聚己内酯与聚羟基丁酸戊酸酯的脱氮性能对比

以可生物降解聚合物聚己内酯(PCL)和聚羟基丁酸戊酸酯(PHBV)作为反硝化缓释碳源和微生物载体,利用清水释碳和批式反硝化试验选出适用于再生水反硝化深度脱氮生物滤池的可生物降解碳源滤料,通过比较与分析碳源滤料的表面形态及物质特性和附着微生物的群落特征揭示其性能优越的原因.结果表明,PHBV反硝化启动时间短,反硝化速率高,剩余有机物浓度低,相比PCL具有更稳定持续的反硝化效果.原因是其表面粗糙,且含有大量C—O和CO等亲水性基团,易于微生物附着和降解利用;其表面附着的微生物种类多样,其中发硫菌属(Thiothrix)、假单胞属(Pseudomonas)、菌胶团属(Zoogloea)、黄杆菌属(Flavobacterium)和脱氯菌属(Dechloromonas)等优势菌属均具有异养反硝化功能.因此,PHBV更适合作为再生水反硝化深度脱氮生物滤池的碳源滤料.     

Isolation and characterisation of a carbofuran degrading Burkholderia sp. PCL3 from carbofuran-phytoremediated rhizosphere soil

A bacterial strain capable of degrading carbofuran as the sole carbon source was isolated from carbofuran-phytoremediated rhizosphere soil of rice. A 16S rRNA study identified the strain as Burkholderia sp. (isolate PCL3). Free cells of isolate PCL3 possessed inhibitory-type degradation kinetics with a q _max of 0.087 day^?1 and S _m of 248.76 mg·L^?1. Immobilised PCL3 on corncob and sugarcane bagasse possessed Monod-type degradation kinetics with a q _max of 0.124 and 0.098 day^?1, respectively. The optimal pH and temperature with the highest degradation rate coefficient of carbofuran were pH 7.5 and 35 °C, respectively.     

A review of the biodegradability and utility of poly(caprolactone)

Since the early 1970s, it has been known that exposure of poly(caprolactone) (PCL) to a variety of microorganisms results in biodegradation of this polymer. Besides the ability of PCL to be utilized as a carbon source for microorganisms, it has been demonstrated that, during degradation, carbon dioxide is generated. Soil burial and compost experiments have shown that chain scission of the PCL backbone occurs, mechanical properties of articles prepared from PCL are reduced rapidly, and significant weight loss occurs in a short time period. This inherent biodegradability of PCL, in combination with its ability to be converted by conventional extrusion equipment, allows for the preparation of biodegradable articles that have utility.Paper presented at the Bio/Environmentally Degradable Polymer Society—Third National Meeting, June 6–8, 1994, Boston, Massachusetts.     

可降解聚合物PCL、PBS在低有机污染水中固相反硝化脱氮效果比较

为了解决低有机污染高氮素水中由于低碳氮比而造成的后续脱氮问题,通过设反应填充床,外加固相碳源,对比了2种可降解聚合物PBS和PCL的反硝化效果。结果表明,（1）在进水TN质量浓度维持在14.33～18.31 mg.L-1,HRT为15.6 min时,PBS填充床平均TN去除率为94.93%,高于PCL填充床。（2）PBS填充床平均反硝化速率为13.55 mg.L-1.h-1（以N计）,高于PCL填充床的9.07 mg.L-1.h-（1以N计）。（3）PBS填充床NO3-N、NO2-N、NH3-N的出水质量浓度分别维持在0.37～0.87、0～0.20、0.01～0.07 mg.L-1,优于PCL填充床。（4）PBS和PCL颗粒表面附着的微生物以杆菌为主,伴有少量的弧菌。该研究为日后新型固相碳源的开发提供了科学依据。     

2种BDPs固相反硝化的脱氮效果对比

利用批量和连续流填充床试验对比了2种BDPs(可生物降解聚合物)——PBS(聚丁二酸丁二醇酯)和PCL(聚ε-己内酯)的反硝化效果. 批量试验结果表明,在脱氮稳定阶段,B1(PCL)和B2(PBS)对TN的平均去除率和反硝化速率分别为97.4%、67.0%和7.5、1.8 mg/(L·h),B2均明显优于B1. 连续流试验中,在进水ρ(NO₃--N)为16.8～18.8 mg/L、HRT(水力停留时间)为4.0 h的条件下,L1(PCL填充床)的反硝化速率大于L2(PBS填充床). 但是随着HRT的减小,L1呈现出比L2更快的反硝化速率. L2和L1分别在HRT为2.0和1.5 h时获得最大反硝化速率,分别为7.7和9.3 mg/(L·h). ESEM(环境扫描电子显微镜)观察结果表明,生物膜剥离后,PCL和PBS颗粒表面均出现大量的坑洞,并且PCL颗粒表面坑洞的密集程度远大于PBS. 三维荧光光谱(3D-EEM)分析结果表明,L2和L1出水中的溶解性有机物主要为类色氨酸这类简单的蛋白质和SMP(溶解性微生物代谢产物),并且L1水中SMP的荧光峰强度明显高于L2.      

可降解聚合物PCL、PBS在低有机污染水中固相反硝化脱氮效果比较

为了解决低有机污染高氮素水中由于低碳氮比而造成的后续脱氮问题,通过设反应填充床,外加固相碳源,对比了2种可降解聚合物PBS和PCL的反硝化效果。结果表明,(1)在进水TN质量浓度维持在14.33～18.31 mg.L-1,HRT为15.6 min时,PBS填充床平均TN去除率为94.93%,高于PCL填充床。(2)PBS填充床平均反硝化速率为13.55 mg.L-1.h-1(以N计),高于PCL填充床的9.07 mg.L-1.h-(1以N计)。(3)PBS填充床NO3-N、NO2-N、NH3-N的出水质量浓度分别维持在0.37～0.87、0～0.20、0.01～0.07 mg.L-1,优于PCL填充床。(4)PBS和PCL颗粒表面附着的微生物以杆菌为主,伴有少量的弧菌。该研究为日后新型固相碳源的开发提供了科学依据。     

缓释碳源滤料滤池用于二级出水的深度脱氮

以聚己内酯(PCL)为反硝化电子供体和生物载体,开发出具有脱氮和过滤功能的缓释碳源滤料滤池,并以城市污水处理厂二级出水为原水进行深度脱氮试验,结果表明,在20.1～22.0℃的条件下,进水总氮(TN)质量浓度30.0 mg.L-1,HRT为0.5 h,反硝化负荷达54.0 mg.(L.h)-1时,TN的去除率最高可达98.9%;出水总有机碳(TOC)为6.5～8.4 mg.L-1,比进水增加了2.0～3.0 mg.L-1;出水SS低于4.0 mg.L-1;反硝化过程所需有机碳主要是在微生物作用下缓慢释放,其占到有机碳总释放量的84.2%;对碳源滤料进行扫描电镜观察,发现在其表面形成了致密的生物膜,其中微生物以杆菌和丝状菌为主.     

Biodegradation of carbofuran in sequencing batch reactor augmented with immobilised Burkholderia cepacia PCL3 on corncob

The performance of sequencing batch reactors (SBRs) augmented with immobilised Burkholderia cepacia PCL3 on corncob for biodegradation of carbofuran in basal salt medium (BSM) was studied. A 2.0-L SBR with a working volume of 1.5 L was operated for a total cycle of 48 h, consisting of 1.0 h fill phase, 46 h react phase and 1.0 h decant phase. The initial pH of the feed medium was 7.0. Air was fed into the reactor at a controlled flow rate of 600 mL·min ^?1. The effect of hydraulic retention time (HRT) (14 to 6 days) on carbofuran-degradation efficiency was investigated at a carbofuran concentration in the feed medium of 20 mg·L ^?1. The shortest HRT resulting in complete degradation of carbofuran was 8 days. At 75% of the optimum HRT (6 days), the effects of biostimulation using organic amendments, i.e. molasses, cassava pulp, rice bran and spent yeast, and the effect of carbofuran concentration in the feed medium (20–80 mg·L ^?1) were investigated. The optimum conditions for SBRs were an initial carbofuran concentration of 40 mg·L ^?1 and 0.1 g·L ^?1 of rice bran as a biostimulated amendment. Complete degradation of carbofuran with a first-order kinetic constant (k ₁) of 0.044 h^?1 was achieved under these optimum conditions.     

Physical properties and biodegradability of blends containing poly(ε-caprolactone) and tropical starches

In order to assess feasibility of tropical starches (sago and cassava starches) as biodegradable plastic materials, blending with poly(-caprolactone) (PCL), a biodegradable polymer, was carried out. It was confirmed that the physical properties (tensile strength and elongation) of PCL/sago and PCL/cassava blends were similar to those of PCL/corn blend, suggesting that sago and cassava starches can also be blended with PCL for production of biodegradable plastic. However, the properties of all PCL/starch blends were still low compared with those of polyethylene. Enzymatic degradability evaluation showed that lipase degradation of PCL and-amylase degradation of starch increased as the starch content in the blend increased. Burial test of the blends for 1, 3, and 5 months was carried out and the rate of degradation of the PCL/sago blend was confirmed to be slower than those of PCL/corn and PCL/cassava blends. Observation of the film blends structure by scanning electron microscope revealed that the starch was dispersed in a PCL continuous phase. Furthermore, changes in the film surface before and after enyzme treatments were observed.