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CXLVIl Chemical oxidation , carbon adsorption and bloaugmentatlon sequence treatment of salicylic add

CXLVIll Klnetlca data for Fenton s reagent and Resorcinol 100 mg l

CXLVn shows the reduction of salicylic acid 325 mg 1 to 245.7 mg l by first treating with CMn04. The TOC removal percentage was 24.40 . Further treatment with activated carbons Noth PAC 20B, Norit E Supra USP, Darco KB, Norit SX2, Darco S-51 and Hydrodarco C produced TOC readings 2693 mg 1, 2813 mg 1,3413 mg 1,

CXVI Determining the weight of organic compound adsorbed per unit mass of activated carbon using Freundllch equation

CXVI1 gives the resonance energy of several compounds containing the CONH2 group in which resonance with the structure

CXVII gives the resonance energy of several compounds containing the GONH2 group in which resonance w ith the structure

CXVIl Detemiining the weight of organic compound adsorbed per unit mass of activated carbon using BET equation

CXVIll Determining he weight of organic compound adsorbed per unit mass of activated carbon using Langmuir equation

CXXI Determining the weight of organic compound adsorbed per unit mass of activated carbon using Langmuir equation

CXXII Determining the weight of organic compound adsorbed per unit mass of activated carbon using Freundlich equation

CXXIII Determining the weight of organic compound adsorbed per unit mass of activated carbon using BET equation

CXXIV Determining the weight of organic compound adsorbed per unit mass of activated carbon Using Langmuir equation

CXXV Determining the weight of organic compound adsorbed per unit mass of activated carbon using Freundllch equation

CXXVI Determining the weight of organic compound adsorbed per unit mass of activated carbon using B T equation

CXXVIII. Dipole Moments Calculated from Dielectric Constants of Pure Liquids

CXXVIll Bioaugmentation using LLMO C l In an anaerobic condition Organic compound

CXXX Bloaiigmeniatlon using LLMO 0-1 In an anaerobic condition Organic compound Vanillin

CXXXII Bloaugmentatlon using LLMO C 1 in an anaerobic condition Organic compound

CXXXIII. Dipole Moments of Orgamc j i, i i

CXXXIII. Dipole Moments of Organic, 5, A 1 i

CXXXIV Bloaugmentatlon using LLMO 0 1 in an aerobic condition Organic compound

CXXXIV. Deviations from Ideal Behaviour in Liquid Mixtures

CXXXIX. Heats of Sublimation of Metals

CXXXL Lengths of Some Hydrogen Bonds

CXXXVI Bloaugmentation using LLMO 0 1 In an aerobic condition Organic compound



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