Rock phosphate solubilizing and cellulolytic actinomycete isolates of earthworm casts

Four microbial isolates, OP2, OP3, OP6, and OP7, of earthworm casts ofPontoscolex corethrurus were found to be acid tolerant actinomycetes and efficient rock phosphate (RP) solubilizers that could grow fast on NH₄Cl-enriched or N-free carboxymethyl cellulose or glucose as sole carbon source. CMC (carboxymethyl cellulose) induced production of extracellular cellulase enzyme and the production of reducing sugar in all the isolates. RP solubilizing power was observed to be inversely related to glucose consumption. The most efficient RP solubilizer was found to consume the least glucose. Growth was faster on cellulose than on glucose media. N-free CMC induced greater glucose production than NH₄Cl-enriched CMC medium. Both CMC and glucose media were acidified by all the isolates, however, RP solubilizing power decreased with acidification. Solubilization power was greatest with isolate OP7, which also produced the greatest amount of reducing sugar per gram CMC. Both RP solubilizing power and the cellulolytic efficiency varied among isolates. A minimum of 631 μg P/0.1 g RP and a maximum of 951.4 μg P/0.1 g RP was recorded.     

苯醌对聚合硅酸铁多相UV-Fenton体系的增效机制

通过构建苯醌增效聚合硅酸铁多相UV-Fenton体系,讨论了体系中橙Ⅱ的脱色和降解途径.在研究苯醌浓度对聚合硅酸铁铁离子的释放、Fe²⁺与Fe³⁺之间的转化、H₂O₂分解和·OH生成影响的基础上,提出了苯醌对聚合硅酸铁多相UV-Fenton体系的增效机制.结果表明,随苯醌浓度的增加,其紫外光下光解还原聚合硅酸铁并释放Fe²⁺的程度增大、H₂O₂分解速度加快、产生·OH浓度峰值增高且出现的时间提前;苯醌增效体系释放于溶液中的Fe²⁺可以通过Fenton反应转化成Fe³⁺,反应结束后聚合硅酸铁能重新吸附Fe³⁺并使其浓度降低,避免了增效体系铁离子的二次污染.本研究将为多相催化剂催化过程的调控提供新的视角,为多相光助-芬顿反应在有机废水资源化中的应用提供理论依据和技术支持.     

UV/H2O2 oxidation of tri(2-chloroethyl) phosphate: Intermediate products, degradation pathway and toxicity evaluation

Tri(2-chloroethyl) phosphate (TCEP) with the initial concentration of 5 mg/L was degraded by UV/H₂O₂ oxidation process. The removal rate of TCEP in the UV/H₂O₂ system was 89.1% with the production of Cl^? and PO₄^3? of 0.23 and 0.64 mg/L. The removal rate of total organic carbon of the reaction was 48.8% and the pH reached 3.3 after the reaction. The oxidative degradation process of TCEP in the UV/H₂O₂ system obeyed the first order kinetic reaction with the apparent rate constant of 0.0025 min^?1 (R²=0.9788). The intermediate products were isolated and identified by gas chromatography-mass spectrometer. The addition reaction of HO? and H₂O and the oxidation reaction with H₂O₂ were found during the degradation pathway of 5 mg/L TCEP in the UV/H₂O₂ system. For the first time, environment risk was estimated via the “ecological structure activity relationships” program and acute and chronic toxicity changes of intermediate products were pointed out. The luminescence inhibition rate of photobacterium was used to evaluate the acute toxicity of intermediate products. The results showed that the toxicity of the intermediate products increased with the increase of reaction time, which may be due to the production of chlorine compounds. Some measures should be introduced to the UV/H₂O₂ system to remove the highly toxic Cl-containing compounds, such as a nanofiltration or reverse osmosis unit.     

新型Fe3O4@α-MnO2活化过一硫酸盐降解水中偶氮染料

采用两步水热法制备了新型磁性纳米Fe₃O₄@α-MnO₂复合材料作为催化剂,用于活化过一硫酸盐（PMS）产生强氧化性的硫酸根自由基（SO₄^-·）氧化降解偶氮染料活性黑5（RBK5）.采用透射电子显微镜（TEM）,X射线粉末衍射仪（XRD）和振动样品磁强计（VSM）对制备的催化剂进行表征,证明成功合成了纳米α-MnO₂包覆Fe₃O₄形态的Fe₃O₄@α-MnO₂催化剂,催化剂的饱和磁化强度为39.89emu/g.Fe₃O₄@α-MnO₂催化剂活化PMS与单一的Fe₃O₄和α-MnO₂活化PMS相比,具有更高的催化效率,说明铁锰双金属存在协同作用.同时研究了催化剂的投加量、PMS的浓度和初始pH值等各种因素对RBK5的降解效率以及反应动力学的影响.实验结果表明,Fe₃O₄@α-MnO₂催化剂活化PMS降解RBK5的过程符合准一级反应动力学,在催化剂投加量为1.2g/L,PMS的浓度为4mmol/L,初始pH值为7.0,反应时间为60min的情况下,浓度为30mg/L的RBK5的降解效率可达到91%,此时RBK5的降解速率常数也达到最高值0.023min^-1.此外,通过加入自由基淬灭剂甲醇、叔丁醇和硝基苯判断了Fe₃O₄@α-MnO₂/PMS体系中起主要氧化降解作用的活性物种为SO₄^-·.     

Simultaneous sorption of aqueous phenanthrene and phosphate onto bentonites modified with AlCl3 and CTMAB

The purpose of this work is to synthesize a new type of bentonite sorbent that can simultaneously remove both organic compounds and phosphate from water. Inorganic-organic bentonites (Al-CTMAB-Bent) were synthesized by modifying bentonites with both AlCl₃ and cetyltrimethyl ammonium bromide (CTMAB). Simultaneous sorption of aqueous phenanthrene and phosphate onto Al-CTMAB-Bent was examined. Removal rates of phenanthrene and phosphate from water reached 96.3% and 90.2%, respectively, at their respective initial concentrations of 1 mg/L and 5 mg/L and the added amount of Al-CTMAB-Bent was 1.25 g/L. The residual turbidity of the Al-CTMAB-Bent suspension decreased 81.4% compared to that of organobentonite suspension after a 1 h settling time. Thus, inorganic-organic bentonite can be used to treat wastewater containing both organic pollutants and phosphate. Translated from Environmental Science, 2006, 27(1): 91–94 [译自: 环境科学]     

磷酸三丁酯萃取邻苯二酚的研究

以磷酸三丁酯（TBP）为络合剂，正辛醇，石油醚，氯仿，四氯化碳，环己烷为稀释剂，测定了络合萃取剂对邻苯二酚溶液的相平衡分配比，讨论了稀释剂，盐，体系pH值和磷酸三丁酯（TBP）络合剂的含量对萃取相平衡分配比D的影响，并分析了形成络合物的组成。     

硝酸银滴定法与硫氰酸汞分光光度法测定水中氯化物（Cl^-）的方法比对

用硝酸银滴定法、硫氰酸汞分光光度法分别测定高浓度的考核已知样及低浓度的考核未知样，均合格。说明两种方法都能满足水和废水中氯化物（Cl^-）测定的需要。     

清洁生产是发展云南磷肥工业的必由之路

云南磷矿储量占全国总储量的１９．１３％，将建成全国最大的磷化工基地。造成磷肥工业污染问题的原因一是矿物原料品位低，二是高污染的原料路线，三是非经济生产规模，四是落后的生产管理。要合理有效地利用资源，要使环境能够承载，就必须推行清洁生产，这是云南磷肥工业可持续发展的必由之路。     

论我国磷业发展战略

我国磷矿资源丰富,但长期以来缺乏磷业发展战略部署,磷矿山建设缓慢,磷肥供应不足,造成氮、磷、钾施肥比例失调,全国有2/3的耕地缺磷,其中半数严重缺磷,农业上出现了“报酬递减”现象。本文在分析我国磷业发展概况的基础上进行了磷矿与磷肥需求预测,根据我国农业及磷矿资源分布与有关开发建设条件等,提出了我国磷业发展战略与宏观生产布局,论证了发展磷业应立足国内、以国民经济总体部署为准则、建立4个大型综合性磷业基地、以资源型布点为主,辅以混合型、临海型和消费型布点等磷业发展战略中的重大问题,并提出了发展我国TS形双结构磷业网络的思想。     

Al（Ⅲ）溶液的水解─沉淀特性研究─—磷酸根的作用

采用连续碱滴定方法和Ｘ射线衍射及红外光谱分析，研究了在Ａｌ（Ⅲ）－磷酸根溶液体系中Ａｌ（Ⅲ）的水解－沉淀特性，结果表明，当Ｐ／Ａｌ＞０．０５时，磷酸根对Ａｌ（Ⅲ）的水解－成核－沉淀过程有显的促进作用，描述了磷酸根作用的动力学机理。