Synergistic effect of compatibilizer in organo‐modified layered silicate reinforced butadiene rubber nanocomposites

We have prepared nanocomposites of intercalated and exfoliated organosilicates in butadiene rubber (BR) by using a two‐stage melt blending process. We used X‐ray diffraction and transmission electron microscopy to examine, respectively, the intergallery spacing of the organosilicates and their dispersion in the BR. Marked enhancements in the mechanical and thermal properties of BR occurred when it incorporated <10 parts of organosilicates and the loading ratio of the organosilicate to dicarboxylic acid‐terminated butadiene oligomer was approximately three. In particular, the addition of 10 parts of organosilicate and 3 parts of compatibilizer in the BR led to a more than four‐fold increase in the tensile strength, a 150% increase in modulus at 100% elongation (M100), and 232 and 410% enhancements in the tear strength and elongation at break, respectively, relative to those of neat BR. The degradation temperature for the BR nanocomposite containing only a 10‐part loading of organosilicate was 51°C higher than that of neat BR; these increases reduced, however, to 9–13°C upon the addition of the CTB compatibilizer. In addition, the relative water vapor permeabilities of the BR nanocomposites containing 10 parts of organosilicate—both in the presence and absence of the compatibilizer—reduced to 20% of that of the neat BR. POLYM. ENG. SCI. 46:80–88, 2006. © 2005 Society of Plastics Engineers     

Dielectric and thermal properties of dicyclopentadiene containing bismaleimide and cyanate ester. Part IV

A novel bismaleimide (BMI), bis(4-maleimidophenoxy-3,5-dimethylphenyl)dicyclopentadiene (DCPDBMI), containing a large dicyclopentadiene (DCPD) and aryl ether linkage, was synthesized from bis(4-aminophenoxy-3,5-dimethylphenyl)dicyclopentadiene and maleic anhydride by the usual two-step procedure that included ring-opening addition to give bismaleamic acid, followed by cyclodehydration to bismaleimide. The monomers were characterized by Fourier transform infrared spectroscopy (FT-IR), proton nuclear magnetic resonance (NMR), elemental analyses (EA), and mass spectra (MS). A series of bismaleimide-triazine (BT) resins were prepared from synthesized bismaleimide (DCPDBMI) and then cured with 2,6-dimethyl phenol-dicyclopentadiene dicyanate ester (DCPDCY) at various molar ratios. Thermal properties of cured BT resins (DCPDBMI/DCPDCY) were studied using dielectric analyzer (DEA), dynamic mechanical analyzer (DMA) and thermalgravimetric analyzer (TGA). These data were compared with that of commercial bismaleimide (DDMBMI) cured with bisphenol A dicyanate ester (BADCY). The cured DCPDBMI/DCPDCY exhibits lower dielectric constant, dissipation factor and moisture absorption than those of DDMBMI/BADCY. The effects of blend composition on the glass transition temperatures and thermal stability are discussed.     

Preparation and barrier property of poly(ethylene terephthalate)/clay nanocomposite using clay‐supported catalyst

Poly(ethylene terephthalate) (PET)/clay nanocomposite was prepared by the direct polymerization with clay‐supported catalyst. The reaction degree of catalyst against the cation exchange capacity of clay was 8 wt %. The intercalation of PET chains into the silicate layers was revealed by X‐ray diffraction studies. SEM morphology of the nanocomposite showed a good dispersion of clay‐supported catalyst, ranging from 30 to 100 nm. The intercalated and exfoliated clay‐supported catalyst in PET matrix was also observed by TEM. The improvement of O₂ permeability for PET/clay‐supported catalyst composite films over the pure PET is approximately factors of 11.3–15.6. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4875–4879, 2006     

MRT Letter: High resolution SEM imaging of nano‐architecture of cured urea‐formaldehyde resin using plasma coating of osmium

Nanoarchitecture of cured urea‐formaldehyde (UF) resins was examined with a field‐emission scanning electron microscope (FE‐SEM) after coating samples with osmium, which is considered to produce particles of considerably smaller size compared to other metal coatings used in SEM studies. This method enabled comparison of the nanoarchitecture of UF resins of low (1.0) and high (1.6) formaldehyde/urea (F/U) mole ratios to be made, based on imaging of extremely small size particles as part of UF resin architecture, not described before. Imaging revealed presence of relatively large globular particles (148.084–703.983 nm size range) as well as smaller substructures (28.004–39.604 nm size range) as part of the architecture of 1.0‐mole UF resin. Globular particles were also present in 1.6 mole UF resin, but of considerably smaller size (14.760–50.269 nm). The work presented demonstrates usefulness of osmium coating in unraveling the intricacies of the nanostructural organization of cured UF resins, prompting wider application of this immensely useful but grossly underutilized metal coating type in high resolution SEM examination of biological and materials samples. Microsc. Res. Tech. 76:1108–1111, 2013. © 2013 Wiley Periodicals, Inc.     

Tribological Performance of Oil-Based Lubricants with Carbon-Fe Nanocapsules Additive

The present study investigates the tribological properties of carbon-Fe nanocapsules (CFNCs) under high contact loads. Block-on-ring wear tests are performed using mineral oil lubricants containing CFNC particles with concentrations ranging from 0.01 to 0.1 wt%. In addition, high-resolution electron transmission microscopy (HR-TEM) and scanning electron microscopy (SEM) analysis were conducted on the test samples. The results show that for a contact load of 650 N, a CFNC concentration of 0.07 wt% and a sliding velocity of 1.65 m/s enhance the surface permeability, fill-up properties, and microbearing lubrication mechanism and promote effective reduction in the wear at the surface contact interface.     

β-Si3N4Whiskers Embedded in Oxynitride Glasses: Interfacial Microstructure

Interfacial microstructures in βP-Si₃N₄( w )-Si-Al-Y-O-N-glass systems were investigated by systematically varying the nitrogen content and the Al:Y ratio of the glass matrix. High-resolution and analytical transmission electron microscopy (HREM and AEM) studies revealed that the interfacial microstructure is a function of the glass composition. No interfacial phases were formed in glasses with low Al:Y ratios and in glasses with high Al:Y ratios and low nitrogen content, whereas epitaxial growth of an interfacial layer (100–200 μm thick) on the βP-Si₃N₄( w ) occurred in a glass matrix with high Al:Y ratio and high nitrogen content. The interfacial layer was identified to be a β'-SiAION phase. Interfaces containing the SiAION layer exhibited high debonding energy compared to Si₃N₄( w )–glass interfaces. HREM studies indicated that the lattice-mismatch strain in the SiAION layer was relieved by dislocation formation at the SiAION–Si₃N₄( w ) interface. The difference in interfacial debonding energy was, hence, attributed to the local atomic structure and bonding between the glass-β-Si₃N₄ and the glass–β'-SiAION phases. This observation was clear evidence of the strong influence of glass chemistry on the interfacial debonding behavior by altering the interfacial microstructure.     

Patient thermal comfort requirement for hospital environments in Taiwan

This study examines the comfort criteria of ASHRAE Standard 55-2004 for their applicability in hospital environments. Through an extensive field survey conducted in a university hospital in Taiwan, 927 sets of data have been collected. Above half of the measured samples failed to meet the specifications of Standard 55 comfort zone due to improper humidity control. Acceptability votes by patients exceeded the Standard's 80% criterion, regardless of whether the physical conditions were in or out of the comfort zone. Thermal neutrality, preference and comfort range are compared with other studies conducted in office environments and Standard 55 criteria. Results of chi-square tests revealed that patients’ physical strength significantly effected their thermal requirements. The net effect of health yields a marked difference in thermal neutrality and preference, and also in the comfortable temperature range.     

巷道围岩破坏形式与原岩应力场的关系研究

运用东北大学开发的RFPA2D程序模拟原岩应力变化时巷道围岩破坏过程,了解无裂纹巷道围岩破坏形式与原岩应力的关系。根据模拟结果,在垂直应力大于水平应力的情况下,破坏主要在巷道侧面上发生。反之,在巷道顶板和底板发生。2个应力之比越大,这样的现象越明显。2个应力相同的情况下,在巷道顶底板和两帮都发生破坏。因此巷道破坏形式与垂直水平应力之间的比值有关而与应力大小无关。     

Characterization of raw water for the ozone application measuring ozone consumption rate.

This study was conducted to illustrate an ideal method for characterizing natural waters for ozonation processes in drinking water treatment plants. A specific instrument designed with the flow injection analysis (FIA) technique enabled us to measure accurately the ozone decomposition rate, which was found to consist of two stages: the instantaneous ozone consumption stage and the slower ozone decay stage. The ozone consumption rate was measured at the initial and secondary stages by determining certain parameters called the instantaneous ozone demand (ID) and the pseudo first-order decay rate constant (k(c)). Using the OH*-probe, the yield of OH* per consumed ozone was also measured to determine its potential to produce OH* for the oxidation of micropollutants during the ozonation process. The ozone consumption of the ID values was significant in most natural waters, and substantial amounts of OH* were found to generate during the instantaneous ozone consumption stage. This study also investigated the effects of particulates, ozone doses, and sequential ozone injection on ozone decomposition kinetics and OH* formation yield.     

Characterization of ozone decomposition in a soil slurry: kinetics and mechanism.

A series of soil slurry experiments were performed in a carefully conceived reactor set-up to investigate the characteristics of the catalytic decomposition of ozone on a sand and iron surface. Real time on-line monitoring of ozone in the reaction module was possible using flow injection analysis coupled with a computer-controlled UV detector and data acquisition system. The effects of the soil media and size, ozone dosage, pH and p-CBA as a probe compound were examined at the given experimental conditions. Two apparent phases existed, and ozone instantaneously decomposed within one second in the first phase. These were defined as the instantaneous ozone demand (ID) phase, and the relatively slow decay stage. The interactions of ozone with the soil organic matter (SOM) and metal oxides were attributed mostly to the instantaneous decomposition of ozone. From the probe (p-CBA) experiments, 60-68% of total p-CBA removal occurred during the ID phase. The generation of hydroxyl radicals (OH.) was demonstrated and was closely related with metal oxides as well as SOM. Metal oxides in soil surface were considered to have relatively faster reaction rate with ozone and provide more favorable reactive sites to generate higher amount of OH. than SOM. Even at one-tenth concentration of the sands, a goethite-induced catalytic reaction outfitted the removal rate ofp-CBA among all the soils tested. More than 40% of total p-CBA removal occurred on the soil surface. It was inferred that the radical reaction with the probe compound seemed to take place not only on the soil surface but also in the solid-liquid interface. Ozone decomposition and the reaction between OH. and p-CBA appeared to be independent of any change in pH.