Sulfuric Acids

硫酸
  • 文章类型: Journal Article
    这项研究调查了免疫活性小鼠长期皮肤暴露(16周)于硫酸(SA)的致癌潜力。临床评估,组织病理学分析,进行免疫组织化学分析和生化测定以评估皮肤刺激,氧化应激生物标志物和SA的潜在致癌作用。结果表明,长时间暴露于SA会导致皮肤结构的各种变化,尤其是炎症,毛囊中的肿瘤前期和肿瘤增生,以及角化过度和棘皮病,导致表皮厚度增加98.50±21.6μm。免疫组织化学分析进一步证实了这些观察结果,显示p53和Ki-67的核表达升高,有丝分裂指数为(57.5%±2.5%)。此外,生化分析表明,SA诱导皮肤脂质过氧化,丙二醛含量高,过氧化氢酶活性随之降低。这些发现表明,长时间暴露于SA可以诱发皮肤肿瘤,强调在经常使用SA的环境中需要采取严格的安全措施。这项研究强调了与SA暴露相关的潜在职业健康风险。
    This study investigates the carcinogenic potential of chronic dermal exposure (16 weeks) to sulfuric acid (SA) in immunocompetent mice. Clinical assessments, histopathological analyses, immunohistochemical analyses and biochemical assays were conducted to evaluate skin irritation, oxidative stress biomarkers and the potential carcinogenic effect of SA. Results indicated that prolonged exposure to SA leads to various alterations in skin structure, notably inflammation, preneoplastic and neoplastic proliferation in hair follicles, as well as hyperkeratosis and acanthosis, resulting in an increased epidermal thickness of 98.50 ± 21.6 μm. Immunohistochemistry analysis further corroborates these observations, showcasing elevated nuclear expression of p53 and Ki-67, with a significant mitotic index of (57.5% ± 2.5%). Moreover, biochemical analyses demonstrate that SA induces lipid peroxidation in the skin, evidenced by a high level of Malondialdehyde and a consequential reduction in catalase activity. These findings suggest that prolonged exposure to SA can induce skin neoplasms, highlighting the need for stringent safety measures in environments where SA is frequently used. This study underscores the potential occupational health risks associated with SA exposure.
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  • 文章类型: Journal Article
    生产的日期糖浆产生大量的日期压蛋糕(DPC),纤维和保湿材料,具有通过生物加工产生价值的巨大潜力。然而,DPC的顽固结构影响生物过程中产品的产量。为了提高结构的可及性以及增加碳水化合物的可溶性部分,并促进进一步的酶水解,水热和稀酸(0.5%(v/v)硫酸)预处理作为具有成本效益和可行的方法,在相对较低的温度(80、100、120和140°C)和反应时间(60和90分钟)。然后通过使用纤维素酶和半纤维素的酶混合物的酶后处理来评估预处理的成功。基于总可获得的糖和最少产生的抑制剂,最佳操作条件被认为是在120°C下酸预处理90分钟,总糖收率提高55.02%。为了探索预处理DPC的潜在用途,在120°C下对未处理和酸预处理的DPC进行厌氧消化90分钟。结果表明,预处理提高了总生物制品产量,包括氢,乙醇,和挥发性脂肪酸产量,59.75%。这表明在生物过程中预处理对产物产率的显著影响。
    The production of date syrup yields a substantial amount of date press cake (DPC), fibrous and moisturising material with great potential for generating value through bioprocessing. However, the recalcitrant structure of DPC affects the yield of products in bioprocesses. To boost the accessibility of the structure as well as increase the soluble fraction of carbohydrates and facilitate further enzymatic hydrolysis, hydrothermal and dilute acid (0.5% (v/v) sulfuric acid) pretreatments as cost-effective and feasible methods were applied on DPC at relatively low temperatures (80, 100, 120 and 140 °C) and reaction times (60 and 90 min). The success in pretreatment was then evaluated by a post-enzymatic treatment using an enzyme cocktail of cellulases and hemicelluloses. Based on total accessible sugar with minimum produced inhibitors, an optimal operating condition was considered acid pretreatment at 120 °C for 90 min with a 55.02% increase in total sugar yield. To explore the potential use of pretreated DPC, an anaerobic digestion was conducted on untreated and acid-pretreated DPC at 120 °C for 90 min. The results showed that pretreatment increased the total bioproduct yield, including hydrogen, ethanol, and volatile fatty acid yields, by 59.75%. This demonstrates the significant impact of pretreatment on product yields in a bioprocess.
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  • 文章类型: Journal Article
    传染病是全球水产养殖业和保护计划损失的主要原因。同时,传染病对孵化场饲养和释放到自然栖息地进行保护的鱼类构成重大风险,包括五大湖湖st鱼(AcipenserFulvescens,即,GL-LST)。最近,同种疱疹病毒(湖鱼疱疹病毒2型,即,在两个成年GL-LST群体中检测到LSHV-2)能够在成年和少年GL-LST中诱导疾病和/或死亡。开始开发疾病预防和/或控制方法,体外实验旨在确定LSHV-2对孵化场和水产养殖设施中常用的消毒剂(Virkon®-Aquatic:过氧单硫酸钾;Ovadine®:聚乙烯吡咯烷酮碘复合物;和Perox-Aid®:过氧化氢)的敏感性。将培养的LSHV-2暴露于两种浓度的每种消毒剂(Virkon®-Aquatic:0.5%和1%;Ovadine®:50和100ppm;Perox-Aid®:500和1000ppm),一式两份,持续1、10和30分钟。曝光后,消毒剂被中和,在白st鱼×湖st鱼杂交细胞系(WSxLS)上经过14天的潜伏期后,通过比较有和没有消毒剂暴露的病毒的50%组织培养感染剂量(TCID50/mL)来计算减少百分比.当暴露于Perox-Aid®时,LSHV-2%的降低范围为58.7%至99.5%。当暴露于Ovadine®时,减少的百分比从99.4%到100%不等。最后,当暴露于Virkon®-Aquatic时,对于两种浓度和所有时间点,减少百分比为100%。本文的结果提供了Virkon®-Aquatic和Ovadine®对LSHV-2都是杀病毒的证据,并且可以代表在野外设置下降低病毒传播风险的手段。
    Infectious diseases are a leading cause of losses in the aquaculture industry and conservation programs globally. Simultaneously, infectious diseases pose a substantial risk to fish being hatchery-reared and released into natural habitats for conservation purposes, including the Great Lakes lake sturgeon (Acipenser fulvescens, i.e., GL-LST). Recently, an alloherpesvirus (lake sturgeon herpesvirus 2, i.e., LSHV-2) capable of inducing disease and/or mortality in adult and juvenile GL-LSTs was detected in two adult GL-LST populations. To begin developing disease prevention and/or control methods, in vitro experiments were designed to determine the susceptibility of LSHV-2 to disinfectants commonly used in hatchery and aquaculture facilities (Virkon®-Aquatic: potassium peroxymonosulfate; Ovadine®: polyvinylpyrrolidone iodine complex; and Perox-Aid®: hydrogen peroxide). Cultured LSHV-2 was exposed to each disinfectant at two concentrations (Virkon®-Aquatic: 0.5% and 1%; Ovadine®: 50 and 100 ppm; and Perox-Aid®: 500 and 1000 ppm) in duplicate for durations of 1, 10, and 30 min. Following exposure, the disinfectant was neutralized, and after a 14-day incubation period on a white sturgeon × lake sturgeon hybrid cell line (WSxLS), percent reduction was calculated by comparing the 50% tissue culture infectious doses (TCID50/mL) of the virus with and without disinfectant exposure. When exposed to Perox-Aid®, LSHV-2 percent reduction ranged from 58.7% to 99.5%. When exposed to Ovadine®, the percent reduction ranged from 99.4% to 100%. Lastly, the percent reduction when exposed to Virkon®-Aquatic was 100% for both concentrations and all timepoints. The results herein provide evidence that both Virkon®-Aquatic and Ovadine® are virucidal to LSHV-2 and may represent a means to reduce virus transmission risk under field settings.
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  • 文章类型: Journal Article
    最近对金星酸性云中生命的可能性重新产生了兴趣,这导致了对浓硫酸中有机化学的新研究。我们以前发现,大多数氨基酸在金星云硫酸浓度范围内是稳定的(81%和98%w/w,其余的是水)。自然的下一个问题是二肽,作为更大的肽和蛋白质的前体,在这种环境下是稳定的。我们使用20种同二肽研究了肽键的反应性,发现其中大多数在几周内进行了溶剂分解,在两个硫酸浓度。值得注意的是,存在一些例外。HH和GG二肽在98%w/w硫酸中稳定至少4个月,而II,LL,VV,PP,RR和KK在81%w/w硫酸中抵抗水解至少5周。此外,在98%w/w浓硫酸中研究的二肽的分解过程不同于释放单体氨基酸的标准酸催化水解。尽管在单一浓度下有一些例外,没有同型二肽在所研究的两种酸浓度中表现出稳定性。这表明金星上的任何假想生命都可能需要肽键的功能性替代品,该肽键可以在整个硫酸浓度范围内保持稳定。
    Recent renewed interest in the possibility of life in the acidic clouds of Venus has led to new studies on organic chemistry in concentrated sulfuric acid. We have previously found that the majority of amino acids are stable in the range of Venus\' cloud sulfuric acid concentrations (81% and 98% w/w, the rest being water). The natural next question is whether dipeptides, as precursors to larger peptides and proteins, could be stable in this environment. We investigated the reactivity of the peptide bond using 20 homodipeptides and find that the majority of them undergo solvolysis within a few weeks, at both sulfuric acid concentrations. Notably, a few exceptions exist. HH and GG dipeptides are stable in 98% w/w sulfuric acid for at least 4 months, while II, LL, VV, PP, RR and KK resist hydrolysis in 81% w/w sulfuric acid for at least 5 weeks. Moreover, the breakdown process of the dipeptides studied in 98% w/w concentrated sulfuric acid is different from the standard acid-catalyzed hydrolysis that releases monomeric amino acids. Despite a few exceptions at a single concentration, no homodipeptides have demonstrated stability across both acid concentrations studied. This indicates that any hypothetical life on Venus would likely require a functional substitute for the peptide bond that can maintain stability throughout the range of sulfuric acid concentrations present.
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  • 文章类型: Journal Article
    从废旧锂离子电池中有效回收关键金属对于清洁能源和可持续行业增长至关重要。传统方法通常无法管理大量废物,导致有害气体排放和危险材料。这项研究调查了使用协同浸出从废LIB中回收关键金属的创新方法。第一步优化热处理条件(570°C在空气中2小时),以去除粘合剂材料,同时保持阴极材料的结晶度,X射线衍射(XRD)分析证实。接下来,响应面法(RSM),I-最优,用于检查硫酸(SA)和有机酸(Org,柠檬酸和乙酸)及其在金属浸出时的浓度(SA:0.5-2M和Org:0.1-2M),以实现生态友好的过程。结果表明,向SA中添加柠檬酸更有效,特别是在较低的浓度下,而不是使用乙酸。测试介质以评估还原剂添加的影响。值得注意的是,发现优化的浸出混合物(1.25MSA和0.55M柠檬酸)有效地提取金属,而不需要任何还原剂,如H2O2,突出了其更简单和更环保的回收过程的潜力。进一步的优化确定了理想的固液比(62.5g/L),以最大程度地减少酸的使用。最后,RSM(D-optimal)用于研究时间和温度对浸出的影响,锂的显著回收率达到99%±0.7,98%±0.0对于Co,Ni为90%±6.6,在189min和95°C的优化条件下,Mn为92%±0.4。化学成本分析表明,该方法比常规方法的成本效益高25%。
    Efficient recycling of critical metals from spent lithium-ion batteries is vital for clean energy and sustainable industry growth. Conventional methods often fail to manage large waste volumes, leading to hazardous gas emissions and dangerous materials. This study investigates innovative methods for recovering critical metals from spent LIBs using synergistic leaching. The first step optimized thermal treatment conditions (570 °C for 2 h in air) to remove binder materials while maintaining cathode material crystallinity, confirmed by X-ray diffraction (XRD) analysis. Next, response surface methodology (RSM), I-optimal, was used to examine the synergistic effects of sulfuric acid (SA) and organic acids (Org, citric and acetic acids) and their concentrations (SA: 0.5-2 M and Org: 0.1-2 M) on metal leaching for an eco-friendlier process. Results showed that adding citric acid to SA was more effective, especially at lower concentrations, than using acetic acid. The medium was tested to evaluate the impact of reductant addition. Remarkably, it was discovered that the optimized leaching mixture (1.25 M SA and 0.55 M citric acid) efficiently extracted metals without the need for any reductant like H2O2, highlighting its potential for a simpler and more eco-friendly recycling process. Further optimization identified the ideal solid-to-liquid ratio (62.5 g/L) to minimize acid use. Finally, RSM (D-optimal) was used to investigate the effects of time and temperature on leaching, achieving remarkable recovery rates of 99% ± 0.7 for Li, 98% ± 0.0 for Co, 90% ± 6.6 for Ni, and 92% ± 0.4 for Mn under optimized conditions at 189 min and 95 °C. Chemical cost analysis revealed this method is about 25% more cost-effective than conventional methods.
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  • 文章类型: Journal Article
    邢阳硫酸厂附近的地下水,河南,从七个不同的地点对中国进行了采样,以探索抗生素抗性基因(ARGs)和移动遗传元件(MGEs)的患病率。结果表明,基因aadA,BlaCTX-M,tetA,qnrA,和sul1以100%的频率检测,然后是aac(6')-Ib(85.71%),ermB(85.71%),和tetX(71.42%)。最丰富的ARGs是LSA2中的sul1(1.15×1011拷贝/mL),LSA6中的tetA(4.95×1010拷贝/mL),AAA在LSA2(4.56×109拷贝/毫升),BlaCTX-M在LSA4中(1.19×109拷贝/mL),和ermB在LSA5中(1.07×109拷贝/mL)。此外,在LSA2中,作为1类整合子的标记的intl1作为MGE的一部分出现为最丰富的基因(2.25×1011拷贝/mL),ISR1跟踪(1.57×109拷贝/mL)。环境因素解释了81.34%的ARG变化,intl2和blaCTX-M基因之间具有很强的正相关,以及ISCR1基因和qnrA,tetA,intl2和blaCTX-M.此外,intI1基因与aadA有很强的正相关,tetA,和sul1基因。此外,aac(6')-Ib基因与As相关,Pb,Mg,Ca,和HCO3-。intl2基因也被证明与Cd密切相关。值得注意的是,网络分析强调blaCTX-M是至少五个属的网络中最常见的基因。特别是,乳酸菌,Plesiomonas,和Ligilactacillus证明了与AadA的相关性,qnrA,BlaCTX-M,intI2和ISCR1。基于16SrRNA测序,优势门是变形杆菌,Firmicutes,拟杆菌,酸杆菌,和放线菌,优势属包括假单胞菌属,小杆菌,亚足,Vogesella,链球菌,Plesiomonas,和费氏病菌.这些发现增强了我们对地下水中ARG分布的理解,发出ARG的大量污染和对公共卫生的潜在风险的信号。
    Groundwater near a sulfuric acid plant in Xingyang, Henan, China was sampled from seven distinct sites to explore the prevalence of antibiotic resistance genes (ARGs) and mobile genetic elements (MGEs). Results showed that genes aadA, blaCTX-M, tetA, qnrA, and sul1 were detected with 100% frequency followed by aac(6\')-Ib (85.71%), ermB (85.71%), and tetX (71.42%). Most abundant ARGs were sul1 in LSA2 (1.15 × 1011 copies/mL), tetA in LSA6 (4.95 × 1010 copies/mL), aadA in LSA2 (4.56 × 109 copies/mL), blaCTX-M in LSA4 (1.19 × 109 copies/mL), and ermB in LSA5 (1.07 × 109 copies/mL). Moreover, in LSA2, intl1 as a marker of class 1 integron emerged as the most abundant gene as part of MGE (2.25 × 1011 copies/mL), trailed by ISCR1 (1.57 × 109 copies/mL). Environmental factors explained 81.34% of ARG variations, with a strong positive correlation between the intl2 and blaCTX-M genes, as well as the ISCR1 gene and qnrA, tetA, intl2, and blaCTX-M. Furthermore, the intI1 gene had a strong positive connection with the aadA, tetA, and sul1 genes. Moreover, the aac(6\')-Ib gene was associated with As, Pb, Mg, Ca, and HCO3-. The intl2 gene was also shown to be strongly associated with Cd. Notably, network analysis highlighted blaCTX-M as the most frequently appearing gene across networks of at least five genera. Particularly, Lactobacillus, Plesiomonas, and Ligilactobacillus demonstrated correlations with aadA, qnrA, blaCTX-M, intI2, and ISCR1. Based on 16S rRNA sequencing, the dominant phyla were Proteobacteria, Firmicutes, Bacteroidota, Acidobacteriota, and Actinobacteriota, with dominant genera including Pseudomonas, Ligilactobacillus, Azoarcus, Vogesella, Streptococcus, Plesiomonas, and Ferritrophicum. These findings enhance our understanding of ARG distribution in groundwater, signaling substantial contamination by ARGs and potential risks to public health.
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  • 文章类型: Journal Article
    生物基L-乳酸(L-LA)吸引了工业;然而,现有技术受到有限的生产率和高能耗的困扰。这项研究建立了一种从石竹藻藻胶体(EDP)生产基于大型藻类的L-LA的集成工艺。选择稀酸辅助微泡介导的臭氧分解(DAMMO)用于EDP的臭氧分解以优化D-半乳糖回收。通过单因素优化DAMMO处理,使用0.15MH2SO4在80°C下持续75分钟实现了最大的D-半乳糖回收效率(59.10%)。用3%(w/v)混合微生物细胞(凝结芽孢杆菌ATCC7050和嗜酸乳杆菌14)和发酵残留物进行发酵可获得97.67%的L-LA产量。此外,在重复分批发酵中进一步评估了这种培养方法,并显示出93.30%的平均L-LA产量,为基于大型藻类的L-LA生产提供了一个可行的概念。
    Biobased L-lactic acid (L-LA) appeals to industries; however, existing technologies are plagued by limited productivity and high energy consumption. This study established an integrated process for producing macroalgae-based L-LA from Eucheuma denticulatum phycocolloid (EDP). Dilute acid-assisted microbubbles-mediated ozonolysis (DAMMO) was selected for the ozonolysis of EDP to optimize D-galactose recovery. Through single-factor optimization of DAMMO treatment, a maximum D-galactose recovery efficiency (59.10 %) was achieved using 0.15 M H2SO4 at 80 °C for 75 min. Fermentation with 3 % (w/v) mixed microbial cells (Bacillus coagulans ATCC 7050 and Lactobacillus acidophilus-14) and fermented residues achieved a 97.67 % L-LA yield. Additionally, this culture approach was further evaluated in repeated-batch fermentation and showed an average L-LA yield of 93.30 %, providing a feasible concept for macroalgae-based L-LA production.
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  • 文章类型: Journal Article
    氯氟烃(CFCs)具有强烈的温室效应,是臭氧消耗的最大贡献者。催化去除被认为是在温和条件下消除低浓度CFC的有效途径。关键问题是催化剂由于其表面氟化而容易失活。我们在此报告了在硫酸改性的三维有序大孔氧化钒-二氧化钛负载的Ru(S-Ru/3DOMVTO)催化剂上在不存在或存在水的情况下催化二氯二氟甲烷(CFC-12)去除的比较研究。S-Ru/3DOMVTO催化剂在1800ppm水的存在下,在空速=40000mLg-1h-1下表现出高活性(T90%=278°C)和在60小时内良好的稳定性。由于酸位点量和氧化还原能力的改善,促进了CFC-12的吸附和C-F键的活化。与干燥条件下的情况相比,在水存在下,对CFC-12的催化性能优于S-Ru/3DOMVTO催化剂。水的引入通过补充羟基来减轻表面氟化,通过表面氟物种清洁作用抑制卤化副产物的形成,促进了COX2(X=Cl/F)→羧酸→CO2的反应途径。
    Chlorofluorocarbons (CFCs) exert a strong greenhouse effect and constitute the largest contributor to ozone depletion. Catalytic removal is considered an effective pathway for eliminating low-concentration CFCs under mild conditions. The key issue is the easy deactivation of the catalysts due to their surface fluorination. We herein report a comparative investigation on catalytic dichlorodifluoromethane (CFC-12) removal in the absence or presence of water over the sulfuric-acid-modified three-dimensionally ordered macroporous vanadia-titania-supported Ru (S-Ru/3DOM VTO) catalysts. The S-Ru/3DOM VTO catalyst exhibited high activity (T90% = 278 °C at space velocity = 40 000 mL g-1 h-1) and good stability within 60 h of on-stream reaction in the presence of 1800 ppm of water due to the improvements in acid site amount and redox ability that promoted the adsorption of CFC-12 and the activation of C-F bonds. Compared with the case under dry conditions, catalytic performance for CFC-12 removal was better over the S-Ru/3DOM VTO catalyst in the presence of water. Water introduction mitigated surface fluorination by the replenishment of hydroxyl groups, inhibited the formation of halogenated byproducts via the surface fluorine species cleaning effect, and promoted the reaction pathway of COX2 (X = Cl/F) → carboxylic acid → CO2.
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  • 文章类型: Journal Article
    全球铀产量的60%以上是基于原位回收开采技术。这种开采方法直接属于反应传输模型的应用范围,以优化铀的生产并限制其相关的环境影响。我们提出了一种建模方法,该方法能够表示受使用硫酸进行的ISR测试影响的含水层的自然演变。该模型是根据从ISR试验单元周围的12个监测井获得的长达12年的数据系列进行校准的。通过这种基于过程的方法,我们模拟了在这些情况下可以考虑的几种补救策略的影响。特别是,我们模拟了泵和处理与反渗透相结合的影响,以及通过不同的操作策略通过储层的非影响流体的循环。我们的方法可以比较这些策略的有效性。对于这个小规模的ISR试点,监测自然衰减构成了一个有趣的方法,由于其更快的pH恢复时间相对于泵和处理(5-10年至pH~6),其效率可以通过添加可交换阳离子来提高。如果进行的时间长于ISR开采和/或延迟部署,则未受影响的流体的循环可以减少pH恢复时间。结合对其部署的经济评价,这种建模方法可以帮助采矿运营商从环境和经济的角度选择和设计最佳的补救策略。
    More than 60% of worldwide uranium production is based on the In Situ Recovery mining technique. This exploitation method directly falls within the scope of the applications of reactive transport modelling to optimize uranium production and limit its associated environmental impact. We propose a modelling approach which is able to represent the natural evolution of an aquifer impacted by an ISR test performed using sulfuric acid. The model is calibrated on a 12 year-long data series obtained from 12 monitoring wells surrounding an ISR pilot cell. Through this process-based approach, we simulate the impact of several remediation strategies that can be considered in these contexts. In particular, we model the impact of Pump & Treat combined with reverse osmosis, as well as the circulation of non-impacted fluids through the reservoir with different operating strategies. Our approach allows to compare the effectiveness of these strategies. For this small-scale ISR pilot, monitored natural attenuation constitutes an interesting approach due to its faster pH recovery time with respect to Pump & Treat (5-10 years to pH ∼ 6), whose efficiency can be improved by the addition of exchangeable cations. Circulation of unimpacted fluids can reduce pH recovery times if performed for periods longer than the ISR exploitation and/or deployed with a delay. Combined with an economic evaluation of their deployment, this modelling approach can help the mining operator select and design optimal remediation strategies from an environmental and economical standpoint.
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  • 文章类型: Journal Article
    有效的脱水对于污泥处理和资源回收至关重要。本研究的重点是将厌氧消化后的污泥转化为生物炭以增强污泥脱水。污泥衍生的生物炭进一步用聚丙烯酰胺(PAM-ADBC)改性,并与硫酸改性的蒙脱石(HMTS)一起使用以获得更好的性能。注意到脱水方面的重大进展,即使在降低HMTS(0.1g/gDS)和PAM-ADBC(25g/kgDS)剂量下。这些改进导致毛细管抽吸时间显着增加41.96%(17.2s)和水分含量显着减少20.26%(66.33%),分别,同时保持稳定的pH值。HMTS,与浸出的阳离子,通过电中和分解胞外聚合物结构以释放污泥絮凝物中的内部结合水来改善脱水。同时,PAM-ADBC将污泥颗粒凝结成较大的絮凝物,形成骨架结构,在压缩脱水中排出内部水。本研究介绍了厌氧消化污泥的资源回收方法,并强调了其可持续利用的潜力。
    Effective dewatering is vital for both sludge treatment and resource recovery. This study focuses on converting post-anaerobic digested sludge into biochar to enhance sludge dewatering. The sludge-derived biochar is further modified with polyacrylamide (PAM-ADBC) and applied with sulfuric acid-modified montmorillonite (HMTS) for better performance. Significant advancements in dewatering were noted, even at reduced HMTS (0.1 g/g DS) and PAM-ADBC (25 g/kg DS) dosages. These improvements resulted in a remarkable 41.96% enhancement in capillary suction time (17.2 s) and a notable 20.26% reduction in moisture content (66.33%), respectively, all while maintaining a stable pH level. HMTS, with leached cations, improved dewatering by decomposing the extracellular polymeric substance structure through electro-neutralization to release the internal bound water within sludge flocs. Simultaneously, PAM-ADBC coagulated decomposed sludge particles into larger flocs to form a skeletal structure with itself to discharge internal water in compression dewatering. This study introduces a resource recovery method for anaerobically digested sludge and highlights its potential for sustainable utilization.
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