Large-scale preparation of hierarchical manganese oxide octahedral molecular sieves (OMS-1) composed of nanoplate microspheres via a facile one-pot reflux method

2011 ◽  
Vol 21 (46) ◽  
pp. 18527 ◽  
Author(s):  
Hao-Jie Cui ◽  
Jian-Wen Shi ◽  
Fan Liu ◽  
Ming-Lai Fu
2015 ◽  
Vol 70 (1) ◽  
pp. 29-38 ◽  
Author(s):  
Yuan Luo ◽  
Bao-Qiang Zhang ◽  
Yan-Hong He ◽  
Zhi Guan

AbstractAn acidic ionic liquid 3-methyl-2-(1-sulfobutyl)-1H-imidazolium hydrogensulfate, [BSO3HMIm]HSO4, was used as an efficient catalyst for the synthesis of a variety of pyrrole derivatives via a one-pot, three-component condensation of amines, nitroolefins, and 1,3-dicarbonyl compounds. Good to excellent yields of 72–96% were obtained under reflux in ethanol. The catalyst could easily be recovered and recycled up to six times, resulting in good yields without prolonging the reaction time. This method was also efficient in large-scale preparation. The procedure could be easily expanded to a one-pot, four-component reaction. This ionic liquid-catalyzed reaction provided an environmentally friendly alternative to the synthesis of pyrrole derivatives.


2021 ◽  
Vol 16 (4) ◽  
pp. 1934578X2110076
Author(s):  
Cheng Le-qin ◽  
Ye An-qi ◽  
Zhang Hao-ran ◽  
Zhang Yue-wei ◽  
Li Ling

Ginsenoside Rg5 is a rare secondary ginsenoside with good pharmacological activity. However, preparation of Rg5 is time consuming, gives a low yield and has poor selectivity and efficiency. Therefore, the current study describes an efficient method of preparing ginsenoside Rg5 through conversion of Protopanaxadiol (PPD) type saponins in the presence of a molecular sieve and hydrochloric acid. The PPD type saponins were transformed on the surface of a molecular sieve to obtain ginsenoside Rg5 and most of the generated secondary ginsenoside was dissociates into the reaction solution, avoiding further decomposition. In addition, the optimal experimental conditions were identified to be as follows; 0.5 ml of absolute ethanol, 0.2 mol/L of hydrochloric acid, 12.5 mg of a 4A molecular sieve, a reaction time of 2.5 hours and a reaction temperature of 70 ℃. Under these experimental conditions, yields of upto 63.2% were obtained for ginsenoside Rg5. Moreover, the hydrochloric acid-catalyzed preparation of ginsenoside Rg5 effectively inhibited its decomposition in the presence of a molecular sieve. The method is therefore suitable for laboratory and industrial production with the advantages of large-scale preparation and high-yield.


RSC Advances ◽  
2015 ◽  
Vol 5 (106) ◽  
pp. 87061-87068 ◽  
Author(s):  
Pei Song ◽  
Shan-Shan Li ◽  
Li-Li He ◽  
Jiu-Ju Feng ◽  
Liang Wu ◽  
...  

A rapid one-pot wet-chemical method was developed for large-scale preparation of surface-clean AuPt alloyed nanowire networks with the assistance of N-methylimidazole as a structure-directing agent and a weak stabilizing agent.


RSC Advances ◽  
2016 ◽  
Vol 6 (10) ◽  
pp. 8096-8102 ◽  
Author(s):  
Hongwei Ding ◽  
Yujuan Zhang ◽  
Guangbin Yang ◽  
Shengmao Zhang ◽  
Laigui Yu ◽  
...  

Silver nanowires (AgNWs) with varied diameters were synthesized by a facile and efficient one-pot polyol method. Each run of the reaction with this method can provide more than 10 g of AgNWs.


Nanoscale ◽  
2013 ◽  
Vol 5 (20) ◽  
pp. 9558 ◽  
Author(s):  
Juan Hou ◽  
Jin Yan ◽  
Qi Zhao ◽  
Yi Li ◽  
Hong Ding ◽  
...  

1969 ◽  
Vol 22 (03) ◽  
pp. 577-583 ◽  
Author(s):  
M.M.P Paulssen ◽  
A.C.M.G.B Wouterlood ◽  
H.L.M.A Scheffers

SummaryFactor VIII can be isolated from plasma proteins, including fibrinogen by chromatography on agarose. The best results were obtained with Sepharose 6B. Large scale preparation is also possible when cryoprecipitate is separated by chromatography. In most fractions containing factor VIII a turbidity is observed which may be due to the presence of chylomicrons.The purified factor VIII was active in vivo as well as in vitro.


1992 ◽  
Vol 70 (6) ◽  
pp. 448-454 ◽  
Author(s):  
Ewa Świeżewska ◽  
T. Chojnacki ◽  
W. J. Jankowski ◽  
K. Singh ◽  
J. Olsson

The long chain polyprenols composed of 30 and more isoprene units from leaves of plants belonging to the genera Potentilla and Rosa have been described. They occur in the form of fatty acid esters. The composition of polyprenol mixture was species dependent and its content reached ca. 0.5% wet weight. Large scale preparation of individual polyprenols from a natural polyprenol mixture was performed using time-extended liquid chromatography on the hydrophobic gel Lipidex-5000.Key words: long chain polyprenols, Rosaceae.


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