Properties of zirconia-toughened-alumina prepared via powder processing and colloidal processing routes

Alumina-zirconia composites were prepared by two routes: powder processing, and colloidal processing. Unstabilised zirconia powder was added to alumina in 5 wt%, 10 wt% and 20 wt% quantities. For the colloidal method, zirconium(IV) propoxide solution was added to alumina powder, also in 5 wt%, 10 wt% and 20 wt% quantities. Additions of glacial acetic acid were needed to form stable suspensions. Suspension stability was verified by pH measurements and sedimentation testing. For the powder processed samples Vickers hardness decreased indefinitely with increasing ZrO(2) additions, but for colloidal samples the hardness at first decreased but then increased again above >10 wt% ZrO(2). Elastic modulus (E) values decreased with ZrO(2) additions. However, samples containing 20 wt% zirconia prepared via a colloidal method exhibited a much higher modulus than the powder processed equivalent. This was due to the homogeneous dispersion of zirconia yielding a sample which was less prone to microcracking.     

ELECTRORHEOLOGICAL PROPERTIES OF TALC POWDER/SILICONE OIL SUSPENSIONS UNDER DC FIELDS

In this study, the electrorheological （ER） behavior of suspensions prepared from d50 = 2.4 lam talc powder, dispersed in insulating silicone oil （SO） medium was investigated. Sedimentation stabilities of suspensions （c = 5 wt%） prepared using these talc powder powders were determined to be 78 days. The ER activity of all the suspensions was observed to increase with increasing electric field strength, concentration and decreasing shear rate. The shear stress of talc powder suspensions increased linearly with increasing concentrations of the particles and with the applied electric field strength. Electric field viscosity of all the suspensions decreased sharply with increasing shear rate and showed a typical shear thinning non-Newtonian visco-elastic behavior. Effects of frequency on the ER activity of talc powder/SO system were also investigated.     

ELECTRORHEOLOGICAL PROPERTIES OF DIATOMITE/SILICONE OIL SUSPENSIONS UNDER DC FIELDS

In this study, electrorheological （ER） behavior of suspensions prepared from 3.0 and 9.0 μm diatomite particulate, dispersed in insulating silicone oil （SO） medium was investigated. Sedimentation stabilities of suspensions （c = 5 wt%） prepared using these diatomite powders were determined to be 32 days （d = 3 μm） and 24 days （d = 9 μm）, respectively. ER activity of all the suspensions was observed to increase with increasing electric field strength, concentration and decreasing shear rate. Shear stress of diatomite suspensions increased linearly with increasing concentrations of the particles and with the applied electric field strength. Electric field viscosity of all the suspensions decreased sharply with increasing shear rate and particle size, showing a typical shear thinning non-Newtonian visco-elastic behavior. Effects of high temperature and polar promoter onto ER activity ofdiatomite/SO system were also investigated.     

Shear rheology of micro-fibrillar cellulose aqueous suspensions

Micro-fibrillar cellulose aqueous suspensions with different fiber lengths were prepared by mechanical refining of softwood pulp fiber suspensions at different specific refining energies. Effects of refining energy level, micro-fiber concentration and temperature on the rheological properties of these aqueous suspensions were studied. These microfibers form a three-dimensional network, which displays typical shear-thinning behavior with little thixotropic tendency, at concentrations as low as 0.5 wt%. A viscoelastic analysis showed that these micro-fibrillar cellulose suspensions at different concentrations (from 0.5 to 2 wt%) exhibit a viscoelastic gel-like behavior [G′ > G″ over an extended range of frequencies (ω) and a weak dependency of G′ on ω] at 25 °C. The storage modulus, G′, at 1 rad/s increased strongly upon increasing concentration from 0.5 to 2 wt% following a power law with an exponent of 3.2. However, increasing the temperature decreases the storage modulus, G′, due to weakening or disruption of intermolecular interactions at elevated temperatures. The viscoelastic behavior changes to liquid-like, with G″ > G′ at the investigated frequency range, for the suspensions at 85 °C.     

高热稳定性三聚氰胺聚磷酸盐的合成

以三聚氰胺和磷酸为原料,以去离子水为溶剂,在杂多酸A催化下,制得改性三聚氰胺磷酸盐(MP);将MP在箱式气氛炉中进行多温度段热缩合反应合成了三聚氰胺聚磷酸盐(MPP),其结构经~(31)P NMR,IR和元素分析表征。通过TG对MPP的热稳定性和成炭性能进行了分析。结果表明:MPP失重1%时温度为372.1℃,失重5%时温度为382.7℃,700℃时残炭率为37.36%。     

Proton exchange membrane prepared by blending polybenzimidazole with poly (aminophosphonate ester)

In this article, we report a new amorphous-crystalline polymer blend system consisting of poly (4, 4′-diphenylether-5, 5′-bibenzimidazole) (OPBI) and poly (aminophosphonate ester) (PAPE) polymers, the membranes of which were fabricated using the solution blending route. A series of blend membranes at different ratios were prepared and systematically analysed for chemical interactions, morphological changes and their physico-chemical properties studied for use as proton exchange membrane. While FT-IR spectroscopy established the hydrogen bonding interactions between N–H of OPBI and phosphonate ester group of PAPE, X-ray diffraction studies revealed the development of crystallinity in the membrane matrix. Interestingly, the gradual induction of crystallinity in an amorphous OPBI matrix was found to influence the properties of the blend membranes favourably. For instance, the blend membrane containing 25 wt% PAPE in OPBI matrix displayed the maximum property enhancement in terms of storage modulus, glass transition temperature (T_g), phosphoric acid (PA) doping level (37 mol/OPBI repeat unit) and most importantly proton conductivity (0.135 S/cm at 180 °C) which is almost twice the value for pristine OPBI (0.05 S/cm at 180 °C) under identical conditions. Although improved properties were observed at other blend ratios as well, the studies ascertain that the membrane with 25 wt% PAPE was found to be the threshold ratio up to which properties increase and beyond which i.e. at >25 wt% PAPE, there is a decrement in properties like mechanical stability and proton conductivity. An important reason for this was attributed to the creation of a right balance of amorphous and crystalline domains and appropriate intra and inter-polymer hydrogen bonding interactions in the matrix of 75/25 (OPBI/PAPE) blend membrane.     

Gelation of cellulose nanocrystal suspensions in glycerol

Aqueous suspensions of cellulose nanocrystals (NCC) produced by sulfuric acid hydrolysis of natural cellulose fibres display a number of unique properties. In addition to forming equilibrium chiral nematic phases above some critical concentration, cellulose nanocrystal suspensions tend to gel or aggregate if the stability of the suspension decreases, for example because of a decrease in the surface charge density of sulfate ester groups, or a change in the properties of the suspending medium. Direct incorporation of unmodified nanocrystals into organic media usually leads to aggregation. We have found that it is possible to circumvent this difficulty and form clear thixotropic gels of unmodified NCC in glycerol, by careful evaporation of water from aqueous glycerol suspensions of NCC. The physical gels form at a fairly low (<3 wt%) concentrations of cellulose. The initial composition of the suspension, the temperature and rate of evaporation, and the time resting at room temperature all influence the formation of thixotropic gels. Desulfation of the acid-form nanocrystals, enhanced in the glycerol-rich suspensions, is shown to be a key step in this gelation process.     

Elevation of charring level of polyamide-6,6 films via ionic introduction of phosphoric acid and boric acid esters

Phosphorus and boron containing materials have the feature of increasing char formation, which can be effectively used as flame retardants especially in textiles. This paper discusses the ionic addition of phosphorus and boron esters to polyamide-6,6 (PA66), and its effect on the charring level. A mixture of phosphoric acid–boric acid ester at different degrees of esterification (ED) was prepared and two theoretical mechanisms for the esterification reaction were suggested. Ionically grafted polymer films were prepared by introducing the ester of highest ED to PA66–formic acid solution via three different processes: open air (cold) grafting, ultraviolet irradiation grafting, and hot vacuum oven grafting. Thermogravimetry was conducted for all synthesized esters and films, and the formation of new bonds between the ester and PA66 was verified using Fourier transform infrared spectroscopy.     

Tribochemical reaction dynamics of phosphoric ester lubricant additive by using a hybrid tight-binding quantum chemical molecular dynamics method

To study the atomistic behavior of the phosphoric ester molecule on the nascent Fe surface under boundary lubrication conditions, we adopted a hybrid tight-binding quantum chemical molecular dynamics method. First, we investigated chemical interactions between phosphoric ester and the nascent Fe surface. Phosphoric ester was shown to interact with the nascent Fe surface, forming both covalent and ionic bonds. Formation and dissociation dynamics of covalent bonds during tribochemical reaction was clearly observed during the simulation. The effect of friction condition on the tribochemical reaction dynamics was then studied, and it was indicated that friction would influence the formation and the dissociation of covalent bonds. By using a hybrid tight-binding quantum chemical molecular dynamics method, we obtained insights on initial tribochemical reaction processes for the formation of tribofilm from the phosphoric ester molecule on the nascent Fe surface.     

Effect of surfactant sucrose ester on physical properties of dairy whipped emulsions in relation to those of O/W interfacial layers

Dairy foams were manufactured on a pilot plant with various sucrose ester contents. Oil-in-water emulsions were produced by high-pressure homogenisation of anhydrous milk fat (20 wt%) with an aqueous phase containing skim milk powder (6.5 wt%), sucrose (15 wt%), hydrocolloids (2 wt%), and sucrose esters. Sucrose ester content was varied from 0 to 0.35 wt%. Firmness and stability of dairy foams were determined. The fraction of protein associated with emulsion fat droplets and the compression isotherms of those droplets were determined as a function of sucrose ester content. With less than 0.1 wt% sucrose ester, no foam could be produced. The most firm and stable foams were obtained with ca. 0.1 wt% sucrose ester. The fraction of protein associated with emulsion droplets suddenly falls from 60% at a sucrose ester content lower than 0.1125% down to ca. 10-20% for higher surfactant content. Compression isotherms of emulsion droplets at the air-water interface show that, in the presence of surfactant, emulsion droplets disrupt and spread at the interface whilst without surfactant they become dispersed. This means that the presence of sucrose ester causes some destabilisation of fat droplet interfacial layers. There is hence an optimal sucrose ester content that allows some destabilisation of the oil-water interface without concomitant protein displacement from that interface. Consequently, with the recipe and manufacturing process used to produce dairy foams, there exists a compromise in sucrose ester content with regards to manufacture and shelf-life of dairy foams.     

Improved electrorheological effect in polyaniline nanocomposite suspensions

We prepared polyaniline (PANI)/clay composites that are composed of both PANI-clay nanocomposite particles and pure PANI particles. The PANI-clay nanocomposite particles were made during the polymerization process, wherein PANI particles are attached on the surface of exfoliated clay particles modified by an aminosilane group. The PANI/clay composites were used as electrorheological fluids (ERFs) by dispersing them in silicon oil. The PANI-clay nanocomposite particles, which can form columnar structure under an electric field, strongly enhance the mechanical rigidity of the suspensions. The maximum yield stress of the PANI/clay composite suspensions (15 wt% in silicon oil) was 1.6 kPa at 3 kV/mm, while that of pure PANI was 300 Pa at the same electric field. A mechanism to explain the yield behaviors of the PANI-based nanocomposite suspensions is proposed.     

Electrorheological analysis of nano laden suspensions

The synthesis and characterization of Pb3O2Cl2 nanowires and the electrorheological (ER) properties of carbon nanofiber (CNF), carbon nanotube (CNT) and Pb3O2Cl2 nanowire (NW) laden suspensions is presented. The ER properties were investigated through oscillatory shear experiments. The viscoelastic response in the presence of dc electric fields was analyzed. Actuation behavior for the CNF and NW laden suspensions was observed at low voltages and low concentration of the reinforcements (0.05 wt%). In the case of the CNT laden suspensions, an effect was observed at a concentration of 0.0125 wt%. Positive and negative electrorheological behaviors were observed due to differences in electrical conductivity and polarization mechanisms.     

Preparation of stable aqueous suspensions of antimony-doped tin oxide nanoparticles used for transparent and thermal insulation fluorocarbon coating

In order to prepare the highly stable aqueous suspensions of antimony-doped tin oxide (ATO) used for the transparent and thermal insulation fluorocarbon coating, the effect of sodium polyacrylate (PAAS) and polyvinyl alcohol (PVA) on the stability of the suspensions was investigated. The stability and dispersity of the suspensions were characterized using zeta potential analyzer, ultraviolet–visible spectrophotometer, and scanning electron microscope. No sediments were observed after 6-month storage of the ATO suspensions containing 0.1 wt% PAAS and 2.0 wt% PVA. The reason why aqueous suspensions were capable of stabilization was explained from a theoretical perspective. A new model of steric hindrance for colloid particles stabilized by binary dispersant was proposed, which may have positive contribution to other colloid system containing two dispersants. A nano-composite fluorocarbon coating, exhibiting a good thermal insulation and high transmittance, was formed after ATO suspensions were added in fluorocarbon emulsion. The temperature inside the chamber was decreased by 6.0 °C, and 75.0 % visible light rays could pass through the coating.     

Rhodium fluorapatite catalyst for the synthesis of trisubstituted olefins via cross coupling of Baylis-Hillman adducts and arylboronic acids

Treatment of fluorapatite (prepared by incorporating basic species F(-) in apatite in situ by coprecipitation) with an aqueous solution of RhCl(3) resulted in rhodium-exchanged fluorapatite catalyst (RhFAP), which successfully promoted cross coupling of Baylis-Hillman adducts with arylboronic acids to yield trisubstituted olefins. A variety of arylboronic acids and Baylis-Hillman adducts were converted to the corresponding trisubstituted olefins, demonstrating the versatility of the reaction. The reaction is highly stereoselective. RhFAP was recovered quantitatively by simple filtration and reused with almost consistent activity.     

Recherches sur la formation et la transformation des esters LXXIII Sur la préparation d'acides ω-[aryl (ou aralcoyl ou alcoyl) carbamylamino]-alcoylphosphoriques et sur leur vitesse de scission à divers pH

N-Aryl(or aralkyl or alkyl)carbamoyl-aminoalkyl phosphoric monoesters have been prepared by the reaction of isocyanates R′-N?C?O on the corresponding amino-alkylphosphoric monoesters H₂N? R? OPO₃H₂ in the presence of 2 equivalents of NaOH. The rates of scission of the phosphoric monoester group and occasionally of the phenylcarbamoylamino group of these monoesters have been studied at 100°, in solutions 0.1M in ester and at various pH.     

Synthesis,Characterization and Application of Some Axially Chiral Binaphthyl Phosphoric Acids in Asymmetric Mannich Reaction

Two novel chiral Br?nsted acids 3b and 3c were prepared without involving the complexity of Suzuki coupling. Catalyst 3c bearing two additional hydroxyl groups at 3 and 3′ positions of axially chiral 1,1‐binaphthalene‐2,2′‐diol phosphoric acid was applied in a model Mannich reaction to afford β‐amino ester in high yield (92%) and enantiomeric excess (91%) at low reacting temperature of ?40°C. In addition, those β‐amino ester derivatives with high yields and excellent enatioselectivities were obtained in the presence of catalyst 3c under the above condition.     

Stability of Suspensions of Bioactive Particles Using Hybrid Organic–Inorganic Solutions as Dispersing Media

Functional coatings incorporating different types of particles developed by the sol–gel method have been proposed in the last few years for diverse applications. This work focuses on the preparation of homogeneous coatings prepared from stable suspensions with 10 wt% of glass and glass ceramic particles in a hybrid organic–inorganic solution as dispersing media. For this purpose, the pH was shifted up to 6–7 by adding tetrapropylammonium hydroxide (TPAH) which behaves as a cationic surfactant being probably adsorbed on the particles surface, while the sol maintains stable. Rheological measurements were performed to study the stability of the suspensions prepared at different conditions such as the kind and concentration of dispersant and the pH conditions. After sintering at 450^∘C/30 min, coatings around 2 μ m in thickness were obtained.     

芳纶纤维/SMPU-SiO2复合材料的界面性能研究

选用形状记忆聚氨酯(SMPU)和正硅酸乙酯(TEOS)为前驱体,固体酸对甲基苯磺酸(PTSA)为催化剂,利用空气中的水分为水解水源,通过溶胶-凝胶法原位制备了形状记忆聚氨酯与二氧化硅( SMPU-SiO2)杂化材料,并将杂化材料应用于芳纶纤维增强的柔性复合材料中,以期改善芳纶纤维与基体的界面性能.同时,针对芳纶纤维表面...     

不同松香改性树脂对农药可分散油悬浮剂物理稳定性的影响

研究了添加松香及其改性氢化松香甘油酯、氢化松香季戊四醇酯、松香改性对特辛基苯酚树脂对以油酸甲酯为介质的12.5%氰霜唑·吡唑醚菌酯可分散油悬浮剂物理稳定性及流变特性的影响。傅里叶变换红外光谱表征结果表明,与松香酸相比,氢化松香甘油酯、氢化松香季戊四醇酯和松香改性对特辛基苯酚树脂的羧基吸收峰消失且出现酯基的特征吸收峰。实验中,随加成烷基醇碳链的延长,软化点升高。且随着树脂的质量分数增加,制剂的粘度提高,物理稳定性也相应提高(析油率降低)。流变结果表明,添加松香改性树脂的可分散油悬浮剂体系呈正触变性,且树脂种类对体系的屈服值影响较大,具体表现为:松香改性对特辛基苯酚>氢化松香季戊四醇酯>氢化松香甘油酯>松香,制剂的物理稳定性也呈现相同的趋势。因此,松香改性树脂具有作为可分散油悬浮剂物理稳定剂的应用潜力。     

Density of organic phases in the extraction system tributyl phosphate-phosphoric acid

Data on the density of phosphoric acid solutions in crude TPB and TBP-based commercial extractant for purification of wet-process phosphoric acid are tabulated over the phosphoric acid concentration range 0.62–27.74 wt% (recalculated to P₂O₅).