天然矿物固硫剂及其对煤粉燃烧的影响

选取CaCO₃、Ca(OH)₂质量配比＝3∶2作为主固硫剂，用钙基固硫剂质量的2％的Na₂CO₃对其改性，利用蛭石作为固硫添加剂。在Ca/S＝2.25的情况下,通过固硫实验考察了主固硫剂以及添加剂的加入对固硫率的影响。实验结果表明，煤粉掺入该固硫剂在950℃下燃烧0.5 h，固硫率可以达到85％。还对添加不同固硫剂的煤粉进行热重实验，分析其对煤粉燃烧特性及动力学参数的影响。结果表明，固硫添加剂的加入不但能提高固硫率，还有利于煤的燃烧，减少灰渣的处理量。     

固硫型煤渣烧制水泥熟料的研究初探

发展固硫型煤工业是治理煤烟型大气污染及减少二氧化硫对大气污染的有效途径。燃烧固硫型煤将产生大量固硫煤渣,对环境构成新的威胁。本文从实验探索的角度,研究开发利用固硫渣的途径。实验中对固硫渣做了化学全分析,用Ｘ－射线粉末衍射法（ＸＲＰＤ）对固硫渣及其加入一定量的添加剂后的煅烧产物进行物相鉴定,证实在一定的条件下固硫渣可以烧制成硫铝酸盐水泥熟料     

生物质工业型煤固硫燃烧特性

探讨生物质工业型煤的燃烧特性以及固硫性能,生物质型煤与普通型煤相比,燃烧性能明显改善,着火温度降低３０℃以上,燃烧强度提高２５％以上,提高了固硫效率。     

型煤燃烧过程中石灰石固硫的试验研究（Ⅱ）

采用石灰石作固硫剂，考察其加入量和空气流量对北宿型煤固硫的影响，研究了固硫型煤矿析出特性和石灰石对不同煤的固硫能力。研究表明：石灰石的最佳固硫温度为８００℃、Ｃａ／Ｓ＝２：１；石灰石中所含的杂质对低温固硫有利，煤中所含钙基组分对固硫有利，石灰石对低灰熔点煤高温固硫不利。     

贝壳粉型煤固硫剂固硫的实验及机理研究

以贝壳粉作为型煤固硫剂,用正交实验的方法研究了影响贝壳粉固硫率的主要影响因素,在高温(1 150℃)时固硫效率达到56.6%,比CaCO3的固硫率提高40%以上,具有较好的高温固硫性。分析得知,贝壳的主要成分为CaCO3,其含钙量在40%左右,贝壳中又含有较高的Na等碱金属元素以及Fe,Al和Si等。用X射线粉末衍射法分析了高温(1 150℃)型煤样生成的灰渣,分析了贝壳粉作为型煤固硫剂在高温下具有较高固硫率的机理。发现CaAlSi2O8为主的复合晶体在高温下包裹在CaSO4的表面,抑制了CaSO4的热分解从而有效地提高了固硫率。     

固硫型煤的生产技术和使用效果

针对链式炉炉内脱硫，设计了固硫型煤生产线，通过测试、试验、生产和实际使用，使固硫型煤满足脱硫要求，同时，节能效果也较明显。另外，对固硫剂、粘结剂的选用和配比作了介绍。     

MnO2对煤粉中CaO固硫效率影响机理

采用热力学计算和实验方法对钙硫比n（CaO）/n（S）=2.0条件下不同钙基固硫剂的固硫效果进行了比较,发现：CaO的固硫效率最高。以CaO为固硫剂,研究了添加剂MnO2对CaO固硫效果的影响。结果表明,加入MnO2可以提高CaO的固硫效率,且其含量为1%时对CaO固硫的促进效果最佳。这是因为煤粉燃烧过程中MnO2将逐级分解,分解产物依次为Mn2O3和Mn3O4,锰的氧化物一方面可以催化CaO的固硫反应,另一方面,Mn3O4本身也参与到固硫反应之中,生成MnSO4,从而促进钙基固硫剂的固硫效果。     

复合钙基固硫添加剂对煤固硫与燃烧的影响

利用程序升温燃烧反应技术,考察了高岭土复合的Ca O、Fe2O3-Ca O、Co O-Ca O添加剂对无烟煤的燃烧以及固硫的影响。实验发现,这些添加物质对煤的裂解产物的燃烧都具有促进作用,除了Fe2O3-Ca O-高岭土复合添加剂对煤焦的燃烧有一定阻碍作用之外,其余都具有对煤焦燃烧的促进作用,尤以Co O-Ca O-高岭土复合添加剂的效果最为显著。高岭土复合的硫酸钙本应具有较高的热稳定性,但受到高温下煤焦与CO的还原而分解,所以添加对煤焦具有明显催化燃烧作用的氧化钴,因减少了还原性气氛,稳定了硫酸钙产物而促进了固硫。     

电石渣固硫性能的研究

研究采用电石渣作为固硫剂，探讨了最佳固硫的燃烧温度，电石渣用量和粒径，并掺入适量的Ｆｅ２Ｏ３对电石渣进行改性，发现用电石渣固硫能与其它钙基固硫剂人有很的应用前景。     

浅析电石渣固硫

研究了用电石渣作为固硫剂,探讨了最佳固硫的燃烧温度、电石渣用量和粒径,并掺入适量的 Ｆｅ_２Ｏ_３对电石渣进行改性,发现用电石渣固硫与其他钙基因硫剂相当,具有良好的应用前景。     

钙基矿物固硫剂对不同煤种固硫效果的影响研究

对肥城煤（FC）、淮南煤（HN）和大同煤（DT）3种典型的高中低硫煤作了煤岩学分析,利用DTA、XRD、SEM、光学显微镜和粒度分析仪对钙基矿物添加剂及其固硫灰渣进行了矿物学研究.主要研究了温度、钙硫比、矿物添加剂等因素对煤种固硫率的影响.实验表明,相同的燃烧条件下,不同煤种对碳酸钙适应性有很大差异,淮南煤和肥城煤对碳酸钙的适应性明显好于大同煤,高硫煤更有利于950℃和1050℃下固硫;煤样自身固硫能力较差,碳酸钙固硫效果显著,当Ca/S=4,燃烧温度分别为1050、850和950℃时,肥城煤、大同煤和淮南煤固硫率分别达到最高值（89%、72%和89%）;膨润土促进大同煤固硫,却降低了肥城煤和淮南煤固硫率;钙基矿物添加剂协同作用能更有效地提高低硫煤的固硫效果,在1050℃时,可将固硫率由51%提高到74%.     

钙基矿物固硫剂对不同煤种固硫效果的影响研究

对肥城煤(FC)、淮南煤(HN)和大同煤(DT)3种典型的高中低硫煤作了煤岩学分析,利用DTA、XRD、SEM、光学显微镜和粒度分析仪对钙基矿物添加剂及其固硫灰渣进行了矿物学研究.主要研究了温度、钙硫比、矿物添加剂等因素对煤种固硫率的影响.实验表明,相同的燃烧条件下,不同煤种对碳酸钙适应性有很大差异,淮南煤和肥城煤对碳酸钙的适应性明显好于大同煤,高硫煤更有利于950℃和1050℃下固硫;煤样自身固硫能力较差,碳酸钙固硫效果显著,当Ca/S=4,燃烧温度分别为1050、850和950℃时,肥城煤、大同煤和淮南煤固硫率分别达到最高值(89%、72%和89%);膨润土促进大同煤固硫,却降低了肥城煤和淮南煤固硫率;钙基矿物添加剂协同作用能更有效地提高低硫煤的固硫效果,在1050℃时,可将固硫率由51%提高到74%.     

Supported transition-metal oxide catalysts for reduction of sulfur dioxide with hydrogen to elemental sulfur

This work is for the purpose to find a high performance catalyst for the catalytic reduction of SO2 with H2 as a reducing agent. NiO/gamma-Al2O3 catalyst was found to be the most active catalyst among the seven gamma-Al2O3-supported metal-oxide catalysts tested. With NiO as the active species, of the supports tested, gamma-Al2O3 was the most suitable one and the optimal Ni content was 16 wt%. Using this NiO/gamma-Al2O3 catalyst, we found that the optimal feed ratio of H2/SO2 is 2:1 and the catalyst presulfided with H2 + H2S exhibits a higher performance than that pretreated with H2 or He. XRD patterns reveal that the nickel oxide experienced a transformation to Ni3S2 and NiS, and then to NiS2, the most active nickel sulfide, during the reaction process. The reason for the highest catalyst activity of 16 wt% Ni was attributed to the largest amount of NiS2. Water vapor in the feed gas reactant caused inhibition of catalyst activity, whereas H2S promoted the reduction of SO2. These phenomena were rationalized with the aid of Claus reaction.     

The physical characteristics of sulfur aerosols

A review of the physical characteristics of sulfur-containing aerosols, with respect to size distribution of the physical distributions, sulfur distributions, distribution modal characteristics, nuclei formation rates, aerosol growth characteristics, and in situ measurement, has been made.Physical size distributions can be characterized well by a trimodal model consisting of three additive lognormal distributions.When atmospheric physical aerosol size distributions are characterized by the trimodal model, the following typical modal parameters are observed:1. Nuclei mode – geometric mean size by volume, DGV_n, from 0.015 to 0.04 μm. σ_gn=1.6, nucler mode volumes from 0.0005 over the remote oceans to 9 μm³ cm⁻³ on an urban freeway.2. Accumulation mode – geometric mean size by volume, DGV_a, from 0.15 to 0.5 μm, σ_ga=1.6–2.2 and mode volume concentrations from 1 for very clean marine or continental backgrounds to as high as 300 μm³ cm⁻³ under very polluted conditions in urban areas.3. Coarse particle mode – geometric mean size by volume, DGV_c, from 5 to 30 μm, σ_gn=2–3, and mode volume concentrations from 2 to 1000 μm³ cm⁻³.It has also been concluded that the fine particles (D_p<2 μm) are essentially independent in formation, transformation and removal from the coarse particles (D_p>2 μm).Modal characterization of impactor-measured sulfate size distributions from the literature shows that the sulfate is nearly all in the accumulation mode and has the same size distribution as the physical accumulation mode distribution.Average sulfate aerodynamic geometric mean dia. was found to be 0.48±0.1 μm (0.37±0.1 μm vol. dia.) and σ_g=2.00±0.29. Concentrations range from a low of about 0.04 μg m⁻³ over the remote oceans to over 8 μg m⁻³ under polluted conditions over the continents.Review of the data on nucleation in smog chambers and in the atmosphere suggests that when SO₂, is present, SO₂-to-aerosol conversion dominates the Aitken nuclei count and, indirectly, through coagulation and condensation, the accumulation mode size and concentration. There are indications that nucleation is ubiquitous in the atmosphere, ranging from values as low as 2 cm⁻³ h⁻¹ over the clean remote oceans to a high of 6×10⁶ cm⁻³ h⁻¹ in a power plant plume under sunny conditions.There is considerable theoretical and experimental evidence that even if most of the mass for the condensational growth of the accumulation mode comes from hydrocarbon conversion, sulfur conversion provides most of the nuclei.     

Catalytic reduction of sulfur dioxide with carbon monoxide over tin dioxide for direct sulfur recovery process

SO(2) reduction by CO over SnO(2) catalyst was studied in this work. The parameters were the reaction temperature, space velocity (GHSV) and [CO]/[SO(2)] molar ratio. The optimal temperature, GHSV and [CO]/[SO(2)] molar ratio were 550 degrees C, 8000 h(-1) and 2.0, respectively. Under these conditions, the SO(2) conversion and sulfur selectivity were about 78% and 68%, respectively. The following reaction pathway involving two mechanisms was proposed in SO(2) reduction by CO over SnO(2) catalyst: in the first step involving Redox mechanism, the elemental sulfur was produced by the mobility of the lattice oxygen between SO(2) and SnO(2) surface. In the second step, COS was formed by the side reaction between elemental sulfur and CO or metal sulfide and CO. In the third step involving COS intermediate mechanism, the abundant elemental sulfur was produced by the SO(2) reduction by COS which was produced in the second step and was more effective reducing agent than CO.     

Comparison of retention and output of sulfur in limestone soil and yellow soil and their responses to acid deposition in a small karst catchment of Guizhou Province,Southwest China

Environmental Science and Pollution Research - Investigating the responses of retention and output of sulfur (S) is significant to understand the impact of atmospheric S deposition on the S cycling...     

单质硫冲击对含硫废水中硫细菌与聚糖菌竞争关系的影响

聚糖菌的富集会与硫循环耦合反硝化除磷系统(denitrifying sulfur conversion-associated enhanced biological phosphorous removal,DS-EBPR)内功能种群微生物——硫细菌发生竞争,从而导致除磷效果波动.因此,首先对母反应器中微生物进行了长期驯化,然后通过向批次实验小反应器中投加单质硫,研究单质硫短期冲击对含硫废水中硫细菌与聚糖菌竞争关系的影响.结果表明,经过长期驯化,在母反应器中发现了硫细菌与聚糖菌共存的现象;而短期冲击实验结果表明,在单个周期反应过程中,虽然单质硫的投加对微生物内源物质(聚羟基脂肪酸酯、糖原)转化量、氮磷去除效果影响不大,但其可以提高硫细菌的活性,增加硫转化量,使得硫细菌在与聚糖菌的竞争中取得优势地位.     

Retention of sulfur dioxide by nylon filters

Based on laboratory studies, recovery efficiencies of sulfur dioxide (SO₂) were determined for nylon filters. The nylon filters used in these experiments were found to retain SO₂. A relatively uniform amount (1.7%) was recoverable from each nylon filter, independent of relative humidity. An appreciable portion of SO₂ was unrecoverable, and this increased from 5 to 16% as the RH increased from 28 to 49%. This unrecoverable SO₂ may account for previous reports of a low bias for SO₂ determinations employing filter packs using nylon filters. Additional characterization of nylon filters is recommended prior to their future deployment as an integrative sampling medium for ambient air.