Empirical evaluation of sand filters to evolve practical designs for artificial recharge through dry wells

2021 ◽  
Vol 593 ◽  
pp. 125839
Author(s):  
Gopal Kumar ◽  
D.R. Sena ◽  
B.K. Rao ◽  
R.S. Kurothe ◽  
Nyonand Yadav ◽  
...  
Keyword(s):  
Artificial Recharge ◽  
Empirical Evaluation ◽  
Sand Filters

Issues in artificial recharge

1996 ◽  
Vol 33 (10-11) ◽  
pp. 381-390 ◽  
Author(s):  
Herman Bouwer
Keyword(s):  
Nitrogen Removal ◽  
Vadose Zone ◽  
Artificial Recharge ◽  
Disinfection Byproducts ◽  
Soil Aquifer Treatment ◽  
Sewage Effluent ◽  
Sand Filters ◽  
Normal Water ◽  
Pre Treatment

Interest in artificial recharge with normal water and sewage effluent continues to increase. Issues discussed in this paper include recharge with infiltration basins, soil-aquifer treatment of sewage effluent, potable use of water from aquifers recharged with sewage effluent, nitrogen removal, pre-treatment of sewage effluent, disinfection, well recharge, clogging parameters, superchlorination, disinfection byproducts, vadose zone wells, seepage trenches, and constructed aquifers used as intermittent sand filters.

Semi-empirical evaluation of Sr-Ar difference potentials

1986 ◽  
Vol 47 (7) ◽  
pp. 1149-1154
Author(s):  
Le Quang Rang ◽  
D. Voslamber
Keyword(s):  
Empirical Evaluation ◽  
Difference Potentials ◽  
Semi Empirical

Computationally Augmented Retrosynthesis: Total Synthesis of Paspaline A and Emindole PB

2018 ◽  
Author(s):  
Timothy Newhouse ◽  
Daria E. Kim ◽  
Joshua E. Zweig
Keyword(s):  
Chemical Synthesis ◽  
Total Synthesis ◽  
Small Molecules ◽  
First Principles ◽  
Quantum Chemical ◽  
Computational Analysis ◽  
Empirical Evaluation ◽  
Synthetic Strategy ◽  
Catalyzed Reactions ◽  
Enzyme Catalyzed Reactions

The diverse molecular architectures of terpene natural products are assembled by exquisite enzyme-catalyzed reactions. Successful recapitulation of these transformations using chemical synthesis is hard to predict from first principles and therefore challenging to execute. A means of evaluating the feasibility of such chemical reactions would greatly enable the development of concise syntheses of complex small molecules. Herein, we report the computational analysis of the energetic favorability of a key bio-inspired transformation, which we use to inform our synthetic strategy. This approach was applied to synthesize two constituents of the historically challenging indole diterpenoid class, resulting in a concise route to (–)-paspaline A in 9 steps from commercially available materials and the first pathway to and structural confirmation of emindole PB in 13 steps. This work highlights how traditional retrosynthetic design can be augmented with quantum chemical calculations to reveal energetically feasible synthetic disconnections, minimizing time-consuming and expensive empirical evaluation.

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