Iron(II) Sulfate(VI) from Titania Production as a Raw Material for Preparation of Hydrogen Sulfide Sorbents

A hybrid sorbent material for removal of hydrogen sulfide from air was developed. The material is based on activated carbon and iron compounds obtained from waste iron(II) sulfate(VI) heptahydrate. The iron salt is deposited on the carbonaceous support and subjected to oxidation (Fe²⁺ to Fe³⁺) using atmospheric oxygen under alkaline conditions. An effect of H₂O₂ addition to the process on the composition of the resultant material was also examined. X-ray diffraction (XRD) analyses confirmed easy conversion of waste FeSO₄·7H₂O to iron oxides Fe₃O₄ and FeOOH. The activated carbon supporting iron oxides revealed a higher efficiency in H₂S elimination from air compared to the commercial activated carbon, without any modification.     

Highly dispersed cobalt nanoparticles onto nitrogen-doped carbon nanosheets for efficient hydrogen generation via catalytic hydrolysis of sodium borohydride

Porous carbon nanostructures are promising supports for stabilizing the highly dispersed metal nanoparticles and facilitating the mass transfer during the reaction, which are critical to achieve the high efficiency of hydrogen generation from sodium borohydride dehydrogenation. Herein, the catalytically active porous architectures are simply prepared by using 2-methylimidazole and melamine as reactive sources. The structural and compositional characterizations reveal the coexistence of metallic cobalt and N-doped carbon in porous architectures. Electron microscopy observations indicate that the synthesized products are smartly constructed from the carbon nanosheets with densely dispersed Co nanoparticles. Due to the notable structural features, the prepared Co@NC-600 sample presents the highly efficient activity for catalytic hydrolysis of NaBH₄ with a hydrogen generation rate of 2574 mL min⁻¹ g_cat⁻¹ and an activation energy of 47.6 kJ mol⁻¹. The catalytically active metallic Co and suitable support-effect of N-doped carbon are responsible for catalytic dehydrogenation.     

丙烯腈－苯乙烯共聚物水解磺化产物对泥浆的稳定作用

在实验室条件下对用丙烯腈－苯乙烯共聚物在硫酸存在下的水解磺化产物（ＨＳＡＳ）处理的泥浆性能进行了评定。ＨＳＡＳ处理的泥浆有较小的滤失性，较好的耐盐和抗高温性。     

Development of catalysts for hydrogen generation from hydride compounds

Catalytic hydrolysis of NaBH₄ and NH₃BH₃ has been studied. It was shown that the nature of the support and the active component of the catalyst affect the H₂ generation rate. Despite similar sizes of rhodium particles formed on the surface of different supports (γ-Al₂O₃, TiO₂, carbon), their reactivity is different. Rh/TiO₂ with low rhodium concentration (1 wt.%) is the most active catalyst both in the hydrolysis of NaBH₄ and NH₃BH₃. The obtained results show that the rhodium chloride interaction with titania determines the reactivity of rhodium particles formed under action of NaBH₄ medium. TEM, DRS UV–vis and XPS were used to characterize the catalysts.     

Kinetic study of the hydrolysis of isocyanic acid in the gas phase

The hydrolysis of isocyanic acid in the gaseous phase has been investigated at temperatures between 553 and 613 K by mass spectrometry and evaluated to obtain the corresponding kinetic data. The reaction order and reaction constant have been determined. Finally, the influence of water on the catalysed formation of melamine from isocyanic acid under the operating conditions employed has been investigated in order to determine whether there is a need to try the process gas.     

水解母液生产葡萄糖酸钙新工艺

葡萄糖酸钙的生产一般是以淀粉为原料经液化、糖化、发酵、中和、精制、结晶、干燥制得的。而以母液为原料，其原料成本低，工艺流程短，减少了营养元素的添加，大幅度地降低了生产成本，值得推广。     

土壤腐殖酸对毒死蜱水解的影响

土壤腐殖酸的VIS-UV光谱特征和E465/E665的测定结果表明,各种土壤腐殖酸的VIS-UV吸收曲线相似,但吸收峰强度和E465/E665差异较大,进而推得它们的腐殖化程度排序为:紫色潮土腐殖酸>中性紫色土腐殖酸>酸性紫色土腐殖酸>腐殖土腐殖酸,说明它们在组成上有共同的本性,但结构和性质差异较大。在此基础上,研究它们对毒死蜱水解的影响。结果表明,不同来源土壤腐殖酸均促进了毒死蜱的水解,但它们的影响程度有明显的差异。对于腐殖化程度最低的腐殖土腐殖酸,浓度为120mg L-1时,对毒死蜱水解的促进作用最大,而随着腐殖酸浓度的增大,促进作用却越来越弱;而对于其它三种样品,腐殖酸溶液对毒死蜱水解的促进作用随着腐殖酸浓度增大而加强,其中以腐殖化程度较低的酸性紫色土的促进作用较为明显。可见,毒死蜱的水解速率与土壤腐殖酸的浓度和腐殖化程度有关。其中,腐殖酸腐殖化程度的影响机理主要与腐殖酸的酸性和腐殖酸的吸附—催化作用有关,其具体作用机理有待于进一步从定性和定量方面去研究,以更好地指导毒死蜱农药的合理施用和污染土壤的修复。     

空气湿固化含硅丙烯酸酯的制备与表征

通过甲基丙烯酸甲酯、丙烯酸丁酯、γ-甲基丙烯酰氧丙基三甲氧基硅烷制备了空气湿固化胶黏剂,使其在pH=7时水解交联。采用H1NMR及FTIR和气象色谱对其结构交联情况做了详细分析,并对溶液膜的性能做了一系列的测试比较。     

甲基丙烯酸甲酯（MMA）生产中水解和酯化反应特性的研究

用间歇式搅拌反应器，对丙酮氰醇（ＨＣＮ）法甲基丙烯酸甲酯生产中水解和酯化反应的特性进行了研究。研究表明：（１）甲基丙烯酰胺硫酸盐的水解反应有较高的平衡转化率，其动力学方程为ｋ１＝６．５２×１０＾６ｅｘｐ（－６９．８／ＲＴ）；（２）甲基丙烯酸与甲醇间酯化反应的平衡转化率较低，故生产中必须加以提高。测得的液相和汽－液相酯化反应的活化能分别为４９．４ｋＪ／ｍｏｌ和５４．４ｋＪ／ｍｏｌ。     

Generating hydrogen-rich fuel-cell feeds from dimethyl ether (DME) using physical mixtures of a commercial Cu/Zn/Al2O3 catalyst and several solid–acid catalysts

Homogeneous physical mixtures containing a commercial Cu/ZnO/Al₂O₃ catalyst and a solid–acid catalyst were used to examine the acidity effects on dimethyl ether hydrolysis and their subsequent effects on dimethyl ether steam reforming (DME-SR). The acid catalysts used were zeolites Y [Si/Al = 2.5 and 15: denoted Y(Si/Al)], ZSM-5 [Si/Al = 15, 25, 40, and 140: denoted Z(Si/Al)] and other conventional catalyst supports (ZrO₂, and γ-Al₂O₃). The homogeneous physical mixtures contained equal amounts, by volume, of the solid–acid catalyst and the commercial Cu/ZnO/Al₂O₃ catalyst (BASF K3-110, denoted as K3). The steam reforming of dimethyl ether was carried out in an isothermal packed-bed reactor at ambient pressure.

The most promising physical mixtures for the low-temperature production of hydrogen from DME contained ZSM-5 as the solid–acid catalyst, with hydrogen yields exceeding 90% (T = 275 °C, S/C = 1.5, τ = 1.0 s and P = 0.78 atm) and hydrogen selectivities exceeding 94%, comparable to those observed for methanol steam reforming (MeOH-SR) over BASF K3-110, with values equaling 95% and 99%, respectively (T = 225 °C, S/C = 1.0, τ = 1.0 s and P = 0.78 atm). Large production rates of hydrogen were directly related to the type of acid catalyst used. The hydrogen production activity trend as a function of physical mixture was