Publications by authors named "Yangong Wu"

Over the past 30 years, researchers have developed X-ray-focusing telescopes by employing the principle of total reflection in thin metal films. The Wolter-I focusing mirror with variable-curvature surfaces demands high precision. However, there has been limited investigation into the removal mechanisms for variable-curvature X-ray mandrels, which are crucial for achieving the desired surface roughness and form accuracy, especially in reducing mid-spatial frequency (MSF) errors.

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This paper describes a method for measuring and compensating the roundness error of a larger mandrel manufactured by an ultra-precision diamond-turning lathe aimed to obtain a calibration cylinder with a roundness of less than 0.1 μm. The diamond-turning machine has a cross-stacked hydrostatic guideway, produces a cutting depth and feed movement direction, and a dual-spindle system that is firmly connected to the bed.

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Brightness enhancement film (BEF), as a polyethylene terephthalate (PET) film with the micro-prism array on the surface, is an indispensable core optical component for a back light unit (BLU) in liquid crystal display. Roll-to-roll (RTR) imprinting approach is the most mature and reliable technology to produce the BEF in the industry. Of course, the machining accuracy of the micro-prism array on the roller mold will directly determine the optical performance of BEF manufactured by RTR.

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Slow tool servo (STS) assisted ultra-precision diamond turning is considered as a promising machining process with high accuracy and low cost to generate the large-area micro lens arrays (MLAs) on the roller mold. However, the chatter mark is obvious at the cut-in part of every machined micro lens along the cutting direction, which is a common problem for the generation of MLAs using STS. In this study, a novel forming approach based on STS is presented to fabricate MLAs on the aluminum alloy (6061) roller mold, which is a high-efficiency machining approach in comparison to a traditional method based on STS.

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Thirteen isolates of Class I Newcastle disease virus obtained from healthy poultry in China during 2008 were characterized genotypically in this study. All the isolates were proved to be lentogenic strains based on the deduced amino acid sequence of the Fusion protein gene. Molecular epidemiological analysis showed that 13 isolates could be subdivided into 2 distinct genotypes, 11 isolates belonged to genotype 2, and other 2 isolates belonged to genotype 3.

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Ten representative isolates of Newcastle disease virus (NDV) obtained from outbreaks in waterfowl (geese and ducks) in China since 1997 were characterized both pathotypically and genotypically. The mean death time and intracerebral pathogenicity index were used to evaluate the virulence of the isolates. Pathogenicity tests showed that all 10 isolates were velogenic strains.

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Seventy-nine velogenic Newcastle disease virus (NDV) isolates were obtained from infected chicken flocks during the outbreaks of Newcastle disease (ND) in various regions of the mainland of China in 2006. The F gene fragment (535bp, from nt 47 to 581 of the F gene) which codes the main functional region of the F protein was obtained by RT-PCR and sequenced. All sequences obtained in this study have been submitted to GenBank.

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Fourteen pigeon-origin Newcastle disease virus (NDV) isolates were obtained from sick pigeons in China between 1996 and 2005. The mean death time (MDT) of embryonated eggs and the intracerebral pathogenicity indices (ICPI) were tested to determine the virulence of the field isolates. The result indicated that most isolates were proved to be mesogenic (MDT 60-90 hr and ICPI > 1.

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Eighty-three strains of Newcastle disease virus (NDV) were obtained from outbreaks in chickens, pigeons, geese, and ducks in China in 2005 and characterized genotypically. The main functional region of the F gene (535 nucleotides) was amplified and sequenced. A phylogenetic tree based on nucleotides 47-435 of the F gene was created using sequences from 83 isolates and representative NDV sequences obtained from GenBank.

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