The effect of Isoprenyl Ether polymer molecular structure on cementitious composites

In order to minimize the rapid flow loss issue from the hot weather or during lengthy periods and long-distance transport, the synthesis of the isoprenyl oxy polyethylene ether (T-PEG) was introduced. However, there were scarce amount of reported literature on the influence of main and side chain densities on the fresh and hardened properties of concrete containing T-PEG polymers. This study was conducted to investigate fresh and mechanical properties of cementitious composites containing T-PEG polymers with different main and side chain densities. These T-PEG polymers were comprised of the density ratio of side chain to main chain of 1:1, 1:1.5, 1:2, 1:2.5 and 1:3.5, respectively. The laboratory tests conducted were marsh cone funnel test, standard consistency, flow retention, flexural strength and compressive strength test. The results obtained showed that the increased density ratio of side chain to main chain of T-PEG improves the fluidity of the cement paste and the flow retention ability of the cement mortar. Consequently, the mortar with T2 polymer proved a better performance on mechanical strength tests. In conclusion, the increasing main to side chain densities ratio of T-PEG polymer imposes a significant influence on the fresh and hardened properties of the concrete material produced

In situ growth of redox-active iron-centered nanoparticles on graphene sheets for specific capacitance enhancement

AbstractA fast and facile approach is proposed to enhance the specific capacitance of N-Methyl-2-pyrrolidone (NMP)-exfoliated graphene. Redox-active nickel ferricyanide (NiFeCN) nanoparticles were grown on the surface of graphene sheets using a simple co-precipitation method. Apart from the synergetic effect of graphene as double layer capacitance and NiFeCN as pseudocapacitance in specific capacitance enhancement, the NiFeCN nanoparticles served as the spacer to prevent the graphene sheets agglomeration. The NiFeCN/graphene exhibited specific capacitance of 113.5Fg−1, which was 2 times higher than the NMP-exfoliated graphene (52Fg−1) and 6times higher than the pure NiFeCN (18Fg−1). The findings suggested the NiFeCN/graphene could be the potential candidate for supercapacitor electrode

High Surface Area Activated Carbon from Rice Husk as a High Performance Supercapacitor Electrode

In this study, we report on the application of high surface area activated carbon (AC) derived from rice husks as a supercapacitor electrode. The prepared AC was free from Brønsted or Lewis acid sites, thus making the electrical double layer capacitance as the main charge storage mechanism. Three samples of AC with different surface areas were prepared at different activation temperatures and studied electrochemically using cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy. All AC samples exhibited good electrochemical performance as supercapacitor electrode. The maximum specific capacitance (147 F g−1) was obtained by the AC sample (surface area of 2696 m2 g−1) which was prepared at an activation temperature of 850 °C. Detailed impedance studies revealed the low resistivity (0.23 Ω) of AC sample and the fast frequency response (0.11 s) of the supercapacitor electrode

Selective Conversion of Glucose to 5-Hydroxymethylfurfural by Using L-Type Zeolites with Different Morphologies

In the present work, the morphology of L-type zeolite (LTL topology) has been modified in order to evaluate the influence of several protonated-form LTL-zeolites with different morphologies on their stability and catalytic performance in the conversion of glucose into 5-hydroxymethylfurfural (5-HMF). Physico-chemical characterization of the LTL-based catalysts has revealed that the three types of morphologies (needle, short rod and cylinder) are active, providing complete glucose conversion and high 5-HMF yield values. The addition of CaCl2 had a positive influence on the catalytic performance. It was found that morphology influences the textural and acid properties of LTL-zeolites, and hence their catalytic performance. The best catalytic results have been obtained with the NEEDLE-LTL, showing nanoparticles with a length of 4.46 micrometer a width of 0.63 micrometer, which attains a 5-HMF yield of 63%, at 175 ºC after 90 min of reaction, and a glucose conversion of 88%. The reusability study has revealed a progressive decrease in 5-HMF yield after each catalytic cycle. Different regeneration methods have been essayed without recovering the initial catalytic activity. The presence of organic molecules in micropores has been demonstrated by TG analysis, which are diffcult to remove even after a regeneration process at 550 C.This research was funded by the Spanish Ministry of Economy and Competitiveness (RTI2018-94918-B-C44), FEDER (European Union) funds and FRGS (203/PKIMIA/6711642)

Extractive bioconversion of cyclodextrins by Bacillus cereus cyclodextrin glycosyltransferase in aqueous two-phase system

An extractive bioconversion with Bacillus cereus cyclodextrin glycosyltransferase (CGTase, EC 2.4.1.19) in aqueous two-phase system (ATPS) was investigated for the synthesis and recovery of cyclodextrins (CDs). Optimum condition for the extractive bioconversion of CDs was achieved in ATPS consisted of 7.7% (w/w) polyethylene glycol (PEG) 20,000 and 10.3% (w/w) dextran T500 with volume ratio (VR) of 4.0. Enzymatic conversion of starch occurred mainly in dextran-rich bottom phase whereas the product, CDs was transferred to top phase and a higher partition coefficient of CDs was achieved. Repetitive batch of CDs synthesis was employed by replenishment of the top phase components and addition of starch every 8 h. An average total CDs concentration of 13.7 mg/mL, (4.77 mg/mLα-CD, 5.02 mg/mLβ-CD and 3.91 mg/mLγ-CD) was recovered in the top phase of PEG 20,000/dextran T500 ATPS. This study showed the effectiveness of ATPS application in extractive bioconversion of CDs synthesis with B. cereus CGTase

Micro- and macroscopic observations of the nucleation process and crystal growth of nanosized Cs-pollucite in an organotemplate-free hydrosol

The nucleation and crystal growth of nanoscale cesium pollucite aluminosilicate zeolite (ANA topology) from an organotemplate-free precursor suspension are reported. By using a new and reactive synthesis recipe (5.5SiO2:1Al2O3:6Cs2O:140H2O), zeolite nanocrystals with higher Al content (Si/Al ratio = 2.12) are obtained within 120 min under mild condition (180 °C) which is much faster and safer as compared to those previously reported. The solid initially experiences amorphous phase reorganization before nucleation, crystallization and crystal growth take place. The resulting Cs-pollucite nanocrystals (average size 55 nm) display trapezohedron morphology. The nanocrystals are colloidally stabilized in water and they are very active in base-catalyzed cyanoethylation of dipropylamine reaction, giving 89.6% conversion at 180 °C within 50 min. In addition, high solid yield of nanocrystals (ca. 70%) is also achieved, thus offering a green pathway for synthesizing zeolite nanocrystals with high basicity in large scale

Characterization of partitioning behaviors of immunoglobulin G in polymer-salt aqueous two-phase systems

The partitioning behavior of immunoglobulin G (IgG) in the aqueous two-phase system (ATPS) composed of poly(ethylene glycol) (PEG) and phosphate was studied. The parameters of ATPS exhibiting the pronounced effects on the partitioning behavior of IgG include phase composition, PEG molecular weight, and the addition of sodium chloride (NaCl). The accumulation of IgG at the interface of the ATPS increased drastically as the tie-line length (TLL) was increased. This trend was correlated with a linear relationship relating the natural logarithm of interfacial partition coefficient (ln G) to the difference of PEG concentration between the top phase and the bottom phase (Δ[PEG]), and a good fit was obtained. An attempt was made to correlate the natural logarithm of partition coefficient (ln K) to the presence of NaCl with the proposed linear relationship, ln K = α″ ln [Cl-] + β″. The proposed relationship, which serves as a better description of the underlying mechanics of the protein partitioning behavior in the polymer-salt ATPS, provides a good fit (r2 > 0.95) for the data of IgG partitioning. An optimum recovery of 99.97% was achieved in an ATPS (pH 7.5) composed of 14.0% (w/w) PEG 1450, 12.5% (w/w) phosphate and 5.0% (w/w) NaCl

Extractive Bioconversion of Gamma-Cyclodextrin and Recycling of Cyclodextrin Glycosyltransferase in Liquid Biphasic System Using Thermo-Separating Polymer

An extractive bioconversion conducted on soluble starch with cyclodextrin glycosyltransferase (CGTase) enzyme in ethylene oxide-propylene oxide (EOPO)/potassium phosphates liquid biphasic system (LBS) to extract gamma-cyclodextrin (γ-CD) was examined. A range of EOPO (with potassium phosphates) molecular weights was screen to investigate the effect of the latter on the partioning efficency of CGTase and γ-CD. The results show that the optimal top phase γ-CD yield (74.4%) was reached in 35.0% (w/w) EOPO 970 and 10.0% (w/w) potassium phosphate with 2.0% (w/w) sodium chloride. A theoretical explanation for the effect of NaCl on γ-CD was also presented. After a 2 h bioconversion process, a total of 0.87 mg/mL concentration of γ-CD was produced in the EOPO/ phosphates LBS top phase. After the extraction of top phase from LBS, four continuous repetitive batches were successfully conducted with relative CGTase activity of 1.00, 0.86, 0.45, and 0.40 respectively

Synthesis of Cs-ABW nanozeolite in organotemplate-free system

Cesium-aluminosilicate zeolite nanocrystals with ABW framework structure are synthesized free of organic template using hydrothermal approach. The crystallization process of Cs-ABW zeolite nanocrystals by varying the initial gel molar composition, heating temperature and crystallization time was studied. More detailed investigations of the formation of Cs-ABW nanozeolite using a reactive clear precursor hydrogel (4SiO2:1Al2O3:16Cs2O:160H2O) were then carried out. Fully crystalline Cs-ABW nanozeolites were obtained within 120 min at 180 °C and 22 bar, which is considerably faster and safer in comparison to the currently available method involving treatment at 695 °C, 1000 bar and 46 h. The Cs-ABW nanocrystals have grain shape morphology with a mean size of 32 nm and they do not agglomerate for long durations. The nanosized Cs-ABW zeolite has high alumina content (Si/Al ratio = 1.04). These nanocrystals can be prepared in high solid yield (ca. 82%) thus offering a promising route for large-scale production of highly basic zeolite nanoparticles

Interfacial partitioning behaviour of bovine serum albumin in polymer-salt aqueous two-phase system

A relationship is proposed for the interfacial partitioning of protein in poly(ethylene glycol) (PEG)-phosphate aqueous two-phase system (ATPS). The relationship relates the natural logarithm of interfacial partition coefficient, ln G to the PEG concentration difference between the top and bottom phases, Δ[PEG], with the equation ln G = AΔ[PEG] + B. Results showed that this relationship provides good fits to the partition of bovine serum albumin (BSA) in ATPS which is comprised of phosphate and PEG of four different molecular weight 1450 g/mol, 2000 g/mol, 3350 g/mol and 4000 g/mol, with the tie-line length (TLL) in the range of 44–60% (w/w) at pH 7.0. The decrease of A values with the increase of PEG molecular weight indicates that the correlation between ln G and Δ[PEG] decreases with the increase in PEG molecular weight and the presence of protein–polymer hydrophobic interaction. When temperature was increased, a non-linear relationship of ln G inversely proportional to temperature was observed. The amount of proteins adsorbed at the interface increased proportionally with the amount of BSA loaded whereas the partition coefficient, K remained relatively constant. The relationship proposed could be applied to elucidate interfacial partitioning behaviour of other biomolecules in polymer-salt ATPS