Development of a superporous hydroxyethyl cellulose‐based hydrogel by anionic surfactant micelle templating with fast swelling and superabsorbent properties

The self‐assembling anionic surfactant, sodium n‐dodecyl sulfonate (SDS) micelles were used as pore‐forming templating for fabricating novel superporous hydroxyethyl cellulose‐grafting‐poly(sodium acrylate)/attapulgite (HEC‐g‐PNaA/APT) hydrogels. The network characteristics, morphologies of the hydrogels and removing of SDS micelles from the final product by washing with ethanol/water (v/v, 7 : 3) procedure were determined by Fourier transform infrared spectroscopy and scanning electron microscopy, as well as by determination of swelling ratio, swelling rate, and stimuli response to salts and pHs. The results showed that the added‐SDS concentration significantly affected the morphologies and pore structure of the hydrogel, and 2 mM SDS facilitates to form a homogeneous and well‐defined pore structure in the gel network to extremely improve the swelling ratio and swelling rate. The 2 mM SDS‐added superporous HEC‐based hydrogel not only had highest equilibrium swelling ratio (Q_eq, 1118, 102 g g^?1 in distilled water and 0.9 wt % NaCl solution), rapid swelling rate (k_is, 5.2840 g g s^?1), also showed multistimulus responses to salts and pHs, which may allow its applications in several areas such as adsorption, separation and biomedical materials. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42027.     

Microstructure and properties of carbon fiber sized with pickering emulsion based on graphene oxide sheets and its composite with epoxy resin

The Graphene oxide (GO) sheets were used for preparing the epoxy resin Pickering emulsion. The particle size and the zeta potential of the Pickering emulsion were measured to evaluate its stability. The stable emulsion could be served as the film former of sizing agent for carbon fiber (CF). The effect of the Pickering emulsion stabilized by GO sheets on the properties of CF and the interfacial adhesion property of CF reinforced composite were investigated. Scanning electron microscopy (SEM) images showed that there existed a layer of sizing agent film with GO sheets evenly on the CF surface. Abrasion resistance and stiffness values of CF were tested and the results indicated that the sized CF conformed to the requirement of CF handleability. The interlaminar shear strength (ILSS) test indicated that the interfacial adhesion of the composite could be greatly improved. The fracture surfaces of CF composites were examined by SEM after ILSS tests. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42285.     

表面活性剂对Cu-H_2O和ZrO_2-H_2O纳米流体稳定性的影响

通过添加表面活性剂制备了Cu-H2O和Zr O2-H2O纳米流体,研究了十二烷基苯磺酸钠、十六烷基三甲基溴化铵和辛基苯基聚氧乙烯醚等表面活性剂对Cu-H2O和Zr O2-H2O纳米流体分散稳定性的影响;并利用分子动力学方法计算出不同表面活性剂分子与Cu/Zr O2颗粒表面的相互作用能。结果发现添加表面活性剂可较大程度地提升纳米流体的稳定性,而尤以添加十二烷基苯磺酸钠的效果最为明显,计算结果也显示十二烷基苯磺酸钠分子与Cu/Zr O2间的吸附作用最强。此外,还模拟了SDBS与Cu-H2O纳米流体中Cu颗粒的吸附行为。     

Facile fabrication of superhydrophobic polyaniline structures and their anticorrosive properties

We report a simple approach for the preparation of superhydrophobic polyaniline (PANI) and its application for the corrosion protection coatings. First, PANI was synthesized conventionally by oxidative polymerization with APS. Subsequently, PANI with different wettability was obtained by modification with different surfactants. The surface modification of PANI with three different surfactants (sodium dodecylbenzenesulfonate, polyethylene glycol, and cetyltrimethylammonium bromide) provided excellent surface superhydrophobicity (water contact angle >150°). The structure and morphology of as‐prepared PANI were characterized with Fourier transform infrared, Energy dispersive X‐ray spectroscopy, and Scanning electron microscopy. Corrosion protection performance of PANI with different wettability was evaluated in 3.5% NaCl electrolyte using Tafel polarization curves and electrochemical impedance spectroscopy. The results indicated that various superhydrophobic PANI coatings have better anticorrosion performance as compared to the hydrophilic PANI. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44248.     

Conducting polymerized high‐internal‐phase emulsion/single‐walled carbon nanotube nanocomposite foams: Effect of the aqueous‐phase surfactant type on the morphology and conductivity

Poly(styrene‐co‐divinylbenzene)/single‐walled carbon nanotubes (SWCNTs) polymerized high‐internal‐phase emulsion (polyHIPE) nanocomposite foams were successfully synthesized with various types of aqueous‐phase surfactants. The effects of anionic, cationic, nonionic, and mixed surfactants on the morphology and electrical conductivity of the resulting nanocomposite foams were investigated. The use of an anionic surfactant, sodium dodecylbenzesulfonate (SDBS), did not completely result in the typical polyHIPE nanocomposite foam microstructure because of the partial instability of the high‐internal‐phase emulsion. The nanocomposite foams synthesized by nonionic surfactants, that is, Pluronic F127 and Triton X‐100, and the cationic/anionic mixture, cetyltrimethylammonium bromide/SDBS, exhibited the proper morphology, but the resulting nanocomposite foams were electrically insulators. Interestingly, the use of a Gemini‐like surfactant, sodium dioctylsulfosuccinate (SDOSS), significantly improved both the typical morphology and electrical properties of the resulting nanocomposite foams because of the probable stronger interactions of SDOSS molecules with SWCNTs. The typical morphology of the nanocomposite foam synthesized with the SDOSS/F127 mixed surfactant was significantly improved, but the electrical conductivity decreased to some extent compared with the SDOSS‐synthesized nanocomposite foams. This behavior was attributed to an increase in the tunneling length of the electrons between adjacent SWCNTs. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43883.     

Micellization Behavior of Long-Chain Substituted Alkylguanidinium Surfactants

Surface activity and micelle formation of alkylguanidinium chlorides containing 10, 12, 14 and 16 carbon atoms in the hydrophobic tail were studied by combining conductivity and surface tension measurements with isothermal titration calorimetry. The purity of the resulting surfactants, their temperatures of Cr→LC and LC→I transitions, as well as their propensity of forming birefringent phases, were assessed based on the results of ¹H and ¹³C NMR, differential scanning calorimetry (DSC), and polarizing microscopy studies. Whenever possible, the resulting values of Krafft temperature (T_K), critical micelle concentration (CMC), minimum surface tension above the CMC, chloride counter-ion binding to the micelle, and the standard enthalpy of micelle formation per mole of surfactant (Δ_micH°) were compared to those characterizing alkyltrimethylammonium chlorides or bromides with the same tail lengths. The value of T_K ranged between 292 and 314 K and increased strongly with the increase in the chain length of the hydrophobic tail. Micellization was described as both entropy and enthalpy-driven. Based on the direct calorimetry measurements, the general trends in the CMC with the temperature, hydrophobic tail length, and NaCl addition were found to be similar to those of other types of cationic surfactants. The particularly exothermic character of micellization was ascribed to the hydrogen-binding capacity of the guanidinium head-group.     

Synthesis,Characterization, Surface and Biological Activity of Diquaternary Cationic Surfactants Containing Ester Linkage

Two series of diquaternary cationic surfactants designated as E9Nm and E11Nm having two different alkyl chains in their chemical structure were synthesized. The chemical structures of these surfactants were confirmed using elemental analysis, FTIR and ¹H‐NMR spectra. The surface activities of the different surfactants were determined using surface and interfacial tension at 25 °C. The surface parameters including: critical micelle concentration, effectiveness, efficiency, maximum surface excess and minimum surface area were determined. The surface activities of the cationic surfactants were correlated with their chemical structure. The surface activities of the surfactants increased with increasing the hydrophobic chain length. The adsorption and micellization tendencies of the surfactants in solution were determined using the free energies of adsorption and micellization. The synthesized surfactants were evaluated as biocides against bacteria and fungi. Biocidal activity data showed that a gradual increase in the hydrophobic chain length of the surfactant molecules gradually increases the efficiency of these surfactants as biocides.     

Synthesis and Evaluation of Bis-quaternary-Based Surfactants as Additives for Water-Based Mud

Two series of cationic gemini surfactants, alkanediyl-α,ω-bis[N,N-dimethyl alkyl (octyl or dodecyl)ammonium] dibromide (R-s-R; s = 6, 10, 12 and R = 8 and 12) were prepared and evaluated as additives for water-based mud. The chemical structures of the prepared surfactants were confirmed using FTIR and mass spectroscopy. Surface activity of these compounds has been studied and their surface properties including surface tension, emulsification power, critical micelle concentration, effectiveness, maximum surface excess and minimum surface area were determined. The results showed that the prepared compounds have significant surface activity, especially those of longer hydrophobic chain length. The prepared cationic gemini surfactants were evaluated as viscosifiers and filter loss additives for water-based mud formulated from local Na-montmorillonite clay. XRD analysis was carried out to the Na-montmorillonite clay to determine the interaction of the surfactants with inter layers of the clay structure. Rheological properties, gel strength, thixotropy, filtration properties and the effect of temperature on rheological properties of the water-based mud were studied. The results indicated that the gemini surfactants have a positive effect on the rheological and filtration properties of the Na-montmorillonite clay according to American Petroleum Institute specifications.     

蓝晶石和石英浮选行为的研究（待续）

通过表面张力测试、浮选试验和红外光谱的测定，研究了蓝晶石和石英在阴／阳离子混合表面活性剂系统中的浮选行为。研究结果说明了表面活性剂混合物引起的表面张力下降中的协同作用。在浮选系统中，由于这一协同作用的存在，油酸钠／十二胺的添加导致在很宽的ｐＨ范围内，浮选回收率提高。文中还分析了在阴／阳离子混合表面活性剂系统中捕收剂的吸附机理。     

微通道反应器中工业混合直链烷基苯磺酸盐的连续合成工艺研究

直链烷基苯磺酸是一种重要的阴离子表面活性剂,由其合成的直链烷基苯磺酸盐是价格低廉的表面活性剂之一,广泛应用于洗涤和三次采油等领域。以某煤制油企业的工业混合烯烃生产的直链烷基苯为原料,在微通道反应器中连续合成直链烷基苯磺酸,考察磺化温度、原料摩尔比以及磺化剂浓度等工艺条件对磺酸产物的影响规律,并与纯十六烷基苯磺化规律进行对比。研究发现混合直链烷基苯磺化过程中各个工艺条件对产品收率的影响较大。在反应温度为50℃,SO₃与LAB摩尔比为1.0∶1,停留时间为5.09 s条件下,最终产品中活性物含量可达到94.5%(质量)。同时,设计并搭建了微反应器小试平台,实现连续合成混合烷基苯磺酸盐,磺酸盐产品收率在90%以上,可为该工艺的工业应用提供技术支持。