如何正确认识安全生产方针

我国的安全生产方针是"安全第一,预防为主".这个方针是根据毛泽东同志的批示和我国劳动保护工作的实际情况,逐步从实践中总结出来的.多年来的实践证明,党的安全生产方针是完全正确的.根据这一方针,国家制定了一系列安全生产的政策、法令、法规和规程.根据这一方针,各企业、事业单位做了大量工作,安全生产工作取得了巨大的成就.特别是改革开发的20多年中,在安全生产方针的指导下,我国安全科学有了突飞猛进的发展,安全生产工作有了长足的进步.现就如何正确理解和执行安全生产方针谈谈自己的一点认识和看法.     

判断有机食品的标准是什么?

判断标准1.原料来自于有机农业生产体系或野生天然产品.2.有机食品在生产和加工过程中必须严格遵循有机食品生产、采集、加工、包装、贮藏、运输标准,禁止使用化学合成的农药、化肥、激素、抗生素、食品添加剂等,禁止使     

生产过程中的风险控制和安全管理

生产安全管理可以归纳为生产过程中对人、设备、环境风险因素的评估、控制和消除的综合管理.生产企业在开展安全性评价工作的基础上,通过应用风险控制的基本方法,可以对企业的安全管理起到积极的主导作用,促进安全生产良性循环.     

生命周期评价在我国乙烯行业环境评估中的应用

采用IMPACT 2002+方法对我国的乙烯行业进行了生命周期评价(LCA)研究,分析了包括原油生产、原煤生产、原料生产、乙烯生产和电力生产5个环节在内的13种污染物排放对乙烯行业的环境影响.结果表明,乙烯工业对不可再生能源原油的消耗,对温室效应、呼吸效应和水体酸化等的环境影响潜值最为严重.减少乙烯生产环节和原料生产环节(炼油过程)的SO2、NOx、CO2等气体的排放,以及原油开采过程的CH4逸放,是改善环境影响的关键因素.同时,以石脑油为原料裂解乙烯工艺比以轻烃为原料制乙烯工艺对环境的影响要小.而煤制烯烃工艺对环境影响较大,仍具有一定改进空间.总体来看,经过近十年发展,我国乙烯行业对资源利用效率和缓解尾气排放两方面都有显著的提升.     

异体监督制度在中原油田安全管理中的应用

长期以来,石油石化行业在安全生产方面创造出了一整套的安全生产监督管理规章制度,并且在生产过程中起到了巨大的作用.但是随着形势的变化,安全工作也需要与时俱进.如何进一步抓好安全生产、环境保护和职业卫生工作,如何更好地将安全生产的各项规章制度落实到基层单位的日常工作中去,成为摆在各级领导、尤其是各级安全管理人员面前的一项重要课题.     

汽车涂料生产环节VOCs的排放特征及安全评价

选择某汽车涂料的生产车间为研究对象,根据汽车涂料生产工艺的不同环节,在3个生产车间选定了8个采样点,用气质联用仪分析了汽车涂料车间内不同生产环节的挥发性有机物(volatile organic compounds,VOCs)的种类及浓度水平,并通过比较各种VOC的浓度与国家卫生部规定的工作场所有毒物质职业接触限值中短时接触容许浓度,对车间工人健康的影响进行了评价.结果表明,汽车涂料生产车间内共检测出15种主要的VOCs,包括苯、甲苯、乙苯、二甲苯、乙酸乙酯、乙酸丁酯、甲基异丁基酮、丙二醇甲醚醋酸酯、三甲苯、乙二醇丁醚等,其浓度检出范围为0.51~593.14 mg·m-3.生产车间各生产环节处TVOCs浓度显著不同,同一生产环节不同批次的气体样品中VOCs浓度也存在较大差异.二甲苯和乙酸丁酯是生产车间室内空气的主要VOCs.在生产高峰期部分VOCs浓度超过了工作场所有毒物质职业接触限值,需采取相应控制措施以保障工人健康.     

乳品企业实施清洁生产的机会

清洁生产是我国工业可持续发展的一项重要战略,也是我国污染控制实现由末端治理向全过程控制转变的重大举措.乳制品生产过程消耗大量的水、电,并排放大量的有机污染物.本文针对乳品生产企业的部分生产环节,着重阐述其部分生产环节中如何节能,如何增加产品产量、减少有机污染物的排放,如何实现清洁生产.     

正确认识安全生产责任制的重要性

<安全生产法>的颁布实施为各厂矿企业安全工作的开展提供了有力的法律保障,为全员不断提高安全意识,对企业建立健全安全生产责任制、逐步改善安全生产的软硬件环境,起到了积极的促进作用.可是,有一些单位虽然制定了安全生产责任制,但仅仅是写在纸上、贴在墙上、挂在嘴上,并没有落实在行动上,仍然是重生产、轻安全,责任制度形同虚设.要真正地建立起安全生产责任制,就应该从以下几个方面予以重视.     

遵章守法关爱生命

又到安全生产月. 今年安全生产月的主题是"遵章守法、关爱生命".每年安全生产月的主题都是针对一段时间以来全国范围内比较突出的安全生产问题提出的应对策略.在国家提出的总体策略下,每一个企业再针对本企业安全生产中存在的主要问题,加以分析研究,制定应对措施并加以实施.     

浙江省人为镉排放源与汇时空格局解析

近年来,随着工农业的迅猛发展,大量的人为镉排放对我国生态环境安全构成了严重威胁,而污染源识别在污染治理中具有举足轻重的作用.为此,本文以工农业集产区浙江省为案例,通过文献调研,构建了浙江省人为镉工农业排放因子清单,并采用清单核算法对浙江省人为镉排放的源汇进行了估算.结果表明,浙江省人为镉排放在1995—2017年期间基本呈上升趋势,从1995年的39 t增加到2007的141 t,自2007年以后,浙江省的镉排放量达到了一定的峰值,其排放量在140 t·a^-1左右.其中75%以上的镉通过固废的形式排放进入环境,而进入大气和水体的镉分别约占15%和10%.在所有排放源中,原煤燃烧的镉排放贡献率最大,占总排放量的50%以上;其他排放源从大到小依次是钢铁生产、有色金属冶炼、造纸生产、水泥生产、塑料生产、有色金属开采、油料消费、磷肥生产、蓄电池生产、平板玻璃生产和陶瓷生产.各个地区镉排放表现出较大的空间差异,2015年杭州市和宁波市镉排放量已达到20 t以上,以杭州和宁波为中心的北部区域远远高于南部区域.因此,建议未来浙江省镉污染排放源头治理重点是减少原煤燃烧,其次是钢铁生产、有色金属冶炼、造纸生产、水泥生产,尤其北部区域.     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

Arsenic uptake by arbuscular mycorrhizal maize （Zea mays L.） grown in an arsenic-contaminated soil with added phosphorus

The effects of arbuscular mycorrhizal (AM) fungus (Glomus mosseae) and phosphorus (P) addition (100 mg/kg soil) on arsenic (As) uptake by maize plants (Zea mays L.) from an As-contaminated soil were examined in a glasshouse experiment.Non-mycorrhizal and zero-P addition controls were included.Plant biomass and concentrations and uptake of As,P,and other nutrients,AM colonization,root lengths,and hyphal length densities were determined.The results indicated that addition of P significantly inhibited root colonization and development of extraradical mycelium.Root length and dry weight both increased markedly with mycorrhizal colonization under the zero-P treatments,but shoot and root biomass of AM plants was depressed by P application.AM fungal inoculation decreased shoot As concentrations when no P was added,and shoot and root As concentrations of AM plants increased 2.6 and 1.4 times with P addition,respectively.Shoot and root uptake of P,Mn,Cu,and Zn increased,but shoot Fe uptake decreased by 44.6%,with inoculation, when P was added.P addition reduced shoot P,Fe,Mn,Cu,and Zn uptake of AM plants,but increased root Fe and Mn uptake of the nonmycorrhizal ones.AM colonization therefore appeared to enhance plant tolerance to As in low P soil,and have some potential for the phytostabilization of As-contaminated soil,however,P application may introduce additional environmental risk by increasing soil As mobility.     

Degradation of metabolites accumulated of benzo[a]pyrene by coupling Penicillium Chrysogenum with KMnO4

Several main metabolites of benzo[a]pyrene （BaP） formed by Penicillium chrysogenum, Benzo[a]pyrene-1,6-quinone （BP 1,6- quinone）, trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene （BP 7,8-diol）, 3-hydroxybenzo[a]pyrene （3-OHBP）, were identified by high-performance liquid chromatography （HPLC）. The three metabolites were liable to be accumulated and were hardly further metabolized because of their toxicity to microorganisms. However, their further degradation was essential for the complete degradation of BaP. To enhance their degradation, two methods, degradation by coupling Penicillium chrysogenum with KMnO4 and degradation only by Penicillium chrysogenum, were compared; Meanwhile, the parameters of degradation in the superior method were optimized. The results showed that （1） the method of coupling Penicillium chrysogenum with KMnO4 was better and was the first method to be used in the degradation of BaP and its metabolites; （2） the metabolite, BP 1,6-quinone was the most liable to be accumulated in pure cultures; （3） the effect of degradation was the best when the concentration of KMnO4 in the cultures was 0.01% （w/v）, concentration of the three compounds was 5 mg/L and pH was 6.2. Based on the experimental results, a novel concept with regard to the bioremediation of BaP-contaminated environment was discussed, considering the influence on environmental toxicity of the accumulated metabolites.     

Impact of atrazine and nitrogen fertilizers on the sorption of chlorotoluron in soil and model sorbents

Sorption of chlorotoluron in ammonium sulfate, urea and atrazine multi-solutes system was investigated by batch experiments. The results showed application of nitrogen fertilizers to the soil could affect the behavior of chlorotoluron. At the same concentration of N, sorption of chlorotoluron decreased as the concentration of atrazine increased on the day 0 and 6 in soil, respectively. The sorption of chlorotoluron increased from 0 to 6 d when soils were preincubated with deionized water, ammonium sulfate and urea solution for 6 d. That indicated incubation time was one of the most important factors for the sorption of chlorotoluron in nitrogen fertilizers treatments. The individual sorption isotherms of chlorotoluron in rubbery polymer and silica were strictly linear in single solute system, but there were competition sorption between pesticides or between pesticides and nitrogen fertilizers. That indicated the sorption taken place by concurrent solid-phase dissolution mechanism and sorption on the interface of water-organic matter or water-mineral matter.     

Potential of plant polyphenol oxidases in the decolorization and removal of textile and non-textile dyes

In this study an effort has been made to use plant polyphenol oxidases; potato （Solanum tuberosum） and brinjal （Solanum melongena）, for the treatment of various important dyes used in textile and other industries. The ammonium sulphate fractionated enzyme preparations were used to treat a number of dyes under various experimental conditions. Majority of the treated dyes were maximally decolorized at pH 3.0. Some of the dyes were quickly decolorized whereas others were marginally decolorized. The initial first hour was sufficient for the maximum decolorization of dyes. The rate of decolorization was quite slow on long treatment of dyes. Enhancement in the dye decolorization was noticed on increasing the concentration of enzymes. The complex mixtures of dyes were treated with both preparations of polyphenol oxidases in the buffers of varying pH values. Potato polyphenol oxidase was significantly more effective in decolorizing the dyes to higher extent as compared to the enzyme obtained from brinjal polyphenol oxidase. Decolorization of dyes and their mixtures, followed by the formation of an insoluble precipitate, which could be easily removed simply by centrifugation.     

Removal of heavy metals from sewage sludge by low costing chemical method and recycling in agriculture

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Single and joint effects of pesticides and mercury on soil urease

The influence of two pesticides including chlorimuron-ethyl and furadan and mercury （Hg） on urease activity in 4 soils （meadow burozem and phaeozem） was investigated. The soils were exposed to various concentrations of the two pesticides and Hg individually and simultaneously. Results showed that there was a close relationship between urease activity and organic matter content in soil. Chlorimuron-ethyl and furadan could both activate urease in the 4 soils. The maximum increment of urease activity by chlorimuronethyl was up to 14%-18%. There was almost an equal increase （up to 13%-21%） in the urease activity by furadan. On the contrary, Hg markedly inhibited soil urease activity. A logarithmic equation was used to describe the relationship （P〈0.05） between the concentration of Hg and the activity of soil urease in the 4 tested soils. Semi-effect dose （ED50） values by the stress of Hg based on the inhibition of soil urease in the 4 soils were 88, 5.5, 24 and 20 mg/kg, respectively, according to the calculation of the corresponding equations. The interactive effect of chlorimuron-ethyl or furadan with metal Hg on soil urease was mainly synergic at the highest tested concentrations.     

Isolation and preliminary characterization of a 3-chlorobenzoate degrading bacteria

A study was conducted to compare the diversity of 2-, 3-, and 4-chlorobenzoate degraders in two pristine soils and one contaminated sewage sludge. These samples contained strikingly different populations of mono-chlorobenzoate degraders. Although fewer cultures were isolated in the uncontaminated soils than contaminated one, the ability of microbial populations to mineralize chlorobenzoate was widespread. The 3- and 4-chlorobenzoate degraders were more diverse than the 2-chlorobenzoate degraders. One of the strains isolated from the sewage sludge was obtained. Based on its phenotype, chemotaxonomic properties and 16S rRNA gene, the organism S-7 was classified as Rhodococcus erythropolis. The strain can grow at temperature from 4 to 37℃. It can utilize several （halo）aromatic compounds. Moreover, strain S-7 can grow and use 3-chlorobenzoate as sole carbon source in a temperatures range of 10-30℃ with stoichiometric release of chloride ions. The psychrotolerant ability was significant for bioremediation in low temperature regions. Catechol and chlorocatechol 1,2-dioxygenase activities were present in cell free extracts of the strain, but no （chloro）catechol 2,3- dioxygenase activities was detected. Spectral conversion assays with extracts from R. erythropolis S-7 showed accumulation of a compound with a similar UV spectrum as chloro-cis,cis-muconate from 3-chlorobenzoate. On the basis of these results, we proposed that S-7 degraded 3-chlorobenzoate through the modified ortho-cleave pathway.     

Organochlorine pesticides in soils under different land usage in the Taihu Lake region, China

A field study was conducted in the Taihu Lake region, China in 2004 to reveal the organochlorine pesticide concentrations in soils after the ban of these substances in the year 1983. Thirteen organochlorine pesticides (OCPs) were analyzed in soils from paddy field, tree land and fallow land. Total organochlorine pesticide residues were higher in agricultural soils than in uncultivated fallow land soils. Among all the pesticides, ΣDDX (DDD, DDE and DDT) had the highest concentration for all the soil samples, ranging from 3.10 ng/g to 166.55 ng/g with a mean value of 57.04 ng/g and followed by ΣHCH, ranging from 0.73 ng/g to 60.97 ng/g with a mean value of 24.06 ng/g. Dieldrin, endrin, HCB and α-endosulfan were also found in soils with less than 15 ng/g. Ratios of p,p'-(DDD DDE)/DDT in soils under three land usages were: paddy field ＞ tree land ＞ fallow land, indicating that land usage inlfuenced the degradation of DDT in soils. Ratios of p,p'-(DDD DDE)/DDT ＞1, showing aged residues of DDTs in soils of the Taihu Lake region. The results were discussed with data from a former study that showed very low actual concentrations of HCH and DDT in soils in the Taihu Lake region, but according to the chemical half-lives and their concentrations in soils in 1980s, the concentration of DDT in soils seemed to be underestimated. In any case our data show that the ban on the use of HCH and DDT resulted in a tremendous reduction of these pesticide residues in soils, but there are still high amounts of pesticide residues in soils, which need more remediation processes.     

Sorption of 1-naphthol by plant cuticular fractions

The contribution of aliphatic-rich plant biopolymer to sorption of hydrophobic organic compounds is significantly important because of their preservation and accumulation in the soil environment,but sorption mechanism is still not fully understood.In this study, sorption of 1-naphthol by plant cuticular fractions was examined to better understand the contributions of respective fraction.Toward this end,cuticular materials were isolated from the fruits of tomato by chemical method.The tomato cuticle sheet consisted of waxes (6.5 wt%),cuticular monomer (69.5 wt%),and polysaccharide (24.0 wt%).Isotherms of l-naphthol to the cuticular fractions were nonlinear (N value (0.82-0.90)) at the whole tested concentration ranges.The KodKow ratios for bulk cuticle (TC1),dewaxed cuticle (TC2),cutin (TC4),and desugared cuticle (TC5) were larger than unity,suggested that tomato bulk cuticle and cutin are much powerful solption medium.Sorption capability of cutin (TC4) was 2.4 times higher than the nonsaponifiable fraction (TC3).The 1-naphthol interactions with tomato cuticular materials were governed by both hydrophobic-type interactions and polar (H-bonding) interactions. Removal of the wax and polysaccharide materials from the bulk tomato cuticle caused a significant increase in the sorption ability of the cuticular material.There was a linear negative trend between K_(oc) values and the amount of polysaccharides or fraction's polarities ((N O)/C);while a linear positive relationship between K_(oc) values and the content of cutin monomer (linear R~2=0.993) was observed for present in the cuticular fractions.Predominant sorbent of the hydrophobic organic compounds (HOCs) in the plant cuticular fraction was the cutin monomer,contributing to 91.7% of the total sorption of tomato bulk cuticle.