From Particles to Stabilizing Blocks – Polymerized Ionic Liquids in Aqueous Heterophase Polymerization

Please note that technical editing may introduce minor changes to the text and/or graphics, which may alter content. The journal’s standard Terms & Conditions and the Ethical guidelines still apply. In no event shall the Royal Society of Chemistry be held responsible for any errors or omissions in this Accepted Manuscript or any consequences arising from the use of any information it contains. Accepted Manuscript


Introduction
The search for new stabilizers in heterophase polymerization is an everlasting topic since the very first attempts to copy natural rubber in chemical reactors. The choice of the proper stabilization strategy is extremely crucial because it determines not only the stability of the latex but in addition also the morphology of the latex particles, the polymerization kinetics, and many application properties. [1][2][3] A very recent development in this area is the application of polymerized ionic liquids (PIL) as stabilizers in aqueous heterophase polymerization. [4][5][6][7] Particularly, it has been found that poly (3n-tetradecyl-1-vinylimida-zolium bromide) behaves extraordinarily and appears as kind of ideal colloidal stabilizer for emulsion polymers because it changes from hydrophilic in the wet to hydrophobic in the dry state. Consequently, the hydrophilicity of an emulsion polymer coating, expressed by means of the contact angle of a sessile water drop, made with PIL stabilizer is significantly reduced compared with commonly used emulsifiers. 8 These results support the hypothesis that the stabilizing PIL units are quite mobile and can adopt different conformations. The PIL with long alkyl chains might alternately be considered as kind of polymerized self-assembled, self-organized structures (lyotropic mesophases; or surfactants), considered also as being a subclass of polysoaps, 9 which are key for membrane-based chemical and physical processes. 10,11 Polysoaps are a topic in colloid chemistry already since the 1950-ies. [12][13][14] Ionic liquids are organic salts with quite low melting points (typically below 100 °C) enabling their use as solvents with very particular properties, such as high polarity and ionic conductivity with very special effect on the kinetics of all kinds of chemical reactions. 15 Ionic liquid monomers (ILM) containing a polymerizing double bond in their molecular structure resemble polymerizable surfactants or surface active monomers (surfmers). 16 Like surfmers which are hydrophobically modified water-soluble monomers, ILMs show the typical behavior of self-associating monomers and polymers. [17][18][19][20][21] Before, during, and after polymerization, interactions of the hydrophobic tails can cause quite strong association leading to gel formation even for copolymers where the content of hydrophobically modified units is only about 1 mol-%. 22 Interestingly, the solubility behavior of polymerized dimethylaminoethyl methacrylate salts quarternized with nalkyl bromides (C 8 -C 18 ) 17 is very similar to that of the PIL used in this study. Both are insoluble in water but dissolve in polar organic solvents. Also, the formation of lamellar structures on substrates is observed for partially quarternized poly(styrene-b-2-vinylpyridine) copolymers. 20 These few examples demonstrate the quite far-reaching similarity between PIL and polymerized surface active monomers. In fact, IL monomers are, depending on the influence of the hydrophobic parts either ionic monomers or surfmers (ILsurfmers). Thus, in the family tree of polymers PILs can be spotted somewhere between polyelectrolytes and polysoaps. The molecular architecture of the monomer, particularly the arrangement of the different functional groups (ionic or hydrophilic, hydrophobic, and polymerizable double bond) determines also the properties and the behavior of PIL as it is generally the case in chemistry and also for polymerized amphiphiles. 9 The imidazole group is known to be quite active in nucleophilic catalysis of carboxylic acid derivatives. 23 Polymers bearing imidazole units have a history starting from the early 1960-ies as model compounds for synthetic enzymes based on the observation that the histidine group plays an active role in encymatic hydrolysis. [24][25][26][27][28][29][30][31][32] The first synthetic polymers of this kind mimicking enzymes were homo-and copolymers of 4-vinylimidazole 25 made via free radical polymerization. The first polymerization of vinylimidzolium iodide and methylsulphate salts was described in the open scientific literature only 1973. 33 But already in the 1950ies patents have been filed describing the polymerization of vinylimidazolium salts and possible uses of the (co)polymers. Copolymers containing ionic liquid (IL) moieties (imidazolium cations) have been for the first time described only in 2004. 34,35 These were block copolymers with polystyrene made starting from poly(styrene-b-chloromethyl styrene) precursors. In a subsequent polymer analogous reaction the chloromethyl styrene block was quaternized with 1-methylimidazole in the presence of NaBF 4 to yield the polystyrene-IL block copolymers. In the subsequent years more PIL-containing copolymers have been synthesized via various radical polymerization techniques. Amongst them are random copolymers and block copolymers made via normal free radical and reversible addition-fragmentation transfer (RAFT) polymerization of N-2-thiazolylmethacrylamide and 2-(1-butylimidazolium-3-yl)ethylmethacrylate, respectively, as polymeric ligands in magnetic complexes with Ni 2+ and Nd 3+ . 36 Also, double hydrophilic block copolymers of 3-(1ethylimidazolium-3-yl)propylmethacrylamidobromide and acrylamide or methacrylic acid have been prepared via RAFT polymerization in methanol. 37 Block copolymers with another type of IL group are described in. 20 Starting from poly(styreneb-2-vinylpyridine) made via anionic polymerization and subsequent quarternization of the 2-vinylpyridine units with Li-bis(trifluoromethylsulfonyl)imine the authors obtained polymeric IL-block copolymers with pyridinium cations with tunable lamellae domain size in the bulk block copolymer. All kind of polymers containing IL-moieties are interesting materials because the counterion and solvent stimuli responsiveness of ILs add new properties to these hydrophilic or amphiphilic polymers and promise new materials for new applications. For instance, exchange of the bromide or chloride counterion with bulkier anions such as terafluoroborate, hexafluorophsohpate, or bis(trifluoro-methanesulfonyl) changes the properties of the IL from hydrophilic to hydrophobic. The interested reader can find instructive examples in the following references. [37][38][39][40][41][42][43][44][45] Temperature is an easily applicable trigger for property changes and hence, block copolymers with thermosensitive units became quite popular during the last decades. Thermosensitivity is a very typical and general property for solutions of all polymers. 46 However, poly-Nisopropylacrylamide (PNIPAM) is the most prominent example because its lower critical solution temperature (LCST) of about 32 °C is in an easily accessible range and very attractive for biomedical applications. 47,48 Therefore it is not surprising that nowadays also block copolymers containing PIL and PNIPAM units as temperature responsive component are in the focus of research on the way to produce multiresponsive smart polymers. [49][50][51][52][53][54] To the best of our knowledge the first reports regarding the synthesis of PIL-PNIPAM block copolymers appeared only in 2009. One procedure uses RAFT polymerization in organic solvents starting with the PNIPAM block. 49 The other procedure started from the PIL block with ceric ion redox radical generation in water. 50 In this contribution, we describe the synthesis and characterization of block copolymer particles with poly(vinylimidazolium) groups (particularly poly (3-ntetradecyl-1-vinylimidazolium bromide)) as PIL block. The synthetic strategy takes advantage of the facile and robust ceric ion redox heterophase polymerization technique which has already frequently been applied for block copolymer production, cf. 2, 55-57 and references therein. Aqueous poly (3-n-tetradecyl-1-vinylimidazolium bromide) dispersions, either cross-linked or not, with hydroxymethyl chain ends were used as reductants in the initiation process with ceric ion as oxidant (cf. Scheme 1). Despite the fact, that the PIL reductant is used as suspension and that the final product is a suspension as well, the PIL particles do not serve as simple seed particles in the common sense. We are discussing results regarding the colloidal and morphological characterization of diblock particles with Nisopropylacrylamide (NIPAM), butyl acrylate (BA), butyl methacrylate (BMA), and styrene (STY) as second monomer and triblock copolymer particles with NIPAM as second and BA, or BMA, or STY as third monomer block. In addition we are considering the thermoresponsiveness of the copolymers containing PNIPAM blocks by means of dynamic light scattering and speed of sound data. The block copolymers under consideration consist of very different units with each of them possessing a very particular aggregation behavior under very specific conditions. Consequently, each block has a particular influence on the particles' morphology. The results convincingly reveal quite a high mobility of the hydrophilic blocks (PIL, PNIPAM) arranging themselves in order to minimize the free interfacial energy of the dispersion with substantial influence on the morphology of the particles. The properties of the hydrophobic block have a great influence on the morphology of the dried particles as observed on transmission electron microscopy grids.

Synthesis
Diblock copolymer particles To a 25 mL Duran glass vial, 10 ml of P1 or P2 dispersion (1 wt%) and 0.5 g monomer (STY, or BMA, or BA) were added and the glass vial was sealed with a rubber stopper. The mixture was deoxygenated by purging with nitrogen for 20 min via two syringe needles. Afterwards, the glass vial was placed in a thermostat bath at 60 °C. After stirring for about 5 min, the initiator solution (0.026 g ceric ammonium nitrate in 1 mL water) was injected and the polymerization was continued for 4 hours.

Triblock copolymer synthesis
To a 25 mL Duran glass vial, 20 mL P1 or P2 dispersion (1 wt%) and 0.4 g NIPAM were added and the glass vial was sealed with a rubber stopper. The mixture was deoxygenated by purging with nitrogen for 30 min via two syringe needles. Afterwards, the initiator solution (0.052 g of ceric ammonium nitrate in 1 mL of water) was injected and the polymerization was conducted at room temperature. After 3 hours, 1 g of hydrophobic monomer (either STY, or BMA, or BA) was added and the polymerization was continued at room temperature for 48 h.

Characterization
During the polymerization samples were withdrawn and the solids content (SC) was determined with a HR 73 halogen moisture analyzer (Mettler Toledo, Giessen, Germany). With the SC the monomer conversion was calculated. The reaction products were dialysed against distilled water (dialysis tubing made of regenerated cellulose, type: membra-cell MD44, cutoff 14 kilo-Dalton) and the water was replaced daily. The dialysis was continued until no more change in the conductivity of water in the dialysis bath was detected. This lasted in average about three weeks. If not otherwise stated, only dialysed samples were characterized.
Infrared spectroscopy was carried out with a Varian 1000 FT-IR spectrometer as ATR measurements. The average hydrodynamic particle size is expressed as intensity weighted diameter (D i ) determined with a Nicomp particle sizer (model 380, PSS, USA). The zeta potential was measured with a Zetasizer Nano ZSP (Malvern) at room temperature. The change in the speed of sound was measured with the ResoScan URT System (TF Instruments GmbH, Heidelberg, Germany) based on ultrasound resonator technology. Shape and morphology of the particles was investigated with electron microscopy. Transmission electron microscopy (TEM) was performed with a Zeiss EM 912 Omega microscope operating at 120 kV according to standard procedures (suspension preparation on carbon coated copper grids).

Results and discussion
Block copolymer formation The polymerization strategy as outlined in Scheme 1 which has been applied already several times successfully for the synthesis of a variety of block copolymers relies on a heterogeneous intermediate generated by the collapse of the PNIPAM above the LCST. Starting with a hydrophilic precursor polymer bearing methylol endgroups the precipitated diblock generates an amphiphilic reaction environment enabling the uptake of both hydrophilic and hydrophobic monomers for further block building. This block copolymer formation strategy relies on the following facts. Firstly, the redox initiation is very fast and it lasts only a few minutes. 55 Secondly, the radical termination probability is quite low as only polymeric radicals are involved. 2 The whole process can be typically carried out at temperatures well above the LCST of PNIPAM, thus allowing fast polymerizations.
For 'common' water soluble polymers such as poly(ethylene glycol), poly(styrene sulfonate), poly(diallyldimethyl ammonium chloride) temperature is no issue and the final product is a stable thermoresponsive block copolymer latex. 61 This journal is © The Royal Society of Chemistry 2012 However, the situation changes when PILs are applied as reducing water soluble polymer to synthesize triblock copolymer latexes containing a hydrophobic polymer as third block. In this case, a polymerization temperature above the LCST of PNIPAM causes breakdown of both the latex stability and the polymerization reaction after charging the hydrophobic monomer to the reaction mixture. Interestingly, when the polymerization is conducted at room temperature, colloidal stability is maintained throughout the entire reaction, however on expense of the reaction time which will be extended accordingly. In contrast, diblock copolymer formation can be carried out at any temperature.
The data depicted in Figure 1 show a conversion -time curve for the triblock copolymer formation process at room temperature with sequential NIPAM and STY addition starting with P1. The polymerization of NIPAM (diblock copolymer formation) takes only 3 h to get a monomer conversion higher than 96%. The formation of the hydrophobic block takes much longer (about 38 h to reach a monomer conversion greater than 80%). This huge difference in required polymerization time or polymerization rate reflects the different propagation rate constants between both monomers. 62, 63 Within the present study two different PIL dispersions have been used. P1 and P2 made in the presence and absence of cross-linker (1, 4-butanediyl-3,3'-bis-1-vinylimidazolium dibromide) as described in [58][59][60] . Both, the crosslinked and noncrosslinked PIL, form an aqueous dispersion with a positive zeta potential of about 50 and 60 mV and an average hydrodynamic particle size of about 43 and 28 nm, respectively. The inner morphology of these particles is very peculiar because the PIL molecules arrange themselves in circular lamellae 58-60 consisting of consecutive nonpolar / hydrophobic (alkyl chains) and polar / hydrophilic (ionic) layers. Interestingly, this kind of morphology has been reported for crosslinked and non-crosslinked PIL particles 58,59 and observed only on cryo-TEM micrographs. The PIL particles on normal TEM micrographs in the dried state show different morphologies depending strongly on the concentration and maturation of the PIL dispersion. The conditions during drying in addition to the local properties at the drying spot of the carbon coated copper TEM grid are also of importance. Clearly, PIL particles behave differently compared to normal latex particles made of hydrophobic polymers. The characterization of the block copolymer particles has been carried out in the dispersed and dried state and the results have been used for the characterization of the colloid chemical features and the block copolymer composition (to control the success of the applied polymerization strategy), respectively. For amphiphilic block copolymer particles as under consideration it is important to bear in mind that the morphology as observed by electron microscopy in the dried state must not represent the dispersed state. 64 Typically, hydrophilic polymer chains which are stabilizing the particles in the dispersed state, collapse in the dried state onto the hydrophobic core. Thus, sizing via dynamic light scattering and analysis of electron micrographs leads to different results. All analytics has been carried out with carefully dialyzed samples. The composition of the copolymers has been checked by FT-IR spectroscopy. The expected characteristic absorption bands of the different building blocks were clearly detected and the corresponding wave numbers and assignments are summarized in Table 1.

Zeta potential
Valuable information regarding the morphology of the particles in the dispersed state has been obtained from zeta potential measurements. The zeta potential is the electric potential in the diffuse electrical double layer surrounding the particles measured at the slipping plane which is located in a certain distance from the geometrical particle surface because the particles tow a water layer which contains counter and coions while moving. So, the composition of the electrical double layer in the gap from the particles' surface to the slipping plane determines the potential. For the kind of particles considered here, this value is essentially governed by  the concentration of imidazolium groups at the surface stretching out into the aqueous phase and the concentration of ions (counterions and coions) diffusing inside the gap up to the slipping plane. Model polystyrene particles made with cetyltrimethyl ammonium peroxodisulfate as surfactantinitiator complex possess a positive zeta potential proving that it is not the anionic polymer end group that determines the zeta potential but the surface active cationic counterion which is reaching farther away from the surface. The inverse initiator surfactant complex, that is cationic initiating radicals and anionic dodecylsulfate as counterions, leads to PS particles with negative zeta potential. In this context, it is necessary to recall that for latex particles made surfactant-free with ionic initiators the charge of the polymer endgroup controls the sign of the zeta potential. These findings regarding the zeta potential -determining ions are important for evaluating the zeta potential data obtained for the PILs and block copolymer particles as discussed below. Figure 2 shows clear differences in dependence on the polymer / copolymer composition and, for the block copolymers, these data allow reasonable conclusion regarding the arrangement of the blocks. The most interesting behavior is observed for the diblock copolymers where the PIL diblocks with the hydrophobic partners possess a similar zeta potential like the pure PIL particles. In contrast, for the PIL-PNIPAM diblock particles (P1-N, P2-N) the zeta potential is an order of magnitude lower. However, adding a third hydrophobic block, the zeta potential slightly increases again to values of 15-20 mV. Notably, the increase for the triblocks made with the crosslinked PIL (P1) is higher compared with that for the non-crosslinked PIL (P2) as starting material. These experimental data, particularly the data for the diblock copolymers, lead us to introduce the idea or the principle of relative hydrophilicity (PRH). The PRH means that a given hydrophilic polymer in combination with a more hydrophilic polymer behaves hydrophobic and vice versa. Accordingly and considering PIL and PNIPAM, the less hydrophilic PIL blocks form the core of these diblock copolymer particles. The particles are predominantly stabilized sterically by the PNIPAM blocks and consequently the zeta potential is drastically reduced compared with the PIL hompolymer particles. In contrast, in the diblock copolymer particles with more hydrophobic monomers the PIL blocks stretch into the aqueous phase and ensure the stability of the dispersion. The thermodynamic driving force behind the principle of relative hydrophilicity is the minimization of the free energy which always brings the more hydrophilic component in direct contact to water thus, lowering the excess interfacial free energy. For the triblock copolymers, the third hydrophobic block tries to avoid contact with water at all and moves towards the core of the particles. This causes drastic rearrangements of the particles morphology bringing the PIL units again in closer contact with water as indicated by the moderate increase in the zeta potential.

Figure 2.
Correlation between the zeta potential (ζ) and polymer / block copolymer composition; the grey-and whitefilled symbols represent the polymers with P1 and P2, respectively.

Particle morphology
The particular properties of the PIL stabilizer and the PRH lead to the assumption that the morphology as observed with common TEM in the dried state might not reflect the particles' morphology in the dispersed state 64 and might cause quite huge differences between the hydrodynamic average particle size and the average resulting from enumerating TEM micrographs. Additionally, the properties of the hydrophobic block, particularly the glass transition temperature (T g ), influence the appearance of the dried particles on the TEM grids.
The TEM micrographs of the di-and triblock copolymer particles displayed in Figure 3 and 4, respectively, clearly prove the enormous influence of the nature of the hydrophobic polymer block on the appearance of the polymer dispersions in both the wet state dispersed in water and the dried particles on the TEM grids. Mainly two important conclusions can be drawn. Firstly, the higher the glass transition temperature (T g ) of the hydrophobic block is, the clearer a solid sphere morphology of both the di-and triblock copolymer particles can be seen. T g of the hydrophobic blocks changes in the order PBA (-55 °C) < PBMA (20 °C) < PS (100 °C). 65 Secondly, the differences between the morphology displayed by the diblock copolymer particles with crosslinked and non-crosslinked PIL are significantly larger than the ones observed for the triblock copolymer particles. This is especially obvious comparing the micrographs of P1-BMA and P2-BMA particles. The P1-BMA particles prepared with crosslinked PIL maintain their sphere morphology on TEM micrographs while film formation and microphase separation is observed for P2-BMA particles with non-crosslinked PIL. In general, the influence of crosslinking the PIL starting dispersion is less pronounced than one might expect for 10 mol-% crosslinker relative to the ILM. This indicates that the efficiency of the crosslinker is pretty much limited which is reasonable considering that a significant mismatch is given regarding the molecular size of the ILM and crosslinker. Figure S1 details this behavior by means of additional TEM micrographs.
The combined evaluation of the corresponding average values as measured by DLS at room temperature (Di) and by enumerating TEM micrographs (D) is a way to quantify the only qualitative impressions gained from the TEM    Figure 5).

Figure 5.
Comparison of hydrodynamic diameters from DLS (D i , grey spheres) and average diameters from TEM images (D, black spheres) of PILs and their corresponding block copolymers latexes at room temperature; DLS measurements and preparation of TEM grids at room temperature; lines are just for guiding the eye.
The comparison of the average diameters from DLS and TEM in Figure 5 clearly supports the reservations regarding the applicability of TEM to determine the morphology of this kind of amphiphilic block copolymer particles in the dispersed state. The DLS data (grey spheres) decrease with increasing T g of the hydrophobic block which is particularly clear for the triblock copolymers. The copolymers containing PBA as hydrophobic block expectedly show a strong tendency to film formation thus, leading to the largest particles on the TEM micrographs. For the triblock copolymers with PBMA and PS as hydrophobic block the diameter from the TEM micrographs are much smaller than D i proving the collapse of the hydrophilic blocks in the dried state on the TEM grids. For the triblock copolymers the D i -values from DLS at room temperature are much higher than that of all other samples.
This result is a consequence of the hydrophilicity of the PNIPAM-block at temperatures below its LCST.

Thermoresponsiveness
Both the morphology in the dispersed state and the hydrodynamic particle size depends for the particles containing PNIPAM in one or the other way more or less strongly on the temperature. 66 The changes are initiated by the behavior of PNIPAM which is either hydrophilic or hydrophobic at temperature below or above the LCST, respectively. The temperature sensitivity of the polymers containing NIPAM-blocks was studied by means of DLS and the ultrasound resonator technology (URT). Both are complementary methods allowing to study specific features of the polymer solution state in dependence on temperature. URT technology evaluates the temperature dependence of the difference in the speed of sound (∆U) between the polymer dispersion and water. U depends in fluids on the compressibility and density of the medium. At the lower critical solution temperature of PNIPAM the polymer precipitates and water is released. The overall compressibility of the sample solution increases and hence, the speed of sound decreases compared with pure water. In essence, URT tracks quantitatively changes in layer of water molecules surrounding solutes. 67,68 Contrary, DLS measures the change in the size of the dissolved / dispersed matter. Evaluating the DLS data of charged molecules or particles at different temperatures one must additionally consider the change of the electrostatic interactions. The higher is the temperature the shorter the Bjerrum and the larger the Debye length. Indeed, comparison experiments with electrostatically stabilized, surfactant-free polystyrene latexes show a slight increase of D i with increasing temperature which should be considered in the following discussion (data not shown). The data of Figure S2 prove an analogous behavior for the cationically charged PIL dispersions. Interestingly and regardless whether the particles are crosslinked or not, the temperature dependence (dD i /dT) is for both dispersions very similar. One can now expect that also the temperature sensitivity of P1-N and P2-N is qualitatively identical. The data summarized in Figure 6a and 7a prove that   The data in Figure 6a show that the particle size increases for both samples sharply between 32 and 35 °C. The position of the extreme value in the temperature curve of the first derivative dD i /dT (cf. two lower curves of Figure 7a and 7b) gives the LCST of the particular sample. Another possibility to determine the LCST is the position of the extreme value of the first derivative of the speed of sound (d∆U/dT) in dependence on temperature (upper two curves in Figure 7a and b). For the sample P1-N and P2-N the maximum of dD i /dT and the minimum of d∆U/dT are positioned at the same temperature. This clearly proves that the sharp increase in temperature the particle size in these samples is caused by the change in the solution behavior of the PNIPAM block. The increase of the hydrodynamic diameter above the LCST, which is much steeper than the temperature-caused changes of the electrostatic interactions of the pure PIL (cf. Fig. S2) points towards aggregation processes of the particles. The aggregation is however limited and, at least at such low concentrations as used for the measurements, complete aggregation with macroscopic coagulum formation is prevented by a certain stabilization capability of the PIL chains. In contrast, PNIPAM homopolymer leads to macroscopic coagulum formation (drastic increase in the hydrodynamic size) and block copolymers with styrene sulfonate or diallyldimethylammonium chloride change from transparent solutions to stabile dispersions with PNIPAM core and stabilizing polyelectrolyte shell (decrease in the hydrodynamic size). 61 Obviously at temperatures below the LCST, the PIL-PNIPAM particles are mainly stabilized by the PNIPAM chains and hence, they collapse after the PNIPAM chains turn hydrophobic. Generally, this interpretation is in accordance also with the zeta-potential data (cf. Fig. 2). Interestingly, for all triblock copolymers the DLS and URT data show a distinctly different behavior for the crosslinked (P1) and non-crosslinked (P2) PIL as exemplarily depicted in Figure 6b and 7b for styrene as hydrophobic block. The hydrodynamic diameter of the triblock particles with P1 decrease with increasing temperature and the dD i /dT curves show a clear minimum at the LCST. However, for the triblock copolymer particles with P2 (non-crosslinked) D i initially decreases with increasing temperature but in the range of the LCST D i changes the direction and increases to values larger than those at room temperature (cf. Fig. 6b). Such behavior is in accordance with limited aggregation as already discussed for the behavior of the PIL-PNIPAM diblock particles based on the DLS data. The limited coagulation finds in the URT data only indirect expression as the LCST (extreme value in the d∆U/dT curve) is unchanged but the width of the peak increases. The width of the base of the d∆U/dT curve measures the temperature range in which changes in the speed of sound or in the amount of released water take place. Thus, increasing width as observed for the P2-triblock copolymers is expected for LCST-induced aggregation. A closer look at the base width of the peak in the d∆U/dT -T plots for all samples containing PNIPAM blocks reveals interesting results (Figure 8). In our understanding, this is a significant experimental observation because the width of the base is an expression of the sharpness of the LCST transition which is an important characteristic of thermoresponsive devices. Quite surprisingly, the base width of the peak in the d∆U/dT -T -curves strongly depends on the properties of the hydrophobic block and not so much from the property of the PIL block (crosslinked or non-crosslinked). With increasing T g of the hydrophobic block the base width increases except for heating and cooling of P1-N-S and cooling of P2-N-S. The behavior might be explained considering the temperature where the changes are observed (LCST) in relation to T g of the hydrophobic block. For PBMA and PBA as hydrophobic block the LCST is much higher than T g and hence, they are quite mobile and do not strongly influence the inflow and outflow of water molecules as well as the unfolding and folding of the PNIPAM block during cooling and heating, respectively. For PS as hydrophobic block the situation is, however, different. The PS particles with crosslinked PIL (P1-N-S) are the hardest of the samples under consideration. In these particles, only the PNIPAM chains are mobile in the vicinity of the LCST. For the non-crosslinked PS particles (P2-N-S) the mobility of the PNIPAM is less influenced and hence, during heating the particles follow the trend as expressed by the regression line.
To understand the behavior during cooling it is necessary to remember that the P2 -particles form aggregates at temperatures above the LCST. Dissolution or unfolding of the collapsed PNIPAM chains requires disaggregation which is, compared with P2-N-BA and P2-N-BMA particles, significantly hindered by the hard PS segments. The data collected in Figure 7 show that the LCST value determined by the URT heating curve and DLS measurement coincide quite nicely. In contrast to DLS, URT measurements allow the separate evaluation of the heating and cooling behavior and thus, the determination of two critical solution temperatures and a possible hysteresis. Typically, the critical temperature determined during heating (for precipitation) is greater than that during cooling (for dissolution). This difference, ∆T p-d , depends on the rate of the temperature change (dT/dt) and has a finite value even at dT/dt = 0. 68 This underlines the conclusion that transient and equilibrium (isothermal) studies such as URT and DLS measurements, respectively, must not lead per se to identical results. 69 For the samples in this study, the hysteresis, ∆T p-d , seems not significantly to depend on the composition. ∆T p-d for all samples is with 0.785 ± 0.23 ° in a similar range as observed for block copolymers of very different composition and is mainly determined by the rate of the temperature change (300 mK/min). 57, 68

Summary
The main experimental findings of our investigations are: 1. Within the class of reactive surfactants PIL dispersions represent the first example proving that even polymer dispersions can act as kind of reactive stabilizer for initiating aqueous heterophase polymerizations.

Crosslinked and non-crosslinked PIL dispersions, P1
and P2, respectively, behave similarly in the polymerization reaction. 3. The amphiphilic nature of the PIL chains enables them to adjust their behavior in dependence on the properties of the other block(s) to be either hydrophilic or hydrophobic. 4. In diblock copolymer dispersions of PIL with a hydrophobic second block, the PIL is hydrophilic and stabilizes the particles. 5. In triblock copolymer dispersions with a PNIPAM middle block, the PIL block is hydrophobic and the particles are stabilized by PNIPAM. 6. The PNIPAM containing block copolymer dispersions show an LCST in the range typically observed for PNIPAM homopolymers. 7. The sharpness of the LCST transition depends strongly on the composition of the block copolymer dispersions and is the highest for the triblock copolymer dispersions with polystyrene. 8. Both the diblock copolymer PIL-PNIPAM and the triblock copolymers made with the non-crosslinked PIL dispersion undergo at temperatures higher than the LCST of PNIPAM limited aggregation. 9. The morphology of the dried particles is governed mainly by the glass transition temperature of the hydrophobic block.

Conclusions
The experimental results show the quite easy applicability of suspensions of poly (3-n-tetradecyl-1-vinylimidazolium bromide), either crosslinked or not, in double function during