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玻璃质化

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The method will involve a sequence of ammonification of glass surface, functionalization of carbon nanotube surface, and bonding between the nanotubes.

将奈米碳管与其它材料以一定的比例复合而制备,进而形成一种具有奈米碳管之复合吸附材料所组成之固相萃取柱介质,其合成步骤包括:奈米碳管表面改质官能化,玻璃粒体之载体氨化及最后将两者经缩合剂作用而产生化学键结使奈米碳管批覆在玻璃粒体之载体上。

A kind of polishing wheel installed in the equipments imported from Germany or Czechoslovakia and in the polishing machine for crystal glass decoration, which is made from high flexible macromolecule, aluminum oxide and cerium oxide .

产品描述:一种安装在德国、克进口设备以及国内自主研发的水晶玻璃饰品研磨机上的抛光盘它是由高弹性和高强度的高分子材料与很锋利的抛光性能极佳的氧化铝、化铈等软质磨料进行混合反应而制作。

Description of project: PCC is produced by carbonation, with limestone as raw material. It is mainly used as filler in the manufacturing procedure of rubber, plastics, paper and paints, inks and other industrial produces. Meanwhile, it could be applied to the production of daily chemical products such as tooth powder, toothpaste cosmetics, as well as the organic synthesis, metallurgy, glass, asbestos and ect.

项目概述:轻质碳酸钙是以石灰石为原料,用碳化法制得,主要用于橡胶、塑料、造纸和涂料、油墨等工业中作填充剂,并可用于牙粉、牙膏、化妆品等日用化工制品中,还可以用于有机合成、冶金、玻璃和石棉生产中。

Results: Compared with sham controls, a progressive hyalinization and thicked wall of coronary arteries; perivascular fibrosis and interstitial fibrosis were observed in SAD rats.

结果:与Sham组相比,SAD大鼠心肌内冠状血管管壁呈进行性增厚、玻璃样变,管腔狭窄,血管周围纤维化和间质纤维化,心肌细胞肿胀、坏死和炎细胞浸润。

The results showed that Yb~(3+)-sensitized Tm~(3+)-doped oxyhalide tellurite glasses can be used as a kind of potential host materials for upconversion blue lasers .

结果表明Yb3+敏化Tm3+掺杂氧卤碲酸盐玻璃是一种上转换蓝光激光器的潜在基质材料。

The histopathologic changes included lymphocyte and monocyte infiltration,hyperplasia of synovial cells and small vessels,interstitial fibrosis,hyaline degeneration and cartilaginous metaplasia.The immunohistochemical observations showed that the high expressions of IL-1 and IL-6 were significantly different between the pathologic plicae and the control groups(P<0.01).The positive expressions of IL-1 and IL-6 were the synovial cells and monocyt-lymph cells in the pathologic synovial plicae.The positive expressions of MMP-1 and TIMP-1 have significant difference between the experiment and control group(P<0.01,P<0.05).The expression of MMP-1 was positive in synovial lining cell,monocyte,fibroblast,endothelial cell in small vessel and chondrocyte.The TIMP-1 expression was detected in the synovial lining cells and a small quantity fibroblast.

结果 正常滑膜皱襞和病理性滑膜皱襞在滑膜细胞增生及小血管增生、间质纤维化及玻璃样变、软骨化生组织学改变方面,差异均有显著性(P<0.01);IL-1、IL-6在病理性滑膜皱襞内的增生滑膜细胞、单核及淋巴细胞和在正常滑膜皱襞内的表达差异均有显著性(P<0.01); MMP-1、TIMP-1在病理性滑膜皱襞和正常皱襞内的阳性表达,差异具有显著性(P<0.01,P<0.05),MMP-1在增生滑膜衬里层细胞、单核和纤维母细胞、血管内皮细胞和软骨化生的软骨细胞呈阳性表达;TIMP-1只在滑膜衬里层细胞和少量纤维母细胞有表达。

Some cell dropped into the cavity and became free. Thrombosis or part organization could be seen. The internal elastic layer became thin, disappear or broken. In internal and middle layer existed fibroblasts, fibrocytes and collagen. Some of the wall indicated hyaline change, soomth muscle cell decreased greatly. The massive inflammatory cells invaded the middle and external layer. There were many foam cells in the capsule tissue. Cytoplasm was filled with fatty tissue and cholesterol. some cavities were full of thrombosis. Some thrombosis was fibrosis, the bottom was organization. The surface of the thrombosis existed red blood cell and librae.(2)Elatic fibrila staining: the internal elastic menbrane almost completely disappeared, the intact internal elastic menbran could be seen in the new small vessels.

动脉瘤管壁厚薄明显不均,全层或局部区域显著变薄向外膨出,内皮细胞空泡变性或坏死脱落,部分内皮细胞剥离并突入管腔成游离状,可见血栓形成及部分血栓机化;内弹力板变薄、消失或突然中断;在内膜及中膜部位主要为纤维母细胞、纤维细胞和大片胶原;部分动脉瘤壁呈均质状玻璃样变,平滑肌细胞明显减少;中膜和外膜可见大量的炎性细胞浸润;瘤壁组织有纤维母细胞、纤维细胞、大片胶原成分及较多泡沫细胞,胞浆内充满脂类物质及胆固醇结晶;部分动脉瘤腔内充满血栓,有的血拴已经纤维化,血栓基部机化,血栓表面有红细胞和纤维素。

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This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。

There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.

双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。