虚拟耕地资源与农业经济增长：作用机理及贡献份额研

虚拟耕地资源被广泛认为是缓解国内耕地资源压力和促进农业经济增长的重要举措之一。在论证虚拟耕地资源贸易对农业经济增长作用机理分析的基础上，计算1996~2018年中国主要农产品虚拟耕地资源贸易量，并对虚拟耕地资源对农业经济增长中的贡献份额进行实证分析，为调整对外贸易战略及优化耕地资源策略提供参考。结果表明：虚拟耕地资源可以在更大范围内实现耕地资源的优化配置；主要农产品贸易的巨大逆差决定了中国是虚拟耕地资源净进口大国，其中，油料是虚拟耕地资源净进口量最大的品种；虚拟耕地资源对农业经济增长的贡献率为0.26%，观点得到了佐证。同时，还提出了要试点实施虚拟耕地资源，全力以赴做好贸易政策调整战略；充分利用国内外“两种资源、两个市场”，倒逼主要农产品进行结构调整；努力构建虚拟耕地资源管理新模式，推动农业“走出去”与市场多元化结合等政策建议。     

Gasification characteristics of biomass for tar removal by secondary oxidant injection

Gasification experiments for sawdust were conducted using a fixed bed reactor at 900 °C by varying the secondary oxidant injection ratio to determine the optimal conditions for tar removal along with the enhancement of gasification efficiency. Secondary oxidant was injected as an oxidant at the top zone of the gasifier in varying ratios of 10–30% of the total amount of oxidant. This method was based on the primary method of tar removal and gasification efficiency improvement by thermal cracking of tar. Various gasification performance parameters were evaluated and tar content was estimated by measuring the fluctuation of weight of the activated carbon filter. The results showed that the concentration of tar in the producer gas decreased by injecting the secondary oxidant, even though syngas yield decreased. The recycling potential of the char produced in the gasification experiments was also assessed with the purpose of utilizing char as an adsorbent by determining its surface area and pore volume. The results demonstrated that the char produced from the gasification experiment had similar quality to that of the activated carbon used in this experiment.     

Absorption characteristics of potassium carbonate-based solutions with rate promoters and corrosion inhibitors

In this research, absorbents for CO₂ capture were prepared by blending 30 wt% potassium carbonate, 3 wt% of a rate promoter, and 1 wt% of a corrosion inhibitor. Pipecolic acid, sarcosine, and diethanolamine were chosen as rate promoter candidates. Based on a rate promoter screening test for CO₂ loading capacity and absorption rate, pipecolic acid and sarcosine were selected to be used as rate promoters. 1,2,3-benzotriazole and ammonium thiocyanate were chosen as corrosion inhibitors, and they were mixed with a 30 wt% potassium carbonate-based absorbent mixture containing one of the rate promoters. The absorption rates for four absorbent solutions (30 wt% potassium carbonate?+?3 wt% pipecolic acid?+?1 wt% 1,2,3-benzotriazole, 30 wt% potassium carbonate?+?3 wt% pipecolic acid?+?1 wt% ammonium thiocyanate, 30 wt% potassium carbonate?+?3 wt% sarcosine?+?1 wt% 1,2,3-benzotriazole, and 30 wt% potassium carbonate?+?3 wt% sarcosine?+?1 wt% ammonium thiocyanate) were measured, tabulated, and graphically displayed. These types of absorbents can be used for capturing CO₂ under high temperature and pressure conditions, such as those found in coal-fired power plants.     

Catalytic upgrading pyrolysis of pine sawdust for bio-oil with metal oxides

The catalytic upgrading pyrolysis of pine sawdust was performed at 500 °C with various metal oxides to improve the quality of the bio-oil. The aim of this study was to investigate the potential of the metal oxides instead of traditional zeolites for catalytic upgrading pyrolysis with the analysis of Gas Chromatograph/Mass Spectrometer. In this study, the used catalysts were Calcium-oxide, Magnesium oxide, Titanium dioxide, and Zeolite (Si/Al?=?80). The influence of catalysts on products yields and compositions were investigated. Most metal oxides can enhance the bio-gas with the bio-oil yields decreased. The metal oxides led to a decrease of Acids, Aldehydes, Ketones and an increase of Furfural, Cresols, Catechols in Furans and Phenolics. Among the catalysts, the MgO catalysts was the most effective to convert the high molecular into lights ones (6.65% Cresols) with yield of 20.48% for Furfural. The deoxygenation reaction in bio-oil was suggested to convert oxygenated compounds into the low molecular weight of the materials (6.39% Guaiacols). Thus, the used metal oxides can improve the quality of bio-oil by decreasing undesirable compounds as well as increasing the desirable compounds with low oxygen contents via deoxygenation reaction.     

《环境监测 分析方法标准制修订技术导则》(HJ 168—2010)对土壤环境监测标准制修订适用性探讨

针对土壤环境监测的复杂性和特殊性,从空白试验、检出限、方法验证、质量控制和标准文本等方面,指出了《环境监测分析方法标准制修订技术导则》《HJ 168—2010》对土壤环境监测标准制修订工作的适用性和执行中存在的问题。提出,为保证土壤标准制修订质量和标准执行质量,应研究适宜土壤监测方法标准的质量控制指标体系和评价体系,及时修订《HJ 168—2010》或发布补充要求;对现有土壤监测方法标准进行技术评估,加强对于土壤标准制修订工作的指导和监管。     

Distribution,source, and environmental risk assessment of phthalate esters (PAEs) in water,suspended particulate matter,and sediment of a typical Yangtze River Delta City,China

Phthalates (PAEs) in drinking water sources such as the Yangtze River in developing countries had aroused widespread concern. Here, the water, suspended particulate matter (SPM), and sediment samples were collected from 15 sites in wet and dry seasons in Zhenjiang, for the determination of six PAEs (DMP, DEP, DIBP, DBP, DEHP, and DOP) using the solid-phase extraction (SPE) or ultrasonic extraction coupled with gas chromatography-mass spectrometry (GC-MS). The total concentrations of six PAEs (Σ₆PAEs) spanned a range of 2.65–39.31 μg L^?1 in water, 1.97–34.10 μg g^?1 in SPM, and 0.93–34.70 μg g^?1 in sediment. The partition coefficients (K_d1) of PAEs in water and SPM phase ranged from 0.004 to 3.36 L g^?1 in the wet season and from 0.12 to 2.84 L g^?1 in the dry season. K_d2 of PAEs in water and sediment phase was 0.001–9.75 L g^?1 in the wet season and 0.006–8.05 L g^?1 in the dry season. The dominant PAEs were DIBP, DBP, and DEHP in water and SPM, DIBP, DEHP, and DOP in sediment. The concentration of DBP in water exceeded the China Surface Water Standard. The discharge of domestic sewage and industrial wastewater might be the main potential sources of PAEs. The risk quotient (RQ) method used for the risk assessment revealed that DBP (0.01 < RQ < 1) posed a medium risk, while DIBP and DEHP (RQ > 1) posed a high environmental risk in water, DIBP (RQ > 1) also showed a high risk in sediment.

     

城郊关键带土壤中溶解性有机质的光谱特性及其时空变异

溶解性有机质(DOM)作为地球关键带中物质与能量循环的重要活性组分,其与关键带中诸多重要环境过程有着密切关系.本研究以宁波樟溪流域作为城郊关键带的典型代表区域,采集土壤样品,结合紫外可见光谱(UV-Vis)、三维荧光光谱(3D-EEM)进行特征表征,分析不同类型土壤中DOM的分布特征、影响因素和季节性变化规律.主要结果如下:林地DOC平均含量均大于耕地,其中林地秋季(15.4 mg·L~(-1))林地春季(12.5 mg·L~(-1));耕地秋季(11.9 mg·L~(-1))耕地春季(11.4 mg·L~(-1));DOM结构在紫外可见光谱下表现为耕地DOM芳香化程度(SUVA_(254))、疏水性组分(SUVA_(260))和分子量(S_R)较林地大,其中耕地秋季最为突出;三维荧光光谱结合平行因子分析(PARAFAC)把土壤DOM分为5种组分,主要以富里酸类物质为主(C_1、C_3、C_5),也含有色氨酸、酪氨酸类蛋白质(C_4)和腐殖酸(C_2)等物质,其中耕地春季的腐殖化程度最大,耕地秋季比春季含有较多类蛋白质,林地较耕地含有更多的类蛋白质,林地春秋两季中DOM结构变化不大.