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      CO2 capture on easily regenerable hybrid adsorbents based on polyamines and mesocellular silica foam. Effect of pore volume of the support and polyamine molecular weight

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          Abstract

          Mesocellular foams (MCFs) with a wide range of pore volumes and pore sizes were prepared and impregnated with PEI. CO 2 adsorption on these adsorbents was studied.

          Abstract

          Mesocellular foams (MCFs) with a wide range of pore volumes and pore sizes were prepared by varying a number of synthesis parameters such as ammonium fluoride concentration, effect of swelling agent trimethylbenzene (TMB), equilibration time and calcination heating rate. The obtained MCFs with pore volumes from 0.98 cm 3 g −1 to 4.17 cm 3 g −1 were impregnated with polyethylenimine (PEI) having molecular weights of 800 g mol −1 to 25 000 g mol −1. These organic/inorganic hybrid materials with PEI loadings of 50 to 83% were tested for CO 2 adsorption capacity, kinetics, stability and regenerability. Increasing pore volume and size in MCFs allowed the loading of higher amounts of PEI and a better distribution of PEI in the pores. Access to the active amino sites by CO 2 was consequently facilitated. Adsorption of up to 6 mmol CO 2 per g adsorbent (265 mg g −1) was obtained at 85 °C with the adsorbent containing PEI with a molecular weight of 800 g mol −1 loaded on the support with the highest pore volume. Contrary to expectation, the adsorbents based on PEI with the highest molecular weight had faster desorption kinetics than the ones loaded with lower molecular weight PEIs. On the other hand the CO 2 adsorption kinetics for a given concentration were very similar for all PEIs, regardless of molecular weights. The adsorption capacity of the adsorbents did not decrease over 100 adsorption/desorption cycles at 75 °C. The CO 2 adsorption results obtained here were in the top tier compared to the ones reported in the literature. Preparation of PEI based adsorbents clearly benefited from the utilization of supports with larger pore volume and diameter which in turn led to significantly improved CO 2 adsorption characteristics.

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          Most cited references46

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          Adsorbent materials for carbon dioxide capture from large anthropogenic point sources.

          Since the time of the industrial revolution, the atmospheric CO(2) concentration has risen by nearly 35 % to its current level of 383 ppm. The increased carbon dioxide concentration in the atmosphere has been suggested to be a leading contributor to global climate change. To slow the increase, reductions in anthropogenic CO(2) emissions are necessary. Large emission point sources, such as fossil-fuel-based power generation facilities, are the first targets for these reductions. A benchmark, mature technology for the separation of dilute CO(2) from gas streams is via absorption with aqueous amines. However, the use of solid adsorbents is now being widely considered as an alternative, potentially less-energy-intensive separation technology. This Review describes the CO(2) adsorption behavior of several different classes of solid carbon dioxide adsorbents, including zeolites, activated carbons, calcium oxides, hydrotalcites, organic-inorganic hybrids, and metal-organic frameworks. These adsorbents are evaluated in terms of their equilibrium CO(2) capacities as well as other important parameters such as adsorption-desorption kinetics, operating windows, stability, and regenerability. The scope of currently available CO(2) adsorbents and their critical properties that will ultimately affect their incorporation into large-scale separation processes is presented.
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            CO2 capture by solid adsorbents and their applications: current status and new trends

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              Chemical recycling of carbon dioxide to methanol and dimethyl ether: from greenhouse gas to renewable, environmentally carbon neutral fuels and synthetic hydrocarbons.

              Nature's photosynthesis uses the sun's energy with chlorophyll in plants as a catalyst to recycle carbon dioxide and water into new plant life. Only given sufficient geological time can new fossil fuels be formed naturally. In contrast, chemical recycling of carbon dioxide from natural and industrial sources as well as varied human activities or even from the air itself to methanol or dimethyl ether (DME) and their varied products can be achieved via its capture and subsequent reductive hydrogenative conversion. The present Perspective reviews this new approach and our research in the field over the last 15 years. Carbon recycling represents a significant aspect of our proposed Methanol Economy. Any available energy source (alternative energies such as solar, wind, geothermal, and atomic energy) can be used for the production of needed hydrogen and chemical conversion of CO(2). Improved new methods for the efficient reductive conversion of CO(2) to methanol and/or DME that we have developed include bireforming with methane and ways of catalytic or electrochemical conversions. Liquid methanol is preferable to highly volatile and potentially explosive hydrogen for energy storage and transportation. Together with the derived DME, they are excellent transportation fuels for internal combustion engines (ICE) and fuel cells as well as convenient starting materials for synthetic hydrocarbons and their varied products. Carbon dioxide thus can be chemically transformed from a detrimental greenhouse gas causing global warming into a valuable, renewable and inexhaustible carbon source of the future allowing environmentally neutral use of carbon fuels and derived hydrocarbon products.
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                Author and article information

                Journal
                RSCACL
                RSC Adv.
                RSC Adv.
                Royal Society of Chemistry (RSC)
                2046-2069
                2014
                2014
                : 4
                : 37
                : 19403-19417
                Article
                10.1039/C4RA02145B
                d4e6d9ea-51cf-4668-9b97-e9dcf90c0c08
                © 2014
                History

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