以粉煤灰为原料制备低温CO2吸附剂的工艺参数优化

利用高铝粉煤灰预脱硅液作为载体原料,通过使用胺基化合物对载体改性制备低温CO_2吸附剂.应用6 sigma中的工具,对制备工艺进行优化,得到理想的吸附剂,并对吸附剂样品进行表征.结果表明制备的CO_2吸附剂表现出良好的CO_2吸附性能.此类CO_2吸附剂具有吸附容量高(160 mg·g~(-1))、吸附速率快、对设备腐蚀低、成本低廉等特点,是一种极具工业应用潜力的CO_2吸附剂.     

Effects of surfactants on the combined toxicity of TiO2 nanoparticles and cadmium to Escherichia coli

The combined ecological toxicity of TiO₂ nanoparticles (nano-TiO₂) and heavy metals has been paid more attention. As the common pollutants in water environment, surfactants could affect the properties of nanoparticles and heavy metals, and thus further influence the combined toxicity of nano-TiO₂ and heavy metals. In this study, the effects of sodium dodecyl benzene sulfonate (SDBS) and Tween 80 on the single and combined toxicities of Cd^2 + and nano-TiO₂ to Escherichia coli (E. coli) were examined, and the underlying influence mechanism was further discussed. The results showed both SDBS and Tween 80 enhanced the toxicity of Cd^2 + to E. coli in varying degrees. The reaction of SDBS and Cd^2 + could increase the outer membrane permeability and the bioavailability of Cd, while Tween 80 itself could enhance the outer membrane permeability. The combined toxicity of nano-TiO₂ and Cd^2 + to E. coli in absence of surfactant was antagonistic because of the adsorption of Cd^2 + to nano-TiO₂ particles. However, in the presence of SDBS, both SDBS and nano-TiO₂ influenced the toxicity of Cd^2 +, and also SDBS could adsorb to nano-TiO₂ by binding to Cd^2 +. The combined toxicity was reduced at Cd^2 + lower than 4 mg/L and enhanced at Cd^2 + higher than 4 mg/L under multiple interactions. Tween 80 enhanced the combined toxicity of nano-TiO₂ and Cd^2 + by increasing the outer membrane permeability. Our study firstly elucidated the effects of surfactants on the combined toxicity of nano-TiO₂ and Cd^2 + to bacteria, and the underlying influencing mechanism was proposed.     

Sorption of uranyl ions on TiO2: Effects of pH, contact time, ionic strength, temperature and HA

Sorption of U(VI) onto TiO₂ as functions of pH, ionic strength, contact time, soil humic acid (SHA), solid-to-liquid ratio and temperature was studied under ambient conditions using batch and spectroscopic approaches. The sorption of U(VI) on TiO₂ was significantly dependent on pH and ionic strength. The presence of SHA slightly enhanced the sorption of U(VI) on TiO₂ below pH 4.0, while it inhibited U(VI) sorption in the higher pH range. U(VI) sorption on TiO₂ was favored at high temperatures, and the sorption process was estimated to be endothermic and spontaneous. Reduction of U(VI) to lower valent species was confirmed by X-ray photo-electron spectroscopy analysis. It is very interesting to find that U(VI) sorption on TiO₂ was promoted in solutions with higher back-ground electrolyte concentrations. In the presence of U(VI), higher back-ground electrolyte made more TiO₂ particles aggregate through (001) facets, leading more (101) facets to be exposed. Therefore, the reduction of U(VI) was enhanced by the exposed (101) facets and more U(VI) removal was observed.     

Effects of O3/Cl2 disinfection on corrosion and opportunistic pathogens growth in drinking water distribution systems

The effects of O_3/Cl_2 disinfection on corrosion and the growth of opportunistic pathogens in drinking water distribution systems were studied using annular reactors(ARs).The corrosion process and most probable number(MPN) analysis indicated that the higher content of iron-oxidizing bacteria and iron-reducing bacteria in biofilms of the AR treated with O_3/Cl_2 induced higher Fe_3O_4 formation in corrosion scales.These corrosion scales became more stable than the ones that formed in the AR treated with Cl_2 alone.O_3/Cl_2 disinfection inhibited corrosion and iron release efficiently by changing the content of corrosion-related bacteria.Moreover,ozone disinfection inactivated or damaged the opportunistic pathogens due to its strong oxidizing properties.The damaged bacteria resulting from initial ozone treatment were inactivated by the subsequent chlorine disinfection.Compared with the AR treated with Cl_2 alone,the opportunistic pathogens M.avium and L.pneumophila were not detectable in effluents of the AR treated with O_3/Cl_2,and decreased to(4.60 ± 0.14) and(3.09 ± 0.12) log10(gene copies/g corrosion scales) in biofilms,respectively.The amoeba counts were also lower in the AR treated with O_3/Cl_2.Therefore,O_3/C_l2 disinfection can effectively control opportunistic pathogens in effluents and biofilms of an AR used as a model for a drinking water distribution system.     

Simultaneous removal of arsenic and antimony from mining wastewater using granular TiO2: Batch and field column studies

Coexisting arsenic (As) and antimony (Sb) in mining wastewater is a common and great concern. On-site simultaneous removal of As and Sb from mining wastewater was achieved by using a reusable granular TiO₂ column in this study. To evaluate the accuracy of the scale-up procedure, As and Sb adsorption from wastewater was studied in both large (600 g TiO₂) and small columns (12 g TiO₂) based on the proportional diffusivity rapid small-scale column tests (PD-RSSCTs) design. The comparable As and Sb breakthrough curves obtained from small and large columns confirmed the accuracy of the PD-RSSCT theory in the design of large-scale columns. Meanwhile, the consistent As and Sb adsorption results from batch and column experiments suggested that TiO₂ adsorption for As and Sb can be predicted from bench-scale tests. Charge distribution multi-site complexation (CD-MUSIC) and one-dimensional transport modeling integrated in the PHREEQC program were performed to study the adsorption behaviors of As and Sb on the TiO₂ surface. Coexisting ions, such as Ca^2 +, Mg^2 +, and Si^4 +, play an important role in As and Sb adsorption, and the breakthrough curves were well simulated after considering the compound ion effects. The results from this study highlight the surface reactions of As and Sb on TiO₂ and provide a practical way for on-site remediation of industrial wastewater.     

Lodging in rice can be alleviated by atmospheric CO2 enrichment

The projected increase of atmospheric CO₂ concentration [CO₂] is expected to increase yield of agricultural C₃ crops, but little is known about effects of [CO₂] on lodging that can reduce yield. This study examined the interaction between [CO₂] and nitrogen (N) fertilization on the lodging of rice (Oryza sativa L.) using free-air CO₂ enrichment (FACE) systems installed in paddy fields at Shizukuishi, Iwate, Japan (39°38′N, 140°57′E). Rice plants were grown under two levels of [CO₂] (ambient = 365 μmol mol⁻¹; elevated [CO₂] = 548 μmol mol⁻¹) and three N fertilization regimes: a single initial basal application of controlled-release urea (8 g N m⁻², CRN), split fertilization with a standard amount of ammonium sulfate (9 g N m⁻², MN), and ample N (15 g N m⁻², HN). Lodging score (six ranks at 18° intervals, with larger scores indicating greater bending), yield, and yield components were measured at maturity. The lodging score was significantly higher under HN than under CRN and MN, but lodging was alleviated by elevated [CO₂] under HN. This alleviation was associated with the shortened and thickened lower internodes, but was not associated with a change in the plant's mass moment around the culm base. A positively significant correlation between lodging score and ripening percentage indicated that ripening percentage decreased by 4.5% per one-unit increase in lodging score. These findings will be useful to develop functional algorithm that can be incorporated into mechanistic crop models to predict rice production more accurately in a changing climate and with different cultural practices.     

Thermodynamics of NaHCO3 decomposition during Na2CO3-based CO2 capture

Amine-basedcarbon-capture technologies have been shown to be energetically expensive and to cause significant environmental and epidemiological impacts due to their volatility.Bicarbonate formation from carbon dioxide's reaction with water has been suggested as an effective alternative for capturing CO_2;however,the thermodynamics of this reaction are not well understood.This study experimentally determined the equilibrium constant of sodium bicarbonate(Na HCO_3)decomposition to sodium,water,and carbon dioxide;the study also compared the equilibrium constant to theoretical calculations.Using a combination of experimentation and thermodynamic relationships,the unitless equilibrium constants of the forward and reverse reactions were calculated accurately(error±9%and±4%,respectively).Equilibrium data were calculated using enthalpy and entropy values of each component of Na HCO_3decomposition at temperatures ranging from 25 to 155°C respectively.These results offer more data essential to optimizing Na HCO_3use in environmentally friendly nextgeneration CO_2-capture technologies.     

Adsorption of carbon dioxide on amine-modified TiO2 nanotubes

TiO2 nanotubes (TiNT) were prepared by a hydrothermal treatment and modified by three kinds of amines,namely ethylenediamine,polyetherimide and tetraethylenepentamine (TEPA),to study their CO2 adsorption properties from gas streams.The resultant samples were characterized by X-ray diffraction,transmission electron microscopy,and infrared spectroscopy,as well as low temperature N 2 adsorption.CO2 capture was investigated in a dynamic packed column at 30℃.TEPA-modified TiO2 nanotubes showed the highest adsorption capacity of 167.64 mg/g because it had the highest amino-group content among the three amines.CO2 fixation on TiNT impregnated by TEPA was investigated at 30,50,and 70℃,and the adsorption capacity increased slightly with temperature.Following the adsorption step,the sorbents were regenerated by temperature programmed desorption,and the TiNT-TEPA sample,as CO2 sorbent,was found to be readily regenerated and energy-efficient.The cycle test also revealed that the TiNT-TEPA adsorbent is fairly stable,with only a 5% drop in the adsorption capacity after 10 adsorption/desorption cycles.In addition,the CO2 adsorption behavior was investigated with the deactivation model,and which showed an excellent prediction for the TiNT-TEPA breakthrough curves.     

Yield formation of CO2-enriched inter-subspecific hybrid rice cultivar Liangyoupeijiu under fully open-air field condition in a warm sub-tropical climate

Hybrid rice (Oryza sativa L.) cultivars play an important role in rice production due to its heterosis, resistance to environmental stress and high yield potential. However, no attention has been given to its yield responses to rising atmospheric CO₂ concentration ([CO₂]). To address this need, we conducted a Free Air CO₂ Enrichment (FACE) experiment at Yangzhou, Jiangsu, China, in 2004–2006. A two-line inter-subspecific hybrid rice variety Liangyoupeijiu, recently bred in China, was grown at ambient or elevated (c. 570 μmol mol^?1) [CO₂] under two levels of nitrogen (N) application (12.5 and 25 g N m^?2). Elevated [CO₂] slightly accelerated phenological development (1–2 days), and substantially enhanced grain yield (+30%). The magnitude of yield response to [CO₂] was independent of N fertilization, but greatly varied among years. On average, elevated [CO₂] increased panicle number per unit land area by 8%, due to an increase in maximum tiller number under FACE, while productive tiller ratio remained unaffected. Spikelet number per panicle showed an average increase of 10% due to elevated [CO₂], which was also supported by increased plant height and dry weight per stem. Meanwhile, Elevated [CO₂] caused a significant enhancement in both filled spikelet percentage (+5%) and individual grain mass (+4%). Compared with previous rice FACE studies, this hybrid cultivar appears to profit much more from elevated [CO₂] than inbred japonica cultivars (c. +13%), not only due to its stronger sink generation, but also enhanced capacity to utilize the carbon sources in a high [CO₂] environment. As sufficient intraspecific variation in yield response exists under field conditions, there is a pressing need to identify genotypes which would produce maximum grain yield under projected future [CO₂] levels.     

树脂基固态胺吸附剂室温下对低浓度CO2的吸附性能研究

以大孔甲基丙烯酸酯吸附树脂为载体,聚乙烯亚胺(PEI)为有机胺,采用液相浸渍法制备出固态胺吸附剂,并研究了其在室温下对低浓度CO2的吸附行为.同时,利用氮气吸附、热重分析和扫描电镜表征了材料的物理化学性质,并采用热重法和固定床吸附法考察了材料的CO2吸附性能.结果表明,大孔树脂担载50%PEI(质量分数)时吸附性能最佳,对纯CO2的最大吸附量为175 mg·g-1;CO2的吸附行为由扩散动力学与吸附热力学共同决定,低温有利于提高吸附容量;吸附剂对400 ppm~15%浓度的CO2都具有优异的动态吸附性能,其中对400 ppm CO2的吸附量达到86 mg·g-1,对15%CO2的吸附量达到150 mg·g-1;湿度对吸附起促进作用,相对湿度为10%时,对400 ppm CO2的吸附量提高至139mg·g-1;吸附剂具有优异的循环性能,具有直接空气捕集CO2的潜力.     

Sorbents with high efficiency for CO2 capture based on amines-supported carbon for biogas upgrading

Sorbents for CO_2 capture have been prepared by wet impregnation of a commercial active carbon(Ketjen-black, Akzo Nobel) with two CO_2-philic compounds, polyethylenimine(PEI)and tetraethylenepentamine(TEPA), respectively. The effects of amine amount(from 10 to70 wt.%), CO_2 concentration in the feed, sorption temperature and gas hourly space velocity on the CO_2 capture performance have been investigated. The sorption capacity has been evaluated using the breakthrough method, with a fixed bed reactor equipped with on line gas chromatograph. The samples have been characterized by N_2 adsorption–desorption,scanning electron microscopy and energy dispersive X-ray(SEM/EDX). A promising CO_2 sorption capacity of 6.90 mmol/gsorbenthas been obtained with 70 wt.% of supported TEPA at 70℃ under a stream containing 80 vol% of CO_2. Sorption tests, carried out with simulated biogas compositions(CH_4/CO_2mixtures), have revealed an appreciable CO_2 separation selectivity; stable performance was maintained for 20 adsorption–desorption cycles.     

Modeling increased demand of energy for air conditioners and consequent CO2 emissions to minimize health risks due to climate change in India

Developing countries situated mostly in latitudes that are projected for the highest climate change impact in the twenty-first century will also have a predictable increase in demand on energy sources. India presents us with a unique opportunity to study this phenomenon in a large developing country. This study finds that climate adaptation policies of India should consider the significance of air conditioners (A/Cs) in mitigation of human vulnerability due to unpredictable weather events such as heat waves. However, the energy demand due to air conditioning usage alone will be in the range of an extra ～750,000 GWh to ～1,350,000 GWh with a 3.7 °C increase in surface temperatures under different population scenarios and increasing incomes by the year 2100. We project that residential A/C usage by 2100 will result in CO₂ emissions of 592 Tg to 1064 Tg. This is significant given that India's total contribution to global CO₂ emissions in 2009 was measured at 1670 Tg and country's residential and commercial electricity consumption in 2007 was estimated at 145,000 GWh.     

Fertilization trajectory of the root crop Raphanus sativus across atmospheric pCO2 estimates of the next 300 years

Plant biomass is known to increase in response to elevated atmospheric CO₂ concentration (pCO₂); however, no experiments have quantified the trajectory of crop fertilization across the full range of pCO₂ levels estimated for the next 300 years. Here we quantify the above- and below-ground biomass response of Raphanus sativus (common radish) across eight pCO₂ levels ranging from 348 to 1791 ppmv. We observed a large net biomass increase of 58% above ground and 279% below ground. A large part of the net increase (38% of the above-ground and 53% of the below-ground) represented biomass fertilization at the high levels of pCO₂ (700–1791 ppmv) predicted if fossil fuel emissions continue unabated. The trajectory of below-ground fertilization in R. sativus greatly exceeded a trajectory based on extrapolation of previous experiments for plants grown at pCO₂ < 800 ppmv. Based on the experimental parameters used to grow these plants, we hypothesize that these experiments represent the maximum CO₂ fertilization that can be achieved for this plant growing under low light levels. If the below-ground biomass enhancement that we have quantified for R. sativus represents a generalized root-crop response that can be extrapolated to agricultural systems, below-ground fertilization under very high pCO₂ levels could dramatically augment crop production in some of the poorest nations of the world, provided that water resources are sufficient and sustainable.     

Efficient nitrogen doped porous carbonaceous CO2 adsorbents based on lotus leaf

In this work, the waste biomass lotus leaf was converted into N-doped porous carbonaceous CO₂ adsorbents. The synthesis process includes carbonization of lotus leaf, melamine post-treatment and KOH activation. For the resultant sorbents, high nitrogen content can be contained due to the melamine modification and advanced porous structure were formed by KOH etching. These samples were carefully characterized by different techniques and their CO₂ adsorption properties were investigated in detail. These sorbents hold good CO₂ adsorption abilities, up to 3.87 and 5.89 mmol/g at 25 and 0°C under 1 bar, respectively. By thorough investigation, the combined interplay of N content and narrow microporous volume was found to be responsible for the CO₂ uptake for this series of sorbents. Together with the high CO₂ adsorption abilities, these carbons also display excellent reversibility, high CO₂/N₂ selectivity, applicable heat of adsorption, fast CO₂ adsorption kinetics and good dynamic CO₂ adsorption capacity. This study reveals a universal method of obtaining N-doped porous carbonaceous sorbents from leaves. The low cost of raw materials accompanied by easy synthesis procedure disclose the enormous potential of leaves-based carbons in CO₂ capture as well as many other applications.     

Comparison of absorption rates and absorption capacity of ammonia solvents with MEA and MDEA aqueous blends for CO2 capture

In this work we present the experimental results of absorption rates and absorption capacity for the CO₂ absorption by ammonia (NH₃) aqueous solutions. Experiments are carried out in a thermoregulated Lewis-type cell reactor and are achieved in temperature and concentration ranges of 278–303 K and 2–5wt.% NH₃ respectively. The obtained values for absorption kinetic rates and absorption capacity are compared with those available for alkanolamine solvents, commonly used to absorb CO₂. In order to achieve this comparison, data available in studies about alkanolamine solvents at 303–333 K and 5–50wt.% for alkanolamines solutions were considered. Results show that CO₂ absorption by NH₃ is faster than the one carried out by MDEA, except for 2wt.% NH₃ at 288 K. At 278 K and using aqueous solutions of 3wt.% NH₃, the absorption rate is almost identical to the one reached with MDEA solvent. The highest absorption capacity, also compared with alkanolamine solution, is reached with aqueous solutions of 5wt.% NH₃ at 278 K and 303 K.     

土壤硝化和反硝化微生物群落及活性对大气CO2浓度和温度升高的响应

硝化和反硝化微生物参与土壤氮循环转化过程,大气CO_2浓度和温度升高可能会影响它们的群落结构和活性.本试验依托稻-麦轮作农田系统气候变化平台研究大气CO_2浓度单独升高(CE)、升温(WA)以及两者同时升高(CW)对麦田土壤硝化和反硝化微生物基因丰度、群落结构和活性的影响.结果表明,在小麦分蘖期,大气CO_2浓度和温度升高对氨氧化细菌(AOB)和反硝化细菌丰度没有影响,而在抽穗和成熟期,CO_2浓度单独升高显著提高了氨氧化古菌(AOA)和反硝化细菌丰度,升温处理对其没有显著影响.通过对T-RFLP数据分析发现,大气CO_2浓度和温度升高对土壤AOA、AOB和反硝化细菌群落结构没有显著影响,但是在一定程度上改变了AOA和反硝化细菌多样性.另外,CO_2浓度单独升高处理显著提高了成熟期的土壤硝化速率,不同气候变化处理对反硝化速率没有显著影响.研究表明大气CO_2浓度和温度升高对不同生育期的微生物群落影响存在差异,而且功能微生物对不同气候变化因子处理的响应也各不相同.     

Hollow TiO2 spheres with improved visible light photocatalytic activity synergistically enhanced by multi-stimulative: Morphology advantage, carbonate-doping and the induced Ti3 +

Great efforts have been devoted to improve the photocatalytic activity of TiO_2 in the visible light region. Rational design of the external structure and adjustment of intrinsic electronic status by impurity doping are two main effective ways to achieve this purpose. A facile onepot synthetic approach was developed to prepare C-doped hollow TiO_2 spheres, which simultaneously realized these advantages. The synthesized TiO_2 exhibits a mesoporous hollow spherical structure composed of fine nanocrystals, leading to high specific surface area(~180 m~2/g) and versatile porous texture. Carbonate-doping was achieved by a postthermal treatment at a relatively low temperature(200°C), which makes the absorption edge red-shifted to the visible region of the solar spectrum. Concomitantly, Ti~(3+) induced by C-doping also functions in improving the visible-light photocatalytic activity by reducing the band gap. There exists a synergistic effect from multiple stimulatives to enhance the photocatalytic effect of the prepared TiO_2 catalyst. It is not out of expectation that the asprepared C-doped hollow TiO_2 spheres exhibits an improved photocatalytic activity under visible light irradiation in organic pollutant degradation.     

Protecting the photosynthetic performance of snap bean under free air ozone exposure

Tropospheric ozone(O_3) is a major air pollutant and causes serious injury to vegetation. To protect sensitive plants from O_3 damage, several agrochemicals have been assessed,including cytokinin(e.g., kinetin, KIN) and ethylenediurea(EDU) with cytokinin-like activity.In higher plant, leaves are primarily injured by O_3 and protective agrochemicals are often applied by leaf spraying. To our knowledge, the mitigating abilities of EDU and KIN have not been compared directly in a realistic setup. In the present research, impacts of elevated O3(2 × ambient O_3, 24 hr per day, for 8 days) on an O_3 sensitive line(S156) of snap bean(Phaseolus vulgaris), which is often used for biomonitoring O_3 pollution, were studied in a free air controlled exposure system. The day before starting the O_3 exposure, plants were sprayed with a solution of EDU(300 ppm), KIN(1 mmol/L) or distilled water, to compare their protective abilities. The results demonstrated that 2 × ambient O_3 inhibited net photosynthetic rate and stomatal conductance, increased the minimal fluorescence yield of the dark-adapted state, decreased the maximal quantum yield of PSII photochemistry, and led to visible injury. KIN and EDU alleviated the reduction of the photosynthetic performance, and visible injury under O_3 fumigation. The plants sprayed with EDU showed greater ability to mitigate the O_3 damage than those sprayed with KIN. Chlorophyll fluorescence imaging may have detected more precisely the differences in O_3 response across the leaf than the conventional fluorometer.     

污泥与煤在CO2/O2及N2/O2气氛条件下的混燃特性分析

采集了广州具有代表性的市政污泥,利用热重法对单一污泥、煤及其混合样品在CO_2/O_2及N_2/O_2气氛条件下进行了TG(热重)实验,同时计算了污泥和煤的4个燃烧特性指数,获得了燃烧的动力学参数.实验结果表明,污泥燃烧有4个燃烧阶段,包括水分析出、挥发分析出与燃烧、固定碳的燃烧和无机盐类挥发分解,其中,挥发分析出与燃烧是污泥燃烧的主要阶段;煤掺烧污泥可以提高煤的着火性能.在CO_2/O_2及N_2/O_2燃烧气氛下,增加O_2浓度,污泥与煤混合样的热重曲线整体向低温区移动,微商热重曲线峰值增大,峰宽变小,燃烧性能增强.在CO_2/O_2气氛下,O_2浓度从30%增加到60%时,污泥的挥发分释放特性指数D、可燃性指数C、燃尽指数Cb、综合燃烧特性指数S分别增加了45%、12%、18%、6%.相同O_2浓度条件下,污泥与煤在CO_2/O_2气氛下的着火性能较N_2/O_2气氛滞后,最大峰值变小,高浓度的CO_2抑制其混合样的燃烧.采用Coats-Redfern方程计算得到3个燃烧阶段反应的动力学参数,其中,增加O_2浓度,污泥与煤混合样品的质量平均表观反应活化能Em减小,并且O_2浓度越高越有利于燃烧反应的进行.污泥与煤混合燃烧取n=2可以对挥发分燃烧与固定碳燃尽峰峰前与峰后的反应模型进行描述.     

Mitigation of greenhouse gas emissions by anaerobic digestion of cattle slurry

Biogas treatment of animal manures is an upcoming technology because it is a way of producing renewable energy (biogas). However, little is known about effects of this management strategy on greenhouse gas (GHG) emissions during fermentation, storage, and field application of the substrates compared to untreated slurries. In this study, we compared cattle slurry and cattle slurry with potato starch as additive during the process of fermentation, during storage and after field application. The addition of potato starch strongly enhanced CH₄ production from 4230 l CH₄ m⁻³ to 8625 l CH₄ m⁻³ in the fermenter at a hydraulic retention time (HRT) of 29 days. Extending the HRT to 56 days had only a small effect on the CH₄ production. Methane emissions from stored slurry depended on storage temperature and were highest from unfermented slurry followed by the slurry/starch mixture. Gas emissions from untreated and fermented slurry during storage were further analyzed in a pilot-scale experiment with different levels of covering such as straw cover, a wooden lid and no cover. Emissions of greenhouse gases (CH₄, N₂O, NH₃) were in the range of 14.3–17.1 kg CO₂ eq. m⁻³ during winter (100 day storage period) and 40.5–90.5 kg CO₂ eq. m⁻³ during summer (140 day storage period). A straw cover reduced NH₃ losses, but not overall GHG emissions, whereas a solid cover reduced CH₄ and NH₃ emissions. After field application, there were no significant differences between slurry types in GHG emissions (4.15–8.12 kg CO₂ eq. m⁻³ a⁻¹). GHG emissions from slurry stores were more important than emissions after field application. Co-digestion of slurry with additives such as starch has a large potential to substitute fossil energy by biogas. On a biogas plant, slurry stores should be covered gas-tight in order to eliminate GHG emissions and collect CH₄ for electricity production.