Metallisch leitende Polymere — Jagdgründe für Solitonen?

Polyacetylene is presented as the prototype of a metallic conducting polymer. The concepts of one-dimensional metal physics are illustrated and special attention is drawn to a structural defect called “soliton”. Electrical, magnetic, and optical experiments connected with solitons are discussed. The authors' opinion is expressed that present experimental results do not yet furnish strong evidence for the existence of solitons in polyacetylene, but that the soliton idea is a fruitful stimulus for further investigations and novel applications.     

Effect of algal flocculation on dissolved organic matters using cationic starch modified soils

Modified soils(MSs) are being increasingly used as geo-engineering materials for the sedimentation removal of cyanobacterial blooms. Cationic starch(CS) has been tested as an effective soil modifier, but little is known about its potential impacts on the treated water.This study investigated dissolved organic matters in the bloom water after algal removal using cationic starch modified soils(CS-MSs). Results showed that the dissolved organic carbon(DOC) could be decreased by CS-MS flocculation and the use of higher charge density CS yielded a greater DOC reduction. When CS with the charge density of 0.052, 0.102 and0.293 meq/g were used, DOC was decreased from 3.4 to 3.0, 2.3 and 1.7 mg/L, respectively.The excitation–emission matrix fluorescence spectroscopy and UV254 analysis indicated that CS-MS exhibits an ability to remove some soluble organics, which contributed to the DOC reduction. However, the use of low charge density CS posed a potential risk of DOC increase due to the high CS loading for effective algal removal. When CS with the charge density of 0.044 meq/g was used, DOC was increased from 3.4 to 3.9 mg/L. This study suggested, when CS-MS is used for cyanobacterial bloom removal, the content of dissolved organic matters in the treated water can be controlled by optimizing the charge density of CS. For the settled organic matters, other measures(e.g., capping treatments using oxygen loaded materials) should be jointly applied after algal flocculation.     

水中羟基氧化铁催化臭氧分解和氧化痕量硝基苯的机理探讨

测定了木质颗粒活性炭(GAC)和负载在GAC上的羟基氧化铁(FeOOH)催化水中臭氧分解的速率常数并探讨了催化臭氧分解的途径.以水中几种氧化物表面羟基密度和表面零电荷pH值(pH_zpc)为表征氧化物表面性质的参数,考察了2个参数对催化臭氧氧化水中硝基苯的影响.GAC和负载在GAC上的FeOOH使水中臭氧一级分解速率常数分别提高了68%和108%,用叔丁醇捕获掉生成的羟基自由基后,前者的分解速率常数降低了9%,后者降低了20%.GAC在催化臭氧分解时主要起到吸附剂和还原剂的作用,FeOOH催化臭氧分解过程中促进了羟基自由基生成.氧化物表面羟基密度和催化臭氧氧化水中硝基苯的效果之间没有直接的关系,由氧化物的pH_zpc决定的表面电荷状态与催化氧化效果有关,表面接近电中性时对催化氧化硝基苯有利.高密度的表面羟基会使表面羟基之间形成较强的氢键,使催化作用减弱.     

基于PSD曲线的军用车辆有机涂层防护性能研究

目的 研究两种军用车辆有机涂层的防腐蚀性能.方法 利用两种军用车辆有机涂层作为样本,以湿热、紫外、中性盐雾、酸性盐雾为4个环境因子,组合成多因子综合腐蚀试验,用电化学噪声频域分析处理试验数据,对比研究两种车辆装备涂层的防腐蚀性能.结果 10个周期之后,两种涂层均完全破坏,其中,灰色有机涂层H的初始状态为9.55×108...     

金属飞片对EFI起爆能量的影响

目的降低EFI的发火能量,研究非金属飞片与金属飞片在EFI中的应用。方法采用飞片材料匹配的方法,并选择金属Al与金属Ti,开展金属飞片的设计与制备,得到Al-PI与Ti-PI的金属飞片以及金属飞片-爆炸桥箔metallic flyer,并开展发火摸底试验。结果在不额外对金属飞片进行绝缘处理的情况下,含有金属飞片的EFI均未发火;对金属飞片进行绝缘处理后,含有金属飞片的EFI均可靠发火。采用光子多普勒测速仪(PDV)进行的飞片速度测试结果表明,在充电电压为1200 V时,Ti-PI金属飞片的速度为3604 m/s,金属飞片-爆炸桥箔一体化换能元速度为2986m/s。结论同样的发火电压下,金属飞片-爆炸桥箔一体化换能元的金属飞片速度明显小于绝缘层较厚的金属飞片速度。     

硫酸铁氧化物的表征及其对重金属吸附作用的研究

根据酸性矿山废水污染河流的特征，着重研究了硫酸铁溶液中和沉淀生成的无定形氧化铁颗粒的表面特性及其对重金属离子的吸附作用，并以硝酸铁溶液中和沉淀生成的无定形氧化铁颗粒作对比，同时应用表面络合反应关系求取了该颗粒的表面络合反应的基本特征参数，最后采用简化的表面络合模式计算了该氧化铁颗粒表面与重金属离子，如Ｃｕ＾２＋，Ｃｄ＾２＋和Ｐｂ＾２＋结合的表面络合形成条件稳定常数。     

Electro-oxidation of Ni (II)-citrate complexes at BDD electrode and simultaneous recovery of metallic nickel by electrodeposition

The simultaneous electro-oxidation of Ni (II)-citrate and electrodeposition recovery of nickel metal were attempted in a combined electro-oxidation-electrodeposition reactor with a boron-doped diamond (BDD) anode and a polished titanium cathode. Effects of initial nickel citrate concentration, current density, initial pH, electrode spacing, electrolyte type, and initial electrolyte dosage on electrochemical performance were examined. The efficiencies of Ni (II)-citrate removal and nickel metal recovery were determined to be 100% and over 72%, respectively, under the optimized conditions (10 mA/cm², pH 4.09, 80 mmol/L Na₂SO₄, initial Ni (II)-citrate concentration of 75 mg/L, electrode spacing of 1 cm, and 180 min of electrolysis). Energy consumption increased with increased current density, and the energy consumption was 0.032 kWh/L at a current density of 10 mA/cm² (pH 6.58). The deposits at the cathode were characterized by scanning electron microscopy (SEM), energy-dispersive spectrometry (EDS), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). These characterization results indicated that the purity of metallic nickel in cathodic deposition was over 95%. The electrochemical system exhibited a prospective approach to oxidize metal complexes and recover metallic nickel.     

基于原位PXRF数据的土壤锰、锌污染分布协同克里金插值与高分地图绘制

高分辨率土壤重金属污染绘图(HRMMs)有助于准确识别需要进行风险管控或修复的区域.传统HRMMs基于网格模式土壤采样,开展化学分析并采用地质统计插值方法绘制污染分布地图,成本高、速度慢,且不适合高度异质性污染场地.该研究提出了一种通过多元非线性回归改善便携式X射线荧光分析(PXRF)数据,采用改进的PXRF数据进行协同克里金插值,以及HRMMs地图绘制和重金属污染分布预测的新方法.为了支持模型的建立和验证,选择我国西北某锰、锌污染场地开展研究.结果表明：(1)引入PXRF数据作为协同克里金插值的辅助变量能有效提高插值精度,而校正的PXRF数据可进一步提高空间刻画精度.重金属Mn和Zn的校正PXRF协同克里金插值较原始PXRF协同克里金插值的平均误差分别降低了4.5%和78.2%.(2)主变量点位密度的变化会改变校正后PXRF协同克里金插值的精度.以Zn为例,当主变量点位密度大于4个/(104 m²)时,校正后的PXRF协同克里金插值的精度显著降低.(3)增加辅助变量点位密度可显著提高协同克里金插值精度.当辅助变量点位密度增至7个/(104 m²     

天然沸石中离子交换平衡的离子特异性研究

沸石在改良土壤和保护环境等方面有着广泛的应用,研究沸石离子交换中的特异性效应对更好地利用沸石有着重要意义.碱金属离子在天然斜发沸石中的交换平衡时的最大吸附量存在着明显的特异性效应;对于同价的碱金属离子,其交换吸附能力差异随着离子浓度的降低而增大.这种实验现象不能用库仑力、离子体积、水合作用、色散力、经典诱导力以及表面络合等相关理论进行完整解释.分析发现,根本原因来自离子因量子涨落而产生的极化与沸石颗粒表面电荷产生的强电场之间的相互作用,这种相互作用导致了离子间偶极矩差异随着表面电位的升高而增大,进而使离子-表面吸附能差异增大,并出现不同的交换吸附能力.由于沸石表面电荷密度较高,离子体积效应对其在双电层中的分布也起着比较重要的作用,导致碱金属离子在沸石表面的交换平衡结果在高表面电位(绝对值大于0.2 V)下才表现出较大选择性,与低电荷密度表面上的交换平衡结果存在一定差异.     

常见金属硫化物电化学反应环境效应及其影响因素分析

金属硫化物矿物作为重要的金属矿产资源之一,在自然界广泛分布并易氧化(电化学反应)引起重金属离子和酸性矿山废水污染的环境效应。本文以黄铁矿和黄铜矿为例全面分析了金属硫化物矿物环境效应产生机制,以及影响金属硫化物矿物电化学反应的各种因素,指出了当前研究存在的不足。这对金属硫化物矿区环境污染的源头控制与修复具有重要的指导意义。     

海洋耐镉微生物筛选及其生物学特性

从重金属污染的近海域筛选到一株对镉具有较强抗性和富集能力的微生物Cd20002,该菌株在液体培养基中的最大耐受浓度为1 000 mg/L,在镉浓度达到200 mg/L时,其吸附率高达93.4%,根据形态特征和生理生化鉴定及16S rRNA测序鉴定为蓝杆菌。通过在不同的镉浓度环境对蓝杆菌Cd20002进行培养,测定其生长曲线,并优化菌体生长的条件及其吸附能力。结果表明,蓝杆菌Cd20002既能在重金属镉环境中生存,且富镉能力较强,对水产环境中重金属的生物清排具有重要意义。     

危险废物填埋场复合衬层渗漏分析与污染物运移预测

以我国危险废物填埋场次防渗层采用1 mm高密度聚乙烯(HDPE)土工膜和0.5 m压实粘土衬垫(CCL)组成的复合衬层为研究对象,采用经验公式以及解析方法计算了不同缺陷条件下复合衬层的渗漏率.在此基础上,采用一维污染物对流扩散运移方程对重金属Cd~(2+)、Zn~(2+)、Cu~(2+)、Pb~(2+)击穿复合衬层的时间进行了计算和分析.结果表明:复合衬层渗漏率主要受到复合衬垫界面接触条件,渗滤液水位以及缺陷类型的影响;当复合衬层的漏洞密度为20个·hm~(-2)时,半径为5.64 mm的圆孔型缺陷其最大渗漏率为22.7 m~3·a~(-1)·hm~(-2);当单位面积裂缝长度为200m·hm~(-2)时,宽度为2 mm长度为1 m的裂缝型缺陷其最大渗漏率为42.5 m~3·a~(-1)·hm~(-2);Cd~(2+)可作为重金属污染物击穿复合衬层的指示性污染物,其击穿时间最长为2.74 a,最短为1.38 a;通过改变土工膜下伏土壤衬层的性能或增加土壤衬层厚度可延缓污染物击穿时间.     

金属尾矿作水泥混合材活性试验研究

选取烧失量低于10%,SO3含量低于3%,SiO2、Al2O3含量较高,适于作水泥混合材的6种金属尾矿进行水泥混合材活性试验研究.6种金属尾矿分别按10%、15%、20%、25%、30%与熟料、石膏进行配比.试验结果表明:6种金属尾矿不同掺配比活性试验的R28在68.72%～76.54%之间,高于活性混合材R28为62%的判定指标,由此可认为此6种尾矿均属于活性混合材,可单独用作水泥活性混合材;6种金属尾矿掺配比在小于30%的范围内,水泥安定性、凝结时间等性能指标均符合普通硅酸盐水泥要求;6种金属尾矿掺配比在小于30%的范围内其强度均满足32.5R等级水泥强度要求;尾矿掺配比为10%时,6种金属尾矿除3号尾矿外,均满足42.5R等级水泥强度要求.符合要求的金属尾矿用作水泥混合材,将扩大水泥混合材来源,降低水泥粉磨能耗和成本,实现尾矿的资源化和水泥工业的可持续发展.     

Hydrogen storage methods

Hydrogen exhibits the highest heating value per mass of all chemical fuels. Furthermore, hydrogen is regenerative and environmentally friendly. There are two reasons why hydrogen is not the major fuel of todays energy consumption. First of all, hydrogen is just an energy carrier. And, although it is the most abundant element in the universe, it has to be produced, since on earth it only occurs in the form of water and hydrocarbons. This implies that we have to pay for the energy, which results in a difficult economic dilemma because ever since the industrial revolution we have become used to consuming energy for free. The second difficulty with hydrogen as an energy carrier is its low critical temperature of 33 K (i.e. hydrogen is a gas at ambient temperature). For mobile and in many cases also for stationary applications the volumetric and gravimetric density of hydrogen in a storage material is crucial. Hydrogen can be stored using six different methods and phenomena: (1) high-pressure gas cylinders (up to 800 bar), (2) liquid hydrogen in cryogenic tanks (at 21 K), (3) adsorbed hydrogen on materials with a large specific surface area (at T<100 K), (4) absorbed on interstitial sites in a host metal (at ambient pressure and temperature), (5) chemically bonded in covalent and ionic compounds (at ambient pressure), or (6) through oxidation of reactive metals, e.g. Li, Na, Mg, Al, Zn with water. The most common storage systems are high-pressure gas cylinders with a maximum pressure of 20 MPa (200 bar). New lightweight composite cylinders have been developed which are able to withstand pressures up to 80 MPa (800 bar) and therefore the hydrogen gas can reach a volumetric density of 36 kg·m^–3, approximately half as much as in its liquid state. Liquid hydrogen is stored in cryogenic tanks at 21.2 K and ambient pressure. Due to the low critical temperature of hydrogen (33 K), liquid hydrogen can only be stored in open systems. The volumetric density of liquid hydrogen is 70.8 kg·m^–3, and large volumes, where the thermal losses are small, can cause hydrogen to reach a system mass ratio close to one. The highest volumetric densities of hydrogen are found in metal hydrides. Many metals and alloys are capable of reversibly absorbing large amounts of hydrogen. Charging can be done using molecular hydrogen gas or hydrogen atoms from an electrolyte. The group one, two and three light metals (e.g. Li, Mg, B, Al) can combine with hydrogen to form a large variety of metal–hydrogen complexes. These are especially interesting because of their light weight and because of the number of hydrogen atoms per metal atom, which is two in many cases. Hydrogen can also be stored indirectly in reactive metals such as Li, Na, Al or Zn. These metals easily react with water to the corresponding hydroxide and liberate the hydrogen from the water. Since water is the product of the combustion of hydrogen with either oxygen or air, it can be recycled in a closed loop and react with the metal. Finally, the metal hydroxides can be thermally reduced to metals in a solar furnace. This paper reviews the various storage methods for hydrogen and highlights their potential for improvement and their physical limitations.     

External heating closed-volume thermally activated tube forming: A fundamentally new approach for hydroforming thick-walled tubes

The underlying principles of water’s equation of state (ES) and its associated pressure–volume–temperature (PVT) relationship, are employed for the purpose of producing “ultra-high” pressure within the closed volume of a thick-walled metal tube, resulting in a new and innovative hydroforming process. The process, called “Closed-Volume Thermally Activated” (CVTA) Tube Hydroforming, involves conducting a high level of heat through the walls of a thick-walled, metallic, water-containing closed tube. Experimental validation of the concept is presented, and potential applications are discussed. This work represents a break-through in manufacturing technology, which, when further developed, is expected to enable manufacturers to expand significantly their manufacturing capability.     

Removal of copper from a copper sulphate solution using an ultrasonic-electrolysis process

The application of ultrasonic-electrolysis process for the removal of copper is studied.In the ultrasonic field cavitation acts as jets and agitates the solution and breaks the barrier layer between the cathode surface and the bulk of the solution.Thus increases metal deposition on the cathode surface.The results show that an ultrasonic field is successful for the removal of low copper concentrations in solution.     

非金属矿物在废水处理中的应用研究

用矿物作为污水处理材料,具有储量丰富,方法简单,可去除水中无机和有机污染物,化学和生物性能稳定,容易再生等优点。非金属矿物具有良好的吸附和离子交换性能,在水处理方面有广阔的应用前景。本文介绍了海泡石、镁砂、沸石、膨润土等几种常见的矿物材料在有机废水、重金属废水及含油废水中的研究现状。     

金属氧化物颗粒/水界面上NOM吸附机制的研究

以腐殖酸作为天然有机物(NOM)的代表,研究了腐殖酸分子在金属氧化物(赤铁矿)颗粒/水界面上的吸附特征,分析了pH值和离子强度对界面吸附配位反应的影响,及它们对赤铁矿颗粒表面吸附密度和团聚体粒径的影响.结果表明,吸附密度随pH值的升高而减少,随离子强度的升高而增大;颗粒团聚体粒径随pH值的升高先增大后减小,随离子强度的升高而增大.pH=4时吸附密度最大,为6.22 mg/m2,但此时团聚体粒径最小;pH=5时吸附密度较小,但团聚体粒径较大;pH=8为配位反应等电点,吸附密度和团聚体粒径均较小;pH=10吸附密度最小,为0.50 mg/m2,团聚体粒径也较小.应用SS/SF混合模型初步分析了赤铁矿颗粒/水界面上腐殖酸分子的吸附构型.当pH值较低时,构型多为链状和环状;当pH值较高时,构型多为扫尾状.离子强度越高,链状和扫尾状构型越多;离子强度越低,环状构型越多.     

On the feasibility of producing polymer–metal composites via novel variant of friction stir processing

In this study a novel variant of friction stir processing was developed for producing of polymer metal surface or bulk composites in order to enhance the mechanical, electrical and thermal properties. For this purpose, a novel tooling system was designed consists of a rotating pin, a stationary shoulder and a heating system located inside the shoulder. In present paper, for preliminary study high-density polyethylene and copper powder was selected as polymeric matrix and metallic additive, respectively. Surface quality, microstructure, ultimate tensile strength and the modulus of elasticity were determined for each prepared sample. From experimental tests, it was found that this approach is an efficient method for producing of polymer–metal composites.