Morphology of a melt crystallized iPP/HDPE/hydrogenated hydrocarbon resin blend

The structure, phase structure, morphology, crystallization and melting behavior of isotactic polypropylene (iPP) blended with a master batch (MB), formed by high density polyethylene and hydrogenated hydrocarbon resin (iPP/MB), have been in details investigated by using X-ray diffraction, optical microscopy and differential scanning calorimetry. It was found that the structure and morphology depend on crystallization conditions. A new family of α spherulites of iPP (type I spherulites) can be activated using appropriate crystallization conditions. Nucleation of these spherulites has been explained by using the approach of nucleus migration in polymer blends. Type I spherulites present specific morphological, kinetic and thermal behaviors. In particular it was found that the growth rate of type I spherulites, at a given T_c, is higher than the growth rate of spherulites grown from plain iPP.     

Determination of Iodine Value in Hydrogenated Oils: Comparison of Titration and Gas Chromatography with Flame‐Ionization Detection Methodologies

The United States Food and Drug Administration (FDA) recently issued its final determination that partially hydrogenated oils (PHO) are no longer generally recognized as safe (GRAS) for any use in human food. Consequently, the discrimination between PHO and fully hydrogenated oils (FHO), which is achieved by the iodine value (IV), has become an important regulatory issue. This study compared American Oil Chemists’ Society (AOCS) and International Organization for Standardization (ISO) titration and gas chromatography with flame‐ionization detection (GC‐FID) methodologies for the determination of IV in seven samples of hydrogenated oil, namely coconut, cottonseed (n = 2), palm kernel, palm stearine, and soybean (n = 2) oils. Titrations produced statistically higher IV determinations than those achieved by GC‐FID, for all samples except the FH coconut oil. The unsaponifiable matter content of the hydrogenated oils, which varied from 0.15% to 0.47% of total fat, likely contributed modest increases to the IV by titration. Both methodologies were prone to issues at low IV (~4), with titrations showing greater variability, and GC‐FID being susceptible to incomplete separation, identification, and quantification of all unsaturated fatty acids. The variability observed with titrations could be minimized by careful execution of the titration protocol. Although both approaches successfully discriminated PHO and FHO in the test materials, at low IV (~4), titration is the most accurate method for determining the IV, and the only approach that has been validated in oils with a very low IV (<1).     

Room temperature photoluminescence spectrum modeling of hydrogenated amorphous silicon carbide thin films by a joint density of tail states approach and its application to plasma deposited hydrogenated amorphous silicon carbide thin films

Room temperature photoluminescence (PL) spectrum of hydrogenated amorphous silicon carbide (a-SiC_x:H) thin films was modeled by a joint density of tail states approach. In the frame of these analyses, the density of tail states was defined in terms of empirical Gaussian functions for conduction and valance bands. The PL spectrum was represented in terms of an integral of joint density of states functions and Fermi distribution function. The analyses were performed for various values of energy band gap, Fermi energy and disorder parameter, which is a parameter that represents the width of the energy band tails. Finally, the model was applied to the measured room temperature PL spectra of a-SiC_x:H thin films deposited by plasma enhanced chemical vapor deposition system, with various carbon contents, which were determined by X-ray photoelectron spectroscopy measurements. The energy band gap and disorder parameters of the conduction and valance band tails were determined and compared with the optical energies and Urbach energies, obtained by UV-Visible transmittance measurements. As a result of the analyses, it was observed that the proposed model sufficiently represents the room temperature PL spectra of a-SiC_x:H thin films.     

加氢尾油非临氢降凝动力学模型

结合加氢尾油催化裂解反应体系,利用集总的方法,建立了加氢尾油非临氢降凝五集总动力学模型。以催化降凝装置上得到的实验数据为根据,用Marquardt++算法编写Matlab语言程序进行优化计算,得到了加氢尾油非临氢的反应速率常数、指前因子和活化能。结果表明：该模型对原料和反应条件变化有较好的适应性,能较好预测不同条件下的产率分布和产品组成。     

Chemical-reaction dependence of plasma parameter in reactive silane plasma

Electron temperature in a silane glow-discharge plasma, being an important plasma parameter for determining photo-induced instability in the resulting hydrogenated amorphous silicon (a-Si:H), has been studied under various film-preparation conditions. We have used an optical-emission-intensity ratio of Si^* to SiH^* (I_si*/I_siH^*) which corresponds to the high-energy-tail slope of the electron-energy-distribution function in the plasma as a measure of electron temperature in a reactive silane glow-discharge plasma. We have found quite differently from the conventional non-reactive glow-discharge plasma such as hydrogen plasma that the electron temperature in the silane plasma is strongly modified by the substrate temperature (gas temperature) especially under high silane-gas partial-pressure condition. This anomalous behavior of the electron temperature in the silane plasma has been explained by means of gas-phase-polymerization reaction and electron-attachment process to the polymers in the plasma. The electron temperature has been remarkably reduced when a hydrogen-dilution method and a cathode-heating method are used which are considered to control polymer-formation reactions in the silane plasma together with utilization of conventional electron-temperature-controlling methods such as a very high plasma-excitation frequency and an application of magnetic field for electron-confinement. As a consequence of the reduction of electron temperature in the silane plasma, highly stabilized a-Si:H has been successfully obtained even under high growth rate conditions of 1.5 nm s^-1.     

Separation of nickel catalyst by microfiltration

Ceramic membranes with pore size of 0.1 and 0.2 µm are used for the separation of nickel catalyst. Effect of trans‐membrane pressure (TMP), linear velocity, temperature and nickel content (solute) on flux and rejection has been investigated. The flux increased with increase in pore size of the membrane. The rejection characteristics were similar for 0.1 and 0.2 µm membranes. The nickel content and iodine value of the membrane‐filtered oil was comparable with that of conventional processes. Permeate flux increased with increase in temperature. Flux increased with increase in linear velocity and a marginal rise was observed above 2.09 m/s. The rejection characteristics were only slightly affected by higher linear velocity. The flux improved after back flushing. The average flux was higher with back flushing as compared to continuous (with out back flushing) filtration process. The results indicated that the secondary layer effect was more pronounced in microfiltration. The flux decreased with increase in solute concentration. The rejection characteristics were not affected by solute concentration. The rejection characteristic of the membranes remained unaltered after membranes were repeatedly cleaned with sodium hydroxide and HCl solutions, however, the flux was decreased marginally.     

SH/T0206老化条件下加氢变压器油电气性能及其化学组成的变化研究

根据SH/T0206-1992《变压器油氧化安定性测定方法》对加氢变压器油进行老化试验,收集不同时段的老化样品,测定其电气性能和族组成变化,从而探讨了这些性能与族组成变化的相关关系。     

Influence of hydrogen dilution on structural, electrical and optical properties of hydrogenated nanocrystalline silicon (nc-Si:H) thin films prepared by plasma enhanced chemical vapour deposition (PE-CVD)

Hydrogenated nanocrystalline silicon (nc-Si:H) thin films were deposited from pure silane (SiH₄) and hydrogen (H₂) gas mixture by conventional plasma enhanced chemical vapour deposition (PE-CVD) method at low temperature (200 °C) using high rf power. The structural, optical and electrical properties of these films are carefully and systematically investigated as a function of hydrogen dilution of silane (R). Characterization of these films with low angle X-ray diffraction and Raman spectroscopy revealed that the crystallite size in the films tends to decrease and at same time the volume fraction of crystallites increases with increase in R. The Fourier transform infrared (FTIR) spectroscopic analysis showed at low values of R, the hydrogen is predominantly incorporated in the nc-Si:H films in the mono-hydrogen (SiH) bonding configuration. However, with increasing R the hydrogen bonding in nc-Si:H films shifts from mono-hydrogen (SiH) to di-hydrogen (SiH₂) and (SiH₂)_n complexes. The hydrogen content in the nc-Si:H films decreases with increase in R and was found less than 10 at% over the entire studied range of R. On the other hand, the Tauc's optical band gap remains as high as 2 eV or much higher. The quantum size effect may responsible for higher band gap in nc-Si:H films. A correlation between electrical and structural properties has been found. For optimized deposition conditions, nc-Si:H films with crystallite size 7.67 nm having good degree of crystallinity (84% ) and high band gap (2.25 eV) were obtained with a low hydrogen content (6.5 at%). However, for these optimized conditions, the deposition rate was quite small (1.6 Å/s).     

氢化羧基丁苯橡胶氢化度的测定

用水合肼/双氧水/硫酸亚铁催化体系对羧基丁苯橡胶（XSBR）胶乳加氢,制备氢化羧基丁苯橡胶（HXSBR）。探讨了用碘量法测定XSBR不饱和度和HXSBR氢化度的条件,得到了以庚醇与四氯化碳的混合试剂[V（庚醇）：V（四氯化碳）=0.12:1]为溶剂,反应时间为1.5h,温度为40-45℃的碘量法可以较好地测定HXSBR氢化度,并用溶度参数相近规则选择并解释所用溶剂。     

Microcrystalline/micromorph silicon thin-film solar cells prepared by VHF-GD technique

Hydrogenated microcrystalline silicon prepared at low temperatures by the glow discharge technique is examined here with respect to its role as a new thin-film photovoltaic absorber material. XRD and TEM characterisations reveal that microcrystalline silicon is a semiconductor with a very complex morphology. Microcrystalline p–i–n cells with open-circuit voltages of up to 560–580 mV could be prepared. “Micromorph” tandem solar cells show under outdoor conditions higher short-circuit currents due to the enhanced blue spectra of real sun light and therefore higher efficiencies than under AM1.5 solar simulator conditions. Furthermore, a weak air mass dependence of the short-circuit current density could be observed for such micromorph tandem solar cells. By applying the monolithic series connection based on laser patterning a first micromorph mini-module (total area of 23.6 cm²) with 9% cell conversion efficiency could be fabricated.