检索结果-南通市图书馆

Influence of crystal-transforming agent on the performance and mechanism ofα-high-strength gypsum prepared from FGD gypsum

引用

Particuology 2024年第4期87卷 37-45页

作者： Zhuoyue Xu Xiao Wang Biao Jin Dawang Zhang Hui Li College of Materials Science and Engineering Xi'an University of Architecture and TechnologyXi'an710055China Schoolof Materials and Chemical Engineering Henan University of Urban ConstructionPingdingshan46736China

This paper investigates the impact of flue gas desulfurization(FGD)gypsum's crystal modifier on the characteristics and microcosmic mechanism ofα-high strength gypsum.The results demonstrate that all three crystal modifiers can convert FGD gypsum toα-high-strength gypsum.Citric acid(CA)has the most significant influence onα-high-strength gypsum,and the preparedα-high-strength gypsum is short columnar,with an aspect ratio in the range of 1-3,and has a faster setting time,a larger specific surface area,and a smaller standard consistency,higher compressive strength,greater surface hardness,and smaller crystal particle size.The initial setting time of theα-high-strength gypsum manufactured with CA crystal modifier was decreased by 36%compared to the blank sample,the final setting time was lowered by 37.5%,and the water consumption of the standard consistency was reduced by 8%.The maximum strength is 32 MPa after 2 h,the absolute dry compressive strength is up to 38 MPa,and the surface hardness is improved by 24.43%.

关键词： Flue gas desulfurization gypsum crystal modifier Microscopic mechanism α-high-strength gypsum

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Controllable synthesis of a large TS-1 catalyst for clean epoxidation of a C=C double bond under mild conditions

引用

Frontiers of Chemical Science and Engineering 2023年第6期17卷 772-783页

作者： Xiu Gao Beining Luo Yanping Hong Peihang He Zedong Zhang Guoqiang Wu Jiangxi Key Laboratory of Natural Products and Functional Food Jiangxi Agricultural UniversityNanchang 330045China School of Food Science and Engineering Jiangxi Agricultural UniversityNanchang 330045China

Development of a titanium silicalite-1(TS-1)catalyst with good crystallinity and a four-coordinate Ti framework is critical for efficient catalytic oxidation reaction under mild conditions.Herein,a size-controlled TS-1 zeolite(TS-10.1ACh(acetylcholine))was synthesized via steam-assisted crystallization by introducing acetylcholine as a crystal growth modifier in the preparation process,and TS-10.1ACh was also employed in epoxidations of different substrates containing C=C double bonds.The crystalline sizes of the as-synthesized TS-10.1ACh catalysts were controlled with the acetylcholine content,and characterization results showed that the particle sizes of highly crystalline TS-10.1ACh zeolite reached 3.0μm with a good Ti framework.Throughout the synthetic process,the growth rate of the crystals was accelerated by electrostatic interactions between the connected hydroxyl groups of the acetylcholine modifier and the negatively charged skeleton of the pre-zeolites.Furthermore,the TS-10.1ACh catalyst demonstrated maximum catalytic activity,good selectivity and high stability during epoxidation of allyl chloride.Importantly,the TS-10.1ACh catalyst was also highly versatile and effective with different unsaturated substrates.These findings may provide novel,easily separable and large TS-1 catalysts for efficient and clean industrial epoxidations of C=C double bonds.

关键词： size-controlled TS-1 crystal modifier steam-assisted crystallization epoxidation

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

欢迎您,

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案：

请选择收藏分类：

通借通还

欢迎您,

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：