我国废旧电冰箱聚氨酯泡沫塑料管理现状及对策研究

随着科技进步和电冰箱产品更新换代速度的加快,报废弃电冰箱数量不断增大.冰箱拆解处理产生的大量聚氨酯泡沫塑料,由于其中含有CFCs类发泡剂且其难以降解等,增加了处理难度,如何对其进行有效处理处置成为国内外广泛关注的焦点.目前我国废弃电冰箱聚氨酯泡沫塑料一般送至生活垃圾处理厂进行焚烧或填埋处置,而未进行资源化利用.在调研电冰箱聚氨酯泡沫塑料国内外现有处理处置技术基础上,比较了热能回收法、物理法、化学法、生物法和热解法等处理技术的优缺点,并对其经济性和实用性进行分析.同时分析了我国废电冰箱聚氨酯泡沫塑料环境管理面临的主要问题,结合国家相关管理政策需求,提出了针对性建议.     

防控高温煤岩裂隙的膏体泡沫研制及应用

煤岩裂隙漏风导致的煤自燃火灾严重危害矿井安全生产,在现有防治煤炭自燃材料的基础上,以聚丙烯酰胺（A）、复合表面活性剂（B）、混合粉体（C）为原材料研制了一种防控高温煤岩裂隙的膏体泡沫。采用正交试验法以保水率、发泡倍数、阻化率为指标优选出了最佳的膏体泡沫配方为A4B4C4:A为70 g/L,B为19.5 g/L,C为270 g/L。对膏体泡沫进行了微观形态表征,并从泡孔尺寸大小及分布、液膜颗粒分布、液膜载体吸水等方面对膏体泡沫的保水、吸热和受热稳定机制进行了分析。最后以南方某煤矿复采工作面煤自燃发火为例,分析和判定了302工作面火区分布,采用钻孔压注膏体对火区高温煤岩裂隙进行控制,3d后工作面1-5#钻孔、三石门密闭处CO浓度从520 ppm,465 ppm,523 ppm,305 ppm,289 ppm,750 ppm下降到22 ppm,18 ppm,23 ppm,14 ppm,14 ppm,36 ppm。     

公路隧道压缩空气泡沫系统灭油池火实验研究

为研究压缩空气泡沫与4.65 m2汽油池火作用过程中隧道内温度、热辐射强度、高温烟气等的变化规律,采用30 m×6 m×6 m公路隧道实验模型,考察公路隧道压缩空气泡沫系统对油池火的灭火性能。结果表明:在供给强度为5.1 L/(min·m2)、气液比14∶1条件下,公路隧道压缩空气泡沫系统对于汽油池火具有优异的控灭火能力,控火时间为21 s,灭火时间为27 s,且泡沫性能稳定,抗复燃能力强;压缩空气泡沫对于隧道内高温烟气层扰动很小,不会导致高温烟气下降到隧道下部,故不影响人员逃生疏散;在压缩空气泡沫作用下,隧道顶部及侧壁100 ℃以上高温持续时间均不超过150 s,并且可在30 s内将油池火周围的热辐射强度降至安全范围。     

环氧丙烷储罐空气泡沫灭火试验研究

环氧丙烷为低沸点水溶性可燃液体,由于其饱和蒸汽压大,灭火困难,此前,国内外未对环氧丙烷进行过大型工程应用灭火试验研究。为研究空气泡沫对环氧丙烷储罐的灭火性能,分别对环氧丙烷进行了0．25m^2油盘探索性试验、1．73m^2油盘泡沫灭火剂选型试验和直径3．5m储罐工程应用灭火试验。试验结果表明,空气泡沫难以扑灭环氧丙烷储罐火灾,在直径3．5m储罐上,虽然采用了灭火性能较好的泡沫液,且使用了较大的供给强度和较长的供给时问,但仍难灭火。在试验基础上,对环氧丙烷储罐的消防要求提出了建议。     

乙酸钠作为碳源不同污泥源短程反硝化过程亚硝酸盐积累特性

为探究乙酸钠作为碳源时,不同污泥源外源短程反硝化过程中亚硝酸盐积累特性,采用1号和2号SBR分别接种某污水处理厂二沉池和同步硝化反硝化除磷系统剩余污泥,通过合理控制初始硝酸盐浓度和缺氧时间,实现了短程反硝化的启动,并考察了其在不同初始COD和NO_3~--N浓度条件下的碳、氮去除特性.试验结果表明:以乙酸钠为碳源,1号和2号SBR可分别在21 d和20 d实现短程反硝化的成功启动,且其NO_2~--N积累量和亚硝酸盐积累率(NAR)均维持在较高水平,分别为12. 61 mg·L-1、79. 76%和13. 85 mg·L-1、87. 60%.当2号SBR初始NO_3~--N浓度为20 mg·L-1,且初始COD浓度由60mg·L-1升高至140 mg·L-1时,系统实现最高NO_2~--N积累时间可由160 min逐渐缩短至6 min,同时NO_3~--N比反硝化速率(以VSS计)由3. 84 mg·(g·h)-1增加至7. 35 mg·(g·h)-1,初始COD浓度的提高有利于实现短程反硝化过程NO_2~--N积累. 2号SBR初始COD浓度为100 mg·L-1,当初始NO_3~--N浓度由20 mg·L-1增加至30 mg·L-1时,系统NAR均维持在90%以上,最高可达100%(NO_3~--N初始浓度为25 mg·L-1);当初始NO_3~--N浓度≥35 mg·L-1时,系统COD不足导致NO_3~--N不能被完全还原为NO_2~--N.此外,在不同初始COD浓度(80、100、120 mg·L-1)和NO_3~--N浓度(20、25、30、40 mg·L-1)条件下,2号SBR的脱氮除碳和短程反硝化性能均优于1号SBR.     

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.     

PTA废液回收利用技术

介绍了从精对苯二甲酸（PTA）废液中回收醋酸,邻、对苯二甲酸,醋酸钴锰盐的回收工艺。醋酸得率为90％,邻、对苯二甲酸得率为70％,醋酸钴锰盐得率为95％。该技术成熟、合理,具有较好的经济效益和环境效益。     

Comparative Biodegradation Study of Starch- and Polylactic Acid-Based Materials

The degradation of starch- and polylactic acid-based plastic films by microorganisms extracted from compost was studied in a liquid medium. The various degradation products produced were measured throughout the duration of the experiment, and total carbon balances were estimated. For an easily biodegradable material, the evolution of the way carbon repartitioned between different degradation products was quite similar whatever the experimental condition or the type of substrate. On the other hand, for a resistant material exposed to these microorganisms, the nature of the biodegradation depended strongly on the experimental conditions. In the latter case, a differential scanning calorimetry analysis confirmed the importance of the applied norm on the state of the residual material. The consequences for improved methods of estimation of biodegradability of these materials are discussed.     

Polymer Mineralization in Soils: Effects of Cold Storage on Microbial Populations and Biodegradation Potential

Soil retrieval, processing and storage procedures can have a profound effect on soil microorganisms. In particular, changes in soil microbial populations may adversely affect the biological activity of a soil and drastically alter the soil's potential to mineralize added substrates. The effects of cold storage on the biodegradation of a series of test polymers was investigated using two soils—a synthetic soil mix (SM-L8) and a field soil (Bridgehampton silt loam) from Rhode Island (RI-1). Biodegradation tests were conducted using freshly prepared/collected soil and again following storage at 4°C for 3 to 8 months. Prior to each biodegradation test, the soils were incubated at 60% water-holding capacity (WHC) and 25°C to rejuvenate the microbial populations; the soils were incubated for periods of 48 h (freshly collected soil) or 25 days (soils stored at 4°C). Soil microbial populations were assessed by enumerating different segments of the population on agar plates containing different selective media. Mineralization of the test polymers (cellulose, poly-3-hydroxybutyrate, and starch acetate, d.s. 1.5) was monitored using standard respirometric techniques. Our results demonstrated that cold storage had a generally negative effect on the soil microbial populations themselves but that its effect on the capacity of the soil microorganisms to degrade the test polymers varied between soils and polymer type. Whereas cold storage resulted in dramatic shifts in the community structure of the soil microbial populations, substantial restoration of these populations was possible by first conditioning the soils at 60% WHC and ambient temperatures for 25 days. Likewise, although the effects of cold storage on polymer mineralization varied with the test polymer and soil, these effects could be largely offset by including an initial 25-day stabilization period in the test.     

利用味精厂米渣生产发泡粉和蛋白质灭火剂

将米渣清洗、过滤以除去液化液、糖液,再加水调至130Be,用石灰调为不同pH,在不同时间下进行水解,结果表明当pH为11.5,在蒸气压为0.1MPa条件下,经过3h水解后蛋白质含量最高,可达到6.0%(水解液含量),再过滤、浓缩成为30%的蛋白质液,经过适当配制可成为蛋白质泡沫灭火剂,经过武汉市科威消防材料厂进行灭火测试,结果表明,粘度、沉淀物、发泡倍数、90%火焰控制时间、灭火时间、抗烧时间等指标均达到中华人民共和国公共安全行业标准(GA2191999);将30%的蛋白质液喷雾干燥后,可制备成为食用蛋白质发泡剂。