Utilization of Waste Sorghum Grain for Producing Superabsorbent for Personal Care Products

Modification of useful starch extracted from waste sorghum grains was carried out for production of superabsorbent materials which can be used in personal care products. Starch was extracted using alkali steeping method. It was characterized for swelling power, percentage transmittance and iodine binding values. The extracted starch was modified via graft copolymerization of acrylic acid and acrylamide onto starch to produce biodegradable absorbent material. The changes in modified starch structure were assessed using TGA, FTIR and SEM. The evaluation of enhancement in the properties was done by performing absorption tests. The reaction parameters were optimized to achieve higher graft add-on level and water absorption capacity. The absorbent product was further subjected to saponification for further enhancing its water absorption capacity (368.8 g/g). The product prepared by using optimized parameters of reaction was made highly porous by introducing sodium bicarbonate during the reaction. It showed a significant increase in the rate of water absorption and enhancement in water absorption capacity (380.9 g/g).The modified product showed 101.1 and 77.0 g/g absorption of artificial blood and artificial urine, respectively. This modified product was infused in commercially available sanitary napkin and baby diaper. Further, it was tested for fluid absorption and centrifuge retention capacity and it performed distinctly better than the commercial products. This superabsorbent material showed 12% weight loss after 28 days when biodegradability test by soil burial method was carried out.     

Melatonin Loaded Cardiac Homing Peptide-Functionalized Gold Nanoparticles for the Care of Anti-Cardiac Hypertrophy

Journal of Polymers and the Environment - Myocardial fibrosis is responsible for the current ineffective treatment of heart hypertrophy. Recent research findings have shown that Melatonin (Mel)...     

我国化学工业要承诺并实施责任关怀

介绍了责任关怀产生的缘由、内容、标志、意义及世界化工行业推行责任关怀的现状与方法,指出责任关怀是化工行业不断改善环境、健康和安全行为的承诺,最具标志性的行为是公布年度环境、健康和安全报告,本质是对职工、邻居和公众健康的关爱。分析了我国化工行业推行责任关怀所存在的问题,提出了相应的建议和措施。     

Precise Engineering of Lignin Incorporated Dextran/Glycol Nanomaterials for Wound Dressings for the Care of Anorectal Surgery

Journal of Polymers and the Environment - Lignin-loaded nanoparticles are versatile nanomaterials that may be used in wound healing properties. The current study describes a wound dressing...     

Pilot project of mechanical-biological treatment of waste in Brazil

By mechanical-biological treatment (MBT) of residual municipal solid waste the behaviour of landfills can be significantly improved. After MBT the organic content (COD and BOD5), total organic carbon, and total nitrogen in the leachate, as well as the gas production rate, are reduced to values lower than 90% of the fresh untreated waste. The volume of the stabilized material to be disposed on landfills decreases enormously, by up to 70%. The monitoring effort for a landfill constructed under these conditions is reduced to a minimum and the stabilized material can be used in other ways, as material for reforestation, for cover material or for thermal utilization to produce energy. Environmental conditions are important in MBT, as well as waste characteristics. This paper describes the results of a pilot project of MBT performed in Rio de Janeiro, Brazil. The results have shown that this technology can be used successfully in developing countries, with economy for the society and important results for the environment.     

An evaluation of the performance of multiple passive diffusion devices for indoor air sampling of VOCs

The United States Environmental Protection Agency is considering recommending longer‐term sampling to achieve more accurate time‐weighted‐average detections for indoor air monitoring of volatile organic chemicals. The purpose of the research presented herein was to compare longer sampling times using passive diffusion samplers to the results from shorter‐term testing periods using sorbent tubes and low‐flow pumps (US EPA Method TO‐17) at great frequency for trichloroethene (TCE) in indoor air. A controlled release of TCE in a large room allowed for over two‐orders‐of‐magnitude daily concentration variability over the course of the two‐week monitoring event. The daily concentration measurements by US EPA Method TO‐17 and the passive diffusion samplers were performed in triplicate and had excellent reproducibility. The results of daily tests were averaged and compared with four passive diffusion devices exposed to indoor air for three, seven, ten, and fourteen days in accordance with ASTM D6196‐02. A specific uptake rate for each of the passive devices at the four different time intervals and the statistical significance of the time‐varying uptake rates were evaluated. The performance of each passive diffusion device was determined using a statistical performance criterion. The average concentration for all of the exposure periods could be reliably predicted using the established uptake rates for two of the four passive devices. © 2009 Wiley Periodicals, Inc.     

化工项目环境风险评价中危险物质临界量的界定

在依据HJ 169—2018《建设项目环境风险评价技术导则》进行危险物质临界量界定的实际应用中,发现该导则存在危险物质种类及危险性质涵盖不全的问题。对比研究了与之相关的HJ 169—2004《建设项目环境风险评价技术导则》、HJ 941—2018《企业突发环境事件风险分级方法》、GB 18218—2018《危险化学品重大危险源辨识》、《赛维索指令Ⅲ》等技术规范和标准,构建了基于上述规范的危险物质临界量界定技术路线,为化工项目环境风险评价的实际工作提供借鉴。     

固相萃取—微波衍生化—GC-MS法同时测定水中6种雌激素物质

建立了固相萃取—微波衍生化—气相色谱-质谱联用法快速同时测定水中雌酮（E1）、17α-雌二醇（α-E2）、17β-雌二醇（β-E2）、雌三醇（E3）、17α-乙炔基雌二醇（EE2）、双酚A（BPA）等6种雌激素物质的分析方法,对色谱柱升温程序、固相萃取及衍生化条件进行了优化。色谱柱最佳升温程序为：初始温度50 ℃,保持2 min;以20 ℃/min速率升至260 ℃,保持5 min;最后以10 ℃/min速率升至280 ℃,保持5 min。实验结果表明,在选取 HC-C18萃取小柱、添加双（三甲基硅烷基）三氟乙酰胺（BSTFA）+1%三甲基氯硅烷（TMCS）+吡啶作为衍生化试剂、微波315 W衍生化加热4 min的条件下,6种目标物标准曲线的相关系数均大于0.999,BPA、E1、EE2及E3的线性范围为3~300 ng/L,17α-E2及17β-E2的线性范围为5~300 ng/L,方法检出限为2.0~5.0 ng/L,加标回收率为76.45%~96.24%。     

Migration of radionuclides in porous rock in the presence of colloids: effects of kinetic interactions

This work investigates the colloid-facilitated migration of radionuclides with radioactive decay in porous media. The sorption processes for radionuclides with both the solid matrix and colloids are treated as equilibrium or nonequilibrium. An analytical solution is obtained from a simplified linear equilibrium interaction mechanism. In addition, the adsorption processes for radionuclides with colloids and porous rock can be assumed as nonequilibrium and modeled by the linear kinetic adsorption. The numerical method is employed to solve the coupled colloid and radionuclide transport equations under nonequilibrium sorption assumption. Moreover, the reaction rates of the adsorption processes for radionuclides with the solid matrix and colloids affect the transport characteristics of radionuclides. The fast reaction rate of radionuclides with colloids causes a higher concentration of radionuclides adsorbed on colloids in a dispersed phase and enlarges acceleration caused by colloids. However, the fast reaction rate for radionuclides with solid matrix increases the retardation effect caused by the solid matrix. This work developed a predictive model for the transport of colloid-facilitated radionuclides in porous medium and to assess the importance of various phenomenological coefficients, particularly parameters for the adsorption interactions.     

Projection of landfill stabilization period by time series analysis of leachate quality and transformation trends of VOCs

The purpose of this study was to evaluate suitability of using the time series analysis for selected leachate quantity and quality parameters to forecast the duration of post closure period of a closed landfill. Selected leachate quality parameters (i.e., sodium, chloride, iron, bicarbonate, total dissolved solids (TDS), and ammonium as N) and volatile organic compounds (VOCs) (i.e., vinyl chloride, 1,4-dichlorobenzene, chlorobenzene, benzene, toluene, ethyl benzene, xylenes, total BTEX) were analyzed by the time series multiplicative decomposition model to estimate the projected levels of the parameters. These parameters were selected based on their detection levels and consistency of detection in leachate samples. In addition, VOCs detected in leachate and their chemical transformations were considered in view of the decomposition stage of the landfill. Projected leachate quality trends were analyzed and compared with the maximum contaminant level (MCL) for the respective parameters. Conditions that lead to specific trends (i.e., increasing, decreasing, or steady) and interactions of leachate quality parameters were evaluated. Decreasing trends were projected for leachate quantity, concentrations of sodium, chloride, TDS, ammonia as N, vinyl chloride, 1,4-dichlorobenzene, benzene, toluene, ethyl benzene, xylenes, and total BTEX. Increasing trends were projected for concentrations of iron, bicarbonate, and chlorobenzene. Anaerobic conditions in landfill provide favorable conditions for corrosion of iron resulting in higher concentrations over time. Bicarbonate formation as a byproduct of bacterial respiration during waste decomposition and the lime rock cap system of the landfill contribute to the increasing levels of bicarbonate in leachate. Chlorobenzene is produced during anaerobic biodegradation of 1,4-dichlorobenzene, hence, the increasing trend of chlorobenzene may be due to the declining trend of 1,4-dichlorobenzene. The time series multiplicative decomposition model in general provides an adequate forecast for future planning purposes for the parameters monitored in leachate. The model projections for 1,4-dichlorobenzene were relatively less accurate in comparison to the projections for vinyl chloride and chlorobenzene. Based on the trends observed, future monitoring needs for the selected leachate parameters were identified.     

Structural investigation of catalyst deactivation of Pt/SDB for catalytic oxidation of VOC-containing wastewater

The stability of styrene-divinyl benzene copolymer (SDB)-supported Pt (Pt/SDB) catalysts for destruction of volatile-organic-compound (VOC) in wastewater was examined. The test reaction was wet oxidation of water-containing aliphatic alcohol and formaldehyde at 140 degrees C and 90 psig for 40 h. The catalytic performance tests indicated that activity of the Pt/SDB catalysts could be maintained for VOC concentration of 3 wt.%, whereas the catalysts deactivated rapidly for 10 wt.% VOC containing wastewater. In order to investigate the nature of catalyst deactivation, extended X-ray absorption fine structure (EXAFS) and X-ray absorption near edge (XANES) spectroscopy were used to characterize the fresh and used catalysts. After the reaction, there is no oxidation of Pt clusters observed in EXAFS and XANES spectroscopy suggesting that the oxidation reaction takes places via the adsorbed oxygen. The spectroscopy results further indicated that deactivation of the catalysts were mainly caused by the increase of Pd particle size. After the reaction, the Pt-Pt coordination number has no significant change for the 3 wt.% wastewater whereas increase from 5.6 to 6.2 for 10 wt.% wastewater. Combined with the fact that the catalysts fractured during the reactions, we suggested that Pt agglomeration was mainly caused by thermal migration of the metal clusters.     

Evaluation of sites for the location of WEEE recycling plants in Spain

As a consequence of new European legal regulations for treatment of waste electrical and electronic equipment (WEEE), recycling plants have to be installed in Spain. In this context, this contribution describes a method for ranking of Spanish municipalities according to their appropriateness for the installation of these plants. In order to rank the alternatives, the discrete multi-criteria decision method PROMETHEE (Preference Ranking Organisation METHod for Enrichment Evaluations), combined with a surveys of experts, is applied. As existing plants are located in North and East Spain, a significant concentration of top ranking municipalities can be observed in South and Central Spain. The method does not present an optimal structure of the future recycling system, but provides a selection of good alternatives for potential locations of recycling plants.     

头孢类抗生素生产废水污染与处理现状

分析了头孢类抗生素生产废水的污染现状,指出了废水的来源及主要特征.介绍了目前常用的头孢类抗生素废水处理技术:物化处理技术和生物处理技术,其中厌氧(缺氧)-好氧组合工艺是处理高浓度头孢类抗生素废水的主要方法,提出了头孢类抗生素企业的污染防治对策.     

Effect of aluminum sulfate and cationic polyelectrolytes on the destabilization of emulsified wastes

Emulsified oil in wastewater constitutes a severe problem in the different treatment stages. Aluminum salts have been traditionally used as coagulants in wastewater treatments. Polyelectrolytes are used to coagulate and flocculate colloidal systems. The performance of aluminum sulfate in comparison to polyelectrolytes (chitosan and polyacrylamide) as conditioning chemicals for an emulsion waste was tested, and the predominant mechanisms acting in each case were analyzed. Turbidimetry, jar test, colloidal titration and microscopy were used to test emulsion destabilization. Both charge neutralization and bridge formation were identified and confirmed as mechanisms of interaction of polyelectrolytes with waste constitutents. Charge neutralization would be more important for chitosan than for polyacrylamide treatment. A coincidence between the doses necessary to reach zero colloidal charge and minimum turbidity was observed for polyelectrolytes. The time necessary to produce system clarification was larger for aluminum sulfate than for polyelectrolytes; this time was shortened for higher aluminum sulfate concentration. The pH showed a marked effect on aluminum sulfate performance with the optimum at pH 6; polyelectrolyte action was practically not affected by pH. Polyelectrolyte addition produced the minimum turbidity for the same doses that zero colloidal charge; at higher doses, emulsion was restabilized and became turbid again. However, aluminum sulfate treatment did not produce emulsion restabilization.     

环境治理工程评标的双基点模型及应用

动用多指标综合排序的双基点法，建立了环境治理工程评标的数学模型。应用实例表明，该模型可以为环境治理工程评标提供客观、合理的方法。     

Study of Aging Characteristics of Ternary Blends of Polyethylenes—II

Six film samples of low-density polypropylene (LDPE)/linear LDPE (LLDPE)/high-density polypropylene (HDPE) with varying ratios of LDPE (20–45 ... wt%) and LLDPE (25–50 wt%) having a fixed amount of HDPE at 30 wt% were prepared by blown film extrusion technique. The samples were aged at four different temperatures, 55°, 70°, 85°, and 100°C, for four different time periods in the interval of between 150 hours and up to 600 hours. The change in the structure of various constituents and the formation of various oxygenated (peroxy and hydroperoxy) and unsaturated groups during thermo-oxidative degradation was discussed by infrared spectroscopy. The visiosity-average molecular weight was found to have decreased slowly in the initial aging hours and temperatures, whereas it decreased by 10% with its previous value tensile strength that is, 100°C when aged for 600 hours. The tensile strength of the sample first increased by 67% at 55°C and 89% at 70°C up to 450 hours, whereas the values increased by 52.5% at 85°C and 33.9% at 100°C when aged for 150 hours and then decreased. The percentage elongation at break increased by 2.7% at 55°C and 10.7% at 70°C for 150 and 300 hours of aging, respectively, whereas the percentage decreased when aged at 85°C and 100°C for up to 600 hours of aging. The values of gel content (percent) increased and initial degradation temperature decreased with aging time and temperature.     

Proposal for the integration of decentralised composting of the organic fraction of municipal solid waste into the waste management system of Cuba

Municipal solid waste (MSW) generation and management in Cuba was studied with a view to integrating composting of the organic fractions of MSW into the system. Composting is already included as part of the environmental strategy of the country as an appropriate waste management solution. However, no programme for area-wide implementation yet exists. The evaluation of studies carried out by some Cuban and international organisations showed that organic matter comprises approximately 60-70% of the MSW, with households being the main source. If all organic waste fractions were considered, the theoretical amount of organic waste produced would be approximately 1 Mio. Mg/a, leading to the production of approximately 0.5 Mio. Mg/a of compost. Composting could, therefore, be a suitable solution for treating the organic waste fractions of the MSW. Composting would best be carried out in decentralised systems, since transportation is a problem in Cuba. Furthermore, low technology and low budget composting options should be considered due to the problematic local economic situation. The location for such decentralised composting units would optimally be located at urban agricultural farms, which can be found all over Cuba. These farms are a unique model for sustainable farming in the world, and have a high demand for organic fertiliser. In this paper, options for the collection and impurity-separation in urban areas are discussed, and a stepwise introduction of source-separation, starting with hotel and restaurant waste, is suggested. For rural areas, the implementation of home composting is recommended.     

Screening tests for hazard classification of complex waste materials – Selection of methods

In this study we describe the development of an alternative methodology for hazard characterization of waste materials. Such an alternative methodology for hazard assessment of complex waste materials is urgently needed, because the lack of a validated instrument leads to arbitrary hazard classification of such complex waste materials. False classification can lead to human and environmental health risks and also has important financial consequences for the waste owner. The Hazardous Waste Directive (HWD) describes the methodology for hazard classification of waste materials. For mirror entries the HWD classification is based upon the hazardous properties (H1–15) of the waste which can be assessed from the hazardous properties of individual identified waste compounds or – if not all compounds are identified – from test results of hazard assessment tests performed on the waste material itself. For the latter the HWD recommends toxicity tests that were initially designed for risk assessment of chemicals in consumer products (pharmaceuticals, cosmetics, biocides, food, etc.). These tests (often using mammals) are not designed nor suitable for the hazard characterization of waste materials. With the present study we want to contribute to the development of an alternative and transparent test strategy for hazard assessment of complex wastes that is in line with the HWD principles for waste classification. It is necessary to cope with this important shortcoming in hazardous waste classification and to demonstrate that alternative methods are available that can be used for hazard assessment of waste materials. Next, by describing the pros and cons of the available methods, and by identifying the needs for additional or further development of test methods, we hope to stimulate research efforts and development in this direction. In this paper we describe promising techniques and argument on the test selection for the pilot study that we have performed on different types of waste materials. Test results are presented in a second paper.As the application of many of the proposed test methods is new in the field of waste management, the principles of the tests are described. The selected tests tackle important hazardous properties but refinement of the test battery is needed to fulfil the a priori conditions.     

A review of emerging technologies for remediation of PFASs

The need for remediation of poly‐ and perfluoroalkyl substances (PFASs) is growing as a result of more regulatory attention to this new class of contaminants with diminishing water quality standards being promulgated, commonly in the parts per trillion range. PFASs comprise >3,000 individual compounds, but the focus of analyses and regulations has generally been PFASs termed perfluoroalkyl acids (PFAAs), which are all extremely persistent, can be highly mobile, and are increasingly being reported to bioaccumulate, with understanding of their toxicology evolving. However, there are thousands of polyfluorinated “PFAA precursors”, which can transform in the environment and in higher organisms to create PFAAs as persistent daughter products. Some PFASs can travel miles from their point of release, as they are mobile and persistent, potentially creating large plumes. The use of a conceptual site model (CSM) to define risks posed by specific PFASs to potential receptors is considered essential. Granular activated carbon (GAC) is commonly used as part of interim remedial measures to treat PFASs present in water. Many alternative treatment technologies are being adapted for PFASs or ingenious solutions developed. The diversity of PFASs commonly associated with use of multiple PFASs in commercial products is not commonly assessed. Remedial technologies, which are adsorptive or destructive, are considered for both soils and waters with challenges to their commercial application outlined. Biological approaches to treat PFASs report biotransformation which creates persistent PFAAs, no PFASs can biodegrade. Water treatment technologies applied ex situ could be used in a treatment train approach, for example, to concentrate PFASs and then destroy them on‐site. Dynamic groundwater recirculation can greatly enhance contaminant mass removal via groundwater pumping. This review of technologies for remediation of PFASs describes that:

• GAC may be effective for removal of long‐chain PFAAs, but does not perform well on short‐chain PFAAs and its use for removal of precursors is reported to be less effective;
• Anion‐exchange resins can remove a wider array of long‐ and short‐chain PFAAs, but struggle to treat the shortest chain PFAAs and removal of most PFAA precursors has not been evaluated;
• Ozofractionation has been applied for PFASs at full scale and shown to be effective for removal of total PFASs;
• Chemical oxidation has been demonstrated to be potentially applicable for some PFAAs, but when applied in situ there is concern over the formation of shorter chain PFAAs and ongoing rebound from sorbed precursors;
• Electrochemical oxidation is evolving as a destructive technology for many PFASs, but can create undesirable by‐products such as perchlorate and bromate;
• Sonolysis has been demonstrated as a potential destructive technology in the laboratory but there are significant challenges when considering scale up;
• Soils stabilization approaches are evolving and have been used at full scale but performance need to be assessed using appropriate testing regimes;
• Thermal technologies to treat PFAS‐impacted soils show promise but elevated temperatures (potentially >500 °C) may be required for treatment.

There are a plethora of technologies evolving to manage PFASs but development is in its early stage, so there are opportunities for much ingenuity.