聚乙烯醇在超临界水氧化中降解

以H2O2为氧化剂用间歇式超临界水氧化装置对聚乙烯醇(PVA)废水进行降解研究。通过正交实验,考察了反应温度、压力、时间及氧化剂过氧倍数对降解效果的影响,并且采用GC/MS对液相降解产物进行表征推测其可能降解途径。结果表明:PVA在SCWO体系中能完全降解,反应温度440℃、压力28 MPa、氧化剂过氧倍数4、反应40 min时,COD去除率为99.03%,出水COD=89.09 mg/L。PVA在SCWO体系中降解为烯烃、烯酮、醇和羧酸类中间产物、最终降解为小分子的饱和直链烷烃类液相产物。     

改性聚乙烯醇树脂恒湿性能研究

制备了聚乙烯醇(PVA)吸附性树脂,根据弹药贮存环境湿度的变化,设计了测定产品恒湿性能的实验装置,利用该装置测试表明,该树脂具有一定的恒湿性能,当产品用量为1.5 g、90%RH下预吸湿4 h,其恒湿范围是45.3%~67.7%RH,满足弹药贮存对环境湿度的要求。     

Controlled release formulations of metribuzin: Release kinetics in water and soil

Controlled release (CR) formulations of metribuzin in Polyvinyl chloride [(PVC) (emulsion)], carboxy methyl cellulose (CMC), and carboxy methyl cellulose-kaolinite composite (CMC-KAO), are reported. Kinetics of its release in water and soil was studied in comparison with the commercial formulation (75 DF). Metribuzin from the commercial formulation became non-detectable after 35 days whereas it attained maxima between 35–49 days and became non-detectable after 63 days in the developed products. Amongst the CR formulations, the release in both water and soil was the fastest in CMC and slowest in PVC. The CMC-KAO composite reduced the rate of release as compared to CMC alone. The diffusion exponent (n value) of metribuzin in water and soil ranged from 0.515 to 0.745 and 0.662 to 1.296, respectively in the various formulations. The release was diffusion controlled with half release time (t_1/2) from different controlled release matrices of 12.98 to 47.63 days in water and 16.90 to 51.79 days in soil. It was 3.25 and 4.66 days, respectively in the commercial formulation. The period of optimum availability of metribuzin in water and soil from controlled released formulations ranged from 15.09 to 31.68 and 17.99 to 34.72 days as against 5.03 and 8.80 days in the commercial formulation.     

臭氧氧化—A/O工艺处理PVA废水

采用臭氧氧化—A/O工艺处理聚乙烯醇（PVA）废水,研究了臭氧氧化时间、臭氧流量以及废水pH等因素对臭氧氧化效果的影响。实验结果表明：当气体臭氧质量浓度为30 mg/L、臭氧氧化时间为45 min、臭氧流量为4 L/min、废水pH为8时,PVA质量浓度从进水的93.2 mg/L降至4.5 mg/L;PVA溶液的BOD₅/COD从0.014增加至0.310,可生化性明显改善;臭氧氧化—A/O工艺处理后出水COD降至50 mg/L左右,达到GB 8978—1996《污水综合排放标准》中的一级排放标准;出水PVA质量浓度为1.6 mg/L,明显优于A/O工艺（33.1 mg/L）。     

Extruded Cornstarch-Glycerol-Polyvinyl Alcohol Blends: Mechanical Properties, Morphology, and Biodegradability

Elongation properties of extruded cornstarch were improved by blending with glycerol. Further blending of starch-glycerol with polyvinyl alcohol (PVOH) resulted in significant improvements in both tensile strength (TS) and elongation at break. Samples of starch-glycerol without PVOH equilibrated at 50% relative humidity had a TS of 1.8 MPa and elongation of 113%, whereas those containing PVOH had a TS and elongation of 4 MPa and 150%, respectively. Dynamic mechanical analysis (DMA) of starch-glycerol-PVOH blends showed that decreases in glass transition temperatures (T _g values) were proportional to glycerol content. Scanning electron microscopy (SEM) of fractured surfaces revealed numerous cracks in starch-glycerol (80:20) samples. Cracks were absent in starch-glycerol (70:30) samples. In both blends, many starch granules were exposed at the surface. No exposed starch granules were visible in blends with added PVOH. Starch-glycerol samples incubated in compost lost up to 70% of their dry weight within 22 days. Addition of PVOH lowered both the rate and extent of biodegradation.     

具有共轭结构的CDPVA/ZnO复合光催化剂的制备及其可见光催化性能

CDPVA是一种具有共轭多烯序列的聚乙烯醇(PVA)衍生物。通过低温热处理法制备了CDPVA/ZnO复合光催化剂。表征结果显示,PVA经低温热处理后形成了具有一定共轭结构的CDPVA并包覆于纳米ZnO颗粒表面,提高了光催化剂的可见光响应能力,有效促进了光生空穴和电子的分离。当PVA与纳米ZnO的质量比为1∶100时,CDPVA/ZnO的可见光催化活性最高;在催化剂投加量为0.5 g/L、初始罗丹明B质量浓度为4 mg/L、可见光照射50 min的条件下,罗丹明B降解率为97.51%,明显优于纯纳米ZnO;CDPVA/ZnO循环使用9次后仍保持较高的罗丹明B降解率,表明CDPVA的包覆有效抑制了纳米ZnO的光腐蚀,提高了光催化剂的稳定性。     

聚乙烯醇罐区火灾爆炸事故树分析

通过现场的调研与事故树分析相结合的手段对某厂聚乙烯醇车间聚合罐区火灾爆炸事故的危险因素进行了识别与分析.以该罐区可能发生的火灾爆炸事故作为顶上事件,对可能引发顶上事件的21个基本事件及一个条件事件构建事故树,利用最小割集、最小径集及结构重要性计算手段进行事故风险程度分析,从而确定醋酸乙烯暴聚是聚合罐区的首要危险源,而促发醋酸乙烯暴聚的物料长时间停留、气相氧含量过高、温度控制失效、阻聚剂含量不足等四个基本事件是导致聚合罐区火灾爆炸事故的最危险因素.本文对以上聚合罐区发生火灾爆炸事故的风险因素进行详细定性分析,并在此基础上有针对性的提出了相应的安全预防控制措施.同时,该聚合罐区的事故树分析结论也可以为同类别化工单位罐区的日常运行、设计改造、维护保养等工作提供理论依据.     

CNFM的制备及其协同电动技术修复土壤重金属的研究

首先采用静电纺丝工艺制备壳聚糖纳米纤维膜并优化了其制备条件,将制备的纳米纤维膜协同电动技术对土壤中的重金属（Cu、Cr）进行了修复.结果表明,纳米纤维膜制备的优化条件为：m（壳聚糖CS）/m（聚乙烯醇PVA）为20：80,乙酸质量浓度为20%,混合溶液质量分数为8%;所制备的纳米纤维膜平均直径为37.11nm,对金属的吸附平衡时间为4h.单一的电动修复来处理土壤中的重金属效率较低,Cu和Cr的去除效率仅为34.9%和11.7%;采用电动技术协同壳聚糖纳米纤维膜能显著提高重金属的去除效率,二者的去除效率分别达到了82%和91%.     

处理悬浮聚合法聚氯乙烯离心母液的EGSB反应器中的污泥性质

在EGSB反应器处理低质量浓度PVC离心母液废水的试验研究中,着重检测了反应器内颗粒污泥的性质及其活性影响因素,并用扫描电镜观测了颗粒污泥表面菌体分布情况.结果表明:反应器运行180 d后,当HRT为8 h时,EGSB反应器对PVC离心母液TOC去除率稳定在50%以上;EGSB反应器中颗粒污泥的形状、颜色、粒径分布、沉降速度、元素成分等方面都发生了变化;污泥最大比产甲烷活性为115 mL/(g·d);通过扫描电镜,在颗粒污泥表面观察到一些丝状菌和短杆菌等,但菌体密度不高;营养物质对颗粒污泥活性影响十分明显.      

黑臭河道中聚乙烯醇/海藻酸钠固定微米沸石粉去除氨氮

采用聚乙烯醇和海藻酸钠对微米沸石粉进行固定,通过批次吸附实验探究水凝珠去除氨氮的效果及其机制.结果表明:PAZ-20的投加量超过10 g·L-1时,氨氮去除率达到了 80％之上.pH为3～8时,pH增加对PAZ吸附氨氮影响不大,当pH从9增至11时,氨氮去除率随pH的增大而显著减小,PAZ吸附氨氮的最佳pH为7.水温为5～25℃时,氨氮去除率随温度升高而逐渐上升,25～35℃内略有上升,水温升至401,氨氮去除率有所下降.准二级动力学方程和Langmuir吸附等温线模型能够更好地拟合PAZ吸附氨氮.PAZ-20对于水中阳离子的吸附能力为:K+＞Mg2+＞Na+＞Ca2+.共存阳离子对PAZ吸附氨氮的影响程度为:K+＞Na+＞Ca2+＞Mg2+.扫描电镜和傅里叶红外光谱分析显示微米沸石粉被良好地固定在聚乙烯醇/海藻酸钠中.PAZ可用于黑臭河道的治理,且受共存阳离子的干扰较小.