减氮对华北地区麦玉轮作农田土壤N2O排放调控机理

【目的】探究减氮对华北地区麦玉轮作农田土壤N2O排放调控机制。【方法】冬小麦季和夏玉米季均以不施氮为对照(CK),设置2个施氮量,分别为常规施氮量(纯氮300 kg/hm2,N2)、减氮20%(纯氮240 kg/hm2,N1),研究施氮量对麦玉轮作农田土壤性质及N2O排放通量影响,基于逐步回归分析,研究减氮对麦玉轮作农田土壤N2O排放调控机制。【结果】(1)减氮有效降低了N2O排放通量,且夏玉米季N2O排放通量远高于冬小麦季,夏玉米季由施肥引起的N2O排放量较高。(2)冬小麦季N2O排放通量与环境因子逐步回归公式为:N2O排放通量=181.952+1.450×硝态氮+8.401×铵态氮-0.514×电导率;硝态氮、铵态氮会对冬小麦季N2O排放通量产生显著的正向影响,而电导率会对冬小麦季N2O排放通量产生显著的负向影响。(3)夏玉米季N2O排放通量与环境因子逐步回归公式为:N2O排放通量=-354.606+4.592×硝态氮+157.848×铵态氮;硝态氮、铵态氮会对夏玉米季N2O排放通量产生显著的正向影响。【结论】综上可知,适量减氮显著降低夏玉米季N2O累积排放量和增温潜势,应加强夏玉米季农田水肥管理。

DNDC模型模拟不同施肥水平下旱作麦田土壤N2O排放及其敏感性分析

【目的】研究陇中黄土高原不同施肥水平下旱作麦田土壤N_(2)O的排放特征,验证DNDC模型对N_(2)O排放模拟的适应性。【方法】以甘肃省定西市旱作麦田为对象,设置不施氮肥(0 kg/hm^(2))、低量氮肥(55 kg/hm^(2))、中量氮肥(110 kg/hm^(2))、高量氮肥(220 kg/hm^(2))4种施肥梯度,采用静态箱-气相色谱法对土壤N_(2)O排放通量排放进行田间原位观测。结合试验点连续监测得到的N_(2)O排放通量等实测数据,运用DNDC模型探究多因子对模拟N_(2)O排放的敏感程度。【结果】不同施肥水平下,旱作麦田土壤N_(2)O排放趋势基本一致,且排放通量的大小与施氮量成正相关关系;DNDC模型对4种施肥水平下N_(2)O排放的模拟效果较好,具体表现为不施氮肥(R^(2)=0.88、EF=0.84、P=0.002),低量氮肥(R^(2)=0.92、EF=0.82、P=0.001),中量氮肥(R^(2)=0.86、EF=0.81、P=0.003),高量氮肥(R^(2)=0.84、EF=0.74、P=0.004),表明DNDC模型能够用于模拟不同施肥水平下旱作麦田土壤N_(2)O排放;敏感性分析则显示,相比其他因子,土壤pH值是影响模型模拟N_(2)O排放最为敏感的参数。【结论】为陇中黄土高原旱作麦田N_(2)O排放模型模拟的参数本地化提供基础依据,为今后农田管理措施的优化提供模型基础技术支撑。

High-Resolution Experimental Study on Photodissocaition of N2O

We study the photodissociation dynamics of nitrous oxide using the time-sliced ion veloc- ity imaging technique at three photolysis wavelengths of 134.20, 135.30, and 136.43 nm. The O（^1Sj=0）＋N2（XI∑g＋） product channels were investigated by measuring images of the O（iSj=0） products. Vibrational states of N2（XI∑g＋） products were fully resolved in the images. Product total kinetic energy releases （TKER） and the branching ratios of vibrational states of N2 products were determined. It is found that the most populated vibrational states of N2 products are v--2 and v--3. The angular anisotropy parameters （8 values） were also derived. The β values are very close to 2 at low vibrational states of the correlated N2 （X1 ∑g＋） products at all three photolysis wavelengths, and gradually decrease to about 1.4 at v--7. This indicates the dissociation is mainly through a parallel transition state to form products at lower vibrational states, and the highly vibrational exited products are from a more bent configuration. This is consistent with the observed shift of the most intense rotational structure in the TKER as the vibrational quantum number increases.

High-resolution Infrared Spectroscopy of ^15N2^16O in 1650-3450 cm-1

High-resolution ro-vibrational spectroscopy of ^15N2^16O in 1650-3450 cm-1 region is studied using highly enriched isotopologue sample. The positions of more than 7300 lines of ^15N2^16O isotopologue were measured with a typical accuracy of 5.0×10-4 cm-1. The transitions were rovibrationally assigned on the basis of the global effective Hamiltonian model. The band by band analysis allowed for the determination of the rovibrational parameters of a total of 73 bands. 29 of them are newly reported and more rotational transitions have been observed for the others. The maximum deviation of the preidictions of the effective Hamiltonian model is up to 0.70 cm-1 for the ^15N2^16O species.

Effect of Nd-incorporation and K-modification on catalytic performance of Co3O4 for N2O decomposition

Nd-Co 3O 4 catalysts were prepared by hydrothermal and co-precipitation methods to catalyze the decomposition of N 2O. The catalysts prepared by hydrothermal method showed higher activity. Among the hydrothermal Nd-Co 3O 4 catalysts, the catalyst with Nd/Co molar ratio of 0.01 had higher activity. 0.01Nd-Co 3O 4 catalyst was then impregnated by K 2CO 3 solution to prepare K-modified catalyst. The catalysts were characterized by means of X-ray diffraction (XRD), nitrogen physisorption, scanning electrons microscopy (SEM), X-ray photoelectron spectroscopy (XPS), hydrogen temperature-programmed reduction (H 2-TPR), and oxygen temperature-programmed desorption (O 2-TPD). The results show that Nd-Co 3O 4 and K-modified catalysts exhibit spinel structure. In contrast to bare Nd-Co 3O 4, the K-modified catalyst with higher activity is due to its weaker strength of Co-O bond and easier desorption of surface oxygen species. In addition, over 90% conversion of N 2O can be reached over 0.02K/0.01Nd-Co 3O 4 at 350 ℃ for 40 h under the co-presence of oxygen and steam in feed gases.

Effect of copper precursors on the catalytic performance of Cu-ZSM-5 catalysts in N2O decomposition

Five Cu-ZSM-5 catalysts were obtained by treating Na-ZSM-5 （Si/Al ratio = 15） with aqueous solutions of differ- ent Cu precursors （CuCl2, Cu（NO3）2, CuSO4, Cu（CH3COO）2, and ammoniacal copper （II） complex ion）. After being pretreated in flowing He at 500 ℃ to form active Cu＋, these catalysts exhibited quite different activities in cata- lytic decomposition of N2O. CZM-AC（II） （prepared by ammoniacal copper （II） complex ion） with 9.4 wt% Cu con- tent was the most active among these Cu-ZSM-5 catalysts, achieving almost complete N2I conversion at 400 ℃. CZM-CA （prepared using Cu（ CH3COO）2 as the Cu precursor） with 2.8 wt% Cu content was the second most active catalyst among these Cu-ZSM-5 catalysts, achieving almost complete N2I conversion at 425 ℃. CZM-CC, CZM- CN, and CZM-CS prepared by using CuCl2, Cu（NO3）2, or CuSO4 as the Cu precursor with similar Cu contents （≈1.7 wt%） were the least active among these Cu-ZSM-5 catalysts, achieving ca. 90% N2O conversion at 500 ℃. XRD, ICP, SEM, TEM, EDX-mapping, and CO-IR experiments were conducted to characterize relevant samples. The superior activity of CZM-AC（II） can be attributed to the high contents of total Cu＋ and dimeric Cu＋ among these samples. The influence of co-fed O2 or H2O on the catalytic performance of typical samples was also studied.

Conversion of Fuel-N to N2O and NOx during Coal Combustion in Combustors of Different Scale

With focus on investigating the effect of combustor scale on the conversion of fuel-N to NOx and N20, experiments are carried out in three combustors, including single coal particle combustion test rig, laboratory scale circulating fluidized-bed boiler （CFB） and full scale CFB in this work. For single coal particle combustion, the majority of f-uel-N （65%-82%） is released as NOx, while only a little （less than 8%） fuel-N yields N20. But in labora- tory scale CFB, the conversion of fuel-N to N20 is increases, but the conversion of fuel-N to NOx is quite less than that of single coal particle combustion. This is because much char in CFB can promote the NOx reduction by in- creasing N20 formation. In full scale CFB, both of the conversion of fuel-N to NOx and the conversion of fuel-N to N20 are smaller than laboratory scale CFB.

Prediction of(n,2n)reaction cross-sections of long-lived fission products based on tensor model

Interest has recently emerged in potential applications of(n,2n)reactions of unstable nuclei.Challenges have arisen because of the scarcity of experimental cross-sectional data.This study aims to predict the(n,2n)reaction cross-section of long-lived fission products based on a tensor model.This tensor model is an extension of the collaborative filtering algorithm used for nuclear data.It is based on tensor decomposition and completion to predict(n,2n)reaction cross-sections;the corresponding EXFOR data are applied as training data.The reliability of the proposed tensor model was validated by comparing the calculations with data from EXFOR and different databases.Predictions were made for long-lived fission products such as^(60)Co,^(79)Se,^(93)Zr,^(107)P,^(126)Sn,and^(137)Cs,which provide a predicted energy range to effectively transmute long-lived fission products into shorter-lived or less radioactive isotopes.This method could be a powerful tool for completing(n,2n)reaction cross-sectional data and shows the possibility of selective transmutation of nuclear waste.

Effects of Water Regime and Straw Application in Paddy Rice Season on N2O Emission from Following Wheat Growing Season

A split-plot experiment in a rice-winter wheat rotation system was performed to study the effects of water regime and wheat straw application in rice-growing season on N2O emission from following wheat growing season. Water regime in the rice-growing season was designed as the conventional irrigation (flooding/drainage cycle) and the permanent flooding. Wheat straw was incorporated with three rates of 0, 225 and 450 g m-2 into the paddy soil for each water regime just before rice was transplanted. N2O emission was measured by static chamber-gas chromatograph method. Results from the variance analysis indicated that the permanent flooding in rice-growing season markedly enhanced N2O emission in following wheat growing season (P=0. 003), and that the effect of straw application on N2O emission was distinguished between two water regimes. Under the conventional irrigation, incoporation of wheat straw reduced N2O emission in the following wheat growing season, while there were no significant differences in the emission for the straw application rates of 225 and 450 g m-2. No significant differences in N2O emissions were observed among the three rates of straw application for the permanent flooding regime. In addition, the seasonal variation of N2O emission was regulated by soil temperature and moisture. The daily N2O flux (Y, mg m-2 d-1) can be quantitatively described by soil temperature (T, ℃) and moisture (W, WFPS %) asY=A0+A1T+A2W+A3W2(n=23, R2 ≥0. 4159** )or y=C0+C1W+C2W2(n=23,R2≥0. 4074** ). Compared with the effect of soil temperature on N2O emission, soil moisture was an important factor regulating the seasonal pattern of N2O emission.

V_(2)O_(3)/VO_(2)@S/N-C nanofibers with excellent cycling stability and superior rate capability in aqueous zinc ion batteries

The development of aqueous zinc-ion batteries (AZIBs) marks a significant advancement in the field of sustainable and environmentally friendly energy storage.To address the challenges faced by singlephase vanadium-based oxides,such as poor conductivity and dissolution in electrolytes,this study introduces vacuum S/N doping to fabricate V_(2)O_(3)/VO_(2)@S/N-C nanofibers,improving the cycling stability and enhancing the capacity.The V_(2)O_(3)/VO_(2)@S/N-C electrode exhibits exceptional cyclic stability,retaining a capacity of 133.3 m A h g^(-1)after 30,000 cycles at a high current density of 100 A g^(-1)and a capacity retention of 81.8%after 150,000 cycles at 200 A g^(-1).Characterizations using ex-situ X-ray diffraction and ex-situ X-ray photoelectron spectroscopy reveal co-intercalation of H^(+)and Zn^(2+)in the V_(2)O_(3)/VO_(2)@S/N-C electrode.Due to the presence of S_(2)^(2-),more phases changed to V_(10)O_(24).12H_(2)O,making the V_(2)O_(3)/VO_(2)@S/N-C electrode better reversible.By elucidating the zinc storage mechanism and demonstrating the stable performance of the doped electrode,this work contributes valuable insights into the optimization of the electrode materials for future energy storage solutions.

Experimental Investigation of the Flame Propagation and Flashback Behavior of a Green Propellant Consisting of N2O and C2H4

Regarding the research on alternatives for monopropellant hydrazine, several so called green propellants are currently under investigation or qualification. Aside others, the DLR Institute of Space Propulsion investigates a N20/C2I-I4 premixed green propellant. During the research activities, flashback from the rocket combustion chamber into the feeding system has been identified as a major challenge when using the propellant mixture. This paper shows the results of ignition experiments conducted in a cylindrical, optical accessible ignition chamber. During the ignition and flame propagation process, pressure, temperature and high-speed video data were collected. The high speed video data were used to analyze the flame propagation speed. The obtained propagation speed was about 20 rn/s at ignition, while during further propagation of the flame speeds of up to 120 m/s were measured. Additionally, two different porous materials as flame arresting elements were tested： Porous stainless steel and porous bronze material. For both materials Peclet numbers for flashback were derived. The critical Peclet number for the sintered bronze material was around 20, while for the sintered stainless steel the critical Peclet number seems to be larger than 40. Due to the test results, sintered porous materials seem to be suitable as flashback arresters.

Preparation and Properties of Si2N2O Ceramics for Microwave Sintering Furnaces

Si2N2O ceramics were prepared using amorphous Si3N4 as the raw material and Li2CO3 as the sintering additive through vacuum multi-stage sintering.The influence of the Li2CO3 addition(0%,1%,2%,3%,and 5%,by mass)on the phase composition,the microstructure,the porosity,the mechanical properties,the dielectric constant and the tangent of the dielectric loss angle of the porous Si2N2O ceramics was investigated.The results reveal that a suitable addition of Li2CO3 can promote the generation of Si2N2O but excessive or inadequate Li2CO3 causes decomposition of Si2N2O ceramics.The prepared porous Si2N2O ceramics have good mechanical properties,good thermal shock resistance,and low dielectric properties,which have excellent potential for application in microwave sintering furnaces.

Influence of the Gas Temperature in Ozone Production of Mixture N2-O2

The ozone occurs naturally in the atmosphere and presents a filter of protection, absorbing the radiations wavelengths lower than 310 nm. The industrial generation of ozone is the classical application of the non-equilibrium air plasmas at the atmospheric pressure. A low temperature is needed because the ozone quickly decays at the high temperature. This study is based on a temporal kinetic model for the production of ozone. The chemical kinetics take into account 96 reactions with 19 species atomic and molecular created in the discharge. In this work, the model allows to calculate the temporal evolution of neutral, ionized and excited species concentrations in plasma. The results show the influence of the kinetic on the ozone production yield and on the gas heating by Joule effect.

Correlations between Mineral Nitrogen Contents and Vertical Distribution of N20 Emission Potentials in Tropical Peat Soils Transformed into Oil Palm Plantations in Sarawak, Malaysia

Tropical peat swamp forest beds that have been reclaimed for agricultural use are generally an active source of nitrous oxide （N2O） efflux, however, the mechanism by which reclaimed tropical peat soils promote the emergence of N2O emitters in soil microbial communities remains unclear. The purpose of this study was to reveal the vertical distribution of N2O emission potential and its correlation with mineral nitrogen contents in reclaimed soils. Using a culture-based N2O emission assay, the N2O emission potentials of soil at various depths （0-450 cm） were investigated in two oil palm plantations in Sarawak, Malaysia, which had elapsed times of two years （E2Y） and 10 years （El 0Y） after deforestation, respectively. On the basis of the relationship between the vertical profiles of N2O emission potentials and the contents of mineralized nitrogen in the peat soils at various depths, the impact of land management on soil microbial communities was discussed. The peat soil at plantation site E2Y showed a trend of high N2O production in deep layers （200-400 cm）, whereas the older plantation site E10Y showed considerably more active N2O emission in shallow soil （10-50 cm）. N2O emission potentials among the soil microbial communities at different soil depths at the E10Y site showed positive correlations with NO3- and NH4＋ contents, whereas, soils obtained from the E2Y site had N2O emission potentials that were inversely proportional to the contents of NO3-. This contrasting vertical correlation between N2O-emitting potentials and mineralized nitrogen contents in bulk soils suggests that active N2O emission in deep soil at the E2Y site has maintained the original carbon-nitrogen （C/N） ratio of the peat soil, whereas at EIOY, such a regulatory system has been lost due to advanced soil degradation, leading to dynamic changes in the nitrogen cycle in shallow soil.

High Efficient Photocatalytic Degradation of 3,7-Bis(Dimethylamino)-Phenothiazin-5-Ium Chloride Dye and Kinetics of H2 Evolution of N2H4H2O by Synthesized CdS/NiS Nanocomposite by Electrochemical Method

CdS/NiS nanocomposites were synthesized by electrochemical method. Ni and Cd is one of the important II-VI semiconducting materials with a direct band gap of 3.26 eV which finds applications in electrical conductivity and photo-catalysis. The synthesized nanocomposites were characterized by BET, UV-VIS, XRD, FE-SEM (EDAX) techniques. X-Ray diffraction (XRD) reveals crystallite size to be 23.22 nm which was calculated using Williamson-Hall (W-H) plot method. The energy of the band gap for CdS/NiS could be thus estimated to be 3.26 eV. The photocatalytic activity of the sample was evaluated by the degradation of textile dye methylene Blue (MB) in aqueous solutions under UV radiation. Hydrogen energy is regarded as a promising alternative in terms of energy conversion and storage. Hydrogen Evolution Reaction (HER) was carried out in both visible light and UV light by using Hydrazine (N2H4H2O) in the presence of CdS/NiS nanocomposite. The synthesized photocatalyst shows applicable performance for kinetics of Hydrogen Evolution Reaction (HER) in Visible light and UV light. The decomposition of hydrazine (N2H4H2O) proceeded rapidly to generate free hydrogen rich gas through OH radical contact with CdS/NiS nanocomposite at room temperature. The rate of HER is limited by either proton adsorption onto an active site or evolution of formed hydrogen from the surface. A high Tafel slope is indicative of proton adsorption as the rate limiting step, while a lower Tafel slope (20 - 45 mV) indicates that the evolution of molecules hydrogen from the catalyst is rate limiting. In the present case the Tafel slopes for visible light 23.5 mV and 42.5 mV for UV light. Blank experiments show poor activity for HER i.e. 10.1 - 13.5 mV.

Development and Test of an Experimental Apparatus to Study Thermal-Choking in Ideal Gases and Self-decomposition in Superheated N2O

N2O represents a popular oxidizer for hybrid rocket motors for a variety of reasons, including safety, ease of access and self-pressurization. It is often used as a saturated two-phase fluid in these applications to take advantage of self-pressurization. Recent interest in using this oxidizer in regeneratively cooled engines requires a detailed heat transfer process analysis to the coolant, in order to quantify performance. Since the injection of N2O typically takes place in the two-phase region, our study focuses on heat transfer rates in this region, and extends the region to include superheated vapor. This analysis is critical for these cooling applications, because the exothermic decomposition nature of N2O also means that unchecked heating in the superheated region may result in a runaway reaction in the cooling passages. Furthermore, provided that sufficient heat transfer rates are available, N2O is expected to accelerate in the cooling passages due to Rayleigh flow effects much like those of a calorically perfect gas. The proximity of superheated N2O to its saturated vapor curve, at the conditions studied here, makes the suitability of a perfect gas model questionable, but that benchmarks is still useful. This paper presents the development of an experimental apparatus （a ＂Rayleigh tube＂）, specifically designed to study this problem, and test the analytical methods developed to model it. Since we focus on the development of the apparatus, the data presented were uses primarily calorically perfect gas surrogates, but the goal is to apply the apparatus and method to N2O. The design and construction of the Rayleigh tube is presented, along with preliminary results with perfect gases. Finally, we present preliminary results on heated N2O flow. Using a simple model for predicted dry-out point, we investigate where superheating may be expected to occur. We present estimates of critical heating and compare them to the heat required to achieve self-decomposition.

肥水管理方式对蔬菜田N2O释放影响的模拟研究

通过田间静态箱监测和DNDC模型模拟的方法,对比研究了崇明岛东滩蔬菜田在常规肥水管理和精确滴灌施肥方式下N2O的排放情况,从排放特征、全年通量、单位氮肥N2O损失率以及单位作物产量排放量等方面分析了不同肥水管理方式对旱田土壤N2O排放的影响。结果表明,基于土壤和作物养分平衡管理的精确滴灌施肥技术,由于减少了氮肥施用量并改进了肥水分配方式,提高了肥料的利用效率,在保持农作物产量的基础上减少了N2O的排放。与常规肥水管理方式相比,滴灌施肥区2006年和2007年的N2O排放通量分别减少6.2和6.8kgN·hm-2·a-1,单位氮肥N2O损失率明显降低,2006年和2007年单位产量排放量分别削减53.2%和58.9%。

DO浓度对生活污水硝化过程中N2O产生量的影响

为确定污水脱氮过程中最优的DO浓度和曝气方式,以提高污水处理效率,降低N2O产生量,采用实际生活污水应用小试SBR反应器,重点考察了不同DO浓度条件下,硝化效率和硝化过程中N2O的产生量.结果表明,当DO浓度恒定为0.4mg.L-1时,虽然硝化过程所消耗的能量最低,但其氨氮氧化的速率较低.提高DO浓度,氨氮氧化速率可随之升高.低氨氮生活污水硝化过程中仍有N2O产生.DO浓度为0.4 mg.L-1和0.9 mg.L-1时,污水N2O产生量(以N计)分别为1.5 mg.L-1和1.6mg.L-1;而DO浓度为1.5 mg.L-1和2.0 mg.L-1时,N2O产生量则分别降低至0.5 mg.L-1和0.4 mg.L-1.当DO浓度高于1.5mg.L-1后,继续提高DO浓度,氨氮氧化速率升高的速率变缓,同时N2O产生量大幅降低.因此,从提高污水脱氮效率节能降耗和控制N2O产生量2个角度考虑,生活污水脱氮过程中控制DO浓度在1.5 mg.L-1较为适宜.

氮肥水平对不同土壤N2O排放的影响

鉴于N2O排放量占施用氮肥量的比例即N2O排放系数还有很大不确定性,室外盆栽试验于2002-2003年选取3个供试土壤,各土壤设置对照和低、中、高氮肥水平,全年施尿素量（以N计）分别为334、670和1 004 kg/hm^2.结果表明,水稻生长季,各个土壤的N2O累积排放量与其对照相比的增加量在低、中、高氮肥水平间无明显差异;而小麦生长季,随氮肥施用量增加,各个土壤的N2O累积排放量与其对照相比的增加量在3种氮肥水平之间的差异显著.整个稻麦轮作系统,随氮肥用量的增加明显促进麦田N2O的排放.无论水稻或小麦生长季,对照3个土壤的N2O累积排放量并无显著差异,F土壤（江苏溧水）、G土壤（江苏涟水）和H土壤（江苏农科院）的N2O累积排放量,在水稻生长季分别为168、127和146 mg/m^2;小麦生长季,分别为134、124和168 mg/m^2.在施氮肥后,3个土壤的N2O排放量出现差异,如在中氮水平下,小麦生长季,F土壤、G土壤和H土壤N2O累积排放量分别为976、744和626 mg/m^2.稻麦轮作生长季内,在低氮与中氮2个水平下,不同土壤间N2O排放系数存在显著差异.以1个稻麦轮作周期为时间尺度,F土壤、G土壤和H土壤总的N2O排放系数分别为1.1%±0.23%、0.75%±0.17%和1.01%±0.11%,表明不同土壤对N2O排放系数的影响不同.

京郊典型设施蔬菜地土壤 N2O 排放特征

利用静态暗箱-气相色谱法对北京郊区设施蔬菜地典型种植模式(番茄-白菜-生菜)下土壤N2O排放特征进行了周年(2012年2月22日—2013年2月23日)观测,探讨了不同处理下(即不施氮肥处理(CK)、农民习惯施肥处理(FP)、减氮优化施肥处理(OPT)和减氮优化施肥+硝化抑制剂处理(OPT+DCD))N2O排放特征及土壤温度、土壤湿度、土壤无机氮含量对土壤N2O排放的影响。结果表明:每次施肥+灌溉之后设施蔬菜地会出现明显的N2O排放高峰,持续时间一般为3—5 d。不同处理N2O排放通量变化范围在-0.21—14.26 mg N2O m-2h-1,平均排放通量0.03—0.36 mg N2O m-2h-1。整个蔬菜生长季各处理N2O排放与土壤孔隙含水率(WFPS)均表现出极显著的正相关关系(P<0.01);不施氮处理5 cm深度土壤温度与N2O排放通量呈现显著的正相关关系(P<0.05);各处理N2O排放与土壤表层硝态氮含量具有较一致变化趋势。不同处理下N2O年度排放总量差异显著,依次顺序为FP((20.66±0.91)kg N/hm2)>OPT((12.79±1.33)kg N/hm2)>OPT+DCD((8.03±0.37)kg N/hm2)。与FP处理相比,OPT处理和OPT+DCD处理N2O年排放总量分别减少了38.09%和61.13%。各处理N2O排放系数介于0.36%—0.77%,低于IPCC 1.0%的推荐值。在目前的管理措施下,合理减少施氮量和添加硝化抑制剂是减少设施蔬菜地N2O排放量的有效途径。