15 research outputs found
Parental perspectives on children’s use of portable digital devices
<p>Small portable digital devices (PDDs) – tablets and smartphones – are becoming increasingly popular among children at early ages. In this qualitative study, we applied the theoretical frameworks of <i>self-efficacy</i> and <i>othermothering</i> to examine the perspectives of parents from rural areas regarding the role of PDDs in children of early and primary education age (4–7 years old). We conducted in-depth interviews with parents, observed children at home, and collected artefacts related to children’s PDDs use to capture daily habits, experiences, and attitudes from different angles. Data revealed that parents supported PDDs as entertainment and learning tools. Parents reported improvements in dexterity, memory, attention, and linguistic and mathematical skills, and believed that PDDs positively affect children’s cognitive development. During observations, children exhibited versatility and skill with app navigation for entertainment and educational purposes. Children completed tasks in an independent and efficacious manner that reinforced engagement. Parents seemed to unconsciously transfer to PDDs a cognitive and social role that created another parenting modality as in othermothering. Parents, meanwhile, appeared concerned with uncontrolled overuse of PDDs by children. These findings suggest that parents from rural areas view PDDs as tools that pose opportunities and challenges for entertainment and learning.</p
Relationship between ACS groups and the fractures.
<p>ACS  =  aortic calcifications score.</p><p>*p<0.01 vs G1.</p
Tetraphenylphosphonium Bromide as a Cathode Buffer Layer Material for Highly Efficient Polymer Solar Cells
Here, we introduced
the role of small organic molecule tetraphenylphosphonium bromide
(<b>QPhPBr</b>) as an electron-transporting layer (ETL) material
for fabricating high-efficiency bulk heterojunction polymer solar
cells (PSCs). Their significantly higher power conversion efficiency
(PCE) in well-known active layer devices (PTB7-Th:PC<sub>71</sub>BM,
PBDTTT-CT:PC<sub>71</sub>BM, and P3HT:PC<sub>71</sub>BM) was observed
compared to that of the bare Al cathode. The use of N719 as an ETL
was also demonstrated. Observed data reveal that <b>QPhPBr</b>-based devices exhibit high PCEs up to 9.18, 8.42, and 4.81% from
PTB7-Th, PBDTTT-CT, and P3HT, respectively. For comparisons, the bare
Al devices show PCEs of 5.37, 4.75, and 3.01%, respectively. Moreover,
further enhancement of PSC efficiency (9.83, 8.69, and 5.35%) is achieved
from mixed binary solution of <b>N719:QPhPBr</b> because of
modulated adjustment of the work function of the Al electrode. Our
results indicate the excellent function of tetraphenylphosphonium
bromide and its binary blend as effective small-molecule organic materials
to regulate the metal surface properties and the potential used as
excellent cathode buffer layer materials for realizing high-efficiency
PSCs
Incidence of vertebral and non-vertebral fractures per 100 person-years by age and site.
<p>Incidence of vertebral and non-vertebral fractures was significantly higher in the 60- to 69-year-old group, the 70- to 79-year-old group and the>80-year-old group compared to the 50- to 59-year-old group (p<0.001, respectively). In each group, the vertebral fracture prevalence was significantly higher than for non-vertebral fractures (p<0.001).</p
Investigation on Thermal Degradation of Poly(1,4-butylene terephthalate) Filled with Aluminum Hypophosphite and Trimer by Thermogravimetric Analysis–Fourier Transform Infrared Spectroscopy and Thermogravimetric Analysis–Mass Spectrometry
Flame-retarded
polyÂ(1,4-butylene terephthalate) (PBT) has been
prepared using aluminum hypophosphite (AHP) and triÂ(1-oxo-2,6,7-trioxa-1-phosphabicycloÂ[2,2,2]Âoctane-methyl)Âphosphate
(Trimer). The combustion properties of flame-retarded PBT were evaluated
using limiting oxygen index, UL-94, and cone calorimetry. The cone
calorimeter data indicated that the presence of PBT/AHP/Trimer imparted
a significant smoke-suppressing effect. The thermal degradation properties
of flame-retarded PBT were investigated using thermogravimetric analysis–Fourier
transform infrared and thermogravimetric analysis–mass spectrometry.
For the samples of PBT, PBT/25% AHP, and PBT/AHP/Trimer, the main
gas pyrolysis products were CO<sub>2</sub> and butadiene; the sample
of PBT/AHP/Trimer generated less CO<sub>2</sub> and butadiene and
consequently retained more carbon in the matrix. The amount of phosphorus–oxygen
radicals of PBT/25% AHP was 1.3 times that of PBT/AHP/Trimer, which
indicated that AHP alone showed slightly stronger gaseous phase effect
than the combination of AHP and Trimer. This result is further confirmed
by the analysis of the char residues by X-ray photoelectron spectroscopy
Rechargeable Aqueous Zn–V<sub>2</sub>O<sub>5</sub> Battery with High Energy Density and Long Cycle Life
We
report an aqueous Zn–V<sub>2</sub>O<sub>5</sub> battery
chemistry employing commercial V<sub>2</sub>O<sub>5</sub> cathode,
Zn anode, and 3 M ZnÂ(CF<sub>3</sub>SO<sub>3</sub>)<sub>2</sub> electrolyte.
We elucidate the Zn-storage mechanism in the V<sub>2</sub>O<sub>5</sub> cathode to be that hydrated Zn<sup>2+</sup> can reversibly (de)Âintercalate
through the layered structure. The function of the co-intercalated
H<sub>2</sub>O is revealed to be shielding the electrostatic interactions
between Zn<sup>2+</sup> and the host framework, accounting for the
enhanced kinetics. In addition, the pristine bulk V<sub>2</sub>O<sub>5</sub> gradually evolves into porous nanosheets upon cycling, providing
more active sites for Zn<sup>2+</sup> storage and thus rendering an
initial capacity increase. As a consequence, a reversible capacity
of 470 mAh g<sup>–1</sup> at 0.2 A g<sup>–1</sup> and
a long-term cyclability with 91.1% capacity rentention over 4000 cycles
at 5 A g<sup>–1</sup> are achieved. The combination of the
good battery performance, safety, scalable materials synthesis, and
facile cell assembly indicates this aqueous Zn–V<sub>2</sub>O<sub>5</sub> system is promising for stationary grid storage applications
Mercury Distribution and Deposition in Glacier Snow over Western China
Western China is home to the largest aggregate of glaciers
outside
the polar regions, yet little is known about how the glaciers in this
area affect the transport and cycling of mercury (Hg) regionally and
globally. From 2005 to 2010, extensive glacier snow sampling campaigns
were carried out in 14 snowpits from 9 glaciers over western China,
and the vertical distribution profiles of Hg were obtained. The Total
Hg (THg) concentrations in the glacier snow ranged from <1 to 43.6
ng L<sup>–1</sup>, and exhibited clear seasonal variations
with lower values in summer than in winter. Spatially, higher THg
concentrations were typically observed in glacier snows from the northern
region where atmospheric particulate loading is comparably high. Glacier
snowpit Hg was largely dependent on particulate matters and was associated
with particulate Hg, which is less prone to postdepositional changes,
thus providing a valuable record of atmospheric Hg deposition. Estimated
atmospheric Hg depositional fluxes ranged from 0.74 to 7.89 ÎĽg
m<sup>–2</sup> yr<sup>–1</sup>, agreeing very well with
the global natural values, but are one to two orders of magnitude
lower than that of the neighboring East Asia. Elevated Hg concentrations
were observed in refrozen ice layers in several snowpits subjected
to intense melt, indicating that Hg can be potentially released to
meltwater