Hydrophilic MacroRAFT-Mediated Emulsion Polymerization: Synthesis of Latexes for

Similar documents
Supporting Information. Amphiphilic Block Copolymer Nano-fibers via RAFT- Mediated Polymerization in Aqueous Dispersed System

Supporting Information

Supporting Information

of Polystyrene 4-arm Stars Synthesized by RAFT- Mediated Miniemulsions.

Supporting Information

(Co)polymers by Iodine Transfer Polymerization Initiated

The ph-responsive behaviour of aqueous solutions of poly(acrylic acid) is dependent on molar mass

Bulk ring-opening transesterification polymerization of the renewable δ-decalactone using

Supporting informations for

CHAPTER TWO: EXPERIMENTAL AND INSTRUMENTATION TECHNIQUES

Controlled Structure Polymer Latex by Nitroxide-Mediated Polymerization. Jason S. Ness, Arkema Inc., USA Stéphanie Magnet, Arkema, France

Supporting information

Supplementary Material (ESI) for

Synthesis and characterization of poly(amino acid methacrylate)-stabilized diblock copolymer nanoobjects

Scheme 1: Reaction scheme for the synthesis of p(an-co-mma) copolymer

Supporting Information

c) fitting of the NMR intensity in dependence of the recycle delays 4

SELF-CROSSLINKING WATER BORNE CHEMISTRY FOR EXCELLENT SHELF STABILITY AND ROOM TEMPERATURE CURE

Supporting Information. Sequence-Regulated Copolymers via Tandem Catalysis of Living Radical Polymerization and In Situ Transesterification

Sequence-controlled methacrylic multiblock. copolymers via sulfur-free RAFT emulsion. polymerization

A critical assessment of the mechanisms governing the formation of aqueous biphasic systems composed of protic ionic liquids and polyethylene glycol

SUPPLEMENTARY INFORMATION

Electronic Supporting Information. Oxygen Tolerant Photopolymerization for Ultralow. Volumes

Supporting Information. Crosslinked network development in compatibilized alkyd/acrylic. hybrid latex films for the creation of hard coatings

Supporting Information

Supporting Information

ELECTRONIC SUPPLEMENTARY INFORMATION

Supporting Information

Supporting Information. Nitroxide Mediated Polymerization of methacrylates at moderate temperature

Supplementary Information

Supplementary Material (ESI) for Chemical Communications This journal is (c) The Royal Society of Chemistry 2009

Investigation into the mechanism of photo-mediated RAFT polymerization involving the reversible photolysis of the chain-transfer agent

Polymerization Induced Self-Assembly: Tuning of Nano-Object Morphology by Use of CO 2

Comparison of the Diffusion Coefficients Obtained for Latex Film Formation Studied by FRET and Pyrene Excimer Formation

Well-defined polyethylene-based random, block and bilayered molecular cobrushes

Comparison of Polymer Separation by Size Exclusion Chromatography and Asymmetric Flow Field Flow Fractionation

Measurement techniques

This is a repository copy of All-acrylic film-forming colloidal polymer/silica nanocomposite particles prepared by aqueous emulsion polymerization.

Azaphosphatranes as Structurally Tunable Organocatalysts for Carbonate Synthesis from CO 2 and Epoxides

RAFT /MADIX polymerization of N-vinylcaprolactam in water-ethanol solvent mixtures

Self-Healing Polymers with PEG Oligomer Side Chains. Based on Multiple H-Bonding and Adhesion Properties

Single-ion BAB triblock copolymers as highly efficient electrolytes for lithium-metal batteries

Wavelength-Dependent Photochemistry of Oxime. Ester Photoinitiators

Supplementary Material (ESI) for Chemical Communications This journal is (c) The Royal Society of Chemistry 2008

Mild and efficient bromination of Poly(hydroxyethyl)acrylate and its use towards Ionic-Liquid containing polymers

Polystyrene-block-poly(butyl acrylate) and polystyreneblock-poly[(butyl

Supporting Information

Photocontrolled RAFT Polymerization Mediated by a

SUPPLEMENTARY INFORMATION. Hydrophobic 1-Allyl-3-alkylimidazolium Dicyanamide Ionic Liquids. with Low Densities

Supporting Information

Polymer Inorganic Composites with Dynamic Covalent Mechanochromophore

Well-defined Click-able Copolymers in One-Pot Synthesis

Supporting Information.

Supporting Information

Nitroxide polymer networks formed by Michael addition: on site-cured electrode-active organic coating

CREATING TOMORROW S SOLUTIONS HEAT-SEALABLE COATINGS I PRINTING INKS I INDUSTRIAL COATINGS VINNOL SURFACE COATING RESINS PRODUCT OVERVIEW

Supporting Information

Molecular weight of polymers. Molecular weight of polymers. Molecular weight of polymers. Molecular weight of polymers. H i

SUPPORTING INFORMATION

Photolabile Protecting Groups: A Strategy for Making

Supporting Information

A novel smart polymer responsive to CO 2

One-pot polymer brush synthesis via simultaneous isocyanate coupling chemistry and grafting from RAFT polymerization

Supporting information. ph- and Thermal-Responsive Multishape Memory Hydrogel

High Frequency sonoatrp of 2-Hydroxyethyl Acrylate in an Aqueous Medium

Novel Tri-Block Copolymer of Poly (acrylic acid)-b-poly (2,2,3,3,4,4,4- hexafluorobutyl acrylate)-b-poly (acrylic acid) Prepared via Two-Step

Supporting Information. Precise Synthesis of Poly(N-Acryloyl Amino Acid) Through

Supporting Information. Supramolecular Cross-Links in Poly(Alkyl Methacrylate) Copolymers and Their Impact on the

Supplementary Information. Rational Design of Soluble and Clickable Polymers Prepared by. Conventional Free Radical Polymerization of

Supporting Information

Contents. Phillip R.A. Chivers a and David K. Smith. Department of Chemistry, University of York, Heslington, York, YO10 5DD, UK

Supporting Information

ELECTRONIC SUPPORTING INFORMATION Pentablock star shaped polymers in less than 90 minutes via

Polymers 2017; doi: 1. Structural Characterisation of the Prepared Iniferters, BDC and SBDC

VINNOL SURFACE COATING RESINS PRODUCT OVERVIEW

Supporting Information

Supramolecular hydrogen-bonded photodriven actuators based on an azobenzenecontaining

Synthesis of hydrophilic monomer, 1,4-dibromo-2,5-di[4-(2,2- dimethylpropoxysulfonyl)phenyl]butoxybenzene (Scheme 1).

Anhydrous Proton Conductivities of Squaric Acid Derivatives

Aziridine in Polymers: A Strategy to Functionalize Polymers by Ring- Opening Reaction of Aziridine

Preparation of 1:1 alternating, nucleobase-containing copolymers for use in sequence-controlled polymerization

Polymer analysis by GPC-SEC. Technical Note. Introduction

Platinum nanoparticles in suspension are as efficient as Karstedt s catalyst for alkene hydrosilylation

Supporting information

Supporting Information for:

Synthesis and characterization of innovative well-defined difluorophosphonylated-(co)polymers by RAFT polymerization

Supporting Information. Surface Functionalized Polystyrene Latexes using Itaconate based Surfmers

Redox for Main Polymerization of

/ /

Chemically recyclable alternating copolymers with low polydispersity from

Quick guide to selecting columns and standards for Gel Permeation Chromatography and Size Exclusion Chromatography SELECTION GUIDE

Supplementary Information T. Ebert, a A. Wollbrink, b A. Seifert, a R. John, a and S. Spange a

Accessory Publication

Supporting information

1 Supporting Information. 2 Adhesive RAFT Agents for Controlled Polymerization of Acrylamide: Effect of. 3 Catechol-end R Groups

1 Electronic Supplementary Information (ESI) 2 Healable thermo-reversible functional polymer via RAFT

Molecular Weight Distribution of Living Chains in Polystyrene Pre-pared by Atom Transfer Radical Polymerization

Cationic Alkylaluminum-Complexed Zirconocene Hydrides as Participants in Olefin-Polymerization Catalysis. Supporting Information

Electronic Supplementary Information (ESI)

Hyperbranched Poly(N-(2-Hydroxypropyl) Methacrylamide) via RAFT Self- Condensing Vinyl Polymerization

Transcription:

Hydrophilic MacroRAFT-Mediated Emulsion Polymerization: Synthesis of Latexes for Crosslinked and Surfactant-Free Films Jennifer Lesage de la Haye, 1 Ignacio Martin-Fabiani, 2 Malin Schulz, 3 Joseph L. Keddie, 3* Franck D Agosto, 1* Muriel Lansalot 1* 1 Univ Lyon, Université Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5265, Chemistry, Catalysis, Polymers & Processes (C2P2), 43 Bd du 11 Novembre 1918, 69616 Villeurbanne, France. 2 Department of Materials, Loughborough University, Loughborough, Leicestershire LE11 3TU, United Kingdom. 3 Department of Physics, University of Surrey, Guildford, Surrey GU2 7XH, United Kingdom. SUPPORTING INFORMATION 1

Analytical techniques Nuclear magnetic resonance (NMR). For the synthesis of the macroraft agents, MAA conversion was determined by 1 H NMR spectroscopy in D 2 O at room temperature (Bruker DRX 300) by the relative integration of the protons of the internal reference (1,3,5-trioxane) at 5.1 ppm and the vinylic protons of MAA at 5.6 and 6.0 ppm. Viscosity measurements. The viscosity of latexes was measured using a RFS III rheometer with a Couette geometry (Rheometric Scientific). The measurements were performed on 12 g of latex at 25 C at a shear rate of 200 s -1. Size exclusion chromatography (SEC-THF). Size exclusion chromatography (SEC) measurements were performed in tetrahydrofuran (THF) at 40 C at a flow rate of 1 ml min 1. Before analysis, polymers were modified by methylation of the carboxylic acid groups using trimethylsilyl diazomethane. 1 They were analyzed at a concentration of 4 mg ml 1 after filtration through a 0.45 μm pore-size membrane. The separation was carried out on three columns from Malvern Instruments [PLgel Olexis Guard (300 7.5 mm)]. The setup (Viscotek TDA305) was equipped with a refractive index (RI) detector (λ = 670 nm). The number-average molar mass (M n ), the weight-average molar mass (M w ) and the dispersity (Đ = M w /M n ) were derived from the RI signal by a calibration curve based on poly(methyl methacrylate) standards (PMMA from Polymer Laboratories). Dynamic light scattering (DLS). The particle size (z-average diameter, D z ) and the dispersity of highly diluted samples (PDI) were measured by dynamic light scattering (NanoZS from Malvern Instruments) at 25 C. The data were collected at 173 using the fully automatic mode of the Zetasizer system, and depending on the size distribution, either the monomodal cumulant analysis or the CONTIN analysis was performed. Tensiometry. Surface tension (γ) measurements were carried out with a Krüss tensiometer 2

thermostated at 25 C, on 25 ml samples. The aqueous macroraft solution or the latex was stirred for 15 min to reach the equilibrium temperature and the surface tension was measured using the Wilhelmy plate method. Differential scanning calorimetry (DSC). Thermal characterizations were performed with a differential scanning calorimeter, Mettler Toledo DSC 1, equipped with an auto-sampler and a 120 thermocouples sensor. The temperature and the heat flow of the equipment were calibrated with indium standard. All samples were accurately weighed (around 10 mg) and sealed in aluminum pans. They were heated from -70 C to +120 C at 20 C min 1 with an empty aluminum pan as reference. Two successive heating and cooling were performed and only the second run was considered. Dry nitrogen with a flow rate set at 30 ml min 1 was used as the purge gas. The glass transition temperature (T g ) was measured at the midpoint. The STARe thermal analysis software was used for the calculation. ph measurements. The ph values of the aqueous solutions were measured with a Mettler Toledo SevenEasy ph-meter using a InLab Routine Pro electrode. For the latexes, an InLab Science Pro electrode was used. The electrodes were calibrated with buffer solutions from Mettler Toledo (ph 4.01, 7.00 and 10.00). 3

Table S1. Properties of some surfactant-free latexes prepared in the presence of PMAA 2k macroraft agent. Latex Monomers a wt% M macroraft b n (kg mol -1 ) / Đ c Viscosity d (cp) Film e 2 BA/MMA (60/40) 1.5 111.0 / 3.2 17 T 3 BA/MMA (60/40) 1.0 168.8 / 3.0 8 T 4 f BA/MMA (60/40) 1.0 n.d. n.d. T 5 BA/S (55/45) 1.0 n.d. n.d. O 6 BA/S (55/45) 0.75 n.d. 84 O 7 BA/S/MMA (60/25/15) 0.75 n.d. n.d. T+O 8 BA/S/MMA (60/15/25) 0.75 n.d. n.d. T 9 BA/S/MMA (60/15/25) 1.0 n.d. n.d. T 10 BA/S/MMA (60/15/25) 1.5 95.5 / 3.2 55 T 11 BA/S/MMA (60/10/30) 1.0 n.d. n.d. T 12 BA/S/MMA (60/10/30) 1.5 89.7 / 3.4 37 T All the experiments were performed at 70 C, using 2 mmol L -1 of APS. a Composition of the initial mixture of hydrophobic monomers - Weight fractions are given in brackets. b With respect to the monomers. c Number-average molar mass and dispersity determined by SEC- THF. d Viscosity determined at 200 s -1. e T stands for transparent and O for opaque. f Semi-batch experiment. Figure S1. DSC curves of Latex 2, Latex 3 and Latex 4 (see Table S1 for more information on these samples). 4

Figure S2. Kinetics of the emulsion polymerizations of Latex 2, Latex 3, Latex 10 and Latex 12. (See Table S1 for more information on these samples.) w(log M) M n = 2 kg mol -1 Đ = 1.2 M n = 95.5 kg mol -1 Đ = 3.2 M n = 89.7 kg mol -1 Đ = 3.4 PMAA 2k Latex 2 Latex 3 Latex 10 Latex 12 M n = 111.0 kg mol -1 Đ = 3.2 M n = 168.8 kg mol -1 Đ = 3.0 2.5 4 5.5 7 log M (g mol -1 ) Figure S3: Size exclusion chromatograms of PMAA 2k, Latex 2, Latex 3, Latex 10 and Latex 12 (see Table S1 for more information on these samples). 5

Figure S4. Surface tension (γ) measurements for Latex 3, compared to that of water and various concentrations of aqueous solutions of the macroraft agent PMAA 2k. 6

Table S2. Visual stability test of Latex 3 at 50 C Day 0 Week 1 Day 1 Day 2 Day 3 Day 6 Day 7 Week 2 Week 3 Week 4 ph 7.0 - - - - - - - 7.0 Viscosity (cp) 9 - - - - - - - 9 Particle size (D z, nm) / σ 204 / 0.03 - - - - - - - 197 / 0.02 Sedimentation? No No No No No No No No No Separation into layers? No No No No No No No No No Appearance Comments - Skin forming at the interface 7

Table S3. Properties of the surfactant-free and (self-)crosslinking latexes prepared in the presence of 1 wt% of PMAA 2k macroraft agent. Latex Functional comonomer 13 BuDA 14 DAAm 15 AAEM Monomers a BA/MMA/BuDA (59.0/39.3/1.7) BA/MMA/DAAm (57.5/38.5/4.0) BA/MMA/AAEM (57.5/38.5/4.0) Viscosity b (cp) Film Appearance c Gel fraction d (%) 10 T 96.9 23 T 100.0 e 10 T 100.0 e All the experiments were performed at 70 C, using 2 mmol L -1 of APS and 1 wt% of macroraft. The ph was initially adjusted to 7 by addition of a 1M NaOH solution. a Composition of the initial mixture of hydrophobic monomers. Weight fractions are given in brackets. b Viscosity determined at 200 s -1. c T stands for transparent. d Gel fraction determined by Soxhlet extraction in THF. e After ADH/HMDA addition. Figure S5. Representative large-strain deformation data from latex films with different crosslinking functionalities. Solid lines show data from films that were formed immediately after the crosslinker (ADH or HMDA) was added to the wet latex (14 (green line) and 15 (blue line), respectively). For comparison, data from films that were formed 21 days after adding the crosslinker are also shown (dashed line). Films from Latex 13 (red line), which was internally crosslinked with BuDA, were analyzed in two separate trials at the same times as the crosslinking latexes. 8

Table S4. Mechanical properties of latex films with different cross-linking functionalities (film-formed 21 days after mixing latex and crosslinker) Latex 13 14 + ADH 15 + HMDA Young s modulus (+/-error) (MPa) 7.55 (2.9) 94.12 (6.92) 98.55 (31.08) Tensile strength (+/-error) (MPa) 0.62 (0.22) 10.17 (0.28) 3.99 (1.33) Strain at failure (+/-error) (%) 33 (8) 348 (52) 154 (46) Yield point (+/-error) (MPa) - 2.23 (0.4) 2.52 (0.76) Figure S6. Loss modulus (E ) for four latexes, as are identified in the legend. (See Tables 1, 2 and 3 for more information on these samples). 9

References 1. Couvreur, L.; Lefay, C.; Belleney, J.; Charleux, B.; Guerret, O.; Magnet, S., First Nitroxide-Mediated Controlled Free-Radical Polymerization of Acrylic Acid. Macromolecules 2003, 36, 8260-8267. 10