Carbon dioxide adsorption on amine-impregnated mesoporous materials prepared from spent quartz sand

Mesoporous MCM-41 was synthesized using cetyltrimethyl ammonium bromide (CTAB) as a cationic surfactant and spent quartz sand as the silica source. Modification of the mesoporous structure to create an absorbent was then completed using 3-aminopropyltrimethoxysilane. Amine-Quartz-MCM (The A-Q-MCM) adsorbents were then characterized by N₂ adsorption/desorption, elemental analysis (EA), X-ray fluorescence (XRF), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), as well as the carbon dioxide (CO₂) adsorption/desorption performance. In this study, spent quartz sand was utilized to synthesize Quartz-MCM (Q-MCM) and the amine functionalized material, A-Q-MCM, which exhibited a higher uptake of CO₂ at room temperature compared with the nongrafted material. The results showed that Q-MCM is similar to MCM-41 synthesized using commercial methods. The surface area, pore volume, and pore diameter were found to be as high as 1028 m²/g, 0.907 cm³/g, and 3.04 nm, respectively. Under the condition of CO₂ concentration of 5000 ppm, retention time of 50 cc/min, and the dosage of 1 g/cm³, the mean adsorption capacity of CO₂ onto A-Q-MCM was about 89 mg/g, and the nitrogen content of A-Q-MCM was 2.74%. The adsorption equilibrium was modeled well using a Freundlich isotherm.

Implications:In this study, spent quartz sand was utilized to synthesize Q-MCM. The amine functionalized material exhibited a higher uptake of CO₂ at room temperature compared with the nongrafted material. The results showed that Q-MCM is similar to MCM-41 synthesized using commercial methods. The adsorption equilibrium was modeled well using a Freundlich isotherm.     

Analysis of air quality in Dire Dawa,Ethiopia

Ambient air quality was monitored and analyzed to develop air quality index and its implications for livability and climate change in Dire Dawa, Ethiopia. Using survey research design, 16 georeferenced locations, representing different land uses, were randomly selected and assessed for sulfur dioxide (SO₂), nitrogen dioxide (NO₂), carbon dioxide (CO₂), carbon monoxide (CO),volatile organic compounds (VOCs), and meteorological parameters (temperature and relative humidity). The study found mean concentrations across all land uses for SO₂ of 0.37 ± 0.08 ppm, NO₂ of 0.13 ± 0.17 ppm, CO₂ of 465.65 ± 28.63 ppm, CO of 3.35 ± 2.04 ppm, and VOCs of 1850.67 ± 402 ppm. An air quality index indicated that ambient air quality for SO₂ was very poor, NO₂ ranged from moderate to very poor, whereas CO rating was moderate. Significant positive correlations existed between temperature and NO₂, CO₂, and CO and between humidity and VOCs. Significant relationships were also recorded between CO₂ and NO₂ and between CO and CO₂. Poor urban planning, inadequate pollution control measure, and weak capacity to monitor air quality have implications for energy usage, air quality, and local meteorological parameters, with subsequent feedback into global climate change. Implementation of programs to monitor and control emissions in order to reduce air pollution will provide health, economic, and environmental benefits to the city.

Implications: The need to develop and implement emission control programs to reduce air pollution in Dire Dawa City is urgent. This will provide enormous economic, health, and environmental benefits. It is expected that economic effects of air quality improvement will offset the expenditures for pollution control. Also, strategies that focus on air quality and climate change present a unique opportunity to engage different stakeholders in providing inclusive and sustainable development agenda for Dire Dawa.     

An Evaluation of CO2, Measurements as an Indicator of Air Pollution

Measurements of ambient carbon dioxide (CO₂), made at the Continuous Air Monitoring Program station in downtown Cincinnati, Ohio, and at a rural location near Cincinnati are presented and evaluated to determine the significance of CO₂ data in urban air quality monitoring programs. Through analysis of rural CO₂ data and evaluation of combustion-sources by means of a diffusion model, it is demonstrated that the variation of urban CO₂ concentrations around the prevailing atmosphere background level results from combustion-and noncombustion {natural) sources. The concentration from natural sources can be substantial and in fact override the combustion sources. Because it is not yet practical to predict the contribution of natural sources to urban CO₂ concentrations, data obtained for-this gas have only limited utility as an index of air quality. Significant statistical relationships between CO₂ data and air quality measurements for summer months are shown to result from similar meteorological effects rather than similar sources. A seasonal and spatial variation of ih-ese relationships is postulated and subsequently demonstrated by analysis of CO₂ and air quality measurements from New Orleans, Louisiana, and SU Louis, Missouri.     

Carbon dioxide and methane emissions from the scale model of open dairy lots

To investigate the impacts of major factors on carbon loss via gaseous emissions, carbon dioxide (CO₂) and methane (CH₄) emissions from the ground of open dairy lots were tested by a scale model experiment at various air temperatures (15, 25, and 35 °C), surface velocities (0.4, 0.7, 1.0, and 1.2 m sec^?1), and floor types (unpaved soil floor and brick-paved floor) in controlled laboratory conditions using the wind tunnel method. Generally, CO₂ and CH₄ emissions were significantly enhanced with the increase of air temperature and velocity (P < 0.05). Floor type had different effects on the CO₂ and CH₄ emissions, which were also affected by air temperature and soil characteristics of the floor. Although different patterns were observed on CH₄ emission from the soil and brick floors at different air temperature-velocity combinations, statistical analysis showed no significant difference in CH₄ emissions from different floors (P > 0.05). For CO₂, similar emissions were found from the soil and brick floors at 15 and 25 °C, whereas higher rates were detected from the brick floor at 35 °C (P < 0.05). Results showed that CH₄ emission from the scale model was exponentially related to CO₂ flux, which might be helpful in CH₄ emission estimation from manure management.

Implications: Gaseous emissions from the open lots are largely dependent on outdoor climate, floor systems, and management practices, which are quite different from those indoors. This study assessed the effects of floor types and air velocities on CO₂ and CH₄ emissions from the open dairy lots at various temperatures by a wind tunnel. It provided some valuable information for decision-making and further studies on gaseous emissions from open lots.     

Nitration of polycyclic aromatic hydrocarbons adsorbed to different carriers in a fluidized bed reactor

The reactivity of selected polycyclic aromatic hydrocarbons (PAH) adsorbed to various surfaces has been studied. PAH were adsorbed to silica, alumina or charcoal particles and exposed to ambient concentrations of NO₂ in air in a fluidized bed reactor. The reaction products were analyzed by capillary gas chromatography and gas chromatograpy/mass spectrometry.The results show that silica is a more reactive surface than alumina. The charcoal used showed to be very adsorbtive and too little material was recovered for analyses. The reactivity of the PAH compounds studied decrease in the order perylene > benzo(a)pyrene > pyrene > chrysene > fluoranthene and phenanthrene. The relevance of these results to the assessment of the possible formation of nitro-PAH in the atmosphere is discussed.     

Carbon dioxide capturing technologies: a review focusing on metal organic framework materials (MOFs)

In this study, a relevant literature has been reviewed focusing on the carbon dioxide capture technologies in general, such as amine-based absorption as conventional carbon dioxide capturing technology, aqueous ammonia-based absorption, membranes, and adsorption material (e.g., zeolites, and activated carbons). In more details, metal organic frameworks (MOFs) as new emerging technologies for carbon dioxide adsorption are discussed. The MOFs section is intended to provide a comprehensive overview of MOFs including material characteristics and synthesis, structural features, CO₂ adsorption capacity, heat of adsorption and selectivity of CO₂.     

Removal of SO2 From Flue Gases Using Carbon at Elevated Temperatures

The interaction of a typical flue gas with active charcoal and bituminous coal char at temperatures between 600 and 800°C and atmospheric pressure has been studied. The SO₂ in the flue gas interacts with the carbon to form primarily H₂S, COS, and a carbon-sulfur surface complex. H₂S and COS break through the carbon bed much in advance of SO₂. At 800°C, sulfur retention on the bed exceeds at least 11% before SO₂ breakthrough occurs. The reaction of H₂S and COS with O₂ over active charcoal at 100–140°C to produce sulfur, which deposits on the carbon, has also been studied and found to be feasible. As a result of this study, a new process is outlined for the removal of SO₂ from flue gas, with the ultimate conversion     

An intensive two-week study of an urban CO2 dome in Phoenix,Arizona, USA

Atmospheric CO₂ concentrations were measured prior to dawn and in the middle of the afternoon at a height of 2 m above the ground along four transects through the metropolitan area of Phoenix, Arizona on 14 consecutive days in January 2000. The data revealed the existence of a strong but variable urban CO₂ dome, which at one time exhibited a peak CO₂ concentration at the center of the city that was 75% greater than that of the surrounding rural area. Mean city-center peak enhancements, however, were considerably lower, averaging 43% on weekdays and 38% on weekends; and averaged over the entire commercial sector of the city, they were lower still, registering 30% on weekdays and 23% on weekends. Over the surrounding residential areas, on the other hand, there are no weekday–weekend differences in boundary-layer CO₂ concentration. Furthermore, because of enhanced vertical mixing during the day, near-surface CO₂ concentrations in the afternoon are typically reduced from what they are prior to sunrise. This situation is additionally perturbed by the prevailing southwest-to-northeast flow of air at that time of day, which lowers afternoon CO₂ concentrations on the southern and western edges of the city still more, as a consequence of the importation of pristine rural air. The southwest-to-northeast flow of air also sometimes totally compensates for the afternoon vertical-mixing-induced loss of CO₂ from areas on the northern and eastern sides of the city, as a consequence of the northeastward advection of CO₂ emanating from the central, southern and western sectors of the city. Hence, although complex, the nature of the urban CO₂ dome of Phoenix, Arizona, is readily understandable in terms of basic meteorological phenomena and their interaction with human activities occurring at the land/air interface.     

Recovering CO2 From Large− and Medium-Size Stationary Combustors

This paper summarizes the results of research conducted at Ar-gonne National Laboratory (ANL) to develop and design a novel method for the recovery of CO₂ from flue gases. The basic process concept Involves the combustion of a hydrocarbon fuel using a mixture of oxygen and carbon dioxide (or CO₂ and H₂0) rather than air as the oxidant, which results In a product stream that contains primarily CO₂ and H₂O. This stream Is then dried and conditioned to meet the specifications of the end user, A slip stream of CO₂ (or CO₂, and H₂0) is used as a diluent in the combustion chamberto maintain a flame temperature equivalent to the temperature that would otherwise be obtained using air as an oxidant. The cost-effectiveness of the process in recovering C0₂ is dependent on the scale of the operation, the type of fuel used, the cost of oxygen, and the cost of capital. The sensitivity of the cost of the recovered C0₂ to these variables Is discussed, and a model for estimating the cost of CO₂ recovered using the ANL process Is presented.     

The effects of air pollution on human mortality: does gender difference matter in African countries?

The relationship between environmental factors and human health has long been a concern among academic researchers. We use two indicators of environmental pollution, namely particulate matter (PM₁₀) and carbon dioxide (CO₂) to examine the effects of poor air quality on human mortality. This study explores an issue that has largely been ignored, particularly in the African literature, where the effect of air pollution on human mortality could be influenced by gender specification. We analyse a panel data from 35 African countries and our result suggests that the elevated levels of PM₁₀ and CO₂ have a significant effect on the increasing mortality rates in infants, under-five children and adults. Although the effect of poor air quality on adults is found to differ between genders, such difference is not statistically significant. We conclude that the air pollution effects, on average, are similar between genders in the African countries.     

On the origins of night-time NO at a rural measurement site

Mixing ratios for NO and NO₂ were measured during 1980/1981 at Deuselbach, a rural site in Germany. The data are analyzed with regard to the occurrence of nocturnal NO signals and their origins. Anthropogenic influences arising from road traffic and home heating activities are identified by their dependence on wind direction. An additional non-directional component is found to exist. It shows up most frequently in summer and when it occurs, the NO mixing ratio increases with rising temperature indicating a biological origin of night-time NO. The temporal behavior of night-time NO is usually correlated with that of CO₂ but anticorrelated to that of O₃. This shows that NO is brought upwards to the air intake of the NO_x monitor from lower levels and that the source of the non-directional component of nocturnal NO is the earth's surface. The release of NO from soils is known from other work and this process is probably also responsible for the present observations. A flux estimate agrees with soil fluxes reported by other authors. The accumulation of NO in the surface air layer under stagnant conditions leads to the appearance of a morning peak of NO after sunrise when increased vertical mixing brings NO rich air up to the monitoring level. During summer, the morning peak may override the NO peak expected to occur at noon due to the photodissociation of NO₂.     

Exposure to moderate concentrations of tropospheric ozone impairs tree stomatal response to carbon dioxide

With rising concentrations of both atmospheric carbon dioxide (CO₂) and tropospheric ozone (O₃), it is important to better understand the interacting effects of these two trace gases on plant physiology affecting land-atmosphere gas exchange. We investigated the effect of growth under elevated CO₂ and O₃, singly and in combination, on the primary short-term stomatal response to CO₂ concentration in paper birch at the Aspen FACE experiment. Leaves from trees grown in elevated CO₂ and/or O₃ exhibited weaker short-term responses of stomatal conductance to both an increase and a decrease in CO₂ concentration from current ambient level. The impairement of the stomatal CO₂ response by O₃ most likely developed progressively over the growing season as assessed by sap flux measurements. Our results suggest that expectations of plant water-savings and reduced stomatal air pollution uptake under rising atmospheric CO₂ may not hold for northern hardwood forests under concurrently rising tropospheric O₃.     

Continuous observations of carbon dioxide at Mace Head,Ireland from 1995 to 1999 and its net European ecosystem exchange

A 5-yr record of continuous high-frequency carbon dioxide CO₂ observations over the 1995–1999 period for the Mace Head Atmospheric Research Station has been examined to reveal a complex interplay between local- and regional-scale sources and sinks. During the winter months, an additional CO₂ source, over and above fossil fuel combustion, is required to support the observed concentrations of CO₂ in European regionally polluted air masses. During the summer months, an additional CO₂ sink is required. Over the entire study period, the additional net European ecosystem exchange source–sink required is –0.36±0.4 Gtonne C yr⁻¹.     

Airborne co2 measurements in the Arctic during spring 1983

A set of flask air samples collected from aircraft in March and April 1983 during the Arctic Gas and Aerosol Sampling Program has been analyzed for CO₂ concentration. The results show CO₂ variations of several ppm in the Arctic troposphere, and qualitative agreement with measurements made on air samples collected at the surface. The CO₂ measurements together with air-mass characteristics determined during the flights show that CO₂ concentrations in the Arctic result from mixing of polluted air transported into the Arctic from lower latitudes with cleaner air of maritime and continental origins. The CO₂ concentration is found to increase or decrease with altitude which is probably dependent on the details of transport and the presence or absence of marine sources and/or sinks.     

Catalytic gasification of biomass (<Emphasis Type="Italic">Miscanthus</Emphasis>) enhanced by CO<Subscript>2</Subscript> sorption

The main objective of this work concerns the coupling of biomass gasification reaction and CO₂ sorption. The study shows the feasibility to promote biomass steam gasification in a dense fluidized bed reactor with CO₂ sorption to enhance tar removal and hydrogen production. It also proves the efficiency of CaO-Ca₁₂Al₁₄O₃₃/olivine bi-functional materials to reduce heavy tar production. Experiments have been carried out in a fluidized bed gasifier using steam as the fluidizing medium to improve hydrogen production. Bed materials consisting of CaO-based oxide for CO₂ sorption (CaO-Ca₁₂Al₁₄O₃₃) deposited on olivine for tar reduction were synthesized, their structural and textural properties were characterized by Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), and temperature-programmed reduction (TPR) methods, and the determination of their sorption capacity and stability analyzed by thermogravimetric analysis (TGA). It appears that this CaO-Ca₁₂Al₁₄O₃₃/olivine sorbent/catalyst presents a good CO₂ sorption stability (for seven cycles of carbonation/decarbonation). Compared to olivine and Fe/olivine in a fixed bed reactor for steam reforming of toluene chosen as tar model compound, it shows a better hydrogen production rate and a lower CO₂ selectivity due to its sorption on the CaO phase. In the biomass steam gasification, the use of CaO-Ca₁₂Al₁₄O₃₃/olivine as bed material at 700 °C leads to a higher H₂ production than olivine at 800 °C thanks to CO₂ sorption. Similar tar concentration and lighter tar production (analyzed by HPLC/UV) are observed. At 700 °C, sorbent addition allows to halve tar content and to eliminate the heaviest tars.     

不同改性方式对竹炭净化气态氮氧化物效果的影响

为了研究不同表面改性方法对竹炭空气净化效果的影响,测定了化学药剂活化、超声处理、微波处理后的改性竹炭对低浓度氮氧化物的净化效果。结果表明:活化剂浸渍后的竹炭,对氮氧化物净化效率降低,净化速度减慢;微波功率越大、辐照时间越长,改性后竹炭对氮氧化物处理效率越大,但辐照时间达到一定程度后,竹炭对氮氧化物的处理效率增大变得缓慢;超声处理后的竹炭对NO的处理效率比改性前有明显提高。BET测试结果表明,竹炭产品用微波和超声处理后,平均孔径、微孔表面积和比表面积均比活化前增大;而经过活化剂浸渍后,微孔面积和比表面积都显著下降。因此建议采用微波及超声方式对竹炭进行活化。     

Early atmospheric detection of carbon dioxide from carbon capture and storage sites

The early atmospheric detection of carbon dioxide (CO₂) leaks from carbon capture and storage (CCS) sites is important both to inform remediation efforts and to build and maintain public support for CCS in mitigating greenhouse gas emissions. A gas analysis system was developed to assess the origin of plumes of air enriched in CO₂, as to whether CO₂ is from a CCS site or from the oxidation of carbon compounds. The system measured CO₂ and O₂ concentrations for different plume samples relative to background air and calculated the gas differential concentration ratio (GDCR = ?ΔO₂/ΔCO₂). The experimental results were in good agreement with theoretical calculations that placed GDCR values for a CO₂ leak at 0.21, compared with GDCR values of 1–1.8 for the combustion of carbon compounds. Although some combustion plume samples deviated in GDCR from theoretical, the very low GDCR values associated with plumes from CO₂ leaks provided confidence that this technology holds promise in providing a tool for the early detection of CO₂ leaks from CCS sites. Implications: This work contributes to the development of a cost-effective technology for the early detection of leaks from sites where CO₂ has been injected into the subsurface to enhance oil recovery or to permanently store the gas as a strategy for mitigating climate change. Such technology will be important in building public confidence regarding the safety and security of carbon capture and storage sites.     

Absorption of Gaseous Air Pollutants By a Standardized Plant Canopy

Concentration profiles for hydrogen fluoride(HF), sulfur dioxide(SO₂), ozone (O₃), nitrogen dioxide(NO₂), and nitric oxide(NO) generated in a standardized alfalfa canopy are presented. Wind, light, temperature, and carbon dioxide(CO₂) profiles, canopy pollutant uptake rates, and canopy structural data are also given. Canopy pollutant concentration profile characteristics were studied to evaluate the relative potentials for major air pollutants to penetrate into canopies. The study was conducted in an environmental growth chamber equipped to control automatically environmental conditions and monitor continuously gas exchange rates. HF, SO₂, and NO₂ profiles suggested that these gases were removed efficiently by the upper portion of the canopy as well as by the immediate subsurface vegetation. The steady state HF profile showed the greatest displacement within the canopy. The NO profile was displaced the least. The uptake rate of NO by plants was apparently too slow in comparison with gas transport and mixing within the canopy to affect the internal profile substantially. O₃ appeared to be readily deposited on the surface tissues, but the deeper tissues in the canopy had less effect on the concentration profile. Data are also presented to show the relationship between NO₂ concentration within the canopy and changes in the air concentration above the vegetation. The results indicated that gas transport between the atmosphere and canopy interior was rapid. The data presented should be of current interest to agriculturists, researchers, administrators, and environmental planners concerned with effects of air pollutants on plants and on the fate of pollutants in the microenvironment.     

On understanding the land–ocean CO2 contrast over the Bay of Bengal: A case study during 2009 summer monsoon

Ship-based observations of atmospheric carbon dioxide (CO₂) concentration over the Bay of Bengal (BoB) between 17 July 2009 and 17 Aug 2009 offered an excellent opportunity to evaluate the land–ocean contrast of surface CO₂ and facilitated its comparison with model simulated CO₂ concentrations. Elevated values of CO₂ with large variability near the coastal region and relatively low values with correspondingly lower variability over the open ocean suggest that this observed CO₂ variability over the ocean essentially captures the differences in terrestrial and oceanic CO₂ fluxes. Although the region under investigation is well known for its atmospheric intraseasonal oscillations of Indian summer monsoon during July and August, the limited duration of observations performed from a moving ship in a research cruise, is not able to capture any high-frequency variability of atmospheric CO₂ concentrations. But band-passed sea surface temperature and wind anomalies do indicate strong intraseasonal variability over the study region during the observational period. The synoptic data, albeit quite short in duration, thus offer a clear benchmark for abrupt variability of CO₂ concentration between land and ocean.     

UTILIZATION OF AGRICULTURAL WASTE CORN COB FOR THE PREPARATION OF CARBON ADSORBENT

In the present study, a series of activated carbons were prepared from agricultural waste corn cob by chemical and physical activations with potassium hydroxide (KOH)/potassium carbonate (K₂CO₃) and carbon dioxide (CO₂). The effect of process variables such as impregnation ratio, impregnation time, activation temperature and soaking time of CO₂ was studied in order to relate these preparation parameters with the physical properties of final carbon products. The resulting activated carbons were characterized by nitrogen adsorption[ch-[chdesorption isotherms at 77 K. The surface areas and pore volumes of carbons were estimated by the BET equation, the Langmuir equation and the t-plot method. Under the experimental conditions investigated, the main parameters in the activation of corn cob were found to be the impregnation ratio and activation temperature. The soaking time of CO₂ is another important variable, which had a strong effect on the pore volume development. The BET surface area and total pore volume were as large as about 2000 m²/g and about 1.0 cm³/g, respectively. This study showed that the activation of agricultural waste corn cob with KOH/K₂CO₃ and CO₂ was suitable for the preparation of large-surface-area activated carbons.