价

The extracting ability of substituted monoamide can be highly influenced by its structure, especially when it extracts te-travalent actinides.

取代单酰胺的萃取能力受结构的影响很大，尤其对 4价锕系元素，可以设计不同结构的酰胺来萃取分离4价和 6价锕系金属，国内外在该类萃取剂的性能研究方面做了大量工作。

Variations 52.3 Exceeding 15 Percent If, on the issue of the Taking-Over Certificate for the whole of the Works, it is found that as a result of: all varied work valued under Sub-Clause 52.1 and 52.2, and all adjustments upon measurement of the estimated quantities set out in the Bill of Quantities, excluding Provisional Sums, daywork and adjustments of price made under Clause 70, But not from any other cause, there have been additions to or deductions from the Contract Price which taken together are in excess of 15 per cent of the "Effective Contract Price"(which for the purposes of this Sub-Clause shall mean the Contract Price excluding Provisional Sums, and allowance for dayworks, if any) then and in such event (subject to Any action already taken under any other Sub-Clause of this Clause), after due consultation by the Engineer with the Employer and the Contractor, there shall be added to or deducted from the Contract Price such further further sum as may be agreed between the Contractor and the Engineer or, failing agreement, determined by the Engineer having regard to the Contractor's Site and general overhead costs of the Contract.

如果在签发整个工程接收证书时，发现由于： 47 超过百分之 52.3 十五(15%)的变更所有按第52.1款和52.2款规定作价的全部变更工程；对工程量清单中开列的估算数量进行计量所做的全部调整费用，但不包括所有暂定金额，计日工作费用及按本文第 70 条规定所作的价格调整。而并非由于任何其他原因，当加到或从合同价中减去的金额总和超过了有效合同价格就本款而言，应指不包括暂定金额和计日工(如有的话的合同价的 15%时，那么，工程师应在与承包人和业主协商后，在考虑据本款采取的任何步骤后，再将合同价减少或增加一笔工程师与承包人协商的调整金额，若不能达成一致意见，则由工程师考虑承包人的现场管理费用及总管理费开文后确定此数额。

At diakinesis, 0.2 tetravalents, 0.05 hexavalents and 0.05 octovalents per pollen mother cell were detected, which was absent in cultivated cucumber. In 30% PMCs, crossed chromosomes occurred at diakinesis.

在减数分裂终变期，平均每个花粉母细胞有0.2个四价体、0.05个六价体和0.05个八价体，约30%的花粉母细胞中存在拉十字的染色体。

Centromeres could be identified easily on the bivalents at diplotene, so it was convenient to analyse the karyotype.

结果表明，日本沼虾染色体数n=52，2n=104，据双线期二价体的相对长度、着丝点位置以及形态诸方面的特点分析了核型，共分为A，B，C，D4个染色体组，核型组成是N=37M+4ST+11T；初级精母细胞减数分裂前期I可分为细线期/偶线期、粗线期、双线期和终变期5个时期，双线期的二价体存在弥散阶段，核仁明显，且双线期二价体着丝点清晰，给核型分析带来了方便。

According to AAS data, Fe, Ni and Mn in pits dissolved into ions in form of divalence, and Cr in form of trivalence both in the presence and absence of PD.

结果表明：304不锈钢蚀孔内，铬元素以三价，铁、镍和锰以二价离子形式溶解，缓蚀剂PD不改变各元素溶解的价态。

Zero-valent iron and fluidize technique was successfully integrated in this study for nitrate removal, with three related processes developed, namely fluidized zero valent iron reactor, two fluidized ZVI reactors system, and pressurized CO2/zero valent iron system.

中文摘要本论文成功结合零价铁与流体化技术发展出零价铁流体化反应器、双流体化反应系统以及加压式零价铁流体化反应器等三种处理程序应用於水中硝酸盐之处理。

Nanoscale zero valent iron particles were synthesized by reductive method in aqueous phase. The crystal structure, morphology and size of the particles were characterized using X-ray diffraction and transmission electron microscopy. The influence of temperature, initial acid fuchsine concentration, nanoscale zero valent iron dosage and pH on the removal of acid fuchsine by the particles was studied, and the removal mechanism of acid fuchsine was discussed.

摘 要：采用液相还原法制备零价纳米铁粒子；用X射线衍射和透射电镜表征该样品的晶体结构、颗粒形貌与尺寸；研究温度、酸性品红初始浓度、纳米零价铁加入量及溶液pH值对零价纳米铁粒子脱除酸性品红的影响，并对酸性品红的脱除机理进行讨论。

The result showed that the one-valence cationsaccelerate the hydration process of α-hemihydrate gypsum greatly because they improvethe dispersed degree of α-hemihydrate gypsum particles due to the remarkable effect ofincreasing theζpotential; the effects of bivalent and trivalent cations on ζpotentialdecrease in turn, compared with monovalent cations, the effects on both the disperseddegree of α-hemihydrate gypsum particles and the setting time of paste are little.

研究还表明：由于一价阳离子能较大程度地提高石膏浆体的ζ电位，因而有效地提高了石膏颗粒的分散程度，对α半水石膏的水化加速作用很大，而二、三价离子对石膏浆体的ζ电位影响依次减小，对半水石膏颗粒的分散程度和浆体凝结时间的影响均不如一价阳离子作用大。

In chapter 2 and 3, experimentally, using the Angular-Resolved high-resolution fast Electron Energy Loss Spectrometer , at the condition of 2. 5 keV incident energy and 50-60 meV energy resolution, we measured the Optical Oscillator Strength Density Spectra for the excitations of 4p, 4s or 3d electron. The oscillator strengths for excitations of the valent shell 4p electron were obtained, and comparisons were done between presently experimental and previously experimental and theoretical results. The experimental results of different groups agree with each other approximately, but the semi-experientially theoretical results do not match with the experimental results. The delayed maximum in the photoabsorption spectra was discussed. It should arise from the transition of 4p→∈d. For the excitation of the inner-valent 4s electron, the discrepancies for the resonant structures in previous electron-impact results and photoionization results were clarified in present work, which confirms again that the fast electron impact method is suitable to measure the optical oscillator strengths. The autoionization Rydberg series 4s〓ns (n=5, 6, 7) and 4s〓nd (n=4, 5, 6, 7) were identified without ambiguity by the measurement at 0°, 2° and 4°scattering angles. The energy levels and natural widths of the excitations of Kr3d and Ar2p inner shell, including optically allowed and forbidden transitions, were determined. The widths of these inner shell excitations are nearly the same, which was interpreted by the Resonant Auger effect .

在第二章和第三章，实验上，使用角分辨的高能量分辨快电子能量损失谱仪，在2.5keV电子入射能量和50-60meV能量分辨下，测量了Kr原子由价壳层4p到内价壳层4s，再到内壳层3d电子激发的光学振子强度密度谱；得到了价壳层4p电子激发束缚态的光学振子强度，与前人实验和半经验理论结果作了细致的比较，说明几家实验是比较符合的，但半经验的理论计算存在问题；分析了光吸收谱中的延迟极大现象，说明在第一电离阈值以上几个eV范围内的极大值源于4p→εd跃迁产生的延迟极大；对于内价壳层4s激发的自电离区，澄清了前人实验中电子碰撞方法和光学方法在共振结构上存在差异的问题，再一次肯定了快电子碰撞方法是获得绝对光学振子强度的一种好方法；通过在非0°散射角的测量（如2°和4°），清楚地标识了4s电子激发的光学禁戒跃迁自电离里德堡系列4s〓ns（n=5，6，7）和4s〓nd（n=4，5，6，7）；通过在0°和4°散射角的测量，观测并标识了几个新的内壳层光学禁戒跃迁能级，得到了Kr原子3d和Ar原子2p内壳层激发态（包括光学允许和禁戒跃迁形成的）的能级位置和自然宽度，用共振俄歇效应解释了这些内壳层激发态（不管是光学允许还是禁戒跃迁产生的）的自然宽度彼此比较接近的原因。

The formal potentials in cyclic voltammograms of these 3+ valence complexes are followed: Co〓-TPPS (-0.08V )＞Fe〓TPPS (-0.14V)＞Mn〓-TPPS (-0.23V). The electrochemical reaction of Mn〓-TPPS is reversible, and both of Co〓-TPPS and Fe〓-TPPS are quasi-reversible. The standard heterogeneous rate constants of Co〓-TPPS and Fe〓-TPPS were determined to be 1. 4×10〓cm/s and 1.4×10〓cm/s respectively. The rates of electrode reaction are as followed: Mn〓-TPPS＞Co〓-TPPS＞Fe〓-TPPS, e.i. Mn〓-TPPS is the most easily oxidized by the dissolved oxygen, and Fe〓-TPPS is oxidized slower than Co〓-TPPS. Ni〓-TPPS can not be oxidized. It is considered that oxygen plays an important role in the valence change of central metal atom and the rate of electron transfer in some metalloporphyrins.

三价金属卟啉络合物在循环伏安图上可得到三价到二价的还原和氧化响应，电极电位从大到小排列为：Co〓-TPPS(-0.08V)＞Fe〓-TPPS(-0.14V)＞Mn〓-TPPS(-0.23V)，电极反应可逆性也不相同，Mn〓-TPPS是可逆过程，Co〓-TPPS、Fe〓-TPPS是准可逆过程，实验测得Co〓-TPPS的标准电极反应速率常数ks＝1.4×10〓cm/s，Fe〓-TPPS的ks＝1.4×10〓cm/s，电极反应的速率从大到小为：Mn〓-TPPS＞Co〓-TPPS＞Fe〓-TPPS，即Mn〓-TPPS最容易被溶解氧所氧化，Fe〓-TPPS被氧化的速度最慢，Ni〓-TMPyP不能被氧化，因此我们认为溶解氧对金属卟啉中心离子的价态和电子转移速率起着重要作用。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。