B.
Khorshidi
a,
T.
Thundat
b,
B. A.
Fleck
a and
M.
Sadrzadeh
*a
aDepartment of Mechanical Engineering, University of Alberta, 6-074 NINT Building, Edmonton, AB T6G 2G8, Canada. E-mail: sadrzade@ualberta.ca; Fax: +1 (780) 492 2200; Tel: +1 (780) 492 9099
bDepartment of Chemical and Material Engineering, University of Alberta, 7-026 ECERF, Edmonton, AB T6G 2V4, Canada
First published on 15th June 2015
Preparation of thin film composite (TFC) polyamide (PA) membranes by interfacial polymerization (IP) reaction is remarkably sensitive to the interactions between synthesis parameters. Here we report the effect of the simultaneous change in four synthesis parameters, namely monomers concentrations (m-phenylenediamine, MPD, and trimesoyl chloride, TMC), reaction time and curing temperature, on the surface morphology and on the permeation properties of TFC membranes. By varying several synthesis parameters at the same time using a Taguchi robust design (L9 orthogonal arrays), it was found that monomers concentration and curing temperature significantly affected water permeation by creating a substantial change in morphology of the PA films. More importantly, a strong interaction between monomers concentration was observed, which demonstrates the importance of smart adjustment of these parameters in the preparation process. Permeation properties were justified by thickness and by the cross-link density of the synthesized films; the latter was found to be more influential. Based on analysis of variance (ANOVA), the contribution of the synthesis parameters towards change in water permeation was determined as: curing temperature (40.7%) > MPD concentration (28%) ∼ TMC concentration (27.8%) > reaction time (1.9%). The findings will provide valuable guidelines to develop practical low cost, robust and high performance membranes by changing the curing temperature and the monomer concentrations as critical parameters.
Reference | Studied parameters | Experimental strategy | Range of performancea | Major results |
---|---|---|---|---|
a All reports used RO test cell to study membranes performance except ref. 12 which only used Fourier transform infrared (FTIR) spectroscopy for membrane characterization. b Reacting monomers are m-phenylenediamine (MPD) and trimesoyl chloride (TMC) for all studies except ref. 11 which used 5-chloroformyloxyisophthaloyl chloride (CFIC) in organic solution. | ||||
Chai and Krantz, 1994 (ref. 5) | Monomers concentration,b reaction time | OFAT | - PA thickness increased with increase in TMC concentration and reaction time, but did not change when MPD concentration increased | |
- Water flux dramatically decreased with increase in reaction time | ||||
Rao et al., 1997 (ref. 6) | Reaction time, curing time and temperature | OFAT | - Flux and rejection increased with increase in reaction time up to 60 s, but rejection decreased dramatically for higher reaction time | |
- Increasing curing temp. up to 75 °C improved both flux and rejection, higher curing temperature lowered the flux substantially | ||||
Rao et al., 2003 (ref. 7) | Reaction and curing time and temperature | Not specified | - Decreasing the reaction time and curing temperature resulted in thinner membranes with higher water flux | |
- Salt rejection was reported to be insensitive to modified conditions | ||||
Song et al., 2005 (ref. 8) | Monomers concentration, reaction time | OFAT | - Permeation flux increased with increase in reaction time at low TMC concentration; the opposite trend was reported at high TMC concentration | |
- Increasing MPD concentration improved salt rejection but lowered the water flux | ||||
Roh et al., 2006 (ref. 9) | Monomers concentration | OFAT | - PA film thickness increased with increase in both MPD and TMC concentrations | |
- Surface hydrophilicity increased by increasing TMC concentration, but decreased as MPD concentration increased | ||||
Ghosh et al., 2008 (ref. 10) | Organic solvent properties, curing time and temperature | Not specified | - High surface tension, low viscosity solvents led to higher permeation performance for membranes | |
- Flux and rejection increased with increase in curing temperature | ||||
Liu et al., 2008 (ref. 11) | Reaction time, pH of water solution, curing time and temperature | OFAT | - Increasing reaction time reduced permeation flux and improved salt rejection | |
- Water permeation increased with increase in TMC concentration | ||||
- Both water flux and rejection increased with increase in curing temperature | ||||
Jin and Su 2009 (ref. 12) | Monomers concentration, reaction time and temperature | OFAT | NA | - Increasing MPD/TMC concentration ratio and reaction time resulted in PA film with more hydrophilic –COOH group at the surface |
Xie et al., 2012 (ref. 13) | Monomers concentration, thermal treatment method | OFAT | - There was an optimum range for monomers concentration to obtain high water flux | |
- Salt passage was not sensitive to change in monomers concentration | ||||
- Thermal treatment did not cause any significant effect on transport properties of membranes | ||||
Klaysom et al., 2013 (ref. 14) | Monomers concentration, reaction time | OFAT | - Water flux decreased with increase in MPD concentration and reaction time | |
- Membranes performance did not changed with TMC concentration except for low values where water flux dropped with increase in TMC concentration |
The studies reviewed in Table 1, suffer from the limitation that the synergistic effects of synthesis parameters were not investigated as most experiments were conducted using the one-factor-at-a-time (OFAT) method where only one factor (variable) was changed at each experimental trial. Although OFAT leads to clearly expressed conclusions, the chance of missing optimum conditions and not observing the covariance between parameters is high in this approach.15,16 Thus, existing results should be interpreted with caution, and the widely accepted hypotheses for the effect of synthesis conditions require further revaluation to be extrapolated to novel practices.
In the current work, we present a systematic study of the effect of simultaneous changes of synthesis conditions on surface morphology, and permeation properties of TFC membranes. Four important synthesis parameters, namely monomer concentration, reaction time and heat curing temperature were considered as influential factors. The experimental trials were arranged using a robust design of experiment (DOE) method known as Taguchi to minimize the number of experiments while quantifying the significance of each parameter and obtaining valuable information about the inter-relationship between the parameters. The results obtained by the Taguchi method were verified by synthesizing additional confirmation membranes and linking the change in permeation properties to the alteration of membrane morphology. A detailed interaction analysis of monomers concentrations was conducted to find ranges of concentrations for which synthesized membranes did not follow the predicted behaviour. The interaction analysis provided valuable guidelines for fabricating a range of salt rejecting membranes from loose NF to tight RO.
(1) |
The general steps of applying the Taguchi method are (i) determining the quality characteristic of interest and designing the OAs matrix of experiments by identifying the controllable factors and their corresponding levels, (ii) running the designed experiments and analysing data by determining the average factor effects, and (iii) conducting confirmation experiments to verify the extracted trends and predicted results. The control variables investigated in the present study and their corresponding levels and arrangement in the L9 (4 three-level factors) array are presented in Table 2. Each run was replicated twice (18 membranes were synthesized in total) to evaluate the repeatability of membrane formation.
Run | Controllable factors | |||
---|---|---|---|---|
MPD concentration (wt%) | TMC concentration (wt%) | Reaction time (s) | Curing temperature (°C) | |
M1 | 1 | 0.15 | 15 | 25 |
M2 | 1 | 0.25 | 30 | 55 |
M3 | 1 | 0.35 | 60 | 85 |
M4 | 1.5 | 0.15 | 30 | 85 |
M5 | 1.5 | 0.25 | 60 | 25 |
M6 | 1.5 | 0.35 | 15 | 55 |
M7 | 2 | 0.15 | 60 | 55 |
M8 | 2 | 0.25 | 15 | 85 |
M9 | 2 | 0.35 | 30 | 25 |
X-ray photoelectron spectroscopy (XPS) is used for analyzing elemental composition (C, O, N) for the top 1–10 nm of the membranes surface. The TFC membranes examined using a Kratos AXIS ULTRA spectrometer equipped with a monochromatic Al Kα X-ray source. The source was run at a power of 210 W (14 mA, 15 kV) using a hybrid lens with a spot size of 700 μm × 400 μm. Survey spectra were collected with a pass energy of 160 eV, step size of 0.4 eV, and sweep time of 100 s in the range of 0–1100 eV. High resolution spectra for C, O and N elements were collected with pass energy of 20 eV, step size of 0.1 eV, and sweep time of 200 s.
The permeation properties of the TFC membranes were evaluated using a crossflow membrane filtration system used previously.19 The performance measurements were carried out at a trans-membrane pressure of 1.52 MPa and at a feed flow rate of 1 L min−1, corresponding to the laminar crossflow of Reynolds number Re = 730.
Water flux (JW) at steady state was obtained by measuring the volume of water (ΔV) passed through the filtration surface (A) during the specific time period of sample collection (Δt):
(2) |
The apparent salt rejection was calculated by measuring the concentration of salt in the permeate after 3 h filtration of 2000 ppm NaCl solution at 25 °C as follows:
(3) |
The amine/acyl chloride (–NH2/–COCl) molar ratio in Fig. 2 is a criterion showing the amount of reactive functional groups present in polymerization reaction. This ratio is calculated by converting the initial mass concentration of MPD and TMC in their corresponding solvents to molar concentration considering the numbers of –NH2 and –COCl functional group in each monomer (two –NH2 and three –COCl groups). According to Fig. 2, the membranes with low molar ratio (–NH2/–COCl < 7) showed significantly different flux/rejection behaviour compared to other membranes. As will be shown later, very high molar ratio (–NH2/–COCl > 30) also changes the separation performance of composite membranes considerably. The –NH2/–COCl molar ratio directly affects the rate of monomers diffusion and polymerization reaction at the surface, which subsequently changes the resulting morphology and water permeation of membranes. The detailed explanation of the effect of monomer concentration on the properties of synthesized PA films is discussed in the following section.
The extracted trends using Taguchi marginal graphs can be verified by comparing the performances of membranes synthesized by only changing the levels of one specific factor when all other factors maintained constant. Since no two runs in the L9 matrix are comparable, 11 extra confirmation membranes were prepared at combinations, which were not considered in Table 2. The synthesis conditions and permeation performance of these confirmation membranes are presented in Table 3. Taguchi predicted flux and rejection in this table are calculated by Taguchi transfer function (a linear model) that will be explained in ANOVA section. By comparing the permeation results of C1 vs. C2 and C3 vs. C4, it is confirmed that membranes prepared at higher MPD concentration showed lower water flux and higher salt rejection.
Confirmation tests | Controllable factors | Results | ||||||
---|---|---|---|---|---|---|---|---|
MPD concentration (wt%) | TMC concentration (wt%) | Reaction time (s) | Curing temperature (°C) | Average water flux (LMH) | Taguchi predicted flux (LMH) | Average salt rejection (%) | Taguchi predicted rejection (%) | |
C1 | 1 | 0.15 | 15 | 55 | 20.9 | 42.8 | 96.9 | 95.7 |
C2 | 2 | 0.15 | 15 | 55 | 19.6 | 12.8 | 97.4 | 98 |
C3 | 1 | 0.35 | 15 | 55 | 79.1 | 72.8 | 91.4 | 93 |
C4 | 2 | 0.35 | 15 | 55 | 42.5 | 42.8 | 96.2 | 95.3 |
C5 | 1 | 0.15 | 15 | 85 | 15.6 | 31 | 97.5 | 96.4 |
C6 | 2 | 0.15 | 30 | 55 | 19.4 | 13.3 | 97.6 | 97.8 |
C7 | 3 | 0.15 | 15 | 55 | 110.5 | — | 72.1 | — |
C8 | 3 | 0.35 | 15 | 55 | 30.6 | — | 96.7 | — |
C9 | 1 | 0.25 | 15 | 55 | 46.0 | 56 | 95.2 | 94.6 |
C10 | 2 | 0.25 | 15 | 55 | 26.0 | 25 | 96.4 | 97 |
C11 | 3 | 0.25 | 15 | 55 | 15.3 | — | 97.1 | — |
In order to explain the observed trends in Fig. 3 and 4, the mechanism of PA formation via interfacial polymerization should be understood. The IP reaction initiates at the surface when the MPD/water impregnated PES support is brought into contact with TMC/organic solvent solution. Since water and organic solvent are immiscible, the polymerization reaction occurs at the water/organic interface.23–25 In most IP reactions, the MPD concentration in water is much larger than the TMC concentration in the organic solvent, due to negligible solubility, vigorous reaction of the acyl chloride monomer with water and good solubility of amine in organic solvent.5,10 Hence, the IP reaction is believed to be mainly controlled by diffusion of MPD molecules to the reaction zone and thus the polymer film grows from the water/organic interface toward the bulk of the organic solution.26,27 However, the growth of the PA film does not follow a linear increase over the reaction time. Immediately after the contact of the two monomers solution the water/organic interface provides an empty platform for fast reaction of MPD and TMC molecules to form an ultrathin incipient (core) PA film at the PES surface. After that, polymerization shifts to a slow growth stage where the MPD diffusion and thus reaction rate slows down significantly due to presence of the incipient (core) layer.28 The result of polymerization at this stage is the formation of a second layer with the so-called ridge-and-valley morphology which covers the core layer.10,13,27 The separation performance of the final PA layer depends not only on the overall film thickness (the thicker the film is, the lower the water permeates), but also on the cross-link density of the internal structure.13 It is worth mentioning that cross-link density of polymer corresponds directly with its crystallinity. The crystallinity is primarily determined by the chain flexibility and the volume fraction of polymer. The transport mechanism through a dense membrane like the most of polyamide TFC RO membranes is by the molecular diffusion of permeants through the free volume elements between the polymer chains which are varying due to thermal motion of the chains.29 Hence, the crystallinity can significantly affect the water permeability by varying the space between the polymer chains (the higher the crystallinity the lower the permeation flux).30 The polyamide active layer in TFC membranes is a semi-crystalline polymer which its degree of crystallinity could not be measured directly. This is due to the fact that the very thin layer of PA, synthesized by in situ polymerization, is not detachable from the PES support to be used for further tests on crystallinity. Therefore, in the present work, the discussions on the density and/or crystallinity of the membranes are provided based on the pure water flux and salt rejection results.
It was shown by Freger31 that the cross-link density of the PA film is not uniform across the cross-section where the incipient thin film is proposed to be the densest and actual selective layer over the whole structure.31,32 Since the monomer diffusion and reaction rate in the slow growth stage strongly depend on the mass transfer resistance of the core layer, any factor which changes the properties of this layer (in terms of the thickness and cross-link density) will affect the final morphology and separation performance of the resulting films.
Regarding the Fig. 3a, the flux decline with the increase in MPD concentration could be attributed to the increase in the overall thickness of the PA film during the course of polymerization. At higher MPD concentration, there will be a larger driving force for MPD to diffuse through the initially formed PA film. The increase in the number of available MPD molecules in the reaction zone promotes polymerization, thus increases the membrane internal resistance toward water passage by forming a thicker PA film with bigger ridge-and-valley structure at the surface.13
The observed trend for the influence of the TMC concentration was also confirmed by comparing the permeation flux of confirmation membranes C1 vs. C3 and C2 vs. C4 as presented in Table 3.
It is a widely held view that in a typical IP reaction, an increase in the TMC concentration decreases the amine to acyl chloride molar ratio (–NH2/–COCl) and results in a thinner but denser PA active film with lower water flux in overall.13,32 Surface images of the membranes made at high TMC concentration (C3) in this study also confirmed the formation of a thin and dense film at the surface (based on more resemblance of PES and C3 surface morphology). However, significant increase in the water flux with increasing in TMC concentration (from 20.9 LMH in C1 to 79.1 LMH in C3), not predicted by the above hypothesis, reveals the complex influence of the film thickness and density on the transport properties of membranes.
The thickness and cross-link density of PA layer were measured by TEM and XPS analyses, respectively to approve above discussion. The cross-linking density of the whole PA active layer (not merely the incipient layer) can be obtained with the following equation:33
(4) |
(5) |
Using eqn (5), the value of m and n can be calculated based on the O/N ratio obtained from XPS data. For example, for the C1 and C3 membranes shown in Fig. 5, the XPS results are presented in Table 4. As can be seen, the cross-linking density of C1 and C3 are 28% and 69%, respectively, which confirms our hypothesis about the higher density of C3 membrane. However, it must be noted that, the density of the core layer, which is commonly used to justify conclusions (e.g. change in surface morphology) cannot be measured with characterization tests because it is covered by the outer loose layer. In the present study, we qualitatively discussed and compared the density of core layer for different membranes by noting that the mass transfer resistance of the incipient layer to MPD diffusion is directly related to its density. As mentioned earlier, in the case of denser core layer, the mass transfer resistance against diffusion of MPD diffusion is larger and thus less ridge-and-valley morphology forms on the surface.
Fig. 5 FESEM surface and TEM cross-section images of confirmation test membranes: PES support, C1 (MPD 1 wt%, TMC 0.15 wt%) and C3 (MPD 1 wt%, TMC 0.35 wt%) to study the effect of TMC concentration. The levels of other parameters are presented in Table 3. |
Sample | Atomic concentration (%) | Cross-linking density (%) | |||
---|---|---|---|---|---|
O 1s | N 1s | C 1s | S 2p | ||
C1 | 14.74 | 9.03 | 75.97 | 0.25 | 28 |
C3 | 12.75 | 10.31 | 76.72 | 0.23 | 69 |
The surface FESEM and cross-section TEM images of two confirmation test membranes along with PES substrate are shown in Fig. 5. Unlike microporous PES supports which have a relatively smooth and featherless morphology, C1 had a tortuous and ridge-and-valley structure at its surface.25 However, by increasing the TMC concentration from 0.1 wt% (C1) to 0.35 wt% (C3), the morphology changed to a nodular structure with small microprotuberances at the surface. This again confirms formation of a denser PA core layer which hindered diffusion of MPD, thereby prevented film growth and formation of ridge-and-valley features on the surface. Moreover, the TEM images illustrate that increasing the TMC concentration results in a marked decrease in PA film thickness which is highly desirable for reducing the hydraulic resistance of membrane against water permeation.
The substantial change in surface morphology and the absence of ridge-and-valley structure at the surface by increasing TMC concentration is a proof of concept for formation of a thin and dense core layer at the early stage of IP reaction. At higher TMC concentration, due to the presence of a higher number of TMC molecules in the reaction zone, the incipient PA layer became dense enough that hindered MPD molecules to diffuse to organic phase and form a thick ridge-and-valley structure during the time of IP reaction. There are two likely causes for such a significant increase in permeation flux by increasing the TMC concentration: first, there is a marked decrease in the thickness of the PA active layer as it is shown by TEM images in Fig. 5, which decreases membrane resistance against mass transfer and eventually increases the water flux. Second, a thinner active layer is more prone to be affected by the subsurface morphology (e.g. porosity and roughness of the support) than the thicker ones, the presence of any open nanopores at the substrate due to incomplete coverage by the thin film may manifest themselves by increasing the water flux and lowering the salt rejection.
The typical trade-off behaviour between salt rejection and water flux was also observed in confirmation experiments. According to Table 3, increasing TMC concentration from 0.1 wt% (C1) to 0.35 wt% (C3) increased water flux significantly (almost four times), but decreased the salt rejection slightly from 96.9% to 91.4%. The salt rejection results from the confirmation experiments (C1–C4) show the dramatic role of monomers concentration. The range of results varies from high rejection/low flux RO membranes to low rejection/high flux NF membranes.
Fig. 6 FESEM surface morphologies of Taguchi base membrane M1 (cured at 25 °C) and confirmation test membranes C1 (cured at 55 °C) and C5 (cured at 85 °C) to study the effect of curing temperature. The levels of other parameters are presented in Table 3. |
Based on the IP reaction mechanism, prolonging the reaction time should increase film thickness and thus membrane resistance to water flow. However, a negligible shift in flux and rejection with the change in reaction time reveals that the growth of the PA film after 15 s was insignificant and implies that the permeation was mainly controlled by the dense core layer which was rapidly formed at the surface.
Fig. 7 Two-way interaction plot for MPD and TMC concentration (reaction time: 15 s, curing temperature: 55 °C). |
Fig. 7 shows that MPD concentration induced different effects on permeation flux when TMC changed from 0.15 wt% to 0.35 wt% in organic solution. At MPD concentration of 1 wt%, the water flux significantly improved from 20.9 LMH (C1) to 79.1 LMH (C3) with the increase in TMC concentration. When MPD concentration in aqueous phase increased to 2 wt%, the rate of flux enhancement decreased, which supports the accepted hypothesis that membranes become thicker with higher internal resistance at higher MPD concentrations. However, at 3 wt% MPD, the trend was different: water flux first dropped dramatically from 110.5 LMH in C7 to 15.3 LMH in C11, then increased to 30.6 LMH in C8 with further increase in the TMC concentration.
The SEM images of C2, C4, C7 and C8 membranes (Fig. 8) provide clear evidence that the unexpected shift in water flux was the result of a significant change in the surface structure of the membranes. The C7 membrane, prepared at high MPD (3 wt%) and low TMC (0.15 wt%) concentrations, had completely different morphology from previously seen ridge-and-valley and nodular structures. The markedly thick and fully formed PA film at the surface of this membrane reveals that due to the lack of sufficient TMC molecules, the incipient core layer was not dense enough to slow down the polymer growth at the surface. Therefore, rapid diffusion of MPD molecules to the reaction zone in the organic phase resulted in a thick but loose structure with high water flux and low salt rejection. By increasing the TMC concentration to 0.35 wt% in C8, the active layer became dense again and the surface morphology transformed to a nodular structure, similar to C3 and C4 membranes which were similarly prepared at high TMC concentration.
According to the interaction plot (Fig. 7), it can be concluded the widely accepted view that the lower amine/acyl chloride molar ratio (closer to unity) results in a denser polyamide film with lower water flux,13,28,32,34 cannot be simply generalized to all practices. The flux and rejection of the PA films is directly related to the surface structure and more specifically to the cross-link density of the core layer which are controlled by initial concentration of both monomers at the beginning of IP reaction rather than a single molar ratio. The very high (31.6 in C7) and low (4.51 in C2) molar ratio in our experiments resulted in high flux membranes at the expense of salt rejection decline, suggesting that there is an acceptable range of monomer concentration which yields salt rejecting NF and RO membranes with desirable water flux (>90%). In order to make TFC membranes with tailored properties, this range must be first identified by considering the monomer concentration interaction at very high and low molar ratios.
(6) |
(7) |
SSe = SST − (SSA + SSB + …) | (8) |
The ratio of factor variance to error variance (known as F-ratio) is an important statistical parameter, which is used to estimate the significance of a factor. It is calculated as follows:
(9) |
If the calculated F-ratio for a factor is larger than the extracted F from table (F-table can be obtained from statistical tables using DOFA and DOFe for different risks, α), it can be concluded that the influence of the factor on the results is significant and cannot be ignored. In fact, it shows that the change in a response is due to the alteration of the level of that factor and not because of noise factors. Table 5 presents the analysis of variance of experimental results based on water flux data. According to this table, the calculated F-ratio for all factors was greater than the extracted F-table (F = 4.26) with 95% confidence (α = 0.05) which means all factors had significant effect on the response.
Factor | SSa | DOFb | Variance | F-ratioc | P d (%) |
---|---|---|---|---|---|
a Sum of squares. b Degree of freedom. c F-table for α (risk) = 0.05 is F = 4.26. d Percent contribution of each factor on response (SSA/SST). | |||||
Curing temperature (°C) | 3977 | 2 | 1988 | 111.0 | 40.7 |
MPD concentration (%) | 2733 | 2 | 1366 | 76.3 | 28.0 |
TMC concentration (%) | 2720 | 2 | 1360 | 75.9 | 27.8 |
Reaction time (s) | 187 | 2 | 94 | 5.2 | 1.9 |
Error (%) | 161 | 9 | 18 | — | — |
The percent contribution of each factor (P) can also be evaluated by considering the sum of squares values using the equation PA = SSA/SST × 100. According to the P values presented in Table 5, curing temperature had the highest contribution (40.7%) to the variance in the water permeation in comparison to other factors. The MPD and TMC concentrations had similar contribution to permeate flux, 28% and 27.8%, respectively. Reaction time, as was observed in the marginal plots (Fig. 2), had the minimum contribution (1.9%) on the response. It must be noted that the extracted contribution values are limited to the levels of control factors considered in this study and could be different for a different set of factor combinations.
Using the Taguchi method, a prediction model (transfer function) is developed by the following equation to predict the performance of TFC membranes at the levels which are not considered in the L9 table.35
(10) |
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