Composition dependences of thermodynamical properties associated with Pb-free ternary,quaternary, and quinary solder systems

In the present study, Chou’s General Solution Model (GSM) has been used to predict the enthalpy and partial enthalpies of mixing of the liquid Ag–In–Sn ternary, Ag–In–Sn–Zn quaternary, and Ag–Au–In–Sn–Zn quinary systems. These are of technical importance to optimize lead-free solder alloys, in selected cross-sections: x_In/x_Sn = 0.5/0.5 (ternary), Au–In_0.1–Sn_0.8–Zn_0.1, Ag–In_0.1–Sn_0.8–Zn_0.1 (quaternary), and t = x_Au/x_In = 1, x_In = x_Sn = x_Zn (quinary) at 1173, 773, and 773 K, respectively. Moreover, the activity of In content in the ternary alloy system Ag–In–Sn has been calculated and its result is compared with that determined from the experiment, while the activities of Ag contents associated with the alloys mentioned above have been calculated. The other traditional models such as of Colinet, Kohler, Muggianu, Toop, and Hillert are also included in calculations. Comparing those calculated from the proposed GSM with those determined from experimental measurements, it is seen that this model becomes considerably realistic in computerization for estimating thermodynamic properties in multicomponent systems.     

Synthesis and spectroelectrochemistry of dithieno(3,2‐b:2′,3′‐d)pyrrole derivatives

New π‐conjugated polymers containing dithieno(3,2‐b:2′,3′‐d)pyrrole (DTP) were successfully synthesized via electropolymerization. The effect of structural differences on the electrochemical and optoelectronic properties of the 4‐[4H‐dithieno(3,2‐b:2′,3′‐d)pyrrol‐4‐yl]aniline (DTP–aryl–NH₂), 10‐[4H‐dithiyeno(3,2‐b:2′,3′‐d)pirol‐4‐il]dekan‐1‐amine (DTP–alkyl–NH₂), and 1,10‐bis[4H‐dithieno(3,2‐b:2′,3′‐d)pyrrol‐4‐yl] decane (DTP–alkyl–DTP) were investigated. The corresponding polymers were characterized by cyclic voltammetry, NMR (¹H‐NMR and ¹³C‐NMR), and ultraviolet–visible spectroscopy. Changes in the electronic nature of the functional groups led to variations in the electrochemical properties of the π‐conjugated systems. The electroactive polymer films revealed redox couples and exhibited electrochromic behavior. The replacement of the DTP–alkyl–DTP unit with DTP–aryl–NH₂ and DTP–alkyl–NH₂ resulted in a lower oxidation potential. Both the poly(10‐(4H‐Dithiyeno[3,2‐b:2′,3′‐d]pirol‐4‐il)dekan‐1‐amin) (poly(DTP–alkyl–NH₂)) and poly(1,10‐bis(4H‐dithieno[3,2‐b:2′,3′‐d]pyrrol‐4‐yl) decane) (poly(DTP–alkyl–DTP)) films showed multicolor electrochromism and also fast switching times (<1 s) in the visible and near infrared regions. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40701.     

Preparation and evaluation of linseed oil based alkyd paints

Alkyd resins are produced with reaction of oil or fatty oil, polyol and polyacid. Alkyd resins are commonly used in coating and paint industry due to ease of application in changing environmental conditions. Linseed oil based paints executed all requirements of technical properties, drying time, storage properties, simplicity in maintenance, appearance, economy, etc. In this study, linseed oil based alkyd resins having different oil contents were synthesized     

牛奶蛋白纤维(第Ⅰ部分)

牛奶蛋白纤维是一种新颖的工业生产纤维,中国已拥有2项发明专利.2004年它就已经通过了国际生态纺织品Oeko-Tex标准100认证.牛奶蛋白纤维是利用新型生物工程技术将牛奶去水脱脂,加工成适用于湿法纺丝工艺的蛋白浆后制得的纤维.它对皮肤友好,手感舒适,色彩鲜艳,具有很好的可染性.牛奶蛋白纤维可以纯纺或与羊绒、蚕丝、棉、毛、麻及其他纤维混纺.     

Effect of calcium hydroxide removal techniques on the bond strength of root canal sealers

To evaluate the influence of calcium-hydroxide(CH) with different vehicles on the push-out bond strength of different canal sealers to radicular dentin. 152 decrowned single-rooted human teeth were used. After preparation of root canals with nickel-titanium rotary files, 8 roots served as control groups. Then, the roots were divided as follows: (1) Calasept and (2) Surepaste (n = 72). Roots were further subgrouped according to the CH removal techniques: (1) %17 ethylenediaminetetraacetic acid (EDTA) + rotary file, (2) %17EDTA + hand file, and (3) %17EDTA (n = 24). Eight roots from each group sectioned longitudinally, divided into two pairs and photographed by stereomicroscope (n = 16). The remaining 16 roots in CH intracanal dressing groups were further divided into 2 subgroups according to the sealer used: (1) AH-Plus-jet and (2) Apexit-Plus (n = 8). Bond strengths of the root canal sealers to root canal dentin were measured using a push-out test setup. The data were statistically analyzed using multivariate analysis of variance p = 0.05. The push-out bond strength values were significantly affected by type of vehicle and the removal techniques (p < 0.05). The mean bond strength of AH-Plus-jet was significantly higher than Apexit-Plus, regardless of type of vehicle and the removal techniques (p < 0.05). There was no difference between vehicles on CH removal (p > 0.05). When examining the removal techniques, only irrigation with %17 EDTA left significantly larger amount of residue (p < 0.05). AH-Plus-jet showed better dislocation resistance than Apexit-Plus. Type of vehicle does not play a fundamental role in the degree of persistence of CH residues on the dentin walls. Instrumentation improves the removal efficiency of CH from root canal.     

Persistence Heterogeneity Testing in Panels with Interactive Fixed Effects

We consider large N,T panel data models with fixed effects, a common factor allowing for cross‐section dependence, and persistent data and shocks, which are assumed fractionally integrated. In a basic setup, the main interest is on the fractional parameter of the idiosyncratic component, which is estimated in first differences after factor removal by projection on the cross‐section average. The pooled conditional‐sum‐of‐squares estimate is consistent but the normal asymptotic distribution might not be centred, requiring the time series dimension to grow faster than the cross‐section size for correction. We develop tests of homogeneity of dynamics, including the degree of integration, that have no trivial power under local departures from the null hypothesis of a non‐negligible fraction of cross‐section units. A simulation study shows that our estimates and tests have good performance even in moderately small panels.     

Removal of metal ions using lignite in aqueous solution—Low cost biosorbents

Turkish lignite can be used as a new adsorption material for removing some toxic metals from aqueous solution. The adsorption of lignite (brown young coals) to remove copper (Cu²⁺), lead (Pb²⁺), and nickel (Ni²⁺) from aqueous solutions was studied as a function of pH, contact time, metal concentration and temperature. Adsorption equilibrium was achieved between 40 and 70 min for all studied cations except Pb²⁺, which is between 10 and 30 min. The adsorption capacities are 17.8 mg/g for Cu²⁺, 56.7 mg/g for Pb²⁺, 13.0 mg/g for Ni²⁺ for BC₁ (Ilg?n lignite) and 18.9 mg/g for Cu²⁺, 68.5 mg/g for Pb²⁺, 12.0 mg/g for Ni²⁺ for BC₂ (Beysehir lignite) and 7.2 mg/g for Cu²⁺, 62.3 mg/g for Pb²⁺, 5.4 mg/g for Ni²⁺ for AC (activated carbon). More than 67% of studied cations were removed by BC₁ and 60% BC₂, respectively from aqueous solution in single step. Whereas about 30% of studied cations except Pb²⁺, which is 90%, were removed by activated carbon. Effective removal of metal ions was demonstrated at pH values of 3.8–5.5. The adsorption isotherms were measured at 20 °C, using adsorptive solutions at the optimum pH value to determine the adsorption capacity. The Langmuir adsorption isotherm was used to describe observed sorption phenomena. The rise in temperature caused a slight decrease in the value of the equilibrium constant (K_c) for the sorption of metal ions. The mechanism for cations removal by the lignite includes ion exchange, complexation and sorption. The process is very efficient especially in the case of low concentrations of pollutants in aqueous solution, where common methods are either economically unfavorable or technically complicated.