天天日夜夜,久久老女人,人人爱国产,91视频青青草

手機(jī)版

掃一掃,手機(jī)訪問

關(guān)于我們 加入收藏

麥克默瑞提克(上海)儀器有限公司

15 年金牌會(huì)員

已認(rèn)證

撥打電話
獲取底價(jià)
提交后,商家將派代表為您專人服務(wù)
立即發(fā)送
點(diǎn)擊提交代表您同意 《用戶服務(wù)協(xié)議》
當(dāng)前位置:
美國麥克儀器 >公司動(dòng)態(tài) >

每周分享

每周分享
美國麥克儀器  2015-03-23  |  閱讀:1293

手機(jī)掃碼查看

每周分享:Hydrothermally stable regenerable catalytic supports for aqueous-phase conversion of biomass

今天給大家分享的是201410月份 Catalysis Today》上發(fā)表的一篇名為:Hydrothermally stable regenerable catalytic supports for aqueous-phase conversion of biomass

 

文章摘要如下:

The hydrothermal stability of TiO2- and ZrO2-based materials was studied by exposing the samples to liquid water at 523 K for 60 h in a batch reactor. No phase transformation or loss in BET surface area was observed for TiO2-based materials that had initial BET surface area of less than 52 m2/g. In contrast, the BET surface area decreased and the primary crystallite size increased for all ZrO2-based materials tested. The BET surface area decreased and the primary crystallite size increased for high BET surface area TiO2 (156 m2/g) and ZrO2 (246 m2/g). Silica-containing TiO2 only lost 30% of its high BET surface area (from 128 to 90 m2/g). In contrast a material composed of silica–phosphate–ZrO2 lost 56–72% of its BET surface area. Using the crystalline TiO2 as a support, we prepared and tested a Pt–ReOx/TiO2 catalyst for hydrodeoxygenation of sorbitol. Pt–ReOx/TiO2 was almost 2 times more active on a total Pt basis than Pt–ReOx/C catalyst. Between 0.1 and 0.9 wt% of coke formed on the catalyst surface after reaction depending on the reaction conditions. The coke could be removed and the catalyst activity completely regenerated by an oxidation-reduction treatment. The catalyst showed only minimal change in BET surface area, TiO2 phase and TiO2 crystallite size after more than 163 h of time on stream. The CO chemisorption of Pt–ReOx/TiO2 increased after reaction which was probably due to migration of ReOx species away from the Pt during the reaction.

 

該文章中材料表征采用的是美國麥克儀器AutoChem 2920

 

詳情可參考下面鏈接:

http://www.sciencedirect.com/science/article/pii/S092058611400220X


留言咨詢
(我們會(huì)第一時(shí)間聯(lián)系您)
關(guān)閉
留言類型:
     
*姓名:
*電話:
*單位:
Email:
*留言內(nèi)容:
(請(qǐng)留下您的聯(lián)系方式,以便工作人員及時(shí)與您聯(lián)系?。?/div>
亚洲AV极品无码专区在线观看| 国产夜夜嗨| 日本伊人高清不卡一区| 国产欧美一区二区精品性| 中文人妻视频| 你懂的国产| 亚洲精品色午夜无码专区日韩| 69天堂网| 日韩久久一区二区免费| 国产黄在线观看免费观看| 亚洲色欲色欲欲www在线| 国产成人一区二区三区影院| 高清日韩一区二区| 国产欧美久久一区二区| 国产精品免费av片在线观看| 第二期国产欧美| 蜜桃视频入口| 成人精品一区二区三区电影| 亚洲区与欧美区| 天天网综合| 欧美美女后入网站| 日韩一级一区| 国产精品无码素人福利免费| 欧美性熟妇| 日本少妇嗷嗷叫| 欧美韩日人妻精品一区二区三区| 久久精品国内一区二区三区| 免费在线观看你懂的| 久久久久久久爱我久久久久| 日本亚洲中文字幕不卡| 精品久久一区二区三区| 亚洲黄色网址| 老太做爰xxxⅹ性xxxhd| 国产黄a三级三级三级av在线看| 奶水视频精品一区| 日韩欧美亚州天堂| 日韩殴美精品| av在线你懂得| 国产成人无码精品久久久免费| 超碰在线免费视频| 在线看日韩观看av|