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Porous structure and surface area of oxide, reduced and sulphided forms of alumina-supported cobalt molybdena catalyst 氧化铝负载的钼钴催化剂的氧化、还原和硫化形式的多孔结构和表面积
Surface Technology Pub Date : 1985-12-01 DOI: 10.1016/0376-4583(85)90096-2
Zenon Sarbak
{"title":"Porous structure and surface area of oxide, reduced and sulphided forms of alumina-supported cobalt molybdena catalyst","authors":"Zenon Sarbak","doi":"10.1016/0376-4583(85)90096-2","DOIUrl":"10.1016/0376-4583(85)90096-2","url":null,"abstract":"<div><p>The porous structure and surface area of alumina-supported cobalt molybdena catalysts were examined as functions of their activation conditions. It was revealed that the process of reduction by hydrogen as well as simultaneous reduction — sulphiding by a hydrogen and hydrogen sulphide mixture — results in the disappearance of pores of larger diameters. This is caused by the formation of monomeric, dimeric and/or polymeric species on pore surfaces as a result of thermal activation in hydrogen and H<sub>2</sub>-H<sub>2</sub>S atmospheres.</p><p>On the basis of the shapes of the hysteresis loops of nitrogen adsorption-desorption isotherms and on <em>t</em> plots of the samples investigated it was found that the dominant pores are those with diameters in the mesopore range.</p><p>The shapes of the mesopores resemble tubular capillaries with diameters o of various size and/or tubular capillaries with short necks and wide sloping bodies. Some of the mesopores can be closed at one end.</p><p>The uniformity of pore sizes appearing after the H<sub>2</sub>-H<sub>2</sub>S treatment provides good conditions for the diffusion of reactant molecules of large diameter. This is especially important for such catalytic reactions as depolymerization of asphaltenes, hydrodemetallization of metal porphyrins and other hydrotreatment processes.</p></div>","PeriodicalId":22037,"journal":{"name":"Surface Technology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1985-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0376-4583(85)90096-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87834115","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
The kinetics of organic film growth during the cathodic electrodeposition process 阴极电沉积过程中有机膜生长动力学研究
Surface Technology Pub Date : 1985-12-01 DOI: 10.1016/0376-4583(85)90098-6
V.B. Mišković, M.D. Maksimović
{"title":"The kinetics of organic film growth during the cathodic electrodeposition process","authors":"V.B. Mišković,&nbsp;M.D. Maksimović","doi":"10.1016/0376-4583(85)90098-6","DOIUrl":"10.1016/0376-4583(85)90098-6","url":null,"abstract":"<div><p>The kinetics and the mechanism of organic film growth during the cathodic electrodeposition process are investigated by galvanostatic and constant voltage methods. Constant voltage experiments carried out at lower voltages enabled the more accurate observation of current density changes and enabled the proposal of a mathematical model which gives a consistent picture of film growth kinetics. It was shown that the film thickness increases with time but a limiting value was not achieved.</p></div>","PeriodicalId":22037,"journal":{"name":"Surface Technology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1985-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0376-4583(85)90098-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88653469","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
The flocculation of cellulose powders with polymer flocculants 高分子絮凝剂对纤维素粉的絮凝作用
Surface Technology Pub Date : 1985-12-01 DOI: 10.1016/0376-4583(85)90101-3
Asif S. Bhatti, David Dollimore, J.I. Bhatty, O. Behar, L. Davies
{"title":"The flocculation of cellulose powders with polymer flocculants","authors":"Asif S. Bhatti,&nbsp;David Dollimore,&nbsp;J.I. Bhatty,&nbsp;O. Behar,&nbsp;L. Davies","doi":"10.1016/0376-4583(85)90101-3","DOIUrl":"10.1016/0376-4583(85)90101-3","url":null,"abstract":"<div><p>The flocculation of pure cellulose, of mercerized cellulose and of cellulose treated with dilute nitric acid has been studied. The adsorption of polymer flocculants on the cellulose is described and results interpreted. Acid pretreatment caused maximum adsorption and flocculation.</p><p>The sedimentation behaviour of concentrated cellulose suspensions has been investigated for the determination of the “nominal radius” of cellulose particles and of related parameters.</p></div>","PeriodicalId":22037,"journal":{"name":"Surface Technology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1985-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0376-4583(85)90101-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88100853","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Sorption-desorption studies on alumina pretreated with acids: I. The anionic dye orange II 酸预处理氧化铝的吸附-解吸研究:1 .阴离子染料橙
Surface Technology Pub Date : 1985-12-01 DOI: 10.1016/0376-4583(85)90094-9
V.K. Jain, G.L. Mundhara, Ramesh K. Mishra, J.S. Tiwari
{"title":"Sorption-desorption studies on alumina pretreated with acids: I. The anionic dye orange II","authors":"V.K. Jain,&nbsp;G.L. Mundhara,&nbsp;Ramesh K. Mishra,&nbsp;J.S. Tiwari","doi":"10.1016/0376-4583(85)90094-9","DOIUrl":"10.1016/0376-4583(85)90094-9","url":null,"abstract":"<div><p>Brockmann alumina was subjected to chemical pretreatment with <em>HNO</em><sub>3</sub>, <em>H</em><sub>2</sub><em>SO</em><sub>4</sub> and <em>H</em><sub>3</sub><em>PO</em><sub>4</sub> of various concentrations, and samples of surface phase <em>pH</em> 3.5 − 8.5 (<em>HNO</em><sub>3</sub><em>Al</em><sub>2</sub><em>O</em><sub>3</sub>(<em>n</em>), <em>H</em><sub>2</sub><em>SO</em><sub>4</sub>-treated <em>Al</em><sub>2</sub><em>O</em><sub>3</sub>(<em>s</em>)) and <em>pH</em> 4.0 − 8.0 (<em>H</em><sub>3</sub><em>PO</em><sub>4</sub>-treated <em>Al</em><sub>2</sub><em>O</em><sub>3</sub>(<em>p</em>)) were prepared. Sorption-desorption behaviour of the anionic dye Orange II (C.I.15510) with change in pH on these substrates was studied. Quantitative sorption is shown at <em>pH</em> ⩽ 4.0 (<em>Al</em><sub>2</sub><em>O</em><sub>3</sub>(<em>n</em>)), and a maximum is observed at <em>pH</em> 5.0 (<em>Al</em><sub>2</sub><em>O</em><sub>3</sub>(<em>s</em>)) and <em>pH</em> 3.0 (<em>Al</em><sub>2</sub><em>O</em><sub>3</sub>(<em>p</em>)). Variation in the amount of sorption with time (10 min – 72 h), temperature (30 – 60 °C) and regeneration of the substrates with aqueous inorganic electrolytes is also reported. Desorption efficacy of the anions is in the order <em>PO</em><sub>4</sub><sup>3−</sup> &gt;<em>SO</em><sub>4</sub><sup>2−</sup> &gt;<em>NO</em><sub>3</sub><sup>−</sup>. The acid treatment, and hence the specifically adsorbed anions (<em>NO</em><sub>3</sub><sup>−</sup>, <em>SO</em><sub>4</sub><sup>2−</sup>, <em>PO</em><sub>4</sub><sup>3−</sup>), appears to lower the isoelectric pH of alumina (pH 8.0). The results show the involvement of anion-exchange properties of the alumina.</p></div>","PeriodicalId":22037,"journal":{"name":"Surface Technology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1985-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0376-4583(85)90094-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83565949","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 12
Electrochemical aspects of steel corrosion in sea water 钢在海水中腐蚀的电化学方面
Surface Technology Pub Date : 1985-12-01 DOI: 10.1016/0376-4583(85)90100-1
J. Sefaja, J. Malina
{"title":"Electrochemical aspects of steel corrosion in sea water","authors":"J. Sefaja,&nbsp;J. Malina","doi":"10.1016/0376-4583(85)90100-1","DOIUrl":"10.1016/0376-4583(85)90100-1","url":null,"abstract":"<div><p>Electrochemical determinations of the corrosion parameters of construction steel DIN St 12 and an experimental alloy (2.8 wt.% Cr) were made in synthetic sea water under defined hydrodynamic conditions. The direct method of measuring polarization resistance was used as well as voltammetric and comparative analytical methods.</p><p>Experimental results clearly indicated an influence of oxygen on the kinetics of the corrosion process, which could be seen as a change of the control mechanism as the oxygen concentration was varied.</p><p>It was shown that the alloying element chromium has a beneficial influence on the corrosion characteristics of the reference steel.</p></div>","PeriodicalId":22037,"journal":{"name":"Surface Technology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1985-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0376-4583(85)90100-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75604580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Sorption-desorption studies on alumina pretreated with acids: II. Oxyanions on HNO3-treated alumina 酸预处理氧化铝的吸附-解吸研究II。hno3处理氧化铝上的氧阴离子
Surface Technology Pub Date : 1985-12-01 DOI: 10.1016/0376-4583(85)90095-0
Ramesh K. Mishra, G.L. Mundhara, V.K. Jain, J.S. Tiwari
{"title":"Sorption-desorption studies on alumina pretreated with acids: II. Oxyanions on HNO3-treated alumina","authors":"Ramesh K. Mishra,&nbsp;G.L. Mundhara,&nbsp;V.K. Jain,&nbsp;J.S. Tiwari","doi":"10.1016/0376-4583(85)90095-0","DOIUrl":"10.1016/0376-4583(85)90095-0","url":null,"abstract":"<div><p>Sorption-desorption behaviour of three oxyanions (<em>MnO</em><sub>4</sub><sup>−</sup>, <em>CrO</em><sub>4</sub><sup>2-</sup> and <em>VO</em><sub>3</sub><sup>−</sup>) on chromatographic alumina pretreated with HNO<sub>3</sub> is described. The sorption is found to be pH dependent, and has maxima at surface pH values of 3.5 (<em>MnO</em><sub>4</sub><sup>−</sup>), 2.5 (<em>VO</em><sub>3</sub><sup>−</sup>) and 2.0 (<em>CrO</em><sub>4</sub><sup>2−</sup>). The affinity of MnO<sub>4</sub><sup>-</sup> and CrO<sub>4</sub><sup>2-</sup> is almost negligible at surface pH values of 5.5 or more. However, VO<sub>3</sub><sup>-</sup> shows affinity for the substrate in the pH range 5.0 - 8.8. The monovalent anion appears to be sorbed, primarily via electrostatic interaction with the surface sites created by the acid treatment. The CrO<sub>4</sub><sup>2-</sup> appears to involve ion exchange and weak chemical interactions. Mixtures of the oxyanions have been separated (binary and ternary) by column chromatography using inorganic electrolytes as eluents.</p></div>","PeriodicalId":22037,"journal":{"name":"Surface Technology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1985-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0376-4583(85)90095-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88104933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
The impedance of the porous cadmium electrode in alkali 多孔镉电极在碱中的阻抗
Surface Technology Pub Date : 1985-12-01 DOI: 10.1016/0376-4583(85)90099-8
R.T. Barton, M. Hughes, S.A.G.R. Karunathilaka, P.J. Mitchell, N.A. Hampson
{"title":"The impedance of the porous cadmium electrode in alkali","authors":"R.T. Barton,&nbsp;M. Hughes,&nbsp;S.A.G.R. Karunathilaka,&nbsp;P.J. Mitchell,&nbsp;N.A. Hampson","doi":"10.1016/0376-4583(85)90099-8","DOIUrl":"10.1016/0376-4583(85)90099-8","url":null,"abstract":"<div><p>The porous cadmium electrode in alkali has been studied using the impedance technique applied to minielectrodes (area, 1 cm<sup>2</sup>) of conventional sintered structure. It is shown that in a wide frequency domain the electrode behaviour confirms to that of a filmed porous electrode under charge-transfer and diffusion control. In the lower frequency domain the electrode behaviour is more complicated and it is concluded that the frequency response was modified by intruding phase formation effects which were relaxed out at the higher frequencies.</p></div>","PeriodicalId":22037,"journal":{"name":"Surface Technology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1985-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0376-4583(85)90099-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76806707","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Electrodeposition of catalytically active nickel powder from sulphate baths: Effect of some operating variables 硫酸盐浴电沉积催化活性镍粉:一些操作变量的影响
Surface Technology Pub Date : 1985-12-01 DOI: 10.1016/0376-4583(85)90097-4
A.M. Abd El-Halim , R.M. Khalil
{"title":"Electrodeposition of catalytically active nickel powder from sulphate baths: Effect of some operating variables","authors":"A.M. Abd El-Halim ,&nbsp;R.M. Khalil","doi":"10.1016/0376-4583(85)90097-4","DOIUrl":"10.1016/0376-4583(85)90097-4","url":null,"abstract":"<div><p>Fine-grained nickel powder has been successfully electrodeposited from a very dilute all-sulphate bath of the composition 0.0125 moll<sup>−1</sup> NiSO<sub>4</sub> · 7H<sub>2</sub>O, 0.23 moll<sup>−1</sup> (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub>, 0.1 moll<sup>−1</sup> H<sub>3</sub>BO<sub>3</sub> and 0.07moll<sup>−1</sup> Na<sub>2</sub>SO<sub>4</sub> · 10H<sub>2</sub>O. The current efficiency of the deposition process and the surface morphology, as well as the catalytic activity of the electrodeposited nickel powder towards the decomposition of 0.4% H<sub>2</sub>O<sub>2</sub> solution, were found to be fundamentally influenced by the operating variables pH, current density and duration of the electrolysis. X-ray diffraction studies revealed that the nickel powder is free from oxide and hydroxide contaminations. Under the optimum operating conditions (<em>pH</em> = 7.7 <em>j</em> = 13.3 A <em>dm</em><sup>−2</sup> and <em>t</em> = 10 min) the selected bath produced a nickel deposit characterized by catalytic activity approaching 100% with a deposition efficiency around 18%.</p></div>","PeriodicalId":22037,"journal":{"name":"Surface Technology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1985-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0376-4583(85)90097-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86176035","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
The corrosion behaviour of nickel in molten NaNO3KNO3 eutectic 镍在熔融NaNO3KNO3共晶中的腐蚀行为
Surface Technology Pub Date : 1985-11-01 DOI: 10.1016/0376-4583(85)90116-5
A. Baraka, R.M.S. Baraka, A. Abdel-Razik
{"title":"The corrosion behaviour of nickel in molten NaNO3KNO3 eutectic","authors":"A. Baraka,&nbsp;R.M.S. Baraka,&nbsp;A. Abdel-Razik","doi":"10.1016/0376-4583(85)90116-5","DOIUrl":"10.1016/0376-4583(85)90116-5","url":null,"abstract":"<div><p>The corrosion (oxidation) of nickel in molten (Na, K)NO<sub>3</sub> eutectic has been investigated at temperatures ranging from 250 °C to 450 °C, for exposure periods of up to 12 h. The results of both weight-gain and potential measurements under open-circuit conditions reveal the formation of a passivating film consisting mainly of NiO. The thickening of the oxide film proceeds according to a parabolic law, at a rate depending on the temperature of the melt. The activation energy of the process was estimated to be 14.95 kcal mol<sup>−1</sup>, indicating that the oxidation process of nickel is determined by diffusion of nickel in the form of ions and electrons via vacancies and holes. A break was observed in the parabolic plots at higher temperatures; this may indicate a change in the mechanism of film growth. The results are discussed in terms of oxidation kinetics data for nickel in both molten nitrates and air at high temperatures.</p></div>","PeriodicalId":22037,"journal":{"name":"Surface Technology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1985-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0376-4583(85)90116-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90674801","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Studies on anodizing of aluminium in alkaline electrolyte using alternating current 铝在碱性电解液中交流阳极氧化的研究
Surface Technology Pub Date : 1985-11-01 DOI: 10.1016/0376-4583(85)90117-7
S. John, V. Balasubramanian, B.A. Shenoi
{"title":"Studies on anodizing of aluminium in alkaline electrolyte using alternating current","authors":"S. John,&nbsp;V. Balasubramanian,&nbsp;B.A. Shenoi","doi":"10.1016/0376-4583(85)90117-7","DOIUrl":"10.1016/0376-4583(85)90117-7","url":null,"abstract":"<div><p>The work reported in this paper concerns a study of the anodizing of aluminium in alkaline electrolyte based on borax (sodium tetraborate) using alternating current. Coating thicknesses of 11 μm were produced from 50 g l<sup>−1</sup> borax solution the pH of which is adjusted with sodium hydroxide to a value of 10.5 at 65 °C, using a current density of 1.5 A dm<sup>−2</sup>. The effect of bath composition, temperature, current density, anodizing time and pH on the rate of build up of oxide coating and their relation to anodizing voltage and coating ratio were studied.</p></div>","PeriodicalId":22037,"journal":{"name":"Surface Technology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1985-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0376-4583(85)90117-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85935966","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
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