Changing dynamics of the Chinese automotive industry : the impact of foreign investment, technology transfer, and WTO membership

Thesis (S.M.M.O.T.)--Massachusetts Institute of Technology, Sloan School of Management, Management of Technology Program, 2003.Includes bibliographical references (leaves 79-82).This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.The Chinese automotive industry was established 50 years ago with the technology transfer of a truck production system from the Soviet Union. Since then, it developed into a decentralized and fragmented truck industry layout due to the self-reliant and defensive policies set forth by the central government. Over the past two decades, China has obtained substantial and modern passenger car production systems with a large sum of foreign direct investment (FDI) and comprehensive technology transfer from global carmakers in Europe, the U.S., and Japan. This research studies the 50- year development history of the Chinese automotive industry and seeks to understand the role of the Chinese protectionist automotive industry policies and the impact of FDI and technology transfer. China officially entered the World Trade Organization (WTO) in November 2001 and committed to end the 50 years of protectionism. The WTO membership is expected to inject fierce market competition into the Chinese automotive industry and ultimately propel the industry to a new level. My research attempts to forecast what might happen in the coming years. My research included site visits and personal interviews with seven senior executives from Chinese automotive firms located in Beijing, Shanghai, and Guangzhou, as well as three academic experts on the Chinese automotive industry at the Tsinghua University. This research finds that China has benefited significantly from foreign investment and technology transfers. China was able to leapfrog from 1950s-level automotive production systems into 1990s-level advanced technologies, and the gap with world standards continues to narrow. My research also indicates the protectionist automotive industry policies China had before the WTO accession have seriously hindered China's ability to achieve the full potential impact that FDI could have made. The lack of coherent policies between protection and competition has caused the Chinese automotive industry to remain fragmented and uncompetitive. The lack of competition and restrictions on foreign equity has delayed the speed of technology transfers and China's development of full automotive design and production capabilities. China will stride in the post-WTO era. However, the protectionism, particular from regional and local governments, is likely to continue and hinder the full impact of benefits from the WTO membership.by Michael Y. Lee.S.M.M.O.T

Notes on two-parameter quantum groups, (II)

This paper is the sequel to [HP1] to study the deformed structures and representations of two-parameter quantum groups $U_{r,s}(\mathfrak{g})$ associated to the finite dimensional simple Lie algebras \mg. An equivalence of the braided tensor categories \O^{r,s} and \O^{q} is explicitly established.Comment: 21 page

Reconfigurable ferromagnetic liquid droplets.

Solid ferromagnetic materials are rigid in shape and cannot be reconfigured. Ferrofluids, although reconfigurable, are paramagnetic at room temperature and lose their magnetization when the applied magnetic field is removed. Here, we show a reversible paramagnetic-to-ferromagnetic transformation of ferrofluid droplets by the jamming of a monolayer of magnetic nanoparticles assembled at the water-oil interface. These ferromagnetic liquid droplets exhibit a finite coercivity and remanent magnetization. They can be easily reconfigured into different shapes while preserving the magnetic properties of solid ferromagnets with classic north-south dipole interactions. Their translational and rotational motions can be actuated remotely and precisely by an external magnetic field, inspiring studies on active matter, energy-dissipative assemblies, and programmable liquid constructs

Two Higgs Bi-doublet Left-Right Model With Spontaneous P and CP Violation

A left-right symmetric model with two Higgs bi-doublet is shown to be a consistent model for both spontaneous P and CP violation. The flavor changing neutral currents can be suppressed by the mechanism of approximate global U(1) family symmetry. We calculate the constraints from neural $K$ meson mass difference $\Delta m_K$ and demonstrate that a right-handed gauge boson $W_2$ contribution in box-diagrams with mass well below 1 TeV is allowed due to a cancellation caused by a light charged Higgs boson with a mass range $150 \sim 300$ GeV. The $W_2$ contribution to $\epsilon_K$ can be suppressed from appropriate choice of additional CP phases appearing in the right-handed Cabbibo-Kobayashi-Maskawa matrix. The model is also found to be fully consistent with $B^0$ mass difference $\Delta m_B$, and the mixing-induced CP violation quantity $\sin2\beta_{J/\psi}$, which is usually difficult for the model with only one Higgs bi-doublet. The new physics beyond the standard model can be directly searched at the colliders LHC and ILC.Comment: 25 pages, 6 figures, typos corrected, 1 figure added, published versio

Cell responses and hemocompatibility of g-HA/PLA composites

The objective of this study was to investigate the hemocompatibility and cell responses to some novel poly(L-lactide) (PLA) composites containing surface modified hydroxyapatite particles for potential applications as a bone substitute material. The surface of hydroxyapatite (HA) particles was first grafted with L-lactic acid oligomers to form grafted HA (g-HA) particles. The g-HA particles were further blended with PLA to prepare g-HA/PLA composites. Our previous study has shown significant improvement in tensile properties of these materials due to the enhanced interfacial adhesion between the polymer matrix and HA particles. To further investigate the potential applications of these composites in bone repair and other orthopedic surgeries, a series of in vitro and in vivo experiments were conducted to examine the cell responses and hemocompatibility of the materials. In vitro experiments showed that the g-HA/PLA composites were well tolerated by the L-929 cells. Hemolysis of the composites was lower than that of pure PLA. Subcutaneous implantation demonstrated that the g-HA/PLA composites were more favorable than the control materials for soft tissue responses. The results suggested that the g-HA/PLA composites are promising and safe materials with potential applications in tissue engineering

Direct numerical simulation of a tip-leakage flow in a planar duct with a longitudinal slit

A planar duct flow configuration with a cross-flow injected from a longitudinal slit close to the upper wall of the duct is studied by using a direct numerical simulation approach to explore the underlying flow mechanism in relation to the tip-leakage vortex (TLV), which is one of the most important flow phenomena in turbomachinery. Major characteristics of TLV in a rotor of turbomachinery are identified in the current flow model. The analysis of mean and instantaneous flow fields reveals that the interaction between the main (axial) flow and jet (cross) flow is the primary source of the generation of the TLV. The evolution of the TLV is then investigated, and a vortex breakup phenomenon is identified. The evolution of TLV can be divided into three phases, i.e. the formation phase, the break-up phase, and the diffusion phase. Mean streamlines and turbulence kinetic energy (TKE) budgets are analysed, showing that the high TKE central spot in the formation phase is due to the interaction between highly swirling vortex filaments and mean velocity gradient. In the outer part of the TLV, the TKE is mainly produced in the shear-layer and transported towards the centre by the turbulence transport

DiffSplice: The Genome-Wide Detection of Differential Splicing Events with RNA-Seq

The RNA transcriptome varies in response to cellular differentiation as well as environmental factors, and can be characterized by the diversity and abundance of transcript isoforms. Differential transcription analysis, the detection of differences between the transcriptomes of different cells, may improve understanding of cell differentiation and development and enable the identification of biomarkers that classify disease types. The availability of high-throughput short-read RNA sequencing technologies provides in-depth sampling of the transcriptome, making it possible to accurately detect the differences between transcriptomes. In this article, we present a new method for the detection and visualization of differential transcription. Our approach does not depend on transcript or gene annotations. It also circumvents the need for full transcript inference and quantification, which is a challenging problem because of short read lengths, as well as various sampling biases. Instead, our method takes a divide-and-conquer approach to localize the difference between transcriptomes in the form of alternative splicing modules (ASMs), where transcript isoforms diverge. Our approach starts with the identification of ASMs from the splice graph, constructed directly from the exons and introns predicted from RNA-seq read alignments. The abundance of alternative splicing isoforms residing in each ASM is estimated for each sample and is compared across sample groups. A non-parametric statistical test is applied to each ASM to detect significant differential transcription with a controlled false discovery rate. The sensitivity and specificity of the method have been assessed using simulated data sets and compared with other state-of-the-art approaches. Experimental validation using qRT-PCR confirmed a selected set of genes that are differentially expressed in a lung differentiation study and a breast cancer data set, demonstrating the utility of the approach applied on experimental biological data sets. The software of DiffSplice is available at http://www.netlab.uky.edu/p/bioinfo/DiffSplice