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  • TITLE
  • CERTIFICATE
  • DECLARATION
  • ACKNOWLEDGEMENT
  • CONTENTS
  • PREFACE
  • 1. CRYSTAL GROWTH: THEORY AND TECHNIQUES
  • 1.1 Introduction
  • 1.2 Thermodynamics of crystal growth
  • 1.3 Nucleation
  • 1.4 Crystal growth theories
  • 1.4.1 Surface energy theory
  • 1.4.2 Diffusion theory
  • 1.4.3 Surface nucleation theory
  • 1.4.4 Screw dislocation theory
  • 1.5 Crystal growth techniques
  • 1.5.1 Growth form solids
  • 1.5.2 Growth from vapour
  • 1.5.3 Growth from melt
  • 1.5.4 Growth from solution
  • References
  • 2. GEL METHOD AND RARE EARTH OXALATE CRYSTALS
  • 2.1 Introduction
  • 2.2 Hydrosilica gel
  • 2.3 Gelation mechanism and gel structure
  • 2.4 Advantages of gel
  • 2.5 Crystallization in gel
  • 2.5.1 Chemical reaction method
  • 2.5.2 Chemical reduction method
  • 2.5.3 Solubility reduction method
  • 2.5.4 Complex dilution method
  • 2.6 Nucleation control in gel
  • 2.7 Rare earth oxalate crystals
  • References
  • 3. CHARACTERIZATION TECHNIQUES
  • 3.1 Introduction
  • 3.2 Optical microscopy
  • 3.3 Etching studies
  • 3.4 Microhardness studies
  • 3.5 X-ray diffractometry
  • 3.6 Infrared spectroscopy
  • 3.7 UV-visible - NIR spectroscopy
  • 3.8 Laser Raman spectroscopy
  • 3.9 Thermal analysis
  • 3.10 Electron spectroscopy for chemical analysis (ESCA)
  • 3.11 Energy dispersive analysis by X-rays (EDAX)
  • 3.12 Fluorescence spectroscopy
  • References
  • 4. GROWTH STUDIES
  • 4.1 Introduction
  • 4.2 Chemistry associated with growth
  • 4.3 Hydrosilica gel as growth medium
  • 4.4 Preparation of hydrosilica gel
  • 4.5 Preparation of supernatant solution
  • 4.6 Growth of lanthanum samarium oxalate crystals
  • 4.7 Growth of lanthanum neodymium oxalate crystals
  • 4.8 Growth kinetics
  • 4.8.1 Effect of density of the gel
  • 4.8.2 Effect of pH of the gel
  • 4.8.3 Effect of ageing of the gel
  • 4.8.4 Effect of concentration of the reactants
  • a. Effect of concentration of inner reactant
  • b. Effect of concentration of the feed solution
  • 4.8.5 Effect of acidity of the feed solution
  • 4.9 Conclusion
  • References
  • 5. MICROTOPOGRAPHIC STUDIES
  • 5.1 Introduction
  • 5.2 Morphology of the crystals
  • 5.3 Microscopic studies
  • 5.4 Etching studies
  • 5.4.1 Kinetics of etching
  • 5.4.2 Dissolution studies of LSO and LNO crystals
  • 5.4.3 Selection of the etchant
  • 5.4.4 Etching on (100) face
  • 5.4.5 Etching on (110) face
  • 5.4.6 Discussion on etching studies
  • 5.5 Microhardness studies
  • 5.5.1 Microhardness studies of LSO and LNO crystals
  • References
  • 6. CHARACTERIZATION STUDIES
  • 6.1 X-ray analysis
  • 6.1.1 XRD studies on LSO
  • 6.1.2 XRD studies on LNO V
  • 6.2 IR absorption studies
  • 6.2.1 IR spectrum of C-SO 6.
  • 6.2.2 IR spectrum of LNO
  • 6.3 UV - visible spectral studies
  • 6.3.1 UV-visible spectrum of LSO
  • 6.3.2 LTV-visible spectrum of LNO
  • 6.4 Thermal analysis
  • 6.4.1 TGA and DTA of LSO
  • 6.4.2 TGA and DTA of LNO
  • 6.5 XPS studies
  • 6.5.1 XPS of LSO
  • 6.5.2 XPS of LNO
  • 6.6 Energy dispersive X-ray analysis (EDAX)
  • 6.6.1 EDAX of LSO
  • 6.6.2 EDAX of LNO
  • 6.7 Laser Raman spectral studies
  • 6.7.1 Laser Raman spectrum of LSO
  • 6.7.2 Laser Raman spectrum of LNO
  • 6.8 Fluorescence studies
  • 6.8.1 Fluorescence in LSO
  • 6.8.2 Fluorescence in LNO
  • References
  • 7. CONCLUSION
  • 7.1 Introduction
  • 7 2 Conclusions
  • 7.3 Scope for further studies
  • References