Research of Immobilization of Transglutaminase on Polypropylene Microporous Membranes

2011 ◽  
Vol 341-342 ◽  
pp. 338-344 ◽  
Author(s):  
Zhi Guo Na ◽  
Xue Fei Wang ◽  
Yong Qiang Ma ◽  
Lei Qian ◽  
Hong Yu Yan
Keyword(s):  
Ferrous Sulfate ◽  
Monomer Concentration ◽  
Cross Linking ◽  
Sulfate Concentration ◽  
Microporous Membranes ◽  
Activation Time ◽  
Reaction Conditions ◽  
Ammonium Ferrous Sulfate ◽  
Optimal Reaction ◽  
Grafting Degree

Activated ozone as the carrier，crylic acid as the monomer and glutaraldehyde as the cross-linking agent were used to research the immobilization of transglutaminase on polypropylene microporous membranes. The effect of ozone activation time，grafting time，grafting temperature，monomer concentration and ammonium ferrous sulfate concentration on grafting degree were studied, the Immobilization conditions were also studied. We found the optimal reaction conditions as following: consistency of hexamethylendiamine was 15%，at 50°C for 120min and consistency，at 30°C for 45minites，consistency of enzyme was 15mg/mL at 4°C. So the immobilized amount of protein could come to 30.23mg/g membrane and the activity of immobilized MTG come to 16.9U/g membrane.

The Effects of the Reaction Conditions on the Grafting Degree of SiO2-g-PMAA Particle

2012 ◽  
Vol 581-582 ◽  
pp. 301-304
Author(s):  
Ke Hong Zhang ◽  
Hui Xiao ◽  
Jun Juan Du
Keyword(s):  
Silica Gel ◽  
Reaction Temperature ◽  
Methacrylic Acid ◽  
Graft Polymerization ◽  
Monomer Concentration ◽  
Reaction Conditions ◽  
Grafted Polymer ◽  
Limiting Value ◽  
Methacryloxypropyl Trimethoxysilane ◽  
Grafting Degree

Modified MPS-SiO2 particle was obtained by the bonding of 3-methacryloxypropyl trimethoxysilane (KH-570) on the surface of silica gel particle. The methacrylic acid (MMA) monomers were grafted on the surface of MPS-SiO2 particle to prepare the grafting particles SiO2-g-PMAA. The effects of reaction conditions on the graft degree were explored. The results indicate that the MMA monomers can be easily grafted on the surface of silica gel particle by using the method of graft polymerization. During the graft polymerization, the grafted polymer layer is a hindrance to the subsequent graft polymerization. Then the grafting degree of the polymer under a certain condition has a limiting value. The reaction conditions, such as monomer concentration, the amount of initiator, reaction temperature, have remarkably influence on the graft polymerization of SiO2-g-PMAA.

The Comparison of Physicochemical Properties of Four Cross-Linked Sodium Hyaluronate Gels with Different Cross-Linking Agents

2011 ◽  
Vol 396-398 ◽  
pp. 1506-1512
Author(s):  
Yu Jia Cui ◽  
Wei Guo Wang ◽  
Peng Li ◽  
Yong Liang Zhao ◽  
Ya Nan Gu ◽  
...  
Keyword(s):  
Physicochemical Properties ◽  
Intrinsic Viscosity ◽  
Dynamic Viscosity ◽  
Sodium Hyaluronate ◽  
Chemical Properties ◽  
Cross Linking ◽  
Reaction Conditions ◽  
Physical And Chemical ◽  
Optimal Reaction

Abstract：PurposeThe physicochemical properties of four Cross-linked sodium hyaluronate gels(CHA) with different cross-linking agents were conpared.In order to research out the different stability and Enzyme-resistant properties of these CHA.Methods The CHA hydrogels were prepared with different cross-linking agents, such as PEG20000, PDE, BDDE and ADH. The optimal reaction conditions were determined by single factor experiment. Dynamic viscosity was tested by Stabinger method. Intrinsic viscosity was tested by Uzziah's viscosity method. The in vitro Enzyme-resistant properties of CHA-gels were analysed by carbazole and spectrophotometry. Results The concentrations of NaOH/HCl, concentrations of HA and the ratio of cross-linking agent to HA were significant conditions which influenced the physicochemical properties of CHA gels. PDE-CHA and PEG20000 gels have best Dynamic viscosity, PDE-CHA gel has best Intrinsic viscosity, ADH-CHA and BDDE-CHA gels have better Enzyme-resistant properties than PEG20000-CHA and PDE-CHA gels.Conclusion The CHA-gel prepared under optimal reaction conditions have different physical and chemical properties, which set foundation for developing double cross-linked gel with both excellent stability and Enzyme-resistant properties.

Synthesis of Super Absorbent Resin from Starch/Bentonite

2013 ◽  
Vol 873 ◽  
pp. 708-712 ◽  
Author(s):  
Rui Jie Wang ◽  
Lian Wei Yang ◽  
Han Dan Zhang ◽  
Tie Jun Geng
Keyword(s):  
Acrylic Acid ◽  
Absorption Rate ◽  
Pure Water ◽  
Weight Ratio ◽  
Cross Linking ◽  
Key Factors ◽  
Reaction Conditions ◽  
Factors Affecting ◽  
Optimal Reaction ◽  
Radiation Time

The compound super absorbent resin was synthesized by starch, bentonite, acrylic acid and acrylamide, using microwave irradiation. Some key factors affecting the solution absorbency of the polymer such as the amount of bentonite, acrylamide, initiator and cross-linking agent have been discussed. The results showed that the optimal reaction conditions of cross-linking agent, initiator, neutralization degree, bentonite, phosphate starch are 0.045%, 0.32%, 70%, 10%, 3% when the weight ratio of acrylic acid and acrylamide was 2:1, the microwave power was 800W, the radiation time was 15min. Under the conditions, the pure water absorption rate of super absorbent resin was up to 796g/g. when the weight ratio of acrylic acid and acrylamide was 1:1, the absorption rate of 0.9% NaCl was 95g/g.

Synthesis of Phosphonates via Michaelis-Arbuzov Reaction

2017 ◽  
Vol 14 (6) ◽  
pp. 883-903 ◽  
Author(s):  
Boppudi Hari Babu ◽  
Gandavaram Syam Prasad ◽  
Chamarthi Naga Raju ◽  
Mandava Venkata Basaveswara Rao
Keyword(s):  
Reaction Times ◽  
Biologically Active ◽  
Fine Tuning ◽  
Arbuzov Reaction ◽  
Reaction Conditions ◽  
Solvent Type ◽  
Potential Applications ◽  
Synthetic Methodologies ◽  
Optimal Reaction ◽  
The Arbuzov Reaction

Background: Michaelis–Arbuzov reaction has played a key role for the synthesis of dialkyl or diaryl phosphonates by reacting various alkyl or aryl halides with trialkyl or triaryl phosphite. This reaction is very versatile in the formation of P-C bond from the reaction of aliphatic halides with phosphinites or phosphites to yield phosphonates, phosphinates, phosphine oxides. The Arbuzov reaction developed some methodologies, possible mechanistic pathways, selectivity, potential applications and biologically active various phosphonates. Objective: The synthesis of phosphonates via Michaelis–Arbuzov reaction with many new and fascinating methodologies were developed and disclosed in the literature, and these are explored in this review. Conclusion: This review has discussed past developments and vast potential applications of Arbuzov reaction in the synthesis of organophosphonates. As presented in this review, various synthetic methodologies were developed to prepare a large variety of phosphonates. Improvements in the reaction conditions of Lewis-acid mediated Arbuzov rearrangement as well as the development of MW-assisted Arbuzov rearrangement were discussed. Finally, to achieve high selectivities and yields, fine-tuning of reaction conditions including solvent type, temperature, and optimal reaction times to be considered.

Amperometric assay of vitamin C using an ascorbate oxidase enzyme electrode

1979 ◽  
Vol 44 (11) ◽  
pp. 3395-3404 ◽  
Author(s):  
Pavel Posádka ◽  
Lumír Macholán
Keyword(s):  
Ascorbic Acid ◽  
Vitamin C ◽  
Oxygen Electrode ◽  
Ascorbate Oxidase ◽  
Current Response ◽  
Reaction Conditions ◽  
Long Term Storage ◽  
Oxidase Enzyme ◽  
Optimal Reaction

An oxygen electrode of the Clark type, coated by a thin, active layer of chemically insolubilized ascorbate oxidase from squash peelings specifically detects by measuring oxygen uptake 10 to 400 μg of ascorbic acid in 3 ml of phosphate buffer. The record of current response to substrate addition lasts 1-2 min. The ascorbic acid values determined in various samples of fruit juices are in good agreement with the data obtained by titration and polarography. The suitable composition of the membrane and its lifetime and stability during long-term storage are described; optimal reaction conditions of vitamin C determination and the possibilities of interference of other compounds are also examined. Of the 35 phenols, aromatic amines and acids tested chlorogenic acid only can cause a positive error provided that the enzyme membrane has been prepared from ascorbate oxidase of high purity.

scholarly journals A Novel Pseudomonas geniculata AGE Family Epimerase/Isomerase and Its Application in d-Mannose Synthesis

Foods ◽  
2020 ◽  
Vol 9 (12) ◽  
pp. 1809
Author(s):  
Zhanzhi Liu ◽  
Ying Li ◽  
Jing Wu ◽  
Sheng Chen
Keyword(s):  
3D Structure ◽  
Three Dimensional ◽  
Optimal Temperature ◽  
Reaction Conditions ◽  
Enzymatic Production ◽  
Physiological Properties ◽  
Potential Applications ◽  
Kinetics Of ◽  
Optimal Reaction ◽  
Gene Age

d-mannose has exhibited excellent physiological properties in the food, pharmaceutical, and feed industries. Therefore, emerging attention has been applied to enzymatic production of d-mannose due to its advantage over chemical synthesis. The gene age of N-acetyl-d-glucosamine 2-epimerase family epimerase/isomerase (AGEase) derived from Pseudomonas geniculata was amplified, and the recombinant P. geniculata AGEase was characterized. The optimal temperature and pH of P. geniculata AGEase were 60 °C and 7.5, respectively. The Km, kcat, and kcat/Km of P. geniculata AGEase for d-mannose were 49.2 ± 8.5 mM, 476.3 ± 4.0 s−1, and 9.7 ± 0.5 s−1·mM−1, respectively. The recombinant P. geniculata AGEase was classified into the YihS enzyme subfamily in the AGE enzyme family by analyzing its substrate specificity and active center of the three-dimensional (3D) structure. Further studies on the kinetics of different substrates showed that the P. geniculata AGEase belongs to the d-mannose isomerase of the YihS enzyme. The P. geniculata AGEase catalyzed the synthesis of d-mannose with d-fructose as a substrate, and the conversion rate was as high as 39.3% with the d-mannose yield of 78.6 g·L−1 under optimal reaction conditions of 200 g·L−1d-fructose and 2.5 U·mL−1P. geniculata AGEase. This novel P. geniculata AGEase has potential applications in the industrial production of d-mannose.

scholarly journals Efficient Degradation of Mordant Blue 9 Using the Fenton-Activated Persulfate System

Water ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 2532 ◽  
Author(s):  
Md. Nahid Pervez ◽  
Felix Y. Telegin ◽  
Yingjie Cai ◽  
Dongsheng Xia ◽  
Tiziano Zarra ◽  
...  
Keyword(s):  
Butyl Alcohol ◽  
Textile Dye ◽  
Oh Radicals ◽  
Operational Parameters ◽  
Reaction Conditions ◽  
Tert Butyl Alcohol ◽  
Initial Ph ◽  
Fe Complex ◽  
Optimal Reaction ◽  
Activated Persulfate

In this study, a Fenton-activated persulfate (Fe2+/PS) system was introduced for the efficient degradation of Mordant Blue 9 (MB 9) as a textile dye in an aqueous solution. Results showed that the degradation of MB 9 was markedly influenced by operational parameters, such as initial pH, PS concentration, Fe2+ concentration, and initial dye concentration. Optimal reaction conditions were then determined. Inorganic anions, such as Cl− and HCO3−, enhanced the degradation efficiency of MB 9 under optimal conditions. Addition of HCO3− reduced the degradation performance of MB 9, whereas the addition of Cl− increased the degradation percentage of MB 9. In addition, quenching experiments were conducted using methanol and tert-butyl alcohol as scavengers, and methanol was identified as an effective scavenger. Thus, the degradation of MB 9 was attributed to S O 4 • − and •OH radicals. The degradation and mineralization efficiency of MB 9 was significantly reduced using the conventional Fenton process i.e., Fe2+/ hydrogen peroxide (HP) because of the formation of a Fe complex during degradation. Meanwhile, the Fe2+/persulfate (PS) system improved the degradation and mineralization performance.

scholarly journals Software-guided microscale flow calorimeter for efficient acquisition of thermokinetic data

2021 ◽  
Author(s):  
Timothy Aljoscha Frede ◽  
Marlene Dietz ◽  
Norbert Kockmann
Keyword(s):  
Design Of Experiments ◽  
Process Development ◽  
Reaction Conditions ◽  
Experimental Conditions ◽  
Flow Calorimeter ◽  
Microscale Flow ◽  
Increased Sensitivity ◽  
Important Time ◽  
Optimal Reaction

AbstractFast chemical process development is inevitably linked to an optimized determination of thermokinetic data of chemical reactions. A miniaturized flow calorimeter enables increased sensitivity when examining small amounts of reactants in a short time compared to traditional batch equipment. Therefore, a methodology to determine optimal reaction conditions for calorimetric measurement experiments was developed and is presented in this contribution. Within the methodology, short-cut calculations are supplemented by computational fluid dynamics (CFD) simulations for a better representation of the hydrodynamics within the microreactor. This approach leads to the effective design of experiments. Unfavourable experimental conditions for kinetics experiments are determined in advance and therefore, need not to be considered during design of experiments. The methodology is tested for an instantaneous acid-base reaction. Good agreement of simulations was obtained with experimental data. Thus, the prediction of the hydrodynamics is enabled and the first steps towards a digital twin of the calorimeter are performed. The flow rates proposed by the methodology are tested for the determination of reaction enthalpy and showed that reasonable experimental settings resulted. Graphical abstract A methodology is suggested to evaluate optimal reaction conditions for efficientacquisition of kinetic data. The experimental design space is limited by thestepwise determination of important time scales based on specified input data.

scholarly journals Synthesis of propylene carbonate from urea and 1,2-propylene glycol over metal carbonates

2011 ◽  
Vol 17 (3) ◽  
pp. 323-331 ◽  
Author(s):  
Jiancheng Zhou ◽  
Wu Dongfang ◽  
Birong Zhang ◽  
Yali Guo
Keyword(s):  
Reaction Time ◽  
Propylene Glycol ◽  
Propylene Carbonate ◽  
Reaction Temperature ◽  
Reaction Conditions ◽  
Lead Carbonate ◽  
Synthetic Process ◽  
Metal Carbonates ◽  
Optimal Reaction ◽  
Mixed Carbonate

A series of single-metal carbonates and Pb-Zn mixed-metal carbonates were prepared as catalysts for alcoholysis of urea with 1,2-propylene glycol (PG) for the synthesis of propylene carbonate (PC). The mixed carbonates all show much better catalytic activities than the single carbonates, arising from a strong synergistic effect between the two crystalline phases, hydrozincite and lead carbonate. The mixed carbonate with Pb/Zn=1:2 gives the highest yield of PC, followed by the mixed carbonate with Pb/Zn=1:3. Furthermore, Taguchi method was used to optimize the synthetic process for improving the yield of PC. It is shown that the reaction temperature is the most significant factor affecting the yield of PC, followed by the reaction time, and that the optimal reaction conditions are the reaction time at 5 hours, the reaction temperature at 180 oC and the catalyst amount at 1.8 wt%, resulting in the highest PC yield of 96.3%.

Lipase-Catalyzed Acyl-L-Carnitines Synthesis in [Bmim]PF6 Ionic Liquid

2009 ◽  
Vol 5 (1) ◽  
Author(s):  
Jin-qiang Tian ◽  
Qiang Wang ◽  
Zhong-yuan Zhang
Keyword(s):  
Ionic Liquid ◽  
Lipase Activity ◽  
Molecular Sieves ◽  
Reaction Medium ◽  
Molar Ratio ◽  
Reaction Conditions ◽  
Optimal Reaction ◽  
Better Than

In order to significantly improve the biosynthesis of acyl-L-carnitines catalyzed by lipase, there must be an efficient and suitable reaction medium that is not only polar but also hydrophobic. [Bmim]PF6, which satisfies the above two requirements, was applied as the medium. The optimal reaction conditions were: for isovaleryl-L-carnitine, 0.22aW, 200mg molecular sieves, 60ºC, 4:1 of molar ratio (fatty acid:L-carnitine), 150rpm and 60h; for octanoyl-L-carnitine and palmitoyl-L-carnitine, 0.22aW, 250 mg molecular sieves, 5:1 of molar ratio (fatty acid:L-carnitine), 200rpm, 48h, 60ºC (octanoyl-L-carnitine) and 65ºC (palmitoyl-L-carnitine). Their overall yields could reach 59.14%, 90.79% and 98.03%, respectively. The yields of isovaleryl-L-carnitine, octanoyl-L-carnitine and palmitoyl-L-carnitine in [Bmim]PF6 were 16.21%, 73.67% and 44.22 % more than those in acetonitrile, respectively. [Bmim]PF6 as the medium was better than acetonitrile. It could not only enhance the yields of acyl-L-carnitines, but also protect the lipase activity.

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