Skip navigation

Contributed by Daniel Teitelbaum, Pollution Prevention Team Lead, Toxics Release Inventory Program, US EPA


For more than two decades, EPA’s Toxics Release Inventory (TRI) Program has required industrial facilities to disclose both their environmental releases and the measures they’ve taken to keep toxic chemicals out of our air, water, and land.  It was only recently, however, that the TRI Program began promoting this treasure trove of pollution prevention (P2) data as a resource for identifying demonstrably-effective green practices.



More than 10,000 source reduction activities are reported to TRI each year, but can we tell which ones actually reduce releases? A rigorous statistical analysis of all TRI data shows that the average effect is highest for the reporting categories that include raw material (e.g., feedstock chemical) substitution and switches to aqueous cleaners from solvents. And a separate analysis of the pharmaceutical sector indicates that green chemistry practices contributed to dramatic reductions in the early-to-mid 2000s.


But more meaningful insights lie ahead. Beginning with reports due July 1 of this year, facilities will have the opportunity to report the estimated annual reduction associated with each newly implemented P2 activity. This information will shed new light on which types of practices (including six new green chemistry categories added in 2012) are having the biggest impact on companies’ environmental footprints. As always, facilities that implemented green chemistry will also be encouraged to highlight their successes by submitting a more detailed narrative in the optional P2 section of the form (see video).



As TRI was founded on transparency, EPA has continually sought to increase the accessibility of TRI data on corporate sustainability. To this end, all of the facility-level P2 information and environmental metrics presented in the TRI P2 Search Tool are now available at the parent company-level as well. This means you can now compare toxic chemical management and greenhouse gas emissions data at the corporate level and see what each parent company is doing to prevent the release of pollutants to the environment.  You can also explore differences in P2 and waste management practices at different facilities within the same parent company – it’s your right to know.


To access TRI's P2 data and learn about reporting P2 to TRI, visit







“The Nexus Blog” is a sister publication of “The Nexus” newsletter. To sign up for the newsletter, please email, or if you have an ACS ID, login to your email preferences and select “The Nexus” to subscribe.



To read other posts, go to Green Chemistry: The Nexus Blog home.

Contributed by Tiffany N. Ellison, Joseph R. Fortunak, Frederick E. Nytko III, Howard University, Department of Chemistry


Some time ago (December, 2012) we published a story about the work being done by Professor Joseph Fortunak and his research group at Howard University (HU) in Washington, DC. This communication is an update on that story.  Last year (2014) Dr. Fortunak estimates he was in nineteen countries including Equatorial Guinea, Nigeria, Tanzania, South Africa, Nicaragua, Brazil, Switzerland, and China. Before joining HU in 2004, Dr. Fortunak spent over twenty years in the pharmaceutical industry, contributing to the launch of over a dozen new drugs and a similar number of new generic products during that time. Howard University is an HBCU (Historically Black College/University) founded in 1867 to provide higher education for freed slaves. Howard has had a PhD program in Chemistry since 1954 and has trained over 20% of the African-American PhD Chemists in the United States.


Picture2.pngThese details are pertinent to this “update report” because the mission of Howard University meshes with Professor Fortunak’s work. Dr. Fortunak and his group members concentrate their efforts on developing new chemistry and technologies for the more efficient, less expensive production of essential medicines of assured quality. The results of this work are shared with pharmaceutical manufacturers in India and China who produce essential medicines for the treatment of HIV/AIDS, malaria, TB, and opportunistic infections. Dr. Fortunak’s work was awarded the ACS Astellas Foundation Award in 2009 for “Chemistry Impact on Human Health.” This research continues in collaboration with the World Health Organization, UNITAID, the William J. Clinton Health Access Initiative, and the Medicines Patent Pool.  An article in the Wall Street Journal (May 13, 2011) by Mark Schoofs described how Mr. Adrian Williams, an MSc student in the group, made a lasting impact on the availability of medicines for HIV/AIDS for low- and middle-income countries by improving the process chemistry for making the drug tenofovir disoproxil fumarate.  This chemistry was published in the Organic Process Research and Development Journal (2010).


Mount Kilimanjaro.jpgOne particular interest is the collaboration between HU and the St. Luke Foundation/Kilimanjaro School of Pharmacy (SLF/KSP) in Moshi, Tanzania.  Moshi is the nearest city to Mount Kilimanjaro, African’s tallest mountain. The area is a favorite with adventurous tourists because Kilimanjaro can be climbed in a several day trek without special equipment, while other famous sites including Olduvai Gorge, the Serengeti Desert, and Ngorongoro Crater are in close proximity.


Sister Zita Ekeocha is the founder and Director of the IPAT (Industrial Pharmacy Advanced Training) at the KSP, while Mr. Wilson Mlaki is the Principal of the School.  The IPAT is taught by faculty from the United States, including Dr. Fortunak and other individuals whose varied experiences in pharmaceutical R&D and manufacturing complement each other well.  The German organization GiZ (Deutsche Gesellschaft für Internationale Zusammenarbeiten) has provided support to build a pilot plant for pharmaceutical production at the SLF/KSP.  With support from the United Nations Industrial Development Organization (UNIDO) the IPAT has provided advanced training in pharmaceutical manufacturing and Current Good Manufacturing Practice (cGMP) to National Drug Regulators, University faculty, and pharmaceutical professionals since 2008.  With occasional courses being offered in a sequence either two or three times per year, approximately 120 participants have completed the core curriculum of four, two-week, full-time courses in drug discovery, development, GMP, and drug regulation.


Dr. Fortunak’s students (notably, Tiffany N. Ellison and Drs. Joseph Williams Jr. and Christopher L. King) have developed new instructional materials and taught at various IPAT courses in Moshi.  Dr. King was awarded an ACS GREET Fellowship (Graduate Research Experiences, Education, and Training) to support part of his work for the KSP. The research work done by these students has so far contributed to five publications and six invited presentations at various research symposia, including at the Gordon Research Conferences “Green Chemistry Conference” in Hong Kong (August, 2014).  Several African participants have also been able to visit Howard University as a result of these collaborations. One recent outcome from these collaborations has been the submission of a book chapter on “The Business Case for Green Chemistry in Drug Discovery” co-authored by Professors Fortunak and Simon Xiang of Howard University, and the African scientists Drs. Harriet Kamendi (Ghana) and Martins Emeje (Nigeria).


Tablet press 2.jpgThe IPAT program has recently divided its efforts in two directions. Purdue University (PU) is offering a Master’s degree to individuals who take additional, online courses and continue through a Purdue sequence. The original IPAT program continues, and the SLF/KSP efforts include transfer of the original program to other African Universities including the University of Ibadan in Nigeria.  These efforts are overseen by Dr. Fortunak.  Ibadan is also developing their own Master’s degree curriculum as part of this continuing collaboration with HU, and Howard is also helping the KSP to develop a Bachelor’s degree program in Industrial Pharmacy.


Synthesis-of-ACTs-at-KSP.jpgOther, exciting aspects of this collaboration have come into being since our last report.  In 2013 the United Nations ANDI (African Innovation for New Drugs and Diagnostics) Program designated the SLF/KSP as a Center of Excellence for drug training and manufacturing.  In 2013 the US FDA also taught a one-week Course in advanced topics for Abbreviated New Drug Applications (ANDAs, generic drug marketing) at the KSP. Participants from 19 African countries attended this training, overseen by (the late) Dr. Beverly Corey who until recently headed the US FDA/Africa. The SLF/KSP was distinguished with a US FDA Honor Award in 2013 for Excellence and Innovation in Regulatory Sciences for this Course In 2014 the SLF/KSP was also designated a Regulatory Center of Excellence (RCORE) in drug regulation by the African Medicines Harmonization program, an effort funded by the Bill and Melinda Gates Foundation. In 2013 Dr. Fortunak was also part of a Team award from the African Union (AU) for Social Responsibility. The AU represents the entire membership of fifty-four independent African nations.


Joe2.jpgAnd so, efforts continue on this fruitful collaboration. As Dr. Fortunak notes,“there is never enough funding” for work such as this.  The importance of this type of an approach to new science and technology is sometimes difficult to qualify for traditional research grant awards. Any readers who are interested in their organization possibly supporting these efforts are urged to contact Dr. Fortunak directly.This work carries both short-term and long-term rewards. Four African companies have used their IPAT training to good effect, and have manufacturing facilities that have been certified as cGMP-compliant by the US FDA and/or the World Health Organization “Pre-Qualification of Medicines Program.” Over the long term, the training of people contributes to economic development, job creation, and national independence and self-determination for creating access to medicines. The most rewarding part of these efforts is the personal interactions that result from international experience in training and in research.



1) KSP Pilot Plant, 2) Mount Kilimanjaro, 3) Tablet press at KSP Pilot Plant, 4) Synthesis of ACTs at KSP Pilot Plant, 5) Dr. Joeseph Fortunak with Sister Zita Ekeocha (Director, KSP IPAT Program) and Mr. Wilson Mlaki (Principal of KSP).



“The Nexus Blog” is a sister publication of “The Nexus” newsletter. To sign up for the newsletter, please email, or if you have an ACS ID, login to your email preferences and select “The Nexus” to subscribe.


To read other posts, go to Green Chemistry: The Nexus Blog home.

The ACS Green Chemistry Institute® would like to thank the 43 corporations that worked collaboratively and non-competitively throughout 2014 to catalyze the integration of sustainable and green chemistry and engineering in the global chemical enterprise. Beginning in 2005 with just three companies on one Roundtable, there are now four Roundtables serving 43 members. The ACS GCI Industrial Roundtables are a proven concept, demonstrating that collaboration among peer companies can effectively provide value directly to the company, as well as to the collective industry, in designing more sustainable processes and products, a pursuit that is imperative for a sustainable business and environment.


Hydraulic Fracturing Roundtable


Building on efforts initiated in 2013 to create a Roundtable to improve the sustainability profile of hydraulic fracturing through green chemistry, in June 2014 the ACS GCI Hydraulic Fracturing Roundtable opened for membership. The group welcomed nine founding members: Apache Corporation, BASF, The Dow Chemical Co., The Lubrizol Corporation, Marathon Oil Company, Nalco Champion (An Ecolab Company), Rockwater Energy Solutions, Solvay USA Inc., and Trican Well Service. The appointed co-chairs are Danny Durham from Apache Corporation and Dave Long of the ACS GCI Board.


In partnership with Clean Production Action, members are provided 40 GreenScreen assessments of widely used fracturing chemicals (an $8,700 value). These assessments are able to be used internally by member companies to better determine the sustainability profile of their fracturing chemicals and identify where replacements might be needed. The newly formed Roundtable also organized a session at the 18th Annual Green Chemistry and Engineering Conference titled “Exploring Greener Approaches to Hydraulic Fracturing.” The session was chaired and organized by Danny Durham of Apache Corporation, and featured academic and industrial presentations on progress and improvements to fracturing chemicals. Moving forward in 2015, the Roundtable will establish annual goals supporting the strategic priorities including an analysis of data from hydraulic fracturing well reports.


Chemical Manufacturer’s Roundtable


Last year the Chemical Manufacturer’s Roundtable conducted a scouting survey to better understand the current implementation of green chemistry in the chemical manufacturing sector. In 2014, they published (in ACS Sustainable Chemistry & Engineering) the findings of a survey on the current implementation of green chemistry in the chemical manufacturing sector and identified actionable projects. Moving forward, the Roundtable seeks to evaluate how members can better highlight the process metrics they use, track green chemistry implementation across the industry, and define research, development, and demonstration needs for industrial application of green chemistry. A major focus area for the Roundtable is reducing the energy required to manufacture products. Building on the work to define opportunities for alternative separation technologies, the ACS GCI Roundtables (led by the Chemical Manufacturers), submitted a proposal for consideration for the NIST Advanced Manufacturing Technology Planning Grant.


The Roundtable also organized sessions at ACS GCI’s 18th Annual Green Chemistry and Engineering Conference in Bethesda, MD. “Greening the Supply Chain Using Biobased Chemicals” was organized by Paul Williams (Arizona Chemical) and Bogdan Comanita (Market Chemica on behalf of Penn A Kem). Alan Phillips (Arizona Chemical) chaired the session on-site. A tools and metrics related session was organized and chaired by Robert Giraud of DuPont. Throughout the year the Roundtable also hosted several distinguished guest speakers at their bimonthly meetings, including Ron Buckhalt (U.S. Department of Agriculture), Blandine Trouille (U.S. Department of Commerce), Nancy Jackson (U.S. Department of State), Rich Engler (U.S. EPA), and I.S. Jawahir (Institute for Sustainable Manufacturing at University of Kentucky). In May, a transition in Roundtable leadership occurred when Paul Williams’ (Arizona Chemical) term as co-chair came to a close, and Amit Sehgal of Solvay USA Inc. was voted in as the new co-chair.


Formulators’ Roundtable


In order to identify key industry needs for formulated consumer products, this year the Formulators’ Roundtable collaborated closely with Dr. Philip Jessop, Professor of Chemistry at Queen’s University and ACS GCI Board Member, on a manuscript defining opportunities for greener alternatives. The group identified 10 classes of components (such as chelants and sequestering agents, corrosion inhibitors, fragrance raw materials, and more) that are in need of replacement as well as the characteristics that ideal replacements should possess. The manuscript has been submitted for publication. Continuing discussions from 2013, the Roundtable acted as an industry voice, engaged the fragrance suppliers and developers, third party reviewers, and the U.S. EPA to enable informed discussions on the interim fragrance criteria and the design of more sustainable alternatives.


The Roundtable facilitated regular conversations with the U.S. EPA to learn about the current status of the Design for the Environment program, a hazard-based calculator being developed to assist fragrance houses and to stay abreast of the fragrance deadline, and several other topics. Furthermore, the Roundtable engaged with guest speakers at their bi-monthly meetings including:

  • Suzanne Hartigan (Director, Science Policy and Regulatory Affairs) and Megan Ekstrom (Manager, Government Affairs) of International Fragrance Association-North America to explore opportunities to collaborate in the development of greener products
  • Clive Davies, Joyce Parker, and Aly Lorenz of the U.S. EPA’s Design for the Environment Program Branch, provided an overview of their new criteria and calculator for fragrances. At the GC&E conference the Roundtable organized two sessions on defining greener and more sustainable consumer products. Chaired by Phil Sliva of Amway, the presentations featured industry professionals discussing topics ranging from hazard data transparency to life cycle assessment for greener products.


Pharmaceutical Roundtable


In its 9th year, the ACS GCI Pharmaceutical Roundtable continued to deliver on their four strategic priorities (inform and influence the research agenda, tools for innovation, education resource, and global collaboration) and welcomed a new member, Cubist Pharmaceuticals. David Leahy of Bristol-Myers Squibb completed his two-year tenure as a co-chair, and the group voted in John Tucker of Amgen as his successor.


This year several grants were awarded by the Roundtable to inform and influence the research agenda:

  • $100,000 to  Professor Paul Chirik of Princeton University for base metal-catalyzed cross-coupling in the pharmaceutical industry
  • $100,000 to Professor Neal Mankad of University of Illinois at Chicago for a bimetallic approach to iron-catalyzed coupling reactions
  • $50,000 to Professor Daniel Weix of University of Rochester for the synthesis of alkylated arenes and heteroarenes from the cross-coupling of heteroaromatic halides in non-amide solvents
  • $50,000 to Professors Matthias Beller and Elisabetta Alberico of the Leibniz-Institut für Katalyse for ligand-metal cooperative catalysis for the mild and selective synthesis of amines


The Roundtable also continued development on several of their established tools that can assist chemists, engineers, academics, students, and other professionals to incorporate greener chemistry into their research. The Biopharma team initiated a Process Mass Intensity benchmarking activity and collected best engineering practices. There were initial efforts to expand the solvent selection guide and fill data gaps in the existing guide. Furthermore, the reagent selection guide was enhanced, including the development of original reagent guides and the expansion of guides donated by member companies. These guides provide background on important transformations in the pharmaceutical industry, and evaluate potential reagents based on greenness, wide utility, and scalability.


Finally, in efforts to build and contribute to education resource, as well as collaborate globally, the Roundtable continued collaborations with the IQ Working Group to create training sessions in green chemistry for industrial chemists. The group also explored collaboration opportunities with IMI CHEM21 on an education and training work plan for students, industrial scientists and engineers, and other stakeholders. Another highlight was continuing a collaboration with a previous grant winner. Professor Neil Garg, as part of an extension of his 2012 Roundtable grant, published a manuscript on greener methodologies for Suzuki couplings in ACS Catalysis and an article highlighting the related undergraduate lab experiment in J. Chem. Ed. The Roundtable organized and chaired six sessions at the 18th Green Chemistry & Engineering Conference. The in-person meetings were held in Paris, France (hosted by Sanofi), Bethesda, MD (hosted by ACS GCI), and Rahway, NJ (hosted by Merck & Co., Inc.). All meetings were also web-based to assure global participation.


Roundtables at GC&E


Once again, in addition to hosting their in-person meetings and organizing technical sessions, all four roundtables sponsored and organized a poster reception in conjunction with the Annual Green Chemistry and Engineering Conference. In its fourth year, the ACS GCI Roundtable Poster Reception was a highly focused networking event with posters featuring a wide range of industrially relevant green chemistry work presented by industry professionals, professors, and students. Attendees consistently praise the reception as being “an excellent venue for interacting with individuals from all phases of the chemical supply chain” and to meet other professionals doing similar work. In each of the past four years the event has been held, over 72% of attendees have indicated they learned about a greener technology of potential relevance to their organization. Sponsors for the event were Florida Chemical Company, Inc. of Flotek, ILSI Health and Environmental Sciences Institute (HESI), and Launch.



“The Nexus Blog” is a sister publication of “The Nexus” newsletter. To sign up for the newsletter, please email, or if you have an ACS ID, login to your email preferences and select “The Nexus” to subscribe.


To read other posts, go to Green Chemistry: The Nexus Blog home.

In the early 2000s, the director of the ACS Green Chemistry Institute®, Dr. Paul Anastas, initiated a discussion with the Dr. Berkeley “Buzz” Cue, a leader in green chemistry at Pfizer, about the possibility of starting a collaborative group that would work to catalyze the broader adoption of green chemistry and engineering in the pharmaceutical industry. These discussions turned into meetings, and in 2005 the ACS GCI Pharmaceutical Roundtable was established.


Ten years later the Roundtable looks back at an impressive set of accomplishments, and the roundtable concept has led to the establishment of three other ACS GCI roundtables—Formulators’ in 2007, Chemical Manufacturer’s in 2009 and Hydraulic Fracturing in 2014.



Click on the infographic to see it in full size


"Since its creation in 2005, the ACS GCI Pharmaceutical Roundtable has been driving the development of innovative ‘green’ approaches to address some of the most important sustainability challenges in the manufacturing of pharmaceuticals," says Dr. Juan Colberg, Technology & Innovation, Pharmaceutical Sciences, Worldwide Research and Development, Pfizer and Co-Chair of the ACS GCI Pharmaceutical Roundtable.  "Over the last 10 years and through the Roundtable’s grant program, we have been able to make significant advancements such as greener solvent alternatives, less toxic catalytic conditions and biocatalytic transformations."


Some of the key accomplishments of the Roundtable include the development of a common solvent selection guide; a process mass intensity calculator and reagent guide; publication of an article outlining key research areas that has been cited 347 times and helped set the agenda for the Roundtable’s grant program (look for an update article later this year); $1.58 million dollars in grants awarded; and numerous publications, presentations and symposia.


"As we look ahead with our collaboration, the Roundtable will continue to sponsor exciting research and development in green alternatives," continues Colberg. "By working together, we can help develop processes that are more sustainable, environmentally sound and cost-effective."



This year, the Roundtable will be holding three events in honor of its anniversary:


Green Chemistry Makes a Difference: Innovations Leading to a More Sustainable Pharmaceutical Industry

The call for posters is open through February 28th for this one-day symposium to be held April 16, 2015, at F. Hoffmann-La Roche in Basel, Switzerland. Registration is free and limited, so if you are interested in attending, please register soon!


19th Annual Green Chemistry & Engineering Conference

The Roundtable is putting together a day-long symposium on green chemistry accomplishments in the pharmaceutical industry over the last 10 years and challenges on the horizon in North Bethesda, Maryland, July 14-16, 2015. Additionally, many other sessions of relevance to the industry will be featured. The call for papers remains open for these sessions through March 13, 2015.


Green Chemistry Makes a Difference: Pharmaceutical Industry/Academic Collaborations

The Roundtable will organize two sessions covering green chemistry organic chemistry topics at the 250th ACS National Meeting & Exposition in Boston during August 16-20, 2015.


Congratulations to the Roundtable! Current members include Amgen; AstraZeneca; Boehringer-Ingelheim Pharmaceuticals, Inc.; Bristol-Myers Squibb; Cubist Pharmaceuticals; Codexis; Dr. Reddy’s Laboratories Ltd.; Eli Lilly and Company; F. Hoffman-La Roche Ltd.; GlaxoSmithKline; Johnson & Johnson; Merck & Co., Inc.; Novartis; Pfizer Inc.; Sanofi and ACS GCI.


Find out more at



“The Nexus Blog” is a sister publication of “The Nexus” newsletter. To sign up for the newsletter, please email, or if you have an ACS ID, login to your email preferences and select “The Nexus” to subscribe.


To read other posts, go to Green Chemistry: The Nexus Blog home.

This month we have dedicated The Nexus to green chemistry and public health, and at the nexus of these issues is the pharmaceutical industry and their innovation processes. As an industry dedicated to developing products that can save people’s lives, typically the primary priority in the innovation process has been ensuring that the drug works rather than guaranteeing that the synthesis will lead to the most efficient or safest possible manufacturing process. Therefore what often goes unrecognized in the drug discovery phase is that huge amounts of waste can be generated in pharmaceutical production processes, and that waste (including volatile organic solvents) can be toxic or difficult to manage. With nearly 25-100 kg of waste being produced for each kilogram of drug in a pharmaceutical plant’s optimized process (a metric known as process mass intensity), there is much room to reduce the impact of the manufacturing process on public health and the environment.


Greener chemistry and engineering is an upstream approach to addressing waste, pollution, and resource issues through toxicity reduction, biodegradability, energy efficiency, and more. For 20 years, the U.S. Environmental Protection Agency (EPA) has sponsored the Presidential Green Chemistry Challenge Awards (PGCCA), in partnership with the American Chemical Society, and it is the premier recognition for sustainable innovation in chemistry. Five awards are given every year to highlight greener groundbreaking science in the chemical enterprise. Winners are chosen if their developments reduce waste, improve efficiency, are commercially viable, and are equally or more cost effective. Over the past two decades the pharmaceutical science has been one of the more active sectors in this sphere, having received 11 awards thus far.


At the time of the inception of the award some companies were beginning to green their pharmaceutical processes, but there was no comprehensive strategy across the industry to understand their relative waste footprint or incorporate greener practices. Most improvements were driven by Manufacturing or Environmental Health & Safety departments, rather than Research & Development. While there many instances of more sustainable processes prior to the mid-1990s, one of the most widely cited examples of greener chemistry is the first pharmaceutical PGCCA recipient in 1997—BHC Company (now BASF Corporation) and their virtually waste free synthesis of Ibuprofen (an active ingredient in many over-the-counter pain relievers). The original process required six stoichiometric steps and wasted more than half of the material introduced in the process. The greener innovation generated the same active ingredient but required only three catalytic steps, doubled the utilization of the inputs, and introduced a byproduct recovery step.


By 2005, after 10 years of the PGCCA, four more awards had been given in the pharmaceutical industry. Lilly Research Laboratories (1999) eliminated huge amounts of chromium and solvent waste from an epilepsy drug process, and in 2000 Roche Colorado Corporation (now CordenPharma Colorado) removed two hazardous waste streams and 11 materials from their process for an antiviral agent (Cytovene) for immune-compromised patients (including those with AIDS). Pfizer (2002) transformed their process for the active ingredient in Zoloft (a depression treatment) that dramatically reduced waste and solvent use, and doubled their yield, and Bristol-Myers Squibb (2004) created an alternative synthetic approach to Paclitaxel (active ingredient in the cancer drug, Taxol) so that it no longer needed to be harvested from the ecologically sensitive Pacific yew tree.


Beyond the awards, green chemistry activity was continuing to build in the industry. Pfizer had developed an in-house and cross-departmental green chemistry program and this model began to be replicated by other major players in the industry. Furthermore, it was at this time that the ACS Green Chemistry Institute founded the Pharmaceutical Roundtable. Eli Lilly, Merck & Co., Inc., and Pfizer were the initial members and the mission of the group was to catalyze the implementation of green chemistry and engineering in the global pharmaceutical industry. They came together to identify critical challenges faced by the industry and created strategic priorities to address them (informing and influencing the research agenda, creating tools for innovation, engaging as an education resource and collaborating globally).


Now, after 20 years of PGCCA, most major pharmaceutical companies are adopting green chemistry in some fashion and are incorporating greener practices in their drug discovery stage so that their processes are safer and the final products can be scaled more efficiently.  The ACS GCI Pharmaceutical Roundtable has 15 members (and growing), and these are the companies that are dominating the PGCCA. Three more industrial pharmaceutical awards have been given; two exclusively to Merck & Co., Inc. (in 2005 and 2006), one to Codexis, Inc. (2006), and one to both companies for a collaborative innovation (2010)—both companies are Roundtable members. As academic-industrial partnerships became even more of a goal in the industry, we have started to see notable academic developments with commercial potential. In 2012, Codexis, Inc. collaborated with Professor Yi Tang from University of California, Los Angeles to create a single-step biocatalytic process to synthesize simvastatin (a cholesterol drug). And just last year, Professor Shannon Stahl of the University of Wisconsin-Madison won for his aerobic oxidation developments for pharmaceutical synthesis, which utilize oxygen from air to oxidize through a new catalytic, mild condition, and highly selective method (replacing the need for hazardous inputs such as chlorinated solvents).


There has been dramatic growth in green innovation in the pharmaceutical industry, and from discovery to scale, it is clear to see that the chemistry done at every phase of drug development has huge implications for public health and the sustainability of the industry. There have been many successes and increased adoption throughout all aspects of companies’ processes, but there are still huge gains to be made. Improvements to process mass intensity are still needed, the dominance of batch processes over flow chemistry holds strong, and the inclusion of generic companies in this green paradigm has yet to fully blossom. There are some companies who are starting to work with suppliers to integrate green chemistry throughout their supply chain, but it is not yet the norm. Outsourcing of the drug discovery phase is growing in the industry, so increasingly a company strategy focused on green and sustainable innovation is needed, as well as continued partnerships with academia to further the research agenda. With these needs, we can surely expect the continuation of green developments in the pharmaceutical industry and we can count on the PGCCA to keep recognizing the top innovators who can deliver on these needs—keep an eye out this summer, when the 2015 PGCCA awards are announced in July to see the next wave of innovation and learn how their science can change the world.




“The Nexus Blog” is a sister publication of “The Nexus” newsletter. To sign up for the newsletter, please email, or if you have an ACS ID, login to your email preferences and select “The Nexus” to subscribe.


To read other posts, go to Green Chemistry: The Nexus Blog home.

Contributed by David Constable, Director, ACS Green Chemistry Institute®


In late January I had the opportunity to attend the LAUNCH forum. In case you are not familiar with LAUNCH, you can find out more about it here.  This year the LAUNCH partners developed a green chemistry challenge and through a well-established process identified 10 innovators to participate in this year’s forum. These 10 innovators started by making a pitch to the LAUNCH council members in attendance and then rotated from group to group to solicit feedback. The purpose of bringing the innovators and the council together was to provide the innovators with connections to people and potential resources that might assist with moving their business forward. It’s really a simple process when you break it down, and it provides a great opportunity for innovators to extend their reach in a short period of time.


Being a part of the entire process brought home, once again, the difficulty in moving an innovation from proof of concept to commercialization. It seems to me that many think that when an innovation is “green,” it’s harder to move that kind of innovation forward than it is to move a “normal” innovation into the marketplace. Conversely, there are some who believe that because an innovation is “green,” it should enjoy either a price premium, or it will somehow be more attractive to investors, banks, etc. The reality is that any innovation in the chemical and allied industries is difficult to commercialize, and one should never bank on a price premium for something they think is greener or more sustainable than an existing product. Markets are markets and they’re pretty unforgiving. And while game-changing innovations are more likely to make it, there are no guarantees that they will.


I can’t highlight all the innovations that were presented but I thought I would highlight a few that I think are worth watching.  First is Grow Plastics, a relatively simple innovation that lightweights a plastic item such as a cup, bowl, plate, a meat tray, etc., while still providing higher performance at a competitive cost to a plastic such as styrofoam.   The fact that Grow Plastics uses PLA and no plasticizers is a definite “green” advantage, but what will capture the market is price and performance.  Establishing and growing the market in the Northwest U.S. makes a lot of sense given moves to ban styrofoam.


Next is Bioamber, a company that is looking to produce succinic acid through sugar fermentation utilizing a modified yeast. Some might argue that yeast is a better platform than what close competitor Myriant uses, but both companies face an uphill battle in getting chemists to begin using succinic acid to create new chemicals and polymers. They also need to demonstrate that they have a reliable supply chain and can supply the volumes at the desired quality. The interesting thing is that despite examples of higher performance or the development of a more desirable property (hardness, durability, softness, etc.) of new molecules utilizing succinic acid both companies still face the uphill battle of displacing an existing product and supply chain that is tried, tested and has customer approval.


Next there is Ancatt, a potentially disruptive anti-corrosion technology that doesn’t use Cr or Zn. Ancatt was an ACS GCI Business Competition winner in June of 2012 and their technology has all the appearances of being a winner. The challenge here is for the company to find a trusted partner to help move this from limited concept demonstrations to widespread commercial use. It is challenging for any innovator to move from the laboratory to pilot and full-scale production, and in an entrenched industry like the painting and coatings industry, there isn’t a simple or clear path. Like many other technologies, breaking into a low-margin commodity business is extraordinarily challenging, no matter how disruptive the technology.


Finally, there is Mango Materials, a company that is looking to make a biodegradable plastic, PHA, from waste methane at wastewater treatment plants. There are a variety of issues with moving this from demonstration to scale, but it appears that Mango Materials is making good progress. It is exciting to see waste methane that is generally not being well utilized at the moment and converting it into a plastic that is biodegradable without the higher temperature composting requirements of PLA.  PHA still has a number of uphill battles as a plastic, but Mango Materials appears to have identified a commercial use that represents a great starting place for establishing a market and a steady cash stream that they can build on and diversify into other markets. If they manage to sort out the pilot plant funding, I think we can expect great things from them in the future.


It is always great to see innovations and innovators who are making inroads towards implementing green chemistry and engineering in business. I remain optimistic that these companies will make great progress and have a very positive impact on the world. I hope to see this trend accelerate.


As always, please do let me know what you think.






“The Nexus Blog” is a sister publication of “The Nexus” newsletter. To sign up for the newsletter, please email, or if you have an ACS ID, login to your email preferences and select “The Nexus” to subscribe.


To read other posts, go to Green Chemistry: The Nexus Blog home.

Contributed by Marie Bourgeois PhD, MPH Research Assistant Professor Center for Environmental/Occupational, Risk Analysis and Management Department of Environmental and Occupational Health, University of South Florida College of Public Health


For decades, the development of new chemicals has outpaced our ability to adequately assess risks potentially posed by exposure. Permissible Exposure Limits (PELs), set by OSHA to protect the health of America’s workforce, are a great example of the existing backlog. Fewer than 600 PELs have been established for common industrial chemicals. However, the Chemical and Product Categories database (CPCat) has catalogued over 40,000 chemicals currently used in different consumer products. While every effort is made to assure the safety of these chemicals, toxicity information is limited or absent for the majority of these compounds. Traditional testing methods are time consuming, expensive, heavily reliant on laboratory animals and frequently limited in scope. Stakeholders all agreed it was time for a new approach.


In 2007, the National Academies published ‘Toxicity Testing in the 21st Century’. This report highlighted the shortcomings of traditional testing methods, advocating a shift from whole animal based testing, to ‘toxicity pathway’ cellular and tissue based testing. It also stressed the utility of dose-response extrapolation of cellular response to toxicants to potential adverse effects in human systems. Report authors recommended continued use of real world data including biomonitoring results from projects such as NHANES. Perhaps most importantly, the report described an adaptive approach to risk assessment that stressed placing risk in context; some risks require rapid testing results from a single environmental agent while others may need a multitude of chemicals screened. Restricting testing to the most hazardous compounds is an economical approach to minimize adverse human health effects. The effort to modernize testing required the development of new tools.


ToxCast and similar tools provide methods of predictive toxicology suitable for the 21st century. ToxCast, or Toxicity Forecasting, is part of the US Environmental Protection Agency’s National Center for Computational Toxicology (EPA/NCCT) Research initiative to generate bioactivity profiles for chemicals posing the greatest risk to human health. ToxCast uses multiple in vitro assays to predict in vivo effects. Phase I profiled 320 chemicals as a ‘Proof of Concept’ in 2009. These chemicals were chosen because decades of existing data in the literature permitted validation via one to one comparison. Well correlated experimental results derived from the approximately 500 in vitro assays and 75 in vivo endpoints demonstrated the reliability of the ToxCast methodology. Phase II examined 2000 chemicals from categories including food additives, ‘green alternatives’ to existing industrial chemicals, nanomaterials and consumer products that were never released. The testing utilized 700 high throughput screening (HTS) assays running the gamut of cellular responses and signaling pathways.


ToxCast chemical data is publicly available via Interactive Chemical Safety for Sustainability Dashboards (iCSS). Other CompTox tools and resources include ACToR (Aggregated Computational Toxicology Resource), ToxRefDB (Toxicity Reference Database), DSSTox (Distributed Structure- Searchable Toxicity Database), ExpoCast (Exposure Forecaster) and Virtual Tissues. These tools provide searchable toxicity testing results, access to thirty years of animal studies, structural information, exposure predictions and virtual tissue models that map existing research to computer simulations of expected effects using an adverse outcome pathway approach. ToxCast data also becomes part of Tox21.


Tox21, as the collaboration between the EPA, National Institute of Environmental Health Sciences (NIEHS)/National Toxicology Program (NTP), National Center for Advancing Translational Sciences (NCATS)/NIH Chemical Genomics Center (NCGC) and the U.S. Food and Drug Administration (FDA) became known, utilizes robotic technology to conduct HTS of chemicals of interest.  HTS shortens test times required for data generation by covering a large range of test concentrations using 1536 well microtiter plates. Tox21 currently screens approximately 10,000 chemicals using biochemical and cellular HTS assays.


The overall goals of ToxCast/Tox21 include creating and screening a large library of chemicals, the creation of HTS assays for pathways, linkage of HTS results to adverse human health effects and identification of toxicity pathways. ToxCast/Tox21 runs multiple assays per target and multiple targets per pathway to develop a prioritization index (ToxPi) for each chemical.


     ToxPi = f(HTS assays + Chemical properties + Pathways)


In the future, additional information on exposure, chemical properties or QSAR models may also be incorporated.


     ToxPi = f(Exposure + Chemical properties + In vitro assays + Pathways)


The EPA formed partnerships with academic, industrial and governmental agencies to revolutionize toxicity and risk assessment. ToxCast data is currently being used by screening programs in Endocrine Disruption, Toxic Substances Control Act and Safe Drinking Water Act to prioritize chemical testing and set contaminant candidate lists.


So what does this mean to the average public health toxicologist? A risk assessment typically proceeds in 4 steps: hazard identification, generation of dose-response data, exposure assessment and risk characterization. Simply put, ToxCast/Tox21 moves the starting line up. A toxicologist looking for information on a priority chemical can begin with any one of these databases. They might check to see if a priority index had been established for their chemical(s) of interest. They could check Tox21, ToxRefDB, ToxExpo and iCSS for previously run in vivo studies and exposure assessments. A toxicologist could even use the virtual tissue models to predict adverse outcomes. This information may not obviate the use of research animals but it should lead to more informed experimental designs. Armed with this data, toxicologists everywhere will be better prepared to design a study that answers their objectives.


For more information:






CSS Dashboards:

CompTox Tools:

Chemical Safety for Sustainability Research Program:



Virtual Liver:

Virtual Embryo:

ToxCast and Tox21: High Throughput Screening for Hazard & Risk of Environmental Chemicals:




Dix et al (2006) “The ToxCast Program for Prioritizing Toxicity Testing of Environmental Chemicals.” Toxicological Sciences.


Judson et al. (2010) “Analysis of Eight Oil Spill Dispersants Using Rapid, In Vitro Tests for Endocrine and Other Biological Activity" Environmental Science and Technology.


Reif et al. (2010) “Endocrine Profiling and Prioritization of Environmental Chemicals Using ToxCast Data.” Environmental Health Perspectives.


Rotroff et al (2010) “Incorporating Human Dosimetry and Exposure into High Throughput In Vitro Toxicity.” Toxicological Sciences.




“The Nexus Blog” is a sister publication of “The Nexus” newsletter. To sign up for the newsletter, please email, or if you have an ACS ID, login to your email preferences and select “The Nexus” to subscribe.


To read other posts, go to Green Chemistry: The Nexus Blog home.

By Eric J. Beckman, Bevier Professor Engineering, Department of Chemical Engineering, University of Pittsburgh; Co-Director, Mascaro Center for Sustainable Innovation; Co-founder, Cohera Medical Inc.


On February 4 of this year, the U.S. Food and Drug Administration approved TissuGlu, the primary product being developed by Cohera Medical Inc., as the first internal tissue adhesive authorized for use in the United States. The approval this year is the culmination of over eight years of laboratory and clinical developments by the company that Michael Buckley (oral and maxillofacial surgeon) and I spun out of the University of Pittsburgh in late 2005. I myself spent three years working full-time on TissuGlu’s development during an entrepreneurial leave from the University (2007-2009) and hence played an active role in the rollercoaster ride that working at a startup involves.


The technology that became TissuGlu was a somewhat serendipitous development, in that Dr. Buckley and I were researching an entirely different project; it was Michael who noted that surgeons (at that time) did not possess an approved adhesive for use internally that was both strong and safe – it was the identification of this business opportunity that led us to postpone the initial project (as it runs out forever) and devote full time to creation of an adhesive.


TissuGlu is designed to adhere flaps of tissue (such as created during abdominoplasty) to reduce fluid accumulation and in many cases eliminate the need for post-operative drains. The adhesive is applied dropwise during surgery using a single-use applicator, cures in approximately 30 minutes, and then resorbs slowly into benign fragments as the patient heals.


Needless to say, successfully creating anything molecular that is designed to be used inside the human body means that safety of the ingredients, the cured product, and the degradation fragments is paramount. TissuGlu is a urethane prepolymer adhesive; a urethane system was chosen because it can be employed as a single-part product (no mixing or other preparation in the clinical setting), cures through contact with moisture, and can covalently bond to functional groups commonly found at tissue surfaces (allowing for good adherence). Urethanes are potentially valuable as biomaterials because their structure allows for a reasonably confident prediction as to how they will hydrolyze.


Industrial and consumer urethane adhesives often employ aromatic isocyanates as building blocks; the known tendency of these to revert to aromatic diamines during degradation precludes their use in a surgical adhesive, and hence we chose the ethyl ester of lysine di-isocyanate to construct TissuGlu; because this material was not readily available commercially, the company developed a scalable manufacturing process in parallel to product development and clinical work.


Typically, urethane prepolymers are synthesized in the presence of a metal catalyst (often tin, but other metals such as zirconium can be used) – these are all cytotoxic to varying degrees and hence the manufacturing of the product proceeds in the absence of catalyst – a slower process but a safer product.


In addition to safety, the product design had to meet certain other criteria to render it attractive to surgeons and patients alike. The adhesive should cure relatively quickly (minutes) yet not too quickly to allow surgeons time to re-approximate tissue if needed. The viscosity of the material should be sufficiently low that it could be delivered from the applicator easily, yet if it were too thin it could “run” on tissue surfaces that are often anything but horizontal. The latter is a classic example of a potential design trade-off; if we add a diluent to reduce viscosity (a plus), the presence of the diluent could make the glue too runny and also slow cure time (owing to simple dilution). Our solution was a volatile diluent (non-toxic, non-flammable) that evaporated quickly upon contact with the 37C tissue.


Design of the applicator, though not a “chemical” issue, was a crucial part of the design, partly because competing products (many of which were two-part) employed relatively clumsy devices that required significant training and clogged readily. While a reusable applicator might have been desirable from a green perspective, potentially serious safety issues surrounding the collection, reconditioning, resterilization, and reuse of the device prompted the company to opt for single-use. In the end, the applicator resembles a glue gun; its ergonomic design allows clinicians to learn to use the product in minutes. Preparation in the operating room requires simply opening the package and flipping a single switch from red to green.


TissuGlu passed all of the preclinical testing required by the European Union and demonstrated safety in a 40-patient human clinical trial in Germany in 2009-2010. This led to E.U. approval in 2011 (the CE Mark); TissuGlu has since been used in over 1500 patients without any device-related safety issues. Approval in the U.S. required an additional series of preclinical tests (including carcinogenicity) that again demonstrated the product’s safety. Following two clinical trials in the U.S., the FDA General and Plastic Surgery Devices Panel of the Medical Devices Advisory Committee voted on August 1, 2014 to recommend TissuGlu for eventual approval; after discussions on indication, labeling, and patient brochure, the product received its approval.




“The Nexus Blog” is a sister publication of “The Nexus” newsletter. To sign up for the newsletter, please email, or if you have an ACS ID, login to your email preferences and select “The Nexus” to subscribe.


To read other posts, go to Green Chemistry: The Nexus Blog home.

Contributed by Professor R. K. Sharma, University of Delhi, Honorary Secretary, Royal Society of Chemistry (London), North India Section Coordinator, Green Chemistry Network Centre


The 5th Asia-Oceania Conference, jointly organized by the Royal Society of Chemistry, London; North India Section, Green Chemistry Network Centre, New Delhi; and The Energy and Resources Institute, New Delhi, formally began on 15th January in a spectacular manner at India Habitat Centre, Lodhi Road, New Delhi.


This international event was fifth in a series of successful meetings on Green and Sustainable Chemistry. Since the onset of AOC-1 in Tokyo (2007), there has been a tradition of associating a broad theme to the entire conference each year namely-“Expansion” in Beijing AOC-2 (2009), “Innovations” in Melbourne AOC-3 (2011), “Opportunities” in Taiwan AOC-4 (2013). Continuing this custom, the theme for this year was decided as “Capabilities” with the motive to unveil the potentials of twelve green chemistry principles and to demonstrate the capabilities of green chemistry for a sustainable future.


The conference was focused to showcase the capabilities ‘Green and Sustainable Chemistry’ can offer to the world for harnessing the same product and services but through a greener route. It was categorized under four themes including: Green Chemistry and Health, Sustainability and Industrial Processes, Green Chemistry Education, and Advancing Global Green Chemistry: Collaborations among academia, government and industry.


Over 300 participants attended this three days conference which included an inaugural lecture by Prof. James Clark, a special session addressed by World Leaders of Green Chemistry, four Plenary Lectures, 12 Keynote Lectures, an opinion exchange between students, cultural program, 44 oral and 72 poster presentations. Academicians, experts from industries, research scholars, graduate and postdoctoral students from twelve countries across the globe participated and represented the different themes of green and sustainable chemistry. Persons from the media were also present to cover the entire event.


6.jpgThe special video conferencing session on the very first day, addressed by the world leaders of green chemistry, i.e. Prof. Paul T. Anastas, Director,Yale University’s Center for Green Chemistry and Green Engineering, USA; Dr. John C. Warner, President and Chief Technology Officer, Warner Babcock Institute for Green Chemistry, USA; Prof. James Clark, Director, Green Chemistry Centre of Excellence, University of York, UK; and Dr. David Constable, Director, American Chemical Society, Green Chemistry Institute (ACS GCI), USA, marked an exhilarating start to the conference.


Group Discussion and opinion exchange between students of JACI (Japan Association for Chemical Innovation) and University of Delhi took place during lunch on the 16th of January. The facilitators did an excellent job of engaging the students and making green chemistry and engineering relevant to their studies.


On day two and three, during the poster presentation session, the entire zone was packed with delegates eager to hear how young minds have utilized green and sustainable chemistry for the futuristic development. The much informative conference erupted into a spectacle of colour on day two with the Cultural Evening including music and performances, and the place was alive with sound, colour and excitement.


12.jpgThe highly motivating three-day event was filled with great amount of combined knowledge and experience culminated in generating several productive inputs for the future growth of green chemistry. With great pride the delegates came on to the stage to receive their momentos to a roaring round of applause and the experts declared the name of winners for "Young Scientist", oral presentation and poster presentation awards. To conclude the event, Prof. R. K. Sharma and Dr. Alok Adholeya, as conference chairs, presented the overview of the amazing conference and gave the highlights for the next conference (AOC-6 GSC) going to be held in Hong-Kong.


Attached are more pictures from the conference.



“The Nexus Blog” is a sister publication of “The Nexus” newsletter. To sign up for the newsletter, please email, or if you have an ACS ID, login to your email preferences and select “The Nexus” to subscribe.


To read other posts, go to Green Chemistry: The Nexus Blog home.

Recently we asked Dr. C.N. Sivaramakrishnan, a distinguished senior scientist from the Society of Dyes & Colorists in India to respond to some questions to give us a sense of the sustainability challenges and opportunities in the dyeing industry in India. The ACS GCI published Part One in January 2015 and below it Part Two.


Q: Is there a particular case study that you would highlight as a success story [of more sustainable dyeing in India]?


A: Arvind Mills is one of the largest integrated textile mills in India and popular for producing world renowned 'Denim' brand jeans. It supplies to almost all the famous jeans, trousers, and garments making units in the world. The unit is located at a distance of approximately 40 kms away from the city of Ahmadabad, Gujarat, India and has been set up on 385 acres of land.


The unit may be an example for end-of-pipe pollution abatement technology for achieving a zero discharge of liquid effluent. It is a fact that integrated textile mills are a water intensive industry. From that point, achieving zero discharge deserves special mention and appreciation. The only source of water here is ground water. Ahmadabad is a developing city, and like all other developing cities, rapid ground water depletion is an important environmental issue in the area. The State Pollution Control Board has restricted the extraction of the ground water. It is because of this compulsion as well as from their quest for making the product cost effective, the unit has adopted suitable measures to bring down the cost of utilities with the support from their research and development wing.


Zero discharge means the entire effluent that is being generated from the different unit operations in the process plants are recycled in the process. For this the unit has adopted a multi-prong approach ranging from the separation of raw effluent on the basis of pollution load to judicious mixing and blending, after primary treatment, with the other highly concentrated pollution load-bearing effluent at the appropriate level of the treatment procedure to the adoption of proper tertiary and polishing treatment technology for making the effluent suitable for reuse in the process without hampering the quality of the product.


Water consumption pattern: Major contributions of raw effluent are from the sizing & desizing, scouring, dyeing and bleaching, and mercerizing sections of the industry. Apart from these main unit operations, a substantial quantity of effluent is generated from the humidification section. Concentration of pollutants and quantity of effluent from these sections may vary depending upon the scale of production, chemicals used and technologies adopted. The following table may give an idea for raw water requirements in similar types of industries. Water loss is approximately 20 percent, mainly from the humidification section.


dyes chart.png


Considering that the unit produces 180 gsm of fabrics with the width of 140 – 150 cm (approximately 59 inches), water requirements come out to be approximately 24.3 litres kg of fabrics produced. The unit produces 5 million meters of fabric with different product mixes as per customer requirements. It generates 10 MLD of process effluent. The same can also be verified considering the average consumption of 24.3 litres per meter of different type of above mentioned product mix.



Flow rate of the effluent generation from different unit operations are given in the table

dyes chart2.png


Effluent characteristics and its treatment facility: Effluent characteristics of a textile unit depend on the type of fabrics being processed, the colors used, whether printing is done, on the chemicals used during mercerization, and the dye fixing process. Apart from the main processes, a substantial quantity, in fact a major quantity of effluent is generated from the washing carried out in between successive processes. For example, in the dye house, after dyeing activity, fixation of dye is one of the most important stages. Usually, 70-80% of fixation is practicable and the rest, i.e. 20% of the dye used, comes out in the effluent generated due to washing. Effluent generated from the dye house has a high concentration of pollutant as compared to other processes in the textile processing unit. It also contains a high amount of inorganic salts like sodium sulphate or sodium chloride, which is used for dye fixing and acts as an electrolyte.


Another important unit operation is mercerization. Mercerization imparts the shining characteristic to the fabric. Washing after mercerization generates typical effluent containing caustic solution and other impurities. In the case of fabrics, caustic is used, but in the case of polyester, sulphuric acid is used. Bleaching is done by peroxide method.


The unit has an elaborate effluent treatment plant consisting of judicious segregation of effluent stream on the basis of pollution load and mixing of the same at an appropriate stage. The treatment processes may be divided into three parts namely i) main treatment facility, ii) pre-treatment (prior to reverse osmosis) and iii) reverse osmosis.


Main treatment facility: Streams of effluent generated from the sizing & de-sizing, bleaching & mercerizing and humidification sections are subjected to physico-chemical processes, i.e. the effluent is collected in an equalization tank. After pH adjustment and addition of poly electrolytes (as coagulant), the effluent is sent to the clarifier for sedimentation.


Effluent from the dye house is collected separately in an equalization tank where pH is adjusted and a chemical is added in acidic medium (pH 5.5) to decolorize the effluent. The unit uses a chemical (brand name Micro plus) which is claimed to act as a color removal agent. This effluent is then mixed with the entire effluent from the mercerized, sizing & humidification sections. These effluents are then fed into the primary clarifier followed by a conventional biological system comprising of degradation of organic components by microorganisms followed by sedimentation in a clarifier and return of bio-mass to the aeration unit.


In the aeration unit, retention time is approximately 16 hrs, MLSS is kept at 2500 and DO level is maintained at 2.5 to 3.0.


Sludge generated from the biological treatment facilities are sent to a sludge drying bed and leachate is sent back to the aeration unit. Effluent is then sent to the primary or pre-treatment facility. The unit has a large storage tank capable of holding 10ML of treated effluent.


Pre-treatment facility: Pretreatment or primary treatment facilities are adopted before the effluent is subjected to reverse osmosis. This stage comprises of two unit operations in succession: turbocirculator followed by pressure sand filter. The turbo circulator is basically a flash mixer.


After main treatment facility, poly aluminum chloride, poly electrolyte are added in the effluent and are passed to turbo-circulator and then to the sand filter before being subjected to reverse osmosis. The unit has intermediate storage tank (capacity 2400 cu.m) for storage of the treated effluent.


Reverse Osmosis: After pre-treatment the effluent is sent to the reverse osmosis plant. Osmosis, as we know, is a natural process and is the tendency of two liquids of different concentrations separated by a semi-permeable membrane, to move from low to high concentrations for chemical potential equilibrium. But in reverse osmosis (RO), when high pressure is applied, liquid moves from high concentration to lower concentration. RO is a method that removes many types of large molecules and ions from solutions by applying pressure to the solution when it is on one side of a membrane. The result is that the impurities  are retained on the pressurized side of the membrane and the pure water is allowed to pass to the other side. The reject of the reverse osmosis plant is fed into the desalination plant (thermal). Backwash of the sand filter is fed into the main treatment facility.


Reject of the reverse osmosis plant is fed into the desalination plant (thermal). Backwash of the sand filter is fed into the main treatment facility.


Other salient features: In the textile industries there are certain processes which generate typical effluent that require special treatment since its recovery gives the cost benefit to the entrepreneur. One such treatment process is the caustic recovery plant.


The caustic recovery plant is a multiple effect evaporator followed by condenser. Recovered caustic is reused and water (effluent) is recycled. It saves approximately 30% of the raw material (caustic soda) cost even after considering the operating cost of the caustic recovery unit. Caustic requirement for this unit is approximately 10 MT/day on 25 % concentration basis. Out of the 10 MT of caustic, 0.5 % is retained by the fabric and the rest goes to the effluent.

Total cost of treating the effluent for the said unit is approximately Rs. 45/ cu.m. of effluent including RO plant cost.






“The Nexus Blog” is a sister publication of “The Nexus” newsletter. To sign up for the newsletter, please email, or if you have an ACS ID, login to your email preferences and select “The Nexus” to subscribe.


To read other posts, go to Green Chemistry: The Nexus Blog home.

Filter Blog

By date: By tag: