An alkaline phosphatase from Bacillus amyloliquefaciens YP6 of new application in biodegradation of five broad-spectrum organophosphorus pesticides

In recent decades, biodegradation has been considered a promising and eco-friendly way to eliminate organophosphorus pesticides (OPs) from the environment. To enrich current biodegrading-enzyme resources, an alkaline phosphatase (AP3) from Bacillus amyloliquefaciens YP6 was characterized and utilized to test the potential for new applications in the biodegradation of five broad-spectrum OPs. Characterization of AP3 demonstrated that activity was optimal at 40?°C and pH 10.3. The activity of AP3 was enhanced by Mg²⁺, Ca²⁺, and Cu²⁺, and strongly inhibited by Mn²⁺, EDTA, and L-Cys. Compared to disodium phenyl phosphate, p-nitrophenyl phosphate (pNPP) was more suitable to AP3, and the V_m, K_m, k_cat, k_cat/K_m values of AP3 for pNPP were 4,033?U mg^?1, 12.2?mmol L^?1, 3.3?×?10⁶ s^?1, and 2.7?×?10⁸ s^?1mol^?1L, respectively. Degradation of the five OPs, which included chlorpyrifos, dichlorvos, dipterex, phoxim, and triazophos, was 18.7%, 53.0%, 5.5%, 68.3%, and 96.3%, respectively, after treatment with AP3 for 1?h. After treatment of the OP for 8?h, AP3 activities remained more than 80%, with the exception of phoxim. It can be postulated that AP3 may have a broad OP-degradation ability and could possibly provide excellent potential for biodegradation and bioremediation in polluted ecosystems.     

废弃SCR催化剂中钒和钨的浸出及回收

采用NaOH溶液一次性浸出废弃SCR催化剂中的钒和钨,并用硫酸对浸出液进行除杂,再利用NH4Cl和硫酸分步对浸出液中的钒和钨进行沉淀回收。在NaOH质量分数40%、液固比8、浸出时间4 h、浸出温度90℃的最佳碱浸条件下,钒和钨的浸出率分别达到90.44%和84.49%。除杂过程的铝去除率达到100%,硅去除率达到77.56%。在沉钒pH为8.0、n(NH_4~+)∶n(V)为4的最佳沉钒条件下,钒回收率达到82.79%。在n(SO_4~(2-))∶n(W)为2的最佳沉钨条件下,钨回收率达到76.41%。     

卤素法电镀锡阳极泥中锡的碱浸回收及动力学分析

以NaOH溶液为浸出剂,采用碱浸法回收卤素法电镀锡阳极泥中的锡,考察了浸出效果的影响因素,并对浸出过程的动力学进行了研究。实验结果表明:在NaOH质量浓度200 g/L、反应温度90℃、液固比6、反应时间240 min的最佳工艺条件下,锡的浸出率约为98%;最佳工艺条件下,浸出液中的氟离子对后续锌粉置换回收锡没有影响;在303.15~363.15 K范围内,该浸出过程主要受内扩散控制,反应活化能为9.725 k J/mol。     

废无汞碱性电池极性材料制备锰锌铁氧体磁性纳米颗粒

以硝酸浸取废无汞碱性电池极性材料,再加入硝酸铁及蔗糖生成前驱体,最后通过焙烧制得锰锌铁氧体磁性纳米颗粒。优化了酸浸和焙烧条件,采用FTIR和DTA-TG技术研究了前驱体的形成和热解过程,采用XRD、FTIR、TEM技术和振动样品磁强计对锰锌铁氧体进行了表征。结果表明:废无汞碱性电池极性材料酸浸的最佳条件为H_2O_2加入量3%(w)、液固比10 mL/g、稀硝酸浓度4 mol/L、浸取温度40℃,该条件下浸取10 min锰和锌的浸出率均可达100%;所得前驱体为葡萄糖酸盐,其最佳焙烧条件为焙烧温度450℃、焙烧时间2 h;最佳条件下所得锰锌铁氧体为尖晶石型Mn_(0.5)Zn_(0.5)Fe_2O_4,其颗粒为球形、大小均匀,且磁性能优良。     

分光光度法测定地表水中总氮的监测质量控制指标研究

运用碱性过硫酸钾-紫外分光光度法对总氮的标准样品及实际样品进行研究分析,通过全国多家实验室的大量监测数据,得出了当前常用的精密度及准确度方面质量控制指标的建议值。研究表明：标准样品在0.5~3.5mg/L浓度范围内,相对标准偏差RSD≤5.0%;室间相对标准偏差RSD′≤10%;相对误差RE≤±10%;实际样品在0.07~10mg/L浓度范围内时,相对偏差RD≤10.0%;加标回收率范围为90%~110%。     

Study on sulfur migration in activated carbon adsorption-desorption cycle: Effect of alkali/alkaline earth metals

Activated carbon (AC) has been widely used in the removal of SO₂ from flue gas owing to its well-developed pore structure and abundant functional groups. Herein, the effect of alkali/alkaline earth metals on sulfur migration was investigated based on the dynamic adsorption and temperature programmed desorption experiment. The adsorption and desorption properties of six types of AC (three commercial and three laboratory-made) were carried out on a fixed-bed experimental device, and the physical and chemical properties of samples were determined by X-ray fluorescence, X-ray diffraction, scanning electron microscopy/energy dispersive X-ray, and X-ray photoelectron spectroscopy analysis. The experimental results showed that the adsorbed SO₂ cannot be completely desorbed by increasing the regeneration temperature (350 – 850°C), while the SO₂ fixed in the AC combines with the Ca-based minerals in the ash to form a stable sulfate. For different samples, higher ash content, higher CaO content in the ash and a more developed pore structure lead to a higher SO₂ fixation rate. Moreover, the multiple adsorption-desorption cycles experiment showed that the effect of SO₂ fixation is mainly reflected in the first cycle, after which the adsorption and desorption amount are approximately the same. This study elucidates the effect of alkali/alkaline earth metals on the adsorption-desorption cycle of AC, which provides a deeper understanding of sulfur migration in the AC flue gas desulfurization process.     

方解石基组配钝化剂与低积累玉米协同修复效果

针对典型北方碱性镉和铅复合污染农田土壤,开展土壤钝化与低积累农作物协同修复田间试验,以方解石作为主量钝化材料,分别复配少量熟石灰、沸石粉和生物炭形成组配钝化剂.研究在CL(方解石+熟石灰)、CZ(方解石+沸石)、CB(方解石+生物炭)和CLZB(方解石+熟石灰+沸石+生物炭)不同组配条件下,对土壤理化性质、重金属Cd和...     

基质投加方式对污泥碱性发酵性能的影响

为了研究低温条件(15±2)℃下投加方式对剩余污泥碱性发酵的影响,将剩余污泥分别在NaOH、KOH、Ca(OH)2和混合碱(Ca(OH)2和KOH) 4种碱性(pH=10±0.2)系统中进行发酵,并在系统稳定后依次改变污泥投加方式(1次投加污泥、平均2次投加和平均3次投加),分别对发酵体系的剩余污泥溶液化、溶解性蛋白质、溶解性多糖、挥发性脂肪酸(SCFAs)和关键酶(水解酶和辅酶420(F420))进行研究.研究发现,4种碱性发酵体系中,不同投加方式对剩余污泥的水解和酸化性能具有显著的影响,其中SCOD随着污泥投加次数的增加略有减小,但是发酵液中可溶性的蛋白质和多糖有增加趋势.水解酶活性随着污泥投加次数的增加而降低,但是在NaOH和KOH发酵体系中,辅酶420随着投加次数的增加而增大,混合碱发酵体系中其活性基本不变,而在Ca(OH)2发酵体系中其活性则降低.NaOH、KOH和混合碱发酵体系产酸能力随投加次数的增加而下降,但是Ca(OH)2 发酵体系酸化能力则先增大后少量降低,由此发现,Ca(OH)2发酵体系水解及产酸能力较为稳定,同时该体系中乙酸/SCFAs最大,高于其他发酵体系的10%左右.     

厦门周边水库浮游植物碱性磷酸酶活性研究

从2010年6月初至12月末,对厦门周边九龙江江东水库、厦门大学芙蓉湖和情人湖三个淡水湖库进行两周一次的连续采样,开展水体总碱性磷酸酶活性(APA)的研究。从营养盐和叶绿素a水平看,三个湖库属不同的富营养化程度:芙蓉湖>情人湖>江东水库。群落水平的总碱性磷酸酶活性和溶解性磷酸盐(SRP)浓度的结果表明,三处水体均呈现群落水平上的磷胁迫状态;不同水体的浮游植物群落结构存在显著差异,同时不同浮游植物的磷胁迫亦不同,蓝藻是芙蓉湖的绝对优势类群且标记率较低,绿藻是情人湖和江东水库的优势类群,且标记率较高。群落组成在一定程度上可以反映浮游植物群落的磷胁迫状态。     

泉州湾河口湿地土壤脲酶和磷酸酶活性研究

本文对泉州湾河口湿地不同区域(上游、中游和下游)、不同红树植被下土壤脲酶和磷酸酶活性在不同季节的变化规律进行了研究。结果表明:土壤脲酶和磷酸酶活性存在极显著的相关性;两种酶在不同区域间均无显著差异,季节变化均表现为春季大于秋季;有红树植被的土壤脲酶和磷酸酶活性皆大于空地和裸地,土壤脲酶不同红树植被下无显著差异,磷酸酶则表现为百年生桐花树和互花米草显著高于其余植被,秋茄和白骨壤次之。随着土壤垂直深度的增加,脲酶和磷酸酶活性整体上表现为逐渐降低的趋势,湿地土壤脲酶和磷酸酶活性受植被类型和根系生长状况显著影响。以上结果为泉州湾河口湿地的生态修复与环境保护提供了一定的理论依据。