黄土高原半干旱区覆膜玉米土壤温度的变异特征

黄土高原半干旱丘陵山区受特殊的地理、地形以及水文气象条件的影响,造成农业生产播种难、出苗率低等问题,严重制约着农业的发展,但通过覆膜坐水技术能够起到抗旱保墒、提高地温、改善土壤肥效等作用。以哲单7号玉米ZeamaysL为供试品种,在设置对比试验小区（覆膜与不覆膜）的基础上,通过分析覆膜玉米土壤温度变异特征,描述了覆膜后增温、提墒、增产的过程,研究结果表明：覆膜处理与不覆膜处理相比,增温最明显的时期出现在出苗到拔节阶段,且10cm．和20cm处的温差表现为最大,可增温2．5℃左右,而后期增温减慢,播种后覆膜增温为玉米发芽生长提供了良好的生长环境,大大提高了出苗率,为作物节水增产提供了必要条件。     

Influence of haze pollution on water-soluble chemical species in PM2.5 and size-resolved particles at an urban site during fall

To investigate the influence of haze on the chemical composition and formation processes of ambient aerosol particles,PM_(2.5) and size-segregated aerosol particles were collected daily during fall at an urban site of Gwangju,Korea.During the study period,the total concentration of secondary ionic species(SIS) contributed an average of 43.9% to the PM_(2.5) ,whereas the contribution of SIS to the PM_(2.5) during the haze period was 62.3%.The NO_3 and SO~(2-)_4 concentrations in PM_(2.5) during the haze period were highly elevated,being 13.4 and 5.0 times higher than those during non-haze period,respectively.The PM,NO~-_3,SO~(2-)_4,oxalate,water-soluble organic carbon(WSOC),and humic-like substances(HULIS) had tri-modal size distributions peaks at 0.32,1.0,and 5.2 μm during the non-haze and haze periods.However,during the non-haze period they exhibited dominant size distributions at the condensation mode peaking at 0.32 μm,while on October 21 when the heaviest haze event occurred,they had predominant droplet mode size distributions peaking at 1.00 μm.Moreover,strong correlations of WSOC and HULIS with SO~(2-)_4,oxalate,and K+at particle sizes of 1.8 μm indicate that secondary processes and emissions from biomass burning could be responsible for WSOC and HULIS formations.It was found that the factors affecting haze formation could be the local stable synoptic conditions,including the weak surface winds and high surface pressures,the long-range transportation of haze from eastern China and upwind regions of the Korean peninsula,as well as the locally emitted and produced aerosol particles.     

进口废塑料环境保护管理研究

随着塑料资源的大量消耗,废塑料的利用引起了社会的高度重视。工艺简单,投入成本少,入行门槛低导致部分废塑料加工利用企业技术水平低、管理模式差、环境污染重。为规范进口废塑料行业,通过调研统计、实验分析、咨询论证和研究了进口废塑料环境保护管理规定,对进口废塑料企业的规模、设备、人员和管理等方面提出了要求,为进一步规范提升进口废塑料行业提供技术支撑。     

吉林省主要覆膜作物地膜残留情况调查

通过文献调研、问卷调查和典型样点采集的方法对吉林省3种主要覆膜作物的地膜残留情况进行调查分析,结果表明：地膜残留量与覆膜年限、地膜回收方式以及种植作物种类密切相关。随覆膜时间的延长地膜残留量有增加的趋势。3种模式地膜残留量由高到低为：瓜菜模式〉玉米连作模式〉花生连作模式,连续覆膜10年,3种模式的地膜残留量分别为30、28.35 kg·hm^-2和15.9kg·hm^-2。以一级污染水平作为标准（75 kg·hm^-2）,覆膜量每年按75～150 kg·hm^-2、年残留率按1.2%～4.02%计,估算吉林省安全使用地膜的年限约为12～83年。     

吸能让位防冲支护结构与围岩协同作用体系研究*

为防治冲击地压危害,减小人员伤亡与经济损失,采用数值计算方法建立吸能让位防冲液压支架与围岩协同作用体系模型,计算支架和围岩组合体系在静载和冲击载荷作用下的受力状态。结果表明:静载条件下,受煤层影响巷道右侧拱肩位置应力值与塑性应变相对最大,此处最易发生破坏;吸能装置在静载条件下没有发生压缩变形,表明吸能装置不会影响支架正常工作;竖向冲击荷载条件下,受煤层结构影响巷道右侧拱肩处等效塑性应变值增大相对比较明显,吸能防冲支架中间液压柱与右侧液压柱水平位移变化相对最明显;冲击地压发生过程中,支架与围岩间相互作用力变化较大,总体可分为振动段、平稳段、上升段、波动段4个阶段。     

吉林市“白色污染”概况及防治措施建议

“白色污染”是中国城市特有的环境污染。在各种公共场所到处都能看见大量废弃的塑料制品,他们从自然界而来,由人类制造,但是这些废弃的塑料制品最终归于大自然时却不易被自然所消纳,从而严重影响了大自然的生态环境。首先介绍了“白色污染”的概念及其危害;然后对吉林市塑料方便袋的使用情况进行了调查,并以此反映吉林市“白色污染”的概况;最后针对中国当前“白色污染”治理过程中的不足提出了针对性的建议,以期达到能够有效缓解或根治“白色污染”的目的。     

3D打印技术在固体废弃物资源循环中的应用

打印材料是限制3D打印技术发展和推广应用的瓶颈问题,目前已经发现部分固体废弃物与3D打印的契合度很高,可以用于制备3D打印材料.本文综述了4类可以用于3D打印的固体废弃物,包括硅铝基废弃物、农林废弃物、废旧塑料和废旧金属,着重讨论了这4类废弃物制备3D打印材料的方法以及废弃物的添加对原打印材料造成的影响,同时分析了当前废弃物制备3D打印材料需要解决的问题,并对废弃物基3D打印材料的发展趋势进行了展望.     

A large-scale outdoor atmospheric simulation smog chamber for studying atmospheric photochemical processes: Characterization and preliminary application

Understanding the formation mechanisms of secondary air pollution is very important for the formulation of air pollution control countermeasures in China. Thus, a large-scale outdoor atmospheric simulation smog chamber was constructed at Chinese Research Academy of Environmental Sciences (the CRAES Chamber), which was designed for simulating the atmospheric photochemical processes under the conditions close to the real atmospheric environment. The chamber consisted of a 56-m³ fluorinated ethylene propylene (FEP) Teflon film reactor, an electrically-driven stainless steel alloy shield, an auxiliary system, and multiple detection instrumentations. By performing a series of characterization experiments, we obtained basic parameters of the CRAES chamber, such as the mixing ability, the background reactivity, and the wall loss rates of gaseous compounds (propene, NO, NO₂, ozone) and aerosols (ammonium sulfate). Oxidation experiments were also performed to study the formation of ozone and secondary organic aerosol (SOA), including α-pinene ozonolysis, propene and 1,3,5-trimethylbenzene photooxidation. Temperature and seed effects on the vapor wall loss and SOA yields were obtained in this work: higher temperature and the presence of seed could reduce the vapor wall loss; SOA yield was found to depend inversely on temperature, and the presence of seed could increase SOA yield. The seed was suggested to be used in the chamber to reduce the interaction between the gas phase and chamber walls. The results above showed that the CRAES chamber was reliable and could meet the demands for investigating tropospheric chemistry.     

Primary and secondary organic aerosol in an urban/industrial site: Sources, health implications and the role of plastic enriched waste burning

PM10 samples were collected from an urban/industrial site nearby Athens, where uncontrolled burning activities occur. PAHs, monocarboxylic, dicarboxylic, hydroxycarboxylic and aromatic acids, tracers from BVOC oxidation, biomass burning tracers and bisphenol A were determined. PAH, monocarboxylic acids, biomass burning tracers and bisphenol A were increased during autumn/winter, while BSOA tracers, dicarboxylic- and hydroxycarboxylic acids during summer. Regarding aromatic acids, different sources and formation mechanisms were indicated as benzoic, phthalic and trimellitic acids were peaked during summer whereas p-toluic, isophthalic and terephthalic were more abundant during autumn/winter. The Benzo[a]pyrene-equivalent carcinogenic power, carcinogenic and mutagenic activities were calculated showing significant (p < 0.05) increases during the colder months. Palmitic, succinic and malic acids were the most abundant monocarboxylic, dicarboxylic and hydrocarboxylic acids during the entire sampling period. Isoprene oxidation was the most significant contributor to BSOA as the isoprene-SOA compounds were two times more abundant than the pinene-SOA (13.4 ± 12.3 and 6.1 ± 2.9 ng/m³, respectively). Ozone has significant impact on the formation of many studied compounds showing significant correlations with: isoprene-SOA (r = 0.77), hydrocarboxylic acids (r = 0.69), pinene-SOA (r = 0.63),dicarboxylic acids (r = 0.58), and the sum of phthalic, benzoic and trimellitic acids (r = 0.44). PCA demonstrated five factors that could explain sources including plastic enriched waste burning (30.8%), oxidation of unsaturated fatty acids (23.0%), vehicle missions and cooking (9.2%), biomass burning (7.7%) and oxidation of VOCs (5.8%). The results highlight the significant contribution of plastic waste uncontrolled burning to the overall air quality degradation.     

Effect of environmental parameters on the degradability of polymer films in laboratory-scale composting reactors

Previous research in our laboratory reported a convenient laboratory-scale composting test method to study the weight loss of polymer films in aerobic thermophilic (53°C) reactors maintained at a 60% moisture content. The laboratory-scale compost reactors contained the following synthetic compost mixture (percentage on dry-weight basis): tree leaves (45.0), shredded paper (16.5), food (6.7), meat (5.8), cow manure (17.5), sawdust (1.9), aluminum and steel shavings (2.4), glass beads (1.3), urea (1.9), and a compost seed (1.0) which is designated Mix-1 in this work. To simplify the laboratory-scale compost weight loss test method and better understand how compost mixture compositions and environmental parameters affect the rate of plastic degradation, a systematic variation of the synthetic mixture composition as well as the moisture content was carried out. Cellulose acetate (CA) with a degree of substitution (DS) value of 1.7 and cellophane films were chosen as test polymer substrates for this work. The extent of CA DS-1.7 and cellophane weight loss as a function of the exposure time remained unchanged when the metal and glass components of the mixture were excluded in Mix-2. Further study showed that large variations in the mixture composition such as the replacement of tree leaves, food, meat, and sawdust with steam-exploded wood and alfalfa (forming Mix-C) could be made with little or no change in the time dependence of CA DS-1.7 film weight loss. In contrast, substituting tree leaves, food, meat, cow manure, and sawdust with steam-exploded wood in combination with either Rabbit Choice (Mix-D) or starch and urea (Mix-E) resulted in a significant time increase (from 7 to 12 days) for the complete disappearance of CA DS-1.7 films. Interestingly, in this work no direct correlation was observed between the C/N ratio (which ranged from 13.9 to 61.4) and the CA DS-1.7 film weight loss. Decreasing moisture contents of the compost Mix-2 from 60 and 50 and 40% resulted in dramatic changes in polymer degradation such that CA DS-1.7 showed an increase in the time period for a complete disappearance of polymer films from 6 to 16 and 30 days, respectively.Guest Editor: Dr. Graham Swift, Rohm & Haas.Paper presented at the Bio/Environmentally Degradable Polymer Society—Second National Meeting, August 19–21, 1993, Chicago, Illinois.