创新价值链视角下企业创新效率差异及影响因素分析——基于江苏省国家高新区企业的验证

中国经济新常态背景下,高新区企业创新增效提质是增强高新区创新能力的内生动力.从创新价值链视角出发,将企业创新过程分为技术开发阶段和经济转化阶段,运用两阶段DEA模型分别对2016年江苏省12个国家高新区、11个技术领域以及各高新区内不同技术类型企业的整体和分阶段创新效率进行测度,并构建Tobit回归模型探究每个阶段企业创新效率的影响因素.研究表明:(1)江苏省国家高新区整体创新效率有较大提升空间,其中技术开发效率表现优于经济转化效率.(2)高创新效率的技术领域集中在电子与信息、新材料等,生物医药、环境保护和光机电一体化等技术领域整体创新效率处于较低水平.(3)以各阶段创新效率均值为分界,划分创新资源利用的四种模式,大部分高新区企业处于高开发-低转化和低开发-高转化型模式,存在技术创新与经济转化联系不够紧密的现象.(4)资本投入水平、劳动力的“质”和“量”、政府支持力度对企业创新效率的影响存在明显的阶段差异性.最后,根据研究结果,从强化知识交流网络、集聚多元化人才、调整资源投入产出评估方式及采取扬优补短式效率提升路径四个方面给出提升高新区企业创新效率的政策建议.     

A combined radical and non-radical oxidation processes for efficient degradation of Acid Orange 7 in the homogeneous Cu(II)/PMS system: important role of chloride

Environmental Science and Pollution Research - Trace copper ion (Cu(II)) in water and wastewater can trigger peroxymonosulfate (PMS) activation to oxidize organic compounds, but it only works under...     

Coupled electrochemical methods for nitrogen and phosphorus recovery from wastewater: a review

Environmental Chemistry Letters - Declining mineral resources, high fertilizer production cost and widespread eutrophication are calling for the recovery of nitrogen and phosphorus from wastewaters...     

Analytical methods for microplastics in the environment: a review

Environmental Chemistry Letters - Microplastic pollution is a recently discovered threat to ecosystems requiring the development of new analytical methods. Here, we review classical and advanced...     

高燃速推进剂成型过程中的安全性分析

为研究高燃速推进剂成型过程中的安全性,根据配方组成和工艺条件,对其压伸过程的热点形成因素进行了理论分析,并采用热-结构耦合方法,选择有限元软件ABAQUS对其不同工艺条件下的压伸过程进行了建模分析。结果表明:在压伸过程中,物料在收缩段承受的压力最大,且温度变化显著。物料中残留的气泡是影响高燃速推进剂压伸成型过程安全性的主要因素。当物料中有残留气泡时,随压伸过程所加的载荷不同,气泡的最高温度会显著上升,载荷为15MPa时,气泡的最高温度可达139.3℃;载荷为20 MPa时,温度可达264.2℃。     

液液萃取-固相萃取-气质联用测定指甲中的多溴联苯醚与多氯联苯

利用液液萃取(LLE)与固相萃取法(SPE)提取和净化人体指甲中的多溴联苯醚(PBDEs)和多氯联苯(PCBs),经浓硫酸除脂后,利用气相色谱-质谱联用仪(GC-MS)测定PBDEs和PCBs.对提取溶剂比例、净化柱类型(复合硅胶柱与固相萃取柱)、固相萃取条件(洗脱溶剂及体积)以及脂肪的去除方法进行了优化,加标回收率较前人基础上均有明显提高.加标回收试验结果显示,PBDEs和PCBs平均基质加标回收率分别为90%—110%和71%—102%,空白加标回收率分别为70%—110%和60%—100%之间,仪器检出限(IDL)分别为0.034—0.120μg·L~(-1)和0.032—0.392μg·L~(-1).本方法快速、简单、高效,能够满足指甲中PBDEs和PCBs的分析.同时本研究利用该方法对电子垃圾拆解地区居民的指甲样品进行测定,PBDEs和PCBs平均浓度分别为623 ng·g~(-1)和148 ng·g~(-1),BDE(-154、-153、-183、-209)和PCB(-8、-28、-52、-66、-101、-77、-118、-153、-187)在所有样品中均检出,女性指甲中PBDEs与PCBs的浓度普遍高于男性.     

Determination of 27 pharmaceuticals and personal care products (PPCPs) in water: The benefit of isotope dilution

• Isotope dilution method was developed for the determination of 27 PPCPs in water. • The established method was successfully applied to different types of water samples. • The correction effect of corresponding 27 ILSs over 70 d was investigated. • Benefit of isotopic dilution method was illustrated for three examples. Pharmaceuticals and personal care products (PPCPs) are a unique group of emerging and non-persistent contaminants. In this study, 27 PPCPs in various water samples were extracted by solid phase extraction (SPE), and determined by isotope dilution method using liquid chromatography coupled to tandem triple quadruple mass spectrometer (LC-MS/MS). A total of 27 isotopically labeled standards (ILSs) were applied to correct the concentration of PPCPs in spiked ultrapure water, drinking water, river, effluent and influent sewage. The corrected recoveries were 73%–122% with the relative standard deviation (RSD)<16%, except for acetaminophen. The matrix effect for all kinds of water samples was<22% and the method quantitation limits (MQLs) were 0.45–8.6 ng/L. The developed method was successfully applied on environmental water samples. The SPE extracts of spiked ultrapure water, drinking water, river and wastewater effluent were stored for 70 days, and the ILSs-corrected recoveries of 27 PPCPs were obtained to evaluate the correction ability of ILSs in the presence of variety interferences. The recoveries of 27 PPCPs over 70 days were within the scope of 72%–140% with the recovery variation<37% in all cases. The isotope dilution method seems to be of benefit when the extract has to be stored for long time before the instrument analysis.     

Biological conversion pathways of sulfate reduction ammonium oxidation in anammox consortia

• The SRAO phenomena tended to occur only under certain conditions. • High amount of biomass and non-anaerobic condition is requirement for SRAO. • Anammox bacteria cannot oxidize ammonium with sulfate as electron acceptor. • AOB and AnAOB are mainly responsible for ammonium conversion. • Heterotrophic sulfate reduction mainly contributed to sulfate conversion. For over two decades, sulfate reduction with ammonium oxidation (SRAO) had been reported from laboratory experiments. SRAO was considered an autotrophic process mediated by anammox bacteria, in which ammonium as electron donor was oxidized by the electron acceptor sulfate. This process had been attributed to observed transformations of nitrogenous and sulfurous compounds in natural environments. Results obtained differed largely for the conversion mole ratios (ammonium/sulfate), and even the intermediate and final products of sulfate reduction. Thus, the hypothesis of biological conversion pathways of ammonium and sulfate in anammox consortia is implausible. In this study, continuous reactor experiments (with working volume of 3.8L) and batch tests were conducted under normal anaerobic (0.2≤DO<0.5 mg/L) / strict anaerobic (DO<0.2 mg/L) conditions with different biomass proportions to verify the SRAO phenomena and identify possible pathways behind substrate conversion. Key findings were that SRAO occurred only in cases of high amounts of inoculant biomass under normal anaerobic condition, while absent under strict anaerobic conditions for same anammox consortia. Mass balance and stoichiometry were checked based on experimental results and the thermodynamics proposed by previous studies were critically discussed. Thus anammox bacteria do not possess the ability to oxidize ammonium with sulfate as electron acceptor and the assumed SRAO could, in fact, be a combination of aerobic ammonium oxidation, anammox and heterotrophic sulfate reduction processes.     

Metagenomic analysis reveals the effects of cotton straw–derived biochar on soil nitrogen transformation in drip-irrigated cotton field

Environmental Science and Pollution Research - Biochar has been widely accepted as a soil amendment to improve nitrogen (N) use efficiency, but the effect of biochar on N transformation metabolic...     

原子荧光法测定水中汞的原子化条件研究

分别采用热原子化原子荧光法(热汞法)和冷原子化原子荧光法(冷汞法)测定水中汞,比较了两种方法的检出限、线性相关系数、准确度和精密度的差异。冷汞法和热汞法的检出限分别为0.003和0.01μg/L,标准曲线相关系数分别为0.999 9和0.999 7,加标回收率范围分别为102%~106%和106%~113%。结果表明,冷汞法比热汞法具有更低的检出限,灵敏度和准确度也略优于热汞法。对于冷汞法,提高负高压有利于提高方法的灵敏度、准确度,并具有更低的方法检出限。