Recovery of pyruvic acid with weakly basic polymeric sorbents

BACKGROUND: Carboxylic acids are among the most important substances that can be manufactured from biomass. However, the recovery of carboxylic acids from fermentation broths presents a challenging separation problem. To avoid the production of waste salts and net consumption of chemicals in the calcium carboxylate salt process, the use of reversible chemical complexation with polymeric sorbents and extractants is attractive for carboxylic acid recovery. Pyruvic acid is widely used in the manufacture of medicines, pesticides and foodstuffs and can be produced by fermentation. Since the acidity of pyruvic acid (pK_a = 2.49) is stronger than that of normal carboxylic acids, and as few reports on the recovery of pyruvic acid are available, the sorption of pyruvic acid from aqueous solution on two types of weakly basic polymeric sorbent, tertiary amine D301R and primary amine D392, was investigated over a wide pH range and at various salt (MgSO₄) concentrations. RESULTS: Overloading adsorption of pyruvic acid on both weakly basic polymeric sorbents occurred, with the overloading of D392 being greater than that of D301R. The adsorption of pyruvic acid on both sorbents was greatly affected by the solution pH and the salt concentration in the aqueous phase. An overloading model was able to predict the experimental uptake data very well. CONCLUSION: Solution pH is one of the most important operating conditions, and both polymeric sorbents D392 and D301R can be used to recover pyruvic acid from dilute aqueous solution with high efficiency at a solution pH around 2. The uptake by D392 is greater than that by D301R owing to steric hindrance of the tertiary amine. Copyright © 2008 Society of Chemical Industry     

Numerical simulation of substrate effects on spinodal decomposition in polymer binary mixture: Effects of the surface potential

The surface-directed spinodal decomposition (SDSD) of polymer binary mixture with different values of surface potential is numerically simulated in three-dimension (3D) by cell dynamic systems (CDS). Furthermore, the growth laws of the wetting layer are theoretically analyzed by the current equation and the dynamical scaling. The results show that the thickness of the wetting layer increases with the increasing surface potential. The crossover, which is later for larger values of surface potential, appears in the evolution curve of the wetting layer. Before the crossover, the growth law is the surface potential dependant growth law. Subsequently, the growth law is the typical Lifshitz-Slyozov (LS) growth law. The results indicate that the surface potential can result in the mutual transformation between completely wetting and partially wetting for the substrate interface. It can be found that the higher surface potential leads to the faster and stronger transmission of the effect of the substrate on the spinodal decomposition in the bulk.     

Microstructure and mechanical behaviour of semi-solid die-casting AZ91D magnesium alloy

Microstructures and mechanical properties of an AZ91D magnesium alloy prepared with semi-solid die-casting (SSDC) were characterized in as-cast conditions. The SSDC alloy exhibits a unique microstructure featuring primary α-Mg globules uniformly distributed in the matrix of fine secondary α-Mg grains and β-Mg₁₇Al₁₂ intermetallic. High ultimate tensile strength and elongation have been achieved before fracture. Observations on the vertical-section microstructure of the fractured sample by scanning electron microscopy (SEM) show that the crack mainly originated from the brittle fracture of the eutectic phase causes the interface decohesion of the ductile Mg phase, making fracture a rather critical event. Before that, the deformation of ductile α-Mg phase in the matrix as well as the “pulling out” of primary α-Mg phase combines to provide the SSDC alloy a certain strain.     

Kinetics and mechanism of carbothermic reduction of magnesia

The reaction between MgO and graphite powders under flowing argon atmosphere was studied using a dynamic thermogravimetric method. In the temperature range 293 to 1973 K, the effects of compacting pressure, magnesia/carbon ratio, heating rate, Ar carrier-gas flow rate, and CO-partial pressure were investigated. An experimentally determined reaction mechanism was proposed and discussed. The reduction process could be divided into two stages. The first stage includes the direct reaction between MgO and graphite particles and partial gas-solid reaction at relatively low temperature (below 1750 K). The overall reaction rate depends on the solid phase-boundary reaction between magnesia and carbon particles. The second stage is the gas-solid reaction between CO and MgO, which determines the overall reaction rate. The apparent activation energies of the two stages were estimated to be 208.29 and 374.13 kJ/mol, respectively.     

Solution-chemistry analysis of ammonium bicarbonate consumption in rare-earth-element precipitation

A solution-chemistry analysis is applied to estimating the consumption of ammonium bicarbonate in the recovery of rare-earth (RE) elements from leachates of weathered clays. The theoretical analysis shows that a two-step process is needed for recovering RE from the leachates of the weathered clays by precipitation using ammonium bicarbonate. The first step is a precipitation at solution pH 5 to remove impurities such as Fe and Al. The second step is to precipitate RE by adjusting the solution pH above 8. The consumption of ammonium bicarbonate was found to depend on the concentration of RE elements and impurities in the leachates. The total amount of ammonium bicarbonate consumption for the entire process was determined experimentally, and the results showed an excellent agreement with that calculated based on solution-chemistry analysis. The decomposition of H₂CO₃ was identified as one of the main causes of ammonium bicarbonate overdose, accounting for up to 41 pct in comparison to 20 pct consumption for the removal of impurities. The amount of ammonium bicarbonate required in terms of the NH₄HCO₃: RE₂O₃ (RE oxides) molar ratio was found to be 4:1 for maximal RE recovery. An overall RE recovery around 90 pct was achieved with a product purity being about 90 pct.     

小生境遗传算法AVOA反演

采用具有水平对称轴的横向各向同性(HTI)模型研究裂缝性油气藏,P波振幅随炮检距和方位角变化(AVOA),表现出较强的方位各向异性特征。本文基于Ruger提出的HTI介质模型的P波反射系数公式,利用由基准测线和另外两条与之呈45°、90°测线的P波反射系数的相对差异估算裂缝方位;同时引入小生境遗传算法,对基准测线和与之呈90°测线的P波反射系数差进行反演,得到了较高精度的纵、横波波速比和Thomsen各向异性参数。     

Wrinkling of corrugated skin sandwich panels

Compression wrinkling of composite sandwich panels with corrugated skins was investigated numerically, analytically and experimentally. Semi-circular and sine-wave shaped corrugations were studied. The corrugations significantly increased wrinkling strength when compared with equal mass flat panels. Semi-circular corrugations proved to be highly preferable to sine-wave shaped corrugations due to localized buckling in the latter. Over 40 fiberglass and foam core sandwich specimens were manufactured with semi-circular skin corrugations. These specimens were tested to failure, providing confirmation of the numerical and analytical results.     

Formation and surface modification of self-assembled films with acrylated hyperbranched poly(ester-amine) as the outmost layer

An acrylated hyperbranched poly(ester-amine) (HPEA) synthesized from piperazine and trimethylolpropanetriacrylate at a molar ratio of 1:1.42 was used as the polycation to form self-assembled films by layer-by-layer dipping with poly(sodium-p-styrenesulfonate) as the polyanion. The surface morphology and hydrophilicity of the films with HPEA as the outmost layer were controlled by adjusting the solution pH of HPEA. Due to the existence of many acrylate groups, the films with HPEA as the outmost layer were further reacted with a series of reagents, including piperazine, piperidine, laurylamine and p-phenylenediamine. The surface reactions of the films depended on both the nature of the reagents and the morphology of the initial surface. In the presence of the strong basic amines, piperazine and piperidine, the films dissolved extensively into the solution. In the case of laurylamine, a modified film with an opaque appearance was obtained due to the crystallization of long alkyl chains. With the weak basic amine p-phenylenediamine as the reactant, the film was effectively modified without any change in the surface morphology.