35 research outputs found
Experimental Investigation on the Early Stage Spray Characteristics with Biodiesel and Diesel
[EN] The early stage spray characteristics have a great impact on the secondary atomization progress, and thus affect
the engine combustion and emission performances. The experimental investigation of the early stage spray
behaviors with biodiesel and diesel was carried out by employing a laser-based Mie-scattering method. The
results show that the spray tip penetration for biodiesel is higher than that for diesel at the early stage spray under
the same injection pressure. Moreover, the early stage spray tip penetration can be longer under high injection
pressures for two fuels. Besides, the early stage spray cone angle for biodiesel is narrower than that for diesel,
and the spray cone angle is especially higher than biodiesel by 25.8% after start of injection time of 0.01ms.
Furthermore, under the same injection condition, the difference of early stage spray area between diesel and
biodiesel is not obvious, while the spray volume for biodiesel is larger than that for diesel, and also the spray
volume can be enlarged by increasing injection pressure for both fuels.This work was supported by the contribution of China postdoctoral fund projects [grant number2013M530236];
The projects of ‘Six talent peak’ [grant number 2014-ZBZZ-014]; Research start-up found projects of Jiangsu
university [grant number 13JDG104]; Natural Science Foundation of Jiangsu Province of China [grant number
BK20150520];The Priority Academic Program Development of Jiangsu Higher Education Institutions [PAPD]Yu, S.; Yin, B.; Wen, S.; Li, X.; Jia, H.; Yu, J. (2017). Experimental Investigation on the Early Stage Spray Characteristics with Biodiesel and Diesel. En Ilass Europe. 28th european conference on Liquid Atomization and Spray Systems. Editorial Universitat Politècnica de València. 473-479. https://doi.org/10.4995/ILASS2017.2017.4651OCS47347
Satellite Content and Halo Mass of Galaxy Clusters: Comparison between Red-Sequence and Halo-based Optical Cluster Finders
Cluster cosmology depends critically on how the optical clusters are selected
from imaging surveys. We compare the conditional luminosity function (CLF) and
weak lensing halo masses between two different cluster samples at fixed
richness, detected within the same volume () using the
red-sequence and halo-based methods. After calibrating our CLF deprojection
method against mock galaxy samples, we measure the 3D CLFs by cross-correlating
clusters with SDSS photometric galaxies. As expected, the CLFs of the
red-sequence and halo-based finders exhibit redder and bluer populations,
respectively. We also find significant shape discrepancies between the two CLFs
at the faint end, where the red-sequence clusters show a strong deficit of
faint galaxies but a bump at , while the halo-based clusters
host an increasing number of blue satellites. By comparing the subsamples of
clusters that have a match between the two catalogues to those without matches,
we discover that the CLF shape depends sensitively on the cluster centroiding.
However, the average weak lensing halo mass between the matched and non-matched
clusters are roughly consistent with each other in either cluster sample. Since
the colour preferences of the two cluster finders are almost orthogonal, such a
consistency indicates that the scatter in the mass-richness relation of either
cluster sample is close to random. Therefore, while the choice of how optical
clusters are identified impacts the satellite content, our result suggests that
it should not introduce strong systematics biases in cluster cosmology.Comment: 17 pages, 12 figures, 6 table
Dark against luminous matter around isolated central galaxies: a comparative study between modern surveys and Illustris-TNG
Based on independent shear measurements using the DECaLS/DR8 imaging data, we
measure the weak lensing signals around isolated central galaxies (ICGs) from
SDSS/DR7 at . The projected stellar mass density profiles of
surrounding satellite galaxies are further deduced, using photometric sources
from the Hyper Suprime-Cam (HSC) survey (pDR3). The signals of ICGs their
extended stellar halos are taken from Wang et al.(2021). All measurements are
compared with predictions by the Illustris-TNG300-1 simulation. We find,
overall, a good agreement between observation and TNG300. In particular, a
correction to the stellar mass of massive observed ICGs is applied based on the
calibration of He et al.(2013), which brings a much better agreement with
TNG300 predicted lensing signals at . In real
observation, red ICGs are hosted by more massive dark matter halos, have more
satellites and more extended stellar halos than blue ICGs at fixed stellar
mass. However, in TNG300 there are more satellites around blue ICGs at fixed
stellar mass, and the outer stellar halos of red and blue ICGs are similar. The
stellar halos of TNG galaxies are more extended compared with real observed
galaxies, especially for blue ICGs with . We find
the same trend for TNG100 galaxies and for true halo central galaxies. The
tensions between TNG and real galaxies might indicate that satellite
disruptions are stronger in TNG. In both TNG300 and observation, satellites
approximately trace the underlying dark matter distribution beyond
, but the fraction of total stellar mass in TNG300 does not show
the same radial distribution as real galaxies.Comment: 28 pages, 12 figure
DESI Legacy Imaging Surveys Data Release 9: Cosmological Constraints from Galaxy Clustering and Weak Lensing using the Minimal Bias Model
We present a tentative constraint on cosmological parameters and
from a joint analysis of galaxy clustering and galaxy-galaxy lensing
from DESI Legacy Imaging Surveys Data Release 9 (DR9), covering approximately
10000 square degrees and spanning the redshift range of 0.1 to 0.9. To study
the dependence of cosmological parameters on lens redshift, we divide lens
galaxies into seven approximately volume-limited samples, each with an equal
width in photometric redshift. To retrieve the intrinsic projected correlation
function from the lens samples, we employ a novel method
to account for redshift uncertainties. Additionally, we measured the
galaxy-galaxy lensing signal for each lens sample,
using source galaxies selected from the shear catalog by applying our
\texttt{Fourier\_Quad} pipeline to DR9 images. We model these observables
within the flat CDM framework, employing the minimal bias model. To
ensure the reliability of the minimal bias model, we apply conservative scale
cuts: and , for and
, respectively. Our findings suggest a mild tendency
that increases with lens redshift,
although this trend is only marginally significant. When we combine low
redshift samples, the value of is determined to be ,
consistent with the Planck results but significantly higher than the 3
2pt analysis by 2-5. Despite the fact that further refinements in
measurements and modeling could improve the accuracy of our results, the
consistency with standard values demonstrates the potential of our method for
more precise and accurate cosmology in the future.Comment: slightly different with the published versio
Halo Properties and Mass Functions of Groups/Clusters from the DESI Legacy Imaging Surveys DR9
Based on a large group/cluster catalog recently constructed from the DESI
Legacy Imaging Surveys DR9 using an extended halo-based group finder, we
measure and model the group-galaxy weak lensing signals for groups/clusters in
a few redshift bins within redshift range . Here, the
background shear signals are obtained based on the DECaLS survey shape catalog
derived with the \textsc{Fourier\_Quad} method. We divide the lens samples into
5 equispaced redshift bins and 7 mass bins, which allow us to probe the
redshift and mass dependence of the lensing signals and hence the resulting
halo properties. In addition to these sample selections, we have also checked
the signals around different group centers, e.g., brightest central galaxy
(BCG), luminosity weighted center and number weighted center. We use a lensing
model that includes off-centering to describe the lensing signals we measure
for all mass and redshift bins. The results demonstrate that our model
predictions for the halo masses, bias and concentrations are stable and
self-consistent among different samples for different group centers. Taking
advantage of the very large and complete sample of groups/clusters, as well as
the reliable estimation of their halo masses, we provide measurements of the
cumulative halo mass functions up to redshift , with a mass precision at
dex.Comment: revised version submitted to Ap
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Inhibition of the prolyl isomerase Pin1 enhances the ability of sorafenib to induce cell death and inhibit tumor growth in hepatocellular carcinoma
Hepatocellular carcinoma (HCC) is the sixth most common cancer, but is the second leading cause of cancer deaths, partially due to its heterogeneity and drug resistance. Sorafenib is the only medical treatment with a proven efficacy against advanced HCC, but its overall clinical efficacy is still modest. Therefore, a major challenge is how to improve its therapeutic efficacy. The unique prolyl isomerase Pin1 regulates numerous cancer-driving pathways. Notably, Pin1 is overexpressed in about 70% HBV-positive HCC patients and contributes to HCC tumorigenesis. However, the role of Pin1 in the efficacy of sorafenib against HCC is unknown. Here we found that sorafenib down-regulated Pin1 mRNA and protein expression, likely through inhibition of Pin1 transcription by the Rb/E2F pathway. Importantly, Pin1 knockdown potently enhanced the ability of sorafenib to induce cell death in HCC, which was further supported by the findings that Pin1 knockdown led to stabilization of Fbxw7 and destabilization of Mcl-1. Furthermore, all-trans retinoic acid (ATRA), a known anticancer drug that inhibits and ultimately induces degradation of active Pin1 in cancer cells, also potently sensitized HCC cells to sorafenib-induced cell death at least in part through a caspase-dependent manner. Moreover, ATRA also synergistically enhanced the ability of sorafenib to reduce Pin1 and inhibit tumor growth of HCC in mouse xenograft models. Collectively, these results not only demonstrate that Pin1 down-regulation is a key event underlying the anti-tumor effects of sorafenib, but also uncover that Pin1 inhibitors offer a novel approach to enhance the therapeutic efficacy of sorafenib against HCC