scholarly journals Hydrothermal carbonization of fructose—effect of salts and reactor stirring on the growth and formation of carbon spheres

2021 ◽  
Author(s):  
Dennis Jung ◽  
Gözde Duman ◽  
Michael Zimmermann ◽  
Andrea Kruse ◽  
Jale Yanik
Keyword(s):  
Growth Mechanism ◽  
Formation Rate ◽  
Reaction Times ◽  
Kinetic Studies ◽  
Hydrothermal Carbonization ◽  
Sphere Diameter ◽  
Carbon Spheres ◽  
Reaction Conditions ◽  
Reaction Rate Constants ◽  
State Of Matter

AbstractHydrothermal carbonization (HTC) has become a promising technology for the production of hydrochar and carbon spheres. Several studies indicate a strong dependency of the reaction conditions on the sphere diameter. The usage of additives, such as salts, is one possibility to increase the size of the spheres. However, the growth mechanism which leads to larger particles is not fully understood. In this work, kinetic studies of HTC with fructose were performed with different salts as additives. The growth of the particles (the increase in size) has been compared to the formation rates (increase in yield) of hydrochar by using the reaction rate constants from the kinetic model. The results indicate that the acceleration of the growth rate is independent of the formation rate. It is therefore assumed that coagulation, as a growth mechanism, took place. With longer reaction times, the particles reached a stable particle size, independently from the added salts; therefore, it was assumed that the particles underwent some sort of solidification. The state of matter can therefore be described as an intermediate state between liquid and solid, similar to mesophase pitch. Experiments with a stirrer resulted in squashed particles, which supports the model, that the particles exhibit emulsion-like behavior.

Synthesis of Colloidal Carbon Spheres by Hydrothermal Carbonization of Glucose at Different Initial pH

2011 ◽  
Vol 685 ◽  
pp. 123-129 ◽  
Author(s):  
Guo Hui Jiang ◽  
Xue Qing Xu ◽  
Gang Xu
Keyword(s):  
Hydrothermal Reaction ◽  
Glucose Solution ◽  
Hydrothermal Carbonization ◽  
Size Distributions ◽  
Carbon Spheres ◽  
Growth Mechanisms ◽  
Reaction Conditions ◽  
Ph Values ◽  
Initial Ph ◽  
Hydrothermal Reaction Time

In this paper, carbon spheres with different size distributions are obtained by hydrothermal carbonization of glucose via varying the reaction conditions including concentration of glucose solution, hydrothermal reaction time and the initial pH values of solutions. The initial pH values of glucose solutions play an important role in the size distribution of the carbon spheres. The formation and growth mechanisms of carbon spheres at different initial pH levels are discussed and proposed.

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.

scholarly journals Self-Assembled Bimetallic Aluminum-Salen Catalyst for the Cyclic Carbonates Synthesis

Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 4097
Author(s):  
Wooyong Seong ◽  
Hyungwoo Hahm ◽  
Seyong Kim ◽  
Jongwoo Park ◽  
Khalil A. Abboud ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Self Assembly ◽  
Reaction Pathway ◽  
Kinetic Studies ◽  
Cyclic Carbonate ◽  
Reaction Conditions ◽  
Formation Reaction ◽  
X Ray ◽  
Carbonate Formation ◽  
Salen Aluminum

Bimetallic bis-urea functionalized salen-aluminum catalysts have been developed for cyclic carbonate synthesis from epoxides and CO2. The urea moiety provides a bimetallic scaffold through hydrogen bonding, which expedites the cyclic carbonate formation reaction under mild reaction conditions. The turnover frequency (TOF) of the bis-urea salen Al catalyst is three times higher than that of a μ-oxo-bridged catalyst, and 13 times higher than that of a monomeric salen aluminum catalyst. The bimetallic reaction pathway is suggested based on urea additive studies and kinetic studies. Additionally, the X-ray crystal structure of a bis-urea salen Ni complex supports the self-assembly of the bis-urea salen metal complex through hydrogen bonding.

scholarly journals Hydrothermal Carbonization (HTC) of Seaweed (Macroalgae) for Producing Hydrochar

Energies ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1805
Author(s):  
Neel Patel ◽  
Bishnu Acharya ◽  
Prabir Basu
Keyword(s):  
Batch Reactor ◽  
Reaction Times ◽  
Hydrothermal Carbonization ◽  
Process Conditions ◽  
Maritime Provinces ◽  
Heating Value ◽  
Direct Combustion ◽  
Ecological Problems ◽  
Liquid Slurry ◽  
Work Done

Waste seaweed that is collected at coastal regions of maritime provinces in Canada is creating ecological problems as it promotes an anoxic event, which produces nearly zero dissolved oxygen in water along with hydrogen sulfide emission. The work done in this study attempts to address this issue by producing a coal-like solid hydrochar and nutritious liquid slurry (processed water) by employing a rather recent thermo-chemical process called hydrothermal carbonization (HTC) on the seaweed. The HTC was carried out in a batch reactor system for three different reaction temperatures, 180 °C, 200 °C, 220 °C, and three different reaction times, 30, 60, and 120 min. Each of the produced hydrochars was characterized by different analytical methods. The effects of the process conditions on the yield and the properties of the hydrochar and process water were examined. The hydrochar produced at 220 °C and 120 min showed the highest carbon content (48.5%) and heating value (18.93 MJ/kg). The energy density and carbon to nitrogen (C/N) ratio in the hydrochar increased significantly as compared to raw seaweed. Moreover, HTC reduced the ash yield and volatile compounds of the seaweed. Thus, hydrochar can be used as a fuel for direct combustion, in soil remediation, or in carbon sequestration applications.

scholarly journals Microwave-Assisted Asinger Synthesis of Thiazolines

2020 ◽  
Vol 3 (1) ◽  
pp. 27
Author(s):  
Raúl Eduardo Gordillo-Cruz ◽  
Liliana Gonzalez-Reyes ◽  
Milton Coporo-Reyes ◽  
Nieves Zavala-Segovia ◽  
Bernardo A. Frontana-Uribe ◽  
...  
Keyword(s):  
Microwave Irradiation ◽  
Reaction Times ◽  
Reaction Conditions ◽  
Microwave Assisted

An array of 2,4-disubstituted thiazolines was obtained through Asinger reaction approach from the straightforward treatment of diverse aldehydes/ketones with 1-mercaptopropan-2-one, in the presence of NH3 assisted by microwave irradiation, displaying similar and sometimes higher yields, as well as shorter reaction times that traditional Asinger reaction conditions at room and lower temperatures.

Efficient and Reusable Silica Gel Supported Metal Ionic Liquid Catalysts for Palmitic Acid Esterification to Biodiesel

2021 ◽  
Vol 43 (1) ◽  
pp. 1-1
Author(s):  
Guo Yingwei Guo Yingwei ◽  
Chen Xuedan Chen Xuedan ◽  
Yan Shiting Yan Shiting ◽  
Zhang Zhengliang Zhang Zhengliang ◽  
Chen Yuqin Chen Yuqin ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Palmitic Acid ◽  
Silica Gel ◽  
High Surface ◽  
High Surface Area ◽  
Kinetic Studies ◽  
Catalytic Performance ◽  
Reaction Conditions ◽  
Acid Esterification ◽  
Supported Metal

A series of silica gel (SG) supported metal ionic liquid catalysts (x[Bmim]Cl-CrCl3/SG) were synthesized and exploited for the esterification of palmitic acid (PA) with methanol (ML) to produce biodiesel efficiently. The 10%[Bmim]Cl-CrCl3/SG catalyst with high surface area and desirable acidity exhibited the best catalytic performance and reusability after six consecutive running cycles. Based on the response surface analysis, the optimal reaction conditions were obtained as follows: methanol/acid mole ratio = 11:1 mol/mol, catalyst amount = 5.3 wt%, reaction time = 65 min, as well as reaction temperature = 373 K, reaching to a biodiesel yield of 96.1%. Further kinetic studies demonstrated that the esterification of PA with ML obeyed 1.41 order kinetics for acid concentration with the activation energy of 16.88 kJ/mol

scholarly journals The Eschenmoser coupling reaction under continuous-flow conditions

2011 ◽  
Vol 7 ◽  
pp. 1164-1172 ◽  
Author(s):  
Sukhdeep Singh ◽  
J Michael Köhler ◽  
Andreas Schober ◽  
G Alexander Groß
Keyword(s):  
Continuous Flow ◽  
Elevated Temperatures ◽  
Reaction Times ◽  
Coupling Reaction ◽  
Flow Chemistry ◽  
Flow Conditions ◽  
Reaction Conditions ◽  
Bond Forming ◽  
Carbon Carbon Bond ◽  
Reaction Proceeds

The Eschenmoser coupling is a useful carbon–carbon bond forming reaction which has been used in various different synthesis strategies. The reaction proceeds smoothly if S-alkylated ternary thioamides or thiolactames are used. In the case of S-alkylated secondary thioamides or thiolactames, the Eschenmoser coupling needs prolonged reaction times and elevated temperatures to deliver valuable yields. We have used a flow chemistry system to promote the Eschenmoser coupling under enhanced reaction conditions in order to convert the demanding precursors such as S-alkylated secondary thioamides and thiolactames in an efficient way. Under pressurized reaction conditions at about 220 °C, the desired Eschenmoser coupling products were obtained within 70 s residence time. The reaction kinetics was investigated and 15 examples of different building block combinations are given.

Facile Synthesis, Morphology Evolution and Tunable Luminescence of NaGdF4:Yb,Er Nanorods with Various Aspect Ratios

NANO ◽  
2018 ◽  
Vol 13 (08) ◽  
pp. 1850093 ◽  
Author(s):  
Shasha Gai ◽  
Jiqing Jiao ◽  
Wei Wei ◽  
Yao Li ◽  
Lihua Liu ◽  
...  
Keyword(s):  
Energy Level ◽  
Hydrothermal Method ◽  
Growth Mechanism ◽  
Morphology Evolution ◽  
Schematic Diagram ◽  
Facile Synthesis ◽  
Reaction Conditions ◽  
Facile Hydrothermal Method ◽  
Aspect Ratios ◽  
Lower Temperature

The well-defined NaGdF4:Yb,Er nanorods (NRs) with various aspect ratios were synthesized using a facile hydrothermal method. The morphology and crystal phase of NRs could be controlled by reaction conditions. NaGdF4:Yb,Er NRs with various aspect ratios could be synthesized and their upconversion (UC) luminescence was tuned. It is displayed that the NRs with aspect ratios about 5 exhibited the strongest UC luminescence among samples. The growth mechanism and morphology transition of NRs had been deduced by schematic diagram. And UC mechanism had been determined by energy level diagrams. Compared with previous reports, the work provided a facial method for UCNRs with various aspect ratios at lower temperature.

scholarly journals Development of the technique for quality control of 1,3-bis(3,4-dicyanophenoxy)benzene by HPLC

2021 ◽  
Vol 16 (1) ◽  
pp. 88-98
Author(s):  
Z. N. Shchekoldina ◽  
A. A. Bogolyubov ◽  
A. Yu. Zakharov ◽  
B. A. Bulgakov ◽  
A. V. Babkin ◽  
...  
Keyword(s):  
Quality Control ◽  
High Performance ◽  
Raw Materials ◽  
Reaction Times ◽  
Kinetic Studies ◽  
Reversed Phase ◽  
Quantitative Chemical Analysis ◽  
Practical Applications ◽  
Good Convergence ◽  
Quantitative Hplc Analysis

Objectives. Determination of target products and byproducts is necessary for the quality control of phthalonitrile monomer synthesis as well as production scaling and performing related kinetic studies. High-performance liquid chromatography (HPLC) is a simple and affordable method for quantitative chemical analysis, which also verifies the quality of raw materials. The objective of this study was to develop an HPLC technique for determining the composition of the reaction mixture in the synthesis of 1,3-bis(3,4-dicyanophenoxy)benzene (DPB).Methods. Reversed-phase HPLC was used to quantitatively analyze the reaction mixture.Results. A simple and rapid method for the quantitative HPLC analysis of phthalonitrile monomers and their mixtures with reagents was developed. Reaction times and the accumulation of byproducts were also studied.Conclusions. The successful performance of the developed technique allows us to recommend it for practical applications. The results obtained for reactors of different sizes have good convergence, and DPB synthesis was successfully scaled up to intermediate scale equipment.

Efficient synthesis of pyrido[2,3-d]pyrimidine-7-carboxylic acids catalyzed by a TiO2/SiO2 nanocomposite in aqueous media at room temperature

2018 ◽  
Vol 73 (9) ◽  
pp. 641-645 ◽  
Author(s):  
Sepehr Sadegh-Samiei ◽  
Shahrzad Abdolmohammadi
Keyword(s):  
Heterogeneous Catalyst ◽  
Carboxylic Acids ◽  
Room Temperature ◽  
Aqueous Media ◽  
Reaction Times ◽  
Molar Ratio ◽  
Efficient Synthesis ◽  
Reaction Conditions ◽  
Moderate Reaction ◽  
Recyclable Heterogeneous Catalyst

AbstractA novel and efficient synthesis of eight 5-aryl-1,3-dimethyl-2,4-dioxo-1,2,3,4,5,8-hexahydropyrido[2,3-d]pyrimidine-7-carboxylic acids using a TiO2/SiO2 nanocomposite with a molar ratio of 1:1 as a recyclable heterogeneous catalyst is described. The desired products, five of which are new, are formed in short reaction times (2–3 h) with high to excellent yields (94%–98%) under very moderate reaction conditions (room temperature, aqueous media).

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