The Comparison of Criticism on Modern Humanism by Marxism and Post-modernism

马克思主义与后现代主义对现代人文主义都作了严厉的批判。本文分别以尼采、海德格尔、利奥塔和德里达等为例 ,具体说明了马克思主义与后现代主义对人文主义批判在本质上的不同 ,指出马克思主义对人文主义的批判是后现代主义永远无法超越的

社会网络与农村非正规金融研究——基于衡水市饶阳县的调查分析

以河北省衡水市饶阳县的邵村、君香、高桥和北善4个村庄所做的168份问卷为基础,进行社会网络与非正规金融机构的调查研究。研究表明:以礼金支出为度量因素的社会网络对非正规金融机构的发展有正面促进作用;正规金融机构与非正规金融机构之间也存在正相关的关系,二者共同促进发展。但是非正规金融机构的发展还不完善,还需要采取一些对策来促进非正规金融机构的健康发展。河北省社会科学规划课题“非正规金融、中小企业融资路径选择对策研究——基于河北省调研数据”(HB14CL081)、农村金融与基层创业发展研究(JRSHZ-2016-01140)、“普惠金融；精准扶贫与美丽乡村建设”路径研究(201603020211)、普惠金融与精准扶贫研究(2016074)阶段性成果

高速电镀银漂洗水的近零排放技术

利用逆流漂洗和逆流蒸发联合装置实现高速电镀银漂洗水的近零排放。该联合装置中逆流漂洗由三级漂洗槽组成,而逆流蒸发包含电镀槽、填料蒸发器、过滤机和风机等。实际镀液实验表明,在保持一定的液位水平和第三槽漂洗水的浓度小于20 mg/L的前提下,系统运行稳定,没有向外界排放含银漂洗废水,新鲜漂洗水用量比原来节省超过90%,实现电镀银过程的节水高效和漂洗水近零排放

血流感染的耐碳青霉烯类鲍曼不动杆菌的分子机制及临床研究

目的探讨血流感染的耐碳青霉烯类鲍曼不动杆菌（CRAB）耐药机制,分析菌株同源性及患者的临床特征,为CRAB的感染控制提供实验依据。方法采用Bact/Alert 3D全自动血培养系统进行血培养,细菌鉴定和药敏使用Vitek-2 Compact全自动微生物分析系统。对2010年6月—2016年5月临床血流感染患者分离到的27株碳青霉烯类药物（亚胺培南和/或美罗培南MIC≥16μg/m L）耐药的CRAB复苏菌株,重新采用Vitek-MS质谱分析仪鉴定,采用改良Hodge试验检测碳青霉烯酶,PCR法检测B类酶基因(blaNDM、blaIMP和blaVIM)和D类酶基因(blaOXA-23、blaOXA-24、blaOXA-51和blaOXA-58)并测序比对。采用MALDI-TOF分析菌株同源性,并分析患者的临床资料及感染相关信息。结果血流感染的CRAB绝大多数对常用抗生素耐药。27株CRAB改良Hodge试验均阳性。所有CRAB均未检测到B类酶基因(blaNDM、blaIMP和blaVIM);25株CRAB同时检测到blaOXA-23和blaOXA-51;另2株CRAB则为blaOXA-58阳性。采用Vitek-MS进行同源性分析,细菌分成3大簇（Ⅰ型13株、Ⅱ型12株、Ⅲ型2株）。85.2%（25/27）患者来自重症监护病房或专科的监护病床,原发感染灶以肺部炎症最常见（11例）。所有的患者在血培养出CRAB前的30d内均有抗菌药物使用史,使用频率较高的抗菌药物有:碳青霉烯类、氟喹诺酮类、头霉素类。15例CRAB血流感染患者死亡。结论厦门地区的CRAB以D类产碳青霉烯酶OXA-23和OXA-51最为多见。CRAB血流感染的原发感染多为肺部炎症。福建省卫生联合资金面上项目(No.2016J01643

芳樟树叶乙醇提取物的抗癌作用

探讨了芳樟树叶乙醇提取物各部分的抗癌作用。采用系统溶剂法从芳樟树叶得到一系列提取物,运用MTT和集落形成实验法考察各提取物对体外培养的人肺癌95-D细胞、人口腔表皮样癌KB细胞和肝癌HepG2细胞增殖的影响。结果发现石油醚部分A1、氯仿部分A2和乙酸乙酯部分A3对3种肿瘤细胞的增殖和集落形成均有不同程度的抑制作用,且给药量与细胞抑制和集落形成明显的正相关关系。因此,芳樟树叶乙醇提取物在体外有明显的抗肿瘤作用,且抗癌有效组分很可能在它的石油醚部分、氯仿部分以及乙酸乙酯部分

HYDROTHERMAL SYNTHESIS AND MAGNETIC PROPERTIES OF NANOSIZED NICKEL ZINC FERRITE POWDER

用水热法分别在200℃和220℃下反应5h制备了纳米级镍锌铁氧体(Ni0.5Zn0.5Fe2O4)粉体。用X射线衍射(X-ray diffraction,XRD)分析合成的纳米Ni0.5Zn0.5Fe2O4的物相,结果表明:200℃水热反应5h得到的纳米Ni0.5Zn0.5Fe2O4粉体中含有γ-Fe2O3,220℃水热反应5h可以得到纯纳米Ni0.5Zn0.5Fe2O4粉体。用透射电镜(transmission electronmicroscope,TEM)、Mssbauer谱(Mssbauer spectroscopy,MS)、Fourier红外分析(Fourier transform infrared spectroscopy,FTIR)、振动样品磁强计(vibrating sample magnetometer,VSM)等方法表征纯纳米Ni0.5Zn0.5Fe2O4粉体。TEM结果表明:纳米Ni0.5Zn0.5Fe2O4粉体粒子为球形,粒径约为20nm。室温MS结果表明:大部分纳米Ni0.5Zn0.5Fe2O4粉体粒子表现出铁磁性,少量的表现出超顺磁性。FTIR分析表明:样品在577cm-1和420cm-1处出现NiZn铁氧体的特征峰。磁滞回线结果表明:纳米Ni0.5Zn0.5Fe2O4粉体粒子的饱和磁化强度为38.14A?m2/kg,剩磁为17.32A?m2/kg,矫顽力为29275.29A/m。Nanosized nickel zinc ferrite(Ni0.5Zn0.5Fe2O4)powder was synthesized by the hydrothermal synthesis method at 200℃ and 220 ℃for 5h,respectively.An X-ray diffraction(XRD)was adopted for the characterization of Ni0.5Zn0.5Fe2O4 powder.It is concluded that the Ni0.5Zn0.5Fe2O4 powder containedγ-Fe2O3 when it is synthesized at 200 ℃for 5h,and pure Ni0.5Zn0.5Fe2O4 powder were prepared by the hydrothermal synthesis at 220 ℃for 5h.The pure powder was characterized by a transmission electron micro-scope(TEM),Mssbauer spectrum(MS),Fourier transform spectroscopy(FTIR),and magnometry using a vibrating sample magne-tometer(VSM).The TEM results show that Ni0.5Zn0.5Fe2O4 nanoparticles are round,and are about 20 nm in diameter.The MS results reveal that most of the Ni0.5Zn0.5Fe2O4 nanoparticles show ferromagnetism and a small quantity of Ni0.5Zn0.5Fe2O4 exhibit superpara-magnetic relaxation.The FTIR results show that the bands at 577 cm-1 and 420 cm-1 are the characteristic bands of NiZn ferrite.The saturated magnetization,remanence and coercivity of Ni0.5Zn0.5Fe2O4 powder are 38.14 A·m2/kg,17.32 A·m2/kg and 29 275.29 A/m,respectively.The powder exhibits good magnetic properties.深圳大学科研(4CHQ)资助项

脉冲电源电解处理含氰含银电镀废水

利用脉冲电源从含氰含银电镀废水中回收银和去除氰,对比了脉冲电源与直流电源对含氰镀银废水的处理效果,系统研究了脉冲电源的电解电压、占空比和脉冲频率等参数对电能消耗、银回收率和除氰率的影响。结果表明,脉冲电源较直流电源能更加有效降低阳极的超电位,减少电极的极化,从而降低槽电压,进而有效地降低电能消耗。脉冲电源的优化参数是:脉冲电压2.0V,脉冲频率1200Hz,占空比50%。在循环流速100ml.min-1,pH值10～11,曝气速率1.0L·min-1的实验条件下,通入电解电压2.0V、脉冲频率1200Hz以及占空比50%的脉冲电源,电解2.0h后,银回收率高达99%,除氰率达到86%

Abundance and production of bacteria and their correlations with environmental factor

以2014年8月南海北部海水样品为研究对象,利用平板计数法和流式细胞仪计数法对南海北部表层和垂直海域可培养细菌和细菌总数分布状况进行研究,对细菌; 生产力进行测定,并结合环境因子进行相关性分析。结果表明:珠江口到南海北部海域,水平方向可培养细菌总数变化范围是3.70*10~2 ~; 1.42*10~3 CFU/mL,细菌总数变化范围是5.12 * 10~5 ~1.61 * 10~6; cells/mL,细菌生产力的变化范围是0.03 ~0.40 mg/m~3/h;垂直方向上可培养细菌变化范围是1.08 *10~3 ~9.00; *10~3 CFU/mL,细菌生产力变化范围是0.01 ~0.08; mg/m~3/h,其中表层海水中的细菌生产力明显高于底层。与环境因子相关性分析表明,水平方向上,影响南海北部表层海水细菌总数和细菌生产力的主要因; 素是温度、盐度、硝酸盐(NO_3-N)、硅酸盐(SiO_3-Si)、亚硝酸盐(NO_2-N)和磷酸盐(PO_4-P)(P<0.05);垂直方向上; ,影响南海北部可培养细菌总数的主要因素是NO_2-N(P<0.05),影响细菌生产力的主要影响因素是温度和盐度(P; <0.05)。可见,南海北部表层海水中细菌总数高于可培养细菌总数2; ~3个数量级,表明该海域表层海水存在大量不可培养细菌;细菌的生命活动在海水表层相较底层更为活跃。Distribution of abundance and production of bacteria and their; correlations with environmental factor were investigated, using plate; count method and flow cytometry, in the surface and vertical waters of; the northern south China sea in August 2014. The cultivable bacterial; abundance ranged from 3.70 * 10~2 CFU/mL to 1.42 * 10~3 CFU/ mL, the; total bacterial abundance ranged from 5.12 * 10~5 cells/mL to 1.61 *; 10~6 cells/mL and the bacterial productions varied from 0.03 mg/m~3/h to; 0.40 mg/m~3/h in horizontal distribution. In vertical distribution, the; cultivable bacterial abundance ranged from 1.08 * 10~3 CFU/mL to 9.00 *; 10~3 CFU/mL and the bacterial productions varied from 0.01 mg/m~3/h to; 0.08 mg/m~3/h, respectively. The correlation analysis results showed; that the environmental factors affecting the abundance of total bacteria; and bacterial productivity included temperature, salinity,; nitrate(NO_3-N),silicate (SiO_3-Si), nitrite (NO_2-N),and phosphate; (PO_4-P) (P<0.05). NO_2-N was the main influencing factor to cultivable; bacteria abundance (P < 0.05), while bacterial productivity was highly; correlated with temperature and salinity in vertical distribution of; northern south China sea (P < 0.05). The total bacterial abundance was 2; ~ 3 orders of magnitude higher than cultivable bacteria, suggesting that; there were many uncultured bacterium in surface water of northern south; China sea and bacterial activities in the surface maybe more active than; in the bottom.全球变化与海气交互作用; 国家重点研发计划全球变化及应对专项; 海洋公益性行业科研专

Diversity of CO_2 fixation gene in the surface waters of northern South China Sea in the Calvin cycle

为揭示南海北部表层海水中参与卡尔文循环的固碳基因多样性及其与环境因子的关系,本研究以卡尔文循环中的关键酶核酮糖-1,5-二磷酸羧化酶/加氧酶(Rubis CO)的Ⅰ、Ⅱ型基因(cbbL、cbbM)作为分子标记,采用Illumina Miseq高通量测序技术对海水中的固碳基因多样性进行分析,并结合多元统计分析的方法,探讨了固碳基因多样性与环境因子的关系.结果显示,在南海北部表层海水中,含cbbL基因固碳基因主要归属于变形菌门(Proteobacteria)、蓝藻门(Cyanobacteria)和厚壁菌门(Firmicutes),其中,优势亚群分别是γ-变形菌亚门(45.3%)、蓝细菌(30.9%)和β-变形杆菌亚门(23.8%);而含cbbM基因的固碳菌群未检测到;近岸的A9站位与其他站位物种组成有一定的差异,异着色菌属(Allochromatium)、硫杆菌属(Thiobacillus)和硫单胞菌属(Thiohalomonas)为其特有菌属.相关性和冗余分析(RDA)结果显示,含cbbL基因的固碳基因丰度与水温、盐度呈显著负相关(p<0.01),与硝酸盐、亚硝酸盐、硅酸盐呈显著正相关(p<0.01).To elucidate the diversity of CO_2 fixation and its relationship with environmental factors in surface water of northern South China Sea,the coding gene form I( cbbL) and form II( cbbM)( that encodes Ribulose-1,5-biphosphate carboxylase/oxygenase( Rubis CO) were chosen as biomarkers in Calvin-Benson-Bassham cycle( a common carbon fixation pathway for chemolithoautotrophic microorganisms) to analyze the carbon sequestration gene diversity. The Illumina Miseq sequencing method and multivariate statistical analysis were employed. The cbbM gene was not detected in any of samples,while the cbbL gene was found in all samples. The cbbL-containing genetic communities were dominated by Proteobacteria,Cyanobacteria and Firmicutes,in which γ-Proteobacteria( 45. 3%),Cyanobacteria( 30. 9%),β-Proteobacteria( 23. 8%) were predominant subpopulation. There were differences between the nearshore station of A9 with other stations,in which Allochromatiu,Thiobacillus and Thiohalomonas were unique species in A9 station.Relativity and redundancy analysis suggest that water temperature, salinity, nitrate, nitrite, silicate were highly statistically significant factors.Temperature and salinity were positively( p < 0. 01),while the other three factors negatively influenced CO_2 fixation gene of cbbL gene abundance( p <0. 01).全球变化与海气交互作用专项(No.GASI-03-01-02-05);; 海洋公益性行业科研专项(No.201305030,201405007)~

Electric-field-induced selective catalysis of single-molecule reaction

随着单分子电学检测技术的迅速发展，分子电子学的研究不再局限于分子电子学器件的构筑及其电学性质的测量，而且扩展到单分子尺度化学反应过程的探索。然而目前相关的研究仍然局限于理论计算方面，在单分子尺度上实时监测和调控化学反应的活性和选择性是化学领域的长期目标和挑战。针对这一挑战，洪文晶教授课题组与程俊教授课题组合作，自主研发了精密科学仪器，将单个有机分子定向连接在两个末端尺寸为原子级的电极之间，解决了化学反应中分子取向控制的问题.理论计算结果证实了定向电场可以有效地稳定化学反应的过渡态，从而降低反应能垒。该研究工作在化学化工学院洪文晶教授、程俊教授、能源材料化学协同创新中心（iChEM）刘俊扬副研究员的共同指导下完成，由硕士研究生黄晓艳、iChEM博士研究生唐淳、博士研究生李洁琼以及兰州大学的陈力川博士作为共同第一作者，化学化工学院师佳副教授、陈招斌高级工程师、夏海平教授和田中群教授，萨本栋微纳研究院杨扬副教授、环境与生态学院白敏冬教授以及兰州大学张浩力教授参与了研究工作的讨论并给予指导，博士后乐家波、博士研究生郑珏婷、张佩（已毕业）、李瑞豪、李晓慧也参与了研究工作。Oriented external electric fields (OEEFs) offer a unique chance to tune catalytic selectivity by orienting the alignment of the electric field along the axis of the activated bond for a specific chemical reaction; however, they remain a key experimental challenge. Here, we experimentally and theoretically investigated the OEEF-induced selective catalysis in a two-step cascade reaction of the Diels-Alder addition followed by an aromatization process. Characterized by the mechanically controllable break junction (MCBJ) technique in the nanogap and confirmed by nuclear magnetic resonance (NMR) in bottles, OEEFs are found to selectively catalyze the aromatization reaction by one order of magnitude owing to the alignment of the electric field on the reaction axis. Meanwhile, the Diels-Alder reaction remained unchanged since its reaction axis is orthogonal to the electric fields. This orientation-selective catalytic effect of OEEFs reveals that chemical reactions can be selectively manipulated through the elegant alignment between the electric fields and the reaction axis.This work was supported by the National Key R&D Program of China (2017YFA0204902), the National Natural Science Foundation of China (21722305, 21703188, 21673195, 21621091, 51733004, 51525303, and 91745103), the China Postdoctoral Science Foundation (2017M622060), and the Young Thousand Talents Project of China. 该工作得到国家自然科学基金委（21722305、21703188、21673195、51733004、51525303、91745103），国家重点研发计划课题（2017YFA0204902），中国博士后面上基金（2017M622060）的资助，以及固体表面物理化学国家重点实验室、醇醚酯化工清洁生产国家工程实验室、能源材料化学协同创新中心的支持