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Anand Mohan Yadav Nikkam Suresh Abhishek Sundaram Pravesh Painkra Ashish Kumar Raja Md Arshad 《Journal of Dispersion Science and Technology》2018,39(5):754-764
The high cost of the bridging liquid subdues the implementation and commercialization of oil agglomeration process. To overcome this problem, waste oils from different sectors were used in this present study. The performance of the process was assessed based on the responses like ash rejection and organic matter recovery. The aim of the present study was to investigate the usage of waste oils from different sectors and to optimize and analyze the behavioral pattern showcased by different variables (pulp density, oil dosage, agglomeration time and oil type) using response surface methodology (Box-Behnken design). Experimental investigation shows that the optimum pulp density, oil dosage, agglomeration time and oil type condition obtained as 3%, 15%, 15?min and waste engine oil, respectively. At optimum condition, the % ash rejection and % organic matter recovery obtained as 63.94% and 81.8%, respectively. 相似文献
95.
Mechanism of Evolution of Koneramine Complexes from One‐Pot Reactions: Snapshots of Intermediates Offer Facile Routes to New Dipicolylamines
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Sakthi Raje Nandakishor Mondivagu Manoj Chahal Prof. Ray J. Butcher Prof. Raja Angamuthu 《化学:亚洲杂志》2018,13(11):1458-1466
Koneramines (LROR′, R=Ph or Ts; R′=Me, iPr) and their complexes were found to emerge from the system of pyridine‐2‐carboxaldehyde and N‐phenyl/tosylethylenediamine when a primary or secondary alcohol was used as solvent. Imidazolidinylpyridines (LR, R=Ph or Ts) became major emergents whereas hemi‐aminals (LROH, R=Ph or Ts) are minor emergents of the system when tertiary butanol was used as the solvent; the bulky tertiary butyl group prevented the addition of alcohol to the iminium ion that diverted the equilibrium towards imidazolidinylpyridines. By playing with the components of the reaction mixture, crystals of the metastable intermediates bound to copper(II) and/or zinc(II) were obtained and the structures were determined by X‐ray diffraction analysis. The reported results shed light on how to control the emergents of the multicomponent reaction mixture that forms koneramines. Reactivity studies of the intermediates pave the way for a new type of koneramine complexes that are new dipicolylamines where the two pyridine moieties of the resulting koneramine are not the same. 相似文献
96.
Synthesis and Reversible Hydration of a Pseudoprotein,a Fully Organic Polymeric Desiccant by Multiple Single‐Crystal‐to‐Single‐Crystal Transformations
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Raja Mohanrao Prof. Dr. Kana M. Sureshan 《Angewandte Chemie (International ed. in English)》2018,57(38):12435-12439
A diphenylalanine derivative, N3‐Phe‐Phe‐NHCH2CCH, was designed for topochemical azide–alkyne cycloaddition (TAAC) polymerization. This dipeptide adopted β‐sheet arrangement as designed, in its crystals, but the azide and alkyne were not fitly aligned for their topochemical reaction. However, the voids present around these groups allowed them to attain a reactive geometry upon heating and their consequent TAAC polymerization to a pseudoprotein in a single‐crystal‐to‐single‐crystal (SCSC) fashion. This motion led to the creation of channels in the product crystal and it absorbed water from the surroundings to fill these channels as H‐bonded water wire. The pseudoprotein undergo reversible hydration/dehydration in SCSC fashion many times under mild conditions: hydration at low relative humidity and dehydration at low temperature. Vapor sorption analyses suggest that this fully organic polymer might be useful as an energy‐efficient desiccant material for controlling indoor humidity. 相似文献
97.
Let Abe an affine domain of dimension nover an algebraically closed field kof characteristic 0. Let I A[T]be a local complete intersection ideal of height nsuch that I/I2 is generated by n elements. It is proved that there exists a projective A[T]module Pof rank nsuch that Iis a surjective image of P. 相似文献
98.
Simon G. Bott Alan P. Marchand Duddu Raja Gopal 《Journal of chemical crystallography》1993,23(11):849-855
The syntheses and crystal structures of pentacyclo[9.4.1.05,14.07,13.012,15]hexadecane-3,9-dione (2), a novel C16 diketone with potential inclusion ability, and the products of the reaction of2 withn-butyllithium andmeso-erythritol (i.e.,meso-1,2,3,4-butanetetrol) are described. Crystal data:2·H2O, orthorhombic,Pmmn,a=10.7385(8),b=9.0188(6),c=6.8411(4)Å,V=662.55(7)Å3, andR=0.039 (379 reflections);3 (product from reaction withn-butyllithium), triclinic,P¯1,a=8.7192(7),b=10.9351(8),c=12.1842(8)Å,=68.933(5),=75.850(6), =80.309(6)°,V=1047.0(1)Å3, andR=0.081 (1811 reflections);4 (product from reaction with erythritol), triclinic,P¯1,a=7.7224(8),b=10.1976(8),c=10.7021(9)Å,=85.405(7),=85.766(8), =76.056(7)°,V=814.0(1)Å3, andR=0.052 (1471 reflections). 相似文献
99.
Venkatachalam G Raja N Pandiarajan D Ramesh R 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2008,71(3):884-891
An interesting series of binuclear ruthenium(III) Schiff base complexes bearing bis-salophen/bis-naphophen units of the general composition [(EPh(3))(X)Ru-L-Ru(X)(EPh(3))] (where E=P or As; X=Cl or Br; L=binucleating dianionic tetradentate ligands) have been synthesized and characterized by analytical (elemental analysis, magnetic susceptibility measurements), spectral (FT-IR, UV-vis and EPR) and electrochemical methods. These ruthenium(III) complexes have two N(2)O(2) metal binding sites, which are linked to each other with a biphenyl bridge and acts as potential catalyst for oxidation of wide range of primary and secondary alcohols to corresponding aldehydes or ketones with moderate to high conversion in the presence of N-methylmorpholine-N-oxide (NMO). The formation of high-valent Ru(V)=O species as a catalytic active intermediate is proposed for the catalytic processes. 相似文献
100.
Raja CR Paramasivam P Vijayan N 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2008,69(4):1146-1149
A novel organic non-linear optical organic single crystal of 4-phenylpyridinium hydrogen squarate (4PHS) has been synthesized and successfully grown from aqueous solutions by slow evaporation solution growth method. In the present investigation the title compound has been synthesized by taking equimolar quantity of 4-phenylpyridine and squaric acid and mixed thoroughly using double distilled water as the solvent. The prepared concentrated solution was placed in an undisturbed condition, and then the solution was periodically inspected. The good quality single crystals have been harvested in a time span of 3 weeks. Then the grown crystal was characterized as single crystal XRD, differential thermal analysis, thermogravimetric analysis, FTIR, UV-vis-NIR, SHG, (1)H NMR and (13)C NMR analyses, respectively. The observed results from the characterization analyses show its suitability for NLO applications when compared with some of the existing organic crystals. The relative second harmonic generation of this grown crystal was found to be five times higher than that of KDP crystal. The UV cut-off wavelength and decomposition temperature of this grown crystal were also comparatively better. (1)H NMR and (13)C NMR spectroscopic studies were employed to elucidate the structure of the grown specimen. 相似文献