Eco-friendly synthesis for MCM-41 nanoporous materials using the non-reacted reagents in mother liquor
© Ng et al.; licensee Springer. 2013
Received: 1 February 2013
Accepted: 27 February 2013
Published: 4 March 2013
Skip to main content
© Ng et al.; licensee Springer. 2013
Received: 1 February 2013
Accepted: 27 February 2013
Published: 4 March 2013
Nanoporous materials such as Mobil composite material number 41 (MCM-41) are attractive for applications such as catalysis, adsorption, supports, and carriers. Green synthesis of MCM-41 is particularly appealing because the chemical reagents are useful and valuable. We report on the eco-friendly synthesis of MCM-41 nanoporous materials via multi-cycle approach by re-using the non-reacted reagents in supernatant as mother liquor after separating the solid product. This approach was achieved via minimal requirement of chemical compensation where additional fresh reactants were added into the mother liquor followed by pH adjustment after each cycle of synthesis. The solid product of each successive batch was collected and characterized while the non-reacted reagents in supernatant can be recovered and re-used to produce subsequent cycle of MCM-41. The multi-cycle synthesis is demonstrated up to three times in this research. This approach suggests a low cost and eco-friendly synthesis of nanoporous material since less waste is discarded after the product has been collected, and in addition, product yield can be maintained at the high level.
Mobil composite material number 41 (MCM-41) is a mesoporous material that was first discovered in 1992[1, 2]. It has a hexagonal array of uniformly sized one-dimensional mesopores with a pore diameter of 2 to 10 nm. The research on these nanoporous materials is of interest especially in catalysis, adsorption, supports, and carriers due to its excellent properties such as high surface area, high thermal stability, high hydrophobicity, and tunable acidity[3, 4]. Furthermore, the pore size of MCM-41 can be tailored by using surfactants with different chain lengths and/or auxiliary structure-directing agent[5, 6].
Several methods such as hydrothermal and solvothermal treatments have been used for the synthesis of MCM-41 meso-ordered material[7–9]. The concept of all these approaches is to terminate the synthesis process after the synthesis is complete; the nanomaterials are formed in sol suspensions and are recovered by filtration or centrifugation. The remaining synthesis solution is usually discarded after the nanoporous materials are collected. However, these conventional methods bring several drawbacks to the environment and industry. For instance, large amounts of initial reactants which remain unused in the remaining solution, including the expensive organic surfactant template, silica and corrosive solvent such as NaOH, is discarded during the recovering of mesostructured particles. This causes the synthesis of nanoporous material an uneconomical process; it is not cost effective for chemical industries. Moreover, the disposal of unused chemical reagents especially the surfactant template after the synthesis results in severe health hazard and adverse environmental effect[10, 11]. Thus, any new insight regarding the replacing, recycling, or reusing of the valuable chemicals in the synthesis of nanoporous materials is highly appreciated.
Recently, the use of electronic (e-waste) and natural wastes such as coal fly ash[13–17] and rice husk ash as silica sources for the preparation of MCM-41 has been reported. In general, the ashes and electronic resin waste are treated with sodium hydroxide to extract the silica out before their introduction into the MCM-41 synthesis solution. With this strategy, the inorganic waste is re-used, and it can be converted into more valuable and useful materials which may have important economic implications. In the environmental aspect, converting silica waste into nanoporous materials such as MCM-41 may provide another way for preserving the environment.
Although eco-friendly synthesis on MCM-41 using natural wastes has been reported to date, there is no study on the synthesis of MCM-41 by recycling the mother liquid. One of the reasons is that the change in the molar composition and the pH of the precursor solution will have a profound impact on the resulting materials, i.e., no solid product, amorphous, new or mixture of two mesophases (lamellar, cubic, disordered) will be formed instead of the desired single hexagonal mesophase. In this work, MCM-41 is prepared with a green synthesis strategy by reusing non-reacted reagents remaining in the synthesis solution followed by supplementary compensation of the consumed chemicals and pH adjustment. The chemical compositions of mother liquor and solid product of each cycle were then characterized by using dry solid mass analysis, thermogravimetry (TG)/differential thermal analysis (DTA), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), 29Si magic-angle-spinning (MAS) solid-state nuclear magnetic resonance (NMR), transmission electron microscopy (TEM), atomic absorption spectrometry (AAS) and N2 adsorption-desorption analyses.
The mother liquor was separated via filtration, and the water from the filtrate was partially evaporated at 55°C for 16 h to enable compensation analysis. For the MCM-41 wet filter cake on clay filter, the mass of water in it was estimated by measuring the mass of the solid before and after drying at 60°C for 14 h. The dried solid was then allowed to redisperse again in water, and the solid product was purified by washing with distilled water until the pH of the solid became 7.0. The purified solid was dried at 80°C overnight, and the mass of purified solid was measured again.
Prior to the second and third synthesis cycles, the chemical composition of the non-reacted solutions was analyzed (please refer to the ‘Characterization’ subsection) and was adjusted to the original one by adding the required amount of CTABr, sodium silicate, and water. The H2SO4 was then added slowly under stirring until a pH of approximately 11.0 was reached using a pH meter (Ohaus Starter 3000, Parsippany, NJ, USA) to monitor the pH of the solution. The MCM-41 nanoporous materials prepared from the first, second, and third synthesis cycles will be denoted as M-1, M-2, and M-3, respectively.
The organic template in the as-synthesized MCM-41 was removed and recovered through extraction by refluxing the solid (1.5 g) in 1 M hydrobromic acid ethanolic solution (500 mL) at 75°C for 24 h. The template-free MCM-41 was filtered, washed with ethanol, and dried for 10 h at 100°C in vacuum. On the other hand, the ethanol in the filtrate solution was distilled out at 80°C, and the surfactant was recrystallized in a mixture solution of acetone/ethanol (95:5 in volume) after the acid in the solution was neutralized. The recrystallized CTABr white solid was purified with ethanol and dried at 70°C overnight.
X-ray powder diffraction patterns were recorded using a Siemens D5000 Kristalloflex diffractometer (Munich, Germany) with a monochromated Cu Kα radiation in the angular range from 1.7° to 10° (2θ) with a scanning speed of 0.02°·s−1. TEM was performed using a Philips CM-12 microscope (Amsterdam, The Netherlands) with an accelerating voltage of 300 kV. The silica content was measured using an AAnalyst 200 atomic absorption spectrometer (PerkinElmer, Waltham, MA, USA). The organic template moiety in the sample was determined using a Mettler TGA SDTA851 instrument (Mettler-Toledo, Columbus, OH, USA) with a heating rate of 10°C·min−1 under nitrogen flow. Nitrogen adsorption-desorption analysis was conducted using a Micromeritics ASAP 2010 instrument (Norcross, GA, USA). The template-free sample was first degassed at 250°C for 3 h followed by nitrogen adsorption measurement at −196°C. The surface physicochemical properties were then calculated using the Brunauer-Emmett-Teller (BET) and the Barrett-Joyner-Halenda (BJH) models. Solid-state 29Si-MAS-NMR spectra were recorded using a Bruker Ultrashield 300 spectrometer (Madison, WI, USA) operating at 300 MHz with tetramethylsilane as a reference. The measurement was carried out at 79.4 MHz and single-contact cross-polarization pulse program was used. The spectra were acquired with a pulse length of 2.7 μs, a repetition time of 6 s, and a contact time of 4 ms. The FTIR spectra of the as-synthesized solid products were obtained with a PerkinElmer spectrometer (System 2000) using the KBr pellet technique (KBr/sample weight ratio = 150:1).
Compensated chemicals added into non-reacted mother liquor for MCM-41 synthesis cycles and MCM-41 solid yield
Non-reacted mother liquor (g)
Solid yield, gram (wt.%)b
8.034 g (73.6%)
pH was determined to be the most important of the investigated synthesis parameters in affecting pore ordering and mesophase. The solubility and the rate of dissolution of silica increases with the increasing pH resulted in a decrease of the total interfacial area and a more long-range pore ordering[24, 25]. High pH results in fast and complete hydrolysis where polymerization can occur within a few minutes. When the pH of the precursor solution decreased (higher acidity), it was observed that the intensity of diffraction peaks in the XRD pattern decreased, suggesting a considerable decrease of pore ordering.
It is important to note that little to no-solid product was formed in the re-used mother liquor before chemical compensation due to insufficient chemicals present in the precursor solution. Thus, supplementary compensation of the consumed chemicals onto mother liquor and pH adjustment are needed before proceeding to the second cycle of synthesis. One should note that amorphous, lamellar, or cubic phase was obtained as single or mixed products when the chemical composition and the pH of the solution were not correctly adjusted (e.g., template/H2O ratio is high).
The XRD results were further confirmed by TEM analysis. Long-range order of the hexagonal pore arrays could be seen in M-1, and the observation was well agreed with the XRD study (inset of Figure 2a). On the other hand, M-2 and M-3 showed a lower ordering degree than M-1. Nevertheless, the hexagonal periodicity of the mesophase of three MCM-41 samples was basically maintained.
The solid yield of the MCM-41 silica materials for the three subsequent cycles was calculated to be 73.6, 71.9, and 78.3 wt.%, respectively, according to dry mass solid analysis (Table 1). Thus, the solid product yield was considerably high and constant for three subsequent cycles. These results are suggesting that the re-use of the non-reacted precursor solutions is possible as the surfactant template is completely preserved and does not decompose during hydrothermal treatment at mild hydrothermal condition (100°C). Additionally, no organic template and inorganic solution are disposed to the environment, and the chemicals are re-used entirely (CTABr surfactant occluded in MCM-41 framework is extracted out and can be re-used after purification), and thus, this method is revealed as benign to the environment.
In addition, the presence of absorption bands at 1,206 and 1,056 cm−1 could be assigned to the asymmetric stretching vibrations of Si-O-Si, while the symmetric stretching vibrations of Si-O-Si resonated at 777 and 616 cm−1. Moreover, the IR band at 442 cm−1 was attributed to the bending vibration of Si-O-Si. A small signal was also detected at 964 cm−1 which was due to the bending mode of surface Si-OH. Low intensity of this signal indicated that only a small amount of silanol group was present in the MCM-41 samples.
29 Si-MAS-NMR deconvolution results
TG analysis is a powerful analytical technique that can be used to determine the organic components of a material by monitoring the weight loss as the specimen is heated. Using this technique, the amount of organic template is consumed in the synthesis (occluded in as-synthesized MCM-41), thus can be estimated (Note: the quantity of template lost during the purification process of the samples is also taken into account). It was found that the CTA+/SiO2 molar ratios of M-1, M-2, and M-3 were 0.16, 0.14, and 0.13, respectively, which were in the range of 0.1 to 0.2, a value previously found for a well-organized hexagonal mesophase. From this chemical analysis, it appeared that six to eight SiO− groups compensated one CTA+ organic cation.
The TG curves of three as-synthesized samples had a similar shape with slight difference in the percentage of weight loss (please refer to Additional file1: Figure S1). In the first stage, the weight loss of approximately 6% at below 130°C was attributed to desorption of water. In the second (weight loss of 33% to 38% at 130°C to 340°C) and third (weight loss of approximately 4% at 340°C to 550°C) stages, the weight losses were due to the thermal decomposition of organic template via Hofmann elimination. In the fourth stage, at the temperature above 500°C, the weight loss was caused by the condensation of silanol groups to form siloxane bonds. From the TG results, it can be summarized that the MCM-41 nanoporous silica synthesized from three subsequent cycles contained almost the same amount of template (total weight loss of 36 to 41 wt.% in the range of 120°C to 500°C), demonstrating that the consumption of the organic template during the formation of MCM-41 was almost constant in each step of the multi-cycle synthesis.
Textural properties of the MCM-41 samples
Unit cell, a0(nm)a
Pore size (nm)b
Surface area, SBET(m2·g−1)
Pore volume, Vtotal(cm3·g−1)
Total chemical reagents used for conventional and multi-step syntheses of MCM-41
Amount of chemical saved (%)
Total chemicals consumed
Meanwhile, the CTABr in the as-synthesized samples was successfully recovered after solvent extraction using ethanolic solution (please refer to Additional file1: Figure S2). It was found that the product yield of CTABr after re-crystallization and purification was 84.6%. The regenerated CTABr can be re-used back for the synthesis of MCM-41 which further reduced the cost and consumption of expensive organic template. Furthermore, the ethanol solution used in organic template extraction can be distilled, separated, and re-used without disposing to the environment.
In short, the low consumption of expensive and harmful chemical reagents is demonstrated; thus, large cost saving and environment protection are achieved. Moreover, this method might offer as another green synthesis for other important nanoporous molecular sieves such as SBA-15, MCM-48, chiral mesoporous silica, KIT-1, etc., where the product yield is considerably maintained by re-using the same non-reacted initial reagents, thus decreasing the synthesis cost, making possible the chemical process to be environmentally benign.
In summary, using a simple multi-cycle method, MCM-41 nanoporous materials can be synthesized in a more eco-friendly and economical way. The obtained samples in three subsequent cycles exhibited remarkable high-BET specific surface area (above 500 m2·g−1) and high pore volume (above 0.60 cm3·g−1) while maintaining its well-ordered hexagonal mesostructure. The MCM-41 synthesized from the three subsequent batches had also almost similar degree of ordering, morphology, yield, pore size, and chemical composition.
The multi-cycle synthesis approach in this work is beneficial from the environmental perspective because the amount of waste produced is minimized by recycling synthesis materials which results in environmental problems. This approach is also beneficial in terms of economic perspective as re-use of chemical reactants reduces the production cost in chemical industries.
JYG is a MSc student of the University Sains Malaysia (USM). EPN is an associate professor at the USM. TCL is a professor at the University of Malaya. RRM is an assistant professor at the Institute Teknologi Bandung.
The authors are grateful for the financial support from FRGS (203/PKIMIA/6711185) grant.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.