Understanding Surface Energy

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Understanding Surface Energy Anett Kondor Surface Measurement Systems Ltd. 6 th October 2015

What is the SE; Why it is important to measure and How it can be measured?

Basics Atoms in the centre of a material are surrounded by other atoms some of the surface electrons could interact with atoms surrounding the material. To quantify the ability of the surface to react. 1 st Law: all systems try to reach their lowest energy levels. - metals surface oxidation

Surface Energy Materials with high surface energy are easier to wet and adhere to than those with low surface energy. Surface energy components according by Fowkes: Dispersive component physical long range interactions, measured by the series of n-alkanes Lewis acid-base component chemical short range interactions, measured by two mono-functional polar solvents T s d s ab s [J/m 2 ] l - Surface tension of liquid

Introduction of the SE The surface energy is a very informative and important parameter of solids. 1 st development for surface energy and acid/base interactions** of IGC was for polymers and composite materials. Knowledge of surface energetics is important in the formulation design of multi-component systems and the prediction of processing performance. Ability to measure the surface energy of various materials is essential for ensuring compatibility between the given base material and the top coating one wishes to apply onto it or other materials one wishes to attach to it. *Laub, R.J. and Pecsok, R.L., Physicochemical Applications of Gas Chromatography. 1978, New York: John Wiley & Sons. ** Schultz, J., Lavielle, L., and Martin, C., The role of the interface in carbon fibre epoxy composites. J. of Adhesion, 1987. 23(1): p45-60.

Examples for Importance of Surface Energy 1. Paper Industry printing quality strongly influenced by the structural and chemical properties of the paper surface 2. Building Industry to evaluate adhesion of bituminous crack sealant to aggregates 3. Medical Care to bond a resin to a tooth

Modify Surface Energy Investigation the influence of surface treatments Common industrial process for tuning the surface energy of materials to application needs.

Pharmaceutical Powders* Selected chemical and solid-state material properties, usually constitute the critical variables of a pharmaceutical manufacturing process * Dilip M. Parikh, American Pharmaceutical Society (2006) An Overview of the Properties of Pharmaceutical Powders and their Effects on Processibility

Pharmaceutical Powders* Tablet strength is controlled by formation of intermolecular forces over the areas of contact between the particles. The strength of these bonding forces is controlled by surface energy.* Knowledge of the wettability and surface energy of pharmaceutical solids is important in the design of pharmaceutical formulations.* If the surface energies of the individual compounds are known, the work of adhesion or cohesion can be obtained. * Dilip M. Parikh, American Pharmaceutical Society (2006) An Overview of the Properties of Pharmaceutical Powders and their Effects on Processibility

Increasing Surface Energy Relationship with other properties Wettability Cohesion Process-induced Disorder Adhesion

Relationship with other properties BUT it is not correlate linearly with everything Surface Energy Linear relation Property of solid/mix Complex relation Surface Energy Property of solid/mix Surface Energy No relation Property of solid/mix Note: Does not mean that the surface energy value is wrong or not useful

How we can measure? Contact Angle (CA) technique Atomic Force Microscope (AFM) Washburn capillary rise technique Invers Gas Chromatography (IGC) Wetting Balance IGC is the most commonly successfully used technique for surface energy analysis of powders and fibres.

SEA vs. CA and AFM Surface Energy Analyzer (SEA) Contact Angle (CA) Atomic Force Microscopy (AFM) Powder, fibres, nano particles, granules, films and semi -solids Surface heterogeneity Very good reproducibility (RSD%=1) Vary conditions (temperature and RH) Flat, smooth, homogenous and inert macroscopic substrate Specific point of the flat surface varying one - ambient condition Thin flat, molecular level Three way (x, y, z) Scatter and irreproducible Strict controlled- low humidity level, controlled and known loads Comparison Table available online on SMS website

Reliability of the igc-sea results Uncertainty of the measurement Experiment to experiment Mean value R 2 SD RSD BET SSA By IGC-SEA 0.2876 0.2788 m 2 /g 0.9993-0.9996 0.0027 0.0060 m 2 /g 0.94-2.16% y d by Peak Max by IGC-SEA 34.43 34.15 mj/m 2 0.9998-1.0000 0.15 0.38 mj/m 2 0.45 1.10% y d by Peak COM by IGC-SEA 38.74 39.16 mj/m 2 0.9994-0.9996 0.14 0.27 mj/m 2 0.37 0.69% Reference: SMS - TN807 Repeatability Part 1

IGC Introduction Gas phase sorption technique Inverse Gas Chromatography (IGC) principles*: 1st developed in 1950s. Focus of physicochemical studies on the kinetic information and thermodynamic quantities from sorption equilibria. Earlier work for catalytic materials, e.g. activated carbon, alumina and silica. Powerful physico-chemical characterization tool for powders, fibres, films, particulates, semi-solids. 1 st development for surface energy and acid/base interactions** was for polymers and composite materials. *Laub, R.J. and Pecsok, R.L., Physicochemical Applications of Gas Chromatography. 1978, New York: John Wiley & Sons. ** Schultz, J., Lavielle, L., and Martin, C., The role of the interface in carbon fibre epoxy composites. J. of Adhesion, 1987. 23(1): p45-60.

Animation by L. Teng, Surface Measurement Systems IGC Principles

Properties measured by IGC-SEA The IGC-SEA provides unique access to the following physico-chemical properties of a wide range of solid materials in a controlled humidity environment: Dispersive and Polar Surface Energies Heats and Entropies of Adsorption Acid/Base Interactions and Specific pair Interaction Parameter (I sp ) BET SSA - Specific Surface Area Phase Transitions Sorption Isotherms Permeability, Solubility and Diffusion Competitive (Multicomponent) Adsorption Thermodynamic Work of Cohesion and Adhesion Surface Energy heterogeneity mapping Constantly extend the applications future applications e.g. Chemisorption

igc-sea Introduction 2 nd generation chromatographic sorption instrument Compact design - Reduced footprint: 450 mm (18 ) x 450 mm (18 ) x 700 mm (27.5 ) 12 vapor reservoirs (50 ml) 2 column oven design: 20 to 150 C Flame Ionization Detector (FID) User Friendly Control and Analysis Software Background Humidity Controller Safety Features: Hydrogen Leak & Organic Vapor Leak Detectors

Applications Surface treatment studies Evaluation of the pre-treatments Batch-to batch variation study Formulation design Surface characterization Influence of humidity for BET Surface Area And about hundred publications so far.

Acknowledgements Every Colleagues at Surface Measurement Systems Collaborators Dr Daryl Williams (Imperial College London) Dr Jerry Heng (Imperial College London) Dr Daniel Burnett (Surface Measurement Systems) Dr Jiyi Khoo (GSK) Dr Majid Naderi (Surface Measurement Systems) Dr Raimundo Ho (Abbott Laboratories) Dr Sarah Dilworth (AstraZeneca) Prof John Watts (University of Surrey) Dr Steven Hinder (University of Surrey) Dr Frank Thielmann (Novartis) Dr Gavin Reynolds (AstraZeneca) Dr David Wilson (AstraZeneca)

Thank you for your attention! Head Office: United States Office: Surface Measurement Systems, Ltd. Surface Measurement Systems, Ltd, NA 5 Wharfside, Rosemont Road 2125 28th Street SW, Suite 1 London HA0 4PE, UK Allentown PA, 18103 Tel: +44 (0)20 8795 9400 Tel: +1 610 798 8299 Fax: +44 (0)20 8795 9401 Fax: +1 610 798 0334 Email: science@surfacemeasurementsystems.com