<?xml version="1.0" encoding="UTF-8"?>
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<title>Chemical Engineering</title>
<link href="http://repository.enu.kz/handle/enu/15588" rel="alternate"/>
<subtitle/>
<id>http://repository.enu.kz/handle/enu/15588</id>
<updated>2026-04-03T23:18:15Z</updated>
<dc:date>2026-04-03T23:18:15Z</dc:date>
<entry>
<title>Wet Chemical Synthesis of AlxGa1−xAs Nanostructures: Investigation of Properties and Growth Mechanisms</title>
<link href="http://repository.enu.kz/handle/enu/29758" rel="alternate"/>
<author>
<name>Suchikova, Yana</name>
</author>
<author>
<name>Kovachov, Sergii</name>
</author>
<author>
<name>Bohdanov, Ihor</name>
</author>
<author>
<name>Konuhova, Marina</name>
</author>
<author>
<name>Zhydachevskyy, Yaroslav</name>
</author>
<author>
<name>Kumarbekov, Kuat</name>
</author>
<author>
<name>Pankratov, Vladimir</name>
</author>
<author>
<name>Popov, Anatoli I.</name>
</author>
<id>http://repository.enu.kz/handle/enu/29758</id>
<updated>2026-03-04T19:04:35Z</updated>
<published>2024-01-01T00:00:00Z</published>
<summary type="text">Wet Chemical Synthesis of AlxGa1−xAs Nanostructures: Investigation of Properties and Growth Mechanisms
Suchikova, Yana; Kovachov, Sergii; Bohdanov, Ihor; Konuhova, Marina; Zhydachevskyy, Yaroslav; Kumarbekov, Kuat; Pankratov, Vladimir; Popov, Anatoli I.
This study focuses on the wet chemical synthesis of AlxGa1−xAs nanostructures, highlighting how different deposition conditions affect the film morphology and material properties.&#13;
Electrochemical etching was used to texture GaAs substrates, enhancing mechanical adhesion and&#13;
chemical bonding. Various deposition regimes, including voltage switching, gradual voltage increase,&#13;
and pulsed voltage, were applied to explore their impact on the film growth mechanisms. SEM&#13;
analysis revealed distinct morphologies, EDX confirmed variations in aluminum content, Raman&#13;
spectroscopy detected structural disorders, and XRD analysis demonstrated peak position shifts. The&#13;
findings emphasize the versatility and cost-effectiveness of wet electrochemical methods for fabricating high-quality AlxGa1−xAs films with tailored properties, showing potential for optoelectronic&#13;
devices, high-efficiency solar cells, and other advanced semiconductor applications.
</summary>
<dc:date>2024-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Variation in the Bandgap of Amorphous Zinc Tin Oxide: Investigating the Thickness Dependence via In Situ STS</title>
<link href="http://repository.enu.kz/handle/enu/29757" rel="alternate"/>
<author>
<name>Callaghan, Peter J.</name>
</author>
<author>
<name>Caffrey, David</name>
</author>
<author>
<name>Zhussupbekov, Kuanysh</name>
</author>
<author>
<name>Berman, Samuel</name>
</author>
<author>
<name>Zhussupbekova, Ainur</name>
</author>
<author>
<name>Smith, Christopher M.</name>
</author>
<author>
<name>Shvets, Igor V.</name>
</author>
<id>http://repository.enu.kz/handle/enu/29757</id>
<updated>2026-03-04T19:01:17Z</updated>
<published>2024-01-01T00:00:00Z</published>
<summary type="text">Variation in the Bandgap of Amorphous Zinc Tin Oxide: Investigating the Thickness Dependence via In Situ STS
Callaghan, Peter J.; Caffrey, David; Zhussupbekov, Kuanysh; Berman, Samuel; Zhussupbekova, Ainur; Smith, Christopher M.; Shvets, Igor V.
Amorphous transparent conducting oxides (aTCOs) have seen substantial interest in recent years due to the&#13;
significant benefits that they can bring to transparent electronic&#13;
devices. One such material of promise is amorphous ZnxSn1−xOy&#13;
(a-ZTO). a-ZTO possesses many attractive properties for a TCO&#13;
such as high transparency in the visible range, tunable charge&#13;
carrier concentration, electron mobility, and only being composed&#13;
of common and abundant elements. In this work, we employ a&#13;
combination of UV−vis spectrophotometry, X-ray photoemission&#13;
spectroscopy, and in situ scanning tunneling spectroscopy to&#13;
investigate a 0.33 eV blue shift in the optical bandgap of a-ZTO,&#13;
which we conclude to be due to quantum confinement effects.
</summary>
<dc:date>2024-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Three-dimensional carbon coated and high mass-loaded NiO@Ni foam anode with high specific capacity for lithium ion batteries</title>
<link href="http://repository.enu.kz/handle/enu/29756" rel="alternate"/>
<author>
<name>Issatayev, Nurbolat</name>
</author>
<author>
<name>Abdumutaliyeva, Diana</name>
</author>
<author>
<name>Tashenov, Yerbolat</name>
</author>
<author>
<name>Yeskozha, Dossym</name>
</author>
<author>
<name>Seipiyev, Adilkhan</name>
</author>
<author>
<name>Bakenov, Zhumabay</name>
</author>
<author>
<name>Nurpeissova, Arailym</name>
</author>
<id>http://repository.enu.kz/handle/enu/29756</id>
<updated>2026-03-04T19:01:34Z</updated>
<published>2024-01-01T00:00:00Z</published>
<summary type="text">Three-dimensional carbon coated and high mass-loaded NiO@Ni foam anode with high specific capacity for lithium ion batteries
Issatayev, Nurbolat; Abdumutaliyeva, Diana; Tashenov, Yerbolat; Yeskozha, Dossym; Seipiyev, Adilkhan; Bakenov, Zhumabay; Nurpeissova, Arailym
Nickel oxide (NiO) is known for its remarkable theoretical specific capacity, making it a highly appealing&#13;
option for electrode materials in electrochemical energy storage applications. Nevertheless, its practical&#13;
use is limited by poor electrochemical performance and complicated electrode fabrication processes. To&#13;
address these issues, we propose a new anode design comprising an intermediate NiO nanoarray layer&#13;
and a carbon coating layer grown directly on a three-dimensional (3D) conductive nickel foam substrate,&#13;
designated as C@NiO@Ni foam. This anode with a high NiO mass loading of 5–6 mg cm−2 is fabricated&#13;
by a two-step process: thermal oxidation of the nickel foam, followed by carbon coating. The 3D&#13;
architecture, with its large surface area, significantly enhances the contact between the electrode and&#13;
electrolyte, thereby shortening the Li-ion diffusion pathway. Additionally, the carbon layer plays a crucial&#13;
role in accommodating the volume changes of NiO during cycling, preventing the detachment of NiO&#13;
from the Ni foam substrate, and enhancing the electronic conductivity of the C@NiO@Ni foam. The&#13;
resulting porous C@NiO@Ni anode was thoroughly analyzed using scanning electron microscopy (SEM),&#13;
X-ray diffraction (XRD), and energy-dispersive X-ray spectroscopy (EDS). When used as an anode&#13;
material for lithium-ion batteries (LIBs), this anode showcased an impressive reversible capacity of&#13;
around 678 mA h g−1 at 0.1C after 100 cycles. Furthermore, it demonstrated excellent electrochemical&#13;
performance at a high current, sustaining a specific capacity of 387 mA h g−1 at 1C after 100 cycles.
</summary>
<dc:date>2024-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>The Vitamin C Enantiomers Possess a Comparable Potency in the Induction of Oxidative Stress in Cancer Cells but Differ in Their Toxicity</title>
<link href="http://repository.enu.kz/handle/enu/29755" rel="alternate"/>
<author>
<name>Begimbetova, Dinara</name>
</author>
<author>
<name>Burska, Agata N.</name>
</author>
<author>
<name>Baltabekova, Aidana</name>
</author>
<author>
<name>Kussainova, Assiya</name>
</author>
<author>
<name>Kukanova, Assiya</name>
</author>
<author>
<name>Fazyl, Fatima</name>
</author>
<author>
<name>Ibragimova, Milana</name>
</author>
<author>
<name>Manekenova, Kenzhekyz</name>
</author>
<author>
<name>Makishev, Abay</name>
</author>
<author>
<name>Bersimbaev, Rakhmetkazhi I.</name>
</author>
<author>
<name>Sarbassov, Dos D.</name>
</author>
<id>http://repository.enu.kz/handle/enu/29755</id>
<updated>2026-03-04T19:01:58Z</updated>
<published>2024-01-01T00:00:00Z</published>
<summary type="text">The Vitamin C Enantiomers Possess a Comparable Potency in the Induction of Oxidative Stress in Cancer Cells but Differ in Their Toxicity
Begimbetova, Dinara; Burska, Agata N.; Baltabekova, Aidana; Kussainova, Assiya; Kukanova, Assiya; Fazyl, Fatima; Ibragimova, Milana; Manekenova, Kenzhekyz; Makishev, Abay; Bersimbaev, Rakhmetkazhi I.; Sarbassov, Dos D.
The use of vitamin C (VC) in high doses demonstrates a potent tumor suppressive effect by&#13;
mediating a glucose-dependent oxidative stress in Kirsten rat sarcoma (KRAS) mutant cancer cells.&#13;
VC with arsenic trioxide (ATO) is a promising drug combination that might lead to the development&#13;
of effective cancer therapeutics. Considering that a tumor suppressive effect of VC requires its highdose administration, it is of interest to examine the toxicity of two enantiomers of VC (enantiomer&#13;
d-optical isomer D-VC and natural l-optical isomer L-VC) in vitro and in vivo. We show that the&#13;
combinations of L-VC with ATO and D-VC with ATO induced a similar cytotoxic oxidative stress in&#13;
KrasG12D-expressing mutant cancer cells as indicated by a substantial increase in reactive oxidative&#13;
species (ROS) production and depolarization of mitochondria. To examine the L-VC and D-VC&#13;
toxicity effects, we administered high doses of D-VC and L-VC to CD1 mice and carried out an&#13;
evaluation of their toxic effects. The daily injections of L-VC at a dose of 9.2 g/kg for 18 days were&#13;
lethal to mice, while 80% of mice remained alive following the similar high-dose administration of&#13;
D-VC. Following the drug injection courses and histopathological studies, we determined that a&#13;
natural form of VC (L-VC) is more harmful and toxic to mice when compared to the effects caused by&#13;
the similar doses of D-VC. Thus, our study indicates that the two enantiomers of VC have a similar&#13;
potency in the induction of oxidative stress in cancer cells, but D-VC has a distinctive lower toxicity&#13;
in mice compared to L-VC. While the mechanism of a distinctive toxicity between D-VC and L-VC&#13;
is yet to be defined, our finding marks D-VC as a more preferable option compared to its natural&#13;
enantiomer L-VC in clinical settings.
</summary>
<dc:date>2024-01-01T00:00:00Z</dc:date>
</entry>
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