ABS塑料三价黑铬电镀工艺与故障处理

介绍了ABS塑料电镀三价黑铬的工艺流程,主要包括除油,亲水,粗化,中和,预浸,催化,加速,化学镀镍,活化,镀铜,微蚀,镀光亮镍,镀三价黑铬,钝化和烘干.给出了三价黑铬镀液的配方,阐述了各组分的作用及工艺奈件对镀层的影响,介绍了常见故障的处理方法.     

ZnO-Al_2O_3-B_2O_3-SiO_2系微晶玻璃与可伐合金的润湿性能

研制了一种新型的与可伐熔封的ZnO-Al_2O_3-B_2O_3-SiO_2系微晶玻璃,研究了不同工艺条件下微晶玻璃与可伐合金间的润湿角大小,结果表明,熔封气氛和熔封温度对润湿性能影响很大,熔封时间影响最小.采用最佳的工艺条件,其润湿性能与现有的其它玻璃润湿性能相似.同时发现玻璃与可伐合金间的润湿角保持在10°～30°之间能得到质量良好的熔封产品.在基本不改变传统工艺制度的条件下,可完成锌铝硼硅系微晶玻璃与可伐合金的熔封,即利用排蜡过程同时完成微晶玻璃的形核,熔封后在稍低温度保温或减慢冷却速度可以完成微晶玻璃的结晶过程.锌铝硼硅系微晶玻璃与预氧化可伐合金的封接依靠玻璃中的SiO_2与FeO或Fe_3O4发生界面反应形成牢固的结合.     

化学水浴沉积CdS薄膜晶相结构及性质

采用CBD法在醋酸镉溶液体系中制备CdS半导体薄膜，研究了溶液组份的浓度对CdS结晶结构的影响．增加乙酸胺的浓度、提高溶液的pH值有利于生成立方晶CdS，反之则易于生成六方晶CdS．无论立方相还是六方相CdS薄膜，电阻率均在10~4～10~5Ω·cm范围，结晶均匀细致．用六方晶为主和立方晶为主的CdS制备的CIGS太阳电池最高效率分别达到12.10%和12.17%．     

Effect of magnesium content on the stress exponent and effective stress in the steady state creep of Al-Mg alloys

The stress exponent of steady state creep,n, and the internal ( _i) and effective stresses ( _e) have been determined using the strain transient dip test for a series of polycrystalline Al-Mg alloys creep tested at 300° C and compared with previously published data. The internal or dislocation back stress, _i, varied with applied stress,, but was insensitive to magnesium content of the alloy, being represented by the empirical equation _i=1.084 ^1.802. Such an applied stress dependence of _i can be explained by using an equation for _i of the form _i (dislocation density)^1/2 and published values for the stress dependence of dislocation density. Values of the friction stress, _f, derived using the equation _e/=(1–c) (1– _f/), indicate that _f is not dependent on the magnesium content. A constant value of _f can best be rationalized by postulating that the creep dislocation structure is relatively insensitive to the magnesium content of the alloy.On leave from Engineering Materials Department, University of Windsor, Windsor, Ontario N9B 3P4, Canada.     

基于可调谐光纤环形镜滤波器的多波长布里渊掺铒光纤激光器

通过使用非线性放大的光纤环形 镜滤波器(AFLMF),构造了一种新颖的多波长布里渊掺铒光纤激光器(E DFL)线形结构。非线性AFLMF由掺铒光纤放大器(EDFA,由980n m泵浦抽运 一段EDF构成)、偏振控制器(PC)和耦合器构成,减少了腔内基于波长的损耗,并且能够灵 活地控制反射 光以及激光腔内输入和输出光的强度。在布里渊泵浦功率为25mW、 980nm泵浦功率为200mW时,获得了波 长间隔为0.08nm的14个波长的激光输出以及50nm的可调谐范围。通过调节980nm抽运光功率、PC以及布里渊泵浦光波长,实现了可调谐的多波长输出。研究 了980nm抽运光功率以及PC对斯托克斯光波数的影响。     

Icons improve older and younger adults' comprehension of medication information

We examined whether timeline icons improved older and younger adults' comprehension of medication information. In Experiment 1, comprehension of instructions with the icon (icon/text format) and without the icon (text-only format) was assessed by questions about information that was (a) implicit in the text but depicted explicitly by the icon (total dose in a 24 hour period), (b) stated and depicted in the icon/text condition (medication dose and times), and (c) stated but not depicted by the icon (e.g., side effects). In a separate task, participants also recalled medication instructions (with or without the icon) after a study period. We found that questions about dose and time information were answered more quickly and accurately when the icon was present in the instructions. Notably, icon benefits were greater for information that was implicit rather than stated in the text. This finding suggests that icons can improve older and younger adults' comprehension by reducing the need to draw some inferences. The icon also reduced effective study time (study time per item recalled). In Experiment 2, icon benefits did not occur for a less integrated version of the timeline icon that, like the text, required participants to integrate dose and time information in order to identify the total daily dose. The integrated version of the icon again improved comprehension, as in Experiment 1, as well as drawing inferences from memory. These findings show that integrated timeline icons improved comprehension primarily by aiding the integration of dose and time information. These findings are discussed in terms of a situation model approach to comprehension.     

Definition of natural T cell antigens with mimicry epitopes obtained from dedicated synthetic peptide libraries

Progress has recently been made in the use of synthetic peptide libraries for the identification of T cell-stimulating ligands. T cell epitopes identified from synthetic libraries are mimics of natural epitopes. Here we show how the mimicry epitopes obtained from synthetic peptide libraries enable unambiguous identification of natural T cell Ags. Synthetic peptide libraries were screened with Mycobacterium tuberculosis-reactive and -autoreactive T cell clones. In two cases, database homology searches with mimicry epitopes isolated from a dedicated synthetic peptide library allowed immediate identification of the natural antigenic protein. In two other cases, an amino acid pattern that reflected the epitope requirements of the T cell was determined by substitution and omission mixture analysis. Subsequently, the natural Ag was identified from databases using this refined pattern. This approach opens new perspectives for rapid and reliable Ag definition, representing a feasible alternative to the biochemical and genetic approaches described thus far.     

Pattern formation in chick feather development: distribution of beta 1-integrin in normal and scaleless embryos

We have examined the immunolocalization of beta 1-integrin during feather development in the spino-lumbar tract of the backskin from normal and scaleless chick embryos. beta 1-integrin appears during early feather development in three distinct phases which correspond to important developmental events. The first phase (5-5 1/2 days of incubation; Hamburger and Hamilton [H.H.] stage 27) represents the period prior to the formation of dermis. During this phase, beta 1-integrin antiserum labels mesenchymal cells located in the central region of the spino-lumbar tract where the initiation site for feather development is located. The second phase (5 1/2-7 1/2 days of incubation; H.H. stages 28-32) corresponds to the period during which dermis is formed. The cells that make up the dermis are readily distinguished by their lack of beta 1-integrin immunostaining. The third phase (7 1/2-10 days of incubation; H.H. stages 33-36) begins with the sudden appearance of beta 1-integrin in the central and lateral regions of the dermis. The pattern of beta 1-integrin immunostaining in scaleless backskin becomes different from that of normal backskin during this phase. In normal backskin the dermal condensations of feather germs are not labeled with the beta 1-integrin antiserum. This produces a heterogeneous immunostaining pattern very similar to the pattern seen for Type I collagen (Mauger et al. [1982] Dev. Biol. 94:93-105). In contrast, homogeneous immunostaining is observed in the dermis of scaleless backskin. The initial time of appearance, manner of appearance, and pattern of integrin expression in the third phase suggest that beta 1-integrin may be involved in the stabilization of the feather pattern. We also observed the appearance of beta 1-integrin on the epidermal basal cells during the time of feather follicle formation. The beta 1-integrin antiserum reacts strongly with the baso-lateral surfaces of normal basal cells, yet the basal surfaces of the scaleless basal cells are unstained. This lack of immunostaining along the basal surfaces of the scaleless basal cells may relate to the abnormal adhesion between the epidermis and dermis in scaleless backskin.