STUDI REDUKSI EMISI GAS KARBON DIOKSIDA DENGAN MENGKONVERSI MENJADI PRECIPITATED CALCIUM CARBONATE (PCC) MENGGUNAKAN METODE KARBONASI DOI Open Access
Nuryoto Nuryoto,

Heri Heriyanto,

Leli Rahmawati

и другие.

JST (Jurnal Sains dan Teknologi), Год журнала: 2024, Номер 13(2), С. 205 - 216

Опубликована: Июль 25, 2024

Gas CO2 dapat mengakibatkan pemanasan global dan pada kadar tertentu mempengaruhi kesehatan manusia. Dalam rangka untuk menjaga di lingkungan dalam kondisi normal, maka penelitian ini mencoba mengkonversi menjadi precipitated calcium carbonate (PCC), yaitu dengan mengontakan gas Ca(OH)2. Tujuan dari adalah mempelajari menganalisa pengaruh kecepatan pengadukan, tekanan sistem reaksi, waktu interaksi pembuatan Precipitated Calcium Carbonate (PCC) menggunakan reaktor semi batch. Penelitian dilakukan hidrostatis 980-9800 Pa, 400 500 rpm, laju alir 2 liter/menit, 15 - 60 menit. Hasil menunjukan bahwa interaksi, pengadukan mempunyai terhadap reaksi antara Ca(OH)2, produk PCC yang dihasilkan. Kondisi operasi optimum diperoleh 9800 menit massa dihasilkan sebesar 7,99 gram.

Thermochemical CO2 Reduction to Methanol over Metal-Based Single-Atom Catalysts (SACs): Outlook and Challenges for Developments DOI

Huibo Zhao,

Xiaochen Liu,

Chunyang Zeng

и другие.

Journal of the American Chemical Society, Год журнала: 2024, Номер 146(34), С. 23649 - 23662

Опубликована: Авг. 20, 2024

The conversion of thermodynamically inert CO

Язык: Английский

Процитировано

20

Efficient Cu–Zn–Al/LDH Catalysts for CO2-to-Methanol Conversion DOI
Xing Cui, Mingsheng Luo, Yang Zhi

и другие.

Energy & Fuels, Год журнала: 2025, Номер unknown

Опубликована: Янв. 28, 2025

Язык: Английский

Процитировано

1

Reaction Mechanisms and Applications of Single Atom Catalysts for Thermal-Catalytic Carbon Dioxide Hydrogenation Toward Oxygenates DOI
Fei Wang, Yicheng Liu,

Mengke Peng

и другие.

ACS Catalysis, Год журнала: 2024, Номер 14(21), С. 16434 - 16458

Опубликована: Окт. 23, 2024

Thermo-catalytic CO2 hydrogenation to high-value oxygenates has been regarded as one of the most powerful strategies that can potentially alleviate excessive emissions. However, due high chemical stability and variability pathways, it is still challenging achieve highly active selective hydrogenation. Single atom catalysts (SACs) with ultrahigh metal utilization efficiency extraordinary electronic features have displayed growing importance for thermo-catalytic multiple developed improve performances. Here, we review breakthroughs in developing SACs efficient toward common (CO, HCOOH, CH3OH, CH3CH2OH) following order: first, an analysis reaction mechanisms thermodynamics challenges reactions; second, a summary SAs designed by dividing them into two categories single- dual-sites; third, discussion support effects focus on approaches regulating strong metal–support interaction (MSI). Summarily, current future perspectives develop higher-performance are presented. We expect this bring more design inspiration trigger innovation catalytic evolution materials eventually benefit achievement carbon-neutrality goal.

Язык: Английский

Процитировано

8

Single‐Atom Pt Loaded on MOF‐Derived Porous TiO2 with Maxim‐ized Pt Atom Utilization for Selective Hydrogenation of Halonitro‐benzene DOI

Mingchun Guo,

Qiangqiang Meng, Ming‐Liang Gao

и другие.

Angewandte Chemie International Edition, Год журнала: 2024, Номер unknown

Опубликована: Окт. 29, 2024

Abstract The location control of single atoms relative to supports is challenging for single‐atom catalysts, leading a large proportion inaccessible buried under supports. Herein, “sequential thermal transition” strategy developed afford Pt preferentially dispersed on the outer surface TiO 2 . Specifically, Ti‐MOF confining nanoparticles converted NPs and composite coated by carbon (Pt &TiO @C‐800) at 800 °C in N Subsequent thermal‐driven atomization 600 air produce decorated 1 /TiO ‐600). resulting ‐600 exhibits superior p ‐chloroaniline ( ‐CAN) selectivity (99 %) ‐400 (45 much better activity than @TiO with randomly both outside inside hydrogenation ‐chloronitrobenzene ‐CNB). Mechanism investigations reveal that achieves 100 % accessibility preferably adsorbs –NO group ‐CNB while weakly –Cl ‐CAN, promoting catalytic selectivity.

Язык: Английский

Процитировано

6

Multiscale structural regulation of Two-Dimensional materials for photocatalytic reduction of CO2 DOI

Junyan Wu,

Lina Zhao,

Xu Gao

и другие.

Progress in Materials Science, Год журнала: 2024, Номер unknown, С. 101386 - 101386

Опубликована: Окт. 1, 2024

Язык: Английский

Процитировано

5

The Relationship between Electronic Behavior of Single Atom Catalysts and CO2 Reduction to Oxygenates DOI

Fenghai Cao,

Guangbo Liu, Xianbiao Wang

и другие.

EnergyChem, Год журнала: 2024, Номер 6(6), С. 100141 - 100141

Опубликована: Ноя. 1, 2024

Язык: Английский

Процитировано

3

Anchoring Cu on Zirconium-oxo nodes in a pore-confined metal-organic framework for CO2 hydrogenation to methanol DOI

Chaosheng Bao,

Ying-Fei Huo,

Yanting Li

и другие.

Chemical Engineering Journal, Год журнала: 2024, Номер unknown, С. 158610 - 158610

Опубликована: Дек. 1, 2024

Язык: Английский

Процитировано

3

Steering CO2 electroreduction to hydrocarbons over 2D thiol-based conductive metal-organic framework DOI

Qiu‐Jin Wu,

Duan‐Hui Si, Yuliang Dong

и другие.

Science Bulletin, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Room-temperature CO2-to-carbon conversion facilitated by copper-gallium liquid metal DOI
Xiao Dong Chen, Jiacheng Liu, Qing Wang

и другие.

Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 160589 - 160589

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

Highly efficient photoenzymatic CO2 reduction via integrated structural design of porphyrin covalent organic framework on Ti3C2T (MXene) DOI
Zhipeng Huang, Shuli Bai,

Ping Wei

и другие.

Separation and Purification Technology, Год журнала: 2025, Номер unknown, С. 132943 - 132943

Опубликована: Апрель 1, 2025

Язык: Английский

Процитировано

0