Some Studies on Starch Carbamate

Starch carbamate was prepared by reacting maize starch with urea using solid state technique. The different factors affecting this reaction were studied. These factors include urea concentration, type of starch, reaction and duration. The carbamate extent and carbamation reaction efficiency (%) were traced by estimating the nitrogen content of the reaction product. Solubility, viscosity and total ester content of starch carbamate samples were estimated. The carbamate extent increases by increasing urea concentration as well as reaction temperature and duration. Increasing the reaction temperature and duration has the same effect on carbamation reaction efficiency (%), while increasing urea concentration do the reverse. The solubility (%) of starch carbamate samples depends on urea concentration, reaction temperature and duration as well as the type of starch used. The maximum solubility obtained was 63% and 43% for starch carbamate derived from pregelled and native starch, respectively. Tentative mechanism for the reaction between starch and urea has been proposed.     

Steerable Microinvasive Probes for Localized Drug Delivery to Deep Tissue

Enhanced understanding of neuropathologies has created a need for more advanced tools. Current neural implants result in extensive glial scarring and are not able to highly localize drug delivery due to their size. Smaller implants reduce surgical trauma and improve spatial resolution, but such a reduction requires improvements in device design to enable accurate and chronic implantation in subcortical structures. Flexible needle steering techniques offer improved control over implant placement, but often require complex closed‐loop control for accurate implantation. This study reports the development of steerable microinvasive neural implants (S‐MINIs) constructed from borosilicate capillaries (OD = 60 µm, ID = 20 µm) that do not require closed‐loop guidance or guide tubes. S‐MINIs reduce glial scarring 3.5‐fold compared to prior implants. Bevel steered needles are utilized for open‐loop targeting of deep‐brain structures. This study demonstrates a sinusoidal relationship between implant bevel angle and the trajectory radius of curvature both in vitro and ex vivo. This relationship allows for bevel‐tipped capillaries to be steered to a target with an average error of 0.23 mm ± 0.19 without closed‐loop control. Polished microcapillaries present a new microinvasive tool for chronic, predictable targeting of pathophysiological structures without the need for closed‐loop feedback and complex imaging.     

Formation and Phase Behavior of Winsor Type III <Emphasis Type="Italic">Jatropha curcas</Emphasis>-Based Microemulsion Systems

The formation and phase behavior of Jatropha curcas-based microemulsion systems, which could potentially be used in enhanced oil recovery applications, has been investigated. Winsor type III microemulsions were obtained by adding n-octane to Winsor type I microemulsion systems prepared using various concentrations of alkyl polyglucoside (APG). To optimize the formulation of type III microemulsion systems, five different types of co-surfactants, i.e. normal butyl alcohol (NBA), isobutyl alcohol, isopropyl alcohol, fatty acid alcohol C8 (FAC8) and fatty acid alcohol C8/C10 (FAC8/C10) were used. The microemulsion phase behavior was determined along with particle size distributions by dynamic light scattering measurements. Results show that the optimum Winston type III system can be achieved by mixing 3 wt% of NBA, 1 wt% APG and 3 wt% NaCl. At the optimum formulation, the IFT reached a minimum value (0.016 mN/m) and formed very small emulsion droplets with a narrow particle size distribution.     

Utilization of aluminum sludge and aluminum slag (dross) for the manufacture of calcium aluminate cement

Four calcium aluminate cement mixes were manufactured from aluminum sludge as a source of calcium oxide and Al₂O₃ and aluminum slag (dross) as a source of aluminum oxide with some additions of pure alumina. The mixes were composed of 35–50% aluminum sludge, 37.50–48.75% aluminum slag (dross) and 12.50–16.25% aluminum oxide. The mixed were processed then sintered at different firing temperatures up to 1500 °C or 1550 °C. The mineralogical compositions of the fired mixes investigated using X-ray diffraction indicated that the fired mixes composed of variable contents of calcium aluminate (CA), calciumdialuminate (CA₂), calciumhexaaluminate (CA₆) in addition to some content of magnesium aluminate spinel (MA). Sintering parameters (bulk density, apparent porosity and linear change) and mechanical properties (cold crushing strength) of the fired briquettes were tested at different firing temperature. Refractoriness of the cement samples manufactured at the optimum firing temperature was detected. Cementing properties (water of consistency, setting time and compressive strength as a function of curing time up to 28 days of hydration) of pasted prepared from the manufactured cement mixes at the selected optimum firing temperatures (1400 °C or 1500 °C) were also tested. Cement mixes manufactured from 45 to 50% aluminum sludge, 37.50–41.25% aluminum slag (dross) with 12.50–13.75% alumina were selected as the optimum mixes for manufacturing calcium aluminate cement since they satisfy the requirements of the international standard specifications regarding cementing and refractory properties as a result of their content of CA (the main hydraulic phase in calcium aluminate cement) and CA₂(the less hydraulic but more refractory phase). Although the recognized high refractoriness of CA₆, its formation affect badly the cementing properties of the other non-optimum mixes.     

Facile synthesis of novel optically active poly(amide‐imide)s containing N,N′‐(pyromellitoyl)‐bis‐l‐phenylalanine diacid chloride and 5,5‐disubstituted hydantoin derivatives under microwave irradiation

Pyromellitic dianhydride (1,2,4,5‐benzenetetracarboxylic acid 1,2,4,5‐dianhydide) (1) was reacted with L‐phenylalanine (2) in a mixture of acetic acid and pyridine (3 : 2) at room temperature, then was refluxed at 90–100°C and N,N′‐(Pyromellitoyl)‐bis‐L ‐phenylalanine diacid (3) was obtained in quantitative yield. The imide‐acid (3) was converted to N,N′‐(Pyromellitoyl)‐bis‐L ‐phenylalanine diacid chloride (4) by reaction with thionyl chloride. Rapid and highly efficient synthesis of poly(amide‐imide)s (6a–f) was achieved under microwave irradiation by using a domestic microwave oven from the polycondensation reactions of N,N′‐(Pyromellitoyl)‐bis‐L ‐phenylalanine diacid chloride (4) with six different derivatives of 5,5‐disubstituted hydantoin compounds (5a–f) in the presence of a small amount of a polar organic medium that acts as a primary microwave absorber. Suitable organic media was o‐cresol. The polycondensation proceeded rapidly, compared with the conventional melt polycondensation and solution polycondensation, and was almost completed within 10 min, giving a series of poly(amide‐imide)s with inherent viscosities about 0.28–0.44 dL/g. The resulting poly(amide‐imide)s were obtained in high yield and are optically active and thermally stable. All of the above compounds were fully characterized by means of FTIR spectroscopy, elemental analyses, inherent viscosity (η_inh), solubility test and specific rotation. Thermal properties of the poly(amide‐imide)s were investigated using thermal gravimetric analysis (TGA). © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 516–524, 2004     

Synthesis and properties of new thermally stable poly(amide-imide)s containing flexible ether moieties

Six new poly(amide-imide)s (PAIs) 8a-f were synthesized from the direct polycondensation reaction of 1,1-bis[4-(trimellitimido)phenoxy]methane 6 with various aromatic diamine 7a–f. The polymerization reactions produced a series of thermally stable and organosoluble PAIs with high yield and good inherent viscosity. The resulted polymers were fully characterized by means of FTIR and ¹H-NMR spectroscopy, elemental analyses, inherent viscosity, and solubility tests. Also thermal properties of the PAIs 8a–f were investigated using thermal gravimetric analysis (TGA) and derivative of thermaogravimetric (DTG) analysis. dicarboxylic acid 6 was synthesized from the reaction of 1,1-bis[4-aminophenoxy]methane 4 with trimellitic anhydride 5 in a solution of glacial acetic acid/pyridine (Py) at refluxing temperature.     

Application of GA-Optimized ANNs to Predict the Water Content,CO2 and H2S Absorption Capacity of Diethanolamine (DEA) in Khangiran Gas Sweetening Plant

Theoretical Foundations of Chemical Engineering - In this work, with the aim of accurate prediction of water content, H2S and CO2 absorption capacity of diethanolamine (DEA) solvent in Khangiran...     

Copper Ion Cementation in Presence of a Magnetic Field

The effect of an electromagnetic field (EMF) on the rate of copper(II) cementation from copper sulfate solutions on a rotating iron cylinder was investigated. The studied variables were cylinder rotation speed, magnetic field strength, and magnetic field direction. The application of EMF increased the rate of cementation in both parallel and perpendicular direction of the magnetic field where the latter proved to be more effective. The rate of mass transfer under an EMF was found to be more than doubled. The enhancement of copper recovery in presence of the EMF is due to the induced motion of Fe⁺ⁿ in the solution which is limited to a certain range of cylinder rotation speed. The power consumption for cementation of copper could be significantly reduced by utilizing EMF.     

Herschel‐Bulkley rheological parameters of a novel environmentally friendly lightweight biopolymer drilling fluid from xanthan gum and starch

This article summarizes a concise investigation on the effect of concentration of the four main components of a novel lightweight drilling fluid, i.e., glass bubbles, xanthan gum, starch, and clay, to the Herschel‐Bulkley rheological model parameters. The three parameters of Herschel‐Bulkley model, i.e., yield stress, fluid consistency, and fluid index were calculated by fitting the experimental data of shear stress as a function of rate of shear to the model. Results indicate that the increment of the amount of four main components increase the yield stress of the final fluid as the flow resistance is increased. Furthermore, the result also showed that the calculated fluid consistency of the drilling fluid appears to be strongly dependent on the presence of glass bubbles, xanthan gum, and clay. However, the fluid consistency appears not to be affected by the presence of starch. It is also concluded that the presence of glass bubbles, xanthan gum, and clay in the fluid tends to determine the final fluid to behave as pseudoplastic. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Photoconductivity and photoluminescence under bias in GaInNAs/GaAs MQW p-i-n structures

The low temperature photoluminescence under bias (PLb) and the photoconductivity (PC) of a p-i-n GaInNAs/GaAs multiple quantum well sample have been investigated. Under optical excitation with photons of energy greater than the GaAs bandgap, PC and PLb results show a number of step-like increases when the sample is reverse biased. The nature of these steps, which depends upon the temperature, exciting wavelength and intensity and the number of quantum wells (QWs) in the device, is explained in terms of thermionic emission and negative charge accumulation due to the low confinement of holes in GaInNAs QWs. At high temperature, thermal escape from the wells becomes much more dominant and the steps smear out.