16 research outputs found
Tracking Inter-Regional Carbon Flows: A Hybrid Network Model
The
mitigation of anthropogenic carbon emissions has moved beyond
the local scale because they diffuse across boundaries, and the consumption
that triggers emissions has become regional and global. A precondition
of effective mitigation is to explicitly assess inter-regional transfer
of emissions. This study presents a hybrid network model to track
inter-regional carbon flows by combining network analysis and inputâoutput
analysis. The direct, embodied, and controlled emissions associated
with regions are quantified for assessing various types of carbon
flow. The network-oriented metrics called âcontrolled emissionsâ
is proposed to cover the amount of carbon emissions that can be mitigated
within a region by adjusting its consumption. The case study of the
JingâJinâJi Area suggests that CO<sub>2</sub> emissions
embodied in products are only partially controlled by a region from
a network perspective. Controlled carbon accounted for about 70% of
the total embodied carbon flows, while household consumption only
controlled about 25% of Beijingâs emissions, much lower than
its proportion of total embodied carbon. In addition to quantifying
emissions, the model can pinpoint the dominant processes and sectors
of emissions transfer across regions. This technique is promising
for searching efficient pathways of coordinated emissions control
across various regions connected by trade
Changing Urban Carbon Metabolism over Time: Historical Trajectory and Future Pathway
Cities are expected to play a major
role in carbon emissions mitigation.
A key step in decoupling urban economy from carbon emissions is to
understand the full impact of socioeconomic development on urban metabolism
over time. Herein, we establish a system-based framework for modeling
the variation of urban carbon metabolism through time by integrating
a metabolic flow inventory, inputâoutput model, and network
analysis. Using Beijing as a case study, we track the historical trajectory
of carbon flows embodied in urban final consumption over 1985â2012.
We find that while the tendency of increase in direct carbon emission
continues within this time frame, consumption-based carbon footprint
might have peaked around 2010. Significant transitions in emission
intensity and roles sectors play in transferring carbon over the period
are important signs of decoupling urban development from carbonization.
Our further analysis of driving factors reveals a strong competition
between efficiency gains and consumption level rise, showing a cumulative
contribution of â584% and 494% to total carbon footprint, respectively.
Projection into a future pathway suggests there is still a great potential
for carbon mitigation for the city, but a strong mitigation plan is
required to achieve such decarbonization before 2030. By bridging
temporal metabolic model and socioeconomic planning, this framework
fills one of the main gaps between monitoring of urban metabolism
and design of a low-carbon economy
Network Environ Perspective for Urban Metabolism and Carbon Emissions: A Case Study of Vienna, Austria
Cities are considered major contributors to global warming,
where carbon emissions are highly embedded in the overall urban metabolism.
To examine urban metabolic processes and emission trajectories we
developed a carbon flux model based on Network Environ Analysis (NEA).
The mutual interactions and control situation within the urban ecosystem
of Vienna were examined, and the system-level properties of the cityâs
carbon metabolism were assessed. Regulatory strategies to minimize
carbon emissions were identified through the tracking of the possible
pathways that affect these emission trajectories. Our findings suggest
that indirect flows have a strong bearing on the mutual and control
relationships between urban sectors. The metabolism of a city is considered
self-mutualistic and sustainable only when the local and distal environments
are embraced. Energy production and construction were found to be
two factors with a major impact on carbon emissions, and whose regulation
is only effective via ad-hoc pathways. In comparison with the original
life-cycle tracking, the application of NEA was better at revealing
details from a mechanistic aspect, which is crucial for informed sustainable
urban management
Nonzero-Sum Relationships in Mitigating Urban Carbon Emissions: A Dynamic Network Simulation
The
âstove-pipeâ way of thinking has been mostly
used in mitigating carbon emissions and managing socioeconomics because
of its convenience of implementation. However, systems-oriented approaches
become imperative in pursuit of an efficient regulation of carbon
emissions from systems as complicated as urban systems. The aim of
this paper is to establish a dynamic network approach that is capable
of assessing the effectiveness of carbon emissions mitigation in a
more holistic way. A carbon metabolic network is constructed by modeling
the carbon flows between economic sectors and environment. With the
network shocked by interventions to the sectoral carbon flows, indirect
emissions from the city are accounted for under certain carbon mitigation
strategies. The nonzero-sum relationships between sectors and environmental
components are identified based on utility analysis, which synthesize
the nature of direct and indirect network interactions. The results
of the case study of Beijing suggest that the stove-pipe mitigation
strategies targeted the economic sectors might be not as efficient
as they were expected. A direct cutting in material or energy import
to the sectors may result in a rebound in indirect emissions and thus
fails to achieve the carbon mitigation goal of the city as a whole.
A promising way of foreseeing the dynamic mechanism of emissions is
to analyze the nonzero-sum relationships between important urban components.
Thinking cities as systems of interactions, the network approach is
potentially a strong tool for appraising and filtering mitigation
strategies of carbon emissions
1950-1951 Yunus Nadi mĂŒkafatı:Milli MĂŒcadeleye ait bir hatıra:Milli MĂŒcadele nasıl baĆladı?
Taha Toros ArĆivi, Dosya Adı: Milli MĂŒcadeleUnutma Ä°stanbul projesi Ä°stanbul Kalkınma Ajansı'nın 2016 yılı "Yenilikçi ve Yaratıcı Ä°stanbul Mali Destek Programı" kapsamında desteklenmiĆtir. Proje No: TR10/16/YNY/010
Ibutilide treatment alters mRNA levels of ER stress markers GRP78, GRP94 and calumenin in tunicamycin treated RNC.
<p>mRNA expression of GRP78, GRP94 and calumenin were analyzed by real-time PCRin RNC treated with either tunicamycin alone (model), tunicamycin pre-treated with ibutilide (treatment) or untreated cells (control). All data are shown as mean ± SE (<i>n</i> = 3 per group). **p<0.01, ***p<0.001.</p
Anion De/Intercalation in Nickel Hydroxychloride Microspheres: A Mechanistic Study of Structural Impact on Energy Storage Performance of Multianion-Containing Layered Materials
Electrochemical
cation de/intercalation has long been investigated for energy-relevant
applications, while anion de/intercalation is comparatively highly
challenging, although promising for promoting the performance of materials.
Herein, layered nickel hydroxychloride was selected as a model multianion-containing
inorganic functional material to study. Hierarchical flower-like microspheres
self-assembled from nanosheets were synthesized via a solvothermal
method. The as-prepared nickel hydroxychloride was built up from neutral
layers of [NiÂ(OH)<sub>3/3</sub>Cl<sub>3/3</sub>] octahedra, showing
an expanded interlayer spacing of 0.57 nm. With this unique microstructure,
Cl<sup>â</sup> deintercalation and OH<sup>â</sup> intercalation
were accomplished through an effective nonelectrochemical process.
The nickel hydroxychloride NiÂ(OH)<sub>0.99</sub>Cl<sub>1.01</sub> with
a maximum Cl<sup>â</sup> ion content was found to possess the
largest interlayer spacing, which when first employed as electrode
materials for supercapacitor, delivered an ultrahigh specific capacitance
of 3831 F/g at a current density of 1 A/g. For the latter case, NiÂ(OH)<sub>2.18</sub>(H<sub>3</sub>O)<sub>0.18</sub> with a maximum OH<sup>â</sup> content showed a specific capacitance of 1489 F/g at 1 A/g. Expanded
interlayer spacing associated with the anion de/intercalation is the
key that enhances ion diffusion kinetics between layers. The methodology
of anion de/intercalation reported in this work would provide hints
of exploring novel multianion-containing materials with anion de/intercalation
necessary for high-performance energy applications
Ibutilide treatment alters protein expression of ER stress markers GRP78, GRP94 and calumenin in tunicamycin treated RNC.
<p>Protein levels GRP78 and GRP94 and calumenin were analyzed from lysates derived from RNC treated with either tunicamycin alone (model), tunicamycin and ibutilide (treatment) or untreated cardiomyocytes (control). Representative immunoblots of lysate immunoblotted with antibodies specific for (A) GRP78, (B) GRP94 or (C) Calumenin. Quantification of band densitometry is shown adjacent to the corresponding blot. All data are shown as mean ± SE (<i>n</i> = 3 per group). *p<0.5, **p<0.01, ***p<0.001.</p
Optimum Preferential Oxidation Performance of CeO<sub>2</sub>âCuO<sub><i>x</i></sub>âRGO Composites through Interfacial Regulation
Interfacial
regulation offers a promising route to rationally and effectively
design advanced materials for CO preferential oxidation. Herein, we
initiated an interfacial regulation of CeO<sub>2</sub>âCuO<sub><i>x</i></sub>âRGO composites by adjusting the addition
sequence of the components during the support formation. The presence
of RGO along with the sequence tuning of the components is confirmed
to survey the changes of the oxidation state of copper species, the
content and distribution of the Cu<sup>+</sup> site, and the synergistic
interactions between CuâCe mixed oxides and reduced graphene
oxide (RGO) over the catalysts. These catalysts were systematically
characterized by inductively coupled plasma, X-ray diffraction, transmission
electron microscopy/high-resolution transmission electron microscopy,
hydrogen temperature-programmed reduction, X-ray photoelectron spectra,
thermal gravimetric analysis, Raman spectra, and in situ diffuse reflectance
infrared Fourier transform spectroscopy measurements. The results
show that RGO is favorable for the generation of Cu<sup>+</sup> and
the dispersion of copperâcerium species in the as-prepared
catalysts. Furthermore, by multi-interfacial regulation of the CeO<sub>2</sub>âCuO<sub><i>x</i></sub>âRGO composites,
the catalyst CeO<sub>2</sub>/CuO<sub><i>x</i></sub>âRGO
exhibits a strikingly high catalytic oxidation activity at a low temperature
coupled with a broader operation temperature window (i.e., CO conversion
>99.0%, 140â220 °C) in the CO-selective oxidation reaction,
which has been attributed to the high content of the active species
Cu<sup>+</sup> enriched on the surface, the highly dispersed copper
oxide clusters subjected to a strong interaction with ceria, and the
synergistic interactions between CuâCe mixed oxides and RGO
Ibutilide treatment attenuates tunicamycin induced increase in Bax/ Bcl-2 ratio.
<p>Protein expression of Bax and Bcl-2 were analyzed from lysate derived from RNC treated with either tunicamycin alone (model), tunicamycin and ibutilide (treatment) or untreated cardiomyocytes (control). Representative immunoblots of lysate immunoblotted with antibodies specific for Bax or BCL-2 are shown. The quantification of normalized band densitometry of Bax was divided by that of Bcl-2 and the results are graphed. All data are shown as mean ± SE (<i>n</i> = 3 per group). *p<0.5, **p<0.01, ***p<0.001.</p