱土（MMT）表面原位生长层状双氢氧化物（LDH），获得了层状双氢氧化物@蒙脱土（LDH@MMT）。通过XRD、SEM、FTIR对LDH@MMT进行了表征。结果表明，LDH和MMT通过氢键复合在一起，呈花状结构。将其引入花椒籽油（ZBMSO）中制得层状双氢氧化物@蒙脱土/改性花椒籽油（LDH@MMT/MZBMSO），TEM结果表明：LDH@MMT均匀分散在MZBMSO中。将其应用于皮革加脂工艺，结果表明：与MZBMSO加脂坯革相比，当LDH@MMT的质量占ZBMSO的12%时，LDH@MMT/MZBMSO加脂坯革阻燃性能明显提高，加脂坯革氧指数由22.8%提升至28.3%，有焰燃烧时间由87 s减少到43 s，热释放速率降低了43.6%，总热释放速率降低了73.6%，产烟速率降低了63.5%；LDH@MMT包裹在坯革纤维表面，形成的“曲折路径”可减缓热量及烟气的释放，燃烧后在纤维表面形成致密碳层进一步阻隔坯革燃烧过程中释放的热量、烟气，并隔绝氧气，从而提升了加脂坯革的阻燃抑烟性能。