CO2 emissions from tropical drained peat in Sumatra,Indonesia

With the increasing use of tropical peatland for agricultural development, documentation of the rate of carbon dioxide (CO₂) emissions is becoming important for national greenhouse gas inventories. The objective of this study was to evaluate soil-surface CO₂ fluxes from drained peat under different land-use systems in Riau and Jambi Provinces, Sumatra, Indonesia. Increase of CO₂ concentration was tracked in measurement chambers using an Infrared Gas Analyzer (IRGA, LI-COR 820 model). The results showed that CO₂ flux under oil palm (Elaeis guineensis) plantations ranged from 34?±?16 and 45?±?25 Mg CO₂ ha^–1 year^–1 in two locations in Jambi province to 66?±?25 Mg CO₂ ha^–1 year^–1 for a site in Riau. For adjacent plots within 3.2 km in the Kampar Peninsula, Riau, CO₂ fluxes from an oil palm plantation, an Acacia plantation, a secondary forest and a rubber plantation were 66?±?25, 59?±?19, 61?±?25, 52?±?17 Mg ha^–1 year^–1, respectively, while on bare land sites it was between 56?±?30 and 67?±?24 Mg CO₂ ha^–1 year^–1, indicating no significant differences among the different land-use systems in the same landscape. Unexplained site variation seems to dominate over land use in influencing CO₂ flux. CO₂ fluxes varied with time of day (p?<?0.001) with the noon flux as the highest, suggesting an overestimate of the mean flux values with the absence of night-time measurements. In general, CO₂ flux increased with the depth of water table, suggesting the importance of keeping the peat as wet as possible.     

A metal-OH group modification strategy to prepare highly-hydrophobic MIL-53-Al for efficient acetone capture under humid conditions

A series of highly-hydrophobic MIL-53-Al (MIL = Materials of Institut Lavoisier) frameworks synthesized via decoration of the Al-OH groups by alkyl phosphonic acid were developed as adsorbents for removing acetone from humid gas streams. The newly prepared materials were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), N₂ adsorption-desorption and thermogravimetric analysis (TGA). Their adsorption behaviors toward acetone vapor under dry and wet conditions were studied subsequently. Results showed that alkyl phosphonic acid was successfully grafted into MIL-53-Al skeleton through coordinating interaction with Al³⁺ generating [email protected]_x (x = 12, 14, 18). The [email protected]_x exhibited similar crystal structure and thermal stability to parent MIL-53-Al. Furthermore, the modified materials showed significantly enhanced hydrophobicity. The water vapor uptake of [email protected]₁₄ decreased by 72.55% at 75% relative humidity (RH). Dynamic adsorption experiments demonstrated that water vapor had almost no effect on the acetone adsorption performance of [email protected]₁₄. Under the condition of 90% RH, the acetone adsorption capacity of [email protected]₁₄ was 102.98% higher than that of MIL-53-Al. Notably, [email protected]₁₄ presented excellent adsorption reversibility and regeneration performance in 10 adsorption-desorption cycles. Taken together, the strategy of metal-OH group modification is an attractive way to improve the acetone adsorption performance over metal-organic frameworks (MOFs) under humid conditions. Besides, [email protected]₁₄ would be deemed as a promising candidate for capturing acetone in high moisture environment.     

Mediterranean shrublands carbon sequestration: environmental and economic benefits

To date, only a few attempts have been done to estimate the contribution of Mediterranean ecosystems to the global carbon cycle. Within this context, shrub species, composition and structure of the Mediterranean shrublands developing along the Latium coast (Italy) were analyzed in order to evaluate their contribution to carbon (C) sequestration, also taking into consideration the economic benefits at a national level. The considered shrublands had a shrub density of 1,200?±?500 shrubs ha^?1. Shrubs were classified into small (S), medium (M) and large (L), according to their volume (V) and leaf area index (LAI). The total yearly carbon dioxide (CO₂) sequestration per species (SC_y) was calculated multiplying the total photosynthetic leaf surface area (spt) of each species by the mean yearly photosynthetic rate and the total yearly photosynthetic activity time (in hours). Q. ilex and A. unedo had the highest SC_y (46.2?±?15.8 kg CO₂ year^?1, mean value), followed by P. latifolia (17.5?±?6.2 kg CO₂ year^?1), E. arborea, E. multiflora, C. incanus, P. lentiscus, R. officinalis, and S. aspera (6.8?±?4.2 kg CO₂ year^?1, mean value). The total yearly CO₂ sequestration per shrub (SC_shy) was 149?±?5 kg CO₂ year^?1 in L, decreasing 30 % in M and 80 % in S shrubs. Taking into account the frequency of S, M and L and their SC_shy, the total CO₂ sequestration of the Mediterranean maquis was quantified in 80 Mg CO₂ ha^?1?year^?1, corresponding to 22 Mg C ha^?1?year^?1. From a monetary viewpoint, this quantity could be valued to more than 500 US$ ha^?1?year^?1. Extending this benefit to the Mediterranean shrublands throughout the whole country, we obtained a nationwide estimated annual benefit in the order of $500 million.     

Structures and catalytic performances of Me/SAPO-34 (Me = Mn, Ni, Co) catalysts for low-tem perature SCR of NOx by ammonia

Me/SAPO-34 (Me = Mn, Ni, Co) series of catalysts were prepared by a wetness impregnation method and investigated for the selective catalytic reduction of nitrogen oxides with ammonia (NH₃-SCR). Among them, Mn/SAPO-34 catalyst was found as the most promising candidate based on its superior low-temperature activity. The catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy images (TEM), nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), temperature programmed reduction and desorption (TPR and TPD), and diffuse reflectance infrared Fourier transformed spectroscopy (DRIFTS) of NH₃/NO_x adsorption. Mn/SAPO-34 is obviously different from Ni/SAPO-34 and Co/SAPO-34 in the active species state and distribution. Surface MnO_x species which play an essential role in NO oxidation and NO₂ adsorption, act as better active sites than nickel and cobalt mostly in the form of the aluminates and silicates.     

Root- and peat-based CO2 emissions from oil palm plantations

Measured carbon dioxide (CO₂) flux from peat soils using the closed chamber technique combines root-related (autotrophic + heterotrophic where rhizosphere organisms are involved) and peat-based (heterotrophic) respiration. The latter contributes to peat loss while the former is linked to recent CO₂ removal through photosynthesis. The objective of this study was to separate root- from peat-based respiration. The study was conducted on peatland under 6 and 15 year old oil palm (Elaeis guineensis Jacq.) plantations in Jambi Province, Indonesia in 2011 to 2012. CO₂ emissions were measured in the field from 25 cm diameter and 25 cm tall closed chambers using an infrared gas analyser. Root sampling and CO₂ emissions measurements were at distances of 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, and 4.5 m from the centre of the base of the palm tree. The emission rate for the six and 15 year old oil palm plantations at ≥3.0 m from the centre of the tree were 38.2?±?9.5 and 34.1?±?15.9 Mg CO₂ ha^?1 yr^?1, respectively. At distances <2.5 m, total respiration linearly decreased with distances from the trees. Heterotrophic respirations were 86 % of the 44.7?±?11.2 and 71 % of 47.8?±?21.3 Mg CO₂ ha^?1 yr^?1 of weighted surface flux, respectively for the 6 and 15 year old plantations. We propose that CO₂ flux measurements in oil palm plantations made at a distance of ≥3 m from the tree centre be used to represent the heterotrophic respiration that is relevant for the environmental impact assessment.     

Capture of carbon dioxide from flue gas on TEPA-grafted metal-organic framework Mg2(dobdc)

Carbon dioxide （CO2） adsorption on a standard metal-organic framework Mg2（dobdc） （Mg/DOBDC or Mg-MOF-74） and a tetraethylenepentamine （TEPA） modified Mgz（dobdc） （TEPA-Mg/DOBDC） were investigated and compared. The structural information, surface chemistry and thermal behavior of the adsorbent samples were characterized by X-ray powder diffraction （XRD）, infrared spectroscopy （IR）, thermogravimetric analysis （TGA） and nitrogen adsorption-desorption isotherm analysis. CO2 adsorption capacity was measured by dynamic adsorption experiments with N2-CO2 mixed gases at 60℃. Results showed that the CO2 adsorption capacity of Mg/DOBDC was significantly improved after amine modification, with an increase from 2.67 to 6.06 mmol CO2/g adsorbent. Moreover, CO2 adsorption on the TEPA-Mg/DOBDC adsorbent was promoted by water vapor, and the adsorption capacity was enhanced to 8.31 mmol CO2/g absorbent. The adsorption capacity of the TEPA-Mg/DOBDC adsorbent dropped only 3% after 5 consecutive adsorption]desorption cycles. Therefore, this kind of adsorbent can be considered as a promising material for the capture of CO2 from flue gas.     

Improvement of the activity and SO2 tolerance of Sb-modified Mn/PG catalysts for NH3-SCR at a low temperature

A series of MnM/palygorskite (PG) (M = La, W, Mo, Sb, Mg) catalysts was prepared by the wetness co-impregnation method for low-temperature selective catalytic reduction (SCR) of NO with NH₃. Conversion efficiency followed the order Sb > Mo > La > W > Mg. A combination of various physico-chemical techniques was used to investigate the influence of Sb-modified Mn/PG catalysts. MnSb_0.156/PG catalyst showed highest NO conversion at low temperatures in the presence of SO₂ which reveals that addition of Sb oxides effectively enhances the SCR activity of catalysts. A SO₂ step-wise study showed that MnSb_0.156/PG catalyst displays higher durable resistance to SO₂ than Mn/PG catalyst, where the sulfating of active phase is greatly inhibited after Sb doping. Scanning electron microscopy and X-ray diffraction results showed that Sb loading enhances the dispersion of Mn oxides on the carrier surface. According to the results of characterization analyses, it is suggested that the main reason for the deactivation of Mn/PG is the formation of manganese sulfates which cause the permanent deactivation of Mn-based catalysts. For Sb-doped Mn/PG catalyst, SO_x ad-species formed were mainly combined with SbO_x rather than MnO_x. This preferential interaction between SbO_x and SO₂ effectively shields the MnO_x as active species from being sulfated by SO₂ resulting in the improvement of SO₂ tolerance on Sb-added catalyst. Multiple information support that, owing to the addition of Sb, original formed MnO_x crystallite has been completely transformed into highly dispersed amorphous phase accounting for higher SCR activity.     

Eutectic mixture promoted CO2 sorption on MgO-TiO2 composite at elevated temperature

The development of carbon dioxide(CO_2) sorbents that can operate at elevated temperatures is significant for the advancement of pre-combustion capture technologies.Recently, promoter-based systems composed of alkali/alkaline earth metal nitrates and/or carbonates have been considered as next-generation solid sorbents due to their improved CO_2 uptake and kinetics. However, obtaining stable MgO sorbents against temperature swing regeneration still remained challenging. Herein, we report MgO-TiO_2 solid sorbents promoted by eutectic mixture(KNO_3 and LiNO_3) for elevated temperature CO_2 sorption. The developed sorbents show improved CO_2 sorption capacity, which may be attributed to the alternative CO_2 sorption pathway provided by the ionization of highly dispersed MgO in the eutectic mixture. The MgO-TiO_2 framework was also shown to assist in retaining the MgO configuration by constraining its interaction with CO_2. Furthermore, it is demonstrated that constructing composite structures is essential to improve the CO_2 sorption characteristics,mainly recyclability, at elevated temperatures. The developed promoter integrated sorbents showed exceptionally high CO_2 sorption capacity of 30 wt.% at an elevated temperature(300°C) with pronounced stability under temperature swing operation.     

Greenhouse gas emission factors for land use and land-use change in Southeast Asian peatlands

Tropical peat swamp forests, which are predominantly located in Southeast Asia (SEA) and play a prominent role as a global carbon store, are being intensively degraded and converted to agricultural lands and tree plantations. For national inventories, updated estimates of peat emissions of greenhouse gases (GHG) from land use (LU) and land-use change in the tropics are required. In this context, we reviewed the scientific literature and calculated emission factors of peat net emissions of carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) in seven representative LU categories for SEA i.e. intact peat swamp forest, degraded forest (logged, drained and affected by fire), mixed croplands and shrublands, rice fields, oil palm, Acacia crassicarpa and sago palm plantations. Peat net CO₂ uptake from or emissions to the atmosphere were assessed using a mass balance approach. The balance included main peat C inputs through litterfall and root mortality and outputs via organic matter mineralization and dissolved organic carbon. Peat net CO₂ loss rate from degraded forest, croplands and shrublands, rice fields, oil palm, A. crassicarpa and sago palm plantations amounted to 19.4?±?9.4, 41.0?±?6.7, 25.6?±?11.5, 29.9?±?10.6, 71.8?±?12.7 and 5.2?±?5.1 Mg CO₂ ha^?1 y^?1, respectively. Total peat GHG losses amounted to 20.9?±?9.4, 43.8?±?6.8, 36.1?±?12.9, 30.4?±?10.6, 72?±?12.8 and 8.6?±?5.3 Mg CO₂-equivalent ha^?1 y^?1 in the same LU categories, respectively. A single land-clearing fire would result in additional emissions of 493.6?±?156.0 Mg CO₂-equivalent ha^?1.     

On-going nitrification in chloraminated drinking water distribution system (DWDS) is conditioned by hydraulics and disinfection strategies

Within the drinking water distribution system (DWDS) using chloramine as disinfectant, nitrification caused by nitrifying bacteria is increasingly becoming a concern as it poses a great challenge for maintaining water quality. To investigate efficient control strategies, operational conditions including hydraulic regimes and disinfectant scenarios were controlled within a flow cell experimental facility. Two test phases were conducted to investigate the effects on the extent of nitrification of three flow rates (Q = 2, 6, and 10 L/min) and four disinfection scenarios (total Cl₂=1 mg/L, Cl₂/NH₃-N=3:1; total Cl₂=1 mg/L, Cl₂/NH₃-N=5:1; total Cl₂=5 mg/L, Cl₂/NH₃-N=3:1; and total Cl₂=5 mg/L, Cl₂/NH₃-N=5:1). Physico-chemical parameters and nitrification indicators were monitored during the tests. The characteristics of biofilm extracellular polymetric substance (EPS) were evaluated after the experiment. The main results from the study indicate that nitrification is affected by hydraulic conditions and the process tends to be severe when the fluid flow transforms from laminar to turbulent (2300<Re<4000). Increasing disinfectant concentration and optimizing Cl₂/NH₃-N mass ratio were found to inhibit nitrification to some extend when the system was running at turbulent condition (Q = 10 L/min, Re = 5535). EPS extracted from biofilm that was established at the flow rate of 6 L/min had greater carbohydrate/protein ratio. Furthermore, several nitrification indicators were evaluated for their prediction efficiency and the results suggest that the change of nitrite, together with total organic carbon (TOC) and turbidity can indicate nitrification potential efficiently.     

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.     

Impacts of land use,restoration, and climate change on tropical peat carbon stocks in the twenty-first century: implications for climate mitigation

The climate mitigation potential of tropical peatlands has gained increased attention as Southeast Asian peatlands are being deforested, drained and burned at very high rates, causing globally significant carbon dioxide (CO₂) emissions to the atmosphere. We used a process-based dynamic tropical peatland model to explore peat carbon (C) dynamics of several management scenarios within the context of simulated twenty-first century climate change. Simulations of all scenarios with land use, including restoration, indicated net C losses over the twenty-first century ranging from 10 to 100 % of pre-disturbance values. Fire can be the dominant C-loss pathway, particularly in the drier climate scenario we tested. Simulated 100 years of oil palm (Elaeis guineensis) cultivation with an initial prescribed burn resulted in 2400–3000 Mg CO₂?ha^?1 total emissions. Simulated restoration following one 25-year oil palm rotation reduced total emissions to 440–1200 Mg CO₂?ha^?1, depending on climate. These results suggest that even under a very optimistic scenario of hydrological and forest restoration and the wettest climate regime, only about one third of the peat C lost to the atmosphere from 25 years of oil palm cultivation can be recovered in the following 75 years if the site is restored. Emissions from a simulated land degradation scenario were most sensitive to climate, with total emissions ranging from 230 to 10,600 Mg CO₂?ha^?1 over 100 years for the wettest and driest dry season scenarios, respectively. The large difference was driven by increased fire probability. Therefore, peat fire suppression is an effective management tool to maintain tropical peatland C stocks in the near term and should be a high priority for climate mitigation efforts. In total, we estimate emissions from current cleared peatlands and peatlands converted to oil palm in Southeast Asia to be 8.7 Gt CO₂ over 100 years with a moderate twenty-first century climate. These emissions could be minimized by effective fire suppression and hydrological restoration.     

Government environmental control measures on CO2 emission during the 2014 Youth Olympic Games in Nanjing: Perspectives from a top-down approach

Strict air pollution control measures were conducted during the Youth Olympic Games（YOG） period at Nanjing city and surrounding areas in August 2014.This event provides a unique chance to evaluate the effect of government control measures on regional atmospheric pollution and greenhouse gas emissions.Many previous studies have observed significant reductions of atmospheric pollution species and improvement in air quality,while no study has quantified its synergism on anthropogenic CO₂...     

Is CO2 flux from oil palm plantations on peatland controlled by soil moisture and/or soil and air temperatures?

Measurements of carbon dioxide (CO₂) flux at the soil surface of oil palm (Elaeis guineensis Jacq.) plantations on peatlands typically exhibit considerable temporal and spatial variation, which challenges the derivation of emission factors required in land use discussions. We tested 20 cm surface soil moisture content, and the diurnal patterns in soil and air temperatures as CO₂ flux controls during an annual measurement schedule in a 15-year-old oil palm plantation in Jambi Province, Sumatra, Indonesia. A total of 480 CO₂ flux measurements were obtained using an Infrared Gas Analyser (IRGA) at six different time intervals each day. Samples were recorded at 20 observation points distributed along four transects located 15, 42, 50, 70, and 84 m from the edge of the drainage canal. Results showed CO₂ flux exhibited no relationship to soil and air temperature, however values tended to increase with volumetric soil moisture content; the highest annual flux of 55 Mg ha^?1 yr^?1 was observed at mid-day, when air temperature was highest, and lowest at dawn when soil and air temperatures were lowest. CO₂ flux decreased consistent with distance from the drainage canal, suggesting a higher flux with a deeper water table. This result indicates a shallow water table must be maintained. The annual mean CO₂ flux of 46?±?30 Mg CO₂ ha^?1 yr^?1 was comparable to other studies, and can be set as a baseline emissions factor for areas with similar land use and peat characteristics.     

Survival of Norovirus Surrogate on Various Food-Contact Surfaces

Norovirus (NoV) is an environmental threat to humans, which spreads easily from one infected person to another, causing foodborne and waterborne diseases. Therefore, precautions against NoV infection are important in the preparation of food. The aim of this study was to investigate the survival of murine norovirus (MNV), as a NoV surrogate, on six different food-contact surfaces: ceramic, wood, rubber, glass, stainless steel, and plastic. We inoculated 10⁵ PFU of MNV onto the six different surface coupons that were then kept at room temperature for 28 days. On the food-contact surfaces, the greatest reduction in MNV was 2.28 log₁₀ PFU/coupon, observed on stainless steel, while the lowest MNV reduction was 1.29 log₁₀ PFU/coupon, observed on wood. The rank order of MNV reduction, from highest to lowest, was stainless steel, plastic, rubber, glass, ceramic, and wood. The values of d _R (time required to reduce the virus by 90 %) on survival plots of MNV determined by a modified Weibull model were 277.60 h (R ² = 0.99) on ceramic, 492.59 h (R ² = 0.98) on wood, 173.56 h on rubber (R ² = 0.98), 97.18 h (R ² = 0.94) on glass, 91.76 h (R ² = 0.97) on stainless steel, and 137.74 h (R ² = 0.97) on plastic. The infectivity of MNV on all food-contact surfaces remained after 28 days. These results show that MNV persists in an infective state on various food-contact surfaces for long periods. This study may provide valuable information for the control of NoV on various food-contact surfaces, in order to prevent foodborne disease.     

CO2 capture performance of bi-functional activated bleaching earth modified with basic-alcoholic solution and functionalization with monoethanolamine: isotherms, kinetics and thermodynamics

CO_2 capture performance of bifunctional activated bleaching earth(ABE) was investigated at atmospheric pressure. The sorbents were characterized by means of X-ray diffraction(XRD), Brunauer–Emmett–Teller(BET), Caron-Hydrogen-Nitrogen analysis(CHN), Fourier transform infrared(FT-IR) and thermal gravimetric analysis(TGA). The CO_2 capacity was enhanced via basic-modification and monoethanolamine(MEA) loading of the ABE sorbent to obtain a bifunctional surface property. Here, basic-modified calcined ABE with a 30 wt.%MEA loading(SAB-30) showed the highest CO_2 capture capacity, but this was decreased with excess MEA loading( 30 wt.%). At a 10%(V/V) initial CO_2 concentration feed, the maximum capacity of SAB-30 increased from 2.71 mmol/g at 30℃(without adding moisture to the feed) to 3.3 mmol/g at 50℃ when adding 10%(V/V) moisture to the feed. Increasing the moisture concentration further reduced the maximum CO_2 capacity due to the blocking effect of the excess moisture on the sorbent surface. However, SAB-30 could completely capture CO_2 even in a 100%(V/V) initial CO_2 concentration feed. A maximum CO_2 capacity of5.7 mmol/g for SAB-30 was achieved at 30℃. Varying the ratio of sorbent weight to total flow rate of the gas stream had no discernible effect on the equilibrium CO_2 capture capacity. Avrami's equation and Toth's isotherm model provided a good fitting for the data and suggested the presence of more than one reaction pathway in the CO_2 capture process and the heterogeneous adsorption surface of SAB-30. Thermodynamics studies revealed that CO_2 capture on the bifunctional SAB-30 is feasible, spontaneous and exothermic in nature.     

Will funding to Reduce Emissions from Deforestation and (forest) Degradation (REDD+) stop conversion of peat swamps to oil palm in orangutan habitat in Tripa in Aceh,Indonesia?

Tripa is the last remaining peat-swamp forest that harbours a potentially viable Sumatran orangutan (Pongo abelii) sub-population in a formally but not effectively protected area. It appears to be a simple showcase where current efforts to financially support reducing emissions from deforestation and forest degradation (REDD+) converge with biodiversity and social co-benefits. In practice, however, situation is more complex. REDD+ efforts interact with global palm oil trade and regulatory approaches (the moratorium) to achieve national goals for emissions reduction under umbrella of nationally appropriate mitigation actions (NAMA). To contextualize this debate, we assessed (i) land-use history and formal basis of palm-oil companies’ rights; (ii) carbon (C) stocks, historical emission levels and potential emissions that can be avoided; (iii) economic benefits of land-use options and opportunity costs of avoiding emissions; (iv) biodiversity and environmental services; and (v) alternative options for “high C stock development” and employment generation. Natural forest cover declined (54 % in 1995, 18 % in 2009) while oil palm increased 4–39 %. Aboveground C stocks decreased from 148 Mg ha^?1 in 1990 to 61 Mg ha^?1 in 2009, leading to average annual emissions of 14.5 Mg (carbon dioxide) CO₂e ha^?1 year^?1. While 41 % of these emissions yield less than American Dollar (USD) 5 of current economic benefits per Mg CO₂e emitted and might be compensated by REDD+, nearly all new emissions derive from a breach of existing laws, regulations and voluntary palm-oil standards. Substantial investment in alternative employment is needed, rather than carbon payments per se, to support livelihoods in a low carbon emissions economy.     

Synthesis of mesoporous Cu/Mg/Fe layered double hydroxide and its adsorption performance for arsenate in aqueous solutions

The mesoporous Cu/Mg/Fe layered double hydroxide(Cu/Mg/Fe-LDH) with carbonate intercalation was synthesized and used for the removal of arsenate from aqueous solutions.The Cu/Mg/Fe-LDH was characterized by Fourier transform infrared spectrometry,X-ray diffraction crystallography,scanning electron microscopy,X-ray photoelectron spectroscopy and Brunauer-Emmett-Teller.Effects of various physico-chemical parameters such as pH,adsorbent dosage,contact time and initial arsenate concentration on the adsorption of arsenate onto Cu/Mg/Fe-LDH were investigated.Results showed that it was efficient for the removal of arsenate,and the removal efficiency of arsenate increased with the increment of the adsorbent dosage,while the arsenate adsorption capacity decreased with increase of initial pH from 3 to 11.The adsorption isotherms can be well described by the Langmuir model with R 2 > 0.99.Its adsorption kinetics followed the pseudo second-order kinetic model.Coexisting ions such as HPO42-,CO32-,SO42and NO3could compete with arsenate for adsorption sites on the Cu/Mg/Fe-LDH.The adsorption of arsenate on the adsorbent can be mainly attributed to the ion exchange process.It was found that the synthesized Cu/Mg/Fe-LDH can reduce the arsenate concentration down to a final level of < 10 μg/L under the experimental conditions,and makes it a potential material for the decontamination of arsenate polluted water.     

磁性Mg/Al-LDHs制备条件对其吸附除磷性能的影响

为提高粉末状水滑石吸附剂的工程应用性,采用共沉淀法制备了磁性Mg/Al水滑石(Layered Double Hydroxides,LDHs).结合XRD、FTIR、SEM及VSM等材料表征结果,考察了制备条件(磁基质投加量、金属物质的量比和层间阴离子)对其吸附除磷性能、磁学性能及结构特征的影响.结果表明,在Fe_3O_4与Mg~(2+)物质的量比为0.02、Mg/Al物质的量比为2∶1和层间阴离子为Cl~-/OH~-的条件下制备出的磁性Mg/Al-LDHs对TP吸附性能最好,平衡吸附量可达49.60 mg·g~(-1);比饱和磁化强度为2.78 emu·g~(-1),能够实现吸附剂的快速高效磁分离回收.层间阴离子种类对水滑石焙烧前后吸附除磷性能有一定的影响:经高温焙烧后,层间含有CO■的水滑石吸磷能力虽有所提高,但仍低于无CO■型LDHs.因此,在水滑石制备过程中避免使用碳酸盐作为共沉碱原料,这样无需焙烧即可获得较高吸磷能力的吸附剂.     

Enhanced activation of peroxydisulfate by strontium modified BiFeO3perovskite for ciprofloxacin degradation

A series of Sr-doped BiFeO₃ perovskites (Bi_1-xSr_xFeO₃, BSFO) fabricated via sol-gel method was applied as peroxydisulfate (PDS) activator for ciprofloxacin (CIP) degradation. Various technologies were used to characterize the morphology and physicochemical features of prepared BSFO samples and the results indicated that Sr was successfully inserted into the perovskites lattice. The catalytic performance of BiFeO₃ was significantly boosted by strontium doping. Specifically, Bi_0.9Sr_0.1FeO₃ (0.1BSFO) exhibited the highest catalytic performance for PDS activation to remove CIP, where 95% of CIP (10 mg/L) could be degraded with the addition of 1 g/L 0.1BSFO and 1 mmol/L PDS within 60 min. Moreover, 0.1BSFO displayed high reusability and stability with lower metal leaching. Weak acidic condition was preferred to neutral and alkaline conditions in 0.1BSFO/PDS system. The boosted catalytic performance can be interpreted as the lower oxidation state of Fe and the existence of affluent oxygen vacancies generated by Sr doping, that induced the formation of singlet oxygen (¹O₂) which was confirmed as the dominant reactive species by radical scavenging studies and electron spin resonance (ESR) tests. The catalytic oxidation mechanism related to major ¹O₂ and minor free radicals was proposed. Current study opens a new avenue to develop effective A-site modified perovskite and expands their application for PDS activation in wastewater remediation.